Item | Value |
---|---|
geneid | 259266 |
ensemblid | ENSG00000066279.19 |
hgncid | 19048 |
symbol | ASPM |
name | assembly factor for spindle microtubules |
refseq_nuc | NM_018136.5 |
refseq_prot | NP_060606.3 |
ensembl_nuc | ENST00000367409.9 |
ensembl_prot | ENSP00000356379.4 |
mane_status | MANE Select |
chr | chr1 |
start | 197084127 |
end | 197146669 |
strand | - |
ver | v1.2 |
region | chr1:197084127-197146669 |
region5000 | chr1:197079127-197151669 |
regionname0 | ASPM_chr1_197084127_197146669 |
regionname5000 | ASPM_chr1_197079127_197151669 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 3477 | 167 | 50 | 29 | 66 | 4 | 17 | 52 | ASPM_chr1_197079127_197151669 | ASPM | MANRR others(3472): Show |
chr1 | 197079127 | 197151669 |
a0002 | 0/0 | 3477 | 58 | 5 | 15 | 27 | 0 | 11 | 22 | ASPM_chr1_197079127_197151669 | ASPM | MANRR others(3472): Show |
chr1 | 197079127 | 197151669 |
a0003 | 0/0 | 3477 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | MANRR others(3472): Show |
chr1 | 197079127 | 197151669 |
a0004 | 0/0 | 3477 | 7 | 0 | 0 | 7 | 0 | 0 | 5 | ASPM_chr1_197079127_197151669 | ASPM | MANRR others(3472): Show |
chr1 | 197079127 | 197151669 |
a0005 | 1/0 | 3477 | 3 | 0 | 2 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | MANRR others(3472): Show |
chr1 | 197079127 | 197151669 |
a0006 | 0/0 | 3477 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | MANRR others(3472): Show |
chr1 | 197079127 | 197151669 |
a0007 | 0/0 | 3477 | 3 | 0 | 2 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | MANRR others(3472): Show |
chr1 | 197079127 | 197151669 |
a0008 | 0/0 | 3477 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | MANRR others(3472): Show |
chr1 | 197079127 | 197151669 |
a0009 | 0/0 | 3477 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | MANRR others(3472): Show |
chr1 | 197079127 | 197151669 |
a0010 | 0/0 | 3477 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | MANRR others(3472): Show |
chr1 | 197079127 | 197151669 |
a0011 | 0/0 | 3477 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | MANRR others(3472): Show |
chr1 | 197079127 | 197151669 |
a0012 | 0/0 | 3477 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | ASPM_chr1_197079127_197151669 | ASPM | MANRR others(3472): Show |
chr1 | 197079127 | 197151669 |
a0013 | 0/0 | 3477 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | ASPM_chr1_197079127_197151669 | ASPM | MANRR others(3472): Show |
chr1 | 197079127 | 197151669 |
a0014 | 0/0 | 3477 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | ASPM_chr1_197079127_197151669 | ASPM | MANRR others(3472): Show |
chr1 | 197079127 | 197151669 |
a0015 | 0/0 | 3477 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | ASPM_chr1_197079127_197151669 | ASPM | MANRR others(3472): Show |
chr1 | 197079127 | 197151669 |
a0016 | 0/0 | 3477 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | MANRR others(3472): Show |
chr1 | 197079127 | 197151669 |
a0017 | 0/0 | 3477 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | MANRR others(3472): Show |
chr1 | 197079127 | 197151669 |
a0018 | 0/0 | 3477 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | ASPM_chr1_197079127_197151669 | ASPM | MANRR others(3472): Show |
chr1 | 197079127 | 197151669 |
a0019 | 0/0 | 3477 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | MANRR others(3472): Show |
chr1 | 197079127 | 197151669 |
a0020 | 0/0 | 3477 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ASPM_chr1_197079127_197151669 | ASPM | MANRR others(3472): Show |
chr1 | 197079127 | 197151669 |
a0021 | 0/0 | 3477 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | MANRR others(3472): Show |
chr1 | 197079127 | 197151669 |
a0022 | 0/0 | 3477 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | MANRR others(3472): Show |
chr1 | 197079127 | 197151669 |
a0023 | 0/0 | 3477 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | MANRR others(3472): Show |
chr1 | 197079127 | 197151669 |
a0024 | 0/0 | 3477 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | MANRR others(3472): Show |
chr1 | 197079127 | 197151669 |
a0025 | 0/0 | 3477 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ASPM_chr1_197079127_197151669 | ASPM | MANRR others(3472): Show |
chr1 | 197079127 | 197151669 |
a0026 | 0/0 | 3477 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | MANRR others(3472): Show |
chr1 | 197079127 | 197151669 |
a0027 | 0/0 | 3477 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | MANRR others(3472): Show |
chr1 | 197079127 | 197151669 |
a0028 | 0/0 | 3477 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ASPM_chr1_197079127_197151669 | ASPM | MANRR others(3472): Show |
chr1 | 197079127 | 197151669 |
a0029 | 0/0 | 3477 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ASPM_chr1_197079127_197151669 | ASPM | MANRR others(3472): Show |
chr1 | 197079127 | 197151669 |
a0030 | 0/0 | 3477 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ASPM_chr1_197079127_197151669 | ASPM | MANRR others(3472): Show |
chr1 | 197079127 | 197151669 |
a0031 | 0/0 | 3477 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ASPM_chr1_197079127_197151669 | ASPM | MANRR others(3472): Show |
chr1 | 197079127 | 197151669 |
a0032 | 0/0 | 3477 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ASPM_chr1_197079127_197151669 | ASPM | MANRR others(3472): Show |
chr1 | 197079127 | 197151669 |
a0033 | 0/0 | 3477 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ASPM_chr1_197079127_197151669 | ASPM | MANRR others(3472): Show |
chr1 | 197079127 | 197151669 |
a0034 | 0/0 | 3477 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ASPM_chr1_197079127_197151669 | ASPM | MANRR others(3472): Show |
chr1 | 197079127 | 197151669 |
a0035 | 0/0 | 3477 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ASPM_chr1_197079127_197151669 | ASPM | MANRR others(3472): Show |
chr1 | 197079127 | 197151669 |
a0036 | 0/0 | 3477 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | MANRR others(3472): Show |
chr1 | 197079127 | 197151669 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 10431 | 64 | 2 | 14 | 41 | 1 | 6 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0001c0003 | 0/0 | 10431 | 56 | 12 | 11 | 25 | 2 | 6 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0001c0004 | 0/1 | 10431 | 34 | 26 | 3 | 0 | 0 | 4 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0001c0008 | 0/0 | 10431 | 4 | 4 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0001c0022 | 0/0 | 10431 | 2 | 2 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0001c0026 | 0/0 | 10431 | 1 | 0 | 0 | 0 | 0 | 1 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0001c0028 | 0/0 | 10431 | 1 | 0 | 0 | 0 | 1 | 0 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0001c0031 | 0/0 | 10431 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0001c0033 | 0/0 | 10431 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0001c0034 | 0/0 | 10431 | 1 | 0 | 1 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0001c0039 | 0/0 | 10431 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0001c0045 | 0/0 | 10431 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0002c0002 | 0/0 | 10431 | 57 | 5 | 15 | 26 | 0 | 11 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0002c0040 | 0/0 | 10431 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0003c0007 | 0/0 | 10431 | 4 | 4 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0003c0012 | 0/0 | 10431 | 3 | 3 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0004c0005 | 0/0 | 10431 | 7 | 0 | 0 | 7 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0005c0011 | 1/0 | 10431 | 3 | 0 | 2 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0006c0006 | 0/0 | 10431 | 4 | 4 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0007c0015 | 0/0 | 10431 | 3 | 0 | 2 | 0 | 1 | 0 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0008c0016 | 0/0 | 10431 | 3 | 3 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0009c0010 | 0/0 | 10431 | 3 | 3 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0010c0009 | 0/0 | 10431 | 3 | 3 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0011c0013 | 0/0 | 10431 | 3 | 3 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0012c0014 | 0/0 | 10431 | 3 | 0 | 0 | 3 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0013c0018 | 0/0 | 10431 | 2 | 0 | 0 | 0 | 1 | 1 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0014c0023 | 0/0 | 10431 | 2 | 0 | 0 | 0 | 1 | 1 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0015c0017 | 0/0 | 10431 | 2 | 0 | 0 | 2 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0016c0025 | 0/0 | 10431 | 2 | 2 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0017c0024 | 0/0 | 10431 | 2 | 2 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0018c0021 | 0/0 | 10431 | 2 | 0 | 0 | 0 | 0 | 2 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0019c0019 | 0/0 | 10431 | 2 | 2 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0020c0020 | 0/0 | 10431 | 2 | 0 | 0 | 2 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0021c0048 | 0/0 | 10431 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0022c0027 | 0/0 | 10431 | 1 | 0 | 1 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0023c0037 | 0/0 | 10431 | 1 | 0 | 1 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0024c0041 | 0/0 | 10431 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0025c0044 | 0/0 | 10431 | 1 | 0 | 0 | 0 | 0 | 1 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0026c0043 | 0/0 | 10431 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0027c0032 | 0/0 | 10431 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0028c0030 | 0/0 | 10431 | 1 | 0 | 0 | 0 | 0 | 1 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0029c0049 | 0/0 | 10431 | 1 | 0 | 0 | 0 | 0 | 1 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0030c0046 | 0/0 | 10431 | 1 | 0 | 0 | 0 | 0 | 1 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0031c0038 | 0/0 | 10431 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0032c0047 | 0/0 | 10431 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0033c0035 | 0/0 | 10431 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0034c0042 | 0/0 | 10431 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0035c0036 | 0/0 | 10431 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 | ||
a0036c0029 | 0/0 | 10431 | 1 | 0 | 0 | 0 | 1 | 0 | ASPM_chr1_197079127_197151669 | ASPM | ATGGC others(10426): Show |
chr1 | 197079127 | 197151669 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 10863 | 63 | 2 | 14 | 40 | 1 | 6 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0001c0001t0009 | 0/0 | 10863 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0001c0003t0001 | 0/0 | 10863 | 55 | 12 | 11 | 24 | 2 | 6 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0001c0003t0008 | 0/0 | 10863 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0001c0004t0002 | 0/1 | 10863 | 34 | 26 | 3 | 0 | 0 | 4 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0001c0008t0001 | 0/0 | 10863 | 4 | 4 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0001c0022t0001 | 0/0 | 10863 | 2 | 2 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0001c0026t0001 | 0/0 | 10863 | 1 | 0 | 0 | 0 | 0 | 1 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0001c0028t0001 | 0/0 | 10863 | 1 | 0 | 0 | 0 | 1 | 0 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0001c0031t0002 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0001c0033t0002 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0001c0034t0001 | 0/0 | 10863 | 1 | 0 | 1 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0001c0039t0001 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0001c0045t0001 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0002c0002t0001 | 0/0 | 10863 | 55 | 5 | 14 | 26 | 0 | 10 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0002c0002t0007 | 0/0 | 10863 | 2 | 0 | 1 | 0 | 0 | 1 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0002c0040t0001 | 0/0 | 10863 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0003c0007t0002 | 0/0 | 10863 | 4 | 4 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0003c0012t0002 | 0/0 | 10863 | 3 | 3 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0004c0005t0003 | 0/0 | 10863 | 7 | 0 | 0 | 7 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0005c0011t0002 | 1/0 | 10863 | 3 | 0 | 2 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0006c0006t0005 | 0/0 | 10863 | 4 | 4 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0007c0015t0001 | 0/0 | 10863 | 3 | 0 | 2 | 0 | 1 | 0 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0008c0016t0001 | 0/0 | 10863 | 3 | 3 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0009c0010t0002 | 0/0 | 10863 | 3 | 3 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0010c0009t0002 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0010c0009t0006 | 0/0 | 10863 | 2 | 2 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0011c0013t0004 | 0/0 | 10863 | 3 | 3 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0012c0014t0001 | 0/0 | 10863 | 3 | 0 | 0 | 3 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0013c0018t0001 | 0/0 | 10863 | 2 | 0 | 0 | 0 | 1 | 1 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0014c0023t0001 | 0/0 | 10863 | 2 | 0 | 0 | 0 | 1 | 1 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0015c0017t0001 | 0/0 | 10863 | 2 | 0 | 0 | 2 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0016c0025t0004 | 0/0 | 10863 | 2 | 2 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0017c0024t0004 | 0/0 | 10863 | 2 | 2 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0018c0021t0001 | 0/0 | 10863 | 2 | 0 | 0 | 0 | 0 | 2 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0019c0019t0001 | 0/0 | 10863 | 2 | 2 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0020c0020t0001 | 0/0 | 10863 | 2 | 0 | 0 | 2 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0021c0048t0001 | 0/0 | 10863 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0022c0027t0001 | 0/0 | 10863 | 1 | 0 | 1 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0023c0037t0001 | 0/0 | 10863 | 1 | 0 | 1 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0024c0041t0001 | 0/0 | 10863 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0025c0044t0001 | 0/0 | 10863 | 1 | 0 | 0 | 0 | 0 | 1 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0026c0043t0001 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0027c0032t0002 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0028c0030t0002 | 0/0 | 10863 | 1 | 0 | 0 | 0 | 0 | 1 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0029c0049t0001 | 0/0 | 10863 | 1 | 0 | 0 | 0 | 0 | 1 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0030c0046t0001 | 0/0 | 10863 | 1 | 0 | 0 | 0 | 0 | 1 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0031c0038t0001 | 0/0 | 10863 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0032c0047t0001 | 0/0 | 10863 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0033c0035t0001 | 0/0 | 10863 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0034c0042t0001 | 0/0 | 10863 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0035c0036t0001 | 0/0 | 10863 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
a0036c0029t0002 | 0/0 | 10863 | 1 | 0 | 0 | 0 | 1 | 0 | ASPM_chr1_197079127_197151669 | ASPM | AGAGT others(10858): Show |
chr1 | 197079127 | 197151669 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 14 | 1 | 7 | 3 | 1 | 2 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0001t0001g0006 | 0/0 | 4 | 1 | 2 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0001t0009g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0003t0001g0002 | 0/0 | 10 | 0 | 2 | 8 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0003t0001g0005 | 0/0 | 5 | 1 | 3 | 0 | 1 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0003t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0003t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0003t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0003t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0003t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0003t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0003t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0003t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0003t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0003t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0003t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0003t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0003t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0003t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0003t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0003t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0003t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0003t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0003t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0003t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0003t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0003t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0003t0008g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0004t0002g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0004t0002g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0004t0002g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0004t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0004t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0004t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0004t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0004t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0004t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0004t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0004t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0004t0002g0059 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0004t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0004t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0004t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0004t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0004t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0004t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0004t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0004t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0004t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0004t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0004t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0004t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0004t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0004t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0004t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0004t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0004t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0004t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0004t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0008t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0008t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0008t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0008t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0022t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0026t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0028t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0031t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0033t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0034t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0039t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0001c0045t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0002c0002t0001g0003 | 0/0 | 8 | 0 | 5 | 1 | 0 | 2 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0002c0002t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0002c0002t0001g0007 | 0/0 | 4 | 1 | 1 | 0 | 0 | 2 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0002c0002t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0002c0002t0001g0013 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0002c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0002c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0002c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0002c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0002c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0002c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0002c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0002c0002t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0002c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0002c0002t0007g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0002c0002t0007g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0002c0040t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0003c0007t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0003c0007t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0003c0007t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0003c0012t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0003c0012t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0004c0005t0003g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0004c0005t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0004c0005t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0004c0005t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0004c0005t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0004c0005t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0005c0011t0002g0008 | 1/0 | 3 | 0 | 2 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0006c0006t0005g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0006c0006t0005g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0006c0006t0005g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0007c0015t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0007c0015t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0007c0015t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0008c0016t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0009c0010t0002g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0009c0010t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0010c0009t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0010c0009t0006g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0011c0013t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0011c0013t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0011c0013t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0012c0014t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0012c0014t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0013c0018t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0014c0023t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0015c0017t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0015c0017t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0016c0025t0004g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0017c0024t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0017c0024t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0018c0021t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0019c0019t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0020c0020t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0020c0020t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0021c0048t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0022c0027t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0023c0037t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0024c0041t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0025c0044t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0026c0043t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0027c0032t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0028c0030t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0029c0049t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0030c0046t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0031c0038t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0032c0047t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0033c0035t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0034c0042t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0035c0036t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
a0036c0029t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0013 | c0018 | t0001 | g0035 | EUR | GBR | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG00099 | hp2 | a0007 | c0015 | t0001 | g0100 | EUR | GBR | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG00140 | hp1 | a0014 | c0023 | t0001 | g0032 | EUR | GBR | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG00140 | hp2 | a0001 | c0003 | t0001 | g0005 | EUR | GBR | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG00423 | hp1 | a0002 | c0002 | t0001 | g0161 | EAS | CHS | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG00438 | hp2 | a0021 | c0048 | t0001 | g0133 | EAS | CHS | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG00544 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | CHS | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG00597 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | CHS | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG00609 | hp1 | a0001 | c0003 | t0001 | g0015 | EAS | CHS | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG00639 | hp1 | a0007 | c0015 | t0001 | g0093 | AMR | PUR | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG00639 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG00735 | hp2 | a0022 | c0027 | t0001 | g0137 | AMR | PUR | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0147 | AMR | PUR | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG00738 | hp2 | a0001 | c0003 | t0001 | g0198 | AMR | PUR | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG00741 | hp2 | a0002 | c0002 | t0001 | g0158 | AMR | PUR | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG01069 | hp1 | a0005 | c0011 | t0002 | g0008 | AMR | PUR | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0152 | AMR | PUR | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG01070 | hp2 | a0001 | c0003 | t0001 | g0005 | AMR | PUR | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG01071 | hp1 | a0001 | c0003 | t0001 | g0005 | AMR | PUR | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG01071 | hp2 | a0005 | c0011 | t0002 | g0008 | AMR | PUR | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG01074 | hp1 | a0001 | c0003 | t0001 | g0005 | AMR | PUR | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG01074 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0155 | AMR | PUR | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0165 | AMR | PUR | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG01099 | hp2 | a0001 | c0003 | t0001 | g0187 | AMR | PUR | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG01106 | hp2 | a0002 | c0002 | t0001 | g0162 | AMR | PUR | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG01168 | hp1 | a0001 | c0003 | t0001 | g0002 | AMR | PUR | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG01175 | hp1 | a0001 | c0004 | t0002 | g0080 | AMR | PUR | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG01175 | hp2 | a0007 | c0015 | t0001 | g0110 | AMR | PUR | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG01192 | hp1 | a0001 | c0004 | t0002 | g0061 | AMR | PUR | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG01192 | hp2 | a0001 | c0003 | t0001 | g0207 | AMR | PUR | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG01255 | hp1 | a0001 | c0003 | t0001 | g0197 | AMR | CLM | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG01256 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | CLM | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | CLM | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG01261 | hp2 | a0023 | c0037 | t0001 | g0192 | AMR | CLM | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG01346 | hp1 | a0001 | c0004 | t0002 | g0057 | AMR | CLM | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG01358 | hp1 | a0002 | c0002 | t0007 | g0154 | AMR | CLM | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG01433 | hp1 | a0001 | c0034 | t0001 | g0174 | AMR | CLM | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG01433 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | CLM | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0013 | AMR | CLM | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG01515 | hp2 | a0001 | c0003 | t0001 | g0206 | EUR | IBS | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG01884 | hp1 | a0001 | c0004 | t0002 | g0077 | AFR | ACB | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG01884 | hp2 | a0002 | c0002 | t0001 | g0146 | AFR | ACB | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG01891 | hp1 | a0001 | c0004 | t0002 | g0082 | AFR | ACB | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG01891 | hp2 | a0001 | c0031 | t0002 | g0085 | AFR | ACB | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG01934 | hp2 | a0002 | c0002 | t0001 | g0013 | AMR | PEL | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02004 | hp1 | a0001 | c0003 | t0001 | g0002 | AMR | PEL | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02015 | hp1 | a0002 | c0002 | t0001 | g0156 | EAS | KHV | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02015 | hp2 | a0001 | c0003 | t0001 | g0195 | EAS | KHV | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02055 | hp1 | a0001 | c0004 | t0002 | g0074 | AFR | ACB | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02055 | hp2 | a0001 | c0004 | t0002 | g0062 | AFR | ACB | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02056 | hp1 | a0015 | c0017 | t0001 | g0185 | EAS | KHV | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02071 | hp2 | a0002 | c0002 | t0001 | g0138 | EAS | KHV | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02145 | hp1 | a0001 | c0008 | t0001 | g0097 | AFR | ACB | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02145 | hp2 | a0006 | c0006 | t0005 | g0212 | AFR | ACB | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02148 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PEL | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02148 | hp2 | a0001 | c0003 | t0001 | g0182 | AMR | PEL | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02155 | hp1 | a0002 | c0002 | t0001 | g0160 | EAS | CDX | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CDX | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02165 | hp1 | a0024 | c0041 | t0001 | g0140 | EAS | CDX | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02257 | hp2 | a0001 | c0004 | t0002 | g0066 | AFR | ACB | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02258 | hp1 | a0003 | c0007 | t0002 | g0022 | AFR | ACB | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02258 | hp2 | a0001 | c0003 | t0001 | g0178 | AFR | ACB | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02280 | hp1 | a0008 | c0016 | t0001 | g0011 | AFR | ACB | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02280 | hp2 | a0001 | c0039 | t0001 | g0168 | AFR | ACB | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02293 | hp2 | a0001 | c0003 | t0001 | g0190 | AMR | PEL | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02451 | hp1 | a0001 | c0004 | t0002 | g0076 | AFR | ACB | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02451 | hp2 | a0001 | c0004 | t0002 | g0058 | AFR | ACB | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02523 | hp2 | a0004 | c0005 | t0003 | g0040 | EAS | KHV | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02622 | hp1 | a0003 | c0007 | t0002 | g0022 | AFR | GWD | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02622 | hp2 | a0009 | c0010 | t0002 | g0063 | AFR | GWD | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02630 | hp1 | a0001 | c0008 | t0001 | g0096 | AFR | GWD | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02630 | hp2 | a0001 | c0004 | t0002 | g0053 | AFR | GWD | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02647 | hp1 | a0001 | c0004 | t0002 | g0081 | AFR | GWD | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02647 | hp2 | a0001 | c0003 | t0001 | g0177 | AFR | GWD | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02698 | hp1 | a0025 | c0044 | t0001 | g0163 | SAS | PJL | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02698 | hp2 | a0001 | c0004 | t0002 | g0019 | SAS | PJL | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02717 | hp1 | a0006 | c0006 | t0005 | g0213 | AFR | GWD | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02717 | hp2 | a0001 | c0004 | t0002 | g0064 | AFR | GWD | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02723 | hp1 | a0001 | c0004 | t0002 | g0070 | AFR | GWD | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02723 | hp2 | a0010 | c0009 | t0006 | g0016 | AFR | GWD | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02735 | hp2 | a0001 | c0003 | t0001 | g0194 | SAS | PJL | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02809 | hp1 | a0003 | c0007 | t0002 | g0067 | AFR | GWD | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02809 | hp2 | a0002 | c0002 | t0001 | g0136 | AFR | GWD | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02818 | hp1 | a0001 | c0003 | t0001 | g0036 | AFR | GWD | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02818 | hp2 | a0011 | c0013 | t0004 | g0046 | AFR | GWD | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02886 | hp1 | a0001 | c0008 | t0001 | g0094 | AFR | GWD | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02886 | hp2 | a0001 | c0004 | t0002 | g0065 | AFR | GWD | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02895 | hp1 | a0003 | c0007 | t0002 | g0069 | AFR | GWD | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02895 | hp2 | a0001 | c0004 | t0002 | g0021 | AFR | GWD | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02896 | hp1 | a0016 | c0025 | t0004 | g0024 | AFR | GWD | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02896 | hp2 | a0001 | c0003 | t0001 | g0186 | AFR | GWD | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02897 | hp1 | a0016 | c0025 | t0004 | g0024 | AFR | GWD | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02897 | hp2 | a0001 | c0004 | t0002 | g0021 | AFR | GWD | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02965 | hp1 | a0017 | c0024 | t0004 | g0089 | AFR | ESN | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02965 | hp2 | a0001 | c0004 | t0002 | g0018 | AFR | ESN | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02970 | hp1 | a0001 | c0004 | t0002 | g0084 | AFR | ESN | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02970 | hp2 | a0001 | c0003 | t0001 | g0005 | AFR | ESN | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02976 | hp1 | a0011 | c0013 | t0004 | g0047 | AFR | ESN | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02976 | hp2 | a0001 | c0004 | t0002 | g0018 | AFR | ESN | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0007 | SAS | PJL | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG03017 | hp2 | a0018 | c0021 | t0001 | g0029 | SAS | PJL | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG03041 | hp1 | a0011 | c0013 | t0004 | g0048 | AFR | GWD | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG03041 | hp2 | a0001 | c0004 | t0002 | g0050 | AFR | GWD | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG03098 | hp1 | a0008 | c0016 | t0001 | g0011 | AFR | MSL | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG03098 | hp2 | a0001 | c0003 | t0001 | g0037 | AFR | MSL | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG03130 | hp1 | a0003 | c0012 | t0002 | g0023 | AFR | ESN | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG03130 | hp2 | a0001 | c0003 | t0001 | g0037 | AFR | ESN | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG03139 | hp1 | a0006 | c0006 | t0005 | g0038 | AFR | ESN | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG03139 | hp2 | a0019 | c0019 | t0001 | g0033 | AFR | ESN | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG03209 | hp1 | a0009 | c0010 | t0002 | g0020 | AFR | MSL | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG03209 | hp2 | a0001 | c0003 | t0001 | g0196 | AFR | MSL | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG03225 | hp1 | a0009 | c0010 | t0002 | g0020 | AFR | MSL | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG03225 | hp2 | a0026 | c0043 | t0001 | g0095 | AFR | MSL | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG03239 | hp1 | a0001 | c0004 | t0002 | g0054 | SAS | PJL | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0013 | SAS | PJL | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG03453 | hp1 | a0001 | c0004 | t0002 | g0075 | AFR | MSL | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG03453 | hp2 | a0001 | c0022 | t0001 | g0034 | AFR | MSL | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG03486 | hp1 | a0001 | c0003 | t0001 | g0181 | AFR | MSL | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG03486 | hp2 | a0003 | c0012 | t0002 | g0023 | AFR | MSL | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG03490 | hp1 | a0002 | c0002 | t0001 | g0151 | SAS | PJL | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG03492 | hp1 | a0002 | c0002 | t0001 | g0164 | SAS | PJL | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG03492 | hp2 | a0018 | c0021 | t0001 | g0029 | SAS | PJL | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG03516 | hp1 | a0001 | c0003 | t0001 | g0184 | AFR | ESN | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG03516 | hp2 | a0001 | c0004 | t0002 | g0049 | AFR | ESN | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG03540 | hp1 | a0027 | c0032 | t0002 | g0083 | AFR | GWD | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG03540 | hp2 | a0001 | c0004 | t0002 | g0052 | AFR | GWD | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG03654 | hp1 | a0028 | c0030 | t0002 | g0056 | SAS | PJL | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0144 | SAS | PJL | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG03688 | hp1 | a0013 | c0018 | t0001 | g0035 | SAS | STU | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG03688 | hp2 | a0001 | c0004 | t0002 | g0019 | SAS | STU | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG03704 | hp1 | a0029 | c0049 | t0001 | g0208 | SAS | PJL | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG03704 | hp2 | a0030 | c0046 | t0001 | g0129 | SAS | PJL | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG03710 | hp1 | a0001 | c0004 | t0002 | g0055 | SAS | PJL | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG03710 | hp2 | a0002 | c0002 | t0001 | g0143 | SAS | PJL | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG03831 | hp1 | a0001 | c0003 | t0001 | g0193 | SAS | BEB | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | BEB | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG03927 | hp1 | a0001 | c0003 | t0001 | g0199 | SAS | BEB | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG03927 | hp2 | a0002 | c0002 | t0007 | g0166 | SAS | BEB | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0007 | SAS | BEB | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0003 | SAS | BEB | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG04184 | hp2 | a0001 | c0003 | t0001 | g0180 | SAS | BEB | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG04199 | hp1 | a0002 | c0002 | t0001 | g0145 | SAS | STU | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | STU | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG04204 | hp1 | a0001 | c0003 | t0001 | g0205 | SAS | STU | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG04204 | hp2 | a0001 | c0026 | t0001 | g0044 | SAS | STU | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG04228 | hp2 | a0002 | c0002 | t0001 | g0003 | SAS | STU | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18612 | hp1 | a0001 | c0001 | t0009 | g0211 | EAS | CHB | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18612 | hp2 | a0004 | c0005 | t0003 | g0039 | EAS | CHB | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18906 | hp1 | a0001 | c0004 | t0002 | g0073 | AFR | YRI | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18906 | hp2 | a0001 | c0004 | t0002 | g0079 | AFR | YRI | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18940 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18940 | hp2 | a0031 | c0038 | t0001 | g0106 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18943 | hp1 | a0032 | c0047 | t0001 | g0132 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18943 | hp2 | a0001 | c0003 | t0001 | g0015 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18944 | hp1 | a0001 | c0003 | t0001 | g0015 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18945 | hp1 | a0004 | c0005 | t0003 | g0017 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18947 | hp1 | a0001 | c0003 | t0001 | g0172 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18947 | hp2 | a0020 | c0020 | t0001 | g0102 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18949 | hp2 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18952 | hp2 | a0012 | c0014 | t0001 | g0027 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18953 | hp1 | a0012 | c0014 | t0001 | g0027 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18953 | hp2 | a0015 | c0017 | t0001 | g0183 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18960 | hp1 | a0033 | c0035 | t0001 | g0203 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18964 | hp1 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18965 | hp1 | a0001 | c0003 | t0001 | g0014 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18966 | hp2 | a0002 | c0002 | t0001 | g0142 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18969 | hp1 | a0004 | c0005 | t0003 | g0017 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18969 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18972 | hp1 | a0004 | c0005 | t0003 | g0041 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18972 | hp2 | a0020 | c0020 | t0001 | g0101 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18973 | hp1 | a0001 | c0003 | t0001 | g0014 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18975 | hp2 | a0001 | c0003 | t0001 | g0201 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18978 | hp1 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18980 | hp2 | a0002 | c0002 | t0001 | g0139 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18987 | hp2 | a0002 | c0040 | t0001 | g0148 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18988 | hp2 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18998 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19000 | hp1 | a0001 | c0003 | t0001 | g0179 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19001 | hp1 | a0001 | c0003 | t0001 | g0173 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19003 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19005 | hp1 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19005 | hp2 | a0001 | c0003 | t0001 | g0175 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19006 | hp1 | a0004 | c0005 | t0003 | g0042 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19007 | hp1 | a0002 | c0002 | t0001 | g0167 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19010 | hp1 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19010 | hp2 | a0001 | c0003 | t0008 | g0189 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19011 | hp1 | a0034 | c0042 | t0001 | g0141 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19011 | hp2 | a0012 | c0014 | t0001 | g0118 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19012 | hp2 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19030 | hp1 | a0008 | c0016 | t0001 | g0011 | AFR | LWK | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19030 | hp2 | a0001 | c0008 | t0001 | g0128 | AFR | LWK | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19043 | hp1 | a0019 | c0019 | t0001 | g0033 | AFR | LWK | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19043 | hp2 | a0017 | c0024 | t0004 | g0088 | AFR | LWK | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19057 | hp1 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19060 | hp2 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19063 | hp2 | a0001 | c0003 | t0001 | g0209 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19065 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19066 | hp2 | a0001 | c0003 | t0001 | g0171 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19068 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19072 | hp1 | a0004 | c0005 | t0003 | g0043 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19072 | hp2 | a0001 | c0003 | t0001 | g0014 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19076 | hp1 | a0001 | c0003 | t0001 | g0204 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19079 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19083 | hp2 | a0001 | c0003 | t0001 | g0188 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19086 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19088 | hp1 | a0035 | c0036 | t0001 | g0191 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19089 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19240 | hp1 | a0001 | c0004 | t0002 | g0078 | AFR | YRI | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA19240 | hp2 | a0001 | c0003 | t0001 | g0036 | AFR | YRI | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA20129 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | ASW | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA20129 | hp2 | a0010 | c0009 | t0006 | g0016 | AFR | ASW | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA20752 | hp1 | a0036 | c0029 | t0002 | g0060 | EUR | TSI | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA20752 | hp2 | a0001 | c0028 | t0001 | g0051 | EUR | TSI | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA20905 | hp1 | a0001 | c0003 | t0001 | g0176 | SAS | GIH | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA20905 | hp2 | a0014 | c0023 | t0001 | g0032 | SAS | GIH | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02109 | hp1 | a0006 | c0006 | t0005 | g0038 | AFR | ACB | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02109 | hp2 | a0001 | c0033 | t0002 | g0071 | AFR | ACB | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02486 | hp1 | a0001 | c0045 | t0001 | g0202 | AFR | ACB | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG02486 | hp2 | a0002 | c0002 | t0001 | g0150 | AFR | ACB | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG03471 | hp1 | a0001 | c0004 | t0002 | g0086 | AFR | MSL | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG03471 | hp2 | a0010 | c0009 | t0002 | g0045 | AFR | MSL | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG06807 | hp1 | a0001 | c0004 | t0002 | g0072 | AFR | USA | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
HG06807 | hp2 | a0002 | c0002 | t0001 | g0153 | AFR | USA | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA18955 | hp2 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA20300 | hp1 | a0001 | c0022 | t0001 | g0034 | AFR | USA | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | USA | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA21309 | hp1 | a0003 | c0012 | t0002 | g0068 | AFR | LWK | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
NA21309 | hp2 | a0001 | c0003 | t0001 | g0200 | AFR | LWK | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
homoSapiens | chm13v2 | a0001 | c0004 | t0002 | g0059 | REF | REF | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
homoSapiens | grch38p0 | a0005 | c0011 | t0002 | g0008 | REF | REF | ASPM_chr1_197079127_197151669 | ASPM | chr1 | 197079127 | 197151669 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:197088356 | C | T | 1 | a0024 | 1 | HG02165.hp1 | missense_variant | MODERATE | c.10061G>A | p.Arg3354Gln | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 26/28 | 10293/10863 | 10061/10434 | 3354/3477 | chr1 | 197088356 | |||
chr1:197090081 | A | G | 1 | a0033 | 1 | NA18960.hp1 | missense_variant | MODERATE | c.9833T>C | p.Val3278Ala | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 25/28 | 10065/10863 | 9833/10434 | 3278/3477 | chr1 | 197090081 | |||
chr1:197090252 | T | C | 1 | a0011 | 3 | HG02818.hp2 HG02976.hp1 HG03041.hp1 |
missense_variant | MODERATE | c.9773A>G | p.His3258Arg | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 24/28 | 10005/10863 | 9773/10434 | 3258/3477 | chr1 | 197090252 | |||
chr1:197090947 | T | G | 1 | a0018 | 2 | HG03017.hp2 HG03492.hp2 |
missense_variant | MODERATE | c.9539A>C | p.Gln3180Pro | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 23/28 | 9771/10863 | 9539/10434 | 3180/3477 | chr1 | 197090947 | |||
chr1:197091956 | A | C | 1 | a0014 | 2 | HG00140.hp1 NA20905.hp2 |
missense_variant | MODERATE | c.9395T>G | p.Leu3132Arg | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 22/28 | 9627/10863 | 9395/10434 | 3132/3477 | chr1 | 197091956 | |||
chr1:197093245 | C | T | 1 | a0020 | 2 | NA18947.hp2 NA18972.hp2 |
missense_variant | MODERATE | c.9101G>A | p.Cys3034Tyr | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 21/28 | 9333/10863 | 9101/10434 | 3034/3477 | chr1 | 197093245 | |||
chr1:197100799 | C | A | 1 | a0035 | 1 | NA19088.hp1 | missense_variant | MODERATE | c.8452G>T | p.Ala2818Ser | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/28 | 8684/10863 | 8452/10434 | 2818/3477 | chr1 | 197100799 | |||
chr1:197100802 | C | A | 1 | a0015 | 2 | HG02056.hp1 NA18953.hp2 |
missense_variant | MODERATE | c.8449G>T | p.Ala2817Ser | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/28 | 8681/10863 | 8449/10434 | 2817/3477 | chr1 | 197100802 | |||
chr1:197100996 | A | C | 1 | a0019 | 2 | HG03139.hp2 NA19043.hp1 |
missense_variant | MODERATE | c.8255T>G | p.Met2752Arg | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/28 | 8487/10863 | 8255/10434 | 2752/3477 | chr1 | 197100996 | |||
chr1:197101312 | G | T | 6 | a0002 a0014 a0022 others(3): Show |
64 | HG00140.hp1 HG00423.hp1 HG00639.hp2 others(61): Show |
missense_variant | MODERATE | c.7939C>A | p.Leu2647Ile | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/28 | 8171/10863 | 7939/10434 | 2647/3477 | chr1 | 197101312 | |||
chr1:197101391 | C | G | 2 | a0007 a0030 |
4 | HG00099.hp2 HG00639.hp1 HG01175.hp2 others(1): Show |
missense_variant | MODERATE | c.7860G>C | p.Gln2620His | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/28 | 8092/10863 | 7860/10434 | 2620/3477 | chr1 | 197101391 | |||
chr1:197101464 | A | G | 2 | a0004 a0011 |
10 | HG02523.hp2 HG02818.hp2 HG02976.hp1 others(7): Show |
missense_variant | MODERATE | c.7787T>C | p.Val2596Ala | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/28 | 8019/10863 | 7787/10434 | 2596/3477 | chr1 | 197101464 | |||
chr1:197101567 | T | C | 6 | a0002 a0014 a0022 others(3): Show |
64 | HG00140.hp1 HG00423.hp1 HG00639.hp2 others(61): Show |
missense_variant | MODERATE | c.7684A>G | p.Ser2562Gly | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/28 | 7916/10863 | 7684/10434 | 2562/3477 | chr1 | 197101567 | |||
chr1:197101686 | A | C | 2 | a0016 a0017 |
4 | HG02896.hp1 HG02897.hp1 HG02965.hp1 others(1): Show |
stop_gained | HIGH | c.7565T>G | p.Leu2522* | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/28 | 7797/10863 | 7565/10434 | 2522/3477 | chr1 | 197101686 | |||
chr1:197101771 | A | G | 35 | a0001 a0002 a0003 others(32): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
missense_variant | MODERATE | c.7480T>C | p.Tyr2494His | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/28 | 7712/10863 | 7480/10434 | 2494/3477 | chr1 | 197101771 | |||
chr1:197101776 | C | T | 1 | a0012 | 3 | NA18952.hp2 NA18953.hp1 NA19011.hp2 |
missense_variant | MODERATE | c.7475G>A | p.Arg2492Lys | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/28 | 7707/10863 | 7475/10434 | 2492/3477 | chr1 | 197101776 | |||
chr1:197102137 | T | C | 1 | a0035 | 1 | NA19088.hp1 | missense_variant | MODERATE | c.7114A>G | p.Arg2372Gly | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/28 | 7346/10863 | 7114/10434 | 2372/3477 | chr1 | 197102137 | |||
chr1:197102524 | C | A | 1 | a0027 | 1 | HG03540.hp1 | missense_variant | MODERATE | c.6727G>T | p.Val2243Leu | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/28 | 6959/10863 | 6727/10434 | 2243/3477 | chr1 | 197102524 | |||
chr1:197103430 | A | G | 2 | a0004 a0011 |
10 | HG02523.hp2 HG02818.hp2 HG02976.hp1 others(7): Show |
missense_variant | MODERATE | c.5821T>C | p.Cys1941Arg | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/28 | 6053/10863 | 5821/10434 | 1941/3477 | chr1 | 197103430 | |||
chr1:197103467 | C | G | 1 | a0028 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.5784G>C | p.Gln1928His | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/28 | 6016/10863 | 5784/10434 | 1928/3477 | chr1 | 197103467 | |||
chr1:197103622 | C | T | 1 | a0008 | 3 | HG02280.hp1 HG03098.hp1 NA19030.hp1 |
missense_variant | MODERATE | c.5629G>A | p.Ala1877Thr | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/28 | 5861/10863 | 5629/10434 | 1877/3477 | chr1 | 197103622 | |||
chr1:197103672 | G | A | 2 | a0004 a0011 |
10 | HG02523.hp2 HG02818.hp2 HG02976.hp1 others(7): Show |
missense_variant | MODERATE | c.5579C>T | p.Ala1860Val | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/28 | 5811/10863 | 5579/10434 | 1860/3477 | chr1 | 197103672 | |||
chr1:197104045 | G | C | 2 | a0016 a0017 |
4 | HG02896.hp1 HG02897.hp1 HG02965.hp1 others(1): Show |
missense_variant | MODERATE | c.5206C>G | p.Gln1736Glu | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/28 | 5438/10863 | 5206/10434 | 1736/3477 | chr1 | 197104045 | |||
chr1:197104066 | G | A | 2 | a0023 a0029 |
2 | HG01261.hp2 HG03704.hp1 |
missense_variant | MODERATE | c.5185C>T | p.Arg1729Trp | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/28 | 5417/10863 | 5185/10434 | 1729/3477 | chr1 | 197104066 | |||
chr1:197104168 | G | A | 2 | a0006 a0011 |
7 | HG02109.hp1 HG02145.hp2 HG02717.hp1 others(4): Show |
missense_variant | MODERATE | c.5083C>T | p.Arg1695Cys | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/28 | 5315/10863 | 5083/10434 | 1695/3477 | chr1 | 197104168 | |||
chr1:197104188 | G | A | 2 | a0004 a0011 |
10 | HG02523.hp2 HG02818.hp2 HG02976.hp1 others(7): Show |
missense_variant | MODERATE | c.5063C>T | p.Thr1688Ile | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/28 | 5295/10863 | 5063/10434 | 1688/3477 | chr1 | 197104188 | |||
chr1:197104276 | C | A | 1 | a0034 | 1 | NA19011.hp1 | missense_variant | MODERATE | c.4975G>T | p.Val1659Phe | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/28 | 5207/10863 | 4975/10434 | 1659/3477 | chr1 | 197104276 | |||
chr1:197104815 | T | C | 1 | a0026 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.4436A>G | p.Lys1479Arg | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/28 | 4668/10863 | 4436/10434 | 1479/3477 | chr1 | 197104815 | |||
chr1:197105038 | G | A | 1 | a0013 | 2 | HG00099.hp1 HG03688.hp1 |
missense_variant | MODERATE | c.4213C>T | p.Arg1405Cys | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/28 | 4445/10863 | 4213/10434 | 1405/3477 | chr1 | 197105038 | |||
chr1:197121994 | C | T | 1 | a0009 | 3 | HG02622.hp2 HG03209.hp1 HG03225.hp1 |
missense_variant | MODERATE | c.3791G>A | p.Arg1264His | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 16/28 | 4023/10863 | 3791/10434 | 1264/3477 | chr1 | 197121994 | |||
chr1:197122009 | C | T | 1 | a0036 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.3776G>A | p.Arg1259Lys | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 16/28 | 4008/10863 | 3776/10434 | 1259/3477 | chr1 | 197122009 | |||
chr1:197124127 | C | T | 1 | a0031 | 1 | NA18940.hp2 | missense_variant | MODERATE | c.3373G>A | p.Ala1125Thr | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 13/28 | 3605/10863 | 3373/10434 | 1125/3477 | chr1 | 197124127 | |||
chr1:197124231 | G | A | 2 | a0003 a0010 |
10 | HG02258.hp1 HG02622.hp1 HG02723.hp2 others(7): Show |
missense_variant | MODERATE | c.3269C>T | p.Ser1090Phe | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 13/28 | 3501/10863 | 3269/10434 | 1090/3477 | chr1 | 197124231 | |||
chr1:197128602 | G | A | 1 | a0025 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.2824C>T | p.Arg942Cys | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 10/28 | 3056/10863 | 2824/10434 | 942/3477 | chr1 | 197128602 | |||
chr1:197133502 | T | C | 1 | a0030 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.2267A>G | p.Tyr756Cys | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 6/28 | 2499/10863 | 2267/10434 | 756/3477 | chr1 | 197133502 | |||
chr1:197133551 | T | A | 2 | a0016 a0017 |
4 | HG02896.hp1 HG02897.hp1 HG02965.hp1 others(1): Show |
missense_variant | MODERATE | c.2218A>T | p.Ile740Leu | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 6/28 | 2450/10863 | 2218/10434 | 740/3477 | chr1 | 197133551 | |||
chr1:197139806 | C | A | 1 | a0008 | 3 | HG02280.hp1 HG03098.hp1 NA19030.hp1 |
missense_variant | MODERATE | c.1987G>T | p.Ala663Ser | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/28 | 2219/10863 | 1987/10434 | 663/3477 | chr1 | 197139806 | |||
chr1:197142801 | T | C | 2 | a0016 a0017 |
4 | HG02896.hp1 HG02897.hp1 HG02965.hp1 others(1): Show |
missense_variant | MODERATE | c.1451A>G | p.Asn484Ser | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 3/28 | 1683/10863 | 1451/10434 | 484/3477 | chr1 | 197142801 | |||
chr1:197142867 | T | C | 1 | a0016 | 2 | HG02896.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.1385A>G | p.Tyr462Cys | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 3/28 | 1617/10863 | 1385/10434 | 462/3477 | chr1 | 197142867 | |||
chr1:197142928 | G | C | 1 | a0032 | 1 | NA18943.hp1 | missense_variant | MODERATE | c.1324C>G | p.Gln442Glu | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 3/28 | 1556/10863 | 1324/10434 | 442/3477 | chr1 | 197142928 | |||
chr1:197142964 | T | C | 1 | a0011 | 3 | HG02818.hp2 HG02976.hp1 HG03041.hp1 |
missense_variant | MODERATE | c.1288A>G | p.Arg430Gly | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 3/28 | 1520/10863 | 1288/10434 | 430/3477 | chr1 | 197142964 | |||
chr1:197143245 | G | T | 1 | a0004 | 7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
missense_variant | MODERATE | c.1007C>A | p.Thr336Lys | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 3/28 | 1239/10863 | 1007/10434 | 336/3477 | chr1 | 197143245 | |||
chr1:197143315 | T | C | 1 | a0021 | 1 | HG00438.hp2 | missense_variant | MODERATE | c.937A>G | p.Ile313Val | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 3/28 | 1169/10863 | 937/10434 | 313/3477 | chr1 | 197143315 | |||
chr1:197143319 | G | C | 1 | a0029 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.933C>G | p.Ser311Arg | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 3/28 | 1165/10863 | 933/10434 | 311/3477 | chr1 | 197143319 | |||
chr1:197143347 | C | T | 1 | a0004 | 7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
missense_variant | MODERATE | c.905G>A | p.Cys302Tyr | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 3/28 | 1137/10863 | 905/10434 | 302/3477 | chr1 | 197143347 | |||
chr1:197143408 | T | G | 1 | a0004 | 7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
missense_variant | MODERATE | c.844A>C | p.Asn282His | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 3/28 | 1076/10863 | 844/10434 | 282/3477 | chr1 | 197143408 | |||
chr1:197143606 | C | T | 1 | a0022 | 1 | HG00735.hp2 | missense_variant | MODERATE | c.646G>A | p.Glu216Lys | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 3/28 | 878/10863 | 646/10434 | 216/3477 | chr1 | 197143606 | |||
chr1:197143608 | T | G | 2 | a0016 a0017 |
4 | HG02896.hp1 HG02897.hp1 HG02965.hp1 others(1): Show |
missense_variant | MODERATE | c.644A>C | p.Glu215Ala | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 3/28 | 876/10863 | 644/10434 | 215/3477 | chr1 | 197143608 | |||
chr1:197146215 | C | T | 1 | a0010 | 3 | HG02723.hp2 HG03471.hp2 NA20129.hp2 |
missense_variant | MODERATE | c.223G>A | p.Ala75Thr | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 1/28 | 455/10863 | 223/10434 | 75/3477 | chr1 | 197146215 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:197088421 | A | G | 1 | a0001c0022 | 2 | HG03453.hp2 NA20300.hp1 |
synonymous_variant | LOW | c.9996T>C | p.Thr3332Thr | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 26/28 | 10228/10863 | 9996/10434 | 3332/3477 | chr1 | 197088421 | |||
chr1:197101085 | A | G | 1 | a0004c0005 | 7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
synonymous_variant | LOW | c.8166T>C | p.Tyr2722Tyr | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/28 | 8398/10863 | 8166/10434 | 2722/3477 | chr1 | 197101085 | |||
chr1:197101334 | T | C | 2 | a0001c0039 a0019c0019 |
3 | HG02280.hp2 HG03139.hp2 NA19043.hp1 |
synonymous_variant | LOW | c.7917A>G | p.Lys2639Lys | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/28 | 8149/10863 | 7917/10434 | 2639/3477 | chr1 | 197101334 | |||
chr1:197101577 | G | A | 7 | a0002c0002 a0002c0040 a0014c0023 others(4): Show |
64 | HG00140.hp1 HG00423.hp1 HG00639.hp2 others(61): Show |
synonymous_variant | LOW | c.7674C>T | p.Ile2558Ile | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/28 | 7906/10863 | 7674/10434 | 2558/3477 | chr1 | 197101577 | |||
chr1:197101646 | C | T | 10 | a0001c0001 a0001c0026 a0007c0015 others(7): Show |
79 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(76): Show |
synonymous_variant | LOW | c.7605G>A | p.Val2535Val | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/28 | 7837/10863 | 7605/10434 | 2535/3477 | chr1 | 197101646 | |||
chr1:197101685 | T | C | 40 | a0001c0001 a0001c0003 a0001c0008 others(37): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
synonymous_variant | LOW | c.7566A>G | p.Leu2522Leu | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/28 | 7798/10863 | 7566/10434 | 2522/3477 | chr1 | 197101685 | |||
chr1:197101898 | C | T | 2 | a0001c0039 a0019c0019 |
3 | HG02280.hp2 HG03139.hp2 NA19043.hp1 |
synonymous_variant | LOW | c.7353G>A | p.Leu2451Leu | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/28 | 7585/10863 | 7353/10434 | 2451/3477 | chr1 | 197101898 | |||
chr1:197102072 | A | T | 1 | a0002c0040 | 1 | NA18987.hp2 | synonymous_variant | LOW | c.7179T>A | p.Ala2393Ala | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/28 | 7411/10863 | 7179/10434 | 2393/3477 | chr1 | 197102072 | |||
chr1:197102228 | G | A | 1 | a0003c0012 | 3 | HG03130.hp1 HG03486.hp2 NA21309.hp1 |
synonymous_variant | LOW | c.7023C>T | p.Ile2341Ile | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/28 | 7255/10863 | 7023/10434 | 2341/3477 | chr1 | 197102228 | |||
chr1:197102549 | T | C | 1 | a0001c0033 | 1 | HG02109.hp2 | synonymous_variant | LOW | c.6702A>G | p.Gln2234Gln | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/28 | 6934/10863 | 6702/10434 | 2234/3477 | chr1 | 197102549 | |||
chr1:197103290 | T | C | 7 | a0002c0002 a0002c0040 a0014c0023 others(4): Show |
64 | HG00140.hp1 HG00423.hp1 HG00639.hp2 others(61): Show |
synonymous_variant | LOW | c.5961A>G | p.Gln1987Gln | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/28 | 6193/10863 | 5961/10434 | 1987/3477 | chr1 | 197103290 | |||
chr1:197104802 | T | C | 7 | a0002c0002 a0002c0040 a0014c0023 others(4): Show |
64 | HG00140.hp1 HG00423.hp1 HG00639.hp2 others(61): Show |
synonymous_variant | LOW | c.4449A>G | p.Lys1483Lys | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/28 | 4681/10863 | 4449/10434 | 1483/3477 | chr1 | 197104802 | |||
chr1:197117942 | G | T | 1 | a0011c0013 | 3 | HG02818.hp2 HG02976.hp1 HG03041.hp1 |
synonymous_variant | LOW | c.3912C>A | p.Ile1304Ile | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/28 | 4144/10863 | 3912/10434 | 1304/3477 | chr1 | 197117942 | |||
chr1:197122407 | A | T | 37 | a0001c0001 a0001c0003 a0001c0008 others(34): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
synonymous_variant | LOW | c.3579T>A | p.Ser1193Ser | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 14/28 | 3811/10863 | 3579/10434 | 1193/3477 | chr1 | 197122407 | |||
chr1:197124900 | C | T | 10 | a0001c0003 a0001c0028 a0001c0034 others(7): Show |
67 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(64): Show |
synonymous_variant | LOW | c.3138G>A | p.Arg1046Arg | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 12/28 | 3370/10863 | 3138/10434 | 1046/3477 | chr1 | 197124900 | |||
chr1:197129196 | G | A | 1 | a0001c0045 | 1 | HG02486.hp1 | synonymous_variant | LOW | c.2751C>T | p.Ala917Ala | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 9/28 | 2983/10863 | 2751/10434 | 917/3477 | chr1 | 197129196 | |||
chr1:197133462 | T | C | 1 | a0011c0013 | 3 | HG02818.hp2 HG02976.hp1 HG03041.hp1 |
synonymous_variant | LOW | c.2307A>G | p.Ala769Ala | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 6/28 | 2539/10863 | 2307/10434 | 769/3477 | chr1 | 197133462 | |||
chr1:197139816 | A | G | 2 | a0001c0028 a0001c0034 |
2 | HG01433.hp1 NA20752.hp2 |
synonymous_variant | LOW | c.1977T>C | p.Ile659Ile | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/28 | 2209/10863 | 1977/10434 | 659/3477 | chr1 | 197139816 | |||
chr1:197143403 | G | A | 32 | a0001c0001 a0001c0003 a0001c0008 others(29): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
synonymous_variant | LOW | c.849C>T | p.Ser283Ser | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 3/28 | 1081/10863 | 849/10434 | 283/3477 | chr1 | 197143403 | |||
chr1:197146357 | G | T | 1 | a0001c0026 | 1 | HG04204.hp2 | synonymous_variant | LOW | c.81C>A | p.Pro27Pro | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 1/28 | 313/10863 | 81/10434 | 27/3477 | chr1 | 197146357 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:197084166 | A | G | 1 | a0002c0002t0007 | 2 | HG01358.hp1 HG03927.hp2 |
3_prime_UTR_variant | MODIFIER | c.*158T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 28/28 | 158 | chr1 | 197084166 | ||||||
chr1:197084243 | G | A | 40 | a0001c0001t0001 a0001c0001t0009 a0001c0003t0001 others(37): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
3_prime_UTR_variant | MODIFIER | c.*81C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 28/28 | 81 | chr1 | 197084243 | ||||||
chr1:197084246 | G | C | 1 | a0001c0003t0008 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*78C>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 28/28 | 78 | chr1 | 197084246 | ||||||
chr1:197084264 | G | A | 3 | a0011c0013t0004 a0016c0025t0004 a0017c0024t0004 |
7 | HG02818.hp2 HG02896.hp1 HG02897.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*60C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 28/28 | 60 | chr1 | 197084264 | ||||||
chr1:197146446 | C | A | 1 | a0001c0001t0009 | 1 | NA18612.hp1 | 5_prime_UTR_variant | MODIFIER | c.-9G>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 1/28 | 9 | chr1 | 197146446 | ||||||
chr1:197146547 | G | A | 1 | a0006c0006t0005 | 4 | HG02109.hp1 HG02145.hp2 HG02717.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-110C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 1/28 | 110 | chr1 | 197146547 | ||||||
chr1:197146551 | G | T | 1 | a0004c0005t0003 | 7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-114C>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 1/28 | 114 | chr1 | 197146551 | ||||||
chr1:197146614 | C | T | 1 | a0004c0005t0003 | 7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-177G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 1/28 | 177 | chr1 | 197146614 | ||||||
chr1:197146634 | A | G | 1 | a0010c0009t0006 | 2 | HG02723.hp2 NA20129.hp2 |
5_prime_UTR_variant | MODIFIER | c.-197T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 1/28 | 197 | chr1 | 197146634 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:197084431 | T | TA | 53 | a0001c0004t0002g0053 a0001c0039t0001g0168 a0002c0002t0001g0003 others(50): Show |
77 | HG00140.hp1 HG00423.hp1 HG00639.hp2 others(74): Show |
splice_region_variant&intron_variant | LOW | c.10332-6dupT | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 27/27 | chr1 | 197084431 | |||||||
chr1:197084463 | GTTC | G | 3 | a0001c0004t0002g0072 a0001c0004t0002g0074 a0001c0004t0002g0084 |
3 | HG02055.hp1 HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.10332-40_10332-38d others(5): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 27/27 | chr1 | 197084463 | |||||||
chr1:197084629 | C | T | 6 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(3): Show |
7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.10332-203G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 27/27 | chr1 | 197084629 | |||||||
chr1:197084788 | C | A | 1 | a0001c0031t0002g0085 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.10332-362G>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 27/27 | chr1 | 197084788 | |||||||
chr1:197085144 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.10332-718C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 27/27 | chr1 | 197085144 | |||||||
chr1:197085213 | T | C | 6 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(3): Show |
7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.10332-787A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 27/27 | chr1 | 197085213 | |||||||
chr1:197085477 | T | C | 1 | a0007c0015t0001g0093 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.10332-1051A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 27/27 | chr1 | 197085477 | |||||||
chr1:197085734 | CA | C | 3 | a0016c0025t0004g0024 a0017c0024t0004g0088 a0017c0024t0004g0089 |
4 | HG02896.hp1 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.10331+1068delT | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 27/27 | chr1 | 197085734 | |||||||
chr1:197085812 | C | T | 3 | a0006c0006t0005g0038 a0006c0006t0005g0212 a0006c0006t0005g0213 |
4 | HG02109.hp1 HG02145.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.10331+991G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 27/27 | chr1 | 197085812 | |||||||
chr1:197085821 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.10331+982C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 27/27 | chr1 | 197085821 | |||||||
chr1:197085839 | T | C | 5 | a0001c0004t0002g0018 a0001c0004t0002g0052 a0001c0004t0002g0053 others(2): Show |
6 | HG02451.hp2 HG02630.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.10331+964A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 27/27 | chr1 | 197085839 | |||||||
chr1:197085861 | A | G | 42 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0007 others(39): Show |
64 | HG00140.hp1 HG00423.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.10331+942T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 27/27 | chr1 | 197085861 | |||||||
chr1:197086042 | A | G | 1 | a0003c0012t0002g0068 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.10331+761T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 27/27 | chr1 | 197086042 | |||||||
chr1:197086255 | G | C | 1 | a0018c0021t0001g0029 | 2 | HG03017.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.10331+548C>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 27/27 | chr1 | 197086255 | |||||||
chr1:197086310 | A | G | 1 | a0027c0032t0002g0083 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.10331+493T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 27/27 | chr1 | 197086310 | |||||||
chr1:197086326 | C | T | 1 | a0001c0004t0002g0049 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.10331+477G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 27/27 | chr1 | 197086326 | |||||||
chr1:197086441 | G | A | 1 | a0002c0002t0001g0155 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.10331+362C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 27/27 | chr1 | 197086441 | |||||||
chr1:197086652 | T | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(161): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.10331+151A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 27/27 | chr1 | 197086652 | |||||||
chr1:197086795 | T | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(161): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
splice_region_variant&intron_variant | LOW | c.10331+8A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 27/27 | chr1 | 197086795 | |||||||
chr1:197086979 | A | T | 3 | a0016c0025t0004g0024 a0017c0024t0004g0088 a0017c0024t0004g0089 |
4 | HG02896.hp1 HG02897.hp1 HG02965.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.10162-7T>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 26/27 | chr1 | 197086979 | |||||||
chr1:197087045 | C | A | 4 | a0001c0008t0001g0094 a0001c0008t0001g0096 a0001c0008t0001g0097 others(1): Show |
4 | HG02145.hp1 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.10162-73G>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 26/27 | chr1 | 197087045 | |||||||
chr1:197087177 | C | T | 2 | a0001c0001t0001g0109 a0001c0001t0001g0111 |
2 | HG00741.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.10162-205G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 26/27 | chr1 | 197087177 | |||||||
chr1:197087203 | T | C | 1 | a0011c0013t0004g0048 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.10162-231A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 26/27 | chr1 | 197087203 | |||||||
chr1:197087333 | C | T | 2 | a0001c0004t0002g0076 a0001c0004t0002g0078 |
2 | HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.10162-361G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 26/27 | chr1 | 197087333 | |||||||
chr1:197087531 | TATTATAG others(11): Show |
T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(52): Show |
80 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.10162-577_10162-56 others(22): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 26/27 | chr1 | 197087531 | |||||||
chr1:197087559 | A | G | 1 | a0001c0004t0002g0062 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.10162-587T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 26/27 | chr1 | 197087559 | |||||||
chr1:197087638 | C | T | 1 | a0002c0002t0001g0146 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.10161+618G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 26/27 | chr1 | 197087638 | |||||||
chr1:197088112 | T | A | 3 | a0006c0006t0005g0038 a0006c0006t0005g0212 a0006c0006t0005g0213 |
4 | HG02109.hp1 HG02145.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.10161+144A>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 26/27 | chr1 | 197088112 | |||||||
chr1:197088604 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.9985-172C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 25/27 | chr1 | 197088604 | |||||||
chr1:197088788 | G | A | 1 | a0009c0010t0002g0063 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.9985-356C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 25/27 | chr1 | 197088788 | |||||||
chr1:197088906 | T | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(149): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.9985-474A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 25/27 | chr1 | 197088906 | |||||||
chr1:197089006 | AATAAC | A | 42 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0007 others(39): Show |
64 | HG00140.hp1 HG00423.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.9985-579_9985-575d others(7): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 25/27 | chr1 | 197089006 | |||||||
chr1:197089085 | G | C | 4 | a0001c0008t0001g0094 a0001c0008t0001g0096 a0001c0008t0001g0097 others(1): Show |
4 | HG02145.hp1 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.9985-653C>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 25/27 | chr1 | 197089085 | |||||||
chr1:197089250 | C | T | 177 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(174): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.9984+680G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 25/27 | chr1 | 197089250 | |||||||
chr1:197089298 | A | G | 1 | a0033c0035t0001g0203 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.9984+632T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 25/27 | chr1 | 197089298 | |||||||
chr1:197089695 | T | G | 1 | a0026c0043t0001g0095 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.9984+235A>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 25/27 | chr1 | 197089695 | |||||||
chr1:197089871 | A | G | 6 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(3): Show |
7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.9984+59T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 25/27 | chr1 | 197089871 | |||||||
chr1:197090426 | C | T | 2 | a0003c0012t0002g0023 a0003c0012t0002g0068 |
3 | HG03130.hp1 HG03486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.9637-38G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 23/27 | chr1 | 197090426 | |||||||
chr1:197090639 | A | G | 1 | a0002c0002t0001g0153 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.9636+211T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 23/27 | chr1 | 197090639 | |||||||
chr1:197090734 | C | T | 5 | a0002c0002t0001g0007 a0002c0002t0001g0013 a0002c0002t0001g0144 others(2): Show |
10 | HG01106.hp2 HG01433.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.9636+116G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 23/27 | chr1 | 197090734 | |||||||
chr1:197090742 | T | C | 1 | a0001c0001t0001g0113 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.9636+108A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 23/27 | chr1 | 197090742 | |||||||
chr1:197090748 | G | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(152): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.9636+102C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 23/27 | chr1 | 197090748 | |||||||
chr1:197090762 | A | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(149): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.9636+88T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 23/27 | chr1 | 197090762 | |||||||
chr1:197090781 | AG | A | 3 | a0016c0025t0004g0024 a0017c0024t0004g0088 a0017c0024t0004g0089 |
4 | HG02896.hp1 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.9636+68delC | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 23/27 | chr1 | 197090781 | |||||||
chr1:197090798 | A | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(149): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.9636+52T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 23/27 | chr1 | 197090798 | |||||||
chr1:197091116 | T | C | 1 | a0001c0033t0002g0071 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.9445-75A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 22/27 | chr1 | 197091116 | |||||||
chr1:197091228 | CTG | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(161): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.9445-189_9445-188d others(4): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 22/27 | chr1 | 197091228 | |||||||
chr1:197091290 | C | T | 2 | a0001c0039t0001g0168 a0019c0019t0001g0033 |
3 | HG02280.hp2 HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.9445-249G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 22/27 | chr1 | 197091290 | |||||||
chr1:197091653 | A | T | 42 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0007 others(39): Show |
64 | HG00140.hp1 HG00423.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.9444+254T>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 22/27 | chr1 | 197091653 | |||||||
chr1:197091772 | T | C | 1 | a0001c0039t0001g0168 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.9444+135A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 22/27 | chr1 | 197091772 | |||||||
chr1:197091796 | C | T | 3 | a0016c0025t0004g0024 a0017c0024t0004g0088 a0017c0024t0004g0089 |
4 | HG02896.hp1 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.9444+111G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 22/27 | chr1 | 197091796 | |||||||
chr1:197091846 | T | C | 1 | a0001c0004t0002g0066 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.9444+61A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 22/27 | chr1 | 197091846 | |||||||
chr1:197092427 | A | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(161): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.9295-371T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 21/27 | chr1 | 197092427 | |||||||
chr1:197092610 | T | C | 2 | a0016c0025t0004g0024 a0017c0024t0004g0089 |
3 | HG02896.hp1 HG02897.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.9294+442A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 21/27 | chr1 | 197092610 | |||||||
chr1:197092989 | C | T | 1 | a0002c0002t0001g0167 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.9294+63G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 21/27 | chr1 | 197092989 | |||||||
chr1:197093293 | G | A | 1 | a0001c0008t0001g0097 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.9085-32C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 20/27 | chr1 | 197093293 | |||||||
chr1:197093344 | T | C | 3 | a0016c0025t0004g0024 a0017c0024t0004g0088 a0017c0024t0004g0089 |
4 | HG02896.hp1 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.9085-83A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 20/27 | chr1 | 197093344 | |||||||
chr1:197093362 | A | T | 3 | a0016c0025t0004g0024 a0017c0024t0004g0088 a0017c0024t0004g0089 |
4 | HG02896.hp1 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.9085-101T>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 20/27 | chr1 | 197093362 | |||||||
chr1:197093461 | C | T | 1 | a0001c0008t0001g0097 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.9085-200G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 20/27 | chr1 | 197093461 | |||||||
chr1:197093690 | A | T | 177 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(174): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.9084+394T>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 20/27 | chr1 | 197093690 | |||||||
chr1:197093749 | A | T | 3 | a0016c0025t0004g0024 a0017c0024t0004g0088 a0017c0024t0004g0089 |
4 | HG02896.hp1 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.9084+335T>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 20/27 | chr1 | 197093749 | |||||||
chr1:197093793 | T | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(149): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.9084+291A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 20/27 | chr1 | 197093793 | |||||||
chr1:197093953 | C | T | 2 | a0003c0012t0002g0023 a0003c0012t0002g0068 |
3 | HG03130.hp1 HG03486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.9084+131G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 20/27 | chr1 | 197093953 | |||||||
chr1:197094222 | C | T | 42 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0007 others(39): Show |
64 | HG00140.hp1 HG00423.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.8988-42G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 19/27 | chr1 | 197094222 | |||||||
chr1:197094476 | G | C | 3 | a0001c0008t0001g0094 a0001c0008t0001g0096 a0026c0043t0001g0095 |
3 | HG02630.hp1 HG02886.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.8988-296C>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 19/27 | chr1 | 197094476 | |||||||
chr1:197094617 | C | A | 6 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(3): Show |
7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.8988-437G>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 19/27 | chr1 | 197094617 | |||||||
chr1:197094711 | A | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(161): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.8988-531T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 19/27 | chr1 | 197094711 | |||||||
chr1:197095239 | C | G | 1 | a0001c0004t0002g0055 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.8987+759G>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 19/27 | chr1 | 197095239 | |||||||
chr1:197095366 | G | A | 104 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(101): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.8987+632C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 19/27 | chr1 | 197095366 | |||||||
chr1:197095454 | TA | T | 108 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(105): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.8987+543delT | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 19/27 | chr1 | 197095454 | |||||||
chr1:197095483 | G | C | 1 | a0001c0001t0001g0114 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.8987+515C>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 19/27 | chr1 | 197095483 | |||||||
chr1:197095496 | T | C | 1 | a0001c0004t0002g0079 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.8987+502A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 19/27 | chr1 | 197095496 | |||||||
chr1:197095696 | A | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(149): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.8987+302T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 19/27 | chr1 | 197095696 | |||||||
chr1:197095719 | G | A | 5 | a0001c0001t0001g0099 a0001c0001t0001g0105 a0001c0001t0001g0117 others(2): Show |
5 | NA18943.hp1 NA18975.hp1 NA19079.hp2 others(2): Show |
intron_variant | MODIFIER | c.8987+279C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 19/27 | chr1 | 197095719 | |||||||
chr1:197095767 | T | TGTA | 164 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(161): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.8987+230_8987+231i others(5): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 19/27 | chr1 | 197095767 | |||||||
chr1:197096211 | T | C | 1 | a0001c0039t0001g0168 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.8821-47A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/27 | chr1 | 197096211 | |||||||
chr1:197096449 | CAT | C | 2 | a0001c0039t0001g0168 a0019c0019t0001g0033 |
3 | HG02280.hp2 HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.8821-287_8821-286d others(4): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/27 | chr1 | 197096449 | |||||||
chr1:197096944 | T | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(149): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.8821-780A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/27 | chr1 | 197096944 | |||||||
chr1:197097149 | A | C | 1 | a0001c0003t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.8821-985T>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/27 | chr1 | 197097149 | |||||||
chr1:197097275 | C | T | 1 | a0001c0004t0002g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.8821-1111G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/27 | chr1 | 197097275 | |||||||
chr1:197097318 | G | A | 2 | a0001c0004t0002g0064 a0001c0004t0002g0065 |
2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.8821-1154C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/27 | chr1 | 197097318 | |||||||
chr1:197097594 | A | G | 6 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(3): Show |
7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.8821-1430T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/27 | chr1 | 197097594 | |||||||
chr1:197097614 | T | C | 5 | a0001c0004t0002g0018 a0001c0004t0002g0052 a0001c0004t0002g0053 others(2): Show |
6 | HG02451.hp2 HG02630.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.8821-1450A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/27 | chr1 | 197097614 | |||||||
chr1:197097618 | C | T | 2 | a0001c0039t0001g0168 a0019c0019t0001g0033 |
3 | HG02280.hp2 HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.8821-1454G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/27 | chr1 | 197097618 | |||||||
chr1:197097790 | G | C | 4 | a0001c0008t0001g0094 a0001c0008t0001g0096 a0001c0008t0001g0097 others(1): Show |
4 | HG02145.hp1 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.8821-1626C>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/27 | chr1 | 197097790 | |||||||
chr1:197097971 | G | C | 1 | a0001c0003t0001g0187 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.8821-1807C>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/27 | chr1 | 197097971 | |||||||
chr1:197097981 | T | G | 1 | a0001c0001t0001g0115 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.8821-1817A>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/27 | chr1 | 197097981 | |||||||
chr1:197098001 | A | AAT | 3 | a0001c0004t0002g0080 a0001c0004t0002g0081 a0001c0004t0002g0082 |
3 | HG01175.hp1 HG01891.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.8821-1839_8821-183 others(6): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/27 | chr1 | 197098001 | |||||||
chr1:197098001 | AAT | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(55): Show |
84 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.8821-1839_8821-183 others(6): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/27 | chr1 | 197098001 | |||||||
chr1:197098008 | A | T | 4 | a0001c0008t0001g0094 a0001c0008t0001g0096 a0001c0008t0001g0097 others(1): Show |
4 | HG02145.hp1 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.8821-1844T>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/27 | chr1 | 197098008 | |||||||
chr1:197098019 | C | G | 3 | a0006c0006t0005g0038 a0006c0006t0005g0212 a0006c0006t0005g0213 |
4 | HG02109.hp1 HG02145.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.8821-1855G>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/27 | chr1 | 197098019 | |||||||
chr1:197098173 | C | T | 1 | a0004c0005t0003g0042 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.8821-2009G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/27 | chr1 | 197098173 | |||||||
chr1:197098186 | G | GAT | 42 | a0001c0031t0002g0085 a0002c0002t0001g0003 a0002c0002t0001g0004 others(39): Show |
64 | HG00140.hp1 HG00423.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.8821-2024_8821-202 others(6): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/27 | chr1 | 197098186 | |||||||
chr1:197098186 | GAT | G | 6 | a0001c0001t0001g0009 a0001c0001t0001g0121 a0001c0001t0001g0123 others(3): Show |
8 | HG00423.hp2 HG00438.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.8821-2024_8821-202 others(6): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/27 | chr1 | 197098186 | |||||||
chr1:197098188 | T | G | 1 | a0001c0003t0001g0181 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.8821-2024A>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/27 | chr1 | 197098188 | |||||||
chr1:197098202 | T | TAA | 3 | a0016c0025t0004g0024 a0017c0024t0004g0088 a0017c0024t0004g0089 |
4 | HG02896.hp1 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.8821-2040_8821-203 others(6): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/27 | chr1 | 197098202 | |||||||
chr1:197098579 | A | T | 6 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(3): Show |
7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.8820+1852T>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/27 | chr1 | 197098579 | |||||||
chr1:197098667 | T | C | 1 | a0001c0031t0002g0085 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.8820+1764A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/27 | chr1 | 197098667 | |||||||
chr1:197098782 | T | C | 2 | a0001c0004t0002g0052 a0001c0004t0002g0053 |
2 | HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.8820+1649A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/27 | chr1 | 197098782 | |||||||
chr1:197098785 | G | A | 1 | a0001c0031t0002g0085 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.8820+1646C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/27 | chr1 | 197098785 | |||||||
chr1:197098919 | T | A | 1 | a0019c0019t0001g0033 | 2 | HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.8820+1512A>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/27 | chr1 | 197098919 | |||||||
chr1:197099070 | C | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(51): Show |
79 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.8820+1361G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/27 | chr1 | 197099070 | |||||||
chr1:197099145 | T | C | 1 | a0010c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.8820+1286A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/27 | chr1 | 197099145 | |||||||
chr1:197099225 | AT | A | 5 | a0001c0001t0001g0026 a0001c0003t0001g0190 a0001c0004t0002g0070 others(2): Show |
6 | HG02293.hp2 HG02723.hp1 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.8820+1205delA | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/27 | chr1 | 197099225 | |||||||
chr1:197099314 | A | T | 6 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(3): Show |
7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.8820+1117T>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/27 | chr1 | 197099314 | |||||||
chr1:197099500 | G | T | 4 | a0001c0008t0001g0094 a0001c0008t0001g0096 a0001c0008t0001g0097 others(1): Show |
4 | HG02145.hp1 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.8820+931C>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/27 | chr1 | 197099500 | |||||||
chr1:197099782 | TG | T | 3 | a0011c0013t0004g0046 a0011c0013t0004g0047 a0011c0013t0004g0048 |
3 | HG02818.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.8820+648delC | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/27 | chr1 | 197099782 | |||||||
chr1:197099874 | A | C | 1 | a0001c0003t0001g0200 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.8820+557T>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/27 | chr1 | 197099874 | |||||||
chr1:197100125 | A | G | 3 | a0011c0013t0004g0046 a0011c0013t0004g0047 a0011c0013t0004g0048 |
3 | HG02818.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.8820+306T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/27 | chr1 | 197100125 | |||||||
chr1:197100424 | G | C | 1 | a0027c0032t0002g0083 | 1 | HG03540.hp1 | splice_region_variant&intron_variant | LOW | c.8820+7C>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 18/27 | chr1 | 197100424 | |||||||
chr1:197105248 | C | T | 2 | a0001c0004t0002g0052 a0001c0004t0002g0053 |
2 | HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.4066-63G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197105248 | |||||||
chr1:197105365 | C | T | 1 | a0001c0003t0001g0193 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.4066-180G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197105365 | |||||||
chr1:197105407 | T | A | 2 | a0001c0031t0002g0085 a0001c0033t0002g0071 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.4066-222A>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197105407 | |||||||
chr1:197105525 | T | A | 1 | a0001c0001t0001g0115 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.4066-340A>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197105525 | |||||||
chr1:197105621 | A | G | 2 | a0002c0002t0001g0139 a0002c0002t0001g0170 |
2 | NA18980.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.4066-436T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197105621 | |||||||
chr1:197105825 | T | G | 4 | a0001c0001t0001g0091 a0001c0001t0001g0125 a0012c0014t0001g0027 others(1): Show |
5 | NA18952.hp2 NA18953.hp1 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.4066-640A>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197105825 | |||||||
chr1:197105942 | G | C | 3 | a0006c0006t0005g0038 a0006c0006t0005g0212 a0006c0006t0005g0213 |
4 | HG02109.hp1 HG02145.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.4066-757C>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197105942 | |||||||
chr1:197106072 | T | G | 1 | a0001c0033t0002g0071 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4066-887A>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197106072 | |||||||
chr1:197106197 | G | C | 3 | a0016c0025t0004g0024 a0017c0024t0004g0088 a0017c0024t0004g0089 |
4 | HG02896.hp1 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.4066-1012C>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197106197 | |||||||
chr1:197106274 | T | C | 1 | a0001c0001t0001g0116 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.4066-1089A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197106274 | |||||||
chr1:197106454 | T | A | 1 | a0001c0004t0002g0081 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.4066-1269A>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197106454 | |||||||
chr1:197106486 | T | C | 2 | a0015c0017t0001g0183 a0015c0017t0001g0185 |
2 | HG02056.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.4066-1301A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197106486 | |||||||
chr1:197106492 | T | TA | 3 | a0016c0025t0004g0024 a0017c0024t0004g0088 a0017c0024t0004g0089 |
4 | HG02896.hp1 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.4066-1308dupT | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197106492 | |||||||
chr1:197106679 | C | A | 2 | a0001c0039t0001g0168 a0019c0019t0001g0033 |
3 | HG02280.hp2 HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.4066-1494G>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197106679 | |||||||
chr1:197106978 | C | A | 7 | a0003c0007t0002g0022 a0003c0007t0002g0067 a0003c0007t0002g0069 others(4): Show |
10 | HG02258.hp1 HG02622.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.4066-1793G>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197106978 | |||||||
chr1:197107029 | C | T | 1 | a0001c0004t0002g0049 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4066-1844G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197107029 | |||||||
chr1:197107064 | C | T | 104 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(101): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.4066-1879G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197107064 | |||||||
chr1:197107232 | G | C | 1 | a0001c0003t0001g0186 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.4066-2047C>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197107232 | |||||||
chr1:197107272 | C | T | 1 | a0019c0019t0001g0033 | 2 | HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.4066-2087G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197107272 | |||||||
chr1:197107634 | C | T | 1 | a0026c0043t0001g0095 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4066-2449G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197107634 | |||||||
chr1:197107649 | T | C | 8 | a0002c0002t0001g0004 a0002c0002t0001g0012 a0002c0002t0001g0138 others(5): Show |
15 | HG02056.hp2 HG02071.hp2 HG02165.hp1 others(12): Show |
intron_variant | MODIFIER | c.4066-2464A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197107649 | |||||||
chr1:197107748 | A | G | 2 | a0001c0031t0002g0085 a0001c0033t0002g0071 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.4066-2563T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197107748 | |||||||
chr1:197107841 | T | C | 1 | a0002c0002t0001g0138 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.4066-2656A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197107841 | |||||||
chr1:197107928 | T | C | 1 | a0011c0013t0004g0046 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4066-2743A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197107928 | |||||||
chr1:197108217 | G | GA | 107 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(104): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.4066-3033dupT | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197108217 | |||||||
chr1:197108261 | T | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(105): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.4066-3076A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197108261 | |||||||
chr1:197108386 | T | C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(51): Show |
79 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.4066-3201A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197108386 | |||||||
chr1:197108470 | A | G | 1 | a0001c0004t0002g0070 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4066-3285T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197108470 | |||||||
chr1:197108521 | A | G | 1 | a0001c0039t0001g0168 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4066-3336T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197108521 | |||||||
chr1:197108530 | C | T | 4 | a0001c0008t0001g0094 a0001c0008t0001g0096 a0001c0008t0001g0097 others(1): Show |
4 | HG02145.hp1 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.4066-3345G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197108530 | |||||||
chr1:197108563 | T | C | 3 | a0011c0013t0004g0046 a0011c0013t0004g0047 a0011c0013t0004g0048 |
3 | HG02818.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.4066-3378A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197108563 | |||||||
chr1:197108732 | AG | A | 6 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(3): Show |
7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.4066-3548delC | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197108732 | |||||||
chr1:197108832 | G | T | 1 | a0019c0019t0001g0033 | 2 | HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.4066-3647C>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197108832 | |||||||
chr1:197108935 | T | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(161): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.4066-3750A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197108935 | |||||||
chr1:197108945 | T | C | 1 | a0001c0001t0001g0119 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.4066-3760A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197108945 | |||||||
chr1:197108971 | C | CA | 24 | a0001c0001t0001g0028 a0001c0001t0001g0117 a0001c0001t0001g0119 others(21): Show |
27 | HG01192.hp2 HG01891.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.4066-3787dupT | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197108971 | |||||||
chr1:197108971 | CA | C | 41 | a0001c0001t0001g0109 a0001c0001t0001g0123 a0001c0003t0001g0197 others(38): Show |
63 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(60): Show |
intron_variant | MODIFIER | c.4066-3787delT | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197108971 | |||||||
chr1:197108971 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0135 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.4066-3797_4066-378 others(15): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197108971 | |||||||
chr1:197108972 | A | C | 3 | a0016c0025t0004g0024 a0017c0024t0004g0088 a0017c0024t0004g0089 |
4 | HG02896.hp1 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.4066-3787T>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197108972 | |||||||
chr1:197109101 | T | C | 1 | a0001c0004t0002g0079 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.4066-3916A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197109101 | |||||||
chr1:197109155 | AAGAT | A | 2 | a0001c0039t0001g0168 a0019c0019t0001g0033 |
3 | HG02280.hp2 HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.4066-3974_4066-397 others(8): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197109155 | |||||||
chr1:197109206 | C | CAA | 164 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(161): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.4066-4022_4066-402 others(6): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197109206 | |||||||
chr1:197109270 | T | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(149): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.4066-4085A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197109270 | |||||||
chr1:197109277 | C | G | 4 | a0001c0008t0001g0094 a0001c0008t0001g0096 a0001c0008t0001g0097 others(1): Show |
4 | HG02145.hp1 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.4066-4092G>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197109277 | |||||||
chr1:197109412 | C | A | 1 | a0001c0004t0002g0062 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4066-4227G>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197109412 | |||||||
chr1:197109457 | A | G | 1 | a0019c0019t0001g0033 | 2 | HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.4066-4272T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197109457 | |||||||
chr1:197109466 | A | T | 1 | a0001c0001t0001g0108 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.4066-4281T>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197109466 | |||||||
chr1:197109757 | G | A | 5 | a0001c0004t0002g0072 a0001c0004t0002g0073 a0001c0004t0002g0074 others(2): Show |
5 | HG02055.hp1 HG02970.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.4066-4572C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197109757 | |||||||
chr1:197109782 | T | A | 3 | a0001c0004t0002g0070 a0001c0004t0002g0076 a0001c0004t0002g0078 |
3 | HG02451.hp1 HG02723.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.4066-4597A>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197109782 | |||||||
chr1:197109836 | T | G | 2 | a0001c0003t0001g0181 a0001c0003t0001g0196 |
2 | HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.4066-4651A>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197109836 | |||||||
chr1:197110000 | T | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(161): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.4066-4815A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197110000 | |||||||
chr1:197110046 | A | C | 1 | a0001c0004t0002g0072 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4066-4861T>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197110046 | |||||||
chr1:197110339 | T | C | 9 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(6): Show |
10 | HG02523.hp2 HG02818.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.4066-5154A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197110339 | |||||||
chr1:197110447 | G | T | 1 | a0001c0031t0002g0085 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.4066-5262C>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197110447 | |||||||
chr1:197110516 | G | T | 6 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(3): Show |
7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.4066-5331C>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197110516 | |||||||
chr1:197110541 | C | A | 164 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(161): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.4066-5356G>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197110541 | |||||||
chr1:197110599 | G | C | 3 | a0001c0001t0001g0121 a0001c0004t0002g0077 a0001c0004t0002g0086 |
3 | HG00423.hp2 HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4066-5414C>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197110599 | |||||||
chr1:197110695 | A | G | 2 | a0001c0039t0001g0168 a0019c0019t0001g0033 |
3 | HG02280.hp2 HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.4066-5510T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197110695 | |||||||
chr1:197110906 | G | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(161): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.4066-5721C>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197110906 | |||||||
chr1:197111073 | A | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(174): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.4066-5888T>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197111073 | |||||||
chr1:197111219 | A | T | 9 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(6): Show |
10 | HG02523.hp2 HG02818.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.4066-6034T>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197111219 | |||||||
chr1:197111330 | A | C | 6 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(3): Show |
7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.4066-6145T>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197111330 | |||||||
chr1:197111572 | C | T | 1 | a0001c0003t0001g0171 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.4065+6217G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197111572 | |||||||
chr1:197111637 | G | A | 4 | a0002c0002t0001g0157 a0006c0006t0005g0038 a0006c0006t0005g0212 others(1): Show |
5 | HG02109.hp1 HG02145.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.4065+6152C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197111637 | |||||||
chr1:197111845 | C | T | 6 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(3): Show |
7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.4065+5944G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197111845 | |||||||
chr1:197111907 | T | C | 1 | a0001c0003t0001g0194 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.4065+5882A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197111907 | |||||||
chr1:197112058 | G | A | 3 | a0006c0006t0005g0038 a0006c0006t0005g0212 a0006c0006t0005g0213 |
4 | HG02109.hp1 HG02145.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.4065+5731C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197112058 | |||||||
chr1:197112112 | T | C | 1 | a0001c0033t0002g0071 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4065+5677A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197112112 | |||||||
chr1:197112149 | A | G | 3 | a0006c0006t0005g0038 a0006c0006t0005g0212 a0006c0006t0005g0213 |
4 | HG02109.hp1 HG02145.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.4065+5640T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197112149 | |||||||
chr1:197112198 | G | A | 1 | a0001c0031t0002g0085 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.4065+5591C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197112198 | |||||||
chr1:197112254 | G | A | 4 | a0001c0039t0001g0168 a0016c0025t0004g0024 a0017c0024t0004g0088 others(1): Show |
5 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4065+5535C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197112254 | |||||||
chr1:197112266 | C | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(52): Show |
80 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.4065+5523G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197112266 | |||||||
chr1:197112552 | G | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(52): Show |
80 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.4065+5237C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197112552 | |||||||
chr1:197112734 | C | A | 1 | a0001c0003t0001g0206 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.4065+5055G>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197112734 | |||||||
chr1:197112816 | T | G | 1 | a0027c0032t0002g0083 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4065+4973A>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197112816 | |||||||
chr1:197112821 | C | T | 1 | a0002c0002t0001g0031 | 2 | NA18978.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.4065+4968G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197112821 | |||||||
chr1:197112912 | T | G | 1 | a0006c0006t0005g0212 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4065+4877A>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197112912 | |||||||
chr1:197113004 | T | C | 3 | a0011c0013t0004g0046 a0011c0013t0004g0047 a0011c0013t0004g0048 |
3 | HG02818.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.4065+4785A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197113004 | |||||||
chr1:197113046 | A | C | 1 | a0001c0001t0001g0120 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4065+4743T>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197113046 | |||||||
chr1:197113218 | C | T | 1 | a0002c0002t0001g0169 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.4065+4571G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197113218 | |||||||
chr1:197113503 | T | A | 1 | a0028c0030t0002g0056 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4065+4286A>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197113503 | |||||||
chr1:197113684 | A | G | 2 | a0002c0002t0001g0152 a0002c0002t0001g0165 |
2 | HG01069.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.4065+4105T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197113684 | |||||||
chr1:197113760 | G | A | 1 | a0001c0022t0001g0034 | 2 | HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.4065+4029C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197113760 | |||||||
chr1:197114008 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4065+3781C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197114008 | |||||||
chr1:197114009 | T | C | 2 | a0001c0004t0002g0049 a0001c0004t0002g0050 |
2 | HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.4065+3780A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197114009 | |||||||
chr1:197114029 | T | TAGTGTCT others(5): Show |
163 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(160): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.4065+3759_4065+376 others(16): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197114029 | |||||||
chr1:197114066 | T | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(157): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.4065+3723A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197114066 | |||||||
chr1:197114099 | A | G | 3 | a0001c0004t0002g0080 a0001c0004t0002g0081 a0001c0004t0002g0082 |
3 | HG01175.hp1 HG01891.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.4065+3690T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197114099 | |||||||
chr1:197114146 | T | C | 1 | a0001c0003t0001g0180 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.4065+3643A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197114146 | |||||||
chr1:197114199 | G | A | 164 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(161): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.4065+3590C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197114199 | |||||||
chr1:197114382 | A | T | 3 | a0011c0013t0004g0046 a0011c0013t0004g0047 a0011c0013t0004g0048 |
3 | HG02818.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.4065+3407T>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197114382 | |||||||
chr1:197114477 | C | T | 3 | a0002c0002t0001g0004 a0002c0002t0001g0012 a0002c0002t0001g0142 |
10 | HG02056.hp2 NA18940.hp1 NA18944.hp2 others(7): Show |
intron_variant | MODIFIER | c.4065+3312G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197114477 | |||||||
chr1:197114532 | C | T | 1 | a0001c0003t0001g0186 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.4065+3257G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197114532 | |||||||
chr1:197114561 | A | G | 1 | a0001c0001t0001g0107 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.4065+3228T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197114561 | |||||||
chr1:197114780 | G | A | 9 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(6): Show |
10 | HG02523.hp2 HG02818.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.4065+3009C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197114780 | |||||||
chr1:197114809 | C | T | 1 | a0019c0019t0001g0033 | 2 | HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.4065+2980G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197114809 | |||||||
chr1:197114960 | A | G | 9 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(6): Show |
10 | HG02523.hp2 HG02818.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.4065+2829T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197114960 | |||||||
chr1:197115013 | C | T | 152 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(149): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.4065+2776G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197115013 | |||||||
chr1:197115088 | G | T | 1 | a0001c0008t0001g0128 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4065+2701C>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197115088 | |||||||
chr1:197115105 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.4065+2684A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197115105 | |||||||
chr1:197115119 | C | T | 2 | a0001c0031t0002g0085 a0001c0033t0002g0071 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.4065+2670G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197115119 | |||||||
chr1:197115270 | G | A | 9 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(6): Show |
10 | HG02523.hp2 HG02818.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.4065+2519C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197115270 | |||||||
chr1:197115276 | C | T | 2 | a0003c0007t0002g0067 a0003c0007t0002g0069 |
2 | HG02809.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.4065+2513G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197115276 | |||||||
chr1:197115333 | T | G | 42 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0007 others(39): Show |
64 | HG00140.hp1 HG00423.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.4065+2456A>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197115333 | |||||||
chr1:197115398 | A | G | 6 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(3): Show |
7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.4065+2391T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197115398 | |||||||
chr1:197115727 | C | G | 42 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0007 others(39): Show |
64 | HG00140.hp1 HG00423.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.4065+2062G>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197115727 | |||||||
chr1:197115754 | G | C | 1 | a0001c0003t0001g0195 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.4065+2035C>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197115754 | |||||||
chr1:197115886 | A | C | 2 | a0002c0002t0001g0151 a0002c0002t0001g0164 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.4065+1903T>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197115886 | |||||||
chr1:197115898 | C | A | 1 | a0022c0027t0001g0137 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.4065+1891G>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197115898 | |||||||
chr1:197116299 | G | C | 1 | a0001c0031t0002g0085 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.4065+1490C>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197116299 | |||||||
chr1:197116410 | T | C | 1 | a0001c0004t0002g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4065+1379A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197116410 | |||||||
chr1:197116425 | A | T | 2 | a0002c0002t0001g0139 a0002c0002t0001g0170 |
2 | NA18980.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.4065+1364T>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197116425 | |||||||
chr1:197116444 | A | C | 4 | a0001c0003t0001g0014 a0001c0003t0001g0171 a0001c0003t0001g0172 others(1): Show |
6 | NA18947.hp1 NA18965.hp1 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.4065+1345T>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197116444 | |||||||
chr1:197116523 | T | C | 7 | a0003c0007t0002g0022 a0003c0007t0002g0067 a0003c0007t0002g0069 others(4): Show |
10 | HG02258.hp1 HG02622.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.4065+1266A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197116523 | |||||||
chr1:197116546 | T | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(149): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.4065+1243A>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197116546 | |||||||
chr1:197116680 | G | A | 1 | a0001c0031t0002g0085 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.4065+1109C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197116680 | |||||||
chr1:197116900 | T | G | 1 | a0001c0001t0001g0122 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.4065+889A>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197116900 | |||||||
chr1:197117000 | T | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(52): Show |
80 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.4065+789A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197117000 | |||||||
chr1:197117041 | T | C | 2 | a0001c0003t0001g0181 a0001c0003t0001g0196 |
2 | HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.4065+748A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197117041 | |||||||
chr1:197117139 | T | C | 2 | a0001c0003t0001g0036 a0001c0003t0001g0184 |
3 | HG02818.hp1 HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.4065+650A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197117139 | |||||||
chr1:197117265 | TA | T | 6 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(3): Show |
7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.4065+523delT | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197117265 | |||||||
chr1:197117473 | G | C | 3 | a0011c0013t0004g0046 a0011c0013t0004g0047 a0011c0013t0004g0048 |
3 | HG02818.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.4065+316C>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197117473 | |||||||
chr1:197117539 | C | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(152): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.4065+250G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197117539 | |||||||
chr1:197117716 | T | C | 3 | a0011c0013t0004g0046 a0011c0013t0004g0047 a0011c0013t0004g0048 |
3 | HG02818.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.4065+73A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 17/27 | chr1 | 197117716 | |||||||
chr1:197118007 | G | A | 2 | a0001c0003t0001g0197 a0001c0003t0001g0198 |
2 | HG00738.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.3871-24C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 16/27 | chr1 | 197118007 | |||||||
chr1:197118037 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3871-54A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 16/27 | chr1 | 197118037 | |||||||
chr1:197118155 | C | T | 2 | a0011c0013t0004g0046 a0011c0013t0004g0047 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.3871-172G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 16/27 | chr1 | 197118155 | |||||||
chr1:197118156 | G | A | 1 | a0001c0039t0001g0168 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3871-173C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 16/27 | chr1 | 197118156 | |||||||
chr1:197118234 | T | C | 3 | a0011c0013t0004g0046 a0011c0013t0004g0047 a0011c0013t0004g0048 |
3 | HG02818.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3871-251A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 16/27 | chr1 | 197118234 | |||||||
chr1:197118355 | T | C | 1 | a0002c0002t0001g0162 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3871-372A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 16/27 | chr1 | 197118355 | |||||||
chr1:197118453 | T | C | 1 | a0001c0008t0001g0097 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3871-470A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 16/27 | chr1 | 197118453 | |||||||
chr1:197118565 | T | C | 1 | a0001c0031t0002g0085 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3871-582A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 16/27 | chr1 | 197118565 | |||||||
chr1:197118641 | T | C | 9 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(6): Show |
10 | HG02523.hp2 HG02818.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.3871-658A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 16/27 | chr1 | 197118641 | |||||||
chr1:197118966 | G | A | 1 | a0002c0002t0001g0142 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.3871-983C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 16/27 | chr1 | 197118966 | |||||||
chr1:197119088 | T | C | 42 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0007 others(39): Show |
64 | HG00140.hp1 HG00423.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.3871-1105A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 16/27 | chr1 | 197119088 | |||||||
chr1:197119173 | G | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(149): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.3871-1190C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 16/27 | chr1 | 197119173 | |||||||
chr1:197119326 | A | C | 9 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(6): Show |
10 | HG02523.hp2 HG02818.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.3871-1343T>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 16/27 | chr1 | 197119326 | |||||||
chr1:197119619 | G | GCC | 164 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(161): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.3871-1637_3871-163 others(6): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 16/27 | chr1 | 197119619 | |||||||
chr1:197119808 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.3871-1825C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 16/27 | chr1 | 197119808 | |||||||
chr1:197119863 | C | T | 7 | a0001c0003t0001g0005 a0001c0003t0001g0186 a0001c0003t0001g0187 others(4): Show |
11 | HG00140.hp2 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.3871-1880G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 16/27 | chr1 | 197119863 | |||||||
chr1:197119897 | C | G | 4 | a0001c0008t0001g0094 a0001c0008t0001g0096 a0001c0008t0001g0097 others(1): Show |
4 | HG02145.hp1 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.3871-1914G>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 16/27 | chr1 | 197119897 | |||||||
chr1:197120167 | T | G | 1 | a0001c0034t0001g0174 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3870+1748A>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 16/27 | chr1 | 197120167 | |||||||
chr1:197120218 | TGAGAAAA others(34): Show |
T | 1 | a0001c0039t0001g0168 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3870+1656_3870+169 others(45): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 16/27 | chr1 | 197120218 | |||||||
chr1:197120529 | C | T | 2 | a0015c0017t0001g0183 a0015c0017t0001g0185 |
2 | HG02056.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.3870+1386G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 16/27 | chr1 | 197120529 | |||||||
chr1:197120678 | G | A | 1 | a0001c0003t0001g0182 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.3870+1237C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 16/27 | chr1 | 197120678 | |||||||
chr1:197120710 | T | C | 8 | a0003c0007t0002g0022 a0003c0007t0002g0067 a0003c0007t0002g0069 others(5): Show |
11 | HG02258.hp1 HG02622.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.3870+1205A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 16/27 | chr1 | 197120710 | |||||||
chr1:197120884 | A | C | 3 | a0011c0013t0004g0046 a0011c0013t0004g0047 a0011c0013t0004g0048 |
3 | HG02818.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3870+1031T>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 16/27 | chr1 | 197120884 | |||||||
chr1:197120901 | G | C | 6 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(3): Show |
7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.3870+1014C>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 16/27 | chr1 | 197120901 | |||||||
chr1:197120911 | G | C | 1 | a0007c0015t0001g0093 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3870+1004C>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 16/27 | chr1 | 197120911 | |||||||
chr1:197121209 | A | C | 1 | a0001c0003t0001g0184 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3870+706T>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 16/27 | chr1 | 197121209 | |||||||
chr1:197121559 | T | C | 1 | a0018c0021t0001g0029 | 2 | HG03017.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.3870+356A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 16/27 | chr1 | 197121559 | |||||||
chr1:197121621 | C | T | 3 | a0011c0013t0004g0046 a0011c0013t0004g0047 a0011c0013t0004g0048 |
3 | HG02818.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3870+294G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 16/27 | chr1 | 197121621 | |||||||
chr1:197121625 | G | A | 1 | a0001c0001t0001g0134 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.3870+290C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 16/27 | chr1 | 197121625 | |||||||
chr1:197121890 | T | C | 1 | a0001c0039t0001g0168 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3870+25A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 16/27 | chr1 | 197121890 | |||||||
chr1:197122053 | A | C | 1 | a0001c0003t0001g0206 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.3742-10T>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 15/27 | chr1 | 197122053 | |||||||
chr1:197122120 | A | G | 1 | a0001c0033t0002g0071 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3741+39T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 15/27 | chr1 | 197122120 | |||||||
chr1:197122305 | T | C | 1 | a0001c0003t0001g0037 | 2 | HG03098.hp2 HG03130.hp2 |
splice_region_variant&intron_variant | LOW | c.3599-4A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 14/27 | chr1 | 197122305 | |||||||
chr1:197122351 | T | C | 1 | a0002c0002t0001g0158 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3598+37A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 14/27 | chr1 | 197122351 | |||||||
chr1:197122609 | C | A | 3 | a0006c0006t0005g0038 a0006c0006t0005g0212 a0006c0006t0005g0213 |
4 | HG02109.hp1 HG02145.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.3391-14G>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 13/27 | chr1 | 197122609 | |||||||
chr1:197122626 | C | T | 1 | a0001c0008t0001g0094 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3391-31G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 13/27 | chr1 | 197122626 | |||||||
chr1:197122656 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3391-61A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 13/27 | chr1 | 197122656 | |||||||
chr1:197122678 | T | C | 42 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0007 others(39): Show |
64 | HG00140.hp1 HG00423.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.3391-83A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 13/27 | chr1 | 197122678 | |||||||
chr1:197122893 | T | C | 1 | a0008c0016t0001g0011 | 3 | HG02280.hp1 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3391-298A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 13/27 | chr1 | 197122893 | |||||||
chr1:197122955 | T | A | 1 | a0027c0032t0002g0083 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3391-360A>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 13/27 | chr1 | 197122955 | |||||||
chr1:197122976 | A | G | 2 | a0002c0002t0001g0136 a0002c0002t0001g0147 |
2 | HG00738.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.3391-381T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 13/27 | chr1 | 197122976 | |||||||
chr1:197123116 | T | C | 2 | a0001c0039t0001g0168 a0019c0019t0001g0033 |
3 | HG02280.hp2 HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3391-521A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 13/27 | chr1 | 197123116 | |||||||
chr1:197123143 | C | T | 1 | a0006c0006t0005g0213 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3391-548G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 13/27 | chr1 | 197123143 | |||||||
chr1:197123303 | T | C | 1 | a0001c0022t0001g0034 | 2 | HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3391-708A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 13/27 | chr1 | 197123303 | |||||||
chr1:197123892 | T | C | 9 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(6): Show |
10 | HG02523.hp2 HG02818.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.3390+218A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 13/27 | chr1 | 197123892 | |||||||
chr1:197123948 | T | C | 3 | a0016c0025t0004g0024 a0017c0024t0004g0088 a0017c0024t0004g0089 |
4 | HG02896.hp1 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.3390+162A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 13/27 | chr1 | 197123948 | |||||||
chr1:197123968 | A | T | 189 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(186): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.3390+142T>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 13/27 | chr1 | 197123968 | |||||||
chr1:197124588 | G | A | 1 | a0002c0002t0001g0159 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.3169-257C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 12/27 | chr1 | 197124588 | |||||||
chr1:197124702 | T | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(148): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.3168+168A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 12/27 | chr1 | 197124702 | |||||||
chr1:197124992 | G | C | 6 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(3): Show |
7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.3083-37C>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 11/27 | chr1 | 197124992 | |||||||
chr1:197125228 | A | G | 1 | a0015c0017t0001g0183 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2937-37T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 10/27 | chr1 | 197125228 | |||||||
chr1:197125362 | A | G | 3 | a0011c0013t0004g0046 a0011c0013t0004g0047 a0011c0013t0004g0048 |
3 | HG02818.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2937-171T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 10/27 | chr1 | 197125362 | |||||||
chr1:197125737 | T | C | 1 | a0002c0002t0001g0147 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2937-546A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 10/27 | chr1 | 197125737 | |||||||
chr1:197125814 | A | G | 9 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(6): Show |
10 | HG02523.hp2 HG02818.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.2937-623T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 10/27 | chr1 | 197125814 | |||||||
chr1:197125831 | T | A | 42 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0007 others(39): Show |
64 | HG00140.hp1 HG00423.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.2937-640A>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 10/27 | chr1 | 197125831 | |||||||
chr1:197125851 | G | A | 1 | a0001c0004t0002g0021 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2937-660C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 10/27 | chr1 | 197125851 | |||||||
chr1:197126167 | G | A | 1 | a0001c0004t0002g0075 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2937-976C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 10/27 | chr1 | 197126167 | |||||||
chr1:197126266 | C | A | 3 | a0016c0025t0004g0024 a0017c0024t0004g0088 a0017c0024t0004g0089 |
4 | HG02896.hp1 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2937-1075G>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 10/27 | chr1 | 197126266 | |||||||
chr1:197126356 | G | A | 2 | a0002c0002t0001g0160 a0002c0002t0001g0161 |
2 | HG00423.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.2937-1165C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 10/27 | chr1 | 197126356 | |||||||
chr1:197126427 | G | A | 1 | a0001c0003t0001g0199 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2937-1236C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 10/27 | chr1 | 197126427 | |||||||
chr1:197126439 | C | CA | 8 | a0001c0004t0002g0018 a0001c0004t0002g0049 a0001c0004t0002g0057 others(5): Show |
10 | HG01346.hp1 HG02451.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.2937-1249dupT | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 10/27 | chr1 | 197126439 | |||||||
chr1:197126454 | AAAAAAAA others(7): Show |
A | 1 | a0019c0019t0001g0033 | 2 | HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2937-1277_2937-126 others(18): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 10/27 | chr1 | 197126454 | |||||||
chr1:197126462 | AAAAAAG | A | 94 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(91): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.2937-1277_2937-127 others(10): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 10/27 | chr1 | 197126462 | |||||||
chr1:197126463 | AAAAAG | A | 10 | a0001c0001t0001g0112 a0001c0001t0001g0116 a0001c0003t0001g0036 others(7): Show |
11 | HG01099.hp1 HG01175.hp2 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.2937-1277_2937-127 others(9): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 10/27 | chr1 | 197126463 | |||||||
chr1:197126464 | AAAAG | A | 39 | a0001c0008t0001g0094 a0002c0002t0001g0003 a0002c0002t0001g0004 others(36): Show |
59 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.2937-1277_2937-127 others(8): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 10/27 | chr1 | 197126464 | |||||||
chr1:197126465 | AAAG | A | 8 | a0001c0008t0001g0096 a0001c0008t0001g0097 a0001c0039t0001g0168 others(5): Show |
8 | HG00423.hp1 HG02145.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.2937-1277_2937-127 others(7): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 10/27 | chr1 | 197126465 | |||||||
chr1:197126467 | AG | A | 22 | a0001c0004t0002g0019 a0001c0004t0002g0021 a0001c0033t0002g0071 others(19): Show |
26 | HG02109.hp1 HG02109.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.2937-1277delC | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 10/27 | chr1 | 197126467 | |||||||
chr1:197126468 | G | A | 41 | a0001c0004t0002g0018 a0001c0004t0002g0019 a0001c0004t0002g0049 others(38): Show |
45 | HG01069.hp1 HG01071.hp2 HG01175.hp1 others(42): Show |
intron_variant | MODIFIER | c.2937-1277C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 10/27 | chr1 | 197126468 | |||||||
chr1:197126585 | G | A | 3 | a0011c0013t0004g0046 a0011c0013t0004g0047 a0011c0013t0004g0048 |
3 | HG02818.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2937-1394C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 10/27 | chr1 | 197126585 | |||||||
chr1:197126710 | G | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(104): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.2937-1519C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 10/27 | chr1 | 197126710 | |||||||
chr1:197127005 | T | C | 58 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(55): Show |
86 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.2936+1485A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 10/27 | chr1 | 197127005 | |||||||
chr1:197127128 | G | A | 1 | a0001c0033t0002g0071 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2936+1362C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 10/27 | chr1 | 197127128 | |||||||
chr1:197127350 | T | G | 160 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(157): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.2936+1140A>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 10/27 | chr1 | 197127350 | |||||||
chr1:197127385 | C | T | 1 | a0027c0032t0002g0083 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2936+1105G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 10/27 | chr1 | 197127385 | |||||||
chr1:197127402 | C | T | 1 | a0001c0039t0001g0168 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2936+1088G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 10/27 | chr1 | 197127402 | |||||||
chr1:197127431 | T | G | 9 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(6): Show |
10 | HG02523.hp2 HG02818.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.2936+1059A>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 10/27 | chr1 | 197127431 | |||||||
chr1:197127469 | C | A | 1 | a0020c0020t0001g0102 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2936+1021G>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 10/27 | chr1 | 197127469 | |||||||
chr1:197127572 | C | G | 3 | a0011c0013t0004g0046 a0011c0013t0004g0047 a0011c0013t0004g0048 |
3 | HG02818.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2936+918G>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 10/27 | chr1 | 197127572 | |||||||
chr1:197127590 | G | A | 163 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(160): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.2936+900C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 10/27 | chr1 | 197127590 | |||||||
chr1:197127614 | C | T | 1 | a0019c0019t0001g0033 | 2 | HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2936+876G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 10/27 | chr1 | 197127614 | |||||||
chr1:197127712 | T | C | 3 | a0016c0025t0004g0024 a0017c0024t0004g0088 a0017c0024t0004g0089 |
4 | HG02896.hp1 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2936+778A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 10/27 | chr1 | 197127712 | |||||||
chr1:197127823 | T | C | 1 | a0001c0004t0002g0078 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2936+667A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 10/27 | chr1 | 197127823 | |||||||
chr1:197127956 | A | G | 9 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(6): Show |
10 | HG02523.hp2 HG02818.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.2936+534T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 10/27 | chr1 | 197127956 | |||||||
chr1:197127992 | CG | C | 6 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(3): Show |
7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.2936+497delC | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 10/27 | chr1 | 197127992 | |||||||
chr1:197128082 | G | A | 1 | a0001c0003t0001g0037 | 2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2936+408C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 10/27 | chr1 | 197128082 | |||||||
chr1:197128263 | T | G | 1 | a0001c0003t0001g0200 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2936+227A>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 10/27 | chr1 | 197128263 | |||||||
chr1:197128293 | G | A | 6 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(3): Show |
7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.2936+197C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 10/27 | chr1 | 197128293 | |||||||
chr1:197128343 | G | GA | 137 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(134): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.2936+146dupT | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 10/27 | chr1 | 197128343 | |||||||
chr1:197128343 | G | GAA | 12 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0003t0001g0172 others(9): Show |
19 | HG01106.hp2 HG01433.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.2936+145_2936+146d others(4): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 10/27 | chr1 | 197128343 | |||||||
chr1:197128355 | A | C | 6 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(3): Show |
7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.2936+135T>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 10/27 | chr1 | 197128355 | |||||||
chr1:197128761 | AAAAT | A | 42 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0007 others(39): Show |
64 | HG00140.hp1 HG00423.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.2761-100_2761-97de others(5): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 9/27 | chr1 | 197128761 | |||||||
chr1:197128804 | C | T | 6 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(3): Show |
7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.2761-139G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 9/27 | chr1 | 197128804 | |||||||
chr1:197128898 | A | G | 6 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(3): Show |
7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.2761-233T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 9/27 | chr1 | 197128898 | |||||||
chr1:197129013 | G | C | 180 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(177): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.2760+174C>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 9/27 | chr1 | 197129013 | |||||||
chr1:197129142 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2760+45C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 9/27 | chr1 | 197129142 | |||||||
chr1:197129378 | A | C | 4 | a0001c0008t0001g0094 a0001c0008t0001g0096 a0001c0008t0001g0097 others(1): Show |
4 | HG02145.hp1 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2630-61T>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 8/27 | chr1 | 197129378 | |||||||
chr1:197129381 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2630-64T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 8/27 | chr1 | 197129381 | |||||||
chr1:197129385 | T | C | 1 | a0001c0004t0002g0079 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2630-68A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 8/27 | chr1 | 197129385 | |||||||
chr1:197129700 | G | T | 1 | a0001c0001t0001g0103 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2629+215C>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 8/27 | chr1 | 197129700 | |||||||
chr1:197129741 | T | C | 1 | a0001c0004t0002g0082 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2629+174A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 8/27 | chr1 | 197129741 | |||||||
chr1:197129787 | T | G | 1 | a0001c0001t0001g0127 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2629+128A>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 8/27 | chr1 | 197129787 | |||||||
chr1:197129886 | G | A | 1 | a0002c0002t0001g0136 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2629+29C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 8/27 | chr1 | 197129886 | |||||||
chr1:197130187 | T | G | 3 | a0016c0025t0004g0024 a0017c0024t0004g0088 a0017c0024t0004g0089 |
4 | HG02896.hp1 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2488-131A>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 7/27 | chr1 | 197130187 | |||||||
chr1:197130334 | A | T | 1 | a0019c0019t0001g0033 | 2 | HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2488-278T>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 7/27 | chr1 | 197130334 | |||||||
chr1:197130355 | A | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(149): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.2488-299T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 7/27 | chr1 | 197130355 | |||||||
chr1:197130434 | T | C | 42 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0007 others(39): Show |
64 | HG00140.hp1 HG00423.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.2488-378A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 7/27 | chr1 | 197130434 | |||||||
chr1:197130576 | G | A | 6 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(3): Show |
7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.2488-520C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 7/27 | chr1 | 197130576 | |||||||
chr1:197130689 | A | G | 1 | a0001c0008t0001g0094 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2488-633T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 7/27 | chr1 | 197130689 | |||||||
chr1:197130843 | C | T | 2 | a0020c0020t0001g0101 a0020c0020t0001g0102 |
2 | NA18947.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.2488-787G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 7/27 | chr1 | 197130843 | |||||||
chr1:197130860 | A | ATT | 1 | a0001c0003t0001g0015 | 3 | HG00609.hp1 NA18943.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.2488-805_2488-804i others(4): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 7/27 | chr1 | 197130860 | |||||||
chr1:197130861 | C | A | 1 | a0001c0003t0001g0015 | 3 | HG00609.hp1 NA18943.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.2488-805G>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 7/27 | chr1 | 197130861 | |||||||
chr1:197131087 | G | T | 1 | a0001c0039t0001g0168 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2488-1031C>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 7/27 | chr1 | 197131087 | |||||||
chr1:197131294 | G | C | 6 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(3): Show |
7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.2487+991C>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 7/27 | chr1 | 197131294 | |||||||
chr1:197131365 | T | C | 2 | a0001c0039t0001g0168 a0019c0019t0001g0033 |
3 | HG02280.hp2 HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2487+920A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 7/27 | chr1 | 197131365 | |||||||
chr1:197131375 | A | T | 6 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(3): Show |
7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.2487+910T>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 7/27 | chr1 | 197131375 | |||||||
chr1:197131426 | C | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(148): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.2487+859G>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 7/27 | chr1 | 197131426 | |||||||
chr1:197131467 | T | C | 3 | a0001c0004t0002g0080 a0001c0004t0002g0081 a0001c0004t0002g0082 |
3 | HG01175.hp1 HG01891.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.2487+818A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 7/27 | chr1 | 197131467 | |||||||
chr1:197131557 | C | CT | 55 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(52): Show |
80 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.2487+727dupA | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 7/27 | chr1 | 197131557 | |||||||
chr1:197131751 | G | A | 1 | a0001c0001t0001g0134 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2487+534C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 7/27 | chr1 | 197131751 | |||||||
chr1:197131883 | C | A | 3 | a0016c0025t0004g0024 a0017c0024t0004g0088 a0017c0024t0004g0089 |
4 | HG02896.hp1 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2487+402G>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 7/27 | chr1 | 197131883 | |||||||
chr1:197131892 | C | T | 42 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0007 others(39): Show |
64 | HG00140.hp1 HG00423.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.2487+393G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 7/27 | chr1 | 197131892 | |||||||
chr1:197131975 | T | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(161): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.2487+310A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 7/27 | chr1 | 197131975 | |||||||
chr1:197131991 | T | C | 5 | a0001c0004t0002g0072 a0001c0004t0002g0073 a0001c0004t0002g0074 others(2): Show |
5 | HG02055.hp1 HG02970.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.2487+294A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 7/27 | chr1 | 197131991 | |||||||
chr1:197132024 | G | A | 6 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(3): Show |
7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.2487+261C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 7/27 | chr1 | 197132024 | |||||||
chr1:197132133 | C | T | 3 | a0002c0002t0001g0150 a0004c0005t0003g0041 a0004c0005t0003g0043 |
3 | HG02486.hp2 NA18972.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.2487+152G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 7/27 | chr1 | 197132133 | |||||||
chr1:197132160 | G | T | 2 | a0001c0039t0001g0168 a0019c0019t0001g0033 |
3 | HG02280.hp2 HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2487+125C>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 7/27 | chr1 | 197132160 | |||||||
chr1:197132173 | C | A | 42 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0007 others(39): Show |
64 | HG00140.hp1 HG00423.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.2487+112G>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 7/27 | chr1 | 197132173 | |||||||
chr1:197132372 | CAAATAAG others(5): Show |
C | 1 | a0001c0003t0001g0173 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2420-32_2420-21del others(12): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 6/27 | chr1 | 197132372 | |||||||
chr1:197132491 | T | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(107): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.2420-139A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 6/27 | chr1 | 197132491 | |||||||
chr1:197132587 | G | T | 1 | a0002c0002t0001g0149 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2420-235C>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 6/27 | chr1 | 197132587 | |||||||
chr1:197132597 | A | G | 3 | a0002c0002t0001g0138 a0002c0002t0001g0139 a0002c0002t0001g0170 |
3 | HG02071.hp2 NA18980.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.2420-245T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 6/27 | chr1 | 197132597 | |||||||
chr1:197132964 | G | A | 1 | a0006c0006t0005g0213 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2419+386C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 6/27 | chr1 | 197132964 | |||||||
chr1:197133037 | T | C | 9 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(6): Show |
10 | HG02523.hp2 HG02818.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.2419+313A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 6/27 | chr1 | 197133037 | |||||||
chr1:197133044 | C | T | 1 | a0007c0015t0001g0100 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2419+306G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 6/27 | chr1 | 197133044 | |||||||
chr1:197133060 | C | T | 2 | a0002c0002t0001g0169 a0002c0040t0001g0148 |
2 | NA18964.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.2419+290G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 6/27 | chr1 | 197133060 | |||||||
chr1:197133061 | G | A | 3 | a0011c0013t0004g0046 a0011c0013t0004g0047 a0011c0013t0004g0048 |
3 | HG02818.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2419+289C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 6/27 | chr1 | 197133061 | |||||||
chr1:197133146 | G | A | 8 | a0001c0004t0002g0021 a0001c0004t0002g0049 a0001c0004t0002g0050 others(5): Show |
10 | HG02055.hp2 HG02622.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.2419+204C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 6/27 | chr1 | 197133146 | |||||||
chr1:197133293 | C | A | 6 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(3): Show |
7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.2419+57G>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 6/27 | chr1 | 197133293 | |||||||
chr1:197133338 | C | T | 2 | a0002c0002t0001g0136 a0002c0002t0001g0147 |
2 | HG00738.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2419+12G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 6/27 | chr1 | 197133338 | |||||||
chr1:197133615 | A | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(52): Show |
80 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.2174-20T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 5/27 | chr1 | 197133615 | |||||||
chr1:197133681 | C | T | 1 | a0002c0002t0001g0146 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2174-86G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 5/27 | chr1 | 197133681 | |||||||
chr1:197133709 | A | C | 169 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(166): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.2174-114T>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 5/27 | chr1 | 197133709 | |||||||
chr1:197133796 | C | T | 42 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0007 others(39): Show |
64 | HG00140.hp1 HG00423.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.2174-201G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 5/27 | chr1 | 197133796 | |||||||
chr1:197133806 | A | G | 8 | a0002c0002t0001g0004 a0002c0002t0001g0012 a0002c0002t0001g0138 others(5): Show |
15 | HG02056.hp2 HG02071.hp2 HG02165.hp1 others(12): Show |
intron_variant | MODIFIER | c.2174-211T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 5/27 | chr1 | 197133806 | |||||||
chr1:197133896 | TAA | T | 2 | a0001c0039t0001g0168 a0019c0019t0001g0033 |
3 | HG02280.hp2 HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2174-303_2174-302d others(4): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 5/27 | chr1 | 197133896 | |||||||
chr1:197133944 | T | C | 6 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(3): Show |
7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.2174-349A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 5/27 | chr1 | 197133944 | |||||||
chr1:197134053 | G | A | 3 | a0011c0013t0004g0046 a0011c0013t0004g0047 a0011c0013t0004g0048 |
3 | HG02818.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2174-458C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 5/27 | chr1 | 197134053 | |||||||
chr1:197134175 | A | T | 6 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(3): Show |
7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.2174-580T>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 5/27 | chr1 | 197134175 | |||||||
chr1:197134250 | T | A | 1 | a0001c0022t0001g0034 | 2 | HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2174-655A>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 5/27 | chr1 | 197134250 | |||||||
chr1:197134250 | T | TA | 103 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(100): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.2174-656dupT | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 5/27 | chr1 | 197134250 | |||||||
chr1:197134250 | T | TAA | 8 | a0001c0001t0001g0099 a0001c0001t0001g0130 a0004c0005t0003g0017 others(5): Show |
9 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(6): Show |
intron_variant | MODIFIER | c.2174-657_2174-656d others(4): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 5/27 | chr1 | 197134250 | |||||||
chr1:197134252 | A | AT | 42 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0007 others(39): Show |
64 | HG00140.hp1 HG00423.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.2174-658_2174-657i others(3): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 5/27 | chr1 | 197134252 | |||||||
chr1:197134253 | A | T | 1 | a0001c0031t0002g0085 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2174-658T>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 5/27 | chr1 | 197134253 | |||||||
chr1:197134425 | G | GA | 177 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(174): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.2173+670dupT | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 5/27 | chr1 | 197134425 | |||||||
chr1:197134473 | C | T | 1 | a0002c0002t0001g0145 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2173+623G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 5/27 | chr1 | 197134473 | |||||||
chr1:197134479 | G | A | 3 | a0011c0013t0004g0046 a0011c0013t0004g0047 a0011c0013t0004g0048 |
3 | HG02818.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2173+617C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 5/27 | chr1 | 197134479 | |||||||
chr1:197134827 | A | C | 5 | a0001c0004t0002g0072 a0001c0004t0002g0073 a0001c0004t0002g0074 others(2): Show |
5 | HG02055.hp1 HG02970.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.2173+269T>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 5/27 | chr1 | 197134827 | |||||||
chr1:197134845 | G | A | 163 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(160): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.2173+251C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 5/27 | chr1 | 197134845 | |||||||
chr1:197134976 | T | C | 3 | a0001c0004t0002g0019 a0001c0004t0002g0061 a0036c0029t0002g0060 |
4 | HG01192.hp1 HG02698.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.2173+120A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 5/27 | chr1 | 197134976 | |||||||
chr1:197135019 | TA | T | 152 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(149): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.2173+76delT | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 5/27 | chr1 | 197135019 | |||||||
chr1:197135566 | A | G | 1 | a0001c0031t0002g0085 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2027-324T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197135566 | |||||||
chr1:197135623 | C | CT | 19 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0003t0001g0171 others(16): Show |
20 | HG02055.hp2 HG02071.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.2027-382dupA | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197135623 | |||||||
chr1:197135623 | C | CTT | 8 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0041 others(5): Show |
10 | HG02109.hp1 HG02145.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.2027-383_2027-382d others(4): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197135623 | |||||||
chr1:197135623 | CT | C | 9 | a0001c0001t0001g0131 a0001c0003t0001g0178 a0001c0003t0001g0204 others(6): Show |
9 | HG01081.hp2 HG01515.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.2027-382delA | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197135623 | |||||||
chr1:197135737 | G | A | 3 | a0011c0013t0004g0046 a0011c0013t0004g0047 a0011c0013t0004g0048 |
3 | HG02818.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2027-495C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197135737 | |||||||
chr1:197135836 | C | A | 3 | a0016c0025t0004g0024 a0017c0024t0004g0088 a0017c0024t0004g0089 |
4 | HG02896.hp1 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2027-594G>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197135836 | |||||||
chr1:197136032 | T | C | 2 | a0001c0039t0001g0168 a0019c0019t0001g0033 |
3 | HG02280.hp2 HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2027-790A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197136032 | |||||||
chr1:197136239 | T | C | 6 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(3): Show |
7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.2027-997A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197136239 | |||||||
chr1:197136241 | A | G | 1 | a0002c0002t0001g0012 | 3 | NA18952.hp1 NA18998.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.2027-999T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197136241 | |||||||
chr1:197136281 | C | T | 1 | a0017c0024t0004g0088 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2027-1039G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197136281 | |||||||
chr1:197136377 | G | A | 1 | a0008c0016t0001g0011 | 3 | HG02280.hp1 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2027-1135C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197136377 | |||||||
chr1:197136406 | T | G | 158 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(155): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.2027-1164A>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197136406 | |||||||
chr1:197136486 | T | A | 1 | a0001c0033t0002g0071 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2027-1244A>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197136486 | |||||||
chr1:197136540 | GAAGTT | G | 3 | a0011c0013t0004g0046 a0011c0013t0004g0047 a0011c0013t0004g0048 |
3 | HG02818.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2027-1303_2027-129 others(9): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197136540 | |||||||
chr1:197136769 | A | C | 1 | a0002c0002t0001g0144 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2027-1527T>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197136769 | |||||||
chr1:197136796 | T | C | 6 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(3): Show |
7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.2027-1554A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197136796 | |||||||
chr1:197137046 | CAG | C | 6 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(3): Show |
7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.2027-1806_2027-180 others(6): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197137046 | |||||||
chr1:197137097 | T | C | 1 | a0001c0003t0001g0205 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2027-1855A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197137097 | |||||||
chr1:197137119 | C | T | 152 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(149): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.2027-1877G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197137119 | |||||||
chr1:197137474 | C | T | 152 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(149): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.2027-2232G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197137474 | |||||||
chr1:197137540 | G | C | 1 | a0001c0004t0002g0061 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2026+2227C>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197137540 | |||||||
chr1:197137584 | G | A | 1 | a0001c0001t0001g0006 | 4 | HG02004.hp2 HG02165.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.2026+2183C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197137584 | |||||||
chr1:197137593 | G | A | 1 | a0002c0002t0001g0143 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2026+2174C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197137593 | |||||||
chr1:197137658 | A | T | 6 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(3): Show |
7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.2026+2109T>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197137658 | |||||||
chr1:197137669 | T | C | 17 | a0001c0004t0002g0021 a0001c0004t0002g0049 a0001c0004t0002g0050 others(14): Show |
20 | HG02055.hp2 HG02523.hp2 HG02622.hp2 others(17): Show |
intron_variant | MODIFIER | c.2026+2098A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197137669 | |||||||
chr1:197137690 | G | A | 1 | a0001c0001t0001g0010 | 3 | NA18960.hp2 NA18965.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.2026+2077C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197137690 | |||||||
chr1:197137749 | G | A | 3 | a0006c0006t0005g0038 a0006c0006t0005g0212 a0006c0006t0005g0213 |
4 | HG02109.hp1 HG02145.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2026+2018C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197137749 | |||||||
chr1:197137877 | G | A | 3 | a0016c0025t0004g0024 a0017c0024t0004g0088 a0017c0024t0004g0089 |
4 | HG02896.hp1 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2026+1890C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197137877 | |||||||
chr1:197137964 | TTTATC | T | 3 | a0016c0025t0004g0024 a0017c0024t0004g0088 a0017c0024t0004g0089 |
4 | HG02896.hp1 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2026+1798_2026+180 others(9): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197137964 | |||||||
chr1:197138307 | CT | C | 3 | a0016c0025t0004g0024 a0017c0024t0004g0088 a0017c0024t0004g0089 |
4 | HG02896.hp1 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2026+1459delA | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197138307 | |||||||
chr1:197138345 | C | T | 1 | a0002c0002t0001g0143 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2026+1422G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197138345 | |||||||
chr1:197138378 | C | T | 2 | a0001c0003t0001g0177 a0001c0003t0001g0178 |
2 | HG02258.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2026+1389G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197138378 | |||||||
chr1:197138412 | C | T | 1 | a0001c0003t0001g0176 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2026+1355G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197138412 | |||||||
chr1:197138446 | G | A | 6 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(3): Show |
7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.2026+1321C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197138446 | |||||||
chr1:197138482 | G | C | 6 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(3): Show |
7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.2026+1285C>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197138482 | |||||||
chr1:197138512 | G | C | 1 | a0001c0004t0002g0066 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2026+1255C>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197138512 | |||||||
chr1:197138590 | G | T | 2 | a0001c0039t0001g0168 a0019c0019t0001g0033 |
3 | HG02280.hp2 HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2026+1177C>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197138590 | |||||||
chr1:197138670 | T | G | 6 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(3): Show |
7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.2026+1097A>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197138670 | |||||||
chr1:197138716 | A | G | 6 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(3): Show |
7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.2026+1051T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197138716 | |||||||
chr1:197138762 | G | T | 2 | a0001c0031t0002g0085 a0001c0033t0002g0071 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.2026+1005C>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197138762 | |||||||
chr1:197138882 | A | T | 3 | a0011c0013t0004g0046 a0011c0013t0004g0047 a0011c0013t0004g0048 |
3 | HG02818.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2026+885T>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197138882 | |||||||
chr1:197138987 | T | C | 9 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(6): Show |
10 | HG02523.hp2 HG02818.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.2026+780A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197138987 | |||||||
chr1:197139140 | A | G | 1 | a0001c0003t0001g0175 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2026+627T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197139140 | |||||||
chr1:197139297 | A | G | 161 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(158): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.2026+470T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197139297 | |||||||
chr1:197139319 | G | A | 3 | a0016c0025t0004g0024 a0017c0024t0004g0088 a0017c0024t0004g0089 |
4 | HG02896.hp1 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2026+448C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197139319 | |||||||
chr1:197139361 | C | T | 6 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(3): Show |
7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.2026+406G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197139361 | |||||||
chr1:197139454 | G | A | 2 | a0001c0039t0001g0168 a0019c0019t0001g0033 |
3 | HG02280.hp2 HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2026+313C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197139454 | |||||||
chr1:197139463 | C | G | 6 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(3): Show |
7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.2026+304G>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197139463 | |||||||
chr1:197139563 | C | T | 152 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(149): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.2026+204G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197139563 | |||||||
chr1:197139588 | T | C | 1 | a0001c0003t0001g0206 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2026+179A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 4/27 | chr1 | 197139588 | |||||||
chr1:197139912 | C | T | 164 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(161): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.1922-41G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 3/27 | chr1 | 197139912 | |||||||
chr1:197139949 | G | A | 1 | a0001c0022t0001g0034 | 2 | HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1922-78C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 3/27 | chr1 | 197139949 | |||||||
chr1:197140429 | C | T | 4 | a0001c0003t0001g0014 a0001c0003t0001g0171 a0001c0003t0001g0172 others(1): Show |
6 | NA18947.hp1 NA18965.hp1 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.1922-558G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 3/27 | chr1 | 197140429 | |||||||
chr1:197140454 | T | C | 1 | a0001c0003t0001g0207 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1922-583A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 3/27 | chr1 | 197140454 | |||||||
chr1:197140610 | C | CAGTAT | 3 | a0016c0025t0004g0024 a0017c0024t0004g0088 a0017c0024t0004g0089 |
4 | HG02896.hp1 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1922-744_1922-740d others(7): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 3/27 | chr1 | 197140610 | |||||||
chr1:197140723 | A | G | 3 | a0016c0025t0004g0024 a0017c0024t0004g0088 a0017c0024t0004g0089 |
4 | HG02896.hp1 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1922-852T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 3/27 | chr1 | 197140723 | |||||||
chr1:197140858 | G | A | 1 | a0001c0031t0002g0085 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1922-987C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 3/27 | chr1 | 197140858 | |||||||
chr1:197141052 | C | T | 3 | a0016c0025t0004g0024 a0017c0024t0004g0088 a0017c0024t0004g0089 |
4 | HG02896.hp1 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1922-1181G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 3/27 | chr1 | 197141052 | |||||||
chr1:197141091 | G | T | 8 | a0002c0002t0001g0004 a0002c0002t0001g0012 a0002c0002t0001g0138 others(5): Show |
15 | HG02056.hp2 HG02071.hp2 HG02165.hp1 others(12): Show |
intron_variant | MODIFIER | c.1922-1220C>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 3/27 | chr1 | 197141091 | |||||||
chr1:197141184 | T | TA | 120 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(117): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.1921+1146dupT | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 3/27 | chr1 | 197141184 | |||||||
chr1:197141201 | T | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(161): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.1921+1130A>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 3/27 | chr1 | 197141201 | |||||||
chr1:197141310 | G | A | 3 | a0006c0006t0005g0038 a0006c0006t0005g0212 a0006c0006t0005g0213 |
4 | HG02109.hp1 HG02145.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1921+1021C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 3/27 | chr1 | 197141310 | |||||||
chr1:197141361 | A | G | 9 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(6): Show |
10 | HG02523.hp2 HG02818.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.1921+970T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 3/27 | chr1 | 197141361 | |||||||
chr1:197141479 | T | C | 3 | a0011c0013t0004g0046 a0011c0013t0004g0047 a0011c0013t0004g0048 |
3 | HG02818.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1921+852A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 3/27 | chr1 | 197141479 | |||||||
chr1:197141692 | A | G | 161 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(158): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.1921+639T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 3/27 | chr1 | 197141692 | |||||||
chr1:197141733 | G | A | 3 | a0011c0013t0004g0046 a0011c0013t0004g0047 a0011c0013t0004g0048 |
3 | HG02818.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1921+598C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 3/27 | chr1 | 197141733 | |||||||
chr1:197141743 | CT | C | 3 | a0011c0013t0004g0046 a0011c0013t0004g0047 a0011c0013t0004g0048 |
3 | HG02818.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1921+587delA | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 3/27 | chr1 | 197141743 | |||||||
chr1:197141767 | C | G | 3 | a0011c0013t0004g0046 a0011c0013t0004g0047 a0011c0013t0004g0048 |
3 | HG02818.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1921+564G>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 3/27 | chr1 | 197141767 | |||||||
chr1:197141920 | C | T | 9 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(6): Show |
10 | HG02523.hp2 HG02818.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.1921+411G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 3/27 | chr1 | 197141920 | |||||||
chr1:197142031 | C | T | 3 | a0016c0025t0004g0024 a0017c0024t0004g0088 a0017c0024t0004g0089 |
4 | HG02896.hp1 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1921+300G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 3/27 | chr1 | 197142031 | |||||||
chr1:197142071 | TAGG | T | 1 | a0008c0016t0001g0011 | 3 | HG02280.hp1 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1921+257_1921+259d others(5): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 3/27 | chr1 | 197142071 | |||||||
chr1:197142095 | C | G | 1 | a0001c0004t0002g0070 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1921+236G>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 3/27 | chr1 | 197142095 | |||||||
chr1:197142110 | TTTG | T | 6 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(3): Show |
7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.1921+218_1921+220d others(5): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 3/27 | chr1 | 197142110 | |||||||
chr1:197142277 | A | C | 6 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(3): Show |
7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.1921+54T>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 3/27 | chr1 | 197142277 | |||||||
chr1:197143836 | A | G | 3 | a0011c0013t0004g0046 a0011c0013t0004g0047 a0011c0013t0004g0048 |
3 | HG02818.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.442-26T>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 2/27 | chr1 | 197143836 | |||||||
chr1:197143943 | G | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(148): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.441+14C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 2/27 | chr1 | 197143943 | |||||||
chr1:197144443 | C | T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(160): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.298-343G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 1/27 | chr1 | 197144443 | |||||||
chr1:197144463 | G | A | 6 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(3): Show |
7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.298-363C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 1/27 | chr1 | 197144463 | |||||||
chr1:197144587 | C | T | 6 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(3): Show |
7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.298-487G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 1/27 | chr1 | 197144587 | |||||||
chr1:197144763 | C | T | 1 | a0002c0002t0001g0136 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.298-663G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 1/27 | chr1 | 197144763 | |||||||
chr1:197144917 | T | C | 1 | a0001c0001t0001g0134 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.298-817A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 1/27 | chr1 | 197144917 | |||||||
chr1:197144986 | G | A | 1 | a0002c0002t0001g0169 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.298-886C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 1/27 | chr1 | 197144986 | |||||||
chr1:197145070 | G | T | 1 | a0002c0002t0001g0170 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.298-970C>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 1/27 | chr1 | 197145070 | |||||||
chr1:197145079 | T | A | 1 | a0002c0002t0001g0170 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.298-979A>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 1/27 | chr1 | 197145079 | |||||||
chr1:197145097 | T | C | 1 | a0001c0001t0001g0135 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.298-997A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 1/27 | chr1 | 197145097 | |||||||
chr1:197145152 | G | A | 1 | a0001c0003t0001g0209 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.297+989C>T | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 1/27 | chr1 | 197145152 | |||||||
chr1:197145273 | G | C | 1 | a0002c0002t0001g0013 | 3 | HG01496.hp1 HG01934.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.297+868C>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 1/27 | chr1 | 197145273 | |||||||
chr1:197145304 | T | C | 6 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(3): Show |
7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.297+837A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 1/27 | chr1 | 197145304 | |||||||
chr1:197145307 | C | T | 2 | a0001c0004t0002g0049 a0001c0004t0002g0050 |
2 | HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.297+834G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 1/27 | chr1 | 197145307 | |||||||
chr1:197145328 | A | C | 7 | a0003c0007t0002g0022 a0003c0007t0002g0067 a0003c0007t0002g0069 others(4): Show |
10 | HG02258.hp1 HG02622.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.297+813T>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 1/27 | chr1 | 197145328 | |||||||
chr1:197145791 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.297+350G>A | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 1/27 | chr1 | 197145791 | |||||||
chr1:197145795 | T | G | 9 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(6): Show |
10 | HG02523.hp2 HG02818.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.297+346A>C | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 1/27 | chr1 | 197145795 | |||||||
chr1:197145797 | T | C | 6 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(3): Show |
7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.297+344A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 1/27 | chr1 | 197145797 | |||||||
chr1:197145845 | A | AATATATA others(7): Show |
1 | a0011c0013t0004g0048 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.297+282_297+295dup others(14): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 1/27 | chr1 | 197145845 | |||||||
chr1:197145845 | A | AATATATA others(9): Show |
1 | a0011c0013t0004g0047 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.297+280_297+295dup others(16): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 1/27 | chr1 | 197145845 | |||||||
chr1:197145845 | A | AATATATA others(11): Show |
1 | a0011c0013t0004g0046 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.297+278_297+295dup others(18): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 1/27 | chr1 | 197145845 | |||||||
chr1:197145845 | A | AATATATA others(13): Show |
1 | a0004c0005t0003g0043 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.297+276_297+295dup others(20): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 1/27 | chr1 | 197145845 | |||||||
chr1:197145845 | AAT | A | 24 | a0001c0004t0002g0070 a0001c0004t0002g0072 a0001c0004t0002g0073 others(21): Show |
27 | HG01175.hp1 HG01884.hp1 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.297+294_297+295del others(2): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 1/27 | chr1 | 197145845 | |||||||
chr1:197145845 | AATAT | A | 62 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(59): Show |
88 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.297+292_297+295del others(4): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 1/27 | chr1 | 197145845 | |||||||
chr1:197145845 | AATATAT | A | 46 | a0001c0022t0001g0034 a0001c0039t0001g0168 a0002c0002t0001g0003 others(43): Show |
72 | HG00140.hp1 HG00423.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.297+290_297+295del others(6): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 1/27 | chr1 | 197145845 | |||||||
chr1:197145845 | AATATATA others(1): Show |
A | 46 | a0001c0003t0001g0002 a0001c0003t0001g0005 a0001c0003t0001g0014 others(43): Show |
66 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.297+288_297+295del others(8): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 1/27 | chr1 | 197145845 | |||||||
chr1:197145868 | A | ATATATAT others(14): Show |
3 | a0004c0005t0003g0017 a0004c0005t0003g0041 a0004c0005t0003g0042 |
4 | NA18945.hp1 NA18969.hp1 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.297+272_297+273ins others(21): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 1/27 | chr1 | 197145868 | |||||||
chr1:197145868 | A | ATATATAT others(18): Show |
1 | a0004c0005t0003g0040 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.297+272_297+273ins others(25): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 1/27 | chr1 | 197145868 | |||||||
chr1:197145868 | A | ATATATAT others(20): Show |
1 | a0004c0005t0003g0039 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.297+272_297+273ins others(27): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 1/27 | chr1 | 197145868 | |||||||
chr1:197145871 | A | AT | 6 | a0004c0005t0003g0017 a0004c0005t0003g0039 a0004c0005t0003g0040 others(3): Show |
7 | HG02523.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.297+269dupA | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 1/27 | chr1 | 197145871 | |||||||
chr1:197145874 | GAC | G | 3 | a0011c0013t0004g0046 a0011c0013t0004g0047 a0011c0013t0004g0048 |
3 | HG02818.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.297+265_297+266del others(2): Show |
ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 1/27 | chr1 | 197145874 | |||||||
chr1:197145976 | T | C | 1 | a0001c0001t0001g0210 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.297+165A>G | ASPM | ENSG00000066279.19 | transcript | ENST00000367409.9 | protein_coding | 1/27 | chr1 | 197145976 |