Item | Value |
---|---|
geneid | 4330 |
ensemblid | ENSG00000169184.7 |
hgncid | 7180 |
symbol | MN1 |
name | MN1 proto-oncogene, transcriptional regulator |
refseq_nuc | NM_002430.3 |
refseq_prot | NP_002421.3 |
ensembl_nuc | ENST00000302326.5 |
ensembl_prot | ENSP00000304956.4 |
mane_status | MANE Select |
chr | chr22 |
start | 27748277 |
end | 27801756 |
strand | - |
ver | v1.2 |
region | chr22:27748277-27801756 |
region5000 | chr22:27743277-27806756 |
regionname0 | MN1_chr22_27748277_27801756 |
regionname5000 | MN1_chr22_27743277_27806756 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1320 | 317 | 68 | 64 | 138 | 13 | 32 | 103 | MN1_chr22_27743277_27806756 | MN1 | MFGLD others(1315): Show |
chr22 | 27743277 | 27806756 |
a0002 | 0/0 | 1321 | 50 | 18 | 10 | 16 | 4 | 2 | 10 | MN1_chr22_27743277_27806756 | MN1 | MFGLD others(1316): Show |
chr22 | 27743277 | 27806756 |
a0003 | 0/0 | 1318 | 12 | 5 | 3 | 4 | 0 | 0 | 3 | MN1_chr22_27743277_27806756 | MN1 | MFGLD others(1313): Show |
chr22 | 27743277 | 27806756 |
a0004 | 0/0 | 1320 | 5 | 0 | 3 | 0 | 1 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | MFGLD others(1315): Show |
chr22 | 27743277 | 27806756 |
a0005 | 0/0 | 1319 | 3 | 2 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | MFGLD others(1314): Show |
chr22 | 27743277 | 27806756 |
a0006 | 0/0 | 1320 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | MFGLD others(1315): Show |
chr22 | 27743277 | 27806756 |
a0007 | 0/0 | 1320 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | MFGLD others(1315): Show |
chr22 | 27743277 | 27806756 |
a0008 | 0/0 | 1326 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | MFGLD others(1321): Show |
chr22 | 27743277 | 27806756 |
a0009 | 0/0 | 1320 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | MFGLD others(1315): Show |
chr22 | 27743277 | 27806756 |
a0010 | 0/0 | 1320 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | MFGLD others(1315): Show |
chr22 | 27743277 | 27806756 |
a0011 | 0/0 | 1320 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | MFGLD others(1315): Show |
chr22 | 27743277 | 27806756 |
a0012 | 0/0 | 1320 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | MFGLD others(1315): Show |
chr22 | 27743277 | 27806756 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 3960 | 286 | 44 | 62 | 133 | 13 | 32 | MN1_chr22_27743277_27806756 | MN1 | ATGTT others(3955): Show |
chr22 | 27743277 | 27806756 | ||
a0001c0005 | 0/0 | 3960 | 10 | 8 | 2 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | ATGTT others(3955): Show |
chr22 | 27743277 | 27806756 | ||
a0001c0008 | 0/0 | 3960 | 4 | 4 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | ATGTT others(3955): Show |
chr22 | 27743277 | 27806756 | ||
a0001c0009 | 0/0 | 3960 | 4 | 4 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | ATGTT others(3955): Show |
chr22 | 27743277 | 27806756 | ||
a0001c0010 | 0/0 | 3960 | 3 | 3 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | ATGTT others(3955): Show |
chr22 | 27743277 | 27806756 | ||
a0001c0012 | 0/0 | 3960 | 3 | 0 | 0 | 3 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | ATGTT others(3955): Show |
chr22 | 27743277 | 27806756 | ||
a0001c0013 | 0/0 | 3960 | 2 | 2 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | ATGTT others(3955): Show |
chr22 | 27743277 | 27806756 | ||
a0001c0014 | 0/0 | 3960 | 2 | 2 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | ATGTT others(3955): Show |
chr22 | 27743277 | 27806756 | ||
a0001c0016 | 0/0 | 3960 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | ATGTT others(3955): Show |
chr22 | 27743277 | 27806756 | ||
a0001c0019 | 0/0 | 3960 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | ATGTT others(3955): Show |
chr22 | 27743277 | 27806756 | ||
a0001c0021 | 0/0 | 3960 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | ATGTT others(3955): Show |
chr22 | 27743277 | 27806756 | ||
a0002c0002 | 0/0 | 3963 | 29 | 1 | 8 | 14 | 4 | 2 | MN1_chr22_27743277_27806756 | MN1 | ATGTT others(3958): Show |
chr22 | 27743277 | 27806756 | ||
a0002c0003 | 0/0 | 3963 | 14 | 12 | 2 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | ATGTT others(3958): Show |
chr22 | 27743277 | 27806756 | ||
a0002c0006 | 0/0 | 3963 | 5 | 5 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | ATGTT others(3958): Show |
chr22 | 27743277 | 27806756 | ||
a0002c0020 | 0/0 | 3963 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | ATGTT others(3958): Show |
chr22 | 27743277 | 27806756 | ||
a0002c0022 | 0/0 | 3963 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | ATGTT others(3958): Show |
chr22 | 27743277 | 27806756 | ||
a0003c0004 | 0/0 | 3954 | 12 | 5 | 3 | 4 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | ATGTT others(3949): Show |
chr22 | 27743277 | 27806756 | ||
a0004c0007 | 0/0 | 3960 | 5 | 0 | 3 | 0 | 1 | 1 | MN1_chr22_27743277_27806756 | MN1 | ATGTT others(3955): Show |
chr22 | 27743277 | 27806756 | ||
a0005c0011 | 0/0 | 3957 | 3 | 2 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | ATGTT others(3952): Show |
chr22 | 27743277 | 27806756 | ||
a0006c0015 | 0/0 | 3960 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | ATGTT others(3955): Show |
chr22 | 27743277 | 27806756 | ||
a0007c0018 | 0/0 | 3960 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | ATGTT others(3955): Show |
chr22 | 27743277 | 27806756 | ||
a0008c0025 | 0/0 | 3978 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | ATGTT others(3973): Show |
chr22 | 27743277 | 27806756 | ||
a0009c0024 | 0/0 | 3960 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | ATGTT others(3955): Show |
chr22 | 27743277 | 27806756 | ||
a0010c0023 | 0/0 | 3960 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | ATGTT others(3955): Show |
chr22 | 27743277 | 27806756 | ||
a0011c0017 | 0/0 | 3960 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | ATGTT others(3955): Show |
chr22 | 27743277 | 27806756 | ||
a0012c0026 | 0/0 | 3960 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | ATGTT others(3955): Show |
chr22 | 27743277 | 27806756 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 7814 | 68 | 6 | 20 | 24 | 2 | 14 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7809): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0002 | 0/0 | 7815 | 58 | 15 | 19 | 13 | 5 | 6 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7810): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0003 | 0/0 | 7814 | 27 | 0 | 1 | 24 | 0 | 2 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7809): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0004 | 0/0 | 7815 | 20 | 0 | 4 | 15 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7810): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0005 | 0/0 | 7814 | 10 | 0 | 5 | 4 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7809): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0006 | 0/0 | 7814 | 9 | 1 | 0 | 8 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7809): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0007 | 0/0 | 7813 | 8 | 1 | 0 | 7 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7808): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0008 | 0/0 | 7815 | 8 | 0 | 1 | 0 | 3 | 4 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7810): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0009 | 0/0 | 7836 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7831): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0010 | 0/0 | 7814 | 6 | 0 | 0 | 5 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7809): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0011 | 0/0 | 7815 | 5 | 0 | 0 | 5 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7810): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0012 | 0/0 | 7813 | 5 | 0 | 0 | 5 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7808): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0013 | 0/0 | 7815 | 5 | 0 | 0 | 5 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7810): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0016 | 0/0 | 7814 | 2 | 2 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7809): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0017 | 0/0 | 7815 | 2 | 0 | 2 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7810): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0020 | 0/0 | 7815 | 2 | 0 | 1 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7810): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0021 | 0/0 | 7816 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7811): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0022 | 0/0 | 7814 | 3 | 0 | 0 | 3 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7809): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0023 | 0/0 | 7835 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7830): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0024 | 0/0 | 7835 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7830): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0025 | 0/0 | 7835 | 2 | 1 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7830): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0026 | 0/0 | 7815 | 2 | 0 | 0 | 2 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7810): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0027 | 0/0 | 7814 | 2 | 0 | 2 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7809): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0028 | 0/0 | 7814 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7809): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0029 | 0/0 | 7814 | 2 | 0 | 2 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7809): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0030 | 0/0 | 7815 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7810): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0031 | 0/0 | 7815 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7810): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0032 | 0/0 | 7814 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7809): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0033 | 0/0 | 7816 | 2 | 2 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7811): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0034 | 0/0 | 7815 | 2 | 0 | 0 | 2 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7810): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0037 | 0/0 | 7814 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7809): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0044 | 0/0 | 7834 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7829): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0045 | 0/0 | 7835 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7830): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0046 | 0/0 | 7834 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7829): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0047 | 0/0 | 7813 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7808): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0050 | 0/0 | 7815 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7810): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0051 | 0/0 | 7815 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7810): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0052 | 0/0 | 7815 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7810): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0053 | 0/0 | 7814 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7809): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0054 | 0/0 | 7814 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7809): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0055 | 0/0 | 7814 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7809): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0056 | 0/0 | 7813 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7808): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0057 | 0/0 | 7814 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7809): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0058 | 0/0 | 7814 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7809): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0059 | 0/0 | 7814 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7809): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0060 | 0/0 | 7815 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7810): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0061 | 0/0 | 7816 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7811): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0062 | 0/0 | 7815 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7810): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0063 | 0/0 | 7813 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7808): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0064 | 0/0 | 7815 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7810): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0065 | 0/0 | 7815 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7810): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0066 | 0/0 | 7815 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7810): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0067 | 0/0 | 7815 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7810): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0068 | 0/0 | 7814 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7809): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0069 | 0/0 | 7813 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7808): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0074 | 0/0 | 7813 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7808): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0075 | 0/0 | 7814 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7809): Show |
chr22 | 27743277 | 27806756 |
a0001c0001t0076 | 0/0 | 7816 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7811): Show |
chr22 | 27743277 | 27806756 |
a0001c0005t0002 | 0/0 | 7815 | 3 | 3 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7810): Show |
chr22 | 27743277 | 27806756 |
a0001c0005t0006 | 0/0 | 7814 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7809): Show |
chr22 | 27743277 | 27806756 |
a0001c0005t0009 | 0/0 | 7836 | 2 | 1 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7831): Show |
chr22 | 27743277 | 27806756 |
a0001c0005t0016 | 0/0 | 7814 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7809): Show |
chr22 | 27743277 | 27806756 |
a0001c0005t0028 | 0/0 | 7814 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7809): Show |
chr22 | 27743277 | 27806756 |
a0001c0005t0043 | 0/0 | 7835 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7830): Show |
chr22 | 27743277 | 27806756 |
a0001c0005t0049 | 0/0 | 7815 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7810): Show |
chr22 | 27743277 | 27806756 |
a0001c0008t0018 | 0/0 | 7814 | 2 | 2 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7809): Show |
chr22 | 27743277 | 27806756 |
a0001c0008t0035 | 0/0 | 7812 | 2 | 2 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7807): Show |
chr22 | 27743277 | 27806756 |
a0001c0009t0002 | 0/0 | 7815 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7810): Show |
chr22 | 27743277 | 27806756 |
a0001c0009t0006 | 0/0 | 7814 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7809): Show |
chr22 | 27743277 | 27806756 |
a0001c0009t0021 | 0/0 | 7816 | 2 | 2 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7811): Show |
chr22 | 27743277 | 27806756 |
a0001c0010t0014 | 0/0 | 7835 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7830): Show |
chr22 | 27743277 | 27806756 |
a0001c0010t0024 | 0/0 | 7835 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7830): Show |
chr22 | 27743277 | 27806756 |
a0001c0010t0040 | 0/0 | 7836 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7831): Show |
chr22 | 27743277 | 27806756 |
a0001c0012t0001 | 0/0 | 7814 | 2 | 0 | 0 | 2 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7809): Show |
chr22 | 27743277 | 27806756 |
a0001c0012t0020 | 0/0 | 7815 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7810): Show |
chr22 | 27743277 | 27806756 |
a0001c0013t0001 | 0/0 | 7814 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7809): Show |
chr22 | 27743277 | 27806756 |
a0001c0013t0048 | 0/0 | 7813 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7808): Show |
chr22 | 27743277 | 27806756 |
a0001c0014t0018 | 0/0 | 7814 | 2 | 2 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7809): Show |
chr22 | 27743277 | 27806756 |
a0001c0016t0003 | 0/0 | 7814 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7809): Show |
chr22 | 27743277 | 27806756 |
a0001c0019t0004 | 0/0 | 7815 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7810): Show |
chr22 | 27743277 | 27806756 |
a0001c0021t0007 | 0/0 | 7813 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7808): Show |
chr22 | 27743277 | 27806756 |
a0002c0002t0001 | 0/0 | 7817 | 6 | 0 | 2 | 4 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7812): Show |
chr22 | 27743277 | 27806756 |
a0002c0002t0002 | 0/0 | 7818 | 3 | 0 | 1 | 2 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7813): Show |
chr22 | 27743277 | 27806756 |
a0002c0002t0003 | 0/0 | 7817 | 3 | 0 | 1 | 1 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7812): Show |
chr22 | 27743277 | 27806756 |
a0002c0002t0004 | 0/0 | 7818 | 5 | 0 | 0 | 1 | 4 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7813): Show |
chr22 | 27743277 | 27806756 |
a0002c0002t0005 | 0/0 | 7817 | 2 | 0 | 0 | 2 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7812): Show |
chr22 | 27743277 | 27806756 |
a0002c0002t0006 | 0/0 | 7817 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7812): Show |
chr22 | 27743277 | 27806756 |
a0002c0002t0007 | 0/0 | 7816 | 3 | 0 | 1 | 2 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7811): Show |
chr22 | 27743277 | 27806756 |
a0002c0002t0017 | 0/0 | 7818 | 2 | 0 | 2 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7813): Show |
chr22 | 27743277 | 27806756 |
a0002c0002t0023 | 0/0 | 7838 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7833): Show |
chr22 | 27743277 | 27806756 |
a0002c0002t0030 | 0/0 | 7818 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7813): Show |
chr22 | 27743277 | 27806756 |
a0002c0002t0031 | 0/0 | 7818 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7813): Show |
chr22 | 27743277 | 27806756 |
a0002c0002t0070 | 0/0 | 7816 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7811): Show |
chr22 | 27743277 | 27806756 |
a0002c0003t0009 | 0/0 | 7839 | 2 | 2 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7834): Show |
chr22 | 27743277 | 27806756 |
a0002c0003t0014 | 0/0 | 7838 | 3 | 2 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7833): Show |
chr22 | 27743277 | 27806756 |
a0002c0003t0015 | 0/0 | 7837 | 4 | 4 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7832): Show |
chr22 | 27743277 | 27806756 |
a0002c0003t0019 | 0/0 | 7839 | 2 | 1 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7834): Show |
chr22 | 27743277 | 27806756 |
a0002c0003t0039 | 0/0 | 7839 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7834): Show |
chr22 | 27743277 | 27806756 |
a0002c0003t0041 | 0/0 | 7838 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7833): Show |
chr22 | 27743277 | 27806756 |
a0002c0003t0042 | 0/0 | 7837 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7832): Show |
chr22 | 27743277 | 27806756 |
a0002c0006t0036 | 0/0 | 7839 | 2 | 2 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7834): Show |
chr22 | 27743277 | 27806756 |
a0002c0006t0071 | 0/0 | 7838 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7833): Show |
chr22 | 27743277 | 27806756 |
a0002c0006t0072 | 0/0 | 7838 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7833): Show |
chr22 | 27743277 | 27806756 |
a0002c0006t0073 | 0/0 | 7838 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7833): Show |
chr22 | 27743277 | 27806756 |
a0002c0020t0005 | 0/0 | 7817 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7812): Show |
chr22 | 27743277 | 27806756 |
a0002c0022t0002 | 0/0 | 7818 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7813): Show |
chr22 | 27743277 | 27806756 |
a0003c0004t0001 | 0/0 | 7808 | 4 | 1 | 2 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7803): Show |
chr22 | 27743277 | 27806756 |
a0003c0004t0002 | 0/0 | 7809 | 4 | 3 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7804): Show |
chr22 | 27743277 | 27806756 |
a0003c0004t0005 | 0/0 | 7808 | 3 | 0 | 0 | 3 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7803): Show |
chr22 | 27743277 | 27806756 |
a0003c0004t0016 | 0/0 | 7808 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7803): Show |
chr22 | 27743277 | 27806756 |
a0004c0007t0001 | 0/0 | 7814 | 3 | 0 | 2 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7809): Show |
chr22 | 27743277 | 27806756 |
a0004c0007t0002 | 0/0 | 7815 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7810): Show |
chr22 | 27743277 | 27806756 |
a0004c0007t0008 | 0/0 | 7815 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7810): Show |
chr22 | 27743277 | 27806756 |
a0005c0011t0004 | 0/0 | 7812 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7807): Show |
chr22 | 27743277 | 27806756 |
a0005c0011t0009 | 0/0 | 7833 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7828): Show |
chr22 | 27743277 | 27806756 |
a0005c0011t0019 | 0/0 | 7833 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7828): Show |
chr22 | 27743277 | 27806756 |
a0006c0015t0005 | 0/0 | 7814 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7809): Show |
chr22 | 27743277 | 27806756 |
a0007c0018t0002 | 0/0 | 7815 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7810): Show |
chr22 | 27743277 | 27806756 |
a0008c0025t0032 | 0/0 | 7832 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7827): Show |
chr22 | 27743277 | 27806756 |
a0009c0024t0009 | 0/0 | 7836 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7831): Show |
chr22 | 27743277 | 27806756 |
a0010c0023t0038 | 0/0 | 7815 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7810): Show |
chr22 | 27743277 | 27806756 |
a0011c0017t0003 | 0/0 | 7814 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7809): Show |
chr22 | 27743277 | 27806756 |
a0012c0026t0001 | 0/0 | 7814 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | GTTGC others(7809): Show |
chr22 | 27743277 | 27806756 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0106 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0215 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0004g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0004g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0004g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0004g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0004g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0004g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0004g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0004g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0004g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0004g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0004g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0004g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0004g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0004g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0004g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0005g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0005g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0005g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0005g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0005g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0005g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0005g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0005g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0005g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0005g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0006g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0006g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0006g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0006g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0006g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0006g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0006g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0006g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0006g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0007g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0007g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0007g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0007g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0007g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0007g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0007g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0007g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0008g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0008g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0008g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0008g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0008g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0008g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0008g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0008g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0009g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0010g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0010g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0010g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0010g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0010g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0010g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0011g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0011g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0011g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0011g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0011g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0012g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0012g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0012g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0012g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0012g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0013g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0013g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0013g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0013g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0013g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0016g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0016g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0017g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0017g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0020g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0020g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0021g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0022g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0022g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0022g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0023g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0024g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0025g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0025g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0026g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0026g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0027g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0027g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0028g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0029g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0029g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0030g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0031g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0032g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0033g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0033g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0034g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0034g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0037g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0044g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0045g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0046g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0047g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0050g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0051g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0052g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0053g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0054g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0055g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0056g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0057g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0058g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0059g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0060g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0061g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0062g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0063g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0064g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0065g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0066g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0067g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0068g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0069g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0074g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0075g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0076g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0005t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0005t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0005t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0005t0006g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0005t0009g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0005t0009g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0005t0016g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0005t0028g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0005t0043g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0005t0049g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0008t0018g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0008t0018g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0008t0035g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0008t0035g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0009t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0009t0006g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0009t0021g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0010t0014g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0010t0024g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0010t0040g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0012t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0012t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0012t0020g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0013t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0013t0048g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0014t0018g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0014t0018g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0016t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0019t0004g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0021t0007g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0003g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0003g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0003g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0004g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0004g0362 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0004g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0004g0368 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0005g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0005g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0006g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0007g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0007g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0007g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0017g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0017g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0023g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0030g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0031g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0070g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0003t0009g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0003t0009g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0003t0014g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0003t0014g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0003t0014g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0003t0015g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0003t0015g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0003t0015g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0003t0015g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0003t0019g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0003t0019g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0003t0039g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0003t0041g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0003t0042g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0006t0036g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0006t0071g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0006t0072g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0006t0073g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0020t0005g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0022t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0003c0004t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0003c0004t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0003c0004t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0003c0004t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0003c0004t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0003c0004t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0003c0004t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0003c0004t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0003c0004t0005g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0003c0004t0016g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0004c0007t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0004c0007t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0004c0007t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0004c0007t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0004c0007t0008g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0005c0011t0004g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0005c0011t0009g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0005c0011t0019g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0006c0015t0005g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0007c0018t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0008c0025t0032g0370 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0009c0024t0009g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0010c0023t0038g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0011c0017t0003g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0012c0026t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0051 | g0165 | EUR | GBR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0101 | EUR | GBR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00140 | hp1 | a0001 | c0001 | t0008 | g0057 | EUR | GBR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0146 | EUR | GBR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00280 | hp1 | a0001 | c0001 | t0005 | g0170 | EUR | FIN | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00280 | hp2 | a0001 | c0001 | t0008 | g0067 | EUR | FIN | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0094 | EUR | FIN | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0066 | EUR | FIN | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0282 | EAS | CHS | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00423 | hp1 | a0001 | c0001 | t0011 | g0167 | EAS | CHS | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00423 | hp2 | a0001 | c0001 | t0004 | g0351 | EAS | CHS | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | CHS | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00438 | hp2 | a0002 | c0002 | t0004 | g0366 | EAS | CHS | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00558 | hp2 | a0001 | c0001 | t0004 | g0303 | EAS | CHS | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00609 | hp2 | a0001 | c0001 | t0012 | g0355 | EAS | CHS | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00621 | hp1 | a0002 | c0002 | t0001 | g0259 | EAS | CHS | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00621 | hp2 | a0003 | c0004 | t0001 | g0244 | EAS | CHS | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00639 | hp2 | a0001 | c0001 | t0029 | g0061 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00642 | hp2 | a0002 | c0002 | t0002 | g0260 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00673 | hp1 | a0001 | c0001 | t0013 | g0329 | EAS | CHS | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | CHS | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00733 | hp1 | a0002 | c0002 | t0007 | g0254 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00733 | hp2 | a0004 | c0007 | t0008 | g0274 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00738 | hp1 | a0001 | c0001 | t0027 | g0180 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00741 | hp1 | a0001 | c0001 | t0005 | g0191 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00741 | hp2 | a0003 | c0004 | t0001 | g0240 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01069 | hp1 | a0001 | c0001 | t0029 | g0190 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01069 | hp2 | a0002 | c0002 | t0017 | g0364 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01070 | hp2 | a0001 | c0001 | t0004 | g0340 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01071 | hp2 | a0002 | c0002 | t0017 | g0363 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01081 | hp2 | a0001 | c0001 | t0031 | g0296 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01099 | hp1 | a0001 | c0001 | t0058 | g0234 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01099 | hp2 | a0001 | c0001 | t0017 | g0354 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0129 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01109 | hp1 | a0001 | c0001 | t0027 | g0107 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01167 | hp1 | a0003 | c0004 | t0001 | g0242 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01167 | hp2 | a0001 | c0001 | t0030 | g0194 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01175 | hp2 | a0001 | c0001 | t0062 | g0062 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01192 | hp1 | a0003 | c0004 | t0002 | g0243 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01243 | hp1 | a0001 | c0005 | t0006 | g0050 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01243 | hp2 | a0002 | c0003 | t0014 | g0035 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0145 | AMR | CLM | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01255 | hp2 | a0001 | c0001 | t0017 | g0353 | AMR | CLM | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0090 | AMR | CLM | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0265 | AMR | CLM | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0089 | AMR | CLM | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0091 | AMR | CLM | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0137 | AMR | CLM | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01261 | hp2 | a0004 | c0007 | t0001 | g0272 | AMR | CLM | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01346 | hp1 | a0001 | c0001 | t0004 | g0335 | AMR | CLM | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01358 | hp1 | a0001 | c0001 | t0005 | g0085 | AMR | CLM | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01358 | hp2 | a0001 | c0001 | t0004 | g0334 | AMR | CLM | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0111 | AMR | CLM | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01433 | hp2 | a0002 | c0002 | t0031 | g0369 | AMR | CLM | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01496 | hp1 | a0001 | c0005 | t0009 | g0017 | AMR | CLM | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01496 | hp2 | a0002 | c0003 | t0019 | g0033 | AMR | CLM | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01515 | hp1 | a0002 | c0002 | t0004 | g0368 | EUR | IBS | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0207 | EUR | IBS | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01516 | hp1 | a0002 | c0002 | t0004 | g0008 | EUR | IBS | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01516 | hp2 | a0004 | c0007 | t0001 | g0273 | EUR | IBS | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01517 | hp1 | a0002 | c0002 | t0004 | g0008 | EUR | IBS | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0208 | EUR | IBS | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01884 | hp1 | a0002 | c0003 | t0015 | g0027 | AFR | ACB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01884 | hp2 | a0002 | c0003 | t0039 | g0029 | AFR | ACB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0233 | AFR | ACB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0225 | AFR | ACB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01928 | hp1 | a0001 | c0001 | t0005 | g0179 | AMR | PEL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01934 | hp1 | a0001 | c0001 | t0046 | g0039 | AMR | PEL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01934 | hp2 | a0001 | c0001 | t0005 | g0188 | AMR | PEL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0141 | AMR | PEL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01952 | hp2 | a0001 | c0001 | t0020 | g0168 | AMR | PEL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01975 | hp1 | a0001 | c0001 | t0005 | g0078 | AMR | PEL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01978 | hp1 | a0002 | c0002 | t0001 | g0264 | AMR | PEL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0297 | AMR | PEL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0227 | AMR | PEL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02004 | hp1 | a0001 | c0001 | t0004 | g0293 | AMR | PEL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0110 | AMR | PEL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02015 | hp1 | a0001 | c0001 | t0013 | g0344 | EAS | KHV | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02015 | hp2 | a0001 | c0001 | t0004 | g0281 | EAS | KHV | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0356 | EAS | KHV | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02027 | hp2 | a0002 | c0020 | t0005 | g0249 | EAS | KHV | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02040 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | KHV | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | KHV | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02055 | hp1 | a0003 | c0004 | t0001 | g0247 | AFR | ACB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02055 | hp2 | a0001 | c0001 | t0069 | g0371 | AFR | ACB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | KHV | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0320 | EAS | KHV | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02071 | hp1 | a0001 | c0001 | t0012 | g0321 | EAS | KHV | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02074 | hp1 | a0002 | c0002 | t0005 | g0255 | EAS | KHV | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02074 | hp2 | a0002 | c0002 | t0007 | g0263 | EAS | KHV | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02080 | hp1 | a0001 | c0001 | t0013 | g0299 | EAS | KHV | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02080 | hp2 | a0001 | c0001 | t0026 | g0044 | EAS | KHV | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02083 | hp1 | a0001 | c0001 | t0004 | g0350 | EAS | KHV | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0312 | EAS | KHV | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0337 | EAS | KHV | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02132 | hp2 | a0001 | c0001 | t0010 | g0304 | EAS | KHV | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0349 | EAS | KHV | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02135 | hp2 | a0002 | c0002 | t0003 | g0367 | EAS | KHV | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02145 | hp1 | a0001 | c0001 | t0009 | g0021 | AFR | ACB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02145 | hp2 | a0002 | c0003 | t0042 | g0031 | AFR | ACB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02148 | hp2 | a0002 | c0002 | t0003 | g0361 | AMR | PEL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | CDX | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | CDX | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02257 | hp1 | a0001 | c0014 | t0018 | g0372 | AFR | ACB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02257 | hp2 | a0002 | c0003 | t0015 | g0025 | AFR | ACB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02258 | hp2 | a0001 | c0009 | t0006 | g0268 | AFR | ACB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0128 | AMR | PEL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02280 | hp1 | a0001 | c0005 | t0002 | g0055 | AFR | ACB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02280 | hp2 | a0003 | c0004 | t0002 | g0246 | AFR | ACB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0127 | AMR | PEL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02293 | hp2 | a0001 | c0001 | t0008 | g0095 | AMR | PEL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02451 | hp1 | a0001 | c0005 | t0049 | g0053 | AFR | ACB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02451 | hp2 | a0003 | c0004 | t0016 | g0248 | AFR | ACB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02523 | hp1 | a0001 | c0001 | t0004 | g0348 | EAS | KHV | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0342 | EAS | KHV | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02572 | hp1 | a0002 | c0003 | t0015 | g0026 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02572 | hp2 | a0001 | c0001 | t0074 | g0383 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02602 | hp1 | a0001 | c0001 | t0032 | g0358 | SAS | PJL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0100 | SAS | PJL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02622 | hp1 | a0001 | c0010 | t0024 | g0014 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02622 | hp2 | a0001 | c0001 | t0016 | g0226 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02630 | hp1 | a0001 | c0001 | t0061 | g0224 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0200 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0237 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02647 | hp2 | a0001 | c0001 | t0021 | g0075 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02683 | hp1 | a0001 | c0001 | t0008 | g0102 | SAS | PJL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0117 | SAS | PJL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02698 | hp1 | a0006 | c0015 | t0005 | g0046 | SAS | PJL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02717 | hp1 | a0002 | c0003 | t0014 | g0030 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02717 | hp2 | a0001 | c0001 | t0059 | g0232 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02735 | hp1 | a0001 | c0001 | t0008 | g0229 | SAS | PJL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0139 | SAS | PJL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02738 | hp1 | a0001 | c0001 | t0025 | g0040 | SAS | PJL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02738 | hp2 | a0002 | c0002 | t0003 | g0365 | SAS | PJL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02809 | hp1 | a0002 | c0006 | t0071 | g0380 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02809 | hp2 | a0001 | c0001 | t0044 | g0041 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02818 | hp1 | a0002 | c0003 | t0041 | g0028 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02818 | hp2 | a0001 | c0001 | t0033 | g0327 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02886 | hp1 | a0002 | c0006 | t0036 | g0009 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02886 | hp2 | a0001 | c0001 | t0025 | g0042 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02895 | hp1 | a0001 | c0009 | t0021 | g0006 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02895 | hp2 | a0001 | c0001 | t0006 | g0220 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02896 | hp1 | a0001 | c0008 | t0035 | g0375 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02896 | hp2 | a0001 | c0013 | t0001 | g0048 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02897 | hp1 | a0001 | c0009 | t0021 | g0006 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02897 | hp2 | a0001 | c0008 | t0035 | g0376 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02922 | hp1 | a0001 | c0005 | t0002 | g0049 | AFR | ESN | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0150 | AFR | ESN | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02970 | hp1 | a0001 | c0010 | t0014 | g0012 | AFR | ESN | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02970 | hp2 | a0001 | c0005 | t0002 | g0051 | AFR | ESN | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0058 | AFR | ESN | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02976 | hp2 | a0002 | c0003 | t0015 | g0024 | AFR | ESN | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03041 | hp1 | a0002 | c0006 | t0036 | g0009 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03041 | hp2 | a0001 | c0001 | t0075 | g0382 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03098 | hp1 | a0003 | c0004 | t0002 | g0245 | AFR | MSL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03098 | hp2 | a0001 | c0001 | t0023 | g0020 | AFR | MSL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03130 | hp1 | a0001 | c0008 | t0018 | g0374 | AFR | ESN | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03130 | hp2 | a0002 | c0002 | t0023 | g0036 | AFR | ESN | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03139 | hp1 | a0001 | c0010 | t0040 | g0013 | AFR | ESN | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03139 | hp2 | a0001 | c0005 | t0028 | g0052 | AFR | ESN | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0112 | AFR | ESN | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03195 | hp2 | a0001 | c0001 | t0060 | g0196 | AFR | ESN | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03209 | hp1 | a0001 | c0009 | t0002 | g0269 | AFR | MSL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03209 | hp2 | a0001 | c0001 | t0016 | g0119 | AFR | MSL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03225 | hp1 | a0005 | c0011 | t0009 | g0015 | AFR | MSL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03225 | hp2 | a0001 | c0001 | t0057 | g0238 | AFR | MSL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0308 | SAS | PJL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03453 | hp1 | a0001 | c0014 | t0018 | g0373 | AFR | MSL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03453 | hp2 | a0001 | c0001 | t0076 | g0384 | AFR | MSL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0210 | AFR | MSL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03486 | hp2 | a0001 | c0005 | t0016 | g0054 | AFR | MSL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03516 | hp1 | a0001 | c0013 | t0048 | g0047 | AFR | ESN | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0231 | AFR | ESN | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0216 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0228 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03579 | hp1 | a0001 | c0005 | t0009 | g0018 | AFR | MSL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03579 | hp2 | a0001 | c0001 | t0028 | g0235 | AFR | MSL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03654 | hp2 | a0007 | c0018 | t0002 | g0239 | SAS | PJL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03669 | hp1 | a0004 | c0007 | t0002 | g0271 | SAS | PJL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0197 | SAS | PJL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0093 | SAS | PJL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03710 | hp2 | a0005 | c0011 | t0004 | g0279 | SAS | PJL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03831 | hp1 | a0002 | c0002 | t0006 | g0266 | SAS | BEB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03831 | hp2 | a0001 | c0001 | t0055 | g0142 | SAS | BEB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | BEB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | BEB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | BEB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0301 | SAS | BEB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG04115 | hp1 | a0008 | c0025 | t0032 | g0370 | SAS | STU | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG04115 | hp2 | a0001 | c0001 | t0008 | g0143 | SAS | STU | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0204 | SAS | BEB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG04184 | hp2 | a0001 | c0001 | t0037 | g0010 | SAS | BEB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG04199 | hp1 | a0001 | c0001 | t0024 | g0019 | SAS | STU | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG04199 | hp2 | a0001 | c0001 | t0004 | g0339 | SAS | STU | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | STU | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | STU | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | STU | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | STU | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18522 | hp1 | a0002 | c0003 | t0019 | g0034 | AFR | YRI | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18522 | hp2 | a0005 | c0011 | t0019 | g0016 | AFR | YRI | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18612 | hp1 | a0001 | c0001 | t0007 | g0198 | EAS | CHB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18612 | hp2 | a0001 | c0012 | t0001 | g0277 | EAS | CHB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18747 | hp1 | a0001 | c0001 | t0022 | g0292 | EAS | CHB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18747 | hp2 | a0001 | c0001 | t0005 | g0118 | EAS | CHB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18906 | hp1 | a0001 | c0021 | t0007 | g0250 | AFR | YRI | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18906 | hp2 | a0002 | c0006 | t0073 | g0379 | AFR | YRI | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18940 | hp1 | a0001 | c0001 | t0004 | g0322 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18940 | hp2 | a0001 | c0001 | t0054 | g0175 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18941 | hp1 | a0001 | c0012 | t0020 | g0276 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18941 | hp2 | a0001 | c0001 | t0007 | g0096 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18942 | hp1 | a0001 | c0001 | t0010 | g0307 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18942 | hp2 | a0003 | c0004 | t0005 | g0001 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18944 | hp1 | a0001 | c0001 | t0022 | g0316 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18944 | hp2 | a0001 | c0001 | t0006 | g0218 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0341 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18945 | hp2 | a0002 | c0002 | t0007 | g0258 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18947 | hp1 | a0001 | c0001 | t0003 | g0311 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18947 | hp2 | a0001 | c0001 | t0004 | g0286 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18950 | hp1 | a0001 | c0001 | t0012 | g0330 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18950 | hp2 | a0001 | c0001 | t0007 | g0134 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18951 | hp1 | a0001 | c0001 | t0034 | g0309 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18951 | hp2 | a0001 | c0001 | t0006 | g0160 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18959 | hp1 | a0001 | c0001 | t0004 | g0357 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18960 | hp1 | a0001 | c0001 | t0005 | g0086 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18960 | hp2 | a0001 | c0001 | t0056 | g0152 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18962 | hp2 | a0001 | c0001 | t0034 | g0283 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18964 | hp2 | a0001 | c0001 | t0004 | g0345 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18965 | hp1 | a0010 | c0023 | t0038 | g0011 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18965 | hp2 | a0001 | c0001 | t0003 | g0290 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18966 | hp1 | a0001 | c0001 | t0006 | g0154 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18966 | hp2 | a0001 | c0001 | t0020 | g0186 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18967 | hp1 | a0001 | c0001 | t0010 | g0305 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18967 | hp2 | a0002 | c0002 | t0002 | g0253 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18968 | hp1 | a0001 | c0001 | t0010 | g0310 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18969 | hp1 | a0001 | c0001 | t0067 | g0284 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18969 | hp2 | a0001 | c0019 | t0004 | g0360 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18970 | hp1 | a0001 | c0001 | t0006 | g0217 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18971 | hp1 | a0001 | c0001 | t0065 | g0294 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18971 | hp2 | a0002 | c0002 | t0001 | g0256 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18974 | hp1 | a0002 | c0022 | t0002 | g0251 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18974 | hp2 | a0001 | c0001 | t0007 | g0097 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18979 | hp1 | a0001 | c0001 | t0004 | g0289 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18979 | hp2 | a0001 | c0001 | t0050 | g0199 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18980 | hp1 | a0001 | c0016 | t0003 | g0280 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18980 | hp2 | a0001 | c0001 | t0011 | g0070 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18981 | hp1 | a0001 | c0001 | t0003 | g0326 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18983 | hp2 | a0001 | c0001 | t0006 | g0185 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18984 | hp1 | a0001 | c0001 | t0013 | g0347 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0352 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18992 | hp1 | a0001 | c0001 | t0026 | g0045 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18993 | hp2 | a0001 | c0001 | t0012 | g0298 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0252 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18994 | hp2 | a0001 | c0001 | t0003 | g0332 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18995 | hp1 | a0001 | c0001 | t0012 | g0315 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18998 | hp1 | a0001 | c0001 | t0007 | g0187 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0302 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18999 | hp1 | a0001 | c0001 | t0003 | g0343 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19000 | hp1 | a0002 | c0002 | t0001 | g0261 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19000 | hp2 | a0001 | c0001 | t0006 | g0108 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19004 | hp1 | a0001 | c0001 | t0066 | g0317 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0300 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19005 | hp1 | a0001 | c0001 | t0047 | g0125 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19005 | hp2 | a0002 | c0002 | t0030 | g0262 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19007 | hp1 | a0002 | c0002 | t0005 | g0267 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0325 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19009 | hp1 | a0001 | c0001 | t0004 | g0324 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19009 | hp2 | a0003 | c0004 | t0005 | g0001 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19010 | hp1 | a0001 | c0001 | t0011 | g0109 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19010 | hp2 | a0001 | c0001 | t0010 | g0306 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19030 | hp1 | a0002 | c0003 | t0014 | g0022 | AFR | LWK | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | LWK | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19043 | hp1 | a0001 | c0001 | t0053 | g0205 | AFR | LWK | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0151 | AFR | LWK | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19056 | hp1 | a0001 | c0001 | t0006 | g0130 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19056 | hp2 | a0001 | c0001 | t0011 | g0121 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19060 | hp2 | a0002 | c0002 | t0070 | g0378 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19063 | hp1 | a0001 | c0001 | t0003 | g0318 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19063 | hp2 | a0001 | c0001 | t0007 | g0114 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19064 | hp1 | a0001 | c0001 | t0052 | g0081 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19064 | hp2 | a0001 | c0001 | t0004 | g0328 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19065 | hp1 | a0011 | c0017 | t0003 | g0359 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19065 | hp2 | a0003 | c0004 | t0005 | g0001 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19066 | hp1 | a0001 | c0001 | t0005 | g0195 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0291 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19070 | hp2 | a0001 | c0001 | t0063 | g0285 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19077 | hp1 | a0002 | c0002 | t0002 | g0257 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19077 | hp2 | a0001 | c0001 | t0013 | g0346 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19078 | hp1 | a0001 | c0001 | t0005 | g0123 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19078 | hp2 | a0001 | c0001 | t0004 | g0295 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0323 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19081 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0338 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19087 | hp1 | a0001 | c0012 | t0001 | g0278 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19087 | hp2 | a0001 | c0001 | t0022 | g0333 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0288 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19088 | hp2 | a0001 | c0001 | t0064 | g0313 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19089 | hp2 | a0001 | c0001 | t0006 | g0158 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19090 | hp1 | a0001 | c0001 | t0007 | g0122 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19090 | hp2 | a0001 | c0001 | t0011 | g0178 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19091 | hp2 | a0001 | c0001 | t0003 | g0314 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19240 | hp1 | a0002 | c0003 | t0009 | g0032 | AFR | YRI | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | YRI | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA20129 | hp1 | a0001 | c0001 | t0045 | g0043 | AFR | ASW | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ASW | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA20752 | hp1 | a0002 | c0002 | t0004 | g0362 | EUR | TSI | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA20752 | hp2 | a0001 | c0001 | t0010 | g0319 | EUR | TSI | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA20805 | hp1 | a0001 | c0001 | t0008 | g0144 | EUR | TSI | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0060 | EUR | TSI | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA20905 | hp1 | a0001 | c0001 | t0008 | g0131 | SAS | GIH | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA20905 | hp2 | a0012 | c0026 | t0001 | g0275 | SAS | GIH | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01123 | hp2 | a0004 | c0007 | t0001 | g0270 | AMR | CLM | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02109 | hp1 | a0001 | c0001 | t0033 | g0287 | AFR | ACB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02109 | hp2 | a0002 | c0006 | t0072 | g0381 | AFR | ACB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02486 | hp1 | a0001 | c0001 | t0007 | g0088 | AFR | ACB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0201 | AFR | ACB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02559 | hp1 | a0001 | c0008 | t0018 | g0377 | AFR | ACB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02559 | hp2 | a0001 | c0001 | t0068 | g0331 | AFR | ACB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | MSL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03471 | hp2 | a0003 | c0004 | t0002 | g0241 | AFR | MSL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG06807 | hp1 | a0009 | c0024 | t0009 | g0037 | AFR | USA | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG06807 | hp2 | a0002 | c0003 | t0009 | g0023 | AFR | USA | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0336 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | USA | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0135 | AFR | USA | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA21309 | hp1 | a0001 | c0005 | t0043 | g0038 | AFR | LWK | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | LWK | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0215 | REF | REF | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0106 | REF | REF | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:27797603 | C | A | 1 | a0011 | 1 | NA19065.hp1 | missense_variant | MODERATE | c.2941G>T | p.Ala981Ser | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 4154/7814 | 2941/3963 | 981/1320 | chr22 | 27797603 | |||
chr22:27798238 | G | C | 1 | a0007 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.2306C>G | p.Ala769Gly | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 3519/7814 | 2306/3963 | 769/1320 | chr22 | 27798238 | |||
chr22:27798761 | C | T | 2 | a0002 a0006 |
2 | HG02698.hp1 NA18974.hp1 |
missense_variant | MODERATE | c.1783G>A | p.Val595Met | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 2996/7814 | 1783/3963 | 595/1320 | chr22 | 27798761 | |||
chr22:27798906 | CTGCTGT | C | 1 | a0003 | 12 | HG00621.hp2 HG00741.hp2 HG01167.hp1 others(9): Show |
disruptive_inframe_deletion | MODERATE | c.1632_1637delACAGCA | p.Gln545_Gln546del | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 2850/7814 | 1632/3963 | 544/1320 | chr22 | 27798906 | |||
chr22:27798924 | T | TTGC | 1 | a0002 | 15 | HG01243.hp2 HG01496.hp2 HG01884.hp1 others(12): Show |
disruptive_inframe_insertion | MODERATE | c.1617_1619dupGCA | p.Gln540dup | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 2832/7814 | 1619/3963 | 540/1320 | chr22 | 27798924 | |||
chr22:27798945 | T | TTGC | 1 | a0002 | 35 | HG00438.hp2 HG00621.hp1 HG00642.hp2 others(32): Show |
disruptive_inframe_insertion | MODERATE | c.1596_1598dupGCA | p.Gln533dup | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 2811/7814 | 1598/3963 | 533/1320 | chr22 | 27798945 | |||
chr22:27798945 | TTGC | T | 1 | a0005 | 3 | HG03225.hp1 HG03710.hp2 NA18522.hp2 |
disruptive_inframe_deletion | MODERATE | c.1596_1598delGCA | p.Gln533del | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 2811/7814 | 1596/3963 | 532/1320 | chr22 | 27798945 | |||
chr22:27799021 | G | A | 1 | a0010 | 1 | NA18965.hp1 | missense_variant | MODERATE | c.1523C>T | p.Ser508Leu | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 2736/7814 | 1523/3963 | 508/1320 | chr22 | 27799021 | |||
chr22:27799043 | G | A | 1 | a0009 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.1501C>T | p.Pro501Ser | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 2714/7814 | 1501/3963 | 501/1320 | chr22 | 27799043 | |||
chr22:27799398 | C | A | 1 | a0004 | 5 | HG00733.hp2 HG01123.hp2 HG01261.hp2 others(2): Show |
missense_variant | MODERATE | c.1146G>T | p.Gln382His | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 2359/7814 | 1146/3963 | 382/1320 | chr22 | 27799398 | |||
chr22:27799618 | T | TGCTGCTG others(11): Show |
1 | a0008 | 1 | HG04115.hp1 | conservative_inframe_insertion | MODERATE | c.908_925dupCCCAGCAG others(10): Show |
p.Pro303_Gln308dup | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 2138/7814 | 925/3963 | 309/1320 | chr22 | 27799618 | |||
chr22:27800048 | C | A | 1 | a0012 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.496G>T | p.Gly166Cys | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 1709/7814 | 496/3963 | 166/1320 | chr22 | 27800048 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:27797109 | C | T | 3 | a0001c0010 a0001c0013 a0002c0003 |
19 | HG01243.hp2 HG01496.hp2 HG01884.hp1 others(16): Show |
synonymous_variant | LOW | c.3435G>A | p.Pro1145Pro | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 4648/7814 | 3435/3963 | 1145/1320 | chr22 | 27797109 | |||
chr22:27797610 | C | T | 1 | a0001c0016 | 1 | NA18980.hp1 | synonymous_variant | LOW | c.2934G>A | p.Gln978Gln | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 4147/7814 | 2934/3963 | 978/1320 | chr22 | 27797610 | |||
chr22:27798072 | G | A | 1 | a0001c0014 | 2 | HG02257.hp1 HG03453.hp1 |
synonymous_variant | LOW | c.2472C>T | p.Cys824Cys | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 3685/7814 | 2472/3963 | 824/1320 | chr22 | 27798072 | |||
chr22:27798465 | G | A | 1 | a0001c0019 | 1 | NA18969.hp2 | synonymous_variant | LOW | c.2079C>T | p.Pro693Pro | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 3292/7814 | 2079/3963 | 693/1320 | chr22 | 27798465 | |||
chr22:27798759 | C | T | 5 | a0001c0005 a0001c0010 a0001c0013 others(2): Show |
34 | HG01243.hp1 HG01243.hp2 HG01496.hp1 others(31): Show |
synonymous_variant | LOW | c.1785G>A | p.Val595Val | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 2998/7814 | 1785/3963 | 595/1320 | chr22 | 27798759 | |||
chr22:27798924 | T | C | 1 | a0001c0021 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.1620A>G | p.Gln540Gln | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 2833/7814 | 1620/3963 | 540/1320 | chr22 | 27798924 | |||
chr22:27798945 | T | C | 1 | a0001c0008 | 4 | HG02559.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
synonymous_variant | LOW | c.1599A>G | p.Gln533Gln | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 2812/7814 | 1599/3963 | 533/1320 | chr22 | 27798945 | |||
chr22:27798981 | G | A | 1 | a0001c0009 | 4 | HG02258.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
synonymous_variant | LOW | c.1563C>T | p.Ser521Ser | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 2776/7814 | 1563/3963 | 521/1320 | chr22 | 27798981 | |||
chr22:27799020 | C | G | 1 | a0010c0023 | 1 | NA18965.hp1 | synonymous_variant | LOW | c.1524G>C | p.Ser508Ser | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 2737/7814 | 1524/3963 | 508/1320 | chr22 | 27799020 | |||
chr22:27799989 | G | T | 1 | a0002c0006 | 5 | HG02109.hp2 HG02809.hp1 HG02886.hp1 others(2): Show |
synonymous_variant | LOW | c.555C>A | p.Ala185Ala | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 1768/7814 | 555/3963 | 185/1320 | chr22 | 27799989 | |||
chr22:27800136 | G | A | 1 | a0001c0012 | 3 | NA18612.hp2 NA18941.hp1 NA19087.hp1 |
synonymous_variant | LOW | c.408C>T | p.Tyr136Tyr | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 1621/7814 | 408/3963 | 136/1320 | chr22 | 27800136 | |||
chr22:27800238 | C | G | 1 | a0001c0010 | 3 | HG02622.hp1 HG02970.hp1 HG03139.hp1 |
synonymous_variant | LOW | c.306G>C | p.Pro102Pro | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 1519/7814 | 306/3963 | 102/1320 | chr22 | 27800238 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:27748391 | GA | G | 22 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0010 others(19): Show |
49 | HG00609.hp2 HG00733.hp1 HG01243.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*2523delT | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 2523 | chr22 | 27748391 | ||||||
chr22:27748469 | A | G | 1 | a0001c0001t0037 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2446T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 2446 | chr22 | 27748469 | ||||||
chr22:27748636 | T | G | 11 | a0001c0001t0005 a0001c0001t0020 a0001c0001t0022 others(8): Show |
26 | HG00280.hp1 HG00741.hp1 HG01358.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2279A>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 2279 | chr22 | 27748636 | ||||||
chr22:27748777 | G | T | 1 | a0001c0001t0050 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2138C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 2138 | chr22 | 27748777 | ||||||
chr22:27748879 | A | G | 1 | a0001c0001t0064 | 1 | NA19088.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2036T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 2036 | chr22 | 27748879 | ||||||
chr22:27748897 | C | T | 1 | a0002c0006t0072 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2018G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 2018 | chr22 | 27748897 | ||||||
chr22:27749000 | C | T | 2 | a0001c0001t0068 a0002c0006t0071 |
2 | HG02559.hp2 HG02809.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1915G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 1915 | chr22 | 27749000 | ||||||
chr22:27749093 | C | T | 1 | a0001c0001t0056 | 1 | NA18960.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1822G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 1822 | chr22 | 27749093 | ||||||
chr22:27749156 | G | T | 1 | a0001c0001t0055 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1759C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 1759 | chr22 | 27749156 | ||||||
chr22:27749160 | G | A | 10 | a0001c0001t0005 a0001c0001t0020 a0001c0001t0022 others(7): Show |
25 | HG00280.hp1 HG00741.hp1 HG01358.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1755C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 1755 | chr22 | 27749160 | ||||||
chr22:27749226 | G | A | 10 | a0001c0001t0017 a0001c0001t0044 a0001c0001t0051 others(7): Show |
16 | HG00099.hp1 HG01069.hp2 HG01071.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1689C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 1689 | chr22 | 27749226 | ||||||
chr22:27749265 | T | C | 1 | a0001c0001t0057 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1650A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 1650 | chr22 | 27749265 | ||||||
chr22:27749339 | G | A | 1 | a0001c0001t0029 | 2 | HG00639.hp2 HG01069.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1576C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 1576 | chr22 | 27749339 | ||||||
chr22:27749517 | G | A | 4 | a0001c0001t0011 a0001c0001t0013 a0001c0001t0052 others(1): Show |
12 | HG00423.hp1 HG00673.hp1 HG02015.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1398C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 1398 | chr22 | 27749517 | ||||||
chr22:27749545 | A | T | 1 | a0001c0001t0054 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1370T>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 1370 | chr22 | 27749545 | ||||||
chr22:27749546 | A | G | 2 | a0001c0001t0028 a0001c0005t0028 |
2 | HG03139.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1369T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 1369 | chr22 | 27749546 | ||||||
chr22:27749547 | C | T | 1 | a0001c0001t0054 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1368G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 1368 | chr22 | 27749547 | ||||||
chr22:27749548 | C | A | 1 | a0001c0001t0054 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1367G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 1367 | chr22 | 27749548 | ||||||
chr22:27749549 | A | C | 1 | a0001c0001t0054 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1366T>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 1366 | chr22 | 27749549 | ||||||
chr22:27749550 | C | A | 1 | a0001c0001t0054 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1365G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 1365 | chr22 | 27749550 | ||||||
chr22:27749551 | C | T | 1 | a0001c0001t0054 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1364G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 1364 | chr22 | 27749551 | ||||||
chr22:27749553 | C | G | 1 | a0001c0001t0054 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1362G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 1362 | chr22 | 27749553 | ||||||
chr22:27749555 | C | G | 1 | a0001c0001t0054 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1360G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 1360 | chr22 | 27749555 | ||||||
chr22:27749558 | C | G | 1 | a0001c0001t0054 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1357G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 1357 | chr22 | 27749558 | ||||||
chr22:27749560 | C | T | 1 | a0001c0001t0054 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1355G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 1355 | chr22 | 27749560 | ||||||
chr22:27749617 | C | T | 9 | a0001c0001t0008 a0001c0001t0027 a0001c0001t0031 others(6): Show |
17 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1298G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 1298 | chr22 | 27749617 | ||||||
chr22:27749618 | A | C | 1 | a0001c0010t0040 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1297T>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 1297 | chr22 | 27749618 | ||||||
chr22:27749683 | C | T | 2 | a0001c0001t0021 a0001c0009t0021 |
3 | HG02647.hp2 HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1232G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 1232 | chr22 | 27749683 | ||||||
chr22:27749937 | C | T | 6 | a0001c0001t0044 a0001c0001t0074 a0001c0005t0049 others(3): Show |
10 | HG01884.hp1 HG02257.hp2 HG02451.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*978G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 978 | chr22 | 27749937 | ||||||
chr22:27750065 | G | A | 1 | a0001c0001t0052 | 1 | NA19064.hp1 | 3_prime_UTR_variant | MODIFIER | c.*850C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 850 | chr22 | 27750065 | ||||||
chr22:27750141 | T | A | 2 | a0001c0001t0058 a0001c0001t0069 |
2 | HG01099.hp1 HG02055.hp2 |
3_prime_UTR_variant | MODIFIER | c.*774A>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 774 | chr22 | 27750141 | ||||||
chr22:27750147 | C | T | 1 | a0002c0003t0039 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*768G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 768 | chr22 | 27750147 | ||||||
chr22:27750225 | A | G | 1 | a0001c0001t0054 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*690T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 690 | chr22 | 27750225 | ||||||
chr22:27750288 | CG | C | 6 | a0001c0001t0044 a0001c0001t0053 a0001c0001t0074 others(3): Show |
10 | HG01884.hp1 HG02257.hp2 HG02572.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*626delC | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 626 | chr22 | 27750288 | ||||||
chr22:27750289 | G | A | 1 | a0001c0001t0046 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*626C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 626 | chr22 | 27750289 | ||||||
chr22:27750403 | T | C | 1 | a0002c0003t0041 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*512A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 512 | chr22 | 27750403 | ||||||
chr22:27750424 | T | C | 1 | a0001c0001t0059 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*491A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 491 | chr22 | 27750424 | ||||||
chr22:27750747 | G | A | 6 | a0001c0001t0011 a0001c0001t0013 a0001c0001t0030 others(3): Show |
15 | HG00423.hp1 HG00673.hp1 HG01167.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*168C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 168 | chr22 | 27750747 | ||||||
chr22:27750780 | A | AG | 50 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(47): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
3_prime_UTR_variant | MODIFIER | c.*134dupC | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 134 | chr22 | 27750780 | ||||||
chr22:27750781 | G | GA | 6 | a0001c0001t0011 a0001c0001t0013 a0001c0001t0030 others(3): Show |
15 | HG00423.hp1 HG00673.hp1 HG01167.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*133dupT | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 133 | chr22 | 27750781 | ||||||
chr22:27750781 | G | GGA | 8 | a0001c0001t0021 a0001c0001t0033 a0001c0001t0060 others(5): Show |
11 | HG01496.hp2 HG02109.hp1 HG02630.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*133_*134insTC | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 133 | chr22 | 27750781 | ||||||
chr22:27750782 | A | G | 11 | a0001c0001t0016 a0001c0001t0044 a0001c0001t0074 others(8): Show |
18 | HG01243.hp2 HG01884.hp1 HG02257.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*133T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 133 | chr22 | 27750782 | ||||||
chr22:27750794 | C | T | 2 | a0001c0001t0047 a0001c0001t0063 |
2 | NA19005.hp1 NA19070.hp2 |
3_prime_UTR_variant | MODIFIER | c.*121G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 121 | chr22 | 27750794 | ||||||
chr22:27800547 | T | G | 1 | a0010c0023t0038 | 1 | NA18965.hp1 | 5_prime_UTR_variant | MODIFIER | c.-4A>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 4 | chr22 | 27800547 | ||||||
chr22:27800736 | C | G | 1 | a0001c0001t0026 | 2 | HG02080.hp2 NA18992.hp1 |
5_prime_UTR_variant | MODIFIER | c.-193G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 193 | chr22 | 27800736 | ||||||
chr22:27800752 | A | G | 1 | a0010c0023t0038 | 1 | NA18965.hp1 | 5_prime_UTR_variant | MODIFIER | c.-209T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 209 | chr22 | 27800752 | ||||||
chr22:27800922 | G | A | 28 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0010 others(25): Show |
98 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(95): Show |
5_prime_UTR_variant | MODIFIER | c.-379C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 379 | chr22 | 27800922 | ||||||
chr22:27801015 | T | C | 1 | a0001c0005t0043 | 1 | NA21309.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-472A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | chr22 | 27801015 | |||||||
chr22:27801027 | A | G | 1 | a0010c0023t0038 | 1 | NA18965.hp1 | 5_prime_UTR_variant | MODIFIER | c.-484T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 484 | chr22 | 27801027 | ||||||
chr22:27801138 | G | A | 4 | a0001c0001t0025 a0001c0001t0044 a0001c0001t0045 others(1): Show |
5 | HG01934.hp1 HG02738.hp1 HG02809.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-595C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 595 | chr22 | 27801138 | ||||||
chr22:27801274 | CG | C | 4 | a0001c0001t0069 a0001c0008t0018 a0001c0008t0035 others(1): Show |
7 | HG02055.hp2 HG02257.hp1 HG02559.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-732delC | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 732 | chr22 | 27801274 | ||||||
chr22:27801317 | C | CTCGGCAG others(14): Show |
27 | a0001c0001t0009 a0001c0001t0023 a0001c0001t0024 others(24): Show |
37 | HG01243.hp2 HG01496.hp1 HG01496.hp2 others(34): Show |
5_prime_UTR_variant | MODIFIER | c.-795_-775dupACGCAG others(15): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 775 | chr22 | 27801317 | ||||||
chr22:27801318 | T | C | 1 | a0002c0002t0070 | 1 | NA19060.hp2 | 5_prime_UTR_variant | MODIFIER | c.-775A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 775 | chr22 | 27801318 | ||||||
chr22:27801399 | G | C | 1 | a0010c0023t0038 | 1 | NA18965.hp1 | 5_prime_UTR_variant | MODIFIER | c.-856C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 856 | chr22 | 27801399 | ||||||
chr22:27801401 | C | G | 1 | a0010c0023t0038 | 1 | NA18965.hp1 | 5_prime_UTR_variant | MODIFIER | c.-858G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 858 | chr22 | 27801401 | ||||||
chr22:27801424 | C | A | 4 | a0002c0006t0036 a0002c0006t0071 a0002c0006t0072 others(1): Show |
5 | HG02109.hp2 HG02809.hp1 HG02886.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-881G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 881 | chr22 | 27801424 | ||||||
chr22:27801529 | G | A | 1 | a0010c0023t0038 | 1 | NA18965.hp1 | 5_prime_UTR_variant | MODIFIER | c.-986C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 986 | chr22 | 27801529 | ||||||
chr22:27801530 | A | T | 1 | a0010c0023t0038 | 1 | NA18965.hp1 | 5_prime_UTR_variant | MODIFIER | c.-987T>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 987 | chr22 | 27801530 | ||||||
chr22:27801613 | G | C | 3 | a0001c0001t0074 a0001c0001t0075 a0001c0001t0076 |
3 | HG02572.hp2 HG03041.hp2 HG03453.hp2 |
5_prime_UTR_variant | MODIFIER | c.-1070C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 1070 | chr22 | 27801613 | ||||||
chr22:27801741 | C | G | 1 | a0001c0001t0037 | 1 | HG04184.hp2 | 5_prime_UTR_variant | MODIFIER | c.-1198G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 1198 | chr22 | 27801741 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:27751201 | C | T | 43 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0077 others(40): Show |
43 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.3782-105G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27751201 | |||||||
chr22:27751202 | G | A | 3 | a0001c0001t0017g0354 a0001c0001t0051g0165 a0004c0007t0001g0273 |
3 | HG00099.hp1 HG01099.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.3782-106C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27751202 | |||||||
chr22:27751310 | T | C | 43 | a0001c0001t0001g0149 a0001c0001t0001g0192 a0001c0001t0001g0193 others(40): Show |
44 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.3782-214A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27751310 | |||||||
chr22:27751310 | T | G | 6 | a0001c0001t0016g0119 a0001c0005t0043g0038 a0001c0009t0021g0006 others(3): Show |
7 | HG02451.hp2 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.3782-214A>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27751310 | |||||||
chr22:27751316 | T | C | 9 | a0001c0001t0006g0220 a0001c0001t0044g0041 a0001c0001t0045g0043 others(6): Show |
9 | HG01243.hp2 HG02257.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.3782-220A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27751316 | |||||||
chr22:27751387 | T | C | 1 | a0001c0001t0052g0081 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.3782-291A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27751387 | |||||||
chr22:27751419 | T | A | 1 | a0001c0001t0062g0062 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3782-323A>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27751419 | |||||||
chr22:27751437 | C | T | 3 | a0001c0001t0003g0311 a0001c0001t0005g0118 a0002c0002t0005g0267 |
3 | NA18747.hp2 NA18947.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.3782-341G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27751437 | |||||||
chr22:27751489 | G | A | 48 | a0001c0001t0001g0005 a0001c0001t0001g0149 a0001c0001t0001g0181 others(45): Show |
50 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.3782-393C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27751489 | |||||||
chr22:27751492 | G | A | 1 | a0001c0001t0002g0136 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3782-396C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27751492 | |||||||
chr22:27751492 | G | T | 1 | a0001c0005t0009g0018 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3782-396C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27751492 | |||||||
chr22:27751638 | G | A | 6 | a0001c0001t0002g0231 a0001c0001t0045g0043 a0001c0005t0028g0052 others(3): Show |
6 | HG02257.hp1 HG03139.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.3782-542C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27751638 | |||||||
chr22:27751708 | G | A | 2 | a0001c0014t0018g0372 a0002c0003t0009g0032 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3782-612C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27751708 | |||||||
chr22:27751943 | G | A | 8 | a0001c0001t0001g0171 a0001c0001t0001g0223 a0001c0001t0002g0157 others(5): Show |
8 | HG00621.hp2 HG02074.hp2 NA18992.hp2 others(5): Show |
intron_variant | MODIFIER | c.3782-847C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27751943 | |||||||
chr22:27752310 | G | T | 8 | a0001c0001t0002g0201 a0001c0001t0058g0234 a0001c0001t0059g0232 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.3782-1214C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27752310 | |||||||
chr22:27752339 | G | T | 1 | a0001c0001t0050g0199 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.3782-1243C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27752339 | |||||||
chr22:27752825 | G | A | 112 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0056 others(109): Show |
115 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.3782-1729C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27752825 | |||||||
chr22:27752840 | G | A | 1 | a0001c0001t0075g0382 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3782-1744C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27752840 | |||||||
chr22:27753072 | G | A | 1 | a0001c0001t0069g0371 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3782-1976C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27753072 | |||||||
chr22:27753172 | A | C | 197 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0056 others(194): Show |
201 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.3782-2076T>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27753172 | |||||||
chr22:27753215 | C | T | 1 | a0001c0001t0005g0191 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3782-2119G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27753215 | |||||||
chr22:27753705 | C | A | 43 | a0001c0001t0001g0084 a0001c0001t0002g0065 a0001c0001t0002g0066 others(40): Show |
45 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.3782-2609G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27753705 | |||||||
chr22:27753739 | G | A | 1 | a0001c0001t0002g0201 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3782-2643C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27753739 | |||||||
chr22:27753786 | C | T | 10 | a0001c0001t0002g0093 a0001c0001t0002g0117 a0001c0001t0002g0139 others(7): Show |
10 | HG00738.hp1 HG01109.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.3782-2690G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27753786 | |||||||
chr22:27753821 | G | C | 1 | a0006c0015t0005g0046 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3782-2725C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27753821 | |||||||
chr22:27753843 | C | T | 6 | a0001c0001t0001g0149 a0001c0001t0002g0228 a0001c0001t0068g0331 others(3): Show |
6 | HG02559.hp2 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.3782-2747G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27753843 | |||||||
chr22:27753940 | C | T | 12 | a0001c0001t0001g0079 a0001c0001t0002g0213 a0001c0001t0003g0338 others(9): Show |
12 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.3782-2844G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27753940 | |||||||
chr22:27754010 | C | G | 58 | a0001c0001t0001g0068 a0001c0001t0001g0084 a0001c0001t0001g0159 others(55): Show |
61 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.3782-2914G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27754010 | |||||||
chr22:27754066 | G | A | 5 | a0001c0005t0016g0054 a0001c0013t0001g0048 a0001c0013t0048g0047 others(2): Show |
5 | HG01884.hp1 HG02572.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3782-2970C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27754066 | |||||||
chr22:27754121 | A | G | 321 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0056 others(318): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.3782-3025T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27754121 | |||||||
chr22:27754221 | G | A | 1 | a0001c0012t0001g0278 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.3782-3125C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27754221 | |||||||
chr22:27754227 | C | T | 2 | a0001c0001t0002g0092 a0002c0002t0002g0253 |
2 | NA18967.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.3782-3131G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27754227 | |||||||
chr22:27754257 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3782-3161C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27754257 | |||||||
chr22:27754494 | A | G | 5 | a0001c0001t0002g0112 a0001c0001t0002g0231 a0001c0001t0069g0371 others(2): Show |
5 | HG01243.hp2 HG02055.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.3782-3398T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27754494 | |||||||
chr22:27754505 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3782-3409C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27754505 | |||||||
chr22:27754744 | G | A | 13 | a0001c0001t0001g0079 a0001c0001t0002g0213 a0001c0001t0003g0338 others(10): Show |
13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-3648C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27754744 | |||||||
chr22:27754756 | G | A | 2 | a0001c0001t0027g0107 a0001c0001t0027g0180 |
2 | HG00738.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.3782-3660C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27754756 | |||||||
chr22:27754826 | C | T | 2 | a0001c0005t0043g0038 a0002c0003t0014g0022 |
2 | NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3782-3730G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27754826 | |||||||
chr22:27754827 | G | A | 56 | a0001c0001t0001g0068 a0001c0001t0001g0083 a0001c0001t0001g0084 others(53): Show |
59 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.3782-3731C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27754827 | |||||||
chr22:27754848 | C | A | 1 | a0001c0001t0004g0295 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.3782-3752G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27754848 | |||||||
chr22:27754875 | C | A | 12 | a0001c0001t0001g0079 a0001c0001t0002g0213 a0001c0001t0003g0338 others(9): Show |
12 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.3782-3779G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27754875 | |||||||
chr22:27754978 | C | T | 1 | a0001c0001t0011g0070 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.3782-3882G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27754978 | |||||||
chr22:27755022 | C | A | 1 | a0003c0004t0002g0241 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3782-3926G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27755022 | |||||||
chr22:27755132 | C | G | 109 | a0001c0001t0001g0004 a0001c0001t0001g0080 a0001c0001t0001g0104 others(106): Show |
111 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.3782-4036G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27755132 | |||||||
chr22:27755226 | C | A | 4 | a0001c0001t0001g0099 a0001c0001t0001g0169 a0001c0001t0037g0010 others(1): Show |
4 | HG03704.hp1 HG03710.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.3782-4130G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27755226 | |||||||
chr22:27755420 | G | A | 2 | a0001c0001t0002g0201 a0002c0003t0039g0029 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.3782-4324C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27755420 | |||||||
chr22:27755602 | C | G | 11 | a0001c0001t0001g0079 a0001c0001t0002g0213 a0001c0001t0003g0338 others(8): Show |
11 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.3782-4506G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27755602 | |||||||
chr22:27755645 | C | A | 2 | a0001c0009t0006g0268 a0002c0003t0009g0023 |
2 | HG02258.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3782-4549G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27755645 | |||||||
chr22:27755685 | A | G | 322 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0056 others(319): Show |
330 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.3782-4589T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27755685 | |||||||
chr22:27755729 | C | T | 4 | a0001c0001t0002g0071 a0001c0001t0002g0233 a0001c0009t0006g0268 others(1): Show |
4 | HG01192.hp2 HG01891.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.3782-4633G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27755729 | |||||||
chr22:27755801 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3782-4705C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27755801 | |||||||
chr22:27755837 | G | A | 76 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0064 others(73): Show |
77 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.3782-4741C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27755837 | |||||||
chr22:27755839 | G | A | 6 | a0001c0001t0001g0159 a0001c0001t0060g0196 a0001c0001t0074g0383 others(3): Show |
6 | HG01496.hp1 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.3782-4743C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27755839 | |||||||
chr22:27755883 | T | C | 6 | a0001c0001t0001g0159 a0001c0001t0060g0196 a0001c0001t0074g0383 others(3): Show |
6 | HG01496.hp1 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.3782-4787A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27755883 | |||||||
chr22:27755977 | G | A | 3 | a0001c0001t0001g0084 a0001c0001t0001g0164 a0001c0001t0001g0221 |
3 | HG01123.hp1 HG02273.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.3782-4881C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27755977 | |||||||
chr22:27756213 | T | C | 2 | a0001c0001t0005g0085 a0001c0001t0005g0179 |
2 | HG01358.hp1 HG01928.hp1 |
intron_variant | MODIFIER | c.3782-5117A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27756213 | |||||||
chr22:27756254 | G | A | 3 | a0001c0001t0001g0113 a0001c0001t0002g0115 a0001c0001t0007g0114 |
3 | HG00438.hp1 NA18959.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.3782-5158C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27756254 | |||||||
chr22:27756281 | T | G | 1 | a0001c0016t0003g0280 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.3782-5185A>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27756281 | |||||||
chr22:27756370 | C | A | 1 | a0001c0001t0004g0281 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.3782-5274G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27756370 | |||||||
chr22:27756385 | G | A | 9 | a0001c0001t0001g0236 a0001c0001t0002g0058 a0001c0001t0002g0150 others(6): Show |
9 | HG01891.hp2 HG02630.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.3782-5289C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27756385 | |||||||
chr22:27756613 | G | A | 129 | a0001c0001t0001g0004 a0001c0001t0001g0079 a0001c0001t0001g0080 others(126): Show |
131 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.3782-5517C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27756613 | |||||||
chr22:27756648 | G | A | 1 | a0001c0005t0016g0054 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3782-5552C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27756648 | |||||||
chr22:27756651 | A | G | 75 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0064 others(72): Show |
76 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.3782-5555T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27756651 | |||||||
chr22:27756810 | C | T | 4 | a0001c0001t0002g0117 a0001c0001t0002g0139 a0001c0001t0024g0019 others(1): Show |
4 | HG02683.hp2 HG02735.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.3782-5714G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27756810 | |||||||
chr22:27756868 | A | C | 1 | a0001c0005t0016g0054 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3782-5772T>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27756868 | |||||||
chr22:27757178 | G | A | 2 | a0001c0001t0002g0231 a0002c0003t0014g0035 |
2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3782-6082C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27757178 | |||||||
chr22:27757252 | C | G | 1 | a0002c0002t0006g0266 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3782-6156G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27757252 | |||||||
chr22:27757334 | G | C | 13 | a0001c0001t0001g0079 a0001c0001t0002g0213 a0001c0001t0003g0338 others(10): Show |
13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-6238C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27757334 | |||||||
chr22:27757349 | G | A | 2 | a0001c0005t0043g0038 a0002c0003t0014g0022 |
2 | NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3782-6253C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27757349 | |||||||
chr22:27757691 | G | A | 1 | a0001c0001t0057g0238 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3782-6595C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27757691 | |||||||
chr22:27757802 | C | T | 2 | a0001c0001t0001g0184 a0001c0001t0006g0185 |
2 | NA18983.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.3782-6706G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27757802 | |||||||
chr22:27757813 | T | C | 1 | a0001c0001t0032g0358 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3782-6717A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27757813 | |||||||
chr22:27757868 | A | C | 323 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0056 others(320): Show |
330 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.3782-6772T>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27757868 | |||||||
chr22:27758150 | C | T | 4 | a0001c0001t0001g0159 a0001c0005t0009g0017 a0001c0010t0024g0014 others(1): Show |
4 | HG01496.hp1 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.3782-7054G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27758150 | |||||||
chr22:27758218 | G | A | 1 | a0002c0003t0015g0024 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3782-7122C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27758218 | |||||||
chr22:27758378 | T | C | 13 | a0001c0001t0001g0079 a0001c0001t0002g0213 a0001c0001t0003g0338 others(10): Show |
13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-7282A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27758378 | |||||||
chr22:27758622 | C | G | 13 | a0001c0001t0001g0079 a0001c0001t0002g0213 a0001c0001t0003g0338 others(10): Show |
13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-7526G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27758622 | |||||||
chr22:27758630 | G | T | 306 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0056 others(303): Show |
312 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(309): Show |
intron_variant | MODIFIER | c.3782-7534C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27758630 | |||||||
chr22:27758665 | C | T | 13 | a0001c0001t0001g0079 a0001c0001t0002g0213 a0001c0001t0003g0338 others(10): Show |
13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-7569G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27758665 | |||||||
chr22:27758671 | C | T | 13 | a0001c0001t0001g0079 a0001c0001t0002g0213 a0001c0001t0003g0338 others(10): Show |
13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-7575G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27758671 | |||||||
chr22:27758754 | C | T | 1 | a0001c0001t0069g0371 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3782-7658G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27758754 | |||||||
chr22:27758961 | G | T | 1 | a0002c0003t0019g0034 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3782-7865C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27758961 | |||||||
chr22:27759000 | A | G | 13 | a0001c0001t0001g0079 a0001c0001t0002g0213 a0001c0001t0003g0338 others(10): Show |
13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-7904T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27759000 | |||||||
chr22:27759197 | C | A | 4 | a0001c0013t0001g0048 a0001c0013t0048g0047 a0002c0003t0015g0026 others(1): Show |
4 | HG01884.hp1 HG02572.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.3782-8101G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27759197 | |||||||
chr22:27759212 | C | G | 4 | a0001c0001t0001g0116 a0001c0001t0001g0183 a0001c0001t0003g0320 others(1): Show |
4 | HG00558.hp1 HG00609.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.3782-8116G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27759212 | |||||||
chr22:27759235 | G | A | 13 | a0001c0001t0001g0079 a0001c0001t0002g0213 a0001c0001t0003g0338 others(10): Show |
13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-8139C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27759235 | |||||||
chr22:27759241 | G | A | 8 | a0001c0001t0001g0140 a0001c0001t0001g0163 a0001c0001t0001g0174 others(5): Show |
8 | HG01168.hp1 HG01928.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.3782-8145C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27759241 | |||||||
chr22:27759309 | C | A | 1 | a0001c0005t0016g0054 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3782-8213G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27759309 | |||||||
chr22:27759344 | CAA | C | 10 | a0001c0001t0001g0173 a0001c0001t0001g0222 a0001c0001t0002g0197 others(7): Show |
10 | HG00280.hp2 HG01106.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.3782-8250_3782-824 others(6): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27759344 | |||||||
chr22:27759361 | G | A | 1 | a0001c0005t0009g0018 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3782-8265C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27759361 | |||||||
chr22:27759416 | C | T | 22 | a0001c0001t0002g0060 a0001c0001t0002g0066 a0001c0001t0002g0145 others(19): Show |
22 | HG00323.hp2 HG00639.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.3782-8320G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27759416 | |||||||
chr22:27759458 | C | T | 1 | a0002c0002t0002g0260 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3782-8362G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27759458 | |||||||
chr22:27759459 | G | A | 13 | a0001c0001t0001g0079 a0001c0001t0002g0213 a0001c0001t0003g0338 others(10): Show |
13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-8363C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27759459 | |||||||
chr22:27759464 | G | A | 137 | a0001c0001t0001g0004 a0001c0001t0001g0080 a0001c0001t0001g0082 others(134): Show |
140 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.3782-8368C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27759464 | |||||||
chr22:27759468 | C | T | 15 | a0001c0001t0001g0236 a0001c0001t0002g0058 a0001c0001t0002g0150 others(12): Show |
15 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.3782-8372G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27759468 | |||||||
chr22:27759689 | C | A | 2 | a0001c0001t0004g0351 a0001c0001t0034g0309 |
2 | HG00423.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.3782-8593G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27759689 | |||||||
chr22:27759842 | TG | T | 13 | a0001c0001t0001g0079 a0001c0001t0002g0213 a0001c0001t0003g0338 others(10): Show |
13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-8747delC | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27759842 | |||||||
chr22:27759975 | TG | T | 10 | a0001c0001t0001g0173 a0001c0001t0001g0222 a0001c0001t0002g0197 others(7): Show |
10 | HG00280.hp2 HG01106.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.3782-8880delC | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27759975 | |||||||
chr22:27759999 | C | T | 2 | a0001c0014t0018g0372 a0002c0003t0009g0032 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3782-8903G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27759999 | |||||||
chr22:27760004 | G | A | 17 | a0001c0001t0001g0236 a0001c0001t0002g0058 a0001c0001t0002g0150 others(14): Show |
17 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.3782-8908C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27760004 | |||||||
chr22:27760075 | C | T | 2 | a0001c0005t0043g0038 a0002c0003t0014g0022 |
2 | NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3782-8979G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27760075 | |||||||
chr22:27760430 | GC | G | 4 | a0001c0013t0001g0048 a0001c0013t0048g0047 a0002c0003t0015g0026 others(1): Show |
4 | HG01884.hp1 HG02572.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.3782-9335delG | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27760430 | |||||||
chr22:27760509 | T | TA | 159 | a0001c0001t0001g0004 a0001c0001t0001g0079 a0001c0001t0001g0080 others(156): Show |
162 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.3782-9414dupT | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27760509 | |||||||
chr22:27760518 | T | G | 1 | a0009c0024t0009g0037 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3782-9422A>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27760518 | |||||||
chr22:27760720 | G | A | 1 | a0001c0001t0069g0371 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3782-9624C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27760720 | |||||||
chr22:27760728 | A | C | 1 | a0001c0001t0026g0045 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.3782-9632T>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27760728 | |||||||
chr22:27760800 | A | G | 146 | a0001c0001t0001g0004 a0001c0001t0001g0080 a0001c0001t0001g0082 others(143): Show |
149 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.3782-9704T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27760800 | |||||||
chr22:27760869 | C | T | 1 | a0002c0003t0014g0030 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3782-9773G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27760869 | |||||||
chr22:27761048 | C | T | 1 | a0001c0001t0002g0117 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3782-9952G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27761048 | |||||||
chr22:27761218 | T | C | 79 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0064 others(76): Show |
80 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.3782-10122A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27761218 | |||||||
chr22:27761221 | T | TTC | 13 | a0001c0001t0001g0079 a0001c0001t0002g0213 a0001c0001t0003g0338 others(10): Show |
13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-10127_3782-10 others(8): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27761221 | |||||||
chr22:27761313 | T | C | 32 | a0001c0001t0001g0173 a0001c0001t0001g0222 a0001c0001t0002g0060 others(29): Show |
32 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.3782-10217A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27761313 | |||||||
chr22:27761413 | T | A | 3 | a0001c0001t0001g0116 a0001c0001t0003g0320 a0001c0001t0003g0356 |
3 | HG00558.hp1 HG02027.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.3782-10317A>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27761413 | |||||||
chr22:27761427 | TG | T | 14 | a0001c0001t0001g0079 a0001c0001t0002g0213 a0001c0001t0003g0338 others(11): Show |
14 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.3782-10332delC | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27761427 | |||||||
chr22:27761432 | G | A | 2 | a0001c0005t0043g0038 a0002c0003t0014g0022 |
2 | NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3782-10336C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27761432 | |||||||
chr22:27761432 | GA | G | 120 | a0001c0001t0001g0004 a0001c0001t0001g0080 a0001c0001t0001g0084 others(117): Show |
122 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.3782-10337delT | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27761432 | |||||||
chr22:27761433 | A | G | 29 | a0001c0001t0001g0173 a0001c0001t0001g0183 a0001c0001t0001g0222 others(26): Show |
29 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.3782-10337T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27761433 | |||||||
chr22:27761434 | A | G | 1 | a0001c0001t0062g0062 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3782-10338T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27761434 | |||||||
chr22:27761611 | G | A | 2 | a0001c0001t0001g0124 a0001c0001t0003g0301 |
2 | HG03654.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.3782-10515C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27761611 | |||||||
chr22:27761748 | G | A | 3 | a0001c0001t0007g0088 a0001c0001t0008g0144 a0001c0001t0010g0319 |
3 | HG02486.hp1 NA20752.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.3782-10652C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27761748 | |||||||
chr22:27761753 | G | A | 2 | a0001c0001t0030g0194 a0004c0007t0001g0273 |
2 | HG01167.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.3782-10657C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27761753 | |||||||
chr22:27761760 | C | T | 2 | a0001c0001t0008g0067 a0002c0002t0031g0369 |
2 | HG00280.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.3782-10664G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27761760 | |||||||
chr22:27761768 | G | A | 5 | a0001c0001t0003g0290 a0001c0013t0001g0048 a0001c0013t0048g0047 others(2): Show |
5 | HG01884.hp1 HG02572.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3782-10672C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27761768 | |||||||
chr22:27761852 | A | G | 1 | a0001c0005t0002g0049 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3782-10756T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27761852 | |||||||
chr22:27761882 | G | A | 5 | a0001c0001t0009g0021 a0001c0005t0049g0053 a0001c0008t0018g0374 others(2): Show |
5 | HG02145.hp1 HG02451.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.3782-10786C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27761882 | |||||||
chr22:27761982 | T | C | 13 | a0001c0001t0001g0079 a0001c0001t0002g0213 a0001c0001t0003g0338 others(10): Show |
13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-10886A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27761982 | |||||||
chr22:27762026 | G | T | 13 | a0001c0001t0001g0079 a0001c0001t0002g0213 a0001c0001t0003g0338 others(10): Show |
13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-10930C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762026 | |||||||
chr22:27762066 | C | A | 13 | a0001c0001t0001g0079 a0001c0001t0002g0213 a0001c0001t0003g0338 others(10): Show |
13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-10970G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762066 | |||||||
chr22:27762071 | G | C | 1 | a0001c0001t0001g0099 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3782-10975C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762071 | |||||||
chr22:27762073 | A | G | 13 | a0001c0001t0001g0079 a0001c0001t0002g0213 a0001c0001t0003g0338 others(10): Show |
13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-10977T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762073 | |||||||
chr22:27762131 | T | C | 1 | a0003c0004t0001g0247 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3782-11035A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762131 | |||||||
chr22:27762187 | T | A | 16 | a0001c0001t0001g0126 a0001c0001t0002g0087 a0001c0001t0002g0136 others(13): Show |
16 | HG00423.hp1 HG02071.hp1 NA18940.hp1 others(13): Show |
intron_variant | MODIFIER | c.3782-11091A>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762187 | |||||||
chr22:27762258 | C | T | 1 | a0001c0012t0001g0278 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.3782-11162G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762258 | |||||||
chr22:27762297 | A | G | 2 | a0001c0001t0002g0201 a0002c0003t0039g0029 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.3782-11201T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762297 | |||||||
chr22:27762369 | A | C | 1 | a0001c0001t0003g0318 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3782-11273T>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762369 | |||||||
chr22:27762426 | C | T | 16 | a0001c0001t0002g0065 a0001c0001t0002g0093 a0001c0001t0002g0210 others(13): Show |
16 | HG00735.hp2 HG00738.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.3782-11330G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762426 | |||||||
chr22:27762555 | C | G | 1 | a0001c0001t0062g0062 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3782-11459G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762555 | |||||||
chr22:27762586 | T | C | 3 | a0001c0001t0033g0287 a0001c0001t0033g0327 a0001c0001t0061g0224 |
3 | HG02109.hp1 HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3782-11490A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762586 | |||||||
chr22:27762602 | C | T | 1 | a0003c0004t0002g0243 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3782-11506G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762602 | |||||||
chr22:27762612 | C | T | 1 | a0001c0005t0016g0054 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3782-11516G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762612 | |||||||
chr22:27762661 | C | T | 30 | a0001c0001t0001g0076 a0001c0001t0001g0083 a0001c0001t0001g0084 others(27): Show |
32 | HG00438.hp2 HG00621.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.3782-11565G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762661 | |||||||
chr22:27762722 | C | T | 22 | a0001c0001t0001g0183 a0001c0001t0002g0060 a0001c0001t0002g0066 others(19): Show |
22 | HG00323.hp2 HG00609.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.3782-11626G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762722 | |||||||
chr22:27762756 | G | A | 2 | a0001c0009t0021g0006 a0003c0004t0016g0248 |
3 | HG02451.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3782-11660C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762756 | |||||||
chr22:27762820 | C | T | 17 | a0001c0001t0001g0183 a0001c0001t0002g0060 a0001c0001t0002g0066 others(14): Show |
17 | HG00323.hp2 HG00609.hp1 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.3782-11724G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762820 | |||||||
chr22:27762865 | G | A | 13 | a0001c0001t0001g0079 a0001c0001t0002g0213 a0001c0001t0003g0338 others(10): Show |
13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-11769C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762865 | |||||||
chr22:27762879 | G | GCTTGAGC others(1): Show |
8 | a0001c0001t0001g0159 a0001c0001t0021g0075 a0001c0001t0059g0232 others(5): Show |
8 | HG01496.hp1 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.3782-11791_3782-11 others(14): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762879 | |||||||
chr22:27762924 | C | T | 15 | a0001c0001t0002g0065 a0001c0001t0002g0093 a0001c0001t0002g0210 others(12): Show |
15 | HG00735.hp2 HG00738.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.3782-11828G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762924 | |||||||
chr22:27762925 | G | A | 1 | a0001c0001t0002g0231 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3782-11829C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762925 | |||||||
chr22:27762930 | C | G | 1 | a0001c0001t0003g0302 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.3782-11834G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762930 | |||||||
chr22:27762998 | C | T | 1 | a0001c0001t0011g0121 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.3782-11902G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762998 | |||||||
chr22:27763022 | G | C | 2 | a0001c0005t0043g0038 a0002c0003t0014g0022 |
2 | NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3782-11926C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763022 | |||||||
chr22:27763097 | AAAAACAA others(3): Show |
A | 5 | a0001c0001t0002g0155 a0001c0001t0006g0160 a0001c0001t0010g0305 others(2): Show |
5 | NA18942.hp1 NA18951.hp2 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.3782-12011_3782-12 others(16): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763097 | |||||||
chr22:27763126 | T | C | 1 | a0001c0001t0002g0182 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.3782-12030A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763126 | |||||||
chr22:27763240 | C | T | 3 | a0001c0001t0076g0384 a0002c0003t0019g0033 a0002c0003t0019g0034 |
3 | HG01496.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.3782-12144G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763240 | |||||||
chr22:27763323 | C | T | 8 | a0001c0001t0001g0159 a0001c0001t0002g0201 a0001c0001t0021g0075 others(5): Show |
8 | HG01496.hp1 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.3782-12227G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763323 | |||||||
chr22:27763359 | C | T | 13 | a0001c0001t0001g0079 a0001c0001t0002g0213 a0001c0001t0003g0338 others(10): Show |
13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-12263G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763359 | |||||||
chr22:27763372 | G | A | 2 | a0001c0001t0007g0198 a0001c0001t0022g0333 |
2 | NA18612.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.3782-12276C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763372 | |||||||
chr22:27763388 | G | A | 11 | a0001c0001t0001g0138 a0001c0001t0001g0173 a0001c0001t0001g0222 others(8): Show |
11 | HG00280.hp2 HG01106.hp1 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.3782-12292C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763388 | |||||||
chr22:27763497 | A | T | 13 | a0001c0001t0001g0079 a0001c0001t0002g0213 a0001c0001t0003g0338 others(10): Show |
13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-12401T>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763497 | |||||||
chr22:27763546 | T | G | 11 | a0001c0001t0001g0138 a0001c0001t0001g0173 a0001c0001t0001g0222 others(8): Show |
11 | HG00280.hp2 HG01106.hp1 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.3782-12450A>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763546 | |||||||
chr22:27763555 | G | T | 13 | a0001c0001t0001g0079 a0001c0001t0002g0213 a0001c0001t0003g0338 others(10): Show |
13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-12459C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763555 | |||||||
chr22:27763623 | C | T | 13 | a0001c0001t0001g0079 a0001c0001t0002g0213 a0001c0001t0003g0338 others(10): Show |
13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-12527G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763623 | |||||||
chr22:27763661 | G | A | 3 | a0001c0001t0011g0167 a0001c0001t0011g0178 a0002c0002t0001g0261 |
3 | HG00423.hp1 NA19000.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.3782-12565C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763661 | |||||||
chr22:27763674 | A | T | 1 | a0002c0003t0014g0030 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3782-12578T>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763674 | |||||||
chr22:27763684 | G | A | 223 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0056 others(220): Show |
227 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.3782-12588C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763684 | |||||||
chr22:27763702 | T | C | 315 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0056 others(312): Show |
321 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(318): Show |
intron_variant | MODIFIER | c.3782-12606A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763702 | |||||||
chr22:27763760 | T | C | 225 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0056 others(222): Show |
229 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.3782-12664A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763760 | |||||||
chr22:27763806 | A | C | 13 | a0001c0001t0001g0079 a0001c0001t0002g0213 a0001c0001t0003g0338 others(10): Show |
13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-12710T>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763806 | |||||||
chr22:27763818 | G | A | 1 | a0001c0001t0064g0313 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.3782-12722C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763818 | |||||||
chr22:27763874 | G | C | 13 | a0001c0001t0001g0079 a0001c0001t0002g0213 a0001c0001t0003g0338 others(10): Show |
13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-12778C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763874 | |||||||
chr22:27763915 | C | G | 13 | a0001c0001t0001g0079 a0001c0001t0002g0213 a0001c0001t0003g0338 others(10): Show |
13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-12819G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763915 | |||||||
chr22:27763929 | G | A | 1 | a0001c0012t0001g0277 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3782-12833C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763929 | |||||||
chr22:27763952 | A | G | 1 | a0001c0001t0053g0205 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3782-12856T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763952 | |||||||
chr22:27763971 | C | T | 13 | a0001c0001t0001g0079 a0001c0001t0002g0213 a0001c0001t0003g0338 others(10): Show |
13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-12875G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763971 | |||||||
chr22:27764059 | G | C | 17 | a0001c0001t0001g0236 a0001c0001t0002g0058 a0001c0001t0002g0150 others(14): Show |
17 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.3782-12963C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27764059 | |||||||
chr22:27764062 | G | A | 13 | a0001c0001t0001g0079 a0001c0001t0002g0213 a0001c0001t0003g0338 others(10): Show |
13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-12966C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27764062 | |||||||
chr22:27764086 | T | C | 317 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0056 others(314): Show |
323 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(320): Show |
intron_variant | MODIFIER | c.3782-12990A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27764086 | |||||||
chr22:27764110 | C | A | 1 | a0001c0001t0022g0333 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.3782-13014G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27764110 | |||||||
chr22:27764112 | G | T | 4 | a0001c0013t0001g0048 a0001c0013t0048g0047 a0002c0003t0015g0026 others(1): Show |
4 | HG01884.hp1 HG02572.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.3782-13016C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27764112 | |||||||
chr22:27764201 | C | T | 2 | a0001c0005t0043g0038 a0002c0003t0014g0022 |
2 | NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3782-13105G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27764201 | |||||||
chr22:27764222 | G | A | 4 | a0001c0013t0001g0048 a0001c0013t0048g0047 a0002c0003t0015g0026 others(1): Show |
4 | HG01884.hp1 HG02572.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.3782-13126C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27764222 | |||||||
chr22:27764353 | C | T | 13 | a0001c0001t0001g0079 a0001c0001t0002g0213 a0001c0001t0003g0338 others(10): Show |
13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-13257G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27764353 | |||||||
chr22:27764419 | C | T | 228 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0056 others(225): Show |
232 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.3782-13323G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27764419 | |||||||
chr22:27764551 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.3782-13455G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27764551 | |||||||
chr22:27764755 | G | A | 1 | a0001c0001t0053g0205 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3782-13659C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27764755 | |||||||
chr22:27764855 | G | A | 13 | a0001c0001t0001g0079 a0001c0001t0002g0213 a0001c0001t0003g0338 others(10): Show |
13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-13759C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27764855 | |||||||
chr22:27764984 | T | G | 314 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0056 others(311): Show |
320 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(317): Show |
intron_variant | MODIFIER | c.3782-13888A>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27764984 | |||||||
chr22:27764996 | G | C | 211 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0056 others(208): Show |
215 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.3782-13900C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27764996 | |||||||
chr22:27765038 | T | C | 1 | a0001c0001t0002g0100 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3782-13942A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27765038 | |||||||
chr22:27765158 | C | T | 1 | a0001c0001t0025g0042 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3782-14062G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27765158 | |||||||
chr22:27765181 | T | G | 1 | a0001c0001t0004g0340 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.3782-14085A>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27765181 | |||||||
chr22:27765249 | T | C | 14 | a0001c0001t0001g0079 a0001c0001t0002g0213 a0001c0001t0003g0338 others(11): Show |
14 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.3782-14153A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27765249 | |||||||
chr22:27765370 | A | G | 1 | a0001c0001t0057g0238 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3782-14274T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27765370 | |||||||
chr22:27765422 | AG | A | 249 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0056 others(246): Show |
253 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.3782-14327delC | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27765422 | |||||||
chr22:27765423 | G | A | 16 | a0001c0001t0001g0079 a0001c0001t0002g0213 a0001c0001t0003g0318 others(13): Show |
16 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.3782-14327C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27765423 | |||||||
chr22:27765509 | C | T | 7 | a0001c0001t0001g0149 a0001c0001t0002g0228 a0001c0001t0023g0020 others(4): Show |
7 | HG02559.hp2 HG02809.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.3782-14413G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27765509 | |||||||
chr22:27765553 | C | G | 1 | a0001c0005t0016g0054 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3782-14457G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27765553 | |||||||
chr22:27765715 | A | G | 71 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0076 others(68): Show |
73 | HG00323.hp2 HG00438.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.3782-14619T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27765715 | |||||||
chr22:27765817 | G | C | 12 | a0001c0001t0001g0132 a0001c0001t0001g0138 a0001c0001t0001g0140 others(9): Show |
12 | HG00280.hp2 HG01106.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.3782-14721C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27765817 | |||||||
chr22:27765909 | C | T | 1 | a0001c0001t0005g0195 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.3782-14813G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27765909 | |||||||
chr22:27765943 | C | T | 4 | a0001c0001t0001g0064 a0001c0001t0002g0214 a0002c0002t0017g0363 others(1): Show |
4 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.3782-14847G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27765943 | |||||||
chr22:27766105 | C | T | 1 | a0001c0001t0005g0086 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.3782-15009G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27766105 | |||||||
chr22:27766116 | T | C | 1 | a0001c0001t0053g0205 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3782-15020A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27766116 | |||||||
chr22:27766152 | C | T | 21 | a0001c0001t0001g0236 a0001c0001t0002g0058 a0001c0001t0002g0150 others(18): Show |
21 | HG01884.hp1 HG01891.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.3782-15056G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27766152 | |||||||
chr22:27766825 | C | T | 1 | a0001c0001t0058g0234 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3782-15729G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27766825 | |||||||
chr22:27766826 | G | A | 2 | a0001c0005t0043g0038 a0002c0003t0014g0022 |
2 | NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3782-15730C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27766826 | |||||||
chr22:27766859 | G | A | 1 | a0001c0001t0045g0043 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3782-15763C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27766859 | |||||||
chr22:27766870 | G | A | 1 | a0001c0001t0002g0111 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3782-15774C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27766870 | |||||||
chr22:27766995 | G | T | 1 | a0001c0010t0040g0013 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3782-15899C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27766995 | |||||||
chr22:27767046 | A | T | 1 | a0001c0001t0024g0019 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3782-15950T>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27767046 | |||||||
chr22:27767211 | C | G | 1 | a0002c0003t0042g0031 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3782-16115G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27767211 | |||||||
chr22:27767264 | G | A | 2 | a0001c0001t0001g0126 a0001c0001t0003g0326 |
2 | NA18981.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.3782-16168C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27767264 | |||||||
chr22:27767358 | G | A | 80 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0073 others(77): Show |
81 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.3782-16262C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27767358 | |||||||
chr22:27767475 | C | A | 1 | a0002c0003t0015g0027 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3782-16379G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27767475 | |||||||
chr22:27767621 | T | C | 3 | a0001c0001t0009g0021 a0001c0008t0018g0374 a0001c0014t0018g0373 |
3 | HG02145.hp1 HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3782-16525A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27767621 | |||||||
chr22:27767710 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3782-16614G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27767710 | |||||||
chr22:27767715 | C | T | 1 | a0001c0001t0010g0304 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3782-16619G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27767715 | |||||||
chr22:27767782 | G | T | 2 | a0001c0005t0043g0038 a0002c0003t0014g0022 |
2 | NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3782-16686C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27767782 | |||||||
chr22:27767811 | A | G | 16 | a0001c0001t0001g0173 a0001c0001t0002g0065 a0001c0001t0002g0093 others(13): Show |
16 | HG00735.hp2 HG00738.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.3782-16715T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27767811 | |||||||
chr22:27767979 | G | A | 1 | a0002c0002t0001g0265 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3782-16883C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27767979 | |||||||
chr22:27768006 | A | G | 134 | a0001c0001t0001g0004 a0001c0001t0001g0079 a0001c0001t0001g0113 others(131): Show |
137 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.3782-16910T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27768006 | |||||||
chr22:27768062 | T | G | 101 | a0001c0001t0001g0004 a0001c0001t0001g0113 a0001c0001t0001g0126 others(98): Show |
103 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.3782-16966A>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27768062 | |||||||
chr22:27768081 | G | C | 7 | a0001c0001t0001g0149 a0001c0001t0002g0228 a0001c0001t0059g0232 others(4): Show |
7 | HG02559.hp2 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.3782-16985C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27768081 | |||||||
chr22:27768218 | A | C | 3 | a0001c0001t0023g0020 a0001c0001t0069g0371 a0001c0013t0001g0048 |
3 | HG02055.hp2 HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3782-17122T>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27768218 | |||||||
chr22:27768262 | T | C | 4 | a0001c0001t0001g0163 a0001c0001t0002g0227 a0001c0001t0020g0168 others(1): Show |
4 | HG01952.hp2 HG01978.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.3782-17166A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27768262 | |||||||
chr22:27768546 | C | A | 2 | a0001c0001t0001g0140 a0001c0001t0008g0095 |
2 | HG01928.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.3782-17450G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27768546 | |||||||
chr22:27768591 | G | A | 5 | a0001c0001t0001g0068 a0001c0001t0017g0353 a0001c0001t0017g0354 others(2): Show |
6 | HG00099.hp1 HG01099.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.3782-17495C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27768591 | |||||||
chr22:27768640 | T | A | 1 | a0001c0001t0002g0100 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3782-17544A>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27768640 | |||||||
chr22:27768803 | C | T | 1 | a0001c0001t0069g0371 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3782-17707G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27768803 | |||||||
chr22:27768824 | T | G | 1 | a0001c0001t0001g0098 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3782-17728A>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27768824 | |||||||
chr22:27768864 | C | T | 3 | a0001c0001t0023g0020 a0001c0001t0069g0371 a0001c0013t0001g0048 |
3 | HG02055.hp2 HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3782-17768G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27768864 | |||||||
chr22:27769015 | T | C | 21 | a0001c0001t0001g0183 a0001c0001t0002g0060 a0001c0001t0002g0066 others(18): Show |
21 | HG00323.hp2 HG00609.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.3782-17919A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769015 | |||||||
chr22:27769113 | T | G | 12 | a0001c0001t0001g0104 a0001c0001t0001g0132 a0001c0001t0001g0138 others(9): Show |
12 | HG00280.hp2 HG01106.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.3782-18017A>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769113 | |||||||
chr22:27769346 | A | G | 225 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0056 others(222): Show |
229 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.3782-18250T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769346 | |||||||
chr22:27769430 | T | C | 3 | a0001c0001t0023g0020 a0001c0001t0069g0371 a0001c0013t0001g0048 |
3 | HG02055.hp2 HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3782-18334A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769430 | |||||||
chr22:27769552 | A | ATTTTTTT others(2): Show |
28 | a0001c0001t0001g0104 a0001c0001t0001g0132 a0001c0001t0001g0138 others(25): Show |
28 | HG00438.hp1 HG00558.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.3782-18465_3782-18 others(15): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769552 | |||||||
chr22:27769552 | A | ATTTTTTT others(3): Show |
105 | a0001c0001t0001g0004 a0001c0001t0001g0079 a0001c0001t0001g0113 others(102): Show |
107 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.3782-18466_3782-18 others(16): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769552 | |||||||
chr22:27769552 | A | ATTTTTTT others(4): Show |
74 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0074 others(71): Show |
75 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.3782-18467_3782-18 others(17): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769552 | |||||||
chr22:27769552 | A | ATTTTTTT others(5): Show |
32 | a0001c0001t0001g0064 a0001c0001t0001g0073 a0001c0001t0001g0105 others(29): Show |
33 | HG00408.hp1 HG00609.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.3782-18468_3782-18 others(18): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769552 | |||||||
chr22:27769552 | A | ATTTTTTT others(6): Show |
37 | a0001c0001t0001g0099 a0001c0001t0001g0124 a0001c0001t0001g0149 others(34): Show |
40 | HG00735.hp1 HG01081.hp1 HG01167.hp1 others(37): Show |
intron_variant | MODIFIER | c.3782-18469_3782-18 others(19): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769552 | |||||||
chr22:27769552 | A | ATTTTTTT others(7): Show |
41 | a0001c0001t0001g0005 a0001c0001t0001g0063 a0001c0001t0001g0068 others(38): Show |
42 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.3782-18470_3782-18 others(20): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769552 | |||||||
chr22:27769552 | A | ATTTTTTT others(8): Show |
3 | a0001c0001t0001g0181 a0001c0001t0002g0146 a0001c0001t0003g0336 |
3 | HG00140.hp2 HG00639.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.3782-18471_3782-18 others(21): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769552 | |||||||
chr22:27769552 | A | ATTTTTTT others(13): Show |
2 | a0001c0001t0053g0205 a0001c0005t0016g0054 |
2 | HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3782-18457_3782-18 others(26): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769552 | |||||||
chr22:27769552 | A | ATTTTTTT others(14): Show |
1 | a0001c0021t0007g0250 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3782-18457_3782-18 others(27): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769552 | |||||||
chr22:27769570 | TGAGACAG others(32): Show |
T | 2 | a0001c0001t0023g0020 a0001c0001t0069g0371 |
2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3782-18513_3782-18 others(45): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769570 | |||||||
chr22:27769573 | GACAGAGT others(33): Show |
G | 1 | a0001c0013t0001g0048 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3782-18517_3782-18 others(46): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769573 | |||||||
chr22:27769612 | G | A | 2 | a0001c0001t0023g0020 a0001c0001t0069g0371 |
2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3782-18516C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769612 | |||||||
chr22:27769613 | C | G | 2 | a0001c0001t0023g0020 a0001c0001t0069g0371 |
2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3782-18517G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769613 | |||||||
chr22:27769709 | C | T | 15 | a0001c0001t0001g0079 a0001c0001t0002g0213 a0001c0001t0003g0318 others(12): Show |
15 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.3782-18613G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769709 | |||||||
chr22:27769720 | T | A | 1 | a0001c0001t0002g0060 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3782-18624A>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769720 | |||||||
chr22:27769762 | C | G | 263 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0056 others(260): Show |
268 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.3782-18666G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769762 | |||||||
chr22:27769790 | G | A | 3 | a0001c0001t0023g0020 a0001c0001t0069g0371 a0001c0013t0001g0048 |
3 | HG02055.hp2 HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3782-18694C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769790 | |||||||
chr22:27769819 | G | A | 142 | a0001c0001t0001g0004 a0001c0001t0001g0079 a0001c0001t0001g0113 others(139): Show |
145 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.3782-18723C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769819 | |||||||
chr22:27769863 | AT | A | 131 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0073 others(128): Show |
133 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.3782-18768delA | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769863 | |||||||
chr22:27770032 | T | C | 1 | a0003c0004t0016g0248 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3782-18936A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27770032 | |||||||
chr22:27770095 | T | C | 1 | a0001c0001t0008g0229 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3782-18999A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27770095 | |||||||
chr22:27770105 | C | T | 1 | a0001c0001t0002g0237 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3782-19009G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27770105 | |||||||
chr22:27770152 | C | T | 1 | a0001c0005t0002g0055 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3782-19056G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27770152 | |||||||
chr22:27770296 | C | T | 2 | a0001c0005t0043g0038 a0002c0003t0014g0022 |
2 | NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3782-19200G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27770296 | |||||||
chr22:27770315 | G | A | 15 | a0001c0001t0001g0079 a0001c0001t0002g0213 a0001c0001t0003g0318 others(12): Show |
15 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.3782-19219C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27770315 | |||||||
chr22:27770414 | C | G | 39 | a0001c0001t0001g0005 a0001c0001t0001g0063 a0001c0001t0001g0064 others(36): Show |
42 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(39): Show |
intron_variant | MODIFIER | c.3782-19318G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27770414 | |||||||
chr22:27770447 | AATCATGT others(2): Show |
A | 141 | a0001c0001t0001g0004 a0001c0001t0001g0079 a0001c0001t0001g0113 others(138): Show |
144 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.3782-19360_3782-19 others(15): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27770447 | |||||||
chr22:27770458 | T | C | 2 | a0001c0009t0021g0006 a0003c0004t0016g0248 |
3 | HG02451.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3782-19362A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27770458 | |||||||
chr22:27770482 | C | A | 24 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0103 others(21): Show |
25 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.3782-19386G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27770482 | |||||||
chr22:27770518 | C | T | 1 | a0001c0001t0002g0094 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.3782-19422G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27770518 | |||||||
chr22:27770575 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.3782-19479G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27770575 | |||||||
chr22:27770662 | TTTATTTT others(61): Show |
T | 26 | a0001c0001t0001g0079 a0001c0001t0001g0149 a0001c0001t0002g0213 others(23): Show |
27 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.3782-19634_3782-19 others(74): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27770662 | |||||||
chr22:27770872 | T | C | 19 | a0001c0001t0001g0183 a0001c0001t0002g0060 a0001c0001t0002g0066 others(16): Show |
19 | HG00323.hp2 HG00609.hp1 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.3782-19776A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27770872 | |||||||
chr22:27770935 | C | T | 8 | a0001c0001t0001g0079 a0001c0001t0002g0213 a0001c0001t0003g0318 others(5): Show |
8 | HG00673.hp2 HG02015.hp1 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.3782-19839G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27770935 | |||||||
chr22:27771096 | G | A | 1 | a0001c0001t0062g0062 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3782-20000C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27771096 | |||||||
chr22:27771136 | A | G | 4 | a0001c0001t0001g0159 a0001c0005t0009g0017 a0001c0010t0024g0014 others(1): Show |
4 | HG01496.hp1 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.3782-20040T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27771136 | |||||||
chr22:27771163 | A | G | 1 | a0001c0001t0002g0216 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3782-20067T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27771163 | |||||||
chr22:27771219 | C | CTT | 22 | a0001c0001t0001g0079 a0001c0001t0001g0149 a0001c0001t0002g0213 others(19): Show |
24 | HG00673.hp2 HG01243.hp2 HG02015.hp1 others(21): Show |
intron_variant | MODIFIER | c.3782-20125_3782-20 others(8): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27771219 | |||||||
chr22:27771219 | C | CTTT | 26 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0177 others(23): Show |
26 | HG01192.hp2 HG02055.hp1 HG02451.hp1 others(23): Show |
intron_variant | MODIFIER | c.3782-20126_3782-20 others(9): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27771219 | |||||||
chr22:27771219 | CT | C | 142 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0063 others(139): Show |
149 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.3782-20124delA | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27771219 | |||||||
chr22:27771219 | CTT | C | 13 | a0001c0001t0001g0208 a0001c0001t0002g0137 a0001c0001t0002g0202 others(10): Show |
13 | HG00558.hp2 HG01070.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-20125_3782-20 others(8): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27771219 | |||||||
chr22:27771219 | CTTTT | C | 40 | a0001c0001t0001g0098 a0001c0001t0001g0116 a0001c0001t0001g0169 others(37): Show |
40 | HG00140.hp2 HG00558.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.3782-20127_3782-20 others(10): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27771219 | |||||||
chr22:27771219 | CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0002g0225 a0001c0001t0025g0042 a0002c0003t0041g0028 |
3 | HG01891.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3782-20135_3782-20 others(18): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27771219 | |||||||
chr22:27771297 | T | C | 1 | a0001c0001t0006g0154 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3782-20201A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27771297 | |||||||
chr22:27771433 | C | T | 1 | a0002c0002t0007g0254 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3782-20337G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27771433 | |||||||
chr22:27771535 | T | G | 18 | a0001c0001t0001g0149 a0001c0001t0001g0230 a0001c0001t0002g0150 others(15): Show |
19 | HG01243.hp2 HG02257.hp2 HG02809.hp1 others(16): Show |
intron_variant | MODIFIER | c.3782-20439A>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27771535 | |||||||
chr22:27771647 | C | T | 1 | a0001c0001t0003g0349 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3782-20551G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27771647 | |||||||
chr22:27771687 | G | A | 1 | a0002c0002t0003g0361 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.3782-20591C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27771687 | |||||||
chr22:27771920 | T | A | 1 | a0001c0001t0001g0153 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.3782-20824A>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27771920 | |||||||
chr22:27772071 | G | A | 1 | a0001c0001t0023g0020 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3782-20975C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27772071 | |||||||
chr22:27772110 | C | A | 1 | a0001c0010t0024g0014 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3782-21014G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27772110 | |||||||
chr22:27772264 | C | T | 90 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0073 others(87): Show |
94 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.3782-21168G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27772264 | |||||||
chr22:27772345 | C | T | 1 | a0002c0003t0014g0030 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3782-21249G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27772345 | |||||||
chr22:27772346 | G | A | 1 | a0001c0001t0066g0317 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.3782-21250C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27772346 | |||||||
chr22:27772359 | A | G | 74 | a0001c0001t0001g0056 a0001c0001t0001g0064 a0001c0001t0001g0068 others(71): Show |
77 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.3782-21263T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27772359 | |||||||
chr22:27772386 | A | C | 2 | a0001c0001t0002g0233 a0001c0021t0007g0250 |
2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3782-21290T>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27772386 | |||||||
chr22:27772495 | G | C | 78 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0073 others(75): Show |
82 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.3782-21399C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27772495 | |||||||
chr22:27772503 | C | G | 4 | a0001c0001t0002g0071 a0001c0001t0002g0200 a0001c0001t0023g0020 others(1): Show |
4 | HG01192.hp2 HG02630.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.3782-21407G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27772503 | |||||||
chr22:27772597 | C | T | 66 | a0001c0001t0001g0002 a0001c0001t0001g0080 a0001c0001t0001g0082 others(63): Show |
67 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.3782-21501G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27772597 | |||||||
chr22:27772691 | C | T | 1 | a0001c0001t0004g0303 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.3782-21595G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27772691 | |||||||
chr22:27772796 | T | C | 6 | a0001c0001t0001g0098 a0001c0001t0002g0089 a0001c0001t0002g0090 others(3): Show |
6 | HG00140.hp1 HG01167.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.3782-21700A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27772796 | |||||||
chr22:27772817 | T | C | 2 | a0001c0005t0049g0053 a0001c0013t0001g0048 |
2 | HG02451.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.3782-21721A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27772817 | |||||||
chr22:27772852 | C | CCAT | 20 | a0001c0001t0001g0098 a0001c0001t0001g0104 a0001c0001t0002g0065 others(17): Show |
20 | HG00673.hp2 HG00735.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.3782-21759_3782-21 others(9): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27772852 | |||||||
chr22:27772852 | C | CCATCAT | 34 | a0001c0001t0001g0099 a0001c0001t0001g0105 a0001c0001t0001g0149 others(31): Show |
35 | HG01243.hp1 HG01496.hp2 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.3782-21762_3782-21 others(12): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27772852 | |||||||
chr22:27772852 | C | CCATCATC others(2): Show |
3 | a0001c0001t0069g0371 a0001c0009t0021g0006 a0003c0004t0016g0248 |
4 | HG02055.hp2 HG02451.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.3782-21765_3782-21 others(15): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27772852 | |||||||
chr22:27772880 | CATCATA | C | 76 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0073 others(73): Show |
80 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.3782-21790_3782-21 others(12): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27772880 | |||||||
chr22:27772886 | A | C | 5 | a0001c0001t0001g0164 a0001c0001t0002g0233 a0001c0005t0049g0053 others(2): Show |
5 | HG01123.hp1 HG01891.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.3782-21790T>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27772886 | |||||||
chr22:27772959 | G | C | 1 | a0001c0001t0003g0301 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3782-21863C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27772959 | |||||||
chr22:27772959 | G | T | 1 | a0001c0001t0008g0131 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3782-21863C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27772959 | |||||||
chr22:27773072 | C | G | 2 | a0001c0001t0016g0119 a0001c0013t0048g0047 |
2 | HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3782-21976G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27773072 | |||||||
chr22:27773089 | C | T | 2 | a0001c0014t0018g0372 a0003c0004t0001g0247 |
2 | HG02055.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.3782-21993G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27773089 | |||||||
chr22:27773099 | A | T | 1 | a0002c0003t0009g0023 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3782-22003T>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27773099 | |||||||
chr22:27773149 | C | T | 1 | a0002c0002t0006g0266 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3782-22053G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27773149 | |||||||
chr22:27773318 | A | G | 3 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 |
3 | NA18992.hp2 NA19011.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.3782-22222T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27773318 | |||||||
chr22:27773469 | A | G | 2 | a0001c0001t0002g0151 a0001c0001t0075g0382 |
2 | HG03041.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3782-22373T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27773469 | |||||||
chr22:27773501 | AC | A | 7 | a0001c0001t0002g0112 a0001c0001t0076g0384 a0001c0005t0049g0053 others(4): Show |
7 | HG01496.hp2 HG02451.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.3782-22406delG | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27773501 | |||||||
chr22:27773511 | C | T | 149 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0068 others(146): Show |
154 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.3782-22415G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27773511 | |||||||
chr22:27773533 | C | A | 324 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(321): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.3782-22437G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27773533 | |||||||
chr22:27773553 | G | A | 1 | a0001c0001t0010g0310 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.3782-22457C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27773553 | |||||||
chr22:27773589 | T | A | 1 | a0001c0001t0001g0120 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.3782-22493A>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27773589 | |||||||
chr22:27773804 | G | A | 5 | a0001c0001t0002g0150 a0001c0001t0002g0216 a0001c0001t0044g0041 others(2): Show |
5 | HG02109.hp2 HG02809.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.3782-22708C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27773804 | |||||||
chr22:27773907 | G | C | 2 | a0001c0009t0021g0006 a0003c0004t0016g0248 |
3 | HG02451.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3782-22811C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27773907 | |||||||
chr22:27773961 | T | G | 81 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0073 others(78): Show |
85 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.3781+22802A>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27773961 | |||||||
chr22:27774043 | C | A | 91 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0073 others(88): Show |
95 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.3781+22720G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774043 | |||||||
chr22:27774046 | C | A | 1 | a0001c0001t0001g0161 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3781+22717G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774046 | |||||||
chr22:27774156 | G | C | 1 | a0001c0001t0054g0175 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3781+22607C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774156 | |||||||
chr22:27774158 | C | A | 1 | a0001c0001t0054g0175 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3781+22605G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774158 | |||||||
chr22:27774161 | A | C | 1 | a0001c0001t0054g0175 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3781+22602T>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774161 | |||||||
chr22:27774163 | G | T | 1 | a0001c0001t0054g0175 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3781+22600C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774163 | |||||||
chr22:27774166 | C | T | 1 | a0001c0001t0054g0175 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3781+22597G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774166 | |||||||
chr22:27774167 | T | G | 1 | a0001c0001t0054g0175 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3781+22596A>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774167 | |||||||
chr22:27774168 | C | A | 1 | a0001c0001t0054g0175 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3781+22595G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774168 | |||||||
chr22:27774170 | C | G | 1 | a0001c0001t0054g0175 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3781+22593G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774170 | |||||||
chr22:27774172 | G | T | 1 | a0001c0001t0054g0175 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3781+22591C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774172 | |||||||
chr22:27774178 | A | C | 96 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0073 others(93): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.3781+22585T>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774178 | |||||||
chr22:27774229 | C | T | 144 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0098 others(141): Show |
146 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.3781+22534G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774229 | |||||||
chr22:27774292 | C | T | 42 | a0001c0001t0001g0077 a0001c0001t0001g0083 a0001c0001t0001g0126 others(39): Show |
43 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.3781+22471G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774292 | |||||||
chr22:27774505 | T | C | 2 | a0001c0001t0002g0233 a0001c0021t0007g0250 |
2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3781+22258A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774505 | |||||||
chr22:27774606 | A | G | 1 | a0001c0001t0002g0201 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3781+22157T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774606 | |||||||
chr22:27774623 | A | G | 1 | a0001c0005t0016g0054 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3781+22140T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774623 | |||||||
chr22:27774686 | C | A | 1 | a0002c0002t0023g0036 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3781+22077G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774686 | |||||||
chr22:27774702 | G | A | 75 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0073 others(72): Show |
79 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.3781+22061C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774702 | |||||||
chr22:27774708 | G | A | 1 | a0001c0001t0002g0093 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3781+22055C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774708 | |||||||
chr22:27774726 | G | A | 1 | a0001c0001t0003g0337 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3781+22037C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774726 | |||||||
chr22:27774726 | G | C | 2 | a0001c0001t0002g0233 a0001c0021t0007g0250 |
2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3781+22037C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774726 | |||||||
chr22:27774735 | A | T | 106 | a0001c0001t0001g0064 a0001c0001t0001g0068 a0001c0001t0001g0076 others(103): Show |
108 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.3781+22028T>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774735 | |||||||
chr22:27774802 | G | A | 1 | a0002c0002t0007g0258 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.3781+21961C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774802 | |||||||
chr22:27774834 | T | C | 3 | a0001c0001t0004g0334 a0001c0001t0004g0335 a0001c0001t0025g0040 |
3 | HG01346.hp1 HG01358.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.3781+21929A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774834 | |||||||
chr22:27774858 | T | C | 6 | a0001c0001t0002g0112 a0001c0001t0002g0200 a0001c0001t0076g0384 others(3): Show |
6 | HG01496.hp2 HG02630.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.3781+21905A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774858 | |||||||
chr22:27774904 | C | T | 2 | a0001c0001t0002g0233 a0001c0021t0007g0250 |
2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3781+21859G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774904 | |||||||
chr22:27775056 | C | T | 6 | a0001c0001t0002g0112 a0001c0001t0002g0200 a0001c0001t0076g0384 others(3): Show |
6 | HG01496.hp2 HG02630.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.3781+21707G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27775056 | |||||||
chr22:27775325 | C | T | 2 | a0001c0001t0006g0217 a0001c0001t0012g0298 |
2 | NA18970.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.3781+21438G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27775325 | |||||||
chr22:27775399 | G | A | 1 | a0001c0001t0026g0044 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.3781+21364C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27775399 | |||||||
chr22:27775522 | C | T | 32 | a0001c0001t0001g0153 a0001c0001t0001g0209 a0001c0001t0002g0071 others(29): Show |
32 | HG00438.hp2 HG01099.hp1 HG01192.hp2 others(29): Show |
intron_variant | MODIFIER | c.3781+21241G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27775522 | |||||||
chr22:27775948 | G | GA | 92 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0073 others(89): Show |
97 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.3781+20814dupT | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27775948 | |||||||
chr22:27776056 | C | G | 3 | a0001c0001t0003g0300 a0001c0001t0003g0336 a0001c0001t0013g0299 |
3 | HG02080.hp1 NA18955.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.3781+20707G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27776056 | |||||||
chr22:27776102 | G | A | 7 | a0001c0001t0001g0159 a0001c0001t0006g0220 a0001c0001t0023g0020 others(4): Show |
7 | HG01243.hp2 HG02717.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.3781+20661C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27776102 | |||||||
chr22:27776248 | T | C | 3 | a0001c0001t0002g0089 a0001c0001t0002g0090 a0001c0001t0002g0091 |
3 | HG01256.hp2 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.3781+20515A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27776248 | |||||||
chr22:27776251 | G | A | 1 | a0002c0002t0002g0260 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3781+20512C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27776251 | |||||||
chr22:27776300 | G | A | 2 | a0001c0001t0006g0220 a0001c0001t0010g0319 |
2 | HG02895.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.3781+20463C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27776300 | |||||||
chr22:27776473 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3781+20290A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27776473 | |||||||
chr22:27776543 | G | A | 12 | a0001c0001t0001g0149 a0001c0001t0002g0228 a0001c0001t0053g0205 others(9): Show |
13 | HG02055.hp2 HG02717.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.3781+20220C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27776543 | |||||||
chr22:27776556 | C | A | 1 | a0001c0001t0001g0099 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3781+20207G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27776556 | |||||||
chr22:27776589 | T | G | 298 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0056 others(295): Show |
305 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.3781+20174A>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27776589 | |||||||
chr22:27776697 | C | T | 1 | a0001c0016t0003g0280 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.3781+20066G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27776697 | |||||||
chr22:27777015 | G | A | 2 | a0001c0001t0002g0092 a0001c0001t0007g0097 |
2 | NA18974.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.3781+19748C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777015 | |||||||
chr22:27777026 | G | A | 24 | a0001c0001t0001g0153 a0001c0001t0001g0209 a0001c0001t0002g0071 others(21): Show |
24 | HG00438.hp2 HG01099.hp1 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.3781+19737C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777026 | |||||||
chr22:27777042 | G | A | 202 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0073 others(199): Show |
207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.3781+19721C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777042 | |||||||
chr22:27777059 | C | T | 4 | a0001c0001t0002g0237 a0001c0001t0009g0021 a0001c0001t0016g0226 others(1): Show |
4 | HG02145.hp1 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.3781+19704G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777059 | |||||||
chr22:27777092 | C | T | 1 | a0005c0011t0019g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3781+19671G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777092 | |||||||
chr22:27777159 | C | T | 1 | a0001c0014t0018g0373 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3781+19604G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777159 | |||||||
chr22:27777163 | A | T | 3 | a0001c0001t0007g0198 a0001c0001t0012g0355 a0001c0001t0050g0199 |
3 | HG00609.hp2 NA18612.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.3781+19600T>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777163 | |||||||
chr22:27777208 | T | C | 7 | a0001c0001t0001g0159 a0001c0001t0006g0220 a0001c0001t0023g0020 others(4): Show |
7 | HG01243.hp2 HG02717.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.3781+19555A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777208 | |||||||
chr22:27777440 | G | A | 1 | a0001c0001t0057g0238 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3781+19323C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777440 | |||||||
chr22:27777533 | TA | T | 198 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0074 others(195): Show |
203 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.3781+19229delT | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777533 | |||||||
chr22:27777533 | TAA | T | 10 | a0001c0001t0001g0073 a0001c0001t0001g0159 a0001c0001t0001g0181 others(7): Show |
10 | HG00639.hp1 HG01257.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.3781+19228_3781+19 others(8): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777533 | |||||||
chr22:27777547 | A | AG | 84 | a0001c0001t0001g0056 a0001c0001t0001g0064 a0001c0001t0001g0068 others(81): Show |
86 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.3781+19215_3781+19 others(7): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777547 | |||||||
chr22:27777557 | GA | G | 84 | a0001c0001t0001g0056 a0001c0001t0001g0064 a0001c0001t0001g0068 others(81): Show |
86 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.3781+19205delT | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777557 | |||||||
chr22:27777559 | A | G | 1 | a0001c0001t0045g0043 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3781+19204T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777559 | |||||||
chr22:27777582 | A | G | 172 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0056 others(169): Show |
178 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.3781+19181T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777582 | |||||||
chr22:27777656 | C | G | 1 | a0001c0001t0058g0234 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3781+19107G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777656 | |||||||
chr22:27777686 | G | A | 1 | a0001c0001t0008g0067 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3781+19077C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777686 | |||||||
chr22:27777702 | T | TAC | 255 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0056 others(252): Show |
261 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.3781+19059_3781+19 others(8): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777702 | |||||||
chr22:27777714 | C | G | 1 | a0002c0003t0009g0032 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3781+19049G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777714 | |||||||
chr22:27777777 | G | A | 9 | a0001c0001t0001g0149 a0001c0001t0002g0228 a0001c0001t0053g0205 others(6): Show |
10 | HG02055.hp2 HG02717.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.3781+18986C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777777 | |||||||
chr22:27777877 | C | CA | 22 | a0001c0001t0001g0149 a0001c0001t0002g0225 a0001c0001t0002g0228 others(19): Show |
24 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.3781+18885dupT | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777877 | |||||||
chr22:27777910 | T | C | 293 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0056 others(290): Show |
300 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.3781+18853A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777910 | |||||||
chr22:27777911 | C | T | 5 | a0001c0001t0002g0058 a0001c0001t0002g0210 a0001c0001t0068g0331 others(2): Show |
5 | HG02559.hp2 HG02976.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.3781+18852G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777911 | |||||||
chr22:27777969 | G | A | 1 | a0005c0011t0019g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3781+18794C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777969 | |||||||
chr22:27778122 | G | A | 1 | a0001c0001t0057g0238 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3781+18641C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27778122 | |||||||
chr22:27778193 | G | T | 1 | a0001c0001t0074g0383 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3781+18570C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27778193 | |||||||
chr22:27778304 | G | A | 1 | a0001c0001t0003g0290 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3781+18459C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27778304 | |||||||
chr22:27778352 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3781+18411G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27778352 | |||||||
chr22:27778432 | C | G | 1 | a0003c0004t0001g0247 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3781+18331G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27778432 | |||||||
chr22:27778433 | G | A | 1 | a0001c0005t0016g0054 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3781+18330C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27778433 | |||||||
chr22:27778609 | G | A | 42 | a0001c0001t0001g0056 a0001c0001t0001g0079 a0001c0001t0001g0084 others(39): Show |
42 | HG00621.hp1 HG00741.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.3781+18154C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27778609 | |||||||
chr22:27778644 | C | T | 50 | a0001c0001t0001g0056 a0001c0001t0001g0079 a0001c0001t0001g0084 others(47): Show |
51 | HG00621.hp1 HG00741.hp1 HG01243.hp1 others(48): Show |
intron_variant | MODIFIER | c.3781+18119G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27778644 | |||||||
chr22:27778702 | C | T | 2 | a0001c0001t0002g0233 a0001c0021t0007g0250 |
2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3781+18061G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27778702 | |||||||
chr22:27778710 | C | G | 1 | a0001c0001t0005g0086 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.3781+18053G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27778710 | |||||||
chr22:27778836 | G | A | 1 | a0002c0003t0009g0032 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3781+17927C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27778836 | |||||||
chr22:27778961 | G | A | 4 | a0001c0001t0002g0065 a0001c0008t0018g0377 a0002c0002t0004g0362 others(1): Show |
4 | HG00735.hp2 HG01261.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.3781+17802C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27778961 | |||||||
chr22:27778981 | G | C | 301 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(298): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.3781+17782C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27778981 | |||||||
chr22:27779007 | C | G | 1 | a0001c0001t0002g0225 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3781+17756G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27779007 | |||||||
chr22:27779174 | C | T | 135 | a0001c0001t0001g0056 a0001c0001t0001g0064 a0001c0001t0001g0068 others(132): Show |
137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.3781+17589G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27779174 | |||||||
chr22:27779244 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3781+17519A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27779244 | |||||||
chr22:27779402 | G | A | 2 | a0001c0001t0002g0058 a0005c0011t0019g0016 |
2 | HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3781+17361C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27779402 | |||||||
chr22:27779529 | A | G | 1 | a0001c0001t0037g0010 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3781+17234T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27779529 | |||||||
chr22:27779753 | G | A | 175 | a0001c0001t0001g0056 a0001c0001t0001g0064 a0001c0001t0001g0068 others(172): Show |
177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.3781+17010C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27779753 | |||||||
chr22:27779754 | C | G | 1 | a0001c0001t0057g0238 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3781+17009G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27779754 | |||||||
chr22:27779783 | C | T | 1 | a0002c0003t0019g0033 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3781+16980G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27779783 | |||||||
chr22:27780170 | G | A | 12 | a0001c0001t0001g0104 a0001c0001t0002g0201 a0001c0001t0002g0213 others(9): Show |
12 | HG00673.hp2 HG02080.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.3781+16593C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27780170 | |||||||
chr22:27780422 | T | TCCAGGGT others(2): Show |
3 | a0001c0001t0001g0236 a0001c0001t0002g0151 a0001c0001t0075g0382 |
3 | HG03041.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3781+16332_3781+16 others(15): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27780422 | |||||||
chr22:27780518 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.3781+16245T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27780518 | |||||||
chr22:27780733 | C | T | 1 | a0001c0001t0008g0143 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3781+16030G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27780733 | |||||||
chr22:27780789 | A | G | 32 | a0001c0001t0001g0230 a0001c0001t0001g0236 a0001c0001t0002g0065 others(29): Show |
32 | HG00735.hp2 HG01243.hp1 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.3781+15974T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27780789 | |||||||
chr22:27780842 | G | A | 4 | a0001c0001t0001g0077 a0001c0001t0001g0083 a0001c0001t0052g0081 others(1): Show |
4 | NA18941.hp1 NA18949.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.3781+15921C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27780842 | |||||||
chr22:27780909 | CTA | C | 26 | a0001c0001t0001g0230 a0001c0001t0002g0065 a0001c0001t0002g0112 others(23): Show |
26 | HG00735.hp2 HG01243.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.3781+15852_3781+15 others(8): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27780909 | |||||||
chr22:27780934 | A | AT | 34 | a0001c0001t0001g0230 a0001c0001t0002g0065 a0001c0001t0002g0112 others(31): Show |
34 | HG00735.hp2 HG01243.hp1 HG01261.hp2 others(31): Show |
intron_variant | MODIFIER | c.3781+15828dupA | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27780934 | |||||||
chr22:27780957 | G | C | 5 | a0001c0001t0002g0059 a0002c0003t0015g0024 a0002c0003t0015g0025 others(2): Show |
5 | HG02145.hp2 HG02257.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.3781+15806C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27780957 | |||||||
chr22:27781297 | A | G | 1 | a0001c0005t0002g0055 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3781+15466T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27781297 | |||||||
chr22:27781366 | C | T | 1 | a0001c0001t0028g0235 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3781+15397G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27781366 | |||||||
chr22:27781515 | G | A | 4 | a0001c0001t0002g0065 a0001c0008t0018g0377 a0002c0002t0004g0362 others(1): Show |
4 | HG00735.hp2 HG01261.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.3781+15248C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27781515 | |||||||
chr22:27781707 | G | A | 2 | a0001c0001t0002g0201 a0001c0001t0076g0384 |
2 | HG02486.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3781+15056C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27781707 | |||||||
chr22:27781900 | G | A | 3 | a0001c0001t0025g0042 a0001c0010t0014g0012 a0002c0003t0014g0022 |
3 | HG02886.hp2 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3781+14863C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27781900 | |||||||
chr22:27782022 | G | A | 37 | a0001c0001t0001g0056 a0001c0001t0001g0079 a0001c0001t0001g0084 others(34): Show |
37 | HG00408.hp2 HG00621.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.3781+14741C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27782022 | |||||||
chr22:27782117 | C | T | 1 | a0001c0001t0002g0117 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3781+14646G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27782117 | |||||||
chr22:27782213 | C | T | 54 | a0001c0001t0001g0056 a0001c0001t0001g0079 a0001c0001t0001g0084 others(51): Show |
54 | HG00408.hp2 HG00423.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.3781+14550G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27782213 | |||||||
chr22:27782214 | G | A | 1 | a0002c0003t0014g0035 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3781+14549C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27782214 | |||||||
chr22:27782329 | G | A | 2 | a0001c0001t0004g0328 a0001c0001t0012g0330 |
2 | NA18950.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.3781+14434C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27782329 | |||||||
chr22:27782437 | A | T | 31 | a0001c0001t0001g0230 a0001c0001t0002g0065 a0001c0001t0002g0112 others(28): Show |
31 | HG00735.hp2 HG01243.hp1 HG01261.hp2 others(28): Show |
intron_variant | MODIFIER | c.3781+14326T>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27782437 | |||||||
chr22:27782526 | C | T | 2 | a0001c0001t0010g0319 a0002c0002t0004g0368 |
2 | HG01515.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.3781+14237G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27782526 | |||||||
chr22:27782602 | T | C | 34 | a0001c0001t0001g0230 a0001c0001t0001g0236 a0001c0001t0002g0065 others(31): Show |
34 | HG00735.hp2 HG01243.hp1 HG01261.hp2 others(31): Show |
intron_variant | MODIFIER | c.3781+14161A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27782602 | |||||||
chr22:27782637 | T | A | 2 | a0001c0001t0002g0201 a0001c0001t0076g0384 |
2 | HG02486.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3781+14126A>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27782637 | |||||||
chr22:27782663 | T | C | 14 | a0001c0001t0001g0230 a0001c0001t0002g0150 a0001c0001t0002g0216 others(11): Show |
14 | HG01884.hp1 HG02055.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.3781+14100A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27782663 | |||||||
chr22:27782706 | G | C | 1 | a0001c0001t0001g0064 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3781+14057C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27782706 | |||||||
chr22:27782942 | T | C | 1 | a0001c0001t0057g0238 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3781+13821A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27782942 | |||||||
chr22:27782960 | G | A | 21 | a0001c0001t0001g0159 a0001c0001t0001g0236 a0001c0001t0002g0065 others(18): Show |
21 | HG00735.hp2 HG01243.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.3781+13803C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27782960 | |||||||
chr22:27782973 | C | T | 1 | a0001c0001t0057g0238 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3781+13790G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27782973 | |||||||
chr22:27782979 | G | C | 1 | a0001c0001t0001g0098 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3781+13784C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27782979 | |||||||
chr22:27783133 | C | CT | 46 | a0001c0001t0001g0080 a0001c0001t0001g0082 a0001c0001t0001g0149 others(43): Show |
46 | HG00423.hp1 HG00438.hp2 HG01099.hp1 others(43): Show |
intron_variant | MODIFIER | c.3781+13629dupA | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27783133 | |||||||
chr22:27783133 | CT | C | 11 | a0001c0001t0001g0120 a0001c0001t0001g0212 a0001c0001t0002g0112 others(8): Show |
11 | HG01243.hp1 HG01496.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.3781+13629delA | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27783133 | |||||||
chr22:27783247 | G | A | 56 | a0001c0001t0001g0056 a0001c0001t0001g0079 a0001c0001t0001g0084 others(53): Show |
56 | HG00408.hp2 HG00423.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.3781+13516C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27783247 | |||||||
chr22:27783296 | T | G | 1 | a0001c0001t0004g0351 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.3781+13467A>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27783296 | |||||||
chr22:27783343 | G | A | 1 | a0001c0009t0021g0006 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3781+13420C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27783343 | |||||||
chr22:27783592 | C | A | 8 | a0001c0001t0002g0112 a0001c0001t0002g0200 a0001c0005t0002g0049 others(5): Show |
8 | HG01243.hp1 HG01496.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.3781+13171G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27783592 | |||||||
chr22:27783835 | T | C | 310 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(307): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.3781+12928A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27783835 | |||||||
chr22:27783852 | A | AGTCCGAA others(1): Show |
3 | a0001c0001t0001g0124 a0001c0001t0002g0060 a0001c0001t0003g0301 |
3 | HG03654.hp1 HG03927.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.3781+12903_3781+12 others(14): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27783852 | |||||||
chr22:27783868 | C | T | 26 | a0001c0001t0001g0076 a0001c0001t0001g0236 a0001c0001t0002g0172 others(23): Show |
26 | HG00609.hp2 HG01243.hp2 HG01993.hp1 others(23): Show |
intron_variant | MODIFIER | c.3781+12895G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27783868 | |||||||
chr22:27783879 | C | T | 2 | a0001c0001t0045g0043 a0001c0001t0069g0371 |
2 | HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3781+12884G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27783879 | |||||||
chr22:27783961 | C | T | 3 | a0001c0001t0016g0119 a0002c0003t0015g0026 a0002c0003t0015g0027 |
3 | HG01884.hp1 HG02572.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.3781+12802G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27783961 | |||||||
chr22:27784323 | C | A | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | HG03017.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.3781+12440G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27784323 | |||||||
chr22:27784446 | A | G | 1 | a0001c0001t0002g0071 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3781+12317T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27784446 | |||||||
chr22:27784527 | CTAAAGTT | C | 19 | a0001c0001t0001g0064 a0001c0001t0001g0068 a0001c0001t0001g0166 others(16): Show |
20 | HG00099.hp1 HG00642.hp1 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.3781+12229_3781+12 others(13): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27784527 | |||||||
chr22:27784561 | G | C | 6 | a0001c0001t0002g0087 a0001c0001t0002g0155 a0001c0001t0002g0156 others(3): Show |
6 | NA18966.hp1 NA18992.hp2 NA19011.hp2 others(3): Show |
intron_variant | MODIFIER | c.3781+12202C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27784561 | |||||||
chr22:27784690 | A | G | 2 | a0001c0001t0002g0151 a0001c0001t0075g0382 |
2 | HG03041.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3781+12073T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27784690 | |||||||
chr22:27784720 | G | A | 10 | a0001c0001t0002g0213 a0001c0001t0003g0300 a0001c0001t0003g0336 others(7): Show |
10 | HG00621.hp1 HG00673.hp2 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.3781+12043C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27784720 | |||||||
chr22:27784869 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3781+11894G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27784869 | |||||||
chr22:27785024 | G | T | 2 | a0001c0001t0002g0071 a0002c0002t0023g0036 |
2 | HG01192.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.3781+11739C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785024 | |||||||
chr22:27785056 | C | CCA | 36 | a0001c0001t0001g0063 a0001c0001t0001g0079 a0001c0001t0002g0065 others(33): Show |
36 | HG00673.hp2 HG00735.hp2 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.3781+11705_3781+11 others(8): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785056 | |||||||
chr22:27785056 | C | CCACA | 17 | a0001c0001t0001g0113 a0001c0001t0001g0116 a0001c0001t0001g0166 others(14): Show |
17 | HG00558.hp1 HG00621.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.3781+11703_3781+11 others(10): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785056 | |||||||
chr22:27785056 | C | CCACACA | 24 | a0001c0001t0001g0126 a0001c0001t0001g0164 a0001c0001t0001g0222 others(21): Show |
25 | HG00099.hp1 HG01081.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.3781+11701_3781+11 others(12): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785056 | |||||||
chr22:27785056 | C | CCACACAC others(1): Show |
17 | a0001c0001t0001g0076 a0001c0001t0002g0202 a0001c0001t0003g0343 others(14): Show |
18 | HG00423.hp2 HG01515.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.3781+11699_3781+11 others(14): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785056 | |||||||
chr22:27785056 | C | CCACACAC others(3): Show |
21 | a0001c0001t0001g0064 a0001c0001t0001g0068 a0001c0001t0001g0147 others(18): Show |
21 | HG00642.hp1 HG01175.hp1 HG01975.hp2 others(18): Show |
intron_variant | MODIFIER | c.3781+11697_3781+11 others(16): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785056 | |||||||
chr22:27785056 | C | CCACACAC others(5): Show |
3 | a0001c0001t0004g0357 a0001c0001t0066g0317 a0001c0012t0001g0278 |
3 | NA18959.hp1 NA19004.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.3781+11695_3781+11 others(18): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785056 | |||||||
chr22:27785056 | C | CCACACAC others(7): Show |
3 | a0001c0001t0003g0311 a0001c0001t0004g0348 a0001c0001t0026g0045 |
3 | HG02523.hp1 NA18947.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.3781+11693_3781+11 others(20): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785056 | |||||||
chr22:27785056 | CCA | C | 18 | a0001c0001t0001g0056 a0001c0001t0001g0148 a0001c0001t0002g0100 others(15): Show |
18 | HG00741.hp2 HG01099.hp1 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.3781+11705_3781+11 others(8): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785056 | |||||||
chr22:27785056 | CCACA | C | 101 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0073 others(98): Show |
105 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.3781+11703_3781+11 others(10): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785056 | |||||||
chr22:27785056 | CCACACA | C | 42 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0104 others(39): Show |
42 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.3781+11701_3781+11 others(12): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785056 | |||||||
chr22:27785056 | CCACACAC others(1): Show |
C | 7 | a0001c0001t0002g0087 a0001c0001t0002g0112 a0001c0001t0002g0155 others(4): Show |
7 | HG03195.hp1 NA18966.hp1 NA18992.hp2 others(4): Show |
intron_variant | MODIFIER | c.3781+11699_3781+11 others(14): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785056 | |||||||
chr22:27785056 | CCACACAC others(9): Show |
C | 1 | a0002c0002t0023g0036 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3781+11691_3781+11 others(22): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785056 | |||||||
chr22:27785101 | T | G | 1 | a0001c0001t0001g0083 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.3781+11662A>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785101 | |||||||
chr22:27785223 | G | C | 2 | a0001c0001t0002g0071 a0002c0002t0023g0036 |
2 | HG01192.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.3781+11540C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785223 | |||||||
chr22:27785225 | C | T | 3 | a0001c0001t0002g0151 a0001c0001t0075g0382 a0001c0009t0021g0006 |
4 | HG02895.hp1 HG02897.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.3781+11538G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785225 | |||||||
chr22:27785259 | C | T | 1 | a0001c0001t0002g0129 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3781+11504G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785259 | |||||||
chr22:27785332 | C | G | 1 | a0002c0003t0009g0032 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3781+11431G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785332 | |||||||
chr22:27785378 | G | C | 1 | a0001c0001t0001g0211 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3781+11385C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785378 | |||||||
chr22:27785406 | T | C | 5 | a0001c0001t0016g0119 a0001c0013t0001g0048 a0001c0013t0048g0047 others(2): Show |
5 | HG01884.hp1 HG02572.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3781+11357A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785406 | |||||||
chr22:27785411 | C | T | 164 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(161): Show |
169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.3781+11352G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785411 | |||||||
chr22:27785448 | A | C | 310 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(307): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.3781+11315T>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785448 | |||||||
chr22:27785510 | C | T | 2 | a0001c0001t0002g0071 a0003c0004t0002g0241 |
2 | HG01192.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3781+11253G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785510 | |||||||
chr22:27785746 | G | GC | 61 | a0001c0001t0001g0056 a0001c0001t0001g0077 a0001c0001t0001g0082 others(58): Show |
62 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.3781+11016dupG | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785746 | |||||||
chr22:27785746 | GC | G | 31 | a0001c0001t0001g0063 a0001c0001t0001g0099 a0001c0001t0001g0223 others(28): Show |
31 | HG00741.hp2 HG01099.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.3781+11016delG | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785746 | |||||||
chr22:27785746 | GCC | G | 70 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0073 others(67): Show |
74 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.3781+11015_3781+11 others(8): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785746 | |||||||
chr22:27785753 | C | CA | 58 | a0001c0001t0001g0002 a0001c0001t0001g0098 a0001c0001t0001g0103 others(55): Show |
59 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(56): Show |
intron_variant | MODIFIER | c.3781+11009_3781+11 others(7): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785753 | |||||||
chr22:27785790 | A | G | 2 | a0001c0005t0002g0051 a0001c0005t0028g0052 |
2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3781+10973T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785790 | |||||||
chr22:27786304 | C | T | 2 | a0001c0001t0002g0071 a0003c0004t0002g0241 |
2 | HG01192.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3781+10459G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27786304 | |||||||
chr22:27786430 | A | AAC | 30 | a0001c0001t0001g0056 a0001c0001t0001g0077 a0001c0001t0001g0080 others(27): Show |
30 | HG00408.hp2 HG01081.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.3781+10331_3781+10 others(8): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27786430 | |||||||
chr22:27786430 | A | AACAC | 7 | a0001c0001t0001g0079 a0001c0001t0001g0221 a0001c0005t0002g0051 others(4): Show |
7 | HG02300.hp1 HG02451.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.3781+10329_3781+10 others(10): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27786430 | |||||||
chr22:27786522 | G | A | 10 | a0001c0001t0001g0076 a0001c0001t0002g0069 a0001c0001t0002g0202 others(7): Show |
10 | HG01081.hp1 HG01993.hp1 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.3781+10241C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27786522 | |||||||
chr22:27786548 | G | A | 1 | a0001c0001t0001g0005 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.3781+10215C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27786548 | |||||||
chr22:27786740 | C | T | 2 | a0001c0001t0002g0071 a0003c0004t0002g0241 |
2 | HG01192.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3781+10023G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27786740 | |||||||
chr22:27786782 | C | T | 1 | a0001c0001t0002g0203 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.3781+9981G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27786782 | |||||||
chr22:27786835 | C | T | 2 | a0001c0001t0002g0071 a0003c0004t0002g0241 |
2 | HG01192.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3781+9928G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27786835 | |||||||
chr22:27786842 | G | GCA | 99 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0073 others(96): Show |
103 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.3781+9919_3781+992 others(6): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27786842 | |||||||
chr22:27786842 | G | GCACA | 6 | a0001c0001t0003g0349 a0001c0001t0004g0335 a0001c0001t0005g0195 others(3): Show |
6 | HG01346.hp1 HG02135.hp1 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.3781+9917_3781+992 others(8): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27786842 | |||||||
chr22:27786842 | G | GCGCACAC others(5): Show |
2 | a0001c0001t0002g0071 a0003c0004t0002g0241 |
2 | HG01192.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3781+9920_3781+992 others(16): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27786842 | |||||||
chr22:27786842 | GCA | G | 8 | a0001c0001t0001g0149 a0001c0001t0001g0230 a0001c0001t0002g0216 others(5): Show |
8 | HG02109.hp2 HG02809.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.3781+9919_3781+992 others(6): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27786842 | |||||||
chr22:27786844 | A | G | 1 | a0001c0001t0001g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3781+9919T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27786844 | |||||||
chr22:27786895 | G | A | 1 | a0001c0001t0057g0238 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3781+9868C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27786895 | |||||||
chr22:27786955 | A | T | 1 | a0001c0001t0026g0045 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.3781+9808T>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27786955 | |||||||
chr22:27786982 | T | G | 1 | a0001c0001t0003g0311 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.3781+9781A>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27786982 | |||||||
chr22:27787225 | T | C | 1 | a0001c0001t0004g0348 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3781+9538A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27787225 | |||||||
chr22:27787238 | G | A | 2 | a0002c0003t0019g0033 a0002c0003t0019g0034 |
2 | HG01496.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.3781+9525C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27787238 | |||||||
chr22:27787318 | T | C | 2 | a0001c0001t0002g0071 a0003c0004t0002g0241 |
2 | HG01192.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3781+9445A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27787318 | |||||||
chr22:27787380 | A | G | 1 | a0001c0001t0005g0078 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3781+9383T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27787380 | |||||||
chr22:27787387 | G | A | 1 | a0002c0003t0039g0029 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3781+9376C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27787387 | |||||||
chr22:27787665 | G | T | 5 | a0001c0001t0045g0043 a0001c0001t0059g0232 a0001c0001t0069g0371 others(2): Show |
5 | HG01516.hp2 HG02055.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.3781+9098C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27787665 | |||||||
chr22:27787917 | C | T | 1 | a0001c0001t0006g0218 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.3781+8846G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27787917 | |||||||
chr22:27787997 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.3781+8766C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27787997 | |||||||
chr22:27788001 | G | C | 5 | a0001c0005t0002g0051 a0001c0005t0016g0054 a0001c0005t0028g0052 others(2): Show |
5 | HG02451.hp1 HG02451.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.3781+8762C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27788001 | |||||||
chr22:27788147 | G | A | 16 | a0001c0001t0001g0113 a0001c0001t0001g0116 a0001c0001t0002g0065 others(13): Show |
16 | HG00438.hp1 HG00558.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.3781+8616C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27788147 | |||||||
chr22:27788189 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3781+8574C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27788189 | |||||||
chr22:27788301 | A | G | 2 | a0001c0001t0045g0043 a0001c0001t0069g0371 |
2 | HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3781+8462T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27788301 | |||||||
chr22:27788309 | T | C | 5 | a0001c0001t0016g0119 a0001c0013t0001g0048 a0001c0013t0048g0047 others(2): Show |
5 | HG01884.hp1 HG02572.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3781+8454A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27788309 | |||||||
chr22:27788325 | G | A | 1 | a0001c0001t0002g0228 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3781+8438C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27788325 | |||||||
chr22:27788340 | G | T | 3 | a0001c0001t0001g0098 a0001c0001t0008g0057 a0003c0004t0001g0242 |
3 | HG00140.hp1 HG01167.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3781+8423C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27788340 | |||||||
chr22:27788363 | A | G | 5 | a0001c0001t0016g0119 a0001c0013t0001g0048 a0001c0013t0048g0047 others(2): Show |
5 | HG01884.hp1 HG02572.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3781+8400T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27788363 | |||||||
chr22:27788364 | C | T | 2 | a0001c0001t0002g0071 a0003c0004t0002g0241 |
2 | HG01192.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3781+8399G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27788364 | |||||||
chr22:27788454 | A | G | 1 | a0001c0001t0001g0171 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.3781+8309T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27788454 | |||||||
chr22:27788545 | C | A | 4 | a0001c0001t0002g0225 a0001c0005t0009g0017 a0001c0005t0009g0018 others(1): Show |
4 | HG01496.hp1 HG01891.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.3781+8218G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27788545 | |||||||
chr22:27788619 | CT | C | 12 | a0001c0001t0001g0077 a0001c0001t0002g0151 a0001c0001t0002g0225 others(9): Show |
13 | HG01243.hp1 HG01496.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.3781+8143delA | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27788619 | |||||||
chr22:27788680 | T | TGTGTGTG others(9): Show |
1 | a0001c0016t0003g0280 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.3781+8067_3781+808 others(20): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27788680 | |||||||
chr22:27788680 | TGTGTGTG others(9): Show |
T | 5 | a0001c0001t0016g0119 a0001c0013t0001g0048 a0001c0013t0048g0047 others(2): Show |
5 | HG01884.hp1 HG02572.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3781+8067_3781+808 others(20): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27788680 | |||||||
chr22:27788690 | T | C | 5 | a0001c0001t0002g0071 a0001c0001t0002g0151 a0001c0001t0075g0382 others(2): Show |
6 | HG01192.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.3781+8073A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27788690 | |||||||
chr22:27788693 | A | G | 2 | a0001c0001t0002g0071 a0003c0004t0002g0241 |
2 | HG01192.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3781+8070T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27788693 | |||||||
chr22:27788723 | G | A | 2 | a0001c0001t0004g0350 a0001c0001t0012g0355 |
2 | HG00609.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.3781+8040C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27788723 | |||||||
chr22:27789033 | G | A | 1 | a0001c0001t0009g0021 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3781+7730C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27789033 | |||||||
chr22:27789251 | GATCTTCT others(17): Show |
G | 10 | a0001c0001t0003g0314 a0001c0001t0003g0343 a0001c0001t0004g0345 others(7): Show |
10 | HG02015.hp1 HG02523.hp1 NA18964.hp2 others(7): Show |
intron_variant | MODIFIER | c.3781+7488_3781+751 others(28): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27789251 | |||||||
chr22:27789438 | A | G | 17 | a0001c0001t0001g0113 a0001c0001t0001g0116 a0001c0001t0002g0065 others(14): Show |
17 | HG00438.hp1 HG00558.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.3781+7325T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27789438 | |||||||
chr22:27789464 | T | G | 46 | a0001c0001t0001g0153 a0001c0001t0001g0207 a0001c0001t0001g0208 others(43): Show |
46 | HG00438.hp2 HG00733.hp1 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.3781+7299A>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27789464 | |||||||
chr22:27789489 | C | T | 1 | a0001c0001t0008g0067 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3781+7274G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27789489 | |||||||
chr22:27789537 | C | T | 2 | a0001c0014t0018g0372 a0001c0014t0018g0373 |
2 | HG02257.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3781+7226G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27789537 | |||||||
chr22:27789677 | C | A | 2 | a0001c0014t0018g0372 a0001c0014t0018g0373 |
2 | HG02257.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3781+7086G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27789677 | |||||||
chr22:27789989 | G | A | 3 | a0001c0001t0033g0327 a0001c0001t0061g0224 a0002c0020t0005g0249 |
3 | HG02027.hp2 HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3781+6774C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27789989 | |||||||
chr22:27790097 | T | C | 1 | a0004c0007t0001g0270 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3781+6666A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27790097 | |||||||
chr22:27790112 | C | T | 1 | a0001c0001t0003g0297 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.3781+6651G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27790112 | |||||||
chr22:27790139 | G | A | 3 | a0001c0001t0002g0213 a0001c0001t0003g0337 a0001c0001t0011g0070 |
3 | HG00673.hp2 HG02132.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.3781+6624C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27790139 | |||||||
chr22:27790157 | C | T | 1 | a0001c0001t0002g0128 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.3781+6606G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27790157 | |||||||
chr22:27790181 | C | T | 2 | a0003c0004t0001g0247 a0003c0004t0002g0246 |
2 | HG02055.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.3781+6582G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27790181 | |||||||
chr22:27790299 | G | A | 51 | a0001c0001t0001g0063 a0001c0001t0001g0124 a0001c0001t0001g0126 others(48): Show |
52 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.3781+6464C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27790299 | |||||||
chr22:27790301 | A | G | 72 | a0001c0001t0001g0063 a0001c0001t0001g0113 a0001c0001t0001g0116 others(69): Show |
73 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.3781+6462T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27790301 | |||||||
chr22:27790369 | A | G | 1 | a0002c0003t0009g0032 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3781+6394T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27790369 | |||||||
chr22:27790382 | A | G | 57 | a0001c0001t0001g0063 a0001c0001t0001g0124 a0001c0001t0001g0126 others(54): Show |
58 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.3781+6381T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27790382 | |||||||
chr22:27790522 | C | A | 1 | a0001c0001t0004g0335 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3781+6241G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27790522 | |||||||
chr22:27790589 | G | A | 1 | a0011c0017t0003g0359 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.3781+6174C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27790589 | |||||||
chr22:27790787 | T | C | 52 | a0001c0001t0001g0063 a0001c0001t0001g0124 a0001c0001t0001g0126 others(49): Show |
53 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.3781+5976A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27790787 | |||||||
chr22:27790847 | T | A | 1 | a0008c0025t0032g0370 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3781+5916A>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27790847 | |||||||
chr22:27790958 | C | G | 1 | a0001c0001t0005g0170 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3781+5805G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27790958 | |||||||
chr22:27790971 | C | T | 26 | a0001c0001t0001g0056 a0001c0001t0001g0077 a0001c0001t0001g0079 others(23): Show |
26 | HG00408.hp2 HG01257.hp1 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.3781+5792G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27790971 | |||||||
chr22:27791318 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3781+5445C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27791318 | |||||||
chr22:27791389 | G | A | 1 | a0001c0001t0005g0086 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.3781+5374C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27791389 | |||||||
chr22:27791408 | A | G | 49 | a0001c0001t0001g0063 a0001c0001t0001g0124 a0001c0001t0001g0126 others(46): Show |
49 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.3781+5355T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27791408 | |||||||
chr22:27791749 | A | T | 1 | a0001c0001t0002g0112 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3781+5014T>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27791749 | |||||||
chr22:27791785 | T | C | 2 | a0001c0001t0010g0319 a0002c0002t0004g0368 |
2 | HG01515.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.3781+4978A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27791785 | |||||||
chr22:27791790 | A | T | 1 | a0001c0001t0059g0232 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3781+4973T>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27791790 | |||||||
chr22:27792014 | C | T | 2 | a0001c0001t0024g0019 a0002c0002t0006g0266 |
2 | HG03831.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.3781+4749G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792014 | |||||||
chr22:27792105 | A | C | 1 | a0001c0001t0002g0202 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3781+4658T>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792105 | |||||||
chr22:27792112 | A | C | 1 | a0001c0001t0059g0232 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3781+4651T>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792112 | |||||||
chr22:27792215 | T | C | 49 | a0001c0001t0001g0063 a0001c0001t0001g0124 a0001c0001t0001g0126 others(46): Show |
49 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.3781+4548A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792215 | |||||||
chr22:27792229 | C | T | 3 | a0001c0001t0002g0087 a0001c0001t0004g0295 a0001c0001t0065g0294 |
3 | NA18971.hp1 NA19078.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.3781+4534G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792229 | |||||||
chr22:27792230 | G | A | 22 | a0001c0001t0001g0076 a0001c0001t0002g0069 a0001c0001t0002g0202 others(19): Show |
22 | HG00621.hp1 HG00673.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.3781+4533C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792230 | |||||||
chr22:27792317 | C | CAT | 26 | a0001c0001t0001g0002 a0001c0001t0001g0098 a0001c0001t0001g0099 others(23): Show |
27 | HG00099.hp2 HG00408.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.3781+4444_3781+444 others(6): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792317 | |||||||
chr22:27792317 | C | CATAT | 15 | a0001c0001t0001g0209 a0001c0001t0002g0071 a0001c0001t0002g0094 others(12): Show |
15 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.3781+4442_3781+444 others(8): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792317 | |||||||
chr22:27792317 | C | CATATAT | 13 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0002g0089 others(10): Show |
13 | HG01099.hp1 HG01256.hp2 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.3781+4440_3781+444 others(10): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792317 | |||||||
chr22:27792317 | C | CATATATA others(3): Show |
7 | a0001c0001t0002g0145 a0001c0001t0007g0088 a0001c0001t0008g0057 others(4): Show |
7 | HG00140.hp1 HG01255.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.3781+4436_3781+444 others(14): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792317 | |||||||
chr22:27792317 | CAT | C | 42 | a0001c0001t0001g0063 a0001c0001t0001g0132 a0001c0001t0001g0133 others(39): Show |
42 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.3781+4444_3781+444 others(6): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792317 | |||||||
chr22:27792317 | CATAT | C | 25 | a0001c0001t0001g0056 a0001c0001t0001g0077 a0001c0001t0001g0120 others(22): Show |
25 | HG00639.hp2 HG01884.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.3781+4442_3781+444 others(8): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792317 | |||||||
chr22:27792317 | CATATAT | C | 67 | a0001c0001t0001g0068 a0001c0001t0001g0079 a0001c0001t0001g0080 others(64): Show |
70 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.3781+4440_3781+444 others(10): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792317 | |||||||
chr22:27792317 | CATATATA others(1): Show |
C | 83 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0064 others(80): Show |
89 | HG00280.hp1 HG00408.hp2 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.3781+4438_3781+444 others(12): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792317 | |||||||
chr22:27792317 | CATATATA others(3): Show |
C | 37 | a0001c0001t0001g0076 a0001c0001t0001g0113 a0001c0001t0001g0116 others(34): Show |
37 | HG00438.hp1 HG00558.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.3781+4436_3781+444 others(14): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792317 | |||||||
chr22:27792317 | CATATATA others(5): Show |
C | 8 | a0001c0001t0002g0213 a0001c0001t0003g0337 a0001c0001t0011g0070 others(5): Show |
8 | HG00621.hp1 HG00673.hp2 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.3781+4434_3781+444 others(16): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792317 | |||||||
chr22:27792317 | CATATATA others(7): Show |
C | 3 | a0001c0001t0003g0338 a0001c0001t0005g0123 a0001c0001t0007g0122 |
3 | NA19078.hp1 NA19081.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.3781+4432_3781+444 others(18): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792317 | |||||||
chr22:27792317 | CATATATA others(9): Show |
C | 2 | a0001c0001t0007g0198 a0001c0001t0050g0199 |
2 | NA18612.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.3781+4430_3781+444 others(20): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792317 | |||||||
chr22:27792351 | T | A | 41 | a0001c0001t0001g0063 a0001c0001t0001g0124 a0001c0001t0001g0126 others(38): Show |
41 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.3781+4412A>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792351 | |||||||
chr22:27792351 | T | TAA | 3 | a0001c0001t0002g0072 a0001c0001t0003g0302 a0001c0001t0062g0062 |
3 | HG00738.hp2 HG01175.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.3781+4411_3781+441 others(6): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792351 | |||||||
chr22:27792409 | C | T | 2 | a0001c0001t0003g0312 a0001c0001t0003g0342 |
2 | HG02083.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.3781+4354G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792409 | |||||||
chr22:27792552 | G | A | 2 | a0001c0001t0002g0071 a0003c0004t0002g0241 |
2 | HG01192.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3781+4211C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792552 | |||||||
chr22:27792653 | C | T | 3 | a0001c0001t0009g0021 a0001c0001t0045g0043 a0001c0001t0069g0371 |
3 | HG02055.hp2 HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.3781+4110G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792653 | |||||||
chr22:27792707 | G | A | 1 | a0001c0001t0002g0117 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3781+4056C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792707 | |||||||
chr22:27792709 | G | A | 1 | a0001c0001t0005g0118 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3781+4054C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792709 | |||||||
chr22:27792894 | C | G | 7 | a0001c0001t0002g0228 a0001c0001t0009g0021 a0001c0001t0045g0043 others(4): Show |
8 | HG02055.hp2 HG02145.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.3781+3869G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792894 | |||||||
chr22:27792896 | C | G | 14 | a0001c0001t0001g0149 a0001c0001t0001g0230 a0001c0001t0002g0071 others(11): Show |
14 | HG01192.hp2 HG01243.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.3781+3867G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792896 | |||||||
chr22:27792911 | C | T | 3 | a0001c0001t0002g0151 a0001c0001t0075g0382 a0001c0009t0021g0006 |
4 | HG02895.hp1 HG02897.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.3781+3852G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792911 | |||||||
chr22:27793183 | C | T | 8 | a0001c0001t0001g0076 a0001c0001t0002g0069 a0001c0001t0002g0202 others(5): Show |
8 | HG01081.hp1 HG02040.hp2 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.3781+3580G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27793183 | |||||||
chr22:27793299 | CTG | C | 12 | a0001c0001t0001g0149 a0001c0001t0001g0230 a0001c0001t0002g0150 others(9): Show |
12 | HG01243.hp2 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.3781+3462_3781+346 others(6): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27793299 | |||||||
chr22:27793331 | ATTACAAA others(47): Show |
A | 14 | a0001c0001t0001g0149 a0001c0001t0001g0230 a0001c0001t0002g0071 others(11): Show |
14 | HG01192.hp2 HG01243.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.3781+3378_3781+343 others(58): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27793331 | |||||||
chr22:27793399 | C | A | 6 | a0001c0001t0016g0119 a0001c0001t0021g0075 a0001c0013t0001g0048 others(3): Show |
6 | HG01884.hp1 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.3781+3364G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27793399 | |||||||
chr22:27793468 | C | T | 4 | a0001c0001t0002g0151 a0001c0001t0075g0382 a0001c0009t0021g0006 others(1): Show |
5 | HG02895.hp1 HG02897.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.3781+3295G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27793468 | |||||||
chr22:27793681 | T | C | 7 | a0001c0001t0002g0225 a0001c0005t0002g0049 a0001c0005t0006g0050 others(4): Show |
7 | HG01243.hp1 HG01496.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.3781+3082A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27793681 | |||||||
chr22:27793699 | T | C | 25 | a0001c0001t0001g0149 a0001c0001t0001g0230 a0001c0001t0002g0071 others(22): Show |
25 | HG01192.hp2 HG01243.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.3781+3064A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27793699 | |||||||
chr22:27793720 | CA | C | 9 | a0001c0001t0001g0076 a0001c0001t0002g0069 a0001c0001t0002g0202 others(6): Show |
9 | HG01081.hp1 HG01993.hp1 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.3781+3042delT | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27793720 | |||||||
chr22:27793756 | C | T | 1 | a0001c0001t0009g0021 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3781+3007G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27793756 | |||||||
chr22:27793834 | G | A | 10 | a0001c0001t0001g0149 a0001c0001t0001g0230 a0001c0001t0002g0150 others(7): Show |
10 | HG02109.hp2 HG02809.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.3781+2929C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27793834 | |||||||
chr22:27793839 | C | T | 3 | a0001c0001t0002g0087 a0001c0001t0004g0295 a0001c0001t0065g0294 |
3 | NA18971.hp1 NA19078.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.3781+2924G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27793839 | |||||||
chr22:27793899 | G | A | 9 | a0001c0001t0001g0076 a0001c0001t0001g0148 a0001c0001t0002g0069 others(6): Show |
9 | HG01081.hp1 HG01361.hp1 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.3781+2864C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27793899 | |||||||
chr22:27793960 | A | C | 10 | a0001c0001t0001g0149 a0001c0001t0001g0230 a0001c0001t0002g0150 others(7): Show |
10 | HG02109.hp2 HG02809.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.3781+2803T>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27793960 | |||||||
chr22:27793988 | G | A | 2 | a0001c0001t0002g0071 a0003c0004t0002g0241 |
2 | HG01192.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3781+2775C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27793988 | |||||||
chr22:27794178 | A | G | 1 | a0001c0001t0001g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3781+2585T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27794178 | |||||||
chr22:27794217 | G | A | 3 | a0001c0001t0004g0334 a0001c0001t0004g0335 a0001c0001t0025g0040 |
3 | HG01346.hp1 HG01358.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.3781+2546C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27794217 | |||||||
chr22:27794246 | A | G | 22 | a0001c0001t0001g0056 a0001c0001t0001g0077 a0001c0001t0001g0079 others(19): Show |
22 | HG00408.hp2 HG01257.hp1 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.3781+2517T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27794246 | |||||||
chr22:27794426 | A | T | 45 | a0001c0001t0001g0063 a0001c0001t0001g0124 a0001c0001t0001g0126 others(42): Show |
45 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.3781+2337T>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27794426 | |||||||
chr22:27794463 | C | A | 1 | a0001c0001t0001g0120 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.3781+2300G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27794463 | |||||||
chr22:27794493 | G | A | 11 | a0001c0001t0002g0213 a0001c0001t0003g0300 a0001c0001t0003g0336 others(8): Show |
11 | HG00621.hp1 HG00673.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.3781+2270C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27794493 | |||||||
chr22:27794498 | G | A | 2 | a0001c0001t0008g0067 a0001c0012t0020g0276 |
2 | HG00280.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.3781+2265C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27794498 | |||||||
chr22:27794610 | A | C | 1 | a0001c0001t0002g0233 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3781+2153T>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27794610 | |||||||
chr22:27794743 | T | C | 1 | a0002c0002t0005g0267 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.3781+2020A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27794743 | |||||||
chr22:27794813 | TG | T | 194 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0064 others(191): Show |
202 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.3781+1949delC | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27794813 | |||||||
chr22:27794814 | G | GT | 5 | a0001c0005t0002g0051 a0001c0005t0016g0054 a0001c0005t0028g0052 others(2): Show |
5 | HG02451.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.3781+1948dupA | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27794814 | |||||||
chr22:27794814 | G | T | 4 | a0001c0001t0002g0228 a0001c0001t0053g0205 a0002c0006t0036g0009 others(1): Show |
5 | HG02886.hp1 HG03041.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3781+1949C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27794814 | |||||||
chr22:27794816 | TG | T | 52 | a0001c0001t0001g0063 a0001c0001t0001g0124 a0001c0001t0001g0126 others(49): Show |
52 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.3781+1946delC | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27794816 | |||||||
chr22:27794817 | G | T | 203 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0064 others(200): Show |
212 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(209): Show |
intron_variant | MODIFIER | c.3781+1946C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27794817 | |||||||
chr22:27794817 | GT | G | 39 | a0001c0001t0001g0116 a0001c0001t0001g0207 a0001c0001t0001g0208 others(36): Show |
39 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.3781+1945delA | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27794817 | |||||||
chr22:27794821 | T | G | 249 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0063 others(246): Show |
258 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.3781+1942A>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27794821 | |||||||
chr22:27795213 | C | T | 1 | a0001c0001t0033g0287 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3781+1550G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27795213 | |||||||
chr22:27795289 | C | T | 2 | a0002c0003t0014g0030 a0002c0003t0039g0029 |
2 | HG01884.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.3781+1474G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27795289 | |||||||
chr22:27795517 | G | A | 2 | a0001c0001t0008g0229 a0001c0001t0032g0358 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.3781+1246C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27795517 | |||||||
chr22:27795522 | G | T | 1 | a0001c0001t0011g0070 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.3781+1241C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27795522 | |||||||
chr22:27795713 | C | CTA | 8 | a0001c0001t0001g0236 a0001c0005t0043g0038 a0001c0010t0040g0013 others(5): Show |
8 | HG01884.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.3781+1048_3781+104 others(6): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27795713 | |||||||
chr22:27795722 | T | TAC | 89 | a0001c0001t0001g0068 a0001c0001t0001g0206 a0001c0001t0001g0207 others(86): Show |
89 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.3781+1039_3781+104 others(6): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27795722 | |||||||
chr22:27795722 | TAC | T | 9 | a0001c0001t0001g0230 a0001c0001t0002g0069 a0001c0001t0002g0231 others(6): Show |
9 | HG01081.hp1 HG01243.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.3781+1039_3781+104 others(6): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27795722 | |||||||
chr22:27795724 | C | T | 21 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0076 others(18): Show |
21 | HG00408.hp1 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.3781+1039G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27795724 | |||||||
chr22:27795726 | C | T | 1 | a0001c0001t0069g0371 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3781+1037G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27795726 | |||||||
chr22:27795740 | C | T | 1 | a0001c0001t0023g0020 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3781+1023G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27795740 | |||||||
chr22:27795858 | T | G | 43 | a0001c0001t0001g0230 a0001c0001t0001g0236 a0001c0001t0002g0231 others(40): Show |
43 | HG01099.hp1 HG01243.hp1 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.3781+905A>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27795858 | |||||||
chr22:27795907 | G | T | 14 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0068 others(11): Show |
14 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(11): Show |
intron_variant | MODIFIER | c.3781+856C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27795907 | |||||||
chr22:27795938 | C | T | 1 | a0001c0001t0046g0039 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.3781+825G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27795938 | |||||||
chr22:27796008 | T | C | 2 | a0001c0001t0009g0021 a0001c0001t0023g0020 |
2 | HG02145.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.3781+755A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27796008 | |||||||
chr22:27796435 | G | A | 21 | a0001c0005t0002g0049 a0001c0005t0002g0051 a0001c0005t0002g0055 others(18): Show |
21 | HG01243.hp1 HG01243.hp2 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.3781+328C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27796435 | |||||||
chr22:27796555 | T | C | 1 | a0002c0020t0005g0249 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3781+208A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27796555 | |||||||
chr22:27796563 | G | T | 1 | a0001c0001t0001g0056 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3781+200C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27796563 | |||||||
chr22:27796580 | G | T | 1 | a0001c0001t0004g0281 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.3781+183C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27796580 |