Item | Value |
---|---|
geneid | 55746 |
ensemblid | ENSG00000069248.12 |
hgncid | 18016 |
symbol | NUP133 |
name | nucleoporin 133 |
refseq_nuc | NM_018230.3 |
refseq_prot | NP_060700.2 |
ensembl_nuc | ENST00000261396.6 |
ensembl_prot | ENSP00000261396.3 |
mane_status | MANE Select |
chr | chr1 |
start | 229440259 |
end | 229508341 |
strand | - |
ver | v1.2 |
region | chr1:229440259-229508341 |
region5000 | chr1:229435259-229513341 |
regionname0 | NUP133_chr1_229440259_229508341 |
regionname5000 | NUP133_chr1_229435259_229513341 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 1156 | 163 | 30 | 33 | 69 | 9 | 21 | 51 | NUP133_chr1_229435259_229513341 | NUP133 | MFPAA others(1151): Show |
chr1 | 229435259 | 229513341 |
a0002 | 0/1 | 1156 | 49 | 13 | 12 | 18 | 2 | 3 | 13 | NUP133_chr1_229435259_229513341 | NUP133 | MFPAA others(1151): Show |
chr1 | 229435259 | 229513341 |
a0003 | 0/0 | 1156 | 35 | 31 | 2 | 1 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | MFPAA others(1151): Show |
chr1 | 229435259 | 229513341 |
a0004 | 0/0 | 1156 | 14 | 0 | 13 | 0 | 0 | 1 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | MFPAA others(1151): Show |
chr1 | 229435259 | 229513341 |
a0005 | 0/0 | 1156 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | MFPAA others(1151): Show |
chr1 | 229435259 | 229513341 |
a0006 | 0/0 | 1156 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | MFPAA others(1151): Show |
chr1 | 229435259 | 229513341 |
a0007 | 0/0 | 1156 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | MFPAA others(1151): Show |
chr1 | 229435259 | 229513341 |
a0008 | 0/0 | 1156 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | MFPAA others(1151): Show |
chr1 | 229435259 | 229513341 |
a0009 | 0/0 | 1156 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | MFPAA others(1151): Show |
chr1 | 229435259 | 229513341 |
a0010 | 0/0 | 1156 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | MFPAA others(1151): Show |
chr1 | 229435259 | 229513341 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 3468 | 155 | 28 | 32 | 67 | 8 | 19 | NUP133_chr1_229435259_229513341 | NUP133 | ATGTT others(3463): Show |
chr1 | 229435259 | 229513341 | ||
a0001c0007 | 0/0 | 3468 | 4 | 0 | 1 | 0 | 1 | 2 | NUP133_chr1_229435259_229513341 | NUP133 | ATGTT others(3463): Show |
chr1 | 229435259 | 229513341 | ||
a0001c0009 | 0/0 | 3468 | 2 | 2 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | ATGTT others(3463): Show |
chr1 | 229435259 | 229513341 | ||
a0001c0012 | 0/0 | 3468 | 2 | 0 | 0 | 2 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | ATGTT others(3463): Show |
chr1 | 229435259 | 229513341 | ||
a0002c0002 | 0/1 | 3468 | 36 | 1 | 11 | 18 | 2 | 3 | NUP133_chr1_229435259_229513341 | NUP133 | ATGTT others(3463): Show |
chr1 | 229435259 | 229513341 | ||
a0002c0005 | 0/0 | 3468 | 12 | 12 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | ATGTT others(3463): Show |
chr1 | 229435259 | 229513341 | ||
a0002c0015 | 0/0 | 3468 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | ATGTT others(3463): Show |
chr1 | 229435259 | 229513341 | ||
a0003c0003 | 0/0 | 3468 | 33 | 30 | 1 | 1 | 1 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | ATGTT others(3463): Show |
chr1 | 229435259 | 229513341 | ||
a0003c0011 | 0/0 | 3468 | 2 | 1 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | ATGTT others(3463): Show |
chr1 | 229435259 | 229513341 | ||
a0004c0004 | 0/0 | 3468 | 14 | 0 | 13 | 0 | 0 | 1 | NUP133_chr1_229435259_229513341 | NUP133 | ATGTT others(3463): Show |
chr1 | 229435259 | 229513341 | ||
a0005c0006 | 0/0 | 3468 | 8 | 8 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | ATGTT others(3463): Show |
chr1 | 229435259 | 229513341 | ||
a0006c0008 | 0/0 | 3468 | 2 | 2 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | ATGTT others(3463): Show |
chr1 | 229435259 | 229513341 | ||
a0007c0010 | 0/0 | 3468 | 2 | 0 | 0 | 0 | 0 | 2 | NUP133_chr1_229435259_229513341 | NUP133 | ATGTT others(3463): Show |
chr1 | 229435259 | 229513341 | ||
a0008c0013 | 0/0 | 3468 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | ATGTT others(3463): Show |
chr1 | 229435259 | 229513341 | ||
a0009c0014 | 0/0 | 3468 | 1 | 0 | 0 | 0 | 0 | 1 | NUP133_chr1_229435259_229513341 | NUP133 | ATGTT others(3463): Show |
chr1 | 229435259 | 229513341 | ||
a0010c0016 | 0/0 | 3468 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | ATGTT others(3463): Show |
chr1 | 229435259 | 229513341 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 5208 | 149 | 26 | 32 | 65 | 8 | 17 | NUP133_chr1_229435259_229513341 | NUP133 | CTCTT others(5203): Show |
chr1 | 229435259 | 229513341 |
a0001c0001t0004 | 0/0 | 5208 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | CTCTT others(5203): Show |
chr1 | 229435259 | 229513341 |
a0001c0001t0008 | 0/0 | 5208 | 2 | 0 | 0 | 0 | 0 | 2 | NUP133_chr1_229435259_229513341 | NUP133 | CTCTT others(5203): Show |
chr1 | 229435259 | 229513341 |
a0001c0001t0014 | 0/0 | 5208 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | CTCTT others(5203): Show |
chr1 | 229435259 | 229513341 |
a0001c0001t0015 | 0/0 | 5208 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | CTCTT others(5203): Show |
chr1 | 229435259 | 229513341 |
a0001c0001t0016 | 0/0 | 5208 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | CTCTT others(5203): Show |
chr1 | 229435259 | 229513341 |
a0001c0007t0001 | 0/0 | 5208 | 4 | 0 | 1 | 0 | 1 | 2 | NUP133_chr1_229435259_229513341 | NUP133 | CTCTT others(5203): Show |
chr1 | 229435259 | 229513341 |
a0001c0009t0001 | 0/0 | 5208 | 2 | 2 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | CTCTT others(5203): Show |
chr1 | 229435259 | 229513341 |
a0001c0012t0001 | 0/0 | 5208 | 2 | 0 | 0 | 2 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | CTCTT others(5203): Show |
chr1 | 229435259 | 229513341 |
a0002c0002t0001 | 0/0 | 5208 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | CTCTT others(5203): Show |
chr1 | 229435259 | 229513341 |
a0002c0002t0002 | 0/1 | 5208 | 31 | 0 | 10 | 16 | 2 | 2 | NUP133_chr1_229435259_229513341 | NUP133 | CTCTT others(5203): Show |
chr1 | 229435259 | 229513341 |
a0002c0002t0010 | 0/0 | 5208 | 2 | 0 | 0 | 1 | 0 | 1 | NUP133_chr1_229435259_229513341 | NUP133 | CTCTT others(5203): Show |
chr1 | 229435259 | 229513341 |
a0002c0002t0011 | 0/0 | 5208 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | CTCTT others(5203): Show |
chr1 | 229435259 | 229513341 |
a0002c0002t0012 | 0/0 | 5208 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | CTCTT others(5203): Show |
chr1 | 229435259 | 229513341 |
a0002c0005t0005 | 0/0 | 5208 | 12 | 12 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | CTCTT others(5203): Show |
chr1 | 229435259 | 229513341 |
a0002c0015t0005 | 0/0 | 5208 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | CTCTT others(5203): Show |
chr1 | 229435259 | 229513341 |
a0003c0003t0001 | 0/0 | 5208 | 3 | 3 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | CTCTT others(5203): Show |
chr1 | 229435259 | 229513341 |
a0003c0003t0002 | 0/0 | 5208 | 2 | 2 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | CTCTT others(5203): Show |
chr1 | 229435259 | 229513341 |
a0003c0003t0003 | 0/0 | 5208 | 2 | 2 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | CTCTT others(5203): Show |
chr1 | 229435259 | 229513341 |
a0003c0003t0004 | 0/0 | 5208 | 13 | 10 | 1 | 1 | 1 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | CTCTT others(5203): Show |
chr1 | 229435259 | 229513341 |
a0003c0003t0006 | 0/0 | 5209 | 8 | 8 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | CTCTT others(5204): Show |
chr1 | 229435259 | 229513341 |
a0003c0003t0007 | 0/0 | 5208 | 4 | 4 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | CTCTT others(5203): Show |
chr1 | 229435259 | 229513341 |
a0003c0003t0013 | 0/0 | 5208 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | CTCTT others(5203): Show |
chr1 | 229435259 | 229513341 |
a0003c0011t0009 | 0/0 | 5208 | 2 | 1 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | CTCTT others(5203): Show |
chr1 | 229435259 | 229513341 |
a0004c0004t0003 | 0/0 | 5208 | 14 | 0 | 13 | 0 | 0 | 1 | NUP133_chr1_229435259_229513341 | NUP133 | CTCTT others(5203): Show |
chr1 | 229435259 | 229513341 |
a0005c0006t0001 | 0/0 | 5208 | 7 | 7 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | CTCTT others(5203): Show |
chr1 | 229435259 | 229513341 |
a0005c0006t0017 | 0/0 | 5208 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | CTCTT others(5203): Show |
chr1 | 229435259 | 229513341 |
a0006c0008t0004 | 0/0 | 5208 | 2 | 2 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | CTCTT others(5203): Show |
chr1 | 229435259 | 229513341 |
a0007c0010t0001 | 0/0 | 5208 | 2 | 0 | 0 | 0 | 0 | 2 | NUP133_chr1_229435259_229513341 | NUP133 | CTCTT others(5203): Show |
chr1 | 229435259 | 229513341 |
a0008c0013t0003 | 0/0 | 5208 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | CTCTT others(5203): Show |
chr1 | 229435259 | 229513341 |
a0009c0014t0002 | 0/0 | 5208 | 1 | 0 | 0 | 0 | 0 | 1 | NUP133_chr1_229435259_229513341 | NUP133 | CTCTT others(5203): Show |
chr1 | 229435259 | 229513341 |
a0010c0016t0003 | 0/0 | 5208 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | CTCTT others(5203): Show |
chr1 | 229435259 | 229513341 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0056 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0008g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0008g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0014g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0015g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0001t0016g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0007t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0007t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0007t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0007t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0009t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0009t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0012t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0001c0012t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0002t0002g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0002t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0002t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0002t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0002t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0002t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0002t0002g0241 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0002t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0002t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0002t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0002t0010g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0002t0010g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0002t0011g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0002t0012g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0005t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0005t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0005t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0005t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0005t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0005t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0005t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0005t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0005t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0005t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0005t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0005t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0002c0015t0005g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0003c0003t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0003c0003t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0003c0003t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0003c0003t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0003c0003t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0003c0003t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0003c0003t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0003c0003t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0003c0003t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0003c0003t0004g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0003c0003t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0003c0003t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0003c0003t0004g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0003c0003t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0003c0003t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0003c0003t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0003c0003t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0003c0003t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0003c0003t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0003c0003t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0003c0003t0006g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0003c0003t0006g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0003c0003t0006g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0003c0003t0006g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0003c0003t0006g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0003c0003t0006g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0003c0003t0006g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0003c0003t0006g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0003c0003t0007g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0003c0003t0007g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0003c0003t0007g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0003c0003t0007g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0003c0003t0013g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0003c0011t0009g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0003c0011t0009g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0004c0004t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0004c0004t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0004c0004t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0004c0004t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0004c0004t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0004c0004t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0004c0004t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0004c0004t0003g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0004c0004t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0004c0004t0003g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0004c0004t0003g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0004c0004t0003g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0004c0004t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0004c0004t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0005c0006t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0005c0006t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0005c0006t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0005c0006t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0005c0006t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0005c0006t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0005c0006t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0005c0006t0017g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0006c0008t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0006c0008t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0007c0010t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0007c0010t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0008c0013t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0009c0014t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
a0010c0016t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0002 | g0244 | EUR | GBR | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG00099 | hp2 | a0001 | c0007 | t0001 | g0173 | EUR | GBR | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0211 | EUR | GBR | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG00140 | hp2 | a0002 | c0002 | t0002 | g0249 | EUR | GBR | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0142 | EUR | FIN | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0061 | EUR | FIN | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG00438 | hp2 | a0002 | c0002 | t0002 | g0236 | EAS | CHS | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG00733 | hp1 | a0002 | c0002 | t0002 | g0250 | AMR | PUR | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG00738 | hp2 | a0002 | c0002 | t0002 | g0214 | AMR | PUR | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG00741 | hp1 | a0002 | c0002 | t0002 | g0226 | AMR | PUR | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01071 | hp1 | a0002 | c0002 | t0002 | g0224 | AMR | PUR | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01074 | hp2 | a0002 | c0002 | t0002 | g0256 | AMR | PUR | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01106 | hp1 | a0002 | c0002 | t0002 | g0222 | AMR | PUR | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01106 | hp2 | a0003 | c0011 | t0009 | g0136 | AMR | PUR | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01167 | hp2 | a0004 | c0004 | t0003 | g0230 | AMR | PUR | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01168 | hp1 | a0002 | c0002 | t0002 | g0217 | AMR | PUR | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01243 | hp1 | a0003 | c0003 | t0004 | g0109 | AMR | PUR | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01243 | hp2 | a0001 | c0007 | t0001 | g0172 | AMR | PUR | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01256 | hp2 | a0002 | c0002 | t0002 | g0009 | AMR | CLM | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01258 | hp2 | a0002 | c0002 | t0002 | g0009 | AMR | CLM | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01261 | hp1 | a0004 | c0004 | t0003 | g0229 | AMR | CLM | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01261 | hp2 | a0002 | c0015 | t0005 | g0031 | AMR | CLM | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01358 | hp1 | a0002 | c0002 | t0011 | g0247 | AMR | CLM | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0135 | EUR | IBS | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0195 | EUR | IBS | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01516 | hp1 | a0003 | c0003 | t0004 | g0112 | EUR | IBS | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0194 | EUR | IBS | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01884 | hp1 | a0001 | c0009 | t0001 | g0208 | AFR | ACB | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01884 | hp2 | a0002 | c0005 | t0005 | g0032 | AFR | ACB | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01928 | hp1 | a0004 | c0004 | t0003 | g0257 | AMR | PEL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01934 | hp1 | a0004 | c0004 | t0003 | g0259 | AMR | PEL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01943 | hp2 | a0004 | c0004 | t0003 | g0225 | AMR | PEL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01952 | hp1 | a0004 | c0004 | t0003 | g0228 | AMR | PEL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01975 | hp1 | a0004 | c0004 | t0003 | g0220 | AMR | PEL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01978 | hp2 | a0004 | c0004 | t0003 | g0251 | AMR | PEL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01981 | hp1 | a0004 | c0004 | t0003 | g0216 | AMR | PEL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01993 | hp1 | a0004 | c0004 | t0003 | g0253 | AMR | PEL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02004 | hp1 | a0002 | c0002 | t0002 | g0246 | AMR | PEL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02004 | hp2 | a0004 | c0004 | t0003 | g0261 | AMR | PEL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02015 | hp2 | a0002 | c0002 | t0002 | g0245 | EAS | KHV | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02040 | hp2 | a0003 | c0003 | t0004 | g0111 | EAS | KHV | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02074 | hp2 | a0002 | c0002 | t0002 | g0218 | EAS | KHV | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02080 | hp1 | a0002 | c0002 | t0002 | g0238 | EAS | KHV | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02145 | hp1 | a0002 | c0005 | t0005 | g0029 | AFR | ACB | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CDX | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | CDX | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02257 | hp1 | a0003 | c0003 | t0006 | g0123 | AFR | ACB | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02258 | hp1 | a0003 | c0003 | t0006 | g0129 | AFR | ACB | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02280 | hp1 | a0003 | c0003 | t0004 | g0132 | AFR | ACB | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02300 | hp1 | a0004 | c0004 | t0003 | g0258 | AMR | PEL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02451 | hp1 | a0003 | c0011 | t0009 | g0137 | AFR | ACB | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02572 | hp1 | a0003 | c0003 | t0003 | g0134 | AFR | GWD | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02615 | hp2 | a0003 | c0003 | t0002 | g0116 | AFR | GWD | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02622 | hp1 | a0005 | c0006 | t0001 | g0015 | AFR | GWD | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02622 | hp2 | a0003 | c0003 | t0004 | g0106 | AFR | GWD | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02630 | hp1 | a0003 | c0003 | t0007 | g0263 | AFR | GWD | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02647 | hp1 | a0005 | c0006 | t0001 | g0018 | AFR | GWD | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02647 | hp2 | a0001 | c0009 | t0001 | g0011 | AFR | GWD | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02698 | hp1 | a0002 | c0002 | t0002 | g0243 | SAS | PJL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02717 | hp1 | a0003 | c0003 | t0004 | g0110 | AFR | GWD | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02717 | hp2 | a0001 | c0001 | t0004 | g0147 | AFR | GWD | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02723 | hp1 | a0003 | c0003 | t0006 | g0126 | AFR | GWD | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02735 | hp2 | a0004 | c0004 | t0003 | g0252 | SAS | PJL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02809 | hp1 | a0005 | c0006 | t0001 | g0017 | AFR | GWD | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02809 | hp2 | a0003 | c0003 | t0006 | g0127 | AFR | GWD | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02886 | hp1 | a0005 | c0006 | t0001 | g0012 | AFR | GWD | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02886 | hp2 | a0003 | c0003 | t0006 | g0128 | AFR | GWD | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02895 | hp1 | a0002 | c0005 | t0005 | g0022 | AFR | GWD | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02895 | hp2 | a0002 | c0002 | t0001 | g0242 | AFR | GWD | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02896 | hp2 | a0008 | c0013 | t0003 | g0013 | AFR | GWD | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02897 | hp2 | a0002 | c0005 | t0005 | g0035 | AFR | GWD | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02965 | hp2 | a0003 | c0003 | t0004 | g0120 | AFR | ESN | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02976 | hp1 | a0003 | c0003 | t0007 | g0265 | AFR | ESN | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG03041 | hp1 | a0003 | c0003 | t0007 | g0266 | AFR | GWD | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG03041 | hp2 | a0003 | c0003 | t0004 | g0118 | AFR | GWD | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG03098 | hp1 | a0005 | c0006 | t0001 | g0020 | AFR | MSL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG03098 | hp2 | a0003 | c0003 | t0004 | g0133 | AFR | MSL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG03130 | hp1 | a0003 | c0003 | t0001 | g0023 | AFR | ESN | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG03130 | hp2 | a0003 | c0003 | t0001 | g0050 | AFR | ESN | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG03139 | hp1 | a0003 | c0003 | t0006 | g0122 | AFR | ESN | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG03195 | hp1 | a0005 | c0006 | t0001 | g0014 | AFR | ESN | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG03225 | hp1 | a0003 | c0003 | t0003 | g0113 | AFR | MSL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG03225 | hp2 | a0003 | c0003 | t0006 | g0124 | AFR | MSL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG03453 | hp2 | a0003 | c0003 | t0013 | g0267 | AFR | MSL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG03486 | hp1 | a0006 | c0008 | t0004 | g0024 | AFR | MSL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG03486 | hp2 | a0003 | c0003 | t0007 | g0264 | AFR | MSL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG03491 | hp1 | a0007 | c0010 | t0001 | g0206 | SAS | PJL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG03491 | hp2 | a0001 | c0001 | t0008 | g0105 | SAS | PJL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG03492 | hp1 | a0007 | c0010 | t0001 | g0207 | SAS | PJL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG03492 | hp2 | a0001 | c0001 | t0008 | g0164 | SAS | PJL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG03516 | hp1 | a0002 | c0005 | t0005 | g0036 | AFR | ESN | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG03516 | hp2 | a0003 | c0003 | t0004 | g0108 | AFR | ESN | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG03540 | hp2 | a0005 | c0006 | t0017 | g0019 | AFR | GWD | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG03579 | hp1 | a0003 | c0003 | t0004 | g0121 | AFR | MSL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG03579 | hp2 | a0002 | c0005 | t0005 | g0027 | AFR | MSL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG03669 | hp2 | a0009 | c0014 | t0002 | g0248 | SAS | PJL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG03710 | hp1 | a0002 | c0002 | t0010 | g0232 | SAS | PJL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG03927 | hp1 | a0001 | c0007 | t0001 | g0171 | SAS | BEB | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | BEB | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG03942 | hp2 | a0002 | c0002 | t0002 | g0219 | SAS | BEB | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | STU | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | STU | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | BEB | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG04184 | hp2 | a0001 | c0007 | t0001 | g0157 | SAS | BEB | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | STU | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | STU | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | YRI | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA18522 | hp2 | a0003 | c0003 | t0002 | g0117 | AFR | YRI | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA18747 | hp1 | a0002 | c0002 | t0010 | g0223 | EAS | CHB | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | CHB | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA18906 | hp1 | a0003 | c0003 | t0006 | g0125 | AFR | YRI | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA18906 | hp2 | a0001 | c0001 | t0014 | g0039 | AFR | YRI | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA18954 | hp1 | a0002 | c0002 | t0002 | g0255 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA18957 | hp2 | a0001 | c0012 | t0001 | g0076 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA18967 | hp2 | a0002 | c0002 | t0002 | g0233 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA18968 | hp1 | a0002 | c0002 | t0002 | g0239 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA18968 | hp2 | a0001 | c0012 | t0001 | g0075 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA18977 | hp2 | a0002 | c0002 | t0002 | g0221 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA18980 | hp1 | a0001 | c0001 | t0016 | g0038 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA18980 | hp2 | a0002 | c0002 | t0002 | g0234 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA18983 | hp2 | a0001 | c0001 | t0015 | g0183 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA18989 | hp2 | a0002 | c0002 | t0002 | g0237 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA18998 | hp1 | a0002 | c0002 | t0012 | g0231 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | LWK | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA19030 | hp2 | a0002 | c0005 | t0005 | g0025 | AFR | LWK | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA19043 | hp1 | a0002 | c0005 | t0005 | g0030 | AFR | LWK | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA19043 | hp2 | a0002 | c0005 | t0005 | g0026 | AFR | LWK | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA19054 | hp1 | a0002 | c0002 | t0002 | g0254 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA19060 | hp1 | a0002 | c0002 | t0002 | g0235 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA19079 | hp2 | a0002 | c0002 | t0002 | g0240 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA19082 | hp2 | a0002 | c0002 | t0002 | g0262 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA19085 | hp2 | a0002 | c0002 | t0002 | g0227 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA19087 | hp1 | a0002 | c0002 | t0002 | g0215 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA19240 | hp1 | a0003 | c0003 | t0004 | g0119 | AFR | YRI | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA19240 | hp2 | a0002 | c0005 | t0005 | g0028 | AFR | YRI | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA20129 | hp1 | a0002 | c0005 | t0005 | g0034 | AFR | ASW | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA20129 | hp2 | a0003 | c0003 | t0004 | g0115 | AFR | ASW | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0199 | EUR | TSI | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | GIH | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | GIH | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG01123 | hp2 | a0004 | c0004 | t0003 | g0260 | AMR | CLM | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02109 | hp1 | a0003 | c0003 | t0001 | g0209 | AFR | ACB | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG06807 | hp1 | a0005 | c0006 | t0001 | g0016 | AFR | USA | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
HG06807 | hp2 | a0002 | c0005 | t0005 | g0033 | AFR | USA | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | USA | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA20300 | hp2 | a0010 | c0016 | t0003 | g0114 | AFR | USA | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | LWK | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
NA21309 | hp2 | a0006 | c0008 | t0004 | g0021 | AFR | LWK | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
homoSapiens | chm13v2 | a0002 | c0002 | t0002 | g0241 | REF | REF | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0056 | REF | REF | NUP133_chr1_229435259_229513341 | NUP133 | chr1 | 229435259 | 229513341 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:229458256 | C | T | 3 | a0004 a0008 a0010 |
16 | HG01123.hp2 HG01167.hp2 HG01261.hp1 others(13): Show |
missense_variant | MODERATE | c.2885G>A | p.Arg962His | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/26 | 2977/5208 | 2885/3471 | 962/1156 | chr1 | 229458256 | |||
chr1:229470657 | C | T | 1 | a0007 | 2 | HG03491.hp1 HG03492.hp1 |
missense_variant | MODERATE | c.1999G>A | p.Ala667Thr | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 15/26 | 2091/5208 | 1999/3471 | 667/1156 | chr1 | 229470657 | |||
chr1:229486489 | G | A | 1 | a0006 | 2 | HG03486.hp1 NA21309.hp2 |
missense_variant | MODERATE | c.1382C>T | p.Pro461Leu | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 11/26 | 1474/5208 | 1382/3471 | 461/1156 | chr1 | 229486489 | |||
chr1:229487591 | T | C | 8 | a0002 a0003 a0004 others(5): Show |
110 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(107): Show |
missense_variant | MODERATE | c.1217A>G | p.Gln406Arg | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 10/26 | 1309/5208 | 1217/3471 | 406/1156 | chr1 | 229487591 | |||
chr1:229487612 | G | A | 1 | a0009 | 1 | HG03669.hp2 | missense_variant&splice_region_variant | MODERATE | c.1196C>T | p.Ser399Phe | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 10/26 | 1288/5208 | 1196/3471 | 399/1156 | chr1 | 229487612 | |||
chr1:229495987 | T | C | 6 | a0002 a0004 a0005 others(3): Show |
74 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(71): Show |
missense_variant | MODERATE | c.880A>G | p.Ile294Val | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 7/26 | 972/5208 | 880/3471 | 294/1156 | chr1 | 229495987 | |||
chr1:229500814 | C | T | 3 | a0005 a0006 a0008 |
11 | HG02622.hp1 HG02647.hp1 HG02809.hp1 others(8): Show |
missense_variant | MODERATE | c.455G>A | p.Ser152Asn | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 4/26 | 547/5208 | 455/3471 | 152/1156 | chr1 | 229500814 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:229441991 | C | T | 1 | a0002c0015 | 1 | HG01261.hp2 | synonymous_variant | LOW | c.3384G>A | p.Ala1128Ala | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 26/26 | 3476/5208 | 3384/3471 | 1128/1156 | chr1 | 229441991 | |||
chr1:229449164 | T | C | 1 | a0003c0011 | 2 | HG01106.hp2 HG02451.hp1 |
synonymous_variant | LOW | c.3207A>G | p.Leu1069Leu | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/26 | 3299/5208 | 3207/3471 | 1069/1156 | chr1 | 229449164 | |||
chr1:229486415 | A | G | 11 | a0002c0002 a0002c0005 a0002c0015 others(8): Show |
110 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(107): Show |
synonymous_variant | LOW | c.1456T>C | p.Leu486Leu | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 11/26 | 1548/5208 | 1456/3471 | 486/1156 | chr1 | 229486415 | |||
chr1:229487545 | G | A | 1 | a0001c0007 | 4 | HG00099.hp2 HG01243.hp2 HG03927.hp1 others(1): Show |
synonymous_variant | LOW | c.1263C>T | p.Asn421Asn | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 10/26 | 1355/5208 | 1263/3471 | 421/1156 | chr1 | 229487545 | |||
chr1:229495904 | G | A | 2 | a0002c0005 a0002c0015 |
13 | HG01261.hp2 HG01884.hp2 HG02145.hp1 others(10): Show |
synonymous_variant | LOW | c.963C>T | p.Thr321Thr | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 7/26 | 1055/5208 | 963/3471 | 321/1156 | chr1 | 229495904 | |||
chr1:229495997 | C | T | 1 | a0010c0016 | 1 | NA20300.hp2 | synonymous_variant | LOW | c.870G>A | p.Thr290Thr | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 7/26 | 962/5208 | 870/3471 | 290/1156 | chr1 | 229495997 | |||
chr1:229498292 | A | T | 1 | a0001c0009 | 2 | HG01884.hp1 HG02647.hp2 |
synonymous_variant | LOW | c.663T>A | p.Ile221Ile | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 6/26 | 755/5208 | 663/3471 | 221/1156 | chr1 | 229498292 | |||
chr1:229499774 | A | G | 5 | a0002c0002 a0002c0005 a0002c0015 others(2): Show |
63 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(60): Show |
synonymous_variant | LOW | c.558T>C | p.Tyr186Tyr | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 5/26 | 650/5208 | 558/3471 | 186/1156 | chr1 | 229499774 | |||
chr1:229500804 | T | C | 1 | a0001c0012 | 2 | NA18957.hp2 NA18968.hp2 |
synonymous_variant | LOW | c.465A>G | p.Leu155Leu | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 4/26 | 557/5208 | 465/3471 | 155/1156 | chr1 | 229500804 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:229440340 | G | C | 1 | a0003c0003t0007 | 4 | HG02630.hp1 HG02976.hp1 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1564C>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 26/26 | 1564 | chr1 | 229440340 | ||||||
chr1:229440388 | T | C | 1 | a0002c0002t0011 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1516A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 26/26 | 1516 | chr1 | 229440388 | ||||||
chr1:229440389 | C | G | 7 | a0002c0002t0002 a0002c0002t0010 a0002c0002t0011 others(4): Show |
45 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1515G>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 26/26 | 1515 | chr1 | 229440389 | ||||||
chr1:229440401 | G | GT | 1 | a0003c0003t0006 | 8 | HG02257.hp1 HG02258.hp1 HG02723.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1502dupA | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 26/26 | 1502 | chr1 | 229440401 | ||||||
chr1:229440419 | C | T | 1 | a0001c0001t0008 | 2 | HG03491.hp2 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1485G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 26/26 | 1485 | chr1 | 229440419 | ||||||
chr1:229440420 | G | A | 1 | a0002c0002t0012 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1484C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 26/26 | 1484 | chr1 | 229440420 | ||||||
chr1:229440426 | G | A | 1 | a0001c0001t0015 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1478C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 26/26 | 1478 | chr1 | 229440426 | ||||||
chr1:229440483 | C | T | 5 | a0001c0001t0004 a0003c0003t0004 a0003c0003t0007 others(2): Show |
21 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1421G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 26/26 | 1421 | chr1 | 229440483 | ||||||
chr1:229440512 | C | T | 1 | a0003c0003t0013 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1392G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 26/26 | 1392 | chr1 | 229440512 | ||||||
chr1:229440580 | G | C | 2 | a0002c0005t0005 a0002c0015t0005 |
13 | HG01261.hp2 HG01884.hp2 HG02145.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1324C>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 26/26 | 1324 | chr1 | 229440580 | ||||||
chr1:229440587 | C | A | 1 | a0001c0001t0016 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1317G>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 26/26 | 1317 | chr1 | 229440587 | ||||||
chr1:229440869 | T | C | 6 | a0001c0001t0004 a0003c0003t0004 a0003c0003t0007 others(3): Show |
23 | HG01106.hp2 HG01243.hp1 HG01516.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1035A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 26/26 | 1035 | chr1 | 229440869 | ||||||
chr1:229440979 | T | C | 1 | a0005c0006t0017 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*925A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 26/26 | 925 | chr1 | 229440979 | ||||||
chr1:229441090 | A | G | 1 | a0001c0001t0014 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*814T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 26/26 | 814 | chr1 | 229441090 | ||||||
chr1:229441218 | C | T | 19 | a0001c0001t0004 a0002c0002t0002 a0002c0002t0010 others(16): Show |
99 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*686G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 26/26 | 686 | chr1 | 229441218 | ||||||
chr1:229441494 | G | A | 1 | a0003c0011t0009 | 2 | HG01106.hp2 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*410C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 26/26 | 410 | chr1 | 229441494 | ||||||
chr1:229441728 | T | C | 1 | a0002c0002t0010 | 2 | HG03710.hp1 NA18747.hp1 |
3_prime_UTR_variant | MODIFIER | c.*176A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 26/26 | 176 | chr1 | 229441728 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:229442058 | A | C | 3 | a0001c0001t0001g0006 a0001c0001t0001g0100 a0001c0001t0001g0182 |
4 | NA18962.hp1 NA18977.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.3335-18T>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229442058 | |||||||
chr1:229442144 | C | T | 6 | a0003c0003t0007g0263 a0003c0003t0007g0264 a0003c0003t0007g0265 others(3): Show |
6 | HG02630.hp1 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.3335-104G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229442144 | |||||||
chr1:229442433 | G | C | 1 | a0001c0001t0014g0039 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3335-393C>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229442433 | |||||||
chr1:229442578 | T | C | 2 | a0001c0001t0001g0070 a0001c0001t0001g0074 |
2 | HG00609.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.3335-538A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229442578 | |||||||
chr1:229442714 | C | CT | 5 | a0001c0001t0001g0095 a0001c0001t0001g0099 a0001c0001t0001g0201 others(2): Show |
5 | HG00741.hp2 HG01123.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.3335-675dupA | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229442714 | |||||||
chr1:229442714 | CT | C | 80 | a0002c0002t0002g0009 a0002c0002t0002g0214 a0002c0002t0002g0215 others(77): Show |
81 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.3335-675delA | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229442714 | |||||||
chr1:229442714 | CTT | C | 17 | a0001c0001t0004g0147 a0003c0003t0004g0106 a0003c0003t0004g0108 others(14): Show |
17 | HG01106.hp2 HG01243.hp1 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.3335-676_3335-675d others(4): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229442714 | |||||||
chr1:229442725 | T | A | 1 | a0001c0001t0001g0096 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.3335-685A>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229442725 | |||||||
chr1:229442829 | C | G | 2 | a0003c0011t0009g0136 a0003c0011t0009g0137 |
2 | HG01106.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.3335-789G>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229442829 | |||||||
chr1:229442895 | T | C | 101 | a0001c0001t0001g0010 a0001c0001t0001g0054 a0001c0001t0004g0147 others(98): Show |
102 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.3335-855A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229442895 | |||||||
chr1:229443047 | G | C | 78 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0044 others(75): Show |
80 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.3335-1007C>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229443047 | |||||||
chr1:229443068 | C | T | 44 | a0002c0002t0002g0009 a0002c0002t0002g0214 a0002c0002t0002g0215 others(41): Show |
45 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.3335-1028G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229443068 | |||||||
chr1:229443091 | G | A | 2 | a0003c0011t0009g0136 a0003c0011t0009g0137 |
2 | HG01106.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.3335-1051C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229443091 | |||||||
chr1:229443202 | A | AT | 5 | a0001c0001t0001g0006 a0001c0001t0001g0100 a0001c0001t0001g0101 others(2): Show |
6 | NA18962.hp1 NA18977.hp1 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.3335-1163dupA | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229443202 | |||||||
chr1:229443202 | AT | A | 9 | a0001c0001t0001g0054 a0001c0001t0004g0147 a0003c0003t0004g0118 others(6): Show |
9 | HG02280.hp1 HG02717.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.3335-1163delA | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229443202 | |||||||
chr1:229443492 | A | C | 1 | a0003c0003t0001g0023 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3334+1422T>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229443492 | |||||||
chr1:229443548 | T | C | 4 | a0001c0001t0001g0104 a0001c0001t0001g0154 a0001c0001t0001g0169 others(1): Show |
4 | HG01123.hp1 HG01168.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.3334+1366A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229443548 | |||||||
chr1:229443561 | A | T | 2 | a0003c0011t0009g0136 a0003c0011t0009g0137 |
2 | HG01106.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.3334+1353T>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229443561 | |||||||
chr1:229443614 | T | G | 30 | a0002c0005t0005g0022 a0002c0005t0005g0025 a0002c0005t0005g0026 others(27): Show |
30 | HG01123.hp2 HG01167.hp2 HG01261.hp1 others(27): Show |
intron_variant | MODIFIER | c.3334+1300A>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229443614 | |||||||
chr1:229443649 | C | T | 2 | a0002c0002t0002g0222 a0002c0002t0002g0226 |
2 | HG00741.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.3334+1265G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229443649 | |||||||
chr1:229443669 | A | G | 2 | a0003c0011t0009g0136 a0003c0011t0009g0137 |
2 | HG01106.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.3334+1245T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229443669 | |||||||
chr1:229443676 | C | T | 2 | a0003c0011t0009g0136 a0003c0011t0009g0137 |
2 | HG01106.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.3334+1238G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229443676 | |||||||
chr1:229443677 | G | A | 6 | a0003c0003t0007g0263 a0003c0003t0007g0264 a0003c0003t0007g0265 others(3): Show |
6 | HG02630.hp1 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.3334+1237C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229443677 | |||||||
chr1:229443681 | T | C | 2 | a0003c0003t0007g0263 a0003c0003t0007g0264 |
2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.3334+1233A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229443681 | |||||||
chr1:229443723 | A | AT | 7 | a0001c0001t0001g0010 a0001c0001t0001g0052 a0001c0001t0001g0079 others(4): Show |
7 | HG00597.hp1 HG00735.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.3334+1190dupA | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229443723 | |||||||
chr1:229443723 | AT | A | 18 | a0001c0001t0001g0055 a0001c0001t0001g0067 a0001c0001t0001g0156 others(15): Show |
18 | HG01261.hp2 HG01884.hp2 HG01943.hp1 others(15): Show |
intron_variant | MODIFIER | c.3334+1190delA | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229443723 | |||||||
chr1:229443723 | ATT | A | 47 | a0002c0002t0002g0009 a0002c0002t0002g0214 a0002c0002t0002g0215 others(44): Show |
48 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.3334+1189_3334+119 others(6): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229443723 | |||||||
chr1:229443723 | ATTT | A | 37 | a0001c0001t0004g0147 a0002c0002t0010g0223 a0003c0003t0003g0134 others(34): Show |
37 | HG01123.hp2 HG01167.hp2 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.3334+1188_3334+119 others(7): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229443723 | |||||||
chr1:229443759 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3334+1155G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229443759 | |||||||
chr1:229443894 | C | CT | 9 | a0001c0001t0001g0203 a0001c0001t0004g0147 a0003c0003t0004g0118 others(6): Show |
9 | HG00741.hp2 HG02280.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.3334+1019dupA | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229443894 | |||||||
chr1:229443894 | CT | C | 12 | a0001c0001t0001g0037 a0001c0001t0001g0061 a0001c0001t0001g0067 others(9): Show |
12 | HG00323.hp2 HG01074.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.3334+1019delA | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229443894 | |||||||
chr1:229443894 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0096 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.3334+1009_3334+101 others(15): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229443894 | |||||||
chr1:229443913 | TTTTTTA | T | 7 | a0003c0003t0004g0106 a0003c0003t0004g0108 a0003c0003t0004g0109 others(4): Show |
7 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.3334+995_3334+1000 others(9): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229443913 | |||||||
chr1:229443917 | TTA | T | 22 | a0002c0002t0002g0239 a0002c0002t0002g0243 a0002c0002t0002g0262 others(19): Show |
22 | HG01106.hp2 HG01123.hp2 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.3334+995_3334+996d others(4): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229443917 | |||||||
chr1:229443918 | TA | T | 64 | a0002c0002t0002g0009 a0002c0002t0002g0214 a0002c0002t0002g0215 others(61): Show |
65 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.3334+995delT | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229443918 | |||||||
chr1:229443919 | A | T | 16 | a0001c0001t0004g0147 a0002c0002t0002g0219 a0003c0003t0001g0023 others(13): Show |
16 | HG02280.hp1 HG02630.hp1 HG02717.hp2 others(13): Show |
intron_variant | MODIFIER | c.3334+995T>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229443919 | |||||||
chr1:229444104 | G | A | 2 | a0003c0003t0001g0050 a0003c0003t0001g0209 |
2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.3334+810C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229444104 | |||||||
chr1:229444117 | G | A | 1 | a0003c0003t0006g0123 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3334+797C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229444117 | |||||||
chr1:229444232 | G | A | 21 | a0001c0001t0004g0147 a0003c0003t0004g0106 a0003c0003t0004g0108 others(18): Show |
21 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.3334+682C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229444232 | |||||||
chr1:229444398 | T | C | 1 | a0010c0016t0003g0114 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3334+516A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229444398 | |||||||
chr1:229444474 | A | G | 75 | a0002c0002t0002g0009 a0002c0002t0002g0214 a0002c0002t0002g0215 others(72): Show |
76 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.3334+440T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229444474 | |||||||
chr1:229444476 | T | C | 2 | a0003c0011t0009g0136 a0003c0011t0009g0137 |
2 | HG01106.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.3334+438A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229444476 | |||||||
chr1:229444507 | G | T | 2 | a0003c0003t0001g0050 a0003c0003t0001g0209 |
2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.3334+407C>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229444507 | |||||||
chr1:229444516 | G | A | 2 | a0003c0003t0001g0050 a0003c0003t0001g0209 |
2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.3334+398C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229444516 | |||||||
chr1:229444584 | G | T | 1 | a0010c0016t0003g0114 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3334+330C>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229444584 | |||||||
chr1:229444680 | T | G | 21 | a0001c0001t0004g0147 a0003c0003t0004g0106 a0003c0003t0004g0108 others(18): Show |
21 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.3334+234A>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229444680 | |||||||
chr1:229444846 | C | CA | 42 | a0002c0002t0002g0009 a0002c0002t0002g0214 a0002c0002t0002g0215 others(39): Show |
43 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.3334+67dupT | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229444846 | |||||||
chr1:229444855 | A | C | 1 | a0001c0001t0001g0070 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3334+59T>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 25/25 | chr1 | 229444855 | |||||||
chr1:229445047 | T | C | 2 | a0003c0011t0009g0136 a0003c0011t0009g0137 |
2 | HG01106.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.3246-45A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229445047 | |||||||
chr1:229445239 | C | T | 98 | a0001c0001t0004g0147 a0002c0002t0002g0009 a0002c0002t0002g0214 others(95): Show |
99 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.3246-237G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229445239 | |||||||
chr1:229445349 | T | C | 1 | a0001c0001t0001g0192 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.3246-347A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229445349 | |||||||
chr1:229445360 | A | G | 3 | a0001c0001t0001g0130 a0001c0001t0001g0152 a0001c0001t0001g0210 |
3 | HG00735.hp2 HG01255.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.3246-358T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229445360 | |||||||
chr1:229445419 | T | C | 109 | a0001c0001t0004g0147 a0002c0002t0002g0009 a0002c0002t0002g0214 others(106): Show |
110 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.3246-417A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229445419 | |||||||
chr1:229445444 | G | A | 2 | a0003c0011t0009g0136 a0003c0011t0009g0137 |
2 | HG01106.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.3246-442C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229445444 | |||||||
chr1:229445517 | G | A | 2 | a0002c0002t0010g0223 a0002c0002t0010g0232 |
2 | HG03710.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.3246-515C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229445517 | |||||||
chr1:229445560 | C | T | 1 | a0003c0003t0001g0050 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3246-558G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229445560 | |||||||
chr1:229445718 | A | G | 1 | a0003c0003t0001g0023 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3246-716T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229445718 | |||||||
chr1:229445744 | A | G | 13 | a0002c0005t0005g0022 a0002c0005t0005g0025 a0002c0005t0005g0026 others(10): Show |
13 | HG01261.hp2 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.3246-742T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229445744 | |||||||
chr1:229445775 | G | T | 1 | a0003c0003t0006g0127 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3246-773C>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229445775 | |||||||
chr1:229446107 | T | C | 2 | a0003c0003t0002g0116 a0003c0003t0002g0117 |
2 | HG02615.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.3246-1105A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229446107 | |||||||
chr1:229446120 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3246-1118C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229446120 | |||||||
chr1:229446134 | C | T | 7 | a0003c0003t0004g0106 a0003c0003t0004g0108 a0003c0003t0004g0109 others(4): Show |
7 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.3246-1132G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229446134 | |||||||
chr1:229446186 | C | T | 2 | a0003c0011t0009g0136 a0003c0011t0009g0137 |
2 | HG01106.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.3246-1184G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229446186 | |||||||
chr1:229446341 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3246-1339C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229446341 | |||||||
chr1:229446350 | G | A | 1 | a0001c0007t0001g0157 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3246-1348C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229446350 | |||||||
chr1:229446385 | G | A | 12 | a0001c0001t0001g0004 a0001c0001t0001g0040 a0001c0001t0001g0042 others(9): Show |
13 | HG00544.hp1 HG00639.hp2 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.3246-1383C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229446385 | |||||||
chr1:229446477 | C | T | 1 | a0001c0001t0001g0037 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.3246-1475G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229446477 | |||||||
chr1:229446525 | C | T | 1 | a0008c0013t0003g0013 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3246-1523G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229446525 | |||||||
chr1:229446569 | A | G | 2 | a0003c0011t0009g0136 a0003c0011t0009g0137 |
2 | HG01106.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.3246-1567T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229446569 | |||||||
chr1:229446607 | A | G | 98 | a0001c0001t0004g0147 a0002c0002t0002g0009 a0002c0002t0002g0214 others(95): Show |
99 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.3246-1605T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229446607 | |||||||
chr1:229446711 | G | T | 1 | a0001c0001t0001g0040 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.3246-1709C>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229446711 | |||||||
chr1:229446744 | T | A | 30 | a0001c0001t0004g0147 a0003c0003t0004g0106 a0003c0003t0004g0108 others(27): Show |
30 | HG01106.hp2 HG01243.hp1 HG01516.hp1 others(27): Show |
intron_variant | MODIFIER | c.3246-1742A>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229446744 | |||||||
chr1:229446776 | TAAAAC | T | 23 | a0001c0001t0004g0147 a0003c0003t0004g0106 a0003c0003t0004g0108 others(20): Show |
23 | HG01106.hp2 HG01243.hp1 HG01516.hp1 others(20): Show |
intron_variant | MODIFIER | c.3246-1779_3246-177 others(9): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229446776 | |||||||
chr1:229446795 | C | T | 1 | a0002c0002t0001g0242 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.3246-1793G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229446795 | |||||||
chr1:229446864 | C | T | 1 | a0003c0003t0003g0113 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3246-1862G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229446864 | |||||||
chr1:229446892 | C | T | 2 | a0003c0003t0002g0116 a0003c0003t0002g0117 |
2 | HG02615.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.3246-1890G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229446892 | |||||||
chr1:229447014 | C | G | 43 | a0002c0002t0002g0009 a0002c0002t0002g0214 a0002c0002t0002g0215 others(40): Show |
44 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.3246-2012G>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229447014 | |||||||
chr1:229447049 | G | A | 26 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(23): Show |
28 | HG00544.hp1 HG00639.hp2 HG01975.hp2 others(25): Show |
intron_variant | MODIFIER | c.3246-2047C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229447049 | |||||||
chr1:229447102 | C | A | 6 | a0003c0003t0007g0263 a0003c0003t0007g0264 a0003c0003t0007g0265 others(3): Show |
6 | HG02630.hp1 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.3245+2024G>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229447102 | |||||||
chr1:229447111 | T | G | 5 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(2): Show |
5 | HG00597.hp1 HG00609.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.3245+2015A>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229447111 | |||||||
chr1:229447268 | C | T | 2 | a0003c0011t0009g0136 a0003c0011t0009g0137 |
2 | HG01106.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.3245+1858G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229447268 | |||||||
chr1:229447513 | C | T | 3 | a0001c0001t0001g0146 a0001c0001t0001g0156 a0001c0001t0001g0174 |
3 | HG02055.hp1 HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3245+1613G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229447513 | |||||||
chr1:229447629 | T | C | 21 | a0001c0001t0004g0147 a0003c0003t0004g0106 a0003c0003t0004g0108 others(18): Show |
21 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.3245+1497A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229447629 | |||||||
chr1:229447738 | G | A | 1 | a0003c0003t0001g0209 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3245+1388C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229447738 | |||||||
chr1:229447758 | G | C | 7 | a0003c0003t0004g0106 a0003c0003t0004g0108 a0003c0003t0004g0109 others(4): Show |
7 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.3245+1368C>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229447758 | |||||||
chr1:229447800 | C | T | 98 | a0001c0001t0004g0147 a0002c0002t0002g0009 a0002c0002t0002g0214 others(95): Show |
99 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.3245+1326G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229447800 | |||||||
chr1:229448053 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3245+1073A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229448053 | |||||||
chr1:229448158 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3245+968C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229448158 | |||||||
chr1:229448171 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3245+955C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229448171 | |||||||
chr1:229448384 | C | T | 21 | a0001c0001t0004g0147 a0003c0003t0004g0106 a0003c0003t0004g0108 others(18): Show |
21 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.3245+742G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229448384 | |||||||
chr1:229448670 | A | G | 75 | a0002c0002t0002g0009 a0002c0002t0002g0214 a0002c0002t0002g0215 others(72): Show |
76 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.3245+456T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229448670 | |||||||
chr1:229448710 | C | CTGG | 98 | a0001c0001t0004g0147 a0002c0002t0002g0009 a0002c0002t0002g0214 others(95): Show |
99 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.3245+415_3245+416i others(5): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229448710 | |||||||
chr1:229448726 | TG | T | 15 | a0001c0001t0004g0147 a0003c0003t0004g0106 a0003c0003t0004g0108 others(12): Show |
15 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.3245+399delC | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229448726 | |||||||
chr1:229448759 | T | C | 23 | a0001c0001t0004g0147 a0003c0003t0004g0106 a0003c0003t0004g0108 others(20): Show |
23 | HG01106.hp2 HG01243.hp1 HG01516.hp1 others(20): Show |
intron_variant | MODIFIER | c.3245+367A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229448759 | |||||||
chr1:229448816 | G | C | 1 | a0003c0003t0004g0111 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.3245+310C>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229448816 | |||||||
chr1:229448873 | T | G | 98 | a0001c0001t0004g0147 a0002c0002t0002g0009 a0002c0002t0002g0214 others(95): Show |
99 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.3245+253A>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229448873 | |||||||
chr1:229448942 | T | C | 2 | a0003c0011t0009g0136 a0003c0011t0009g0137 |
2 | HG01106.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.3245+184A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 24/25 | chr1 | 229448942 | |||||||
chr1:229449274 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.3181-84G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229449274 | |||||||
chr1:229449328 | A | G | 5 | a0001c0001t0001g0155 a0001c0001t0001g0179 a0001c0001t0001g0189 others(2): Show |
5 | HG02155.hp2 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.3181-138T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229449328 | |||||||
chr1:229449353 | G | A | 7 | a0001c0001t0004g0147 a0003c0003t0004g0118 a0003c0003t0004g0119 others(4): Show |
7 | HG02280.hp1 HG02717.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.3181-163C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229449353 | |||||||
chr1:229449370 | C | CT | 45 | a0001c0001t0001g0177 a0002c0002t0002g0214 a0002c0002t0002g0215 others(42): Show |
45 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.3181-181dupA | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229449370 | |||||||
chr1:229449502 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3181-312C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229449502 | |||||||
chr1:229449513 | A | G | 98 | a0001c0001t0004g0147 a0002c0002t0002g0009 a0002c0002t0002g0214 others(95): Show |
99 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.3181-323T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229449513 | |||||||
chr1:229449563 | G | A | 1 | a0002c0002t0002g0254 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.3181-373C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229449563 | |||||||
chr1:229449849 | T | TTATATAT others(19): Show |
1 | a0001c0001t0004g0147 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3181-660_3181-659i others(28): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229449849 | |||||||
chr1:229449851 | T | A | 3 | a0001c0001t0004g0147 a0003c0003t0004g0132 a0003c0003t0004g0133 |
3 | HG02280.hp1 HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3181-661A>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229449851 | |||||||
chr1:229449851 | T | TTA | 21 | a0001c0001t0001g0139 a0001c0001t0001g0178 a0004c0004t0003g0216 others(18): Show |
21 | HG01123.hp2 HG01167.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.3181-663_3181-662d others(4): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229449851 | |||||||
chr1:229449851 | T | TTATA | 12 | a0001c0001t0001g0138 a0001c0001t0001g0140 a0001c0001t0001g0141 others(9): Show |
12 | HG01515.hp2 HG01993.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.3181-665_3181-662d others(6): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229449851 | |||||||
chr1:229449851 | T | TTATATA | 10 | a0001c0001t0001g0190 a0002c0005t0005g0025 a0002c0005t0005g0026 others(7): Show |
10 | HG01261.hp2 HG01884.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.3181-667_3181-662d others(8): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229449851 | |||||||
chr1:229449851 | T | TTATATAT others(1): Show |
18 | a0002c0002t0002g0009 a0002c0002t0002g0214 a0002c0002t0002g0217 others(15): Show |
19 | HG00099.hp1 HG00738.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.3180+666_3181-662d others(10): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229449851 | |||||||
chr1:229449851 | T | TTATATAT others(3): Show |
16 | a0002c0002t0002g0215 a0002c0002t0002g0218 a0002c0002t0002g0221 others(13): Show |
16 | HG00140.hp2 HG00733.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.3180+664_3181-662d others(12): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229449851 | |||||||
chr1:229449851 | T | TTATATAT others(5): Show |
6 | a0002c0002t0002g0222 a0002c0002t0002g0226 a0002c0002t0002g0235 others(3): Show |
6 | HG00741.hp1 HG01106.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.3180+662_3181-662d others(14): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229449851 | |||||||
chr1:229449851 | T | TTATATAT others(7): Show |
5 | a0002c0002t0002g0233 a0002c0002t0002g0234 a0002c0002t0002g0236 others(2): Show |
5 | HG00438.hp2 HG01074.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.3180+660_3181-662d others(16): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229449851 | |||||||
chr1:229449851 | T | TTATATAT others(9): Show |
1 | a0008c0013t0003g0013 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3180+658_3181-662d others(18): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229449851 | |||||||
chr1:229449871 | A | T | 1 | a0001c0001t0001g0057 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3180+654T>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229449871 | |||||||
chr1:229449873 | A | AT | 5 | a0001c0001t0001g0067 a0001c0001t0001g0087 a0001c0001t0001g0103 others(2): Show |
5 | HG00438.hp1 HG02723.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.3180+651dupA | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229449873 | |||||||
chr1:229449873 | A | ATATATAT others(6): Show |
1 | a0003c0003t0004g0115 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3180+651_3180+652i others(15): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229449873 | |||||||
chr1:229449873 | A | ATATATAT others(28): Show |
1 | a0003c0003t0004g0133 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3180+651_3180+652i others(37): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229449873 | |||||||
chr1:229449873 | A | ATATATAT others(24): Show |
1 | a0003c0003t0004g0132 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3180+651_3180+652i others(33): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229449873 | |||||||
chr1:229449873 | A | ATATATAT others(22): Show |
1 | a0003c0003t0013g0267 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3180+651_3180+652i others(31): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229449873 | |||||||
chr1:229449873 | A | ATATATAT others(6): Show |
1 | a0003c0003t0004g0111 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.3180+651_3180+652i others(15): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229449873 | |||||||
chr1:229449873 | A | ATATATAT others(8): Show |
1 | a0003c0003t0004g0106 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3180+651_3180+652i others(17): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229449873 | |||||||
chr1:229449873 | A | ATATATAT others(6): Show |
2 | a0003c0003t0004g0108 a0003c0003t0004g0112 |
2 | HG01516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3180+651_3180+652i others(15): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229449873 | |||||||
chr1:229449873 | A | ATATATAT others(8): Show |
2 | a0003c0003t0004g0109 a0003c0003t0004g0110 |
2 | HG01243.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.3180+651_3180+652i others(17): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229449873 | |||||||
chr1:229449873 | A | T | 5 | a0001c0001t0001g0049 a0001c0001t0001g0053 a0001c0001t0001g0057 others(2): Show |
5 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.3180+652T>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229449873 | |||||||
chr1:229449873 | AT | A | 46 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(43): Show |
49 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.3180+651delA | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229449873 | |||||||
chr1:229449873 | ATT | A | 7 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0058 others(4): Show |
7 | HG02155.hp1 HG03942.hp1 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.3180+650_3180+651d others(4): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229449873 | |||||||
chr1:229449874 | T | TA | 11 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0081 others(8): Show |
11 | HG01884.hp1 HG02647.hp2 HG03017.hp2 others(8): Show |
intron_variant | MODIFIER | c.3180+650_3180+651i others(3): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229449874 | |||||||
chr1:229449874 | T | TATATA | 3 | a0001c0001t0001g0083 a0001c0001t0001g0193 a0001c0001t0001g0194 |
3 | HG00738.hp1 HG01516.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.3180+650_3180+651i others(7): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229449874 | |||||||
chr1:229449874 | T | TATATATA others(14): Show |
1 | a0003c0003t0004g0119 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3180+650_3180+651i others(23): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229449874 | |||||||
chr1:229449874 | T | TATATATA others(16): Show |
3 | a0003c0003t0004g0118 a0003c0003t0004g0120 a0003c0003t0004g0121 |
3 | HG02965.hp2 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.3180+650_3180+651i others(25): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229449874 | |||||||
chr1:229449875 | T | A | 135 | a0001c0001t0001g0007 a0001c0001t0001g0041 a0001c0001t0001g0044 others(132): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.3180+650A>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229449875 | |||||||
chr1:229449876 | T | A | 26 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0081 others(23): Show |
27 | HG00408.hp2 HG00738.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.3180+649A>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229449876 | |||||||
chr1:229449877 | T | A | 7 | a0001c0001t0001g0146 a0001c0001t0001g0156 a0001c0001t0001g0166 others(4): Show |
7 | HG01515.hp2 HG01952.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.3180+648A>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229449877 | |||||||
chr1:229449878 | T | A | 8 | a0003c0003t0001g0050 a0003c0003t0004g0118 a0003c0003t0004g0119 others(5): Show |
8 | HG02965.hp2 HG02976.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.3180+647A>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229449878 | |||||||
chr1:229449879 | T | A | 75 | a0002c0002t0002g0009 a0002c0002t0002g0214 a0002c0002t0002g0215 others(72): Show |
76 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.3180+646A>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229449879 | |||||||
chr1:229449880 | T | A | 2 | a0003c0003t0007g0265 a0003c0003t0007g0266 |
2 | HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3180+645A>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229449880 | |||||||
chr1:229449883 | T | A | 45 | a0002c0002t0002g0009 a0002c0002t0002g0214 a0002c0002t0002g0215 others(42): Show |
46 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.3180+642A>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229449883 | |||||||
chr1:229449884 | T | A | 30 | a0002c0005t0005g0022 a0002c0005t0005g0025 a0002c0005t0005g0026 others(27): Show |
30 | HG01123.hp2 HG01167.hp2 HG01261.hp1 others(27): Show |
intron_variant | MODIFIER | c.3180+641A>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229449884 | |||||||
chr1:229449887 | T | A | 43 | a0002c0002t0002g0009 a0002c0002t0002g0215 a0002c0002t0002g0217 others(40): Show |
44 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.3180+638A>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229449887 | |||||||
chr1:229449888 | T | A | 6 | a0002c0005t0005g0022 a0002c0005t0005g0030 a0002c0005t0005g0033 others(3): Show |
6 | HG02895.hp1 HG02897.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.3180+637A>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229449888 | |||||||
chr1:229450023 | G | A | 4 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0187 others(1): Show |
4 | HG01943.hp1 NA19009.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.3180+502C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229450023 | |||||||
chr1:229450036 | C | G | 15 | a0001c0001t0004g0147 a0003c0003t0004g0106 a0003c0003t0004g0108 others(12): Show |
15 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.3180+489G>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229450036 | |||||||
chr1:229450122 | C | G | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | NA19009.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.3180+403G>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229450122 | |||||||
chr1:229450425 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3180+100A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229450425 | |||||||
chr1:229450449 | T | C | 7 | a0003c0003t0004g0106 a0003c0003t0004g0108 a0003c0003t0004g0109 others(4): Show |
7 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.3180+76A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229450449 | |||||||
chr1:229450461 | G | A | 7 | a0002c0005t0005g0025 a0002c0005t0005g0026 a0002c0005t0005g0027 others(4): Show |
7 | HG01261.hp2 HG01884.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.3180+64C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 23/25 | chr1 | 229450461 | |||||||
chr1:229450681 | G | A | 1 | a0001c0009t0001g0208 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3100-76C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 22/25 | chr1 | 229450681 | |||||||
chr1:229450715 | T | TTTTG | 49 | a0002c0002t0002g0009 a0002c0002t0002g0214 a0002c0002t0002g0215 others(46): Show |
50 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.3100-114_3100-111d others(6): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 22/25 | chr1 | 229450715 | |||||||
chr1:229450739 | T | G | 98 | a0001c0001t0001g0094 a0001c0001t0001g0144 a0001c0001t0004g0147 others(95): Show |
99 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.3100-134A>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 22/25 | chr1 | 229450739 | |||||||
chr1:229450898 | G | GT | 45 | a0002c0002t0002g0009 a0002c0002t0002g0214 a0002c0002t0002g0215 others(42): Show |
46 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.3100-294dupA | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 22/25 | chr1 | 229450898 | |||||||
chr1:229451210 | G | A | 2 | a0001c0012t0001g0075 a0001c0012t0001g0076 |
2 | NA18957.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.3100-605C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 22/25 | chr1 | 229451210 | |||||||
chr1:229451344 | A | T | 7 | a0003c0003t0004g0106 a0003c0003t0004g0108 a0003c0003t0004g0109 others(4): Show |
7 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.3100-739T>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 22/25 | chr1 | 229451344 | |||||||
chr1:229451386 | A | G | 101 | a0001c0001t0004g0147 a0002c0002t0002g0009 a0002c0002t0002g0214 others(98): Show |
102 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.3100-781T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 22/25 | chr1 | 229451386 | |||||||
chr1:229451405 | TA | T | 75 | a0002c0002t0002g0009 a0002c0002t0002g0214 a0002c0002t0002g0215 others(72): Show |
76 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.3100-801delT | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 22/25 | chr1 | 229451405 | |||||||
chr1:229451562 | C | G | 6 | a0003c0003t0007g0263 a0003c0003t0007g0264 a0003c0003t0007g0265 others(3): Show |
6 | HG02630.hp1 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.3100-957G>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 22/25 | chr1 | 229451562 | |||||||
chr1:229451628 | A | ATAAC | 23 | a0001c0001t0004g0147 a0003c0003t0004g0106 a0003c0003t0004g0108 others(20): Show |
23 | HG01106.hp2 HG01243.hp1 HG01516.hp1 others(20): Show |
intron_variant | MODIFIER | c.3099+896_3099+897i others(6): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 22/25 | chr1 | 229451628 | |||||||
chr1:229451754 | T | C | 2 | a0001c0001t0001g0084 a0001c0001t0001g0091 |
2 | NA19002.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.3099+771A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 22/25 | chr1 | 229451754 | |||||||
chr1:229451912 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3099+613A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 22/25 | chr1 | 229451912 | |||||||
chr1:229452076 | A | T | 6 | a0003c0003t0007g0263 a0003c0003t0007g0264 a0003c0003t0007g0265 others(3): Show |
6 | HG02630.hp1 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.3099+449T>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 22/25 | chr1 | 229452076 | |||||||
chr1:229452389 | C | T | 1 | a0002c0002t0002g0233 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.3099+136G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 22/25 | chr1 | 229452389 | |||||||
chr1:229452481 | T | G | 1 | a0001c0001t0001g0202 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3099+44A>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 22/25 | chr1 | 229452481 | |||||||
chr1:229452679 | T | C | 1 | a0001c0001t0001g0058 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2981-36A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229452679 | |||||||
chr1:229453212 | G | A | 1 | a0003c0003t0013g0267 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2981-569C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229453212 | |||||||
chr1:229453215 | TCCC | T | 20 | a0001c0001t0004g0147 a0003c0003t0004g0106 a0003c0003t0004g0108 others(17): Show |
20 | HG01516.hp1 HG02040.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.2981-575_2981-573d others(5): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229453215 | |||||||
chr1:229453219 | C | T | 20 | a0001c0001t0004g0147 a0003c0003t0004g0106 a0003c0003t0004g0108 others(17): Show |
20 | HG01516.hp1 HG02040.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.2981-576G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229453219 | |||||||
chr1:229453222 | A | AAGCTTAA others(175): Show |
21 | a0001c0001t0004g0147 a0003c0003t0004g0106 a0003c0003t0004g0108 others(18): Show |
21 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.2981-580_2981-579i others(184): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229453222 | |||||||
chr1:229453264 | A | T | 98 | a0001c0001t0004g0147 a0002c0002t0002g0009 a0002c0002t0002g0214 others(95): Show |
99 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.2981-621T>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229453264 | |||||||
chr1:229453426 | A | G | 2 | a0003c0011t0009g0136 a0003c0011t0009g0137 |
2 | HG01106.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2981-783T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229453426 | |||||||
chr1:229453459 | G | A | 1 | a0002c0002t0011g0247 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2981-816C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229453459 | |||||||
chr1:229453489 | G | C | 2 | a0003c0011t0009g0136 a0003c0011t0009g0137 |
2 | HG01106.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2981-846C>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229453489 | |||||||
chr1:229453633 | T | C | 21 | a0001c0001t0004g0147 a0003c0003t0004g0106 a0003c0003t0004g0108 others(18): Show |
21 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.2981-990A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229453633 | |||||||
chr1:229453823 | T | C | 21 | a0001c0001t0004g0147 a0003c0003t0004g0106 a0003c0003t0004g0108 others(18): Show |
21 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.2981-1180A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229453823 | |||||||
chr1:229453920 | A | AT | 93 | a0001c0001t0004g0147 a0002c0002t0002g0009 a0002c0002t0002g0214 others(90): Show |
94 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.2981-1278dupA | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229453920 | |||||||
chr1:229453964 | T | A | 6 | a0003c0003t0007g0263 a0003c0003t0007g0264 a0003c0003t0007g0265 others(3): Show |
6 | HG02630.hp1 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2981-1321A>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229453964 | |||||||
chr1:229454082 | A | G | 2 | a0003c0011t0009g0136 a0003c0011t0009g0137 |
2 | HG01106.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2981-1439T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229454082 | |||||||
chr1:229454086 | G | A | 2 | a0003c0011t0009g0136 a0003c0011t0009g0137 |
2 | HG01106.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2981-1443C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229454086 | |||||||
chr1:229454184 | A | G | 6 | a0003c0003t0007g0263 a0003c0003t0007g0264 a0003c0003t0007g0265 others(3): Show |
6 | HG02630.hp1 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2981-1541T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229454184 | |||||||
chr1:229454299 | C | T | 101 | a0001c0001t0004g0147 a0002c0002t0002g0009 a0002c0002t0002g0214 others(98): Show |
102 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.2981-1656G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229454299 | |||||||
chr1:229454303 | C | T | 75 | a0002c0002t0002g0009 a0002c0002t0002g0214 a0002c0002t0002g0215 others(72): Show |
76 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.2981-1660G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229454303 | |||||||
chr1:229454460 | A | G | 2 | a0003c0011t0009g0136 a0003c0011t0009g0137 |
2 | HG01106.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2981-1817T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229454460 | |||||||
chr1:229454478 | A | G | 1 | a0002c0002t0010g0232 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2981-1835T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229454478 | |||||||
chr1:229454484 | G | A | 6 | a0002c0002t0002g0227 a0002c0002t0002g0234 a0002c0002t0002g0236 others(3): Show |
6 | HG00438.hp2 HG02080.hp1 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.2981-1841C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229454484 | |||||||
chr1:229454597 | C | T | 15 | a0001c0001t0004g0147 a0003c0003t0004g0106 a0003c0003t0004g0108 others(12): Show |
15 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.2981-1954G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229454597 | |||||||
chr1:229454848 | C | T | 7 | a0001c0001t0004g0147 a0003c0003t0004g0118 a0003c0003t0004g0119 others(4): Show |
7 | HG02280.hp1 HG02717.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.2981-2205G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229454848 | |||||||
chr1:229454886 | TA | T | 15 | a0001c0001t0004g0147 a0003c0003t0004g0106 a0003c0003t0004g0108 others(12): Show |
15 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.2981-2244delT | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229454886 | |||||||
chr1:229455028 | C | T | 1 | a0001c0001t0001g0008 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2981-2385G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229455028 | |||||||
chr1:229455088 | G | C | 2 | a0001c0001t0001g0131 a0001c0001t0001g0151 |
2 | HG01192.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.2981-2445C>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229455088 | |||||||
chr1:229455108 | T | C | 1 | a0001c0001t0001g0192 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2981-2465A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229455108 | |||||||
chr1:229455735 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2980+2426G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229455735 | |||||||
chr1:229455748 | A | G | 9 | a0004c0004t0003g0216 a0004c0004t0003g0220 a0004c0004t0003g0225 others(6): Show |
9 | HG01167.hp2 HG01261.hp1 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.2980+2413T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229455748 | |||||||
chr1:229455851 | T | C | 75 | a0002c0002t0002g0009 a0002c0002t0002g0214 a0002c0002t0002g0215 others(72): Show |
76 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.2980+2310A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229455851 | |||||||
chr1:229455920 | T | C | 21 | a0001c0001t0004g0147 a0003c0003t0004g0106 a0003c0003t0004g0108 others(18): Show |
21 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.2980+2241A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229455920 | |||||||
chr1:229456066 | T | C | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | NA19009.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.2980+2095A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229456066 | |||||||
chr1:229456135 | C | G | 1 | a0001c0001t0001g0150 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2980+2026G>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229456135 | |||||||
chr1:229456186 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2980+1975A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229456186 | |||||||
chr1:229456226 | A | G | 21 | a0001c0001t0004g0147 a0003c0003t0004g0106 a0003c0003t0004g0108 others(18): Show |
21 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.2980+1935T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229456226 | |||||||
chr1:229456487 | T | C | 1 | a0003c0003t0001g0023 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2980+1674A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229456487 | |||||||
chr1:229456571 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2980+1590T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229456571 | |||||||
chr1:229456585 | G | C | 75 | a0002c0002t0002g0009 a0002c0002t0002g0214 a0002c0002t0002g0215 others(72): Show |
76 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.2980+1576C>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229456585 | |||||||
chr1:229456743 | G | GTA | 89 | a0001c0001t0004g0147 a0002c0002t0002g0009 a0002c0002t0002g0214 others(86): Show |
90 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.2980+1416_2980+141 others(6): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229456743 | |||||||
chr1:229456743 | G | GTATA | 7 | a0002c0002t0002g0235 a0003c0003t0007g0263 a0003c0003t0007g0264 others(4): Show |
7 | HG02630.hp1 HG02976.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.2980+1414_2980+141 others(8): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229456743 | |||||||
chr1:229456758 | C | T | 15 | a0001c0001t0004g0147 a0003c0003t0004g0106 a0003c0003t0004g0108 others(12): Show |
15 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.2980+1403G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229456758 | |||||||
chr1:229456772 | TAC | T | 4 | a0003c0003t0004g0118 a0003c0003t0004g0119 a0003c0003t0004g0120 others(1): Show |
4 | HG02965.hp2 HG03041.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2980+1387_2980+138 others(6): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229456772 | |||||||
chr1:229456792 | T | C | 30 | a0002c0005t0005g0022 a0002c0005t0005g0025 a0002c0005t0005g0026 others(27): Show |
30 | HG01123.hp2 HG01167.hp2 HG01261.hp1 others(27): Show |
intron_variant | MODIFIER | c.2980+1369A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229456792 | |||||||
chr1:229456818 | T | G | 1 | a0003c0003t0004g0115 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2980+1343A>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229456818 | |||||||
chr1:229456841 | T | C | 1 | a0003c0003t0001g0023 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2980+1320A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229456841 | |||||||
chr1:229456913 | A | G | 109 | a0001c0001t0004g0147 a0002c0002t0002g0009 a0002c0002t0002g0214 others(106): Show |
110 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.2980+1248T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229456913 | |||||||
chr1:229457366 | A | T | 1 | a0003c0003t0004g0120 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2980+795T>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229457366 | |||||||
chr1:229457440 | A | C | 6 | a0001c0001t0001g0049 a0001c0001t0001g0064 a0001c0001t0001g0065 others(3): Show |
6 | HG02109.hp2 HG02258.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2980+721T>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229457440 | |||||||
chr1:229457441 | C | A | 6 | a0001c0001t0001g0049 a0001c0001t0001g0064 a0001c0001t0001g0065 others(3): Show |
6 | HG02109.hp2 HG02258.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2980+720G>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229457441 | |||||||
chr1:229457445 | C | T | 21 | a0001c0001t0004g0147 a0003c0003t0004g0106 a0003c0003t0004g0108 others(18): Show |
21 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.2980+716G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229457445 | |||||||
chr1:229457578 | A | T | 43 | a0002c0002t0002g0009 a0002c0002t0002g0214 a0002c0002t0002g0215 others(40): Show |
44 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.2980+583T>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229457578 | |||||||
chr1:229457643 | C | G | 96 | a0001c0001t0004g0147 a0002c0002t0002g0009 a0002c0002t0002g0214 others(93): Show |
97 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.2980+518G>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229457643 | |||||||
chr1:229457679 | T | A | 1 | a0002c0002t0002g0219 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2980+482A>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229457679 | |||||||
chr1:229457754 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2980+407C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229457754 | |||||||
chr1:229457923 | A | T | 21 | a0001c0001t0004g0147 a0003c0003t0004g0106 a0003c0003t0004g0108 others(18): Show |
21 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.2980+238T>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 21/25 | chr1 | 229457923 | |||||||
chr1:229458394 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2845-98C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 20/25 | chr1 | 229458394 | |||||||
chr1:229458474 | A | G | 15 | a0001c0001t0004g0147 a0003c0003t0004g0106 a0003c0003t0004g0108 others(12): Show |
15 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.2845-178T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 20/25 | chr1 | 229458474 | |||||||
chr1:229458563 | A | G | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(70): Show |
79 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.2845-267T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 20/25 | chr1 | 229458563 | |||||||
chr1:229458711 | A | AT | 73 | a0001c0001t0001g0144 a0001c0001t0001g0189 a0002c0002t0002g0009 others(70): Show |
74 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.2845-416dupA | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 20/25 | chr1 | 229458711 | |||||||
chr1:229458711 | AT | A | 21 | a0001c0001t0001g0212 a0001c0001t0004g0147 a0003c0003t0004g0106 others(18): Show |
21 | HG01167.hp1 HG01243.hp1 HG01516.hp1 others(18): Show |
intron_variant | MODIFIER | c.2845-416delA | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 20/25 | chr1 | 229458711 | |||||||
chr1:229459059 | T | C | 75 | a0002c0002t0002g0009 a0002c0002t0002g0214 a0002c0002t0002g0215 others(72): Show |
76 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.2845-763A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 20/25 | chr1 | 229459059 | |||||||
chr1:229459147 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2845-851A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 20/25 | chr1 | 229459147 | |||||||
chr1:229459253 | T | C | 13 | a0004c0004t0003g0216 a0004c0004t0003g0220 a0004c0004t0003g0225 others(10): Show |
13 | HG01123.hp2 HG01167.hp2 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.2845-957A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 20/25 | chr1 | 229459253 | |||||||
chr1:229459502 | T | C | 8 | a0003c0003t0006g0122 a0003c0003t0006g0123 a0003c0003t0006g0124 others(5): Show |
8 | HG02257.hp1 HG02258.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.2844+1109A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 20/25 | chr1 | 229459502 | |||||||
chr1:229459834 | T | C | 1 | a0003c0003t0006g0127 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2844+777A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 20/25 | chr1 | 229459834 | |||||||
chr1:229459910 | T | C | 2 | a0001c0001t0001g0142 a0001c0001t0001g0211 |
2 | HG00140.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.2844+701A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 20/25 | chr1 | 229459910 | |||||||
chr1:229460057 | A | C | 1 | a0010c0016t0003g0114 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2844+554T>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 20/25 | chr1 | 229460057 | |||||||
chr1:229460097 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2844+514A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 20/25 | chr1 | 229460097 | |||||||
chr1:229460104 | A | G | 6 | a0003c0003t0007g0263 a0003c0003t0007g0264 a0003c0003t0007g0265 others(3): Show |
6 | HG02630.hp1 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2844+507T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 20/25 | chr1 | 229460104 | |||||||
chr1:229460269 | C | T | 1 | a0008c0013t0003g0013 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2844+342G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 20/25 | chr1 | 229460269 | |||||||
chr1:229460314 | G | A | 31 | a0001c0001t0001g0008 a0001c0001t0001g0045 a0001c0001t0001g0099 others(28): Show |
32 | HG00738.hp1 HG01074.hp1 HG01515.hp2 others(29): Show |
intron_variant | MODIFIER | c.2844+297C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 20/25 | chr1 | 229460314 | |||||||
chr1:229460315 | C | A | 30 | a0001c0001t0001g0008 a0001c0001t0001g0045 a0001c0001t0001g0099 others(27): Show |
31 | HG00738.hp1 HG01074.hp1 HG01515.hp2 others(28): Show |
intron_variant | MODIFIER | c.2844+296G>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 20/25 | chr1 | 229460315 | |||||||
chr1:229460442 | A | G | 1 | a0001c0001t0001g0062 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2844+169T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 20/25 | chr1 | 229460442 | |||||||
chr1:229460513 | A | G | 83 | a0002c0002t0002g0009 a0002c0002t0002g0214 a0002c0002t0002g0215 others(80): Show |
84 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.2844+98T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 20/25 | chr1 | 229460513 | |||||||
chr1:229460818 | C | T | 2 | a0001c0001t0001g0130 a0001c0001t0001g0210 |
2 | HG00735.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.2686-49G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 19/25 | chr1 | 229460818 | |||||||
chr1:229460996 | A | C | 1 | a0001c0001t0001g0089 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2686-227T>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 19/25 | chr1 | 229460996 | |||||||
chr1:229461004 | G | A | 1 | a0003c0003t0003g0113 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2686-235C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 19/25 | chr1 | 229461004 | |||||||
chr1:229461037 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2686-268G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 19/25 | chr1 | 229461037 | |||||||
chr1:229461246 | T | C | 2 | a0003c0011t0009g0136 a0003c0011t0009g0137 |
2 | HG01106.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2686-477A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 19/25 | chr1 | 229461246 | |||||||
chr1:229461319 | A | T | 2 | a0001c0001t0001g0084 a0001c0001t0001g0091 |
2 | NA19002.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.2686-550T>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 19/25 | chr1 | 229461319 | |||||||
chr1:229461409 | G | A | 2 | a0001c0001t0001g0057 a0001c0001t0001g0068 |
2 | HG02630.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2686-640C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 19/25 | chr1 | 229461409 | |||||||
chr1:229461531 | C | T | 14 | a0004c0004t0003g0216 a0004c0004t0003g0220 a0004c0004t0003g0225 others(11): Show |
14 | HG01123.hp2 HG01167.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.2686-762G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 19/25 | chr1 | 229461531 | |||||||
chr1:229461621 | A | G | 7 | a0001c0001t0004g0147 a0003c0003t0004g0118 a0003c0003t0004g0119 others(4): Show |
7 | HG02280.hp1 HG02717.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.2686-852T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 19/25 | chr1 | 229461621 | |||||||
chr1:229461641 | A | C | 3 | a0001c0001t0001g0041 a0001c0001t0001g0046 a0001c0001t0001g0107 |
3 | NA18951.hp2 NA19000.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.2686-872T>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 19/25 | chr1 | 229461641 | |||||||
chr1:229461746 | T | C | 1 | a0002c0002t0002g0262 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2686-977A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 19/25 | chr1 | 229461746 | |||||||
chr1:229461848 | T | C | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | HG01074.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.2686-1079A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 19/25 | chr1 | 229461848 | |||||||
chr1:229461880 | T | A | 106 | a0001c0001t0004g0147 a0002c0002t0002g0009 a0002c0002t0002g0214 others(103): Show |
107 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.2686-1111A>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 19/25 | chr1 | 229461880 | |||||||
chr1:229461887 | C | CT | 7 | a0003c0003t0007g0263 a0003c0003t0007g0264 a0003c0003t0007g0265 others(4): Show |
7 | HG01261.hp1 HG02630.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.2686-1119dupA | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 19/25 | chr1 | 229461887 | |||||||
chr1:229461887 | C | CTT | 10 | a0003c0011t0009g0136 a0003c0011t0009g0137 a0005c0006t0001g0012 others(7): Show |
10 | HG01106.hp2 HG02451.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.2686-1120_2686-111 others(6): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 19/25 | chr1 | 229461887 | |||||||
chr1:229461948 | A | G | 75 | a0002c0002t0002g0009 a0002c0002t0002g0214 a0002c0002t0002g0215 others(72): Show |
76 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.2686-1179T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 19/25 | chr1 | 229461948 | |||||||
chr1:229461952 | T | C | 106 | a0001c0001t0004g0147 a0002c0002t0002g0009 a0002c0002t0002g0214 others(103): Show |
107 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.2686-1183A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 19/25 | chr1 | 229461952 | |||||||
chr1:229461953 | G | A | 14 | a0003c0003t0007g0263 a0003c0003t0007g0264 a0003c0003t0007g0265 others(11): Show |
14 | HG02622.hp1 HG02630.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.2686-1184C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 19/25 | chr1 | 229461953 | |||||||
chr1:229462032 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2686-1263G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 19/25 | chr1 | 229462032 | |||||||
chr1:229462040 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2686-1271A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 19/25 | chr1 | 229462040 | |||||||
chr1:229462095 | G | A | 1 | a0003c0003t0002g0116 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2686-1326C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 19/25 | chr1 | 229462095 | |||||||
chr1:229462169 | C | T | 29 | a0001c0001t0004g0147 a0003c0003t0004g0106 a0003c0003t0004g0108 others(26): Show |
29 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(26): Show |
intron_variant | MODIFIER | c.2685+1374G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 19/25 | chr1 | 229462169 | |||||||
chr1:229462207 | A | C | 1 | a0006c0008t0004g0021 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2685+1336T>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 19/25 | chr1 | 229462207 | |||||||
chr1:229462466 | C | G | 2 | a0001c0007t0001g0171 a0001c0007t0001g0172 |
2 | HG01243.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.2685+1077G>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 19/25 | chr1 | 229462466 | |||||||
chr1:229462472 | T | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0054 a0001c0001t0014g0039 |
3 | HG02145.hp2 HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2685+1071A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 19/25 | chr1 | 229462472 | |||||||
chr1:229462564 | AT | A | 5 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0212 others(2): Show |
5 | HG01167.hp1 HG02896.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2685+978delA | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 19/25 | chr1 | 229462564 | |||||||
chr1:229462585 | A | AG | 16 | a0003c0003t0007g0263 a0003c0003t0007g0264 a0003c0003t0007g0265 others(13): Show |
16 | HG01106.hp2 HG02451.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.2685+957dupC | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 19/25 | chr1 | 229462585 | |||||||
chr1:229462747 | G | A | 1 | a0003c0003t0001g0023 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2685+796C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 19/25 | chr1 | 229462747 | |||||||
chr1:229463008 | G | A | 1 | a0002c0002t0011g0247 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2685+535C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 19/25 | chr1 | 229463008 | |||||||
chr1:229463170 | C | T | 44 | a0002c0002t0002g0009 a0002c0002t0002g0214 a0002c0002t0002g0215 others(41): Show |
45 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.2685+373G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 19/25 | chr1 | 229463170 | |||||||
chr1:229463208 | G | A | 16 | a0004c0004t0003g0216 a0004c0004t0003g0220 a0004c0004t0003g0225 others(13): Show |
16 | HG01123.hp2 HG01167.hp2 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.2685+335C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 19/25 | chr1 | 229463208 | |||||||
chr1:229463289 | C | A | 1 | a0003c0003t0004g0115 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2685+254G>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 19/25 | chr1 | 229463289 | |||||||
chr1:229463320 | A | C | 14 | a0003c0003t0007g0263 a0003c0003t0007g0264 a0003c0003t0007g0265 others(11): Show |
14 | HG02622.hp1 HG02630.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.2685+223T>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 19/25 | chr1 | 229463320 | |||||||
chr1:229463468 | A | C | 1 | a0001c0001t0016g0038 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2685+75T>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 19/25 | chr1 | 229463468 | |||||||
chr1:229463478 | T | C | 44 | a0002c0002t0002g0009 a0002c0002t0002g0214 a0002c0002t0002g0215 others(41): Show |
45 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.2685+65A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 19/25 | chr1 | 229463478 | |||||||
chr1:229463692 | A | C | 31 | a0001c0001t0004g0147 a0003c0003t0004g0106 a0003c0003t0004g0108 others(28): Show |
31 | HG01106.hp2 HG01243.hp1 HG01516.hp1 others(28): Show |
intron_variant | MODIFIER | c.2552-16T>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 18/25 | chr1 | 229463692 | |||||||
chr1:229463903 | T | C | 1 | a0002c0002t0002g0221 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2552-227A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 18/25 | chr1 | 229463903 | |||||||
chr1:229463950 | C | T | 1 | a0003c0003t0003g0113 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2552-274G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 18/25 | chr1 | 229463950 | |||||||
chr1:229464008 | G | C | 73 | a0001c0001t0004g0147 a0002c0002t0002g0009 a0002c0002t0002g0214 others(70): Show |
74 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.2552-332C>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 18/25 | chr1 | 229464008 | |||||||
chr1:229464009 | G | A | 1 | a0006c0008t0004g0024 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2552-333C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 18/25 | chr1 | 229464009 | |||||||
chr1:229464193 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2551+431G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 18/25 | chr1 | 229464193 | |||||||
chr1:229464349 | C | T | 1 | a0003c0003t0003g0134 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2551+275G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 18/25 | chr1 | 229464349 | |||||||
chr1:229464379 | G | C | 1 | a0001c0001t0014g0039 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2551+245C>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 18/25 | chr1 | 229464379 | |||||||
chr1:229464441 | A | G | 1 | a0002c0015t0005g0031 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2551+183T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 18/25 | chr1 | 229464441 | |||||||
chr1:229464456 | G | A | 5 | a0003c0003t0007g0263 a0003c0003t0007g0264 a0003c0003t0007g0265 others(2): Show |
5 | HG02630.hp1 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2551+168C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 18/25 | chr1 | 229464456 | |||||||
chr1:229464460 | T | C | 1 | a0010c0016t0003g0114 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2551+164A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 18/25 | chr1 | 229464460 | |||||||
chr1:229464535 | C | T | 1 | a0001c0001t0008g0164 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2551+89G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 18/25 | chr1 | 229464535 | |||||||
chr1:229464589 | A | C | 74 | a0002c0002t0002g0009 a0002c0002t0002g0214 a0002c0002t0002g0215 others(71): Show |
75 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.2551+35T>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 18/25 | chr1 | 229464589 | |||||||
chr1:229465137 | T | C | 14 | a0003c0003t0007g0263 a0003c0003t0007g0264 a0003c0003t0007g0265 others(11): Show |
14 | HG02622.hp1 HG02630.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.2300-262A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 17/25 | chr1 | 229465137 | |||||||
chr1:229465267 | C | A | 103 | a0001c0001t0004g0147 a0002c0002t0002g0009 a0002c0002t0002g0214 others(100): Show |
104 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.2299+153G>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 17/25 | chr1 | 229465267 | |||||||
chr1:229465288 | G | C | 8 | a0005c0006t0001g0012 a0005c0006t0001g0014 a0005c0006t0001g0015 others(5): Show |
8 | HG02622.hp1 HG02647.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.2299+132C>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 17/25 | chr1 | 229465288 | |||||||
chr1:229465576 | T | C | 2 | a0003c0003t0001g0050 a0003c0003t0001g0209 |
2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2200-57A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 16/25 | chr1 | 229465576 | |||||||
chr1:229465869 | C | A | 14 | a0001c0001t0004g0147 a0003c0003t0004g0106 a0003c0003t0004g0108 others(11): Show |
14 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.2200-350G>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 16/25 | chr1 | 229465869 | |||||||
chr1:229465892 | C | CA | 51 | a0001c0001t0001g0058 a0001c0001t0001g0093 a0001c0001t0001g0131 others(48): Show |
52 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.2200-374dupT | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 16/25 | chr1 | 229465892 | |||||||
chr1:229465892 | C | CAA | 32 | a0002c0005t0005g0022 a0002c0005t0005g0025 a0002c0005t0005g0026 others(29): Show |
32 | HG01106.hp2 HG01123.hp2 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.2200-375_2200-374d others(4): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 16/25 | chr1 | 229465892 | |||||||
chr1:229465892 | CA | C | 8 | a0005c0006t0001g0012 a0005c0006t0001g0014 a0005c0006t0001g0015 others(5): Show |
8 | HG02622.hp1 HG02647.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.2200-374delT | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 16/25 | chr1 | 229465892 | |||||||
chr1:229465926 | G | A | 110 | a0001c0001t0004g0147 a0002c0002t0001g0242 a0002c0002t0002g0009 others(107): Show |
111 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.2200-407C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 16/25 | chr1 | 229465926 | |||||||
chr1:229466129 | G | A | 15 | a0001c0001t0004g0147 a0003c0003t0007g0263 a0003c0003t0007g0264 others(12): Show |
15 | HG02622.hp1 HG02630.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.2199+505C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 16/25 | chr1 | 229466129 | |||||||
chr1:229466209 | T | G | 17 | a0001c0001t0004g0147 a0003c0003t0007g0263 a0003c0003t0007g0264 others(14): Show |
17 | HG01106.hp2 HG02451.hp1 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.2199+425A>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 16/25 | chr1 | 229466209 | |||||||
chr1:229466253 | G | A | 6 | a0003c0003t0004g0118 a0003c0003t0004g0119 a0003c0003t0004g0120 others(3): Show |
6 | HG02280.hp1 HG02965.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.2199+381C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 16/25 | chr1 | 229466253 | |||||||
chr1:229466285 | T | A | 1 | a0001c0001t0001g0064 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2199+349A>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 16/25 | chr1 | 229466285 | |||||||
chr1:229466333 | A | C | 107 | a0001c0001t0004g0147 a0002c0002t0001g0242 a0002c0002t0002g0009 others(104): Show |
108 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.2199+301T>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 16/25 | chr1 | 229466333 | |||||||
chr1:229466334 | GA | G | 178 | a0001c0001t0001g0008 a0001c0001t0001g0041 a0001c0001t0001g0044 others(175): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.2199+299delT | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 16/25 | chr1 | 229466334 | |||||||
chr1:229466481 | A | G | 1 | a0002c0002t0002g0236 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2199+153T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 16/25 | chr1 | 229466481 | |||||||
chr1:229466537 | C | A | 90 | a0001c0001t0004g0147 a0002c0002t0001g0242 a0002c0002t0002g0009 others(87): Show |
91 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.2199+97G>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 16/25 | chr1 | 229466537 | |||||||
chr1:229466996 | T | TTTTA | 182 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0044 others(179): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.2077-244_2077-241d others(6): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 15/25 | chr1 | 229466996 | |||||||
chr1:229467070 | A | C | 46 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(43): Show |
47 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.2077-314T>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 15/25 | chr1 | 229467070 | |||||||
chr1:229467348 | C | G | 1 | a0003c0003t0003g0134 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2077-592G>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 15/25 | chr1 | 229467348 | |||||||
chr1:229467372 | A | T | 1 | a0001c0001t0001g0070 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2077-616T>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 15/25 | chr1 | 229467372 | |||||||
chr1:229467643 | C | CTA | 15 | a0001c0001t0004g0147 a0003c0003t0007g0263 a0003c0003t0007g0264 others(12): Show |
15 | HG02622.hp1 HG02630.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.2077-889_2077-888d others(4): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 15/25 | chr1 | 229467643 | |||||||
chr1:229467797 | C | A | 1 | a0001c0001t0001g0139 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2077-1041G>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 15/25 | chr1 | 229467797 | |||||||
chr1:229467857 | C | A | 15 | a0001c0001t0004g0147 a0003c0003t0007g0263 a0003c0003t0007g0264 others(12): Show |
15 | HG02622.hp1 HG02630.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.2077-1101G>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 15/25 | chr1 | 229467857 | |||||||
chr1:229467918 | A | G | 1 | a0003c0003t0004g0118 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2077-1162T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 15/25 | chr1 | 229467918 | |||||||
chr1:229467923 | C | CA | 13 | a0001c0001t0001g0047 a0001c0001t0001g0060 a0001c0001t0001g0063 others(10): Show |
13 | HG00639.hp1 HG00639.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.2077-1168dupT | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 15/25 | chr1 | 229467923 | |||||||
chr1:229467923 | C | CAA | 14 | a0003c0003t0004g0106 a0003c0003t0004g0108 a0003c0003t0004g0109 others(11): Show |
14 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.2077-1169_2077-116 others(6): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 15/25 | chr1 | 229467923 | |||||||
chr1:229468067 | T | C | 1 | a0001c0001t0001g0201 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2077-1311A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 15/25 | chr1 | 229468067 | |||||||
chr1:229468111 | G | A | 1 | a0001c0007t0001g0157 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2077-1355C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 15/25 | chr1 | 229468111 | |||||||
chr1:229468214 | A | C | 1 | a0001c0001t0001g0180 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2077-1458T>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 15/25 | chr1 | 229468214 | |||||||
chr1:229468245 | T | C | 1 | a0003c0003t0003g0134 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2077-1489A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 15/25 | chr1 | 229468245 | |||||||
chr1:229468394 | G | A | 1 | a0001c0001t0001g0191 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2077-1638C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 15/25 | chr1 | 229468394 | |||||||
chr1:229468438 | C | T | 2 | a0003c0003t0007g0265 a0003c0003t0007g0266 |
2 | HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2077-1682G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 15/25 | chr1 | 229468438 | |||||||
chr1:229468733 | T | G | 1 | a0003c0003t0003g0113 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2076+1847A>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 15/25 | chr1 | 229468733 | |||||||
chr1:229468748 | T | C | 1 | a0003c0003t0001g0023 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2076+1832A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 15/25 | chr1 | 229468748 | |||||||
chr1:229468912 | C | T | 15 | a0001c0001t0004g0147 a0003c0003t0007g0263 a0003c0003t0007g0264 others(12): Show |
15 | HG02622.hp1 HG02630.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.2076+1668G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 15/25 | chr1 | 229468912 | |||||||
chr1:229468929 | G | A | 4 | a0001c0001t0001g0150 a0001c0001t0001g0176 a0001c0001t0001g0177 others(1): Show |
4 | HG01074.hp1 HG02293.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.2076+1651C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 15/25 | chr1 | 229468929 | |||||||
chr1:229468942 | G | T | 74 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(71): Show |
75 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.2076+1638C>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 15/25 | chr1 | 229468942 | |||||||
chr1:229469049 | C | T | 13 | a0002c0005t0005g0022 a0002c0005t0005g0025 a0002c0005t0005g0026 others(10): Show |
13 | HG01261.hp2 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.2076+1531G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 15/25 | chr1 | 229469049 | |||||||
chr1:229469175 | G | T | 7 | a0001c0001t0004g0147 a0003c0003t0007g0263 a0003c0003t0007g0264 others(4): Show |
7 | HG02630.hp1 HG02717.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.2076+1405C>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 15/25 | chr1 | 229469175 | |||||||
chr1:229469293 | C | T | 1 | a0008c0013t0003g0013 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2076+1287G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 15/25 | chr1 | 229469293 | |||||||
chr1:229469506 | A | G | 1 | a0001c0001t0001g0188 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2076+1074T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 15/25 | chr1 | 229469506 | |||||||
chr1:229469805 | C | G | 1 | a0006c0008t0004g0021 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2076+775G>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 15/25 | chr1 | 229469805 | |||||||
chr1:229469870 | A | G | 29 | a0002c0005t0005g0022 a0002c0005t0005g0025 a0002c0005t0005g0026 others(26): Show |
29 | HG01123.hp2 HG01167.hp2 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.2076+710T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 15/25 | chr1 | 229469870 | |||||||
chr1:229469910 | C | T | 1 | a0006c0008t0004g0024 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2076+670G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 15/25 | chr1 | 229469910 | |||||||
chr1:229469952 | G | A | 29 | a0002c0005t0005g0022 a0002c0005t0005g0025 a0002c0005t0005g0026 others(26): Show |
29 | HG01123.hp2 HG01167.hp2 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.2076+628C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 15/25 | chr1 | 229469952 | |||||||
chr1:229470247 | A | T | 2 | a0003c0003t0006g0123 a0003c0003t0006g0124 |
2 | HG02257.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2076+333T>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 15/25 | chr1 | 229470247 | |||||||
chr1:229470284 | T | C | 1 | a0002c0002t0002g0245 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2076+296A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 15/25 | chr1 | 229470284 | |||||||
chr1:229470287 | C | CA | 49 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(46): Show |
50 | HG00140.hp2 HG00438.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.2076+292dupT | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 15/25 | chr1 | 229470287 | |||||||
chr1:229470287 | CAA | C | 45 | a0001c0001t0004g0147 a0002c0005t0005g0022 a0002c0005t0005g0025 others(42): Show |
45 | HG01106.hp2 HG01167.hp2 HG01261.hp1 others(42): Show |
intron_variant | MODIFIER | c.2076+291_2076+292d others(4): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 15/25 | chr1 | 229470287 | |||||||
chr1:229470309 | C | A | 1 | a0008c0013t0003g0013 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2076+271G>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 15/25 | chr1 | 229470309 | |||||||
chr1:229470478 | G | T | 4 | a0001c0007t0001g0157 a0001c0007t0001g0171 a0001c0007t0001g0172 others(1): Show |
4 | HG00099.hp2 HG01243.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.2076+102C>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 15/25 | chr1 | 229470478 | |||||||
chr1:229470506 | C | T | 2 | a0003c0003t0004g0132 a0003c0003t0004g0133 |
2 | HG02280.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2076+74G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 15/25 | chr1 | 229470506 | |||||||
chr1:229470839 | A | C | 1 | a0002c0002t0002g0233 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1852-35T>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229470839 | |||||||
chr1:229471195 | C | A | 1 | a0001c0001t0001g0064 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1852-391G>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229471195 | |||||||
chr1:229471253 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1852-449G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229471253 | |||||||
chr1:229471455 | T | C | 15 | a0001c0001t0004g0147 a0003c0003t0007g0263 a0003c0003t0007g0264 others(12): Show |
15 | HG02622.hp1 HG02630.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.1852-651A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229471455 | |||||||
chr1:229471759 | C | A | 45 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(42): Show |
46 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.1852-955G>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229471759 | |||||||
chr1:229471946 | T | C | 16 | a0004c0004t0003g0216 a0004c0004t0003g0220 a0004c0004t0003g0225 others(13): Show |
16 | HG01123.hp2 HG01167.hp2 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.1852-1142A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229471946 | |||||||
chr1:229471979 | T | C | 1 | a0003c0003t0001g0209 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1852-1175A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229471979 | |||||||
chr1:229472005 | C | A | 2 | a0003c0003t0001g0050 a0003c0003t0001g0209 |
2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1852-1201G>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229472005 | |||||||
chr1:229472085 | C | T | 7 | a0001c0001t0004g0147 a0003c0003t0007g0263 a0003c0003t0007g0264 others(4): Show |
7 | HG02630.hp1 HG02717.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1852-1281G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229472085 | |||||||
chr1:229472095 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1852-1291C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229472095 | |||||||
chr1:229472102 | G | A | 13 | a0002c0005t0005g0022 a0002c0005t0005g0025 a0002c0005t0005g0026 others(10): Show |
13 | HG01261.hp2 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1852-1298C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229472102 | |||||||
chr1:229472250 | C | T | 1 | a0008c0013t0003g0013 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1852-1446G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229472250 | |||||||
chr1:229472318 | C | CA | 12 | a0001c0001t0001g0052 a0001c0001t0001g0089 a0001c0001t0001g0095 others(9): Show |
12 | HG00544.hp1 HG00735.hp1 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.1852-1515dupT | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229472318 | |||||||
chr1:229472318 | CA | C | 84 | a0001c0001t0001g0037 a0001c0001t0001g0149 a0001c0001t0001g0155 others(81): Show |
85 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(82): Show |
intron_variant | MODIFIER | c.1852-1515delT | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229472318 | |||||||
chr1:229472356 | T | G | 1 | a0003c0003t0013g0267 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1852-1552A>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229472356 | |||||||
chr1:229472419 | G | A | 51 | a0001c0001t0004g0147 a0002c0005t0005g0022 a0002c0005t0005g0025 others(48): Show |
51 | HG01123.hp2 HG01167.hp2 HG01243.hp1 others(48): Show |
intron_variant | MODIFIER | c.1852-1615C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229472419 | |||||||
chr1:229472534 | G | T | 29 | a0002c0005t0005g0022 a0002c0005t0005g0025 a0002c0005t0005g0026 others(26): Show |
29 | HG01123.hp2 HG01167.hp2 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.1852-1730C>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229472534 | |||||||
chr1:229472542 | T | C | 102 | a0001c0001t0004g0147 a0002c0002t0001g0242 a0002c0002t0002g0009 others(99): Show |
103 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.1852-1738A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229472542 | |||||||
chr1:229472628 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1852-1824T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229472628 | |||||||
chr1:229472707 | C | CAT | 18 | a0001c0001t0001g0049 a0001c0001t0001g0053 a0001c0001t0001g0064 others(15): Show |
18 | HG00544.hp1 HG02015.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1852-1905_1852-190 others(6): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229472707 | |||||||
chr1:229472707 | C | CATACATA others(3): Show |
15 | a0002c0005t0005g0022 a0002c0005t0005g0030 a0002c0005t0005g0033 others(12): Show |
15 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.1852-1904_1852-190 others(14): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229472707 | |||||||
chr1:229472707 | C | CATACATA others(5): Show |
17 | a0003c0003t0007g0266 a0004c0004t0003g0216 a0004c0004t0003g0220 others(14): Show |
17 | HG01123.hp2 HG01167.hp2 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.1852-1904_1852-190 others(16): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229472707 | |||||||
chr1:229472707 | C | CATACATA others(7): Show |
4 | a0001c0001t0004g0147 a0003c0003t0007g0263 a0003c0003t0007g0265 others(1): Show |
4 | HG02630.hp1 HG02717.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1852-1904_1852-190 others(18): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229472707 | |||||||
chr1:229472707 | C | CATACATA others(9): Show |
5 | a0002c0005t0005g0026 a0002c0005t0005g0029 a0002c0005t0005g0032 others(2): Show |
5 | HG01261.hp2 HG01884.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.1852-1904_1852-190 others(20): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229472707 | |||||||
chr1:229472707 | C | CATACATA others(11): Show |
3 | a0002c0005t0005g0025 a0002c0005t0005g0027 a0002c0005t0005g0028 |
3 | HG03579.hp2 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1852-1904_1852-190 others(22): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229472707 | |||||||
chr1:229472707 | C | CATACATA others(17): Show |
1 | a0003c0003t0004g0120 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1852-1904_1852-190 others(28): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229472707 | |||||||
chr1:229472707 | C | CATACATA others(25): Show |
2 | a0003c0003t0004g0132 a0003c0003t0004g0133 |
2 | HG02280.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1852-1904_1852-190 others(36): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229472707 | |||||||
chr1:229472707 | C | CATACATA others(33): Show |
1 | a0003c0003t0004g0121 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1852-1904_1852-190 others(44): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229472707 | |||||||
chr1:229472707 | C | CATACATA others(37): Show |
1 | a0003c0003t0004g0118 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1852-1904_1852-190 others(48): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229472707 | |||||||
chr1:229472707 | C | CATACATA others(43): Show |
1 | a0003c0003t0004g0119 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1852-1904_1852-190 others(54): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229472707 | |||||||
chr1:229472707 | C | CATAT | 7 | a0005c0006t0001g0012 a0005c0006t0001g0014 a0005c0006t0001g0016 others(4): Show |
7 | HG02647.hp1 HG02809.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1852-1907_1852-190 others(8): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229472707 | |||||||
chr1:229472707 | C | CATATACA others(5): Show |
1 | a0003c0003t0001g0050 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1852-1904_1852-190 others(16): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229472707 | |||||||
chr1:229472707 | C | CATATATA others(5): Show |
1 | a0003c0003t0001g0209 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1852-1915_1852-190 others(16): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229472707 | |||||||
chr1:229472707 | C | CATATATA others(13): Show |
2 | a0003c0003t0006g0123 a0003c0003t0006g0124 |
2 | HG02257.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1852-1923_1852-190 others(24): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229472707 | |||||||
chr1:229472707 | C | CATATATA others(15): Show |
4 | a0002c0002t0002g0249 a0003c0003t0006g0126 a0003c0003t0006g0128 others(1): Show |
4 | HG00140.hp2 HG02258.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1852-1904_1852-190 others(26): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229472707 | |||||||
chr1:229472707 | C | CATATATA others(17): Show |
7 | a0002c0002t0002g0215 a0002c0002t0002g0226 a0002c0002t0002g0240 others(4): Show |
7 | HG00741.hp1 HG02015.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1852-1904_1852-190 others(28): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229472707 | |||||||
chr1:229472707 | C | CATATATA others(19): Show |
2 | a0002c0002t0002g0254 a0002c0002t0002g0256 |
2 | HG01074.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.1852-1904_1852-190 others(30): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229472707 | |||||||
chr1:229472707 | C | CATATATA others(21): Show |
10 | a0002c0002t0002g0221 a0002c0002t0002g0222 a0002c0002t0002g0233 others(7): Show |
10 | HG01106.hp1 HG01358.hp1 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.1852-1904_1852-190 others(32): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229472707 | |||||||
chr1:229472707 | C | CATATATA others(25): Show |
3 | a0002c0002t0001g0242 a0002c0002t0002g0262 a0003c0011t0009g0136 |
3 | HG01106.hp2 HG02895.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1852-1904_1852-190 others(36): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229472707 | |||||||
chr1:229472707 | C | CATATATA others(27): Show |
7 | a0002c0002t0002g0219 a0002c0002t0002g0224 a0002c0002t0002g0234 others(4): Show |
7 | HG00438.hp2 HG01071.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1852-1904_1852-190 others(38): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229472707 | |||||||
chr1:229472707 | C | CATATATA others(29): Show |
4 | a0002c0002t0002g0217 a0002c0002t0002g0250 a0002c0002t0010g0232 others(1): Show |
4 | HG00733.hp1 HG01168.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1852-1904_1852-190 others(40): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229472707 | |||||||
chr1:229472707 | C | CATATATA others(31): Show |
5 | a0002c0002t0002g0009 a0002c0002t0002g0218 a0002c0002t0002g0227 others(2): Show |
6 | HG00099.hp1 HG01256.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1852-1904_1852-190 others(42): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229472707 | |||||||
chr1:229472707 | C | CATATATA others(33): Show |
1 | a0002c0002t0002g0239 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1852-1904_1852-190 others(44): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229472707 | |||||||
chr1:229472707 | C | CATATATA others(35): Show |
2 | a0002c0002t0002g0214 a0009c0014t0002g0248 |
2 | HG00738.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1852-1904_1852-190 others(46): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229472707 | |||||||
chr1:229472727 | T | TATATATA others(20): Show |
1 | a0002c0002t0002g0238 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1852-1924_1852-192 others(31): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229472727 | |||||||
chr1:229472728 | G | A | 14 | a0003c0003t0004g0106 a0003c0003t0004g0108 a0003c0003t0004g0109 others(11): Show |
14 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.1852-1924C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229472728 | |||||||
chr1:229472825 | A | G | 1 | a0006c0008t0004g0024 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1852-2021T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229472825 | |||||||
chr1:229473039 | G | A | 2 | a0003c0011t0009g0136 a0003c0011t0009g0137 |
2 | HG01106.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1852-2235C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229473039 | |||||||
chr1:229473091 | C | A | 4 | a0001c0001t0001g0062 a0001c0001t0001g0088 a0001c0012t0001g0075 others(1): Show |
4 | NA18948.hp1 NA18957.hp2 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.1852-2287G>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229473091 | |||||||
chr1:229473165 | T | C | 1 | a0003c0003t0006g0124 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1852-2361A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229473165 | |||||||
chr1:229473243 | G | A | 29 | a0002c0005t0005g0022 a0002c0005t0005g0025 a0002c0005t0005g0026 others(26): Show |
29 | HG01123.hp2 HG01167.hp2 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.1851+2395C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229473243 | |||||||
chr1:229473263 | C | A | 21 | a0001c0001t0004g0147 a0003c0003t0004g0106 a0003c0003t0004g0108 others(18): Show |
21 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.1851+2375G>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229473263 | |||||||
chr1:229473286 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1851+2352A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229473286 | |||||||
chr1:229473341 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1851+2297C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229473341 | |||||||
chr1:229473397 | A | G | 1 | a0006c0008t0004g0021 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1851+2241T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229473397 | |||||||
chr1:229473515 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1851+2123C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229473515 | |||||||
chr1:229473534 | G | A | 1 | a0003c0003t0003g0134 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1851+2104C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229473534 | |||||||
chr1:229473599 | A | T | 1 | a0006c0008t0004g0021 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1851+2039T>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229473599 | |||||||
chr1:229473672 | G | T | 36 | a0001c0001t0004g0147 a0002c0005t0005g0022 a0002c0005t0005g0025 others(33): Show |
36 | HG01123.hp2 HG01167.hp2 HG01261.hp1 others(33): Show |
intron_variant | MODIFIER | c.1851+1966C>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229473672 | |||||||
chr1:229473688 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1851+1950G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229473688 | |||||||
chr1:229473714 | A | G | 110 | a0001c0001t0004g0147 a0002c0002t0001g0242 a0002c0002t0002g0009 others(107): Show |
111 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.1851+1924T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229473714 | |||||||
chr1:229473721 | G | A | 14 | a0003c0003t0004g0106 a0003c0003t0004g0108 a0003c0003t0004g0109 others(11): Show |
14 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.1851+1917C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229473721 | |||||||
chr1:229473735 | C | T | 1 | a0002c0002t0002g0222 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1851+1903G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229473735 | |||||||
chr1:229473859 | G | C | 14 | a0003c0003t0004g0106 a0003c0003t0004g0108 a0003c0003t0004g0109 others(11): Show |
14 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.1851+1779C>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229473859 | |||||||
chr1:229473904 | AT | A | 29 | a0002c0005t0005g0022 a0002c0005t0005g0025 a0002c0005t0005g0026 others(26): Show |
29 | HG01123.hp2 HG01167.hp2 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.1851+1733delA | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229473904 | |||||||
chr1:229473905 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1851+1733A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229473905 | |||||||
chr1:229473970 | C | T | 29 | a0002c0005t0005g0022 a0002c0005t0005g0025 a0002c0005t0005g0026 others(26): Show |
29 | HG01123.hp2 HG01167.hp2 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.1851+1668G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229473970 | |||||||
chr1:229474048 | A | C | 1 | a0003c0003t0013g0267 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1851+1590T>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229474048 | |||||||
chr1:229474113 | A | T | 13 | a0002c0005t0005g0022 a0002c0005t0005g0025 a0002c0005t0005g0026 others(10): Show |
13 | HG01261.hp2 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1851+1525T>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229474113 | |||||||
chr1:229474118 | C | T | 29 | a0002c0005t0005g0022 a0002c0005t0005g0025 a0002c0005t0005g0026 others(26): Show |
29 | HG01123.hp2 HG01167.hp2 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.1851+1520G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229474118 | |||||||
chr1:229474119 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1851+1519C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229474119 | |||||||
chr1:229474120 | A | T | 29 | a0001c0001t0004g0147 a0003c0003t0004g0106 a0003c0003t0004g0108 others(26): Show |
29 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(26): Show |
intron_variant | MODIFIER | c.1851+1518T>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229474120 | |||||||
chr1:229474322 | A | G | 15 | a0001c0001t0004g0147 a0003c0003t0007g0263 a0003c0003t0007g0264 others(12): Show |
15 | HG02622.hp1 HG02630.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.1851+1316T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229474322 | |||||||
chr1:229474382 | C | A | 29 | a0001c0001t0004g0147 a0003c0003t0004g0106 a0003c0003t0004g0108 others(26): Show |
29 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(26): Show |
intron_variant | MODIFIER | c.1851+1256G>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229474382 | |||||||
chr1:229474403 | TA | T | 29 | a0002c0005t0005g0022 a0002c0005t0005g0025 a0002c0005t0005g0026 others(26): Show |
29 | HG01123.hp2 HG01167.hp2 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.1851+1234delT | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229474403 | |||||||
chr1:229474424 | A | G | 1 | a0004c0004t0003g0252 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1851+1214T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229474424 | |||||||
chr1:229474460 | A | C | 1 | a0003c0003t0001g0023 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1851+1178T>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229474460 | |||||||
chr1:229474512 | T | C | 1 | a0008c0013t0003g0013 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1851+1126A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229474512 | |||||||
chr1:229474770 | G | A | 1 | a0002c0002t0002g0246 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1851+868C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229474770 | |||||||
chr1:229474844 | T | C | 2 | a0003c0011t0009g0136 a0003c0011t0009g0137 |
2 | HG01106.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1851+794A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229474844 | |||||||
chr1:229474918 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1851+720G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229474918 | |||||||
chr1:229474935 | T | C | 1 | a0001c0001t0001g0177 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1851+703A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229474935 | |||||||
chr1:229475098 | C | CAATA | 5 | a0001c0001t0004g0147 a0003c0003t0007g0263 a0003c0003t0007g0264 others(2): Show |
5 | HG02630.hp1 HG02717.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1851+536_1851+539d others(6): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229475098 | |||||||
chr1:229475098 | CAATAAAT others(1): Show |
C | 8 | a0005c0006t0001g0012 a0005c0006t0001g0014 a0005c0006t0001g0015 others(5): Show |
8 | HG02622.hp1 HG02647.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1851+532_1851+539d others(10): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229475098 | |||||||
chr1:229475125 | A | T | 1 | a0003c0003t0003g0113 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1851+513T>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229475125 | |||||||
chr1:229475126 | C | A | 1 | a0003c0003t0003g0113 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1851+512G>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229475126 | |||||||
chr1:229475130 | C | T | 1 | a0003c0003t0013g0267 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1851+508G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229475130 | |||||||
chr1:229475165 | T | C | 14 | a0003c0003t0004g0106 a0003c0003t0004g0108 a0003c0003t0004g0109 others(11): Show |
14 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.1851+473A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229475165 | |||||||
chr1:229475173 | G | A | 46 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(43): Show |
47 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.1851+465C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229475173 | |||||||
chr1:229475188 | G | A | 8 | a0005c0006t0001g0012 a0005c0006t0001g0014 a0005c0006t0001g0015 others(5): Show |
8 | HG02622.hp1 HG02647.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1851+450C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229475188 | |||||||
chr1:229475254 | T | G | 1 | a0001c0001t0001g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1851+384A>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229475254 | |||||||
chr1:229475277 | G | A | 21 | a0001c0001t0004g0147 a0003c0003t0004g0106 a0003c0003t0004g0108 others(18): Show |
21 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.1851+361C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229475277 | |||||||
chr1:229475297 | A | G | 2 | a0001c0001t0001g0163 a0001c0001t0001g0168 |
2 | HG03017.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1851+341T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229475297 | |||||||
chr1:229475401 | CTT | C | 4 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(1): Show |
4 | HG02055.hp2 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1851+235_1851+236d others(4): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229475401 | |||||||
chr1:229475571 | A | G | 58 | a0001c0001t0004g0147 a0002c0005t0005g0022 a0002c0005t0005g0025 others(55): Show |
58 | HG01123.hp2 HG01167.hp2 HG01243.hp1 others(55): Show |
intron_variant | MODIFIER | c.1851+67T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229475571 | |||||||
chr1:229475630 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG01943.hp1 | splice_region_variant&intron_variant | LOW | c.1851+8C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 14/25 | chr1 | 229475630 | |||||||
chr1:229475808 | C | T | 29 | a0001c0001t0004g0147 a0003c0003t0004g0106 a0003c0003t0004g0108 others(26): Show |
29 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(26): Show |
intron_variant | MODIFIER | c.1757-76G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 13/25 | chr1 | 229475808 | |||||||
chr1:229475858 | C | T | 2 | a0001c0001t0001g0010 a0005c0006t0017g0019 |
2 | HG02145.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1757-126G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 13/25 | chr1 | 229475858 | |||||||
chr1:229475875 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1757-143G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 13/25 | chr1 | 229475875 | |||||||
chr1:229475905 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1757-173G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 13/25 | chr1 | 229475905 | |||||||
chr1:229475972 | G | A | 1 | a0001c0001t0001g0199 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1757-240C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 13/25 | chr1 | 229475972 | |||||||
chr1:229475977 | G | A | 2 | a0002c0002t0010g0223 a0002c0002t0010g0232 |
2 | HG03710.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.1757-245C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 13/25 | chr1 | 229475977 | |||||||
chr1:229475979 | A | G | 29 | a0001c0001t0004g0147 a0003c0003t0004g0106 a0003c0003t0004g0108 others(26): Show |
29 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(26): Show |
intron_variant | MODIFIER | c.1757-247T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 13/25 | chr1 | 229475979 | |||||||
chr1:229475998 | C | G | 1 | a0003c0003t0013g0267 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1757-266G>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 13/25 | chr1 | 229475998 | |||||||
chr1:229476003 | G | A | 6 | a0001c0001t0004g0147 a0003c0003t0007g0263 a0003c0003t0007g0264 others(3): Show |
6 | HG02630.hp1 HG02717.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1757-271C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 13/25 | chr1 | 229476003 | |||||||
chr1:229476028 | A | T | 4 | a0003c0003t0004g0118 a0003c0003t0004g0119 a0003c0003t0004g0120 others(1): Show |
4 | HG02965.hp2 HG03041.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1757-296T>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 13/25 | chr1 | 229476028 | |||||||
chr1:229476031 | C | A | 1 | a0002c0002t0002g0219 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1757-299G>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 13/25 | chr1 | 229476031 | |||||||
chr1:229476032 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1757-300G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 13/25 | chr1 | 229476032 | |||||||
chr1:229476057 | C | T | 1 | a0003c0003t0003g0134 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1757-325G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 13/25 | chr1 | 229476057 | |||||||
chr1:229476072 | G | A | 16 | a0004c0004t0003g0216 a0004c0004t0003g0220 a0004c0004t0003g0225 others(13): Show |
16 | HG01123.hp2 HG01167.hp2 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.1757-340C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 13/25 | chr1 | 229476072 | |||||||
chr1:229476087 | G | A | 1 | a0001c0001t0001g0192 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1757-355C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 13/25 | chr1 | 229476087 | |||||||
chr1:229476339 | G | T | 1 | a0010c0016t0003g0114 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1757-607C>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 13/25 | chr1 | 229476339 | |||||||
chr1:229476384 | T | G | 14 | a0003c0003t0004g0106 a0003c0003t0004g0108 a0003c0003t0004g0109 others(11): Show |
14 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.1757-652A>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 13/25 | chr1 | 229476384 | |||||||
chr1:229476722 | A | G | 29 | a0001c0001t0004g0147 a0003c0003t0004g0106 a0003c0003t0004g0108 others(26): Show |
29 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(26): Show |
intron_variant | MODIFIER | c.1756+875T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 13/25 | chr1 | 229476722 | |||||||
chr1:229476835 | T | G | 29 | a0001c0001t0004g0147 a0003c0003t0004g0106 a0003c0003t0004g0108 others(26): Show |
29 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(26): Show |
intron_variant | MODIFIER | c.1756+762A>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 13/25 | chr1 | 229476835 | |||||||
chr1:229476928 | C | CAA | 14 | a0002c0005t0005g0022 a0002c0005t0005g0026 a0002c0005t0005g0028 others(11): Show |
14 | HG01261.hp2 HG01884.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1756+667_1756+668d others(4): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 13/25 | chr1 | 229476928 | |||||||
chr1:229476928 | C | CAAA | 17 | a0002c0005t0005g0025 a0002c0005t0005g0027 a0003c0003t0004g0106 others(14): Show |
17 | HG01123.hp2 HG01243.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.1756+666_1756+668d others(5): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 13/25 | chr1 | 229476928 | |||||||
chr1:229476928 | C | CAAAA | 15 | a0001c0001t0004g0147 a0003c0003t0004g0108 a0003c0003t0004g0110 others(12): Show |
15 | HG01167.hp2 HG01934.hp1 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.1756+665_1756+668d others(6): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 13/25 | chr1 | 229476928 | |||||||
chr1:229476930 | AAAAAAAA others(4): Show |
A | 1 | a0003c0003t0013g0267 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1756+656_1756+666d others(13): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 13/25 | chr1 | 229476930 | |||||||
chr1:229476941 | C | A | 54 | a0001c0001t0004g0147 a0002c0005t0005g0022 a0002c0005t0005g0025 others(51): Show |
54 | HG01123.hp2 HG01167.hp2 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.1756+656G>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 13/25 | chr1 | 229476941 | |||||||
chr1:229476961 | G | C | 1 | a0001c0001t0001g0061 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1756+636C>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 13/25 | chr1 | 229476961 | |||||||
chr1:229476995 | A | T | 110 | a0001c0001t0004g0147 a0002c0002t0001g0242 a0002c0002t0002g0009 others(107): Show |
111 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.1756+602T>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 13/25 | chr1 | 229476995 | |||||||
chr1:229477301 | A | G | 29 | a0001c0001t0004g0147 a0003c0003t0004g0106 a0003c0003t0004g0108 others(26): Show |
29 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(26): Show |
intron_variant | MODIFIER | c.1756+296T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 13/25 | chr1 | 229477301 | |||||||
chr1:229477384 | G | A | 1 | a0002c0002t0002g0239 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1756+213C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 13/25 | chr1 | 229477384 | |||||||
chr1:229477395 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1756+202C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 13/25 | chr1 | 229477395 | |||||||
chr1:229477439 | C | CA | 17 | a0001c0001t0001g0153 a0003c0003t0003g0134 a0004c0004t0003g0220 others(14): Show |
17 | HG01167.hp2 HG01261.hp1 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.1756+157dupT | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 13/25 | chr1 | 229477439 | |||||||
chr1:229477439 | CAA | C | 14 | a0003c0003t0004g0106 a0003c0003t0004g0108 a0003c0003t0004g0109 others(11): Show |
14 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.1756+156_1756+157d others(4): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 13/25 | chr1 | 229477439 | |||||||
chr1:229477461 | G | T | 1 | a0003c0003t0007g0263 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1756+136C>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 13/25 | chr1 | 229477461 | |||||||
chr1:229477572 | C | T | 14 | a0002c0002t0002g0215 a0002c0002t0002g0218 a0002c0002t0002g0221 others(11): Show |
14 | HG00438.hp2 HG02074.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.1756+25G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 13/25 | chr1 | 229477572 | |||||||
chr1:229477583 | T | C | 2 | a0002c0002t0001g0242 a0002c0002t0002g0009 |
3 | HG01256.hp2 HG01258.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1756+14A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 13/25 | chr1 | 229477583 | |||||||
chr1:229477931 | C | T | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | HG01074.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1593-171G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229477931 | |||||||
chr1:229478158 | A | T | 29 | a0002c0005t0005g0022 a0002c0005t0005g0025 a0002c0005t0005g0026 others(26): Show |
29 | HG01123.hp2 HG01167.hp2 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.1593-398T>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229478158 | |||||||
chr1:229478216 | A | C | 1 | a0004c0004t0003g0220 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1593-456T>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229478216 | |||||||
chr1:229478301 | T | A | 1 | a0003c0003t0001g0023 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1593-541A>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229478301 | |||||||
chr1:229478313 | G | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | NA19009.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1593-553C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229478313 | |||||||
chr1:229478454 | G | C | 2 | a0001c0001t0001g0130 a0001c0001t0001g0210 |
2 | HG00735.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1593-694C>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229478454 | |||||||
chr1:229478455 | G | T | 29 | a0002c0005t0005g0022 a0002c0005t0005g0025 a0002c0005t0005g0026 others(26): Show |
29 | HG01123.hp2 HG01167.hp2 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.1593-695C>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229478455 | |||||||
chr1:229478539 | C | T | 13 | a0002c0005t0005g0022 a0002c0005t0005g0025 a0002c0005t0005g0026 others(10): Show |
13 | HG01261.hp2 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1593-779G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229478539 | |||||||
chr1:229478550 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1593-790C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229478550 | |||||||
chr1:229478654 | A | G | 29 | a0002c0005t0005g0022 a0002c0005t0005g0025 a0002c0005t0005g0026 others(26): Show |
29 | HG01123.hp2 HG01167.hp2 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.1593-894T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229478654 | |||||||
chr1:229478715 | C | T | 107 | a0001c0001t0004g0147 a0002c0002t0001g0242 a0002c0002t0002g0009 others(104): Show |
108 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.1593-955G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229478715 | |||||||
chr1:229478732 | G | A | 1 | a0003c0003t0001g0023 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1593-972C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229478732 | |||||||
chr1:229478772 | T | C | 1 | a0003c0003t0003g0134 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1593-1012A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229478772 | |||||||
chr1:229478909 | C | T | 29 | a0002c0005t0005g0022 a0002c0005t0005g0025 a0002c0005t0005g0026 others(26): Show |
29 | HG01123.hp2 HG01167.hp2 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.1593-1149G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229478909 | |||||||
chr1:229478913 | T | C | 1 | a0003c0003t0001g0209 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1593-1153A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229478913 | |||||||
chr1:229478941 | C | A | 2 | a0001c0001t0001g0184 a0001c0001t0001g0198 |
2 | HG03710.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1593-1181G>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229478941 | |||||||
chr1:229479214 | A | C | 14 | a0002c0002t0002g0243 a0004c0004t0003g0216 a0004c0004t0003g0220 others(11): Show |
14 | HG01167.hp2 HG01261.hp1 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.1593-1454T>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229479214 | |||||||
chr1:229479328 | T | C | 4 | a0001c0001t0001g0062 a0001c0001t0001g0088 a0001c0012t0001g0075 others(1): Show |
4 | NA18948.hp1 NA18957.hp2 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.1593-1568A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229479328 | |||||||
chr1:229479485 | T | G | 2 | a0007c0010t0001g0206 a0007c0010t0001g0207 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1593-1725A>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229479485 | |||||||
chr1:229479690 | AGTG | A | 3 | a0002c0005t0005g0030 a0002c0005t0005g0034 a0002c0005t0005g0036 |
3 | HG03516.hp1 NA19043.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1593-1933_1593-193 others(7): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229479690 | |||||||
chr1:229479695 | C | A | 3 | a0002c0005t0005g0030 a0002c0005t0005g0034 a0002c0005t0005g0036 |
3 | HG03516.hp1 NA19043.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1593-1935G>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229479695 | |||||||
chr1:229479838 | T | A | 31 | a0002c0005t0005g0022 a0002c0005t0005g0025 a0002c0005t0005g0026 others(28): Show |
31 | HG01106.hp2 HG01261.hp2 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.1593-2078A>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229479838 | |||||||
chr1:229479854 | C | T | 2 | a0003c0011t0009g0136 a0003c0011t0009g0137 |
2 | HG01106.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1593-2094G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229479854 | |||||||
chr1:229480525 | G | C | 1 | a0001c0001t0001g0202 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1593-2765C>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229480525 | |||||||
chr1:229480613 | C | A | 1 | a0003c0011t0009g0137 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1593-2853G>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229480613 | |||||||
chr1:229480741 | C | T | 1 | a0003c0003t0006g0127 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1593-2981G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229480741 | |||||||
chr1:229480746 | A | G | 11 | a0005c0006t0001g0012 a0005c0006t0001g0014 a0005c0006t0001g0015 others(8): Show |
11 | HG02622.hp1 HG02647.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.1593-2986T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229480746 | |||||||
chr1:229480748 | G | A | 1 | a0003c0003t0001g0023 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1593-2988C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229480748 | |||||||
chr1:229480852 | A | AT | 25 | a0001c0001t0001g0070 a0001c0001t0001g0074 a0001c0001t0001g0162 others(22): Show |
25 | HG00609.hp1 HG01106.hp2 HG02040.hp2 others(22): Show |
intron_variant | MODIFIER | c.1593-3093dupA | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229480852 | |||||||
chr1:229480852 | A | ATT | 12 | a0003c0003t0001g0023 a0003c0003t0003g0113 a0003c0003t0004g0106 others(9): Show |
12 | HG01243.hp1 HG01516.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1593-3094_1593-309 others(6): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229480852 | |||||||
chr1:229480852 | AT | A | 60 | a0001c0001t0001g0063 a0001c0001t0001g0077 a0001c0001t0001g0102 others(57): Show |
61 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.1593-3093delA | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229480852 | |||||||
chr1:229480852 | ATT | A | 12 | a0004c0004t0003g0252 a0005c0006t0001g0012 a0005c0006t0001g0014 others(9): Show |
12 | HG02622.hp1 HG02647.hp1 HG02735.hp2 others(9): Show |
intron_variant | MODIFIER | c.1593-3094_1593-309 others(6): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229480852 | |||||||
chr1:229480946 | T | C | 73 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(70): Show |
74 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1592+3108A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229480946 | |||||||
chr1:229481011 | T | C | 109 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(106): Show |
110 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.1592+3043A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229481011 | |||||||
chr1:229481029 | C | T | 1 | a0002c0002t0002g0250 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1592+3025G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229481029 | |||||||
chr1:229481195 | G | GT | 5 | a0003c0003t0001g0023 a0003c0003t0003g0113 a0003c0011t0009g0136 others(2): Show |
5 | HG01106.hp2 HG02451.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1592+2858dupA | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229481195 | |||||||
chr1:229481285 | G | A | 1 | a0002c0002t0002g0219 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1592+2769C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229481285 | |||||||
chr1:229481459 | A | G | 1 | a0006c0008t0004g0024 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1592+2595T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229481459 | |||||||
chr1:229481511 | A | G | 1 | a0003c0003t0001g0023 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1592+2543T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229481511 | |||||||
chr1:229481647 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1592+2407G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229481647 | |||||||
chr1:229481648 | G | A | 4 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(1): Show |
4 | HG02055.hp2 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1592+2406C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229481648 | |||||||
chr1:229481684 | G | C | 10 | a0003c0003t0002g0116 a0003c0003t0002g0117 a0003c0003t0006g0122 others(7): Show |
10 | HG02257.hp1 HG02258.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1592+2370C>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229481684 | |||||||
chr1:229481698 | C | CA | 65 | a0001c0001t0001g0074 a0001c0001t0014g0039 a0002c0002t0001g0242 others(62): Show |
66 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.1592+2355dupT | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229481698 | |||||||
chr1:229481698 | CAA | C | 11 | a0005c0006t0001g0012 a0005c0006t0001g0014 a0005c0006t0001g0015 others(8): Show |
11 | HG02622.hp1 HG02647.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.1592+2354_1592+235 others(6): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229481698 | |||||||
chr1:229481914 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1592+2140G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229481914 | |||||||
chr1:229481930 | T | C | 11 | a0005c0006t0001g0012 a0005c0006t0001g0014 a0005c0006t0001g0015 others(8): Show |
11 | HG02622.hp1 HG02647.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.1592+2124A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229481930 | |||||||
chr1:229482404 | C | A | 6 | a0002c0005t0005g0022 a0002c0005t0005g0030 a0002c0005t0005g0033 others(3): Show |
6 | HG02895.hp1 HG02897.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1592+1650G>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229482404 | |||||||
chr1:229482582 | A | G | 1 | a0003c0003t0003g0134 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1592+1472T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229482582 | |||||||
chr1:229482761 | C | T | 1 | a0001c0001t0001g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1592+1293G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229482761 | |||||||
chr1:229482887 | C | T | 62 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(59): Show |
63 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1592+1167G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229482887 | |||||||
chr1:229482952 | C | A | 1 | a0003c0003t0003g0134 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1592+1102G>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229482952 | |||||||
chr1:229482959 | A | G | 11 | a0005c0006t0001g0012 a0005c0006t0001g0014 a0005c0006t0001g0015 others(8): Show |
11 | HG02622.hp1 HG02647.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.1592+1095T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229482959 | |||||||
chr1:229483067 | G | A | 1 | a0004c0004t0003g0252 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1592+987C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229483067 | |||||||
chr1:229483141 | C | G | 49 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(46): Show |
50 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.1592+913G>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229483141 | |||||||
chr1:229483229 | C | G | 1 | a0005c0006t0017g0019 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1592+825G>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229483229 | |||||||
chr1:229483659 | C | T | 10 | a0003c0003t0002g0116 a0003c0003t0002g0117 a0003c0003t0006g0122 others(7): Show |
10 | HG02257.hp1 HG02258.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1592+395G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229483659 | |||||||
chr1:229483683 | C | T | 1 | a0003c0003t0002g0117 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1592+371G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229483683 | |||||||
chr1:229483696 | C | CA | 58 | a0001c0001t0001g0037 a0001c0001t0001g0046 a0001c0001t0001g0047 others(55): Show |
59 | HG00099.hp1 HG00438.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.1592+357dupT | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229483696 | |||||||
chr1:229483696 | C | CAA | 10 | a0001c0001t0001g0167 a0001c0001t0001g0175 a0002c0002t0002g0214 others(7): Show |
10 | HG00438.hp1 HG00597.hp2 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.1592+356_1592+357d others(4): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229483696 | |||||||
chr1:229483696 | CA | C | 33 | a0001c0001t0001g0010 a0001c0001t0001g0162 a0001c0001t0001g0163 others(30): Show |
33 | HG01261.hp2 HG01884.hp2 HG02145.hp1 others(30): Show |
intron_variant | MODIFIER | c.1592+357delT | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229483696 | |||||||
chr1:229483696 | CAA | C | 11 | a0003c0003t0002g0116 a0003c0003t0002g0117 a0003c0003t0004g0106 others(8): Show |
11 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.1592+356_1592+357d others(4): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229483696 | |||||||
chr1:229483696 | CAAAAAAA others(6): Show |
C | 9 | a0005c0006t0001g0012 a0005c0006t0001g0014 a0005c0006t0001g0015 others(6): Show |
9 | HG02622.hp1 HG02647.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1592+345_1592+357d others(15): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229483696 | |||||||
chr1:229483769 | T | C | 34 | a0001c0001t0001g0008 a0001c0001t0001g0145 a0001c0001t0001g0146 others(31): Show |
35 | HG00438.hp1 HG00642.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.1592+285A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229483769 | |||||||
chr1:229483777 | T | C | 11 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0037 others(8): Show |
13 | HG00408.hp1 HG00544.hp2 HG00609.hp1 others(10): Show |
intron_variant | MODIFIER | c.1592+277A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229483777 | |||||||
chr1:229483843 | C | T | 5 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(2): Show |
5 | HG00597.hp1 HG00609.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.1592+211G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 12/25 | chr1 | 229483843 | |||||||
chr1:229484240 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1501-95C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 11/25 | chr1 | 229484240 | |||||||
chr1:229484385 | T | A | 1 | a0002c0002t0011g0247 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1501-240A>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 11/25 | chr1 | 229484385 | |||||||
chr1:229484405 | A | T | 1 | a0005c0006t0001g0020 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1501-260T>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 11/25 | chr1 | 229484405 | |||||||
chr1:229484568 | T | C | 11 | a0005c0006t0001g0012 a0005c0006t0001g0014 a0005c0006t0001g0015 others(8): Show |
11 | HG02622.hp1 HG02647.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.1501-423A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 11/25 | chr1 | 229484568 | |||||||
chr1:229484649 | G | A | 62 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(59): Show |
63 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1501-504C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 11/25 | chr1 | 229484649 | |||||||
chr1:229484876 | ACAAAATG | A | 14 | a0002c0002t0002g0215 a0002c0002t0002g0218 a0002c0002t0002g0221 others(11): Show |
14 | HG00438.hp2 HG02074.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.1501-738_1501-732d others(9): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 11/25 | chr1 | 229484876 | |||||||
chr1:229484883 | G | A | 48 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(45): Show |
49 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.1501-738C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 11/25 | chr1 | 229484883 | |||||||
chr1:229484938 | C | T | 62 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(59): Show |
63 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1501-793G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 11/25 | chr1 | 229484938 | |||||||
chr1:229485251 | C | T | 2 | a0003c0003t0003g0113 a0010c0016t0003g0114 |
2 | HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1501-1106G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 11/25 | chr1 | 229485251 | |||||||
chr1:229485632 | A | C | 5 | a0002c0005t0005g0025 a0002c0005t0005g0026 a0002c0005t0005g0027 others(2): Show |
5 | HG02145.hp1 HG03579.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.1500+739T>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 11/25 | chr1 | 229485632 | |||||||
chr1:229485882 | G | T | 1 | a0001c0001t0001g0097 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1500+489C>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 11/25 | chr1 | 229485882 | |||||||
chr1:229485975 | C | A | 11 | a0003c0003t0003g0113 a0005c0006t0001g0012 a0005c0006t0001g0014 others(8): Show |
11 | HG02622.hp1 HG02647.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.1500+396G>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 11/25 | chr1 | 229485975 | |||||||
chr1:229486145 | C | T | 13 | a0002c0005t0005g0022 a0002c0005t0005g0025 a0002c0005t0005g0026 others(10): Show |
13 | HG01261.hp2 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1500+226G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 11/25 | chr1 | 229486145 | |||||||
chr1:229486322 | T | TAAAAAAT others(296): Show |
6 | a0003c0003t0002g0116 a0003c0003t0006g0122 a0003c0003t0006g0123 others(3): Show |
6 | HG02257.hp1 HG02258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1500+48_1500+49ins others(303): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 11/25 | chr1 | 229486322 | |||||||
chr1:229486322 | T | TAAAAAAT others(297): Show |
3 | a0003c0003t0002g0117 a0003c0003t0006g0124 a0003c0003t0006g0128 |
3 | HG02886.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1500+48_1500+49ins others(304): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 11/25 | chr1 | 229486322 | |||||||
chr1:229486325 | A | AAAATAAA others(302): Show |
1 | a0003c0003t0003g0113 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1500+45_1500+46ins others(309): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 11/25 | chr1 | 229486325 | |||||||
chr1:229486325 | A | AAAATAAA others(297): Show |
1 | a0003c0003t0006g0127 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1500+45_1500+46ins others(304): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 11/25 | chr1 | 229486325 | |||||||
chr1:229486325 | A | AAAATAAA others(301): Show |
1 | a0005c0006t0001g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1500+45_1500+46ins others(308): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 11/25 | chr1 | 229486325 | |||||||
chr1:229486325 | A | AAAATAAA others(301): Show |
1 | a0008c0013t0003g0013 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1500+45_1500+46ins others(308): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 11/25 | chr1 | 229486325 | |||||||
chr1:229486325 | A | AAAATAAA others(301): Show |
4 | a0005c0006t0001g0012 a0005c0006t0001g0016 a0005c0006t0001g0017 others(1): Show |
4 | HG02809.hp1 HG02886.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1500+45_1500+46ins others(308): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 11/25 | chr1 | 229486325 | |||||||
chr1:229486325 | A | AAAATAAA others(301): Show |
1 | a0005c0006t0001g0015 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1500+45_1500+46ins others(308): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 11/25 | chr1 | 229486325 | |||||||
chr1:229486325 | A | AAAATAAA others(303): Show |
1 | a0010c0016t0003g0114 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1500+45_1500+46ins others(310): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 11/25 | chr1 | 229486325 | |||||||
chr1:229486325 | A | AAAATAAA others(301): Show |
1 | a0005c0006t0001g0018 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1500+45_1500+46ins others(308): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 11/25 | chr1 | 229486325 | |||||||
chr1:229486325 | A | AAAATAAA others(301): Show |
1 | a0005c0006t0017g0019 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1500+45_1500+46ins others(308): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 11/25 | chr1 | 229486325 | |||||||
chr1:229486583 | T | C | 2 | a0003c0011t0009g0136 a0003c0011t0009g0137 |
2 | HG01106.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1343-55A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 10/25 | chr1 | 229486583 | |||||||
chr1:229486761 | C | T | 1 | a0002c0002t0002g0219 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1343-233G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 10/25 | chr1 | 229486761 | |||||||
chr1:229486903 | GA | G | 28 | a0001c0001t0001g0007 a0001c0001t0001g0143 a0001c0001t0001g0151 others(25): Show |
29 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(26): Show |
intron_variant | MODIFIER | c.1343-376delT | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 10/25 | chr1 | 229486903 | |||||||
chr1:229486903 | GAAAAAAA others(3): Show |
G | 10 | a0003c0003t0002g0116 a0003c0003t0002g0117 a0003c0003t0006g0122 others(7): Show |
10 | HG02257.hp1 HG02258.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1343-385_1343-376d others(12): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 10/25 | chr1 | 229486903 | |||||||
chr1:229486904 | A | G | 5 | a0001c0001t0001g0104 a0001c0001t0001g0154 a0001c0001t0001g0169 others(2): Show |
5 | HG00639.hp1 HG01123.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.1343-376T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 10/25 | chr1 | 229486904 | |||||||
chr1:229487020 | A | G | 2 | a0003c0011t0009g0136 a0003c0011t0009g0137 |
2 | HG01106.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1342+446T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 10/25 | chr1 | 229487020 | |||||||
chr1:229487116 | A | G | 62 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(59): Show |
63 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1342+350T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 10/25 | chr1 | 229487116 | |||||||
chr1:229487283 | A | C | 1 | a0004c0004t0003g0261 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1342+183T>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 10/25 | chr1 | 229487283 | |||||||
chr1:229487384 | G | C | 62 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(59): Show |
63 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1342+82C>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 10/25 | chr1 | 229487384 | |||||||
chr1:229487390 | T | C | 104 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(101): Show |
105 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1342+76A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 10/25 | chr1 | 229487390 | |||||||
chr1:229487662 | A | ATTTG | 62 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(59): Show |
63 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1195-53_1195-50dup others(4): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 9/25 | chr1 | 229487662 | |||||||
chr1:229487838 | A | AT | 15 | a0001c0001t0001g0001 a0001c0001t0001g0040 a0001c0001t0001g0052 others(12): Show |
16 | HG00735.hp1 HG01074.hp1 HG01981.hp2 others(13): Show |
intron_variant | MODIFIER | c.1195-226dupA | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 9/25 | chr1 | 229487838 | |||||||
chr1:229487838 | AT | A | 26 | a0001c0001t0001g0066 a0001c0001t0001g0153 a0001c0001t0001g0155 others(23): Show |
26 | HG00099.hp2 HG01106.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.1195-226delA | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 9/25 | chr1 | 229487838 | |||||||
chr1:229487838 | ATT | A | 18 | a0002c0002t0002g0217 a0002c0002t0002g0219 a0002c0002t0002g0233 others(15): Show |
18 | HG01168.hp1 HG02622.hp1 HG02809.hp1 others(15): Show |
intron_variant | MODIFIER | c.1195-227_1195-226d others(4): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 9/25 | chr1 | 229487838 | |||||||
chr1:229487838 | ATTT | A | 59 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(56): Show |
60 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.1195-228_1195-226d others(5): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 9/25 | chr1 | 229487838 | |||||||
chr1:229487874 | C | T | 1 | a0010c0016t0003g0114 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1195-261G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 9/25 | chr1 | 229487874 | |||||||
chr1:229487887 | A | G | 1 | a0001c0001t0001g0078 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1195-274T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 9/25 | chr1 | 229487887 | |||||||
chr1:229487918 | T | A | 73 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(70): Show |
74 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1195-305A>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 9/25 | chr1 | 229487918 | |||||||
chr1:229488005 | G | A | 4 | a0003c0003t0007g0263 a0003c0003t0007g0264 a0003c0003t0007g0265 others(1): Show |
4 | HG02630.hp1 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1195-392C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 9/25 | chr1 | 229488005 | |||||||
chr1:229488066 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1195-453C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 9/25 | chr1 | 229488066 | |||||||
chr1:229488128 | G | A | 62 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(59): Show |
63 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1195-515C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 9/25 | chr1 | 229488128 | |||||||
chr1:229488149 | A | T | 62 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(59): Show |
63 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1195-536T>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 9/25 | chr1 | 229488149 | |||||||
chr1:229488663 | T | C | 2 | a0003c0003t0003g0113 a0010c0016t0003g0114 |
2 | HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1195-1050A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 9/25 | chr1 | 229488663 | |||||||
chr1:229488676 | TC | T | 4 | a0002c0002t0002g0217 a0002c0002t0002g0262 a0004c0004t0003g0259 others(1): Show |
4 | HG01168.hp1 HG01934.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1195-1064delG | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 9/25 | chr1 | 229488676 | |||||||
chr1:229488677 | C | T | 69 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(66): Show |
70 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.1195-1064G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 9/25 | chr1 | 229488677 | |||||||
chr1:229488678 | A | T | 4 | a0002c0002t0002g0217 a0002c0002t0002g0262 a0004c0004t0003g0259 others(1): Show |
4 | HG01168.hp1 HG01934.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1195-1065T>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 9/25 | chr1 | 229488678 | |||||||
chr1:229488821 | C | T | 2 | a0006c0008t0004g0021 a0006c0008t0004g0024 |
2 | HG03486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1194+1134G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 9/25 | chr1 | 229488821 | |||||||
chr1:229488832 | G | T | 1 | a0001c0001t0001g0131 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1194+1123C>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 9/25 | chr1 | 229488832 | |||||||
chr1:229488833 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1194+1122G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 9/25 | chr1 | 229488833 | |||||||
chr1:229489189 | A | C | 1 | a0003c0003t0001g0023 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1194+766T>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 9/25 | chr1 | 229489189 | |||||||
chr1:229489272 | C | T | 14 | a0002c0002t0002g0215 a0002c0002t0002g0218 a0002c0002t0002g0221 others(11): Show |
14 | HG00438.hp2 HG02074.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.1194+683G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 9/25 | chr1 | 229489272 | |||||||
chr1:229489275 | C | T | 2 | a0002c0002t0002g0254 a0002c0002t0002g0255 |
2 | NA18954.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.1194+680G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 9/25 | chr1 | 229489275 | |||||||
chr1:229489314 | G | A | 1 | a0005c0006t0001g0018 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1194+641C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 9/25 | chr1 | 229489314 | |||||||
chr1:229489426 | C | T | 1 | a0002c0002t0002g0218 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1194+529G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 9/25 | chr1 | 229489426 | |||||||
chr1:229489702 | C | T | 1 | a0001c0001t0004g0147 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1194+253G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 9/25 | chr1 | 229489702 | |||||||
chr1:229490125 | G | A | 1 | a0003c0003t0004g0132 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1047-23C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229490125 | |||||||
chr1:229490365 | T | C | 1 | a0006c0008t0004g0024 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1047-263A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229490365 | |||||||
chr1:229490401 | T | TA | 20 | a0001c0001t0001g0101 a0001c0001t0001g0155 a0001c0001t0001g0188 others(17): Show |
20 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.1047-300dupT | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229490401 | |||||||
chr1:229490401 | TA | T | 25 | a0001c0001t0001g0077 a0001c0001t0001g0212 a0002c0005t0005g0022 others(22): Show |
25 | HG01167.hp1 HG01261.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.1047-300delT | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229490401 | |||||||
chr1:229490412 | A | C | 1 | a0002c0002t0002g0226 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1047-310T>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229490412 | |||||||
chr1:229490419 | A | T | 61 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(58): Show |
62 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.1047-317T>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229490419 | |||||||
chr1:229490575 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1047-473G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229490575 | |||||||
chr1:229490719 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1047-617A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229490719 | |||||||
chr1:229490739 | C | G | 62 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(59): Show |
63 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1047-637G>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229490739 | |||||||
chr1:229490779 | G | A | 9 | a0005c0006t0001g0012 a0005c0006t0001g0014 a0005c0006t0001g0015 others(6): Show |
9 | HG02622.hp1 HG02647.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1047-677C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229490779 | |||||||
chr1:229490882 | T | A | 1 | a0003c0003t0004g0133 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1047-780A>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229490882 | |||||||
chr1:229490930 | G | A | 1 | a0001c0001t0001g0010 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1047-828C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229490930 | |||||||
chr1:229490940 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1047-838G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229490940 | |||||||
chr1:229490950 | T | TA | 61 | a0001c0001t0001g0040 a0002c0002t0001g0242 a0002c0002t0002g0009 others(58): Show |
62 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.1047-849dupT | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229490950 | |||||||
chr1:229491085 | A | G | 62 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(59): Show |
63 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1047-983T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229491085 | |||||||
chr1:229491144 | C | G | 62 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(59): Show |
63 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1047-1042G>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229491144 | |||||||
chr1:229491158 | C | T | 19 | a0003c0003t0003g0134 a0003c0003t0004g0106 a0003c0003t0004g0108 others(16): Show |
19 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.1047-1056G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229491158 | |||||||
chr1:229491211 | G | A | 1 | a0003c0003t0001g0050 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1047-1109C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229491211 | |||||||
chr1:229491223 | T | C | 33 | a0003c0003t0001g0050 a0003c0003t0001g0209 a0003c0003t0002g0116 others(30): Show |
33 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(30): Show |
intron_variant | MODIFIER | c.1047-1121A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229491223 | |||||||
chr1:229491368 | G | A | 1 | a0001c0007t0001g0157 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1047-1266C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229491368 | |||||||
chr1:229491474 | A | G | 13 | a0002c0005t0005g0032 a0002c0015t0005g0031 a0005c0006t0001g0012 others(10): Show |
13 | HG01261.hp2 HG01884.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1047-1372T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229491474 | |||||||
chr1:229491505 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1047-1403C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229491505 | |||||||
chr1:229491587 | T | C | 1 | a0003c0003t0001g0209 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1047-1485A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229491587 | |||||||
chr1:229491647 | G | A | 5 | a0003c0003t0007g0263 a0003c0003t0007g0264 a0003c0003t0007g0265 others(2): Show |
5 | HG02630.hp1 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1047-1545C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229491647 | |||||||
chr1:229491783 | A | C | 13 | a0002c0005t0005g0022 a0002c0005t0005g0025 a0002c0005t0005g0026 others(10): Show |
13 | HG01261.hp2 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1047-1681T>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229491783 | |||||||
chr1:229491919 | A | T | 62 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(59): Show |
63 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1047-1817T>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229491919 | |||||||
chr1:229491975 | T | C | 62 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(59): Show |
63 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1047-1873A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229491975 | |||||||
chr1:229492107 | A | AT | 9 | a0001c0001t0001g0052 a0001c0001t0001g0094 a0001c0001t0001g0097 others(6): Show |
9 | HG01168.hp1 HG01952.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1047-2006dupA | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229492107 | |||||||
chr1:229492128 | C | T | 62 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(59): Show |
63 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1047-2026G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229492128 | |||||||
chr1:229492137 | A | G | 104 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(101): Show |
105 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1047-2035T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229492137 | |||||||
chr1:229492163 | G | A | 1 | a0001c0001t0001g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1047-2061C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229492163 | |||||||
chr1:229492168 | G | A | 3 | a0003c0003t0003g0134 a0003c0003t0004g0132 a0003c0003t0004g0133 |
3 | HG02280.hp1 HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1047-2066C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229492168 | |||||||
chr1:229492240 | G | A | 2 | a0001c0012t0001g0075 a0001c0012t0001g0076 |
2 | NA18957.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.1047-2138C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229492240 | |||||||
chr1:229492398 | C | T | 11 | a0005c0006t0001g0012 a0005c0006t0001g0014 a0005c0006t0001g0015 others(8): Show |
11 | HG02622.hp1 HG02647.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.1047-2296G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229492398 | |||||||
chr1:229492797 | A | G | 4 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(1): Show |
4 | HG02055.hp2 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1047-2695T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229492797 | |||||||
chr1:229492820 | G | C | 31 | a0001c0001t0001g0008 a0001c0001t0001g0145 a0001c0001t0001g0149 others(28): Show |
32 | HG00438.hp1 HG00642.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.1046+2675C>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229492820 | |||||||
chr1:229492923 | A | T | 64 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(61): Show |
65 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.1046+2572T>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229492923 | |||||||
chr1:229493049 | A | T | 1 | a0003c0003t0001g0209 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1046+2446T>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229493049 | |||||||
chr1:229493303 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1046+2192C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229493303 | |||||||
chr1:229493306 | T | C | 62 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(59): Show |
63 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1046+2189A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229493306 | |||||||
chr1:229493498 | C | A | 62 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(59): Show |
63 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1046+1997G>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229493498 | |||||||
chr1:229493988 | G | A | 11 | a0005c0006t0001g0012 a0005c0006t0001g0014 a0005c0006t0001g0015 others(8): Show |
11 | HG02622.hp1 HG02647.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.1046+1507C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229493988 | |||||||
chr1:229494129 | C | CA | 6 | a0003c0003t0004g0118 a0003c0003t0004g0119 a0003c0003t0004g0120 others(3): Show |
6 | HG02280.hp1 HG02965.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1046+1365dupT | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229494129 | |||||||
chr1:229494416 | C | G | 1 | a0001c0001t0001g0160 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1046+1079G>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229494416 | |||||||
chr1:229494416 | C | T | 73 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(70): Show |
74 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1046+1079G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229494416 | |||||||
chr1:229494445 | T | G | 2 | a0002c0002t0002g0249 a0002c0002t0002g0250 |
2 | HG00140.hp2 HG00733.hp1 |
intron_variant | MODIFIER | c.1046+1050A>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229494445 | |||||||
chr1:229494815 | G | A | 10 | a0003c0003t0002g0116 a0003c0003t0002g0117 a0003c0003t0003g0113 others(7): Show |
10 | HG02257.hp1 HG02258.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1046+680C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229494815 | |||||||
chr1:229494966 | A | G | 1 | a0003c0003t0001g0023 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1046+529T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229494966 | |||||||
chr1:229494972 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1046+523C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229494972 | |||||||
chr1:229495365 | C | T | 74 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(71): Show |
75 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.1046+130G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229495365 | |||||||
chr1:229495446 | T | C | 73 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(70): Show |
74 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1046+49A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 8/25 | chr1 | 229495446 | |||||||
chr1:229495577 | T | C | 11 | a0005c0006t0001g0012 a0005c0006t0001g0014 a0005c0006t0001g0015 others(8): Show |
11 | HG02622.hp1 HG02647.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.976-12A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 7/25 | chr1 | 229495577 | |||||||
chr1:229495631 | C | A | 2 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
2 | HG01192.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.976-66G>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 7/25 | chr1 | 229495631 | |||||||
chr1:229495643 | G | A | 2 | a0003c0011t0009g0136 a0003c0011t0009g0137 |
2 | HG01106.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.976-78C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 7/25 | chr1 | 229495643 | |||||||
chr1:229495680 | G | A | 1 | a0003c0003t0001g0050 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.976-115C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 7/25 | chr1 | 229495680 | |||||||
chr1:229495830 | G | A | 6 | a0001c0001t0001g0049 a0001c0001t0001g0064 a0001c0001t0001g0065 others(3): Show |
6 | HG02109.hp2 HG02258.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.975+62C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 7/25 | chr1 | 229495830 | |||||||
chr1:229496060 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.820-13C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 6/25 | chr1 | 229496060 | |||||||
chr1:229496295 | G | A | 62 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(59): Show |
63 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.820-248C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 6/25 | chr1 | 229496295 | |||||||
chr1:229496331 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.820-284C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 6/25 | chr1 | 229496331 | |||||||
chr1:229496451 | C | T | 62 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(59): Show |
63 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.820-404G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 6/25 | chr1 | 229496451 | |||||||
chr1:229496491 | C | A | 186 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0104 others(183): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.820-444G>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 6/25 | chr1 | 229496491 | |||||||
chr1:229496608 | G | A | 2 | a0003c0003t0001g0050 a0003c0003t0001g0209 |
2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.820-561C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 6/25 | chr1 | 229496608 | |||||||
chr1:229496866 | T | C | 14 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0210 others(11): Show |
14 | HG00735.hp2 HG01255.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.820-819A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 6/25 | chr1 | 229496866 | |||||||
chr1:229496889 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.820-842A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 6/25 | chr1 | 229496889 | |||||||
chr1:229496891 | G | T | 62 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(59): Show |
63 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.820-844C>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 6/25 | chr1 | 229496891 | |||||||
chr1:229496973 | T | C | 12 | a0003c0003t0002g0116 a0003c0003t0002g0117 a0003c0003t0003g0113 others(9): Show |
12 | HG02257.hp1 HG02258.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.820-926A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 6/25 | chr1 | 229496973 | |||||||
chr1:229497018 | C | G | 1 | a0002c0002t0012g0231 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.820-971G>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 6/25 | chr1 | 229497018 | |||||||
chr1:229497121 | A | C | 1 | a0004c0004t0003g0251 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.819+1015T>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 6/25 | chr1 | 229497121 | |||||||
chr1:229497214 | T | C | 7 | a0003c0003t0004g0106 a0003c0003t0004g0108 a0003c0003t0004g0109 others(4): Show |
7 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.819+922A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 6/25 | chr1 | 229497214 | |||||||
chr1:229497305 | G | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0085 |
3 | NA18960.hp1 NA18983.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.819+831C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 6/25 | chr1 | 229497305 | |||||||
chr1:229497309 | C | A | 62 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(59): Show |
63 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.819+827G>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 6/25 | chr1 | 229497309 | |||||||
chr1:229497512 | T | C | 1 | a0003c0003t0003g0134 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.819+624A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 6/25 | chr1 | 229497512 | |||||||
chr1:229497557 | C | T | 2 | a0003c0003t0006g0123 a0003c0003t0006g0124 |
2 | HG02257.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.819+579G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 6/25 | chr1 | 229497557 | |||||||
chr1:229497624 | A | G | 77 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0210 others(74): Show |
78 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.819+512T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 6/25 | chr1 | 229497624 | |||||||
chr1:229497824 | C | T | 62 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(59): Show |
63 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.819+312G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 6/25 | chr1 | 229497824 | |||||||
chr1:229497852 | T | C | 14 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0210 others(11): Show |
14 | HG00735.hp2 HG01255.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.819+284A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 6/25 | chr1 | 229497852 | |||||||
chr1:229497963 | A | G | 1 | a0003c0003t0001g0023 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.819+173T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 6/25 | chr1 | 229497963 | |||||||
chr1:229498313 | A | G | 2 | a0004c0004t0003g0257 a0004c0004t0003g0258 |
2 | HG01928.hp1 HG02300.hp1 |
splice_region_variant&intron_variant | LOW | c.649-7T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 5/25 | chr1 | 229498313 | |||||||
chr1:229498544 | G | C | 2 | a0001c0001t0001g0004 a0001c0001t0001g0085 |
3 | NA18960.hp1 NA18983.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.649-238C>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 5/25 | chr1 | 229498544 | |||||||
chr1:229498622 | G | A | 2 | a0001c0001t0001g0191 a0005c0006t0017g0019 |
2 | HG03540.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.649-316C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 5/25 | chr1 | 229498622 | |||||||
chr1:229498626 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.649-320G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 5/25 | chr1 | 229498626 | |||||||
chr1:229498649 | G | T | 62 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(59): Show |
63 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.649-343C>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 5/25 | chr1 | 229498649 | |||||||
chr1:229498650 | G | T | 62 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(59): Show |
63 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.649-344C>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 5/25 | chr1 | 229498650 | |||||||
chr1:229498666 | G | A | 1 | a0001c0001t0001g0192 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.649-360C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 5/25 | chr1 | 229498666 | |||||||
chr1:229498699 | T | C | 1 | a0003c0003t0001g0023 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.649-393A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 5/25 | chr1 | 229498699 | |||||||
chr1:229498713 | G | A | 2 | a0003c0011t0009g0136 a0003c0011t0009g0137 |
2 | HG01106.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.649-407C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 5/25 | chr1 | 229498713 | |||||||
chr1:229498763 | G | GA | 11 | a0001c0001t0001g0093 a0001c0001t0001g0145 a0005c0006t0001g0012 others(8): Show |
11 | HG02074.hp1 HG02622.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.649-458dupT | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 5/25 | chr1 | 229498763 | |||||||
chr1:229498763 | GA | G | 62 | a0001c0001t0001g0159 a0002c0002t0001g0242 a0002c0002t0002g0009 others(59): Show |
63 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.649-458delT | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 5/25 | chr1 | 229498763 | |||||||
chr1:229499119 | T | C | 11 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0037 others(8): Show |
13 | HG00408.hp1 HG00544.hp2 HG00609.hp1 others(10): Show |
intron_variant | MODIFIER | c.648+565A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 5/25 | chr1 | 229499119 | |||||||
chr1:229499153 | G | C | 1 | a0005c0006t0001g0020 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.648+531C>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 5/25 | chr1 | 229499153 | |||||||
chr1:229499336 | T | C | 16 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0210 others(13): Show |
16 | HG00735.hp2 HG01255.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.648+348A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 5/25 | chr1 | 229499336 | |||||||
chr1:229499396 | C | T | 14 | a0004c0004t0003g0216 a0004c0004t0003g0220 a0004c0004t0003g0225 others(11): Show |
14 | HG01123.hp2 HG01167.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.648+288G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 5/25 | chr1 | 229499396 | |||||||
chr1:229499520 | T | G | 49 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(46): Show |
50 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.648+164A>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 5/25 | chr1 | 229499520 | |||||||
chr1:229499561 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.648+123C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 5/25 | chr1 | 229499561 | |||||||
chr1:229499634 | A | C | 1 | a0001c0001t0001g0158 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.648+50T>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 5/25 | chr1 | 229499634 | |||||||
chr1:229499864 | C | T | 1 | a0003c0003t0003g0113 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.514-46G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 4/25 | chr1 | 229499864 | |||||||
chr1:229499945 | A | C | 1 | a0002c0002t0002g0227 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.514-127T>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 4/25 | chr1 | 229499945 | |||||||
chr1:229500120 | A | G | 62 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(59): Show |
63 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.514-302T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 4/25 | chr1 | 229500120 | |||||||
chr1:229500202 | C | T | 1 | a0004c0004t0003g0257 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.514-384G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 4/25 | chr1 | 229500202 | |||||||
chr1:229500641 | A | G | 109 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(106): Show |
110 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.513+115T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 4/25 | chr1 | 229500641 | |||||||
chr1:229500694 | C | T | 1 | a0002c0002t0002g0226 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.513+62G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 4/25 | chr1 | 229500694 | |||||||
chr1:229501093 | G | A | 1 | a0003c0003t0001g0023 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.406-230C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 3/25 | chr1 | 229501093 | |||||||
chr1:229501185 | C | A | 2 | a0001c0001t0001g0146 a0001c0001t0001g0156 |
2 | HG02055.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.406-322G>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 3/25 | chr1 | 229501185 | |||||||
chr1:229501550 | C | T | 62 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(59): Show |
63 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.405+449G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 3/25 | chr1 | 229501550 | |||||||
chr1:229501572 | G | T | 1 | a0005c0006t0001g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.405+427C>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 3/25 | chr1 | 229501572 | |||||||
chr1:229501633 | T | C | 12 | a0003c0003t0001g0023 a0005c0006t0001g0012 a0005c0006t0001g0014 others(9): Show |
12 | HG02622.hp1 HG02647.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.405+366A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 3/25 | chr1 | 229501633 | |||||||
chr1:229501667 | C | T | 74 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(71): Show |
75 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.405+332G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 3/25 | chr1 | 229501667 | |||||||
chr1:229501756 | A | T | 110 | a0001c0007t0001g0157 a0002c0002t0001g0242 a0002c0002t0002g0009 others(107): Show |
111 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.405+243T>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 3/25 | chr1 | 229501756 | |||||||
chr1:229501898 | C | A | 74 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(71): Show |
75 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.405+101G>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 3/25 | chr1 | 229501898 | |||||||
chr1:229502134 | T | G | 62 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(59): Show |
63 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.302-32A>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229502134 | |||||||
chr1:229502324 | C | T | 10 | a0003c0003t0002g0116 a0003c0003t0002g0117 a0003c0003t0006g0122 others(7): Show |
10 | HG02257.hp1 HG02258.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.302-222G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229502324 | |||||||
chr1:229502417 | A | G | 74 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(71): Show |
75 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.302-315T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229502417 | |||||||
chr1:229502515 | T | C | 62 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(59): Show |
63 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.302-413A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229502515 | |||||||
chr1:229502558 | C | CA | 28 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(25): Show |
28 | HG00597.hp1 HG00609.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.302-457dupT | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229502558 | |||||||
chr1:229502558 | C | CAA | 60 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(57): Show |
61 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.302-458_302-457dup others(2): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229502558 | |||||||
chr1:229502558 | C | CAAA | 13 | a0002c0002t0002g0262 a0002c0005t0005g0029 a0003c0003t0001g0023 others(10): Show |
13 | HG01978.hp2 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.302-459_302-457dup others(3): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229502558 | |||||||
chr1:229502558 | CA | C | 9 | a0001c0001t0001g0051 a0001c0001t0001g0084 a0001c0001t0001g0085 others(6): Show |
9 | HG01256.hp1 HG02976.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.302-457delT | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229502558 | |||||||
chr1:229502558 | CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0001g0211 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.302-471_302-457del others(15): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229502558 | |||||||
chr1:229502596 | T | C | 1 | a0003c0003t0001g0023 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.302-494A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229502596 | |||||||
chr1:229502693 | G | C | 49 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(46): Show |
50 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.302-591C>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229502693 | |||||||
chr1:229502797 | T | TA | 9 | a0001c0001t0001g0083 a0001c0001t0001g0107 a0001c0001t0001g0146 others(6): Show |
9 | HG01106.hp2 HG02055.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.302-696dupT | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229502797 | |||||||
chr1:229502797 | TA | T | 19 | a0001c0001t0001g0049 a0001c0001t0001g0104 a0001c0001t0001g0153 others(16): Show |
19 | HG01071.hp1 HG01168.hp2 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.302-696delT | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229502797 | |||||||
chr1:229502797 | TAA | T | 11 | a0002c0005t0005g0030 a0005c0006t0001g0014 a0005c0006t0001g0015 others(8): Show |
11 | HG02622.hp1 HG02647.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.302-697_302-696del others(2): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229502797 | |||||||
chr1:229502890 | T | C | 6 | a0001c0001t0001g0102 a0001c0001t0001g0130 a0001c0001t0001g0199 others(3): Show |
6 | HG00735.hp2 HG02738.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.302-788A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229502890 | |||||||
chr1:229503004 | A | G | 12 | a0003c0003t0001g0023 a0005c0006t0001g0012 a0005c0006t0001g0014 others(9): Show |
12 | HG02622.hp1 HG02647.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.302-902T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229503004 | |||||||
chr1:229503005 | C | T | 1 | a0002c0002t0010g0223 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.302-903G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229503005 | |||||||
chr1:229503096 | T | C | 10 | a0003c0003t0002g0116 a0003c0003t0002g0117 a0003c0003t0006g0122 others(7): Show |
10 | HG02257.hp1 HG02258.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.302-994A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229503096 | |||||||
chr1:229503135 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.302-1033C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229503135 | |||||||
chr1:229503220 | T | C | 10 | a0003c0003t0002g0116 a0003c0003t0002g0117 a0003c0003t0006g0122 others(7): Show |
10 | HG02257.hp1 HG02258.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.302-1118A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229503220 | |||||||
chr1:229503234 | C | T | 3 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0003c0003t0001g0023 |
3 | HG01192.hp2 HG01255.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.302-1132G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229503234 | |||||||
chr1:229503337 | A | C | 75 | a0001c0001t0001g0131 a0002c0002t0001g0242 a0002c0002t0002g0009 others(72): Show |
76 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.302-1235T>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229503337 | |||||||
chr1:229503360 | A | G | 1 | a0003c0003t0001g0023 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.302-1258T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229503360 | |||||||
chr1:229503382 | C | A | 13 | a0001c0001t0001g0131 a0003c0003t0001g0023 a0005c0006t0001g0012 others(10): Show |
13 | HG01255.hp1 HG02622.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.302-1280G>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229503382 | |||||||
chr1:229503527 | G | A | 1 | a0004c0004t0003g0252 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.302-1425C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229503527 | |||||||
chr1:229503805 | T | A | 1 | a0003c0003t0007g0266 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.302-1703A>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229503805 | |||||||
chr1:229503978 | AAT | A | 75 | a0001c0001t0001g0131 a0002c0002t0001g0242 a0002c0002t0002g0009 others(72): Show |
76 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.302-1878_302-1877d others(4): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229503978 | |||||||
chr1:229503990 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.302-1888A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229503990 | |||||||
chr1:229504415 | G | C | 1 | a0002c0002t0002g0256 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.301+1625C>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229504415 | |||||||
chr1:229504450 | C | T | 1 | a0001c0001t0001g0150 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.301+1590G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229504450 | |||||||
chr1:229504724 | T | C | 62 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(59): Show |
63 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.301+1316A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229504724 | |||||||
chr1:229504870 | C | T | 74 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(71): Show |
75 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.301+1170G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229504870 | |||||||
chr1:229504896 | A | C | 1 | a0008c0013t0003g0013 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.301+1144T>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229504896 | |||||||
chr1:229505024 | A | G | 109 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(106): Show |
110 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.301+1016T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229505024 | |||||||
chr1:229505164 | C | T | 62 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(59): Show |
63 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.301+876G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229505164 | |||||||
chr1:229505258 | G | C | 7 | a0003c0003t0004g0106 a0003c0003t0004g0108 a0003c0003t0004g0109 others(4): Show |
7 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.301+782C>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229505258 | |||||||
chr1:229505325 | T | C | 19 | a0003c0003t0003g0134 a0003c0003t0004g0106 a0003c0003t0004g0108 others(16): Show |
19 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.301+715A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229505325 | |||||||
chr1:229505331 | T | G | 74 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(71): Show |
75 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.301+709A>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229505331 | |||||||
chr1:229505508 | T | G | 1 | a0003c0003t0003g0134 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.301+532A>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229505508 | |||||||
chr1:229505564 | T | TA | 39 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(36): Show |
41 | HG00544.hp1 HG00735.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.301+475dupT | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229505564 | |||||||
chr1:229505564 | T | TAA | 40 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0002c0002t0001g0242 others(37): Show |
41 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.301+474_301+475dup others(2): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229505564 | |||||||
chr1:229505564 | T | TAAA | 8 | a0002c0002t0002g0215 a0002c0002t0002g0218 a0002c0002t0002g0219 others(5): Show |
8 | HG01074.hp2 HG01993.hp1 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.301+473_301+475dup others(3): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229505564 | |||||||
chr1:229505564 | TA | T | 26 | a0001c0001t0001g0049 a0001c0001t0001g0104 a0001c0001t0001g0142 others(23): Show |
26 | HG00323.hp1 HG01168.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.301+475delT | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229505564 | |||||||
chr1:229505564 | TAAAAAAA others(8): Show |
T | 7 | a0003c0003t0004g0106 a0003c0003t0004g0108 a0003c0003t0004g0109 others(4): Show |
7 | HG01243.hp1 HG01516.hp1 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.301+461_301+475del others(15): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229505564 | |||||||
chr1:229505610 | G | A | 2 | a0007c0010t0001g0206 a0007c0010t0001g0207 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.301+430C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229505610 | |||||||
chr1:229505625 | G | A | 1 | a0006c0008t0004g0024 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.301+415C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229505625 | |||||||
chr1:229505649 | G | A | 15 | a0001c0001t0001g0006 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
16 | HG01358.hp2 HG01515.hp1 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.301+391C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229505649 | |||||||
chr1:229505711 | A | G | 2 | a0003c0011t0009g0136 a0003c0011t0009g0137 |
2 | HG01106.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.301+329T>C | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 2/25 | chr1 | 229505711 | |||||||
chr1:229506429 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.183-271A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 1/25 | chr1 | 229506429 | |||||||
chr1:229506449 | G | GT | 39 | a0001c0001t0001g0010 a0001c0001t0001g0037 a0001c0001t0001g0040 others(36): Show |
39 | HG00323.hp1 HG01243.hp1 HG01261.hp2 others(36): Show |
intron_variant | MODIFIER | c.183-292dupA | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 1/25 | chr1 | 229506449 | |||||||
chr1:229506449 | G | GTT | 55 | a0001c0001t0001g0107 a0002c0002t0001g0242 a0002c0002t0002g0009 others(52): Show |
56 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.183-293_183-292dup others(2): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 1/25 | chr1 | 229506449 | |||||||
chr1:229506449 | G | GTTT | 6 | a0002c0002t0002g0215 a0002c0002t0002g0217 a0002c0002t0002g0218 others(3): Show |
6 | HG01168.hp1 HG01981.hp1 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.183-294_183-292dup others(3): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 1/25 | chr1 | 229506449 | |||||||
chr1:229506539 | T | C | 4 | a0004c0004t0003g0257 a0004c0004t0003g0258 a0004c0004t0003g0259 others(1): Show |
4 | HG01123.hp2 HG01928.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.183-381A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 1/25 | chr1 | 229506539 | |||||||
chr1:229506630 | G | A | 2 | a0003c0011t0009g0136 a0003c0011t0009g0137 |
2 | HG01106.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.183-472C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 1/25 | chr1 | 229506630 | |||||||
chr1:229506638 | G | A | 73 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(70): Show |
74 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.183-480C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 1/25 | chr1 | 229506638 | |||||||
chr1:229506648 | T | C | 1 | a0001c0009t0001g0208 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.183-490A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 1/25 | chr1 | 229506648 | |||||||
chr1:229506677 | C | T | 4 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(1): Show |
4 | HG02055.hp2 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.183-519G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 1/25 | chr1 | 229506677 | |||||||
chr1:229506752 | T | A | 77 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0104 others(74): Show |
79 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.183-594A>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 1/25 | chr1 | 229506752 | |||||||
chr1:229506770 | T | C | 62 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(59): Show |
63 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.183-612A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 1/25 | chr1 | 229506770 | |||||||
chr1:229506796 | G | A | 1 | a0003c0003t0001g0023 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.183-638C>T | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 1/25 | chr1 | 229506796 | |||||||
chr1:229506821 | T | TA | 169 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0107 others(166): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.183-664dupT | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 1/25 | chr1 | 229506821 | |||||||
chr1:229506821 | T | TAA | 6 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0002c0002t0002g0262 others(3): Show |
6 | HG00140.hp1 HG02004.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.183-665_183-664dup others(2): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 1/25 | chr1 | 229506821 | |||||||
chr1:229506866 | G | C | 1 | a0001c0001t0001g0212 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.183-708C>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 1/25 | chr1 | 229506866 | |||||||
chr1:229506905 | C | T | 74 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(71): Show |
75 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.183-747G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 1/25 | chr1 | 229506905 | |||||||
chr1:229506993 | G | T | 74 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(71): Show |
75 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.183-835C>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 1/25 | chr1 | 229506993 | |||||||
chr1:229507005 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.183-847A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 1/25 | chr1 | 229507005 | |||||||
chr1:229507070 | T | C | 1 | a0003c0003t0013g0267 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.183-912A>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 1/25 | chr1 | 229507070 | |||||||
chr1:229507119 | A | C | 1 | a0001c0009t0001g0011 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.182+949T>G | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 1/25 | chr1 | 229507119 | |||||||
chr1:229507524 | AT | A | 49 | a0002c0002t0001g0242 a0002c0002t0002g0009 a0002c0002t0002g0214 others(46): Show |
50 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.182+543delA | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 1/25 | chr1 | 229507524 | |||||||
chr1:229507533 | C | T | 1 | a0001c0001t0001g0010 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.182+535G>A | NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 1/25 | chr1 | 229507533 | |||||||
chr1:229507877 | AATCAACT others(1): Show |
A | 5 | a0003c0003t0007g0263 a0003c0003t0007g0264 a0003c0003t0007g0265 others(2): Show |
5 | HG02630.hp1 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.182+183_182+190del others(8): Show |
NUP133 | ENSG00000069248.12 | transcript | ENST00000261396.6 | protein_coding | 1/25 | chr1 | 229507877 |