Item | Value |
---|---|
geneid | 81609 |
ensemblid | ENSG00000143376.14 |
hgncid | 20073 |
symbol | SNX27 |
name | sorting nexin 27 |
refseq_nuc | NM_001330723.2 |
refseq_prot | NP_001317652.1 |
ensembl_nuc | ENST00000458013.7 |
ensembl_prot | ENSP00000400333.2 |
mane_status | MANE Select |
chr | chr1 |
start | 151612050 |
end | 151699080 |
strand | + |
ver | v1.2 |
region | chr1:151612050-151699080 |
region5000 | chr1:151607050-151704080 |
regionname0 | SNX27_chr1_151612050_151699080 |
regionname5000 | SNX27_chr1_151607050_151704080 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 541 | 359 | 94 | 56 | 159 | 12 | 36 | 119 | SNX27_chr1_151607050_151704080 | SNX27 | MADED others(536): Show |
chr1 | 151607050 | 151704080 |
a0002 | 0/0 | 541 | 6 | 0 | 0 | 6 | 0 | 0 | 6 | SNX27_chr1_151607050_151704080 | SNX27 | MADED others(536): Show |
chr1 | 151607050 | 151704080 |
a0003 | 0/0 | 500 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | MADED others(495): Show |
chr1 | 151607050 | 151704080 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1623 | 353 | 89 | 56 | 158 | 12 | 36 | SNX27_chr1_151607050_151704080 | SNX27 | ATGGC others(1618): Show |
chr1 | 151607050 | 151704080 | ||
a0001c0003 | 0/0 | 1623 | 2 | 2 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ATGGC others(1618): Show |
chr1 | 151607050 | 151704080 | ||
a0001c0004 | 0/0 | 1623 | 2 | 2 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ATGGC others(1618): Show |
chr1 | 151607050 | 151704080 | ||
a0001c0006 | 0/0 | 1623 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ATGGC others(1618): Show |
chr1 | 151607050 | 151704080 | ||
a0001c0007 | 0/0 | 1623 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ATGGC others(1618): Show |
chr1 | 151607050 | 151704080 | ||
a0002c0002 | 0/0 | 1623 | 6 | 0 | 0 | 6 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ATGGC others(1618): Show |
chr1 | 151607050 | 151704080 | ||
a0003c0005 | 0/0 | 1623 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ATGGC others(1618): Show |
chr1 | 151607050 | 151704080 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6436 | 43 | 7 | 11 | 18 | 4 | 3 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6431): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0002 | 0/0 | 6442 | 21 | 4 | 5 | 9 | 2 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6437): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0003 | 0/0 | 6433 | 13 | 0 | 0 | 12 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6428): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0004 | 0/0 | 6437 | 13 | 0 | 2 | 9 | 0 | 2 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6432): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0005 | 0/0 | 6446 | 13 | 0 | 0 | 13 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6441): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0006 | 0/0 | 6433 | 11 | 2 | 3 | 1 | 1 | 4 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6428): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0007 | 1/0 | 6441 | 11 | 3 | 3 | 0 | 2 | 2 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6436): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0008 | 0/0 | 6437 | 11 | 0 | 2 | 9 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6432): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0009 | 0/0 | 6437 | 8 | 1 | 2 | 2 | 0 | 3 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6432): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0010 | 0/0 | 6441 | 8 | 3 | 0 | 3 | 0 | 2 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6436): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0011 | 0/0 | 6451 | 7 | 0 | 2 | 3 | 0 | 2 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6446): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0012 | 0/0 | 6441 | 6 | 6 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6436): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0013 | 0/0 | 6449 | 6 | 1 | 2 | 3 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6444): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0014 | 0/0 | 6447 | 6 | 0 | 1 | 5 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6442): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0015 | 0/0 | 6437 | 3 | 3 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6432): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0016 | 0/0 | 6448 | 5 | 5 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6443): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0017 | 0/0 | 6433 | 5 | 0 | 0 | 5 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6428): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0018 | 0/0 | 6449 | 5 | 2 | 0 | 3 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6444): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0019 | 0/0 | 6441 | 5 | 5 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6436): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0020 | 0/0 | 6443 | 5 | 0 | 2 | 1 | 0 | 2 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6438): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0021 | 0/0 | 6438 | 4 | 0 | 1 | 3 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6433): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0022 | 0/0 | 6421 | 3 | 0 | 3 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6416): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0023 | 0/0 | 6437 | 3 | 0 | 0 | 3 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6432): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0024 | 0/0 | 6437 | 3 | 0 | 2 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6432): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0025 | 0/0 | 6445 | 3 | 1 | 0 | 1 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6440): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0026 | 0/0 | 6450 | 3 | 0 | 1 | 1 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6445): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0027 | 0/0 | 6454 | 3 | 0 | 0 | 3 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6449): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0028 | 0/0 | 6443 | 3 | 3 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6438): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0029 | 0/0 | 6455 | 3 | 0 | 0 | 2 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6450): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0030 | 0/0 | 6451 | 3 | 0 | 0 | 3 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6446): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0031 | 0/0 | 6445 | 2 | 2 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6440): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0032 | 0/0 | 6437 | 2 | 0 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6432): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0033 | 0/0 | 6433 | 2 | 0 | 2 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6428): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0034 | 0/0 | 6434 | 2 | 0 | 0 | 1 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6429): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0035 | 0/0 | 6437 | 2 | 0 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6432): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0036 | 0/0 | 6461 | 2 | 0 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6456): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0037 | 0/0 | 6441 | 2 | 0 | 2 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6436): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0038 | 0/0 | 6449 | 2 | 2 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6444): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0039 | 0/0 | 6434 | 2 | 0 | 0 | 1 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6429): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0040 | 0/0 | 6434 | 2 | 0 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6429): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0041 | 0/0 | 6458 | 2 | 0 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6453): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0042 | 0/0 | 6443 | 2 | 1 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6438): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0043 | 0/0 | 6442 | 2 | 1 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6437): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0045 | 0/0 | 6446 | 2 | 0 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6441): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0046 | 0/0 | 6443 | 2 | 2 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6438): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0047 | 0/0 | 6444 | 2 | 2 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6439): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0048 | 0/0 | 6459 | 2 | 0 | 2 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6454): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0049 | 0/0 | 6444 | 2 | 0 | 0 | 1 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6439): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0050 | 0/0 | 6454 | 2 | 0 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6449): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0051 | 0/0 | 6438 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6433): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0052 | 0/0 | 6449 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6444): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0053 | 0/0 | 6433 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6428): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0054 | 0/0 | 6449 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6444): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0055 | 0/0 | 6441 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6436): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0056 | 0/0 | 6433 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6428): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0057 | 0/0 | 6442 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6437): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0058 | 0/0 | 6432 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6427): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0059 | 0/0 | 6436 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6431): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0060 | 0/0 | 6440 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6435): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0061 | 0/0 | 6435 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6430): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0062 | 0/0 | 6451 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6446): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0063 | 0/0 | 6435 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6430): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0064 | 0/0 | 6433 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6428): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0065 | 0/0 | 6445 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6440): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0066 | 0/0 | 6448 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6443): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0067 | 0/0 | 6429 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6424): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0068 | 0/0 | 6438 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6433): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0069 | 0/0 | 6441 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6436): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0070 | 0/0 | 6441 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6436): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0071 | 0/0 | 6445 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6440): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0072 | 0/0 | 6446 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6441): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0073 | 0/0 | 6453 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6448): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0074 | 0/0 | 6445 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6440): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0075 | 0/0 | 6449 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6444): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0077 | 0/0 | 6436 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6431): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0078 | 0/1 | 6456 | 1 | 0 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6451): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0079 | 0/0 | 6448 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6443): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0080 | 0/0 | 6436 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6431): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0081 | 0/0 | 6448 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6443): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0082 | 0/0 | 6452 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6447): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0083 | 0/0 | 6436 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6431): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0084 | 0/0 | 6442 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6437): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0085 | 0/0 | 6434 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6429): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0086 | 0/0 | 6438 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6433): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0087 | 0/0 | 6446 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6441): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0088 | 0/0 | 6454 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6449): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0089 | 0/0 | 6458 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6453): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0090 | 0/0 | 6442 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6437): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0091 | 0/0 | 6442 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6437): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0092 | 0/0 | 6437 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6432): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0093 | 0/0 | 6449 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6444): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0094 | 0/0 | 6453 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6448): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0095 | 0/0 | 6437 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6432): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0096 | 0/0 | 6445 | 1 | 0 | 0 | 0 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6440): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0097 | 0/0 | 6447 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6442): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0098 | 0/0 | 6447 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6442): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0099 | 0/0 | 6459 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6454): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0100 | 0/0 | 6450 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6445): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0101 | 0/0 | 6440 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6435): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0102 | 0/0 | 6443 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6438): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0103 | 0/0 | 6432 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6427): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0104 | 0/0 | 6444 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6439): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0105 | 0/0 | 6438 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6433): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0106 | 0/0 | 6442 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6437): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0107 | 0/0 | 6442 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6437): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0108 | 0/0 | 6443 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6438): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0109 | 0/0 | 6443 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6438): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0110 | 0/0 | 6443 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6438): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0111 | 0/0 | 6427 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6422): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0112 | 0/0 | 6447 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6442): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0113 | 0/0 | 6435 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6430): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0114 | 0/0 | 6440 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6435): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0115 | 0/0 | 6444 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6439): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0116 | 0/0 | 6448 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6443): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0117 | 0/0 | 6452 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6447): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0118 | 0/0 | 6452 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6447): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0119 | 0/0 | 6445 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6440): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0120 | 0/0 | 6452 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6447): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0121 | 0/0 | 6453 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6448): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0122 | 0/0 | 6456 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6451): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0123 | 0/0 | 6426 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6421): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0124 | 0/0 | 6442 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6437): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0125 | 0/0 | 6448 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6443): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0126 | 0/0 | 6446 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6441): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0127 | 0/0 | 6447 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6442): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0128 | 0/0 | 6446 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6441): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0129 | 0/0 | 6450 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6445): Show |
chr1 | 151607050 | 151704080 |
a0001c0001t0130 | 0/0 | 6436 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6431): Show |
chr1 | 151607050 | 151704080 |
a0001c0003t0044 | 0/0 | 6438 | 2 | 2 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6433): Show |
chr1 | 151607050 | 151704080 |
a0001c0004t0015 | 0/0 | 6437 | 2 | 2 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6432): Show |
chr1 | 151607050 | 151704080 |
a0001c0006t0076 | 0/0 | 6457 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6452): Show |
chr1 | 151607050 | 151704080 |
a0001c0007t0003 | 0/0 | 6433 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6428): Show |
chr1 | 151607050 | 151704080 |
a0002c0002t0001 | 0/0 | 6436 | 6 | 0 | 0 | 6 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6431): Show |
chr1 | 151607050 | 151704080 |
a0003c0005t0002 | 0/0 | 6442 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | ACCCC others(6437): Show |
chr1 | 151607050 | 151704080 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0004g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0004g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0004g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0005g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0005g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0005g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0005g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0005g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0005g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0005g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0005g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0005g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0005g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0005g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0005g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0005g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0006g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0006g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0006g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0006g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0006g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0006g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0006g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0006g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0006g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0006g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0006g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0007g0085 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0007g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0007g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0007g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0007g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0007g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0007g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0007g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0007g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0007g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0007g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0008g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0008g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0008g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0008g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0008g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0008g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0008g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0008g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0008g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0008g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0008g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0009g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0009g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0009g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0009g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0009g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0009g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0009g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0009g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0010g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0010g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0010g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0010g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0010g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0010g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0010g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0010g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0011g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0011g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0011g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0011g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0011g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0011g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0011g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0012g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0012g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0012g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0012g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0012g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0012g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0013g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0013g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0013g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0013g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0013g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0013g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0014g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0014g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0014g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0014g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0014g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0014g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0015g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0015g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0015g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0016g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0016g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0016g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0016g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0016g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0017g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0017g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0017g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0017g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0017g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0018g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0018g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0018g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0018g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0018g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0019g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0019g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0019g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0019g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0019g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0020g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0020g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0020g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0020g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0020g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0021g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0021g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0021g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0022g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0022g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0022g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0023g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0023g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0023g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0024g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0024g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0024g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0025g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0025g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0025g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0026g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0026g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0026g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0027g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0027g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0027g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0028g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0028g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0028g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0029g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0029g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0029g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0030g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0030g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0030g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0031g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0032g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0032g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0033g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0033g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0034g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0034g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0035g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0035g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0036g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0036g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0037g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0037g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0038g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0038g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0039g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0039g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0040g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0040g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0041g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0042g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0042g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0043g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0043g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0045g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0045g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0046g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0046g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0047g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0047g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0048g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0048g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0049g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0049g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0050g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0050g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0051g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0052g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0053g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0054g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0055g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0056g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0057g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0058g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0059g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0060g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0061g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0062g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0063g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0064g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0065g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0066g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0067g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0068g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0069g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0070g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0071g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0072g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0073g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0074g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0075g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0077g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0078g0009 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0079g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0080g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0081g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0082g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0083g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0084g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0085g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0086g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0087g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0088g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0089g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0090g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0091g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0092g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0093g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0094g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0095g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0096g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0097g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0098g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0099g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0100g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0101g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0102g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0103g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0104g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0105g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0106g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0107g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0108g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0109g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0110g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0111g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0112g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0113g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0114g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0115g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0116g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0117g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0118g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0119g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0120g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0121g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0122g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0123g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0124g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0125g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0126g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0127g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0128g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0129g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0130g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0003t0044g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0003t0044g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0004t0015g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0004t0015g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0006t0076g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0007t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0002c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0003c0005t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0007 | g0176 | EUR | GBR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00099 | hp2 | a0001 | c0001 | t0025 | g0173 | EUR | GBR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00280 | hp1 | a0001 | c0001 | t0034 | g0177 | EUR | FIN | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0269 | EUR | FIN | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0220 | EUR | FIN | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0180 | EUR | FIN | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00408 | hp1 | a0001 | c0001 | t0071 | g0139 | EAS | CHS | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00408 | hp2 | a0001 | c0001 | t0124 | g0048 | EAS | CHS | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00423 | hp1 | a0001 | c0001 | t0030 | g0045 | EAS | CHS | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00423 | hp2 | a0001 | c0001 | t0089 | g0312 | EAS | CHS | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00438 | hp1 | a0001 | c0001 | t0013 | g0260 | EAS | CHS | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00438 | hp2 | a0001 | c0001 | t0004 | g0242 | EAS | CHS | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00544 | hp1 | a0001 | c0001 | t0021 | g0338 | EAS | CHS | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00544 | hp2 | a0001 | c0001 | t0114 | g0079 | EAS | CHS | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00597 | hp1 | a0001 | c0001 | t0005 | g0062 | EAS | CHS | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | CHS | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00609 | hp1 | a0001 | c0001 | t0005 | g0059 | EAS | CHS | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0117 | EAS | CHS | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00639 | hp1 | a0001 | c0001 | t0093 | g0274 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0179 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00642 | hp1 | a0001 | c0001 | t0004 | g0240 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00642 | hp2 | a0001 | c0001 | t0022 | g0186 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00673 | hp2 | a0001 | c0001 | t0005 | g0056 | EAS | CHS | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00735 | hp2 | a0001 | c0001 | t0024 | g0343 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00738 | hp1 | a0001 | c0001 | t0021 | g0174 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00741 | hp1 | a0001 | c0001 | t0033 | g0342 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00741 | hp2 | a0001 | c0001 | t0121 | g0083 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01071 | hp1 | a0001 | c0001 | t0014 | g0050 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01071 | hp2 | a0001 | c0001 | t0007 | g0157 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01074 | hp1 | a0001 | c0001 | t0008 | g0193 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01074 | hp2 | a0001 | c0001 | t0006 | g0170 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01099 | hp1 | a0001 | c0001 | t0013 | g0264 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0178 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01167 | hp2 | a0001 | c0001 | t0070 | g0345 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01168 | hp1 | a0001 | c0001 | t0079 | g0275 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01168 | hp2 | a0001 | c0001 | t0060 | g0163 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01175 | hp2 | a0001 | c0001 | t0026 | g0299 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01192 | hp2 | a0001 | c0001 | t0009 | g0175 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01255 | hp1 | a0001 | c0001 | t0048 | g0049 | AMR | CLM | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01255 | hp2 | a0001 | c0001 | t0007 | g0149 | AMR | CLM | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01256 | hp1 | a0001 | c0001 | t0022 | g0136 | AMR | CLM | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01256 | hp2 | a0001 | c0001 | t0048 | g0065 | AMR | CLM | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01257 | hp1 | a0001 | c0001 | t0037 | g0192 | AMR | CLM | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01257 | hp2 | a0001 | c0001 | t0007 | g0150 | AMR | CLM | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01258 | hp1 | a0001 | c0001 | t0022 | g0133 | AMR | CLM | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01258 | hp2 | a0001 | c0001 | t0037 | g0194 | AMR | CLM | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | CLM | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01261 | hp2 | a0001 | c0001 | t0006 | g0172 | AMR | CLM | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01346 | hp1 | a0001 | c0001 | t0020 | g0053 | AMR | CLM | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0148 | AMR | CLM | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | CLM | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01433 | hp1 | a0001 | c0001 | t0004 | g0253 | AMR | CLM | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01433 | hp2 | a0001 | c0001 | t0011 | g0051 | AMR | CLM | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0224 | EUR | IBS | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01515 | hp2 | a0001 | c0001 | t0007 | g0162 | EUR | IBS | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0271 | EUR | IBS | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0296 | EUR | IBS | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01884 | hp1 | a0001 | c0001 | t0006 | g0114 | AFR | ACB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01884 | hp2 | a0001 | c0001 | t0015 | g0352 | AFR | ACB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01934 | hp1 | a0001 | c0001 | t0006 | g0101 | AMR | PEL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01934 | hp2 | a0001 | c0001 | t0072 | g0159 | AMR | PEL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01975 | hp1 | a0001 | c0001 | t0033 | g0158 | AMR | PEL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01975 | hp2 | a0001 | c0001 | t0057 | g0346 | AMR | PEL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01978 | hp1 | a0001 | c0001 | t0024 | g0347 | AMR | PEL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02004 | hp1 | a0001 | c0001 | t0013 | g0263 | AMR | PEL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02004 | hp2 | a0001 | c0001 | t0008 | g0191 | AMR | PEL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02015 | hp1 | a0001 | c0001 | t0009 | g0167 | EAS | KHV | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02040 | hp1 | a0001 | c0001 | t0042 | g0309 | EAS | KHV | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02040 | hp2 | a0001 | c0001 | t0064 | g0147 | EAS | KHV | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0315 | AFR | ACB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0288 | AFR | ACB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | KHV | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | KHV | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02071 | hp2 | a0001 | c0001 | t0126 | g0041 | EAS | KHV | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02074 | hp1 | a0001 | c0001 | t0045 | g0097 | EAS | KHV | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02074 | hp2 | a0001 | c0001 | t0006 | g0183 | EAS | KHV | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02080 | hp1 | a0001 | c0001 | t0005 | g0077 | EAS | KHV | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02080 | hp2 | a0001 | c0001 | t0056 | g0181 | EAS | KHV | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02083 | hp1 | a0001 | c0001 | t0005 | g0029 | EAS | KHV | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02083 | hp2 | a0001 | c0001 | t0128 | g0044 | EAS | KHV | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0327 | EAS | KHV | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02129 | hp2 | a0001 | c0001 | t0065 | g0012 | EAS | KHV | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02132 | hp1 | a0001 | c0001 | t0023 | g0141 | EAS | KHV | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02132 | hp2 | a0001 | c0001 | t0026 | g0292 | EAS | KHV | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02145 | hp1 | a0001 | c0001 | t0118 | g0018 | AFR | ACB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02145 | hp2 | a0001 | c0001 | t0091 | g0331 | AFR | ACB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02148 | hp2 | a0001 | c0001 | t0122 | g0052 | AMR | PEL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02155 | hp1 | a0001 | c0001 | t0092 | g0266 | EAS | CDX | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02155 | hp2 | a0001 | c0001 | t0005 | g0074 | EAS | CDX | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02165 | hp1 | a0001 | c0001 | t0051 | g0067 | EAS | CDX | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | CDX | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02257 | hp1 | a0001 | c0001 | t0119 | g0073 | AFR | ACB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02257 | hp2 | a0001 | c0001 | t0055 | g0350 | AFR | ACB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02258 | hp1 | a0001 | c0001 | t0094 | g0093 | AFR | ACB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02258 | hp2 | a0001 | c0001 | t0016 | g0108 | AFR | ACB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02273 | hp2 | a0001 | c0001 | t0011 | g0055 | AMR | PEL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02280 | hp1 | a0001 | c0001 | t0016 | g0113 | AFR | ACB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02280 | hp2 | a0001 | c0001 | t0102 | g0016 | AFR | ACB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02300 | hp1 | a0001 | c0001 | t0020 | g0057 | AMR | PEL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02300 | hp2 | a0001 | c0001 | t0009 | g0155 | AMR | PEL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02451 | hp1 | a0001 | c0001 | t0047 | g0358 | AFR | ACB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02451 | hp2 | a0001 | c0001 | t0103 | g0026 | AFR | ACB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02523 | hp1 | a0001 | c0001 | t0005 | g0036 | EAS | KHV | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02572 | hp1 | a0001 | c0001 | t0105 | g0014 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02572 | hp2 | a0001 | c0001 | t0015 | g0354 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02602 | hp1 | a0001 | c0001 | t0011 | g0080 | SAS | PJL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02602 | hp2 | a0001 | c0001 | t0007 | g0185 | SAS | PJL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02615 | hp1 | a0001 | c0001 | t0054 | g0351 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02615 | hp2 | a0001 | c0001 | t0019 | g0332 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02622 | hp1 | a0001 | c0001 | t0083 | g0231 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02622 | hp2 | a0001 | c0001 | t0082 | g0091 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02647 | hp1 | a0001 | c0001 | t0016 | g0105 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02647 | hp2 | a0001 | c0001 | t0043 | g0255 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02698 | hp1 | a0001 | c0001 | t0059 | g0166 | SAS | PJL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02698 | hp2 | a0001 | c0001 | t0113 | g0068 | SAS | PJL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02717 | hp1 | a0001 | c0001 | t0104 | g0357 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02717 | hp2 | a0001 | c0004 | t0015 | g0348 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02723 | hp1 | a0001 | c0001 | t0012 | g0286 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02723 | hp2 | a0001 | c0001 | t0052 | g0359 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02735 | hp1 | a0001 | c0001 | t0026 | g0301 | SAS | PJL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02738 | hp1 | a0001 | c0001 | t0006 | g0102 | SAS | PJL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02738 | hp2 | a0001 | c0001 | t0010 | g0337 | SAS | PJL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02809 | hp1 | a0001 | c0001 | t0012 | g0329 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02809 | hp2 | a0001 | c0001 | t0013 | g0276 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02818 | hp1 | a0001 | c0001 | t0117 | g0089 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02818 | hp2 | a0001 | c0001 | t0015 | g0353 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02895 | hp1 | a0001 | c0001 | t0028 | g0023 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02895 | hp2 | a0001 | c0003 | t0044 | g0100 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02896 | hp1 | a0001 | c0001 | t0058 | g0341 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02896 | hp2 | a0001 | c0001 | t0106 | g0021 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02922 | hp1 | a0001 | c0001 | t0053 | g0349 | AFR | ESN | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02922 | hp2 | a0001 | c0001 | t0007 | g0340 | AFR | ESN | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02965 | hp1 | a0001 | c0001 | t0110 | g0015 | AFR | ESN | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02965 | hp2 | a0001 | c0001 | t0019 | g0335 | AFR | ESN | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02970 | hp1 | a0001 | c0001 | t0063 | g0199 | AFR | ESN | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02970 | hp2 | a0001 | c0004 | t0015 | g0355 | AFR | ESN | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02976 | hp1 | a0001 | c0001 | t0046 | g0019 | AFR | ESN | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02976 | hp2 | a0001 | c0001 | t0066 | g0112 | AFR | ESN | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0306 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03041 | hp2 | a0001 | c0001 | t0111 | g0022 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03098 | hp1 | a0001 | c0001 | t0031 | g0007 | AFR | MSL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03098 | hp2 | a0001 | c0001 | t0101 | g0094 | AFR | MSL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03130 | hp1 | a0001 | c0001 | t0116 | g0098 | AFR | ESN | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03130 | hp2 | a0001 | c0001 | t0019 | g0325 | AFR | ESN | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03139 | hp1 | a0001 | c0001 | t0075 | g0281 | AFR | ESN | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03139 | hp2 | a0001 | c0001 | t0081 | g0090 | AFR | ESN | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03195 | hp1 | a0001 | c0001 | t0007 | g0318 | AFR | ESN | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03195 | hp2 | a0001 | c0001 | t0100 | g0096 | AFR | ESN | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03209 | hp1 | a0001 | c0001 | t0090 | g0004 | AFR | MSL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03209 | hp2 | a0001 | c0001 | t0025 | g0319 | AFR | MSL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03225 | hp1 | a0001 | c0001 | t0031 | g0007 | AFR | MSL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03225 | hp2 | a0001 | c0001 | t0097 | g0197 | AFR | MSL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03239 | hp1 | a0001 | c0001 | t0080 | g0270 | SAS | PJL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03239 | hp2 | a0001 | c0001 | t0007 | g0164 | SAS | PJL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03453 | hp1 | a0001 | c0001 | t0012 | g0283 | AFR | MSL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03453 | hp2 | a0001 | c0001 | t0019 | g0330 | AFR | MSL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03486 | hp1 | a0001 | c0001 | t0028 | g0024 | AFR | MSL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03486 | hp2 | a0001 | c0001 | t0012 | g0004 | AFR | MSL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0131 | SAS | PJL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0294 | SAS | PJL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03492 | hp2 | a0001 | c0001 | t0039 | g0132 | SAS | PJL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03516 | hp1 | a0001 | c0001 | t0010 | g0279 | AFR | ESN | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03516 | hp2 | a0001 | c0001 | t0007 | g0317 | AFR | ESN | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03540 | hp1 | a0001 | c0001 | t0074 | g0282 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03540 | hp2 | a0001 | c0001 | t0109 | g0020 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03579 | hp1 | a0001 | c0001 | t0018 | g0322 | AFR | MSL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03579 | hp2 | a0001 | c0001 | t0038 | g0111 | AFR | MSL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03654 | hp1 | a0001 | c0001 | t0112 | g0030 | SAS | PJL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03654 | hp2 | a0001 | c0001 | t0009 | g0165 | SAS | PJL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03688 | hp1 | a0001 | c0001 | t0020 | g0075 | SAS | STU | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03688 | hp2 | a0001 | c0001 | t0009 | g0168 | SAS | STU | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03704 | hp1 | a0001 | c0001 | t0024 | g0344 | SAS | PJL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03704 | hp2 | a0001 | c0001 | t0020 | g0060 | SAS | PJL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03710 | hp1 | a0001 | c0001 | t0006 | g0171 | SAS | PJL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03710 | hp2 | a0001 | c0001 | t0086 | g0289 | SAS | PJL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03831 | hp1 | a0001 | c0001 | t0006 | g0119 | SAS | BEB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03831 | hp2 | a0001 | c0001 | t0049 | g0082 | SAS | BEB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | BEB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03834 | hp2 | a0001 | c0001 | t0006 | g0169 | SAS | BEB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03927 | hp1 | a0001 | c0001 | t0010 | g0257 | SAS | BEB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03927 | hp2 | a0001 | c0001 | t0011 | g0046 | SAS | BEB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03942 | hp1 | a0001 | c0001 | t0009 | g0184 | SAS | BEB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03942 | hp2 | a0001 | c0001 | t0029 | g0034 | SAS | BEB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG04115 | hp1 | a0001 | c0001 | t0043 | g0336 | SAS | STU | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG04115 | hp2 | a0001 | c0001 | t0004 | g0222 | SAS | STU | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG04184 | hp1 | a0001 | c0001 | t0120 | g0037 | SAS | BEB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG04184 | hp2 | a0001 | c0001 | t0004 | g0218 | SAS | BEB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18522 | hp1 | a0001 | c0001 | t0046 | g0017 | AFR | YRI | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18522 | hp2 | a0001 | c0001 | t0047 | g0084 | AFR | YRI | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0323 | EAS | CHB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18612 | hp2 | a0001 | c0001 | t0021 | g0001 | EAS | CHB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18906 | hp1 | a0001 | c0001 | t0062 | g0198 | AFR | YRI | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18906 | hp2 | a0001 | c0001 | t0009 | g0320 | AFR | YRI | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18939 | hp1 | a0001 | c0001 | t0017 | g0146 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18939 | hp2 | a0001 | c0001 | t0005 | g0032 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18941 | hp1 | a0002 | c0002 | t0001 | g0228 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18941 | hp2 | a0001 | c0001 | t0013 | g0258 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18942 | hp1 | a0001 | c0001 | t0050 | g0095 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18944 | hp1 | a0001 | c0001 | t0129 | g0031 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18944 | hp2 | a0001 | c0001 | t0017 | g0152 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18946 | hp1 | a0001 | c0001 | t0029 | g0064 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18946 | hp2 | a0001 | c0001 | t0008 | g0104 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18947 | hp1 | a0001 | c0001 | t0069 | g0143 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18947 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18948 | hp2 | a0001 | c0001 | t0027 | g0302 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18949 | hp1 | a0001 | c0001 | t0004 | g0216 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18949 | hp2 | a0001 | c0001 | t0011 | g0054 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18950 | hp2 | a0001 | c0001 | t0098 | g0326 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18951 | hp2 | a0001 | c0001 | t0010 | g0256 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18953 | hp1 | a0001 | c0001 | t0023 | g0135 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18953 | hp2 | a0001 | c0001 | t0027 | g0304 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18954 | hp1 | a0002 | c0002 | t0001 | g0226 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18954 | hp2 | a0001 | c0001 | t0035 | g0154 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18960 | hp1 | a0001 | c0001 | t0041 | g0006 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18961 | hp1 | a0001 | c0001 | t0004 | g0204 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18961 | hp2 | a0001 | c0001 | t0035 | g0151 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18962 | hp1 | a0001 | c0001 | t0011 | g0069 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18962 | hp2 | a0001 | c0001 | t0008 | g0247 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18963 | hp1 | a0001 | c0001 | t0005 | g0081 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18963 | hp2 | a0001 | c0001 | t0004 | g0237 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18965 | hp1 | a0001 | c0001 | t0125 | g0039 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18965 | hp2 | a0001 | c0001 | t0041 | g0006 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18966 | hp1 | a0001 | c0007 | t0003 | g0142 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18966 | hp2 | a0001 | c0001 | t0008 | g0250 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18967 | hp1 | a0001 | c0001 | t0040 | g0156 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18967 | hp2 | a0001 | c0001 | t0004 | g0206 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18971 | hp1 | a0001 | c0001 | t0008 | g0208 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18972 | hp1 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18972 | hp2 | a0001 | c0001 | t0087 | g0311 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18973 | hp2 | a0001 | c0001 | t0004 | g0234 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18975 | hp2 | a0001 | c0001 | t0050 | g0066 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18979 | hp1 | a0001 | c0001 | t0008 | g0249 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18979 | hp2 | a0001 | c0001 | t0068 | g0130 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18980 | hp1 | a0001 | c0001 | t0077 | g0188 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18982 | hp1 | a0001 | c0001 | t0085 | g0310 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18982 | hp2 | a0001 | c0001 | t0020 | g0076 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18983 | hp1 | a0001 | c0001 | t0017 | g0153 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18983 | hp2 | a0001 | c0001 | t0004 | g0254 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18984 | hp1 | a0001 | c0001 | t0014 | g0071 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18985 | hp1 | a0001 | c0001 | t0010 | g0261 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18985 | hp2 | a0001 | c0001 | t0030 | g0035 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18986 | hp1 | a0001 | c0001 | t0008 | g0251 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18986 | hp2 | a0001 | c0001 | t0018 | g0300 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18988 | hp1 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18988 | hp2 | a0001 | c0001 | t0014 | g0040 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18991 | hp1 | a0001 | c0001 | t0108 | g0088 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18991 | hp2 | a0002 | c0002 | t0001 | g0202 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18992 | hp1 | a0001 | c0001 | t0004 | g0207 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18992 | hp2 | a0001 | c0001 | t0039 | g0116 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18997 | hp1 | a0003 | c0005 | t0002 | g0297 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18998 | hp2 | a0001 | c0001 | t0123 | g0063 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18999 | hp2 | a0001 | c0001 | t0030 | g0047 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19000 | hp2 | a0001 | c0001 | t0029 | g0086 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19001 | hp1 | a0001 | c0001 | t0045 | g0027 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19001 | hp2 | a0001 | c0001 | t0008 | g0201 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19003 | hp1 | a0001 | c0001 | t0005 | g0061 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0356 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19004 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19005 | hp2 | a0001 | c0001 | t0032 | g0209 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19009 | hp1 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19009 | hp2 | a0001 | c0001 | t0017 | g0126 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19011 | hp1 | a0001 | c0001 | t0040 | g0144 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19011 | hp2 | a0001 | c0001 | t0115 | g0078 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19012 | hp1 | a0001 | c0001 | t0036 | g0305 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19012 | hp2 | a0001 | c0001 | t0036 | g0160 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19030 | hp1 | a0001 | c0001 | t0028 | g0025 | AFR | LWK | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19030 | hp2 | a0001 | c0001 | t0042 | g0314 | AFR | LWK | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19043 | hp1 | a0001 | c0001 | t0016 | g0110 | AFR | LWK | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0339 | AFR | LWK | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19057 | hp2 | a0001 | c0001 | t0010 | g0262 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19058 | hp1 | a0001 | c0001 | t0017 | g0145 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19058 | hp2 | a0001 | c0001 | t0014 | g0058 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19060 | hp1 | a0001 | c0001 | t0127 | g0042 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19060 | hp2 | a0001 | c0001 | t0021 | g0001 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19062 | hp1 | a0001 | c0001 | t0023 | g0118 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19062 | hp2 | a0001 | c0001 | t0014 | g0070 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19066 | hp1 | a0001 | c0001 | t0025 | g0182 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19066 | hp2 | a0001 | c0001 | t0027 | g0303 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19067 | hp1 | a0001 | c0001 | t0049 | g0033 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19067 | hp2 | a0001 | c0001 | t0034 | g0115 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19068 | hp1 | a0001 | c0001 | t0014 | g0043 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19068 | hp2 | a0001 | c0001 | t0009 | g0328 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19070 | hp1 | a0001 | c0001 | t0073 | g0161 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19070 | hp2 | a0001 | c0001 | t0013 | g0259 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19074 | hp1 | a0001 | c0001 | t0018 | g0127 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19074 | hp2 | a0001 | c0001 | t0018 | g0290 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19080 | hp1 | a0001 | c0001 | t0008 | g0248 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19080 | hp2 | a0001 | c0001 | t0107 | g0087 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19081 | hp1 | a0001 | c0001 | t0008 | g0245 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19081 | hp2 | a0001 | c0001 | t0005 | g0028 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19083 | hp1 | a0001 | c0001 | t0004 | g0272 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19083 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19084 | hp1 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19084 | hp2 | a0001 | c0001 | t0032 | g0200 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19087 | hp1 | a0001 | c0001 | t0005 | g0038 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19087 | hp2 | a0001 | c0001 | t0099 | g0308 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19091 | hp1 | a0001 | c0001 | t0130 | g0243 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19091 | hp2 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | YRI | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19240 | hp2 | a0001 | c0001 | t0010 | g0278 | AFR | YRI | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | ASW | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA20129 | hp2 | a0001 | c0001 | t0018 | g0321 | AFR | ASW | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA20752 | hp1 | a0001 | c0001 | t0006 | g0103 | EUR | TSI | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA20752 | hp2 | a0001 | c0001 | t0096 | g0265 | EUR | TSI | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA20905 | hp1 | a0001 | c0001 | t0067 | g0128 | SAS | GIH | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA20905 | hp2 | a0001 | c0001 | t0088 | g0307 | SAS | GIH | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02109 | hp1 | a0001 | c0001 | t0016 | g0106 | AFR | ACB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02109 | hp2 | a0001 | c0006 | t0076 | g0334 | AFR | ACB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02486 | hp1 | a0001 | c0001 | t0010 | g0277 | AFR | ACB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02486 | hp2 | a0001 | c0001 | t0012 | g0284 | AFR | ACB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ACB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02559 | hp2 | a0001 | c0001 | t0038 | g0109 | AFR | ACB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03471 | hp1 | a0001 | c0001 | t0012 | g0285 | AFR | MSL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03471 | hp2 | a0001 | c0001 | t0019 | g0333 | AFR | MSL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG06807 | hp1 | a0001 | c0001 | t0095 | g0092 | AFR | USA | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0316 | AFR | USA | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18955 | hp1 | a0001 | c0001 | t0061 | g0187 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18955 | hp2 | a0001 | c0001 | t0011 | g0072 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | USA | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA20300 | hp2 | a0001 | c0001 | t0084 | g0107 | AFR | USA | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA21309 | hp1 | a0001 | c0003 | t0044 | g0099 | AFR | LWK | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA21309 | hp2 | a0001 | c0001 | t0006 | g0008 | AFR | LWK | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
homoSapiens | chm13v2 | a0001 | c0001 | t0078 | g0009 | REF | REF | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
homoSapiens | grch38p0 | a0001 | c0001 | t0007 | g0085 | REF | REF | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:151660833 | A | G | 1 | a0002 | 6 | NA18941.hp1 NA18947.hp2 NA18954.hp1 others(3): Show |
missense_variant | MODERATE | c.772A>G | p.Met258Val | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 4/12 | 924/6441 | 772/1626 | 258/541 | chr1 | 151660833 | |||
chr1:151693022 | A | T | 1 | a0003 | 1 | NA18997.hp1 | stop_gained | HIGH | c.1501A>T | p.Lys501* | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 10/12 | 1653/6441 | 1501/1626 | 501/541 | chr1 | 151693022 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:151612219 | G | A | 1 | a0001c0003 | 2 | HG02895.hp2 NA21309.hp1 |
synonymous_variant | LOW | c.18G>A | p.Gly6Gly | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/12 | 170/6441 | 18/1626 | 6/541 | chr1 | 151612219 | |||
chr1:151662183 | C | T | 1 | a0001c0007 | 1 | NA18966.hp1 | synonymous_variant | LOW | c.819C>T | p.Ser273Ser | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/12 | 971/6441 | 819/1626 | 273/541 | chr1 | 151662183 | |||
chr1:151666010 | T | C | 1 | a0001c0004 | 2 | HG02717.hp2 HG02970.hp2 |
splice_region_variant&synonymous_variant | LOW | c.984T>C | p.Phe328Phe | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/12 | 1136/6441 | 984/1626 | 328/541 | chr1 | 151666010 | |||
chr1:151683361 | C | T | 1 | a0001c0006 | 1 | HG02109.hp2 | synonymous_variant | LOW | c.1155C>T | p.Val385Val | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/12 | 1307/6441 | 1155/1626 | 385/541 | chr1 | 151683361 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:151612124 | G | A | 1 | a0001c0001t0051 | 1 | HG02165.hp1 | 5_prime_UTR_variant | MODIFIER | c.-78G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/12 | 78 | chr1 | 151612124 | ||||||
chr1:151612151 | G | A | 1 | a0001c0001t0052 | 1 | HG02723.hp2 | 5_prime_UTR_variant | MODIFIER | c.-51G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/12 | 51 | chr1 | 151612151 | ||||||
chr1:151694519 | T | TA | 6 | a0001c0001t0015 a0001c0001t0031 a0001c0001t0053 others(3): Show |
10 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*105dupA | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 106 | INFO_REALIGN_3_PRIME | chr1 | 151694519 | |||||
chr1:151694718 | C | T | 1 | a0001c0001t0130 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*301C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 301 | chr1 | 151694718 | ||||||
chr1:151694941 | T | C | 1 | a0001c0001t0032 | 2 | NA19005.hp2 NA19084.hp2 |
3_prime_UTR_variant | MODIFIER | c.*524T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 524 | chr1 | 151694941 | ||||||
chr1:151694948 | G | A | 1 | a0001c0001t0056 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*531G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 531 | chr1 | 151694948 | ||||||
chr1:151695136 | G | A | 1 | a0001c0001t0057 | 1 | HG01975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*719G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 719 | chr1 | 151695136 | ||||||
chr1:151695242 | A | G | 43 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0014 others(40): Show |
83 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*825A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 825 | chr1 | 151695242 | ||||||
chr1:151695353 | T | C | 1 | a0001c0001t0102 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*936T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 936 | chr1 | 151695353 | ||||||
chr1:151695410 | C | CT | 37 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0010 others(34): Show |
108 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*1019dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 1020 | INFO_REALIGN_3_PRIME | chr1 | 151695410 | |||||
chr1:151695410 | C | CTT | 11 | a0001c0001t0042 a0001c0001t0043 a0001c0001t0049 others(8): Show |
14 | HG00741.hp2 HG02040.hp1 HG02148.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1018_*1019dupTT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 1020 | INFO_REALIGN_3_PRIME | chr1 | 151695410 | |||||
chr1:151695410 | C | CTTTT | 11 | a0001c0001t0005 a0001c0001t0030 a0001c0001t0050 others(8): Show |
26 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1016_*1019dupTTTT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 1020 | INFO_REALIGN_3_PRIME | chr1 | 151695410 | |||||
chr1:151695410 | CT | C | 10 | a0001c0001t0052 a0001c0001t0058 a0001c0001t0059 others(7): Show |
11 | HG01168.hp2 HG02572.hp1 HG02698.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1019delT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 1019 | INFO_REALIGN_3_PRIME | chr1 | 151695410 | |||||
chr1:151695410 | CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0103 a0001c0001t0104 |
2 | HG02451.hp2 HG02717.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1009_*1019delTTTT others(7): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 1009 | INFO_REALIGN_3_PRIME | chr1 | 151695410 | |||||
chr1:151695449 | C | G | 6 | a0001c0001t0028 a0001c0001t0106 a0001c0001t0109 others(3): Show |
9 | HG02895.hp1 HG02895.hp2 HG02896.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1032C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 1032 | chr1 | 151695449 | ||||||
chr1:151695460 | G | A | 1 | a0001c0001t0112 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1043G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 1043 | chr1 | 151695460 | ||||||
chr1:151695605 | T | G | 33 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0014 others(30): Show |
69 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*1188T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 1188 | chr1 | 151695605 | ||||||
chr1:151695658 | C | G | 2 | a0001c0001t0062 a0001c0001t0063 |
2 | HG02970.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1241C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 1241 | chr1 | 151695658 | ||||||
chr1:151695819 | A | C | 75 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(72): Show |
203 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(200): Show |
3_prime_UTR_variant | MODIFIER | c.*1402A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 1402 | chr1 | 151695819 | ||||||
chr1:151696003 | A | G | 3 | a0001c0001t0019 a0001c0001t0091 a0001c0006t0076 |
7 | HG02109.hp2 HG02145.hp2 HG02615.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1586A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 1586 | chr1 | 151696003 | ||||||
chr1:151696063 | A | G | 5 | a0001c0001t0028 a0001c0001t0106 a0001c0001t0109 others(2): Show |
7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1646A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 1646 | chr1 | 151696063 | ||||||
chr1:151696097 | T | C | 1 | a0001c0001t0064 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1680T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 1680 | chr1 | 151696097 | ||||||
chr1:151696219 | C | T | 4 | a0001c0001t0012 a0001c0001t0074 a0001c0001t0075 others(1): Show |
9 | HG02486.hp2 HG02723.hp1 HG02809.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1802C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 1802 | chr1 | 151696219 | ||||||
chr1:151696258 | G | A | 1 | a0001c0001t0077 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1841G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 1841 | chr1 | 151696258 | ||||||
chr1:151696371 | T | A | 6 | a0001c0001t0016 a0001c0001t0038 a0001c0001t0065 others(3): Show |
11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1954T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 1954 | chr1 | 151696371 | ||||||
chr1:151696461 | T | TTTTC | 13 | a0001c0001t0014 a0001c0001t0025 a0001c0001t0030 others(10): Show |
23 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2085_*2088dupTTTC | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2089 | INFO_REALIGN_3_PRIME | chr1 | 151696461 | |||||
chr1:151696461 | T | TTTTCTTT others(1): Show |
11 | a0001c0001t0011 a0001c0001t0018 a0001c0001t0026 others(8): Show |
25 | HG00741.hp2 HG01175.hp2 HG01433.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2081_*2088dupTTTC others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2089 | INFO_REALIGN_3_PRIME | chr1 | 151696461 | |||||
chr1:151696461 | T | TTTTCTTT others(5): Show |
6 | a0001c0001t0027 a0001c0001t0029 a0001c0001t0073 others(3): Show |
10 | HG02148.hp2 HG02717.hp1 HG03942.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2077_*2088dupTTTC others(8): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2089 | INFO_REALIGN_3_PRIME | chr1 | 151696461 | |||||
chr1:151696461 | T | TTTTCTTT others(9): Show |
5 | a0001c0001t0041 a0001c0001t0048 a0001c0001t0089 others(2): Show |
7 | HG00423.hp2 HG01255.hp1 HG01256.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2073_*2088dupTTTC others(12): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2089 | INFO_REALIGN_3_PRIME | chr1 | 151696461 | |||||
chr1:151696461 | T | TTTTCTTT others(13): Show |
1 | a0001c0001t0036 | 2 | NA19012.hp1 NA19012.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2069_*2088dupTTTC others(16): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2089 | INFO_REALIGN_3_PRIME | chr1 | 151696461 | |||||
chr1:151696461 | TTTTC | T | 14 | a0001c0001t0009 a0001c0001t0017 a0001c0001t0021 others(11): Show |
34 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*2085_*2088delTTTC | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2085 | INFO_REALIGN_3_PRIME | chr1 | 151696461 | |||||
chr1:151696461 | TTTTCTTT others(1): Show |
T | 11 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0033 others(8): Show |
36 | HG00280.hp1 HG00609.hp2 HG00741.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*2081_*2088delTTTC others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2081 | INFO_REALIGN_3_PRIME | chr1 | 151696461 | |||||
chr1:151696461 | TTTTCTTT others(5): Show |
T | 1 | a0001c0001t0067 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2077_*2088delTTTC others(8): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2077 | INFO_REALIGN_3_PRIME | chr1 | 151696461 | |||||
chr1:151696461 | TTTTCTTT others(13): Show |
T | 1 | a0001c0001t0022 | 3 | HG00642.hp2 HG01256.hp1 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2069_*2088delTTTC others(16): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2069 | INFO_REALIGN_3_PRIME | chr1 | 151696461 | |||||
chr1:151696471 | T | C | 1 | a0001c0001t0105 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2054T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2054 | chr1 | 151696471 | ||||||
chr1:151696486 | TTTCTTTC others(13): Show |
T | 1 | a0001c0001t0123 | 1 | NA18998.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2077_*2096delTTTC others(16): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2077 | INFO_REALIGN_3_PRIME | chr1 | 151696486 | |||||
chr1:151696490 | T | G | 2 | a0001c0001t0008 a0001c0001t0037 |
4 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2073T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2073 | chr1 | 151696490 | ||||||
chr1:151696490 | T | TTTCTTTC others(1): Show |
5 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0061 others(2): Show |
11 | NA18946.hp2 NA18947.hp2 NA18951.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2080_*2081insGTTC others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2081 | INFO_REALIGN_3_PRIME | chr1 | 151696490 | |||||
chr1:151696490 | T | TTTCTTTC others(9): Show |
1 | a0002c0002t0001 | 2 | NA18941.hp1 NA19009.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2080_*2081insGTTC others(12): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2081 | INFO_REALIGN_3_PRIME | chr1 | 151696490 | |||||
chr1:151696494 | T | G | 4 | a0001c0001t0016 a0001c0001t0038 a0001c0001t0084 others(1): Show |
9 | HG02109.hp1 HG02155.hp1 HG02258.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2077T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2077 | chr1 | 151696494 | ||||||
chr1:151696494 | TTTCTTTC others(5): Show |
T | 3 | a0001c0001t0002 a0001c0001t0019 a0001c0001t0042 |
4 | HG02056.hp1 HG02615.hp2 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2085_*2096delTTTC others(8): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2085 | INFO_REALIGN_3_PRIME | chr1 | 151696494 | |||||
chr1:151696498 | T | G | 12 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(9): Show |
23 | HG00642.hp1 HG01074.hp1 HG01257.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2081T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2081 | chr1 | 151696498 | ||||||
chr1:151696498 | T | TTTCG | 4 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0046 others(1): Show |
8 | HG02280.hp2 HG02486.hp1 HG03516.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2084_*2085insGTTC | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2085 | INFO_REALIGN_3_PRIME | chr1 | 151696498 | |||||
chr1:151696498 | T | TTTCGTTC others(5): Show |
4 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0063 others(1): Show |
12 | HG00735.hp1 HG00738.hp2 HG02148.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2084_*2085insGTTC others(8): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2085 | INFO_REALIGN_3_PRIME | chr1 | 151696498 | |||||
chr1:151696498 | T | TTTCTTTC others(1): Show |
4 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0020 others(1): Show |
9 | HG01167.hp1 HG01261.hp1 HG01346.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2105_*2112dupGTTC others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2113 | INFO_REALIGN_3_PRIME | chr1 | 151696498 | |||||
chr1:151696498 | T | TTTCTTTC others(9): Show |
4 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(1): Show |
12 | HG01433.hp1 HG01515.hp1 HG02735.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2097_*2112dupGTTC others(12): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2113 | INFO_REALIGN_3_PRIME | chr1 | 151696498 | |||||
chr1:151696498 | T | TTTCTTTC others(17): Show |
3 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 |
6 | HG00673.hp1 HG02273.hp1 HG03834.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2089_*2112dupGTTC others(20): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2113 | INFO_REALIGN_3_PRIME | chr1 | 151696498 | |||||
chr1:151696498 | T | TTTCTTTC others(5): Show |
7 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0010 others(4): Show |
11 | HG00438.hp2 HG01175.hp1 HG02486.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2088_*2089insTTTC others(8): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2089 | INFO_REALIGN_3_PRIME | chr1 | 151696498 | |||||
chr1:151696498 | T | TTTCTTTC others(13): Show |
6 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0019 others(3): Show |
10 | HG01346.hp2 HG03098.hp2 HG03453.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2088_*2089insTTTC others(16): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2089 | INFO_REALIGN_3_PRIME | chr1 | 151696498 | |||||
chr1:151696498 | T | TTTCTTTC others(21): Show |
2 | a0001c0001t0001 a0001c0001t0008 |
2 | NA18950.hp1 NA19001.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2088_*2089insTTTC others(24): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2089 | INFO_REALIGN_3_PRIME | chr1 | 151696498 | |||||
chr1:151696498 | T | TTTCTTTC others(29): Show |
1 | a0001c0001t0008 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2088_*2089insTTTC others(32): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2089 | INFO_REALIGN_3_PRIME | chr1 | 151696498 | |||||
chr1:151696498 | T | TTTCTTTC others(9): Show |
6 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0019 others(3): Show |
7 | HG02015.hp2 HG02300.hp1 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2088_*2089insTTTC others(12): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2089 | INFO_REALIGN_3_PRIME | chr1 | 151696498 | |||||
chr1:151696498 | T | TTTCTTTC others(17): Show |
3 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0091 |
7 | HG00280.hp2 HG01516.hp1 HG01978.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2088_*2089insTTTC others(20): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2089 | INFO_REALIGN_3_PRIME | chr1 | 151696498 | |||||
chr1:151696498 | T | TTTCTTTC others(25): Show |
2 | a0001c0001t0001 a0001c0001t0008 |
4 | HG00323.hp1 NA18962.hp2 NA18979.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2088_*2089insTTTC others(28): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2089 | INFO_REALIGN_3_PRIME | chr1 | 151696498 | |||||
chr1:151696498 | T | TTTCTTTC others(13): Show |
1 | a0001c0001t0001 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2088_*2089insTTTC others(16): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2089 | INFO_REALIGN_3_PRIME | chr1 | 151696498 | |||||
chr1:151696498 | T | TTTCTTTC others(21): Show |
1 | a0001c0001t0001 | 2 | HG01081.hp2 NA18960.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2088_*2089insTTTC others(24): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2089 | INFO_REALIGN_3_PRIME | chr1 | 151696498 | |||||
chr1:151696498 | TTTCTTTC others(1): Show |
T | 2 | a0001c0001t0002 a0001c0001t0019 |
7 | HG00323.hp2 HG00639.hp2 HG01099.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2105_*2112delGTTC others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2105 | INFO_REALIGN_3_PRIME | chr1 | 151696498 | |||||
chr1:151696502 | T | G | 4 | a0001c0001t0016 a0001c0001t0038 a0001c0001t0084 others(1): Show |
9 | HG02109.hp1 HG02155.hp1 HG02258.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2085T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2085 | chr1 | 151696502 | ||||||
chr1:151696502 | TTTCG | T | 4 | a0001c0001t0002 a0001c0001t0020 a0001c0001t0049 others(1): Show |
8 | HG01081.hp1 HG01192.hp1 HG01516.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2089_*2092delGTTC | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2089 | INFO_REALIGN_3_PRIME | chr1 | 151696502 | |||||
chr1:151696502 | TTTCGTTC others(5): Show |
T | 2 | a0001c0001t0028 a0001c0001t0106 |
4 | HG02895.hp1 HG02896.hp2 HG03486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2089_*2100delGTTC others(8): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2089 | INFO_REALIGN_3_PRIME | chr1 | 151696502 | |||||
chr1:151696502 | TTTCGTTC others(13): Show |
T | 1 | a0001c0001t0109 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2089_*2108delGTTC others(16): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2089 | INFO_REALIGN_3_PRIME | chr1 | 151696502 | |||||
chr1:151696505 | C | CTTTCTTT others(9): Show |
1 | a0001c0001t0043 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2088_*2089insTTTC others(12): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2089 | chr1 | 151696505 | ||||||
chr1:151696506 | G | T | 17 | a0001c0001t0002 a0001c0001t0014 a0001c0001t0016 others(14): Show |
27 | HG00423.hp2 HG01175.hp2 HG02055.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*2089G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2089 | chr1 | 151696506 | ||||||
chr1:151696506 | GTTCTTTC others(17): Show |
G | 1 | a0001c0001t0110 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2097_*2120delGTTC others(20): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2097 | INFO_REALIGN_3_PRIME | chr1 | 151696506 | |||||
chr1:151696510 | T | G | 4 | a0001c0001t0016 a0001c0001t0038 a0001c0001t0084 others(1): Show |
9 | HG02109.hp1 HG02155.hp1 HG02258.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2093T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2093 | chr1 | 151696510 | ||||||
chr1:151696514 | G | A | 2 | a0001c0001t0079 a0001c0001t0093 |
2 | HG00639.hp1 HG01168.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2097G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2097 | chr1 | 151696514 | ||||||
chr1:151696514 | G | T | 4 | a0001c0001t0016 a0001c0001t0038 a0001c0001t0084 others(1): Show |
9 | HG02109.hp1 HG02155.hp1 HG02258.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2097G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2097 | chr1 | 151696514 | ||||||
chr1:151696514 | GTTCTTTC others(9): Show |
G | 1 | a0001c0001t0111 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2105_*2120delGTTC others(12): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2105 | INFO_REALIGN_3_PRIME | chr1 | 151696514 | |||||
chr1:151696518 | T | G | 4 | a0001c0001t0016 a0001c0001t0038 a0001c0001t0084 others(1): Show |
9 | HG02109.hp1 HG02155.hp1 HG02258.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2101T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2101 | chr1 | 151696518 | ||||||
chr1:151696522 | G | GTTCT | 6 | a0001c0001t0010 a0001c0001t0043 a0001c0001t0055 others(3): Show |
14 | HG02129.hp2 HG02257.hp2 HG02486.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2126_*2129dupTTCT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2130 | INFO_REALIGN_3_PRIME | chr1 | 151696522 | |||||
chr1:151696522 | G | GTTCTTTC others(5): Show |
6 | a0001c0001t0013 a0001c0001t0054 a0001c0001t0079 others(3): Show |
11 | HG00438.hp1 HG00639.hp1 HG01099.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2112_*2113insGTTC others(8): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2113 | INFO_REALIGN_3_PRIME | chr1 | 151696522 | |||||
chr1:151696522 | G | GTTCTTTC others(9): Show |
3 | a0001c0001t0062 a0001c0001t0082 a0001c0001t0094 |
3 | HG02258.hp1 HG02622.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2112_*2113insGTTC others(12): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2113 | INFO_REALIGN_3_PRIME | chr1 | 151696522 | |||||
chr1:151696522 | G | T | 14 | a0001c0001t0016 a0001c0001t0027 a0001c0001t0028 others(11): Show |
24 | HG02109.hp1 HG02155.hp1 HG02258.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2105G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2105 | chr1 | 151696522 | ||||||
chr1:151696522 | GTTCT | G | 3 | a0001c0001t0017 a0001c0001t0035 a0001c0001t0040 |
9 | NA18939.hp1 NA18944.hp2 NA18954.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2126_*2129delTTCT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2126 | INFO_REALIGN_3_PRIME | chr1 | 151696522 | |||||
chr1:151696526 | T | G | 1 | a0001c0001t0080 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2109T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2109 | chr1 | 151696526 | ||||||
chr1:151696530 | T | G | 40 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0014 others(37): Show |
80 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*2113T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2113 | chr1 | 151696530 | ||||||
chr1:151696651 | G | GT | 6 | a0001c0001t0021 a0001c0001t0034 a0001c0001t0052 others(3): Show |
10 | HG00280.hp1 HG00544.hp1 HG00738.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2252dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2253 | INFO_REALIGN_3_PRIME | chr1 | 151696651 | |||||
chr1:151696651 | GTTTT | G | 2 | a0001c0001t0008 a0001c0001t0032 |
13 | HG01074.hp1 HG02004.hp2 NA18946.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2249_*2252delTTTT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2249 | INFO_REALIGN_3_PRIME | chr1 | 151696651 | |||||
chr1:151696651 | GTTTTT | G | 29 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0010 others(26): Show |
105 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*2248_*2252delTTTT others(1): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2248 | INFO_REALIGN_3_PRIME | chr1 | 151696651 | |||||
chr1:151696668 | T | TTTTC | 36 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0014 others(33): Show |
74 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*2252_*2253insTTCT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2253 | INFO_REALIGN_3_PRIME | chr1 | 151696668 | |||||
chr1:151696668 | T | TTTTTC | 6 | a0001c0001t0030 a0001c0001t0108 a0001c0001t0114 others(3): Show |
8 | HG00423.hp1 HG00544.hp2 HG00741.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2252_*2253insTTTC others(1): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2253 | INFO_REALIGN_3_PRIME | chr1 | 151696668 | |||||
chr1:151696669 | T | TTTTTTTC | 3 | a0001c0001t0016 a0001c0001t0038 a0001c0001t0066 |
8 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2252_*2253insTTTT others(3): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2253 | chr1 | 151696669 | ||||||
chr1:151696683 | T | C | 1 | a0001c0001t0101 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2266T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2266 | chr1 | 151696683 | ||||||
chr1:151696688 | C | T | 4 | a0001c0001t0024 a0001c0001t0033 a0001c0001t0058 others(1): Show |
7 | HG00735.hp2 HG00741.hp1 HG01167.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2271C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2271 | chr1 | 151696688 | ||||||
chr1:151696966 | C | T | 75 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(72): Show |
203 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(200): Show |
3_prime_UTR_variant | MODIFIER | c.*2549C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2549 | chr1 | 151696966 | ||||||
chr1:151697079 | C | A | 26 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(23): Show |
110 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*2662C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2662 | chr1 | 151697079 | ||||||
chr1:151697215 | T | G | 2 | a0001c0001t0116 a0001c0001t0119 |
2 | HG02257.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2798T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2798 | chr1 | 151697215 | ||||||
chr1:151697225 | TA | T | 27 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0014 others(24): Show |
62 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*2811delA | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2811 | INFO_REALIGN_3_PRIME | chr1 | 151697225 | |||||
chr1:151697521 | C | A | 81 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(78): Show |
214 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(211): Show |
3_prime_UTR_variant | MODIFIER | c.*3104C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 3104 | chr1 | 151697521 | ||||||
chr1:151697614 | G | A | 1 | a0001c0001t0065 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3197G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 3197 | chr1 | 151697614 | ||||||
chr1:151697912 | G | A | 1 | a0001c0001t0083 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3495G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 3495 | chr1 | 151697912 | ||||||
chr1:151698114 | CAG | C | 42 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0014 others(39): Show |
82 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*3698_*3699delAG | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 3698 | chr1 | 151698114 | ||||||
chr1:151698123 | A | C | 1 | a0001c0001t0126 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3706A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 3706 | chr1 | 151698123 | ||||||
chr1:151698210 | C | G | 3 | a0001c0001t0047 a0001c0001t0116 a0001c0001t0119 |
4 | HG02257.hp1 HG02451.hp1 HG03130.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3793C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 3793 | chr1 | 151698210 | ||||||
chr1:151698377 | C | T | 5 | a0001c0001t0028 a0001c0001t0106 a0001c0001t0109 others(2): Show |
7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3960C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 3960 | chr1 | 151698377 | ||||||
chr1:151698751 | G | A | 36 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0014 others(33): Show |
73 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*4334G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 4334 | chr1 | 151698751 | ||||||
chr1:151698879 | T | C | 7 | a0001c0001t0003 a0001c0001t0023 a0001c0001t0039 others(4): Show |
22 | HG00408.hp1 HG00609.hp2 HG02132.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*4462T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 4462 | chr1 | 151698879 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:151612549 | G | A | 1 | a0001c0001t0006g0008 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.311+37G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151612549 | |||||||
chr1:151612774 | C | G | 1 | a0001c0001t0052g0359 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.311+262C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151612774 | |||||||
chr1:151612841 | T | G | 1 | a0001c0001t0001g0010 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.311+329T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151612841 | |||||||
chr1:151612890 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.311+378G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151612890 | |||||||
chr1:151612981 | C | G | 2 | a0001c0001t0047g0358 a0001c0001t0104g0357 |
2 | HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.311+469C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151612981 | |||||||
chr1:151613067 | C | T | 1 | a0001c0001t0001g0356 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.311+555C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151613067 | |||||||
chr1:151613332 | C | T | 9 | a0001c0001t0015g0352 a0001c0001t0015g0353 a0001c0001t0015g0354 others(6): Show |
10 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.311+820C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151613332 | |||||||
chr1:151613742 | C | T | 7 | a0001c0001t0024g0343 a0001c0001t0024g0344 a0001c0001t0024g0347 others(4): Show |
7 | HG00735.hp2 HG00741.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.311+1230C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151613742 | |||||||
chr1:151613852 | G | C | 2 | a0001c0001t0005g0013 a0001c0001t0065g0012 |
2 | HG02129.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.311+1340G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151613852 | |||||||
chr1:151613895 | T | C | 1 | a0001c0001t0052g0359 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.311+1383T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151613895 | |||||||
chr1:151613898 | C | T | 1 | a0001c0001t0007g0340 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.311+1386C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151613898 | |||||||
chr1:151613919 | C | T | 1 | a0001c0001t0001g0339 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.311+1407C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151613919 | |||||||
chr1:151613948 | A | AATTTT | 270 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(267): Show |
276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.311+1438_311+1442d others(7): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151613948 | ||||||
chr1:151614064 | T | C | 9 | a0001c0001t0015g0352 a0001c0001t0015g0353 a0001c0001t0015g0354 others(6): Show |
10 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.311+1552T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151614064 | |||||||
chr1:151614178 | A | G | 2 | a0001c0003t0044g0099 a0001c0003t0044g0100 |
2 | HG02895.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.311+1666A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151614178 | |||||||
chr1:151614442 | G | C | 2 | a0001c0003t0044g0099 a0001c0003t0044g0100 |
2 | HG02895.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.311+1930G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151614442 | |||||||
chr1:151614564 | C | T | 1 | a0001c0001t0021g0338 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.311+2052C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151614564 | |||||||
chr1:151614709 | T | G | 3 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0103 |
3 | HG01934.hp1 HG02738.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.311+2197T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151614709 | |||||||
chr1:151614772 | A | C | 2 | a0001c0001t0010g0337 a0001c0001t0043g0336 |
2 | HG02738.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.311+2260A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151614772 | |||||||
chr1:151615327 | G | C | 1 | a0001c0001t0065g0012 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.311+2815G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151615327 | |||||||
chr1:151615404 | G | A | 1 | a0001c0001t0104g0357 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.311+2892G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151615404 | |||||||
chr1:151615437 | T | C | 1 | a0001c0001t0008g0104 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.311+2925T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151615437 | |||||||
chr1:151615773 | G | A | 9 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(6): Show |
9 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.311+3261G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151615773 | |||||||
chr1:151615803 | T | A | 283 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(280): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.311+3291T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151615803 | |||||||
chr1:151616151 | G | A | 1 | a0001c0001t0065g0012 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.311+3639G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151616151 | |||||||
chr1:151616259 | G | A | 86 | a0001c0001t0002g0148 a0001c0001t0002g0178 a0001c0001t0002g0179 others(83): Show |
87 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.311+3747G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151616259 | |||||||
chr1:151616339 | A | G | 146 | a0001c0001t0002g0005 a0001c0001t0002g0148 a0001c0001t0002g0178 others(143): Show |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.311+3827A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151616339 | |||||||
chr1:151616441 | T | A | 1 | a0001c0001t0105g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.311+3929T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151616441 | |||||||
chr1:151616678 | A | G | 2 | a0001c0001t0001g0280 a0001c0001t0001g0339 |
2 | HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.311+4166A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151616678 | |||||||
chr1:151616887 | G | A | 5 | a0001c0001t0001g0002 a0001c0001t0001g0189 a0001c0001t0001g0190 others(2): Show |
6 | NA18951.hp1 NA18955.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.311+4375G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151616887 | |||||||
chr1:151616938 | C | T | 2 | a0001c0003t0044g0099 a0001c0003t0044g0100 |
2 | HG02895.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.311+4426C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151616938 | |||||||
chr1:151617219 | C | A | 2 | a0001c0003t0044g0099 a0001c0003t0044g0100 |
2 | HG02895.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.311+4707C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151617219 | |||||||
chr1:151617263 | T | TTTTA | 25 | a0001c0001t0001g0273 a0001c0001t0010g0277 a0001c0001t0010g0278 others(22): Show |
25 | HG00639.hp1 HG00642.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.311+4780_311+4783d others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151617263 | ||||||
chr1:151617263 | TTTTA | T | 6 | a0001c0001t0008g0191 a0001c0001t0008g0193 a0001c0001t0037g0192 others(3): Show |
6 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.311+4780_311+4783d others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151617263 | ||||||
chr1:151617364 | C | T | 1 | a0001c0001t0103g0026 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.311+4852C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151617364 | |||||||
chr1:151617371 | C | A | 1 | a0001c0001t0006g0114 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.311+4859C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151617371 | |||||||
chr1:151617373 | G | C | 1 | a0001c0001t0001g0195 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.311+4861G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151617373 | |||||||
chr1:151617535 | C | T | 1 | a0001c0004t0015g0355 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.311+5023C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151617535 | |||||||
chr1:151617589 | G | T | 3 | a0001c0001t0002g0327 a0001c0001t0009g0328 a0001c0001t0098g0326 |
3 | HG02129.hp1 NA18950.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.311+5077G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151617589 | |||||||
chr1:151617730 | A | G | 1 | a0001c0001t0007g0185 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.311+5218A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151617730 | |||||||
chr1:151617803 | T | C | 2 | a0001c0001t0047g0358 a0001c0001t0104g0357 |
2 | HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.311+5291T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151617803 | |||||||
chr1:151617834 | G | A | 7 | a0001c0001t0028g0023 a0001c0001t0028g0024 a0001c0001t0028g0025 others(4): Show |
7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.311+5322G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151617834 | |||||||
chr1:151617878 | G | GT | 9 | a0001c0001t0017g0145 a0001c0001t0017g0152 a0001c0001t0029g0086 others(6): Show |
9 | HG02083.hp2 HG02165.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.311+5389dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151617878 | ||||||
chr1:151617878 | GT | G | 32 | a0001c0001t0002g0005 a0001c0001t0002g0148 a0001c0001t0002g0178 others(29): Show |
33 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.311+5389delT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151617878 | ||||||
chr1:151617878 | GTT | G | 129 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0215 others(126): Show |
130 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.311+5388_311+5389d others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151617878 | ||||||
chr1:151617878 | GTTT | G | 99 | a0001c0001t0001g0002 a0001c0001t0001g0189 a0001c0001t0001g0190 others(96): Show |
102 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.311+5387_311+5389d others(5): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151617878 | ||||||
chr1:151617878 | GTTTT | G | 13 | a0001c0001t0001g0224 a0001c0001t0016g0105 a0001c0001t0016g0106 others(10): Show |
13 | HG01515.hp1 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.311+5386_311+5389d others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151617878 | ||||||
chr1:151617880 | T | A | 1 | a0001c0001t0034g0115 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.311+5368T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151617880 | |||||||
chr1:151617887 | T | G | 9 | a0001c0001t0015g0352 a0001c0001t0015g0353 a0001c0001t0015g0354 others(6): Show |
10 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.311+5375T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151617887 | |||||||
chr1:151617889 | T | G | 9 | a0001c0001t0012g0004 a0001c0001t0012g0283 a0001c0001t0012g0284 others(6): Show |
9 | HG02486.hp2 HG02723.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.311+5377T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151617889 | |||||||
chr1:151617967 | C | G | 5 | a0001c0001t0015g0352 a0001c0001t0015g0353 a0001c0001t0015g0354 others(2): Show |
5 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.311+5455C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151617967 | |||||||
chr1:151618131 | G | T | 4 | a0001c0001t0046g0017 a0001c0001t0046g0019 a0001c0001t0102g0016 others(1): Show |
4 | HG02145.hp1 HG02280.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.311+5619G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151618131 | |||||||
chr1:151618177 | A | G | 7 | a0001c0001t0019g0325 a0001c0001t0019g0330 a0001c0001t0019g0332 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.311+5665A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151618177 | |||||||
chr1:151618258 | A | G | 16 | a0001c0001t0012g0004 a0001c0001t0012g0283 a0001c0001t0012g0284 others(13): Show |
16 | HG02109.hp2 HG02145.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.311+5746A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151618258 | |||||||
chr1:151618473 | CT | C | 5 | a0001c0001t0015g0352 a0001c0001t0015g0353 a0001c0001t0015g0354 others(2): Show |
5 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.311+5962delT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151618473 | |||||||
chr1:151618564 | A | G | 1 | a0001c0001t0004g0272 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.311+6052A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151618564 | |||||||
chr1:151618588 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.311+6076G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151618588 | |||||||
chr1:151618885 | C | T | 1 | a0001c0001t0012g0329 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.311+6373C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151618885 | |||||||
chr1:151618935 | G | C | 7 | a0001c0001t0028g0023 a0001c0001t0028g0024 a0001c0001t0028g0025 others(4): Show |
7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.311+6423G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151618935 | |||||||
chr1:151619011 | C | CA | 7 | a0001c0001t0003g0117 a0001c0001t0006g0119 a0001c0001t0023g0118 others(4): Show |
7 | HG00609.hp2 HG02129.hp2 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.311+6511dupA | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151619011 | ||||||
chr1:151619011 | CA | C | 107 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(104): Show |
110 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.311+6511delA | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151619011 | ||||||
chr1:151619158 | T | A | 11 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(8): Show |
11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.311+6646T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151619158 | |||||||
chr1:151619295 | C | G | 2 | a0001c0001t0002g0323 a0001c0001t0002g0324 |
2 | NA18612.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.311+6783C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151619295 | |||||||
chr1:151619308 | T | C | 7 | a0001c0001t0028g0023 a0001c0001t0028g0024 a0001c0001t0028g0025 others(4): Show |
7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.311+6796T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151619308 | |||||||
chr1:151619753 | T | G | 1 | a0001c0001t0055g0350 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.311+7241T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151619753 | |||||||
chr1:151620212 | G | A | 1 | a0001c0001t0005g0028 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.311+7700G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151620212 | |||||||
chr1:151620231 | A | G | 1 | a0001c0001t0034g0115 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.311+7719A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151620231 | |||||||
chr1:151620422 | T | C | 1 | a0001c0003t0044g0099 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.311+7910T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151620422 | |||||||
chr1:151620425 | T | C | 1 | a0001c0001t0065g0012 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.311+7913T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151620425 | |||||||
chr1:151620512 | G | GT | 111 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(108): Show |
114 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.311+8001dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151620512 | ||||||
chr1:151620694 | C | CT | 102 | a0001c0001t0001g0280 a0001c0001t0001g0339 a0001c0001t0002g0148 others(99): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.311+8195dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151620694 | ||||||
chr1:151620694 | C | CTT | 111 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(108): Show |
114 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.311+8194_311+8195d others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151620694 | ||||||
chr1:151620758 | C | T | 5 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(2): Show |
5 | HG00280.hp2 HG01081.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.311+8246C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151620758 | |||||||
chr1:151620804 | C | T | 11 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(8): Show |
11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.311+8292C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151620804 | |||||||
chr1:151620983 | C | T | 20 | a0001c0001t0004g0272 a0001c0001t0010g0256 a0001c0001t0010g0257 others(17): Show |
20 | HG00438.hp1 HG00639.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.311+8471C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151620983 | |||||||
chr1:151621039 | G | A | 1 | a0001c0001t0002g0287 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.311+8527G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151621039 | |||||||
chr1:151621068 | A | G | 1 | a0001c0001t0101g0094 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.311+8556A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151621068 | |||||||
chr1:151621196 | A | C | 1 | a0001c0001t0065g0012 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.311+8684A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151621196 | |||||||
chr1:151621737 | T | G | 1 | a0001c0001t0065g0012 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.311+9225T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151621737 | |||||||
chr1:151621807 | G | C | 7 | a0001c0001t0028g0023 a0001c0001t0028g0024 a0001c0001t0028g0025 others(4): Show |
7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.311+9295G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151621807 | |||||||
chr1:151622052 | C | A | 2 | a0001c0001t0003g0121 a0001c0001t0003g0122 |
2 | NA19000.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.311+9540C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151622052 | |||||||
chr1:151622078 | A | G | 1 | a0001c0001t0043g0255 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.311+9566A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151622078 | |||||||
chr1:151622335 | A | T | 3 | a0001c0001t0002g0315 a0001c0001t0002g0316 a0001c0001t0042g0314 |
3 | HG02055.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.311+9823A>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151622335 | |||||||
chr1:151622499 | T | G | 2 | a0001c0001t0001g0195 a0001c0001t0001g0203 |
2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.311+9987T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151622499 | |||||||
chr1:151622589 | A | G | 1 | a0001c0001t0006g0183 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.311+10077A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151622589 | |||||||
chr1:151622744 | A | G | 7 | a0001c0001t0081g0090 a0001c0001t0082g0091 a0001c0001t0094g0093 others(4): Show |
7 | HG02258.hp1 HG02622.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.311+10232A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151622744 | |||||||
chr1:151622859 | G | A | 1 | a0001c0001t0019g0330 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.311+10347G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151622859 | |||||||
chr1:151623153 | T | A | 335 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(332): Show |
341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.311+10641T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151623153 | |||||||
chr1:151623155 | T | A | 12 | a0001c0001t0008g0191 a0001c0001t0028g0023 a0001c0001t0028g0024 others(9): Show |
12 | HG02004.hp2 HG02129.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.311+10643T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151623155 | |||||||
chr1:151623181 | G | A | 5 | a0001c0001t0003g0121 a0001c0001t0003g0122 a0001c0001t0003g0123 others(2): Show |
5 | NA18971.hp2 NA19000.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.311+10669G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151623181 | |||||||
chr1:151623224 | T | C | 3 | a0001c0001t0002g0315 a0001c0001t0002g0316 a0001c0001t0042g0314 |
3 | HG02055.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.311+10712T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151623224 | |||||||
chr1:151623265 | C | T | 11 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(8): Show |
11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.311+10753C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151623265 | |||||||
chr1:151623292 | C | T | 1 | a0001c0001t0049g0082 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.311+10780C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151623292 | |||||||
chr1:151623308 | T | A | 1 | a0001c0001t0075g0281 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.311+10796T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151623308 | |||||||
chr1:151623319 | T | G | 16 | a0001c0001t0012g0004 a0001c0001t0012g0283 a0001c0001t0012g0284 others(13): Show |
16 | HG02109.hp2 HG02145.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.311+10807T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151623319 | |||||||
chr1:151623430 | G | A | 20 | a0001c0001t0004g0272 a0001c0001t0010g0256 a0001c0001t0010g0257 others(17): Show |
20 | HG00438.hp1 HG00639.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.311+10918G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151623430 | |||||||
chr1:151623691 | C | T | 1 | a0001c0001t0002g0313 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.311+11179C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151623691 | |||||||
chr1:151623692 | G | A | 1 | a0001c0001t0005g0029 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.311+11180G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151623692 | |||||||
chr1:151623725 | C | T | 1 | a0001c0001t0005g0081 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.311+11213C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151623725 | |||||||
chr1:151623948 | T | C | 1 | a0001c0001t0002g0288 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.311+11436T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151623948 | |||||||
chr1:151623953 | T | A | 2 | a0001c0001t0046g0017 a0001c0001t0118g0018 |
2 | HG02145.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.311+11441T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151623953 | |||||||
chr1:151623954 | A | T | 270 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(267): Show |
276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.311+11442A>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151623954 | |||||||
chr1:151624219 | G | C | 4 | a0001c0001t0001g0280 a0001c0001t0001g0339 a0001c0001t0062g0198 others(1): Show |
4 | HG02886.hp1 HG02970.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.311+11707G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151624219 | |||||||
chr1:151624231 | G | A | 1 | a0001c0001t0086g0289 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.311+11719G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151624231 | |||||||
chr1:151624245 | A | C | 9 | a0001c0001t0015g0352 a0001c0001t0015g0353 a0001c0001t0015g0354 others(6): Show |
10 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.311+11733A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151624245 | |||||||
chr1:151624409 | T | TTA | 41 | a0001c0001t0001g0205 a0001c0001t0001g0210 a0001c0001t0001g0211 others(38): Show |
41 | HG00438.hp1 HG00639.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.311+11919_311+1192 others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151624409 | ||||||
chr1:151624409 | T | TTATA | 44 | a0001c0001t0001g0280 a0001c0001t0001g0339 a0001c0001t0002g0005 others(41): Show |
47 | HG00423.hp2 HG00597.hp2 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.311+11917_311+1192 others(8): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151624409 | ||||||
chr1:151624409 | T | TTATATA | 3 | a0001c0001t0002g0293 a0001c0001t0002g0323 a0001c0001t0010g0256 |
3 | HG02056.hp1 NA18612.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.311+11915_311+1192 others(10): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151624409 | ||||||
chr1:151624409 | T | TTATATAT others(1): Show |
3 | a0001c0001t0002g0291 a0001c0001t0018g0290 a0001c0001t0026g0292 |
3 | HG02132.hp2 NA18943.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.311+11913_311+1192 others(12): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151624409 | ||||||
chr1:151624409 | T | TTATATAT others(3): Show |
4 | a0001c0001t0015g0352 a0001c0001t0015g0353 a0001c0001t0015g0354 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.311+11911_311+1192 others(14): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151624409 | ||||||
chr1:151624409 | T | TTATATAT others(5): Show |
2 | a0001c0001t0043g0336 a0001c0001t0054g0351 |
2 | HG02615.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.311+11909_311+1192 others(16): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151624409 | ||||||
chr1:151624409 | TTA | T | 77 | a0001c0001t0002g0148 a0001c0001t0002g0178 a0001c0001t0002g0179 others(74): Show |
78 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.311+11919_311+1192 others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151624409 | ||||||
chr1:151624431 | A | G | 3 | a0001c0001t0006g0102 a0001c0001t0025g0182 a0001c0001t0052g0359 |
3 | HG02723.hp2 HG02738.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.311+11919A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151624431 | |||||||
chr1:151624433 | G | A | 6 | a0001c0001t0003g0121 a0001c0001t0006g0102 a0001c0001t0010g0337 others(3): Show |
6 | HG02723.hp2 HG02738.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.311+11921G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151624433 | |||||||
chr1:151624434 | TA | T | 3 | a0001c0001t0006g0102 a0001c0001t0025g0182 a0001c0001t0052g0359 |
3 | HG02723.hp2 HG02738.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.311+11923delA | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151624434 | |||||||
chr1:151624435 | A | AT | 12 | a0001c0001t0002g0315 a0001c0001t0008g0191 a0001c0001t0008g0193 others(9): Show |
12 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.311+11937dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151624435 | ||||||
chr1:151624435 | A | ATATATAT others(6): Show |
1 | a0001c0001t0010g0337 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.311+11924_311+1192 others(17): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151624435 | ||||||
chr1:151624512 | A | G | 1 | a0001c0001t0026g0292 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.311+12000A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151624512 | |||||||
chr1:151624618 | G | A | 77 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(74): Show |
79 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.311+12106G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151624618 | |||||||
chr1:151624683 | C | T | 1 | a0001c0001t0056g0181 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.311+12171C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151624683 | |||||||
chr1:151624744 | T | C | 1 | a0001c0001t0018g0290 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.311+12232T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151624744 | |||||||
chr1:151625003 | T | C | 1 | a0001c0001t0102g0016 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.311+12491T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151625003 | |||||||
chr1:151625169 | G | A | 1 | a0001c0001t0052g0359 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.311+12657G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151625169 | |||||||
chr1:151625184 | G | C | 89 | a0001c0001t0002g0148 a0001c0001t0003g0117 a0001c0001t0003g0120 others(86): Show |
90 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.311+12672G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151625184 | |||||||
chr1:151625185 | T | C | 130 | a0001c0001t0002g0005 a0001c0001t0002g0148 a0001c0001t0002g0178 others(127): Show |
133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.311+12673T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151625185 | |||||||
chr1:151625220 | G | C | 7 | a0001c0001t0028g0023 a0001c0001t0028g0024 a0001c0001t0028g0025 others(4): Show |
7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.311+12708G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151625220 | |||||||
chr1:151625276 | G | A | 1 | a0001c0001t0046g0019 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.311+12764G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151625276 | |||||||
chr1:151625277 | C | G | 1 | a0001c0001t0046g0019 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.311+12765C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151625277 | |||||||
chr1:151625277 | C | T | 1 | a0001c0001t0065g0012 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.311+12765C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151625277 | |||||||
chr1:151625278 | G | T | 1 | a0001c0001t0046g0019 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.311+12766G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151625278 | |||||||
chr1:151625279 | G | A | 1 | a0001c0001t0046g0019 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.311+12767G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151625279 | |||||||
chr1:151625287 | C | G | 146 | a0001c0001t0002g0005 a0001c0001t0002g0148 a0001c0001t0002g0178 others(143): Show |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.311+12775C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151625287 | |||||||
chr1:151625463 | G | A | 2 | a0001c0003t0044g0099 a0001c0003t0044g0100 |
2 | HG02895.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.311+12951G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151625463 | |||||||
chr1:151625515 | A | G | 20 | a0001c0001t0004g0272 a0001c0001t0010g0256 a0001c0001t0010g0257 others(17): Show |
20 | HG00438.hp1 HG00639.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.311+13003A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151625515 | |||||||
chr1:151625708 | C | T | 1 | a0001c0001t0097g0197 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.312-13180C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151625708 | |||||||
chr1:151625784 | C | CA | 34 | a0001c0001t0001g0215 a0001c0001t0001g0217 a0001c0001t0001g0219 others(31): Show |
34 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.312-13087dupA | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151625784 | ||||||
chr1:151625846 | G | GC | 3 | a0001c0001t0001g0205 a0001c0001t0004g0204 a0001c0001t0004g0206 |
3 | HG00673.hp1 NA18961.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.312-13041dupC | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151625846 | ||||||
chr1:151626019 | C | T | 2 | a0001c0001t0047g0358 a0001c0001t0104g0357 |
2 | HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.312-12869C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151626019 | |||||||
chr1:151626204 | G | C | 1 | a0001c0001t0052g0359 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.312-12684G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151626204 | |||||||
chr1:151626265 | CT | C | 21 | a0001c0001t0004g0272 a0001c0001t0010g0256 a0001c0001t0010g0257 others(18): Show |
21 | HG00438.hp1 HG00639.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.312-12611delT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151626265 | ||||||
chr1:151626277 | TG | T | 8 | a0001c0001t0016g0106 a0001c0001t0016g0108 a0001c0001t0016g0110 others(5): Show |
8 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.312-12610delG | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151626277 | |||||||
chr1:151626278 | G | T | 4 | a0001c0001t0016g0105 a0001c0001t0052g0359 a0001c0001t0097g0197 others(1): Show |
4 | HG02647.hp1 HG02723.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.312-12610G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151626278 | |||||||
chr1:151626283 | T | C | 9 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(6): Show |
9 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.312-12605T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151626283 | |||||||
chr1:151626479 | T | G | 1 | a0001c0001t0018g0290 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.312-12409T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151626479 | |||||||
chr1:151626607 | C | T | 77 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(74): Show |
79 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.312-12281C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151626607 | |||||||
chr1:151626680 | C | T | 11 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(8): Show |
11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.312-12208C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151626680 | |||||||
chr1:151626699 | C | CTAAA | 4 | a0001c0001t0095g0092 a0001c0001t0105g0014 a0001c0003t0044g0099 others(1): Show |
4 | HG02572.hp1 HG02895.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.312-12163_312-1216 others(8): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151626699 | ||||||
chr1:151626699 | C | CTAAATAA others(5): Show |
9 | a0001c0001t0015g0352 a0001c0001t0015g0353 a0001c0001t0015g0354 others(6): Show |
10 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.312-12171_312-1216 others(16): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151626699 | ||||||
chr1:151626699 | CTAAATAA others(1): Show |
C | 77 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(74): Show |
79 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.312-12167_312-1216 others(12): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151626699 | ||||||
chr1:151626791 | G | T | 89 | a0001c0001t0002g0148 a0001c0001t0003g0117 a0001c0001t0003g0120 others(86): Show |
90 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.312-12097G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151626791 | |||||||
chr1:151627087 | C | T | 1 | a0001c0001t0004g0254 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.312-11801C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151627087 | |||||||
chr1:151627396 | G | T | 1 | a0001c0001t0016g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.312-11492G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151627396 | |||||||
chr1:151627643 | G | A | 2 | a0001c0001t0062g0198 a0001c0001t0063g0199 |
2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.312-11245G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151627643 | |||||||
chr1:151627719 | C | T | 2 | a0001c0003t0044g0099 a0001c0003t0044g0100 |
2 | HG02895.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.312-11169C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151627719 | |||||||
chr1:151627741 | TGTTCTAT others(3): Show |
T | 89 | a0001c0001t0002g0148 a0001c0001t0003g0117 a0001c0001t0003g0120 others(86): Show |
90 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.312-11138_312-1112 others(14): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151627741 | ||||||
chr1:151627890 | C | A | 1 | a0001c0001t0018g0290 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.312-10998C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151627890 | |||||||
chr1:151627890 | C | T | 1 | a0001c0001t0118g0018 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.312-10998C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151627890 | |||||||
chr1:151627965 | G | A | 270 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(267): Show |
276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.312-10923G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151627965 | |||||||
chr1:151628006 | G | GT | 12 | a0001c0001t0009g0184 a0001c0001t0011g0080 a0001c0001t0026g0299 others(9): Show |
12 | HG00280.hp1 HG00544.hp2 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.312-10863dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151628006 | ||||||
chr1:151628006 | GT | G | 103 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(100): Show |
106 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.312-10863delT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151628006 | ||||||
chr1:151628151 | C | T | 2 | a0001c0003t0044g0099 a0001c0003t0044g0100 |
2 | HG02895.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.312-10737C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151628151 | |||||||
chr1:151628155 | C | T | 1 | a0001c0001t0013g0276 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.312-10733C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151628155 | |||||||
chr1:151628264 | A | G | 1 | a0001c0001t0097g0197 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.312-10624A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151628264 | |||||||
chr1:151628302 | C | T | 7 | a0001c0001t0028g0023 a0001c0001t0028g0024 a0001c0001t0028g0025 others(4): Show |
7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.312-10586C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151628302 | |||||||
chr1:151628347 | A | G | 4 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0271 others(1): Show |
4 | HG00280.hp2 HG01081.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.312-10541A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151628347 | |||||||
chr1:151628578 | T | C | 1 | a0001c0001t0010g0257 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.312-10310T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151628578 | |||||||
chr1:151628579 | A | G | 2 | a0001c0001t0002g0298 a0001c0001t0089g0312 |
2 | HG00423.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.312-10309A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151628579 | |||||||
chr1:151628596 | C | T | 9 | a0001c0001t0012g0004 a0001c0001t0012g0283 a0001c0001t0012g0284 others(6): Show |
9 | HG02486.hp2 HG02723.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.312-10292C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151628596 | |||||||
chr1:151628655 | T | G | 1 | a0001c0001t0052g0359 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.312-10233T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151628655 | |||||||
chr1:151628669 | G | T | 1 | a0001c0001t0105g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.312-10219G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151628669 | |||||||
chr1:151628751 | A | G | 1 | a0001c0001t0105g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.312-10137A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151628751 | |||||||
chr1:151628925 | GTT | G | 3 | a0001c0001t0019g0325 a0001c0001t0019g0332 a0001c0001t0019g0333 |
3 | HG02615.hp2 HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.312-9960_312-9959d others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151628925 | ||||||
chr1:151629083 | CT | C | 9 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(6): Show |
9 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.312-9801delT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151629083 | ||||||
chr1:151629203 | T | C | 1 | a0001c0001t0097g0197 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.312-9685T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151629203 | |||||||
chr1:151629211 | T | TTGTACTA others(2727): Show |
1 | a0001c0001t0016g0105 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.312-9664_312-9663i others(2736): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151629211 | ||||||
chr1:151629211 | T | TTGTACTA others(2726): Show |
2 | a0001c0001t0016g0106 a0001c0001t0066g0112 |
2 | HG02109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.312-9664_312-9663i others(2735): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151629211 | ||||||
chr1:151629211 | T | TTGTACTA others(2727): Show |
3 | a0001c0001t0016g0108 a0001c0001t0016g0113 a0001c0001t0084g0107 |
3 | HG02258.hp2 HG02280.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.312-9664_312-9663i others(2736): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151629211 | ||||||
chr1:151629211 | T | TTGTACTA others(2726): Show |
2 | a0001c0001t0016g0110 a0001c0001t0038g0109 |
2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.312-9664_312-9663i others(2735): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151629211 | ||||||
chr1:151629211 | T | TTGTACTA others(2727): Show |
1 | a0001c0001t0038g0111 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.312-9664_312-9663i others(2736): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151629211 | ||||||
chr1:151629256 | A | G | 146 | a0001c0001t0002g0005 a0001c0001t0002g0148 a0001c0001t0002g0178 others(143): Show |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.312-9632A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151629256 | |||||||
chr1:151629385 | C | T | 1 | a0001c0001t0007g0176 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.312-9503C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151629385 | |||||||
chr1:151629402 | C | T | 1 | a0001c0001t0004g0253 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.312-9486C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151629402 | |||||||
chr1:151629451 | G | A | 7 | a0001c0001t0028g0023 a0001c0001t0028g0024 a0001c0001t0028g0025 others(4): Show |
7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.312-9437G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151629451 | |||||||
chr1:151629453 | A | G | 77 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(74): Show |
79 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.312-9435A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151629453 | |||||||
chr1:151629458 | T | TAC | 23 | a0001c0001t0002g0294 a0001c0001t0004g0272 a0001c0001t0007g0340 others(20): Show |
23 | HG00438.hp1 HG00639.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.312-9429_312-9428d others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151629458 | ||||||
chr1:151629478 | C | CAT | 19 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(16): Show |
19 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.312-9410_312-9409i others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151629478 | |||||||
chr1:151629478 | C | CGT | 258 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(255): Show |
264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.312-9409_312-9408d others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151629478 | ||||||
chr1:151629496 | C | T | 111 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(108): Show |
114 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.312-9392C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151629496 | |||||||
chr1:151629509 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.312-9379A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151629509 | |||||||
chr1:151629539 | A | G | 89 | a0001c0001t0002g0148 a0001c0001t0003g0117 a0001c0001t0003g0120 others(86): Show |
90 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.312-9349A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151629539 | |||||||
chr1:151629585 | A | G | 1 | a0001c0001t0019g0330 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.312-9303A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151629585 | |||||||
chr1:151629586 | A | AT | 19 | a0001c0001t0001g0189 a0001c0001t0001g0214 a0001c0001t0005g0081 others(16): Show |
19 | HG01192.hp2 HG02109.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.312-9287dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151629586 | ||||||
chr1:151629686 | C | CGATTCTC others(7): Show |
1 | a0001c0001t0115g0078 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.312-9201_312-9188d others(16): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151629686 | ||||||
chr1:151629711 | G | A | 1 | a0001c0001t0002g0295 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.312-9177G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151629711 | |||||||
chr1:151629897 | A | T | 106 | a0001c0001t0002g0148 a0001c0001t0003g0117 a0001c0001t0003g0120 others(103): Show |
107 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.312-8991A>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151629897 | |||||||
chr1:151629899 | A | T | 158 | a0001c0001t0002g0005 a0001c0001t0002g0148 a0001c0001t0002g0178 others(155): Show |
161 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.312-8989A>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151629899 | |||||||
chr1:151630030 | G | A | 1 | a0001c0001t0017g0146 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.312-8858G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151630030 | |||||||
chr1:151630110 | C | CA | 113 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(110): Show |
116 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.312-8765dupA | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151630110 | ||||||
chr1:151630171 | A | G | 283 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(280): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.312-8717A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151630171 | |||||||
chr1:151630215 | G | A | 1 | a0001c0001t0120g0037 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.312-8673G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151630215 | |||||||
chr1:151630276 | A | T | 11 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(8): Show |
11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.312-8612A>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151630276 | |||||||
chr1:151630298 | T | G | 9 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(6): Show |
9 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.312-8590T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151630298 | |||||||
chr1:151630371 | A | G | 1 | a0001c0001t0102g0016 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.312-8517A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151630371 | |||||||
chr1:151630711 | A | G | 283 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(280): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.312-8177A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151630711 | |||||||
chr1:151630755 | C | T | 1 | a0001c0001t0105g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.312-8133C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151630755 | |||||||
chr1:151630761 | C | T | 77 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(74): Show |
79 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.312-8127C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151630761 | |||||||
chr1:151630784 | A | G | 9 | a0001c0001t0015g0352 a0001c0001t0015g0353 a0001c0001t0015g0354 others(6): Show |
10 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.312-8104A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151630784 | |||||||
chr1:151630860 | C | T | 56 | a0001c0001t0003g0117 a0001c0001t0003g0120 a0001c0001t0003g0121 others(53): Show |
56 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.312-8028C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151630860 | |||||||
chr1:151630896 | G | A | 1 | a0001c0001t0004g0207 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.312-7992G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151630896 | |||||||
chr1:151630957 | G | A | 9 | a0001c0001t0001g0011 a0001c0001t0001g0196 a0001c0001t0001g0215 others(6): Show |
9 | HG00323.hp1 HG00735.hp1 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.312-7931G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151630957 | |||||||
chr1:151631027 | G | A | 1 | a0001c0001t0010g0256 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.312-7861G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151631027 | |||||||
chr1:151631136 | A | G | 10 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(7): Show |
10 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.312-7752A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151631136 | |||||||
chr1:151631197 | TTCTAGTA | T | 5 | a0002c0002t0001g0003 a0002c0002t0001g0202 a0002c0002t0001g0226 others(2): Show |
6 | NA18941.hp1 NA18947.hp2 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.312-7690_312-7684d others(9): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151631197 | |||||||
chr1:151631284 | T | A | 1 | a0001c0001t0007g0164 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.312-7604T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151631284 | |||||||
chr1:151631343 | G | T | 20 | a0001c0001t0004g0272 a0001c0001t0010g0256 a0001c0001t0010g0257 others(17): Show |
20 | HG00438.hp1 HG00639.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.312-7545G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151631343 | |||||||
chr1:151631461 | A | G | 11 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(8): Show |
11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.312-7427A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151631461 | |||||||
chr1:151631512 | G | T | 1 | a0001c0001t0117g0089 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.312-7376G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151631512 | |||||||
chr1:151631705 | G | T | 2 | a0001c0001t0007g0162 a0001c0001t0060g0163 |
2 | HG01168.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.312-7183G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151631705 | |||||||
chr1:151632024 | A | G | 77 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(74): Show |
79 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.312-6864A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151632024 | |||||||
chr1:151632154 | C | T | 11 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(8): Show |
11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.312-6734C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151632154 | |||||||
chr1:151632322 | T | TTC | 11 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(8): Show |
11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.312-6566_312-6565i others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151632322 | |||||||
chr1:151632411 | T | C | 269 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(266): Show |
275 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.312-6477T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151632411 | |||||||
chr1:151632502 | A | G | 1 | a0001c0001t0085g0310 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.312-6386A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151632502 | |||||||
chr1:151632788 | C | CTTTTCAC others(3): Show |
1 | a0001c0001t0045g0027 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.312-6099_312-6090d others(12): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151632788 | ||||||
chr1:151632810 | C | A | 1 | a0001c0001t0019g0330 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.312-6078C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151632810 | |||||||
chr1:151632833 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.312-6055G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151632833 | |||||||
chr1:151633052 | C | T | 1 | a0001c0001t0097g0197 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.312-5836C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151633052 | |||||||
chr1:151633083 | A | G | 7 | a0001c0001t0028g0023 a0001c0001t0028g0024 a0001c0001t0028g0025 others(4): Show |
7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.312-5805A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151633083 | |||||||
chr1:151633086 | A | G | 1 | a0001c0001t0042g0309 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.312-5802A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151633086 | |||||||
chr1:151633161 | C | T | 1 | a0001c0001t0053g0349 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.312-5727C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151633161 | |||||||
chr1:151633164 | G | T | 7 | a0001c0001t0028g0023 a0001c0001t0028g0024 a0001c0001t0028g0025 others(4): Show |
7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.312-5724G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151633164 | |||||||
chr1:151633215 | A | G | 2 | a0001c0001t0062g0198 a0001c0001t0063g0199 |
2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.312-5673A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151633215 | |||||||
chr1:151633372 | C | T | 1 | a0001c0001t0002g0295 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.312-5516C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151633372 | |||||||
chr1:151633399 | G | A | 3 | a0001c0001t0002g0148 a0001c0001t0007g0149 a0001c0001t0007g0150 |
3 | HG01255.hp2 HG01257.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.312-5489G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151633399 | |||||||
chr1:151633557 | CCA | C | 130 | a0001c0001t0002g0005 a0001c0001t0002g0148 a0001c0001t0002g0178 others(127): Show |
133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.312-5328_312-5327d others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151633557 | ||||||
chr1:151633644 | CA | C | 17 | a0001c0001t0004g0272 a0001c0001t0010g0256 a0001c0001t0010g0257 others(14): Show |
17 | HG00438.hp1 HG00639.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.312-5242delA | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151633644 | ||||||
chr1:151633725 | C | T | 1 | a0001c0001t0052g0359 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.312-5163C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151633725 | |||||||
chr1:151633901 | T | A | 283 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(280): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.312-4987T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151633901 | |||||||
chr1:151633929 | G | A | 282 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(279): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.312-4959G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151633929 | |||||||
chr1:151633966 | A | G | 270 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(267): Show |
276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.312-4922A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151633966 | |||||||
chr1:151633972 | G | GT | 8 | a0001c0001t0005g0077 a0001c0001t0006g0101 a0001c0001t0006g0102 others(5): Show |
8 | HG01934.hp1 HG02080.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.312-4904dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151633972 | ||||||
chr1:151633974 | T | G | 1 | a0001c0006t0076g0334 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.312-4914T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151633974 | |||||||
chr1:151634092 | A | G | 1 | a0001c0001t0012g0284 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.312-4796A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151634092 | |||||||
chr1:151634435 | A | G | 270 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(267): Show |
276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.312-4453A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151634435 | |||||||
chr1:151634601 | T | C | 1 | a0001c0001t0006g0103 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.312-4287T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151634601 | |||||||
chr1:151634670 | G | C | 9 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(6): Show |
9 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.312-4218G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151634670 | |||||||
chr1:151634994 | C | T | 2 | a0001c0001t0001g0195 a0001c0001t0001g0203 |
2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.312-3894C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151634994 | |||||||
chr1:151635292 | C | A | 1 | a0001c0001t0009g0165 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.312-3596C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151635292 | |||||||
chr1:151635576 | C | G | 1 | a0001c0001t0065g0012 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.312-3312C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151635576 | |||||||
chr1:151635620 | A | G | 111 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(108): Show |
114 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.312-3268A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151635620 | |||||||
chr1:151635721 | A | G | 2 | a0001c0001t0018g0321 a0001c0001t0018g0322 |
2 | HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.312-3167A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151635721 | |||||||
chr1:151635733 | G | C | 1 | a0001c0001t0010g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.312-3155G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151635733 | |||||||
chr1:151635954 | C | T | 1 | a0001c0001t0034g0115 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.312-2934C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151635954 | |||||||
chr1:151635966 | A | C | 1 | a0001c0001t0065g0012 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.312-2922A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151635966 | |||||||
chr1:151636083 | G | A | 1 | a0001c0001t0064g0147 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.312-2805G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151636083 | |||||||
chr1:151636115 | C | A | 2 | a0001c0001t0006g0114 a0001c0001t0067g0128 |
2 | HG01884.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.312-2773C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151636115 | |||||||
chr1:151636247 | G | A | 9 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(6): Show |
9 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.312-2641G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151636247 | |||||||
chr1:151636342 | C | T | 6 | a0001c0001t0007g0317 a0001c0001t0007g0318 a0001c0001t0009g0320 others(3): Show |
6 | HG03195.hp1 HG03209.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.312-2546C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151636342 | |||||||
chr1:151636345 | AGGCTGGA others(7): Show |
A | 6 | a0001c0001t0017g0126 a0001c0001t0017g0146 a0001c0001t0017g0152 others(3): Show |
6 | NA18939.hp1 NA18944.hp2 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.312-2539_312-2526d others(16): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151636345 | ||||||
chr1:151636546 | T | C | 279 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.312-2342T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151636546 | |||||||
chr1:151636636 | T | G | 1 | a0001c0001t0106g0021 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.312-2252T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151636636 | |||||||
chr1:151636666 | T | TA | 25 | a0001c0001t0005g0038 a0001c0001t0005g0077 a0001c0001t0014g0040 others(22): Show |
25 | HG02071.hp2 HG02074.hp1 HG02080.hp1 others(22): Show |
intron_variant | MODIFIER | c.312-2198dupA | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151636666 | ||||||
chr1:151636666 | T | TAA | 15 | a0001c0001t0002g0296 a0001c0001t0015g0352 a0001c0001t0015g0353 others(12): Show |
16 | HG01516.hp2 HG01884.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.312-2199_312-2198d others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151636666 | ||||||
chr1:151636666 | TA | T | 223 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0189 others(220): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.312-2198delA | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151636666 | ||||||
chr1:151636716 | CCTAGGGA others(6): Show |
C | 9 | a0001c0001t0028g0023 a0001c0001t0028g0024 a0001c0001t0028g0025 others(6): Show |
9 | HG02895.hp1 HG02895.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.312-2171_312-2159d others(15): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151636716 | |||||||
chr1:151637149 | TC | T | 77 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(74): Show |
79 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.312-1738delC | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151637149 | |||||||
chr1:151637153 | G | GT | 6 | a0001c0001t0019g0325 a0001c0001t0019g0330 a0001c0001t0019g0332 others(3): Show |
6 | HG02109.hp2 HG02145.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.312-1727dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151637153 | ||||||
chr1:151637153 | G | GTTT | 6 | a0001c0001t0012g0283 a0001c0001t0012g0284 a0001c0001t0012g0285 others(3): Show |
6 | HG02486.hp2 HG02723.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.312-1729_312-1727d others(5): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151637153 | ||||||
chr1:151637160 | TTG | T | 79 | a0001c0001t0002g0005 a0001c0001t0002g0178 a0001c0001t0002g0179 others(76): Show |
82 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.312-1726_312-1725d others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151637160 | ||||||
chr1:151637161 | TG | T | 49 | a0001c0001t0002g0148 a0001c0001t0002g0287 a0001c0001t0002g0288 others(46): Show |
49 | HG00280.hp1 HG00423.hp2 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.312-1726delG | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151637161 | |||||||
chr1:151637162 | G | T | 22 | a0001c0001t0001g0221 a0001c0001t0002g0293 a0001c0001t0008g0201 others(19): Show |
22 | HG00735.hp1 HG02056.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.312-1726G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151637162 | |||||||
chr1:151637163 | T | G | 6 | a0001c0001t0001g0221 a0001c0001t0008g0104 a0001c0001t0008g0201 others(3): Show |
6 | HG00735.hp1 NA18946.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.312-1725T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151637163 | |||||||
chr1:151637168 | T | G | 1 | a0001c0001t0065g0012 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.312-1720T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151637168 | |||||||
chr1:151637168 | TTG | T | 9 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0110 others(6): Show |
9 | HG02109.hp1 HG02280.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.312-1718_312-1717d others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151637168 | ||||||
chr1:151637169 | TG | T | 117 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(114): Show |
120 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.312-1718delG | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151637169 | |||||||
chr1:151637170 | G | T | 156 | a0001c0001t0001g0189 a0001c0001t0001g0221 a0001c0001t0002g0005 others(153): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.312-1718G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151637170 | |||||||
chr1:151637173 | T | G | 101 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
103 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.312-1715T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151637173 | |||||||
chr1:151637210 | G | A | 3 | a0002c0002t0001g0003 a0002c0002t0001g0202 a0002c0002t0001g0226 |
4 | NA18947.hp2 NA18954.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.312-1678G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151637210 | |||||||
chr1:151637281 | C | T | 3 | a0001c0001t0046g0017 a0001c0001t0046g0019 a0001c0001t0118g0018 |
3 | HG02145.hp1 HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.312-1607C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151637281 | |||||||
chr1:151637412 | T | C | 1 | a0001c0001t0075g0281 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.312-1476T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151637412 | |||||||
chr1:151637697 | G | A | 2 | a0001c0001t0002g0316 a0001c0001t0042g0314 |
2 | HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.312-1191G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151637697 | |||||||
chr1:151638413 | GTCTC | G | 5 | a0001c0001t0006g0183 a0001c0001t0022g0133 a0001c0001t0022g0136 others(2): Show |
5 | HG00642.hp2 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.312-473_312-470del others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151638413 | ||||||
chr1:151638494 | A | G | 1 | a0001c0001t0021g0338 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.312-394A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151638494 | |||||||
chr1:151638590 | T | C | 1 | a0001c0001t0097g0197 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.312-298T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151638590 | |||||||
chr1:151638714 | A | G | 1 | a0001c0007t0003g0142 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.312-174A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151638714 | |||||||
chr1:151639349 | TTAGA | T | 77 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(74): Show |
79 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.543+234_543+237del others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151639349 | ||||||
chr1:151639472 | G | C | 77 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(74): Show |
79 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.543+353G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151639472 | |||||||
chr1:151639478 | G | T | 1 | a0001c0001t0097g0197 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.543+359G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151639478 | |||||||
chr1:151639525 | A | T | 2 | a0001c0003t0044g0099 a0001c0003t0044g0100 |
2 | HG02895.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.543+406A>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151639525 | |||||||
chr1:151639631 | A | G | 1 | a0001c0001t0097g0197 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.543+512A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151639631 | |||||||
chr1:151639689 | C | T | 1 | a0001c0001t0020g0075 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.543+570C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151639689 | |||||||
chr1:151639898 | T | G | 1 | a0001c0001t0014g0043 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.543+779T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151639898 | |||||||
chr1:151639911 | A | G | 6 | a0001c0001t0007g0317 a0001c0001t0007g0318 a0001c0001t0009g0320 others(3): Show |
6 | HG03195.hp1 HG03209.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+792A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151639911 | |||||||
chr1:151639997 | G | A | 1 | a0001c0001t0128g0044 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.543+878G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151639997 | |||||||
chr1:151640226 | T | G | 1 | a0001c0001t0030g0045 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.543+1107T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151640226 | |||||||
chr1:151640400 | C | T | 2 | a0001c0001t0001g0205 a0001c0001t0004g0204 |
2 | HG00673.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.543+1281C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151640400 | |||||||
chr1:151640522 | G | A | 3 | a0001c0001t0002g0291 a0001c0001t0018g0290 a0001c0001t0026g0292 |
3 | HG02132.hp2 NA18943.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.543+1403G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151640522 | |||||||
chr1:151640550 | T | G | 2 | a0001c0001t0001g0229 a0001c0001t0004g0216 |
2 | HG02523.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.543+1431T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151640550 | |||||||
chr1:151640699 | C | A | 2 | a0001c0001t0062g0198 a0001c0001t0063g0199 |
2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.543+1580C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151640699 | |||||||
chr1:151640869 | C | G | 1 | a0001c0001t0043g0255 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.543+1750C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151640869 | |||||||
chr1:151641012 | A | G | 6 | a0001c0001t0008g0201 a0001c0001t0008g0247 a0001c0001t0008g0248 others(3): Show |
6 | NA18962.hp2 NA18966.hp2 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.543+1893A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151641012 | |||||||
chr1:151641013 | CATT | C | 6 | a0001c0001t0007g0317 a0001c0001t0007g0318 a0001c0001t0009g0320 others(3): Show |
6 | HG03195.hp1 HG03209.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+1895_543+1897d others(5): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151641013 | |||||||
chr1:151641016 | T | G | 1 | a0001c0001t0105g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.543+1897T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151641016 | |||||||
chr1:151641171 | A | G | 1 | a0001c0001t0002g0178 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.543+2052A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151641171 | |||||||
chr1:151641301 | C | A | 1 | a0001c0001t0004g0253 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.543+2182C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151641301 | |||||||
chr1:151641331 | T | A | 1 | a0001c0001t0004g0272 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.543+2212T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151641331 | |||||||
chr1:151641504 | T | C | 2 | a0001c0001t0007g0317 a0001c0001t0009g0320 |
2 | HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.543+2385T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151641504 | |||||||
chr1:151641555 | G | T | 7 | a0001c0001t0028g0023 a0001c0001t0028g0024 a0001c0001t0028g0025 others(4): Show |
7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.543+2436G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151641555 | |||||||
chr1:151641598 | G | GAT | 16 | a0001c0001t0006g0102 a0001c0001t0006g0103 a0001c0001t0007g0317 others(13): Show |
16 | HG00735.hp2 HG00741.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.543+2510_543+2511d others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641598 | ||||||
chr1:151641598 | G | GATAT | 21 | a0001c0001t0005g0074 a0001c0001t0006g0101 a0001c0001t0006g0114 others(18): Show |
22 | HG00099.hp1 HG01168.hp2 HG01515.hp2 others(19): Show |
intron_variant | MODIFIER | c.543+2508_543+2511d others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641598 | ||||||
chr1:151641598 | G | GATATAT | 35 | a0001c0001t0003g0117 a0001c0001t0003g0120 a0001c0001t0003g0121 others(32): Show |
35 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.543+2506_543+2511d others(8): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641598 | ||||||
chr1:151641598 | G | GATATATA others(1): Show |
25 | a0001c0001t0001g0280 a0001c0001t0003g0122 a0001c0001t0003g0129 others(22): Show |
25 | HG01074.hp2 HG02015.hp1 HG02083.hp1 others(22): Show |
intron_variant | MODIFIER | c.543+2504_543+2511d others(10): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641598 | ||||||
chr1:151641598 | G | GATATATA others(3): Show |
23 | a0001c0001t0001g0339 a0001c0001t0002g0294 a0001c0001t0005g0036 others(20): Show |
24 | HG00544.hp1 HG00597.hp1 HG01256.hp2 others(21): Show |
intron_variant | MODIFIER | c.543+2502_543+2511d others(12): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641598 | ||||||
chr1:151641598 | G | GATATATA others(5): Show |
14 | a0001c0001t0002g0316 a0001c0001t0005g0028 a0001c0001t0005g0059 others(11): Show |
14 | HG00423.hp1 HG00609.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.543+2500_543+2511d others(14): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641598 | ||||||
chr1:151641598 | G | GATATATA others(7): Show |
19 | a0001c0001t0002g0148 a0001c0001t0002g0288 a0001c0001t0002g0306 others(16): Show |
19 | HG01175.hp2 HG01255.hp2 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.543+2498_543+2511d others(16): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641598 | ||||||
chr1:151641598 | G | GATATATA others(9): Show |
19 | a0001c0001t0002g0005 a0001c0001t0002g0178 a0001c0001t0002g0179 others(16): Show |
20 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.543+2496_543+2511d others(18): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641598 | ||||||
chr1:151641598 | G | GATATATA others(11): Show |
15 | a0001c0001t0002g0287 a0001c0001t0002g0295 a0001c0001t0002g0296 others(12): Show |
15 | HG01255.hp1 HG01516.hp2 HG02040.hp1 others(12): Show |
intron_variant | MODIFIER | c.543+2494_543+2511d others(20): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641598 | ||||||
chr1:151641598 | G | GATATATA others(13): Show |
13 | a0001c0001t0002g0291 a0001c0001t0002g0293 a0001c0001t0002g0323 others(10): Show |
13 | HG00408.hp2 HG02056.hp1 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.543+2492_543+2511d others(22): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641598 | ||||||
chr1:151641598 | G | GATATATA others(15): Show |
4 | a0001c0001t0014g0043 a0001c0001t0029g0086 a0001c0001t0062g0198 others(1): Show |
4 | HG03654.hp1 NA18906.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.543+2490_543+2511d others(24): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641598 | ||||||
chr1:151641598 | G | GATATATA others(17): Show |
3 | a0001c0001t0020g0075 a0001c0001t0036g0305 a0001c0001t0100g0096 |
3 | HG03195.hp2 HG03688.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.543+2488_543+2511d others(26): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641598 | ||||||
chr1:151641598 | G | GATATATA others(19): Show |
2 | a0001c0001t0005g0013 a0001c0001t0081g0090 |
2 | HG03139.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.543+2486_543+2511d others(28): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641598 | ||||||
chr1:151641598 | G | GATATATA others(21): Show |
1 | a0001c0001t0114g0079 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.543+2484_543+2511d others(30): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641598 | ||||||
chr1:151641598 | GAT | G | 11 | a0001c0001t0005g0081 a0001c0001t0013g0258 a0001c0001t0013g0259 others(8): Show |
11 | HG02280.hp2 HG02735.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.543+2510_543+2511d others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641598 | ||||||
chr1:151641598 | GATAT | G | 28 | a0001c0001t0001g0230 a0001c0001t0004g0272 a0001c0001t0010g0261 others(25): Show |
28 | HG00438.hp1 HG00639.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.543+2508_543+2511d others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641598 | ||||||
chr1:151641598 | GATATAT | G | 3 | a0001c0001t0004g0254 a0001c0001t0008g0208 a0001c0001t0083g0231 |
3 | HG02622.hp1 NA18971.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.543+2506_543+2511d others(8): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641598 | ||||||
chr1:151641598 | GATATATA others(1): Show |
G | 78 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(75): Show |
81 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.543+2504_543+2511d others(10): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641598 | ||||||
chr1:151641598 | GATATATA others(3): Show |
G | 1 | a0001c0001t0001g0189 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.543+2502_543+2511d others(12): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641598 | ||||||
chr1:151641598 | GATATATA others(5): Show |
G | 1 | a0001c0001t0012g0284 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.543+2500_543+2511d others(14): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641598 | ||||||
chr1:151641598 | GATATATA others(7): Show |
G | 15 | a0001c0001t0012g0004 a0001c0001t0012g0283 a0001c0001t0012g0285 others(12): Show |
15 | HG02109.hp2 HG02145.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.543+2498_543+2511d others(16): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641598 | ||||||
chr1:151641631 | C | A | 3 | a0001c0001t0053g0349 a0001c0004t0015g0348 a0001c0004t0015g0355 |
3 | HG02717.hp2 HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.543+2512C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151641631 | |||||||
chr1:151641647 | A | C | 146 | a0001c0001t0002g0005 a0001c0001t0002g0148 a0001c0001t0002g0178 others(143): Show |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.543+2528A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151641647 | |||||||
chr1:151641656 | G | A | 1 | a0001c0001t0046g0019 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.543+2537G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151641656 | |||||||
chr1:151641661 | A | T | 1 | a0001c0001t0046g0019 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.543+2542A>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151641661 | |||||||
chr1:151641682 | C | A | 62 | a0001c0001t0005g0013 a0001c0001t0005g0028 a0001c0001t0005g0029 others(59): Show |
62 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.543+2563C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151641682 | |||||||
chr1:151641694 | T | G | 280 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(277): Show |
286 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.543+2575T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151641694 | |||||||
chr1:151641773 | ATATC | A | 146 | a0001c0001t0002g0005 a0001c0001t0002g0148 a0001c0001t0002g0178 others(143): Show |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.543+2656_543+2659d others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641773 | ||||||
chr1:151641775 | ATC | A | 11 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(8): Show |
11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.543+2658_543+2659d others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641775 | ||||||
chr1:151641800 | ATATAGAT others(81): Show |
A | 1 | a0001c0001t0097g0197 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.543+2706_543+2793d others(90): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641800 | ||||||
chr1:151641821 | A | G | 2 | a0001c0001t0013g0263 a0001c0001t0013g0264 |
2 | HG01099.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.543+2702A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151641821 | |||||||
chr1:151641825 | G | A | 269 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(266): Show |
275 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.543+2706G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151641825 | |||||||
chr1:151641845 | A | AGATATAT others(21): Show |
1 | a0001c0001t0117g0089 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.543+2757_543+2784d others(30): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641845 | ||||||
chr1:151641873 | TGATATAT others(23): Show |
T | 1 | a0001c0001t0102g0016 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.543+2826_543+2855d others(32): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641873 | ||||||
chr1:151641881 | ATATC | A | 9 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(6): Show |
9 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.543+2763_543+2766d others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151641881 | |||||||
chr1:151641918 | CTATAGAT others(55): Show |
C | 1 | a0001c0001t0002g0179 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.543+2829_543+2890d others(64): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641918 | ||||||
chr1:151641931 | TGAGATAT others(25): Show |
T | 1 | a0001c0001t0053g0349 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.543+2815_543+2846d others(34): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641931 | ||||||
chr1:151641948 | C | A | 10 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(7): Show |
10 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.543+2829C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151641948 | |||||||
chr1:151641948 | CTATAGAT others(25): Show |
C | 4 | a0001c0001t0001g0213 a0001c0001t0001g0246 a0001c0001t0004g0207 others(1): Show |
4 | HG02015.hp2 NA18948.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.543+2856_543+2887d others(34): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641948 | ||||||
chr1:151641964 | G | T | 1 | a0001c0001t0046g0019 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.543+2845G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151641964 | |||||||
chr1:151641964 | GAT | G | 258 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(255): Show |
264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.543+2856_543+2857d others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641964 | ||||||
chr1:151641966 | T | TATATATA others(21): Show |
1 | a0001c0001t0065g0012 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.543+2855_543+2856i others(30): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641966 | ||||||
chr1:151641966 | T | TATATATA others(81): Show |
1 | a0001c0001t0105g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.543+2855_543+2856i others(90): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641966 | ||||||
chr1:151641966 | T | TATATATA others(21): Show |
3 | a0001c0001t0006g0170 a0001c0001t0057g0346 a0001c0001t0058g0341 |
3 | HG01074.hp2 HG01975.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.543+2855_543+2856i others(30): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641966 | ||||||
chr1:151641966 | T | TATATATA others(51): Show |
1 | a0001c0001t0026g0292 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.543+2855_543+2856i others(60): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641966 | ||||||
chr1:151641980 | A | C | 150 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(147): Show |
155 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.543+2861A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151641980 | |||||||
chr1:151642010 | A | C | 1 | a0001c0001t0053g0349 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.543+2891A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151642010 | |||||||
chr1:151642094 | C | T | 3 | a0001c0001t0010g0277 a0001c0001t0010g0278 a0001c0001t0010g0279 |
3 | HG02486.hp1 HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.543+2975C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151642094 | |||||||
chr1:151642095 | G | A | 10 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(7): Show |
10 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.543+2976G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151642095 | |||||||
chr1:151642100 | G | A | 1 | a0001c0001t0052g0359 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.543+2981G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151642100 | |||||||
chr1:151642456 | C | T | 1 | a0001c0001t0102g0016 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.543+3337C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151642456 | |||||||
chr1:151642481 | T | G | 2 | a0001c0003t0044g0099 a0001c0003t0044g0100 |
2 | HG02895.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.543+3362T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151642481 | |||||||
chr1:151642677 | C | T | 1 | a0001c0001t0065g0012 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.543+3558C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151642677 | |||||||
chr1:151642679 | C | G | 9 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(6): Show |
9 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.543+3560C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151642679 | |||||||
chr1:151642831 | G | A | 77 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(74): Show |
79 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.543+3712G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151642831 | |||||||
chr1:151642919 | C | T | 89 | a0001c0001t0002g0148 a0001c0001t0003g0117 a0001c0001t0003g0120 others(86): Show |
90 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.543+3800C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151642919 | |||||||
chr1:151642929 | C | T | 3 | a0001c0001t0001g0213 a0001c0001t0001g0246 a0001c0001t0004g0207 |
3 | HG02015.hp2 NA18948.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.543+3810C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151642929 | |||||||
chr1:151642932 | G | A | 1 | a0001c0001t0049g0033 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.543+3813G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151642932 | |||||||
chr1:151642954 | G | GTTTTA | 8 | a0001c0001t0006g0169 a0001c0001t0006g0171 a0001c0001t0006g0172 others(5): Show |
8 | HG01261.hp2 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.543+3855_543+3859d others(7): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151642954 | ||||||
chr1:151642986 | G | A | 1 | a0001c0001t0005g0062 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.543+3867G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151642986 | |||||||
chr1:151643183 | G | A | 1 | a0001c0001t0002g0293 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.543+4064G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151643183 | |||||||
chr1:151643210 | C | T | 146 | a0001c0001t0002g0005 a0001c0001t0002g0148 a0001c0001t0002g0178 others(143): Show |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.543+4091C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151643210 | |||||||
chr1:151643264 | T | TTTTA | 49 | a0001c0001t0001g0011 a0001c0001t0001g0196 a0001c0001t0001g0210 others(46): Show |
49 | HG00323.hp1 HG00735.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.543+4189_543+4192d others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151643264 | ||||||
chr1:151643264 | T | TTTTATTT others(1): Show |
47 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0189 others(44): Show |
50 | HG00280.hp2 HG00438.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.543+4185_543+4192d others(10): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151643264 | ||||||
chr1:151643264 | T | TTTTATTT others(5): Show |
20 | a0001c0001t0001g0195 a0001c0001t0001g0205 a0001c0001t0001g0212 others(17): Show |
20 | HG00438.hp2 HG00673.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.543+4181_543+4192d others(14): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151643264 | ||||||
chr1:151643264 | T | TTTTATTT others(9): Show |
4 | a0001c0001t0004g0204 a0001c0001t0008g0104 a0001c0001t0010g0262 others(1): Show |
4 | HG01099.hp1 NA18946.hp2 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.543+4177_543+4192d others(18): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151643264 | ||||||
chr1:151643264 | TTTTA | T | 15 | a0001c0001t0001g0280 a0001c0001t0005g0038 a0001c0001t0012g0283 others(12): Show |
15 | HG00408.hp2 HG00642.hp2 HG02300.hp1 others(12): Show |
intron_variant | MODIFIER | c.543+4189_543+4192d others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151643264 | ||||||
chr1:151643264 | TTTTATTT others(1): Show |
T | 65 | a0001c0001t0003g0120 a0001c0001t0003g0121 a0001c0001t0003g0122 others(62): Show |
65 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.543+4185_543+4192d others(10): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151643264 | ||||||
chr1:151643264 | TTTTATTT others(5): Show |
T | 74 | a0001c0001t0002g0005 a0001c0001t0002g0148 a0001c0001t0002g0178 others(71): Show |
77 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.543+4181_543+4192d others(14): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151643264 | ||||||
chr1:151643544 | C | T | 1 | a0001c0001t0028g0023 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.543+4425C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151643544 | |||||||
chr1:151643619 | A | G | 1 | a0001c0001t0124g0048 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.543+4500A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151643619 | |||||||
chr1:151643629 | C | T | 2 | a0001c0001t0007g0162 a0001c0001t0060g0163 |
2 | HG01168.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.543+4510C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151643629 | |||||||
chr1:151643638 | A | G | 1 | a0001c0001t0005g0061 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.543+4519A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151643638 | |||||||
chr1:151643656 | T | G | 11 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(8): Show |
11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.543+4537T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151643656 | |||||||
chr1:151643662 | T | A | 9 | a0001c0001t0012g0004 a0001c0001t0012g0283 a0001c0001t0012g0284 others(6): Show |
9 | HG02486.hp2 HG02723.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.543+4543T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151643662 | |||||||
chr1:151643663 | T | A | 16 | a0001c0001t0012g0004 a0001c0001t0012g0283 a0001c0001t0012g0284 others(13): Show |
16 | HG02109.hp2 HG02145.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.543+4544T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151643663 | |||||||
chr1:151643804 | G | T | 9 | a0001c0001t0028g0023 a0001c0001t0028g0024 a0001c0001t0028g0025 others(6): Show |
9 | HG02895.hp1 HG02895.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.543+4685G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151643804 | |||||||
chr1:151643812 | C | T | 1 | a0001c0001t0097g0197 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.543+4693C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151643812 | |||||||
chr1:151643822 | G | A | 9 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(6): Show |
9 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.543+4703G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151643822 | |||||||
chr1:151644200 | T | C | 1 | a0001c0001t0024g0344 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.543+5081T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151644200 | |||||||
chr1:151644232 | C | A | 1 | a0001c0001t0006g0008 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.543+5113C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151644232 | |||||||
chr1:151644588 | C | T | 1 | a0001c0001t0105g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.543+5469C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151644588 | |||||||
chr1:151644645 | T | C | 90 | a0001c0001t0002g0148 a0001c0001t0002g0306 a0001c0001t0003g0117 others(87): Show |
91 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.543+5526T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151644645 | |||||||
chr1:151644865 | A | G | 1 | a0001c0001t0081g0090 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.543+5746A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151644865 | |||||||
chr1:151644916 | A | G | 62 | a0001c0001t0005g0013 a0001c0001t0005g0028 a0001c0001t0005g0029 others(59): Show |
62 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.543+5797A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151644916 | |||||||
chr1:151645064 | T | C | 3 | a0001c0001t0046g0017 a0001c0001t0046g0019 a0001c0001t0118g0018 |
3 | HG02145.hp1 HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.543+5945T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151645064 | |||||||
chr1:151645090 | G | GACC | 7 | a0001c0001t0028g0023 a0001c0001t0028g0024 a0001c0001t0028g0025 others(4): Show |
7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.543+5973_543+5975d others(5): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151645090 | ||||||
chr1:151645279 | T | C | 5 | a0001c0001t0015g0352 a0001c0001t0015g0353 a0001c0001t0015g0354 others(2): Show |
5 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.543+6160T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151645279 | |||||||
chr1:151645511 | C | A | 2 | a0001c0001t0001g0213 a0001c0001t0004g0207 |
2 | NA18948.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.543+6392C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151645511 | |||||||
chr1:151645601 | T | G | 1 | a0001c0001t0008g0104 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.543+6482T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151645601 | |||||||
chr1:151645913 | G | C | 1 | a0001c0001t0102g0016 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.543+6794G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151645913 | |||||||
chr1:151645952 | A | G | 1 | a0001c0001t0004g0253 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.543+6833A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151645952 | |||||||
chr1:151646197 | C | T | 2 | a0001c0001t0047g0358 a0001c0001t0104g0357 |
2 | HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.543+7078C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151646197 | |||||||
chr1:151646210 | C | T | 9 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(6): Show |
9 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.543+7091C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151646210 | |||||||
chr1:151646211 | G | A | 2 | a0001c0001t0065g0012 a0001c0001t0102g0016 |
2 | HG02129.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.543+7092G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151646211 | |||||||
chr1:151646312 | A | G | 4 | a0001c0001t0001g0280 a0001c0001t0001g0339 a0001c0001t0062g0198 others(1): Show |
4 | HG02886.hp1 HG02970.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.543+7193A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151646312 | |||||||
chr1:151646843 | G | C | 1 | a0001c0006t0076g0334 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.543+7724G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151646843 | |||||||
chr1:151646882 | G | GAC | 195 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(192): Show |
197 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.543+7783_543+7784d others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151646882 | ||||||
chr1:151646882 | G | GACAC | 113 | a0001c0001t0002g0148 a0001c0001t0003g0117 a0001c0001t0003g0120 others(110): Show |
115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.543+7781_543+7784d others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151646882 | ||||||
chr1:151646882 | G | GACACAC | 39 | a0001c0001t0002g0005 a0001c0001t0002g0178 a0001c0001t0002g0179 others(36): Show |
41 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.543+7779_543+7784d others(8): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151646882 | ||||||
chr1:151646882 | G | GACACACA others(1): Show |
4 | a0001c0001t0002g0288 a0001c0001t0002g0316 a0001c0001t0042g0314 others(1): Show |
4 | HG02055.hp2 HG06807.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.543+7777_543+7784d others(10): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151646882 | ||||||
chr1:151647079 | A | G | 1 | a0001c0001t0056g0181 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.543+7960A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151647079 | |||||||
chr1:151647132 | C | CT | 255 | a0001c0001t0001g0010 a0001c0001t0001g0195 a0001c0001t0001g0196 others(252): Show |
260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.543+8030dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151647132 | ||||||
chr1:151647237 | G | A | 1 | a0001c0001t0031g0007 | 2 | HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.543+8118G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151647237 | |||||||
chr1:151647292 | C | T | 21 | a0001c0001t0004g0272 a0001c0001t0010g0256 a0001c0001t0010g0257 others(18): Show |
21 | HG00438.hp1 HG00639.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.543+8173C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151647292 | |||||||
chr1:151647439 | C | G | 1 | a0001c0001t0001g0011 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.543+8320C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151647439 | |||||||
chr1:151647598 | T | G | 41 | a0001c0001t0002g0005 a0001c0001t0002g0178 a0001c0001t0002g0179 others(38): Show |
43 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.543+8479T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151647598 | |||||||
chr1:151647682 | G | C | 2 | a0001c0001t0005g0032 a0001c0001t0129g0031 |
2 | NA18939.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.543+8563G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151647682 | |||||||
chr1:151647758 | G | T | 20 | a0001c0001t0004g0272 a0001c0001t0010g0256 a0001c0001t0010g0257 others(17): Show |
20 | HG00438.hp1 HG00639.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.543+8639G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151647758 | |||||||
chr1:151647795 | T | C | 1 | a0001c0001t0102g0016 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.543+8676T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151647795 | |||||||
chr1:151647923 | A | T | 1 | a0001c0001t0023g0118 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.543+8804A>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151647923 | |||||||
chr1:151647992 | T | TA | 10 | a0001c0001t0002g0293 a0001c0001t0002g0295 a0001c0001t0028g0023 others(7): Show |
10 | HG02056.hp1 HG02895.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.543+8884dupA | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151647992 | ||||||
chr1:151648059 | T | G | 1 | a0001c0001t0023g0118 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.543+8940T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151648059 | |||||||
chr1:151648060 | G | T | 1 | a0001c0001t0023g0118 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.543+8941G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151648060 | |||||||
chr1:151648119 | A | G | 11 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(8): Show |
11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.543+9000A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151648119 | |||||||
chr1:151648133 | C | T | 1 | a0001c0001t0007g0340 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.543+9014C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151648133 | |||||||
chr1:151648200 | C | T | 1 | a0001c0001t0043g0255 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.543+9081C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151648200 | |||||||
chr1:151648254 | C | T | 1 | a0001c0001t0065g0012 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.543+9135C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151648254 | |||||||
chr1:151648432 | T | C | 1 | a0001c0001t0065g0012 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.543+9313T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151648432 | |||||||
chr1:151648481 | G | A | 1 | a0001c0001t0002g0288 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.543+9362G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151648481 | |||||||
chr1:151648482 | C | T | 2 | a0001c0003t0044g0099 a0001c0003t0044g0100 |
2 | HG02895.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.543+9363C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151648482 | |||||||
chr1:151648568 | A | C | 12 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(9): Show |
12 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.543+9449A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151648568 | |||||||
chr1:151648658 | A | G | 2 | a0001c0003t0044g0099 a0001c0003t0044g0100 |
2 | HG02895.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.543+9539A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151648658 | |||||||
chr1:151648693 | A | G | 2 | a0001c0001t0001g0236 a0001c0001t0004g0237 |
2 | NA18963.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.544-9542A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151648693 | |||||||
chr1:151648698 | C | T | 1 | a0001c0001t0085g0310 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.544-9537C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151648698 | |||||||
chr1:151648740 | A | C | 146 | a0001c0001t0002g0005 a0001c0001t0002g0148 a0001c0001t0002g0178 others(143): Show |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.544-9495A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151648740 | |||||||
chr1:151648744 | TA | T | 145 | a0001c0001t0002g0005 a0001c0001t0002g0148 a0001c0001t0002g0178 others(142): Show |
148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.544-9490delA | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151648744 | |||||||
chr1:151648745 | A | T | 1 | a0001c0001t0023g0118 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.544-9490A>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151648745 | |||||||
chr1:151648870 | G | A | 9 | a0001c0001t0015g0352 a0001c0001t0015g0353 a0001c0001t0015g0354 others(6): Show |
10 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.544-9365G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151648870 | |||||||
chr1:151649058 | G | A | 4 | a0001c0001t0008g0191 a0001c0001t0008g0193 a0001c0001t0037g0192 others(1): Show |
4 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.544-9177G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151649058 | |||||||
chr1:151649061 | C | T | 1 | a0001c0001t0011g0055 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.544-9174C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151649061 | |||||||
chr1:151649086 | C | T | 1 | a0001c0001t0105g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.544-9149C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151649086 | |||||||
chr1:151649195 | C | T | 9 | a0001c0001t0012g0004 a0001c0001t0012g0283 a0001c0001t0012g0284 others(6): Show |
9 | HG02486.hp2 HG02723.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.544-9040C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151649195 | |||||||
chr1:151649196 | G | A | 130 | a0001c0001t0002g0005 a0001c0001t0002g0148 a0001c0001t0002g0178 others(127): Show |
133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.544-9039G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151649196 | |||||||
chr1:151649317 | A | G | 2 | a0001c0001t0036g0160 a0001c0001t0073g0161 |
2 | NA19012.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.544-8918A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151649317 | |||||||
chr1:151649341 | G | C | 1 | a0001c0001t0074g0282 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.544-8894G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151649341 | |||||||
chr1:151649579 | T | C | 1 | a0001c0001t0105g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.544-8656T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151649579 | |||||||
chr1:151649644 | G | A | 39 | a0001c0001t0002g0005 a0001c0001t0002g0178 a0001c0001t0002g0179 others(36): Show |
41 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.544-8591G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151649644 | |||||||
chr1:151649813 | C | A | 77 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(74): Show |
79 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.544-8422C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151649813 | |||||||
chr1:151649835 | A | G | 1 | a0001c0001t0043g0255 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.544-8400A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151649835 | |||||||
chr1:151650053 | A | C | 147 | a0001c0001t0002g0005 a0001c0001t0002g0148 a0001c0001t0002g0178 others(144): Show |
150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.544-8182A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151650053 | |||||||
chr1:151650135 | A | T | 11 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(8): Show |
11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.544-8100A>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151650135 | |||||||
chr1:151650285 | C | G | 1 | a0001c0001t0059g0166 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.544-7950C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151650285 | |||||||
chr1:151650292 | A | G | 7 | a0001c0001t0028g0023 a0001c0001t0028g0024 a0001c0001t0028g0025 others(4): Show |
7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.544-7943A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151650292 | |||||||
chr1:151650595 | T | C | 1 | a0001c0001t0052g0359 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.544-7640T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151650595 | |||||||
chr1:151650602 | T | A | 3 | a0001c0001t0046g0017 a0001c0001t0046g0019 a0001c0001t0118g0018 |
3 | HG02145.hp1 HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.544-7633T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151650602 | |||||||
chr1:151650603 | T | A | 13 | a0001c0001t0028g0023 a0001c0001t0028g0024 a0001c0001t0028g0025 others(10): Show |
13 | HG02040.hp1 HG02145.hp1 HG02895.hp1 others(10): Show |
intron_variant | MODIFIER | c.544-7632T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151650603 | |||||||
chr1:151650604 | A | T | 18 | a0001c0001t0012g0004 a0001c0001t0012g0283 a0001c0001t0012g0284 others(15): Show |
18 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.544-7631A>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151650604 | |||||||
chr1:151650654 | G | C | 1 | a0001c0001t0105g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.544-7581G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151650654 | |||||||
chr1:151650730 | T | G | 1 | a0001c0001t0065g0012 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.544-7505T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151650730 | |||||||
chr1:151650746 | C | T | 1 | a0001c0001t0059g0166 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.544-7489C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151650746 | |||||||
chr1:151650747 | GGCCTTCC others(3): Show |
G | 1 | a0001c0001t0102g0016 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.544-7486_544-7477d others(12): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151650747 | ||||||
chr1:151650773 | G | C | 10 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(7): Show |
10 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.544-7462G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151650773 | |||||||
chr1:151650808 | C | G | 1 | a0001c0001t0002g0294 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.544-7427C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151650808 | |||||||
chr1:151650886 | C | T | 2 | a0001c0001t0014g0040 a0001c0001t0014g0058 |
2 | NA18988.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.544-7349C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151650886 | |||||||
chr1:151650905 | C | T | 111 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(108): Show |
114 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.544-7330C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151650905 | |||||||
chr1:151650979 | G | T | 2 | a0001c0001t0005g0032 a0001c0001t0129g0031 |
2 | NA18939.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.544-7256G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151650979 | |||||||
chr1:151651010 | C | T | 8 | a0001c0001t0009g0175 a0001c0001t0024g0343 a0001c0001t0024g0344 others(5): Show |
8 | HG00735.hp2 HG00741.hp1 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.544-7225C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651010 | |||||||
chr1:151651015 | A | C | 1 | a0001c0001t0056g0181 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.544-7220A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651015 | |||||||
chr1:151651130 | C | T | 1 | a0001c0001t0043g0255 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.544-7105C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651130 | |||||||
chr1:151651136 | G | C | 2 | a0001c0001t0011g0046 a0001c0001t0114g0079 |
2 | HG00544.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.544-7099G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651136 | |||||||
chr1:151651153 | G | A | 1 | a0001c0001t0065g0012 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.544-7082G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651153 | |||||||
chr1:151651199 | C | T | 77 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(74): Show |
79 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.544-7036C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651199 | |||||||
chr1:151651203 | C | G | 1 | a0001c0001t0052g0359 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.544-7032C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651203 | |||||||
chr1:151651203 | C | T | 4 | a0001c0001t0006g0103 a0001c0001t0047g0358 a0001c0001t0104g0357 others(1): Show |
4 | HG02451.hp1 HG02572.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.544-7032C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651203 | |||||||
chr1:151651225 | G | C | 1 | a0001c0001t0117g0089 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.544-7010G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651225 | |||||||
chr1:151651241 | G | C | 354 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(351): Show |
360 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(357): Show |
intron_variant | MODIFIER | c.544-6994G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651241 | |||||||
chr1:151651278 | G | T | 9 | a0001c0001t0028g0023 a0001c0001t0028g0024 a0001c0001t0028g0025 others(6): Show |
9 | HG02895.hp1 HG02895.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.544-6957G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651278 | |||||||
chr1:151651319 | GGGCGGGG others(43): Show |
G | 1 | a0001c0001t0016g0106 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.544-6880_544-6831d others(52): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151651319 | ||||||
chr1:151651360 | C | T | 1 | a0001c0001t0092g0266 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.544-6875C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651360 | |||||||
chr1:151651402 | G | C | 1 | a0001c0001t0002g0294 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.544-6833G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651402 | |||||||
chr1:151651427 | C | T | 1 | a0001c0001t0043g0255 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.544-6808C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651427 | |||||||
chr1:151651491 | G | A | 1 | a0001c0001t0024g0347 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.544-6744G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651491 | |||||||
chr1:151651569 | G | A | 2 | a0001c0001t0014g0070 a0001c0001t0097g0197 |
2 | HG03225.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.544-6666G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651569 | |||||||
chr1:151651571 | G | A | 77 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(74): Show |
79 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.544-6664G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651571 | |||||||
chr1:151651610 | C | T | 1 | a0001c0001t0031g0007 | 2 | HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.544-6625C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651610 | |||||||
chr1:151651650 | C | A | 4 | a0001c0001t0028g0023 a0001c0001t0028g0024 a0001c0001t0028g0025 others(1): Show |
4 | HG02895.hp1 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.544-6585C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651650 | |||||||
chr1:151651776 | C | T | 1 | a0001c0001t0006g0101 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.544-6459C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651776 | |||||||
chr1:151651777 | G | A | 1 | a0001c0001t0105g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.544-6458G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651777 | |||||||
chr1:151651794 | C | CG | 24 | a0001c0001t0001g0189 a0001c0001t0001g0232 a0001c0001t0001g0238 others(21): Show |
24 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(21): Show |
intron_variant | MODIFIER | c.544-6437dupG | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151651794 | ||||||
chr1:151651807 | G | A | 1 | a0001c0001t0001g0239 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.544-6428G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651807 | |||||||
chr1:151651825 | C | T | 1 | a0001c0001t0046g0019 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.544-6410C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651825 | |||||||
chr1:151651851 | G | A | 1 | a0001c0001t0002g0316 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.544-6384G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651851 | |||||||
chr1:151651901 | G | A | 3 | a0001c0001t0046g0017 a0001c0001t0046g0019 a0001c0001t0118g0018 |
3 | HG02145.hp1 HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.544-6334G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651901 | |||||||
chr1:151651945 | A | G | 3 | a0001c0001t0046g0017 a0001c0001t0046g0019 a0001c0001t0118g0018 |
3 | HG02145.hp1 HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.544-6290A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651945 | |||||||
chr1:151651954 | C | T | 11 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(8): Show |
11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.544-6281C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651954 | |||||||
chr1:151651957 | G | C | 261 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(258): Show |
266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.544-6278G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651957 | |||||||
chr1:151651957 | G | T | 9 | a0001c0001t0015g0352 a0001c0001t0015g0353 a0001c0001t0015g0354 others(6): Show |
10 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.544-6278G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651957 | |||||||
chr1:151651983 | T | C | 1 | a0001c0001t0001g0233 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.544-6252T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651983 | |||||||
chr1:151651993 | G | A | 1 | a0001c0001t0001g0233 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.544-6242G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651993 | |||||||
chr1:151652007 | T | C | 1 | a0001c0001t0001g0233 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.544-6228T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151652007 | |||||||
chr1:151652021 | G | A | 1 | a0001c0001t0001g0233 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.544-6214G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151652021 | |||||||
chr1:151652028 | C | T | 4 | a0001c0001t0001g0225 a0001c0001t0019g0325 a0001c0001t0019g0332 others(1): Show |
4 | HG02615.hp2 HG03130.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.544-6207C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151652028 | |||||||
chr1:151652037 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0233 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.544-6194_544-6193i others(14): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151652037 | ||||||
chr1:151652045 | G | C | 1 | a0001c0001t0001g0233 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.544-6190G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151652045 | |||||||
chr1:151652051 | T | C | 1 | a0001c0001t0001g0233 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.544-6184T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151652051 | |||||||
chr1:151652055 | G | A | 1 | a0001c0001t0009g0165 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.544-6180G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151652055 | |||||||
chr1:151652056 | C | T | 1 | a0001c0001t0093g0274 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.544-6179C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151652056 | |||||||
chr1:151652063 | A | C | 1 | a0001c0001t0001g0233 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.544-6172A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151652063 | |||||||
chr1:151652065 | C | G | 3 | a0001c0001t0002g0148 a0001c0001t0007g0149 a0001c0001t0007g0150 |
3 | HG01255.hp2 HG01257.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.544-6170C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151652065 | |||||||
chr1:151652073 | C | T | 1 | a0001c0001t0012g0284 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.544-6162C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151652073 | |||||||
chr1:151652205 | G | GGGGAGA | 114 | a0001c0001t0001g0236 a0001c0001t0001g0268 a0001c0001t0001g0269 others(111): Show |
116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.544-5993_544-5988d others(8): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151652205 | ||||||
chr1:151652205 | G | GGGGAGAG others(5): Show |
83 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(80): Show |
85 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.544-5999_544-5988d others(14): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151652205 | ||||||
chr1:151652205 | G | GGGGAGAG others(11): Show |
9 | a0001c0001t0001g0189 a0001c0001t0001g0203 a0001c0001t0004g0253 others(6): Show |
9 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.544-6005_544-5988d others(20): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151652205 | ||||||
chr1:151652205 | G | GGGGAGAG others(17): Show |
1 | a0001c0001t0008g0247 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.544-6011_544-5988d others(26): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151652205 | ||||||
chr1:151652205 | GGGGAGA | G | 9 | a0001c0001t0006g0103 a0001c0001t0028g0023 a0001c0001t0028g0024 others(6): Show |
9 | HG02280.hp2 HG02895.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.544-5993_544-5988d others(8): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151652205 | ||||||
chr1:151652205 | GGGGAGAG others(5): Show |
G | 2 | a0001c0001t0062g0198 a0001c0001t0097g0197 |
2 | HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.544-5999_544-5988d others(14): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151652205 | ||||||
chr1:151652205 | GGGGAGAG others(11): Show |
G | 9 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(6): Show |
9 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.544-6005_544-5988d others(20): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151652205 | ||||||
chr1:151652206 | G | GGGAGAGG others(35): Show |
1 | a0001c0001t0126g0041 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.544-6009_544-5968d others(44): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151652206 | ||||||
chr1:151652207 | G | A | 1 | a0001c0001t0065g0012 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.544-6028G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151652207 | |||||||
chr1:151652211 | A | AGGGAGAG others(16): Show |
2 | a0001c0001t0001g0280 a0001c0001t0001g0339 |
2 | HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.544-6006_544-6005i others(25): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151652211 | ||||||
chr1:151652212 | GGGAGAGG others(29): Show |
G | 1 | a0001c0001t0105g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.544-6003_544-5968d others(38): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151652212 | ||||||
chr1:151652236 | G | GGGAGAGG others(5): Show |
1 | a0001c0001t0052g0359 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.544-5987_544-5976d others(14): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151652236 | ||||||
chr1:151652242 | G | GGGAGAGG others(23): Show |
1 | a0001c0001t0088g0307 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.544-5988_544-5987i others(32): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151652242 | ||||||
chr1:151652248 | C | G | 1 | a0001c0001t0112g0030 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.544-5987C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151652248 | |||||||
chr1:151652395 | T | C | 1 | a0001c0001t0009g0328 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.544-5840T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151652395 | |||||||
chr1:151652403 | C | CT | 33 | a0001c0001t0001g0010 a0001c0001t0001g0212 a0001c0001t0002g0288 others(30): Show |
33 | HG00544.hp2 HG00673.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.544-5812dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151652403 | ||||||
chr1:151652510 | G | A | 11 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(8): Show |
11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.544-5725G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151652510 | |||||||
chr1:151652618 | G | A | 1 | a0001c0001t0007g0185 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.544-5617G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151652618 | |||||||
chr1:151652682 | A | G | 1 | a0001c0001t0117g0089 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.544-5553A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151652682 | |||||||
chr1:151652842 | G | T | 1 | a0001c0001t0020g0075 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.544-5393G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151652842 | |||||||
chr1:151652868 | A | G | 2 | a0001c0001t0062g0198 a0001c0001t0063g0199 |
2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.544-5367A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151652868 | |||||||
chr1:151652921 | G | C | 1 | a0001c0001t0008g0251 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.544-5314G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151652921 | |||||||
chr1:151652927 | CT | C | 240 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(237): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.544-5291delT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151652927 | ||||||
chr1:151652991 | G | C | 9 | a0001c0001t0015g0352 a0001c0001t0015g0353 a0001c0001t0015g0354 others(6): Show |
10 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.544-5244G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151652991 | |||||||
chr1:151653014 | G | A | 2 | a0001c0001t0001g0239 a0001c0001t0001g0241 |
2 | NA18942.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.544-5221G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151653014 | |||||||
chr1:151653057 | A | G | 1 | a0001c0001t0062g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.544-5178A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151653057 | |||||||
chr1:151653083 | A | G | 1 | a0001c0001t0032g0200 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.544-5152A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151653083 | |||||||
chr1:151653106 | T | C | 146 | a0001c0001t0002g0005 a0001c0001t0002g0148 a0001c0001t0002g0178 others(143): Show |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.544-5129T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151653106 | |||||||
chr1:151653127 | A | T | 2 | a0001c0003t0044g0099 a0001c0003t0044g0100 |
2 | HG02895.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.544-5108A>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151653127 | |||||||
chr1:151653172 | C | T | 1 | a0001c0001t0028g0024 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.544-5063C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151653172 | |||||||
chr1:151653215 | C | T | 3 | a0001c0001t0011g0054 a0001c0001t0049g0033 a0001c0001t0115g0078 |
3 | NA18949.hp2 NA19011.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.544-5020C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151653215 | |||||||
chr1:151653232 | T | G | 279 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.544-5003T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151653232 | |||||||
chr1:151653266 | TTTG | T | 20 | a0001c0001t0004g0272 a0001c0001t0010g0256 a0001c0001t0010g0257 others(17): Show |
20 | HG00438.hp1 HG00639.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.544-4966_544-4964d others(5): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151653266 | ||||||
chr1:151653313 | A | G | 1 | a0001c0001t0014g0043 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.544-4922A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151653313 | |||||||
chr1:151653434 | C | T | 1 | a0001c0001t0002g0287 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.544-4801C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151653434 | |||||||
chr1:151653439 | G | A | 1 | a0001c0001t0062g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.544-4796G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151653439 | |||||||
chr1:151653636 | G | C | 1 | a0001c0001t0052g0359 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.544-4599G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151653636 | |||||||
chr1:151653683 | A | G | 1 | a0001c0001t0105g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.544-4552A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151653683 | |||||||
chr1:151653750 | G | A | 6 | a0001c0001t0015g0352 a0001c0001t0015g0353 a0001c0001t0015g0354 others(3): Show |
7 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.544-4485G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151653750 | |||||||
chr1:151653768 | G | A | 1 | a0001c0001t0118g0018 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.544-4467G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151653768 | |||||||
chr1:151653827 | GTTTTTTT others(8): Show |
G | 1 | a0001c0001t0105g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.544-4399_544-4385d others(17): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151653827 | ||||||
chr1:151653836 | G | GT | 214 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(211): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.544-4384dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151653836 | ||||||
chr1:151653896 | G | A | 279 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.544-4339G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151653896 | |||||||
chr1:151653920 | C | T | 2 | a0001c0001t0006g0101 a0001c0001t0006g0102 |
2 | HG01934.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.544-4315C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151653920 | |||||||
chr1:151653934 | GT | G | 6 | a0001c0001t0028g0023 a0001c0001t0028g0024 a0001c0001t0028g0025 others(3): Show |
6 | HG02895.hp1 HG02965.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-4300delT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151653934 | |||||||
chr1:151654294 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.544-3941T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151654294 | |||||||
chr1:151654355 | T | G | 11 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(8): Show |
11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.544-3880T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151654355 | |||||||
chr1:151654406 | C | G | 1 | a0001c0001t0057g0346 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.544-3829C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151654406 | |||||||
chr1:151654407 | G | A | 1 | a0001c0001t0014g0071 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.544-3828G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151654407 | |||||||
chr1:151654637 | A | G | 20 | a0001c0001t0004g0272 a0001c0001t0010g0256 a0001c0001t0010g0257 others(17): Show |
20 | HG00438.hp1 HG00639.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.544-3598A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151654637 | |||||||
chr1:151654771 | G | C | 1 | a0001c0001t0069g0143 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.544-3464G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151654771 | |||||||
chr1:151654834 | G | A | 1 | a0001c0001t0006g0101 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.544-3401G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151654834 | |||||||
chr1:151654855 | T | A | 1 | a0001c0001t0019g0335 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.544-3380T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151654855 | |||||||
chr1:151654942 | C | T | 2 | a0001c0001t0062g0198 a0001c0001t0063g0199 |
2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.544-3293C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151654942 | |||||||
chr1:151655068 | G | A | 1 | a0001c0001t0045g0097 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.544-3167G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151655068 | |||||||
chr1:151655094 | T | C | 20 | a0001c0001t0004g0272 a0001c0001t0010g0256 a0001c0001t0010g0257 others(17): Show |
20 | HG00438.hp1 HG00639.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.544-3141T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151655094 | |||||||
chr1:151655128 | A | G | 89 | a0001c0001t0002g0148 a0001c0001t0003g0117 a0001c0001t0003g0120 others(86): Show |
90 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.544-3107A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151655128 | |||||||
chr1:151655397 | G | A | 27 | a0001c0001t0002g0148 a0001c0001t0006g0008 a0001c0001t0007g0149 others(24): Show |
28 | HG00099.hp1 HG00544.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.544-2838G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151655397 | |||||||
chr1:151655682 | G | C | 1 | a0001c0001t0052g0359 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.544-2553G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151655682 | |||||||
chr1:151655686 | C | A | 4 | a0001c0001t0011g0051 a0001c0001t0014g0050 a0001c0001t0048g0049 others(1): Show |
4 | HG01071.hp1 HG01255.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.544-2549C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151655686 | |||||||
chr1:151655714 | C | T | 1 | a0001c0001t0006g0119 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.544-2521C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151655714 | |||||||
chr1:151655754 | C | T | 1 | a0001c0001t0105g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.544-2481C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151655754 | |||||||
chr1:151655776 | A | G | 283 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(280): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.544-2459A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151655776 | |||||||
chr1:151655824 | T | C | 1 | a0001c0001t0065g0012 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.544-2411T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151655824 | |||||||
chr1:151656009 | C | G | 11 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(8): Show |
11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.544-2226C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151656009 | |||||||
chr1:151656050 | C | T | 1 | a0001c0001t0089g0312 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.544-2185C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151656050 | |||||||
chr1:151656066 | A | G | 145 | a0001c0001t0002g0005 a0001c0001t0002g0148 a0001c0001t0002g0178 others(142): Show |
148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.544-2169A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151656066 | |||||||
chr1:151656094 | G | C | 1 | a0001c0001t0102g0016 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.544-2141G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151656094 | |||||||
chr1:151656110 | C | G | 1 | a0001c0001t0065g0012 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.544-2125C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151656110 | |||||||
chr1:151656147 | C | T | 1 | a0001c0001t0002g0296 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.544-2088C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151656147 | |||||||
chr1:151656223 | C | CA | 108 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0189 others(105): Show |
111 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.544-1992dupA | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151656223 | ||||||
chr1:151656223 | C | CAA | 12 | a0001c0001t0001g0010 a0001c0001t0001g0280 a0001c0001t0001g0339 others(9): Show |
12 | HG00438.hp1 HG01175.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.544-1993_544-1992d others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151656223 | ||||||
chr1:151656223 | CA | C | 10 | a0001c0001t0002g0313 a0001c0001t0024g0343 a0001c0001t0024g0344 others(7): Show |
10 | HG00597.hp2 HG00735.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.544-1992delA | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151656223 | ||||||
chr1:151656313 | G | T | 1 | a0001c0001t0033g0342 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.544-1922G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151656313 | |||||||
chr1:151656362 | G | A | 1 | a0001c0001t0003g0117 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.544-1873G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151656362 | |||||||
chr1:151656814 | T | C | 3 | a0001c0001t0053g0349 a0001c0004t0015g0348 a0001c0004t0015g0355 |
3 | HG02717.hp2 HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.544-1421T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151656814 | |||||||
chr1:151656972 | T | C | 3 | a0001c0001t0002g0288 a0001c0001t0002g0316 a0001c0001t0042g0314 |
3 | HG02055.hp2 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.544-1263T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151656972 | |||||||
chr1:151657067 | G | A | 1 | a0001c0001t0065g0012 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.544-1168G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151657067 | |||||||
chr1:151657184 | G | GT | 5 | a0001c0001t0018g0127 a0001c0001t0025g0182 a0001c0001t0036g0160 others(2): Show |
5 | HG01934.hp2 NA19012.hp2 NA19066.hp1 others(2): Show |
intron_variant | MODIFIER | c.544-1044dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151657184 | ||||||
chr1:151657225 | G | A | 9 | a0001c0001t0015g0352 a0001c0001t0015g0353 a0001c0001t0015g0354 others(6): Show |
10 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.544-1010G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151657225 | |||||||
chr1:151657278 | A | G | 3 | a0001c0001t0007g0162 a0001c0001t0007g0176 a0001c0001t0060g0163 |
3 | HG00099.hp1 HG01168.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.544-957A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151657278 | |||||||
chr1:151657482 | A | G | 70 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(67): Show |
72 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.544-753A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151657482 | |||||||
chr1:151657534 | C | A | 1 | a0001c0001t0042g0314 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.544-701C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151657534 | |||||||
chr1:151657534 | C | T | 146 | a0001c0001t0002g0005 a0001c0001t0002g0148 a0001c0001t0002g0178 others(143): Show |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.544-701C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151657534 | |||||||
chr1:151657535 | G | T | 1 | a0001c0001t0007g0164 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.544-700G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151657535 | |||||||
chr1:151657637 | CTT | C | 3 | a0001c0001t0001g0205 a0001c0001t0004g0204 a0001c0001t0004g0206 |
3 | HG00673.hp1 NA18961.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.544-595_544-594del others(2): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151657637 | ||||||
chr1:151657654 | A | T | 1 | a0001c0001t0005g0013 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.544-581A>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151657654 | |||||||
chr1:151657655 | T | A | 1 | a0001c0001t0005g0013 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.544-580T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151657655 | |||||||
chr1:151657759 | G | A | 1 | a0001c0001t0065g0012 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.544-476G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151657759 | |||||||
chr1:151657943 | A | G | 9 | a0001c0001t0028g0023 a0001c0001t0028g0024 a0001c0001t0028g0025 others(6): Show |
9 | HG02895.hp1 HG02895.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.544-292A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151657943 | |||||||
chr1:151657971 | A | C | 1 | a0001c0001t0047g0358 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.544-264A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151657971 | |||||||
chr1:151657981 | A | G | 1 | a0001c0003t0044g0099 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.544-254A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151657981 | |||||||
chr1:151657994 | C | G | 1 | a0001c0001t0105g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.544-241C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151657994 | |||||||
chr1:151658662 | GT | G | 7 | a0001c0001t0028g0023 a0001c0001t0028g0024 a0001c0001t0028g0025 others(4): Show |
7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.736+240delT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 151658662 | ||||||
chr1:151658725 | C | T | 112 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(109): Show |
115 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.736+298C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | chr1 | 151658725 | |||||||
chr1:151658759 | A | G | 1 | a0001c0001t0009g0175 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.736+332A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | chr1 | 151658759 | |||||||
chr1:151658833 | T | C | 1 | a0001c0001t0105g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.736+406T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | chr1 | 151658833 | |||||||
chr1:151658859 | AT | A | 357 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(354): Show |
363 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(360): Show |
intron_variant | MODIFIER | c.736+438delT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 151658859 | ||||||
chr1:151658945 | A | G | 89 | a0001c0001t0002g0148 a0001c0001t0003g0117 a0001c0001t0003g0120 others(86): Show |
90 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.736+518A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | chr1 | 151658945 | |||||||
chr1:151659049 | A | G | 1 | a0001c0001t0065g0012 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.736+622A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | chr1 | 151659049 | |||||||
chr1:151659099 | G | A | 1 | a0001c0001t0097g0197 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.736+672G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | chr1 | 151659099 | |||||||
chr1:151659216 | C | A | 112 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(109): Show |
115 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.736+789C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | chr1 | 151659216 | |||||||
chr1:151659236 | T | TTTTTG | 3 | a0001c0001t0028g0024 a0001c0001t0028g0025 a0001c0001t0111g0022 |
3 | HG03041.hp2 HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.736+835_736+839dup others(5): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 151659236 | ||||||
chr1:151659236 | TTTTTGTT others(3): Show |
T | 2 | a0002c0002t0001g0227 a0002c0002t0001g0228 |
2 | NA18941.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.736+830_736+839del others(10): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 151659236 | ||||||
chr1:151659321 | C | T | 1 | a0001c0001t0065g0012 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.736+894C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | chr1 | 151659321 | |||||||
chr1:151659394 | C | T | 1 | a0001c0001t0065g0012 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.736+967C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | chr1 | 151659394 | |||||||
chr1:151659881 | T | G | 2 | a0001c0001t0003g0117 a0001c0001t0039g0116 |
2 | HG00609.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.737-917T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | chr1 | 151659881 | |||||||
chr1:151659926 | G | A | 1 | a0001c0001t0009g0175 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.737-872G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | chr1 | 151659926 | |||||||
chr1:151660170 | T | C | 129 | a0001c0001t0002g0005 a0001c0001t0002g0148 a0001c0001t0002g0178 others(126): Show |
132 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.737-628T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | chr1 | 151660170 | |||||||
chr1:151660234 | C | T | 7 | a0001c0001t0019g0325 a0001c0001t0019g0330 a0001c0001t0019g0332 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.737-564C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | chr1 | 151660234 | |||||||
chr1:151660240 | G | GT | 9 | a0001c0001t0005g0013 a0001c0001t0006g0102 a0001c0001t0007g0149 others(6): Show |
9 | HG01255.hp2 HG02257.hp2 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.737-541dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 151660240 | ||||||
chr1:151660256 | T | C | 2 | a0001c0001t0001g0280 a0001c0001t0001g0339 |
2 | HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.737-542T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | chr1 | 151660256 | |||||||
chr1:151660452 | C | G | 1 | a0001c0001t0105g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.737-346C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | chr1 | 151660452 | |||||||
chr1:151660611 | T | C | 2 | a0001c0001t0013g0263 a0001c0001t0013g0264 |
2 | HG01099.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.737-187T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | chr1 | 151660611 | |||||||
chr1:151660651 | C | CCA | 4 | a0001c0001t0008g0191 a0001c0001t0008g0193 a0001c0001t0037g0192 others(1): Show |
4 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.737-146_737-145dup others(2): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 151660651 | ||||||
chr1:151660711 | G | T | 1 | a0001c0001t0097g0197 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.737-87G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | chr1 | 151660711 | |||||||
chr1:151661435 | C | A | 9 | a0001c0001t0015g0352 a0001c0001t0015g0353 a0001c0001t0015g0354 others(6): Show |
10 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.801+573C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 4/11 | chr1 | 151661435 | |||||||
chr1:151661529 | C | T | 3 | a0001c0001t0002g0291 a0001c0001t0018g0290 a0001c0001t0026g0292 |
3 | HG02132.hp2 NA18943.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.802-637C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 4/11 | chr1 | 151661529 | |||||||
chr1:151661671 | A | C | 6 | a0001c0001t0001g0010 a0001c0001t0001g0230 a0001c0001t0001g0238 others(3): Show |
6 | HG00642.hp1 HG01167.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.802-495A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 4/11 | chr1 | 151661671 | |||||||
chr1:151661778 | G | T | 2 | a0001c0003t0044g0099 a0001c0003t0044g0100 |
2 | HG02895.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.802-388G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 4/11 | chr1 | 151661778 | |||||||
chr1:151662030 | G | C | 1 | a0001c0001t0014g0050 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.802-136G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 4/11 | chr1 | 151662030 | |||||||
chr1:151662036 | A | AT | 144 | a0001c0001t0002g0005 a0001c0001t0002g0148 a0001c0001t0002g0178 others(141): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.802-123dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 151662036 | ||||||
chr1:151662047 | G | A | 1 | a0001c0001t0095g0092 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.802-119G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 4/11 | chr1 | 151662047 | |||||||
chr1:151662327 | G | A | 83 | a0001c0001t0002g0148 a0001c0001t0003g0117 a0001c0001t0003g0120 others(80): Show |
84 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.906+57G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151662327 | |||||||
chr1:151662354 | G | A | 1 | a0001c0001t0065g0012 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.906+84G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151662354 | |||||||
chr1:151662378 | C | T | 1 | a0001c0001t0084g0107 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.906+108C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151662378 | |||||||
chr1:151662547 | A | G | 1 | a0001c0001t0004g0253 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.906+277A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151662547 | |||||||
chr1:151662552 | C | T | 1 | a0001c0001t0002g0306 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.906+282C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151662552 | |||||||
chr1:151662672 | A | G | 2 | a0001c0001t0001g0205 a0001c0001t0004g0204 |
2 | HG00673.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.906+402A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151662672 | |||||||
chr1:151662706 | A | C | 1 | a0001c0001t0004g0253 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.906+436A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151662706 | |||||||
chr1:151662735 | G | A | 11 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(8): Show |
11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.906+465G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151662735 | |||||||
chr1:151662900 | C | G | 2 | a0001c0003t0044g0099 a0001c0003t0044g0100 |
2 | HG02895.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.906+630C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151662900 | |||||||
chr1:151662901 | G | A | 6 | a0001c0001t0002g0005 a0001c0001t0002g0306 a0001c0001t0002g0315 others(3): Show |
7 | HG01081.hp1 HG01192.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.906+631G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151662901 | |||||||
chr1:151662914 | T | TTTTTCTT others(318): Show |
1 | a0001c0001t0006g0119 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.906+653_906+654ins others(325): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 151662914 | ||||||
chr1:151663152 | A | AT | 8 | a0001c0001t0001g0010 a0001c0001t0002g0315 a0001c0001t0004g0237 others(5): Show |
8 | HG01175.hp1 HG02055.hp1 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.906+898dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 151663152 | ||||||
chr1:151663214 | G | A | 1 | a0001c0001t0008g0248 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.906+944G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151663214 | |||||||
chr1:151663295 | C | T | 1 | a0001c0001t0065g0012 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.906+1025C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151663295 | |||||||
chr1:151663307 | C | T | 2 | a0001c0001t0001g0280 a0001c0001t0001g0339 |
2 | HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.906+1037C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151663307 | |||||||
chr1:151663312 | G | A | 1 | a0001c0001t0097g0197 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.906+1042G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151663312 | |||||||
chr1:151663367 | G | T | 2 | a0001c0001t0001g0219 a0001c0001t0004g0218 |
2 | HG03492.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.906+1097G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151663367 | |||||||
chr1:151663400 | T | C | 78 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(75): Show |
80 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.906+1130T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151663400 | |||||||
chr1:151663444 | C | T | 1 | a0001c0001t0016g0110 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.906+1174C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151663444 | |||||||
chr1:151663487 | T | C | 1 | a0001c0001t0028g0025 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.906+1217T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151663487 | |||||||
chr1:151663766 | A | G | 1 | a0001c0001t0105g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.906+1496A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151663766 | |||||||
chr1:151663792 | T | C | 9 | a0001c0001t0015g0352 a0001c0001t0015g0353 a0001c0001t0015g0354 others(6): Show |
10 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.906+1522T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151663792 | |||||||
chr1:151664122 | C | T | 279 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.907-1811C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151664122 | |||||||
chr1:151664138 | T | C | 1 | a0001c0001t0012g0285 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.907-1795T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151664138 | |||||||
chr1:151664204 | A | T | 2 | a0001c0001t0062g0198 a0001c0001t0063g0199 |
2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.907-1729A>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151664204 | |||||||
chr1:151664208 | A | ATAT | 283 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(280): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.907-1723_907-1721d others(5): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 151664208 | ||||||
chr1:151664261 | GTC | G | 20 | a0001c0001t0004g0272 a0001c0001t0010g0256 a0001c0001t0010g0257 others(17): Show |
20 | HG00438.hp1 HG00639.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.907-1669_907-1668d others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 151664261 | ||||||
chr1:151664338 | G | A | 1 | a0001c0001t0102g0016 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.907-1595G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151664338 | |||||||
chr1:151664427 | A | T | 4 | a0001c0001t0001g0280 a0001c0001t0001g0339 a0001c0001t0062g0198 others(1): Show |
4 | HG02886.hp1 HG02970.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.907-1506A>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151664427 | |||||||
chr1:151664458 | C | T | 1 | a0001c0001t0116g0098 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.907-1475C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151664458 | |||||||
chr1:151664470 | A | G | 16 | a0001c0001t0012g0004 a0001c0001t0012g0283 a0001c0001t0012g0284 others(13): Show |
16 | HG02109.hp2 HG02145.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.907-1463A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151664470 | |||||||
chr1:151664539 | G | A | 1 | a0001c0001t0046g0019 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.907-1394G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151664539 | |||||||
chr1:151664589 | C | T | 21 | a0001c0001t0004g0272 a0001c0001t0010g0256 a0001c0001t0010g0257 others(18): Show |
21 | HG00438.hp1 HG00639.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.907-1344C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151664589 | |||||||
chr1:151664611 | G | T | 2 | a0001c0001t0062g0198 a0001c0001t0063g0199 |
2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.907-1322G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151664611 | |||||||
chr1:151664674 | C | T | 279 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.907-1259C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151664674 | |||||||
chr1:151664715 | A | G | 1 | a0001c0001t0105g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.907-1218A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151664715 | |||||||
chr1:151664858 | T | G | 1 | a0001c0001t0043g0255 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.907-1075T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151664858 | |||||||
chr1:151665062 | G | C | 1 | a0001c0001t0082g0091 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.907-871G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151665062 | |||||||
chr1:151665314 | A | G | 1 | a0001c0001t0102g0016 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.907-619A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151665314 | |||||||
chr1:151665422 | A | C | 1 | a0001c0001t0005g0013 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.907-511A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151665422 | |||||||
chr1:151665523 | G | A | 1 | a0001c0001t0102g0016 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.907-410G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151665523 | |||||||
chr1:151665595 | G | A | 1 | a0001c0001t0105g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.907-338G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151665595 | |||||||
chr1:151665715 | A | G | 1 | a0001c0001t0065g0012 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.907-218A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151665715 | |||||||
chr1:151666327 | A | G | 2 | a0001c0003t0044g0099 a0001c0003t0044g0100 |
2 | HG02895.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.985+316A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151666327 | |||||||
chr1:151666490 | T | C | 1 | a0001c0001t0017g0146 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.985+479T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151666490 | |||||||
chr1:151666588 | T | C | 5 | a0001c0001t0003g0134 a0001c0001t0003g0137 a0001c0001t0003g0138 others(2): Show |
5 | NA18947.hp1 NA18953.hp1 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.985+577T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151666588 | |||||||
chr1:151667017 | C | G | 1 | a0001c0001t0083g0231 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.985+1006C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151667017 | |||||||
chr1:151667025 | G | A | 2 | a0001c0001t0001g0280 a0001c0001t0001g0339 |
2 | HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.985+1014G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151667025 | |||||||
chr1:151667052 | G | A | 1 | a0001c0001t0006g0101 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.985+1041G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151667052 | |||||||
chr1:151667247 | C | CA | 6 | a0001c0001t0015g0352 a0001c0001t0015g0353 a0001c0001t0015g0354 others(3): Show |
7 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.986-1213dupA | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 151667247 | ||||||
chr1:151667247 | C | CAAAAAAA others(1): Show |
35 | a0001c0001t0002g0005 a0001c0001t0002g0178 a0001c0001t0002g0179 others(32): Show |
37 | HG00423.hp2 HG00597.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.986-1220_986-1213d others(10): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 151667247 | ||||||
chr1:151667247 | C | CAAAAAAA others(2): Show |
59 | a0001c0001t0001g0220 a0001c0001t0002g0148 a0001c0001t0002g0288 others(56): Show |
60 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.986-1221_986-1213d others(11): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 151667247 | ||||||
chr1:151667247 | C | CAAAAAAA others(3): Show |
137 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(134): Show |
138 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.986-1222_986-1213d others(12): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 151667247 | ||||||
chr1:151667247 | C | CAAAAAAA others(4): Show |
80 | a0001c0001t0001g0229 a0001c0001t0001g0235 a0001c0001t0001g0246 others(77): Show |
81 | HG00408.hp2 HG00544.hp2 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.986-1223_986-1213d others(13): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 151667247 | ||||||
chr1:151667247 | C | CAAAAAAA others(5): Show |
27 | a0001c0001t0003g0140 a0001c0001t0004g0222 a0001c0001t0005g0028 others(24): Show |
27 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.986-1224_986-1213d others(14): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 151667247 | ||||||
chr1:151667247 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0005g0013 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.986-1213_986-1212i others(15): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 151667247 | ||||||
chr1:151667250 | A | AAAAAAAA others(1): Show |
10 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(7): Show |
10 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.986-1215_986-1214i others(10): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 151667250 | ||||||
chr1:151667386 | G | C | 355 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(352): Show |
361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.986-1086G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151667386 | |||||||
chr1:151667396 | T | G | 1 | a0001c0001t0009g0175 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.986-1076T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151667396 | |||||||
chr1:151667548 | G | A | 1 | a0001c0001t0059g0166 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.986-924G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151667548 | |||||||
chr1:151667563 | C | T | 2 | a0001c0001t0059g0166 a0001c0001t0065g0012 |
2 | HG02129.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.986-909C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151667563 | |||||||
chr1:151667574 | C | T | 1 | a0001c0001t0059g0166 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.986-898C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151667574 | |||||||
chr1:151667591 | C | T | 1 | a0001c0001t0105g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.986-881C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151667591 | |||||||
chr1:151667592 | G | A | 1 | a0001c0001t0059g0166 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.986-880G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151667592 | |||||||
chr1:151667596 | CG | C | 88 | a0001c0001t0002g0148 a0001c0001t0003g0117 a0001c0001t0003g0120 others(85): Show |
89 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.986-873delG | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 151667596 | ||||||
chr1:151667600 | C | T | 1 | a0001c0001t0059g0166 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.986-872C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151667600 | |||||||
chr1:151667632 | C | T | 1 | a0001c0001t0059g0166 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.986-840C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151667632 | |||||||
chr1:151667639 | A | C | 1 | a0001c0001t0059g0166 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.986-833A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151667639 | |||||||
chr1:151667641 | C | T | 1 | a0001c0001t0059g0166 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.986-831C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151667641 | |||||||
chr1:151667652 | C | T | 1 | a0001c0001t0059g0166 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.986-820C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151667652 | |||||||
chr1:151667687 | C | A | 1 | a0001c0001t0059g0166 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.986-785C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151667687 | |||||||
chr1:151667688 | G | A | 26 | a0001c0001t0005g0013 a0001c0001t0005g0028 a0001c0001t0005g0029 others(23): Show |
26 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.986-784G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151667688 | |||||||
chr1:151667689 | T | A | 1 | a0001c0001t0059g0166 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.986-783T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151667689 | |||||||
chr1:151667690 | A | G | 1 | a0001c0001t0059g0166 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.986-782A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151667690 | |||||||
chr1:151667696 | G | A | 1 | a0001c0001t0059g0166 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.986-776G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151667696 | |||||||
chr1:151667738 | A | C | 1 | a0001c0001t0102g0016 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.986-734A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151667738 | |||||||
chr1:151667756 | G | A | 9 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(6): Show |
9 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.986-716G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151667756 | |||||||
chr1:151667826 | C | CA | 11 | a0001c0001t0005g0038 a0001c0001t0010g0261 a0001c0001t0010g0277 others(8): Show |
11 | HG02004.hp1 HG02074.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.986-621dupA | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 151667826 | ||||||
chr1:151667826 | CA | C | 77 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(74): Show |
79 | HG00280.hp2 HG00642.hp1 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.986-621delA | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 151667826 | ||||||
chr1:151667826 | CAA | C | 35 | a0001c0001t0001g0213 a0001c0001t0001g0220 a0001c0001t0001g0239 others(32): Show |
35 | HG00323.hp1 HG00408.hp1 HG01433.hp1 others(32): Show |
intron_variant | MODIFIER | c.986-622_986-621del others(2): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 151667826 | ||||||
chr1:151667826 | CAAA | C | 126 | a0001c0001t0002g0005 a0001c0001t0002g0148 a0001c0001t0002g0178 others(123): Show |
129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.986-623_986-621del others(3): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 151667826 | ||||||
chr1:151668170 | T | C | 4 | a0001c0001t0028g0023 a0001c0001t0028g0024 a0001c0001t0028g0025 others(1): Show |
4 | HG02895.hp1 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.986-302T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151668170 | |||||||
chr1:151668314 | G | A | 1 | a0001c0001t0026g0301 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.986-158G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151668314 | |||||||
chr1:151668452 | G | C | 2 | a0001c0001t0001g0219 a0001c0001t0004g0218 |
2 | HG03492.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.986-20G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151668452 | |||||||
chr1:151669282 | A | C | 1 | a0001c0001t0011g0080 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1149+647A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151669282 | |||||||
chr1:151669459 | C | T | 1 | a0001c0001t0031g0007 | 2 | HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1149+824C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151669459 | |||||||
chr1:151669517 | C | T | 1 | a0001c0001t0105g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1149+882C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151669517 | |||||||
chr1:151669701 | G | A | 1 | a0001c0001t0054g0351 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1149+1066G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151669701 | |||||||
chr1:151669841 | A | G | 292 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(289): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1149+1206A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151669841 | |||||||
chr1:151670092 | TG | T | 5 | a0001c0001t0012g0004 a0001c0001t0012g0285 a0001c0001t0012g0286 others(2): Show |
5 | HG02723.hp1 HG02809.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1149+1460delG | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151670092 | ||||||
chr1:151670369 | A | C | 1 | a0001c0001t0036g0305 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1149+1734A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151670369 | |||||||
chr1:151670431 | C | T | 1 | a0001c0001t0007g0318 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1149+1796C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151670431 | |||||||
chr1:151670512 | C | T | 1 | a0001c0001t0068g0130 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1149+1877C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151670512 | |||||||
chr1:151670674 | C | G | 9 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(6): Show |
9 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1149+2039C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151670674 | |||||||
chr1:151670798 | A | G | 1 | a0001c0001t0029g0034 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1149+2163A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151670798 | |||||||
chr1:151670869 | T | C | 7 | a0001c0001t0006g0170 a0001c0001t0007g0185 a0001c0001t0009g0167 others(4): Show |
7 | HG00099.hp2 HG00738.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.1149+2234T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151670869 | |||||||
chr1:151670885 | T | C | 283 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(280): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.1149+2250T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151670885 | |||||||
chr1:151670902 | A | G | 147 | a0001c0001t0002g0005 a0001c0001t0002g0148 a0001c0001t0002g0178 others(144): Show |
150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.1149+2267A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151670902 | |||||||
chr1:151671058 | A | G | 1 | a0001c0001t0052g0359 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1149+2423A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151671058 | |||||||
chr1:151671236 | C | CT | 8 | a0001c0001t0008g0249 a0001c0001t0010g0277 a0001c0001t0016g0105 others(5): Show |
8 | HG02145.hp1 HG02280.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1149+2617dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151671236 | ||||||
chr1:151671236 | C | CTT | 5 | a0001c0001t0015g0352 a0001c0001t0015g0353 a0001c0001t0015g0354 others(2): Show |
6 | HG01884.hp2 HG02572.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1149+2616_1149+261 others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151671236 | ||||||
chr1:151671236 | CT | C | 39 | a0001c0001t0002g0005 a0001c0001t0002g0178 a0001c0001t0002g0179 others(36): Show |
41 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.1149+2617delT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151671236 | ||||||
chr1:151671255 | A | G | 1 | a0001c0001t0130g0243 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1149+2620A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151671255 | |||||||
chr1:151671297 | G | A | 1 | a0001c0001t0046g0019 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1149+2662G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151671297 | |||||||
chr1:151671609 | G | A | 1 | a0001c0001t0088g0307 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1149+2974G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151671609 | |||||||
chr1:151671817 | C | G | 3 | a0001c0001t0002g0005 a0001c0001t0002g0306 a0001c0001t0002g0315 |
4 | HG01081.hp1 HG01192.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.1149+3182C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151671817 | |||||||
chr1:151671883 | C | T | 1 | a0001c0001t0102g0016 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1149+3248C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151671883 | |||||||
chr1:151671900 | C | T | 1 | a0001c0001t0105g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1149+3265C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151671900 | |||||||
chr1:151671929 | A | G | 9 | a0001c0001t0015g0352 a0001c0001t0015g0353 a0001c0001t0015g0354 others(6): Show |
10 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1149+3294A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151671929 | |||||||
chr1:151671961 | T | G | 355 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(352): Show |
361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.1149+3326T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151671961 | |||||||
chr1:151672462 | A | G | 2 | a0001c0001t0007g0157 a0001c0001t0009g0155 |
2 | HG01071.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1149+3827A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151672462 | |||||||
chr1:151672574 | A | T | 1 | a0001c0001t0085g0310 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1149+3939A>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151672574 | |||||||
chr1:151672730 | T | C | 9 | a0001c0001t0028g0023 a0001c0001t0028g0024 a0001c0001t0028g0025 others(6): Show |
9 | HG02895.hp1 HG02895.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.1149+4095T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151672730 | |||||||
chr1:151672867 | C | CT | 7 | a0001c0001t0002g0178 a0001c0001t0002g0179 a0001c0001t0002g0180 others(4): Show |
7 | HG00323.hp2 HG00639.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.1149+4242dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151672867 | ||||||
chr1:151672877 | T | C | 1 | a0001c0001t0102g0016 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1149+4242T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151672877 | |||||||
chr1:151673181 | T | C | 1 | a0001c0001t0097g0197 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1149+4546T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151673181 | |||||||
chr1:151673442 | A | G | 11 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(8): Show |
11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1149+4807A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151673442 | |||||||
chr1:151674210 | G | GT | 10 | a0001c0001t0001g0280 a0001c0001t0015g0352 a0001c0001t0015g0353 others(7): Show |
11 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1149+5576dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151674210 | ||||||
chr1:151674472 | T | C | 146 | a0001c0001t0002g0005 a0001c0001t0002g0148 a0001c0001t0002g0178 others(143): Show |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.1149+5837T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151674472 | |||||||
chr1:151674531 | T | C | 89 | a0001c0001t0002g0148 a0001c0001t0003g0117 a0001c0001t0003g0120 others(86): Show |
90 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.1149+5896T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151674531 | |||||||
chr1:151674637 | G | A | 1 | a0001c0001t0086g0289 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1149+6002G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151674637 | |||||||
chr1:151674714 | G | A | 2 | a0001c0003t0044g0099 a0001c0003t0044g0100 |
2 | HG02895.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1149+6079G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151674714 | |||||||
chr1:151674926 | T | C | 3 | a0001c0001t0001g0217 a0001c0001t0001g0232 a0001c0001t0001g0273 |
3 | HG01978.hp2 HG02148.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.1149+6291T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151674926 | |||||||
chr1:151674975 | C | T | 2 | a0001c0003t0044g0099 a0001c0003t0044g0100 |
2 | HG02895.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1149+6340C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151674975 | |||||||
chr1:151674976 | G | A | 1 | a0001c0001t0105g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1149+6341G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151674976 | |||||||
chr1:151674982 | G | A | 16 | a0001c0001t0012g0004 a0001c0001t0012g0283 a0001c0001t0012g0284 others(13): Show |
16 | HG02109.hp2 HG02145.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1149+6347G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151674982 | |||||||
chr1:151675101 | A | G | 9 | a0001c0001t0015g0352 a0001c0001t0015g0353 a0001c0001t0015g0354 others(6): Show |
10 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1149+6466A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151675101 | |||||||
chr1:151675409 | CATAGTTA others(23): Show |
C | 1 | a0001c0001t0014g0040 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1149+6775_1149+680 others(34): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151675409 | |||||||
chr1:151675422 | C | T | 147 | a0001c0001t0002g0005 a0001c0001t0002g0148 a0001c0001t0002g0178 others(144): Show |
150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.1149+6787C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151675422 | |||||||
chr1:151675508 | A | G | 1 | a0001c0001t0048g0065 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1149+6873A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151675508 | |||||||
chr1:151675576 | G | C | 1 | a0001c0001t0046g0019 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1149+6941G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151675576 | |||||||
chr1:151675626 | A | G | 10 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(7): Show |
10 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1149+6991A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151675626 | |||||||
chr1:151675716 | ATGATGCT others(12): Show |
A | 1 | a0001c0001t0008g0245 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1149+7084_1149+710 others(23): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151675716 | ||||||
chr1:151675798 | C | G | 1 | a0001c0001t0050g0066 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1149+7163C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151675798 | |||||||
chr1:151675810 | C | CT | 37 | a0001c0001t0003g0122 a0001c0001t0003g0129 a0001c0001t0003g0131 others(34): Show |
37 | HG00280.hp1 HG01074.hp2 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.1149+7210dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151675810 | ||||||
chr1:151675810 | C | CTT | 23 | a0001c0001t0002g0148 a0001c0001t0003g0117 a0001c0001t0003g0120 others(20): Show |
23 | HG00099.hp1 HG00099.hp2 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.1149+7209_1149+721 others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151675810 | ||||||
chr1:151675810 | C | CTTT | 14 | a0001c0001t0003g0125 a0001c0001t0006g0008 a0001c0001t0009g0155 others(11): Show |
14 | HG00735.hp2 HG01168.hp2 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.1149+7208_1149+721 others(7): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151675810 | ||||||
chr1:151675810 | CT | C | 6 | a0001c0001t0007g0318 a0001c0001t0009g0320 a0001c0001t0018g0321 others(3): Show |
6 | HG02258.hp1 HG02622.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1149+7210delT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151675810 | ||||||
chr1:151675810 | CTT | C | 9 | a0001c0001t0002g0288 a0001c0001t0026g0299 a0001c0001t0047g0358 others(6): Show |
9 | HG01175.hp2 HG02055.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1149+7209_1149+721 others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151675810 | ||||||
chr1:151675810 | CTTT | C | 9 | a0001c0001t0002g0178 a0001c0001t0002g0179 a0001c0001t0002g0180 others(6): Show |
9 | HG00323.hp2 HG00597.hp2 HG00639.hp2 others(6): Show |
intron_variant | MODIFIER | c.1149+7208_1149+721 others(7): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151675810 | ||||||
chr1:151675810 | CTTTT | C | 34 | a0001c0001t0002g0005 a0001c0001t0002g0291 a0001c0001t0002g0293 others(31): Show |
36 | HG00423.hp2 HG01081.hp1 HG01192.hp1 others(33): Show |
intron_variant | MODIFIER | c.1149+7207_1149+721 others(8): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151675810 | ||||||
chr1:151675810 | CTTTTT | C | 41 | a0001c0001t0001g0215 a0001c0001t0009g0328 a0001c0001t0010g0257 others(38): Show |
42 | HG00438.hp1 HG00639.hp1 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.1149+7206_1149+721 others(9): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151675810 | ||||||
chr1:151675810 | CTTTTTT | C | 24 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0221 others(21): Show |
24 | HG00280.hp2 HG00438.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.1149+7205_1149+721 others(10): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151675810 | ||||||
chr1:151675810 | CTTTTTTT | C | 57 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(54): Show |
59 | HG00323.hp1 HG00642.hp1 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.1149+7204_1149+721 others(11): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151675810 | ||||||
chr1:151675810 | CTTTTTTT others(1): Show |
C | 10 | a0001c0001t0001g0235 a0001c0001t0001g0280 a0001c0001t0001g0339 others(7): Show |
10 | HG01257.hp1 HG02165.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1149+7203_1149+721 others(12): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151675810 | ||||||
chr1:151675810 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0016g0105 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1149+7197_1149+721 others(18): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151675810 | ||||||
chr1:151675810 | CTTTTTTT others(9): Show |
C | 60 | a0001c0001t0005g0013 a0001c0001t0005g0028 a0001c0001t0005g0029 others(57): Show |
60 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.1149+7195_1149+721 others(20): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151675810 | ||||||
chr1:151675810 | CTTTTTTT others(10): Show |
C | 7 | a0001c0001t0005g0032 a0001c0001t0011g0054 a0001c0001t0023g0141 others(4): Show |
7 | HG00408.hp1 HG02132.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1149+7194_1149+721 others(21): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151675810 | ||||||
chr1:151675810 | CTTTTTTT others(11): Show |
C | 1 | a0001c0001t0052g0359 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1149+7193_1149+721 others(22): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151675810 | ||||||
chr1:151675810 | CTTTTTTT others(12): Show |
C | 1 | a0001c0001t0006g0103 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1149+7192_1149+721 others(23): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151675810 | ||||||
chr1:151675818 | T | C | 3 | a0001c0001t0046g0017 a0001c0001t0046g0019 a0001c0001t0118g0018 |
3 | HG02145.hp1 HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1149+7183T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151675818 | |||||||
chr1:151675821 | T | C | 1 | a0001c0001t0065g0012 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1149+7186T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151675821 | |||||||
chr1:151675830 | T | C | 1 | a0001c0001t0108g0088 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1149+7195T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151675830 | |||||||
chr1:151676006 | T | A | 76 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(73): Show |
78 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1150-7350T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151676006 | |||||||
chr1:151676068 | G | T | 7 | a0001c0001t0028g0023 a0001c0001t0028g0024 a0001c0001t0028g0025 others(4): Show |
7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1150-7288G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151676068 | |||||||
chr1:151676101 | G | T | 11 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(8): Show |
11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1150-7255G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151676101 | |||||||
chr1:151676171 | G | C | 9 | a0001c0001t0015g0352 a0001c0001t0015g0353 a0001c0001t0015g0354 others(6): Show |
10 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1150-7185G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151676171 | |||||||
chr1:151676270 | ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0005g0061 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1150-7042_1150-703 others(14): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | ||||||
chr1:151676270 | ATTTTTTT others(4): Show |
A | 4 | a0001c0001t0017g0152 a0001c0001t0047g0358 a0001c0001t0063g0199 others(1): Show |
4 | HG02451.hp1 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1150-7043_1150-703 others(15): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | ||||||
chr1:151676270 | ATTTTTTT others(5): Show |
A | 5 | a0001c0001t0004g0272 a0001c0001t0005g0029 a0001c0001t0014g0043 others(2): Show |
5 | HG02083.hp1 HG02083.hp2 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.1150-7044_1150-703 others(16): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | ||||||
chr1:151676270 | ATTTTTTT others(6): Show |
A | 9 | a0001c0001t0010g0337 a0001c0001t0030g0035 a0001c0001t0030g0045 others(6): Show |
9 | HG00423.hp1 HG02071.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1150-7045_1150-703 others(17): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | ||||||
chr1:151676270 | ATTTTTTT others(7): Show |
A | 10 | a0001c0001t0005g0013 a0001c0001t0005g0056 a0001c0001t0005g0081 others(7): Show |
10 | HG00673.hp2 HG01099.hp1 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.1150-7046_1150-703 others(18): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | ||||||
chr1:151676270 | ATTTTTTT others(8): Show |
A | 13 | a0001c0001t0002g0294 a0001c0001t0010g0262 a0001c0001t0010g0278 others(10): Show |
13 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.1150-7047_1150-703 others(19): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | ||||||
chr1:151676270 | ATTTTTTT others(9): Show |
A | 32 | a0001c0001t0002g0288 a0001c0001t0002g0295 a0001c0001t0002g0315 others(29): Show |
32 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.1150-7048_1150-703 others(20): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | ||||||
chr1:151676270 | ATTTTTTT others(10): Show |
A | 61 | a0001c0001t0002g0178 a0001c0001t0002g0179 a0001c0001t0002g0180 others(58): Show |
63 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.1150-7049_1150-703 others(21): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | ||||||
chr1:151676270 | ATTTTTTT others(11): Show |
A | 41 | a0001c0001t0002g0005 a0001c0001t0002g0148 a0001c0001t0002g0293 others(38): Show |
42 | HG00408.hp2 HG00597.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1150-7050_1150-703 others(22): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | ||||||
chr1:151676270 | ATTTTTTT others(12): Show |
A | 6 | a0001c0001t0003g0123 a0001c0001t0003g0124 a0001c0001t0003g0125 others(3): Show |
6 | HG02922.hp2 HG03491.hp1 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.1150-7051_1150-703 others(23): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | ||||||
chr1:151676270 | ATTTTTTT others(14): Show |
A | 3 | a0001c0001t0020g0075 a0001c0001t0091g0331 a0001c0001t0122g0052 |
3 | HG02145.hp2 HG02148.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1150-7053_1150-703 others(25): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | ||||||
chr1:151676270 | ATTTTTTT others(15): Show |
A | 9 | a0001c0001t0011g0051 a0001c0001t0014g0050 a0001c0001t0019g0325 others(6): Show |
9 | HG01071.hp1 HG01255.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.1150-7054_1150-703 others(26): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | ||||||
chr1:151676270 | ATTTTTTT others(16): Show |
A | 9 | a0001c0001t0015g0353 a0001c0001t0016g0105 a0001c0001t0016g0108 others(6): Show |
9 | HG02258.hp2 HG02280.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1150-7055_1150-703 others(27): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | ||||||
chr1:151676270 | ATTTTTTT others(17): Show |
A | 19 | a0001c0001t0012g0004 a0001c0001t0012g0283 a0001c0001t0012g0284 others(16): Show |
19 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1150-7056_1150-703 others(28): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | ||||||
chr1:151676270 | ATTTTTTT others(18): Show |
A | 3 | a0001c0001t0096g0265 a0001c0001t0105g0014 a0001c0001t0113g0068 |
3 | HG02572.hp1 HG02698.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1150-7057_1150-703 others(29): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | ||||||
chr1:151676270 | ATTTTTTT others(19): Show |
A | 6 | a0001c0001t0001g0280 a0001c0001t0001g0339 a0001c0001t0031g0007 others(3): Show |
7 | HG02886.hp1 HG02895.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1150-7058_1150-703 others(30): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | ||||||
chr1:151676270 | ATTTTTTT others(21): Show |
A | 6 | a0001c0001t0043g0255 a0001c0001t0081g0090 a0001c0001t0094g0093 others(3): Show |
6 | HG02258.hp1 HG02647.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1150-7060_1150-703 others(32): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | ||||||
chr1:151676270 | ATTTTTTT others(22): Show |
A | 5 | a0001c0001t0005g0074 a0001c0001t0053g0349 a0001c0001t0082g0091 others(2): Show |
5 | HG02155.hp2 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1150-7061_1150-703 others(33): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | ||||||
chr1:151676270 | ATTTTTTT others(23): Show |
A | 1 | a0001c0001t0007g0164 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1150-7062_1150-703 others(34): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | ||||||
chr1:151676270 | ATTTTTTT others(24): Show |
A | 1 | a0001c0001t0014g0058 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1150-7063_1150-703 others(35): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | ||||||
chr1:151676270 | ATTTTTTT others(25): Show |
A | 4 | a0001c0001t0010g0256 a0001c0001t0010g0257 a0001c0001t0013g0258 others(1): Show |
4 | HG03927.hp1 NA18941.hp2 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.1150-7064_1150-703 others(36): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | ||||||
chr1:151676270 | ATTTTTTT others(26): Show |
A | 2 | a0001c0001t0001g0189 a0001c0001t0008g0249 |
2 | NA18979.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.1150-7065_1150-703 others(37): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | ||||||
chr1:151676270 | ATTTTTTT others(27): Show |
A | 71 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(68): Show |
73 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.1150-7066_1150-703 others(38): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | ||||||
chr1:151676270 | ATTTTTTT others(28): Show |
A | 4 | a0001c0001t0001g0213 a0001c0001t0001g0221 a0001c0001t0062g0198 others(1): Show |
4 | HG00735.hp1 NA18906.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.1150-7067_1150-703 others(39): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | ||||||
chr1:151676287 | T | C | 1 | a0001c0001t0029g0034 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1150-7069T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151676287 | |||||||
chr1:151676933 | G | GGT | 12 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(9): Show |
12 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1150-6404_1150-640 others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676933 | ||||||
chr1:151676954 | A | G | 2 | a0001c0001t0021g0338 a0001c0003t0044g0100 |
2 | HG00544.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1150-6402A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151676954 | |||||||
chr1:151677003 | A | G | 7 | a0001c0001t0028g0023 a0001c0001t0028g0024 a0001c0001t0028g0025 others(4): Show |
7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1150-6353A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151677003 | |||||||
chr1:151677104 | C | A | 1 | a0001c0001t0011g0072 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1150-6252C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151677104 | |||||||
chr1:151677141 | A | G | 7 | a0001c0001t0043g0255 a0001c0001t0081g0090 a0001c0001t0082g0091 others(4): Show |
7 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1150-6215A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151677141 | |||||||
chr1:151677150 | T | C | 3 | a0001c0001t0012g0283 a0001c0001t0074g0282 a0001c0001t0075g0281 |
3 | HG03139.hp1 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1150-6206T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151677150 | |||||||
chr1:151677740 | G | A | 4 | a0001c0001t0005g0038 a0001c0001t0045g0027 a0001c0001t0107g0087 others(1): Show |
4 | HG00408.hp2 NA19001.hp1 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.1150-5616G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151677740 | |||||||
chr1:151677865 | C | T | 7 | a0001c0001t0028g0023 a0001c0001t0028g0024 a0001c0001t0028g0025 others(4): Show |
7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1150-5491C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151677865 | |||||||
chr1:151677991 | G | A | 1 | a0001c0001t0008g0249 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1150-5365G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151677991 | |||||||
chr1:151678039 | T | C | 1 | a0001c0001t0050g0066 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1150-5317T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151678039 | |||||||
chr1:151678084 | G | A | 4 | a0001c0001t0008g0104 a0001c0001t0008g0208 a0001c0001t0032g0200 others(1): Show |
4 | NA18946.hp2 NA18971.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.1150-5272G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151678084 | |||||||
chr1:151678271 | C | A | 1 | a0001c0001t0105g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1150-5085C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151678271 | |||||||
chr1:151678289 | T | G | 1 | a0001c0001t0001g0236 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1150-5067T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151678289 | |||||||
chr1:151678352 | A | G | 1 | a0001c0001t0014g0070 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1150-5004A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151678352 | |||||||
chr1:151678505 | A | G | 1 | a0001c0001t0020g0060 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1150-4851A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151678505 | |||||||
chr1:151678540 | G | C | 1 | a0001c0001t0049g0082 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1150-4816G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151678540 | |||||||
chr1:151678704 | A | AT | 83 | a0001c0001t0002g0148 a0001c0001t0003g0117 a0001c0001t0003g0120 others(80): Show |
84 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.1150-4645dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151678704 | ||||||
chr1:151678713 | T | C | 1 | a0001c0001t0052g0359 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1150-4643T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151678713 | |||||||
chr1:151678782 | C | T | 1 | a0001c0001t0116g0098 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1150-4574C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151678782 | |||||||
chr1:151678825 | T | C | 10 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(7): Show |
10 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1150-4531T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151678825 | |||||||
chr1:151678989 | T | C | 1 | a0001c0001t0113g0068 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1150-4367T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151678989 | |||||||
chr1:151679228 | G | T | 9 | a0001c0001t0012g0004 a0001c0001t0012g0283 a0001c0001t0012g0284 others(6): Show |
9 | HG02486.hp2 HG02723.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1150-4128G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151679228 | |||||||
chr1:151679343 | A | G | 1 | a0001c0001t0052g0359 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1150-4013A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151679343 | |||||||
chr1:151679667 | C | G | 1 | a0001c0001t0097g0197 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1150-3689C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151679667 | |||||||
chr1:151679737 | G | A | 1 | a0001c0001t0105g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1150-3619G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151679737 | |||||||
chr1:151679793 | G | A | 77 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(74): Show |
79 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.1150-3563G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151679793 | |||||||
chr1:151679976 | G | A | 2 | a0001c0001t0062g0198 a0001c0001t0063g0199 |
2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1150-3380G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151679976 | |||||||
chr1:151679985 | C | T | 1 | a0001c0001t0052g0359 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1150-3371C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151679985 | |||||||
chr1:151680016 | A | G | 1 | a0001c0001t0008g0245 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1150-3340A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151680016 | |||||||
chr1:151680053 | T | C | 210 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(207): Show |
213 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.1150-3303T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151680053 | |||||||
chr1:151680152 | CT | C | 138 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(135): Show |
141 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.1150-3187delT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151680152 | ||||||
chr1:151680152 | CTT | C | 45 | a0001c0001t0001g0214 a0001c0001t0001g0356 a0001c0001t0002g0005 others(42): Show |
47 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.1150-3188_1150-318 others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151680152 | ||||||
chr1:151680183 | G | A | 7 | a0001c0001t0028g0023 a0001c0001t0028g0024 a0001c0001t0028g0025 others(4): Show |
7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1150-3173G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151680183 | |||||||
chr1:151680386 | C | A | 3 | a0001c0001t0014g0070 a0001c0001t0020g0076 a0001c0001t0029g0064 |
3 | NA18946.hp1 NA18982.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1150-2970C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151680386 | |||||||
chr1:151680435 | C | T | 89 | a0001c0001t0002g0148 a0001c0001t0003g0117 a0001c0001t0003g0120 others(86): Show |
90 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.1150-2921C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151680435 | |||||||
chr1:151680568 | G | C | 1 | a0001c0001t0010g0256 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1150-2788G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151680568 | |||||||
chr1:151680786 | C | G | 1 | a0001c0001t0105g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1150-2570C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151680786 | |||||||
chr1:151680836 | A | C | 117 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(114): Show |
120 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.1150-2520A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151680836 | |||||||
chr1:151680921 | T | G | 5 | a0001c0001t0012g0004 a0001c0001t0012g0285 a0001c0001t0012g0286 others(2): Show |
5 | HG02723.hp1 HG02809.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1150-2435T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151680921 | |||||||
chr1:151681037 | C | T | 1 | a0001c0001t0117g0089 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1150-2319C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151681037 | |||||||
chr1:151681105 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1150-2251C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151681105 | |||||||
chr1:151681231 | C | T | 352 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(349): Show |
358 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(355): Show |
intron_variant | MODIFIER | c.1150-2125C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151681231 | |||||||
chr1:151681235 | C | CT | 19 | a0001c0001t0001g0205 a0001c0001t0002g0288 a0001c0001t0002g0295 others(16): Show |
19 | HG00597.hp2 HG00673.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.1150-2097dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | ||||||
chr1:151681235 | C | CTT | 6 | a0001c0001t0002g0293 a0001c0001t0004g0204 a0001c0001t0010g0257 others(3): Show |
6 | HG02056.hp1 HG02572.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.1150-2098_1150-209 others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | ||||||
chr1:151681235 | C | CTTTTT | 6 | a0001c0001t0010g0277 a0001c0001t0010g0279 a0001c0001t0028g0024 others(3): Show |
6 | HG02486.hp1 HG02896.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1150-2101_1150-209 others(9): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | ||||||
chr1:151681235 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0196 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1150-2106_1150-209 others(14): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | ||||||
chr1:151681235 | C | CTTTTTTT others(4): Show |
4 | a0001c0001t0001g0232 a0001c0001t0008g0193 a0001c0001t0037g0192 others(1): Show |
4 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1150-2107_1150-209 others(15): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | ||||||
chr1:151681235 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0001g0236 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1150-2108_1150-209 others(16): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | ||||||
chr1:151681235 | C | CTTTTTTT others(6): Show |
3 | a0001c0001t0001g0195 a0001c0001t0001g0235 a0001c0001t0004g0272 |
3 | HG02165.hp2 HG02886.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1150-2109_1150-209 others(17): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | ||||||
chr1:151681235 | C | CTTTTTTT others(8): Show |
6 | a0001c0001t0010g0256 a0001c0001t0013g0276 a0001c0001t0043g0336 others(3): Show |
6 | HG00639.hp1 HG01168.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1150-2111_1150-209 others(19): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | ||||||
chr1:151681235 | C | CTTTTTTT others(9): Show |
3 | a0001c0001t0010g0261 a0001c0001t0010g0262 a0001c0001t0092g0266 |
3 | HG02155.hp1 NA18985.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1150-2112_1150-209 others(20): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | ||||||
chr1:151681235 | C | CTTTTTTT others(10): Show |
2 | a0001c0001t0013g0260 a0001c0001t0013g0263 |
2 | HG00438.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.1150-2113_1150-209 others(21): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | ||||||
chr1:151681235 | C | CTTTTTTT others(12): Show |
5 | a0001c0001t0001g0356 a0001c0001t0013g0264 a0001c0001t0130g0243 others(2): Show |
6 | HG01099.hp1 NA18947.hp2 NA18991.hp2 others(3): Show |
intron_variant | MODIFIER | c.1150-2115_1150-209 others(23): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | ||||||
chr1:151681235 | C | CTTTTTTT others(13): Show |
1 | a0002c0002t0001g0226 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1150-2116_1150-209 others(24): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | ||||||
chr1:151681235 | C | CTTTTTTT others(14): Show |
4 | a0001c0001t0010g0337 a0001c0001t0081g0090 a0001c0001t0094g0093 others(1): Show |
4 | HG02258.hp1 HG02738.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1150-2117_1150-209 others(25): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | ||||||
chr1:151681235 | C | CTTTTTTT others(15): Show |
1 | a0001c0001t0101g0094 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1150-2118_1150-209 others(26): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | ||||||
chr1:151681235 | C | CTTTTTTT others(16): Show |
3 | a0001c0001t0001g0273 a0002c0002t0001g0227 a0002c0002t0001g0228 |
3 | HG02273.hp1 NA18941.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1150-2119_1150-209 others(27): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | ||||||
chr1:151681235 | C | CTTTTTTT others(17): Show |
7 | a0001c0001t0001g0190 a0001c0001t0001g0210 a0001c0001t0001g0223 others(4): Show |
7 | HG00738.hp2 HG02523.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.1150-2120_1150-209 others(28): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | ||||||
chr1:151681235 | C | CTTTTTTT others(18): Show |
11 | a0001c0001t0001g0002 a0001c0001t0001g0189 a0001c0001t0001g0246 others(8): Show |
12 | HG00280.hp2 HG00438.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.1150-2097_1150-209 others(29): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | ||||||
chr1:151681235 | C | CTTTTTTT others(19): Show |
7 | a0001c0001t0001g0211 a0001c0001t0001g0213 a0001c0001t0001g0233 others(4): Show |
7 | HG01516.hp1 HG03195.hp2 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.1150-2097_1150-209 others(30): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | ||||||
chr1:151681235 | C | CTTTTTTT others(21): Show |
1 | a0001c0001t0004g0234 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1150-2097_1150-209 others(32): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | ||||||
chr1:151681235 | C | CTTTTTTT others(22): Show |
2 | a0001c0001t0004g0237 a0001c0001t0008g0208 |
2 | NA18963.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1150-2097_1150-209 others(33): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | ||||||
chr1:151681235 | C | CTTTTTTT others(24): Show |
3 | a0001c0001t0001g0203 a0001c0001t0001g0217 a0001c0001t0004g0222 |
3 | HG01978.hp2 HG04115.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1150-2097_1150-209 others(35): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | ||||||
chr1:151681235 | C | CTTTTTTT others(25): Show |
2 | a0001c0001t0001g0224 a0001c0001t0004g0253 |
2 | HG01433.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1150-2097_1150-209 others(36): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | ||||||
chr1:151681235 | C | CTTTTTTT others(28): Show |
1 | a0001c0001t0001g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1150-2097_1150-209 others(39): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | ||||||
chr1:151681235 | C | CTTTTTTT others(29): Show |
1 | a0001c0001t0001g0214 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1150-2097_1150-209 others(40): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | ||||||
chr1:151681235 | C | CTTTTTTT others(32): Show |
2 | a0001c0001t0001g0239 a0001c0001t0004g0207 |
2 | NA18960.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.1150-2097_1150-209 others(43): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | ||||||
chr1:151681235 | C | CTTTTTTT others(33): Show |
1 | a0001c0001t0001g0241 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1150-2097_1150-209 others(44): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | ||||||
chr1:151681235 | CT | C | 17 | a0001c0001t0001g0220 a0001c0001t0012g0004 a0001c0001t0012g0283 others(14): Show |
17 | HG00323.hp1 HG02109.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1150-2097delT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | ||||||
chr1:151681235 | CTT | C | 6 | a0001c0001t0001g0010 a0001c0001t0008g0201 a0001c0001t0008g0245 others(3): Show |
6 | HG01175.hp1 NA18962.hp2 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.1150-2098_1150-209 others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | ||||||
chr1:151681235 | CTTT | C | 8 | a0001c0001t0001g0230 a0001c0001t0001g0238 a0001c0001t0001g0244 others(5): Show |
8 | HG00642.hp1 HG01167.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1150-2099_1150-209 others(7): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | ||||||
chr1:151681235 | CTTTT | C | 22 | a0001c0001t0005g0077 a0001c0001t0005g0081 a0001c0001t0011g0069 others(19): Show |
23 | HG01884.hp2 HG02080.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.1150-2100_1150-209 others(8): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | ||||||
chr1:151681235 | CTTTTT | C | 67 | a0001c0001t0005g0013 a0001c0001t0005g0028 a0001c0001t0005g0029 others(64): Show |
67 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.1150-2101_1150-209 others(9): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | ||||||
chr1:151681404 | G | A | 2 | a0001c0001t0018g0127 a0001c0001t0072g0159 |
2 | HG01934.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1150-1952G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151681404 | |||||||
chr1:151681532 | G | A | 4 | a0001c0001t0005g0038 a0001c0001t0045g0027 a0001c0001t0107g0087 others(1): Show |
4 | HG00408.hp2 NA19001.hp1 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.1150-1824G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151681532 | |||||||
chr1:151681575 | C | G | 11 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(8): Show |
11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1150-1781C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151681575 | |||||||
chr1:151681783 | C | CTTTTTAG others(31): Show |
5 | a0001c0001t0011g0055 a0001c0001t0020g0053 a0001c0001t0020g0057 others(2): Show |
5 | HG00741.hp2 HG01256.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.1150-1571_1150-153 others(42): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681783 | ||||||
chr1:151681952 | C | T | 1 | a0001c0001t0017g0145 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1150-1404C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151681952 | |||||||
chr1:151682313 | T | G | 1 | a0001c0001t0083g0231 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1150-1043T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151682313 | |||||||
chr1:151682512 | G | A | 1 | a0001c0001t0105g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1150-844G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151682512 | |||||||
chr1:151682543 | G | A | 7 | a0001c0001t0028g0023 a0001c0001t0028g0024 a0001c0001t0028g0025 others(4): Show |
7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1150-813G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151682543 | |||||||
chr1:151682545 | A | G | 7 | a0001c0001t0043g0255 a0001c0001t0081g0090 a0001c0001t0082g0091 others(4): Show |
7 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1150-811A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151682545 | |||||||
chr1:151682886 | T | C | 1 | a0001c0001t0002g0295 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1150-470T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151682886 | |||||||
chr1:151682890 | C | T | 1 | a0001c0001t0002g0295 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1150-466C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151682890 | |||||||
chr1:151682891 | T | A | 1 | a0001c0001t0002g0295 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1150-465T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151682891 | |||||||
chr1:151682892 | G | C | 1 | a0001c0001t0002g0295 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1150-464G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151682892 | |||||||
chr1:151682893 | G | A | 1 | a0001c0001t0002g0295 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1150-463G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151682893 | |||||||
chr1:151682894 | G | T | 1 | a0001c0001t0002g0295 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1150-462G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151682894 | |||||||
chr1:151682895 | C | A | 1 | a0001c0001t0002g0295 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1150-461C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151682895 | |||||||
chr1:151682967 | G | A | 1 | a0001c0001t0036g0160 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1150-389G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151682967 | |||||||
chr1:151683051 | C | A | 212 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(209): Show |
215 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(212): Show |
intron_variant | MODIFIER | c.1150-305C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151683051 | |||||||
chr1:151683151 | A | G | 41 | a0001c0001t0002g0005 a0001c0001t0002g0178 a0001c0001t0002g0179 others(38): Show |
43 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.1150-205A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151683151 | |||||||
chr1:151683275 | C | T | 27 | a0001c0001t0004g0272 a0001c0001t0010g0256 a0001c0001t0010g0257 others(24): Show |
27 | HG00438.hp1 HG00639.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.1150-81C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151683275 | |||||||
chr1:151683594 | C | T | 1 | a0001c0001t0105g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1239+149C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151683594 | |||||||
chr1:151683728 | G | A | 1 | a0001c0001t0029g0086 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1239+283G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151683728 | |||||||
chr1:151683850 | A | G | 20 | a0001c0001t0004g0272 a0001c0001t0010g0256 a0001c0001t0010g0257 others(17): Show |
20 | HG00438.hp1 HG00639.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1239+405A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151683850 | |||||||
chr1:151683921 | C | A | 9 | a0001c0001t0015g0352 a0001c0001t0015g0353 a0001c0001t0015g0354 others(6): Show |
10 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1239+476C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151683921 | |||||||
chr1:151684299 | C | G | 1 | a0001c0001t0043g0336 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1239+854C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151684299 | |||||||
chr1:151684418 | G | A | 62 | a0001c0001t0005g0013 a0001c0001t0005g0028 a0001c0001t0005g0029 others(59): Show |
62 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.1239+973G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151684418 | |||||||
chr1:151684598 | T | C | 16 | a0001c0001t0012g0004 a0001c0001t0012g0283 a0001c0001t0012g0284 others(13): Show |
16 | HG02109.hp2 HG02145.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1239+1153T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151684598 | |||||||
chr1:151684635 | C | A | 82 | a0001c0001t0005g0013 a0001c0001t0005g0028 a0001c0001t0005g0029 others(79): Show |
82 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.1239+1190C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151684635 | |||||||
chr1:151684934 | G | A | 2 | a0001c0001t0001g0219 a0001c0001t0004g0218 |
2 | HG03492.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1239+1489G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151684934 | |||||||
chr1:151685190 | T | A | 1 | a0001c0001t0102g0016 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1239+1745T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151685190 | |||||||
chr1:151685360 | T | G | 1 | a0001c0001t0001g0280 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1239+1915T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151685360 | |||||||
chr1:151685368 | A | G | 2 | a0001c0001t0014g0040 a0001c0001t0014g0058 |
2 | NA18988.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.1239+1923A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151685368 | |||||||
chr1:151685419 | C | T | 1 | a0001c0001t0013g0260 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1239+1974C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151685419 | |||||||
chr1:151685479 | C | G | 1 | a0001c0001t0007g0176 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1239+2034C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151685479 | |||||||
chr1:151685677 | G | A | 10 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(7): Show |
10 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1239+2232G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151685677 | |||||||
chr1:151685786 | AAGTAATA others(9): Show |
A | 1 | a0001c0001t0005g0038 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1239+2343_1239+235 others(20): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 151685786 | ||||||
chr1:151685792 | T | G | 7 | a0001c0001t0028g0023 a0001c0001t0028g0024 a0001c0001t0028g0025 others(4): Show |
7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1239+2347T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151685792 | |||||||
chr1:151686067 | G | A | 2 | a0001c0001t0024g0343 a0001c0001t0024g0344 |
2 | HG00735.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1239+2622G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151686067 | |||||||
chr1:151686089 | C | A | 1 | a0001c0001t0033g0342 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1239+2644C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151686089 | |||||||
chr1:151686178 | A | G | 16 | a0001c0001t0012g0004 a0001c0001t0012g0283 a0001c0001t0012g0284 others(13): Show |
16 | HG02109.hp2 HG02145.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1239+2733A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151686178 | |||||||
chr1:151686463 | G | A | 8 | a0001c0001t0011g0054 a0001c0001t0011g0055 a0001c0001t0020g0053 others(5): Show |
8 | HG00741.hp2 HG01256.hp2 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.1239+3018G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151686463 | |||||||
chr1:151686547 | G | A | 11 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(8): Show |
11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1239+3102G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151686547 | |||||||
chr1:151686592 | T | A | 1 | a0001c0001t0052g0359 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1239+3147T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151686592 | |||||||
chr1:151686595 | A | G | 117 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(114): Show |
120 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.1239+3150A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151686595 | |||||||
chr1:151686890 | T | C | 73 | a0001c0001t0005g0013 a0001c0001t0005g0028 a0001c0001t0005g0029 others(70): Show |
73 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.1239+3445T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151686890 | |||||||
chr1:151687311 | G | A | 9 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(6): Show |
9 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1239+3866G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151687311 | |||||||
chr1:151687486 | A | C | 1 | a0001c0001t0018g0290 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1239+4041A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151687486 | |||||||
chr1:151687603 | C | G | 7 | a0001c0001t0043g0255 a0001c0001t0081g0090 a0001c0001t0082g0091 others(4): Show |
7 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1239+4158C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151687603 | |||||||
chr1:151687675 | G | A | 4 | a0001c0001t0003g0120 a0001c0001t0003g0129 a0001c0001t0003g0140 others(1): Show |
4 | NA18943.hp1 NA19062.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.1239+4230G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151687675 | |||||||
chr1:151687863 | G | A | 1 | a0001c0001t0009g0165 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1239+4418G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151687863 | |||||||
chr1:151687902 | C | G | 1 | a0001c0001t0040g0144 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1239+4457C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151687902 | |||||||
chr1:151687945 | C | CA | 9 | a0001c0001t0002g0288 a0001c0001t0002g0295 a0001c0001t0002g0316 others(6): Show |
9 | HG02055.hp2 HG02109.hp2 HG06807.hp2 others(6): Show |
intron_variant | MODIFIER | c.1240-4475dupA | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 151687945 | ||||||
chr1:151687945 | CA | C | 9 | a0001c0001t0001g0268 a0001c0001t0046g0017 a0001c0001t0046g0019 others(6): Show |
9 | HG01081.hp2 HG02145.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1240-4475delA | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 151687945 | ||||||
chr1:151687945 | CAA | C | 202 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(199): Show |
205 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.1240-4476_1240-447 others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 151687945 | ||||||
chr1:151687960 | A | C | 2 | a0001c0001t0001g0229 a0001c0001t0004g0216 |
2 | HG02523.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.1240-4475A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151687960 | |||||||
chr1:151687971 | C | CA | 89 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0189 others(86): Show |
91 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.1240-4453dupA | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 151687971 | ||||||
chr1:151687979 | A | G | 3 | a0001c0001t0046g0017 a0001c0001t0046g0019 a0001c0001t0118g0018 |
3 | HG02145.hp1 HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1240-4456A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151687979 | |||||||
chr1:151688048 | A | G | 7 | a0001c0001t0028g0023 a0001c0001t0028g0024 a0001c0001t0028g0025 others(4): Show |
7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1240-4387A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151688048 | |||||||
chr1:151688139 | A | G | 9 | a0001c0001t0001g0011 a0001c0001t0001g0196 a0001c0001t0001g0215 others(6): Show |
9 | HG00323.hp1 HG00735.hp1 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1240-4296A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151688139 | |||||||
chr1:151688275 | G | A | 1 | a0001c0001t0105g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1240-4160G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151688275 | |||||||
chr1:151688295 | A | G | 1 | a0001c0001t0017g0126 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1240-4140A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151688295 | |||||||
chr1:151688307 | C | A | 1 | a0001c0001t0008g0201 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1240-4128C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151688307 | |||||||
chr1:151688522 | C | T | 2 | a0001c0001t0037g0192 a0001c0001t0037g0194 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1240-3913C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151688522 | |||||||
chr1:151688631 | C | CA | 208 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(205): Show |
211 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(208): Show |
intron_variant | MODIFIER | c.1240-3787dupA | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 151688631 | ||||||
chr1:151688631 | C | CAA | 9 | a0001c0001t0001g0214 a0001c0001t0010g0337 a0001c0001t0043g0255 others(6): Show |
9 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1240-3788_1240-378 others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 151688631 | ||||||
chr1:151688917 | C | A | 2 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
2 | HG01515.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1240-3518C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151688917 | |||||||
chr1:151689107 | C | G | 1 | a0001c0001t0105g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1240-3328C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151689107 | |||||||
chr1:151689108 | A | C | 3 | a0001c0001t0006g0169 a0001c0001t0006g0171 a0001c0001t0006g0172 |
3 | HG01261.hp2 HG03710.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1240-3327A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151689108 | |||||||
chr1:151689116 | C | T | 8 | a0001c0001t0030g0035 a0001c0001t0030g0045 a0001c0001t0030g0047 others(5): Show |
8 | HG00423.hp1 HG02071.hp2 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.1240-3319C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151689116 | |||||||
chr1:151689124 | G | A | 4 | a0001c0001t0046g0017 a0001c0001t0046g0019 a0001c0001t0102g0016 others(1): Show |
4 | HG02145.hp1 HG02280.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1240-3311G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151689124 | |||||||
chr1:151689637 | G | A | 94 | a0001c0001t0005g0013 a0001c0001t0005g0028 a0001c0001t0005g0029 others(91): Show |
94 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.1240-2798G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151689637 | |||||||
chr1:151689737 | C | T | 1 | a0001c0001t0130g0243 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1240-2698C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151689737 | |||||||
chr1:151689762 | A | G | 1 | a0001c0001t0063g0199 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1240-2673A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151689762 | |||||||
chr1:151689850 | CT | C | 109 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(106): Show |
111 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.1240-2573delT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 151689850 | ||||||
chr1:151689917 | C | T | 2 | a0001c0001t0103g0026 a0001c0001t0104g0357 |
2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1240-2518C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151689917 | |||||||
chr1:151690223 | G | A | 1 | a0001c0001t0070g0345 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1240-2212G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151690223 | |||||||
chr1:151690337 | C | T | 1 | a0001c0001t0058g0341 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1240-2098C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151690337 | |||||||
chr1:151690510 | G | T | 7 | a0001c0001t0028g0023 a0001c0001t0028g0024 a0001c0001t0028g0025 others(4): Show |
7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1240-1925G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151690510 | |||||||
chr1:151690616 | G | T | 1 | a0001c0001t0109g0020 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1240-1819G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151690616 | |||||||
chr1:151690617 | T | G | 1 | a0003c0005t0002g0297 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1240-1818T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151690617 | |||||||
chr1:151690638 | G | A | 1 | a0001c0001t0004g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1240-1797G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151690638 | |||||||
chr1:151690662 | G | A | 4 | a0001c0001t0008g0191 a0001c0001t0008g0193 a0001c0001t0037g0192 others(1): Show |
4 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240-1773G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151690662 | |||||||
chr1:151690677 | G | A | 1 | a0001c0001t0096g0265 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1240-1758G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151690677 | |||||||
chr1:151691157 | C | T | 1 | a0001c0001t0065g0012 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1240-1278C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151691157 | |||||||
chr1:151691305 | A | G | 82 | a0001c0001t0005g0013 a0001c0001t0005g0028 a0001c0001t0005g0029 others(79): Show |
82 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.1240-1130A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151691305 | |||||||
chr1:151691356 | A | G | 1 | a0001c0001t0001g0203 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1240-1079A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151691356 | |||||||
chr1:151691387 | G | A | 1 | a0001c0001t0105g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1240-1048G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151691387 | |||||||
chr1:151691466 | G | GT | 25 | a0001c0001t0001g0010 a0001c0001t0001g0232 a0001c0001t0001g0244 others(22): Show |
25 | HG00544.hp2 HG00642.hp1 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.1240-951dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 151691466 | ||||||
chr1:151691875 | T | C | 6 | a0001c0001t0008g0201 a0001c0001t0008g0247 a0001c0001t0008g0248 others(3): Show |
6 | NA18962.hp2 NA18966.hp2 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.1240-560T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151691875 | |||||||
chr1:151691966 | G | A | 1 | a0001c0001t0052g0359 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1240-469G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151691966 | |||||||
chr1:151692402 | C | T | 2 | a0001c0001t0006g0101 a0001c0001t0006g0102 |
2 | HG01934.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1240-33C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151692402 | |||||||
chr1:151692406 | C | CT | 84 | a0001c0001t0001g0011 a0001c0001t0001g0190 a0001c0001t0001g0213 others(81): Show |
84 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(81): Show |
splice_acceptor_variant&intron_variant | HIGH | c.1240-3dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 151692406 | ||||||
chr1:151692406 | C | CTT | 68 | a0001c0001t0001g0002 a0001c0001t0001g0189 a0001c0001t0001g0195 others(65): Show |
70 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(67): Show |
splice_acceptor_variant&intron_variant | HIGH | c.1240-4_1240-3dupTT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 151692406 | ||||||
chr1:151692406 | C | CTTT | 14 | a0001c0001t0001g0010 a0001c0001t0001g0212 a0001c0001t0001g0215 others(11): Show |
14 | HG00280.hp2 HG01081.hp2 HG01167.hp1 others(11): Show |
splice_acceptor_variant&intron_variant | HIGH | c.1240-5_1240-3dupTT others(1): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 151692406 | ||||||
chr1:151692406 | CT | C | 21 | a0001c0001t0007g0162 a0001c0001t0016g0105 a0001c0001t0016g0106 others(18): Show |
21 | HG01515.hp2 HG02109.hp1 HG02145.hp1 others(18): Show |
splice_region_variant&intron_variant | LOW | c.1240-3delT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 151692406 | ||||||
chr1:151692406 | CTT | C | 70 | a0001c0001t0005g0013 a0001c0001t0005g0028 a0001c0001t0005g0029 others(67): Show |
70 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(67): Show |
splice_region_variant&intron_variant | LOW | c.1240-4_1240-3delTT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 151692406 | ||||||
chr1:151692406 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0009g0328 | 1 | NA19068.hp2 | splice_region_variant&intron_variant | LOW | c.1240-13_1240-3delT others(10): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 151692406 | ||||||
chr1:151692667 | TA | T | 5 | a0001c0001t0018g0127 a0001c0001t0036g0160 a0001c0001t0036g0305 others(2): Show |
5 | HG01934.hp2 NA19012.hp1 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.1389+84delA | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 9/11 | chr1 | 151692667 | |||||||
chr1:151692849 | C | T | 11 | a0001c0001t0016g0105 a0001c0001t0016g0106 a0001c0001t0016g0108 others(8): Show |
11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1390-62C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 9/11 | chr1 | 151692849 | |||||||
chr1:151693078 | G | T | 1 | a0003c0005t0002g0297 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1518+39G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 10/11 | chr1 | 151693078 | |||||||
chr1:151693086 | G | GT | 74 | a0001c0001t0005g0013 a0001c0001t0005g0028 a0001c0001t0005g0029 others(71): Show |
74 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.1518+57dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 151693086 | ||||||
chr1:151693125 | T | G | 2 | a0001c0001t0002g0306 a0001c0001t0002g0315 |
2 | HG02055.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1518+86T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 10/11 | chr1 | 151693125 | |||||||
chr1:151693381 | CT | C | 83 | a0001c0001t0005g0013 a0001c0001t0005g0028 a0001c0001t0005g0029 others(80): Show |
83 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.1519-42delT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 10/11 | chr1 | 151693381 | |||||||
chr1:151693549 | T | TG | 5 | a0001c0001t0008g0104 a0001c0001t0008g0208 a0001c0001t0008g0245 others(2): Show |
5 | NA18946.hp2 NA18971.hp1 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.1578+68dupG | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | 151693549 | ||||||
chr1:151693659 | G | C | 2 | a0001c0001t0018g0321 a0001c0001t0018g0322 |
2 | HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1578+176G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 11/11 | chr1 | 151693659 | |||||||
chr1:151693677 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1578+194C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 11/11 | chr1 | 151693677 | |||||||
chr1:151694036 | A | G | 7 | a0001c0001t0028g0023 a0001c0001t0028g0024 a0001c0001t0028g0025 others(4): Show |
7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1579-334A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 11/11 | chr1 | 151694036 | |||||||
chr1:151694325 | G | A | 1 | a0001c0001t0051g0067 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1579-45G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 11/11 | chr1 | 151694325 |