Item | Value |
---|---|
geneid | 4600 |
ensemblid | ENSG00000183486.14 |
hgncid | 7533 |
symbol | MX2 |
name | MX dynamin like GTPase 2 |
refseq_nuc | NM_002463.2 |
refseq_prot | NP_002454.1 |
ensembl_nuc | ENST00000330714.8 |
ensembl_prot | ENSP00000333657.3 |
mane_status | MANE Select |
chr | chr21 |
start | 41362027 |
end | 41409393 |
strand | + |
ver | v1.2 |
region | chr21:41362027-41409393 |
region5000 | chr21:41357027-41414393 |
regionname0 | MX2_chr21_41362027_41409393 |
regionname5000 | MX2_chr21_41357027_41414393 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 715 | 331 | 65 | 65 | 140 | 18 | 41 | 105 | MX2_chr21_41357027_41414393 | MX2 | MSKAH others(710): Show |
chr21 | 41357027 | 41414393 |
a0002 | 0/0 | 715 | 26 | 15 | 3 | 7 | 0 | 1 | 6 | MX2_chr21_41357027_41414393 | MX2 | MSKAH others(710): Show |
chr21 | 41357027 | 41414393 |
a0003 | 0/0 | 715 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | MSKAH others(710): Show |
chr21 | 41357027 | 41414393 |
a0004 | 0/0 | 715 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | MSKAH others(710): Show |
chr21 | 41357027 | 41414393 |
a0005 | 0/0 | 715 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | MSKAH others(710): Show |
chr21 | 41357027 | 41414393 |
a0006 | 0/0 | 715 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | MSKAH others(710): Show |
chr21 | 41357027 | 41414393 |
a0007 | 0/0 | 715 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | MSKAH others(710): Show |
chr21 | 41357027 | 41414393 |
a0008 | 0/0 | 715 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | MSKAH others(710): Show |
chr21 | 41357027 | 41414393 |
a0009 | 0/0 | 715 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | MSKAH others(710): Show |
chr21 | 41357027 | 41414393 |
a0010 | 0/0 | 715 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | MSKAH others(710): Show |
chr21 | 41357027 | 41414393 |
a0011 | 0/0 | 715 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | MSKAH others(710): Show |
chr21 | 41357027 | 41414393 |
a0012 | 0/0 | 715 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | MSKAH others(710): Show |
chr21 | 41357027 | 41414393 |
a0013 | 0/0 | 715 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | MSKAH others(710): Show |
chr21 | 41357027 | 41414393 |
a0014 | 0/0 | 715 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | MSKAH others(710): Show |
chr21 | 41357027 | 41414393 |
a0015 | 0/0 | 715 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | MSKAH others(710): Show |
chr21 | 41357027 | 41414393 |
a0016 | 0/0 | 715 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | MSKAH others(710): Show |
chr21 | 41357027 | 41414393 |
a0017 | 0/0 | 715 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | MSKAH others(710): Show |
chr21 | 41357027 | 41414393 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2145 | 279 | 52 | 63 | 107 | 17 | 38 | MX2_chr21_41357027_41414393 | MX2 | ATGTC others(2140): Show |
chr21 | 41357027 | 41414393 | ||
a0001c0002 | 0/0 | 2145 | 35 | 5 | 1 | 25 | 1 | 3 | MX2_chr21_41357027_41414393 | MX2 | ATGTC others(2140): Show |
chr21 | 41357027 | 41414393 | ||
a0001c0004 | 0/0 | 2145 | 12 | 5 | 0 | 7 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | ATGTC others(2140): Show |
chr21 | 41357027 | 41414393 | ||
a0001c0006 | 0/0 | 2145 | 2 | 1 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | ATGTC others(2140): Show |
chr21 | 41357027 | 41414393 | ||
a0001c0024 | 0/0 | 2145 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | ATGTC others(2140): Show |
chr21 | 41357027 | 41414393 | ||
a0001c0025 | 0/0 | 2145 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | ATGTC others(2140): Show |
chr21 | 41357027 | 41414393 | ||
a0001c0026 | 0/0 | 2145 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | ATGTC others(2140): Show |
chr21 | 41357027 | 41414393 | ||
a0002c0003 | 0/0 | 2145 | 19 | 11 | 1 | 6 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | ATGTC others(2140): Show |
chr21 | 41357027 | 41414393 | ||
a0002c0005 | 0/0 | 2145 | 4 | 2 | 2 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | ATGTC others(2140): Show |
chr21 | 41357027 | 41414393 | ||
a0002c0010 | 0/0 | 2145 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | ATGTC others(2140): Show |
chr21 | 41357027 | 41414393 | ||
a0002c0013 | 0/0 | 2145 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | ATGTC others(2140): Show |
chr21 | 41357027 | 41414393 | ||
a0002c0014 | 0/0 | 2145 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | ATGTC others(2140): Show |
chr21 | 41357027 | 41414393 | ||
a0003c0008 | 0/0 | 2145 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | ATGTC others(2140): Show |
chr21 | 41357027 | 41414393 | ||
a0003c0009 | 0/0 | 2145 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | ATGTC others(2140): Show |
chr21 | 41357027 | 41414393 | ||
a0004c0007 | 0/0 | 2145 | 2 | 2 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | ATGTC others(2140): Show |
chr21 | 41357027 | 41414393 | ||
a0005c0022 | 0/0 | 2145 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | ATGTC others(2140): Show |
chr21 | 41357027 | 41414393 | ||
a0006c0018 | 0/0 | 2145 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | ATGTC others(2140): Show |
chr21 | 41357027 | 41414393 | ||
a0007c0012 | 0/0 | 2145 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | ATGTC others(2140): Show |
chr21 | 41357027 | 41414393 | ||
a0008c0020 | 0/0 | 2145 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | ATGTC others(2140): Show |
chr21 | 41357027 | 41414393 | ||
a0009c0011 | 0/0 | 2145 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | ATGTC others(2140): Show |
chr21 | 41357027 | 41414393 | ||
a0010c0027 | 0/0 | 2145 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | ATGTC others(2140): Show |
chr21 | 41357027 | 41414393 | ||
a0011c0016 | 0/0 | 2145 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | ATGTC others(2140): Show |
chr21 | 41357027 | 41414393 | ||
a0012c0023 | 0/0 | 2145 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | ATGTC others(2140): Show |
chr21 | 41357027 | 41414393 | ||
a0013c0019 | 0/0 | 2145 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | ATGTC others(2140): Show |
chr21 | 41357027 | 41414393 | ||
a0014c0015 | 0/0 | 2145 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | ATGTC others(2140): Show |
chr21 | 41357027 | 41414393 | ||
a0015c0017 | 0/0 | 2145 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | ATGTC others(2140): Show |
chr21 | 41357027 | 41414393 | ||
a0016c0021 | 0/0 | 2145 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | ATGTC others(2140): Show |
chr21 | 41357027 | 41414393 | ||
a0017c0028 | 0/0 | 2145 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | ATGTC others(2140): Show |
chr21 | 41357027 | 41414393 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3406 | 210 | 31 | 59 | 77 | 14 | 28 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3401): Show |
chr21 | 41357027 | 41414393 |
a0001c0001t0002 | 1/0 | 3408 | 37 | 1 | 2 | 22 | 2 | 9 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3403): Show |
chr21 | 41357027 | 41414393 |
a0001c0001t0004 | 0/0 | 3406 | 9 | 9 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3401): Show |
chr21 | 41357027 | 41414393 |
a0001c0001t0005 | 0/0 | 3406 | 5 | 5 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3401): Show |
chr21 | 41357027 | 41414393 |
a0001c0001t0006 | 0/0 | 3404 | 5 | 3 | 2 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3399): Show |
chr21 | 41357027 | 41414393 |
a0001c0001t0007 | 0/0 | 3406 | 2 | 0 | 0 | 2 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3401): Show |
chr21 | 41357027 | 41414393 |
a0001c0001t0008 | 0/0 | 3406 | 2 | 0 | 0 | 2 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3401): Show |
chr21 | 41357027 | 41414393 |
a0001c0001t0009 | 0/0 | 3406 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3401): Show |
chr21 | 41357027 | 41414393 |
a0001c0001t0010 | 0/0 | 3406 | 2 | 0 | 0 | 2 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3401): Show |
chr21 | 41357027 | 41414393 |
a0001c0001t0011 | 0/0 | 3406 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3401): Show |
chr21 | 41357027 | 41414393 |
a0001c0001t0012 | 0/0 | 3406 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3401): Show |
chr21 | 41357027 | 41414393 |
a0001c0001t0013 | 0/0 | 3406 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3401): Show |
chr21 | 41357027 | 41414393 |
a0001c0001t0015 | 0/0 | 3406 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3401): Show |
chr21 | 41357027 | 41414393 |
a0001c0001t0017 | 0/0 | 3404 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3399): Show |
chr21 | 41357027 | 41414393 |
a0001c0001t0018 | 0/0 | 3406 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3401): Show |
chr21 | 41357027 | 41414393 |
a0001c0002t0001 | 0/0 | 3406 | 8 | 0 | 0 | 7 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3401): Show |
chr21 | 41357027 | 41414393 |
a0001c0002t0002 | 0/0 | 3408 | 26 | 4 | 1 | 18 | 0 | 3 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3403): Show |
chr21 | 41357027 | 41414393 |
a0001c0002t0004 | 0/0 | 3406 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3401): Show |
chr21 | 41357027 | 41414393 |
a0001c0004t0003 | 0/0 | 3406 | 12 | 5 | 0 | 7 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3401): Show |
chr21 | 41357027 | 41414393 |
a0001c0006t0001 | 0/0 | 3406 | 2 | 1 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3401): Show |
chr21 | 41357027 | 41414393 |
a0001c0024t0006 | 0/0 | 3404 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3399): Show |
chr21 | 41357027 | 41414393 |
a0001c0025t0001 | 0/0 | 3406 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3401): Show |
chr21 | 41357027 | 41414393 |
a0001c0026t0009 | 0/0 | 3406 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3401): Show |
chr21 | 41357027 | 41414393 |
a0002c0003t0001 | 0/0 | 3406 | 12 | 6 | 1 | 4 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3401): Show |
chr21 | 41357027 | 41414393 |
a0002c0003t0002 | 0/0 | 3408 | 2 | 0 | 0 | 2 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3403): Show |
chr21 | 41357027 | 41414393 |
a0002c0003t0004 | 0/0 | 3406 | 3 | 3 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3401): Show |
chr21 | 41357027 | 41414393 |
a0002c0003t0005 | 0/0 | 3406 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3401): Show |
chr21 | 41357027 | 41414393 |
a0002c0003t0019 | 0/0 | 3404 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3399): Show |
chr21 | 41357027 | 41414393 |
a0002c0005t0003 | 0/0 | 3406 | 4 | 2 | 2 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3401): Show |
chr21 | 41357027 | 41414393 |
a0002c0010t0016 | 0/0 | 3406 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3401): Show |
chr21 | 41357027 | 41414393 |
a0002c0013t0001 | 0/0 | 3406 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3401): Show |
chr21 | 41357027 | 41414393 |
a0002c0014t0001 | 0/0 | 3406 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3401): Show |
chr21 | 41357027 | 41414393 |
a0003c0008t0003 | 0/0 | 3406 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3401): Show |
chr21 | 41357027 | 41414393 |
a0003c0009t0001 | 0/0 | 3406 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3401): Show |
chr21 | 41357027 | 41414393 |
a0004c0007t0001 | 0/0 | 3406 | 2 | 2 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3401): Show |
chr21 | 41357027 | 41414393 |
a0005c0022t0001 | 0/0 | 3406 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3401): Show |
chr21 | 41357027 | 41414393 |
a0006c0018t0002 | 0/0 | 3408 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3403): Show |
chr21 | 41357027 | 41414393 |
a0007c0012t0001 | 0/0 | 3406 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3401): Show |
chr21 | 41357027 | 41414393 |
a0008c0020t0001 | 0/0 | 3406 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3401): Show |
chr21 | 41357027 | 41414393 |
a0009c0011t0001 | 0/0 | 3406 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3401): Show |
chr21 | 41357027 | 41414393 |
a0010c0027t0005 | 0/0 | 3406 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3401): Show |
chr21 | 41357027 | 41414393 |
a0011c0016t0005 | 0/0 | 3406 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3401): Show |
chr21 | 41357027 | 41414393 |
a0012c0023t0014 | 0/0 | 3408 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3403): Show |
chr21 | 41357027 | 41414393 |
a0013c0019t0002 | 0/0 | 3408 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3403): Show |
chr21 | 41357027 | 41414393 |
a0014c0015t0001 | 0/0 | 3406 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3401): Show |
chr21 | 41357027 | 41414393 |
a0015c0017t0001 | 0/0 | 3406 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3401): Show |
chr21 | 41357027 | 41414393 |
a0016c0021t0001 | 0/0 | 3406 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3401): Show |
chr21 | 41357027 | 41414393 |
a0017c0028t0001 | 0/0 | 3406 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | GATGA others(3401): Show |
chr21 | 41357027 | 41414393 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0010 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0282 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0281 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0004g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0004g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0004g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0004g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0004g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0005g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0005g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0005g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0005g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0005g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0006g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0006g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0006g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0006g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0006g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0007g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0008g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0008g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0009g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0010g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0010g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0011g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0012g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0013g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0015g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0017g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0018g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0001g0002 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0004t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0004t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0004t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0004t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0004t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0004t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0004t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0004t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0004t0003g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0004t0003g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0004t0003g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0004t0003g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0006t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0006t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0024t0006g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0025t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0026t0009g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0003t0001g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0003t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0003t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0003t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0003t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0003t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0003t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0003t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0003t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0003t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0003t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0003t0004g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0003t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0003t0005g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0003t0019g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0005t0003g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0005t0003g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0005t0003g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0010t0016g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0013t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0014t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0003c0008t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0003c0009t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0004c0007t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0004c0007t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0005c0022t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0006c0018t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0007c0012t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0008c0020t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0009c0011t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0010c0027t0005g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0011c0016t0005g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0012c0023t0014g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0013c0019t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0014c0015t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0015c0017t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0016c0021t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0017c0028t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0041 | EUR | GBR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0335 | EUR | GBR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0302 | EUR | GBR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0229 | EUR | GBR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0233 | EUR | FIN | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00280 | hp2 | a0001 | c0002 | t0001 | g0002 | EUR | FIN | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0115 | EUR | FIN | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0284 | EUR | FIN | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | CHS | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | CHS | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00423 | hp2 | a0001 | c0002 | t0002 | g0214 | EAS | CHS | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00558 | hp2 | a0001 | c0001 | t0010 | g0001 | EAS | CHS | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | CHS | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00621 | hp1 | a0005 | c0022 | t0001 | g0048 | EAS | CHS | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01069 | hp2 | a0006 | c0018 | t0002 | g0016 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0313 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01106 | hp1 | a0001 | c0006 | t0001 | g0238 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01109 | hp1 | a0007 | c0012 | t0001 | g0243 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01167 | hp1 | a0001 | c0001 | t0006 | g0341 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01169 | hp2 | a0001 | c0001 | t0006 | g0340 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01243 | hp2 | a0002 | c0003 | t0001 | g0024 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01257 | hp1 | a0002 | c0005 | t0003 | g0294 | AMR | CLM | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | CLM | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01258 | hp2 | a0002 | c0005 | t0003 | g0295 | AMR | CLM | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0089 | EUR | IBS | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0153 | EUR | IBS | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01516 | hp2 | a0001 | c0001 | t0011 | g0255 | EUR | IBS | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0090 | EUR | IBS | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01884 | hp1 | a0001 | c0004 | t0003 | g0316 | AFR | ACB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01884 | hp2 | a0001 | c0001 | t0015 | g0289 | AFR | ACB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | ACB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PEL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01993 | hp1 | a0001 | c0002 | t0002 | g0273 | AMR | PEL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02040 | hp1 | a0001 | c0002 | t0002 | g0037 | EAS | KHV | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02040 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02055 | hp1 | a0002 | c0005 | t0003 | g0023 | AFR | ACB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02055 | hp2 | a0001 | c0004 | t0003 | g0323 | AFR | ACB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02071 | hp1 | a0001 | c0026 | t0009 | g0173 | EAS | KHV | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02071 | hp2 | a0001 | c0002 | t0002 | g0165 | EAS | KHV | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02074 | hp1 | a0002 | c0013 | t0001 | g0193 | EAS | KHV | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0337 | EAS | KHV | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | KHV | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0325 | EAS | KHV | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02145 | hp1 | a0002 | c0005 | t0003 | g0023 | AFR | ACB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02145 | hp2 | a0001 | c0001 | t0004 | g0322 | AFR | ACB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02155 | hp1 | a0001 | c0002 | t0002 | g0198 | EAS | CDX | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02155 | hp2 | a0008 | c0020 | t0001 | g0110 | EAS | CDX | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | CDX | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02165 | hp2 | a0001 | c0002 | t0002 | g0126 | EAS | CDX | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02257 | hp1 | a0001 | c0006 | t0001 | g0141 | AFR | ACB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02257 | hp2 | a0009 | c0011 | t0001 | g0242 | AFR | ACB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02280 | hp1 | a0003 | c0009 | t0001 | g0339 | AFR | ACB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02280 | hp2 | a0001 | c0001 | t0017 | g0072 | AFR | ACB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | PEL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02451 | hp1 | a0001 | c0002 | t0002 | g0073 | AFR | ACB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0241 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0268 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02615 | hp2 | a0001 | c0001 | t0005 | g0324 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0065 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02630 | hp2 | a0001 | c0001 | t0005 | g0064 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02647 | hp1 | a0001 | c0004 | t0003 | g0274 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02647 | hp2 | a0002 | c0003 | t0001 | g0298 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02698 | hp1 | a0001 | c0002 | t0002 | g0058 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02723 | hp1 | a0001 | c0001 | t0006 | g0317 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02723 | hp2 | a0002 | c0010 | t0016 | g0329 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0146 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02738 | hp2 | a0001 | c0001 | t0013 | g0092 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02809 | hp1 | a0002 | c0003 | t0004 | g0305 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02886 | hp2 | a0001 | c0002 | t0002 | g0312 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02895 | hp1 | a0001 | c0001 | t0004 | g0066 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02895 | hp2 | a0003 | c0008 | t0003 | g0292 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02896 | hp1 | a0002 | c0003 | t0001 | g0311 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02896 | hp2 | a0001 | c0001 | t0005 | g0254 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | ESN | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02922 | hp2 | a0001 | c0004 | t0003 | g0320 | AFR | ESN | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | ESN | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02965 | hp2 | a0004 | c0007 | t0001 | g0328 | AFR | ESN | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02970 | hp1 | a0002 | c0003 | t0001 | g0300 | AFR | ESN | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02970 | hp2 | a0011 | c0016 | t0005 | g0251 | AFR | ESN | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02976 | hp2 | a0001 | c0002 | t0002 | g0250 | AFR | ESN | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0118 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0097 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03041 | hp2 | a0002 | c0003 | t0005 | g0297 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03098 | hp1 | a0001 | c0001 | t0006 | g0069 | AFR | MSL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03098 | hp2 | a0001 | c0001 | t0005 | g0315 | AFR | MSL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03130 | hp1 | a0001 | c0002 | t0004 | g0074 | AFR | ESN | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03130 | hp2 | a0002 | c0003 | t0004 | g0239 | AFR | ESN | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0063 | AFR | ESN | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03139 | hp2 | a0001 | c0001 | t0012 | g0291 | AFR | ESN | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | ESN | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03195 | hp2 | a0001 | c0001 | t0004 | g0245 | AFR | ESN | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03209 | hp1 | a0001 | c0024 | t0006 | g0330 | AFR | MSL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | MSL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03486 | hp2 | a0002 | c0014 | t0001 | g0071 | AFR | MSL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03490 | hp1 | a0001 | c0002 | t0002 | g0011 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03492 | hp1 | a0001 | c0002 | t0002 | g0011 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03516 | hp1 | a0001 | c0001 | t0006 | g0067 | AFR | ESN | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03540 | hp2 | a0002 | c0003 | t0001 | g0024 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03579 | hp1 | a0012 | c0023 | t0014 | g0249 | AFR | MSL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03654 | hp1 | a0013 | c0019 | t0002 | g0224 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0219 | SAS | STU | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | STU | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | BEB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | BEB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | BEB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | BEB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0130 | SAS | BEB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | BEB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0208 | SAS | STU | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | STU | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0285 | SAS | BEB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0280 | SAS | BEB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | STU | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG04199 | hp2 | a0002 | c0003 | t0001 | g0288 | SAS | STU | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0042 | SAS | STU | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | STU | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0277 | SAS | STU | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | STU | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18522 | hp1 | a0001 | c0004 | t0003 | g0307 | AFR | YRI | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18522 | hp2 | a0002 | c0003 | t0004 | g0304 | AFR | YRI | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18612 | hp1 | a0001 | c0001 | t0010 | g0180 | EAS | CHB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CHB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | CHB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | YRI | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18906 | hp2 | a0001 | c0025 | t0001 | g0331 | AFR | YRI | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18939 | hp2 | a0001 | c0002 | t0002 | g0190 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18943 | hp1 | a0014 | c0015 | t0001 | g0060 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18943 | hp2 | a0001 | c0001 | t0008 | g0166 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18944 | hp2 | a0001 | c0002 | t0002 | g0127 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18950 | hp2 | a0001 | c0002 | t0002 | g0129 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18952 | hp2 | a0001 | c0004 | t0003 | g0124 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18956 | hp1 | a0001 | c0002 | t0002 | g0213 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18957 | hp2 | a0001 | c0004 | t0003 | g0094 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18962 | hp1 | a0001 | c0002 | t0002 | g0104 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18965 | hp1 | a0002 | c0003 | t0002 | g0226 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0336 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18966 | hp1 | a0002 | c0003 | t0001 | g0326 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18966 | hp2 | a0015 | c0017 | t0001 | g0218 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18968 | hp1 | a0001 | c0002 | t0002 | g0189 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18969 | hp1 | a0016 | c0021 | t0001 | g0186 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18972 | hp1 | a0002 | c0003 | t0001 | g0136 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18974 | hp2 | a0001 | c0001 | t0007 | g0018 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18979 | hp1 | a0001 | c0004 | t0003 | g0256 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18980 | hp1 | a0001 | c0002 | t0002 | g0133 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18983 | hp1 | a0001 | c0001 | t0007 | g0018 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18984 | hp1 | a0002 | c0003 | t0001 | g0055 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18984 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18988 | hp2 | a0001 | c0004 | t0003 | g0227 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18994 | hp1 | a0001 | c0002 | t0002 | g0221 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19002 | hp2 | a0001 | c0001 | t0009 | g0332 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19004 | hp2 | a0001 | c0002 | t0002 | g0215 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19007 | hp1 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19009 | hp1 | a0001 | c0001 | t0008 | g0043 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19012 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19030 | hp1 | a0002 | c0003 | t0019 | g0237 | AFR | LWK | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19030 | hp2 | a0001 | c0001 | t0004 | g0248 | AFR | LWK | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19043 | hp1 | a0002 | c0003 | t0001 | g0296 | AFR | LWK | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19043 | hp2 | a0001 | c0001 | t0004 | g0276 | AFR | LWK | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19054 | hp2 | a0001 | c0004 | t0003 | g0128 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19067 | hp1 | a0001 | c0002 | t0002 | g0334 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19078 | hp2 | a0001 | c0004 | t0003 | g0085 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19081 | hp1 | a0001 | c0004 | t0003 | g0086 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19083 | hp1 | a0001 | c0001 | t0018 | g0338 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19086 | hp1 | a0002 | c0003 | t0001 | g0194 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19091 | hp2 | a0002 | c0003 | t0002 | g0197 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19240 | hp1 | a0001 | c0001 | t0005 | g0275 | AFR | YRI | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19240 | hp2 | a0001 | c0001 | t0004 | g0321 | AFR | YRI | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA20129 | hp1 | a0002 | c0003 | t0001 | g0299 | AFR | ASW | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ASW | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0117 | EUR | TSI | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0270 | EUR | TSI | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0102 | EUR | TSI | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0247 | EUR | TSI | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0113 | SAS | GIH | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA20905 | hp2 | a0017 | c0028 | t0001 | g0293 | SAS | GIH | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | ACB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0333 | AFR | ACB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02559 | hp2 | a0010 | c0027 | t0005 | g0272 | AFR | ACB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03471 | hp1 | a0004 | c0007 | t0001 | g0327 | AFR | MSL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03471 | hp2 | a0001 | c0002 | t0002 | g0318 | AFR | MSL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | USA | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | USA | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | LWK | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | LWK | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0282 | REF | REF | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0281 | REF | REF | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr21:41376962 | G | A | 1 | a0003 | 2 | HG02280.hp1 HG02895.hp2 |
missense_variant | MODERATE | c.56G>A | p.Arg19Gln | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 2/14 | 156/3408 | 56/2148 | 19/715 | chr21 | 41376962 | |||
chr21:41377007 | C | T | 1 | a0017 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.101C>T | p.Pro34Leu | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 2/14 | 201/3408 | 101/2148 | 34/715 | chr21 | 41377007 | |||
chr21:41377025 | C | T | 1 | a0010 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.119C>T | p.Pro40Leu | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 2/14 | 219/3408 | 119/2148 | 40/715 | chr21 | 41377025 | |||
chr21:41377123 | C | G | 1 | a0004 | 2 | HG02965.hp2 HG03471.hp1 |
missense_variant | MODERATE | c.217C>G | p.Pro73Ala | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 2/14 | 317/3408 | 217/2148 | 73/715 | chr21 | 41377123 | |||
chr21:41377154 | T | C | 3 | a0002 a0007 a0009 |
28 | HG01109.hp1 HG01243.hp2 HG01257.hp1 others(25): Show |
missense_variant&splice_region_variant | MODERATE | c.248T>C | p.Met83Thr | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 2/14 | 348/3408 | 248/2148 | 83/715 | chr21 | 41377154 | |||
chr21:41377819 | G | A | 1 | a0014 | 1 | NA18943.hp1 | missense_variant | MODERATE | c.280G>A | p.Glu94Lys | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/14 | 380/3408 | 280/2148 | 94/715 | chr21 | 41377819 | |||
chr21:41380103 | G | A | 2 | a0009 a0011 |
2 | HG02257.hp2 HG02970.hp2 |
missense_variant | MODERATE | c.529G>A | p.Glu177Lys | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/14 | 629/3408 | 529/2148 | 177/715 | chr21 | 41380103 | |||
chr21:41390571 | G | A | 1 | a0015 | 1 | NA18966.hp2 | missense_variant | MODERATE | c.739G>A | p.Ala247Thr | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/14 | 839/3408 | 739/2148 | 247/715 | chr21 | 41390571 | |||
chr21:41395721 | A | G | 1 | a0012 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.1006A>G | p.Arg336Gly | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/14 | 1106/3408 | 1006/2148 | 336/715 | chr21 | 41395721 | |||
chr21:41398951 | G | A | 1 | a0007 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.1204G>A | p.Glu402Lys | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 9/14 | 1304/3408 | 1204/2148 | 402/715 | chr21 | 41398951 | |||
chr21:41398969 | G | A | 1 | a0006 | 1 | HG01069.hp2 | missense_variant | MODERATE | c.1222G>A | p.Gly408Arg | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 9/14 | 1322/3408 | 1222/2148 | 408/715 | chr21 | 41398969 | |||
chr21:41403329 | A | C | 1 | a0005 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.1636A>C | p.Asn546His | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/14 | 1736/3408 | 1636/2148 | 546/715 | chr21 | 41403329 | |||
chr21:41403338 | G | A | 1 | a0008 | 1 | HG02155.hp2 | missense_variant | MODERATE | c.1645G>A | p.Val549Ile | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/14 | 1745/3408 | 1645/2148 | 549/715 | chr21 | 41403338 | |||
chr21:41408106 | G | A | 1 | a0016 | 1 | NA18969.hp1 | missense_variant | MODERATE | c.2021G>A | p.Arg674His | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 14/14 | 2121/3408 | 2021/2148 | 674/715 | chr21 | 41408106 | |||
chr21:41408141 | G | A | 1 | a0013 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.2056G>A | p.Ala686Thr | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 14/14 | 2156/3408 | 2056/2148 | 686/715 | chr21 | 41408141 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr21:41377008 | G | A | 1 | a0001c0006 | 2 | HG01106.hp1 HG02257.hp1 |
synonymous_variant | LOW | c.102G>A | p.Pro34Pro | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 2/14 | 202/3408 | 102/2148 | 34/715 | chr21 | 41377008 | |||
chr21:41377077 | T | G | 1 | a0002c0010 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.171T>G | p.Ala57Ala | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 2/14 | 271/3408 | 171/2148 | 57/715 | chr21 | 41377077 | |||
chr21:41377818 | C | T | 2 | a0002c0010 a0002c0014 |
2 | HG02723.hp2 HG03486.hp2 |
synonymous_variant | LOW | c.279C>T | p.Tyr93Tyr | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/14 | 379/3408 | 279/2148 | 93/715 | chr21 | 41377818 | |||
chr21:41382477 | C | T | 1 | a0001c0026 | 1 | HG02071.hp1 | synonymous_variant | LOW | c.645C>T | p.Ser215Ser | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/14 | 745/3408 | 645/2148 | 215/715 | chr21 | 41382477 | |||
chr21:41382555 | C | T | 2 | a0001c0024 a0001c0025 |
2 | HG03209.hp1 NA18906.hp2 |
synonymous_variant | LOW | c.723C>T | p.Ile241Ile | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/14 | 823/3408 | 723/2148 | 241/715 | chr21 | 41382555 | |||
chr21:41399249 | T | C | 3 | a0001c0002 a0002c0013 a0013c0019 |
37 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(34): Show |
synonymous_variant | LOW | c.1326T>C | p.Val442Val | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/14 | 1426/3408 | 1326/2148 | 442/715 | chr21 | 41399249 | |||
chr21:41403313 | C | T | 1 | a0001c0025 | 1 | NA18906.hp2 | synonymous_variant | LOW | c.1620C>T | p.Gly540Gly | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/14 | 1720/3408 | 1620/2148 | 540/715 | chr21 | 41403313 | |||
chr21:41406749 | G | A | 3 | a0001c0004 a0002c0005 a0003c0008 |
17 | HG01257.hp1 HG01258.hp2 HG01884.hp1 others(14): Show |
synonymous_variant | LOW | c.1656G>A | p.Thr552Thr | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 13/14 | 1756/3408 | 1656/2148 | 552/715 | chr21 | 41406749 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr21:41408267 | G | T | 1 | a0002c0003t0019 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*34G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 14/14 | 34 | chr21 | 41408267 | ||||||
chr21:41408273 | A | G | 4 | a0001c0001t0005 a0002c0003t0005 a0010c0027t0005 others(1): Show |
8 | HG02559.hp2 HG02615.hp2 HG02630.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*40A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 14/14 | 40 | chr21 | 41408273 | ||||||
chr21:41408286 | G | A | 1 | a0001c0001t0011 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*53G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 14/14 | 53 | chr21 | 41408286 | ||||||
chr21:41408417 | C | T | 1 | a0001c0001t0010 | 2 | HG00558.hp2 NA18612.hp1 |
3_prime_UTR_variant | MODIFIER | c.*184C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 14/14 | 184 | chr21 | 41408417 | ||||||
chr21:41408452 | C | T | 1 | a0001c0001t0018 | 1 | NA19083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*219C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 14/14 | 219 | chr21 | 41408452 | ||||||
chr21:41408604 | G | C | 3 | a0001c0001t0004 a0001c0002t0004 a0002c0003t0004 |
13 | HG02145.hp2 HG02572.hp1 HG02630.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*371G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 14/14 | 371 | chr21 | 41408604 | ||||||
chr21:41408606 | C | A | 1 | a0001c0001t0012 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*373C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 14/14 | 373 | chr21 | 41408606 | ||||||
chr21:41408683 | T | C | 1 | a0001c0001t0013 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*450T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 14/14 | 450 | chr21 | 41408683 | ||||||
chr21:41408746 | C | A | 3 | a0001c0004t0003 a0002c0005t0003 a0003c0008t0003 |
17 | HG01257.hp1 HG01258.hp2 HG01884.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*513C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 14/14 | 513 | chr21 | 41408746 | ||||||
chr21:41408775 | C | T | 4 | a0001c0001t0006 a0001c0001t0017 a0001c0024t0006 others(1): Show |
8 | HG01167.hp1 HG01169.hp2 HG02280.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*542C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 14/14 | 542 | chr21 | 41408775 | ||||||
chr21:41408818 | C | T | 2 | a0001c0001t0006 a0001c0024t0006 |
6 | HG01167.hp1 HG01169.hp2 HG02723.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*585C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 14/14 | 585 | chr21 | 41408818 | ||||||
chr21:41408940 | C | T | 5 | a0001c0001t0006 a0001c0001t0017 a0001c0024t0006 others(2): Show |
9 | HG01167.hp1 HG01169.hp2 HG02280.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*707C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 14/14 | 707 | chr21 | 41408940 | ||||||
chr21:41409056 | C | A | 1 | a0001c0001t0007 | 2 | NA18974.hp2 NA18983.hp1 |
3_prime_UTR_variant | MODIFIER | c.*823C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 14/14 | 823 | chr21 | 41409056 | ||||||
chr21:41409075 | T | A | 1 | a0001c0001t0008 | 2 | NA18943.hp2 NA19009.hp1 |
3_prime_UTR_variant | MODIFIER | c.*842T>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 14/14 | 842 | chr21 | 41409075 | ||||||
chr21:41409117 | C | T | 2 | a0001c0001t0015 a0012c0023t0014 |
2 | HG01884.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*884C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 14/14 | 884 | chr21 | 41409117 | ||||||
chr21:41409190 | T | C | 5 | a0001c0001t0006 a0001c0001t0017 a0001c0024t0006 others(2): Show |
9 | HG01167.hp1 HG01169.hp2 HG02280.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*957T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 14/14 | 957 | chr21 | 41409190 | ||||||
chr21:41409236 | TAC | T | 38 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(35): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
3_prime_UTR_variant | MODIFIER | c.*1025_*1026delCA | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 14/14 | 1025 | INFO_REALIGN_3_PRIME | chr21 | 41409236 | |||||
chr21:41409236 | TACAC | T | 4 | a0001c0001t0006 a0001c0001t0017 a0001c0024t0006 others(1): Show |
8 | HG01167.hp1 HG01169.hp2 HG02280.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1023_*1026delCACA | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 14/14 | 1023 | INFO_REALIGN_3_PRIME | chr21 | 41409236 | |||||
chr21:41409277 | A | G | 2 | a0001c0001t0009 a0001c0026t0009 |
2 | HG02071.hp1 NA19002.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1044A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 14/14 | 1044 | chr21 | 41409277 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr21:41362064 | G | A | 37 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0027 others(34): Show |
40 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-72+9G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362064 | |||||||
chr21:41362136 | A | G | 13 | a0001c0001t0001g0026 a0001c0001t0001g0333 a0001c0001t0001g0335 others(10): Show |
14 | HG00099.hp2 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.-72+81A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362136 | |||||||
chr21:41362138 | C | T | 13 | a0001c0001t0001g0026 a0001c0001t0001g0333 a0001c0001t0001g0335 others(10): Show |
14 | HG00099.hp2 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.-72+83C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362138 | |||||||
chr21:41362186 | C | T | 16 | a0001c0001t0001g0026 a0001c0001t0001g0333 a0001c0001t0001g0335 others(13): Show |
17 | HG00099.hp2 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.-72+131C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362186 | |||||||
chr21:41362197 | T | C | 1 | a0001c0001t0002g0061 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-72+142T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362197 | |||||||
chr21:41362339 | C | T | 1 | a0002c0003t0001g0326 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-72+284C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362339 | |||||||
chr21:41362367 | T | G | 1 | a0001c0001t0001g0062 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-72+312T>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362367 | |||||||
chr21:41362402 | G | A | 3 | a0001c0001t0001g0009 a0001c0001t0004g0063 a0001c0001t0005g0064 |
4 | HG02630.hp2 HG03139.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-72+347G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362402 | |||||||
chr21:41362485 | A | G | 16 | a0001c0001t0001g0026 a0001c0001t0001g0333 a0001c0001t0001g0335 others(13): Show |
17 | HG00099.hp2 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.-72+430A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362485 | |||||||
chr21:41362487 | T | G | 8 | a0001c0001t0001g0009 a0001c0001t0001g0068 a0001c0001t0004g0063 others(5): Show |
9 | HG02109.hp1 HG02630.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-72+432T>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362487 | |||||||
chr21:41362490 | C | T | 1 | a0001c0002t0001g0325 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-72+435C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362490 | |||||||
chr21:41362491 | G | A | 1 | a0001c0001t0002g0070 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-72+436G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362491 | |||||||
chr21:41362524 | G | A | 4 | a0001c0001t0017g0072 a0001c0002t0002g0073 a0001c0002t0004g0074 others(1): Show |
4 | HG02280.hp2 HG02451.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-72+469G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362524 | |||||||
chr21:41362529 | A | G | 6 | a0001c0001t0001g0009 a0001c0001t0001g0068 a0001c0001t0004g0063 others(3): Show |
7 | HG02109.hp1 HG02630.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.-72+474A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362529 | |||||||
chr21:41362533 | C | T | 40 | a0001c0001t0001g0025 a0001c0001t0001g0290 a0001c0001t0001g0301 others(37): Show |
43 | HG00140.hp1 HG01070.hp1 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.-72+478C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362533 | |||||||
chr21:41362564 | C | A | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0002g0075 |
3 | HG01261.hp2 HG01433.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.-72+509C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362564 | |||||||
chr21:41362564 | C | G | 19 | a0001c0001t0001g0025 a0001c0001t0001g0308 a0001c0001t0001g0309 others(16): Show |
20 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.-72+509C>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362564 | |||||||
chr21:41362720 | A | G | 4 | a0001c0001t0017g0072 a0001c0002t0002g0073 a0001c0002t0004g0074 others(1): Show |
4 | HG02280.hp2 HG02451.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-72+665A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362720 | |||||||
chr21:41362750 | C | CT | 56 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0035 others(53): Show |
61 | HG00099.hp1 HG00408.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.-72+721dupT | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr21 | 41362750 | ||||||
chr21:41362750 | C | CTT | 34 | a0001c0001t0001g0026 a0001c0001t0001g0240 a0001c0001t0001g0244 others(31): Show |
35 | HG00099.hp2 HG00140.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.-72+720_-72+721dup others(2): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr21 | 41362750 | ||||||
chr21:41362750 | CTTTTTTT others(4): Show |
C | 1 | a0010c0027t0005g0272 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-72+711_-72+721del others(11): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr21 | 41362750 | ||||||
chr21:41362751 | T | C | 3 | a0001c0001t0001g0009 a0001c0001t0004g0063 a0001c0001t0005g0064 |
4 | HG02630.hp2 HG03139.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-72+696T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362751 | |||||||
chr21:41362757 | T | C | 9 | a0001c0001t0001g0025 a0001c0001t0001g0308 a0001c0001t0001g0309 others(6): Show |
10 | HG01070.hp2 HG01071.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-72+702T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362757 | |||||||
chr21:41362762 | T | TC | 192 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(189): Show |
212 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.-72+707_-72+708ins others(1): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362762 | |||||||
chr21:41362762 | T | TCTTTTTT others(7): Show |
1 | a0001c0001t0001g0078 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-72+707_-72+708ins others(14): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362762 | |||||||
chr21:41362763 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-72+708T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362763 | |||||||
chr21:41362763 | T | TC | 4 | a0001c0001t0017g0072 a0001c0002t0002g0073 a0001c0002t0004g0074 others(1): Show |
4 | HG02280.hp2 HG02451.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-72+708_-72+709ins others(1): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362763 | |||||||
chr21:41362820 | G | C | 5 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(2): Show |
5 | HG01074.hp2 HG01168.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.-72+765G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362820 | |||||||
chr21:41362899 | C | G | 17 | a0001c0001t0001g0026 a0001c0001t0001g0287 a0001c0001t0001g0333 others(14): Show |
18 | HG00099.hp2 HG01167.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.-72+844C>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362899 | |||||||
chr21:41363006 | G | A | 9 | a0001c0001t0001g0009 a0001c0001t0001g0068 a0001c0001t0001g0235 others(6): Show |
10 | HG02109.hp1 HG02630.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.-72+951G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41363006 | |||||||
chr21:41363039 | G | A | 1 | a0001c0006t0001g0238 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-72+984G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41363039 | |||||||
chr21:41363060 | T | C | 279 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(276): Show |
305 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.-72+1005T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41363060 | |||||||
chr21:41363156 | G | A | 4 | a0001c0001t0017g0072 a0001c0002t0002g0073 a0001c0002t0004g0074 others(1): Show |
4 | HG02280.hp2 HG02451.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-72+1101G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41363156 | |||||||
chr21:41363169 | C | T | 1 | a0001c0001t0005g0324 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-72+1114C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41363169 | |||||||
chr21:41363592 | G | A | 2 | a0001c0004t0003g0085 a0001c0004t0003g0086 |
2 | NA19078.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.-72+1537G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41363592 | |||||||
chr21:41363695 | C | T | 5 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0265 others(2): Show |
5 | HG01258.hp1 HG01981.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-72+1640C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41363695 | |||||||
chr21:41363703 | C | T | 1 | a0001c0001t0001g0034 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-72+1648C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41363703 | |||||||
chr21:41363743 | G | A | 2 | a0004c0007t0001g0327 a0004c0007t0001g0328 |
2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-72+1688G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41363743 | |||||||
chr21:41363792 | G | A | 69 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0240 others(66): Show |
73 | HG00099.hp2 HG00140.hp1 HG01070.hp1 others(70): Show |
intron_variant | MODIFIER | c.-72+1737G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41363792 | |||||||
chr21:41363827 | C | T | 7 | a0001c0001t0001g0021 a0001c0001t0001g0229 a0001c0001t0001g0230 others(4): Show |
8 | HG00140.hp2 HG00280.hp1 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.-72+1772C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41363827 | |||||||
chr21:41363868 | G | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0252 a0001c0001t0001g0253 |
5 | HG02451.hp2 HG02572.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-72+1813G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41363868 | |||||||
chr21:41363906 | G | A | 1 | a0001c0006t0001g0238 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-72+1851G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41363906 | |||||||
chr21:41363945 | C | T | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0002g0075 |
3 | HG01261.hp2 HG01433.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.-72+1890C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41363945 | |||||||
chr21:41364130 | T | C | 1 | a0001c0001t0002g0268 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-72+2075T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41364130 | |||||||
chr21:41364213 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-72+2158C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41364213 | |||||||
chr21:41364271 | C | G | 1 | a0001c0001t0001g0228 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-72+2216C>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41364271 | |||||||
chr21:41364337 | A | G | 1 | a0001c0004t0003g0227 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-72+2282A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41364337 | |||||||
chr21:41364486 | G | A | 13 | a0001c0001t0001g0026 a0001c0001t0001g0333 a0001c0001t0001g0335 others(10): Show |
14 | HG00099.hp2 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.-72+2431G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41364486 | |||||||
chr21:41364499 | C | T | 4 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0002c0003t0001g0136 others(1): Show |
4 | HG02922.hp1 NA18906.hp1 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.-72+2444C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41364499 | |||||||
chr21:41364540 | T | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0252 a0001c0001t0001g0253 |
5 | HG02451.hp2 HG02572.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-72+2485T>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41364540 | |||||||
chr21:41364650 | T | C | 4 | a0001c0001t0017g0072 a0001c0002t0002g0073 a0001c0002t0004g0074 others(1): Show |
4 | HG02280.hp2 HG02451.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-72+2595T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41364650 | |||||||
chr21:41364789 | A | G | 1 | a0011c0016t0005g0251 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-72+2734A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41364789 | |||||||
chr21:41364877 | C | A | 2 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-72+2822C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41364877 | |||||||
chr21:41364900 | G | T | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0002g0075 |
3 | HG01261.hp2 HG01433.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.-72+2845G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41364900 | |||||||
chr21:41365010 | C | T | 13 | a0001c0001t0001g0026 a0001c0001t0001g0333 a0001c0001t0001g0335 others(10): Show |
14 | HG00099.hp2 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.-72+2955C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41365010 | |||||||
chr21:41365047 | A | G | 16 | a0001c0001t0001g0025 a0001c0001t0001g0308 a0001c0001t0001g0309 others(13): Show |
18 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.-72+2992A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41365047 | |||||||
chr21:41365111 | T | C | 2 | a0004c0007t0001g0327 a0004c0007t0001g0328 |
2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-72+3056T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41365111 | |||||||
chr21:41365125 | A | G | 39 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0035 others(36): Show |
42 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.-72+3070A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41365125 | |||||||
chr21:41365141 | G | A | 1 | a0001c0002t0001g0325 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-72+3086G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41365141 | |||||||
chr21:41365203 | A | ATTTG | 20 | a0001c0001t0001g0240 a0001c0001t0001g0244 a0001c0001t0001g0246 others(17): Show |
20 | HG01109.hp1 HG01258.hp1 HG01981.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72+3176_-72+3179d others(6): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr21 | 41365203 | ||||||
chr21:41365203 | ATTTG | A | 265 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(262): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.-72+3176_-72+3179d others(6): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr21 | 41365203 | ||||||
chr21:41365245 | T | C | 1 | a0001c0001t0004g0063 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-72+3190T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41365245 | |||||||
chr21:41365254 | G | A | 40 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0035 others(37): Show |
43 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.-72+3199G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41365254 | |||||||
chr21:41365339 | G | A | 1 | a0001c0006t0001g0238 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-72+3284G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41365339 | |||||||
chr21:41365511 | T | G | 1 | a0001c0001t0009g0332 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-72+3456T>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41365511 | |||||||
chr21:41365609 | C | T | 1 | a0001c0006t0001g0238 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-72+3554C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41365609 | |||||||
chr21:41365664 | A | T | 1 | a0001c0001t0001g0314 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-72+3609A>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41365664 | |||||||
chr21:41365665 | T | A | 1 | a0001c0001t0001g0314 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-72+3610T>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41365665 | |||||||
chr21:41365859 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-72+3804C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41365859 | |||||||
chr21:41365919 | C | T | 1 | a0001c0001t0001g0222 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-72+3864C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41365919 | |||||||
chr21:41365937 | G | A | 1 | a0001c0006t0001g0238 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-72+3882G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41365937 | |||||||
chr21:41365958 | G | A | 2 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-72+3903G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41365958 | |||||||
chr21:41365972 | A | G | 1 | a0001c0002t0002g0221 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-72+3917A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41365972 | |||||||
chr21:41366029 | CT | C | 11 | a0001c0001t0001g0026 a0001c0001t0001g0333 a0001c0001t0001g0335 others(8): Show |
12 | HG00099.hp2 HG02080.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-72+3977delT | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr21 | 41366029 | ||||||
chr21:41366296 | G | T | 1 | a0001c0001t0001g0220 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-72+4241G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41366296 | |||||||
chr21:41366538 | C | T | 1 | a0014c0015t0001g0060 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-72+4483C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41366538 | |||||||
chr21:41366590 | T | C | 3 | a0001c0001t0005g0315 a0001c0001t0006g0317 a0001c0004t0003g0316 |
3 | HG01884.hp1 HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-72+4535T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41366590 | |||||||
chr21:41366869 | G | T | 1 | a0001c0001t0005g0064 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-72+4814G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41366869 | |||||||
chr21:41367173 | G | A | 1 | a0001c0001t0001g0087 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-72+5118G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41367173 | |||||||
chr21:41367261 | A | G | 2 | a0001c0001t0001g0287 a0002c0003t0001g0288 |
2 | HG04199.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-72+5206A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41367261 | |||||||
chr21:41367317 | A | T | 17 | a0001c0001t0001g0009 a0001c0001t0001g0026 a0001c0001t0001g0068 others(14): Show |
19 | HG00099.hp2 HG01192.hp1 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.-72+5262A>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41367317 | |||||||
chr21:41367319 | T | C | 6 | a0001c0001t0001g0010 a0001c0001t0001g0088 a0001c0001t0001g0089 others(3): Show |
7 | HG00738.hp2 HG01515.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.-72+5264T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41367319 | |||||||
chr21:41367418 | G | A | 1 | a0001c0001t0001g0009 | 2 | HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-72+5363G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41367418 | |||||||
chr21:41367422 | G | C | 2 | a0001c0001t0005g0315 a0001c0004t0003g0316 |
2 | HG01884.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-72+5367G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41367422 | |||||||
chr21:41367506 | T | C | 35 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0035 others(32): Show |
38 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.-72+5451T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41367506 | |||||||
chr21:41367688 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-72+5633G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41367688 | |||||||
chr21:41367696 | A | G | 1 | a0001c0001t0002g0219 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-72+5641A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41367696 | |||||||
chr21:41367741 | C | T | 4 | a0001c0001t0001g0301 a0001c0001t0001g0302 a0001c0001t0001g0303 others(1): Show |
4 | HG00140.hp1 HG01070.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-72+5686C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41367741 | |||||||
chr21:41367803 | A | G | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-72+5748A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41367803 | |||||||
chr21:41367843 | G | A | 1 | a0010c0027t0005g0272 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-72+5788G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41367843 | |||||||
chr21:41367851 | C | T | 2 | a0001c0001t0001g0303 a0001c0001t0001g0306 |
2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-72+5796C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41367851 | |||||||
chr21:41367894 | C | T | 46 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0035 others(43): Show |
49 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.-72+5839C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41367894 | |||||||
chr21:41368052 | A | G | 310 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(307): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.-72+5997A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41368052 | |||||||
chr21:41368083 | C | T | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-72+6028C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41368083 | |||||||
chr21:41368287 | C | T | 2 | a0001c0001t0006g0340 a0001c0001t0006g0341 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-72+6232C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41368287 | |||||||
chr21:41368348 | C | T | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-72+6293C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41368348 | |||||||
chr21:41368369 | C | A | 2 | a0004c0007t0001g0327 a0004c0007t0001g0328 |
2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-72+6314C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41368369 | |||||||
chr21:41368561 | A | G | 4 | a0001c0001t0001g0301 a0001c0001t0001g0302 a0001c0001t0001g0303 others(1): Show |
4 | HG00140.hp1 HG01070.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-72+6506A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41368561 | |||||||
chr21:41368572 | C | T | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-72+6517C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41368572 | |||||||
chr21:41368854 | C | T | 1 | a0001c0002t0002g0058 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-72+6799C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41368854 | |||||||
chr21:41368897 | C | T | 8 | a0001c0001t0001g0004 a0001c0001t0001g0212 a0001c0001t0001g0216 others(5): Show |
10 | HG00423.hp2 HG01358.hp1 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.-72+6842C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41368897 | |||||||
chr21:41369022 | G | A | 254 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(251): Show |
280 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.-72+6967G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41369022 | |||||||
chr21:41369284 | A | G | 250 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(247): Show |
273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.-72+7229A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41369284 | |||||||
chr21:41369304 | G | A | 2 | a0001c0024t0006g0330 a0001c0025t0001g0331 |
2 | HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-72+7249G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41369304 | |||||||
chr21:41369305 | G | A | 1 | a0001c0001t0001g0301 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-72+7250G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41369305 | |||||||
chr21:41369399 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-72+7344G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41369399 | |||||||
chr21:41369492 | G | A | 1 | a0002c0003t0019g0237 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-71-7344G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41369492 | |||||||
chr21:41369531 | C | G | 3 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 |
3 | HG03239.hp1 HG03834.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-71-7305C>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41369531 | |||||||
chr21:41369593 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-71-7243G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41369593 | |||||||
chr21:41369617 | G | C | 1 | a0001c0001t0011g0255 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-71-7219G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41369617 | |||||||
chr21:41369802 | G | A | 5 | a0001c0001t0017g0072 a0001c0002t0002g0073 a0001c0002t0004g0074 others(2): Show |
5 | HG02280.hp2 HG02451.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-71-7034G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41369802 | |||||||
chr21:41369819 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-71-7017C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41369819 | |||||||
chr21:41369823 | A | ACCCCTGC others(8): Show |
1 | a0001c0001t0001g0235 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-71-7009_-71-6995d others(17): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr21 | 41369823 | ||||||
chr21:41369850 | T | C | 1 | a0001c0006t0001g0238 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-71-6986T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41369850 | |||||||
chr21:41369883 | G | C | 11 | a0001c0001t0001g0026 a0001c0001t0001g0333 a0001c0001t0001g0335 others(8): Show |
12 | HG00099.hp2 HG02080.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-71-6953G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41369883 | |||||||
chr21:41369998 | A | G | 2 | a0003c0008t0003g0292 a0003c0009t0001g0339 |
2 | HG02280.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-71-6838A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41369998 | |||||||
chr21:41370025 | C | G | 1 | a0001c0001t0001g0005 | 3 | HG02451.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-71-6811C>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41370025 | |||||||
chr21:41370089 | C | A | 2 | a0001c0001t0001g0096 a0001c0001t0002g0097 |
2 | HG03017.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-71-6747C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41370089 | |||||||
chr21:41370109 | C | A | 189 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(186): Show |
209 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.-71-6727C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41370109 | |||||||
chr21:41370285 | C | A | 233 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(230): Show |
254 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.-71-6551C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41370285 | |||||||
chr21:41370442 | G | C | 2 | a0001c0001t0001g0089 a0001c0001t0001g0090 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-71-6394G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41370442 | |||||||
chr21:41370489 | C | T | 1 | a0012c0023t0014g0249 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-71-6347C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41370489 | |||||||
chr21:41370523 | T | G | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-71-6313T>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41370523 | |||||||
chr21:41370537 | G | A | 13 | a0001c0001t0001g0026 a0001c0001t0001g0301 a0001c0001t0001g0302 others(10): Show |
14 | HG00099.hp2 HG00140.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.-71-6299G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41370537 | |||||||
chr21:41370602 | A | G | 305 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(302): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.-71-6234A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41370602 | |||||||
chr21:41370617 | T | G | 1 | a0001c0001t0005g0254 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-71-6219T>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41370617 | |||||||
chr21:41370645 | T | C | 1 | a0001c0001t0005g0275 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-71-6191T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41370645 | |||||||
chr21:41370748 | G | C | 1 | a0001c0001t0004g0241 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-71-6088G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41370748 | |||||||
chr21:41370907 | C | T | 2 | a0001c0001t0001g0303 a0001c0001t0001g0306 |
2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-71-5929C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41370907 | |||||||
chr21:41371184 | G | C | 13 | a0001c0001t0001g0036 a0001c0001t0001g0056 a0001c0001t0001g0206 others(10): Show |
14 | HG00423.hp1 HG00609.hp2 HG02040.hp1 others(11): Show |
intron_variant | MODIFIER | c.-71-5652G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41371184 | |||||||
chr21:41371224 | G | A | 16 | a0001c0001t0001g0025 a0001c0001t0001g0308 a0001c0001t0001g0309 others(13): Show |
17 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.-71-5612G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41371224 | |||||||
chr21:41371343 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-71-5493G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41371343 | |||||||
chr21:41371375 | G | T | 3 | a0001c0002t0002g0073 a0001c0002t0004g0074 a0002c0003t0019g0237 |
3 | HG02451.hp1 HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-71-5461G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41371375 | |||||||
chr21:41371391 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-71-5445G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41371391 | |||||||
chr21:41371397 | C | T | 1 | a0001c0006t0001g0238 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-71-5439C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41371397 | |||||||
chr21:41371400 | G | T | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
207 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.-71-5436G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41371400 | |||||||
chr21:41371569 | C | T | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
207 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.-71-5267C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41371569 | |||||||
chr21:41371596 | C | T | 5 | a0001c0001t0001g0026 a0001c0001t0002g0336 a0001c0001t0002g0337 others(2): Show |
6 | HG02080.hp1 NA18965.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.-71-5240C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41371596 | |||||||
chr21:41371601 | T | G | 1 | a0001c0001t0001g0038 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-71-5235T>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41371601 | |||||||
chr21:41371841 | T | C | 9 | a0001c0001t0001g0009 a0001c0001t0001g0068 a0001c0001t0004g0063 others(6): Show |
10 | HG01167.hp1 HG01169.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.-71-4995T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41371841 | |||||||
chr21:41371869 | G | T | 1 | a0001c0001t0005g0254 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-71-4967G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41371869 | |||||||
chr21:41371894 | A | G | 42 | a0001c0001t0001g0007 a0001c0001t0001g0035 a0001c0001t0001g0036 others(39): Show |
44 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.-71-4942A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41371894 | |||||||
chr21:41372337 | A | C | 311 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(308): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.-71-4499A>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41372337 | |||||||
chr21:41372340 | A | G | 311 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(308): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.-71-4496A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41372340 | |||||||
chr21:41372529 | T | TA | 5 | a0001c0001t0017g0072 a0001c0002t0002g0073 a0001c0002t0004g0074 others(2): Show |
5 | HG02280.hp2 HG02451.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-71-4307_-71-4306i others(3): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41372529 | |||||||
chr21:41372652 | C | T | 1 | a0002c0003t0001g0288 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-71-4184C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41372652 | |||||||
chr21:41372678 | A | G | 311 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(308): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.-71-4158A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41372678 | |||||||
chr21:41372958 | C | T | 100 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0017 others(97): Show |
108 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.-71-3878C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41372958 | |||||||
chr21:41372984 | C | A | 3 | a0001c0001t0004g0276 a0001c0001t0005g0275 a0001c0002t0002g0250 |
3 | HG02976.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-71-3852C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41372984 | |||||||
chr21:41373038 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-71-3798G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41373038 | |||||||
chr21:41373078 | G | T | 3 | a0001c0001t0005g0254 a0004c0007t0001g0327 a0004c0007t0001g0328 |
3 | HG02896.hp2 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-71-3758G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41373078 | |||||||
chr21:41373138 | A | C | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-71-3698A>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41373138 | |||||||
chr21:41373167 | G | A | 1 | a0001c0002t0001g0325 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-71-3669G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41373167 | |||||||
chr21:41373199 | G | GA | 8 | a0001c0001t0001g0009 a0001c0001t0001g0068 a0001c0001t0004g0063 others(5): Show |
9 | HG01167.hp1 HG01169.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-71-3635dupA | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr21 | 41373199 | ||||||
chr21:41373245 | A | G | 62 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0026 others(59): Show |
67 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(64): Show |
intron_variant | MODIFIER | c.-71-3591A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41373245 | |||||||
chr21:41373424 | G | A | 54 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0068 others(51): Show |
56 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.-71-3412G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41373424 | |||||||
chr21:41373487 | G | A | 186 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
206 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.-71-3349G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41373487 | |||||||
chr21:41373521 | G | A | 1 | a0001c0001t0011g0255 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-71-3315G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41373521 | |||||||
chr21:41373617 | G | A | 2 | a0001c0024t0006g0330 a0001c0025t0001g0331 |
2 | HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-71-3219G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41373617 | |||||||
chr21:41373651 | C | T | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
207 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.-71-3185C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41373651 | |||||||
chr21:41373663 | C | T | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | HG02572.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-71-3173C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41373663 | |||||||
chr21:41373805 | T | TA | 28 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0039 others(25): Show |
31 | HG00099.hp2 HG00140.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.-71-3010dupA | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr21 | 41373805 | ||||||
chr21:41373805 | T | TAAA | 45 | a0001c0001t0001g0025 a0001c0001t0001g0068 a0001c0001t0001g0100 others(42): Show |
46 | HG01071.hp1 HG01109.hp1 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.-71-3012_-71-3010d others(5): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr21 | 41373805 | ||||||
chr21:41373805 | TA | T | 9 | a0001c0001t0001g0059 a0001c0001t0001g0087 a0001c0001t0001g0090 others(6): Show |
9 | HG00140.hp2 HG01168.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.-71-3010delA | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr21 | 41373805 | ||||||
chr21:41373846 | G | A | 2 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-71-2990G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41373846 | |||||||
chr21:41373876 | A | G | 1 | a0001c0001t0004g0276 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-71-2960A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41373876 | |||||||
chr21:41373887 | C | G | 1 | a0001c0006t0001g0238 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-71-2949C>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41373887 | |||||||
chr21:41373889 | C | T | 1 | a0001c0001t0005g0254 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-71-2947C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41373889 | |||||||
chr21:41373903 | G | A | 3 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0002g0146 |
3 | HG01109.hp2 HG02735.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-71-2933G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41373903 | |||||||
chr21:41373935 | C | A | 1 | a0001c0004t0003g0307 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-71-2901C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41373935 | |||||||
chr21:41373959 | C | T | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG00597.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.-71-2877C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41373959 | |||||||
chr21:41374154 | C | T | 186 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
206 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.-71-2682C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41374154 | |||||||
chr21:41374229 | T | C | 326 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(323): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.-71-2607T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41374229 | |||||||
chr21:41374305 | G | A | 2 | a0001c0001t0006g0340 a0001c0001t0006g0341 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-71-2531G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41374305 | |||||||
chr21:41374349 | C | G | 114 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(111): Show |
121 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.-71-2487C>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41374349 | |||||||
chr21:41374394 | G | A | 1 | a0001c0002t0002g0273 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-71-2442G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41374394 | |||||||
chr21:41374441 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-71-2395G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41374441 | |||||||
chr21:41374478 | G | A | 1 | a0001c0001t0001g0009 | 2 | HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-71-2358G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41374478 | |||||||
chr21:41374565 | G | A | 1 | a0001c0002t0002g0104 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-71-2271G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41374565 | |||||||
chr21:41374641 | C | G | 186 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
206 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.-71-2195C>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41374641 | |||||||
chr21:41374651 | GGCTGCCA others(8): Show |
G | 183 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(180): Show |
203 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.-71-2182_-71-2168d others(17): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr21 | 41374651 | ||||||
chr21:41374670 | G | A | 1 | a0001c0001t0005g0254 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-71-2166G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41374670 | |||||||
chr21:41374671 | G | A | 5 | a0002c0003t0001g0296 a0002c0003t0005g0297 a0002c0005t0003g0023 others(2): Show |
6 | HG01257.hp1 HG01258.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.-71-2165G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41374671 | |||||||
chr21:41374716 | ACT | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0235 a0001c0001t0001g0236 others(2): Show |
7 | HG02451.hp2 HG02572.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-71-2117_-71-2116d others(4): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr21 | 41374716 | ||||||
chr21:41374725 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-71-2111G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41374725 | |||||||
chr21:41375069 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-71-1767C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41375069 | |||||||
chr21:41375227 | G | A | 3 | a0001c0001t0005g0315 a0001c0001t0006g0317 a0001c0004t0003g0316 |
3 | HG01884.hp1 HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-71-1609G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41375227 | |||||||
chr21:41375255 | G | A | 1 | a0001c0001t0011g0255 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-71-1581G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41375255 | |||||||
chr21:41375308 | C | G | 2 | a0004c0007t0001g0327 a0004c0007t0001g0328 |
2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-71-1528C>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41375308 | |||||||
chr21:41375340 | G | A | 61 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0022 others(58): Show |
66 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(63): Show |
intron_variant | MODIFIER | c.-71-1496G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41375340 | |||||||
chr21:41375454 | G | T | 1 | a0001c0006t0001g0238 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-71-1382G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41375454 | |||||||
chr21:41375589 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-71-1247C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41375589 | |||||||
chr21:41375615 | G | T | 88 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0035 others(85): Show |
93 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.-71-1221G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41375615 | |||||||
chr21:41375885 | G | A | 1 | a0002c0014t0001g0071 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-71-951G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41375885 | |||||||
chr21:41375920 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-71-916G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41375920 | |||||||
chr21:41375949 | T | C | 1 | a0001c0006t0001g0238 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-71-887T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41375949 | |||||||
chr21:41376030 | C | A | 1 | a0001c0002t0002g0011 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-71-806C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41376030 | |||||||
chr21:41376305 | G | A | 177 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(174): Show |
197 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.-71-531G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41376305 | |||||||
chr21:41376308 | C | T | 177 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(174): Show |
197 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.-71-528C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41376308 | |||||||
chr21:41376390 | A | C | 310 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(307): Show |
339 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(336): Show |
intron_variant | MODIFIER | c.-71-446A>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41376390 | |||||||
chr21:41376392 | A | C | 222 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(219): Show |
245 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.-71-444A>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41376392 | |||||||
chr21:41376438 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-71-398C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41376438 | |||||||
chr21:41376546 | TCAACAAC others(2): Show |
T | 48 | a0001c0001t0001g0007 a0001c0001t0001g0035 a0001c0001t0001g0036 others(45): Show |
50 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.-71-279_-71-271del others(9): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr21 | 41376546 | ||||||
chr21:41376555 | A | G | 1 | a0001c0001t0004g0063 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-71-281A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41376555 | |||||||
chr21:41376623 | G | A | 2 | a0001c0001t0001g0154 a0001c0001t0001g0202 |
2 | HG01261.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.-71-213G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41376623 | |||||||
chr21:41376677 | C | G | 1 | a0001c0004t0003g0316 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-71-159C>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41376677 | |||||||
chr21:41376702 | A | G | 17 | a0001c0001t0002g0268 a0001c0001t0004g0276 a0001c0001t0006g0340 others(14): Show |
19 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.-71-134A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41376702 | |||||||
chr21:41376776 | G | A | 2 | a0001c0001t0001g0278 a0001c0001t0001g0279 |
2 | HG00738.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.-71-60G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41376776 | |||||||
chr21:41376802 | C | T | 5 | a0001c0001t0001g0068 a0001c0001t0005g0064 a0001c0001t0006g0067 others(2): Show |
5 | HG02109.hp1 HG02630.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-34C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41376802 | |||||||
chr21:41376812 | G | A | 3 | a0001c0001t0001g0306 a0001c0001t0004g0276 a0001c0002t0002g0250 |
3 | HG02717.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-71-24G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41376812 | |||||||
chr21:41377164 | G | A | 4 | a0001c0002t0002g0318 a0001c0006t0001g0238 a0004c0007t0001g0327 others(1): Show |
4 | HG01106.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.249+9G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 2/13 | chr21 | 41377164 | |||||||
chr21:41377188 | G | A | 2 | a0004c0007t0001g0327 a0004c0007t0001g0328 |
2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.249+33G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 2/13 | chr21 | 41377188 | |||||||
chr21:41377262 | A | G | 197 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(194): Show |
212 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.249+107A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 2/13 | chr21 | 41377262 | |||||||
chr21:41377319 | A | G | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.249+164A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 2/13 | chr21 | 41377319 | |||||||
chr21:41377351 | C | T | 2 | a0004c0007t0001g0327 a0004c0007t0001g0328 |
2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.249+196C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 2/13 | chr21 | 41377351 | |||||||
chr21:41377389 | T | C | 1 | a0001c0002t0002g0318 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.249+234T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 2/13 | chr21 | 41377389 | |||||||
chr21:41377432 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.249+277G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 2/13 | chr21 | 41377432 | |||||||
chr21:41377450 | C | T | 40 | a0001c0001t0001g0022 a0001c0001t0001g0026 a0001c0001t0001g0036 others(37): Show |
43 | HG00140.hp1 HG00423.hp1 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.249+295C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 2/13 | chr21 | 41377450 | |||||||
chr21:41377489 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.250-300C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 2/13 | chr21 | 41377489 | |||||||
chr21:41377634 | G | A | 2 | a0001c0001t0001g0076 a0001c0001t0002g0075 |
2 | HG01433.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.250-155G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 2/13 | chr21 | 41377634 | |||||||
chr21:41377675 | T | C | 8 | a0001c0001t0001g0308 a0001c0001t0005g0275 a0001c0001t0006g0067 others(5): Show |
8 | HG01109.hp1 HG02109.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.250-114T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 2/13 | chr21 | 41377675 | |||||||
chr21:41377682 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.250-107T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 2/13 | chr21 | 41377682 | |||||||
chr21:41377719 | C | T | 2 | a0004c0007t0001g0327 a0004c0007t0001g0328 |
2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.250-70C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 2/13 | chr21 | 41377719 | |||||||
chr21:41377997 | C | T | 2 | a0001c0024t0006g0330 a0001c0025t0001g0331 |
2 | HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.442+16C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41377997 | |||||||
chr21:41378078 | T | C | 1 | a0001c0006t0001g0238 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.442+97T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41378078 | |||||||
chr21:41378125 | AGAGAGAC others(10): Show |
A | 14 | a0001c0001t0001g0035 a0001c0001t0001g0053 a0001c0001t0001g0054 others(11): Show |
14 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.442+157_442+173del others(17): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 41378125 | ||||||
chr21:41378162 | G | C | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | HG02572.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.442+181G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41378162 | |||||||
chr21:41378199 | G | A | 1 | a0001c0006t0001g0238 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.442+218G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41378199 | |||||||
chr21:41378225 | A | AGAGACAG others(74): Show |
13 | a0001c0001t0001g0035 a0001c0001t0001g0053 a0001c0001t0001g0054 others(10): Show |
13 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.442+279_442+280ins others(81): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 41378225 | ||||||
chr21:41378232 | G | A | 2 | a0001c0024t0006g0330 a0001c0025t0001g0331 |
2 | HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.442+251G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41378232 | |||||||
chr21:41378239 | G | GGGAGAGA others(93): Show |
1 | a0001c0001t0001g0278 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.442+285_442+286ins others(100): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 41378239 | ||||||
chr21:41378239 | G | GGGAGAGA others(76): Show |
18 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0025 others(15): Show |
22 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.442+340_442+341ins others(83): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 41378239 | ||||||
chr21:41378284 | T | C | 15 | a0001c0001t0001g0035 a0001c0001t0001g0053 a0001c0001t0001g0054 others(12): Show |
15 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.442+303T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41378284 | |||||||
chr21:41378302 | A | ACTGGGAG others(10): Show |
16 | a0001c0001t0001g0035 a0001c0001t0001g0053 a0001c0001t0001g0054 others(13): Show |
16 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.442+338_442+354dup others(17): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 41378302 | ||||||
chr21:41378302 | A | ACTGGGAG others(93): Show |
92 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0056 others(89): Show |
102 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.442+340_442+341ins others(100): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 41378302 | ||||||
chr21:41378302 | A | ACTGGGAG others(323): Show |
6 | a0001c0001t0001g0244 a0001c0001t0004g0241 a0001c0001t0004g0245 others(3): Show |
6 | HG02572.hp1 HG02886.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.442+340_442+341ins others(330): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 41378302 | ||||||
chr21:41378302 | A | ACTGGGAG others(110): Show |
3 | a0001c0001t0001g0333 a0001c0004t0003g0320 a0001c0004t0003g0323 |
3 | HG02055.hp2 HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.442+340_442+341ins others(117): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 41378302 | ||||||
chr21:41378302 | A | ACTGGGAG others(91): Show |
1 | a0001c0001t0015g0289 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.442+340_442+341ins others(98): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 41378302 | ||||||
chr21:41378344 | G | A | 3 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0280 |
3 | HG00280.hp1 HG01243.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.442+363G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41378344 | |||||||
chr21:41378385 | T | C | 35 | a0001c0001t0001g0035 a0001c0001t0001g0053 a0001c0001t0001g0054 others(32): Show |
37 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.442+404T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41378385 | |||||||
chr21:41378445 | C | T | 2 | a0002c0010t0016g0329 a0002c0014t0001g0071 |
2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.442+464C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41378445 | |||||||
chr21:41378485 | A | G | 55 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0056 others(52): Show |
63 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.442+504A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41378485 | |||||||
chr21:41378524 | C | T | 55 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0056 others(52): Show |
63 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.442+543C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41378524 | |||||||
chr21:41378525 | G | A | 19 | a0001c0001t0001g0035 a0001c0001t0001g0053 a0001c0001t0001g0054 others(16): Show |
19 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.442+544G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41378525 | |||||||
chr21:41378530 | C | T | 2 | a0002c0010t0016g0329 a0002c0014t0001g0071 |
2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.442+549C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41378530 | |||||||
chr21:41378604 | C | A | 2 | a0002c0010t0016g0329 a0002c0014t0001g0071 |
2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.442+623C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41378604 | |||||||
chr21:41378651 | C | T | 19 | a0001c0001t0001g0035 a0001c0001t0001g0053 a0001c0001t0001g0054 others(16): Show |
19 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.442+670C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41378651 | |||||||
chr21:41378652 | A | C | 19 | a0001c0001t0001g0035 a0001c0001t0001g0053 a0001c0001t0001g0054 others(16): Show |
19 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.442+671A>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41378652 | |||||||
chr21:41378727 | A | G | 13 | a0001c0001t0001g0246 a0001c0001t0001g0278 a0001c0001t0001g0287 others(10): Show |
13 | HG01891.hp2 HG01952.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.442+746A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41378727 | |||||||
chr21:41378807 | A | G | 21 | a0001c0001t0001g0035 a0001c0001t0001g0053 a0001c0001t0001g0054 others(18): Show |
21 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.442+826A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41378807 | |||||||
chr21:41378846 | G | A | 2 | a0001c0001t0001g0101 a0001c0001t0001g0105 |
2 | HG01109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.442+865G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41378846 | |||||||
chr21:41378915 | C | T | 100 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0056 others(97): Show |
110 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.442+934C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41378915 | |||||||
chr21:41379005 | A | G | 21 | a0001c0001t0001g0035 a0001c0001t0001g0053 a0001c0001t0001g0054 others(18): Show |
21 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.443-1012A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41379005 | |||||||
chr21:41379031 | G | A | 1 | a0001c0006t0001g0238 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.443-986G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41379031 | |||||||
chr21:41379325 | C | T | 1 | a0002c0003t0004g0239 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.443-692C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41379325 | |||||||
chr21:41379351 | G | A | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.443-666G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41379351 | |||||||
chr21:41379392 | C | G | 1 | a0001c0001t0001g0142 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.443-625C>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41379392 | |||||||
chr21:41379414 | C | T | 3 | a0001c0001t0001g0333 a0001c0004t0003g0320 a0001c0004t0003g0323 |
3 | HG02055.hp2 HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.443-603C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41379414 | |||||||
chr21:41379415 | G | A | 15 | a0001c0001t0001g0246 a0001c0001t0001g0278 a0001c0001t0001g0287 others(12): Show |
15 | HG01884.hp2 HG01891.hp2 HG01952.hp2 others(12): Show |
intron_variant | MODIFIER | c.443-602G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41379415 | |||||||
chr21:41379433 | G | A | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.443-584G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41379433 | |||||||
chr21:41379465 | C | T | 16 | a0001c0001t0001g0246 a0001c0001t0001g0278 a0001c0001t0001g0287 others(13): Show |
16 | HG01884.hp2 HG01891.hp2 HG01952.hp2 others(13): Show |
intron_variant | MODIFIER | c.443-552C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41379465 | |||||||
chr21:41379506 | C | T | 2 | a0001c0001t0001g0188 a0001c0002t0002g0189 |
2 | NA18968.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.443-511C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41379506 | |||||||
chr21:41379614 | A | G | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.443-403A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41379614 | |||||||
chr21:41379637 | A | G | 2 | a0001c0001t0005g0064 a0001c0006t0001g0238 |
2 | HG01106.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.443-380A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41379637 | |||||||
chr21:41379651 | T | C | 3 | a0001c0001t0005g0064 a0001c0006t0001g0238 a0002c0010t0016g0329 |
3 | HG01106.hp1 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.443-366T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41379651 | |||||||
chr21:41379656 | A | G | 105 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0035 others(102): Show |
113 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.443-361A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41379656 | |||||||
chr21:41379681 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.443-336C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41379681 | |||||||
chr21:41379732 | A | G | 63 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0056 others(60): Show |
67 | HG00423.hp1 HG00609.hp2 HG01106.hp1 others(64): Show |
intron_variant | MODIFIER | c.443-285A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41379732 | |||||||
chr21:41379806 | G | A | 10 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0308 others(7): Show |
10 | HG01109.hp1 HG02109.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.443-211G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41379806 | |||||||
chr21:41379924 | C | T | 1 | a0002c0014t0001g0071 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.443-93C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41379924 | |||||||
chr21:41379931 | G | A | 24 | a0001c0001t0001g0125 a0001c0001t0001g0148 a0001c0001t0001g0216 others(21): Show |
28 | HG00280.hp2 HG00423.hp2 HG01993.hp1 others(25): Show |
intron_variant | MODIFIER | c.443-86G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41379931 | |||||||
chr21:41379955 | G | C | 2 | a0001c0001t0005g0064 a0001c0006t0001g0238 |
2 | HG01106.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.443-62G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41379955 | |||||||
chr21:41379960 | G | A | 1 | a0001c0002t0001g0156 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.443-57G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41379960 | |||||||
chr21:41379995 | A | G | 3 | a0001c0001t0005g0064 a0001c0006t0001g0238 a0002c0010t0016g0329 |
3 | HG01106.hp1 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.443-22A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41379995 | |||||||
chr21:41380011 | G | A | 4 | a0001c0001t0006g0317 a0001c0001t0006g0340 a0001c0001t0006g0341 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.443-6G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41380011 | |||||||
chr21:41380011 | G | T | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | splice_region_variant&intron_variant | LOW | c.443-6G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41380011 | |||||||
chr21:41380177 | G | A | 3 | a0001c0001t0005g0064 a0001c0006t0001g0238 a0002c0010t0016g0329 |
3 | HG01106.hp1 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.577+26G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41380177 | |||||||
chr21:41380208 | G | T | 3 | a0001c0001t0001g0333 a0001c0004t0003g0320 a0001c0004t0003g0323 |
3 | HG02055.hp2 HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.577+57G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41380208 | |||||||
chr21:41380229 | G | A | 3 | a0001c0001t0005g0064 a0001c0006t0001g0238 a0002c0010t0016g0329 |
3 | HG01106.hp1 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.577+78G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41380229 | |||||||
chr21:41380324 | G | A | 1 | a0001c0004t0003g0274 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.577+173G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41380324 | |||||||
chr21:41380343 | G | A | 10 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0308 others(7): Show |
10 | HG01109.hp1 HG02109.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.577+192G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41380343 | |||||||
chr21:41380346 | T | C | 6 | a0001c0001t0001g0333 a0001c0001t0005g0064 a0001c0004t0003g0320 others(3): Show |
6 | HG01106.hp1 HG02055.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.577+195T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41380346 | |||||||
chr21:41380411 | A | G | 143 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(140): Show |
157 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.577+260A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41380411 | |||||||
chr21:41380425 | G | C | 7 | a0001c0001t0001g0333 a0001c0001t0005g0064 a0001c0004t0003g0320 others(4): Show |
7 | HG01257.hp1 HG01258.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.577+274G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41380425 | |||||||
chr21:41380431 | C | T | 1 | a0001c0001t0002g0219 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.577+280C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41380431 | |||||||
chr21:41380432 | G | A | 7 | a0001c0001t0001g0333 a0001c0001t0005g0064 a0001c0004t0003g0320 others(4): Show |
7 | HG01257.hp1 HG01258.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.577+281G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41380432 | |||||||
chr21:41380458 | AG | A | 7 | a0001c0001t0001g0333 a0001c0001t0005g0064 a0001c0004t0003g0320 others(4): Show |
7 | HG01106.hp1 HG01257.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.577+310delG | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr21 | 41380458 | ||||||
chr21:41380478 | C | G | 2 | a0003c0008t0003g0292 a0003c0009t0001g0339 |
2 | HG02280.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.577+327C>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41380478 | |||||||
chr21:41380612 | T | C | 1 | a0001c0001t0005g0064 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.577+461T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41380612 | |||||||
chr21:41380638 | C | T | 1 | a0001c0006t0001g0238 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.577+487C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41380638 | |||||||
chr21:41380688 | T | G | 8 | a0001c0001t0001g0333 a0001c0004t0003g0320 a0001c0004t0003g0323 others(5): Show |
8 | HG01106.hp1 HG01257.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.577+537T>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41380688 | |||||||
chr21:41380702 | G | A | 1 | a0001c0001t0015g0289 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.577+551G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41380702 | |||||||
chr21:41380780 | T | A | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.577+629T>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41380780 | |||||||
chr21:41380785 | C | T | 7 | a0001c0001t0001g0333 a0001c0004t0003g0320 a0001c0004t0003g0323 others(4): Show |
7 | HG01106.hp1 HG01257.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.577+634C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41380785 | |||||||
chr21:41380827 | G | A | 1 | a0001c0001t0001g0006 | 2 | HG00639.hp1 HG00642.hp1 |
intron_variant | MODIFIER | c.577+676G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41380827 | |||||||
chr21:41380877 | A | G | 1 | a0001c0002t0002g0198 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.577+726A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41380877 | |||||||
chr21:41381031 | C | A | 1 | a0001c0001t0005g0315 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.577+880C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381031 | |||||||
chr21:41381070 | C | G | 1 | a0001c0006t0001g0238 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.577+919C>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381070 | |||||||
chr21:41381111 | A | G | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.577+960A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381111 | |||||||
chr21:41381127 | T | C | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.577+976T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381127 | |||||||
chr21:41381136 | C | A | 4 | a0001c0001t0001g0333 a0001c0006t0001g0238 a0002c0003t0019g0237 others(1): Show |
4 | HG01106.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.577+985C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381136 | |||||||
chr21:41381137 | G | A | 25 | a0001c0001t0001g0125 a0001c0001t0001g0148 a0001c0001t0001g0216 others(22): Show |
29 | HG00280.hp2 HG00423.hp2 HG01993.hp1 others(26): Show |
intron_variant | MODIFIER | c.577+986G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381137 | |||||||
chr21:41381144 | C | T | 1 | a0001c0002t0002g0318 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.577+993C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381144 | |||||||
chr21:41381201 | T | C | 35 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0068 others(32): Show |
38 | HG01070.hp2 HG01071.hp1 HG01257.hp1 others(35): Show |
intron_variant | MODIFIER | c.577+1050T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381201 | |||||||
chr21:41381221 | A | G | 4 | a0001c0001t0006g0317 a0001c0001t0006g0340 a0001c0001t0006g0341 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.577+1070A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381221 | |||||||
chr21:41381286 | T | C | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | HG02572.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.578-1124T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381286 | |||||||
chr21:41381295 | A | G | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.578-1115A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381295 | |||||||
chr21:41381513 | G | A | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.578-897G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381513 | |||||||
chr21:41381521 | T | C | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.578-889T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381521 | |||||||
chr21:41381542 | G | A | 3 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0002g0157 |
3 | NA18979.hp2 NA19010.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.578-868G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381542 | |||||||
chr21:41381548 | A | G | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.578-862A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381548 | |||||||
chr21:41381610 | G | T | 2 | a0004c0007t0001g0327 a0004c0007t0001g0328 |
2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.578-800G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381610 | |||||||
chr21:41381640 | G | A | 2 | a0001c0001t0002g0130 a0002c0010t0016g0329 |
2 | HG02723.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.578-770G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381640 | |||||||
chr21:41381651 | C | T | 1 | a0001c0001t0004g0063 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.578-759C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381651 | |||||||
chr21:41381663 | C | T | 3 | a0001c0001t0004g0245 a0001c0001t0004g0248 a0002c0010t0016g0329 |
3 | HG02723.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.578-747C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381663 | |||||||
chr21:41381672 | G | A | 129 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(126): Show |
142 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.578-738G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381672 | |||||||
chr21:41381684 | C | CA | 36 | a0001c0001t0001g0036 a0001c0001t0001g0053 a0001c0001t0001g0054 others(33): Show |
36 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.578-703dupA | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr21 | 41381684 | ||||||
chr21:41381684 | CA | C | 57 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0033 others(54): Show |
60 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(57): Show |
intron_variant | MODIFIER | c.578-703delA | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr21 | 41381684 | ||||||
chr21:41381878 | A | G | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.578-532A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381878 | |||||||
chr21:41381957 | A | G | 1 | a0001c0001t0006g0067 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.578-453A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381957 | |||||||
chr21:41382046 | T | C | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.578-364T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41382046 | |||||||
chr21:41382054 | G | A | 1 | a0001c0004t0003g0307 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.578-356G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41382054 | |||||||
chr21:41382269 | T | C | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.578-141T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41382269 | |||||||
chr21:41382327 | G | A | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.578-83G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41382327 | |||||||
chr21:41382636 | G | A | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.732+72G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41382636 | |||||||
chr21:41382926 | T | C | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.732+362T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41382926 | |||||||
chr21:41382995 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.732+431G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41382995 | |||||||
chr21:41382999 | G | A | 1 | a0001c0001t0002g0219 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.732+435G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41382999 | |||||||
chr21:41383003 | G | A | 1 | a0001c0001t0017g0072 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.732+439G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41383003 | |||||||
chr21:41383087 | G | A | 1 | a0001c0001t0001g0160 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.732+523G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41383087 | |||||||
chr21:41383092 | C | T | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.732+528C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41383092 | |||||||
chr21:41383133 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.732+569A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41383133 | |||||||
chr21:41383167 | C | T | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.732+603C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41383167 | |||||||
chr21:41383203 | A | T | 1 | a0001c0001t0001g0121 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.732+639A>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41383203 | |||||||
chr21:41383312 | G | A | 1 | a0001c0001t0011g0255 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.732+748G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41383312 | |||||||
chr21:41383478 | C | T | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.732+914C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41383478 | |||||||
chr21:41383705 | T | C | 1 | a0001c0006t0001g0238 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.732+1141T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41383705 | |||||||
chr21:41383733 | G | A | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.732+1169G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41383733 | |||||||
chr21:41383761 | G | A | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.732+1197G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41383761 | |||||||
chr21:41383799 | G | A | 1 | a0001c0001t0006g0067 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.732+1235G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41383799 | |||||||
chr21:41383899 | A | G | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.732+1335A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41383899 | |||||||
chr21:41383905 | C | T | 2 | a0001c0024t0006g0330 a0001c0025t0001g0331 |
2 | HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.732+1341C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41383905 | |||||||
chr21:41383928 | T | C | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.732+1364T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41383928 | |||||||
chr21:41383985 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.732+1421G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41383985 | |||||||
chr21:41384014 | G | A | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.732+1450G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384014 | |||||||
chr21:41384023 | T | C | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.732+1459T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384023 | |||||||
chr21:41384050 | G | C | 1 | a0001c0001t0002g0337 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.732+1486G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384050 | |||||||
chr21:41384072 | T | G | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.732+1508T>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384072 | |||||||
chr21:41384099 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.732+1535C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384099 | |||||||
chr21:41384139 | A | T | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.732+1575A>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384139 | |||||||
chr21:41384150 | C | A | 1 | a0001c0001t0001g0121 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.732+1586C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384150 | |||||||
chr21:41384219 | G | A | 1 | a0001c0002t0002g0058 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.732+1655G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384219 | |||||||
chr21:41384251 | A | C | 1 | a0001c0001t0001g0121 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.732+1687A>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384251 | |||||||
chr21:41384252 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.732+1688G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384252 | |||||||
chr21:41384348 | T | C | 148 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(145): Show |
161 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.732+1784T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384348 | |||||||
chr21:41384393 | G | A | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.732+1829G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384393 | |||||||
chr21:41384420 | C | T | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.732+1856C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384420 | |||||||
chr21:41384458 | T | A | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.732+1894T>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384458 | |||||||
chr21:41384460 | A | T | 150 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(147): Show |
163 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.732+1896A>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384460 | |||||||
chr21:41384463 | G | T | 9 | a0001c0001t0001g0041 a0001c0001t0001g0095 a0001c0001t0001g0140 others(6): Show |
9 | HG00099.hp1 HG01099.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.732+1899G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384463 | |||||||
chr21:41384494 | T | C | 5 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0002g0045 others(2): Show |
5 | HG02071.hp2 NA18962.hp2 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.732+1930T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384494 | |||||||
chr21:41384572 | T | C | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.732+2008T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384572 | |||||||
chr21:41384577 | C | T | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.732+2013C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384577 | |||||||
chr21:41384610 | G | A | 3 | a0001c0001t0001g0200 a0001c0001t0001g0209 a0001c0001t0001g0210 |
3 | HG03654.hp2 HG03834.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.732+2046G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384610 | |||||||
chr21:41384659 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.732+2095A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384659 | |||||||
chr21:41384685 | C | T | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.732+2121C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384685 | |||||||
chr21:41384708 | G | A | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.732+2144G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384708 | |||||||
chr21:41384732 | T | C | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.732+2168T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384732 | |||||||
chr21:41384794 | G | A | 2 | a0004c0007t0001g0327 a0004c0007t0001g0328 |
2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.732+2230G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384794 | |||||||
chr21:41384810 | G | A | 1 | a0001c0001t0008g0166 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.732+2246G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384810 | |||||||
chr21:41384838 | C | CA | 147 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(144): Show |
160 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.732+2289dupA | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 41384838 | ||||||
chr21:41384872 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.732+2308G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384872 | |||||||
chr21:41384927 | A | T | 1 | a0002c0013t0001g0193 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.732+2363A>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384927 | |||||||
chr21:41385044 | TGTGA | T | 4 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0120 others(1): Show |
4 | HG01168.hp2 HG01169.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.732+2484_732+2487d others(6): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 41385044 | ||||||
chr21:41385069 | A | C | 148 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(145): Show |
161 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.732+2505A>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41385069 | |||||||
chr21:41385140 | T | C | 1 | a0001c0001t0001g0121 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.732+2576T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41385140 | |||||||
chr21:41385157 | G | C | 1 | a0001c0001t0001g0257 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.732+2593G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41385157 | |||||||
chr21:41385162 | C | T | 1 | a0001c0001t0001g0051 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.732+2598C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41385162 | |||||||
chr21:41385163 | G | A | 3 | a0007c0012t0001g0243 a0009c0011t0001g0242 a0011c0016t0005g0251 |
3 | HG01109.hp1 HG02257.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.732+2599G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41385163 | |||||||
chr21:41385173 | A | T | 19 | a0001c0001t0001g0125 a0001c0001t0001g0216 a0001c0001t0001g0287 others(16): Show |
23 | HG00280.hp2 HG00423.hp2 HG01993.hp1 others(20): Show |
intron_variant | MODIFIER | c.732+2609A>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41385173 | |||||||
chr21:41385176 | C | A | 46 | a0001c0001t0001g0095 a0001c0001t0001g0125 a0001c0001t0001g0216 others(43): Show |
52 | HG00280.hp2 HG00423.hp2 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.732+2612C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41385176 | |||||||
chr21:41385425 | A | G | 3 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0002g0040 |
4 | NA18963.hp1 NA19011.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.732+2861A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41385425 | |||||||
chr21:41385554 | G | T | 1 | a0001c0001t0001g0121 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.732+2990G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41385554 | |||||||
chr21:41385587 | A | G | 1 | a0001c0025t0001g0331 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.732+3023A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41385587 | |||||||
chr21:41385607 | T | C | 1 | a0001c0025t0001g0331 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.732+3043T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41385607 | |||||||
chr21:41385693 | A | T | 48 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0021 others(45): Show |
51 | HG00323.hp1 HG00621.hp1 HG01069.hp1 others(48): Show |
intron_variant | MODIFIER | c.732+3129A>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41385693 | |||||||
chr21:41386005 | C | A | 7 | a0001c0001t0001g0095 a0001c0001t0015g0289 a0001c0004t0003g0085 others(4): Show |
7 | HG01884.hp2 NA18946.hp2 NA18957.hp2 others(4): Show |
intron_variant | MODIFIER | c.732+3441C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41386005 | |||||||
chr21:41386175 | A | G | 1 | a0001c0001t0015g0289 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.732+3611A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41386175 | |||||||
chr21:41386199 | A | G | 1 | a0001c0001t0015g0289 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.732+3635A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41386199 | |||||||
chr21:41386219 | C | CA | 47 | a0001c0001t0001g0017 a0001c0001t0001g0027 a0001c0001t0001g0031 others(44): Show |
48 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.732+3685dupA | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 41386219 | ||||||
chr21:41386219 | CA | C | 123 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(120): Show |
135 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.732+3685delA | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 41386219 | ||||||
chr21:41386219 | CAA | C | 37 | a0001c0001t0001g0333 a0001c0001t0002g0040 a0001c0001t0004g0065 others(34): Show |
42 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.732+3684_732+3685d others(4): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 41386219 | ||||||
chr21:41386219 | CAAA | C | 11 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0001g0235 others(8): Show |
12 | HG01167.hp1 HG01169.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.732+3683_732+3685d others(5): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 41386219 | ||||||
chr21:41386219 | CAAAAAAA others(5): Show |
C | 1 | a0001c0004t0003g0323 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.732+3674_732+3685d others(14): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 41386219 | ||||||
chr21:41386219 | CAAAAAAA others(6): Show |
C | 1 | a0002c0003t0001g0300 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.732+3673_732+3685d others(15): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 41386219 | ||||||
chr21:41386236 | A | C | 1 | a0001c0001t0002g0137 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.732+3672A>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41386236 | |||||||
chr21:41386237 | A | C | 58 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(55): Show |
66 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.732+3673A>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41386237 | |||||||
chr21:41386239 | A | C | 3 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0002g0040 |
4 | NA18963.hp1 NA19011.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.732+3675A>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41386239 | |||||||
chr21:41386239 | AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0015g0289 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.732+3679_732+3689d others(13): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 41386239 | ||||||
chr21:41386240 | A | C | 2 | a0001c0001t0012g0291 a0002c0014t0001g0071 |
2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.732+3676A>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41386240 | |||||||
chr21:41386248 | A | G | 2 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.732+3684A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41386248 | |||||||
chr21:41386300 | G | A | 6 | a0001c0001t0001g0095 a0001c0004t0003g0085 a0001c0004t0003g0086 others(3): Show |
6 | NA18946.hp2 NA18957.hp2 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.732+3736G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41386300 | |||||||
chr21:41386368 | T | A | 1 | a0001c0001t0001g0184 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.732+3804T>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41386368 | |||||||
chr21:41386389 | A | G | 1 | a0002c0013t0001g0193 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.732+3825A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41386389 | |||||||
chr21:41386457 | G | C | 1 | a0001c0001t0001g0287 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.732+3893G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41386457 | |||||||
chr21:41386500 | A | G | 10 | a0001c0001t0001g0155 a0001c0001t0001g0333 a0001c0001t0004g0063 others(7): Show |
10 | HG01167.hp1 HG01169.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.732+3936A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41386500 | |||||||
chr21:41386783 | T | C | 72 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(69): Show |
81 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.733-3782T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41386783 | |||||||
chr21:41386790 | G | A | 2 | a0007c0012t0001g0243 a0009c0011t0001g0242 |
2 | HG01109.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.733-3775G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41386790 | |||||||
chr21:41386850 | G | A | 13 | a0001c0001t0001g0303 a0001c0001t0001g0306 a0001c0001t0002g0268 others(10): Show |
15 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.733-3715G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41386850 | |||||||
chr21:41386916 | C | T | 1 | a0001c0024t0006g0330 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.733-3649C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41386916 | |||||||
chr21:41386995 | GAAC | G | 59 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(56): Show |
68 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.733-3555_733-3553d others(5): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 41386995 | ||||||
chr21:41387032 | G | A | 8 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0004g0065 others(5): Show |
8 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.733-3533G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41387032 | |||||||
chr21:41387067 | C | T | 3 | a0002c0003t0001g0298 a0002c0003t0001g0299 a0002c0003t0001g0311 |
3 | HG02647.hp2 HG02896.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.733-3498C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41387067 | |||||||
chr21:41387089 | C | T | 59 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(56): Show |
68 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.733-3476C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41387089 | |||||||
chr21:41387122 | T | C | 1 | a0016c0021t0001g0186 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.733-3443T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41387122 | |||||||
chr21:41387184 | C | T | 60 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(57): Show |
69 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.733-3381C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41387184 | |||||||
chr21:41387206 | G | C | 158 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(155): Show |
174 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.733-3359G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41387206 | |||||||
chr21:41387225 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.733-3340G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41387225 | |||||||
chr21:41387267 | T | C | 1 | a0001c0001t0001g0232 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.733-3298T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41387267 | |||||||
chr21:41387302 | G | A | 2 | a0001c0001t0001g0155 a0001c0024t0006g0330 |
2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.733-3263G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41387302 | |||||||
chr21:41387403 | C | T | 3 | a0001c0001t0001g0333 a0001c0001t0006g0340 a0001c0001t0006g0341 |
3 | HG01167.hp1 HG01169.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.733-3162C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41387403 | |||||||
chr21:41387418 | G | A | 1 | a0001c0001t0001g0102 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.733-3147G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41387418 | |||||||
chr21:41387551 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.733-3014T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41387551 | |||||||
chr21:41387573 | G | C | 155 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(152): Show |
171 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.733-2992G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41387573 | |||||||
chr21:41387665 | C | T | 156 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(153): Show |
172 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.733-2900C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41387665 | |||||||
chr21:41387857 | A | G | 5 | a0001c0001t0001g0333 a0001c0001t0004g0063 a0001c0001t0004g0276 others(2): Show |
5 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.733-2708A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41387857 | |||||||
chr21:41387951 | C | T | 29 | a0001c0001t0001g0121 a0001c0001t0001g0287 a0001c0001t0005g0275 others(26): Show |
34 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.733-2614C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41387951 | |||||||
chr21:41388145 | T | C | 3 | a0001c0001t0006g0067 a0001c0001t0006g0317 a0001c0001t0017g0072 |
3 | HG02280.hp2 HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.733-2420T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41388145 | |||||||
chr21:41388154 | G | T | 1 | a0001c0001t0001g0260 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.733-2411G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41388154 | |||||||
chr21:41388201 | C | T | 1 | a0001c0001t0001g0005 | 3 | HG02451.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.733-2364C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41388201 | |||||||
chr21:41388291 | C | T | 1 | a0001c0002t0002g0273 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.733-2274C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41388291 | |||||||
chr21:41388324 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.733-2241G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41388324 | |||||||
chr21:41388385 | C | T | 1 | a0001c0001t0002g0118 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.733-2180C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41388385 | |||||||
chr21:41388600 | G | A | 6 | a0001c0001t0001g0121 a0001c0002t0001g0002 a0001c0002t0001g0012 others(3): Show |
9 | HG00280.hp2 HG00408.hp2 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.733-1965G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41388600 | |||||||
chr21:41388636 | G | T | 51 | a0001c0001t0001g0121 a0001c0001t0001g0235 a0001c0001t0001g0236 others(48): Show |
58 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.733-1929G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41388636 | |||||||
chr21:41388651 | G | A | 32 | a0001c0001t0001g0095 a0001c0001t0001g0162 a0001c0001t0001g0246 others(29): Show |
32 | HG01257.hp1 HG01258.hp2 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.733-1914G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41388651 | |||||||
chr21:41388868 | A | G | 1 | a0001c0001t0001g0333 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.733-1697A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41388868 | |||||||
chr21:41388906 | A | G | 61 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(58): Show |
70 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.733-1659A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41388906 | |||||||
chr21:41389021 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.733-1544C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41389021 | |||||||
chr21:41389134 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.733-1431G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41389134 | |||||||
chr21:41389152 | G | A | 61 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0026 others(58): Show |
65 | HG00099.hp1 HG00140.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.733-1413G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41389152 | |||||||
chr21:41389157 | G | A | 93 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(90): Show |
107 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.733-1408G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41389157 | |||||||
chr21:41389175 | T | C | 32 | a0001c0001t0001g0121 a0001c0001t0001g0155 a0001c0001t0001g0287 others(29): Show |
37 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.733-1390T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41389175 | |||||||
chr21:41389197 | C | CA | 91 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(88): Show |
105 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.733-1355dupA | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 41389197 | ||||||
chr21:41389231 | A | C | 1 | a0001c0025t0001g0331 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.733-1334A>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41389231 | |||||||
chr21:41389301 | G | A | 5 | a0001c0001t0001g0333 a0001c0001t0004g0063 a0001c0001t0004g0276 others(2): Show |
5 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.733-1264G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41389301 | |||||||
chr21:41389313 | A | G | 2 | a0001c0001t0001g0109 a0001c0001t0001g0145 |
2 | NA19068.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.733-1252A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41389313 | |||||||
chr21:41389317 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.733-1248C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41389317 | |||||||
chr21:41389470 | G | C | 1 | a0001c0001t0001g0006 | 2 | HG00639.hp1 HG00642.hp1 |
intron_variant | MODIFIER | c.733-1095G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41389470 | |||||||
chr21:41389527 | T | G | 1 | a0001c0001t0002g0336 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.733-1038T>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41389527 | |||||||
chr21:41389828 | A | G | 2 | a0001c0001t0005g0254 a0001c0001t0005g0315 |
2 | HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.733-737A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41389828 | |||||||
chr21:41389865 | G | A | 124 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(121): Show |
140 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.733-700G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41389865 | |||||||
chr21:41389888 | T | C | 2 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.733-677T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41389888 | |||||||
chr21:41389910 | T | C | 5 | a0002c0003t0001g0298 a0002c0003t0001g0299 a0002c0003t0001g0311 others(2): Show |
5 | HG02647.hp2 HG02723.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.733-655T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41389910 | |||||||
chr21:41390105 | C | T | 3 | a0001c0001t0001g0015 a0001c0001t0001g0100 a0001c0001t0001g0201 |
4 | HG01358.hp2 HG01516.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.733-460C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41390105 | |||||||
chr21:41390230 | G | A | 124 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(121): Show |
140 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.733-335G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41390230 | |||||||
chr21:41390276 | T | C | 43 | a0001c0001t0001g0095 a0001c0001t0001g0162 a0001c0001t0001g0246 others(40): Show |
45 | HG01109.hp1 HG01243.hp2 HG01496.hp1 others(42): Show |
intron_variant | MODIFIER | c.733-289T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41390276 | |||||||
chr21:41390292 | G | A | 2 | a0001c0001t0012g0291 a0002c0014t0001g0071 |
2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.733-273G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41390292 | |||||||
chr21:41390338 | G | C | 4 | a0001c0001t0006g0067 a0001c0001t0006g0317 a0001c0024t0006g0330 others(1): Show |
4 | HG02723.hp1 HG02723.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.733-227G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41390338 | |||||||
chr21:41390345 | T | C | 147 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(144): Show |
163 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.733-220T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41390345 | |||||||
chr21:41390436 | T | C | 56 | a0001c0001t0001g0003 a0001c0001t0001g0026 a0001c0001t0001g0051 others(53): Show |
59 | HG00558.hp1 HG00673.hp1 HG01106.hp1 others(56): Show |
intron_variant | MODIFIER | c.733-129T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41390436 | |||||||
chr21:41390458 | G | A | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.733-107G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41390458 | |||||||
chr21:41390478 | C | T | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.733-87C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41390478 | |||||||
chr21:41390502 | C | T | 1 | a0001c0002t0002g0129 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.733-63C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41390502 | |||||||
chr21:41390512 | A | G | 23 | a0001c0001t0001g0095 a0001c0001t0001g0162 a0001c0001t0001g0246 others(20): Show |
23 | HG01496.hp1 HG01981.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.733-53A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41390512 | |||||||
chr21:41390529 | C | T | 1 | a0001c0001t0017g0072 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.733-36C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41390529 | |||||||
chr21:41390719 | C | A | 4 | a0001c0001t0001g0277 a0001c0001t0001g0286 a0001c0001t0002g0042 others(1): Show |
4 | HG01192.hp1 HG02683.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.871+16C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41390719 | |||||||
chr21:41390727 | C | T | 15 | a0001c0001t0001g0290 a0001c0001t0001g0303 a0001c0001t0001g0306 others(12): Show |
17 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.871+24C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41390727 | |||||||
chr21:41390806 | A | C | 27 | a0001c0001t0001g0121 a0001c0001t0001g0287 a0001c0001t0018g0338 others(24): Show |
32 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.871+103A>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41390806 | |||||||
chr21:41390822 | G | A | 3 | a0001c0001t0001g0030 a0001c0001t0001g0052 a0005c0022t0001g0048 |
3 | HG00621.hp1 NA18994.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.871+119G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41390822 | |||||||
chr21:41390889 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.871+186C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41390889 | |||||||
chr21:41390959 | T | C | 34 | a0001c0001t0001g0121 a0001c0001t0001g0287 a0001c0001t0006g0067 others(31): Show |
39 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.871+256T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41390959 | |||||||
chr21:41391005 | C | CA | 62 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(59): Show |
71 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.871+316dupA | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 41391005 | ||||||
chr21:41391008 | A | C | 2 | a0001c0001t0004g0065 a0001c0001t0004g0066 |
2 | HG02630.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.871+305A>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41391008 | |||||||
chr21:41391094 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.871+391C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41391094 | |||||||
chr21:41391095 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.871+392G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41391095 | |||||||
chr21:41391119 | G | A | 47 | a0001c0001t0001g0121 a0001c0001t0001g0287 a0001c0001t0001g0290 others(44): Show |
54 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.871+416G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41391119 | |||||||
chr21:41391263 | T | TA | 59 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(56): Show |
68 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.871+568dupA | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 41391263 | ||||||
chr21:41391389 | C | CT | 89 | a0001c0001t0001g0031 a0001c0001t0001g0036 a0001c0001t0001g0078 others(86): Show |
96 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.871+701dupT | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 41391389 | ||||||
chr21:41391425 | C | A | 13 | a0001c0001t0001g0290 a0001c0001t0001g0303 a0001c0001t0001g0306 others(10): Show |
15 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.871+722C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41391425 | |||||||
chr21:41391461 | ACTGTAAC others(2): Show |
A | 5 | a0001c0001t0012g0291 a0001c0001t0015g0289 a0001c0001t0017g0072 others(2): Show |
5 | HG01884.hp2 HG02280.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.871+762_871+770del others(9): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 41391461 | ||||||
chr21:41391503 | C | T | 2 | a0001c0001t0005g0254 a0001c0001t0005g0315 |
2 | HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.871+800C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41391503 | |||||||
chr21:41391530 | A | G | 5 | a0001c0001t0012g0291 a0001c0001t0015g0289 a0001c0001t0017g0072 others(2): Show |
5 | HG01884.hp2 HG02280.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.871+827A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41391530 | |||||||
chr21:41391540 | G | C | 4 | a0001c0001t0012g0291 a0001c0001t0015g0289 a0002c0014t0001g0071 others(1): Show |
4 | HG01884.hp2 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.871+837G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41391540 | |||||||
chr21:41391555 | T | C | 1 | a0001c0001t0001g0036 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.871+852T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41391555 | |||||||
chr21:41391594 | C | T | 1 | a0001c0025t0001g0331 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.871+891C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41391594 | |||||||
chr21:41391712 | A | G | 1 | a0001c0001t0002g0070 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.871+1009A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41391712 | |||||||
chr21:41391789 | C | CT | 9 | a0001c0001t0001g0149 a0001c0001t0001g0333 a0001c0001t0004g0063 others(6): Show |
9 | HG01167.hp1 HG01169.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.871+1100dupT | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 41391789 | ||||||
chr21:41391789 | CT | C | 13 | a0001c0001t0001g0080 a0001c0001t0001g0144 a0001c0001t0001g0175 others(10): Show |
13 | HG01168.hp1 HG01257.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.871+1100delT | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 41391789 | ||||||
chr21:41391789 | CTTTT | C | 105 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(102): Show |
121 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.871+1097_871+1100d others(6): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 41391789 | ||||||
chr21:41391861 | C | T | 5 | a0001c0001t0012g0291 a0001c0001t0015g0289 a0001c0001t0017g0072 others(2): Show |
5 | HG01884.hp2 HG02280.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.871+1158C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41391861 | |||||||
chr21:41391904 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.871+1201G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41391904 | |||||||
chr21:41391934 | G | A | 1 | a0001c0006t0001g0238 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.871+1231G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41391934 | |||||||
chr21:41392013 | A | G | 18 | a0001c0001t0001g0290 a0001c0001t0001g0303 a0001c0001t0001g0306 others(15): Show |
20 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.871+1310A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41392013 | |||||||
chr21:41392028 | T | C | 18 | a0001c0001t0001g0290 a0001c0001t0001g0303 a0001c0001t0001g0306 others(15): Show |
20 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.871+1325T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41392028 | |||||||
chr21:41392070 | CAT | C | 13 | a0001c0001t0001g0290 a0001c0001t0001g0303 a0001c0001t0001g0306 others(10): Show |
15 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.871+1368_871+1369d others(4): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41392070 | |||||||
chr21:41392251 | G | A | 48 | a0001c0001t0001g0121 a0001c0001t0001g0155 a0001c0001t0001g0287 others(45): Show |
55 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.871+1548G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41392251 | |||||||
chr21:41392266 | G | A | 48 | a0001c0001t0001g0121 a0001c0001t0001g0155 a0001c0001t0001g0287 others(45): Show |
55 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.871+1563G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41392266 | |||||||
chr21:41392429 | G | C | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.871+1726G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41392429 | |||||||
chr21:41392526 | T | C | 3 | a0001c0004t0003g0085 a0001c0004t0003g0086 a0001c0004t0003g0227 |
3 | NA18988.hp2 NA19078.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.871+1823T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41392526 | |||||||
chr21:41392628 | C | T | 3 | a0001c0001t0001g0290 a0001c0001t0015g0289 a0012c0023t0014g0249 |
3 | HG01884.hp2 HG01891.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.871+1925C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41392628 | |||||||
chr21:41392644 | T | C | 1 | a0001c0001t0011g0255 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.871+1941T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41392644 | |||||||
chr21:41392666 | C | A | 1 | a0001c0025t0001g0331 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.871+1963C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41392666 | |||||||
chr21:41392704 | T | A | 33 | a0001c0001t0001g0003 a0001c0001t0001g0026 a0001c0001t0001g0033 others(30): Show |
36 | HG00558.hp1 HG00673.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.871+2001T>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41392704 | |||||||
chr21:41392839 | T | C | 9 | a0001c0001t0001g0333 a0001c0001t0004g0063 a0001c0001t0004g0276 others(6): Show |
9 | HG01167.hp1 HG01169.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.871+2136T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41392839 | |||||||
chr21:41392873 | G | A | 4 | a0001c0001t0001g0229 a0001c0001t0001g0263 a0001c0001t0001g0265 others(1): Show |
4 | HG00140.hp2 HG02738.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.871+2170G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41392873 | |||||||
chr21:41392924 | G | A | 1 | a0011c0016t0005g0251 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.871+2221G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41392924 | |||||||
chr21:41393021 | G | A | 59 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(56): Show |
68 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.871+2318G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41393021 | |||||||
chr21:41393110 | C | CA | 13 | a0001c0001t0001g0169 a0001c0001t0001g0209 a0001c0001t0001g0212 others(10): Show |
14 | HG02083.hp2 HG02148.hp1 HG03098.hp1 others(11): Show |
intron_variant | MODIFIER | c.871+2428dupA | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 41393110 | ||||||
chr21:41393110 | C | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0231 |
3 | HG01069.hp1 HG01071.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.871+2407C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41393110 | |||||||
chr21:41393110 | CA | C | 68 | a0001c0001t0001g0038 a0001c0001t0001g0095 a0001c0001t0001g0155 others(65): Show |
73 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.871+2428delA | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 41393110 | ||||||
chr21:41393110 | CAA | C | 44 | a0001c0001t0001g0003 a0001c0001t0001g0026 a0001c0001t0001g0033 others(41): Show |
49 | HG00558.hp1 HG00673.hp1 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.871+2427_871+2428d others(4): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 41393110 | ||||||
chr21:41393120 | A | G | 1 | a0001c0001t0001g0020 | 2 | NA18950.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.871+2417A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41393120 | |||||||
chr21:41393127 | A | G | 21 | a0001c0001t0001g0095 a0001c0001t0001g0162 a0001c0001t0001g0246 others(18): Show |
21 | HG01496.hp1 HG01981.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.871+2424A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41393127 | |||||||
chr21:41393128 | A | G | 3 | a0001c0001t0001g0335 a0001c0001t0002g0208 a0001c0025t0001g0331 |
3 | HG00099.hp2 HG04115.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.871+2425A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41393128 | |||||||
chr21:41393145 | GA | G | 140 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(137): Show |
154 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.872-2432delA | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 41393145 | ||||||
chr21:41393186 | A | C | 1 | a0001c0001t0001g0232 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.872-2401A>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41393186 | |||||||
chr21:41393217 | A | G | 2 | a0001c0001t0004g0321 a0001c0001t0004g0322 |
2 | HG02145.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.872-2370A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41393217 | |||||||
chr21:41393257 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.872-2330G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41393257 | |||||||
chr21:41393460 | C | T | 1 | a0001c0001t0017g0072 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.872-2127C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41393460 | |||||||
chr21:41393544 | C | T | 32 | a0001c0001t0001g0121 a0001c0001t0001g0287 a0001c0001t0017g0072 others(29): Show |
37 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.872-2043C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41393544 | |||||||
chr21:41393577 | T | C | 1 | a0001c0001t0002g0075 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.872-2010T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41393577 | |||||||
chr21:41393629 | A | G | 2 | a0001c0001t0012g0291 a0002c0014t0001g0071 |
2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.872-1958A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41393629 | |||||||
chr21:41393711 | T | TG | 69 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(66): Show |
78 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.872-1875dupG | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 41393711 | ||||||
chr21:41393827 | C | T | 1 | a0001c0001t0006g0069 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.872-1760C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41393827 | |||||||
chr21:41393828 | G | A | 3 | a0001c0001t0001g0258 a0001c0001t0002g0157 a0001c0001t0002g0261 |
3 | NA18979.hp2 NA19000.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.872-1759G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41393828 | |||||||
chr21:41393923 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.872-1664C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41393923 | |||||||
chr21:41394148 | A | G | 1 | a0001c0025t0001g0331 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.872-1439A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394148 | |||||||
chr21:41394161 | C | T | 5 | a0001c0001t0006g0067 a0001c0001t0006g0317 a0001c0001t0006g0340 others(2): Show |
5 | HG01167.hp1 HG01169.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.872-1426C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394161 | |||||||
chr21:41394205 | T | G | 54 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0026 others(51): Show |
62 | HG00558.hp1 HG00673.hp1 HG01106.hp2 others(59): Show |
intron_variant | MODIFIER | c.872-1382T>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394205 | |||||||
chr21:41394278 | T | TC | 186 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(183): Show |
206 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.872-1307dupC | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 41394278 | ||||||
chr21:41394311 | A | G | 1 | a0001c0002t0002g0213 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.872-1276A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394311 | |||||||
chr21:41394314 | C | T | 4 | a0001c0001t0006g0067 a0001c0001t0006g0317 a0001c0024t0006g0330 others(1): Show |
4 | HG02723.hp1 HG02723.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.872-1273C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394314 | |||||||
chr21:41394394 | C | A | 4 | a0001c0001t0006g0317 a0001c0001t0006g0340 a0001c0001t0006g0341 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.872-1193C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394394 | |||||||
chr21:41394413 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.872-1174T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394413 | |||||||
chr21:41394429 | C | A | 8 | a0001c0001t0001g0155 a0001c0001t0006g0067 a0001c0001t0006g0069 others(5): Show |
8 | HG01106.hp1 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.872-1158C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394429 | |||||||
chr21:41394431 | G | A | 4 | a0001c0001t0001g0155 a0001c0001t0015g0289 a0001c0006t0001g0238 others(1): Show |
4 | HG01106.hp1 HG01884.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.872-1156G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394431 | |||||||
chr21:41394431 | G | T | 4 | a0001c0001t0006g0067 a0001c0001t0006g0069 a0001c0001t0006g0340 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.872-1156G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394431 | |||||||
chr21:41394479 | C | T | 2 | a0001c0001t0015g0289 a0012c0023t0014g0249 |
2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.872-1108C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394479 | |||||||
chr21:41394539 | T | C | 12 | a0001c0001t0004g0065 a0001c0001t0004g0066 a0001c0001t0004g0241 others(9): Show |
12 | HG01167.hp1 HG01169.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.872-1048T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394539 | |||||||
chr21:41394541 | C | A | 2 | a0001c0001t0002g0130 a0001c0001t0002g0219 |
2 | HG03688.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.872-1046C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394541 | |||||||
chr21:41394581 | A | G | 6 | a0001c0001t0001g0155 a0001c0001t0001g0333 a0001c0004t0003g0320 others(3): Show |
6 | HG01257.hp1 HG01258.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.872-1006A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394581 | |||||||
chr21:41394652 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.872-935G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394652 | |||||||
chr21:41394680 | T | C | 59 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(56): Show |
66 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.872-907T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394680 | |||||||
chr21:41394731 | G | A | 125 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(122): Show |
139 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(136): Show |
intron_variant | MODIFIER | c.872-856G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394731 | |||||||
chr21:41394865 | G | A | 180 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0015 others(177): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.872-722G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394865 | |||||||
chr21:41394872 | C | T | 2 | a0001c0001t0015g0289 a0012c0023t0014g0249 |
2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.872-715C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394872 | |||||||
chr21:41394873 | G | A | 1 | a0001c0001t0012g0291 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.872-714G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394873 | |||||||
chr21:41394883 | G | C | 17 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0290 others(14): Show |
18 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.872-704G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394883 | |||||||
chr21:41394917 | G | A | 2 | a0001c0001t0001g0228 a0001c0001t0002g0118 |
2 | HG03017.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.872-670G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394917 | |||||||
chr21:41394929 | C | CA | 49 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(46): Show |
55 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.872-652dupA | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 41394929 | ||||||
chr21:41394938 | A | AAG | 25 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0290 others(22): Show |
26 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.872-629_872-628dup others(2): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 41394938 | ||||||
chr21:41394938 | A | AAGAG | 6 | a0001c0001t0001g0333 a0001c0004t0003g0320 a0002c0005t0003g0023 others(3): Show |
7 | HG01257.hp1 HG01258.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.872-631_872-628dup others(4): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 41394938 | ||||||
chr21:41394982 | A | AGAAG | 21 | a0001c0001t0001g0187 a0001c0001t0001g0235 a0001c0001t0001g0236 others(18): Show |
22 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.872-585_872-582dup others(4): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 41394982 | ||||||
chr21:41394982 | AGAAG | A | 10 | a0001c0001t0001g0095 a0001c0001t0018g0338 a0001c0004t0003g0085 others(7): Show |
10 | NA18522.hp1 NA18946.hp2 NA18952.hp2 others(7): Show |
intron_variant | MODIFIER | c.872-585_872-582del others(4): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 41394982 | ||||||
chr21:41394989 | A | G | 1 | a0002c0003t0002g0197 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.872-598A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394989 | |||||||
chr21:41395006 | A | G | 1 | a0001c0001t0008g0043 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.872-581A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41395006 | |||||||
chr21:41395046 | A | G | 1 | a0002c0003t0019g0237 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.872-541A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41395046 | |||||||
chr21:41395052 | G | A | 1 | a0002c0003t0019g0237 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.872-535G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41395052 | |||||||
chr21:41395151 | G | A | 29 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0026 others(26): Show |
35 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.872-436G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41395151 | |||||||
chr21:41395155 | G | T | 1 | a0001c0001t0001g0121 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.872-432G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41395155 | |||||||
chr21:41395206 | G | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0015 others(150): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.872-381G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41395206 | |||||||
chr21:41395263 | AT | A | 290 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(287): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.872-321delT | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 41395263 | ||||||
chr21:41395296 | A | C | 87 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(84): Show |
98 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.872-291A>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41395296 | |||||||
chr21:41395310 | T | C | 1 | a0001c0001t0001g0093 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.872-277T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41395310 | |||||||
chr21:41395345 | C | A | 284 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(281): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.872-242C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41395345 | |||||||
chr21:41395352 | T | C | 6 | a0001c0001t0006g0067 a0001c0001t0006g0069 a0001c0001t0006g0317 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.872-235T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41395352 | |||||||
chr21:41395408 | G | A | 5 | a0001c0001t0004g0065 a0001c0001t0004g0066 a0001c0001t0004g0241 others(2): Show |
5 | HG01884.hp2 HG02572.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.872-179G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41395408 | |||||||
chr21:41395486 | A | G | 7 | a0001c0001t0001g0155 a0001c0001t0005g0064 a0001c0001t0005g0275 others(4): Show |
7 | HG02559.hp2 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.872-101A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41395486 | |||||||
chr21:41395806 | T | C | 295 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(292): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.1070+21T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41395806 | |||||||
chr21:41395967 | C | T | 312 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(309): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.1070+182C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41395967 | |||||||
chr21:41396013 | G | A | 49 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(46): Show |
55 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1070+228G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41396013 | |||||||
chr21:41396189 | G | A | 1 | a0001c0001t0011g0255 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1070+404G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41396189 | |||||||
chr21:41396208 | G | A | 1 | a0002c0003t0002g0197 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1070+423G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41396208 | |||||||
chr21:41396258 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1070+473A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41396258 | |||||||
chr21:41396265 | A | G | 1 | a0001c0004t0003g0316 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1070+480A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41396265 | |||||||
chr21:41396370 | C | T | 241 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(238): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.1070+585C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41396370 | |||||||
chr21:41396472 | G | C | 4 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0206 others(1): Show |
4 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(1): Show |
intron_variant | MODIFIER | c.1070+687G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41396472 | |||||||
chr21:41396487 | C | CAG | 331 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(328): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1070+702_1070+703i others(4): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41396487 | |||||||
chr21:41396634 | T | C | 32 | a0001c0001t0001g0053 a0001c0002t0001g0002 a0001c0002t0001g0012 others(29): Show |
37 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.1070+849T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41396634 | |||||||
chr21:41396792 | A | G | 29 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0026 others(26): Show |
35 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.1071-821A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41396792 | |||||||
chr21:41396859 | C | T | 1 | a0001c0002t0002g0133 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1071-754C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41396859 | |||||||
chr21:41396912 | C | T | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1071-701C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41396912 | |||||||
chr21:41396916 | A | T | 5 | a0001c0004t0003g0320 a0002c0005t0003g0023 a0002c0005t0003g0294 others(2): Show |
6 | HG01257.hp1 HG01258.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.1071-697A>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41396916 | |||||||
chr21:41396934 | G | A | 79 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(76): Show |
90 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.1071-679G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41396934 | |||||||
chr21:41396973 | C | T | 1 | a0001c0002t0002g0198 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1071-640C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41396973 | |||||||
chr21:41397045 | T | G | 315 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(312): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.1071-568T>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41397045 | |||||||
chr21:41397109 | T | C | 1 | a0001c0006t0001g0238 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1071-504T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41397109 | |||||||
chr21:41397136 | G | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0015 others(151): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.1071-477G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41397136 | |||||||
chr21:41397140 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1071-473C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41397140 | |||||||
chr21:41397190 | G | C | 1 | a0001c0001t0002g0268 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1071-423G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41397190 | |||||||
chr21:41397267 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1071-346T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41397267 | |||||||
chr21:41397313 | A | G | 31 | a0001c0001t0001g0155 a0001c0001t0001g0235 a0001c0001t0001g0236 others(28): Show |
32 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1071-300A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41397313 | |||||||
chr21:41397353 | T | A | 6 | a0001c0001t0006g0067 a0001c0001t0006g0069 a0001c0001t0006g0317 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1071-260T>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41397353 | |||||||
chr21:41397432 | TCCTGGCC others(8): Show |
T | 29 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0026 others(26): Show |
35 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.1071-175_1071-161d others(17): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr21 | 41397432 | ||||||
chr21:41397442 | C | T | 3 | a0001c0006t0001g0141 a0002c0003t0001g0296 a0002c0003t0001g0300 |
3 | HG02257.hp1 HG02970.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1071-171C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41397442 | |||||||
chr21:41398016 | A | G | 6 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0206 others(3): Show |
6 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(3): Show |
intron_variant | MODIFIER | c.1149+325A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 8/13 | chr21 | 41398016 | |||||||
chr21:41398224 | G | A | 2 | a0001c0001t0001g0176 a0001c0001t0001g0222 |
2 | HG02083.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.1149+533G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 8/13 | chr21 | 41398224 | |||||||
chr21:41398293 | C | T | 1 | a0002c0003t0004g0304 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1149+602C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 8/13 | chr21 | 41398293 | |||||||
chr21:41398586 | T | C | 6 | a0001c0001t0006g0067 a0001c0001t0006g0069 a0001c0001t0006g0317 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1150-311T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 8/13 | chr21 | 41398586 | |||||||
chr21:41398675 | C | A | 1 | a0008c0020t0001g0110 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1150-222C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 8/13 | chr21 | 41398675 | |||||||
chr21:41398677 | T | G | 1 | a0001c0001t0001g0041 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1150-220T>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 8/13 | chr21 | 41398677 | |||||||
chr21:41398740 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1150-157T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 8/13 | chr21 | 41398740 | |||||||
chr21:41398745 | A | G | 1 | a0001c0001t0007g0018 | 2 | NA18974.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.1150-152A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 8/13 | chr21 | 41398745 | |||||||
chr21:41398828 | A | G | 1 | a0001c0002t0002g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1150-69A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 8/13 | chr21 | 41398828 | |||||||
chr21:41399435 | T | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(209): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1414+98T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41399435 | |||||||
chr21:41399507 | A | G | 172 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0015 others(169): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.1414+170A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41399507 | |||||||
chr21:41399519 | A | C | 206 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(203): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.1414+182A>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41399519 | |||||||
chr21:41399605 | G | T | 2 | a0001c0001t0001g0109 a0001c0001t0001g0145 |
2 | NA19068.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1414+268G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41399605 | |||||||
chr21:41399626 | C | T | 28 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0026 others(25): Show |
34 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.1414+289C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41399626 | |||||||
chr21:41399627 | G | A | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0264 |
3 | HG01261.hp2 HG01433.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.1414+290G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41399627 | |||||||
chr21:41399674 | T | G | 1 | a0001c0001t0001g0122 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1414+337T>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41399674 | |||||||
chr21:41399920 | G | A | 2 | a0001c0001t0001g0244 a0001c0006t0001g0238 |
2 | HG01106.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1414+583G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41399920 | |||||||
chr21:41400177 | T | C | 6 | a0001c0001t0001g0333 a0001c0004t0003g0320 a0002c0005t0003g0023 others(3): Show |
7 | HG01257.hp1 HG01258.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1414+840T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41400177 | |||||||
chr21:41400286 | A | G | 1 | a0001c0006t0001g0238 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1414+949A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41400286 | |||||||
chr21:41400312 | A | G | 6 | a0001c0001t0006g0067 a0001c0001t0006g0069 a0001c0001t0006g0317 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1414+975A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41400312 | |||||||
chr21:41400387 | C | T | 1 | a0001c0001t0012g0291 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1414+1050C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41400387 | |||||||
chr21:41400601 | G | A | 312 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(309): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.1414+1264G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41400601 | |||||||
chr21:41400605 | A | G | 312 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(309): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.1414+1268A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41400605 | |||||||
chr21:41400618 | TA | T | 281 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(278): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.1414+1283delA | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr21 | 41400618 | ||||||
chr21:41400703 | CTTTA | C | 191 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(188): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.1415-1251_1415-124 others(8): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr21 | 41400703 | ||||||
chr21:41400728 | C | T | 2 | a0001c0001t0001g0089 a0001c0001t0001g0090 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1415-1242C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41400728 | |||||||
chr21:41401131 | TACAATTT others(75): Show |
T | 1 | a0012c0023t0014g0249 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1415-817_1415-736d others(84): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr21 | 41401131 | ||||||
chr21:41401161 | A | T | 1 | a0001c0001t0001g0308 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1415-809A>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41401161 | |||||||
chr21:41401323 | G | A | 47 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(44): Show |
54 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.1415-647G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41401323 | |||||||
chr21:41401461 | C | T | 6 | a0001c0001t0005g0064 a0001c0001t0005g0275 a0001c0001t0005g0324 others(3): Show |
6 | HG02559.hp2 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1415-509C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41401461 | |||||||
chr21:41401491 | T | G | 3 | a0002c0003t0001g0298 a0002c0003t0001g0299 a0002c0003t0001g0311 |
3 | HG02647.hp2 HG02896.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1415-479T>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41401491 | |||||||
chr21:41401495 | T | C | 1 | a0001c0001t0001g0264 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1415-475T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41401495 | |||||||
chr21:41401528 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1415-442C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41401528 | |||||||
chr21:41401685 | G | GT | 267 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(264): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.1415-272dupT | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr21 | 41401685 | ||||||
chr21:41401685 | G | GTT | 7 | a0001c0001t0001g0005 a0001c0001t0001g0081 a0001c0001t0001g0103 others(4): Show |
9 | HG01934.hp1 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1415-273_1415-272d others(4): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr21 | 41401685 | ||||||
chr21:41401685 | G | GTTT | 36 | a0001c0001t0001g0006 a0001c0001t0001g0095 a0001c0001t0002g0042 others(33): Show |
38 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1415-274_1415-272d others(5): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr21 | 41401685 | ||||||
chr21:41401784 | C | A | 43 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0026 others(40): Show |
50 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.1415-186C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41401784 | |||||||
chr21:41401895 | T | C | 30 | a0001c0001t0002g0032 a0001c0001t0002g0045 a0001c0001t0002g0061 others(27): Show |
32 | HG00423.hp2 HG01993.hp1 HG02040.hp1 others(29): Show |
intron_variant | MODIFIER | c.1415-75T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41401895 | |||||||
chr21:41402238 | C | T | 4 | a0001c0001t0005g0064 a0001c0001t0005g0324 a0002c0003t0005g0297 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1573+110C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 11/13 | chr21 | 41402238 | |||||||
chr21:41402247 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1573+119G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 11/13 | chr21 | 41402247 | |||||||
chr21:41402298 | G | T | 1 | a0002c0005t0003g0023 | 2 | HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.1573+170G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 11/13 | chr21 | 41402298 | |||||||
chr21:41402402 | C | T | 1 | a0001c0001t0012g0291 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1573+274C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 11/13 | chr21 | 41402402 | |||||||
chr21:41402614 | A | G | 207 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(204): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.1573+486A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 11/13 | chr21 | 41402614 | |||||||
chr21:41402686 | A | G | 196 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(193): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.1573+558A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 11/13 | chr21 | 41402686 | |||||||
chr21:41402709 | A | G | 213 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(210): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.1574-558A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 11/13 | chr21 | 41402709 | |||||||
chr21:41402864 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1574-403G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 11/13 | chr21 | 41402864 | |||||||
chr21:41402998 | C | A | 13 | a0001c0001t0004g0063 a0001c0001t0004g0065 a0001c0001t0004g0066 others(10): Show |
13 | HG01106.hp1 HG02145.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1574-269C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 11/13 | chr21 | 41402998 | |||||||
chr21:41403252 | G | GT | 202 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(199): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.1574-15_1574-14ins others(1): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 11/13 | chr21 | 41403252 | |||||||
chr21:41403253 | C | T | 318 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(315): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.1574-14C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 11/13 | chr21 | 41403253 | |||||||
chr21:41403437 | G | T | 2 | a0001c0001t0001g0107 a0001c0001t0001g0147 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1650+94G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41403437 | |||||||
chr21:41403597 | G | A | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1650+254G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41403597 | |||||||
chr21:41403597 | G | T | 13 | a0001c0001t0004g0063 a0001c0001t0004g0065 a0001c0001t0004g0066 others(10): Show |
13 | HG01106.hp1 HG02145.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1650+254G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41403597 | |||||||
chr21:41403725 | T | C | 2 | a0001c0001t0002g0268 a0001c0002t0002g0250 |
2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1650+382T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41403725 | |||||||
chr21:41403760 | C | T | 49 | a0001c0001t0001g0056 a0001c0001t0002g0008 a0001c0001t0002g0014 others(46): Show |
53 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(50): Show |
intron_variant | MODIFIER | c.1650+417C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41403760 | |||||||
chr21:41403905 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1650+562G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41403905 | |||||||
chr21:41404075 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1650+732G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41404075 | |||||||
chr21:41404118 | C | T | 1 | a0001c0004t0003g0316 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1650+775C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41404118 | |||||||
chr21:41404356 | G | A | 1 | a0001c0001t0002g0061 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1650+1013G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41404356 | |||||||
chr21:41404481 | G | C | 2 | a0001c0001t0015g0289 a0012c0023t0014g0249 |
2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1650+1138G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41404481 | |||||||
chr21:41404521 | C | T | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1650+1178C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41404521 | |||||||
chr21:41404532 | T | A | 6 | a0001c0001t0005g0064 a0001c0001t0005g0275 a0001c0001t0005g0324 others(3): Show |
6 | HG02559.hp2 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1650+1189T>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41404532 | |||||||
chr21:41404642 | G | C | 7 | a0001c0001t0006g0067 a0001c0001t0006g0069 a0001c0001t0006g0317 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1650+1299G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41404642 | |||||||
chr21:41404719 | C | T | 1 | a0001c0004t0003g0316 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1650+1376C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41404719 | |||||||
chr21:41404744 | C | T | 8 | a0001c0001t0006g0067 a0001c0001t0006g0069 a0001c0001t0006g0317 others(5): Show |
8 | HG01167.hp1 HG01169.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1650+1401C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41404744 | |||||||
chr21:41404745 | G | A | 1 | a0001c0001t0002g0070 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1650+1402G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41404745 | |||||||
chr21:41404861 | G | A | 9 | a0001c0001t0005g0064 a0001c0001t0005g0254 a0001c0001t0005g0275 others(6): Show |
9 | HG02559.hp2 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1650+1518G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41404861 | |||||||
chr21:41404873 | C | CA | 14 | a0001c0001t0001g0009 a0001c0001t0001g0107 a0001c0001t0001g0121 others(11): Show |
15 | HG00423.hp2 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1650+1548dupA | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr21 | 41404873 | ||||||
chr21:41404873 | CA | C | 58 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0026 others(55): Show |
66 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.1650+1548delA | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr21 | 41404873 | ||||||
chr21:41404873 | CAA | C | 19 | a0001c0001t0009g0332 a0001c0001t0015g0289 a0001c0004t0003g0085 others(16): Show |
20 | HG01257.hp1 HG01258.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1650+1547_1650+154 others(6): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr21 | 41404873 | ||||||
chr21:41404886 | A | G | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0264 |
3 | HG01261.hp2 HG01433.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.1650+1543A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41404886 | |||||||
chr21:41404898 | G | GA | 8 | a0001c0001t0005g0064 a0001c0001t0005g0254 a0001c0001t0005g0275 others(5): Show |
8 | HG02559.hp2 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1650+1565dupA | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr21 | 41404898 | ||||||
chr21:41405079 | C | T | 2 | a0001c0001t0001g0160 a0001c0001t0001g0225 |
2 | NA18983.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1651-1665C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41405079 | |||||||
chr21:41405162 | T | C | 1 | a0001c0001t0001g0036 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1651-1582T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41405162 | |||||||
chr21:41405198 | G | C | 1 | a0001c0002t0002g0126 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1651-1546G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41405198 | |||||||
chr21:41405272 | A | T | 8 | a0001c0001t0006g0067 a0001c0001t0006g0069 a0001c0001t0006g0317 others(5): Show |
8 | HG01167.hp1 HG01169.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1651-1472A>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41405272 | |||||||
chr21:41405412 | G | A | 1 | a0002c0003t0019g0237 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1651-1332G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41405412 | |||||||
chr21:41405418 | G | A | 1 | a0001c0002t0002g0165 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1651-1326G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41405418 | |||||||
chr21:41405424 | TCAG | T | 8 | a0001c0001t0006g0067 a0001c0001t0006g0069 a0001c0001t0006g0317 others(5): Show |
8 | HG01167.hp1 HG01169.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1651-1319_1651-131 others(7): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41405424 | |||||||
chr21:41405452 | G | T | 4 | a0001c0001t0001g0021 a0001c0001t0001g0116 a0001c0001t0001g0117 others(1): Show |
5 | HG01069.hp1 HG01071.hp2 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.1651-1292G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41405452 | |||||||
chr21:41405501 | C | T | 1 | a0001c0001t0002g0130 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1651-1243C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41405501 | |||||||
chr21:41405502 | G | A | 1 | a0001c0001t0004g0065 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1651-1242G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41405502 | |||||||
chr21:41405650 | A | G | 17 | a0001c0001t0005g0064 a0001c0001t0005g0254 a0001c0001t0005g0275 others(14): Show |
17 | HG01167.hp1 HG01169.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.1651-1094A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41405650 | |||||||
chr21:41405701 | C | CT | 18 | a0001c0001t0001g0019 a0001c0001t0001g0096 a0001c0001t0001g0125 others(15): Show |
19 | HG01975.hp2 HG01978.hp1 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.1651-1022dupT | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr21 | 41405701 | ||||||
chr21:41405701 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0188 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1651-1032_1651-102 others(15): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr21 | 41405701 | ||||||
chr21:41405701 | CTTTTTTT others(5): Show |
C | 9 | a0001c0001t0005g0064 a0001c0001t0005g0254 a0001c0001t0005g0275 others(6): Show |
9 | HG02559.hp2 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1651-1033_1651-102 others(16): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr21 | 41405701 | ||||||
chr21:41405754 | A | G | 211 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(208): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1651-990A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41405754 | |||||||
chr21:41405773 | C | T | 8 | a0001c0001t0006g0067 a0001c0001t0006g0069 a0001c0001t0006g0317 others(5): Show |
8 | HG01167.hp1 HG01169.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1651-971C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41405773 | |||||||
chr21:41405897 | G | GT | 229 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(226): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1651-845dupT | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr21 | 41405897 | ||||||
chr21:41405968 | T | C | 1 | a0001c0001t0001g0257 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1651-776T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41405968 | |||||||
chr21:41406002 | C | G | 1 | a0001c0001t0001g0036 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1651-742C>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41406002 | |||||||
chr21:41406132 | G | A | 1 | a0001c0001t0001g0306 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1651-612G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41406132 | |||||||
chr21:41406229 | C | T | 1 | a0001c0001t0001g0035 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1651-515C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41406229 | |||||||
chr21:41406266 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1651-478G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41406266 | |||||||
chr21:41406457 | T | G | 18 | a0001c0001t0015g0289 a0001c0004t0003g0085 a0001c0004t0003g0086 others(15): Show |
19 | HG01257.hp1 HG01258.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.1651-287T>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41406457 | |||||||
chr21:41406459 | T | A | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(205): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1651-285T>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41406459 | |||||||
chr21:41407129 | T | C | 210 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(207): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1905+131T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 13/13 | chr21 | 41407129 | |||||||
chr21:41407147 | A | G | 2 | a0001c0002t0002g0133 a0001c0002t0002g0198 |
2 | HG02155.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.1905+149A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 13/13 | chr21 | 41407147 | |||||||
chr21:41407199 | A | G | 6 | a0001c0001t0001g0021 a0001c0001t0001g0116 a0001c0001t0001g0117 others(3): Show |
7 | HG01069.hp1 HG01071.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.1905+201A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 13/13 | chr21 | 41407199 | |||||||
chr21:41407201 | T | G | 1 | a0001c0001t0001g0263 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1905+203T>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 13/13 | chr21 | 41407201 | |||||||
chr21:41407259 | A | C | 1 | a0002c0003t0019g0237 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1905+261A>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 13/13 | chr21 | 41407259 | |||||||
chr21:41407283 | G | A | 1 | a0015c0017t0001g0218 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1905+285G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 13/13 | chr21 | 41407283 | |||||||
chr21:41407334 | C | T | 1 | a0001c0002t0002g0037 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1905+336C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 13/13 | chr21 | 41407334 | |||||||
chr21:41407481 | C | T | 12 | a0001c0001t0001g0078 a0001c0001t0001g0120 a0001c0001t0001g0122 others(9): Show |
12 | HG00642.hp2 HG01099.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.1905+483C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 13/13 | chr21 | 41407481 | |||||||
chr21:41407524 | T | C | 1 | a0001c0001t0001g0302 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1906-467T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 13/13 | chr21 | 41407524 | |||||||
chr21:41407548 | C | T | 1 | a0002c0003t0019g0237 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1906-443C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 13/13 | chr21 | 41407548 | |||||||
chr21:41407604 | C | T | 1 | a0001c0006t0001g0238 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1906-387C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 13/13 | chr21 | 41407604 | |||||||
chr21:41407656 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1906-335G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 13/13 | chr21 | 41407656 | |||||||
chr21:41407832 | C | T | 6 | a0001c0001t0012g0291 a0001c0025t0001g0331 a0002c0003t0001g0298 others(3): Show |
6 | HG02647.hp2 HG02896.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1906-159C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 13/13 | chr21 | 41407832 | |||||||
chr21:41407887 | G | A | 7 | a0001c0001t0006g0067 a0001c0001t0006g0069 a0001c0001t0006g0317 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1906-104G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 13/13 | chr21 | 41407887 | |||||||
chr21:41407903 | C | T | 4 | a0001c0001t0001g0025 a0001c0001t0001g0068 a0001c0001t0001g0310 others(1): Show |
5 | HG01070.hp2 HG01071.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1906-88C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 13/13 | chr21 | 41407903 |