Item | Value |
---|---|
geneid | 11093 |
ensemblid | ENSG00000160323.19 |
hgncid | 1366 |
symbol | ADAMTS13 |
name | ADAM metallopeptidase with thrombospondin type 1 motif 13 |
refseq_nuc | NM_139027.6 |
refseq_prot | NP_620596.2 |
ensembl_nuc | ENST00000355699.7 |
ensembl_prot | ENSP00000347927.2 |
mane_status | MANE Select |
chr | chr9 |
start | 133422367 |
end | 133459386 |
strand | + |
ver | v1.2 |
region | chr9:133422367-133459386 |
region5000 | chr9:133417367-133464386 |
regionname0 | ADAMTS13_chr9_133422367_133459386 |
regionname5000 | ADAMTS13_chr9_133417367_133464386 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1371 | 191 | 48 | 22 | 89 | 10 | 20 | 61 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | MHQRH others(1366): Show |
chr9 | 133417367 | 133464386 |
a0002 | 0/0 | 1371 | 75 | 4 | 32 | 22 | 3 | 14 | 17 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | MHQRH others(1366): Show |
chr9 | 133417367 | 133464386 |
a0003 | 0/0 | 1371 | 18 | 9 | 5 | 1 | 2 | 1 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | MHQRH others(1366): Show |
chr9 | 133417367 | 133464386 |
a0004 | 0/0 | 1371 | 10 | 10 | 0 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | MHQRH others(1366): Show |
chr9 | 133417367 | 133464386 |
a0005 | 0/0 | 1371 | 8 | 0 | 0 | 8 | 0 | 0 | 5 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | MHQRH others(1366): Show |
chr9 | 133417367 | 133464386 |
a0006 | 0/0 | 1371 | 7 | 0 | 0 | 7 | 0 | 0 | 7 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | MHQRH others(1366): Show |
chr9 | 133417367 | 133464386 |
a0007 | 0/0 | 1371 | 6 | 0 | 6 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | MHQRH others(1366): Show |
chr9 | 133417367 | 133464386 |
a0008 | 0/0 | 1371 | 5 | 1 | 1 | 0 | 1 | 2 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | MHQRH others(1366): Show |
chr9 | 133417367 | 133464386 |
a0009 | 0/0 | 1371 | 5 | 0 | 0 | 5 | 0 | 0 | 4 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | MHQRH others(1366): Show |
chr9 | 133417367 | 133464386 |
a0010 | 0/0 | 1371 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | MHQRH others(1366): Show |
chr9 | 133417367 | 133464386 |
a0011 | 0/0 | 1371 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | MHQRH others(1366): Show |
chr9 | 133417367 | 133464386 |
a0012 | 0/0 | 1371 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | MHQRH others(1366): Show |
chr9 | 133417367 | 133464386 |
a0013 | 0/0 | 1371 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | MHQRH others(1366): Show |
chr9 | 133417367 | 133464386 |
a0014 | 0/0 | 1371 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | MHQRH others(1366): Show |
chr9 | 133417367 | 133464386 |
a0015 | 0/0 | 1371 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | MHQRH others(1366): Show |
chr9 | 133417367 | 133464386 |
a0016 | 0/0 | 1371 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | MHQRH others(1366): Show |
chr9 | 133417367 | 133464386 |
a0017 | 0/0 | 1371 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | MHQRH others(1366): Show |
chr9 | 133417367 | 133464386 |
a0018 | 0/0 | 1371 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | MHQRH others(1366): Show |
chr9 | 133417367 | 133464386 |
a0019 | 0/0 | 1371 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | MHQRH others(1366): Show |
chr9 | 133417367 | 133464386 |
a0020 | 0/0 | 1371 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | MHQRH others(1366): Show |
chr9 | 133417367 | 133464386 |
a0021 | 0/0 | 1371 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | MHQRH others(1366): Show |
chr9 | 133417367 | 133464386 |
a0022 | 0/0 | 1371 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | MHQRH others(1366): Show |
chr9 | 133417367 | 133464386 |
a0023 | 0/0 | 1371 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | MHQRH others(1366): Show |
chr9 | 133417367 | 133464386 |
a0024 | 0/0 | 1371 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | MHQRH others(1366): Show |
chr9 | 133417367 | 133464386 |
a0025 | 0/0 | 1371 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | MHQRH others(1366): Show |
chr9 | 133417367 | 133464386 |
a0026 | 0/0 | 1371 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | MHQRH others(1366): Show |
chr9 | 133417367 | 133464386 |
a0027 | 0/0 | 1371 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | MHQRH others(1366): Show |
chr9 | 133417367 | 133464386 |
a0028 | 0/0 | 1371 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | MHQRH others(1366): Show |
chr9 | 133417367 | 133464386 |
a0029 | 0/0 | 1371 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | MHQRH others(1366): Show |
chr9 | 133417367 | 133464386 |
a0030 | 0/0 | 1371 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | MHQRH others(1366): Show |
chr9 | 133417367 | 133464386 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 4113 | 159 | 31 | 20 | 82 | 7 | 17 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0001c0005 | 0/0 | 4113 | 9 | 9 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0001c0010 | 0/0 | 4113 | 5 | 2 | 1 | 0 | 1 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0001c0011 | 0/0 | 4113 | 5 | 0 | 0 | 4 | 0 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0001c0017 | 0/0 | 4113 | 3 | 3 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0001c0027 | 0/0 | 4113 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0001c0028 | 0/0 | 4113 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0001c0029 | 0/0 | 4113 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0001c0034 | 0/0 | 4113 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0001c0042 | 0/0 | 4113 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0001c0044 | 0/0 | 4113 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0001c0046 | 0/0 | 4113 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0001c0047 | 0/0 | 4113 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0001c0050 | 0/0 | 4113 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0001c0057 | 0/0 | 4113 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0002c0002 | 0/0 | 4113 | 60 | 0 | 27 | 18 | 3 | 12 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0002c0006 | 0/0 | 4113 | 9 | 2 | 3 | 2 | 0 | 2 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0002c0037 | 0/0 | 4113 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0002c0038 | 0/0 | 4113 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0002c0039 | 0/0 | 4113 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0002c0040 | 0/0 | 4113 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0002c0051 | 0/0 | 4113 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0002c0052 | 0/0 | 4113 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0003c0003 | 0/0 | 4113 | 11 | 4 | 3 | 1 | 2 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0003c0019 | 0/0 | 4113 | 2 | 2 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0003c0030 | 0/0 | 4113 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0003c0031 | 0/0 | 4113 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0003c0032 | 0/0 | 4113 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0003c0033 | 0/0 | 4113 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0003c0035 | 0/0 | 4113 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0004c0004 | 0/0 | 4113 | 9 | 9 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0004c0026 | 0/0 | 4113 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0005c0007 | 0/0 | 4113 | 8 | 0 | 0 | 8 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0006c0008 | 0/0 | 4113 | 7 | 0 | 0 | 7 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0007c0009 | 0/0 | 4113 | 6 | 0 | 6 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0008c0013 | 0/0 | 4113 | 5 | 1 | 1 | 0 | 1 | 2 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0009c0012 | 0/0 | 4113 | 5 | 0 | 0 | 5 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0010c0018 | 0/0 | 4113 | 3 | 3 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0010c0060 | 0/0 | 4113 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0011c0015 | 0/0 | 4113 | 4 | 4 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0012c0014 | 0/0 | 4113 | 4 | 0 | 0 | 4 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0013c0016 | 0/0 | 4113 | 3 | 0 | 2 | 0 | 0 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0014c0023 | 0/0 | 4113 | 2 | 2 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0014c0056 | 0/0 | 4113 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0015c0024 | 0/0 | 4113 | 2 | 0 | 2 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0016c0022 | 0/0 | 4113 | 2 | 0 | 2 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0017c0020 | 0/0 | 4113 | 2 | 2 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0018c0021 | 0/0 | 4113 | 2 | 2 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0019c0025 | 0/0 | 4113 | 2 | 0 | 0 | 0 | 0 | 2 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0020c0048 | 0/0 | 4113 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0021c0049 | 0/0 | 4113 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0022c0041 | 0/0 | 4113 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0023c0036 | 0/0 | 4113 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0024c0055 | 0/0 | 4113 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0025c0053 | 0/0 | 4113 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0026c0059 | 0/0 | 4113 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0027c0058 | 0/0 | 4113 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0028c0043 | 0/0 | 4113 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0029c0054 | 0/0 | 4113 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 | ||
a0030c0045 | 0/0 | 4113 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATGCA others(4108): Show |
chr9 | 133417367 | 133464386 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 4399 | 158 | 30 | 20 | 82 | 7 | 17 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0001c0001t0005 | 0/0 | 4399 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0001c0005t0001 | 0/0 | 4399 | 9 | 9 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0001c0010t0001 | 0/0 | 4399 | 4 | 2 | 1 | 0 | 1 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0001c0010t0006 | 0/0 | 4399 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0001c0011t0001 | 0/0 | 4399 | 5 | 0 | 0 | 4 | 0 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0001c0017t0002 | 0/0 | 4399 | 3 | 3 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0001c0027t0001 | 0/0 | 4399 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0001c0028t0001 | 0/0 | 4399 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0001c0029t0001 | 0/0 | 4399 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0001c0034t0001 | 0/0 | 4399 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0001c0042t0001 | 0/0 | 4399 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0001c0044t0001 | 0/0 | 4399 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0001c0046t0001 | 0/0 | 4399 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0001c0047t0001 | 0/0 | 4399 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0001c0050t0001 | 0/0 | 4399 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0001c0057t0001 | 0/0 | 4399 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0002c0002t0001 | 0/0 | 4399 | 60 | 0 | 27 | 18 | 3 | 12 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0002c0006t0001 | 0/0 | 4399 | 9 | 2 | 3 | 2 | 0 | 2 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0002c0037t0001 | 0/0 | 4399 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0002c0038t0001 | 0/0 | 4399 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0002c0039t0001 | 0/0 | 4399 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0002c0040t0001 | 0/0 | 4399 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0002c0051t0001 | 0/0 | 4399 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0002c0052t0001 | 0/0 | 4399 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0003c0003t0001 | 0/0 | 4399 | 11 | 4 | 3 | 1 | 2 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0003c0019t0001 | 0/0 | 4399 | 2 | 2 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0003c0030t0004 | 0/0 | 4399 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0003c0031t0001 | 0/0 | 4399 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0003c0032t0001 | 0/0 | 4399 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0003c0033t0002 | 0/0 | 4399 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0003c0035t0001 | 0/0 | 4399 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0004c0004t0001 | 0/0 | 4399 | 9 | 9 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0004c0026t0001 | 0/0 | 4399 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0005c0007t0001 | 0/0 | 4399 | 8 | 0 | 0 | 8 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0006c0008t0001 | 0/0 | 4399 | 7 | 0 | 0 | 7 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0007c0009t0001 | 0/0 | 4399 | 6 | 0 | 6 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0008c0013t0001 | 0/0 | 4399 | 5 | 1 | 1 | 0 | 1 | 2 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0009c0012t0001 | 0/0 | 4399 | 5 | 0 | 0 | 5 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0010c0018t0001 | 0/0 | 4399 | 3 | 3 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0010c0060t0001 | 0/0 | 4399 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0011c0015t0001 | 0/0 | 4399 | 4 | 4 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0012c0014t0001 | 0/0 | 4399 | 4 | 0 | 0 | 4 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0013c0016t0001 | 0/0 | 4399 | 3 | 0 | 2 | 0 | 0 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0014c0023t0001 | 0/0 | 4399 | 2 | 2 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0014c0056t0001 | 0/0 | 4399 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0015c0024t0001 | 0/0 | 4399 | 2 | 0 | 2 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0016c0022t0001 | 0/0 | 4399 | 2 | 0 | 2 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0017c0020t0001 | 0/0 | 4399 | 2 | 2 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0018c0021t0001 | 0/0 | 4399 | 2 | 2 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0019c0025t0001 | 0/0 | 4399 | 2 | 0 | 0 | 0 | 0 | 2 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0020c0048t0001 | 0/0 | 4399 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0021c0049t0001 | 0/0 | 4399 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0022c0041t0003 | 0/0 | 4399 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0023c0036t0001 | 0/0 | 4399 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0024c0055t0001 | 0/0 | 4399 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0025c0053t0001 | 0/0 | 4399 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0026c0059t0001 | 0/0 | 4399 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0027c0058t0001 | 0/0 | 4399 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0028c0043t0001 | 0/0 | 4399 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0029c0054t0001 | 0/0 | 4399 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
a0030c0045t0001 | 0/0 | 4399 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | ATTCC others(4394): Show |
chr9 | 133417367 | 133464386 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 8 | 0 | 2 | 1 | 2 | 3 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0003 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0009 | 0/1 | 3 | 0 | 0 | 2 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0020 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0261 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0001t0005g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0005t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0005t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0005t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0005t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0005t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0005t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0005t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0005t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0005t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0010t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0010t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0010t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0010t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0010t0006g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0011t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0011t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0011t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0011t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0011t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0017t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0017t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0017t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0027t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0028t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0029t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0034t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0042t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0044t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0046t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0047t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0050t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0001c0057t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0006 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0013 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0014 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0006t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0006t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0006t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0006t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0006t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0006t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0006t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0006t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0006t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0037t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0038t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0039t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0040t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0051t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0002c0052t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0003c0003t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0003c0003t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0003c0003t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0003c0003t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0003c0003t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0003c0003t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0003c0003t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0003c0003t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0003c0003t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0003c0003t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0003c0003t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0003c0019t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0003c0019t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0003c0030t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0003c0031t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0003c0032t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0003c0033t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0003c0035t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0004c0004t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0004c0004t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0004c0004t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0004c0004t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0004c0004t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0004c0004t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0004c0026t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0005c0007t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0005c0007t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0005c0007t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0005c0007t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0006c0008t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0006c0008t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0006c0008t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0006c0008t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0006c0008t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0006c0008t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0006c0008t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0007c0009t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0007c0009t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0007c0009t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0007c0009t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0007c0009t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0007c0009t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0008c0013t0001g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0008c0013t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0008c0013t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0008c0013t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0009c0012t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0009c0012t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0009c0012t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0009c0012t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0009c0012t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0010c0018t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0010c0018t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0010c0018t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0010c0060t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0011c0015t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0011c0015t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0011c0015t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0012c0014t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0012c0014t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0013c0016t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0013c0016t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0013c0016t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0014c0023t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0014c0023t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0014c0056t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0015c0024t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0016c0022t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0016c0022t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0017c0020t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0017c0020t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0018c0021t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0018c0021t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0019c0025t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0019c0025t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0020c0048t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0021c0049t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0022c0041t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0023c0036t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0024c0055t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0025c0053t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0026c0059t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0027c0058t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0028c0043t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0029c0054t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
a0030c0045t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0010 | t0001 | g0189 | EUR | GBR | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG00099 | hp2 | a0001 | c0050 | t0001 | g0057 | EUR | GBR | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0172 | EUR | GBR | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG00280 | hp1 | a0003 | c0003 | t0001 | g0236 | EUR | FIN | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG00280 | hp2 | a0008 | c0013 | t0001 | g0012 | EUR | FIN | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG00323 | hp1 | a0003 | c0003 | t0001 | g0235 | EUR | FIN | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0203 | EUR | FIN | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG00423 | hp2 | a0009 | c0012 | t0001 | g0065 | EAS | CHS | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG00558 | hp1 | a0020 | c0048 | t0001 | g0292 | EAS | CHS | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG00558 | hp2 | a0005 | c0007 | t0001 | g0001 | EAS | CHS | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG00609 | hp1 | a0002 | c0006 | t0001 | g0083 | EAS | CHS | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG00609 | hp2 | a0001 | c0011 | t0001 | g0156 | EAS | CHS | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | CHS | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | CHS | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG00639 | hp1 | a0021 | c0049 | t0001 | g0157 | AMR | PUR | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG00639 | hp2 | a0002 | c0002 | t0001 | g0106 | AMR | PUR | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG00642 | hp1 | a0002 | c0002 | t0001 | g0089 | AMR | PUR | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG00733 | hp1 | a0002 | c0002 | t0001 | g0082 | AMR | PUR | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG00733 | hp2 | a0008 | c0013 | t0001 | g0012 | AMR | PUR | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG00735 | hp1 | a0003 | c0003 | t0001 | g0271 | AMR | PUR | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0097 | AMR | PUR | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG00738 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | PUR | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG00741 | hp2 | a0013 | c0016 | t0001 | g0113 | AMR | PUR | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01069 | hp1 | a0002 | c0002 | t0001 | g0084 | AMR | PUR | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01069 | hp2 | a0015 | c0024 | t0001 | g0024 | AMR | PUR | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01070 | hp1 | a0002 | c0002 | t0001 | g0085 | AMR | PUR | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0041 | AMR | PUR | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01071 | hp1 | a0015 | c0024 | t0001 | g0024 | AMR | PUR | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0093 | AMR | PUR | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01074 | hp1 | a0007 | c0009 | t0001 | g0245 | AMR | PUR | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01074 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PUR | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | PUR | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01081 | hp2 | a0003 | c0032 | t0001 | g0268 | AMR | PUR | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01099 | hp1 | a0007 | c0009 | t0001 | g0244 | AMR | PUR | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01099 | hp2 | a0010 | c0060 | t0001 | g0198 | AMR | PUR | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0103 | AMR | PUR | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01109 | hp1 | a0001 | c0027 | t0001 | g0272 | AMR | PUR | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01167 | hp1 | a0016 | c0022 | t0001 | g0153 | AMR | PUR | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01167 | hp2 | a0003 | c0033 | t0002 | g0267 | AMR | PUR | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01169 | hp1 | a0016 | c0022 | t0001 | g0045 | AMR | PUR | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01169 | hp2 | a0002 | c0002 | t0001 | g0278 | AMR | PUR | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0014 | AMR | PUR | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0108 | AMR | PUR | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01255 | hp2 | a0002 | c0006 | t0001 | g0098 | AMR | CLM | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | CLM | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0105 | AMR | CLM | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01358 | hp1 | a0001 | c0010 | t0001 | g0195 | AMR | CLM | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01358 | hp2 | a0007 | c0009 | t0001 | g0208 | AMR | CLM | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01433 | hp1 | a0003 | c0003 | t0001 | g0296 | AMR | CLM | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0100 | AMR | CLM | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01496 | hp2 | a0007 | c0009 | t0001 | g0246 | AMR | CLM | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0058 | EUR | IBS | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01515 | hp2 | a0002 | c0002 | t0001 | g0078 | EUR | IBS | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01516 | hp1 | a0001 | c0034 | t0001 | g0062 | EUR | IBS | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01516 | hp2 | a0002 | c0002 | t0001 | g0006 | EUR | IBS | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01517 | hp1 | a0002 | c0002 | t0001 | g0006 | EUR | IBS | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0192 | EUR | IBS | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01884 | hp1 | a0001 | c0005 | t0001 | g0265 | AFR | ACB | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01884 | hp2 | a0003 | c0003 | t0001 | g0270 | AFR | ACB | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01891 | hp2 | a0002 | c0040 | t0001 | g0300 | AFR | ACB | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01928 | hp1 | a0002 | c0052 | t0001 | g0213 | AMR | PEL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01928 | hp2 | a0002 | c0006 | t0001 | g0114 | AMR | PEL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0013 | AMR | PEL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01975 | hp1 | a0002 | c0037 | t0001 | g0088 | AMR | PEL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01975 | hp2 | a0002 | c0002 | t0001 | g0117 | AMR | PEL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01978 | hp1 | a0002 | c0002 | t0001 | g0077 | AMR | PEL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0091 | AMR | PEL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01981 | hp1 | a0002 | c0006 | t0001 | g0115 | AMR | PEL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01981 | hp2 | a0007 | c0009 | t0001 | g0248 | AMR | PEL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0116 | AMR | PEL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02004 | hp2 | a0002 | c0002 | t0001 | g0039 | AMR | PEL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | KHV | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02040 | hp1 | a0002 | c0002 | t0001 | g0150 | EAS | KHV | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | ACB | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02129 | hp2 | a0005 | c0007 | t0001 | g0001 | EAS | KHV | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02135 | hp1 | a0002 | c0002 | t0001 | g0096 | EAS | KHV | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02145 | hp1 | a0001 | c0010 | t0001 | g0306 | AFR | ACB | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02145 | hp2 | a0011 | c0015 | t0001 | g0262 | AFR | ACB | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02148 | hp2 | a0002 | c0002 | t0001 | g0112 | AMR | PEL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0094 | EAS | CDX | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | CDX | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0125 | EAS | CDX | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02257 | hp1 | a0011 | c0015 | t0001 | g0023 | AFR | ACB | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02257 | hp2 | a0002 | c0006 | t0001 | g0040 | AFR | ACB | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02258 | hp2 | a0004 | c0004 | t0001 | g0227 | AFR | ACB | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02273 | hp1 | a0002 | c0002 | t0001 | g0243 | AMR | PEL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02273 | hp2 | a0013 | c0016 | t0001 | g0118 | AMR | PEL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02280 | hp2 | a0004 | c0004 | t0001 | g0011 | AFR | ACB | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0111 | AMR | PEL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02300 | hp2 | a0007 | c0009 | t0001 | g0247 | AMR | PEL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02451 | hp1 | a0022 | c0041 | t0003 | g0031 | AFR | ACB | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02451 | hp2 | a0001 | c0017 | t0002 | g0234 | AFR | ACB | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02523 | hp2 | a0003 | c0003 | t0001 | g0237 | EAS | KHV | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02572 | hp1 | a0003 | c0003 | t0001 | g0071 | AFR | GWD | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02615 | hp1 | a0004 | c0026 | t0001 | g0228 | AFR | GWD | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02615 | hp2 | a0001 | c0001 | t0005 | g0186 | AFR | GWD | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | GWD | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02630 | hp1 | a0010 | c0018 | t0001 | g0274 | AFR | GWD | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02630 | hp2 | a0017 | c0020 | t0001 | g0233 | AFR | GWD | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02647 | hp2 | a0014 | c0023 | t0001 | g0303 | AFR | GWD | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02683 | hp1 | a0013 | c0016 | t0001 | g0035 | SAS | PJL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0104 | SAS | PJL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02717 | hp1 | a0001 | c0010 | t0001 | g0307 | AFR | GWD | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02717 | hp2 | a0023 | c0036 | t0001 | g0259 | AFR | GWD | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02738 | hp2 | a0002 | c0002 | t0001 | g0014 | SAS | PJL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02809 | hp1 | a0004 | c0004 | t0001 | g0229 | AFR | GWD | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02818 | hp1 | a0024 | c0055 | t0001 | g0305 | AFR | GWD | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02818 | hp2 | a0025 | c0053 | t0001 | g0298 | AFR | GWD | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02886 | hp2 | a0018 | c0021 | t0001 | g0197 | AFR | GWD | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02895 | hp1 | a0001 | c0005 | t0001 | g0257 | AFR | GWD | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02895 | hp2 | a0004 | c0004 | t0001 | g0231 | AFR | GWD | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02896 | hp1 | a0001 | c0028 | t0001 | g0273 | AFR | GWD | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02897 | hp1 | a0004 | c0004 | t0001 | g0230 | AFR | GWD | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02965 | hp1 | a0011 | c0015 | t0001 | g0068 | AFR | ESN | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02965 | hp2 | a0002 | c0038 | t0001 | g0107 | AFR | ESN | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | ESN | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03041 | hp2 | a0001 | c0005 | t0001 | g0258 | AFR | GWD | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03098 | hp1 | a0003 | c0030 | t0004 | g0266 | AFR | MSL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03098 | hp2 | a0001 | c0005 | t0001 | g0299 | AFR | MSL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03130 | hp1 | a0004 | c0004 | t0001 | g0026 | AFR | ESN | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03130 | hp2 | a0001 | c0005 | t0001 | g0256 | AFR | ESN | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03139 | hp1 | a0011 | c0015 | t0001 | g0023 | AFR | ESN | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03139 | hp2 | a0010 | c0018 | t0001 | g0275 | AFR | ESN | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ESN | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03195 | hp2 | a0003 | c0019 | t0001 | g0131 | AFR | ESN | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03209 | hp1 | a0010 | c0018 | t0001 | g0073 | AFR | MSL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | MSL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03225 | hp1 | a0018 | c0021 | t0001 | g0190 | AFR | MSL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | MSL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03239 | hp1 | a0002 | c0006 | t0001 | g0277 | SAS | PJL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03453 | hp2 | a0003 | c0003 | t0001 | g0269 | AFR | MSL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03486 | hp1 | a0001 | c0029 | t0001 | g0301 | AFR | MSL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03486 | hp2 | a0014 | c0023 | t0001 | g0309 | AFR | MSL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03491 | hp1 | a0019 | c0025 | t0001 | g0126 | SAS | PJL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0288 | SAS | PJL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03492 | hp2 | a0019 | c0025 | t0001 | g0127 | SAS | PJL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03516 | hp1 | a0026 | c0059 | t0001 | g0076 | AFR | ESN | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03516 | hp2 | a0001 | c0005 | t0001 | g0263 | AFR | ESN | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03540 | hp2 | a0003 | c0035 | t0001 | g0240 | AFR | GWD | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | MSL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03579 | hp2 | a0001 | c0005 | t0001 | g0260 | AFR | MSL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0279 | SAS | PJL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03669 | hp1 | a0002 | c0002 | t0001 | g0037 | SAS | PJL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03704 | hp1 | a0002 | c0006 | t0001 | g0101 | SAS | PJL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | BEB | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03831 | hp2 | a0001 | c0046 | t0001 | g0290 | SAS | BEB | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03834 | hp2 | a0002 | c0002 | t0001 | g0151 | SAS | BEB | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03927 | hp2 | a0002 | c0002 | t0001 | g0086 | SAS | BEB | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0090 | SAS | STU | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | STU | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG04184 | hp1 | a0003 | c0003 | t0001 | g0238 | SAS | BEB | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG04184 | hp2 | a0002 | c0002 | t0001 | g0095 | SAS | BEB | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG04199 | hp1 | a0002 | c0002 | t0001 | g0120 | SAS | STU | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG04199 | hp2 | a0002 | c0002 | t0001 | g0099 | SAS | STU | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0079 | SAS | STU | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG04204 | hp2 | a0001 | c0011 | t0001 | g0215 | SAS | STU | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG04228 | hp1 | a0002 | c0002 | t0001 | g0013 | SAS | STU | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG04228 | hp2 | a0008 | c0013 | t0001 | g0072 | SAS | STU | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | YRI | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18612 | hp1 | a0027 | c0058 | t0001 | g0165 | EAS | CHB | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHB | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | CHB | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18747 | hp2 | a0005 | c0007 | t0001 | g0019 | EAS | CHB | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18906 | hp1 | a0004 | c0004 | t0001 | g0026 | AFR | YRI | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18906 | hp2 | a0014 | c0056 | t0001 | g0304 | AFR | YRI | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18940 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18942 | hp1 | a0006 | c0008 | t0001 | g0032 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18942 | hp2 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18944 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18945 | hp1 | a0002 | c0002 | t0001 | g0092 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18947 | hp2 | a0001 | c0011 | t0001 | g0138 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18951 | hp1 | a0006 | c0008 | t0001 | g0141 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18959 | hp1 | a0002 | c0002 | t0001 | g0087 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18962 | hp2 | a0005 | c0007 | t0001 | g0056 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18964 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18964 | hp2 | a0006 | c0008 | t0001 | g0132 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18966 | hp1 | a0005 | c0007 | t0001 | g0019 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18969 | hp1 | a0009 | c0012 | t0001 | g0033 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18971 | hp1 | a0002 | c0039 | t0001 | g0149 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18975 | hp1 | a0005 | c0007 | t0001 | g0001 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18983 | hp1 | a0009 | c0012 | t0001 | g0034 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18986 | hp2 | a0006 | c0008 | t0001 | g0136 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18988 | hp1 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18990 | hp1 | a0005 | c0007 | t0001 | g0001 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18990 | hp2 | a0001 | c0011 | t0001 | g0155 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18992 | hp1 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18992 | hp2 | a0012 | c0014 | t0001 | g0175 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18995 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA19000 | hp1 | a0006 | c0008 | t0001 | g0135 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA19002 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA19003 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA19004 | hp1 | a0006 | c0008 | t0001 | g0145 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA19007 | hp1 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA19009 | hp2 | a0002 | c0051 | t0001 | g0158 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA19030 | hp1 | a0017 | c0020 | t0001 | g0232 | AFR | LWK | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | LWK | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA19043 | hp1 | a0028 | c0043 | t0001 | g0069 | AFR | LWK | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA19043 | hp2 | a0029 | c0054 | t0001 | g0140 | AFR | LWK | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA19054 | hp1 | a0009 | c0012 | t0001 | g0067 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA19054 | hp2 | a0005 | c0007 | t0001 | g0280 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA19057 | hp1 | a0002 | c0006 | t0001 | g0036 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA19063 | hp2 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA19066 | hp2 | a0012 | c0014 | t0001 | g0003 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA19068 | hp1 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA19068 | hp2 | a0012 | c0014 | t0001 | g0003 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA19077 | hp1 | a0006 | c0008 | t0001 | g0044 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA19077 | hp2 | a0001 | c0057 | t0001 | g0218 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA19081 | hp1 | a0009 | c0012 | t0001 | g0066 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA19081 | hp2 | a0001 | c0044 | t0001 | g0217 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA19085 | hp1 | a0012 | c0014 | t0001 | g0003 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA19088 | hp2 | a0001 | c0047 | t0001 | g0002 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA19240 | hp1 | a0001 | c0042 | t0001 | g0302 | AFR | YRI | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA19240 | hp2 | a0001 | c0005 | t0001 | g0264 | AFR | YRI | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA20129 | hp1 | a0004 | c0004 | t0001 | g0011 | AFR | ASW | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ASW | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | TSI | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA20905 | hp1 | a0001 | c0010 | t0006 | g0030 | SAS | GIH | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA20905 | hp2 | a0008 | c0013 | t0001 | g0075 | SAS | GIH | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG01123 | hp2 | a0003 | c0003 | t0001 | g0295 | AMR | CLM | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02109 | hp2 | a0003 | c0019 | t0001 | g0239 | AFR | ACB | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02486 | hp2 | a0008 | c0013 | t0001 | g0074 | AFR | ACB | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG02559 | hp2 | a0003 | c0031 | t0001 | g0276 | AFR | ACB | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03471 | hp1 | a0003 | c0003 | t0001 | g0070 | AFR | MSL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG03471 | hp2 | a0001 | c0017 | t0002 | g0293 | AFR | MSL | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG06807 | hp1 | a0004 | c0004 | t0001 | g0011 | AFR | USA | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
HG06807 | hp2 | a0001 | c0017 | t0002 | g0294 | AFR | USA | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18955 | hp1 | a0001 | c0011 | t0001 | g0137 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA20300 | hp1 | a0002 | c0006 | t0001 | g0119 | AFR | USA | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA20300 | hp2 | a0001 | c0005 | t0001 | g0255 | AFR | USA | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA21309 | hp1 | a0030 | c0045 | t0001 | g0187 | AFR | LWK | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | LWK | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0009 | REF | REF | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0261 | REF | REF | ADAMTS13_chr9_133417367_133464386 | ADAMTS13 | chr9 | 133417367 | 133464386 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:133422462 | C | T | 5 | a0008 a0010 a0015 others(2): Show |
14 | HG00280.hp2 HG00733.hp2 HG01069.hp2 others(11): Show |
missense_variant | MODERATE | c.19C>T | p.Arg7Trp | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 1/29 | 96/4399 | 19/4116 | 7/1371 | chr9 | 133422462 | |||
chr9:133426023 | C | T | 1 | a0017 | 2 | HG02630.hp2 NA19030.hp1 |
missense_variant | MODERATE | c.500C>T | p.Thr167Met | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 5/29 | 577/4399 | 500/4116 | 167/1371 | chr9 | 133426023 | |||
chr9:133426053 | A | G | 1 | a0027 | 1 | NA18612.hp1 | missense_variant | MODERATE | c.530A>G | p.Tyr177Cys | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 5/29 | 607/4399 | 530/4116 | 177/1371 | chr9 | 133426053 | |||
chr9:133432616 | C | G | 1 | a0009 | 5 | HG00423.hp2 NA18969.hp1 NA18983.hp1 others(2): Show |
missense_variant | MODERATE | c.1016C>G | p.Thr339Arg | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 9/29 | 1093/4399 | 1016/4116 | 339/1371 | chr9 | 133432616 | |||
chr9:133432622 | C | T | 1 | a0029 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.1022C>T | p.Pro341Leu | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 9/29 | 1099/4399 | 1022/4116 | 341/1371 | chr9 | 133432622 | |||
chr9:133433441 | C | T | 1 | a0022 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.1156C>T | p.Arg386Cys | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 10/29 | 1233/4399 | 1156/4116 | 386/1371 | chr9 | 133433441 | |||
chr9:133436862 | C | G | 6 | a0002 a0009 a0013 others(3): Show |
88 | HG00423.hp2 HG00609.hp1 HG00639.hp2 others(85): Show |
missense_variant | MODERATE | c.1342C>G | p.Gln448Glu | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 12/29 | 1419/4399 | 1342/4116 | 448/1371 | chr9 | 133436862 | |||
chr9:133436888 | G | T | 3 | a0011 a0014 a0024 |
8 | HG02145.hp2 HG02257.hp1 HG02647.hp2 others(5): Show |
missense_variant | MODERATE | c.1368G>T | p.Gln456His | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 12/29 | 1445/4399 | 1368/4116 | 456/1371 | chr9 | 133436888 | |||
chr9:133436943 | C | T | 1 | a0006 | 7 | NA18942.hp1 NA18951.hp1 NA18964.hp2 others(4): Show |
missense_variant | MODERATE | c.1423C>T | p.Pro475Ser | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 12/29 | 1500/4399 | 1423/4116 | 475/1371 | chr9 | 133436943 | |||
chr9:133437812 | A | C | 1 | a0023 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.1499A>C | p.Asp500Ala | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 13/29 | 1576/4399 | 1499/4116 | 500/1371 | chr9 | 133437812 | |||
chr9:133440409 | C | G | 3 | a0009 a0015 a0019 |
9 | HG00423.hp2 HG01069.hp2 HG01071.hp1 others(6): Show |
missense_variant | MODERATE | c.1852C>G | p.Pro618Ala | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 16/29 | 1929/4399 | 1852/4116 | 618/1371 | chr9 | 133440409 | |||
chr9:133440431 | G | A | 1 | a0004 | 10 | HG02258.hp2 HG02280.hp2 HG02615.hp1 others(7): Show |
missense_variant | MODERATE | c.1874G>A | p.Arg625His | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 16/29 | 1951/4399 | 1874/4116 | 625/1371 | chr9 | 133440431 | |||
chr9:133442676 | C | A | 1 | a0012 | 4 | NA18992.hp2 NA19066.hp2 NA19068.hp2 others(1): Show |
missense_variant | MODERATE | c.2167C>A | p.Gln723Lys | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 18/29 | 2244/4399 | 2167/4116 | 723/1371 | chr9 | 133442676 | |||
chr9:133442727 | G | A | 2 | a0014 a0024 |
4 | HG02647.hp2 HG02818.hp1 HG03486.hp2 others(1): Show |
missense_variant | MODERATE | c.2218G>A | p.Glu740Lys | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 18/29 | 2295/4399 | 2218/4116 | 740/1371 | chr9 | 133442727 | |||
chr9:133444987 | G | A | 1 | a0030 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.2545G>A | p.Val849Ile | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 20/29 | 2622/4399 | 2545/4116 | 849/1371 | chr9 | 133444987 | |||
chr9:133445787 | C | T | 4 | a0003 a0019 a0022 others(1): Show |
22 | HG00280.hp1 HG00323.hp1 HG00735.hp1 others(19): Show |
missense_variant | MODERATE | c.2699C>T | p.Ala900Val | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 21/29 | 2776/4399 | 2699/4116 | 900/1371 | chr9 | 133445787 | |||
chr9:133445796 | C | T | 1 | a0005 | 8 | HG00558.hp2 HG02129.hp2 NA18747.hp2 others(5): Show |
missense_variant | MODERATE | c.2708C>T | p.Ser903Leu | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 21/29 | 2785/4399 | 2708/4116 | 903/1371 | chr9 | 133445796 | |||
chr9:133449811 | G | A | 1 | a0028 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.2890G>A | p.Val964Met | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/29 | 2967/4399 | 2890/4116 | 964/1371 | chr9 | 133449811 | |||
chr9:133454467 | G | A | 2 | a0008 a0016 |
7 | HG00280.hp2 HG00733.hp2 HG01167.hp1 others(4): Show |
missense_variant | MODERATE | c.3097G>A | p.Ala1033Thr | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 24/29 | 3174/4399 | 3097/4116 | 1033/1371 | chr9 | 133454467 | |||
chr9:133454537 | C | G | 1 | a0028 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.3167C>G | p.Ala1056Gly | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 24/29 | 3244/4399 | 3167/4116 | 1056/1371 | chr9 | 133454537 | |||
chr9:133455322 | G | A | 2 | a0007 a0013 |
9 | HG00741.hp2 HG01074.hp1 HG01099.hp1 others(6): Show |
missense_variant | MODERATE | c.3287G>A | p.Arg1096His | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 25/29 | 3364/4399 | 3287/4116 | 1096/1371 | chr9 | 133455322 | |||
chr9:133456213 | C | T | 1 | a0021 | 1 | HG00639.hp1 | missense_variant&splice_region_variant | MODERATE | c.3545C>T | p.Ala1182Val | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 26/29 | 3622/4399 | 3545/4116 | 1182/1371 | chr9 | 133456213 | |||
chr9:133456653 | G | A | 3 | a0018 a0024 a0025 |
4 | HG02818.hp1 HG02818.hp2 HG02886.hp2 others(1): Show |
missense_variant | MODERATE | c.3658G>A | p.Gly1220Arg | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 27/29 | 3735/4399 | 3658/4116 | 1220/1371 | chr9 | 133456653 | |||
chr9:133457958 | C | T | 1 | a0020 | 1 | HG00558.hp1 | missense_variant | MODERATE | c.3773C>T | p.Ser1258Leu | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 28/29 | 3850/4399 | 3773/4116 | 1258/1371 | chr9 | 133457958 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:133425552 | G | A | 2 | a0015c0024 a0019c0025 |
4 | HG01069.hp2 HG01071.hp1 HG03491.hp1 others(1): Show |
synonymous_variant | LOW | c.354G>A | p.Pro118Pro | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 4/29 | 431/4399 | 354/4116 | 118/1371 | chr9 | 133425552 | |||
chr9:133425555 | C | T | 1 | a0001c0017 | 3 | HG02451.hp2 HG03471.hp2 HG06807.hp2 |
synonymous_variant | LOW | c.357C>T | p.Ser119Ser | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 4/29 | 434/4399 | 357/4116 | 119/1371 | chr9 | 133425555 | |||
chr9:133425943 | T | C | 28 | a0001c0005 a0001c0017 a0001c0027 others(25): Show |
133 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(130): Show |
synonymous_variant | LOW | c.420T>C | p.Ala140Ala | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 5/29 | 497/4399 | 420/4116 | 140/1371 | chr9 | 133425943 | |||
chr9:133426205 | C | T | 1 | a0001c0057 | 1 | NA19077.hp2 | synonymous_variant | LOW | c.546C>T | p.Asp182Asp | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 6/29 | 623/4399 | 546/4116 | 182/1371 | chr9 | 133426205 | |||
chr9:133426241 | C | T | 2 | a0015c0024 a0019c0025 |
4 | HG01069.hp2 HG01071.hp1 HG03491.hp1 others(1): Show |
synonymous_variant | LOW | c.582C>T | p.Gly194Gly | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 6/29 | 659/4399 | 582/4116 | 194/1371 | chr9 | 133426241 | |||
chr9:133430050 | C | T | 4 | a0011c0015 a0014c0023 a0014c0056 others(1): Show |
8 | HG02145.hp2 HG02257.hp1 HG02647.hp2 others(5): Show |
synonymous_variant | LOW | c.936C>T | p.Arg312Arg | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/29 | 1013/4399 | 936/4116 | 312/1371 | chr9 | 133430050 | |||
chr9:133439376 | G | A | 40 | a0001c0005 a0001c0017 a0001c0027 others(37): Show |
155 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
synonymous_variant | LOW | c.1716G>A | p.Thr572Thr | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 15/29 | 1793/4399 | 1716/4116 | 572/1371 | chr9 | 133439376 | |||
chr9:133440354 | C | T | 3 | a0014c0023 a0014c0056 a0024c0055 |
4 | HG02647.hp2 HG02818.hp1 HG03486.hp2 others(1): Show |
synonymous_variant | LOW | c.1797C>T | p.Ile599Ile | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 16/29 | 1874/4399 | 1797/4116 | 599/1371 | chr9 | 133440354 | |||
chr9:133440387 | C | T | 2 | a0003c0019 a0003c0035 |
3 | HG02109.hp2 HG03195.hp2 HG03540.hp2 |
synonymous_variant | LOW | c.1830C>T | p.Ser610Ser | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 16/29 | 1907/4399 | 1830/4116 | 610/1371 | chr9 | 133440387 | |||
chr9:133440456 | C | T | 2 | a0002c0040 a0025c0053 |
2 | HG01891.hp2 HG02818.hp2 |
synonymous_variant | LOW | c.1899C>T | p.Thr633Thr | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 16/29 | 1976/4399 | 1899/4116 | 633/1371 | chr9 | 133440456 | |||
chr9:133443421 | T | C | 41 | a0001c0005 a0001c0010 a0001c0017 others(38): Show |
160 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
synonymous_variant | LOW | c.2280T>C | p.Gly760Gly | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 19/29 | 2357/4399 | 2280/4116 | 760/1371 | chr9 | 133443421 | |||
chr9:133444950 | T | C | 5 | a0001c0027 a0001c0028 a0014c0023 others(2): Show |
6 | HG01109.hp1 HG02647.hp2 HG02818.hp1 others(3): Show |
synonymous_variant | LOW | c.2508T>C | p.Asp836Asp | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 20/29 | 2585/4399 | 2508/4116 | 836/1371 | chr9 | 133444950 | |||
chr9:133445022 | C | T | 1 | a0001c0050 | 1 | HG00099.hp2 | synonymous_variant | LOW | c.2580C>T | p.Val860Val | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 20/29 | 2657/4399 | 2580/4116 | 860/1371 | chr9 | 133445022 | |||
chr9:133449831 | C | T | 2 | a0008c0013 a0016c0022 |
7 | HG00280.hp2 HG00733.hp2 HG01167.hp1 others(4): Show |
synonymous_variant | LOW | c.2910C>T | p.Val970Val | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/29 | 2987/4399 | 2910/4116 | 970/1371 | chr9 | 133449831 | |||
chr9:133454478 | G | A | 2 | a0002c0037 a0015c0024 |
3 | HG01069.hp2 HG01071.hp1 HG01975.hp1 |
synonymous_variant | LOW | c.3108G>A | p.Ser1036Ser | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 24/29 | 3185/4399 | 3108/4116 | 1036/1371 | chr9 | 133454478 | |||
chr9:133454520 | G | A | 1 | a0003c0030 | 1 | HG03098.hp1 | synonymous_variant | LOW | c.3150G>A | p.Val1050Val | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 24/29 | 3227/4399 | 3150/4116 | 1050/1371 | chr9 | 133454520 | |||
chr9:133454529 | G | A | 1 | a0001c0046 | 1 | HG03831.hp2 | synonymous_variant | LOW | c.3159G>A | p.Ala1053Ala | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 24/29 | 3236/4399 | 3159/4116 | 1053/1371 | chr9 | 133454529 | |||
chr9:133454541 | G | A | 1 | a0003c0031 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.3171G>A | p.Ala1057Ala | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 24/29 | 3248/4399 | 3171/4116 | 1057/1371 | chr9 | 133454541 | |||
chr9:133455383 | G | A | 1 | a0028c0043 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.3348G>A | p.Leu1116Leu | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 25/29 | 3425/4399 | 3348/4116 | 1116/1371 | chr9 | 133455383 | |||
chr9:133456673 | G | A | 5 | a0001c0027 a0002c0038 a0003c0032 others(2): Show |
6 | HG01081.hp2 HG01109.hp1 HG02615.hp1 others(3): Show |
synonymous_variant | LOW | c.3678G>A | p.Val1226Val | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 27/29 | 3755/4399 | 3678/4116 | 1226/1371 | chr9 | 133456673 | |||
chr9:133458082 | C | A | 1 | a0003c0035 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.3897C>A | p.Ala1299Ala | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 28/29 | 3974/4399 | 3897/4116 | 1299/1371 | chr9 | 133458082 | |||
chr9:133459000 | C | G | 1 | a0002c0039 | 1 | NA18971.hp1 | synonymous_variant | LOW | c.3936C>G | p.Thr1312Thr | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 29/29 | 4013/4399 | 3936/4116 | 1312/1371 | chr9 | 133459000 | |||
chr9:133459093 | C | T | 1 | a0001c0047 | 1 | NA19088.hp2 | synonymous_variant | LOW | c.4029C>T | p.Ala1343Ala | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 29/29 | 4106/4399 | 4029/4116 | 1343/1371 | chr9 | 133459093 | |||
chr9:133459117 | C | A | 7 | a0001c0011 a0001c0029 a0001c0044 others(4): Show |
71 | HG00609.hp2 HG00639.hp2 HG00642.hp1 others(68): Show |
synonymous_variant | LOW | c.4053C>A | p.Thr1351Thr | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 29/29 | 4130/4399 | 4053/4116 | 1351/1371 | chr9 | 133459117 | |||
chr9:133459135 | G | A | 1 | a0003c0033 | 1 | HG01167.hp2 | synonymous_variant | LOW | c.4071G>A | p.Pro1357Pro | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 29/29 | 4148/4399 | 4071/4116 | 1357/1371 | chr9 | 133459135 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:133422392 | C | G | 1 | a0001c0010t0006 | 1 | NA20905.hp1 | 5_prime_UTR_variant | MODIFIER | c.-52C>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 1/29 | 52 | chr9 | 133422392 | ||||||
chr9:133459257 | C | T | 1 | a0001c0001t0005 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*77C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 29/29 | 77 | chr9 | 133459257 | ||||||
chr9:133459260 | T | C | 1 | a0022c0041t0003 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*80T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 29/29 | 80 | chr9 | 133459260 | ||||||
chr9:133459317 | T | C | 1 | a0003c0030t0004 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*137T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 29/29 | 137 | chr9 | 133459317 | ||||||
chr9:133459348 | C | T | 2 | a0001c0017t0002 a0003c0033t0002 |
4 | HG01167.hp2 HG02451.hp2 HG03471.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*168C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 29/29 | 168 | chr9 | 133459348 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:133422569 | G | A | 1 | a0001c0001t0001g0027 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.105+21G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 1/28 | chr9 | 133422569 | |||||||
chr9:133422800 | G | C | 1 | a0001c0001t0001g0028 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.105+252G>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 1/28 | chr9 | 133422800 | |||||||
chr9:133422814 | C | G | 7 | a0001c0001t0001g0308 a0001c0010t0001g0306 a0001c0010t0001g0307 others(4): Show |
7 | HG02145.hp1 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.105+266C>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 1/28 | chr9 | 133422814 | |||||||
chr9:133422847 | C | T | 1 | a0001c0042t0001g0302 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.106-254C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 1/28 | chr9 | 133422847 | |||||||
chr9:133422897 | T | C | 1 | a0001c0001t0001g0029 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.106-204T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 1/28 | chr9 | 133422897 | |||||||
chr9:133422934 | C | CT | 24 | a0001c0001t0001g0025 a0001c0001t0001g0281 a0001c0001t0001g0282 others(21): Show |
27 | HG00558.hp1 HG00621.hp1 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.106-144dupT | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr9 | 133422934 | ||||||
chr9:133422934 | C | T | 1 | a0001c0029t0001g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.106-167C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 1/28 | chr9 | 133422934 | |||||||
chr9:133422934 | CT | C | 93 | a0001c0001t0001g0043 a0001c0001t0001g0046 a0001c0001t0001g0047 others(90): Show |
103 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.106-144delT | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr9 | 133422934 | ||||||
chr9:133422934 | CTT | C | 11 | a0001c0001t0001g0042 a0002c0002t0001g0037 a0002c0002t0001g0038 others(8): Show |
11 | HG01070.hp2 HG02004.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.106-145_106-144del others(2): Show |
ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr9 | 133422934 | ||||||
chr9:133422934 | CTTTTTTT others(3): Show |
C | 1 | a0022c0041t0003g0031 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.106-153_106-144del others(10): Show |
ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr9 | 133422934 | ||||||
chr9:133422936 | T | C | 1 | a0001c0010t0006g0030 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.106-165T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 1/28 | chr9 | 133422936 | |||||||
chr9:133422967 | G | T | 1 | a0005c0007t0001g0280 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.106-134G>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 1/28 | chr9 | 133422967 | |||||||
chr9:133423072 | G | A | 1 | a0001c0001t0001g0043 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.106-29G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 1/28 | chr9 | 133423072 | |||||||
chr9:133423073 | G | T | 1 | a0005c0007t0001g0280 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.106-28G>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 1/28 | chr9 | 133423073 | |||||||
chr9:133423624 | C | T | 1 | a0002c0002t0001g0125 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.172+457C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 2/28 | chr9 | 133423624 | |||||||
chr9:133423676 | G | A | 3 | a0015c0024t0001g0024 a0019c0025t0001g0126 a0019c0025t0001g0127 |
4 | HG01069.hp2 HG01071.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.172+509G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 2/28 | chr9 | 133423676 | |||||||
chr9:133423720 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.172+553G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 2/28 | chr9 | 133423720 | |||||||
chr9:133423787 | G | A | 1 | a0022c0041t0003g0031 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.173-534G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 2/28 | chr9 | 133423787 | |||||||
chr9:133423809 | C | T | 65 | a0001c0001t0001g0042 a0001c0001t0001g0121 a0001c0001t0001g0122 others(62): Show |
74 | HG00609.hp1 HG00639.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.173-512C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 2/28 | chr9 | 133423809 | |||||||
chr9:133423814 | T | C | 3 | a0001c0001t0001g0029 a0001c0001t0001g0129 a0001c0001t0001g0130 |
3 | HG00408.hp2 NA18983.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.173-507T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 2/28 | chr9 | 133423814 | |||||||
chr9:133423851 | C | T | 1 | a0003c0031t0001g0276 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.173-470C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 2/28 | chr9 | 133423851 | |||||||
chr9:133423852 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.173-469G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 2/28 | chr9 | 133423852 | |||||||
chr9:133423921 | G | A | 1 | a0003c0019t0001g0131 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.173-400G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 2/28 | chr9 | 133423921 | |||||||
chr9:133424110 | C | G | 9 | a0002c0040t0001g0300 a0008c0013t0001g0012 a0008c0013t0001g0072 others(6): Show |
10 | HG00280.hp2 HG00733.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.173-211C>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 2/28 | chr9 | 133424110 | |||||||
chr9:133424172 | A | G | 11 | a0001c0027t0001g0272 a0001c0028t0001g0273 a0002c0040t0001g0300 others(8): Show |
11 | HG00735.hp1 HG01081.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.173-149A>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 2/28 | chr9 | 133424172 | |||||||
chr9:133424252 | C | T | 3 | a0001c0005t0001g0263 a0001c0005t0001g0264 a0001c0005t0001g0265 |
3 | HG01884.hp1 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.173-69C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 2/28 | chr9 | 133424252 | |||||||
chr9:133424254 | T | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.173-67T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 2/28 | chr9 | 133424254 | |||||||
chr9:133424273 | G | A | 3 | a0015c0024t0001g0024 a0019c0025t0001g0126 a0019c0025t0001g0127 |
4 | HG01069.hp2 HG01071.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.173-48G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 2/28 | chr9 | 133424273 | |||||||
chr9:133424303 | C | T | 3 | a0015c0024t0001g0024 a0019c0025t0001g0126 a0019c0025t0001g0127 |
4 | HG01069.hp2 HG01071.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.173-18C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 2/28 | chr9 | 133424303 | |||||||
chr9:133424860 | C | T | 34 | a0001c0001t0001g0308 a0001c0010t0001g0306 a0001c0010t0001g0307 others(31): Show |
36 | HG00280.hp2 HG00423.hp2 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.330+382C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 3/28 | chr9 | 133424860 | |||||||
chr9:133424872 | C | T | 1 | a0001c0001t0001g0308 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.330+394C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 3/28 | chr9 | 133424872 | |||||||
chr9:133424982 | C | G | 1 | a0001c0042t0001g0302 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.330+504C>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 3/28 | chr9 | 133424982 | |||||||
chr9:133425034 | G | T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0250 a0001c0001t0001g0251 others(5): Show |
13 | NA18947.hp1 NA18962.hp1 NA18974.hp2 others(10): Show |
intron_variant | MODIFIER | c.331-495G>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 3/28 | chr9 | 133425034 | |||||||
chr9:133425034 | GACAA | G | 7 | a0001c0001t0001g0249 a0002c0002t0001g0243 a0007c0009t0001g0244 others(4): Show |
7 | HG01074.hp1 HG01099.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.331-490_331-487del others(4): Show |
ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 3/28 | INFO_REALIGN_3_PRIME | chr9 | 133425034 | ||||||
chr9:133425221 | C | T | 1 | a0003c0003t0001g0296 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.331-308C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 3/28 | chr9 | 133425221 | |||||||
chr9:133425304 | T | C | 1 | a0006c0008t0001g0132 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.331-225T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 3/28 | chr9 | 133425304 | |||||||
chr9:133425309 | T | C | 2 | a0001c0001t0001g0133 a0003c0031t0001g0276 |
2 | HG01255.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.331-220T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 3/28 | chr9 | 133425309 | |||||||
chr9:133425390 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.331-139C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 3/28 | chr9 | 133425390 | |||||||
chr9:133425415 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.331-114T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 3/28 | chr9 | 133425415 | |||||||
chr9:133425487 | T | C | 27 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0139 others(24): Show |
34 | HG02015.hp1 HG02015.hp2 HG02040.hp2 others(31): Show |
intron_variant | MODIFIER | c.331-42T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 3/28 | chr9 | 133425487 | |||||||
chr9:133425496 | G | A | 1 | a0002c0002t0001g0077 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.331-33G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 3/28 | chr9 | 133425496 | |||||||
chr9:133425674 | C | T | 2 | a0001c0001t0001g0027 a0001c0001t0001g0064 |
2 | HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.414+62C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 4/28 | chr9 | 133425674 | |||||||
chr9:133425873 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0124 |
2 | HG02602.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.415-65C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 4/28 | chr9 | 133425873 | |||||||
chr9:133425889 | C | T | 1 | a0001c0010t0006g0030 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.415-49C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 4/28 | chr9 | 133425889 | |||||||
chr9:133426122 | T | G | 1 | a0001c0005t0001g0255 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.539+60T>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 5/28 | chr9 | 133426122 | |||||||
chr9:133426180 | A | C | 1 | a0001c0001t0001g0241 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.540-19A>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 5/28 | chr9 | 133426180 | |||||||
chr9:133426349 | T | G | 3 | a0015c0024t0001g0024 a0019c0025t0001g0126 a0019c0025t0001g0127 |
4 | HG01069.hp2 HG01071.hp1 HG03491.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.686+4T>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 6/28 | chr9 | 133426349 | |||||||
chr9:133426419 | G | A | 2 | a0001c0005t0001g0256 a0001c0005t0001g0299 |
2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.686+74G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 6/28 | chr9 | 133426419 | |||||||
chr9:133426453 | G | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0282 |
2 | HG02970.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.686+108G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 6/28 | chr9 | 133426453 | |||||||
chr9:133426474 | G | A | 68 | a0002c0002t0001g0004 a0002c0002t0001g0006 a0002c0002t0001g0007 others(65): Show |
79 | HG00609.hp1 HG00639.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.686+129G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 6/28 | chr9 | 133426474 | |||||||
chr9:133426501 | A | T | 65 | a0002c0002t0001g0004 a0002c0002t0001g0006 a0002c0002t0001g0007 others(62): Show |
75 | HG00609.hp1 HG00639.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.686+156A>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 6/28 | chr9 | 133426501 | |||||||
chr9:133426793 | TTTTTC | T | 5 | a0009c0012t0001g0033 a0009c0012t0001g0034 a0009c0012t0001g0065 others(2): Show |
5 | HG00423.hp2 NA18969.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.686+463_686+467del others(5): Show |
ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chr9 | 133426793 | ||||||
chr9:133426808 | C | CTT | 6 | a0004c0004t0001g0011 a0004c0004t0001g0026 a0004c0004t0001g0227 others(3): Show |
9 | HG02258.hp2 HG02280.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.686+474_686+475dup others(2): Show |
ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chr9 | 133426808 | ||||||
chr9:133426808 | CT | C | 72 | a0001c0001t0001g0008 a0001c0001t0001g0051 a0001c0001t0001g0170 others(69): Show |
83 | HG00609.hp1 HG00639.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.686+475delT | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chr9 | 133426808 | ||||||
chr9:133426901 | G | T | 68 | a0002c0002t0001g0004 a0002c0002t0001g0006 a0002c0002t0001g0007 others(65): Show |
79 | HG00609.hp1 HG00639.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.686+556G>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 6/28 | chr9 | 133426901 | |||||||
chr9:133427302 | C | A | 1 | a0001c0001t0001g0152 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.686+957C>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 6/28 | chr9 | 133427302 | |||||||
chr9:133427322 | G | A | 1 | a0002c0006t0001g0277 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.686+977G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 6/28 | chr9 | 133427322 | |||||||
chr9:133427440 | C | G | 1 | a0001c0001t0001g0063 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.686+1095C>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 6/28 | chr9 | 133427440 | |||||||
chr9:133427610 | A | G | 22 | a0001c0027t0001g0272 a0001c0028t0001g0273 a0001c0034t0001g0062 others(19): Show |
22 | HG00280.hp1 HG00323.hp1 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.687-1024A>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 6/28 | chr9 | 133427610 | |||||||
chr9:133427807 | TA | T | 117 | a0001c0017t0002g0234 a0001c0017t0002g0293 a0001c0017t0002g0294 others(114): Show |
132 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.687-825delA | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chr9 | 133427807 | ||||||
chr9:133427848 | T | G | 3 | a0015c0024t0001g0024 a0019c0025t0001g0126 a0019c0025t0001g0127 |
4 | HG01069.hp2 HG01071.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.687-786T>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 6/28 | chr9 | 133427848 | |||||||
chr9:133427946 | T | C | 81 | a0002c0002t0001g0004 a0002c0002t0001g0006 a0002c0002t0001g0007 others(78): Show |
95 | HG00423.hp2 HG00609.hp1 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.687-688T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 6/28 | chr9 | 133427946 | |||||||
chr9:133428001 | T | A | 1 | a0002c0002t0001g0078 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.687-633T>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 6/28 | chr9 | 133428001 | |||||||
chr9:133428039 | C | T | 6 | a0009c0012t0001g0033 a0009c0012t0001g0034 a0009c0012t0001g0065 others(3): Show |
6 | HG00423.hp2 HG02818.hp2 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.687-595C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 6/28 | chr9 | 133428039 | |||||||
chr9:133428156 | C | CG | 36 | a0001c0017t0002g0234 a0001c0017t0002g0293 a0001c0017t0002g0294 others(33): Show |
37 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.687-478_687-477ins others(1): Show |
ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 6/28 | chr9 | 133428156 | |||||||
chr9:133428157 | A | C | 36 | a0001c0017t0002g0234 a0001c0017t0002g0293 a0001c0017t0002g0294 others(33): Show |
37 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.687-477A>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 6/28 | chr9 | 133428157 | |||||||
chr9:133428188 | C | G | 7 | a0001c0001t0001g0308 a0001c0010t0001g0306 a0001c0010t0001g0307 others(4): Show |
7 | HG02145.hp1 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.687-446C>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 6/28 | chr9 | 133428188 | |||||||
chr9:133428264 | C | T | 3 | a0002c0002t0001g0120 a0002c0002t0001g0151 a0002c0006t0001g0119 |
3 | HG03834.hp2 HG04199.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.687-370C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 6/28 | chr9 | 133428264 | |||||||
chr9:133428373 | G | C | 2 | a0016c0022t0001g0045 a0016c0022t0001g0153 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.687-261G>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 6/28 | chr9 | 133428373 | |||||||
chr9:133428539 | G | T | 2 | a0004c0004t0001g0230 a0004c0004t0001g0231 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.687-95G>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 6/28 | chr9 | 133428539 | |||||||
chr9:133428590 | G | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0154 |
2 | HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.687-44G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 6/28 | chr9 | 133428590 | |||||||
chr9:133428783 | C | T | 1 | a0008c0013t0001g0075 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.824+12C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 7/28 | chr9 | 133428783 | |||||||
chr9:133428784 | C | T | 15 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0043 others(12): Show |
17 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(14): Show |
intron_variant | MODIFIER | c.824+13C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 7/28 | chr9 | 133428784 | |||||||
chr9:133428839 | C | T | 1 | a0001c0044t0001g0217 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.824+68C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 7/28 | chr9 | 133428839 | |||||||
chr9:133428869 | G | A | 4 | a0006c0008t0001g0044 a0006c0008t0001g0132 a0006c0008t0001g0135 others(1): Show |
4 | NA18964.hp2 NA18986.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.824+98G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 7/28 | chr9 | 133428869 | |||||||
chr9:133428882 | T | TCCCACCC others(10): Show |
3 | a0001c0011t0001g0155 a0001c0011t0001g0156 a0001c0044t0001g0217 |
3 | HG00609.hp2 NA18990.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.824+132_824+148dup others(17): Show |
ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr9 | 133428882 | ||||||
chr9:133428956 | C | G | 1 | a0001c0001t0001g0063 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.824+185C>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 7/28 | chr9 | 133428956 | |||||||
chr9:133429094 | A | C | 7 | a0004c0004t0001g0011 a0004c0004t0001g0026 a0004c0004t0001g0227 others(4): Show |
10 | HG02258.hp2 HG02280.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.824+323A>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 7/28 | chr9 | 133429094 | |||||||
chr9:133429096 | C | T | 7 | a0004c0004t0001g0011 a0004c0004t0001g0026 a0004c0004t0001g0227 others(4): Show |
10 | HG02258.hp2 HG02280.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.824+325C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 7/28 | chr9 | 133429096 | |||||||
chr9:133429099 | C | CGCT | 7 | a0004c0004t0001g0011 a0004c0004t0001g0026 a0004c0004t0001g0227 others(4): Show |
10 | HG02258.hp2 HG02280.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.824+330_824+331ins others(3): Show |
ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr9 | 133429099 | ||||||
chr9:133429108 | A | T | 7 | a0004c0004t0001g0011 a0004c0004t0001g0026 a0004c0004t0001g0227 others(4): Show |
10 | HG02258.hp2 HG02280.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.824+337A>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 7/28 | chr9 | 133429108 | |||||||
chr9:133429109 | G | C | 7 | a0004c0004t0001g0011 a0004c0004t0001g0026 a0004c0004t0001g0227 others(4): Show |
10 | HG02258.hp2 HG02280.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.824+338G>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 7/28 | chr9 | 133429109 | |||||||
chr9:133429112 | C | G | 7 | a0004c0004t0001g0011 a0004c0004t0001g0026 a0004c0004t0001g0227 others(4): Show |
10 | HG02258.hp2 HG02280.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.824+341C>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 7/28 | chr9 | 133429112 | |||||||
chr9:133429114 | GT | G | 7 | a0004c0004t0001g0011 a0004c0004t0001g0026 a0004c0004t0001g0227 others(4): Show |
10 | HG02258.hp2 HG02280.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.824+344delT | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 7/28 | chr9 | 133429114 | |||||||
chr9:133429120 | T | C | 78 | a0001c0017t0002g0234 a0001c0017t0002g0293 a0001c0017t0002g0294 others(75): Show |
91 | HG00609.hp1 HG00639.hp2 HG00642.hp1 others(88): Show |
intron_variant | MODIFIER | c.824+349T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 7/28 | chr9 | 133429120 | |||||||
chr9:133429124 | G | T | 7 | a0004c0004t0001g0011 a0004c0004t0001g0026 a0004c0004t0001g0227 others(4): Show |
10 | HG02258.hp2 HG02280.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.824+353G>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 7/28 | chr9 | 133429124 | |||||||
chr9:133429126 | T | C | 7 | a0004c0004t0001g0011 a0004c0004t0001g0026 a0004c0004t0001g0227 others(4): Show |
10 | HG02258.hp2 HG02280.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.824+355T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 7/28 | chr9 | 133429126 | |||||||
chr9:133429128 | C | T | 7 | a0004c0004t0001g0011 a0004c0004t0001g0026 a0004c0004t0001g0227 others(4): Show |
10 | HG02258.hp2 HG02280.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.824+357C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 7/28 | chr9 | 133429128 | |||||||
chr9:133429129 | G | C | 7 | a0004c0004t0001g0011 a0004c0004t0001g0026 a0004c0004t0001g0227 others(4): Show |
10 | HG02258.hp2 HG02280.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.824+358G>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 7/28 | chr9 | 133429129 | |||||||
chr9:133429132 | C | A | 7 | a0004c0004t0001g0011 a0004c0004t0001g0026 a0004c0004t0001g0227 others(4): Show |
10 | HG02258.hp2 HG02280.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.824+361C>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 7/28 | chr9 | 133429132 | |||||||
chr9:133429135 | T | C | 7 | a0004c0004t0001g0011 a0004c0004t0001g0026 a0004c0004t0001g0227 others(4): Show |
10 | HG02258.hp2 HG02280.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.824+364T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 7/28 | chr9 | 133429135 | |||||||
chr9:133429141 | G | A | 7 | a0004c0004t0001g0011 a0004c0004t0001g0026 a0004c0004t0001g0227 others(4): Show |
10 | HG02258.hp2 HG02280.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.824+370G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 7/28 | chr9 | 133429141 | |||||||
chr9:133429155 | C | T | 5 | a0009c0012t0001g0033 a0009c0012t0001g0034 a0009c0012t0001g0065 others(2): Show |
5 | HG00423.hp2 NA18969.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.824+384C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 7/28 | chr9 | 133429155 | |||||||
chr9:133429171 | A | AC | 17 | a0001c0034t0001g0062 a0002c0002t0001g0079 a0003c0003t0001g0070 others(14): Show |
17 | HG00280.hp1 HG00323.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.824+407dupC | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr9 | 133429171 | ||||||
chr9:133429179 | G | C | 22 | a0001c0027t0001g0272 a0001c0028t0001g0273 a0001c0034t0001g0062 others(19): Show |
22 | HG00280.hp1 HG00323.hp1 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.824+408G>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 7/28 | chr9 | 133429179 | |||||||
chr9:133429185 | C | T | 5 | a0009c0012t0001g0033 a0009c0012t0001g0034 a0009c0012t0001g0065 others(2): Show |
5 | HG00423.hp2 NA18969.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.824+414C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 7/28 | chr9 | 133429185 | |||||||
chr9:133429197 | A | C | 1 | a0003c0031t0001g0276 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.824+426A>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 7/28 | chr9 | 133429197 | |||||||
chr9:133429203 | T | C | 1 | a0003c0031t0001g0276 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.824+432T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 7/28 | chr9 | 133429203 | |||||||
chr9:133429216 | G | GT | 10 | a0001c0001t0001g0025 a0001c0001t0001g0216 a0001c0001t0001g0291 others(7): Show |
11 | HG00423.hp2 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.824+446dupT | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr9 | 133429216 | ||||||
chr9:133429303 | C | G | 5 | a0009c0012t0001g0033 a0009c0012t0001g0034 a0009c0012t0001g0065 others(2): Show |
5 | HG00423.hp2 NA18969.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.824+532C>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 7/28 | chr9 | 133429303 | |||||||
chr9:133429376 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.825-563C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 7/28 | chr9 | 133429376 | |||||||
chr9:133429578 | T | C | 38 | a0001c0005t0001g0263 a0001c0027t0001g0272 a0001c0028t0001g0273 others(35): Show |
42 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.825-361T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 7/28 | chr9 | 133429578 | |||||||
chr9:133429609 | C | CT | 78 | a0001c0017t0002g0234 a0001c0017t0002g0293 a0001c0017t0002g0294 others(75): Show |
91 | HG00609.hp1 HG00639.hp2 HG00642.hp1 others(88): Show |
intron_variant | MODIFIER | c.825-329dupT | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr9 | 133429609 | ||||||
chr9:133429769 | T | C | 8 | a0003c0031t0001g0276 a0008c0013t0001g0012 a0008c0013t0001g0072 others(5): Show |
9 | HG00280.hp2 HG00733.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.825-170T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 7/28 | chr9 | 133429769 | |||||||
chr9:133429796 | G | A | 1 | a0002c0002t0001g0080 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.825-143G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 7/28 | chr9 | 133429796 | |||||||
chr9:133429883 | C | T | 1 | a0001c0011t0001g0215 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.825-56C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 7/28 | chr9 | 133429883 | |||||||
chr9:133429936 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG02015.hp2 | splice_region_variant&intron_variant | LOW | c.825-3C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 7/28 | chr9 | 133429936 | |||||||
chr9:133430112 | C | T | 10 | a0008c0013t0001g0012 a0008c0013t0001g0072 a0008c0013t0001g0074 others(7): Show |
12 | HG00280.hp2 HG00733.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.987+11C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | chr9 | 133430112 | |||||||
chr9:133430167 | C | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0154 |
2 | HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.987+66C>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | chr9 | 133430167 | |||||||
chr9:133430170 | A | C | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(298): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.987+69A>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | chr9 | 133430170 | |||||||
chr9:133430338 | G | C | 7 | a0011c0015t0001g0023 a0011c0015t0001g0068 a0011c0015t0001g0262 others(4): Show |
8 | HG02145.hp2 HG02257.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.987+237G>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | chr9 | 133430338 | |||||||
chr9:133430414 | T | G | 21 | a0001c0017t0002g0234 a0001c0017t0002g0293 a0001c0017t0002g0294 others(18): Show |
24 | HG00423.hp2 HG01891.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.987+313T>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | chr9 | 133430414 | |||||||
chr9:133430458 | C | T | 5 | a0009c0012t0001g0033 a0009c0012t0001g0034 a0009c0012t0001g0065 others(2): Show |
5 | HG00423.hp2 NA18969.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.987+357C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | chr9 | 133430458 | |||||||
chr9:133430501 | G | A | 42 | a0001c0017t0002g0234 a0001c0017t0002g0293 a0001c0017t0002g0294 others(39): Show |
46 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.987+400G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | chr9 | 133430501 | |||||||
chr9:133430693 | CTA | C | 75 | a0001c0005t0001g0263 a0001c0005t0001g0265 a0002c0002t0001g0004 others(72): Show |
86 | HG00423.hp2 HG00609.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.987+594_987+595del others(2): Show |
ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr9 | 133430693 | ||||||
chr9:133430694 | TA | T | 52 | a0001c0005t0001g0264 a0001c0017t0002g0234 a0001c0017t0002g0293 others(49): Show |
57 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.987+594delA | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | chr9 | 133430694 | |||||||
chr9:133430695 | A | AT | 15 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0146 others(12): Show |
22 | HG02004.hp1 HG02015.hp1 HG02083.hp1 others(19): Show |
intron_variant | MODIFIER | c.987+609dupT | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr9 | 133430695 | ||||||
chr9:133430695 | A | T | 7 | a0001c0005t0001g0255 a0001c0005t0001g0256 a0001c0005t0001g0257 others(4): Show |
7 | HG02717.hp2 HG02895.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.987+594A>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | chr9 | 133430695 | |||||||
chr9:133430695 | AT | A | 8 | a0001c0001t0001g0022 a0001c0001t0001g0046 a0001c0001t0001g0051 others(5): Show |
8 | HG02615.hp2 HG03540.hp1 NA18612.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+609delT | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr9 | 133430695 | ||||||
chr9:133430746 | C | T | 10 | a0002c0002t0001g0077 a0002c0002t0001g0111 a0002c0002t0001g0112 others(7): Show |
10 | HG00741.hp2 HG01928.hp2 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.987+645C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | chr9 | 133430746 | |||||||
chr9:133430770 | C | G | 67 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0020 others(64): Show |
77 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.987+669C>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | chr9 | 133430770 | |||||||
chr9:133430821 | T | C | 1 | a0001c0005t0001g0257 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.987+720T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | chr9 | 133430821 | |||||||
chr9:133430964 | C | CT | 72 | a0002c0002t0001g0004 a0002c0002t0001g0006 a0002c0002t0001g0007 others(69): Show |
82 | HG00423.hp2 HG00609.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.987+872dupT | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr9 | 133430964 | ||||||
chr9:133430979 | C | A | 10 | a0001c0005t0001g0255 a0001c0005t0001g0256 a0001c0005t0001g0257 others(7): Show |
10 | HG01884.hp1 HG02717.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.987+878C>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | chr9 | 133430979 | |||||||
chr9:133431002 | G | A | 1 | a0002c0002t0001g0081 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.987+901G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | chr9 | 133431002 | |||||||
chr9:133431013 | T | G | 2 | a0016c0022t0001g0045 a0016c0022t0001g0153 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.987+912T>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | chr9 | 133431013 | |||||||
chr9:133431043 | G | A | 1 | a0028c0043t0001g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.987+942G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | chr9 | 133431043 | |||||||
chr9:133431111 | C | T | 65 | a0002c0002t0001g0004 a0002c0002t0001g0006 a0002c0002t0001g0007 others(62): Show |
75 | HG00609.hp1 HG00639.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.987+1010C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | chr9 | 133431111 | |||||||
chr9:133431155 | G | A | 3 | a0011c0015t0001g0023 a0011c0015t0001g0068 a0011c0015t0001g0262 |
4 | HG02145.hp2 HG02257.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.987+1054G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | chr9 | 133431155 | |||||||
chr9:133431216 | T | C | 23 | a0001c0005t0001g0255 a0001c0005t0001g0256 a0001c0005t0001g0257 others(20): Show |
26 | HG01884.hp1 HG02258.hp2 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.987+1115T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | chr9 | 133431216 | |||||||
chr9:133431329 | A | AT | 96 | a0001c0001t0001g0214 a0001c0005t0001g0255 a0001c0005t0001g0256 others(93): Show |
109 | HG00423.hp2 HG00609.hp1 HG00639.hp2 others(106): Show |
intron_variant | MODIFIER | c.987+1243dupT | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr9 | 133431329 | ||||||
chr9:133431329 | AT | A | 6 | a0001c0001t0001g0061 a0001c0001t0001g0249 a0015c0024t0001g0024 others(3): Show |
7 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.987+1243delT | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr9 | 133431329 | ||||||
chr9:133431338 | T | C | 4 | a0003c0003t0001g0070 a0003c0003t0001g0071 a0003c0033t0002g0267 others(1): Show |
4 | HG01167.hp2 HG02572.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.987+1237T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | chr9 | 133431338 | |||||||
chr9:133431353 | G | T | 4 | a0014c0023t0001g0303 a0014c0023t0001g0309 a0014c0056t0001g0304 others(1): Show |
4 | HG02647.hp2 HG02818.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.988-1235G>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | chr9 | 133431353 | |||||||
chr9:133431391 | A | G | 23 | a0001c0005t0001g0255 a0001c0005t0001g0256 a0001c0005t0001g0257 others(20): Show |
26 | HG01884.hp1 HG02258.hp2 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.988-1197A>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | chr9 | 133431391 | |||||||
chr9:133431409 | C | T | 3 | a0002c0002t0001g0007 a0002c0002t0001g0041 a0002c0006t0001g0040 |
5 | HG00738.hp2 HG01070.hp2 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.988-1179C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | chr9 | 133431409 | |||||||
chr9:133431436 | C | T | 2 | a0002c0040t0001g0300 a0025c0053t0001g0298 |
2 | HG01891.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.988-1152C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | chr9 | 133431436 | |||||||
chr9:133431536 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.988-1052C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | chr9 | 133431536 | |||||||
chr9:133431569 | C | T | 1 | a0022c0041t0003g0031 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.988-1019C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | chr9 | 133431569 | |||||||
chr9:133431570 | G | A | 3 | a0001c0001t0001g0025 a0001c0001t0001g0216 a0001c0001t0001g0291 |
4 | HG02280.hp1 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.988-1018G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | chr9 | 133431570 | |||||||
chr9:133431573 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.988-1015C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | chr9 | 133431573 | |||||||
chr9:133431730 | C | T | 2 | a0002c0040t0001g0300 a0025c0053t0001g0298 |
2 | HG01891.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.988-858C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | chr9 | 133431730 | |||||||
chr9:133431815 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.988-773C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | chr9 | 133431815 | |||||||
chr9:133431876 | G | A | 7 | a0004c0004t0001g0011 a0004c0004t0001g0026 a0004c0004t0001g0227 others(4): Show |
10 | HG02258.hp2 HG02280.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.988-712G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | chr9 | 133431876 | |||||||
chr9:133431890 | G | A | 10 | a0001c0005t0001g0255 a0001c0005t0001g0256 a0001c0005t0001g0257 others(7): Show |
10 | HG01884.hp1 HG02717.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.988-698G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | chr9 | 133431890 | |||||||
chr9:133432002 | G | A | 1 | a0001c0017t0002g0293 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.988-586G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | chr9 | 133432002 | |||||||
chr9:133432036 | G | GGC | 69 | a0002c0002t0001g0004 a0002c0002t0001g0006 a0002c0002t0001g0007 others(66): Show |
80 | HG00609.hp1 HG00639.hp2 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.988-550_988-549dup others(2): Show |
ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr9 | 133432036 | ||||||
chr9:133432121 | C | T | 14 | a0001c0017t0002g0234 a0001c0017t0002g0293 a0001c0017t0002g0294 others(11): Show |
17 | HG02258.hp2 HG02280.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.988-467C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | chr9 | 133432121 | |||||||
chr9:133432220 | G | A | 1 | a0002c0002t0001g0082 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.988-368G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | chr9 | 133432220 | |||||||
chr9:133432286 | T | G | 276 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(273): Show |
313 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(310): Show |
intron_variant | MODIFIER | c.988-302T>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | chr9 | 133432286 | |||||||
chr9:133432308 | G | A | 2 | a0001c0042t0001g0302 a0029c0054t0001g0140 |
2 | NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.988-280G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | chr9 | 133432308 | |||||||
chr9:133432352 | GAC | G | 3 | a0002c0006t0001g0036 a0002c0006t0001g0083 a0002c0051t0001g0158 |
3 | HG00609.hp1 NA19009.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.988-232_988-231del others(2): Show |
ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr9 | 133432352 | ||||||
chr9:133432372 | A | T | 2 | a0002c0002t0001g0109 a0002c0002t0001g0110 |
2 | NA18988.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.988-216A>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | chr9 | 133432372 | |||||||
chr9:133432386 | G | A | 1 | a0002c0051t0001g0158 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.988-202G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | chr9 | 133432386 | |||||||
chr9:133432512 | G | A | 5 | a0003c0003t0001g0235 a0003c0003t0001g0236 a0003c0003t0001g0237 others(2): Show |
5 | HG00280.hp1 HG00323.hp1 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.988-76G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 8/28 | chr9 | 133432512 | |||||||
chr9:133432759 | G | A | 4 | a0001c0010t0001g0306 a0015c0024t0001g0024 a0019c0025t0001g0126 others(1): Show |
5 | HG01069.hp2 HG01071.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.1092+67G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 9/28 | chr9 | 133432759 | |||||||
chr9:133432780 | G | A | 3 | a0001c0017t0002g0234 a0001c0017t0002g0293 a0001c0017t0002g0294 |
3 | HG02451.hp2 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1092+88G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 9/28 | chr9 | 133432780 | |||||||
chr9:133432975 | G | A | 7 | a0004c0004t0001g0011 a0004c0004t0001g0026 a0004c0004t0001g0227 others(4): Show |
10 | HG02258.hp2 HG02280.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1092+283G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 9/28 | chr9 | 133432975 | |||||||
chr9:133432981 | CG | C | 53 | a0001c0005t0001g0255 a0001c0005t0001g0256 a0001c0005t0001g0257 others(50): Show |
57 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.1092+296delG | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 9/28 | INFO_REALIGN_3_PRIME | chr9 | 133432981 | ||||||
chr9:133432991 | C | A | 3 | a0001c0005t0001g0263 a0001c0005t0001g0264 a0001c0005t0001g0265 |
3 | HG01884.hp1 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1092+299C>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 9/28 | chr9 | 133432991 | |||||||
chr9:133433011 | T | G | 3 | a0015c0024t0001g0024 a0019c0025t0001g0126 a0019c0025t0001g0127 |
4 | HG01069.hp2 HG01071.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.1092+319T>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 9/28 | chr9 | 133433011 | |||||||
chr9:133433061 | C | T | 7 | a0002c0040t0001g0300 a0009c0012t0001g0033 a0009c0012t0001g0034 others(4): Show |
7 | HG00423.hp2 HG01891.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1093-317C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 9/28 | chr9 | 133433061 | |||||||
chr9:133433227 | G | A | 7 | a0001c0001t0001g0047 a0001c0001t0001g0159 a0001c0001t0001g0160 others(4): Show |
7 | HG00438.hp1 HG00621.hp2 HG00673.hp2 others(4): Show |
intron_variant | MODIFIER | c.1093-151G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 9/28 | chr9 | 133433227 | |||||||
chr9:133433303 | G | A | 13 | a0001c0001t0001g0008 a0001c0001t0001g0142 a0001c0001t0001g0143 others(10): Show |
15 | HG02015.hp1 HG02015.hp2 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.1093-75G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 9/28 | chr9 | 133433303 | |||||||
chr9:133433609 | C | G | 139 | a0001c0005t0001g0255 a0001c0005t0001g0256 a0001c0005t0001g0257 others(136): Show |
155 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.1245-32C>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 10/28 | chr9 | 133433609 | |||||||
chr9:133433721 | G | T | 3 | a0011c0015t0001g0023 a0011c0015t0001g0068 a0011c0015t0001g0262 |
4 | HG02145.hp2 HG02257.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1308+17G>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133433721 | |||||||
chr9:133433808 | C | T | 1 | a0002c0002t0001g0120 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1308+104C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133433808 | |||||||
chr9:133433910 | A | G | 1 | a0002c0002t0001g0150 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1308+206A>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133433910 | |||||||
chr9:133433956 | C | T | 70 | a0002c0002t0001g0004 a0002c0002t0001g0006 a0002c0002t0001g0007 others(67): Show |
81 | HG00609.hp1 HG00639.hp2 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.1308+252C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133433956 | |||||||
chr9:133434013 | T | C | 2 | a0017c0020t0001g0232 a0017c0020t0001g0233 |
2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1308+309T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133434013 | |||||||
chr9:133434027 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1308+323T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133434027 | |||||||
chr9:133434047 | G | C | 4 | a0001c0017t0002g0234 a0001c0017t0002g0293 a0001c0017t0002g0294 others(1): Show |
4 | HG02451.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1308+343G>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133434047 | |||||||
chr9:133434106 | T | A | 10 | a0001c0027t0001g0272 a0003c0003t0001g0070 a0003c0003t0001g0071 others(7): Show |
10 | HG00735.hp1 HG01081.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1308+402T>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133434106 | |||||||
chr9:133434233 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1308+529C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133434233 | |||||||
chr9:133434274 | C | T | 21 | a0001c0027t0001g0272 a0001c0028t0001g0273 a0001c0034t0001g0062 others(18): Show |
21 | HG00280.hp1 HG00323.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.1308+570C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133434274 | |||||||
chr9:133434346 | C | T | 1 | a0002c0039t0001g0149 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1308+642C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133434346 | |||||||
chr9:133434474 | T | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0048 a0027c0058t0001g0165 |
4 | NA18612.hp1 NA18955.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.1308+770T>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133434474 | |||||||
chr9:133434495 | A | C | 70 | a0002c0002t0001g0004 a0002c0002t0001g0006 a0002c0002t0001g0007 others(67): Show |
81 | HG00609.hp1 HG00639.hp2 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.1308+791A>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133434495 | |||||||
chr9:133434520 | T | G | 1 | a0001c0001t0001g0250 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1308+816T>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133434520 | |||||||
chr9:133434521 | G | T | 1 | a0001c0001t0001g0250 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1308+817G>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133434521 | |||||||
chr9:133434600 | C | T | 2 | a0008c0013t0001g0012 a0008c0013t0001g0074 |
3 | HG00280.hp2 HG00733.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1308+896C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133434600 | |||||||
chr9:133434682 | T | G | 1 | a0022c0041t0003g0031 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1308+978T>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133434682 | |||||||
chr9:133434817 | T | C | 67 | a0002c0002t0001g0004 a0002c0002t0001g0006 a0002c0002t0001g0007 others(64): Show |
77 | HG00609.hp1 HG00639.hp2 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.1308+1113T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133434817 | |||||||
chr9:133434917 | G | A | 1 | a0013c0016t0001g0035 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1308+1213G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133434917 | |||||||
chr9:133434976 | G | C | 7 | a0002c0040t0001g0300 a0009c0012t0001g0033 a0009c0012t0001g0034 others(4): Show |
7 | HG00423.hp2 HG01891.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1308+1272G>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133434976 | |||||||
chr9:133435002 | T | C | 67 | a0002c0002t0001g0004 a0002c0002t0001g0006 a0002c0002t0001g0007 others(64): Show |
77 | HG00609.hp1 HG00639.hp2 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.1308+1298T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133435002 | |||||||
chr9:133435011 | T | A | 1 | a0001c0001t0001g0159 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1308+1307T>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133435011 | |||||||
chr9:133435035 | G | T | 3 | a0001c0017t0002g0234 a0001c0017t0002g0293 a0001c0017t0002g0294 |
3 | HG02451.hp2 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1308+1331G>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133435035 | |||||||
chr9:133435084 | G | C | 31 | a0001c0005t0001g0255 a0001c0005t0001g0256 a0001c0005t0001g0257 others(28): Show |
31 | HG00280.hp1 HG00323.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.1308+1380G>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133435084 | |||||||
chr9:133435191 | C | CT | 8 | a0001c0001t0001g0169 a0002c0040t0001g0300 a0009c0012t0001g0033 others(5): Show |
8 | HG00423.hp2 HG01891.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1308+1501dupT | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr9 | 133435191 | ||||||
chr9:133435192 | T | C | 1 | a0001c0001t0001g0250 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1308+1488T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133435192 | |||||||
chr9:133435193 | T | C | 1 | a0022c0041t0003g0031 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1308+1489T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133435193 | |||||||
chr9:133435293 | T | A | 1 | a0002c0002t0001g0037 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1309-1536T>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133435293 | |||||||
chr9:133435372 | G | T | 1 | a0001c0001t0001g0159 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1309-1457G>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133435372 | |||||||
chr9:133435404 | G | T | 67 | a0002c0002t0001g0004 a0002c0002t0001g0006 a0002c0002t0001g0007 others(64): Show |
77 | HG00609.hp1 HG00639.hp2 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.1309-1425G>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133435404 | |||||||
chr9:133435498 | CT | C | 69 | a0002c0002t0001g0004 a0002c0002t0001g0006 a0002c0002t0001g0007 others(66): Show |
80 | HG00609.hp1 HG00639.hp2 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.1309-1320delT | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr9 | 133435498 | ||||||
chr9:133435517 | TTTTC | T | 5 | a0009c0012t0001g0033 a0009c0012t0001g0034 a0009c0012t0001g0065 others(2): Show |
5 | HG00423.hp2 NA18969.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.1309-1300_1309-129 others(8): Show |
ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr9 | 133435517 | ||||||
chr9:133435533 | A | C | 16 | a0001c0005t0001g0260 a0002c0038t0001g0107 a0008c0013t0001g0012 others(13): Show |
18 | HG00280.hp2 HG00733.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1309-1296A>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133435533 | |||||||
chr9:133435590 | C | T | 3 | a0011c0015t0001g0023 a0011c0015t0001g0068 a0011c0015t0001g0262 |
4 | HG02145.hp2 HG02257.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1309-1239C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133435590 | |||||||
chr9:133435592 | C | T | 67 | a0002c0002t0001g0004 a0002c0002t0001g0006 a0002c0002t0001g0007 others(64): Show |
77 | HG00609.hp1 HG00639.hp2 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.1309-1237C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133435592 | |||||||
chr9:133435616 | G | T | 4 | a0014c0023t0001g0303 a0014c0023t0001g0309 a0014c0056t0001g0304 others(1): Show |
4 | HG02647.hp2 HG02818.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1309-1213G>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133435616 | |||||||
chr9:133435617 | C | A | 4 | a0014c0023t0001g0303 a0014c0023t0001g0309 a0014c0056t0001g0304 others(1): Show |
4 | HG02647.hp2 HG02818.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1309-1212C>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133435617 | |||||||
chr9:133435620 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1309-1209C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133435620 | |||||||
chr9:133435654 | C | G | 3 | a0015c0024t0001g0024 a0019c0025t0001g0126 a0019c0025t0001g0127 |
4 | HG01069.hp2 HG01071.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.1309-1175C>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133435654 | |||||||
chr9:133435679 | G | T | 1 | a0001c0001t0001g0159 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1309-1150G>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133435679 | |||||||
chr9:133435687 | G | C | 1 | a0001c0001t0001g0159 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1309-1142G>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133435687 | |||||||
chr9:133435689 | C | G | 1 | a0001c0001t0001g0159 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1309-1140C>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133435689 | |||||||
chr9:133435691 | G | A | 3 | a0005c0007t0001g0019 a0005c0007t0001g0056 a0005c0007t0001g0280 |
4 | NA18747.hp2 NA18962.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.1309-1138G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133435691 | |||||||
chr9:133435696 | A | AT | 67 | a0002c0002t0001g0004 a0002c0002t0001g0006 a0002c0002t0001g0007 others(64): Show |
77 | HG00609.hp1 HG00639.hp2 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.1309-1124dupT | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr9 | 133435696 | ||||||
chr9:133435869 | C | T | 1 | a0003c0003t0001g0271 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1309-960C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133435869 | |||||||
chr9:133435903 | T | C | 16 | a0001c0017t0002g0234 a0001c0017t0002g0293 a0001c0017t0002g0294 others(13): Show |
20 | HG02145.hp2 HG02257.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.1309-926T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133435903 | |||||||
chr9:133435905 | C | T | 3 | a0015c0024t0001g0024 a0019c0025t0001g0126 a0019c0025t0001g0127 |
4 | HG01069.hp2 HG01071.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.1309-924C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133435905 | |||||||
chr9:133435977 | CT | C | 55 | a0001c0001t0001g0017 a0001c0001t0001g0043 a0001c0001t0001g0061 others(52): Show |
58 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.1309-832delT | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr9 | 133435977 | ||||||
chr9:133435980 | T | C | 10 | a0003c0031t0001g0276 a0008c0013t0001g0012 a0008c0013t0001g0072 others(7): Show |
12 | HG00280.hp2 HG00733.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.1309-849T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133435980 | |||||||
chr9:133435981 | T | C | 6 | a0009c0012t0001g0033 a0009c0012t0001g0034 a0009c0012t0001g0065 others(3): Show |
6 | HG00423.hp2 HG03491.hp1 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.1309-848T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133435981 | |||||||
chr9:133435983 | T | C | 3 | a0008c0013t0001g0072 a0015c0024t0001g0024 a0019c0025t0001g0127 |
4 | HG01069.hp2 HG01071.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1309-846T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133435983 | |||||||
chr9:133435984 | T | C | 1 | a0019c0025t0001g0126 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1309-845T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133435984 | |||||||
chr9:133435997 | T | A | 3 | a0011c0015t0001g0023 a0011c0015t0001g0068 a0011c0015t0001g0262 |
4 | HG02145.hp2 HG02257.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1309-832T>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133435997 | |||||||
chr9:133436096 | C | T | 7 | a0001c0005t0001g0255 a0001c0005t0001g0256 a0001c0005t0001g0257 others(4): Show |
7 | HG02717.hp2 HG02895.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1309-733C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133436096 | |||||||
chr9:133436206 | C | T | 7 | a0011c0015t0001g0023 a0011c0015t0001g0068 a0011c0015t0001g0262 others(4): Show |
8 | HG02145.hp2 HG02257.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1309-623C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133436206 | |||||||
chr9:133436242 | T | C | 1 | a0002c0002t0001g0109 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1309-587T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133436242 | |||||||
chr9:133436363 | GCAGTGTG others(2): Show |
G | 67 | a0002c0002t0001g0004 a0002c0002t0001g0006 a0002c0002t0001g0007 others(64): Show |
77 | HG00609.hp1 HG00639.hp2 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.1309-457_1309-449d others(11): Show |
ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr9 | 133436363 | ||||||
chr9:133436383 | G | A | 1 | a0025c0053t0001g0298 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1309-446G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133436383 | |||||||
chr9:133436622 | T | C | 2 | a0001c0042t0001g0302 a0029c0054t0001g0140 |
2 | NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1309-207T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133436622 | |||||||
chr9:133436625 | G | A | 4 | a0008c0013t0001g0012 a0008c0013t0001g0072 a0008c0013t0001g0074 others(1): Show |
5 | HG00280.hp2 HG00733.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1309-204G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133436625 | |||||||
chr9:133436698 | C | T | 4 | a0014c0023t0001g0303 a0014c0023t0001g0309 a0014c0056t0001g0304 others(1): Show |
4 | HG02647.hp2 HG02818.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1309-131C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133436698 | |||||||
chr9:133436781 | C | T | 3 | a0004c0004t0001g0011 a0004c0004t0001g0229 a0004c0026t0001g0228 |
5 | HG02280.hp2 HG02615.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1309-48C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 11/28 | chr9 | 133436781 | |||||||
chr9:133437088 | G | A | 3 | a0015c0024t0001g0024 a0019c0025t0001g0126 a0019c0025t0001g0127 |
4 | HG01069.hp2 HG01071.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.1435+133G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 12/28 | chr9 | 133437088 | |||||||
chr9:133437314 | G | T | 70 | a0002c0002t0001g0004 a0002c0002t0001g0006 a0002c0002t0001g0007 others(67): Show |
81 | HG00609.hp1 HG00639.hp2 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.1435+359G>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 12/28 | chr9 | 133437314 | |||||||
chr9:133437330 | C | T | 21 | a0001c0027t0001g0272 a0001c0028t0001g0273 a0001c0034t0001g0062 others(18): Show |
21 | HG00280.hp1 HG00323.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.1435+375C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 12/28 | chr9 | 133437330 | |||||||
chr9:133437477 | C | T | 8 | a0003c0031t0001g0276 a0008c0013t0001g0012 a0008c0013t0001g0072 others(5): Show |
9 | HG00280.hp2 HG00733.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1436-272C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 12/28 | chr9 | 133437477 | |||||||
chr9:133437488 | C | A | 1 | a0028c0043t0001g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1436-261C>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 12/28 | chr9 | 133437488 | |||||||
chr9:133437509 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1436-240C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 12/28 | chr9 | 133437509 | |||||||
chr9:133437563 | T | C | 77 | a0002c0002t0001g0004 a0002c0002t0001g0006 a0002c0002t0001g0007 others(74): Show |
88 | HG00423.hp2 HG00609.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.1436-186T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 12/28 | chr9 | 133437563 | |||||||
chr9:133437642 | A | G | 2 | a0010c0018t0001g0073 a0010c0018t0001g0275 |
2 | HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1436-107A>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 12/28 | chr9 | 133437642 | |||||||
chr9:133437685 | G | C | 1 | a0002c0037t0001g0088 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1436-64G>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 12/28 | chr9 | 133437685 | |||||||
chr9:133438003 | C | G | 70 | a0002c0002t0001g0004 a0002c0002t0001g0006 a0002c0002t0001g0007 others(67): Show |
81 | HG00609.hp1 HG00639.hp2 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.1584+106C>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 13/28 | chr9 | 133438003 | |||||||
chr9:133438129 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1585-117G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 13/28 | chr9 | 133438129 | |||||||
chr9:133438133 | T | C | 77 | a0002c0002t0001g0004 a0002c0002t0001g0006 a0002c0002t0001g0007 others(74): Show |
88 | HG00423.hp2 HG00609.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.1585-113T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 13/28 | chr9 | 133438133 | |||||||
chr9:133438373 | G | A | 7 | a0002c0040t0001g0300 a0009c0012t0001g0033 a0009c0012t0001g0034 others(4): Show |
7 | HG00423.hp2 HG01891.hp2 HG02818.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.1705+7G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 14/28 | chr9 | 133438373 | |||||||
chr9:133438525 | G | A | 3 | a0003c0019t0001g0131 a0003c0019t0001g0239 a0003c0035t0001g0240 |
3 | HG02109.hp2 HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1705+159G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 14/28 | chr9 | 133438525 | |||||||
chr9:133438544 | C | T | 2 | a0010c0018t0001g0073 a0010c0018t0001g0275 |
2 | HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1705+178C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 14/28 | chr9 | 133438544 | |||||||
chr9:133438614 | C | CA | 5 | a0001c0001t0001g0160 a0001c0001t0001g0191 a0001c0001t0001g0285 others(2): Show |
5 | HG00673.hp2 HG01081.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.1705+256dupA | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 14/28 | INFO_REALIGN_3_PRIME | chr9 | 133438614 | ||||||
chr9:133438622 | A | C | 1 | a0001c0001t0001g0199 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1705+256A>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 14/28 | chr9 | 133438622 | |||||||
chr9:133438636 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1705+270C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 14/28 | chr9 | 133438636 | |||||||
chr9:133438664 | G | A | 10 | a0001c0034t0001g0062 a0003c0003t0001g0235 a0003c0003t0001g0236 others(7): Show |
10 | HG00280.hp1 HG00323.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.1705+298G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 14/28 | chr9 | 133438664 | |||||||
chr9:133438768 | G | C | 66 | a0002c0002t0001g0004 a0002c0002t0001g0006 a0002c0002t0001g0007 others(63): Show |
76 | HG00609.hp1 HG00639.hp2 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.1705+402G>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 14/28 | chr9 | 133438768 | |||||||
chr9:133438771 | G | C | 3 | a0001c0001t0001g0166 a0001c0001t0001g0172 a0001c0001t0001g0173 |
3 | HG00140.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1705+405G>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 14/28 | chr9 | 133438771 | |||||||
chr9:133438873 | T | C | 2 | a0019c0025t0001g0126 a0019c0025t0001g0127 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1706-493T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 14/28 | chr9 | 133438873 | |||||||
chr9:133438885 | C | T | 3 | a0011c0015t0001g0023 a0011c0015t0001g0068 a0011c0015t0001g0262 |
4 | HG02145.hp2 HG02257.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1706-481C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 14/28 | chr9 | 133438885 | |||||||
chr9:133438910 | C | CA | 50 | a0001c0001t0001g0049 a0001c0001t0001g0174 a0001c0001t0001g0242 others(47): Show |
54 | HG00280.hp1 HG00323.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.1706-438dupA | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 14/28 | INFO_REALIGN_3_PRIME | chr9 | 133438910 | ||||||
chr9:133438910 | C | CAA | 9 | a0003c0003t0001g0269 a0003c0003t0001g0296 a0014c0023t0001g0303 others(6): Show |
10 | HG01069.hp2 HG01071.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.1706-439_1706-438d others(4): Show |
ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 14/28 | INFO_REALIGN_3_PRIME | chr9 | 133438910 | ||||||
chr9:133438910 | C | CAAA | 11 | a0002c0002t0001g0087 a0002c0002t0001g0108 a0002c0002t0001g0279 others(8): Show |
11 | HG00423.hp2 HG01192.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.1706-440_1706-438d others(5): Show |
ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 14/28 | INFO_REALIGN_3_PRIME | chr9 | 133438910 | ||||||
chr9:133438910 | C | CAAAA | 54 | a0002c0002t0001g0004 a0002c0002t0001g0006 a0002c0002t0001g0007 others(51): Show |
64 | HG00609.hp1 HG00639.hp2 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.1706-441_1706-438d others(6): Show |
ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 14/28 | INFO_REALIGN_3_PRIME | chr9 | 133438910 | ||||||
chr9:133438910 | C | CAAAAA | 9 | a0002c0002t0001g0077 a0002c0002t0001g0081 a0002c0002t0001g0089 others(6): Show |
9 | HG00642.hp1 HG01928.hp1 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.1706-442_1706-438d others(7): Show |
ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 14/28 | INFO_REALIGN_3_PRIME | chr9 | 133438910 | ||||||
chr9:133438910 | CA | C | 8 | a0001c0001t0001g0055 a0001c0001t0001g0148 a0001c0001t0001g0170 others(5): Show |
8 | HG00639.hp1 HG01256.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1706-438delA | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 14/28 | INFO_REALIGN_3_PRIME | chr9 | 133438910 | ||||||
chr9:133439016 | T | A | 136 | a0001c0005t0001g0255 a0001c0005t0001g0256 a0001c0005t0001g0257 others(133): Show |
152 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.1706-350T>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 14/28 | chr9 | 133439016 | |||||||
chr9:133439111 | G | C | 21 | a0001c0027t0001g0272 a0001c0028t0001g0273 a0001c0034t0001g0062 others(18): Show |
21 | HG00280.hp1 HG00323.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.1706-255G>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 14/28 | chr9 | 133439111 | |||||||
chr9:133439340 | A | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0226 |
3 | HG00673.hp1 HG02056.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1706-26A>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 14/28 | chr9 | 133439340 | |||||||
chr9:133439462 | G | A | 1 | a0003c0031t0001g0276 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1786+16G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 15/28 | chr9 | 133439462 | |||||||
chr9:133439607 | G | C | 72 | a0002c0002t0001g0004 a0002c0002t0001g0006 a0002c0002t0001g0007 others(69): Show |
82 | HG00423.hp2 HG00609.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.1786+161G>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 15/28 | chr9 | 133439607 | |||||||
chr9:133439744 | T | C | 4 | a0014c0023t0001g0303 a0014c0023t0001g0309 a0014c0056t0001g0304 others(1): Show |
4 | HG02647.hp2 HG02818.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1786+298T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 15/28 | chr9 | 133439744 | |||||||
chr9:133439770 | T | C | 4 | a0002c0002t0001g0037 a0002c0002t0001g0084 a0002c0002t0001g0089 others(1): Show |
4 | HG00642.hp1 HG01069.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.1786+324T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 15/28 | chr9 | 133439770 | |||||||
chr9:133439864 | C | G | 1 | a0002c0051t0001g0158 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1786+418C>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 15/28 | chr9 | 133439864 | |||||||
chr9:133439891 | T | C | 21 | a0001c0027t0001g0272 a0001c0028t0001g0273 a0001c0034t0001g0062 others(18): Show |
21 | HG00280.hp1 HG00323.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.1786+445T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 15/28 | chr9 | 133439891 | |||||||
chr9:133439892 | C | G | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1786+446C>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 15/28 | chr9 | 133439892 | |||||||
chr9:133440037 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1787-307G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 15/28 | chr9 | 133440037 | |||||||
chr9:133440122 | C | T | 1 | a0004c0004t0001g0227 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1787-222C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 15/28 | chr9 | 133440122 | |||||||
chr9:133440154 | A | G | 68 | a0002c0002t0001g0004 a0002c0002t0001g0006 a0002c0002t0001g0007 others(65): Show |
78 | HG00609.hp1 HG00639.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.1787-190A>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 15/28 | chr9 | 133440154 | |||||||
chr9:133440293 | G | A | 2 | a0002c0040t0001g0300 a0025c0053t0001g0298 |
2 | HG01891.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1787-51G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 15/28 | chr9 | 133440293 | |||||||
chr9:133440307 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1787-37C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 15/28 | chr9 | 133440307 | |||||||
chr9:133440316 | A | G | 1 | a0001c0001t0001g0285 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1787-28A>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 15/28 | chr9 | 133440316 | |||||||
chr9:133440318 | A | G | 140 | a0001c0005t0001g0255 a0001c0005t0001g0256 a0001c0005t0001g0257 others(137): Show |
156 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.1787-26A>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 15/28 | chr9 | 133440318 | |||||||
chr9:133440337 | C | T | 3 | a0011c0015t0001g0023 a0011c0015t0001g0068 a0011c0015t0001g0262 |
4 | HG02145.hp2 HG02257.hp1 HG02965.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1787-7C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 15/28 | chr9 | 133440337 | |||||||
chr9:133440568 | T | C | 5 | a0001c0005t0001g0263 a0001c0005t0001g0264 a0001c0005t0001g0265 others(2): Show |
5 | HG01884.hp1 HG03516.hp2 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.1968+43T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 16/28 | chr9 | 133440568 | |||||||
chr9:133440617 | C | G | 5 | a0001c0001t0001g0010 a0001c0001t0001g0054 a0001c0001t0001g0166 others(2): Show |
7 | HG00140.hp2 HG00741.hp1 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1968+92C>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 16/28 | chr9 | 133440617 | |||||||
chr9:133440735 | C | T | 7 | a0001c0005t0001g0255 a0001c0005t0001g0256 a0001c0005t0001g0257 others(4): Show |
7 | HG02717.hp2 HG02895.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1968+210C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 16/28 | chr9 | 133440735 | |||||||
chr9:133440751 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1968+226G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 16/28 | chr9 | 133440751 | |||||||
chr9:133440809 | T | C | 1 | a0001c0001t0001g0289 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1968+284T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 16/28 | chr9 | 133440809 | |||||||
chr9:133440812 | A | G | 2 | a0002c0002t0001g0109 a0002c0002t0001g0110 |
2 | NA18988.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1968+287A>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 16/28 | chr9 | 133440812 | |||||||
chr9:133441355 | C | T | 1 | a0022c0041t0003g0031 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1968+830C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 16/28 | chr9 | 133441355 | |||||||
chr9:133441425 | A | G | 1 | a0002c0002t0001g0079 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1968+900A>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 16/28 | chr9 | 133441425 | |||||||
chr9:133441594 | C | T | 7 | a0001c0005t0001g0255 a0001c0005t0001g0256 a0001c0005t0001g0257 others(4): Show |
7 | HG02717.hp2 HG02895.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1969-805C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 16/28 | chr9 | 133441594 | |||||||
chr9:133441794 | T | C | 1 | a0009c0012t0001g0065 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1969-605T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 16/28 | chr9 | 133441794 | |||||||
chr9:133441896 | CT | C | 3 | a0015c0024t0001g0024 a0019c0025t0001g0126 a0019c0025t0001g0127 |
4 | HG01069.hp2 HG01071.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.1969-502delT | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 16/28 | chr9 | 133441896 | |||||||
chr9:133441916 | C | T | 1 | a0002c0002t0001g0038 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1969-483C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 16/28 | chr9 | 133441916 | |||||||
chr9:133441968 | A | G | 21 | a0001c0027t0001g0272 a0001c0028t0001g0273 a0001c0034t0001g0062 others(18): Show |
21 | HG00280.hp1 HG00323.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.1969-431A>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 16/28 | chr9 | 133441968 | |||||||
chr9:133442226 | C | T | 2 | a0002c0002t0001g0105 a0002c0002t0001g0106 |
2 | HG00639.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.1969-173C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 16/28 | chr9 | 133442226 | |||||||
chr9:133442255 | G | C | 1 | a0002c0002t0001g0079 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1969-144G>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 16/28 | chr9 | 133442255 | |||||||
chr9:133442287 | A | G | 21 | a0001c0027t0001g0272 a0001c0028t0001g0273 a0001c0034t0001g0062 others(18): Show |
21 | HG00280.hp1 HG00323.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.1969-112A>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 16/28 | chr9 | 133442287 | |||||||
chr9:133442844 | G | C | 1 | a0028c0043t0001g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2234+101G>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 18/28 | chr9 | 133442844 | |||||||
chr9:133442875 | C | T | 1 | a0001c0001t0001g0225 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2234+132C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 18/28 | chr9 | 133442875 | |||||||
chr9:133442899 | G | T | 1 | a0028c0043t0001g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2234+156G>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 18/28 | chr9 | 133442899 | |||||||
chr9:133442963 | A | G | 1 | a0028c0043t0001g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2234+220A>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 18/28 | chr9 | 133442963 | |||||||
chr9:133443213 | A | G | 8 | a0004c0004t0001g0011 a0004c0004t0001g0026 a0004c0004t0001g0227 others(5): Show |
11 | HG02258.hp2 HG02280.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.2235-163A>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 18/28 | chr9 | 133443213 | |||||||
chr9:133443235 | G | T | 1 | a0001c0001t0001g0250 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2235-141G>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 18/28 | chr9 | 133443235 | |||||||
chr9:133443289 | G | A | 1 | a0002c0002t0001g0150 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2235-87G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 18/28 | chr9 | 133443289 | |||||||
chr9:133443612 | G | A | 3 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0003c0003t0001g0236 |
3 | HG00280.hp1 HG01192.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.2420+51G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 19/28 | chr9 | 133443612 | |||||||
chr9:133443619 | C | T | 2 | a0003c0030t0004g0266 a0014c0023t0001g0309 |
2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2420+58C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 19/28 | chr9 | 133443619 | |||||||
chr9:133443630 | C | T | 1 | a0002c0002t0001g0104 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2420+69C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 19/28 | chr9 | 133443630 | |||||||
chr9:133443675 | C | G | 30 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0053 others(27): Show |
34 | HG00140.hp2 HG00639.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.2420+114C>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 19/28 | chr9 | 133443675 | |||||||
chr9:133443920 | C | G | 3 | a0001c0028t0001g0273 a0001c0029t0001g0301 a0003c0030t0004g0266 |
3 | HG02896.hp1 HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2420+359C>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 19/28 | chr9 | 133443920 | |||||||
chr9:133443971 | G | A | 1 | a0013c0016t0001g0113 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2420+410G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 19/28 | chr9 | 133443971 | |||||||
chr9:133444019 | G | A | 1 | a0002c0051t0001g0158 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2420+458G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 19/28 | chr9 | 133444019 | |||||||
chr9:133444219 | A | T | 1 | a0001c0001t0001g0200 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2421-644A>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 19/28 | chr9 | 133444219 | |||||||
chr9:133444220 | T | C | 1 | a0001c0001t0001g0049 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2421-643T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 19/28 | chr9 | 133444220 | |||||||
chr9:133444280 | A | G | 2 | a0001c0017t0002g0234 a0001c0017t0002g0293 |
2 | HG02451.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2421-583A>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 19/28 | chr9 | 133444280 | |||||||
chr9:133444343 | G | A | 3 | a0001c0005t0001g0263 a0001c0005t0001g0264 a0001c0005t0001g0265 |
3 | HG01884.hp1 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2421-520G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 19/28 | chr9 | 133444343 | |||||||
chr9:133444534 | C | T | 1 | a0001c0005t0001g0260 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2421-329C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 19/28 | chr9 | 133444534 | |||||||
chr9:133444646 | A | C | 7 | a0008c0013t0001g0012 a0008c0013t0001g0072 a0008c0013t0001g0074 others(4): Show |
8 | HG00280.hp2 HG00733.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.2421-217A>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 19/28 | chr9 | 133444646 | |||||||
chr9:133444652 | G | A | 1 | a0001c0001t0001g0220 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2421-211G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 19/28 | chr9 | 133444652 | |||||||
chr9:133444654 | G | A | 1 | a0001c0001t0001g0129 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2421-209G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 19/28 | chr9 | 133444654 | |||||||
chr9:133444720 | A | T | 11 | a0003c0003t0001g0235 a0003c0003t0001g0236 a0003c0003t0001g0237 others(8): Show |
11 | HG00280.hp1 HG00323.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.2421-143A>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 19/28 | chr9 | 133444720 | |||||||
chr9:133445114 | G | A | 5 | a0009c0012t0001g0033 a0009c0012t0001g0034 a0009c0012t0001g0065 others(2): Show |
5 | HG00423.hp2 NA18969.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.2610+62G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 20/28 | chr9 | 133445114 | |||||||
chr9:133445136 | C | G | 1 | a0001c0010t0006g0030 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2610+84C>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 20/28 | chr9 | 133445136 | |||||||
chr9:133445228 | G | A | 2 | a0010c0018t0001g0073 a0010c0018t0001g0275 |
2 | HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2610+176G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 20/28 | chr9 | 133445228 | |||||||
chr9:133445298 | G | A | 1 | a0002c0002t0001g0279 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2610+246G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 20/28 | chr9 | 133445298 | |||||||
chr9:133445437 | T | A | 9 | a0001c0042t0001g0302 a0004c0004t0001g0011 a0004c0004t0001g0026 others(6): Show |
12 | HG02258.hp2 HG02280.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.2611-262T>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 20/28 | chr9 | 133445437 | |||||||
chr9:133445520 | A | T | 2 | a0001c0001t0001g0169 a0001c0001t0001g0182 |
2 | NA18977.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.2611-179A>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 20/28 | chr9 | 133445520 | |||||||
chr9:133445551 | C | T | 6 | a0001c0027t0001g0272 a0001c0028t0001g0273 a0014c0023t0001g0303 others(3): Show |
6 | HG01109.hp1 HG02647.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2611-148C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 20/28 | chr9 | 133445551 | |||||||
chr9:133445552 | G | A | 9 | a0001c0042t0001g0302 a0004c0004t0001g0011 a0004c0004t0001g0026 others(6): Show |
12 | HG02258.hp2 HG02280.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.2611-147G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 20/28 | chr9 | 133445552 | |||||||
chr9:133445557 | C | T | 6 | a0001c0027t0001g0272 a0001c0028t0001g0273 a0014c0023t0001g0303 others(3): Show |
6 | HG01109.hp1 HG02647.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2611-142C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 20/28 | chr9 | 133445557 | |||||||
chr9:133445896 | G | A | 156 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0053 others(153): Show |
174 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.2731+77G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 21/28 | chr9 | 133445896 | |||||||
chr9:133445992 | A | G | 1 | a0001c0001t0001g0254 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2731+173A>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 21/28 | chr9 | 133445992 | |||||||
chr9:133446038 | C | T | 3 | a0001c0001t0001g0027 a0001c0001t0001g0064 a0015c0024t0001g0024 |
4 | HG01069.hp2 HG01071.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2731+219C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 21/28 | chr9 | 133446038 | |||||||
chr9:133446051 | C | T | 8 | a0001c0042t0001g0302 a0004c0004t0001g0026 a0004c0004t0001g0227 others(5): Show |
9 | HG02258.hp2 HG02615.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.2731+232C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 21/28 | chr9 | 133446051 | |||||||
chr9:133446082 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2731+263G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 21/28 | chr9 | 133446082 | |||||||
chr9:133446242 | A | C | 1 | a0001c0011t0001g0156 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2731+423A>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 21/28 | chr9 | 133446242 | |||||||
chr9:133446270 | A | G | 86 | a0001c0001t0001g0002 a0001c0001t0001g0146 a0001c0001t0001g0250 others(83): Show |
101 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.2731+451A>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 21/28 | chr9 | 133446270 | |||||||
chr9:133446331 | C | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0211 |
2 | HG01934.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.2731+512C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 21/28 | chr9 | 133446331 | |||||||
chr9:133446558 | G | T | 108 | a0001c0001t0001g0154 a0001c0001t0001g0200 a0001c0001t0001g0216 others(105): Show |
120 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.2731+739G>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 21/28 | chr9 | 133446558 | |||||||
chr9:133446651 | C | G | 1 | a0028c0043t0001g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2731+832C>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 21/28 | chr9 | 133446651 | |||||||
chr9:133446674 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.2731+855T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 21/28 | chr9 | 133446674 | |||||||
chr9:133446675 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.2731+856C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 21/28 | chr9 | 133446675 | |||||||
chr9:133446758 | T | G | 6 | a0008c0013t0001g0012 a0008c0013t0001g0072 a0008c0013t0001g0074 others(3): Show |
7 | HG00280.hp2 HG00733.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.2731+939T>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 21/28 | chr9 | 133446758 | |||||||
chr9:133446943 | C | T | 6 | a0006c0008t0001g0136 a0009c0012t0001g0033 a0009c0012t0001g0034 others(3): Show |
6 | HG00423.hp2 NA18969.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.2731+1124C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 21/28 | chr9 | 133446943 | |||||||
chr9:133446950 | G | A | 6 | a0001c0001t0001g0010 a0001c0001t0001g0054 a0001c0001t0001g0166 others(3): Show |
8 | HG00140.hp2 HG00741.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2731+1131G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 21/28 | chr9 | 133446950 | |||||||
chr9:133446953 | G | T | 20 | a0001c0011t0001g0215 a0002c0002t0001g0004 a0002c0002t0001g0006 others(17): Show |
27 | HG00642.hp1 HG01069.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.2731+1134G>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 21/28 | chr9 | 133446953 | |||||||
chr9:133446955 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2731+1136T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 21/28 | chr9 | 133446955 | |||||||
chr9:133446998 | T | C | 305 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(302): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.2731+1179T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 21/28 | chr9 | 133446998 | |||||||
chr9:133447108 | G | A | 1 | a0028c0043t0001g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2731+1289G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 21/28 | chr9 | 133447108 | |||||||
chr9:133447190 | G | A | 1 | a0022c0041t0003g0031 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2731+1371G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 21/28 | chr9 | 133447190 | |||||||
chr9:133447248 | A | G | 6 | a0008c0013t0001g0012 a0008c0013t0001g0072 a0008c0013t0001g0074 others(3): Show |
7 | HG00280.hp2 HG00733.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.2732-1351A>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 21/28 | chr9 | 133447248 | |||||||
chr9:133447255 | C | A | 1 | a0001c0001t0001g0193 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2732-1344C>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 21/28 | chr9 | 133447255 | |||||||
chr9:133447275 | A | G | 3 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0002c0006t0001g0098 |
3 | HG01192.hp2 HG01255.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.2732-1324A>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 21/28 | chr9 | 133447275 | |||||||
chr9:133447289 | T | C | 1 | a0001c0005t0001g0264 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2732-1310T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 21/28 | chr9 | 133447289 | |||||||
chr9:133447294 | C | CTCTTT | 120 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0027 others(117): Show |
135 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.2732-1298_2732-129 others(9): Show |
ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 21/28 | INFO_REALIGN_3_PRIME | chr9 | 133447294 | ||||||
chr9:133447335 | A | G | 64 | a0001c0011t0001g0137 a0001c0011t0001g0138 a0001c0011t0001g0155 others(61): Show |
74 | HG00609.hp2 HG00639.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.2732-1264A>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 21/28 | chr9 | 133447335 | |||||||
chr9:133447630 | C | T | 1 | a0003c0031t0001g0276 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2732-969C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 21/28 | chr9 | 133447630 | |||||||
chr9:133447776 | T | C | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(123): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.2732-823T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 21/28 | chr9 | 133447776 | |||||||
chr9:133447790 | C | T | 1 | a0002c0002t0001g0082 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2732-809C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 21/28 | chr9 | 133447790 | |||||||
chr9:133447994 | C | CTT | 6 | a0006c0008t0001g0136 a0009c0012t0001g0033 a0009c0012t0001g0034 others(3): Show |
6 | HG00423.hp2 NA18969.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.2732-592_2732-591d others(4): Show |
ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 21/28 | INFO_REALIGN_3_PRIME | chr9 | 133447994 | ||||||
chr9:133448001 | T | C | 20 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0046 others(17): Show |
24 | HG00280.hp1 HG00323.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.2732-598T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 21/28 | chr9 | 133448001 | |||||||
chr9:133448179 | G | A | 1 | a0002c0002t0001g0079 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2732-420G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 21/28 | chr9 | 133448179 | |||||||
chr9:133448257 | C | T | 2 | a0001c0001t0001g0193 a0001c0001t0001g0287 |
2 | HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.2732-342C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 21/28 | chr9 | 133448257 | |||||||
chr9:133448358 | G | A | 7 | a0001c0001t0001g0018 a0001c0001t0001g0050 a0001c0001t0001g0051 others(4): Show |
8 | HG00621.hp1 NA18939.hp2 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.2732-241G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 21/28 | chr9 | 133448358 | |||||||
chr9:133448541 | C | T | 6 | a0006c0008t0001g0136 a0009c0012t0001g0033 a0009c0012t0001g0034 others(3): Show |
6 | HG00423.hp2 NA18969.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.2732-58C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 21/28 | chr9 | 133448541 | |||||||
chr9:133448579 | T | G | 3 | a0011c0015t0001g0023 a0011c0015t0001g0068 a0011c0015t0001g0262 |
4 | HG02145.hp2 HG02257.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2732-20T>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 21/28 | chr9 | 133448579 | |||||||
chr9:133448783 | C | T | 20 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0046 others(17): Show |
24 | HG00280.hp1 HG00323.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.2861+55C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 22/28 | chr9 | 133448783 | |||||||
chr9:133449133 | C | A | 2 | a0001c0001t0001g0219 a0001c0001t0001g0221 |
2 | NA18945.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.2861+405C>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 22/28 | chr9 | 133449133 | |||||||
chr9:133449163 | C | T | 1 | a0001c0001t0001g0224 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2861+435C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 22/28 | chr9 | 133449163 | |||||||
chr9:133449164 | G | A | 2 | a0002c0002t0001g0085 a0002c0002t0001g0093 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2861+436G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 22/28 | chr9 | 133449164 | |||||||
chr9:133449198 | T | G | 1 | a0001c0005t0001g0264 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2861+470T>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 22/28 | chr9 | 133449198 | |||||||
chr9:133449222 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2861+494C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 22/28 | chr9 | 133449222 | |||||||
chr9:133449253 | C | A | 2 | a0002c0037t0001g0088 a0015c0024t0001g0024 |
3 | HG01069.hp2 HG01071.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.2861+525C>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 22/28 | chr9 | 133449253 | |||||||
chr9:133449262 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2862-521C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 22/28 | chr9 | 133449262 | |||||||
chr9:133449371 | C | T | 17 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0046 others(14): Show |
20 | HG00280.hp1 HG00323.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.2862-412C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 22/28 | chr9 | 133449371 | |||||||
chr9:133449511 | G | C | 19 | a0001c0001t0001g0009 a0001c0001t0001g0049 a0001c0001t0001g0060 others(16): Show |
20 | HG01167.hp2 HG01346.hp1 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.2862-272G>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 22/28 | chr9 | 133449511 | |||||||
chr9:133449522 | C | G | 1 | a0003c0031t0001g0276 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2862-261C>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 22/28 | chr9 | 133449522 | |||||||
chr9:133449556 | C | G | 65 | a0001c0011t0001g0137 a0001c0011t0001g0138 a0001c0011t0001g0155 others(62): Show |
75 | HG00609.hp2 HG00639.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.2862-227C>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 22/28 | chr9 | 133449556 | |||||||
chr9:133450086 | C | G | 7 | a0001c0001t0001g0200 a0002c0040t0001g0300 a0003c0030t0004g0266 others(4): Show |
7 | HG01106.hp2 HG01891.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.3044+121C>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133450086 | |||||||
chr9:133450167 | T | G | 1 | a0002c0040t0001g0300 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3044+202T>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133450167 | |||||||
chr9:133450406 | T | C | 1 | a0001c0005t0001g0264 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3044+441T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133450406 | |||||||
chr9:133450435 | G | T | 1 | a0001c0001t0001g0283 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.3044+470G>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133450435 | |||||||
chr9:133450489 | G | A | 1 | a0022c0041t0003g0031 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3044+524G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133450489 | |||||||
chr9:133450565 | C | CA | 12 | a0001c0001t0001g0047 a0001c0001t0001g0123 a0001c0001t0001g0161 others(9): Show |
12 | HG01081.hp2 HG01109.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.3044+619dupA | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr9 | 133450565 | ||||||
chr9:133450565 | CA | C | 16 | a0001c0001t0001g0061 a0001c0001t0001g0163 a0001c0001t0001g0167 others(13): Show |
16 | HG00140.hp2 HG01256.hp1 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.3044+619delA | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr9 | 133450565 | ||||||
chr9:133450580 | A | G | 2 | a0011c0015t0001g0023 a0011c0015t0001g0068 |
3 | HG02257.hp1 HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3044+615A>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133450580 | |||||||
chr9:133450581 | A | G | 3 | a0001c0001t0001g0210 a0002c0002t0001g0015 a0002c0002t0001g0150 |
4 | HG00423.hp1 HG02040.hp1 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.3044+616A>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133450581 | |||||||
chr9:133450585 | G | A | 1 | a0001c0001t0001g0224 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3044+620G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133450585 | |||||||
chr9:133450684 | G | A | 2 | a0001c0027t0001g0272 a0002c0038t0001g0107 |
2 | HG01109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.3044+719G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133450684 | |||||||
chr9:133450706 | G | A | 1 | a0002c0002t0001g0116 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.3044+741G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133450706 | |||||||
chr9:133450736 | C | T | 6 | a0001c0027t0001g0272 a0002c0038t0001g0107 a0003c0032t0001g0268 others(3): Show |
6 | HG01081.hp2 HG01109.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.3044+771C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133450736 | |||||||
chr9:133450784 | G | T | 7 | a0003c0019t0001g0239 a0004c0004t0001g0011 a0004c0004t0001g0026 others(4): Show |
10 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.3044+819G>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133450784 | |||||||
chr9:133450805 | G | A | 2 | a0002c0037t0001g0088 a0015c0024t0001g0024 |
3 | HG01069.hp2 HG01071.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.3044+840G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133450805 | |||||||
chr9:133450853 | G | C | 6 | a0001c0001t0001g0010 a0001c0001t0001g0054 a0001c0001t0001g0166 others(3): Show |
8 | HG00140.hp2 HG00741.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.3044+888G>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133450853 | |||||||
chr9:133451043 | G | A | 2 | a0001c0001t0001g0128 a0001c0001t0001g0211 |
2 | HG01934.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.3044+1078G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133451043 | |||||||
chr9:133451246 | C | A | 63 | a0001c0011t0001g0137 a0001c0011t0001g0138 a0001c0011t0001g0155 others(60): Show |
73 | HG00609.hp2 HG00639.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.3044+1281C>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133451246 | |||||||
chr9:133451295 | T | C | 2 | a0001c0001t0001g0219 a0001c0001t0001g0221 |
2 | NA18945.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.3044+1330T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133451295 | |||||||
chr9:133451322 | A | G | 1 | a0008c0013t0001g0075 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3044+1357A>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133451322 | |||||||
chr9:133451350 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3044+1385C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133451350 | |||||||
chr9:133451385 | G | A | 2 | a0002c0037t0001g0088 a0015c0024t0001g0024 |
3 | HG01069.hp2 HG01071.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.3044+1420G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133451385 | |||||||
chr9:133451461 | T | A | 1 | a0017c0020t0001g0232 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3044+1496T>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133451461 | |||||||
chr9:133451471 | C | T | 6 | a0001c0027t0001g0272 a0002c0038t0001g0107 a0003c0032t0001g0268 others(3): Show |
6 | HG01081.hp2 HG01109.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.3044+1506C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133451471 | |||||||
chr9:133451628 | C | T | 1 | a0003c0031t0001g0276 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3044+1663C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133451628 | |||||||
chr9:133451774 | C | G | 1 | a0001c0001t0001g0059 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3044+1809C>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133451774 | |||||||
chr9:133451821 | A | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(258): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.3044+1856A>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133451821 | |||||||
chr9:133451894 | C | CA | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(150): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.3044+1951dupA | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr9 | 133451894 | ||||||
chr9:133451894 | C | CAA | 26 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0046 others(23): Show |
29 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.3044+1950_3044+195 others(6): Show |
ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr9 | 133451894 | ||||||
chr9:133451894 | CA | C | 58 | a0001c0001t0001g0216 a0001c0011t0001g0137 a0001c0011t0001g0138 others(55): Show |
68 | HG00609.hp2 HG00639.hp2 HG00733.hp1 others(65): Show |
intron_variant | MODIFIER | c.3044+1951delA | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr9 | 133451894 | ||||||
chr9:133451894 | CAA | C | 8 | a0001c0027t0001g0272 a0002c0002t0001g0104 a0002c0038t0001g0107 others(5): Show |
8 | HG01081.hp2 HG01109.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.3044+1950_3044+195 others(6): Show |
ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr9 | 133451894 | ||||||
chr9:133451990 | A | AT | 7 | a0001c0001t0001g0144 a0002c0002t0001g0037 a0002c0002t0001g0084 others(4): Show |
7 | HG00642.hp1 HG01069.hp1 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.3044+2038dupT | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr9 | 133451990 | ||||||
chr9:133452120 | C | CT | 69 | a0001c0011t0001g0137 a0001c0011t0001g0138 a0001c0011t0001g0155 others(66): Show |
79 | HG00423.hp2 HG00609.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.3044+2167dupT | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr9 | 133452120 | ||||||
chr9:133452197 | C | T | 1 | a0022c0041t0003g0031 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3045-2218C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133452197 | |||||||
chr9:133452199 | G | A | 1 | a0001c0005t0001g0264 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3045-2216G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133452199 | |||||||
chr9:133452205 | T | C | 17 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0046 others(14): Show |
20 | HG00280.hp1 HG00323.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.3045-2210T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133452205 | |||||||
chr9:133452402 | C | G | 6 | a0001c0027t0001g0272 a0002c0038t0001g0107 a0003c0032t0001g0268 others(3): Show |
6 | HG01081.hp2 HG01109.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.3045-2013C>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133452402 | |||||||
chr9:133452456 | C | T | 1 | a0028c0043t0001g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3045-1959C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133452456 | |||||||
chr9:133452486 | A | G | 1 | a0001c0001t0001g0216 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3045-1929A>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133452486 | |||||||
chr9:133452592 | G | A | 6 | a0001c0027t0001g0272 a0002c0038t0001g0107 a0003c0032t0001g0268 others(3): Show |
6 | HG01081.hp2 HG01109.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.3045-1823G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133452592 | |||||||
chr9:133452645 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3045-1770C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133452645 | |||||||
chr9:133452655 | C | A | 2 | a0011c0015t0001g0023 a0011c0015t0001g0068 |
3 | HG02257.hp1 HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3045-1760C>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133452655 | |||||||
chr9:133452945 | T | C | 3 | a0005c0007t0001g0019 a0005c0007t0001g0056 a0005c0007t0001g0280 |
4 | NA18747.hp2 NA18962.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.3045-1470T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133452945 | |||||||
chr9:133453073 | G | A | 7 | a0001c0005t0001g0264 a0001c0027t0001g0272 a0002c0038t0001g0107 others(4): Show |
7 | HG01081.hp2 HG01109.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.3045-1342G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133453073 | |||||||
chr9:133453174 | T | C | 3 | a0002c0037t0001g0088 a0015c0024t0001g0024 a0028c0043t0001g0069 |
4 | HG01069.hp2 HG01071.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.3045-1241T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133453174 | |||||||
chr9:133453208 | G | A | 18 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0046 others(15): Show |
21 | HG00280.hp1 HG00323.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.3045-1207G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133453208 | |||||||
chr9:133453218 | C | T | 1 | a0001c0005t0001g0255 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3045-1197C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133453218 | |||||||
chr9:133453271 | C | T | 1 | a0002c0002t0001g0103 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3045-1144C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133453271 | |||||||
chr9:133453648 | C | T | 6 | a0001c0001t0001g0200 a0002c0040t0001g0300 a0018c0021t0001g0190 others(3): Show |
6 | HG01106.hp2 HG01891.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.3045-767C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133453648 | |||||||
chr9:133453785 | G | A | 2 | a0011c0015t0001g0023 a0011c0015t0001g0068 |
3 | HG02257.hp1 HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3045-630G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133453785 | |||||||
chr9:133453877 | C | T | 1 | a0002c0002t0001g0082 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3045-538C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133453877 | |||||||
chr9:133453946 | T | C | 105 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0046 others(102): Show |
119 | HG00280.hp1 HG00323.hp1 HG00609.hp2 others(116): Show |
intron_variant | MODIFIER | c.3045-469T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133453946 | |||||||
chr9:133454166 | G | C | 63 | a0001c0011t0001g0137 a0001c0011t0001g0138 a0001c0011t0001g0155 others(60): Show |
73 | HG00609.hp2 HG00639.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.3045-249G>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133454166 | |||||||
chr9:133454367 | T | C | 2 | a0002c0037t0001g0088 a0015c0024t0001g0024 |
3 | HG01069.hp2 HG01071.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.3045-48T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133454367 | |||||||
chr9:133454374 | G | A | 2 | a0002c0037t0001g0088 a0015c0024t0001g0024 |
3 | HG01069.hp2 HG01071.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.3045-41G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 23/28 | chr9 | 133454374 | |||||||
chr9:133454743 | G | A | 1 | a0028c0043t0001g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3249+124G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 24/28 | chr9 | 133454743 | |||||||
chr9:133454744 | C | T | 1 | a0028c0043t0001g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3249+125C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 24/28 | chr9 | 133454744 | |||||||
chr9:133454834 | G | C | 1 | a0002c0002t0001g0100 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3249+215G>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 24/28 | chr9 | 133454834 | |||||||
chr9:133454839 | C | T | 1 | a0001c0001t0001g0052 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.3249+220C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 24/28 | chr9 | 133454839 | |||||||
chr9:133454897 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3249+278C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 24/28 | chr9 | 133454897 | |||||||
chr9:133455007 | G | T | 1 | a0003c0031t0001g0276 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3250-278G>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 24/28 | chr9 | 133455007 | |||||||
chr9:133455009 | C | T | 3 | a0001c0001t0001g0047 a0001c0001t0001g0159 a0001c0001t0001g0204 |
3 | NA18939.hp1 NA18966.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.3250-276C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 24/28 | chr9 | 133455009 | |||||||
chr9:133455111 | C | T | 1 | a0002c0002t0001g0095 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3250-174C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 24/28 | chr9 | 133455111 | |||||||
chr9:133455266 | T | C | 7 | a0001c0027t0001g0272 a0002c0038t0001g0107 a0003c0032t0001g0268 others(4): Show |
7 | HG01081.hp2 HG01109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.3250-19T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 24/28 | chr9 | 133455266 | |||||||
chr9:133455480 | C | T | 1 | a0001c0001t0001g0282 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3400+45C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 25/28 | chr9 | 133455480 | |||||||
chr9:133455546 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3400+111C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 25/28 | chr9 | 133455546 | |||||||
chr9:133455576 | G | A | 3 | a0001c0001t0001g0021 a0001c0001t0001g0220 a0001c0001t0001g0224 |
4 | HG00408.hp1 HG02071.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.3400+141G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 25/28 | chr9 | 133455576 | |||||||
chr9:133455593 | AGTGCAGT others(8): Show |
A | 1 | a0001c0001t0001g0251 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3400+161_3400+175d others(17): Show |
ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr9 | 133455593 | ||||||
chr9:133455724 | G | A | 5 | a0006c0008t0001g0032 a0006c0008t0001g0044 a0006c0008t0001g0135 others(2): Show |
5 | NA18942.hp1 NA18951.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.3400+289G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 25/28 | chr9 | 133455724 | |||||||
chr9:133455822 | C | T | 1 | a0010c0060t0001g0198 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.3401-247C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 25/28 | chr9 | 133455822 | |||||||
chr9:133455888 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3401-181C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 25/28 | chr9 | 133455888 | |||||||
chr9:133455920 | C | T | 1 | a0028c0043t0001g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3401-149C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 25/28 | chr9 | 133455920 | |||||||
chr9:133455927 | T | C | 1 | a0001c0001t0001g0027 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3401-142T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 25/28 | chr9 | 133455927 | |||||||
chr9:133455984 | C | G | 7 | a0002c0002t0001g0077 a0002c0002t0001g0097 a0002c0002t0001g0111 others(4): Show |
7 | HG00738.hp1 HG01975.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.3401-85C>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 25/28 | chr9 | 133455984 | |||||||
chr9:133456252 | T | C | 1 | a0003c0031t0001g0276 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3547+37T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 26/28 | chr9 | 133456252 | |||||||
chr9:133456358 | G | T | 1 | a0003c0030t0004g0266 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3547+143G>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 26/28 | chr9 | 133456358 | |||||||
chr9:133456479 | G | T | 1 | a0003c0030t0004g0266 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3548-64G>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 26/28 | chr9 | 133456479 | |||||||
chr9:133456504 | G | A | 1 | a0010c0018t0001g0274 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3548-39G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 26/28 | chr9 | 133456504 | |||||||
chr9:133456510 | G | A | 1 | a0002c0002t0001g0015 | 2 | NA18944.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.3548-33G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 26/28 | chr9 | 133456510 | |||||||
chr9:133456762 | T | C | 3 | a0010c0018t0001g0073 a0010c0018t0001g0275 a0014c0056t0001g0304 |
3 | HG03139.hp2 HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3724+43T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 27/28 | chr9 | 133456762 | |||||||
chr9:133456878 | G | C | 1 | a0001c0005t0001g0264 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3724+159G>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 27/28 | chr9 | 133456878 | |||||||
chr9:133457120 | A | G | 1 | a0014c0023t0001g0309 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3724+401A>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 27/28 | chr9 | 133457120 | |||||||
chr9:133457215 | G | C | 2 | a0001c0001t0001g0219 a0001c0001t0001g0221 |
2 | NA18945.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.3724+496G>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 27/28 | chr9 | 133457215 | |||||||
chr9:133457250 | G | A | 1 | a0001c0001t0005g0186 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3724+531G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 27/28 | chr9 | 133457250 | |||||||
chr9:133457345 | A | T | 5 | a0003c0003t0001g0070 a0003c0003t0001g0071 a0003c0003t0001g0271 others(2): Show |
5 | HG00735.hp1 HG01099.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.3725-565A>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 27/28 | chr9 | 133457345 | |||||||
chr9:133457407 | C | T | 41 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0046 others(38): Show |
46 | HG00280.hp1 HG00323.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.3725-503C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 27/28 | chr9 | 133457407 | |||||||
chr9:133457502 | C | A | 1 | a0001c0011t0001g0215 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3725-408C>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 27/28 | chr9 | 133457502 | |||||||
chr9:133457521 | A | G | 5 | a0003c0003t0001g0070 a0003c0003t0001g0071 a0003c0003t0001g0271 others(2): Show |
5 | HG00735.hp1 HG01099.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.3725-389A>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 27/28 | chr9 | 133457521 | |||||||
chr9:133457580 | G | A | 1 | a0002c0006t0001g0083 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3725-330G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 27/28 | chr9 | 133457580 | |||||||
chr9:133457597 | T | C | 1 | a0001c0005t0001g0299 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3725-313T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 27/28 | chr9 | 133457597 | |||||||
chr9:133457634 | G | T | 1 | a0025c0053t0001g0298 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3725-276G>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 27/28 | chr9 | 133457634 | |||||||
chr9:133457645 | T | C | 1 | a0028c0043t0001g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3725-265T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 27/28 | chr9 | 133457645 | |||||||
chr9:133457715 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3725-195C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 27/28 | chr9 | 133457715 | |||||||
chr9:133458126 | T | C | 6 | a0003c0003t0001g0235 a0003c0003t0001g0236 a0003c0003t0001g0237 others(3): Show |
6 | HG00280.hp1 HG00323.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.3909+32T>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 28/28 | chr9 | 133458126 | |||||||
chr9:133458480 | C | T | 3 | a0002c0037t0001g0088 a0015c0024t0001g0024 a0028c0043t0001g0069 |
4 | HG01069.hp2 HG01071.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.3909+386C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 28/28 | chr9 | 133458480 | |||||||
chr9:133458510 | C | A | 51 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(48): Show |
59 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.3909+416C>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 28/28 | chr9 | 133458510 | |||||||
chr9:133458555 | C | CAAAAAAA | 20 | a0001c0001t0001g0148 a0001c0001t0001g0168 a0001c0005t0001g0257 others(17): Show |
22 | HG00280.hp2 HG00423.hp2 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.3910-404_3910-398d others(9): Show |
ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 28/28 | INFO_REALIGN_3_PRIME | chr9 | 133458555 | ||||||
chr9:133458555 | C | CAAAAAAA others(1): Show |
154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.3910-405_3910-398d others(10): Show |
ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 28/28 | INFO_REALIGN_3_PRIME | chr9 | 133458555 | ||||||
chr9:133458555 | C | CAAAAAAA others(2): Show |
49 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0050 others(46): Show |
53 | HG00408.hp1 HG00438.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.3910-406_3910-398d others(11): Show |
ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 28/28 | INFO_REALIGN_3_PRIME | chr9 | 133458555 | ||||||
chr9:133458555 | C | CAAAAAAA others(3): Show |
5 | a0001c0001t0001g0123 a0001c0001t0001g0212 a0001c0001t0001g0308 others(2): Show |
5 | HG02135.hp2 HG02622.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.3910-407_3910-398d others(12): Show |
ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 28/28 | INFO_REALIGN_3_PRIME | chr9 | 133458555 | ||||||
chr9:133458555 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0207 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.3910-410_3910-398d others(15): Show |
ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 28/28 | INFO_REALIGN_3_PRIME | chr9 | 133458555 | ||||||
chr9:133458555 | CA | C | 19 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0046 others(16): Show |
22 | HG00280.hp1 HG00323.hp1 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.3910-398delA | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 28/28 | INFO_REALIGN_3_PRIME | chr9 | 133458555 | ||||||
chr9:133458632 | A | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(258): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.3910-342A>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 28/28 | chr9 | 133458632 | |||||||
chr9:133458704 | A | T | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(303): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.3910-270A>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 28/28 | chr9 | 133458704 | |||||||
chr9:133458723 | G | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(144): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.3910-251G>C | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 28/28 | chr9 | 133458723 | |||||||
chr9:133458756 | A | G | 8 | a0001c0001t0001g0200 a0001c0001t0005g0186 a0002c0040t0001g0300 others(5): Show |
8 | HG01106.hp2 HG01891.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.3910-218A>G | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 28/28 | chr9 | 133458756 | |||||||
chr9:133458884 | C | T | 2 | a0002c0002t0001g0109 a0002c0002t0001g0110 |
2 | NA18988.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.3910-90C>T | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 28/28 | chr9 | 133458884 | |||||||
chr9:133458885 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3910-89G>A | ADAMTS13 | ENSG00000160323.19 | transcript | ENST00000355699.7 | protein_coding | 28/28 | chr9 | 133458885 |