Item | Value |
---|---|
geneid | 3371 |
ensemblid | ENSG00000041982.17 |
hgncid | 5318 |
symbol | TNC |
name | tenascin C |
refseq_nuc | NM_002160.4 |
refseq_prot | NP_002151.2 |
ensembl_nuc | ENST00000350763.9 |
ensembl_prot | ENSP00000265131.4 |
mane_status | MANE Select |
chr | chr9 |
start | 115019575 |
end | 115118157 |
strand | - |
ver | v1.2 |
region | chr9:115019575-115118157 |
region5000 | chr9:115014575-115123157 |
regionname0 | TNC_chr9_115019575_115118157 |
regionname5000 | TNC_chr9_115014575_115123157 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 2201 | 50 | 7 | 10 | 21 | 4 | 8 | 20 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0002 | 0/0 | 2201 | 47 | 2 | 10 | 26 | 1 | 8 | 21 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0003 | 0/0 | 2201 | 39 | 9 | 4 | 23 | 1 | 2 | 21 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0004 | 0/0 | 2201 | 31 | 6 | 6 | 12 | 0 | 7 | 9 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0005 | 0/0 | 2201 | 24 | 5 | 10 | 2 | 2 | 5 | 0 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0006 | 0/0 | 2201 | 18 | 3 | 8 | 7 | 0 | 0 | 5 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0007 | 0/0 | 2201 | 17 | 0 | 0 | 15 | 0 | 2 | 11 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0008 | 0/0 | 2201 | 15 | 0 | 5 | 1 | 5 | 4 | 0 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0009 | 0/0 | 2201 | 15 | 2 | 5 | 5 | 0 | 3 | 2 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0010 | 0/0 | 2201 | 12 | 0 | 0 | 11 | 0 | 1 | 8 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0011 | 0/0 | 2201 | 11 | 6 | 0 | 4 | 0 | 1 | 1 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0012 | 0/0 | 2201 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0013 | 0/0 | 2201 | 5 | 0 | 0 | 5 | 0 | 0 | 4 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0014 | 0/0 | 2201 | 5 | 2 | 3 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0015 | 0/0 | 2201 | 5 | 4 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0016 | 0/0 | 2201 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0017 | 0/0 | 2201 | 4 | 1 | 0 | 3 | 0 | 0 | 3 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0018 | 0/1 | 2201 | 3 | 0 | 2 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0019 | 0/0 | 2201 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0020 | 0/0 | 2201 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0021 | 0/0 | 2201 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0022 | 0/0 | 2201 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0023 | 0/0 | 2201 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0024 | 0/0 | 2201 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0025 | 0/0 | 2201 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0026 | 0/0 | 2201 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0027 | 0/0 | 2201 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0028 | 0/0 | 2201 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0029 | 0/0 | 2201 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0030 | 1/0 | 2201 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0031 | 0/0 | 2201 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0032 | 0/0 | 2201 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0033 | 0/0 | 2201 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0034 | 0/0 | 2201 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0035 | 0/0 | 2201 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0036 | 0/0 | 2201 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0037 | 0/0 | 2201 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0038 | 0/0 | 2201 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0039 | 0/0 | 2201 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0040 | 0/0 | 2201 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0041 | 0/0 | 2201 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0042 | 0/0 | 2201 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0043 | 0/0 | 2201 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0044 | 0/0 | 2201 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0045 | 0/0 | 2201 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0046 | 0/0 | 2201 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0047 | 0/0 | 2201 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0048 | 0/0 | 2201 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0049 | 0/0 | 2201 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0050 | 0/0 | 2201 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0051 | 0/0 | 2201 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0052 | 0/0 | 2201 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0053 | 0/0 | 2201 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0054 | 0/0 | 2201 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0055 | 0/0 | 2201 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
a0056 | 0/0 | 2201 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | MGAMT others(2196): Show |
chr9 | 115014575 | 115123157 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 0/0 | 6603 | 26 | 3 | 7 | 9 | 4 | 3 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0001c0009 | 0/0 | 6603 | 12 | 3 | 2 | 4 | 0 | 3 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0001c0011 | 0/0 | 6603 | 7 | 0 | 1 | 5 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0001c0024 | 0/0 | 6603 | 4 | 1 | 0 | 3 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0001c0094 | 0/0 | 6603 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0002c0001 | 0/0 | 6603 | 39 | 1 | 10 | 21 | 1 | 6 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0002c0020 | 0/0 | 6603 | 5 | 0 | 0 | 5 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0002c0093 | 0/0 | 6603 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0002c0096 | 0/0 | 6603 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0002c0098 | 0/0 | 6603 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0003c0003 | 0/0 | 6603 | 23 | 2 | 3 | 16 | 1 | 1 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0003c0013 | 0/0 | 6603 | 6 | 0 | 1 | 4 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0003c0027 | 0/0 | 6603 | 3 | 3 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0003c0035 | 0/0 | 6603 | 2 | 2 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0003c0052 | 0/0 | 6603 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0003c0055 | 0/0 | 6603 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0003c0068 | 0/0 | 6603 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0003c0069 | 0/0 | 6603 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0003c0077 | 0/0 | 6603 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0004c0004 | 0/0 | 6603 | 19 | 0 | 3 | 11 | 0 | 5 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0004c0018 | 0/0 | 6603 | 5 | 3 | 0 | 1 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0004c0045 | 0/0 | 6603 | 2 | 0 | 2 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0004c0050 | 0/0 | 6603 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0004c0051 | 0/0 | 6603 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0004c0073 | 0/0 | 6603 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0004c0074 | 0/0 | 6603 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0004c0075 | 0/0 | 6603 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0005c0014 | 0/0 | 6603 | 6 | 0 | 5 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0005c0017 | 0/0 | 6603 | 5 | 0 | 1 | 1 | 0 | 3 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0005c0023 | 0/0 | 6603 | 4 | 0 | 1 | 0 | 2 | 1 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0005c0034 | 0/0 | 6603 | 2 | 0 | 2 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0005c0037 | 0/0 | 6603 | 2 | 2 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0005c0061 | 0/0 | 6603 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0005c0062 | 0/0 | 6603 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0005c0066 | 0/0 | 6603 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0005c0067 | 0/0 | 6603 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0005c0103 | 0/0 | 6603 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0006c0007 | 0/0 | 6603 | 13 | 3 | 6 | 4 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0006c0015 | 0/0 | 6603 | 5 | 0 | 2 | 3 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0007c0006 | 0/0 | 6603 | 14 | 0 | 0 | 14 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0007c0041 | 0/0 | 6603 | 2 | 0 | 0 | 0 | 0 | 2 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0007c0086 | 0/0 | 6603 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0008c0005 | 0/0 | 6603 | 15 | 0 | 5 | 1 | 5 | 4 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0009c0019 | 0/0 | 6603 | 5 | 0 | 4 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0009c0031 | 0/0 | 6603 | 3 | 0 | 1 | 1 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0009c0042 | 0/0 | 6603 | 2 | 0 | 0 | 1 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0009c0044 | 0/0 | 6603 | 2 | 0 | 0 | 2 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0009c0092 | 0/0 | 6603 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0009c0099 | 0/0 | 6603 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0009c0100 | 0/0 | 6603 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0010c0008 | 0/0 | 6603 | 12 | 0 | 0 | 11 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0011c0010 | 0/0 | 6603 | 10 | 6 | 0 | 3 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0011c0076 | 0/0 | 6603 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0012c0012 | 0/0 | 6603 | 7 | 7 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0013c0029 | 0/0 | 6603 | 3 | 0 | 0 | 3 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0013c0040 | 0/0 | 6603 | 2 | 0 | 0 | 2 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0014c0016 | 0/0 | 6603 | 5 | 2 | 3 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0015c0021 | 0/0 | 6603 | 4 | 4 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0015c0059 | 0/0 | 6603 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0016c0022 | 0/0 | 6603 | 4 | 4 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0017c0043 | 0/0 | 6603 | 2 | 0 | 0 | 2 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0017c0095 | 0/0 | 6603 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0017c0101 | 0/0 | 6603 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0018c0026 | 0/1 | 6603 | 3 | 0 | 2 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0019c0032 | 0/0 | 6603 | 3 | 2 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0020c0025 | 0/0 | 6603 | 3 | 2 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0021c0028 | 0/0 | 6603 | 3 | 2 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0022c0033 | 0/0 | 6603 | 3 | 3 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0023c0030 | 0/0 | 6603 | 3 | 0 | 0 | 3 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0024c0082 | 0/0 | 6603 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0024c0083 | 0/0 | 6603 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0025c0038 | 0/0 | 6603 | 2 | 2 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0026c0046 | 0/0 | 6603 | 2 | 2 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0027c0070 | 0/0 | 6603 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0027c0071 | 0/0 | 6603 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0028c0036 | 0/0 | 6603 | 2 | 2 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0029c0039 | 0/0 | 6603 | 2 | 0 | 0 | 2 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0030c0081 | 1/0 | 6603 | 1 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0031c0053 | 0/0 | 6603 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0032c0056 | 0/0 | 6603 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0033c0090 | 0/0 | 6603 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0034c0054 | 0/0 | 6603 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0035c0065 | 0/0 | 6603 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0036c0104 | 0/0 | 6603 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0037c0064 | 0/0 | 6603 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0038c0079 | 0/0 | 6603 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0039c0078 | 0/0 | 6603 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0040c0088 | 0/0 | 6603 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0041c0072 | 0/0 | 6603 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0042c0063 | 0/0 | 6603 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0043c0047 | 0/0 | 6603 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0044c0091 | 0/0 | 6603 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0045c0087 | 0/0 | 6603 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0046c0058 | 0/0 | 6603 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0047c0060 | 0/0 | 6603 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0048c0057 | 0/0 | 6603 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0049c0097 | 0/0 | 6603 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0050c0089 | 0/0 | 6603 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0051c0080 | 0/0 | 6603 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0052c0085 | 0/0 | 6603 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0053c0102 | 0/0 | 6603 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0054c0084 | 0/0 | 6603 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0055c0048 | 0/0 | 6603 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 | ||
a0056c0049 | 0/0 | 6603 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | ATGGG others(6598): Show |
chr9 | 115014575 | 115123157 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001 | 0/0 | 8502 | 18 | 3 | 6 | 4 | 3 | 2 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0001c0002t0003 | 0/0 | 8502 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0001c0002t0008 | 0/0 | 8502 | 4 | 0 | 0 | 3 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0001c0002t0010 | 0/0 | 8501 | 2 | 0 | 1 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8496): Show |
chr9 | 115014575 | 115123157 |
a0001c0002t0013 | 0/0 | 8503 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8498): Show |
chr9 | 115014575 | 115123157 |
a0001c0009t0001 | 0/0 | 8502 | 7 | 0 | 2 | 2 | 0 | 3 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0001c0009t0002 | 0/0 | 8500 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0001c0009t0010 | 0/0 | 8501 | 2 | 0 | 0 | 2 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8496): Show |
chr9 | 115014575 | 115123157 |
a0001c0009t0015 | 0/0 | 8503 | 2 | 2 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8498): Show |
chr9 | 115014575 | 115123157 |
a0001c0011t0001 | 0/0 | 8502 | 5 | 0 | 0 | 4 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0001c0011t0008 | 0/0 | 8502 | 2 | 0 | 1 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0001c0024t0001 | 0/0 | 8502 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0001c0024t0003 | 0/0 | 8502 | 2 | 0 | 0 | 2 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0001c0024t0015 | 0/0 | 8503 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8498): Show |
chr9 | 115014575 | 115123157 |
a0001c0094t0008 | 0/0 | 8502 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0002c0001t0001 | 0/0 | 8502 | 2 | 0 | 0 | 2 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0002c0001t0002 | 0/0 | 8500 | 35 | 1 | 9 | 18 | 1 | 6 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0002c0001t0006 | 0/0 | 8501 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8496): Show |
chr9 | 115014575 | 115123157 |
a0002c0001t0007 | 0/0 | 8500 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0002c0020t0001 | 0/0 | 8502 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0002c0020t0002 | 0/0 | 8500 | 3 | 0 | 0 | 3 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0002c0020t0011 | 0/0 | 8499 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8494): Show |
chr9 | 115014575 | 115123157 |
a0002c0093t0004 | 0/0 | 8500 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0002c0096t0002 | 0/0 | 8500 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0002c0098t0002 | 0/0 | 8500 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0003c0003t0001 | 0/0 | 8502 | 17 | 1 | 1 | 14 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0003c0003t0003 | 0/0 | 8502 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0003c0003t0004 | 0/0 | 8500 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0003c0003t0010 | 0/0 | 8501 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8496): Show |
chr9 | 115014575 | 115123157 |
a0003c0003t0013 | 0/0 | 8503 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8498): Show |
chr9 | 115014575 | 115123157 |
a0003c0003t0019 | 0/0 | 8501 | 2 | 0 | 2 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8496): Show |
chr9 | 115014575 | 115123157 |
a0003c0013t0001 | 0/0 | 8502 | 4 | 0 | 1 | 3 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0003c0013t0008 | 0/0 | 8502 | 2 | 0 | 0 | 1 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0003c0027t0002 | 0/0 | 8500 | 3 | 3 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0003c0035t0004 | 0/0 | 8500 | 2 | 2 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0003c0052t0001 | 0/0 | 8502 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0003c0055t0001 | 0/0 | 8502 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0003c0068t0013 | 0/0 | 8503 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8498): Show |
chr9 | 115014575 | 115123157 |
a0003c0069t0005 | 0/0 | 8501 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8496): Show |
chr9 | 115014575 | 115123157 |
a0003c0077t0004 | 0/0 | 8500 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0004c0004t0001 | 0/0 | 8502 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0004c0004t0002 | 0/0 | 8500 | 18 | 0 | 3 | 10 | 0 | 5 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0004c0018t0004 | 0/0 | 8500 | 5 | 3 | 0 | 1 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0004c0045t0002 | 0/0 | 8500 | 2 | 0 | 2 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0004c0050t0014 | 0/0 | 8502 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0004c0051t0004 | 0/0 | 8500 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0004c0073t0002 | 0/0 | 8500 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0004c0074t0002 | 0/0 | 8500 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0004c0075t0004 | 0/0 | 8500 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0005c0014t0001 | 0/0 | 8502 | 6 | 0 | 5 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0005c0017t0001 | 0/0 | 8502 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0005c0017t0002 | 0/0 | 8500 | 4 | 0 | 1 | 1 | 0 | 2 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0005c0023t0001 | 0/0 | 8502 | 3 | 0 | 0 | 0 | 2 | 1 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0005c0023t0018 | 0/0 | 8502 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0005c0034t0002 | 0/0 | 8500 | 2 | 0 | 2 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0005c0037t0004 | 0/0 | 8500 | 2 | 2 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0005c0061t0002 | 0/0 | 8500 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0005c0062t0026 | 0/0 | 8502 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0005c0066t0002 | 0/0 | 8500 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0005c0067t0002 | 0/0 | 8500 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0005c0103t0012 | 0/0 | 8502 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0006c0007t0005 | 0/0 | 8501 | 10 | 2 | 5 | 3 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8496): Show |
chr9 | 115014575 | 115123157 |
a0006c0007t0022 | 0/0 | 8501 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8496): Show |
chr9 | 115014575 | 115123157 |
a0006c0007t0024 | 0/0 | 8501 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8496): Show |
chr9 | 115014575 | 115123157 |
a0006c0007t0027 | 0/0 | 8500 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0006c0015t0002 | 0/0 | 8500 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0006c0015t0005 | 0/0 | 8501 | 4 | 0 | 2 | 2 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8496): Show |
chr9 | 115014575 | 115123157 |
a0007c0006t0003 | 0/0 | 8502 | 2 | 0 | 0 | 2 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0007c0006t0007 | 0/0 | 8500 | 9 | 0 | 0 | 9 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0007c0006t0016 | 0/0 | 8501 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8496): Show |
chr9 | 115014575 | 115123157 |
a0007c0006t0017 | 0/0 | 8499 | 2 | 0 | 0 | 2 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8494): Show |
chr9 | 115014575 | 115123157 |
a0007c0041t0007 | 0/0 | 8500 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0007c0041t0016 | 0/0 | 8501 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8496): Show |
chr9 | 115014575 | 115123157 |
a0007c0086t0020 | 0/0 | 8500 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0008c0005t0001 | 0/0 | 8502 | 13 | 0 | 4 | 1 | 4 | 4 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0008c0005t0002 | 0/0 | 8500 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0008c0005t0010 | 0/0 | 8501 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8496): Show |
chr9 | 115014575 | 115123157 |
a0009c0019t0002 | 0/0 | 8500 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0009c0019t0011 | 0/0 | 8499 | 4 | 0 | 4 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8494): Show |
chr9 | 115014575 | 115123157 |
a0009c0031t0001 | 0/0 | 8502 | 3 | 0 | 1 | 1 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0009c0042t0008 | 0/0 | 8502 | 2 | 0 | 0 | 1 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0009c0044t0001 | 0/0 | 8502 | 2 | 0 | 0 | 2 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0009c0092t0002 | 0/0 | 8500 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0009c0099t0001 | 0/0 | 8502 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0009c0100t0005 | 0/0 | 8501 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8496): Show |
chr9 | 115014575 | 115123157 |
a0010c0008t0001 | 0/0 | 8502 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0010c0008t0003 | 0/0 | 8502 | 9 | 0 | 0 | 9 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0010c0008t0007 | 0/0 | 8500 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0010c0008t0021 | 0/0 | 8501 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8496): Show |
chr9 | 115014575 | 115123157 |
a0011c0010t0001 | 0/0 | 8502 | 9 | 5 | 0 | 3 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0011c0010t0013 | 0/0 | 8503 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8498): Show |
chr9 | 115014575 | 115123157 |
a0011c0076t0001 | 0/0 | 8502 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0012c0012t0006 | 0/0 | 8501 | 7 | 7 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8496): Show |
chr9 | 115014575 | 115123157 |
a0013c0029t0003 | 0/0 | 8502 | 3 | 0 | 0 | 3 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0013c0040t0003 | 0/0 | 8502 | 2 | 0 | 0 | 2 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0014c0016t0006 | 0/0 | 8501 | 5 | 2 | 3 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8496): Show |
chr9 | 115014575 | 115123157 |
a0015c0021t0004 | 0/0 | 8500 | 4 | 4 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0015c0059t0002 | 0/0 | 8500 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0016c0022t0004 | 0/0 | 8500 | 4 | 4 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0017c0043t0009 | 0/0 | 8501 | 2 | 0 | 0 | 2 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8496): Show |
chr9 | 115014575 | 115123157 |
a0017c0095t0025 | 0/0 | 8500 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0017c0101t0005 | 0/0 | 8501 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8496): Show |
chr9 | 115014575 | 115123157 |
a0018c0026t0006 | 0/1 | 8501 | 3 | 0 | 2 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8496): Show |
chr9 | 115014575 | 115123157 |
a0019c0032t0001 | 0/0 | 8502 | 3 | 2 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0020c0025t0001 | 0/0 | 8502 | 3 | 2 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0021c0028t0012 | 0/0 | 8502 | 3 | 2 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0022c0033t0001 | 0/0 | 8502 | 3 | 3 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0023c0030t0009 | 0/0 | 8501 | 3 | 0 | 0 | 3 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8496): Show |
chr9 | 115014575 | 115123157 |
a0024c0082t0004 | 0/0 | 8500 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0024c0083t0001 | 0/0 | 8502 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0025c0038t0005 | 0/0 | 8501 | 2 | 2 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8496): Show |
chr9 | 115014575 | 115123157 |
a0026c0046t0004 | 0/0 | 8500 | 2 | 2 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0027c0070t0002 | 0/0 | 8500 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0027c0071t0001 | 0/0 | 8502 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0028c0036t0002 | 0/0 | 8500 | 2 | 2 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0029c0039t0003 | 0/0 | 8502 | 2 | 0 | 0 | 2 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0030c0081t0002 | 1/0 | 8500 | 1 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0031c0053t0018 | 0/0 | 8502 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0032c0056t0001 | 0/0 | 8502 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0033c0090t0001 | 0/0 | 8502 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0034c0054t0005 | 0/0 | 8501 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8496): Show |
chr9 | 115014575 | 115123157 |
a0035c0065t0005 | 0/0 | 8501 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8496): Show |
chr9 | 115014575 | 115123157 |
a0036c0104t0028 | 0/0 | 8501 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8496): Show |
chr9 | 115014575 | 115123157 |
a0037c0064t0014 | 0/0 | 8502 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0038c0079t0023 | 0/0 | 8502 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0039c0078t0001 | 0/0 | 8502 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0040c0088t0002 | 0/0 | 8500 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0041c0072t0006 | 0/0 | 8501 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8496): Show |
chr9 | 115014575 | 115123157 |
a0042c0063t0012 | 0/0 | 8502 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0043c0047t0001 | 0/0 | 8502 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0044c0091t0002 | 0/0 | 8500 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0045c0087t0003 | 0/0 | 8502 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0046c0058t0001 | 0/0 | 8502 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0047c0060t0014 | 0/0 | 8502 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0048c0057t0014 | 0/0 | 8502 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0049c0097t0002 | 0/0 | 8500 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0050c0089t0009 | 0/0 | 8501 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8496): Show |
chr9 | 115014575 | 115123157 |
a0051c0080t0003 | 0/0 | 8502 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0052c0085t0003 | 0/0 | 8502 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0053c0102t0001 | 0/0 | 8502 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8497): Show |
chr9 | 115014575 | 115123157 |
a0054c0084t0007 | 0/0 | 8500 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
a0055c0048t0005 | 0/0 | 8501 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8496): Show |
chr9 | 115014575 | 115123157 |
a0056c0049t0002 | 0/0 | 8500 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | GGCCA others(8495): Show |
chr9 | 115014575 | 115123157 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0002t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0002t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0002t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0002t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0002t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0002t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0002t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0002t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0002t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0002t0008g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0002t0008g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0002t0008g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0002t0008g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0002t0010g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0002t0010g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0002t0013g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0009t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0009t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0009t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0009t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0009t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0009t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0009t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0009t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0009t0010g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0009t0010g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0009t0015g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0009t0015g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0011t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0011t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0011t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0011t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0011t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0011t0008g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0011t0008g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0024t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0024t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0024t0003g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0024t0015g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0001c0094t0008g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0001t0006g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0001t0007g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0020t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0020t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0020t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0020t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0020t0011g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0093t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0096t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0002c0098t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0003c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0003c0003t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0003c0003t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0003c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0003c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0003c0003t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0003c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0003c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0003c0003t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0003c0003t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0003c0003t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0003c0003t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0003c0003t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0003c0003t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0003c0003t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0003c0003t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0003c0003t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0003c0003t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0003c0003t0004g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0003c0003t0010g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0003c0003t0013g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0003c0003t0019g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0003c0003t0019g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0003c0013t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0003c0013t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0003c0013t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0003c0013t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0003c0013t0008g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0003c0013t0008g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0003c0027t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0003c0027t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0003c0027t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0003c0035t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0003c0035t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0003c0052t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0003c0055t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0003c0068t0013g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0003c0069t0005g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0003c0077t0004g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0004c0004t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0004c0004t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0004c0004t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0004c0004t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0004c0004t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0004c0004t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0004c0004t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0004c0004t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0004c0004t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0004c0004t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0004c0004t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0004c0004t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0004c0004t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0004c0004t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0004c0004t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0004c0004t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0004c0004t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0004c0004t0002g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0004c0004t0002g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0004c0018t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0004c0018t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0004c0018t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0004c0018t0004g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0004c0018t0004g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0004c0045t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0004c0045t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0004c0050t0014g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0004c0051t0004g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0004c0073t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0004c0074t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0004c0075t0004g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0005c0014t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0005c0014t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0005c0014t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0005c0014t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0005c0014t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0005c0017t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0005c0017t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0005c0017t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0005c0017t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0005c0017t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0005c0023t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0005c0023t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0005c0023t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0005c0023t0018g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0005c0034t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0005c0034t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0005c0037t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0005c0037t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0005c0061t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0005c0062t0026g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0005c0066t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0005c0067t0002g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0005c0103t0012g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0006c0007t0005g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0006c0007t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0006c0007t0005g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0006c0007t0005g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0006c0007t0005g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0006c0007t0005g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0006c0007t0005g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0006c0007t0005g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0006c0007t0005g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0006c0007t0005g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0006c0007t0022g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0006c0007t0024g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0006c0007t0027g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0006c0015t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0006c0015t0005g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0006c0015t0005g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0006c0015t0005g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0007c0006t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0007c0006t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0007c0006t0007g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0007c0006t0007g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0007c0006t0007g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0007c0006t0007g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0007c0006t0007g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0007c0006t0007g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0007c0006t0007g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0007c0006t0007g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0007c0006t0016g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0007c0006t0017g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0007c0006t0017g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0007c0041t0007g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0007c0041t0016g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0007c0086t0020g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0008c0005t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0008c0005t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0008c0005t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0008c0005t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0008c0005t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0008c0005t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0008c0005t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0008c0005t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0008c0005t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0008c0005t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0008c0005t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0008c0005t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0008c0005t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0008c0005t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0008c0005t0010g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0009c0019t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0009c0019t0011g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0009c0019t0011g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0009c0019t0011g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0009c0031t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0009c0031t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0009c0031t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0009c0042t0008g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0009c0042t0008g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0009c0044t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0009c0044t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0009c0092t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0009c0099t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0009c0100t0005g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0010c0008t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0010c0008t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0010c0008t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0010c0008t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0010c0008t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0010c0008t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0010c0008t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0010c0008t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0010c0008t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0010c0008t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0010c0008t0007g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0010c0008t0021g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0011c0010t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0011c0010t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0011c0010t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0011c0010t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0011c0010t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0011c0010t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0011c0010t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0011c0010t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0011c0010t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0011c0010t0013g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0011c0076t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0012c0012t0006g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0012c0012t0006g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0012c0012t0006g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0012c0012t0006g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0012c0012t0006g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0012c0012t0006g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0012c0012t0006g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0013c0029t0003g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0013c0029t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0013c0029t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0013c0040t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0013c0040t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0014c0016t0006g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0014c0016t0006g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0014c0016t0006g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0014c0016t0006g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0014c0016t0006g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0015c0021t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0015c0021t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0015c0021t0004g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0015c0021t0004g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0015c0059t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0016c0022t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0016c0022t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0016c0022t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0016c0022t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0017c0043t0009g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0017c0043t0009g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0017c0095t0025g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0017c0101t0005g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0018c0026t0006g0068 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0018c0026t0006g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0018c0026t0006g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0019c0032t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0019c0032t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0019c0032t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0020c0025t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0020c0025t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0020c0025t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0021c0028t0012g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0021c0028t0012g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0021c0028t0012g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0022c0033t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0022c0033t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0022c0033t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0023c0030t0009g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0023c0030t0009g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0023c0030t0009g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0024c0082t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0024c0083t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0025c0038t0005g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0025c0038t0005g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0026c0046t0004g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0026c0046t0004g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0027c0070t0002g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0027c0071t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0028c0036t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0028c0036t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0029c0039t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0029c0039t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0030c0081t0002g0262 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0031c0053t0018g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0032c0056t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0033c0090t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0034c0054t0005g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0035c0065t0005g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0036c0104t0028g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0037c0064t0014g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0038c0079t0023g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0039c0078t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0040c0088t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0041c0072t0006g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0042c0063t0012g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0043c0047t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0044c0091t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0045c0087t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0046c0058t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0047c0060t0014g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0048c0057t0014g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0049c0097t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0050c0089t0009g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0051c0080t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0052c0085t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0053c0102t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0054c0084t0007g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0055c0048t0005g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
a0056c0049t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0005 | c0023 | t0001 | g0292 | EUR | GBR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG00099 | hp2 | a0008 | c0005 | t0001 | g0115 | EUR | GBR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0290 | EUR | GBR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG00140 | hp2 | a0008 | c0005 | t0001 | g0086 | EUR | GBR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG00280 | hp1 | a0008 | c0005 | t0002 | g0187 | EUR | FIN | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG00280 | hp2 | a0001 | c0002 | t0010 | g0288 | EUR | FIN | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG00323 | hp1 | a0031 | c0053 | t0018 | g0245 | EUR | FIN | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG00323 | hp2 | a0005 | c0023 | t0001 | g0291 | EUR | FIN | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG00408 | hp1 | a0007 | c0086 | t0020 | g0044 | EAS | CHS | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG00408 | hp2 | a0007 | c0006 | t0007 | g0019 | EAS | CHS | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG00423 | hp1 | a0004 | c0004 | t0002 | g0311 | EAS | CHS | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG00423 | hp2 | a0010 | c0008 | t0003 | g0015 | EAS | CHS | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG00558 | hp1 | a0007 | c0006 | t0003 | g0028 | EAS | CHS | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG00558 | hp2 | a0007 | c0006 | t0007 | g0046 | EAS | CHS | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG00597 | hp1 | a0003 | c0013 | t0001 | g0285 | EAS | CHS | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG00597 | hp2 | a0010 | c0008 | t0003 | g0013 | EAS | CHS | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG00609 | hp1 | a0004 | c0004 | t0002 | g0233 | EAS | CHS | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG00609 | hp2 | a0010 | c0008 | t0003 | g0014 | EAS | CHS | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG00621 | hp1 | a0013 | c0029 | t0003 | g0010 | EAS | CHS | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG00621 | hp2 | a0006 | c0015 | t0005 | g0235 | EAS | CHS | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG00642 | hp1 | a0002 | c0001 | t0002 | g0169 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG00642 | hp2 | a0018 | c0026 | t0006 | g0070 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG00733 | hp1 | a0005 | c0014 | t0001 | g0005 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG00733 | hp2 | a0002 | c0001 | t0002 | g0174 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG00738 | hp1 | a0004 | c0075 | t0004 | g0266 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG00738 | hp2 | a0008 | c0005 | t0001 | g0089 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG00741 | hp1 | a0032 | c0056 | t0001 | g0232 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG00741 | hp2 | a0014 | c0016 | t0006 | g0074 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0267 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01069 | hp2 | a0008 | c0005 | t0010 | g0084 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01070 | hp1 | a0033 | c0090 | t0001 | g0116 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01070 | hp2 | a0001 | c0002 | t0010 | g0330 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0302 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01071 | hp2 | a0008 | c0005 | t0001 | g0085 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01074 | hp1 | a0006 | c0015 | t0005 | g0004 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01074 | hp2 | a0001 | c0002 | t0001 | g0276 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01081 | hp1 | a0003 | c0003 | t0019 | g0360 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01081 | hp2 | a0009 | c0019 | t0011 | g0177 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01099 | hp1 | a0003 | c0013 | t0001 | g0304 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01099 | hp2 | a0009 | c0019 | t0011 | g0194 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01109 | hp1 | a0024 | c0083 | t0001 | g0056 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01109 | hp2 | a0005 | c0034 | t0002 | g0198 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01169 | hp1 | a0002 | c0001 | t0002 | g0092 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01169 | hp2 | a0002 | c0001 | t0006 | g0120 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01175 | hp1 | a0003 | c0003 | t0001 | g0279 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01175 | hp2 | a0002 | c0001 | t0002 | g0176 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01192 | hp1 | a0005 | c0062 | t0026 | g0250 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01192 | hp2 | a0002 | c0001 | t0002 | g0173 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01243 | hp1 | a0020 | c0025 | t0001 | g0349 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01243 | hp2 | a0005 | c0034 | t0002 | g0197 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01255 | hp1 | a0006 | c0007 | t0005 | g0298 | AMR | CLM | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0277 | AMR | CLM | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01256 | hp1 | a0005 | c0014 | t0001 | g0314 | AMR | CLM | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01256 | hp2 | a0018 | c0026 | t0006 | g0075 | AMR | CLM | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01257 | hp1 | a0005 | c0014 | t0001 | g0308 | AMR | CLM | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01257 | hp2 | a0009 | c0019 | t0011 | g0003 | AMR | CLM | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01258 | hp1 | a0009 | c0019 | t0011 | g0003 | AMR | CLM | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01258 | hp2 | a0005 | c0014 | t0001 | g0005 | AMR | CLM | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01261 | hp1 | a0014 | c0016 | t0006 | g0069 | AMR | CLM | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01261 | hp2 | a0001 | c0009 | t0001 | g0175 | AMR | CLM | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01346 | hp1 | a0014 | c0016 | t0006 | g0073 | AMR | CLM | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01346 | hp2 | a0005 | c0017 | t0002 | g0076 | AMR | CLM | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0303 | AMR | CLM | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01358 | hp2 | a0004 | c0045 | t0002 | g0231 | AMR | CLM | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01361 | hp1 | a0001 | c0011 | t0008 | g0109 | AMR | CLM | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01361 | hp2 | a0006 | c0007 | t0005 | g0324 | AMR | CLM | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01433 | hp1 | a0005 | c0014 | t0001 | g0299 | AMR | CLM | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01433 | hp2 | a0001 | c0002 | t0001 | g0268 | AMR | CLM | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01496 | hp1 | a0021 | c0028 | t0012 | g0259 | AMR | CLM | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01496 | hp2 | a0005 | c0023 | t0018 | g0361 | AMR | CLM | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01515 | hp1 | a0008 | c0005 | t0001 | g0102 | EUR | IBS | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01515 | hp2 | a0003 | c0003 | t0010 | g0328 | EUR | IBS | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01884 | hp1 | a0006 | c0007 | t0024 | g0212 | AFR | ACB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01884 | hp2 | a0022 | c0033 | t0001 | g0338 | AFR | ACB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01891 | hp1 | a0015 | c0021 | t0004 | g0129 | AFR | ACB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01891 | hp2 | a0022 | c0033 | t0001 | g0127 | AFR | ACB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01928 | hp1 | a0034 | c0054 | t0005 | g0237 | AMR | PEL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01928 | hp2 | a0004 | c0045 | t0002 | g0230 | AMR | PEL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01952 | hp1 | a0006 | c0007 | t0005 | g0270 | AMR | PEL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01952 | hp2 | a0001 | c0009 | t0001 | g0188 | AMR | PEL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01978 | hp1 | a0004 | c0004 | t0002 | g0297 | AMR | PEL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01978 | hp2 | a0008 | c0005 | t0001 | g0118 | AMR | PEL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01981 | hp1 | a0003 | c0003 | t0019 | g0273 | AMR | PEL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01981 | hp2 | a0009 | c0031 | t0001 | g0111 | AMR | PEL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01993 | hp1 | a0002 | c0001 | t0002 | g0184 | AMR | PEL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01993 | hp2 | a0006 | c0007 | t0022 | g0054 | AMR | PEL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02004 | hp1 | a0002 | c0001 | t0002 | g0110 | AMR | PEL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02004 | hp2 | a0006 | c0007 | t0005 | g0295 | AMR | PEL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02015 | hp1 | a0009 | c0042 | t0008 | g0113 | EAS | KHV | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02015 | hp2 | a0011 | c0010 | t0001 | g0211 | EAS | KHV | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02040 | hp1 | a0004 | c0018 | t0004 | g0305 | EAS | KHV | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02040 | hp2 | a0002 | c0001 | t0002 | g0191 | EAS | KHV | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02055 | hp1 | a0020 | c0025 | t0001 | g0347 | AFR | ACB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02055 | hp2 | a0004 | c0073 | t0002 | g0274 | AFR | ACB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02071 | hp1 | a0001 | c0002 | t0001 | g0134 | EAS | KHV | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02071 | hp2 | a0009 | c0099 | t0001 | g0146 | EAS | KHV | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02080 | hp1 | a0002 | c0001 | t0002 | g0195 | EAS | KHV | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02080 | hp2 | a0009 | c0044 | t0001 | g0140 | EAS | KHV | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02083 | hp1 | a0002 | c0001 | t0002 | g0082 | EAS | KHV | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02083 | hp2 | a0003 | c0003 | t0001 | g0336 | EAS | KHV | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02129 | hp1 | a0011 | c0076 | t0001 | g0206 | EAS | KHV | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02129 | hp2 | a0008 | c0005 | t0001 | g0087 | EAS | KHV | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02145 | hp1 | a0036 | c0104 | t0028 | g0341 | AFR | ACB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02145 | hp2 | a0004 | c0018 | t0004 | g0224 | AFR | ACB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02148 | hp1 | a0008 | c0005 | t0001 | g0088 | AMR | PEL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02148 | hp2 | a0006 | c0007 | t0005 | g0287 | AMR | PEL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02155 | hp1 | a0011 | c0010 | t0001 | g0209 | EAS | CDX | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02155 | hp2 | a0002 | c0001 | t0002 | g0157 | EAS | CDX | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02257 | hp1 | a0037 | c0064 | t0014 | g0343 | AFR | ACB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02257 | hp2 | a0038 | c0079 | t0023 | g0193 | AFR | ACB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02258 | hp1 | a0011 | c0010 | t0001 | g0228 | AFR | ACB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02258 | hp2 | a0019 | c0032 | t0001 | g0319 | AFR | ACB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02273 | hp1 | a0004 | c0004 | t0002 | g0300 | AMR | PEL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02273 | hp2 | a0006 | c0015 | t0005 | g0004 | AMR | PEL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02280 | hp1 | a0005 | c0067 | t0002 | g0359 | AFR | ACB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02280 | hp2 | a0003 | c0003 | t0004 | g0337 | AFR | ACB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02300 | hp1 | a0004 | c0004 | t0002 | g0293 | AMR | PEL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02300 | hp2 | a0002 | c0001 | t0002 | g0098 | AMR | PEL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02572 | hp1 | a0015 | c0021 | t0004 | g0254 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02572 | hp2 | a0025 | c0038 | t0005 | g0354 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02602 | hp1 | a0002 | c0001 | t0002 | g0154 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02602 | hp2 | a0040 | c0088 | t0002 | g0097 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02615 | hp1 | a0015 | c0021 | t0004 | g0255 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02615 | hp2 | a0011 | c0010 | t0001 | g0264 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02622 | hp1 | a0004 | c0018 | t0004 | g0226 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02622 | hp2 | a0015 | c0021 | t0004 | g0256 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02630 | hp1 | a0012 | c0012 | t0006 | g0058 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02630 | hp2 | a0019 | c0032 | t0001 | g0316 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02647 | hp1 | a0016 | c0022 | t0004 | g0252 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02647 | hp2 | a0001 | c0009 | t0015 | g0124 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02698 | hp1 | a0004 | c0018 | t0004 | g0334 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02698 | hp2 | a0001 | c0002 | t0008 | g0144 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02723 | hp1 | a0041 | c0072 | t0006 | g0351 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02723 | hp2 | a0002 | c0093 | t0004 | g0122 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02735 | hp1 | a0001 | c0002 | t0001 | g0327 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02735 | hp2 | a0009 | c0019 | t0002 | g0178 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02738 | hp1 | a0004 | c0074 | t0002 | g0286 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02738 | hp2 | a0015 | c0059 | t0002 | g0067 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02809 | hp1 | a0001 | c0009 | t0015 | g0350 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02809 | hp2 | a0026 | c0046 | t0004 | g0339 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02818 | hp1 | a0009 | c0100 | t0005 | g0317 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02818 | hp2 | a0042 | c0063 | t0012 | g0149 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02886 | hp1 | a0043 | c0047 | t0001 | g0358 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02886 | hp2 | a0044 | c0091 | t0002 | g0189 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02895 | hp1 | a0003 | c0027 | t0002 | g0215 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02895 | hp2 | a0005 | c0061 | t0002 | g0257 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02896 | hp1 | a0012 | c0012 | t0006 | g0062 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02896 | hp2 | a0006 | c0007 | t0005 | g0204 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02897 | hp1 | a0003 | c0027 | t0002 | g0218 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02897 | hp2 | a0012 | c0012 | t0006 | g0061 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02922 | hp1 | a0016 | c0022 | t0004 | g0130 | AFR | ESN | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02922 | hp2 | a0004 | c0050 | t0014 | g0345 | AFR | ESN | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02965 | hp1 | a0045 | c0087 | t0003 | g0033 | AFR | ESN | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02965 | hp2 | a0020 | c0025 | t0001 | g0348 | AFR | ESN | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02970 | hp1 | a0012 | c0012 | t0006 | g0059 | AFR | ESN | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02970 | hp2 | a0001 | c0002 | t0001 | g0128 | AFR | ESN | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02976 | hp1 | a0003 | c0027 | t0002 | g0214 | AFR | ESN | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02976 | hp2 | a0027 | c0071 | t0001 | g0355 | AFR | ESN | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03017 | hp1 | a0005 | c0017 | t0002 | g0079 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03017 | hp2 | a0004 | c0004 | t0002 | g0333 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03041 | hp1 | a0016 | c0022 | t0004 | g0131 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03041 | hp2 | a0012 | c0012 | t0006 | g0063 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03098 | hp1 | a0003 | c0003 | t0001 | g0344 | AFR | MSL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03098 | hp2 | a0046 | c0058 | t0001 | g0248 | AFR | MSL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03130 | hp1 | a0028 | c0036 | t0002 | g0202 | AFR | ESN | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03130 | hp2 | a0011 | c0010 | t0013 | g0265 | AFR | ESN | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03139 | hp1 | a0017 | c0095 | t0025 | g0179 | AFR | ESN | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03139 | hp2 | a0003 | c0077 | t0004 | g0356 | AFR | ESN | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03195 | hp1 | a0012 | c0012 | t0006 | g0057 | AFR | ESN | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03195 | hp2 | a0025 | c0038 | t0005 | g0353 | AFR | ESN | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03209 | hp1 | a0022 | c0033 | t0001 | g0126 | AFR | MSL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03209 | hp2 | a0016 | c0022 | t0004 | g0261 | AFR | MSL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03225 | hp1 | a0028 | c0036 | t0002 | g0203 | AFR | MSL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03225 | hp2 | a0021 | c0028 | t0012 | g0260 | AFR | MSL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03239 | hp1 | a0011 | c0010 | t0001 | g0296 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03239 | hp2 | a0001 | c0002 | t0001 | g0275 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03453 | hp1 | a0047 | c0060 | t0014 | g0253 | AFR | MSL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03453 | hp2 | a0005 | c0103 | t0012 | g0091 | AFR | MSL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03490 | hp1 | a0002 | c0098 | t0002 | g0147 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03490 | hp2 | a0008 | c0005 | t0001 | g0196 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03491 | hp1 | a0007 | c0041 | t0016 | g0030 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03491 | hp2 | a0003 | c0003 | t0001 | g0329 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03516 | hp1 | a0014 | c0016 | t0006 | g0072 | AFR | ESN | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03516 | hp2 | a0009 | c0092 | t0002 | g0093 | AFR | ESN | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03579 | hp1 | a0001 | c0024 | t0015 | g0320 | AFR | MSL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03579 | hp2 | a0006 | c0007 | t0005 | g0357 | AFR | MSL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03654 | hp1 | a0009 | c0031 | t0001 | g0182 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03654 | hp2 | a0049 | c0097 | t0002 | g0183 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03669 | hp1 | a0005 | c0017 | t0002 | g0078 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03669 | hp2 | a0004 | c0004 | t0002 | g0280 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03688 | hp1 | a0001 | c0011 | t0001 | g0114 | SAS | STU | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03688 | hp2 | a0001 | c0009 | t0001 | g0101 | SAS | STU | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03704 | hp1 | a0002 | c0001 | t0002 | g0185 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03704 | hp2 | a0005 | c0017 | t0001 | g0081 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03710 | hp1 | a0001 | c0094 | t0008 | g0172 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03710 | hp2 | a0001 | c0009 | t0001 | g0123 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03834 | hp1 | a0002 | c0096 | t0002 | g0156 | SAS | BEB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03834 | hp2 | a0008 | c0005 | t0001 | g0083 | SAS | BEB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03927 | hp1 | a0010 | c0008 | t0001 | g0077 | SAS | BEB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03927 | hp2 | a0009 | c0042 | t0008 | g0112 | SAS | BEB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03942 | hp1 | a0004 | c0004 | t0002 | g0278 | SAS | BEB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03942 | hp2 | a0001 | c0009 | t0001 | g0244 | SAS | BEB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG04115 | hp1 | a0004 | c0004 | t0002 | g0325 | SAS | STU | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG04115 | hp2 | a0002 | c0001 | t0002 | g0186 | SAS | STU | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG04184 | hp1 | a0007 | c0041 | t0007 | g0029 | SAS | BEB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG04184 | hp2 | a0003 | c0013 | t0008 | g0246 | SAS | BEB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG04199 | hp1 | a0008 | c0005 | t0001 | g0121 | SAS | STU | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG04199 | hp2 | a0002 | c0001 | t0002 | g0181 | SAS | STU | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG04204 | hp1 | a0002 | c0001 | t0002 | g0103 | SAS | STU | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG04204 | hp2 | a0008 | c0005 | t0001 | g0119 | SAS | STU | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG04228 | hp1 | a0005 | c0023 | t0001 | g0315 | SAS | STU | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG04228 | hp2 | a0004 | c0004 | t0002 | g0281 | SAS | STU | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18522 | hp1 | a0001 | c0002 | t0001 | g0321 | AFR | YRI | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18522 | hp2 | a0003 | c0069 | t0005 | g0219 | AFR | YRI | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18612 | hp1 | a0005 | c0017 | t0002 | g0080 | EAS | CHB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18612 | hp2 | a0006 | c0015 | t0002 | g0241 | EAS | CHB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18747 | hp1 | a0005 | c0014 | t0001 | g0289 | EAS | CHB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18747 | hp2 | a0002 | c0020 | t0002 | g0148 | EAS | CHB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18906 | hp1 | a0003 | c0035 | t0004 | g0151 | AFR | YRI | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18906 | hp2 | a0004 | c0051 | t0004 | g0342 | AFR | YRI | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18939 | hp1 | a0001 | c0009 | t0001 | g0155 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18939 | hp2 | a0002 | c0001 | t0002 | g0158 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18940 | hp1 | a0003 | c0013 | t0001 | g0282 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18940 | hp2 | a0002 | c0001 | t0002 | g0190 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18942 | hp1 | a0013 | c0029 | t0003 | g0025 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18942 | hp2 | a0007 | c0006 | t0017 | g0012 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18943 | hp1 | a0004 | c0004 | t0002 | g0205 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18943 | hp2 | a0001 | c0009 | t0010 | g0105 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18944 | hp1 | a0006 | c0007 | t0005 | g0222 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18944 | hp2 | a0004 | c0004 | t0001 | g0269 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18945 | hp1 | a0001 | c0009 | t0001 | g0160 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18945 | hp2 | a0050 | c0089 | t0009 | g0022 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18947 | hp1 | a0001 | c0011 | t0001 | g0161 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18947 | hp2 | a0007 | c0006 | t0003 | g0052 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18948 | hp1 | a0001 | c0002 | t0008 | g0139 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18948 | hp2 | a0007 | c0006 | t0007 | g0037 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18950 | hp1 | a0002 | c0020 | t0001 | g0145 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18950 | hp2 | a0029 | c0039 | t0003 | g0042 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18952 | hp1 | a0051 | c0080 | t0003 | g0045 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18952 | hp2 | a0003 | c0003 | t0001 | g0217 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18953 | hp1 | a0007 | c0006 | t0007 | g0035 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18953 | hp2 | a0003 | c0003 | t0001 | g0229 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18954 | hp1 | a0052 | c0085 | t0003 | g0047 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18954 | hp2 | a0004 | c0004 | t0002 | g0220 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18956 | hp1 | a0010 | c0008 | t0003 | g0034 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18956 | hp2 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18959 | hp1 | a0002 | c0001 | t0002 | g0107 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18959 | hp2 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18961 | hp1 | a0013 | c0040 | t0003 | g0040 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18961 | hp2 | a0004 | c0004 | t0002 | g0223 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18963 | hp1 | a0001 | c0009 | t0010 | g0163 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18963 | hp2 | a0006 | c0007 | t0005 | g0221 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18964 | hp1 | a0003 | c0003 | t0001 | g0331 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18964 | hp2 | a0007 | c0006 | t0017 | g0039 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18965 | hp1 | a0023 | c0030 | t0009 | g0031 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18965 | hp2 | a0004 | c0004 | t0002 | g0210 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18966 | hp1 | a0013 | c0040 | t0003 | g0036 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18966 | hp2 | a0002 | c0001 | t0001 | g0104 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18968 | hp1 | a0003 | c0003 | t0001 | g0240 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18968 | hp2 | a0004 | c0004 | t0002 | g0284 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18971 | hp1 | a0003 | c0013 | t0001 | g0272 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18971 | hp2 | a0004 | c0004 | t0002 | g0306 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18972 | hp1 | a0010 | c0008 | t0003 | g0024 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18972 | hp2 | a0003 | c0068 | t0013 | g0323 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18975 | hp1 | a0023 | c0030 | t0009 | g0049 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18975 | hp2 | a0003 | c0003 | t0001 | g0247 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18977 | hp1 | a0009 | c0044 | t0001 | g0335 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18977 | hp2 | a0003 | c0003 | t0001 | g0332 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18981 | hp1 | a0002 | c0001 | t0002 | g0168 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18981 | hp2 | a0004 | c0004 | t0002 | g0313 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18982 | hp1 | a0002 | c0020 | t0011 | g0132 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18982 | hp2 | a0017 | c0043 | t0009 | g0016 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18983 | hp1 | a0004 | c0004 | t0002 | g0312 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18983 | hp2 | a0006 | c0015 | t0005 | g0236 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18984 | hp1 | a0002 | c0001 | t0002 | g0108 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18984 | hp2 | a0053 | c0102 | t0001 | g0143 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18990 | hp1 | a0007 | c0006 | t0007 | g0006 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18990 | hp2 | a0017 | c0043 | t0009 | g0020 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18992 | hp1 | a0002 | c0001 | t0002 | g0099 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18992 | hp2 | a0001 | c0024 | t0003 | g0008 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18993 | hp1 | a0003 | c0003 | t0001 | g0216 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18993 | hp2 | a0013 | c0029 | t0003 | g0026 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18995 | hp1 | a0017 | c0101 | t0005 | g0066 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18995 | hp2 | a0029 | c0039 | t0003 | g0041 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18999 | hp1 | a0006 | c0007 | t0027 | g0294 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA18999 | hp2 | a0001 | c0002 | t0008 | g0137 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19000 | hp1 | a0007 | c0006 | t0007 | g0051 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19000 | hp2 | a0006 | c0007 | t0005 | g0200 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19001 | hp1 | a0003 | c0003 | t0001 | g0239 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19001 | hp2 | a0002 | c0001 | t0001 | g0165 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19002 | hp1 | a0001 | c0011 | t0008 | g0153 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19002 | hp2 | a0002 | c0001 | t0002 | g0167 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19004 | hp1 | a0003 | c0003 | t0001 | g0208 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19004 | hp2 | a0007 | c0006 | t0007 | g0001 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19005 | hp1 | a0002 | c0001 | t0007 | g0018 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19005 | hp2 | a0001 | c0024 | t0003 | g0009 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19007 | hp1 | a0007 | c0006 | t0007 | g0043 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19007 | hp2 | a0003 | c0003 | t0001 | g0310 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19009 | hp1 | a0002 | c0001 | t0002 | g0100 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19009 | hp2 | a0011 | c0010 | t0001 | g0225 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19010 | hp1 | a0003 | c0013 | t0008 | g0309 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19010 | hp2 | a0010 | c0008 | t0003 | g0027 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19030 | hp1 | a0004 | c0018 | t0004 | g0213 | AFR | LWK | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19030 | hp2 | a0011 | c0010 | t0001 | g0064 | AFR | LWK | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19056 | hp1 | a0001 | c0011 | t0001 | g0162 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19056 | hp2 | a0007 | c0006 | t0007 | g0001 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19058 | hp1 | a0003 | c0055 | t0001 | g0238 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19058 | hp2 | a0054 | c0084 | t0007 | g0038 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19060 | hp1 | a0023 | c0030 | t0009 | g0048 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19060 | hp2 | a0009 | c0031 | t0001 | g0166 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19062 | hp1 | a0001 | c0002 | t0008 | g0136 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19062 | hp2 | a0010 | c0008 | t0021 | g0011 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19063 | hp2 | a0055 | c0048 | t0005 | g0243 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19064 | hp1 | a0002 | c0001 | t0002 | g0106 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19064 | hp2 | a0003 | c0003 | t0003 | g0053 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19065 | hp1 | a0002 | c0001 | t0002 | g0094 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19065 | hp2 | a0003 | c0003 | t0001 | g0207 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19066 | hp1 | a0003 | c0003 | t0001 | g0283 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19066 | hp2 | a0002 | c0001 | t0002 | g0002 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19067 | hp1 | a0007 | c0006 | t0016 | g0050 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19067 | hp2 | a0001 | c0011 | t0001 | g0095 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19068 | hp1 | a0010 | c0008 | t0003 | g0017 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19068 | hp2 | a0001 | c0024 | t0001 | g0133 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19074 | hp1 | a0010 | c0008 | t0003 | g0032 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19074 | hp2 | a0001 | c0011 | t0001 | g0164 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19078 | hp1 | a0002 | c0020 | t0002 | g0065 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19078 | hp2 | a0001 | c0002 | t0013 | g0135 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19080 | hp1 | a0003 | c0052 | t0001 | g0234 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19080 | hp2 | a0002 | c0020 | t0002 | g0249 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19082 | hp1 | a0010 | c0008 | t0003 | g0023 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19082 | hp2 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19084 | hp1 | a0002 | c0001 | t0002 | g0171 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19084 | hp2 | a0003 | c0003 | t0001 | g0199 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19087 | hp1 | a0003 | c0003 | t0013 | g0201 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19087 | hp2 | a0002 | c0001 | t0002 | g0096 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19090 | hp1 | a0010 | c0008 | t0007 | g0021 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19090 | hp2 | a0002 | c0001 | t0002 | g0002 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19240 | hp1 | a0012 | c0012 | t0006 | g0060 | AFR | YRI | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA19240 | hp2 | a0014 | c0016 | t0006 | g0071 | AFR | YRI | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA20129 | hp1 | a0011 | c0010 | t0001 | g0227 | AFR | ASW | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA20129 | hp2 | a0005 | c0037 | t0004 | g0152 | AFR | ASW | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA20752 | hp1 | a0008 | c0005 | t0001 | g0090 | EUR | TSI | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA20752 | hp2 | a0002 | c0001 | t0002 | g0125 | EUR | TSI | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0301 | EUR | TSI | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA20805 | hp2 | a0001 | c0002 | t0001 | g0192 | EUR | TSI | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA20905 | hp1 | a0002 | c0001 | t0002 | g0180 | SAS | GIH | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA20905 | hp2 | a0005 | c0066 | t0002 | g0251 | SAS | GIH | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01123 | hp1 | a0002 | c0001 | t0002 | g0170 | AMR | CLM | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG01123 | hp2 | a0019 | c0032 | t0001 | g0318 | AMR | CLM | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02109 | hp1 | a0002 | c0001 | t0002 | g0159 | AFR | ACB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02109 | hp2 | a0035 | c0065 | t0005 | g0326 | AFR | ACB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02486 | hp1 | a0024 | c0082 | t0004 | g0055 | AFR | ACB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02486 | hp2 | a0039 | c0078 | t0001 | g0307 | AFR | ACB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02559 | hp1 | a0005 | c0037 | t0004 | g0271 | AFR | ACB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG02559 | hp2 | a0003 | c0035 | t0004 | g0150 | AFR | ACB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03471 | hp1 | a0048 | c0057 | t0014 | g0346 | AFR | MSL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG03471 | hp2 | a0026 | c0046 | t0004 | g0340 | AFR | MSL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG06807 | hp1 | a0001 | c0002 | t0001 | g0322 | AFR | USA | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
HG06807 | hp2 | a0011 | c0010 | t0001 | g0263 | AFR | USA | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA20300 | hp1 | a0001 | c0009 | t0002 | g0117 | AFR | USA | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA20300 | hp2 | a0021 | c0028 | t0012 | g0258 | AFR | USA | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA21309 | hp1 | a0027 | c0070 | t0002 | g0352 | AFR | LWK | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
NA21309 | hp2 | a0056 | c0049 | t0002 | g0242 | AFR | LWK | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
homoSapiens | chm13v2 | a0018 | c0026 | t0006 | g0068 | REF | REF | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
homoSapiens | grch38p0 | a0030 | c0081 | t0002 | g0262 | REF | REF | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:115021264 | C | T | 1 | a0044 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.6499G>A | p.Val2167Ile | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 28/28 | 6811/8500 | 6499/6606 | 2167/2201 | chr9 | 115021264 | |||
chr9:115023986 | T | C | 1 | a0036 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.6482A>G | p.Asn2161Ser | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/28 | 6794/8500 | 6482/6606 | 2161/2201 | chr9 | 115023986 | |||
chr9:115024090 | G | C | 1 | a0052 | 1 | NA18954.hp1 | missense_variant | MODERATE | c.6378C>G | p.Asp2126Glu | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/28 | 6690/8500 | 6378/6606 | 2126/2201 | chr9 | 115024090 | |||
chr9:115030304 | C | G | 37 | a0001 a0003 a0005 others(34): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
missense_variant | MODERATE | c.6022G>C | p.Glu2008Gln | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 24/28 | 6334/8500 | 6022/6606 | 2008/2201 | chr9 | 115030304 | |||
chr9:115036139 | C | G | 1 | a0019 | 3 | HG01123.hp2 HG02258.hp2 HG02630.hp2 |
missense_variant | MODERATE | c.5615G>C | p.Gly1872Ala | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 21/28 | 5927/8500 | 5615/6606 | 1872/2201 | chr9 | 115036139 | |||
chr9:115038284 | A | C | 1 | a0034 | 1 | HG01928.hp1 | missense_variant | MODERATE | c.5489T>G | p.Val1830Gly | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/28 | 5801/8500 | 5489/6606 | 1830/2201 | chr9 | 115038284 | |||
chr9:115040992 | C | T | 8 | a0006 a0017 a0023 others(5): Show |
31 | HG00621.hp2 HG01074.hp1 HG01255.hp1 others(28): Show |
missense_variant | MODERATE | c.5341G>A | p.Ala1781Thr | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/28 | 5653/8500 | 5341/6606 | 1781/2201 | chr9 | 115040992 | |||
chr9:115046442 | C | T | 1 | a0018 | 2 | HG00642.hp2 HG01256.hp2 |
missense_variant | MODERATE | c.5093G>A | p.Arg1698Gln | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/28 | 5405/8500 | 5093/6606 | 1698/2201 | chr9 | 115046442 | |||
chr9:115046506 | T | A | 36 | a0001 a0003 a0006 others(33): Show |
193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
missense_variant | MODERATE | c.5029A>T | p.Ile1677Leu | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/28 | 5341/8500 | 5029/6606 | 1677/2201 | chr9 | 115046506 | |||
chr9:115057260 | C | T | 1 | a0033 | 1 | HG01070.hp1 | missense_variant | MODERATE | c.4472G>A | p.Arg1491Gln | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/28 | 4784/8500 | 4472/6606 | 1491/2201 | chr9 | 115057260 | |||
chr9:115059808 | C | A | 1 | a0053 | 1 | NA18984.hp2 | missense_variant | MODERATE | c.4228G>T | p.Ala1410Ser | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/28 | 4540/8500 | 4228/6606 | 1410/2201 | chr9 | 115059808 | |||
chr9:115063817 | G | T | 1 | a0056 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.3739C>A | p.Leu1247Ile | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 12/28 | 4051/8500 | 3739/6606 | 1247/2201 | chr9 | 115063817 | |||
chr9:115064759 | G | T | 1 | a0028 | 2 | HG03130.hp1 HG03225.hp1 |
missense_variant | MODERATE | c.3375C>A | p.Ser1125Arg | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 11/28 | 3687/8500 | 3375/6606 | 1125/2201 | chr9 | 115064759 | |||
chr9:115064781 | C | T | 1 | a0016 | 4 | HG02647.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
missense_variant | MODERATE | c.3353G>A | p.Arg1118Gln | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 11/28 | 3665/8500 | 3353/6606 | 1118/2201 | chr9 | 115064781 | |||
chr9:115073620 | C | T | 11 | a0008 a0011 a0020 others(8): Show |
39 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(36): Show |
missense_variant | MODERATE | c.3197G>A | p.Arg1066His | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/28 | 3509/8500 | 3197/6606 | 1066/2201 | chr9 | 115073620 | |||
chr9:115073770 | C | G | 1 | a0055 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.3047G>C | p.Arg1016Pro | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/28 | 3359/8500 | 3047/6606 | 1016/2201 | chr9 | 115073770 | |||
chr9:115077997 | T | C | 3 | a0025 a0027 a0041 |
5 | HG02572.hp2 HG02723.hp1 HG02976.hp2 others(2): Show |
missense_variant | MODERATE | c.2620A>G | p.Ile874Val | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/28 | 2932/8500 | 2620/6606 | 874/2201 | chr9 | 115077997 | |||
chr9:115078036 | C | G | 1 | a0054 | 1 | NA19058.hp2 | missense_variant | MODERATE | c.2581G>C | p.Gly861Arg | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/28 | 2893/8500 | 2581/6606 | 861/2201 | chr9 | 115078036 | |||
chr9:115078069 | C | G | 1 | a0050 | 1 | NA18945.hp2 | missense_variant | MODERATE | c.2548G>C | p.Asp850His | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/28 | 2860/8500 | 2548/6606 | 850/2201 | chr9 | 115078069 | |||
chr9:115078080 | C | T | 1 | a0040 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.2537G>A | p.Arg846His | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/28 | 2849/8500 | 2537/6606 | 846/2201 | chr9 | 115078080 | |||
chr9:115082732 | T | C | 3 | a0016 a0037 a0042 |
6 | HG02257.hp1 HG02647.hp1 HG02818.hp2 others(3): Show |
missense_variant | MODERATE | c.2207A>G | p.Asp736Gly | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 5/28 | 2519/8500 | 2207/6606 | 736/2201 | chr9 | 115082732 | |||
chr9:115084301 | T | C | 28 | a0003 a0004 a0005 others(25): Show |
165 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(162): Show |
missense_variant | MODERATE | c.2039A>G | p.Gln680Arg | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/28 | 2351/8500 | 2039/6606 | 680/2201 | chr9 | 115084301 | |||
chr9:115084460 | T | C | 1 | a0049 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.1880A>G | p.Lys627Arg | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/28 | 2192/8500 | 1880/6606 | 627/2201 | chr9 | 115084460 | |||
chr9:115085918 | C | T | 9 | a0007 a0010 a0013 others(6): Show |
43 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(40): Show |
missense_variant | MODERATE | c.1813G>A | p.Val605Ile | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/28 | 2125/8500 | 1813/6606 | 605/2201 | chr9 | 115085918 | |||
chr9:115086115 | T | C | 48 | a0001 a0002 a0003 others(45): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
missense_variant | MODERATE | c.1616A>G | p.Gln539Arg | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/28 | 1928/8500 | 1616/6606 | 539/2201 | chr9 | 115086115 | |||
chr9:115086223 | C | T | 2 | a0026 a0036 |
3 | HG02145.hp1 HG02809.hp2 HG03471.hp2 |
missense_variant | MODERATE | c.1508G>A | p.Arg503Lys | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/28 | 1820/8500 | 1508/6606 | 503/2201 | chr9 | 115086223 | |||
chr9:115086389 | G | C | 1 | a0032 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.1342C>G | p.Arg448Gly | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/28 | 1654/8500 | 1342/6606 | 448/2201 | chr9 | 115086389 | |||
chr9:115086409 | T | C | 1 | a0048 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.1322A>G | p.Asn441Ser | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/28 | 1634/8500 | 1322/6606 | 441/2201 | chr9 | 115086409 | |||
chr9:115086950 | C | T | 1 | a0020 | 3 | HG01243.hp1 HG02055.hp1 HG02965.hp2 |
missense_variant | MODERATE | c.781G>A | p.Gly261Ser | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/28 | 1093/8500 | 781/6606 | 261/2201 | chr9 | 115086950 | |||
chr9:115087094 | C | T | 2 | a0026 a0036 |
3 | HG02145.hp1 HG02809.hp2 HG03471.hp2 |
missense_variant | MODERATE | c.637G>A | p.Gly213Ser | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/28 | 949/8500 | 637/6606 | 213/2201 | chr9 | 115087094 | |||
chr9:115090576 | A | G | 1 | a0051 | 1 | NA18952.hp1 | missense_variant | MODERATE | c.443T>C | p.Leu148Pro | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/28 | 755/8500 | 443/6606 | 148/2201 | chr9 | 115090576 | |||
chr9:115090585 | C | A | 1 | a0022 | 3 | HG01884.hp2 HG01891.hp2 HG03209.hp1 |
missense_variant | MODERATE | c.434G>T | p.Gly145Val | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/28 | 746/8500 | 434/6606 | 145/2201 | chr9 | 115090585 | |||
chr9:115090676 | C | T | 1 | a0038 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.343G>A | p.Ala115Thr | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/28 | 655/8500 | 343/6606 | 115/2201 | chr9 | 115090676 | |||
chr9:115090694 | G | A | 1 | a0039 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.325C>T | p.Arg109Trp | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/28 | 637/8500 | 325/6606 | 109/2201 | chr9 | 115090694 | |||
chr9:115090921 | C | T | 1 | a0043 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.98G>A | p.Arg33Gln | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/28 | 410/8500 | 98/6606 | 33/2201 | chr9 | 115090921 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:115029385 | C | T | 5 | a0005c0014 a0009c0031 a0009c0044 others(2): Show |
24 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(21): Show |
synonymous_variant | LOW | c.6144G>A | p.Gly2048Gly | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/28 | 6456/8500 | 6144/6606 | 2048/2201 | chr9 | 115029385 | |||
chr9:115029430 | G | A | 4 | a0005c0037 a0005c0066 a0015c0021 others(1): Show |
9 | HG01891.hp1 HG02559.hp1 HG02572.hp1 others(6): Show |
synonymous_variant | LOW | c.6099C>T | p.Arg2033Arg | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/28 | 6411/8500 | 6099/6606 | 2033/2201 | chr9 | 115029430 | |||
chr9:115029451 | G | A | 1 | a0001c0094 | 1 | HG03710.hp1 | synonymous_variant | LOW | c.6078C>T | p.Phe2026Phe | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/28 | 6390/8500 | 6078/6606 | 2026/2201 | chr9 | 115029451 | |||
chr9:115030299 | C | G | 1 | a0005c0062 | 1 | HG01192.hp1 | synonymous_variant | LOW | c.6027G>C | p.Ala2009Ala | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 24/28 | 6339/8500 | 6027/6606 | 2009/2201 | chr9 | 115030299 | |||
chr9:115030320 | C | T | 1 | a0016c0022 | 4 | HG02647.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
synonymous_variant | LOW | c.6006G>A | p.Leu2002Leu | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 24/28 | 6318/8500 | 6006/6606 | 2002/2201 | chr9 | 115030320 | |||
chr9:115035246 | G | T | 2 | a0003c0027 a0028c0036 |
5 | HG02895.hp1 HG02897.hp1 HG02976.hp1 others(2): Show |
synonymous_variant | LOW | c.5745C>A | p.Thr1915Thr | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/28 | 6057/8500 | 5745/6606 | 1915/2201 | chr9 | 115035246 | |||
chr9:115035318 | T | C | 12 | a0001c0002 a0001c0011 a0001c0094 others(9): Show |
56 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(53): Show |
synonymous_variant | LOW | c.5673A>G | p.Arg1891Arg | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/28 | 5985/8500 | 5673/6606 | 1891/2201 | chr9 | 115035318 | |||
chr9:115038268 | G | C | 1 | a0005c0062 | 1 | HG01192.hp1 | synonymous_variant | LOW | c.5505C>G | p.Gly1835Gly | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/28 | 5817/8500 | 5505/6606 | 1835/2201 | chr9 | 115038268 | |||
chr9:115041017 | G | A | 1 | a0003c0068 | 1 | NA18972.hp2 | synonymous_variant | LOW | c.5316C>T | p.Gly1772Gly | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/28 | 5628/8500 | 5316/6606 | 1772/2201 | chr9 | 115041017 | |||
chr9:115042265 | T | C | 36 | a0002c0093 a0003c0027 a0003c0069 others(33): Show |
83 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(80): Show |
synonymous_variant | LOW | c.5202A>G | p.Thr1734Thr | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/28 | 5514/8500 | 5202/6606 | 1734/2201 | chr9 | 115042265 | |||
chr9:115042274 | C | T | 2 | a0005c0037 a0015c0021 |
6 | HG01891.hp1 HG02559.hp1 HG02572.hp1 others(3): Show |
synonymous_variant | LOW | c.5193G>A | p.Arg1731Arg | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/28 | 5505/8500 | 5193/6606 | 1731/2201 | chr9 | 115042274 | |||
chr9:115042292 | C | T | 1 | a0011c0076 | 1 | HG02129.hp1 | synonymous_variant | LOW | c.5175G>A | p.Ser1725Ser | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/28 | 5487/8500 | 5175/6606 | 1725/2201 | chr9 | 115042292 | |||
chr9:115048372 | G | A | 1 | a0017c0095 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.4740C>T | p.Thr1580Thr | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 16/28 | 5052/8500 | 4740/6606 | 1580/2201 | chr9 | 115048372 | |||
chr9:115057157 | C | T | 5 | a0005c0017 a0005c0066 a0009c0019 others(2): Show |
13 | HG01081.hp2 HG01099.hp2 HG01257.hp2 others(10): Show |
synonymous_variant | LOW | c.4575G>A | p.Thr1525Thr | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/28 | 4887/8500 | 4575/6606 | 1525/2201 | chr9 | 115057157 | |||
chr9:115059854 | C | T | 1 | a0004c0073 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.4182G>A | p.Thr1394Thr | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/28 | 4494/8500 | 4182/6606 | 1394/2201 | chr9 | 115059854 | |||
chr9:115073652 | G | A | 6 | a0005c0014 a0007c0041 a0009c0031 others(3): Show |
26 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(23): Show |
synonymous_variant | LOW | c.3165C>T | p.Ala1055Ala | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/28 | 3477/8500 | 3165/6606 | 1055/2201 | chr9 | 115073652 | |||
chr9:115077944 | T | G | 1 | a0002c0096 | 1 | HG03834.hp1 | splice_region_variant&synonymous_variant | LOW | c.2673A>C | p.Thr891Thr | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/28 | 2985/8500 | 2673/6606 | 891/2201 | chr9 | 115077944 | |||
chr9:115078055 | G | A | 3 | a0004c0073 a0004c0074 a0004c0075 |
3 | HG00738.hp1 HG02055.hp2 HG02738.hp1 |
synonymous_variant | LOW | c.2562C>T | p.Asp854Asp | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/28 | 2874/8500 | 2562/6606 | 854/2201 | chr9 | 115078055 | |||
chr9:115078160 | G | A | 1 | a0003c0055 | 1 | NA19058.hp1 | synonymous_variant | LOW | c.2457C>T | p.Ala819Ala | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/28 | 2769/8500 | 2457/6606 | 819/2201 | chr9 | 115078160 | |||
chr9:115081787 | T | G | 7 | a0003c0035 a0005c0061 a0005c0062 others(4): Show |
13 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(10): Show |
synonymous_variant | LOW | c.2389A>C | p.Arg797Arg | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/28 | 2701/8500 | 2389/6606 | 797/2201 | chr9 | 115081787 | |||
chr9:115081803 | C | T | 2 | a0002c0098 a0009c0099 |
2 | HG02071.hp2 HG03490.hp1 |
synonymous_variant | LOW | c.2373G>A | p.Arg791Arg | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/28 | 2685/8500 | 2373/6606 | 791/2201 | chr9 | 115081803 | |||
chr9:115081860 | A | T | 1 | a0040c0088 | 1 | HG02602.hp2 | synonymous_variant | LOW | c.2316T>A | p.Gly772Gly | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/28 | 2628/8500 | 2316/6606 | 772/2201 | chr9 | 115081860 | |||
chr9:115084291 | C | T | 41 | a0001c0009 a0001c0011 a0001c0094 others(38): Show |
162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
synonymous_variant | LOW | c.2049G>A | p.Glu683Glu | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/28 | 2361/8500 | 2049/6606 | 683/2201 | chr9 | 115084291 | |||
chr9:115085922 | T | C | 10 | a0001c0002 a0001c0024 a0002c0020 others(7): Show |
45 | HG00140.hp1 HG00280.hp2 HG01069.hp1 others(42): Show |
synonymous_variant | LOW | c.1809A>G | p.Gln603Gln | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/28 | 2121/8500 | 1809/6606 | 603/2201 | chr9 | 115085922 | |||
chr9:115086264 | G | A | 1 | a0011c0076 | 1 | HG02129.hp1 | synonymous_variant | LOW | c.1467C>T | p.Asp489Asp | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/28 | 1779/8500 | 1467/6606 | 489/2201 | chr9 | 115086264 | |||
chr9:115086786 | G | A | 1 | a0003c0077 | 1 | HG03139.hp2 | synonymous_variant | LOW | c.945C>T | p.Cys315Cys | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/28 | 1257/8500 | 945/6606 | 315/2201 | chr9 | 115086786 | |||
chr9:115087035 | T | C | 56 | a0003c0003 a0003c0013 a0003c0027 others(53): Show |
165 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(162): Show |
synonymous_variant | LOW | c.696A>G | p.Val232Val | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/28 | 1008/8500 | 696/6606 | 232/2201 | chr9 | 115087035 | |||
chr9:115090743 | C | T | 54 | a0003c0003 a0003c0013 a0003c0027 others(51): Show |
162 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(159): Show |
synonymous_variant | LOW | c.276G>A | p.Val92Val | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/28 | 588/8500 | 276/6606 | 92/2201 | chr9 | 115090743 | |||
chr9:115090824 | C | T | 13 | a0003c0052 a0003c0055 a0004c0050 others(10): Show |
20 | HG00323.hp1 HG00621.hp2 HG00741.hp1 others(17): Show |
synonymous_variant | LOW | c.195G>A | p.Ser65Ser | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/28 | 507/8500 | 195/6606 | 65/2201 | chr9 | 115090824 | |||
chr9:115090863 | G | A | 2 | a0026c0046 a0036c0104 |
3 | HG02145.hp1 HG02809.hp2 HG03471.hp2 |
synonymous_variant | LOW | c.156C>T | p.His52His | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/28 | 468/8500 | 156/6606 | 52/2201 | chr9 | 115090863 | |||
chr9:115090932 | G | A | 1 | a0036c0104 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.87C>T | p.Ile29Ile | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/28 | 399/8500 | 87/6606 | 29/2201 | chr9 | 115090932 | |||
chr9:115090944 | G | C | 1 | a0022c0033 | 3 | HG01884.hp2 HG01891.hp2 HG03209.hp1 |
synonymous_variant | LOW | c.75C>G | p.Leu25Leu | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/28 | 387/8500 | 75/6606 | 25/2201 | chr9 | 115090944 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:115019701 | C | T | 1 | a0005c0062t0026 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1456G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 28/28 | 1456 | chr9 | 115019701 | ||||||
chr9:115019916 | C | A | 1 | a0005c0062t0026 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1241G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 28/28 | 1241 | chr9 | 115019916 | ||||||
chr9:115019982 | C | T | 21 | a0003c0069t0005 a0005c0062t0026 a0005c0103t0012 others(18): Show |
39 | HG00621.hp2 HG01074.hp1 HG01192.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*1175G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 28/28 | 1175 | chr9 | 115019982 | ||||||
chr9:115020084 | A | G | 5 | a0001c0002t0008 a0001c0011t0008 a0001c0094t0008 others(2): Show |
11 | HG01361.hp1 HG02015.hp1 HG02698.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1073T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 28/28 | 1073 | chr9 | 115020084 | ||||||
chr9:115020179 | G | A | 7 | a0001c0009t0015 a0001c0024t0015 a0004c0050t0014 others(4): Show |
8 | HG02145.hp1 HG02257.hp1 HG02647.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*978C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 28/28 | 978 | chr9 | 115020179 | ||||||
chr9:115020188 | G | A | 2 | a0005c0023t0018 a0031c0053t0018 |
2 | HG00323.hp1 HG01496.hp2 |
3_prime_UTR_variant | MODIFIER | c.*969C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 28/28 | 969 | chr9 | 115020188 | ||||||
chr9:115020203 | C | G | 106 | a0001c0002t0001 a0001c0002t0003 a0001c0002t0008 others(103): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
3_prime_UTR_variant | MODIFIER | c.*954G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 28/28 | 954 | chr9 | 115020203 | ||||||
chr9:115020212 | A | AT | 67 | a0001c0002t0001 a0001c0002t0003 a0001c0002t0008 others(64): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*944dupA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 28/28 | 944 | chr9 | 115020212 | ||||||
chr9:115020212 | A | ATT | 6 | a0001c0002t0013 a0001c0009t0015 a0001c0024t0015 others(3): Show |
7 | HG02647.hp2 HG02809.hp1 HG03130.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*943_*944dupAA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 28/28 | 944 | chr9 | 115020212 | ||||||
chr9:115020212 | AT | A | 4 | a0002c0020t0011 a0006c0007t0027 a0007c0006t0017 others(1): Show |
8 | HG01081.hp2 HG01099.hp2 HG01257.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*944delA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 28/28 | 944 | chr9 | 115020212 | ||||||
chr9:115020557 | T | A | 1 | a0003c0003t0019 | 2 | HG01081.hp1 HG01981.hp1 |
3_prime_UTR_variant | MODIFIER | c.*600A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 28/28 | 600 | chr9 | 115020557 | ||||||
chr9:115020557 | T | TA | 86 | a0001c0002t0001 a0001c0002t0003 a0001c0002t0008 others(83): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*599dupT | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 28/28 | 599 | chr9 | 115020557 | ||||||
chr9:115020612 | T | C | 2 | a0001c0009t0015 a0001c0024t0015 |
3 | HG02647.hp2 HG02809.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*545A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 28/28 | 545 | chr9 | 115020612 | ||||||
chr9:115020809 | C | T | 1 | a0006c0007t0024 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*348G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 28/28 | 348 | chr9 | 115020809 | ||||||
chr9:115021017 | C | T | 1 | a0038c0079t0023 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*140G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 28/28 | 140 | chr9 | 115021017 | ||||||
chr9:115091051 | G | A | 1 | a0036c0104t0028 | 1 | HG02145.hp1 | 5_prime_UTR_variant | MODIFIER | c.-33C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/28 | 33 | chr9 | 115091051 | ||||||
chr9:115118057 | C | T | 1 | a0006c0007t0022 | 1 | HG01993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-212G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/28 | 27039 | chr9 | 115118057 | ||||||
chr9:115118070 | T | C | 24 | a0001c0002t0003 a0001c0024t0003 a0002c0001t0007 others(21): Show |
50 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(47): Show |
5_prime_UTR_variant | MODIFIER | c.-225A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/28 | 27052 | chr9 | 115118070 | ||||||
chr9:115118078 | A | C | 24 | a0001c0002t0003 a0001c0024t0003 a0002c0001t0007 others(21): Show |
50 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(47): Show |
5_prime_UTR_variant | MODIFIER | c.-233T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/28 | 27060 | chr9 | 115118078 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:115021272 | TA | T | 58 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(55): Show |
58 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(55): Show |
splice_region_variant&intron_variant | LOW | c.6496-6delT | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115021272 | |||||||
chr9:115021283 | A | AG | 3 | a0019c0032t0001g0316 a0019c0032t0001g0318 a0019c0032t0001g0319 |
3 | HG01123.hp2 HG02258.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.6496-17_6496-16ins others(1): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115021283 | |||||||
chr9:115021333 | C | T | 1 | a0001c0011t0001g0161 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.6496-66G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115021333 | |||||||
chr9:115021705 | G | T | 60 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(57): Show |
60 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.6496-438C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115021705 | |||||||
chr9:115021911 | G | C | 1 | a0005c0062t0026g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.6496-644C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115021911 | |||||||
chr9:115022137 | T | C | 15 | a0002c0001t0002g0094 a0002c0001t0002g0096 a0002c0001t0002g0099 others(12): Show |
15 | HG00408.hp2 HG01358.hp2 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.6496-870A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115022137 | |||||||
chr9:115022194 | G | T | 1 | a0002c0001t0002g0094 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.6496-927C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115022194 | |||||||
chr9:115022195 | C | G | 1 | a0015c0021t0004g0254 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.6496-928G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115022195 | |||||||
chr9:115022306 | T | C | 8 | a0005c0037t0004g0152 a0005c0037t0004g0271 a0015c0021t0004g0129 others(5): Show |
8 | HG01891.hp1 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.6496-1039A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115022306 | |||||||
chr9:115022442 | A | C | 35 | a0001c0009t0015g0124 a0001c0009t0015g0350 a0001c0024t0015g0320 others(32): Show |
36 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.6496-1175T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115022442 | |||||||
chr9:115022752 | G | T | 3 | a0003c0035t0004g0150 a0003c0035t0004g0151 a0003c0077t0004g0356 |
3 | HG02559.hp2 HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.6495+1221C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115022752 | |||||||
chr9:115022769 | C | G | 2 | a0037c0064t0014g0343 a0047c0060t0014g0253 |
2 | HG02257.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.6495+1204G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115022769 | |||||||
chr9:115022769 | C | T | 60 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(57): Show |
60 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.6495+1204G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115022769 | |||||||
chr9:115022776 | C | T | 13 | a0002c0093t0004g0122 a0004c0018t0004g0213 a0004c0018t0004g0224 others(10): Show |
13 | HG00408.hp1 HG00738.hp1 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.6495+1197G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115022776 | |||||||
chr9:115022874 | G | A | 35 | a0008c0005t0001g0083 a0008c0005t0001g0085 a0008c0005t0001g0086 others(32): Show |
35 | HG00099.hp2 HG00140.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.6495+1099C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115022874 | |||||||
chr9:115022901 | A | G | 1 | a0036c0104t0028g0341 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.6495+1072T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115022901 | |||||||
chr9:115023005 | C | G | 4 | a0003c0069t0005g0219 a0006c0007t0005g0357 a0025c0038t0005g0353 others(1): Show |
4 | HG02572.hp2 HG03195.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.6495+968G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115023005 | |||||||
chr9:115023037 | C | CA | 127 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(124): Show |
129 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.6495+935dupT | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115023037 | |||||||
chr9:115023037 | C | CAA | 12 | a0001c0009t0015g0124 a0001c0024t0015g0320 a0002c0020t0002g0065 others(9): Show |
12 | HG00597.hp2 HG02572.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.6495+934_6495+935d others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115023037 | |||||||
chr9:115023037 | CA | C | 8 | a0001c0009t0001g0101 a0003c0003t0019g0273 a0004c0004t0002g0223 others(5): Show |
8 | HG01192.hp1 HG01981.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.6495+935delT | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115023037 | |||||||
chr9:115023054 | T | A | 1 | a0029c0039t0003g0042 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.6495+919A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115023054 | |||||||
chr9:115023138 | A | G | 24 | a0001c0009t0002g0117 a0003c0027t0002g0214 a0003c0027t0002g0215 others(21): Show |
25 | HG01081.hp2 HG01099.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.6495+835T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115023138 | |||||||
chr9:115023144 | C | T | 23 | a0005c0014t0001g0005 a0005c0014t0001g0289 a0005c0014t0001g0299 others(20): Show |
24 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.6495+829G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115023144 | |||||||
chr9:115023345 | G | A | 1 | a0004c0004t0002g0313 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.6495+628C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115023345 | |||||||
chr9:115023378 | G | A | 2 | a0035c0065t0005g0326 a0038c0079t0023g0193 |
2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.6495+595C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115023378 | |||||||
chr9:115023476 | G | A | 33 | a0001c0009t0002g0117 a0003c0027t0002g0214 a0003c0027t0002g0215 others(30): Show |
34 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.6495+497C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115023476 | |||||||
chr9:115023655 | A | T | 1 | a0012c0012t0006g0058 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.6495+318T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115023655 | |||||||
chr9:115023703 | G | C | 1 | a0012c0012t0006g0058 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.6495+270C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115023703 | |||||||
chr9:115023729 | G | A | 1 | a0005c0034t0002g0197 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.6495+244C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115023729 | |||||||
chr9:115023837 | T | C | 1 | a0002c0001t0002g0173 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.6495+136A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115023837 | |||||||
chr9:115024229 | G | A | 16 | a0002c0001t0006g0120 a0012c0012t0006g0057 a0012c0012t0006g0058 others(13): Show |
16 | HG00642.hp2 HG00741.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.6332-93C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115024229 | |||||||
chr9:115024462 | T | C | 20 | a0002c0001t0006g0120 a0009c0100t0005g0317 a0012c0012t0006g0057 others(17): Show |
20 | HG00642.hp2 HG00741.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.6332-326A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115024462 | |||||||
chr9:115024472 | C | T | 1 | a0005c0062t0026g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.6332-336G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115024472 | |||||||
chr9:115024481 | T | G | 8 | a0005c0037t0004g0152 a0005c0037t0004g0271 a0015c0021t0004g0129 others(5): Show |
8 | HG01891.hp1 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.6332-345A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115024481 | |||||||
chr9:115024485 | T | A | 1 | a0002c0001t0002g0103 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.6332-349A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115024485 | |||||||
chr9:115024671 | T | C | 1 | a0004c0050t0014g0345 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6332-535A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115024671 | |||||||
chr9:115024767 | G | A | 25 | a0005c0014t0001g0005 a0005c0014t0001g0289 a0005c0014t0001g0299 others(22): Show |
26 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.6332-631C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115024767 | |||||||
chr9:115024855 | A | T | 6 | a0005c0037t0004g0152 a0005c0037t0004g0271 a0015c0021t0004g0129 others(3): Show |
6 | HG01891.hp1 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.6332-719T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115024855 | |||||||
chr9:115024894 | A | C | 224 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(221): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.6332-758T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115024894 | |||||||
chr9:115024995 | C | T | 3 | a0004c0051t0004g0342 a0037c0064t0014g0343 a0047c0060t0014g0253 |
3 | HG02257.hp1 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.6332-859G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115024995 | |||||||
chr9:115025055 | G | A | 26 | a0001c0009t0002g0117 a0003c0027t0002g0214 a0003c0027t0002g0215 others(23): Show |
27 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.6332-919C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115025055 | |||||||
chr9:115025101 | G | A | 4 | a0021c0028t0012g0258 a0021c0028t0012g0259 a0021c0028t0012g0260 others(1): Show |
4 | HG01496.hp1 HG02818.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.6332-965C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115025101 | |||||||
chr9:115025168 | G | T | 2 | a0043c0047t0001g0358 a0046c0058t0001g0248 |
2 | HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.6332-1032C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115025168 | |||||||
chr9:115025387 | C | CT | 128 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(125): Show |
130 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.6331+1146dupA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115025387 | |||||||
chr9:115025459 | C | T | 2 | a0002c0001t0002g0157 a0002c0001t0002g0171 |
2 | HG02155.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.6331+1075G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115025459 | |||||||
chr9:115025680 | T | C | 1 | a0008c0005t0001g0121 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.6331+854A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115025680 | |||||||
chr9:115025739 | G | A | 23 | a0005c0014t0001g0005 a0005c0014t0001g0289 a0005c0014t0001g0299 others(20): Show |
24 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.6331+795C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115025739 | |||||||
chr9:115025753 | A | G | 2 | a0012c0012t0006g0060 a0014c0016t0006g0072 |
2 | HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.6331+781T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115025753 | |||||||
chr9:115025890 | G | C | 1 | a0005c0062t0026g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.6331+644C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115025890 | |||||||
chr9:115025993 | A | G | 1 | a0031c0053t0018g0245 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.6331+541T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115025993 | |||||||
chr9:115026135 | G | A | 3 | a0009c0100t0005g0317 a0035c0065t0005g0326 a0038c0079t0023g0193 |
3 | HG02109.hp2 HG02257.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.6331+399C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115026135 | |||||||
chr9:115026149 | C | G | 4 | a0005c0034t0002g0197 a0005c0034t0002g0198 a0005c0067t0002g0359 others(1): Show |
4 | HG01109.hp2 HG01243.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.6331+385G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115026149 | |||||||
chr9:115026172 | A | T | 1 | a0003c0003t0013g0201 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.6331+362T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115026172 | |||||||
chr9:115026260 | G | C | 1 | a0009c0019t0011g0003 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.6331+274C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115026260 | |||||||
chr9:115026376 | G | A | 23 | a0005c0014t0001g0005 a0005c0014t0001g0289 a0005c0014t0001g0299 others(20): Show |
24 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.6331+158C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115026376 | |||||||
chr9:115026706 | C | T | 2 | a0002c0020t0002g0065 a0002c0020t0002g0249 |
2 | NA19078.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.6170-11G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115026706 | |||||||
chr9:115026723 | G | A | 11 | a0001c0002t0008g0136 a0001c0002t0008g0137 a0001c0002t0008g0139 others(8): Show |
11 | HG01361.hp1 HG02015.hp1 HG02698.hp2 others(8): Show |
intron_variant | MODIFIER | c.6170-28C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115026723 | |||||||
chr9:115026770 | C | T | 23 | a0005c0014t0001g0005 a0005c0014t0001g0289 a0005c0014t0001g0299 others(20): Show |
24 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.6170-75G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115026770 | |||||||
chr9:115026860 | A | G | 1 | a0055c0048t0005g0243 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.6170-165T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115026860 | |||||||
chr9:115027006 | G | A | 2 | a0002c0020t0001g0145 a0004c0004t0001g0269 |
2 | NA18944.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.6170-311C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115027006 | |||||||
chr9:115027024 | G | A | 1 | a0001c0002t0001g0327 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.6170-329C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115027024 | |||||||
chr9:115027024 | G | T | 4 | a0002c0001t0002g0170 a0002c0001t0002g0174 a0002c0001t0002g0176 others(1): Show |
4 | HG00733.hp2 HG01123.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.6170-329C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115027024 | |||||||
chr9:115027118 | A | AAAG | 33 | a0001c0009t0002g0117 a0003c0027t0002g0214 a0003c0027t0002g0215 others(30): Show |
34 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.6170-424_6170-423i others(5): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115027118 | |||||||
chr9:115027119 | A | AAG | 322 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(319): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.6170-425_6170-424i others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115027119 | |||||||
chr9:115027120 | A | AG | 3 | a0003c0035t0004g0150 a0003c0035t0004g0151 a0003c0077t0004g0356 |
3 | HG02559.hp2 HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.6170-426_6170-425i others(3): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115027120 | |||||||
chr9:115027293 | C | G | 14 | a0001c0002t0001g0138 a0001c0002t0001g0141 a0001c0002t0001g0142 others(11): Show |
14 | HG00597.hp1 NA18940.hp1 NA18942.hp1 others(11): Show |
intron_variant | MODIFIER | c.6170-598G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115027293 | |||||||
chr9:115027311 | C | T | 3 | a0003c0035t0004g0150 a0003c0035t0004g0151 a0003c0077t0004g0356 |
3 | HG02559.hp2 HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.6170-616G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115027311 | |||||||
chr9:115027319 | G | GTGGC | 23 | a0005c0014t0001g0005 a0005c0014t0001g0289 a0005c0014t0001g0299 others(20): Show |
24 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.6170-628_6170-625d others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115027319 | |||||||
chr9:115027344 | C | T | 2 | a0005c0017t0002g0079 a0005c0066t0002g0251 |
2 | HG03017.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.6170-649G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115027344 | |||||||
chr9:115027365 | G | A | 2 | a0005c0017t0002g0080 a0038c0079t0023g0193 |
2 | HG02257.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.6170-670C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115027365 | |||||||
chr9:115027421 | C | G | 4 | a0016c0022t0004g0130 a0016c0022t0004g0131 a0016c0022t0004g0252 others(1): Show |
4 | HG02647.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.6170-726G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115027421 | |||||||
chr9:115027475 | A | G | 23 | a0005c0014t0001g0005 a0005c0014t0001g0289 a0005c0014t0001g0299 others(20): Show |
24 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.6170-780T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115027475 | |||||||
chr9:115027525 | G | A | 1 | a0027c0070t0002g0352 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.6170-830C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115027525 | |||||||
chr9:115027704 | G | T | 1 | a0047c0060t0014g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6170-1009C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115027704 | |||||||
chr9:115028139 | T | C | 6 | a0001c0009t0015g0124 a0001c0009t0015g0350 a0001c0024t0015g0320 others(3): Show |
6 | HG02280.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.6169+1221A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028139 | |||||||
chr9:115028323 | C | T | 29 | a0001c0009t0002g0117 a0003c0027t0002g0214 a0003c0027t0002g0215 others(26): Show |
30 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.6169+1037G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028323 | |||||||
chr9:115028396 | G | A | 4 | a0002c0093t0004g0122 a0004c0018t0004g0213 a0004c0018t0004g0224 others(1): Show |
4 | HG02145.hp2 HG02622.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.6169+964C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028396 | |||||||
chr9:115028423 | A | G | 1 | a0002c0001t0002g0082 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.6169+937T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028423 | |||||||
chr9:115028463 | G | T | 1 | a0042c0063t0012g0149 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.6169+897C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028463 | |||||||
chr9:115028623 | C | T | 2 | a0005c0017t0002g0076 a0056c0049t0002g0242 |
2 | HG01346.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.6169+737G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028623 | |||||||
chr9:115028646 | A | C | 52 | a0002c0001t0001g0165 a0002c0001t0002g0002 a0002c0001t0002g0082 others(49): Show |
54 | HG00558.hp1 HG00642.hp1 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.6169+714T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028646 | |||||||
chr9:115028650 | C | T | 2 | a0001c0002t0001g0302 a0001c0002t0010g0330 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.6169+710G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028650 | |||||||
chr9:115028771 | T | C | 1 | a0007c0006t0007g0035 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.6169+589A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028771 | |||||||
chr9:115028874 | C | T | 23 | a0005c0014t0001g0005 a0005c0014t0001g0289 a0005c0014t0001g0299 others(20): Show |
24 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.6169+486G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028874 | |||||||
chr9:115028890 | C | T | 1 | a0005c0062t0026g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.6169+470G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028890 | |||||||
chr9:115028924 | G | GA | 25 | a0002c0001t0002g0094 a0002c0001t0002g0103 a0002c0001t0002g0157 others(22): Show |
26 | HG00609.hp1 HG00733.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.6169+435dupT | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028924 | |||||||
chr9:115028924 | G | GAA | 13 | a0002c0001t0002g0082 a0002c0001t0002g0176 a0002c0001t0002g0191 others(10): Show |
13 | HG01175.hp2 HG01978.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.6169+434_6169+435d others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028924 | |||||||
chr9:115028924 | GA | G | 18 | a0002c0001t0001g0104 a0002c0001t0002g0099 a0002c0001t0002g0106 others(15): Show |
18 | HG00738.hp1 HG01192.hp1 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.6169+435delT | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028924 | |||||||
chr9:115028924 | GAAAAAAA others(3): Show |
G | 7 | a0001c0009t0015g0124 a0001c0009t0015g0350 a0001c0024t0015g0320 others(4): Show |
7 | HG01243.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.6169+426_6169+435d others(12): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028924 | |||||||
chr9:115028924 | GAAAAAAA others(4): Show |
G | 70 | a0001c0009t0001g0101 a0001c0009t0001g0155 a0001c0009t0001g0160 others(67): Show |
70 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.6169+425_6169+435d others(13): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028924 | |||||||
chr9:115028924 | GAAAAAAA others(5): Show |
G | 7 | a0001c0002t0001g0142 a0003c0003t0001g0247 a0003c0003t0001g0331 others(4): Show |
7 | HG00741.hp1 HG01069.hp2 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.6169+424_6169+435d others(14): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028924 | |||||||
chr9:115028924 | GAAAAAAA others(6): Show |
G | 37 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(34): Show |
37 | HG00140.hp1 HG00280.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.6169+423_6169+435d others(15): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028924 | |||||||
chr9:115028924 | GAAAAAAA others(7): Show |
G | 38 | a0001c0002t0001g0277 a0002c0093t0004g0122 a0003c0069t0005g0219 others(35): Show |
39 | HG00621.hp2 HG01074.hp1 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.6169+422_6169+435d others(16): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028924 | |||||||
chr9:115028924 | GAAAAAAA others(8): Show |
G | 22 | a0004c0050t0014g0345 a0005c0014t0001g0005 a0005c0014t0001g0289 others(19): Show |
23 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.6169+421_6169+435d others(17): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028924 | |||||||
chr9:115028924 | GAAAAAAA others(9): Show |
G | 11 | a0002c0001t0006g0120 a0005c0014t0001g0308 a0005c0014t0001g0314 others(8): Show |
11 | HG00642.hp2 HG00741.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.6169+420_6169+435d others(18): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028924 | |||||||
chr9:115028924 | GAAAAAAA others(10): Show |
G | 4 | a0016c0022t0004g0130 a0016c0022t0004g0131 a0016c0022t0004g0252 others(1): Show |
4 | HG02647.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.6169+419_6169+435d others(19): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028924 | |||||||
chr9:115028924 | GAAAAAAA others(13): Show |
G | 13 | a0004c0073t0002g0274 a0004c0074t0002g0286 a0005c0037t0004g0152 others(10): Show |
13 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.6169+416_6169+435d others(22): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028924 | |||||||
chr9:115028924 | GAAAAAAA others(14): Show |
G | 42 | a0001c0002t0008g0136 a0001c0002t0008g0137 a0001c0002t0008g0139 others(39): Show |
44 | HG00099.hp1 HG00323.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.6169+415_6169+435d others(23): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028924 | |||||||
chr9:115028924 | GAAAAAAA others(15): Show |
G | 2 | a0007c0006t0003g0052 a0028c0036t0002g0203 |
2 | HG03225.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.6169+414_6169+435d others(24): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028924 | |||||||
chr9:115028959 | A | G | 3 | a0002c0001t0002g0100 a0002c0020t0002g0148 a0004c0004t0002g0293 |
3 | HG02300.hp1 NA18747.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.6169+401T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028959 | |||||||
chr9:115028994 | C | CT | 121 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(118): Show |
123 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.6169+365dupA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028994 | |||||||
chr9:115029035 | G | GA | 100 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(97): Show |
101 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.6169+324dupT | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115029035 | |||||||
chr9:115029035 | G | GAA | 11 | a0001c0002t0008g0137 a0001c0011t0001g0095 a0002c0001t0002g0096 others(8): Show |
11 | HG00597.hp2 HG00741.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.6169+323_6169+324d others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115029035 | |||||||
chr9:115029035 | GA | G | 45 | a0001c0009t0002g0117 a0002c0001t0001g0165 a0002c0001t0002g0082 others(42): Show |
46 | HG00741.hp2 HG01081.hp2 HG01099.hp2 others(43): Show |
intron_variant | MODIFIER | c.6169+324delT | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115029035 | |||||||
chr9:115029038 | A | G | 1 | a0036c0104t0028g0341 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.6169+322T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115029038 | |||||||
chr9:115029039 | A | C | 4 | a0003c0069t0005g0219 a0006c0007t0005g0357 a0025c0038t0005g0353 others(1): Show |
4 | HG02572.hp2 HG03195.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.6169+321T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115029039 | |||||||
chr9:115029116 | C | T | 1 | a0010c0008t0007g0021 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.6169+244G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115029116 | |||||||
chr9:115029117 | G | A | 1 | a0005c0103t0012g0091 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.6169+243C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115029117 | |||||||
chr9:115029127 | T | A | 4 | a0002c0093t0004g0122 a0004c0018t0004g0213 a0004c0018t0004g0224 others(1): Show |
4 | HG02145.hp2 HG02622.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.6169+233A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115029127 | |||||||
chr9:115029145 | G | A | 1 | a0029c0039t0003g0042 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.6169+215C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115029145 | |||||||
chr9:115029233 | G | C | 2 | a0001c0002t0001g0275 a0001c0002t0001g0277 |
2 | HG01255.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.6169+127C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115029233 | |||||||
chr9:115029338 | T | C | 57 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(54): Show |
57 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.6169+22A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115029338 | |||||||
chr9:115029469 | C | T | 1 | a0002c0001t0002g0158 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.6073-13G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 24/27 | chr9 | 115029469 | |||||||
chr9:115029553 | C | T | 1 | a0009c0092t0002g0093 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.6073-97G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 24/27 | chr9 | 115029553 | |||||||
chr9:115029603 | C | T | 1 | a0001c0002t0001g0277 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.6073-147G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 24/27 | chr9 | 115029603 | |||||||
chr9:115029881 | C | T | 1 | a0005c0062t0026g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.6072+373G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 24/27 | chr9 | 115029881 | |||||||
chr9:115029981 | AT | A | 13 | a0001c0009t0002g0117 a0005c0017t0001g0081 a0005c0017t0002g0076 others(10): Show |
14 | HG01081.hp2 HG01099.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.6072+272delA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 24/27 | chr9 | 115029981 | |||||||
chr9:115029995 | G | C | 56 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(53): Show |
56 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.6072+259C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 24/27 | chr9 | 115029995 | |||||||
chr9:115030064 | G | A | 3 | a0002c0001t0002g0098 a0004c0004t0002g0297 a0004c0004t0002g0300 |
3 | HG01978.hp1 HG02273.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.6072+190C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 24/27 | chr9 | 115030064 | |||||||
chr9:115030117 | C | T | 1 | a0004c0073t0002g0274 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.6072+137G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 24/27 | chr9 | 115030117 | |||||||
chr9:115030147 | G | T | 118 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(115): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.6072+107C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 24/27 | chr9 | 115030147 | |||||||
chr9:115030164 | C | T | 5 | a0003c0027t0002g0214 a0003c0027t0002g0215 a0003c0027t0002g0218 others(2): Show |
5 | HG02895.hp1 HG02897.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.6072+90G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 24/27 | chr9 | 115030164 | |||||||
chr9:115030195 | C | G | 1 | a0004c0018t0004g0334 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.6072+59G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 24/27 | chr9 | 115030195 | |||||||
chr9:115030477 | C | G | 1 | a0003c0003t0019g0360 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.5921-72G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 23/27 | chr9 | 115030477 | |||||||
chr9:115030597 | A | T | 28 | a0005c0014t0001g0005 a0005c0014t0001g0289 a0005c0014t0001g0299 others(25): Show |
29 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.5921-192T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 23/27 | chr9 | 115030597 | |||||||
chr9:115030683 | A | C | 1 | a0002c0001t0007g0018 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.5921-278T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 23/27 | chr9 | 115030683 | |||||||
chr9:115030826 | G | T | 2 | a0001c0024t0003g0008 a0001c0024t0003g0009 |
2 | NA18992.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.5921-421C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 23/27 | chr9 | 115030826 | |||||||
chr9:115030831 | C | T | 1 | a0009c0092t0002g0093 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.5921-426G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 23/27 | chr9 | 115030831 | |||||||
chr9:115030916 | G | A | 1 | a0001c0002t0010g0288 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.5921-511C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 23/27 | chr9 | 115030916 | |||||||
chr9:115030946 | C | T | 1 | a0009c0019t0002g0178 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.5921-541G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 23/27 | chr9 | 115030946 | |||||||
chr9:115031079 | T | G | 9 | a0001c0009t0015g0124 a0001c0009t0015g0350 a0001c0024t0015g0320 others(6): Show |
9 | HG02280.hp2 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.5920+474A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 23/27 | chr9 | 115031079 | |||||||
chr9:115031134 | G | T | 25 | a0008c0005t0001g0083 a0008c0005t0001g0085 a0008c0005t0001g0086 others(22): Show |
25 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(22): Show |
intron_variant | MODIFIER | c.5920+419C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 23/27 | chr9 | 115031134 | |||||||
chr9:115031152 | C | A | 2 | a0001c0002t0001g0302 a0001c0002t0010g0330 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.5920+401G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 23/27 | chr9 | 115031152 | |||||||
chr9:115031179 | G | T | 1 | a0001c0002t0008g0137 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.5920+374C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 23/27 | chr9 | 115031179 | |||||||
chr9:115031269 | T | C | 1 | a0005c0062t0026g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.5920+284A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 23/27 | chr9 | 115031269 | |||||||
chr9:115031356 | G | A | 1 | a0004c0004t0002g0300 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.5920+197C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 23/27 | chr9 | 115031356 | |||||||
chr9:115031378 | C | T | 32 | a0003c0069t0005g0219 a0006c0007t0005g0200 a0006c0007t0005g0204 others(29): Show |
33 | HG00621.hp2 HG01074.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.5920+175G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 23/27 | chr9 | 115031378 | |||||||
chr9:115031383 | T | G | 1 | a0005c0062t0026g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.5920+170A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 23/27 | chr9 | 115031383 | |||||||
chr9:115031387 | C | T | 1 | a0003c0003t0019g0360 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.5920+166G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 23/27 | chr9 | 115031387 | |||||||
chr9:115031453 | G | A | 1 | a0005c0062t0026g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.5920+100C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 23/27 | chr9 | 115031453 | |||||||
chr9:115031514 | T | G | 2 | a0001c0009t0001g0188 a0003c0003t0010g0328 |
2 | HG01515.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.5920+39A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 23/27 | chr9 | 115031514 | |||||||
chr9:115031875 | G | A | 56 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(53): Show |
56 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.5788-190C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115031875 | |||||||
chr9:115032121 | G | T | 1 | a0002c0001t0002g0186 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.5788-436C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115032121 | |||||||
chr9:115032122 | G | T | 1 | a0005c0062t0026g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.5788-437C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115032122 | |||||||
chr9:115032321 | C | T | 1 | a0008c0005t0001g0118 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.5788-636G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115032321 | |||||||
chr9:115032403 | G | A | 3 | a0004c0051t0004g0342 a0037c0064t0014g0343 a0047c0060t0014g0253 |
3 | HG02257.hp1 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.5788-718C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115032403 | |||||||
chr9:115032614 | TG | T | 11 | a0001c0002t0008g0136 a0001c0002t0008g0137 a0001c0002t0008g0139 others(8): Show |
11 | HG01361.hp1 HG02015.hp1 HG02698.hp2 others(8): Show |
intron_variant | MODIFIER | c.5788-930delC | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115032614 | |||||||
chr9:115033009 | C | A | 56 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(53): Show |
56 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.5788-1324G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115033009 | |||||||
chr9:115033153 | C | G | 1 | a0004c0050t0014g0345 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5788-1468G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115033153 | |||||||
chr9:115033285 | C | T | 1 | a0004c0051t0004g0342 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.5788-1600G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115033285 | |||||||
chr9:115033320 | C | G | 2 | a0026c0046t0004g0339 a0026c0046t0004g0340 |
2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.5788-1635G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115033320 | |||||||
chr9:115033864 | T | G | 1 | a0004c0051t0004g0342 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.5787+1340A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115033864 | |||||||
chr9:115034062 | C | T | 16 | a0002c0001t0006g0120 a0012c0012t0006g0057 a0012c0012t0006g0058 others(13): Show |
16 | HG00642.hp2 HG00741.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.5787+1142G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115034062 | |||||||
chr9:115034106 | A | T | 2 | a0004c0018t0004g0305 a0007c0086t0020g0044 |
2 | HG00408.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.5787+1098T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115034106 | |||||||
chr9:115034118 | G | A | 1 | a0001c0009t0001g0160 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.5787+1086C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115034118 | |||||||
chr9:115034132 | A | G | 4 | a0002c0001t0006g0120 a0012c0012t0006g0060 a0014c0016t0006g0072 others(1): Show |
4 | HG01169.hp2 HG01346.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.5787+1072T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115034132 | |||||||
chr9:115034136 | G | A | 1 | a0036c0104t0028g0341 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5787+1068C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115034136 | |||||||
chr9:115034187 | G | A | 1 | a0036c0104t0028g0341 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5787+1017C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115034187 | |||||||
chr9:115034218 | A | G | 1 | a0002c0001t0002g0002 | 2 | NA19066.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.5787+986T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115034218 | |||||||
chr9:115034530 | G | A | 4 | a0002c0001t0002g0168 a0002c0020t0011g0132 a0004c0004t0002g0220 others(1): Show |
4 | NA18954.hp2 NA18961.hp2 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.5787+674C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115034530 | |||||||
chr9:115034683 | G | A | 1 | a0006c0007t0027g0294 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.5787+521C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115034683 | |||||||
chr9:115034706 | T | C | 1 | a0001c0009t0001g0160 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.5787+498A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115034706 | |||||||
chr9:115034707 | T | C | 242 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(239): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.5787+497A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115034707 | |||||||
chr9:115034758 | G | C | 3 | a0002c0001t0002g0100 a0002c0020t0002g0148 a0007c0006t0003g0028 |
3 | HG00558.hp1 NA18747.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.5787+446C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115034758 | |||||||
chr9:115034966 | C | A | 1 | a0002c0001t0002g0186 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.5787+238G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115034966 | |||||||
chr9:115035075 | T | C | 1 | a0008c0005t0002g0187 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.5787+129A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115035075 | |||||||
chr9:115035080 | A | AT | 271 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(268): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.5787+123dupA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115035080 | |||||||
chr9:115035115 | G | A | 27 | a0001c0009t0002g0117 a0003c0027t0002g0214 a0003c0027t0002g0215 others(24): Show |
28 | HG01081.hp2 HG01099.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.5787+89C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115035115 | |||||||
chr9:115035128 | A | G | 1 | a0003c0077t0004g0356 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.5787+76T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115035128 | |||||||
chr9:115035439 | G | T | 4 | a0002c0001t0006g0120 a0012c0012t0006g0060 a0014c0016t0006g0072 others(1): Show |
4 | HG01169.hp2 HG01346.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.5657-105C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 21/27 | chr9 | 115035439 | |||||||
chr9:115035610 | C | T | 1 | a0035c0065t0005g0326 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.5657-276G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 21/27 | chr9 | 115035610 | |||||||
chr9:115035882 | C | T | 1 | a0003c0013t0008g0246 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.5656+216G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 21/27 | chr9 | 115035882 | |||||||
chr9:115035883 | G | A | 23 | a0005c0014t0001g0005 a0005c0014t0001g0289 a0005c0014t0001g0299 others(20): Show |
24 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.5656+215C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 21/27 | chr9 | 115035883 | |||||||
chr9:115035968 | G | A | 1 | a0001c0009t0001g0123 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.5656+130C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 21/27 | chr9 | 115035968 | |||||||
chr9:115035994 | C | T | 1 | a0002c0001t0002g0100 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.5656+104G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 21/27 | chr9 | 115035994 | |||||||
chr9:115036284 | T | C | 1 | a0002c0001t0002g0154 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.5513-43A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115036284 | |||||||
chr9:115036336 | G | A | 1 | a0002c0001t0002g0154 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.5513-95C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115036336 | |||||||
chr9:115036346 | G | A | 3 | a0001c0009t0015g0124 a0001c0009t0015g0350 a0001c0024t0015g0320 |
3 | HG02647.hp2 HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.5513-105C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115036346 | |||||||
chr9:115036532 | T | A | 3 | a0001c0009t0015g0124 a0001c0009t0015g0350 a0001c0024t0015g0320 |
3 | HG02647.hp2 HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.5513-291A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115036532 | |||||||
chr9:115036553 | G | C | 35 | a0001c0009t0002g0117 a0003c0027t0002g0214 a0003c0027t0002g0215 others(32): Show |
36 | HG01081.hp2 HG01099.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.5513-312C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115036553 | |||||||
chr9:115036558 | C | T | 56 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(53): Show |
56 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.5513-317G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115036558 | |||||||
chr9:115036559 | G | A | 1 | a0002c0001t0001g0165 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.5513-318C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115036559 | |||||||
chr9:115036733 | T | C | 1 | a0002c0001t0002g0082 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.5513-492A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115036733 | |||||||
chr9:115036833 | T | C | 1 | a0039c0078t0001g0307 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.5513-592A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115036833 | |||||||
chr9:115036853 | C | T | 1 | a0021c0028t0012g0260 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5513-612G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115036853 | |||||||
chr9:115037056 | C | T | 23 | a0005c0014t0001g0005 a0005c0014t0001g0289 a0005c0014t0001g0299 others(20): Show |
24 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.5513-815G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115037056 | |||||||
chr9:115037202 | A | G | 1 | a0021c0028t0012g0258 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.5513-961T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115037202 | |||||||
chr9:115037422 | T | G | 3 | a0007c0006t0007g0001 a0007c0006t0007g0051 a0007c0006t0016g0050 |
4 | NA19000.hp1 NA19004.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.5512+839A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115037422 | |||||||
chr9:115037475 | G | A | 9 | a0002c0093t0004g0122 a0004c0018t0004g0213 a0004c0018t0004g0224 others(6): Show |
9 | HG00323.hp1 HG00408.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.5512+786C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115037475 | |||||||
chr9:115037521 | A | T | 1 | a0005c0062t0026g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.5512+740T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115037521 | |||||||
chr9:115037525 | A | T | 1 | a0002c0001t0002g0184 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.5512+736T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115037525 | |||||||
chr9:115037589 | G | C | 1 | a0005c0062t0026g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.5512+672C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115037589 | |||||||
chr9:115037778 | C | T | 273 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(270): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.5512+483G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115037778 | |||||||
chr9:115037788 | A | G | 37 | a0001c0009t0002g0117 a0003c0027t0002g0214 a0003c0027t0002g0215 others(34): Show |
38 | HG01081.hp2 HG01099.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.5512+473T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115037788 | |||||||
chr9:115037826 | T | C | 250 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(247): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.5512+435A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115037826 | |||||||
chr9:115037855 | G | T | 1 | a0005c0062t0026g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.5512+406C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115037855 | |||||||
chr9:115037933 | A | G | 1 | a0016c0022t0004g0261 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.5512+328T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115037933 | |||||||
chr9:115038138 | T | A | 41 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(38): Show |
41 | HG00140.hp1 HG00280.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.5512+123A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115038138 | |||||||
chr9:115038193 | C | T | 2 | a0003c0003t0001g0329 a0039c0078t0001g0307 |
2 | HG02486.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.5512+68G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115038193 | |||||||
chr9:115038415 | T | C | 6 | a0002c0020t0001g0145 a0004c0004t0001g0269 a0007c0006t0007g0006 others(3): Show |
6 | NA18944.hp2 NA18948.hp2 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.5393-35A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115038415 | |||||||
chr9:115038667 | G | C | 1 | a0001c0002t0008g0136 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.5393-287C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115038667 | |||||||
chr9:115038792 | C | CCTTTTCT others(10): Show |
3 | a0001c0002t0001g0134 a0001c0002t0013g0135 a0001c0011t0001g0095 |
3 | HG02071.hp1 NA19067.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.5393-429_5393-413d others(19): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115038792 | |||||||
chr9:115038897 | G | A | 56 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(53): Show |
56 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.5393-517C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115038897 | |||||||
chr9:115038909 | C | G | 3 | a0003c0003t0004g0337 a0024c0082t0004g0055 a0027c0070t0002g0352 |
3 | HG02280.hp2 HG02486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.5393-529G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115038909 | |||||||
chr9:115038998 | T | C | 3 | a0019c0032t0001g0316 a0019c0032t0001g0318 a0019c0032t0001g0319 |
3 | HG01123.hp2 HG02258.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.5393-618A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115038998 | |||||||
chr9:115039015 | A | G | 1 | a0028c0036t0002g0203 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.5393-635T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115039015 | |||||||
chr9:115039131 | C | G | 3 | a0004c0051t0004g0342 a0037c0064t0014g0343 a0047c0060t0014g0253 |
3 | HG02257.hp1 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.5393-751G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115039131 | |||||||
chr9:115039191 | C | T | 23 | a0005c0014t0001g0005 a0005c0014t0001g0289 a0005c0014t0001g0299 others(20): Show |
24 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.5393-811G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115039191 | |||||||
chr9:115039215 | C | T | 4 | a0029c0039t0003g0041 a0029c0039t0003g0042 a0051c0080t0003g0045 others(1): Show |
4 | NA18950.hp2 NA18952.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.5393-835G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115039215 | |||||||
chr9:115039337 | A | G | 1 | a0044c0091t0002g0189 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.5393-957T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115039337 | |||||||
chr9:115039679 | C | G | 1 | a0048c0057t0014g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.5392+1262G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115039679 | |||||||
chr9:115039715 | G | T | 1 | a0005c0062t0026g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.5392+1226C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115039715 | |||||||
chr9:115039759 | A | G | 1 | a0027c0071t0001g0355 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5392+1182T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115039759 | |||||||
chr9:115039817 | A | G | 9 | a0001c0009t0015g0124 a0001c0009t0015g0350 a0001c0024t0015g0320 others(6): Show |
9 | HG02280.hp2 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.5392+1124T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115039817 | |||||||
chr9:115039968 | T | A | 16 | a0002c0001t0006g0120 a0012c0012t0006g0057 a0012c0012t0006g0058 others(13): Show |
16 | HG00642.hp2 HG00741.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.5392+973A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115039968 | |||||||
chr9:115040102 | C | A | 1 | a0002c0001t0002g0195 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.5392+839G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115040102 | |||||||
chr9:115040196 | T | A | 3 | a0001c0009t0001g0175 a0003c0003t0019g0273 a0003c0003t0019g0360 |
3 | HG01081.hp1 HG01261.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.5392+745A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115040196 | |||||||
chr9:115040211 | T | G | 2 | a0005c0023t0001g0291 a0005c0023t0001g0292 |
2 | HG00099.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.5392+730A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115040211 | |||||||
chr9:115040281 | C | T | 1 | a0005c0017t0002g0076 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.5392+660G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115040281 | |||||||
chr9:115040344 | C | T | 3 | a0006c0007t0005g0357 a0025c0038t0005g0353 a0025c0038t0005g0354 |
3 | HG02572.hp2 HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.5392+597G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115040344 | |||||||
chr9:115040346 | G | A | 2 | a0026c0046t0004g0339 a0026c0046t0004g0340 |
2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.5392+595C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115040346 | |||||||
chr9:115040418 | T | C | 9 | a0001c0009t0015g0124 a0001c0009t0015g0350 a0001c0024t0015g0320 others(6): Show |
9 | HG02280.hp2 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.5392+523A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115040418 | |||||||
chr9:115040515 | A | G | 1 | a0029c0039t0003g0041 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.5392+426T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115040515 | |||||||
chr9:115040706 | G | T | 21 | a0003c0027t0002g0214 a0003c0027t0002g0215 a0003c0027t0002g0218 others(18): Show |
21 | HG00642.hp2 HG00741.hp2 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.5392+235C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115040706 | |||||||
chr9:115040775 | C | G | 1 | a0001c0009t0001g0175 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.5392+166G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115040775 | |||||||
chr9:115040906 | A | AACAC | 221 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(218): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.5392+31_5392+34dup others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115040906 | |||||||
chr9:115040906 | A | AACACAC | 4 | a0004c0050t0014g0345 a0005c0062t0026g0250 a0009c0100t0005g0317 others(1): Show |
4 | HG01192.hp1 HG02257.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.5392+29_5392+34dup others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115040906 | |||||||
chr9:115041101 | G | C | 10 | a0001c0009t0015g0124 a0001c0009t0015g0350 a0001c0024t0015g0320 others(7): Show |
10 | HG02280.hp2 HG02486.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.5249-17C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041101 | |||||||
chr9:115041232 | C | T | 1 | a0006c0007t0005g0298 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.5249-148G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041232 | |||||||
chr9:115041250 | G | T | 1 | a0005c0067t0002g0359 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.5249-166C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041250 | |||||||
chr9:115041300 | C | CG | 3 | a0003c0052t0001g0234 a0006c0007t0005g0221 a0009c0100t0005g0317 |
3 | HG02818.hp1 NA18963.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.5249-217_5249-216i others(3): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041300 | |||||||
chr9:115041300 | CA | C | 47 | a0001c0009t0001g0155 a0001c0009t0001g0160 a0001c0009t0002g0117 others(44): Show |
47 | HG01081.hp1 HG01109.hp2 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.5249-217delT | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041300 | |||||||
chr9:115041300 | CAG | C | 34 | a0001c0009t0001g0123 a0001c0009t0015g0124 a0001c0024t0003g0008 others(31): Show |
35 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.5249-218_5249-217d others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041300 | |||||||
chr9:115041300 | CAGG | C | 12 | a0001c0009t0015g0350 a0001c0024t0015g0320 a0003c0003t0004g0337 others(9): Show |
12 | HG01361.hp2 HG02280.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.5249-219_5249-217d others(5): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041300 | |||||||
chr9:115041301 | A | G | 36 | a0001c0002t0001g0301 a0001c0002t0001g0303 a0001c0009t0001g0101 others(33): Show |
36 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.5249-217T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041301 | |||||||
chr9:115041303 | G | C | 1 | a0004c0018t0004g0224 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.5249-219C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041303 | |||||||
chr9:115041304 | A | AGCGGG | 13 | a0001c0002t0001g0138 a0001c0002t0001g0141 a0001c0002t0001g0142 others(10): Show |
13 | HG03688.hp1 NA18942.hp1 NA18948.hp1 others(10): Show |
intron_variant | MODIFIER | c.5249-221_5249-220i others(7): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041304 | |||||||
chr9:115041304 | A | AGCGGGG | 21 | a0001c0002t0001g0128 a0001c0002t0001g0267 a0001c0002t0001g0268 others(18): Show |
21 | HG00597.hp1 HG00621.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.5249-221_5249-220i others(8): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041304 | |||||||
chr9:115041304 | A | AGCGGGGG | 14 | a0001c0002t0001g0134 a0001c0002t0001g0192 a0001c0002t0001g0276 others(11): Show |
14 | HG00140.hp1 HG00280.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.5249-221_5249-220i others(9): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041304 | |||||||
chr9:115041304 | A | C | 14 | a0002c0093t0004g0122 a0004c0018t0004g0213 a0004c0018t0004g0226 others(11): Show |
14 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(11): Show |
intron_variant | MODIFIER | c.5249-220T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041304 | |||||||
chr9:115041304 | A | G | 115 | a0001c0002t0001g0301 a0001c0002t0001g0303 a0001c0009t0001g0101 others(112): Show |
116 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(113): Show |
intron_variant | MODIFIER | c.5249-220T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041304 | |||||||
chr9:115041305 | G | C | 9 | a0001c0002t0001g0301 a0001c0002t0001g0303 a0012c0012t0006g0060 others(6): Show |
9 | HG00642.hp2 HG00741.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.5249-221C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041305 | |||||||
chr9:115041307 | G | GC | 35 | a0008c0005t0001g0083 a0008c0005t0001g0085 a0008c0005t0001g0086 others(32): Show |
35 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(32): Show |
intron_variant | MODIFIER | c.5249-224_5249-223i others(3): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041307 | |||||||
chr9:115041307 | G | T | 2 | a0026c0046t0004g0339 a0026c0046t0004g0340 |
2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.5249-223C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041307 | |||||||
chr9:115041308 | GC | G | 3 | a0004c0051t0004g0342 a0037c0064t0014g0343 a0047c0060t0014g0253 |
3 | HG02257.hp1 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.5249-225delG | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041308 | |||||||
chr9:115041309 | C | G | 267 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(264): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.5249-225G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041309 | |||||||
chr9:115041309 | C | T | 1 | a0048c0057t0014g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.5249-225G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041309 | |||||||
chr9:115041311 | G | C | 23 | a0003c0003t0001g0344 a0005c0017t0001g0081 a0005c0017t0002g0076 others(20): Show |
24 | HG01081.hp2 HG01099.hp2 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.5249-227C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041311 | |||||||
chr9:115041312 | G | C | 6 | a0001c0011t0008g0153 a0005c0034t0002g0197 a0005c0034t0002g0198 others(3): Show |
6 | HG01109.hp2 HG01243.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.5249-228C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041312 | |||||||
chr9:115041313 | GGAA | G | 16 | a0001c0002t0001g0301 a0001c0002t0001g0303 a0012c0012t0006g0057 others(13): Show |
16 | HG00642.hp2 HG00741.hp2 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.5249-232_5249-230d others(5): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041313 | |||||||
chr9:115041314 | G | A | 54 | a0004c0050t0014g0345 a0005c0014t0001g0005 a0005c0014t0001g0289 others(51): Show |
56 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.5249-230C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041314 | |||||||
chr9:115041315 | A | G | 182 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.5249-231T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041315 | |||||||
chr9:115041316 | A | G | 5 | a0003c0013t0001g0304 a0012c0012t0006g0059 a0019c0032t0001g0316 others(2): Show |
5 | HG01099.hp1 HG01123.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.5249-232T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041316 | |||||||
chr9:115041332 | C | T | 1 | a0002c0093t0004g0122 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.5249-248G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041332 | |||||||
chr9:115041441 | G | A | 182 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(179): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.5249-357C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041441 | |||||||
chr9:115041553 | A | G | 54 | a0002c0093t0004g0122 a0004c0018t0004g0213 a0004c0018t0004g0224 others(51): Show |
55 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.5249-469T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041553 | |||||||
chr9:115041603 | A | G | 272 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(269): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.5249-519T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041603 | |||||||
chr9:115041748 | C | T | 52 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(49): Show |
52 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.5248+471G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041748 | |||||||
chr9:115042051 | C | T | 1 | a0035c0065t0005g0326 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.5248+168G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115042051 | |||||||
chr9:115042121 | A | C | 10 | a0001c0009t0015g0124 a0001c0009t0015g0350 a0001c0024t0015g0320 others(7): Show |
10 | HG02280.hp2 HG02486.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.5248+98T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115042121 | |||||||
chr9:115042377 | A | T | 1 | a0001c0024t0015g0320 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.5126-36T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115042377 | |||||||
chr9:115042388 | T | C | 17 | a0008c0005t0001g0083 a0008c0005t0001g0085 a0008c0005t0001g0086 others(14): Show |
17 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(14): Show |
intron_variant | MODIFIER | c.5126-47A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115042388 | |||||||
chr9:115042589 | C | T | 3 | a0005c0017t0001g0081 a0005c0017t0002g0076 a0056c0049t0002g0242 |
3 | HG01346.hp2 HG03704.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.5126-248G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115042589 | |||||||
chr9:115042652 | C | G | 1 | a0009c0092t0002g0093 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.5126-311G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115042652 | |||||||
chr9:115042670 | T | G | 6 | a0005c0037t0004g0152 a0005c0037t0004g0271 a0015c0021t0004g0129 others(3): Show |
6 | HG01891.hp1 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.5126-329A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115042670 | |||||||
chr9:115042795 | G | A | 4 | a0016c0022t0004g0130 a0016c0022t0004g0131 a0016c0022t0004g0252 others(1): Show |
4 | HG02647.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.5126-454C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115042795 | |||||||
chr9:115042889 | C | T | 1 | a0036c0104t0028g0341 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5126-548G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115042889 | |||||||
chr9:115042922 | C | G | 37 | a0008c0005t0001g0083 a0008c0005t0001g0085 a0008c0005t0001g0086 others(34): Show |
37 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.5126-581G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115042922 | |||||||
chr9:115043015 | G | A | 272 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(269): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.5126-674C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115043015 | |||||||
chr9:115043067 | A | G | 1 | a0005c0014t0001g0289 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.5126-726T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115043067 | |||||||
chr9:115043150 | A | G | 2 | a0004c0050t0014g0345 a0005c0062t0026g0250 |
2 | HG01192.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.5126-809T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115043150 | |||||||
chr9:115043280 | T | C | 50 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(47): Show |
50 | HG00140.hp1 HG00280.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.5126-939A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115043280 | |||||||
chr9:115043396 | A | T | 1 | a0001c0002t0001g0322 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.5126-1055T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115043396 | |||||||
chr9:115043440 | C | A | 217 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(214): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.5126-1099G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115043440 | |||||||
chr9:115043485 | C | T | 52 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(49): Show |
52 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.5126-1144G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115043485 | |||||||
chr9:115043547 | A | G | 2 | a0004c0050t0014g0345 a0005c0062t0026g0250 |
2 | HG01192.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.5126-1206T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115043547 | |||||||
chr9:115043639 | T | A | 1 | a0028c0036t0002g0203 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.5126-1298A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115043639 | |||||||
chr9:115043736 | A | AAAAC | 221 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(218): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.5126-1399_5126-139 others(8): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115043736 | |||||||
chr9:115043740 | C | A | 6 | a0009c0031t0001g0166 a0010c0008t0003g0013 a0010c0008t0003g0014 others(3): Show |
6 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(3): Show |
intron_variant | MODIFIER | c.5126-1399G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115043740 | |||||||
chr9:115043798 | C | T | 1 | a0009c0042t0008g0112 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.5126-1457G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115043798 | |||||||
chr9:115043966 | C | T | 1 | a0021c0028t0012g0258 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.5126-1625G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115043966 | |||||||
chr9:115044088 | A | G | 2 | a0037c0064t0014g0343 a0047c0060t0014g0253 |
2 | HG02257.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.5126-1747T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115044088 | |||||||
chr9:115044200 | A | G | 1 | a0005c0103t0012g0091 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5126-1859T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115044200 | |||||||
chr9:115044262 | T | TA | 55 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(52): Show |
55 | HG00140.hp1 HG00280.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.5126-1922dupT | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115044262 | |||||||
chr9:115044262 | TA | T | 86 | a0001c0009t0001g0101 a0001c0009t0001g0123 a0001c0009t0001g0155 others(83): Show |
86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.5126-1922delT | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115044262 | |||||||
chr9:115044274 | AC | A | 4 | a0021c0028t0012g0258 a0021c0028t0012g0259 a0021c0028t0012g0260 others(1): Show |
4 | HG01496.hp1 HG02818.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.5126-1934delG | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115044274 | |||||||
chr9:115044384 | G | GAC | 89 | a0001c0002t0008g0139 a0001c0011t0001g0114 a0002c0001t0001g0104 others(86): Show |
90 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.5125+2024_5125+202 others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115044384 | |||||||
chr9:115044384 | G | GACAC | 13 | a0002c0001t0002g0184 a0002c0001t0007g0018 a0003c0013t0008g0246 others(10): Show |
14 | HG01993.hp1 HG02572.hp2 HG02602.hp2 others(11): Show |
intron_variant | MODIFIER | c.5125+2022_5125+202 others(8): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115044384 | |||||||
chr9:115044384 | G | GACACACA others(1): Show |
20 | a0005c0014t0001g0005 a0005c0014t0001g0289 a0005c0014t0001g0299 others(17): Show |
21 | HG00423.hp2 HG00609.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.5125+2018_5125+202 others(12): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115044384 | |||||||
chr9:115044384 | G | GACACACA others(3): Show |
1 | a0010c0008t0003g0024 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.5125+2016_5125+202 others(14): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115044384 | |||||||
chr9:115044384 | GAC | G | 34 | a0004c0051t0004g0342 a0006c0007t0005g0200 a0006c0007t0005g0204 others(31): Show |
35 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.5125+2024_5125+202 others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115044384 | |||||||
chr9:115044384 | GACAC | G | 54 | a0001c0009t0015g0124 a0001c0009t0015g0350 a0001c0024t0001g0133 others(51): Show |
54 | HG01109.hp2 HG01243.hp2 HG01496.hp1 others(51): Show |
intron_variant | MODIFIER | c.5125+2022_5125+202 others(8): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115044384 | |||||||
chr9:115044384 | GACACAC | G | 83 | a0001c0009t0001g0101 a0001c0009t0001g0123 a0001c0009t0001g0155 others(80): Show |
84 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.5125+2020_5125+202 others(10): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115044384 | |||||||
chr9:115044429 | G | A | 2 | a0002c0001t0002g0094 a0002c0001t0002g0159 |
2 | HG02109.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.5125+1981C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115044429 | |||||||
chr9:115044503 | G | A | 4 | a0005c0034t0002g0197 a0005c0034t0002g0198 a0005c0067t0002g0359 others(1): Show |
4 | HG01109.hp2 HG01243.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.5125+1907C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115044503 | |||||||
chr9:115044527 | T | G | 1 | a0021c0028t0012g0258 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.5125+1883A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115044527 | |||||||
chr9:115044608 | A | C | 2 | a0002c0001t0002g0092 a0002c0001t0002g0110 |
2 | HG01169.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.5125+1802T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115044608 | |||||||
chr9:115044707 | G | A | 5 | a0005c0103t0012g0091 a0021c0028t0012g0258 a0021c0028t0012g0259 others(2): Show |
5 | HG01496.hp1 HG02818.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.5125+1703C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115044707 | |||||||
chr9:115044781 | C | T | 1 | a0002c0001t0002g0181 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.5125+1629G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115044781 | |||||||
chr9:115044785 | G | A | 2 | a0004c0050t0014g0345 a0005c0062t0026g0250 |
2 | HG01192.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.5125+1625C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115044785 | |||||||
chr9:115045229 | C | T | 22 | a0003c0027t0002g0214 a0003c0027t0002g0215 a0003c0027t0002g0218 others(19): Show |
22 | HG00642.hp2 HG00741.hp2 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.5125+1181G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115045229 | |||||||
chr9:115045325 | T | C | 1 | a0038c0079t0023g0193 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.5125+1085A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115045325 | |||||||
chr9:115045429 | C | T | 27 | a0006c0007t0005g0200 a0006c0007t0005g0204 a0006c0007t0005g0221 others(24): Show |
28 | HG00621.hp2 HG01074.hp1 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.5125+981G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115045429 | |||||||
chr9:115045541 | A | AT | 71 | a0001c0002t0001g0268 a0001c0009t0001g0101 a0001c0009t0015g0124 others(68): Show |
72 | HG00621.hp2 HG00642.hp2 HG00741.hp1 others(69): Show |
intron_variant | MODIFIER | c.5125+868dupA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115045541 | |||||||
chr9:115045541 | A | ATT | 24 | a0005c0014t0001g0005 a0005c0014t0001g0289 a0005c0014t0001g0299 others(21): Show |
25 | HG00597.hp2 HG00609.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.5125+867_5125+868d others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115045541 | |||||||
chr9:115045541 | AT | A | 11 | a0001c0002t0001g0277 a0001c0002t0010g0330 a0001c0009t0001g0123 others(8): Show |
11 | HG01070.hp2 HG01255.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.5125+868delA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115045541 | |||||||
chr9:115045801 | G | A | 21 | a0003c0027t0002g0214 a0003c0027t0002g0215 a0003c0027t0002g0218 others(18): Show |
21 | HG00642.hp2 HG00741.hp2 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.5125+609C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115045801 | |||||||
chr9:115045841 | G | C | 77 | a0001c0009t0001g0101 a0001c0009t0001g0123 a0001c0009t0001g0155 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.5125+569C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115045841 | |||||||
chr9:115045848 | C | T | 4 | a0002c0001t0002g0170 a0002c0001t0002g0174 a0002c0001t0002g0176 others(1): Show |
4 | HG00733.hp2 HG01123.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.5125+562G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115045848 | |||||||
chr9:115046051 | A | G | 3 | a0006c0007t0005g0357 a0025c0038t0005g0353 a0025c0038t0005g0354 |
3 | HG02572.hp2 HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.5125+359T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115046051 | |||||||
chr9:115046070 | G | GT | 8 | a0004c0018t0004g0305 a0004c0018t0004g0334 a0004c0075t0004g0266 others(5): Show |
8 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(5): Show |
intron_variant | MODIFIER | c.5125+339dupA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115046070 | |||||||
chr9:115046071 | TA | T | 20 | a0002c0020t0001g0145 a0004c0004t0001g0269 a0007c0006t0007g0006 others(17): Show |
20 | HG00642.hp2 HG00741.hp2 HG01256.hp2 others(17): Show |
intron_variant | MODIFIER | c.5125+338delT | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115046071 | |||||||
chr9:115046168 | G | A | 1 | a0017c0095t0025g0179 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.5125+242C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115046168 | |||||||
chr9:115046184 | G | A | 25 | a0005c0014t0001g0005 a0005c0014t0001g0289 a0005c0014t0001g0299 others(22): Show |
26 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.5125+226C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115046184 | |||||||
chr9:115046209 | C | T | 29 | a0006c0007t0005g0200 a0006c0007t0005g0204 a0006c0007t0005g0221 others(26): Show |
30 | HG00621.hp2 HG01074.hp1 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.5125+201G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115046209 | |||||||
chr9:115047211 | G | T | 1 | a0002c0001t0002g0181 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.4853-529C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 16/27 | chr9 | 115047211 | |||||||
chr9:115047240 | C | CT | 86 | a0001c0002t0001g0128 a0001c0002t0001g0141 a0001c0002t0001g0142 others(83): Show |
87 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.4853-559dupA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 16/27 | chr9 | 115047240 | |||||||
chr9:115047240 | C | CTT | 88 | a0001c0002t0001g0134 a0001c0002t0001g0138 a0001c0002t0001g0192 others(85): Show |
89 | HG00597.hp1 HG00621.hp1 HG01081.hp1 others(86): Show |
intron_variant | MODIFIER | c.4853-560_4853-559d others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 16/27 | chr9 | 115047240 | |||||||
chr9:115047240 | C | CTTT | 7 | a0001c0009t0001g0175 a0003c0003t0001g0207 a0003c0003t0001g0208 others(4): Show |
7 | HG01261.hp2 HG03471.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.4853-561_4853-559d others(5): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 16/27 | chr9 | 115047240 | |||||||
chr9:115047361 | T | C | 1 | a0001c0002t0001g0327 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.4853-679A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 16/27 | chr9 | 115047361 | |||||||
chr9:115047362 | G | T | 1 | a0049c0097t0002g0183 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.4853-680C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 16/27 | chr9 | 115047362 | |||||||
chr9:115047403 | T | C | 5 | a0009c0100t0005g0317 a0016c0022t0004g0130 a0016c0022t0004g0131 others(2): Show |
5 | HG02647.hp1 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.4853-721A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 16/27 | chr9 | 115047403 | |||||||
chr9:115047631 | T | C | 1 | a0002c0001t0002g0186 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.4852+629A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 16/27 | chr9 | 115047631 | |||||||
chr9:115047692 | G | A | 1 | a0007c0041t0007g0029 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.4852+568C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 16/27 | chr9 | 115047692 | |||||||
chr9:115047757 | C | T | 56 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(53): Show |
56 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.4852+503G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 16/27 | chr9 | 115047757 | |||||||
chr9:115047838 | T | A | 26 | a0002c0093t0004g0122 a0004c0018t0004g0213 a0004c0018t0004g0224 others(23): Show |
26 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(23): Show |
intron_variant | MODIFIER | c.4852+422A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 16/27 | chr9 | 115047838 | |||||||
chr9:115047879 | A | G | 217 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(214): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.4852+381T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 16/27 | chr9 | 115047879 | |||||||
chr9:115047962 | A | T | 12 | a0005c0017t0001g0081 a0005c0017t0002g0076 a0005c0017t0002g0078 others(9): Show |
13 | HG01081.hp2 HG01099.hp2 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.4852+298T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 16/27 | chr9 | 115047962 | |||||||
chr9:115047971 | G | T | 52 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(49): Show |
52 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.4852+289C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 16/27 | chr9 | 115047971 | |||||||
chr9:115048016 | G | A | 12 | a0002c0093t0004g0122 a0004c0018t0004g0213 a0004c0018t0004g0224 others(9): Show |
12 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(9): Show |
intron_variant | MODIFIER | c.4852+244C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 16/27 | chr9 | 115048016 | |||||||
chr9:115048208 | A | T | 1 | a0002c0001t0002g0181 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.4852+52T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 16/27 | chr9 | 115048208 | |||||||
chr9:115048612 | A | G | 2 | a0009c0042t0008g0112 a0009c0042t0008g0113 |
2 | HG02015.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.4580-80T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115048612 | |||||||
chr9:115048681 | T | G | 3 | a0002c0001t0002g0098 a0004c0004t0002g0297 a0004c0004t0002g0300 |
3 | HG01978.hp1 HG02273.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.4580-149A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115048681 | |||||||
chr9:115048730 | G | A | 3 | a0001c0009t0015g0124 a0001c0009t0015g0350 a0001c0024t0015g0320 |
3 | HG02647.hp2 HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.4580-198C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115048730 | |||||||
chr9:115048879 | G | C | 4 | a0003c0003t0004g0337 a0024c0082t0004g0055 a0027c0070t0002g0352 others(1): Show |
4 | HG02280.hp2 HG02486.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.4580-347C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115048879 | |||||||
chr9:115048906 | G | A | 5 | a0004c0004t0001g0269 a0005c0034t0002g0197 a0005c0034t0002g0198 others(2): Show |
5 | HG01109.hp2 HG01243.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.4580-374C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115048906 | |||||||
chr9:115048926 | T | C | 12 | a0002c0093t0004g0122 a0004c0018t0004g0213 a0004c0018t0004g0224 others(9): Show |
12 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(9): Show |
intron_variant | MODIFIER | c.4580-394A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115048926 | |||||||
chr9:115048987 | C | T | 1 | a0006c0007t0027g0294 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.4580-455G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115048987 | |||||||
chr9:115049036 | G | C | 272 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(269): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.4580-504C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115049036 | |||||||
chr9:115049072 | G | GT | 221 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(218): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.4580-541dupA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115049072 | |||||||
chr9:115049429 | C | T | 1 | a0002c0001t0002g0173 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.4580-897G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115049429 | |||||||
chr9:115049499 | C | T | 4 | a0016c0022t0004g0130 a0016c0022t0004g0131 a0016c0022t0004g0252 others(1): Show |
4 | HG02647.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.4580-967G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115049499 | |||||||
chr9:115049517 | T | C | 223 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(220): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.4580-985A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115049517 | |||||||
chr9:115049592 | G | C | 1 | a0003c0003t0001g0336 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.4580-1060C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115049592 | |||||||
chr9:115049656 | T | A | 4 | a0002c0001t0002g0157 a0002c0001t0002g0171 a0002c0001t0002g0190 others(1): Show |
4 | HG02040.hp2 HG02155.hp2 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.4580-1124A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115049656 | |||||||
chr9:115049677 | AT | A | 216 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(213): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.4580-1146delA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115049677 | |||||||
chr9:115049743 | C | T | 1 | a0034c0054t0005g0237 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.4580-1211G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115049743 | |||||||
chr9:115049790 | G | C | 1 | a0003c0003t0001g0216 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.4580-1258C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115049790 | |||||||
chr9:115049833 | A | T | 22 | a0001c0002t0001g0128 a0001c0002t0001g0267 a0001c0002t0001g0268 others(19): Show |
22 | HG00140.hp1 HG00280.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.4580-1301T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115049833 | |||||||
chr9:115049888 | T | C | 2 | a0004c0050t0014g0345 a0005c0062t0026g0250 |
2 | HG01192.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.4580-1356A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115049888 | |||||||
chr9:115049965 | G | A | 1 | a0005c0023t0001g0292 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.4580-1433C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115049965 | |||||||
chr9:115050021 | A | G | 2 | a0009c0042t0008g0112 a0009c0042t0008g0113 |
2 | HG02015.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.4580-1489T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115050021 | |||||||
chr9:115050066 | A | G | 217 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(214): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.4580-1534T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115050066 | |||||||
chr9:115050121 | A | G | 241 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(238): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.4580-1589T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115050121 | |||||||
chr9:115050252 | T | C | 27 | a0003c0035t0004g0150 a0003c0035t0004g0151 a0003c0077t0004g0356 others(24): Show |
28 | HG01081.hp2 HG01099.hp2 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.4580-1720A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115050252 | |||||||
chr9:115050278 | A | G | 4 | a0021c0028t0012g0258 a0021c0028t0012g0259 a0021c0028t0012g0260 others(1): Show |
4 | HG01496.hp1 HG02818.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.4580-1746T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115050278 | |||||||
chr9:115050347 | G | A | 6 | a0005c0037t0004g0152 a0005c0037t0004g0271 a0015c0021t0004g0129 others(3): Show |
6 | HG01891.hp1 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.4580-1815C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115050347 | |||||||
chr9:115050462 | C | T | 4 | a0016c0022t0004g0130 a0016c0022t0004g0131 a0016c0022t0004g0252 others(1): Show |
4 | HG02647.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.4580-1930G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115050462 | |||||||
chr9:115050498 | T | C | 31 | a0006c0007t0005g0200 a0006c0007t0005g0204 a0006c0007t0005g0221 others(28): Show |
32 | HG00621.hp2 HG01074.hp1 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.4580-1966A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115050498 | |||||||
chr9:115050512 | A | G | 12 | a0002c0093t0004g0122 a0004c0018t0004g0213 a0004c0018t0004g0224 others(9): Show |
12 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(9): Show |
intron_variant | MODIFIER | c.4580-1980T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115050512 | |||||||
chr9:115050612 | C | A | 27 | a0003c0035t0004g0150 a0003c0035t0004g0151 a0003c0077t0004g0356 others(24): Show |
28 | HG01081.hp2 HG01099.hp2 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.4580-2080G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115050612 | |||||||
chr9:115050903 | AC | A | 4 | a0011c0010t0001g0064 a0011c0010t0001g0227 a0011c0010t0001g0228 others(1): Show |
4 | HG02258.hp1 HG02615.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.4580-2372delG | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115050903 | |||||||
chr9:115051056 | G | A | 213 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(210): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.4580-2524C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115051056 | |||||||
chr9:115051085 | G | A | 52 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(49): Show |
52 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.4580-2553C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115051085 | |||||||
chr9:115051148 | G | A | 1 | a0009c0019t0002g0178 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.4580-2616C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115051148 | |||||||
chr9:115051176 | C | T | 213 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(210): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.4580-2644G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115051176 | |||||||
chr9:115051312 | G | T | 213 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(210): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.4580-2780C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115051312 | |||||||
chr9:115051404 | G | A | 1 | a0004c0004t0002g0325 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4580-2872C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115051404 | |||||||
chr9:115051511 | G | T | 1 | a0002c0093t0004g0122 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4580-2979C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115051511 | |||||||
chr9:115051537 | CT | C | 214 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(211): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.4580-3006delA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115051537 | |||||||
chr9:115051588 | A | G | 213 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(210): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.4580-3056T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115051588 | |||||||
chr9:115051641 | G | A | 25 | a0005c0014t0001g0005 a0005c0014t0001g0289 a0005c0014t0001g0299 others(22): Show |
26 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.4580-3109C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115051641 | |||||||
chr9:115051648 | G | A | 1 | a0031c0053t0018g0245 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.4580-3116C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115051648 | |||||||
chr9:115051695 | T | G | 214 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(211): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.4580-3163A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115051695 | |||||||
chr9:115051711 | C | T | 213 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(210): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.4580-3179G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115051711 | |||||||
chr9:115051822 | G | T | 3 | a0022c0033t0001g0126 a0022c0033t0001g0127 a0022c0033t0001g0338 |
3 | HG01884.hp2 HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.4580-3290C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115051822 | |||||||
chr9:115051874 | T | C | 5 | a0005c0103t0012g0091 a0021c0028t0012g0258 a0021c0028t0012g0259 others(2): Show |
5 | HG01496.hp1 HG02818.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.4580-3342A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115051874 | |||||||
chr9:115052023 | T | TATAG | 241 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(238): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.4580-3495_4580-349 others(8): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115052023 | |||||||
chr9:115052079 | C | CATATATA others(19): Show |
1 | a0004c0050t0014g0345 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4580-3548_4580-354 others(30): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115052079 | |||||||
chr9:115052079 | CAT | C | 53 | a0005c0017t0001g0081 a0005c0017t0002g0076 a0005c0017t0002g0078 others(50): Show |
55 | HG00621.hp2 HG01074.hp1 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.4580-3549_4580-354 others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115052079 | |||||||
chr9:115052154 | T | G | 1 | a0002c0001t0002g0191 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.4580-3622A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115052154 | |||||||
chr9:115052475 | C | CAATA | 44 | a0001c0002t0001g0267 a0001c0002t0001g0327 a0001c0009t0001g0244 others(41): Show |
44 | HG00642.hp1 HG00738.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.4580-3947_4580-394 others(8): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115052475 | |||||||
chr9:115052475 | C | CAATAAAT others(1): Show |
29 | a0003c0003t0004g0337 a0004c0018t0004g0305 a0005c0023t0001g0291 others(26): Show |
29 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(26): Show |
intron_variant | MODIFIER | c.4580-3951_4580-394 others(12): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115052475 | |||||||
chr9:115052475 | CAATA | C | 5 | a0001c0002t0001g0128 a0001c0002t0001g0192 a0001c0002t0001g0321 others(2): Show |
5 | HG00323.hp1 HG02970.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.4580-3947_4580-394 others(8): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115052475 | |||||||
chr9:115052475 | CAATAAAT others(1): Show |
C | 57 | a0003c0035t0004g0150 a0003c0035t0004g0151 a0003c0077t0004g0356 others(54): Show |
59 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.4580-3951_4580-394 others(12): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115052475 | |||||||
chr9:115052732 | T | C | 25 | a0005c0014t0001g0005 a0005c0014t0001g0289 a0005c0014t0001g0299 others(22): Show |
26 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.4580-4200A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115052732 | |||||||
chr9:115052757 | G | A | 24 | a0005c0017t0001g0081 a0005c0017t0002g0076 a0005c0017t0002g0078 others(21): Show |
25 | HG01081.hp2 HG01099.hp2 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.4580-4225C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115052757 | |||||||
chr9:115052807 | G | T | 1 | a0005c0062t0026g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.4580-4275C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115052807 | |||||||
chr9:115052945 | G | C | 1 | a0001c0002t0001g0301 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.4579+4208C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115052945 | |||||||
chr9:115052994 | G | A | 77 | a0001c0009t0001g0101 a0001c0009t0001g0123 a0001c0009t0001g0155 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.4579+4159C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115052994 | |||||||
chr9:115053027 | A | G | 3 | a0004c0051t0004g0342 a0037c0064t0014g0343 a0047c0060t0014g0253 |
3 | HG02257.hp1 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.4579+4126T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115053027 | |||||||
chr9:115053143 | G | A | 1 | a0004c0004t0002g0325 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4579+4010C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115053143 | |||||||
chr9:115053147 | G | A | 2 | a0002c0001t0002g0103 a0002c0001t0006g0120 |
2 | HG01169.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.4579+4006C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115053147 | |||||||
chr9:115053234 | T | C | 52 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(49): Show |
52 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.4579+3919A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115053234 | |||||||
chr9:115053268 | C | T | 1 | a0020c0025t0001g0349 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.4579+3885G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115053268 | |||||||
chr9:115053334 | C | T | 272 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(269): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.4579+3819G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115053334 | |||||||
chr9:115053807 | C | A | 213 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(210): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.4579+3346G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115053807 | |||||||
chr9:115053881 | A | C | 27 | a0003c0035t0004g0150 a0003c0035t0004g0151 a0003c0077t0004g0356 others(24): Show |
28 | HG01081.hp2 HG01099.hp2 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.4579+3272T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115053881 | |||||||
chr9:115053937 | T | C | 3 | a0012c0012t0006g0060 a0014c0016t0006g0072 a0014c0016t0006g0073 |
3 | HG01346.hp1 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.4579+3216A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115053937 | |||||||
chr9:115053951 | C | T | 2 | a0002c0001t0002g0169 a0002c0001t0002g0185 |
2 | HG00642.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.4579+3202G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115053951 | |||||||
chr9:115054003 | T | C | 25 | a0005c0014t0001g0005 a0005c0014t0001g0289 a0005c0014t0001g0299 others(22): Show |
26 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.4579+3150A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115054003 | |||||||
chr9:115054009 | T | C | 1 | a0021c0028t0012g0260 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4579+3144A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115054009 | |||||||
chr9:115054091 | G | A | 52 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(49): Show |
52 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.4579+3062C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115054091 | |||||||
chr9:115054092 | C | A | 52 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(49): Show |
52 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.4579+3061G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115054092 | |||||||
chr9:115054148 | C | T | 1 | a0005c0037t0004g0152 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4579+3005G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115054148 | |||||||
chr9:115054257 | C | T | 1 | a0026c0046t0004g0339 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4579+2896G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115054257 | |||||||
chr9:115054328 | G | A | 1 | a0028c0036t0002g0203 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4579+2825C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115054328 | |||||||
chr9:115054385 | T | C | 1 | a0004c0045t0002g0230 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.4579+2768A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115054385 | |||||||
chr9:115054595 | C | T | 1 | a0022c0033t0001g0338 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.4579+2558G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115054595 | |||||||
chr9:115054745 | C | G | 1 | a0004c0074t0002g0286 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.4579+2408G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115054745 | |||||||
chr9:115054776 | A | C | 4 | a0002c0093t0004g0122 a0004c0018t0004g0213 a0004c0018t0004g0224 others(1): Show |
4 | HG02145.hp2 HG02622.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.4579+2377T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115054776 | |||||||
chr9:115054882 | T | G | 1 | a0001c0011t0001g0114 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.4579+2271A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115054882 | |||||||
chr9:115054904 | A | G | 1 | a0004c0075t0004g0266 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.4579+2249T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115054904 | |||||||
chr9:115054995 | T | G | 1 | a0005c0062t0026g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.4579+2158A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115054995 | |||||||
chr9:115055017 | T | C | 4 | a0005c0034t0002g0197 a0005c0034t0002g0198 a0005c0067t0002g0359 others(1): Show |
4 | HG01109.hp2 HG01243.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.4579+2136A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115055017 | |||||||
chr9:115055038 | A | G | 24 | a0005c0017t0001g0081 a0005c0017t0002g0076 a0005c0017t0002g0078 others(21): Show |
25 | HG01081.hp2 HG01099.hp2 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.4579+2115T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115055038 | |||||||
chr9:115055047 | A | G | 268 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(265): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.4579+2106T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115055047 | |||||||
chr9:115055072 | T | G | 52 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(49): Show |
52 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.4579+2081A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115055072 | |||||||
chr9:115055075 | C | T | 24 | a0005c0017t0001g0081 a0005c0017t0002g0076 a0005c0017t0002g0078 others(21): Show |
25 | HG01081.hp2 HG01099.hp2 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.4579+2078G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115055075 | |||||||
chr9:115055126 | T | G | 52 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(49): Show |
52 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.4579+2027A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115055126 | |||||||
chr9:115055317 | G | C | 14 | a0002c0001t0002g0092 a0002c0001t0002g0098 a0002c0001t0002g0108 others(11): Show |
14 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(11): Show |
intron_variant | MODIFIER | c.4579+1836C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115055317 | |||||||
chr9:115055404 | G | A | 87 | a0001c0009t0001g0101 a0001c0009t0001g0123 a0001c0009t0001g0155 others(84): Show |
87 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.4579+1749C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115055404 | |||||||
chr9:115055428 | A | C | 1 | a0002c0001t0002g0159 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4579+1725T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115055428 | |||||||
chr9:115055429 | T | C | 1 | a0002c0001t0002g0159 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4579+1724A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115055429 | |||||||
chr9:115055497 | G | A | 16 | a0005c0017t0001g0081 a0005c0017t0002g0076 a0005c0017t0002g0078 others(13): Show |
17 | HG01081.hp2 HG01099.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.4579+1656C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115055497 | |||||||
chr9:115055522 | C | CA | 165 | a0001c0009t0001g0101 a0001c0009t0001g0123 a0001c0009t0001g0155 others(162): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.4579+1630dupT | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115055522 | |||||||
chr9:115055843 | T | G | 52 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(49): Show |
52 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.4579+1310A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115055843 | |||||||
chr9:115055900 | T | G | 219 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(216): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.4579+1253A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115055900 | |||||||
chr9:115056203 | A | AT | 55 | a0001c0002t0010g0288 a0003c0027t0002g0214 a0003c0027t0002g0215 others(52): Show |
56 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.4579+949dupA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115056203 | |||||||
chr9:115056203 | AT | A | 16 | a0005c0017t0001g0081 a0005c0017t0002g0076 a0005c0017t0002g0078 others(13): Show |
17 | HG01081.hp2 HG01099.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.4579+949delA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115056203 | |||||||
chr9:115056264 | C | A | 1 | a0005c0103t0012g0091 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4579+889G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115056264 | |||||||
chr9:115056289 | C | T | 1 | a0013c0029t0003g0010 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.4579+864G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115056289 | |||||||
chr9:115056539 | C | A | 1 | a0002c0098t0002g0147 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.4579+614G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115056539 | |||||||
chr9:115056557 | C | T | 1 | a0018c0026t0006g0075 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.4579+596G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115056557 | |||||||
chr9:115056584 | G | C | 1 | a0005c0062t0026g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.4579+569C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115056584 | |||||||
chr9:115056696 | C | T | 1 | a0002c0001t0002g0185 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.4579+457G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115056696 | |||||||
chr9:115056724 | A | C | 28 | a0006c0007t0005g0200 a0006c0007t0005g0204 a0006c0007t0005g0221 others(25): Show |
29 | HG00621.hp2 HG01074.hp1 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.4579+429T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115056724 | |||||||
chr9:115056738 | C | T | 3 | a0007c0006t0007g0001 a0007c0006t0007g0051 a0007c0006t0016g0050 |
4 | NA19000.hp1 NA19004.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.4579+415G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115056738 | |||||||
chr9:115057005 | A | T | 1 | a0021c0028t0012g0259 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.4579+148T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115057005 | |||||||
chr9:115057046 | T | C | 1 | a0001c0002t0001g0141 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.4579+107A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115057046 | |||||||
chr9:115057079 | G | A | 1 | a0007c0006t0007g0006 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.4579+74C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115057079 | |||||||
chr9:115057110 | A | T | 50 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(47): Show |
50 | HG00140.hp1 HG00280.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.4579+43T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115057110 | |||||||
chr9:115057150 | T | C | 1 | a0013c0040t0003g0040 | 1 | NA18961.hp1 | splice_region_variant&intron_variant | LOW | c.4579+3A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115057150 | |||||||
chr9:115057469 | GTTAA | G | 52 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(49): Show |
52 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.4307-48_4307-45del others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/27 | chr9 | 115057469 | |||||||
chr9:115057762 | G | T | 4 | a0016c0022t0004g0130 a0016c0022t0004g0131 a0016c0022t0004g0252 others(1): Show |
4 | HG02647.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.4307-337C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/27 | chr9 | 115057762 | |||||||
chr9:115057926 | C | A | 2 | a0001c0002t0001g0134 a0001c0011t0001g0095 |
2 | HG02071.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.4307-501G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/27 | chr9 | 115057926 | |||||||
chr9:115057946 | C | T | 7 | a0001c0009t0015g0124 a0001c0009t0015g0350 a0001c0024t0015g0320 others(4): Show |
7 | HG02280.hp2 HG02486.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.4307-521G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/27 | chr9 | 115057946 | |||||||
chr9:115058241 | G | A | 4 | a0015c0021t0004g0129 a0015c0021t0004g0254 a0015c0021t0004g0255 others(1): Show |
4 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.4307-816C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/27 | chr9 | 115058241 | |||||||
chr9:115058270 | G | C | 27 | a0003c0035t0004g0150 a0003c0035t0004g0151 a0003c0077t0004g0356 others(24): Show |
28 | HG01081.hp2 HG01099.hp2 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.4307-845C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/27 | chr9 | 115058270 | |||||||
chr9:115058303 | T | C | 1 | a0025c0038t0005g0354 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4307-878A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/27 | chr9 | 115058303 | |||||||
chr9:115058360 | T | C | 1 | a0003c0069t0005g0219 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4307-935A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/27 | chr9 | 115058360 | |||||||
chr9:115058363 | C | A | 15 | a0012c0012t0006g0057 a0012c0012t0006g0058 a0012c0012t0006g0059 others(12): Show |
15 | HG00642.hp2 HG00741.hp2 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.4307-938G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/27 | chr9 | 115058363 | |||||||
chr9:115058385 | C | A | 1 | a0001c0094t0008g0172 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.4307-960G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/27 | chr9 | 115058385 | |||||||
chr9:115058408 | A | G | 2 | a0043c0047t0001g0358 a0046c0058t0001g0248 |
2 | HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.4307-983T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/27 | chr9 | 115058408 | |||||||
chr9:115058551 | A | C | 2 | a0009c0100t0005g0317 a0038c0079t0023g0193 |
2 | HG02257.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.4307-1126T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/27 | chr9 | 115058551 | |||||||
chr9:115058747 | A | G | 162 | a0001c0009t0001g0101 a0001c0009t0001g0123 a0001c0009t0001g0155 others(159): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.4306+983T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/27 | chr9 | 115058747 | |||||||
chr9:115058810 | T | A | 2 | a0043c0047t0001g0358 a0046c0058t0001g0248 |
2 | HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.4306+920A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/27 | chr9 | 115058810 | |||||||
chr9:115058864 | C | T | 4 | a0002c0001t0002g0157 a0002c0001t0002g0171 a0002c0001t0002g0190 others(1): Show |
4 | HG02040.hp2 HG02155.hp2 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.4306+866G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/27 | chr9 | 115058864 | |||||||
chr9:115059123 | CT | C | 77 | a0001c0009t0001g0101 a0001c0009t0001g0123 a0001c0009t0001g0155 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.4306+606delA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/27 | chr9 | 115059123 | |||||||
chr9:115059163 | G | A | 4 | a0003c0003t0004g0337 a0024c0082t0004g0055 a0027c0070t0002g0352 others(1): Show |
4 | HG02280.hp2 HG02486.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.4306+567C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/27 | chr9 | 115059163 | |||||||
chr9:115059339 | A | C | 162 | a0001c0009t0001g0101 a0001c0009t0001g0123 a0001c0009t0001g0155 others(159): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.4306+391T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/27 | chr9 | 115059339 | |||||||
chr9:115059380 | G | T | 1 | a0003c0003t0004g0337 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4306+350C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/27 | chr9 | 115059380 | |||||||
chr9:115059467 | A | C | 40 | a0001c0009t0001g0101 a0001c0009t0001g0123 a0001c0009t0001g0155 others(37): Show |
40 | HG01081.hp1 HG01175.hp1 HG01261.hp2 others(37): Show |
intron_variant | MODIFIER | c.4306+263T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/27 | chr9 | 115059467 | |||||||
chr9:115059611 | G | A | 7 | a0003c0027t0002g0214 a0003c0027t0002g0215 a0003c0027t0002g0218 others(4): Show |
7 | HG02895.hp1 HG02897.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.4306+119C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/27 | chr9 | 115059611 | |||||||
chr9:115060073 | C | T | 2 | a0001c0011t0001g0114 a0031c0053t0018g0245 |
2 | HG00323.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.4034-71G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115060073 | |||||||
chr9:115060335 | A | G | 22 | a0003c0027t0002g0214 a0003c0027t0002g0215 a0003c0027t0002g0218 others(19): Show |
22 | HG00642.hp2 HG00741.hp2 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.4034-333T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115060335 | |||||||
chr9:115060522 | A | T | 3 | a0001c0009t0015g0124 a0001c0009t0015g0350 a0001c0024t0015g0320 |
3 | HG02647.hp2 HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.4034-520T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115060522 | |||||||
chr9:115060731 | T | C | 77 | a0001c0009t0001g0101 a0001c0009t0001g0123 a0001c0009t0001g0155 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.4034-729A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115060731 | |||||||
chr9:115060744 | G | A | 6 | a0011c0010t0001g0064 a0011c0010t0001g0227 a0011c0010t0001g0228 others(3): Show |
6 | HG02258.hp1 HG02615.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.4034-742C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115060744 | |||||||
chr9:115060835 | C | T | 160 | a0001c0009t0001g0101 a0001c0009t0001g0123 a0001c0009t0001g0155 others(157): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.4034-833G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115060835 | |||||||
chr9:115060902 | C | T | 16 | a0005c0017t0001g0081 a0005c0017t0002g0076 a0005c0017t0002g0078 others(13): Show |
17 | HG01081.hp2 HG01099.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.4034-900G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115060902 | |||||||
chr9:115061496 | A | G | 243 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(240): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.4033+1421T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115061496 | |||||||
chr9:115061622 | T | C | 84 | a0001c0009t0001g0101 a0001c0009t0001g0123 a0001c0009t0001g0155 others(81): Show |
84 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.4033+1295A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115061622 | |||||||
chr9:115061794 | T | C | 272 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(269): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.4033+1123A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115061794 | |||||||
chr9:115061830 | C | T | 2 | a0001c0011t0001g0114 a0031c0053t0018g0245 |
2 | HG00323.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.4033+1087G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115061830 | |||||||
chr9:115061939 | T | C | 4 | a0003c0003t0004g0337 a0024c0082t0004g0055 a0027c0070t0002g0352 others(1): Show |
4 | HG02280.hp2 HG02486.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.4033+978A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115061939 | |||||||
chr9:115062029 | G | T | 272 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(269): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.4033+888C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115062029 | |||||||
chr9:115062053 | G | A | 161 | a0001c0009t0001g0101 a0001c0009t0001g0123 a0001c0009t0001g0155 others(158): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.4033+864C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115062053 | |||||||
chr9:115062086 | T | C | 1 | a0033c0090t0001g0116 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.4033+831A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115062086 | |||||||
chr9:115062147 | G | A | 1 | a0025c0038t0005g0354 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4033+770C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115062147 | |||||||
chr9:115062196 | G | A | 25 | a0005c0014t0001g0005 a0005c0014t0001g0289 a0005c0014t0001g0299 others(22): Show |
26 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.4033+721C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115062196 | |||||||
chr9:115062367 | G | A | 1 | a0038c0079t0023g0193 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4033+550C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115062367 | |||||||
chr9:115062428 | G | A | 1 | a0008c0005t0001g0121 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4033+489C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115062428 | |||||||
chr9:115062449 | A | G | 1 | a0003c0052t0001g0234 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.4033+468T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115062449 | |||||||
chr9:115062479 | C | T | 1 | a0014c0016t0006g0074 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.4033+438G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115062479 | |||||||
chr9:115062567 | C | T | 25 | a0005c0014t0001g0005 a0005c0014t0001g0289 a0005c0014t0001g0299 others(22): Show |
26 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.4033+350G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115062567 | |||||||
chr9:115062608 | CA | C | 142 | a0001c0002t0008g0136 a0001c0009t0001g0123 a0001c0009t0001g0188 others(139): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.4033+308delT | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115062608 | |||||||
chr9:115062652 | T | C | 4 | a0005c0061t0002g0257 a0022c0033t0001g0126 a0022c0033t0001g0127 others(1): Show |
4 | HG01884.hp2 HG01891.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.4033+265A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115062652 | |||||||
chr9:115062661 | A | G | 25 | a0005c0014t0001g0005 a0005c0014t0001g0289 a0005c0014t0001g0299 others(22): Show |
26 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.4033+256T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115062661 | |||||||
chr9:115062701 | T | G | 1 | a0004c0018t0004g0213 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4033+216A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115062701 | |||||||
chr9:115062742 | T | A | 1 | a0004c0004t0002g0313 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.4033+175A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115062742 | |||||||
chr9:115062761 | G | A | 1 | a0005c0103t0012g0091 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4033+156C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115062761 | |||||||
chr9:115062806 | G | A | 16 | a0005c0017t0001g0081 a0005c0017t0002g0076 a0005c0017t0002g0078 others(13): Show |
17 | HG01081.hp2 HG01099.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.4033+111C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115062806 | |||||||
chr9:115063286 | T | C | 1 | a0042c0063t0012g0149 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3761-97A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 12/27 | chr9 | 115063286 | |||||||
chr9:115063310 | C | T | 1 | a0001c0009t0001g0188 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3761-121G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 12/27 | chr9 | 115063310 | |||||||
chr9:115063312 | T | A | 1 | a0003c0003t0001g0208 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.3761-123A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 12/27 | chr9 | 115063312 | |||||||
chr9:115063325 | G | A | 12 | a0002c0093t0004g0122 a0004c0018t0004g0213 a0004c0018t0004g0224 others(9): Show |
12 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(9): Show |
intron_variant | MODIFIER | c.3761-136C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 12/27 | chr9 | 115063325 | |||||||
chr9:115063646 | G | T | 1 | a0038c0079t0023g0193 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3760+150C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 12/27 | chr9 | 115063646 | |||||||
chr9:115063667 | C | T | 2 | a0005c0023t0001g0291 a0005c0023t0001g0292 |
2 | HG00099.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.3760+129G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 12/27 | chr9 | 115063667 | |||||||
chr9:115063723 | C | T | 1 | a0036c0104t0028g0341 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3760+73G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 12/27 | chr9 | 115063723 | |||||||
chr9:115063729 | A | G | 2 | a0009c0100t0005g0317 a0038c0079t0023g0193 |
2 | HG02257.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.3760+67T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 12/27 | chr9 | 115063729 | |||||||
chr9:115064514 | C | T | 1 | a0003c0003t0001g0240 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.3487+133G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 11/27 | chr9 | 115064514 | |||||||
chr9:115064515 | G | T | 4 | a0014c0016t0006g0069 a0014c0016t0006g0074 a0018c0026t0006g0070 others(1): Show |
4 | HG00642.hp2 HG00741.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.3487+132C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 11/27 | chr9 | 115064515 | |||||||
chr9:115064555 | C | T | 4 | a0005c0034t0002g0197 a0005c0034t0002g0198 a0005c0067t0002g0359 others(1): Show |
4 | HG01109.hp2 HG01243.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.3487+92G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 11/27 | chr9 | 115064555 | |||||||
chr9:115065166 | T | A | 2 | a0002c0001t0002g0169 a0002c0001t0002g0185 |
2 | HG00642.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.3215-247A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115065166 | |||||||
chr9:115065310 | C | T | 15 | a0008c0005t0001g0083 a0008c0005t0001g0085 a0008c0005t0001g0086 others(12): Show |
15 | HG00099.hp2 HG00140.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.3215-391G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115065310 | |||||||
chr9:115065373 | G | A | 51 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(48): Show |
51 | HG00140.hp1 HG00280.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.3215-454C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115065373 | |||||||
chr9:115065561 | T | C | 1 | a0004c0004t0001g0269 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.3215-642A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115065561 | |||||||
chr9:115065563 | A | G | 11 | a0005c0017t0001g0081 a0005c0017t0002g0076 a0005c0017t0002g0078 others(8): Show |
12 | HG01081.hp2 HG01099.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.3215-644T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115065563 | |||||||
chr9:115065700 | A | G | 1 | a0001c0009t0001g0244 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3215-781T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115065700 | |||||||
chr9:115065901 | C | CA | 43 | a0001c0024t0015g0320 a0001c0094t0008g0172 a0002c0001t0001g0165 others(40): Show |
43 | HG00423.hp1 HG00609.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.3215-983dupT | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115065901 | |||||||
chr9:115065901 | CA | C | 39 | a0001c0002t0001g0277 a0001c0009t0001g0155 a0001c0011t0001g0114 others(36): Show |
40 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.3215-983delT | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115065901 | |||||||
chr9:115066154 | T | A | 1 | a0019c0032t0001g0318 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3215-1235A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115066154 | |||||||
chr9:115066195 | C | T | 1 | a0002c0020t0002g0148 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3215-1276G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115066195 | |||||||
chr9:115066214 | G | A | 1 | a0027c0070t0002g0352 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3215-1295C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115066214 | |||||||
chr9:115066309 | C | A | 1 | a0005c0103t0012g0091 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3215-1390G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115066309 | |||||||
chr9:115066338 | G | A | 1 | a0004c0004t0002g0233 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3215-1419C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115066338 | |||||||
chr9:115066394 | T | A | 22 | a0002c0093t0004g0122 a0004c0018t0004g0213 a0004c0018t0004g0224 others(19): Show |
22 | HG00099.hp1 HG00323.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.3215-1475A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115066394 | |||||||
chr9:115066560 | T | A | 11 | a0005c0017t0001g0081 a0005c0017t0002g0076 a0005c0017t0002g0078 others(8): Show |
12 | HG01081.hp2 HG01099.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.3215-1641A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115066560 | |||||||
chr9:115066651 | T | A | 10 | a0002c0093t0004g0122 a0004c0018t0004g0213 a0004c0018t0004g0224 others(7): Show |
10 | HG00099.hp1 HG00323.hp2 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.3215-1732A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115066651 | |||||||
chr9:115066740 | T | C | 1 | a0013c0029t0003g0010 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.3215-1821A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115066740 | |||||||
chr9:115066778 | A | G | 1 | a0001c0002t0001g0301 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3215-1859T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115066778 | |||||||
chr9:115066910 | C | A | 1 | a0003c0003t0001g0208 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.3215-1991G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115066910 | |||||||
chr9:115067196 | G | A | 3 | a0004c0004t0002g0293 a0004c0045t0002g0230 a0004c0045t0002g0231 |
3 | HG01358.hp2 HG01928.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.3215-2277C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115067196 | |||||||
chr9:115067239 | T | G | 1 | a0001c0009t0001g0123 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3215-2320A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115067239 | |||||||
chr9:115067346 | TTTTG | T | 56 | a0003c0027t0002g0214 a0003c0027t0002g0215 a0003c0027t0002g0218 others(53): Show |
57 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(54): Show |
intron_variant | MODIFIER | c.3215-2431_3215-242 others(8): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115067346 | |||||||
chr9:115067435 | C | T | 6 | a0005c0037t0004g0152 a0005c0037t0004g0271 a0015c0021t0004g0129 others(3): Show |
6 | HG01891.hp1 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.3215-2516G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115067435 | |||||||
chr9:115067546 | G | T | 1 | a0012c0012t0006g0063 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3215-2627C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115067546 | |||||||
chr9:115067708 | C | A | 140 | a0001c0009t0001g0101 a0001c0009t0001g0123 a0001c0009t0001g0155 others(137): Show |
141 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.3215-2789G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115067708 | |||||||
chr9:115068509 | C | A | 6 | a0005c0037t0004g0152 a0005c0037t0004g0271 a0015c0021t0004g0129 others(3): Show |
6 | HG01891.hp1 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.3215-3590G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115068509 | |||||||
chr9:115068533 | G | A | 56 | a0003c0027t0002g0214 a0003c0027t0002g0215 a0003c0027t0002g0218 others(53): Show |
57 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(54): Show |
intron_variant | MODIFIER | c.3215-3614C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115068533 | |||||||
chr9:115068759 | A | T | 1 | a0016c0022t0004g0130 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3215-3840T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115068759 | |||||||
chr9:115068793 | T | A | 5 | a0005c0103t0012g0091 a0021c0028t0012g0258 a0021c0028t0012g0259 others(2): Show |
5 | HG01496.hp1 HG02818.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.3215-3874A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115068793 | |||||||
chr9:115068843 | C | T | 5 | a0009c0100t0005g0317 a0016c0022t0004g0130 a0016c0022t0004g0131 others(2): Show |
5 | HG02647.hp1 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.3215-3924G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115068843 | |||||||
chr9:115068914 | T | C | 30 | a0006c0007t0005g0200 a0006c0007t0005g0204 a0006c0007t0005g0221 others(27): Show |
31 | HG00621.hp2 HG01074.hp1 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.3215-3995A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115068914 | |||||||
chr9:115069041 | T | C | 1 | a0002c0001t0002g0181 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3215-4122A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069041 | |||||||
chr9:115069042 | A | G | 4 | a0005c0034t0002g0197 a0005c0034t0002g0198 a0005c0067t0002g0359 others(1): Show |
4 | HG01109.hp2 HG01243.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.3215-4123T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069042 | |||||||
chr9:115069161 | T | A | 1 | a0001c0002t0001g0268 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3215-4242A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069161 | |||||||
chr9:115069225 | G | A | 3 | a0003c0027t0002g0214 a0028c0036t0002g0202 a0028c0036t0002g0203 |
3 | HG02976.hp1 HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3215-4306C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069225 | |||||||
chr9:115069438 | A | G | 55 | a0003c0027t0002g0214 a0003c0027t0002g0215 a0003c0027t0002g0218 others(52): Show |
56 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.3214+4165T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069438 | |||||||
chr9:115069520 | C | A | 22 | a0003c0027t0002g0214 a0003c0027t0002g0215 a0003c0027t0002g0218 others(19): Show |
22 | HG00642.hp2 HG00741.hp2 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.3214+4083G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069520 | |||||||
chr9:115069558 | G | T | 4 | a0016c0022t0004g0130 a0016c0022t0004g0131 a0016c0022t0004g0252 others(1): Show |
4 | HG02647.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.3214+4045C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069558 | |||||||
chr9:115069572 | TTCCCTCC others(53): Show |
T | 1 | a0010c0008t0001g0077 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3214+3971_3214+403 others(64): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069572 | |||||||
chr9:115069597 | T | C | 1 | a0006c0007t0005g0200 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.3214+4006A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069597 | |||||||
chr9:115069602 | C | T | 54 | a0003c0027t0002g0214 a0003c0027t0002g0215 a0003c0027t0002g0218 others(51): Show |
55 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.3214+4001G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069602 | |||||||
chr9:115069602 | CCCTCCCT others(33): Show |
C | 1 | a0043c0047t0001g0358 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3214+3961_3214+400 others(44): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069602 | |||||||
chr9:115069606 | CCCTCCCT others(121): Show |
C | 1 | a0021c0028t0012g0259 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3214+3869_3214+399 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069606 | |||||||
chr9:115069607 | CCTCCCTC others(5): Show |
C | 59 | a0001c0002t0001g0128 a0001c0002t0001g0267 a0001c0002t0001g0268 others(56): Show |
59 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.3214+3984_3214+399 others(16): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069607 | |||||||
chr9:115069610 | C | T | 7 | a0008c0005t0001g0083 a0008c0005t0001g0115 a0008c0005t0001g0121 others(4): Show |
7 | HG00099.hp2 HG01070.hp1 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.3214+3993G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069610 | |||||||
chr9:115069611 | CCTCCCTC others(1): Show |
C | 14 | a0003c0003t0019g0360 a0005c0037t0004g0152 a0005c0037t0004g0271 others(11): Show |
14 | HG01081.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.3214+3984_3214+399 others(12): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069611 | |||||||
chr9:115069614 | CCCTCTCT others(105): Show |
C | 2 | a0021c0028t0012g0258 a0021c0028t0012g0260 |
2 | HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3214+3877_3214+398 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069614 | |||||||
chr9:115069615 | CCTCT | C | 36 | a0001c0009t0001g0155 a0001c0009t0001g0160 a0001c0009t0001g0188 others(33): Show |
36 | HG00099.hp1 HG00323.hp2 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.3214+3984_3214+398 others(8): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069615 | |||||||
chr9:115069618 | CTCTCCCT others(109): Show |
C | 1 | a0042c0063t0012g0149 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3214+3869_3214+398 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069618 | |||||||
chr9:115069619 | T | C | 117 | a0001c0002t0001g0134 a0001c0002t0001g0138 a0001c0002t0001g0141 others(114): Show |
119 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(116): Show |
intron_variant | MODIFIER | c.3214+3984A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069619 | |||||||
chr9:115069622 | C | T | 18 | a0008c0005t0001g0085 a0008c0005t0001g0086 a0008c0005t0001g0087 others(15): Show |
18 | HG00140.hp2 HG00280.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.3214+3981G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069622 | |||||||
chr9:115069626 | C | G | 1 | a0004c0004t0002g0325 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3214+3977G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069626 | |||||||
chr9:115069626 | C | T | 1 | a0013c0029t0003g0010 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.3214+3977G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069626 | |||||||
chr9:115069626 | CCCTCCCT others(93): Show |
C | 3 | a0003c0035t0004g0150 a0003c0035t0004g0151 a0003c0077t0004g0356 |
3 | HG02559.hp2 HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3214+3877_3214+397 others(104): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069626 | |||||||
chr9:115069630 | C | T | 48 | a0001c0002t0001g0138 a0001c0002t0001g0141 a0001c0002t0001g0142 others(45): Show |
48 | HG00099.hp2 HG00738.hp1 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.3214+3973G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069630 | |||||||
chr9:115069630 | CCCTCCCT others(85): Show |
C | 10 | a0005c0017t0001g0081 a0005c0017t0002g0076 a0005c0017t0002g0078 others(7): Show |
11 | HG01081.hp2 HG01099.hp2 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.3214+3881_3214+397 others(96): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069630 | |||||||
chr9:115069634 | C | T | 31 | a0001c0009t0001g0155 a0001c0009t0001g0160 a0001c0009t0001g0188 others(28): Show |
31 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.3214+3969G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069634 | |||||||
chr9:115069634 | CCCTCCCT others(85): Show |
C | 1 | a0004c0018t0004g0226 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3214+3877_3214+396 others(96): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069634 | |||||||
chr9:115069638 | C | T | 1 | a0008c0005t0001g0083 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3214+3965G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069638 | |||||||
chr9:115069638 | CCCTTCCT others(89): Show |
C | 1 | a0005c0017t0002g0079 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3214+3869_3214+396 others(100): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069638 | |||||||
chr9:115069642 | T | C | 99 | a0001c0002t0001g0134 a0001c0002t0001g0138 a0001c0002t0001g0141 others(96): Show |
99 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.3214+3961A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069642 | |||||||
chr9:115069642 | T | TCCTCCCT others(5): Show |
1 | a0002c0001t0002g0002 | 2 | NA19066.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.3214+3949_3214+396 others(16): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069642 | |||||||
chr9:115069642 | T | TCCTCCCT others(9): Show |
7 | a0002c0001t0002g0169 a0002c0001t0002g0185 a0004c0004t0002g0306 others(4): Show |
7 | HG00642.hp1 HG03704.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.3214+3945_3214+396 others(20): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069642 | |||||||
chr9:115069646 | C | T | 1 | a0045c0087t0003g0033 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3214+3957G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069646 | |||||||
chr9:115069647 | C | T | 1 | a0010c0008t0001g0077 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3214+3956G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069647 | |||||||
chr9:115069650 | C | T | 1 | a0036c0104t0028g0341 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3214+3953G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069650 | |||||||
chr9:115069654 | C | CCCTCCCT others(25): Show |
24 | a0002c0001t0002g0100 a0002c0001t0002g0157 a0002c0001t0002g0168 others(21): Show |
24 | HG00558.hp1 HG00733.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.3214+3948_3214+394 others(36): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069654 | |||||||
chr9:115069654 | C | CCCTCCCT others(21): Show |
4 | a0002c0001t0002g0154 a0002c0001t0007g0018 a0007c0006t0007g0035 others(1): Show |
4 | HG02602.hp1 HG02886.hp2 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.3214+3948_3214+394 others(32): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069654 | |||||||
chr9:115069654 | C | CCCTCCCT others(17): Show |
1 | a0002c0001t0001g0165 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.3214+3948_3214+394 others(28): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069654 | |||||||
chr9:115069654 | C | CCCTCCCT others(5): Show |
16 | a0002c0001t0002g0082 a0002c0001t0002g0094 a0002c0001t0002g0096 others(13): Show |
16 | HG00408.hp2 HG01358.hp2 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.3214+3948_3214+394 others(16): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069654 | |||||||
chr9:115069654 | C | T | 3 | a0001c0009t0015g0124 a0001c0009t0015g0350 a0001c0024t0015g0320 |
3 | HG02647.hp2 HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3214+3949G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069654 | |||||||
chr9:115069654 | CCCTCCCT others(65): Show |
C | 6 | a0001c0002t0008g0136 a0001c0002t0008g0139 a0001c0011t0008g0109 others(3): Show |
6 | HG01361.hp1 HG04184.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.3214+3877_3214+394 others(76): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069654 | |||||||
chr9:115069654 | CCCTCCCT others(73): Show |
C | 11 | a0001c0002t0001g0134 a0001c0011t0001g0114 a0002c0093t0004g0122 others(8): Show |
11 | HG00621.hp1 HG01891.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.3214+3869_3214+394 others(84): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069654 | |||||||
chr9:115069658 | C | T | 8 | a0001c0009t0015g0124 a0001c0009t0015g0350 a0001c0024t0015g0320 others(5): Show |
8 | HG02280.hp2 HG02486.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.3214+3945G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069658 | |||||||
chr9:115069658 | CCCTCCCT others(69): Show |
C | 10 | a0001c0002t0001g0138 a0001c0002t0001g0141 a0001c0002t0001g0142 others(7): Show |
10 | HG01070.hp2 HG01071.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.3214+3869_3214+394 others(80): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069658 | |||||||
chr9:115069662 | C | CCCTCCCT others(73): Show |
1 | a0009c0100t0005g0317 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3214+3940_3214+394 others(84): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069662 | |||||||
chr9:115069662 | C | T | 72 | a0002c0001t0002g0092 a0002c0001t0002g0098 a0002c0001t0002g0108 others(69): Show |
73 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.3214+3941G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069662 | |||||||
chr9:115069662 | CCCTCCCT others(1): Show |
C | 29 | a0001c0002t0001g0128 a0001c0002t0001g0267 a0001c0002t0001g0268 others(26): Show |
29 | HG00140.hp1 HG00280.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.3214+3933_3214+394 others(12): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069662 | |||||||
chr9:115069662 | CCCTCCCT others(57): Show |
C | 1 | a0036c0104t0028g0341 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3214+3877_3214+394 others(68): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069662 | |||||||
chr9:115069662 | CCCTCCCT others(65): Show |
C | 2 | a0022c0033t0001g0126 a0022c0033t0001g0127 |
2 | HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.3214+3869_3214+394 others(76): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069662 | |||||||
chr9:115069666 | C | T | 77 | a0001c0009t0001g0101 a0001c0009t0001g0175 a0001c0009t0001g0244 others(74): Show |
78 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(75): Show |
intron_variant | MODIFIER | c.3214+3937G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069666 | |||||||
chr9:115069666 | CCCTT | C | 19 | a0001c0002t0001g0303 a0001c0002t0008g0144 a0001c0011t0001g0095 others(16): Show |
19 | HG00140.hp2 HG00280.hp1 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.3214+3933_3214+393 others(8): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069666 | |||||||
chr9:115069666 | CCCTTCCT others(49): Show |
C | 1 | a0007c0041t0007g0029 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3214+3881_3214+393 others(60): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069666 | |||||||
chr9:115069666 | CCCTTCCT others(53): Show |
C | 22 | a0005c0014t0001g0005 a0005c0014t0001g0299 a0005c0014t0001g0308 others(19): Show |
23 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.3214+3877_3214+393 others(64): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069666 | |||||||
chr9:115069666 | CCCTTCCT others(61): Show |
C | 1 | a0022c0033t0001g0338 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3214+3869_3214+393 others(72): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069666 | |||||||
chr9:115069670 | T | C | 77 | a0001c0009t0001g0101 a0001c0009t0001g0123 a0001c0009t0001g0175 others(74): Show |
78 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.3214+3933A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069670 | |||||||
chr9:115069670 | TCCTC | T | 3 | a0003c0003t0001g0310 a0003c0055t0001g0238 a0013c0040t0003g0040 |
3 | NA18961.hp1 NA19007.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.3214+3929_3214+393 others(8): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069670 | |||||||
chr9:115069670 | TCCTCCCT others(25): Show |
T | 1 | a0005c0062t0026g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3214+3901_3214+393 others(36): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069670 | |||||||
chr9:115069670 | TCCTCCCT others(29): Show |
T | 1 | a0004c0050t0014g0345 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3214+3897_3214+393 others(40): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069670 | |||||||
chr9:115069670 | TCCTCCCT others(73): Show |
T | 1 | a0031c0053t0018g0245 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.3214+3853_3214+393 others(84): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069670 | |||||||
chr9:115069674 | C | T | 69 | a0003c0027t0002g0214 a0003c0027t0002g0215 a0003c0027t0002g0218 others(66): Show |
70 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.3214+3929G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069674 | |||||||
chr9:115069678 | C | T | 29 | a0002c0001t0002g0092 a0002c0001t0002g0098 a0002c0001t0002g0108 others(26): Show |
29 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.3214+3925G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069678 | |||||||
chr9:115069678 | CCCTCCCT others(49): Show |
C | 2 | a0005c0014t0001g0289 a0005c0034t0002g0198 |
2 | HG01109.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.3214+3869_3214+392 others(60): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069678 | |||||||
chr9:115069679 | C | CCTCCCTT others(1): Show |
3 | a0003c0003t0004g0337 a0027c0070t0002g0352 a0048c0057t0014g0346 |
3 | HG02280.hp2 HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3214+3923_3214+392 others(12): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069679 | |||||||
chr9:115069679 | C | CCTTG | 3 | a0001c0009t0015g0124 a0001c0009t0015g0350 a0001c0024t0015g0320 |
3 | HG02647.hp2 HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3214+3923_3214+392 others(8): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069679 | |||||||
chr9:115069682 | C | T | 24 | a0001c0002t0001g0303 a0001c0002t0008g0144 a0001c0094t0008g0172 others(21): Show |
24 | HG00099.hp2 HG01070.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.3214+3921G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069682 | |||||||
chr9:115069682 | CCCTCCCT others(45): Show |
C | 3 | a0005c0023t0001g0291 a0005c0023t0001g0292 a0005c0023t0018g0361 |
3 | HG00099.hp1 HG00323.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.3214+3869_3214+392 others(56): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069682 | |||||||
chr9:115069686 | C | T | 68 | a0001c0002t0001g0128 a0001c0002t0001g0267 a0001c0002t0001g0268 others(65): Show |
70 | HG00140.hp1 HG00280.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.3214+3917G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069686 | |||||||
chr9:115069686 | CCCTCCCT others(33): Show |
C | 1 | a0003c0003t0019g0360 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3214+3877_3214+391 others(44): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069686 | |||||||
chr9:115069686 | CCCTCCCT others(41): Show |
C | 2 | a0004c0051t0004g0342 a0005c0023t0001g0315 |
2 | HG04228.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3214+3869_3214+391 others(52): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069686 | |||||||
chr9:115069690 | C | T | 16 | a0001c0009t0001g0123 a0001c0009t0001g0244 a0002c0001t0002g0173 others(13): Show |
16 | HG01070.hp1 HG01175.hp2 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.3214+3913G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069690 | |||||||
chr9:115069690 | CCCTCCCT others(37): Show |
C | 4 | a0004c0075t0004g0266 a0037c0064t0014g0343 a0038c0079t0023g0193 others(1): Show |
4 | HG00738.hp1 HG02257.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.3214+3869_3214+391 others(48): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069690 | |||||||
chr9:115069694 | C | T | 70 | a0001c0009t0001g0101 a0001c0009t0001g0123 a0001c0009t0001g0175 others(67): Show |
70 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.3214+3909G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069694 | |||||||
chr9:115069694 | CCCTCCCT others(33): Show |
C | 2 | a0004c0018t0004g0334 a0006c0007t0005g0204 |
2 | HG02698.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.3214+3869_3214+390 others(44): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069694 | |||||||
chr9:115069695 | C | T | 50 | a0003c0027t0002g0214 a0003c0027t0002g0215 a0003c0027t0002g0218 others(47): Show |
51 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.3214+3908G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069695 | |||||||
chr9:115069698 | C | CCCTTCCT others(29): Show |
3 | a0007c0006t0007g0001 a0007c0006t0007g0051 a0007c0006t0016g0050 |
4 | NA19000.hp1 NA19004.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.3214+3904_3214+390 others(40): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069698 | |||||||
chr9:115069698 | C | T | 81 | a0001c0009t0001g0101 a0001c0009t0001g0123 a0001c0009t0001g0155 others(78): Show |
81 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.3214+3905G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069698 | |||||||
chr9:115069699 | C | T | 1 | a0045c0087t0003g0033 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3214+3904G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069699 | |||||||
chr9:115069702 | C | CCCTCCCT others(69): Show |
1 | a0002c0001t0002g0195 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3214+3900_3214+390 others(80): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069702 | |||||||
chr9:115069702 | C | CCCTCCCT others(9): Show |
2 | a0002c0001t0002g0190 a0049c0097t0002g0183 |
2 | HG03654.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.3214+3885_3214+390 others(20): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069702 | |||||||
chr9:115069702 | C | CCCTTCCT others(29): Show |
4 | a0002c0001t0002g0173 a0002c0001t0002g0176 a0002c0001t0002g0181 others(1): Show |
4 | HG01175.hp2 HG01192.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.3214+3900_3214+390 others(40): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069702 | |||||||
chr9:115069702 | C | T | 114 | a0001c0009t0001g0101 a0001c0009t0001g0155 a0001c0009t0001g0160 others(111): Show |
114 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.3214+3901G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069702 | |||||||
chr9:115069702 | CCCTCCCT others(25): Show |
C | 24 | a0006c0007t0005g0221 a0006c0007t0005g0222 a0006c0007t0005g0270 others(21): Show |
25 | HG00621.hp2 HG01074.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.3214+3869_3214+390 others(36): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069702 | |||||||
chr9:115069706 | C | T | 60 | a0001c0002t0008g0144 a0001c0009t0001g0155 a0001c0009t0001g0160 others(57): Show |
60 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.3214+3897G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069706 | |||||||
chr9:115069706 | CCCTTCCT others(21): Show |
C | 27 | a0003c0027t0002g0214 a0003c0027t0002g0215 a0003c0027t0002g0218 others(24): Show |
27 | HG00642.hp2 HG00741.hp2 HG01256.hp2 others(24): Show |
intron_variant | MODIFIER | c.3214+3869_3214+389 others(32): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069706 | |||||||
chr9:115069710 | T | C | 39 | a0001c0009t0001g0101 a0001c0009t0001g0123 a0001c0009t0001g0155 others(36): Show |
39 | HG01070.hp1 HG01175.hp1 HG01261.hp2 others(36): Show |
intron_variant | MODIFIER | c.3214+3893A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069710 | |||||||
chr9:115069710 | TCCTTCCT others(37): Show |
T | 3 | a0005c0034t0002g0197 a0005c0067t0002g0359 a0009c0092t0002g0093 |
3 | HG01243.hp2 HG02280.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3214+3849_3214+389 others(48): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069710 | |||||||
chr9:115069714 | T | C | 54 | a0001c0009t0001g0101 a0001c0009t0001g0123 a0001c0009t0001g0155 others(51): Show |
54 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.3214+3889A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069714 | |||||||
chr9:115069714 | T | TCCTC | 3 | a0002c0001t0001g0104 a0004c0004t0002g0210 a0004c0045t0002g0230 |
3 | HG01928.hp2 NA18965.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.3214+3888_3214+388 others(8): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069714 | |||||||
chr9:115069714 | T | TCCTTCCT others(1): Show |
10 | a0002c0001t0002g0002 a0002c0001t0002g0159 a0002c0001t0002g0169 others(7): Show |
11 | HG00642.hp1 HG02109.hp1 HG03017.hp2 others(8): Show |
intron_variant | MODIFIER | c.3214+3888_3214+388 others(12): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069714 | |||||||
chr9:115069714 | T | TCCTTCCT others(61): Show |
2 | a0016c0022t0004g0252 a0016c0022t0004g0261 |
2 | HG02647.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.3214+3888_3214+388 others(72): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069714 | |||||||
chr9:115069718 | T | C | 56 | a0001c0009t0001g0101 a0001c0009t0001g0123 a0001c0009t0001g0155 others(53): Show |
56 | HG00140.hp2 HG00280.hp1 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.3214+3885A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069718 | |||||||
chr9:115069718 | TCCTTCCT others(25): Show |
T | 2 | a0008c0005t0001g0115 a0011c0010t0001g0296 |
2 | HG00099.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.3214+3853_3214+388 others(36): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069718 | |||||||
chr9:115069718 | TCCTTCCT others(49): Show |
T | 2 | a0001c0002t0001g0303 a0004c0018t0004g0213 |
2 | HG01358.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3214+3829_3214+388 others(60): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069718 | |||||||
chr9:115069722 | T | C | 45 | a0001c0009t0001g0155 a0001c0009t0001g0160 a0001c0009t0001g0188 others(42): Show |
45 | HG00140.hp2 HG00280.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.3214+3881A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069722 | |||||||
chr9:115069722 | TCCTTCCT others(13): Show |
T | 1 | a0026c0046t0004g0340 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3214+3861_3214+388 others(24): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069722 | |||||||
chr9:115069722 | TCCTTCCT others(17): Show |
T | 1 | a0026c0046t0004g0339 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3214+3857_3214+388 others(28): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069722 | |||||||
chr9:115069722 | TCCTTCCT others(21): Show |
T | 7 | a0011c0010t0001g0064 a0011c0010t0001g0227 a0011c0010t0001g0228 others(4): Show |
7 | HG02258.hp1 HG02615.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.3214+3853_3214+388 others(32): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069722 | |||||||
chr9:115069722 | TCCTTCCT others(45): Show |
T | 27 | a0001c0002t0001g0267 a0001c0002t0001g0268 a0001c0002t0001g0275 others(24): Show |
27 | HG00140.hp1 HG00280.hp2 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.3214+3829_3214+388 others(56): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069722 | |||||||
chr9:115069726 | T | C | 39 | a0001c0009t0001g0160 a0001c0024t0003g0008 a0001c0024t0003g0009 others(36): Show |
40 | HG00140.hp2 HG00280.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.3214+3877A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069726 | |||||||
chr9:115069726 | TCCTCCCT others(13): Show |
T | 3 | a0008c0005t0001g0121 a0033c0090t0001g0116 a0035c0065t0005g0326 |
3 | HG01070.hp1 HG02109.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.3214+3857_3214+387 others(24): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069726 | |||||||
chr9:115069726 | TCCTCCCT others(17): Show |
T | 5 | a0011c0010t0001g0209 a0011c0076t0001g0206 a0020c0025t0001g0347 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.3214+3853_3214+387 others(28): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069726 | |||||||
chr9:115069726 | TCCTCCCT others(41): Show |
T | 6 | a0001c0002t0001g0128 a0001c0002t0001g0321 a0001c0002t0001g0322 others(3): Show |
6 | HG01099.hp1 HG02698.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.3214+3829_3214+387 others(52): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069726 | |||||||
chr9:115069730 | C | T | 74 | a0001c0009t0001g0101 a0001c0009t0001g0123 a0001c0009t0001g0155 others(71): Show |
76 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.3214+3873G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069730 | |||||||
chr9:115069734 | T | C | 27 | a0003c0055t0001g0238 a0004c0018t0004g0226 a0004c0050t0014g0345 others(24): Show |
29 | HG00140.hp2 HG00280.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.3214+3869A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069734 | |||||||
chr9:115069734 | T | TCCTC | 3 | a0002c0096t0002g0156 a0004c0004t0001g0269 a0007c0006t0007g0043 |
3 | HG03834.hp1 NA18944.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.3214+3865_3214+386 others(8): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069734 | |||||||
chr9:115069734 | TCCTCCCT others(1): Show |
T | 13 | a0001c0009t0001g0101 a0001c0009t0001g0123 a0001c0009t0001g0175 others(10): Show |
13 | HG01261.hp2 HG01981.hp1 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.3214+3861_3214+386 others(12): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069734 | |||||||
chr9:115069734 | TCCTCCCT others(33): Show |
T | 1 | a0005c0103t0012g0091 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3214+3829_3214+386 others(44): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069734 | |||||||
chr9:115069735 | C | T | 1 | a0006c0007t0005g0204 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3214+3868G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069735 | |||||||
chr9:115069738 | C | CCCTT | 24 | a0002c0001t0001g0104 a0002c0001t0002g0002 a0002c0001t0002g0092 others(21): Show |
25 | HG00558.hp2 HG00609.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.3214+3864_3214+386 others(8): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069738 | |||||||
chr9:115069738 | C | CCCTTCCT others(57): Show |
1 | a0016c0022t0004g0130 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3214+3864_3214+386 others(68): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069738 | |||||||
chr9:115069738 | C | T | 57 | a0001c0002t0001g0138 a0001c0002t0001g0141 a0001c0002t0001g0142 others(54): Show |
57 | HG00140.hp2 HG00280.hp1 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.3214+3865G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069738 | |||||||
chr9:115069739 | C | T | 1 | a0038c0079t0023g0193 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3214+3864G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069739 | |||||||
chr9:115069742 | C | T | 48 | a0001c0002t0001g0302 a0001c0002t0010g0330 a0001c0009t0001g0155 others(45): Show |
48 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.3214+3861G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069742 | |||||||
chr9:115069746 | C | CCCTCCCT others(57): Show |
1 | a0016c0022t0004g0131 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3214+3856_3214+385 others(68): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069746 | |||||||
chr9:115069746 | C | T | 40 | a0001c0009t0001g0101 a0001c0009t0010g0105 a0001c0011t0001g0114 others(37): Show |
40 | HG00140.hp2 HG00280.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.3214+3857G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069746 | |||||||
chr9:115069750 | C | CCCTTCCT others(21): Show |
6 | a0001c0009t0015g0124 a0001c0009t0015g0350 a0001c0024t0015g0320 others(3): Show |
6 | HG02280.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.3214+3852_3214+385 others(32): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069750 | |||||||
chr9:115069750 | C | T | 50 | a0004c0051t0004g0342 a0005c0014t0001g0005 a0005c0014t0001g0299 others(47): Show |
51 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.3214+3853G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069750 | |||||||
chr9:115069754 | C | T | 64 | a0003c0027t0002g0214 a0003c0027t0002g0215 a0003c0027t0002g0218 others(61): Show |
65 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.3214+3849G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069754 | |||||||
chr9:115069758 | C | T | 23 | a0001c0002t0008g0136 a0001c0002t0008g0139 a0001c0011t0008g0109 others(20): Show |
24 | HG01081.hp2 HG01099.hp2 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.3214+3845G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069758 | |||||||
chr9:115069762 | C | T | 46 | a0001c0002t0001g0138 a0001c0002t0001g0141 a0001c0002t0001g0142 others(43): Show |
46 | HG00621.hp1 HG01175.hp1 HG01261.hp2 others(43): Show |
intron_variant | MODIFIER | c.3214+3841G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069762 | |||||||
chr9:115069766 | C | T | 73 | a0001c0002t0001g0134 a0001c0002t0001g0138 a0001c0002t0001g0141 others(70): Show |
73 | HG00621.hp1 HG00738.hp1 HG01070.hp2 others(70): Show |
intron_variant | MODIFIER | c.3214+3837G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069766 | |||||||
chr9:115069770 | C | T | 115 | a0001c0002t0001g0134 a0001c0002t0001g0138 a0001c0002t0001g0141 others(112): Show |
115 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.3214+3833G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069770 | |||||||
chr9:115069774 | C | CCCTTCCT others(25): Show |
1 | a0048c0057t0014g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3214+3828_3214+382 others(36): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069774 | |||||||
chr9:115069774 | C | T | 164 | a0001c0002t0001g0134 a0001c0002t0001g0138 a0001c0002t0001g0141 others(161): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.3214+3829G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069774 | |||||||
chr9:115069778 | T | C | 3 | a0002c0001t0002g0002 a0005c0017t0002g0079 a0036c0104t0028g0341 |
4 | HG02145.hp1 HG03017.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.3214+3825A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069778 | |||||||
chr9:115069798 | T | C | 5 | a0023c0030t0009g0048 a0023c0030t0009g0049 a0026c0046t0004g0340 others(2): Show |
5 | HG02886.hp1 HG03098.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.3214+3805A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069798 | |||||||
chr9:115069802 | C | T | 3 | a0023c0030t0009g0048 a0023c0030t0009g0049 a0026c0046t0004g0340 |
3 | HG03471.hp2 NA18975.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.3214+3801G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069802 | |||||||
chr9:115069806 | T | C | 3 | a0023c0030t0009g0048 a0023c0030t0009g0049 a0026c0046t0004g0340 |
3 | HG03471.hp2 NA18975.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.3214+3797A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069806 | |||||||
chr9:115069884 | G | A | 1 | a0005c0014t0001g0289 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3214+3719C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069884 | |||||||
chr9:115069897 | T | C | 1 | a0014c0016t0006g0073 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3214+3706A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069897 | |||||||
chr9:115069943 | G | A | 1 | a0001c0094t0008g0172 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3214+3660C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069943 | |||||||
chr9:115070012 | C | T | 4 | a0002c0001t0002g0168 a0002c0020t0011g0132 a0004c0004t0002g0220 others(1): Show |
4 | NA18954.hp2 NA18961.hp2 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.3214+3591G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115070012 | |||||||
chr9:115070046 | G | A | 1 | a0045c0087t0003g0033 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3214+3557C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115070046 | |||||||
chr9:115070073 | C | T | 7 | a0001c0009t0015g0124 a0001c0009t0015g0350 a0001c0024t0015g0320 others(4): Show |
7 | HG02280.hp2 HG02486.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.3214+3530G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115070073 | |||||||
chr9:115070087 | A | G | 109 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(106): Show |
110 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.3214+3516T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115070087 | |||||||
chr9:115070137 | T | C | 109 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(106): Show |
110 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.3214+3466A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115070137 | |||||||
chr9:115070158 | A | G | 1 | a0005c0037t0004g0271 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3214+3445T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115070158 | |||||||
chr9:115070332 | C | A | 1 | a0036c0104t0028g0341 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3214+3271G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115070332 | |||||||
chr9:115070339 | G | C | 116 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(113): Show |
117 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.3214+3264C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115070339 | |||||||
chr9:115070384 | A | C | 269 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(266): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.3214+3219T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115070384 | |||||||
chr9:115070491 | G | A | 1 | a0007c0006t0017g0012 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.3214+3112C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115070491 | |||||||
chr9:115070522 | C | T | 4 | a0004c0004t0002g0325 a0020c0025t0001g0347 a0020c0025t0001g0348 others(1): Show |
4 | HG01243.hp1 HG02055.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.3214+3081G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115070522 | |||||||
chr9:115070553 | T | C | 1 | a0011c0010t0001g0296 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3214+3050A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115070553 | |||||||
chr9:115070696 | G | A | 37 | a0008c0005t0001g0083 a0008c0005t0001g0085 a0008c0005t0001g0086 others(34): Show |
37 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.3214+2907C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115070696 | |||||||
chr9:115070696 | G | T | 53 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(50): Show |
53 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.3214+2907C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115070696 | |||||||
chr9:115070824 | C | A | 2 | a0001c0002t0001g0302 a0001c0002t0010g0330 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.3214+2779G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115070824 | |||||||
chr9:115070827 | G | A | 269 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(266): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.3214+2776C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115070827 | |||||||
chr9:115070945 | G | A | 2 | a0001c0011t0001g0114 a0031c0053t0018g0245 |
2 | HG00323.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.3214+2658C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115070945 | |||||||
chr9:115070997 | C | T | 1 | a0003c0003t0019g0273 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.3214+2606G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115070997 | |||||||
chr9:115071212 | G | A | 116 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(113): Show |
117 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.3214+2391C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115071212 | |||||||
chr9:115071214 | G | A | 1 | a0009c0100t0005g0317 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3214+2389C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115071214 | |||||||
chr9:115071239 | A | G | 116 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(113): Show |
117 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.3214+2364T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115071239 | |||||||
chr9:115071266 | T | C | 1 | a0008c0005t0001g0102 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3214+2337A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115071266 | |||||||
chr9:115071352 | C | T | 116 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(113): Show |
117 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.3214+2251G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115071352 | |||||||
chr9:115071356 | A | G | 2 | a0022c0033t0001g0127 a0022c0033t0001g0338 |
2 | HG01884.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.3214+2247T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115071356 | |||||||
chr9:115071400 | T | G | 1 | a0003c0077t0004g0356 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3214+2203A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115071400 | |||||||
chr9:115071428 | T | C | 116 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(113): Show |
117 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.3214+2175A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115071428 | |||||||
chr9:115071524 | T | G | 1 | a0015c0059t0002g0067 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3214+2079A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115071524 | |||||||
chr9:115071564 | A | C | 116 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(113): Show |
117 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.3214+2039T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115071564 | |||||||
chr9:115071574 | T | C | 116 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(113): Show |
117 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.3214+2029A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115071574 | |||||||
chr9:115071691 | A | G | 116 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(113): Show |
117 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.3214+1912T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115071691 | |||||||
chr9:115071711 | G | A | 22 | a0002c0093t0004g0122 a0004c0018t0004g0213 a0004c0018t0004g0224 others(19): Show |
22 | HG00099.hp1 HG00323.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.3214+1892C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115071711 | |||||||
chr9:115071747 | A | G | 15 | a0005c0017t0001g0081 a0005c0017t0002g0076 a0005c0017t0002g0078 others(12): Show |
16 | HG01081.hp2 HG01099.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.3214+1856T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115071747 | |||||||
chr9:115071767 | A | G | 1 | a0010c0008t0003g0013 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3214+1836T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115071767 | |||||||
chr9:115071783 | C | T | 53 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(50): Show |
53 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.3214+1820G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115071783 | |||||||
chr9:115071786 | T | G | 3 | a0005c0034t0002g0197 a0005c0034t0002g0198 a0005c0067t0002g0359 |
3 | HG01109.hp2 HG01243.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.3214+1817A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115071786 | |||||||
chr9:115071791 | C | T | 269 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(266): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.3214+1812G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115071791 | |||||||
chr9:115071854 | T | C | 7 | a0001c0009t0015g0124 a0001c0009t0015g0350 a0001c0024t0015g0320 others(4): Show |
7 | HG02280.hp2 HG02486.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.3214+1749A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115071854 | |||||||
chr9:115072112 | C | T | 5 | a0005c0034t0002g0197 a0005c0034t0002g0198 a0005c0067t0002g0359 others(2): Show |
5 | HG01109.hp2 HG01243.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.3214+1491G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115072112 | |||||||
chr9:115072214 | G | A | 22 | a0002c0093t0004g0122 a0004c0018t0004g0213 a0004c0018t0004g0224 others(19): Show |
22 | HG00099.hp1 HG00323.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.3214+1389C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115072214 | |||||||
chr9:115072561 | C | T | 116 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(113): Show |
117 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.3214+1042G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115072561 | |||||||
chr9:115072651 | C | T | 5 | a0009c0100t0005g0317 a0016c0022t0004g0130 a0016c0022t0004g0131 others(2): Show |
5 | HG02647.hp1 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.3214+952G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115072651 | |||||||
chr9:115072652 | G | A | 53 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(50): Show |
53 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.3214+951C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115072652 | |||||||
chr9:115072674 | A | G | 23 | a0003c0027t0002g0214 a0003c0027t0002g0215 a0003c0027t0002g0218 others(20): Show |
23 | HG00642.hp2 HG00741.hp2 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.3214+929T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115072674 | |||||||
chr9:115072817 | A | T | 15 | a0005c0017t0001g0081 a0005c0017t0002g0076 a0005c0017t0002g0078 others(12): Show |
16 | HG01081.hp2 HG01099.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.3214+786T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115072817 | |||||||
chr9:115072902 | C | T | 2 | a0004c0050t0014g0345 a0005c0062t0026g0250 |
2 | HG01192.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.3214+701G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115072902 | |||||||
chr9:115072935 | C | G | 239 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(236): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.3214+668G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115072935 | |||||||
chr9:115072943 | T | G | 239 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(236): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.3214+660A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115072943 | |||||||
chr9:115072975 | A | G | 51 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(48): Show |
51 | HG00140.hp1 HG00280.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.3214+628T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115072975 | |||||||
chr9:115072997 | A | G | 269 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(266): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.3214+606T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115072997 | |||||||
chr9:115073019 | G | A | 3 | a0007c0006t0007g0001 a0007c0006t0007g0051 a0007c0006t0016g0050 |
4 | NA19000.hp1 NA19004.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.3214+584C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115073019 | |||||||
chr9:115073150 | A | G | 1 | a0002c0001t0002g0159 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3214+453T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115073150 | |||||||
chr9:115073322 | A | G | 3 | a0001c0009t0015g0124 a0001c0009t0015g0350 a0001c0024t0015g0320 |
3 | HG02647.hp2 HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3214+281T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115073322 | |||||||
chr9:115073428 | A | G | 5 | a0009c0100t0005g0317 a0016c0022t0004g0130 a0016c0022t0004g0131 others(2): Show |
5 | HG02647.hp1 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.3214+175T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115073428 | |||||||
chr9:115073525 | G | C | 1 | a0004c0004t0002g0300 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.3214+78C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115073525 | |||||||
chr9:115073909 | A | G | 269 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(266): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.2951-43T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115073909 | |||||||
chr9:115074121 | G | A | 116 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(113): Show |
117 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.2951-255C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115074121 | |||||||
chr9:115074166 | A | G | 1 | a0002c0096t0002g0156 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2951-300T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115074166 | |||||||
chr9:115074180 | A | C | 1 | a0036c0104t0028g0341 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2951-314T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115074180 | |||||||
chr9:115074294 | C | G | 1 | a0031c0053t0018g0245 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2951-428G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115074294 | |||||||
chr9:115074297 | A | G | 6 | a0005c0037t0004g0152 a0005c0037t0004g0271 a0015c0021t0004g0129 others(3): Show |
6 | HG01891.hp1 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.2951-431T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115074297 | |||||||
chr9:115074533 | AG | A | 4 | a0021c0028t0012g0258 a0021c0028t0012g0259 a0021c0028t0012g0260 others(1): Show |
4 | HG01496.hp1 HG02818.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2951-668delC | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115074533 | |||||||
chr9:115074768 | CAT | C | 15 | a0005c0017t0001g0081 a0005c0017t0002g0076 a0005c0017t0002g0078 others(12): Show |
16 | HG01081.hp2 HG01099.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.2951-904_2951-903d others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115074768 | |||||||
chr9:115074805 | C | T | 22 | a0003c0027t0002g0214 a0003c0027t0002g0215 a0003c0027t0002g0218 others(19): Show |
22 | HG00642.hp2 HG00741.hp2 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.2951-939G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115074805 | |||||||
chr9:115074863 | C | T | 5 | a0009c0100t0005g0317 a0016c0022t0004g0130 a0016c0022t0004g0131 others(2): Show |
5 | HG02647.hp1 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2951-997G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115074863 | |||||||
chr9:115074918 | C | T | 2 | a0004c0050t0014g0345 a0005c0062t0026g0250 |
2 | HG01192.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2951-1052G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115074918 | |||||||
chr9:115074969 | C | A | 1 | a0011c0010t0001g0264 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2950+1063G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115074969 | |||||||
chr9:115074973 | A | G | 101 | a0001c0009t0001g0123 a0001c0009t0001g0155 a0001c0009t0001g0160 others(98): Show |
102 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.2950+1059T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115074973 | |||||||
chr9:115075042 | G | A | 3 | a0001c0009t0015g0124 a0001c0009t0015g0350 a0001c0024t0015g0320 |
3 | HG02647.hp2 HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2950+990C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115075042 | |||||||
chr9:115075111 | T | G | 2 | a0001c0009t0001g0188 a0003c0003t0010g0328 |
2 | HG01515.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.2950+921A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115075111 | |||||||
chr9:115075240 | A | G | 1 | a0036c0104t0028g0341 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2950+792T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115075240 | |||||||
chr9:115075432 | A | C | 1 | a0011c0010t0001g0264 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2950+600T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115075432 | |||||||
chr9:115075552 | C | G | 1 | a0002c0001t0002g0100 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2950+480G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115075552 | |||||||
chr9:115075561 | C | T | 7 | a0001c0009t0015g0124 a0001c0009t0015g0350 a0001c0024t0015g0320 others(4): Show |
7 | HG02280.hp2 HG02486.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2950+471G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115075561 | |||||||
chr9:115075579 | G | A | 1 | a0047c0060t0014g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2950+453C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115075579 | |||||||
chr9:115075678 | G | A | 2 | a0004c0050t0014g0345 a0005c0062t0026g0250 |
2 | HG01192.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2950+354C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115075678 | |||||||
chr9:115075717 | G | A | 25 | a0005c0014t0001g0005 a0005c0014t0001g0289 a0005c0014t0001g0299 others(22): Show |
26 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.2950+315C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115075717 | |||||||
chr9:115075814 | C | T | 116 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(113): Show |
117 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.2950+218G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115075814 | |||||||
chr9:115075894 | T | C | 3 | a0004c0018t0004g0224 a0024c0083t0001g0056 a0027c0071t0001g0355 |
3 | HG01109.hp1 HG02145.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2950+138A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115075894 | |||||||
chr9:115075987 | G | C | 1 | a0004c0004t0002g0325 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2950+45C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115075987 | |||||||
chr9:115075995 | C | G | 5 | a0009c0100t0005g0317 a0016c0022t0004g0130 a0016c0022t0004g0131 others(2): Show |
5 | HG02647.hp1 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2950+37G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115075995 | |||||||
chr9:115076345 | C | G | 53 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(50): Show |
53 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.2860+45G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 8/27 | chr9 | 115076345 | |||||||
chr9:115076661 | G | A | 7 | a0001c0009t0015g0124 a0001c0009t0015g0350 a0001c0024t0015g0320 others(4): Show |
7 | HG02280.hp2 HG02486.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2675-86C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115076661 | |||||||
chr9:115076724 | T | C | 2 | a0002c0001t0002g0100 a0002c0020t0002g0148 |
2 | NA18747.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.2675-149A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115076724 | |||||||
chr9:115076736 | C | A | 2 | a0004c0050t0014g0345 a0005c0062t0026g0250 |
2 | HG01192.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2675-161G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115076736 | |||||||
chr9:115076779 | C | T | 7 | a0002c0093t0004g0122 a0004c0018t0004g0213 a0004c0018t0004g0224 others(4): Show |
7 | HG02145.hp2 HG02723.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2675-204G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115076779 | |||||||
chr9:115076780 | G | A | 1 | a0009c0100t0005g0317 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2675-205C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115076780 | |||||||
chr9:115076823 | G | T | 1 | a0002c0001t0002g0103 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2675-248C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115076823 | |||||||
chr9:115076948 | A | G | 5 | a0005c0034t0002g0197 a0005c0034t0002g0198 a0005c0067t0002g0359 others(2): Show |
5 | HG01109.hp2 HG01243.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.2675-373T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115076948 | |||||||
chr9:115077110 | A | C | 2 | a0026c0046t0004g0339 a0026c0046t0004g0340 |
2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2675-535T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115077110 | |||||||
chr9:115077111 | A | G | 1 | a0002c0020t0001g0145 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2675-536T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115077111 | |||||||
chr9:115077152 | T | C | 1 | a0007c0006t0007g0006 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2675-577A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115077152 | |||||||
chr9:115077194 | A | T | 1 | a0009c0092t0002g0093 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2675-619T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115077194 | |||||||
chr9:115077257 | T | C | 1 | a0011c0010t0001g0225 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2675-682A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115077257 | |||||||
chr9:115077269 | A | G | 89 | a0001c0009t0001g0101 a0002c0001t0002g0092 a0002c0001t0002g0108 others(86): Show |
90 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.2674+674T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115077269 | |||||||
chr9:115077278 | A | G | 1 | a0004c0004t0002g0333 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2674+665T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115077278 | |||||||
chr9:115077297 | T | C | 26 | a0001c0009t0001g0188 a0001c0009t0002g0117 a0002c0001t0002g0169 others(23): Show |
27 | HG00280.hp1 HG00642.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.2674+646A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115077297 | |||||||
chr9:115077299 | G | A | 1 | a0056c0049t0002g0242 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2674+644C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115077299 | |||||||
chr9:115077299 | GC | G | 16 | a0008c0005t0001g0083 a0008c0005t0001g0085 a0008c0005t0001g0086 others(13): Show |
16 | HG00140.hp2 HG00642.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.2674+643delG | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115077299 | |||||||
chr9:115077303 | G | A | 1 | a0008c0005t0001g0196 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2674+640C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115077303 | |||||||
chr9:115077336 | G | A | 1 | a0001c0011t0001g0114 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2674+607C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115077336 | |||||||
chr9:115077338 | G | C | 98 | a0001c0002t0001g0276 a0001c0009t0001g0101 a0001c0009t0001g0123 others(95): Show |
99 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.2674+605C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115077338 | |||||||
chr9:115077479 | C | T | 38 | a0002c0098t0002g0147 a0004c0004t0001g0269 a0004c0051t0004g0342 others(35): Show |
39 | HG00423.hp2 HG00558.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.2674+464G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115077479 | |||||||
chr9:115077482 | G | T | 16 | a0001c0009t0001g0188 a0005c0017t0001g0081 a0005c0017t0002g0076 others(13): Show |
17 | HG01081.hp2 HG01257.hp2 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.2674+461C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115077482 | |||||||
chr9:115077483 | C | T | 1 | a0006c0007t0005g0324 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2674+460G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115077483 | |||||||
chr9:115077518 | A | G | 31 | a0004c0004t0001g0269 a0007c0006t0003g0028 a0007c0006t0003g0052 others(28): Show |
32 | HG00423.hp2 HG00558.hp1 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.2674+425T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115077518 | |||||||
chr9:115077589 | G | A | 33 | a0002c0098t0002g0147 a0004c0004t0001g0269 a0004c0051t0004g0342 others(30): Show |
33 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.2674+354C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115077589 | |||||||
chr9:115077606 | G | A | 1 | a0008c0005t0001g0196 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2674+337C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115077606 | |||||||
chr9:115077782 | A | G | 105 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(102): Show |
105 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.2674+161T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115077782 | |||||||
chr9:115078422 | T | C | 13 | a0003c0035t0004g0150 a0003c0035t0004g0151 a0005c0061t0002g0257 others(10): Show |
13 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.2405-210A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115078422 | |||||||
chr9:115078463 | G | C | 149 | a0001c0009t0001g0101 a0001c0009t0001g0123 a0001c0009t0001g0155 others(146): Show |
152 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.2405-251C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115078463 | |||||||
chr9:115078482 | G | T | 1 | a0051c0080t0003g0045 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2405-270C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115078482 | |||||||
chr9:115078505 | G | A | 1 | a0003c0003t0001g0332 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2405-293C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115078505 | |||||||
chr9:115078558 | A | T | 151 | a0001c0002t0001g0192 a0001c0009t0001g0101 a0001c0009t0001g0123 others(148): Show |
154 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.2405-346T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115078558 | |||||||
chr9:115078643 | A | G | 124 | a0001c0002t0001g0192 a0001c0009t0001g0101 a0001c0009t0001g0123 others(121): Show |
127 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.2405-431T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115078643 | |||||||
chr9:115079049 | G | GA | 3 | a0001c0002t0001g0134 a0001c0002t0013g0135 a0002c0020t0002g0148 |
3 | HG02071.hp1 NA18747.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.2405-838dupT | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115079049 | |||||||
chr9:115079137 | T | C | 34 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(31): Show |
34 | HG00140.hp1 HG00280.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.2405-925A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115079137 | |||||||
chr9:115079291 | G | T | 354 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(351): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.2405-1079C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115079291 | |||||||
chr9:115079623 | G | C | 354 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(351): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.2405-1411C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115079623 | |||||||
chr9:115079635 | T | C | 1 | a0005c0066t0002g0251 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2405-1423A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115079635 | |||||||
chr9:115079659 | C | T | 43 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(40): Show |
43 | HG00140.hp1 HG00280.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.2405-1447G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115079659 | |||||||
chr9:115079694 | C | T | 19 | a0003c0003t0001g0199 a0003c0003t0001g0207 a0003c0003t0001g0208 others(16): Show |
19 | HG02015.hp2 HG02129.hp1 HG02155.hp1 others(16): Show |
intron_variant | MODIFIER | c.2405-1482G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115079694 | |||||||
chr9:115079994 | C | T | 1 | a0004c0051t0004g0342 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2404+1778G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115079994 | |||||||
chr9:115080006 | A | T | 9 | a0009c0092t0002g0093 a0012c0012t0006g0057 a0012c0012t0006g0058 others(6): Show |
9 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.2404+1766T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115080006 | |||||||
chr9:115080028 | A | G | 215 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(212): Show |
217 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.2404+1744T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115080028 | |||||||
chr9:115080114 | A | G | 6 | a0008c0005t0001g0083 a0008c0005t0001g0085 a0008c0005t0001g0086 others(3): Show |
6 | HG00140.hp2 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.2404+1658T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115080114 | |||||||
chr9:115080190 | A | G | 3 | a0005c0067t0002g0359 a0006c0007t0005g0357 a0043c0047t0001g0358 |
3 | HG02280.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2404+1582T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115080190 | |||||||
chr9:115080259 | C | G | 3 | a0026c0046t0004g0339 a0026c0046t0004g0340 a0036c0104t0028g0341 |
3 | HG02145.hp1 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2404+1513G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115080259 | |||||||
chr9:115080260 | A | T | 3 | a0026c0046t0004g0339 a0026c0046t0004g0340 a0036c0104t0028g0341 |
3 | HG02145.hp1 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2404+1512T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115080260 | |||||||
chr9:115080320 | T | TG | 214 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(211): Show |
216 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.2404+1451dupC | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115080320 | |||||||
chr9:115080322 | A | T | 1 | a0020c0025t0001g0347 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2404+1450T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115080322 | |||||||
chr9:115080327 | T | C | 1 | a0001c0002t0010g0288 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2404+1445A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115080327 | |||||||
chr9:115080367 | G | A | 1 | a0004c0018t0004g0226 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2404+1405C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115080367 | |||||||
chr9:115080442 | T | C | 3 | a0002c0020t0002g0065 a0002c0020t0002g0249 a0017c0101t0005g0066 |
3 | NA18995.hp1 NA19078.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.2404+1330A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115080442 | |||||||
chr9:115080545 | C | T | 1 | a0035c0065t0005g0326 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2404+1227G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115080545 | |||||||
chr9:115080648 | C | T | 3 | a0004c0073t0002g0274 a0004c0074t0002g0286 a0004c0075t0004g0266 |
3 | HG00738.hp1 HG02055.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.2404+1124G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115080648 | |||||||
chr9:115080658 | C | T | 3 | a0005c0037t0004g0152 a0005c0037t0004g0271 a0035c0065t0005g0326 |
3 | HG02109.hp2 HG02559.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2404+1114G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115080658 | |||||||
chr9:115080895 | G | GA | 52 | a0001c0002t0013g0135 a0002c0001t0002g0154 a0002c0001t0002g0176 others(49): Show |
53 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.2404+876dupT | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115080895 | |||||||
chr9:115080895 | GA | G | 121 | a0001c0002t0010g0330 a0001c0009t0001g0188 a0001c0009t0002g0117 others(118): Show |
122 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.2404+876delT | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115080895 | |||||||
chr9:115081143 | C | T | 1 | a0010c0008t0003g0013 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2404+629G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115081143 | |||||||
chr9:115081385 | G | A | 1 | a0003c0003t0001g0332 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2404+387C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115081385 | |||||||
chr9:115081442 | G | A | 1 | a0002c0001t0002g0159 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2404+330C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115081442 | |||||||
chr9:115081635 | C | T | 1 | a0004c0051t0004g0342 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2404+137G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115081635 | |||||||
chr9:115081653 | A | T | 8 | a0012c0012t0006g0057 a0012c0012t0006g0058 a0012c0012t0006g0059 others(5): Show |
8 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.2404+119T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115081653 | |||||||
chr9:115081741 | T | C | 3 | a0005c0067t0002g0359 a0006c0007t0005g0357 a0043c0047t0001g0358 |
3 | HG02280.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2404+31A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115081741 | |||||||
chr9:115081960 | G | A | 169 | a0003c0003t0001g0199 a0003c0003t0001g0207 a0003c0003t0001g0208 others(166): Show |
171 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.2248-32C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 5/27 | chr9 | 115081960 | |||||||
chr9:115081965 | G | T | 1 | a0002c0001t0002g0108 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2248-37C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 5/27 | chr9 | 115081965 | |||||||
chr9:115082236 | C | G | 1 | a0004c0050t0014g0345 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2248-308G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 5/27 | chr9 | 115082236 | |||||||
chr9:115082247 | G | A | 2 | a0001c0002t0001g0302 a0001c0002t0010g0330 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.2248-319C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 5/27 | chr9 | 115082247 | |||||||
chr9:115082372 | C | A | 1 | a0002c0001t0002g0171 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2247+320G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 5/27 | chr9 | 115082372 | |||||||
chr9:115082492 | G | C | 203 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(200): Show |
205 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.2247+200C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 5/27 | chr9 | 115082492 | |||||||
chr9:115082532 | A | G | 6 | a0005c0034t0002g0197 a0005c0034t0002g0198 a0022c0033t0001g0126 others(3): Show |
6 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.2247+160T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 5/27 | chr9 | 115082532 | |||||||
chr9:115082568 | C | T | 1 | a0002c0001t0002g0100 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2247+124G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 5/27 | chr9 | 115082568 | |||||||
chr9:115082578 | C | A | 1 | a0005c0037t0004g0152 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2247+114G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 5/27 | chr9 | 115082578 | |||||||
chr9:115082584 | C | T | 1 | a0006c0015t0005g0235 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2247+108G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 5/27 | chr9 | 115082584 | |||||||
chr9:115082654 | C | T | 11 | a0003c0027t0002g0214 a0003c0027t0002g0215 a0003c0027t0002g0218 others(8): Show |
11 | HG01884.hp1 HG02145.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.2247+38G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 5/27 | chr9 | 115082654 | |||||||
chr9:115082866 | C | T | 1 | a0001c0002t0008g0144 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2132-59G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/27 | chr9 | 115082866 | |||||||
chr9:115082887 | A | G | 1 | a0009c0031t0001g0166 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2132-80T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/27 | chr9 | 115082887 | |||||||
chr9:115083046 | C | T | 45 | a0002c0001t0007g0018 a0007c0006t0003g0028 a0007c0006t0003g0052 others(42): Show |
46 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.2132-239G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/27 | chr9 | 115083046 | |||||||
chr9:115083047 | G | A | 1 | a0048c0057t0014g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2132-240C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/27 | chr9 | 115083047 | |||||||
chr9:115083054 | T | G | 200 | a0001c0002t0001g0128 a0001c0002t0001g0138 a0001c0002t0001g0141 others(197): Show |
202 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.2132-247A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/27 | chr9 | 115083054 | |||||||
chr9:115083068 | A | G | 14 | a0014c0016t0006g0069 a0014c0016t0006g0071 a0014c0016t0006g0072 others(11): Show |
14 | HG00642.hp2 HG00741.hp2 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.2132-261T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/27 | chr9 | 115083068 | |||||||
chr9:115083124 | G | A | 204 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(201): Show |
206 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.2132-317C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/27 | chr9 | 115083124 | |||||||
chr9:115083162 | G | A | 162 | a0003c0003t0001g0199 a0003c0003t0001g0207 a0003c0003t0001g0208 others(159): Show |
164 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.2132-355C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/27 | chr9 | 115083162 | |||||||
chr9:115083170 | G | A | 162 | a0003c0003t0001g0199 a0003c0003t0001g0207 a0003c0003t0001g0208 others(159): Show |
164 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.2132-363C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/27 | chr9 | 115083170 | |||||||
chr9:115083183 | GA | G | 14 | a0014c0016t0006g0069 a0014c0016t0006g0071 a0014c0016t0006g0072 others(11): Show |
14 | HG00642.hp2 HG00741.hp2 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.2132-377delT | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/27 | chr9 | 115083183 | |||||||
chr9:115083310 | C | T | 1 | a0036c0104t0028g0341 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2132-503G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/27 | chr9 | 115083310 | |||||||
chr9:115083332 | A | G | 43 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(40): Show |
43 | HG00140.hp1 HG00280.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.2132-525T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/27 | chr9 | 115083332 | |||||||
chr9:115083380 | C | T | 162 | a0003c0003t0001g0199 a0003c0003t0001g0207 a0003c0003t0001g0208 others(159): Show |
164 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.2132-573G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/27 | chr9 | 115083380 | |||||||
chr9:115083507 | G | A | 1 | a0005c0066t0002g0251 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2132-700C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/27 | chr9 | 115083507 | |||||||
chr9:115083602 | C | CT | 59 | a0001c0002t0013g0135 a0001c0009t0001g0101 a0002c0001t0007g0018 others(56): Show |
60 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.2131+606dupA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/27 | chr9 | 115083602 | |||||||
chr9:115083602 | CT | C | 149 | a0001c0002t0010g0330 a0001c0024t0003g0008 a0002c0020t0011g0132 others(146): Show |
151 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.2131+606delA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/27 | chr9 | 115083602 | |||||||
chr9:115083602 | CTT | C | 17 | a0003c0035t0004g0150 a0003c0035t0004g0151 a0003c0055t0001g0238 others(14): Show |
17 | HG01192.hp1 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.2131+605_2131+606d others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/27 | chr9 | 115083602 | |||||||
chr9:115083638 | A | C | 162 | a0003c0003t0001g0199 a0003c0003t0001g0207 a0003c0003t0001g0208 others(159): Show |
164 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.2131+571T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/27 | chr9 | 115083638 | |||||||
chr9:115083801 | C | T | 135 | a0003c0003t0001g0199 a0003c0003t0001g0207 a0003c0003t0001g0208 others(132): Show |
137 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.2131+408G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/27 | chr9 | 115083801 | |||||||
chr9:115083837 | C | T | 162 | a0003c0003t0001g0199 a0003c0003t0001g0207 a0003c0003t0001g0208 others(159): Show |
164 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.2131+372G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/27 | chr9 | 115083837 | |||||||
chr9:115084140 | C | T | 1 | a0001c0011t0001g0161 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2131+69G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/27 | chr9 | 115084140 | |||||||
chr9:115084171 | A | G | 207 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(204): Show |
209 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.2131+38T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/27 | chr9 | 115084171 | |||||||
chr9:115084577 | G | A | 1 | a0006c0015t0002g0241 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1868-105C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/27 | chr9 | 115084577 | |||||||
chr9:115084701 | C | G | 163 | a0003c0003t0001g0199 a0003c0003t0001g0207 a0003c0003t0001g0208 others(160): Show |
165 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1868-229G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/27 | chr9 | 115084701 | |||||||
chr9:115084706 | G | T | 163 | a0003c0003t0001g0199 a0003c0003t0001g0207 a0003c0003t0001g0208 others(160): Show |
165 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1868-234C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/27 | chr9 | 115084706 | |||||||
chr9:115084771 | A | T | 3 | a0022c0033t0001g0126 a0022c0033t0001g0127 a0022c0033t0001g0338 |
3 | HG01884.hp2 HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1868-299T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/27 | chr9 | 115084771 | |||||||
chr9:115084874 | A | T | 354 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(351): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.1868-402T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/27 | chr9 | 115084874 | |||||||
chr9:115084900 | C | A | 354 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(351): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.1868-428G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/27 | chr9 | 115084900 | |||||||
chr9:115085054 | A | G | 1 | a0003c0027t0002g0214 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1868-582T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/27 | chr9 | 115085054 | |||||||
chr9:115085241 | C | G | 1 | a0025c0038t0005g0354 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1867+623G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/27 | chr9 | 115085241 | |||||||
chr9:115085334 | C | G | 163 | a0003c0003t0001g0199 a0003c0003t0001g0207 a0003c0003t0001g0208 others(160): Show |
165 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1867+530G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/27 | chr9 | 115085334 | |||||||
chr9:115085429 | G | A | 2 | a0003c0003t0001g0199 a0006c0007t0005g0200 |
2 | NA19000.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1867+435C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/27 | chr9 | 115085429 | |||||||
chr9:115085590 | T | C | 354 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(351): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.1867+274A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/27 | chr9 | 115085590 | |||||||
chr9:115085676 | C | T | 1 | a0018c0026t0006g0070 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1867+188G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/27 | chr9 | 115085676 | |||||||
chr9:115085688 | G | A | 2 | a0004c0004t0002g0280 a0004c0004t0002g0281 |
2 | HG03669.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1867+176C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/27 | chr9 | 115085688 | |||||||
chr9:115085790 | C | T | 1 | a0006c0015t0002g0241 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1867+74G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/27 | chr9 | 115085790 | |||||||
chr9:115085833 | A | T | 113 | a0003c0003t0001g0199 a0003c0003t0001g0207 a0003c0003t0001g0208 others(110): Show |
114 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.1867+31T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/27 | chr9 | 115085833 | |||||||
chr9:115085850 | G | T | 1 | a0013c0040t0003g0040 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1867+14C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/27 | chr9 | 115085850 | |||||||
chr9:115087362 | T | G | 150 | a0003c0003t0001g0199 a0003c0003t0001g0207 a0003c0003t0001g0208 others(147): Show |
152 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.458-89A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087362 | |||||||
chr9:115087387 | C | G | 44 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(41): Show |
44 | HG00140.hp1 HG00280.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.458-114G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087387 | |||||||
chr9:115087401 | A | G | 4 | a0001c0002t0013g0135 a0002c0020t0002g0065 a0002c0020t0002g0249 others(1): Show |
4 | NA18995.hp1 NA19078.hp1 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-128T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087401 | |||||||
chr9:115087412 | G | A | 1 | a0003c0077t0004g0356 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.458-139C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087412 | |||||||
chr9:115087443 | C | G | 42 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(39): Show |
42 | HG00140.hp1 HG00280.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.458-170G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087443 | |||||||
chr9:115087471 | T | C | 12 | a0009c0092t0002g0093 a0012c0012t0006g0057 a0012c0012t0006g0058 others(9): Show |
12 | HG02145.hp1 HG02630.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.458-198A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087471 | |||||||
chr9:115087507 | A | T | 1 | a0002c0001t0002g0159 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.458-234T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087507 | |||||||
chr9:115087527 | G | GATGTGT | 5 | a0001c0002t0001g0128 a0009c0100t0005g0317 a0019c0032t0001g0316 others(2): Show |
5 | HG01123.hp2 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.458-255_458-254ins others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087527 | |||||||
chr9:115087527 | G | GGTGT | 8 | a0001c0002t0001g0302 a0001c0002t0008g0137 a0001c0002t0008g0144 others(5): Show |
8 | HG00558.hp2 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.458-258_458-255dup others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087527 | |||||||
chr9:115087527 | G | GGTGTGT | 36 | a0001c0002t0001g0134 a0001c0002t0001g0138 a0001c0002t0001g0141 others(33): Show |
36 | HG00140.hp1 HG00280.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.458-260_458-255dup others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087527 | |||||||
chr9:115087527 | G | GGTGTGTG others(1): Show |
36 | a0001c0002t0001g0301 a0001c0002t0013g0135 a0001c0024t0001g0133 others(33): Show |
37 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.458-262_458-255dup others(8): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087527 | |||||||
chr9:115087527 | G | GGTGTGTG others(3): Show |
3 | a0007c0041t0016g0030 a0010c0008t0001g0077 a0010c0008t0003g0013 |
3 | HG00597.hp2 HG03491.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.458-264_458-255dup others(10): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087527 | |||||||
chr9:115087527 | G | GGTGTGTG others(5): Show |
4 | a0007c0006t0007g0019 a0007c0041t0007g0029 a0017c0043t0009g0016 others(1): Show |
4 | HG00408.hp2 HG04184.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-266_458-255dup others(12): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087527 | |||||||
chr9:115087527 | G | GGTGTGTG others(7): Show |
1 | a0002c0001t0007g0018 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.458-268_458-255dup others(14): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087527 | |||||||
chr9:115087527 | G | GTGTGTGT others(6): Show |
1 | a0007c0006t0007g0006 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.458-255_458-254ins others(13): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087527 | |||||||
chr9:115087527 | GGT | G | 4 | a0002c0001t0002g0099 a0002c0001t0002g0107 a0002c0001t0002g0171 others(1): Show |
4 | HG02071.hp2 NA18959.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.458-256_458-255del others(2): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087527 | |||||||
chr9:115087527 | GGTGT | G | 25 | a0001c0009t0001g0155 a0001c0009t0001g0160 a0001c0009t0001g0175 others(22): Show |
26 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.458-258_458-255del others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087527 | |||||||
chr9:115087527 | GGTGTGT | G | 64 | a0001c0002t0001g0192 a0001c0009t0001g0101 a0001c0009t0001g0123 others(61): Show |
65 | HG00099.hp2 HG00140.hp2 HG00738.hp2 others(62): Show |
intron_variant | MODIFIER | c.458-260_458-255del others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087527 | |||||||
chr9:115087527 | GGTGTGTG others(3): Show |
G | 1 | a0001c0002t0001g0327 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.458-264_458-255del others(10): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087527 | |||||||
chr9:115087527 | GGTGTGTG others(17): Show |
G | 161 | a0003c0003t0001g0199 a0003c0003t0001g0207 a0003c0003t0001g0208 others(158): Show |
163 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.458-278_458-255del others(24): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087527 | |||||||
chr9:115087528 | G | A | 2 | a0001c0002t0001g0321 a0001c0002t0001g0322 |
2 | HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.458-255C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087528 | |||||||
chr9:115087581 | G | A | 1 | a0007c0086t0020g0044 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.458-308C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087581 | |||||||
chr9:115087583 | G | A | 2 | a0005c0034t0002g0197 a0005c0034t0002g0198 |
2 | HG01109.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.458-310C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087583 | |||||||
chr9:115087698 | C | CT | 54 | a0001c0002t0001g0192 a0001c0009t0001g0155 a0001c0009t0001g0160 others(51): Show |
55 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.458-426dupA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087698 | |||||||
chr9:115087698 | CT | C | 49 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(46): Show |
49 | HG00140.hp1 HG00280.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.458-426delA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087698 | |||||||
chr9:115087698 | CTT | C | 152 | a0001c0002t0001g0142 a0001c0002t0001g0303 a0001c0002t0010g0330 others(149): Show |
154 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.458-427_458-426del others(2): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087698 | |||||||
chr9:115087702 | T | TC | 43 | a0002c0001t0007g0018 a0007c0006t0003g0028 a0007c0006t0003g0052 others(40): Show |
44 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.458-430_458-429ins others(1): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087702 | |||||||
chr9:115087703 | T | C | 1 | a0004c0004t0002g0220 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.458-430A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087703 | |||||||
chr9:115087703 | T | TC | 45 | a0001c0009t0001g0101 a0001c0009t0001g0123 a0001c0009t0001g0244 others(42): Show |
46 | HG00099.hp2 HG00140.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.458-431_458-430ins others(1): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087703 | |||||||
chr9:115087704 | T | C | 2 | a0003c0003t0001g0279 a0005c0062t0026g0250 |
2 | HG01175.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.458-431A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087704 | |||||||
chr9:115087705 | T | C | 125 | a0003c0003t0001g0199 a0003c0003t0001g0207 a0003c0003t0001g0208 others(122): Show |
127 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.458-432A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087705 | |||||||
chr9:115087842 | C | T | 1 | a0014c0016t0006g0069 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.458-569G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087842 | |||||||
chr9:115087846 | C | T | 1 | a0001c0009t0001g0101 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.458-573G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087846 | |||||||
chr9:115087862 | C | T | 8 | a0014c0016t0006g0069 a0014c0016t0006g0071 a0014c0016t0006g0072 others(5): Show |
8 | HG00642.hp2 HG00741.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.458-589G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087862 | |||||||
chr9:115087925 | A | C | 1 | a0002c0001t0002g0082 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.458-652T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087925 | |||||||
chr9:115088005 | T | C | 3 | a0026c0046t0004g0339 a0026c0046t0004g0340 a0036c0104t0028g0341 |
3 | HG02145.hp1 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.458-732A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115088005 | |||||||
chr9:115088024 | T | C | 1 | a0011c0076t0001g0206 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.458-751A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115088024 | |||||||
chr9:115088205 | T | C | 1 | a0002c0001t0002g0099 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.458-932A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115088205 | |||||||
chr9:115088283 | G | T | 44 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(41): Show |
44 | HG00140.hp1 HG00280.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.458-1010C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115088283 | |||||||
chr9:115088303 | G | A | 3 | a0026c0046t0004g0339 a0026c0046t0004g0340 a0036c0104t0028g0341 |
3 | HG02145.hp1 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.458-1030C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115088303 | |||||||
chr9:115088322 | A | G | 1 | a0007c0006t0007g0046 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.458-1049T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115088322 | |||||||
chr9:115088427 | T | C | 1 | a0005c0017t0002g0078 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.458-1154A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115088427 | |||||||
chr9:115088442 | C | T | 1 | a0005c0034t0002g0198 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.458-1169G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115088442 | |||||||
chr9:115088612 | A | G | 1 | a0033c0090t0001g0116 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.458-1339T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115088612 | |||||||
chr9:115088625 | T | A | 1 | a0025c0038t0005g0354 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.458-1352A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115088625 | |||||||
chr9:115088702 | A | T | 1 | a0003c0003t0001g0199 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.458-1429T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115088702 | |||||||
chr9:115088751 | T | C | 3 | a0026c0046t0004g0339 a0026c0046t0004g0340 a0036c0104t0028g0341 |
3 | HG02145.hp1 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.458-1478A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115088751 | |||||||
chr9:115089018 | T | C | 5 | a0016c0022t0004g0130 a0016c0022t0004g0131 a0016c0022t0004g0252 others(2): Show |
5 | HG02647.hp1 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.457+1544A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115089018 | |||||||
chr9:115089159 | G | T | 1 | a0037c0064t0014g0343 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.457+1403C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115089159 | |||||||
chr9:115089185 | A | G | 2 | a0003c0035t0004g0150 a0003c0035t0004g0151 |
2 | HG02559.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.457+1377T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115089185 | |||||||
chr9:115089210 | C | T | 46 | a0002c0001t0007g0018 a0007c0006t0003g0028 a0007c0006t0003g0052 others(43): Show |
47 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.457+1352G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115089210 | |||||||
chr9:115089393 | T | C | 162 | a0003c0003t0001g0199 a0003c0003t0001g0207 a0003c0003t0001g0208 others(159): Show |
164 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.457+1169A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115089393 | |||||||
chr9:115089478 | A | ATC | 11 | a0001c0002t0003g0007 a0001c0011t0001g0095 a0002c0001t0001g0104 others(8): Show |
12 | HG02015.hp1 HG02071.hp2 HG02965.hp1 others(9): Show |
intron_variant | MODIFIER | c.457+1082_457+1083d others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115089478 | |||||||
chr9:115089478 | ATC | A | 82 | a0003c0003t0001g0229 a0003c0003t0001g0239 a0003c0003t0001g0240 others(79): Show |
83 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.457+1082_457+1083d others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115089478 | |||||||
chr9:115089478 | ATCTC | A | 78 | a0003c0003t0001g0199 a0003c0003t0001g0207 a0003c0003t0001g0208 others(75): Show |
79 | HG00323.hp1 HG00621.hp2 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.457+1080_457+1083d others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115089478 | |||||||
chr9:115089484 | C | A | 3 | a0020c0025t0001g0347 a0020c0025t0001g0348 a0020c0025t0001g0349 |
3 | HG01243.hp1 HG02055.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.457+1078G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115089484 | |||||||
chr9:115089593 | C | T | 1 | a0009c0092t0002g0093 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.457+969G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115089593 | |||||||
chr9:115089891 | T | C | 43 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(40): Show |
43 | HG00140.hp1 HG00280.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.457+671A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115089891 | |||||||
chr9:115089960 | C | A | 9 | a0003c0035t0004g0150 a0003c0035t0004g0151 a0005c0061t0002g0257 others(6): Show |
9 | HG02257.hp1 HG02559.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.457+602G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115089960 | |||||||
chr9:115090190 | C | T | 1 | a0001c0002t0010g0288 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.457+372G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115090190 | |||||||
chr9:115090209 | T | A | 1 | a0003c0003t0004g0337 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.457+353A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115090209 | |||||||
chr9:115090243 | T | C | 113 | a0003c0003t0001g0199 a0003c0003t0001g0207 a0003c0003t0001g0208 others(110): Show |
114 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.457+319A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115090243 | |||||||
chr9:115090325 | G | T | 1 | a0001c0002t0001g0267 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.457+237C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115090325 | |||||||
chr9:115090398 | C | T | 2 | a0001c0024t0001g0133 a0002c0020t0011g0132 |
2 | NA18982.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.457+164G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115090398 | |||||||
chr9:115091353 | C | T | 45 | a0002c0001t0007g0018 a0007c0006t0003g0028 a0007c0006t0003g0052 others(42): Show |
46 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.-136-199G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115091353 | |||||||
chr9:115092027 | G | A | 13 | a0003c0035t0004g0150 a0003c0035t0004g0151 a0005c0061t0002g0257 others(10): Show |
13 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136-873C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115092027 | |||||||
chr9:115092123 | T | G | 3 | a0026c0046t0004g0339 a0026c0046t0004g0340 a0036c0104t0028g0341 |
3 | HG02145.hp1 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-136-969A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115092123 | |||||||
chr9:115092387 | G | A | 1 | a0005c0103t0012g0091 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-136-1233C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115092387 | |||||||
chr9:115092569 | A | G | 3 | a0020c0025t0001g0347 a0020c0025t0001g0348 a0020c0025t0001g0349 |
3 | HG01243.hp1 HG02055.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-136-1415T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115092569 | |||||||
chr9:115092642 | T | C | 354 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(351): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.-136-1488A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115092642 | |||||||
chr9:115092670 | T | C | 3 | a0020c0025t0001g0347 a0020c0025t0001g0348 a0020c0025t0001g0349 |
3 | HG01243.hp1 HG02055.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-136-1516A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115092670 | |||||||
chr9:115092720 | C | T | 1 | a0021c0028t0012g0258 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-136-1566G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115092720 | |||||||
chr9:115092749 | A | AT | 51 | a0001c0002t0008g0136 a0002c0001t0007g0018 a0002c0098t0002g0147 others(48): Show |
52 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.-136-1596dupA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115092749 | |||||||
chr9:115092749 | AT | A | 142 | a0001c0002t0010g0330 a0002c0001t0002g0107 a0003c0003t0001g0199 others(139): Show |
143 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.-136-1596delA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115092749 | |||||||
chr9:115092749 | ATT | A | 15 | a0003c0027t0002g0214 a0003c0052t0001g0234 a0003c0055t0001g0238 others(12): Show |
16 | HG00323.hp1 HG00621.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-136-1597_-136-159 others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115092749 | |||||||
chr9:115092755 | T | A | 1 | a0005c0062t0026g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-136-1601A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115092755 | |||||||
chr9:115092908 | A | G | 1 | a0004c0051t0004g0342 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-136-1754T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115092908 | |||||||
chr9:115093164 | T | C | 7 | a0001c0011t0008g0109 a0002c0001t0002g0092 a0002c0001t0002g0098 others(4): Show |
7 | HG01169.hp1 HG01361.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136-2010A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115093164 | |||||||
chr9:115093192 | A | C | 8 | a0003c0003t0001g0199 a0003c0003t0001g0207 a0003c0003t0001g0208 others(5): Show |
8 | NA18952.hp2 NA18993.hp1 NA19000.hp2 others(5): Show |
intron_variant | MODIFIER | c.-136-2038T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115093192 | |||||||
chr9:115093228 | G | C | 149 | a0002c0098t0002g0147 a0003c0003t0001g0199 a0003c0003t0001g0207 others(146): Show |
151 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.-136-2074C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115093228 | |||||||
chr9:115093620 | C | CT | 54 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0192 others(51): Show |
54 | HG00140.hp1 HG00280.hp2 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.-136-2467dupA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115093620 | |||||||
chr9:115093620 | CT | C | 6 | a0003c0003t0001g0329 a0005c0062t0026g0250 a0008c0005t0001g0102 others(3): Show |
6 | HG01099.hp2 HG01192.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.-136-2467delA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115093620 | |||||||
chr9:115093648 | A | G | 1 | a0001c0009t0001g0101 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-136-2494T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115093648 | |||||||
chr9:115093765 | A | T | 354 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(351): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.-136-2611T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115093765 | |||||||
chr9:115093832 | G | A | 3 | a0026c0046t0004g0339 a0026c0046t0004g0340 a0036c0104t0028g0341 |
3 | HG02145.hp1 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-136-2678C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115093832 | |||||||
chr9:115093835 | A | C | 206 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(203): Show |
208 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.-136-2681T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115093835 | |||||||
chr9:115093851 | T | G | 13 | a0003c0052t0001g0234 a0003c0055t0001g0238 a0004c0045t0002g0230 others(10): Show |
14 | HG00323.hp1 HG00621.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.-136-2697A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115093851 | |||||||
chr9:115093861 | T | C | 43 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(40): Show |
43 | HG00140.hp1 HG00280.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.-136-2707A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115093861 | |||||||
chr9:115093865 | G | C | 13 | a0003c0052t0001g0234 a0003c0055t0001g0238 a0004c0045t0002g0230 others(10): Show |
14 | HG00323.hp1 HG00621.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.-136-2711C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115093865 | |||||||
chr9:115093915 | G | A | 1 | a0010c0008t0001g0077 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-136-2761C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115093915 | |||||||
chr9:115094025 | A | G | 9 | a0009c0092t0002g0093 a0012c0012t0006g0057 a0012c0012t0006g0058 others(6): Show |
9 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.-136-2871T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094025 | |||||||
chr9:115094039 | C | T | 210 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(207): Show |
212 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.-136-2885G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094039 | |||||||
chr9:115094144 | T | C | 1 | a0002c0001t0006g0120 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-136-2990A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094144 | |||||||
chr9:115094203 | T | C | 1 | a0015c0059t0002g0067 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-136-3049A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094203 | |||||||
chr9:115094205 | C | T | 2 | a0001c0009t0001g0155 a0001c0009t0001g0160 |
2 | NA18939.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.-136-3051G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094205 | |||||||
chr9:115094207 | C | A | 31 | a0003c0052t0001g0234 a0003c0055t0001g0238 a0004c0045t0002g0230 others(28): Show |
32 | HG00323.hp1 HG00621.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.-136-3053G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094207 | |||||||
chr9:115094214 | G | A | 10 | a0014c0016t0006g0069 a0014c0016t0006g0071 a0014c0016t0006g0072 others(7): Show |
10 | HG00642.hp2 HG00741.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.-136-3060C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094214 | |||||||
chr9:115094273 | A | G | 1 | a0001c0002t0003g0007 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-136-3119T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094273 | |||||||
chr9:115094275 | C | T | 89 | a0001c0009t0001g0101 a0001c0009t0001g0123 a0001c0009t0001g0155 others(86): Show |
91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.-136-3121G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094275 | |||||||
chr9:115094518 | G | A | 5 | a0003c0077t0004g0356 a0015c0021t0004g0129 a0015c0021t0004g0254 others(2): Show |
5 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-136-3364C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094518 | |||||||
chr9:115094598 | G | A | 151 | a0001c0002t0001g0128 a0001c0002t0001g0267 a0001c0002t0001g0268 others(148): Show |
152 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.-136-3444C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094598 | |||||||
chr9:115094633 | A | T | 176 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(173): Show |
177 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.-136-3479T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094633 | |||||||
chr9:115094639 | T | C | 1 | a0001c0009t0001g0123 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-136-3485A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094639 | |||||||
chr9:115094814 | CCT | C | 64 | a0001c0002t0008g0144 a0001c0002t0013g0135 a0002c0001t0002g0158 others(61): Show |
65 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.-136-3662_-136-366 others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094814 | |||||||
chr9:115094814 | CCTCTGTG others(3): Show |
C | 6 | a0014c0016t0006g0069 a0014c0016t0006g0074 a0018c0026t0006g0070 others(3): Show |
6 | HG00642.hp2 HG00741.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.-136-3670_-136-366 others(14): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094814 | |||||||
chr9:115094814 | CCTCTGTG others(5): Show |
C | 6 | a0014c0016t0006g0071 a0014c0016t0006g0072 a0014c0016t0006g0073 others(3): Show |
6 | HG01346.hp1 HG01884.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.-136-3672_-136-366 others(16): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094814 | |||||||
chr9:115094814 | CCTCTGTG others(7): Show |
C | 5 | a0004c0051t0004g0342 a0005c0034t0002g0197 a0005c0034t0002g0198 others(2): Show |
5 | HG01109.hp2 HG01243.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.-136-3674_-136-366 others(18): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094814 | |||||||
chr9:115094814 | CCTCTGTG others(11): Show |
C | 1 | a0004c0050t0014g0345 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-136-3678_-136-366 others(22): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094814 | |||||||
chr9:115094814 | CCTCTGTG others(13): Show |
C | 14 | a0001c0009t0001g0244 a0003c0052t0001g0234 a0003c0055t0001g0238 others(11): Show |
15 | HG00323.hp1 HG00621.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-136-3680_-136-366 others(24): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094814 | |||||||
chr9:115094815 | CTCTG | C | 67 | a0001c0002t0001g0128 a0001c0002t0001g0192 a0001c0002t0001g0267 others(64): Show |
68 | HG00280.hp2 HG00597.hp1 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.-136-3665_-136-366 others(8): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094815 | |||||||
chr9:115094815 | CTCTGTG | C | 95 | a0001c0002t0001g0134 a0001c0002t0001g0138 a0001c0002t0001g0141 others(92): Show |
97 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.-136-3667_-136-366 others(10): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094815 | |||||||
chr9:115094815 | CTCTGTGT others(1): Show |
C | 22 | a0001c0002t0001g0268 a0001c0002t0001g0302 a0001c0002t0010g0330 others(19): Show |
22 | HG00099.hp2 HG00738.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.-136-3669_-136-366 others(12): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094815 | |||||||
chr9:115094815 | CTCTGTGT others(3): Show |
C | 10 | a0001c0009t0001g0123 a0002c0001t0002g0106 a0002c0001t0002g0171 others(7): Show |
10 | HG02071.hp2 HG02257.hp2 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.-136-3671_-136-366 others(14): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094815 | |||||||
chr9:115094815 | CTCTGTGT others(5): Show |
C | 4 | a0003c0035t0004g0150 a0003c0035t0004g0151 a0005c0062t0026g0250 others(1): Show |
4 | HG01192.hp1 HG02257.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-136-3673_-136-366 others(16): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094815 | |||||||
chr9:115094815 | CTCTGTGT others(9): Show |
C | 10 | a0004c0004t0002g0297 a0009c0092t0002g0093 a0012c0012t0006g0057 others(7): Show |
10 | HG01978.hp1 HG02630.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.-136-3677_-136-366 others(20): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094815 | |||||||
chr9:115094817 | C | G | 50 | a0001c0002t0001g0290 a0001c0009t0015g0350 a0002c0001t0001g0104 others(47): Show |
50 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.-136-3663G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094817 | |||||||
chr9:115094867 | G | C | 331 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(328): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.-136-3713C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094867 | |||||||
chr9:115094867 | G | GTC | 15 | a0002c0001t0001g0104 a0003c0003t0001g0216 a0004c0004t0002g0205 others(12): Show |
15 | HG00558.hp1 HG01496.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.-136-3714_-136-371 others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094867 | |||||||
chr9:115094867 | G | GTGTC | 9 | a0003c0077t0004g0356 a0007c0006t0007g0037 a0007c0006t0017g0039 others(6): Show |
9 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(6): Show |
intron_variant | MODIFIER | c.-136-3714_-136-371 others(8): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094867 | |||||||
chr9:115095208 | A | G | 346 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(343): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.-136-4054T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095208 | |||||||
chr9:115095210 | G | A | 88 | a0001c0009t0001g0101 a0001c0009t0001g0123 a0001c0009t0001g0155 others(85): Show |
90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.-136-4056C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095210 | |||||||
chr9:115095211 | C | T | 142 | a0001c0009t0001g0101 a0001c0009t0001g0123 a0001c0009t0001g0155 others(139): Show |
145 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.-136-4057G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095211 | |||||||
chr9:115095212 | G | A | 1 | a0005c0103t0012g0091 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-136-4058C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095212 | |||||||
chr9:115095437 | G | A | 3 | a0020c0025t0001g0347 a0020c0025t0001g0348 a0020c0025t0001g0349 |
3 | HG01243.hp1 HG02055.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-136-4283C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095437 | |||||||
chr9:115095444 | GTGTATAT others(207): Show |
G | 44 | a0001c0009t0001g0244 a0003c0003t0001g0229 a0003c0003t0001g0239 others(41): Show |
45 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.-136-4504_-136-429 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095444 | |||||||
chr9:115095446 | G | GTA | 3 | a0003c0035t0004g0150 a0003c0035t0004g0151 a0005c0061t0002g0257 |
3 | HG02559.hp2 HG02895.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-136-4294_-136-429 others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095446 | |||||||
chr9:115095448 | ATATATAT others(173): Show |
A | 5 | a0002c0001t0002g0169 a0002c0001t0002g0173 a0002c0001t0002g0185 others(2): Show |
5 | HG00280.hp1 HG00642.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.-136-4474_-136-429 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095448 | |||||||
chr9:115095450 | ATATATAT others(151): Show |
A | 41 | a0001c0002t0001g0192 a0001c0009t0001g0101 a0001c0009t0001g0155 others(38): Show |
42 | HG00733.hp2 HG01081.hp2 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.-136-4454_-136-429 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095450 | |||||||
chr9:115095450 | ATATATAT others(225): Show |
A | 2 | a0002c0098t0002g0147 a0009c0099t0001g0146 |
2 | HG02071.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.-136-4528_-136-429 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095450 | |||||||
chr9:115095452 | ATATATGT others(149): Show |
A | 5 | a0005c0062t0026g0250 a0020c0025t0001g0347 a0020c0025t0001g0348 others(2): Show |
5 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.-136-4454_-136-429 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095452 | |||||||
chr9:115095472 | ATATATAT others(129): Show |
A | 1 | a0002c0001t0002g0171 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-136-4454_-136-431 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095472 | |||||||
chr9:115095472 | ATATATAT others(215): Show |
A | 23 | a0001c0002t0001g0134 a0001c0002t0001g0138 a0001c0002t0001g0141 others(20): Show |
23 | HG02071.hp1 HG02080.hp2 HG02698.hp2 others(20): Show |
intron_variant | MODIFIER | c.-136-4540_-136-431 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095472 | |||||||
chr9:115095480 | G | GTA | 6 | a0016c0022t0004g0252 a0016c0022t0004g0261 a0026c0046t0004g0339 others(3): Show |
6 | HG02145.hp1 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-136-4328_-136-432 others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095480 | |||||||
chr9:115095482 | A | G | 1 | a0027c0070t0002g0352 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-136-4328T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095482 | |||||||
chr9:115095482 | ATATATAT others(3): Show |
A | 2 | a0010c0008t0003g0024 a0010c0008t0021g0011 |
2 | NA18972.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.-136-4338_-136-432 others(14): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095482 | |||||||
chr9:115095482 | ATATATAT others(205): Show |
A | 2 | a0004c0004t0002g0325 a0004c0018t0004g0213 |
2 | HG04115.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-136-4540_-136-432 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095482 | |||||||
chr9:115095494 | ATATATAT others(193): Show |
A | 131 | a0001c0002t0001g0128 a0001c0002t0001g0267 a0001c0002t0001g0268 others(128): Show |
132 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.-136-4540_-136-434 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095494 | |||||||
chr9:115095496 | ATATATGT others(105): Show |
A | 2 | a0003c0035t0004g0150 a0003c0035t0004g0151 |
2 | HG02559.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-136-4454_-136-434 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095496 | |||||||
chr9:115095496 | ATATATGT others(191): Show |
A | 1 | a0003c0077t0004g0356 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-136-4540_-136-434 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095496 | |||||||
chr9:115095502 | G | A | 1 | a0005c0061t0002g0257 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-136-4348C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095502 | |||||||
chr9:115095502 | GTATATAT others(109): Show |
G | 1 | a0008c0005t0001g0121 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-136-4464_-136-434 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095502 | |||||||
chr9:115095502 | GTATATAT others(153): Show |
G | 41 | a0001c0009t0001g0123 a0001c0009t0002g0117 a0001c0009t0010g0105 others(38): Show |
42 | HG00099.hp2 HG00140.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.-136-4508_-136-434 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095502 | |||||||
chr9:115095504 | A | G | 1 | a0005c0061t0002g0257 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-136-4350T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095504 | |||||||
chr9:115095510 | ATATGTAT others(143): Show |
A | 40 | a0002c0001t0007g0018 a0007c0006t0003g0028 a0007c0006t0003g0052 others(37): Show |
41 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.-136-4506_-136-435 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095510 | |||||||
chr9:115095514 | GTATATAT others(119): Show |
G | 3 | a0026c0046t0004g0339 a0026c0046t0004g0340 a0036c0104t0028g0341 |
3 | HG02145.hp1 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-136-4486_-136-436 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095514 | |||||||
chr9:115095516 | ATATATAT others(171): Show |
A | 1 | a0005c0103t0012g0091 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-136-4540_-136-436 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095516 | |||||||
chr9:115095524 | GTA | G | 3 | a0016c0022t0004g0252 a0016c0022t0004g0261 a0042c0063t0012g0149 |
3 | HG02647.hp1 HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-136-4372_-136-437 others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095524 | |||||||
chr9:115095524 | GTATATAT others(131): Show |
G | 1 | a0038c0079t0023g0193 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-136-4508_-136-437 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095524 | |||||||
chr9:115095524 | GTATATAT others(153): Show |
G | 1 | a0009c0019t0011g0194 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-136-4530_-136-437 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095524 | |||||||
chr9:115095532 | ATATGTAT others(143): Show |
A | 1 | a0010c0008t0003g0034 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-136-4528_-136-437 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095532 | |||||||
chr9:115095532 | ATATGTAT others(165): Show |
A | 1 | a0049c0097t0002g0183 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-136-4550_-136-437 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095532 | |||||||
chr9:115095536 | G | GTATATAT others(5): Show |
1 | a0021c0028t0012g0260 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-136-4394_-136-438 others(16): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095536 | |||||||
chr9:115095538 | ATATATAT others(105): Show |
A | 1 | a0005c0061t0002g0257 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-136-4496_-136-438 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095538 | |||||||
chr9:115095548 | ATATATAT others(149): Show |
A | 1 | a0002c0001t0002g0190 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-136-4550_-136-439 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095548 | |||||||
chr9:115095556 | GTATATAT others(99): Show |
G | 2 | a0010c0008t0003g0024 a0010c0008t0021g0011 |
2 | NA18972.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.-136-4508_-136-440 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095556 | |||||||
chr9:115095568 | ATATATAT others(119): Show |
A | 3 | a0016c0022t0004g0252 a0016c0022t0004g0261 a0042c0063t0012g0149 |
3 | HG02647.hp1 HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-136-4540_-136-441 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095568 | |||||||
chr9:115095576 | G | GTATATAT others(47): Show |
2 | a0021c0028t0012g0258 a0021c0028t0012g0259 |
2 | HG01496.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-136-4423_-136-442 others(58): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095576 | |||||||
chr9:115095598 | ATATATAT others(3): Show |
A | 1 | a0024c0082t0004g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-136-4454_-136-444 others(14): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095598 | |||||||
chr9:115095606 | A | G | 1 | a0024c0083t0001g0056 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-136-4452T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095606 | |||||||
chr9:115095608 | G | A | 1 | a0024c0083t0001g0056 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-136-4454C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095608 | |||||||
chr9:115095608 | G | GTA | 3 | a0021c0028t0012g0258 a0021c0028t0012g0259 a0021c0028t0012g0260 |
3 | HG01496.hp1 HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-136-4456_-136-445 others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095608 | |||||||
chr9:115095640 | A | ATATATAT others(35): Show |
1 | a0021c0028t0012g0260 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-136-4528_-136-448 others(46): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095640 | |||||||
chr9:115095650 | G | GTA | 7 | a0003c0035t0004g0150 a0003c0035t0004g0151 a0005c0062t0026g0250 others(4): Show |
7 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.-136-4498_-136-449 others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095650 | |||||||
chr9:115095662 | A | G | 40 | a0002c0001t0007g0018 a0007c0006t0003g0028 a0007c0006t0003g0052 others(37): Show |
41 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.-136-4508T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095662 | |||||||
chr9:115095670 | A | G | 3 | a0003c0035t0004g0150 a0003c0035t0004g0151 a0005c0061t0002g0257 |
3 | HG02559.hp2 HG02895.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-136-4516T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095670 | |||||||
chr9:115095671 | T | C | 10 | a0014c0016t0006g0069 a0014c0016t0006g0071 a0014c0016t0006g0072 others(7): Show |
10 | HG00642.hp2 HG00741.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.-136-4517A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095671 | |||||||
chr9:115095672 | G | A | 3 | a0003c0035t0004g0150 a0003c0035t0004g0151 a0005c0061t0002g0257 |
3 | HG02559.hp2 HG02895.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-136-4518C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095672 | |||||||
chr9:115095684 | A | G | 1 | a0010c0008t0003g0034 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-136-4530T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095684 | |||||||
chr9:115095692 | A | G | 5 | a0002c0098t0002g0147 a0009c0099t0001g0146 a0026c0046t0004g0339 others(2): Show |
5 | HG02071.hp2 HG02145.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-136-4538T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095692 | |||||||
chr9:115095694 | G | A | 5 | a0002c0098t0002g0147 a0009c0099t0001g0146 a0026c0046t0004g0339 others(2): Show |
5 | HG02071.hp2 HG02145.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-136-4540C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095694 | |||||||
chr9:115095702 | A | G | 1 | a0003c0077t0004g0356 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-136-4548T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095702 | |||||||
chr9:115095704 | G | A | 1 | a0003c0077t0004g0356 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-136-4550C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095704 | |||||||
chr9:115095749 | A | G | 2 | a0005c0034t0002g0197 a0005c0034t0002g0198 |
2 | HG01109.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.-136-4595T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095749 | |||||||
chr9:115095787 | T | A | 8 | a0003c0035t0004g0150 a0003c0035t0004g0151 a0005c0061t0002g0257 others(5): Show |
8 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-136-4633A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095787 | |||||||
chr9:115095866 | G | A | 14 | a0003c0003t0001g0247 a0003c0003t0001g0283 a0003c0003t0001g0310 others(11): Show |
14 | HG00423.hp1 HG00597.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-136-4712C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095866 | |||||||
chr9:115096019 | G | A | 8 | a0010c0008t0003g0023 a0010c0008t0003g0024 a0010c0008t0003g0027 others(5): Show |
8 | NA18942.hp1 NA18956.hp1 NA18972.hp1 others(5): Show |
intron_variant | MODIFIER | c.-136-4865C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115096019 | |||||||
chr9:115096481 | G | A | 6 | a0016c0022t0004g0252 a0016c0022t0004g0261 a0026c0046t0004g0339 others(3): Show |
6 | HG02145.hp1 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-136-5327C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115096481 | |||||||
chr9:115096486 | C | T | 1 | a0004c0004t0002g0233 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-136-5332G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115096486 | |||||||
chr9:115096597 | G | A | 8 | a0009c0092t0002g0093 a0012c0012t0006g0057 a0012c0012t0006g0058 others(5): Show |
8 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-136-5443C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115096597 | |||||||
chr9:115096626 | GA | G | 134 | a0001c0009t0001g0101 a0001c0009t0001g0123 a0001c0009t0001g0155 others(131): Show |
137 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.-136-5473delT | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115096626 | |||||||
chr9:115096638 | A | G | 1 | a0008c0005t0001g0115 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-136-5484T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115096638 | |||||||
chr9:115096663 | C | A | 8 | a0003c0035t0004g0150 a0003c0035t0004g0151 a0005c0061t0002g0257 others(5): Show |
8 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-136-5509G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115096663 | |||||||
chr9:115096717 | T | C | 1 | a0001c0011t0001g0114 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-136-5563A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115096717 | |||||||
chr9:115096989 | G | A | 7 | a0004c0051t0004g0342 a0005c0034t0002g0197 a0005c0034t0002g0198 others(4): Show |
7 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136-5835C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115096989 | |||||||
chr9:115097006 | A | G | 8 | a0009c0092t0002g0093 a0012c0012t0006g0057 a0012c0012t0006g0058 others(5): Show |
8 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-136-5852T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115097006 | |||||||
chr9:115097019 | G | A | 1 | a0004c0051t0004g0342 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-136-5865C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115097019 | |||||||
chr9:115097261 | G | T | 6 | a0005c0017t0001g0081 a0005c0017t0002g0076 a0005c0017t0002g0078 others(3): Show |
6 | HG01346.hp2 HG03017.hp1 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.-136-6107C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115097261 | |||||||
chr9:115097362 | G | A | 46 | a0002c0001t0007g0018 a0007c0006t0003g0028 a0007c0006t0003g0052 others(43): Show |
47 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.-136-6208C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115097362 | |||||||
chr9:115097616 | G | A | 1 | a0006c0007t0005g0270 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-136-6462C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115097616 | |||||||
chr9:115097668 | G | T | 8 | a0003c0035t0004g0150 a0003c0035t0004g0151 a0005c0061t0002g0257 others(5): Show |
8 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-136-6514C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115097668 | |||||||
chr9:115097796 | G | C | 1 | a0006c0007t0024g0212 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-136-6642C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115097796 | |||||||
chr9:115097992 | A | G | 2 | a0005c0017t0002g0079 a0005c0066t0002g0251 |
2 | HG03017.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-136-6838T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115097992 | |||||||
chr9:115098016 | C | T | 138 | a0001c0002t0001g0128 a0001c0002t0001g0267 a0001c0002t0001g0268 others(135): Show |
139 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-136-6862G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115098016 | |||||||
chr9:115098169 | A | C | 5 | a0001c0009t0002g0117 a0008c0005t0001g0115 a0008c0005t0001g0118 others(2): Show |
5 | HG00099.hp2 HG01070.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.-136-7015T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115098169 | |||||||
chr9:115098180 | G | A | 24 | a0001c0002t0001g0134 a0001c0002t0001g0138 a0001c0002t0001g0141 others(21): Show |
24 | HG02071.hp1 HG02071.hp2 HG02080.hp2 others(21): Show |
intron_variant | MODIFIER | c.-136-7026C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115098180 | |||||||
chr9:115098189 | C | T | 137 | a0001c0002t0001g0192 a0001c0009t0001g0101 a0001c0009t0001g0123 others(134): Show |
140 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.-136-7035G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115098189 | |||||||
chr9:115098229 | C | T | 67 | a0001c0002t0001g0134 a0001c0002t0001g0138 a0001c0002t0001g0141 others(64): Show |
68 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.-136-7075G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115098229 | |||||||
chr9:115098285 | G | A | 1 | a0031c0053t0018g0245 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-136-7131C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115098285 | |||||||
chr9:115098672 | G | A | 217 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(214): Show |
219 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.-136-7518C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115098672 | |||||||
chr9:115098762 | C | T | 1 | a0005c0017t0002g0078 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-136-7608G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115098762 | |||||||
chr9:115098764 | C | A | 1 | a0003c0077t0004g0356 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-136-7610G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115098764 | |||||||
chr9:115098938 | A | ATTT | 6 | a0005c0037t0004g0152 a0012c0012t0006g0062 a0022c0033t0001g0126 others(3): Show |
6 | HG00323.hp1 HG01884.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.-136-7787_-136-778 others(7): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115098938 | |||||||
chr9:115098938 | A | ATTTT | 45 | a0001c0009t0001g0244 a0003c0003t0001g0229 a0003c0003t0001g0239 others(42): Show |
46 | HG00609.hp1 HG00621.hp2 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.-136-7788_-136-778 others(8): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115098938 | |||||||
chr9:115098938 | A | ATTTTT | 103 | a0001c0002t0001g0267 a0001c0002t0001g0268 a0001c0002t0001g0275 others(100): Show |
104 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.-136-7789_-136-778 others(9): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115098938 | |||||||
chr9:115098938 | A | ATTTTTT | 19 | a0001c0002t0010g0288 a0003c0003t0001g0279 a0003c0003t0003g0053 others(16): Show |
19 | HG00280.hp2 HG01175.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.-136-7790_-136-778 others(10): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115098938 | |||||||
chr9:115098938 | A | ATTTTTTT | 20 | a0001c0002t0001g0134 a0001c0002t0001g0141 a0001c0002t0001g0142 others(17): Show |
20 | HG02071.hp1 HG02071.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.-136-7791_-136-778 others(11): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115098938 | |||||||
chr9:115098938 | A | T | 2 | a0005c0067t0002g0359 a0043c0047t0001g0358 |
2 | HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-136-7784T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115098938 | |||||||
chr9:115098938 | ATT | A | 120 | a0001c0002t0001g0192 a0001c0009t0001g0101 a0001c0009t0001g0123 others(117): Show |
123 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.-136-7786_-136-778 others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115098938 | |||||||
chr9:115098938 | ATTT | A | 17 | a0001c0009t0002g0117 a0002c0001t0002g0092 a0002c0001t0006g0120 others(14): Show |
17 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(14): Show |
intron_variant | MODIFIER | c.-136-7787_-136-778 others(7): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115098938 | |||||||
chr9:115098938 | ATTTT | A | 9 | a0001c0002t0001g0128 a0001c0002t0001g0321 a0001c0002t0001g0322 others(6): Show |
9 | HG01123.hp2 HG02258.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-136-7788_-136-778 others(8): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115098938 | |||||||
chr9:115099192 | G | A | 220 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(217): Show |
222 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.-136-8038C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115099192 | |||||||
chr9:115099261 | G | C | 46 | a0001c0009t0001g0244 a0003c0003t0001g0229 a0003c0003t0001g0239 others(43): Show |
47 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.-136-8107C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115099261 | |||||||
chr9:115099916 | A | C | 5 | a0003c0077t0004g0356 a0015c0021t0004g0129 a0015c0021t0004g0254 others(2): Show |
5 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-136-8762T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115099916 | |||||||
chr9:115099931 | G | A | 136 | a0001c0002t0001g0192 a0001c0009t0001g0101 a0001c0009t0001g0123 others(133): Show |
139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.-136-8777C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115099931 | |||||||
chr9:115099932 | A | T | 136 | a0001c0002t0001g0192 a0001c0009t0001g0101 a0001c0009t0001g0123 others(133): Show |
139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.-136-8778T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115099932 | |||||||
chr9:115100006 | A | G | 1 | a0005c0067t0002g0359 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-136-8852T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115100006 | |||||||
chr9:115100058 | C | T | 1 | a0006c0007t0022g0054 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-136-8904G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115100058 | |||||||
chr9:115100227 | A | G | 169 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(166): Show |
170 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.-136-9073T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115100227 | |||||||
chr9:115100646 | G | A | 1 | a0015c0021t0004g0255 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-136-9492C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115100646 | |||||||
chr9:115100656 | G | A | 1 | a0002c0001t0002g0159 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-136-9502C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115100656 | |||||||
chr9:115100658 | C | T | 1 | a0001c0024t0001g0133 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-136-9504G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115100658 | |||||||
chr9:115100720 | C | T | 25 | a0001c0002t0001g0134 a0001c0002t0001g0138 a0001c0002t0001g0141 others(22): Show |
25 | HG02071.hp1 HG02071.hp2 HG02080.hp2 others(22): Show |
intron_variant | MODIFIER | c.-136-9566G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115100720 | |||||||
chr9:115100739 | T | G | 6 | a0007c0006t0003g0052 a0007c0006t0007g0001 a0007c0006t0007g0051 others(3): Show |
7 | NA18947.hp2 NA18975.hp1 NA19000.hp1 others(4): Show |
intron_variant | MODIFIER | c.-136-9585A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115100739 | |||||||
chr9:115100775 | G | C | 7 | a0005c0103t0012g0091 a0016c0022t0004g0252 a0016c0022t0004g0261 others(4): Show |
7 | HG02145.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136-9621C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115100775 | |||||||
chr9:115100808 | A | G | 3 | a0016c0022t0004g0252 a0016c0022t0004g0261 a0042c0063t0012g0149 |
3 | HG02647.hp1 HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-136-9654T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115100808 | |||||||
chr9:115100838 | A | G | 1 | a0003c0013t0001g0285 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-136-9684T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115100838 | |||||||
chr9:115100841 | C | T | 1 | a0002c0001t0002g0169 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-136-9687G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115100841 | |||||||
chr9:115100920 | A | T | 2 | a0003c0003t0001g0283 a0004c0004t0002g0284 |
2 | NA18968.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.-136-9766T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115100920 | |||||||
chr9:115101135 | C | T | 24 | a0001c0002t0001g0134 a0001c0002t0001g0138 a0001c0002t0001g0141 others(21): Show |
24 | HG02071.hp1 HG02071.hp2 HG02080.hp2 others(21): Show |
intron_variant | MODIFIER | c.-136-9981G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115101135 | |||||||
chr9:115101175 | G | A | 1 | a0008c0005t0001g0121 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-136-10021C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115101175 | |||||||
chr9:115101204 | C | G | 46 | a0002c0001t0007g0018 a0007c0006t0003g0028 a0007c0006t0003g0052 others(43): Show |
47 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.-136-10050G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115101204 | |||||||
chr9:115101275 | G | A | 1 | a0003c0013t0001g0282 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-136-10121C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115101275 | |||||||
chr9:115101328 | C | G | 9 | a0003c0035t0004g0150 a0003c0035t0004g0151 a0004c0051t0004g0342 others(6): Show |
9 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-136-10174G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115101328 | |||||||
chr9:115101345 | G | T | 3 | a0001c0002t0001g0138 a0001c0002t0001g0141 a0001c0002t0001g0142 |
3 | NA18956.hp2 NA18959.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.-136-10191C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115101345 | |||||||
chr9:115101405 | A | G | 83 | a0001c0002t0001g0134 a0001c0002t0001g0138 a0001c0002t0001g0141 others(80): Show |
84 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.-136-10251T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115101405 | |||||||
chr9:115101493 | G | A | 1 | a0002c0096t0002g0156 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-136-10339C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115101493 | |||||||
chr9:115101587 | A | T | 5 | a0007c0006t0003g0028 a0010c0008t0003g0013 a0010c0008t0003g0014 others(2): Show |
5 | HG00423.hp2 HG00558.hp1 HG00597.hp2 others(2): Show |
intron_variant | MODIFIER | c.-136-10433T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115101587 | |||||||
chr9:115101623 | A | T | 1 | a0002c0001t0002g0103 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-136-10469T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115101623 | |||||||
chr9:115101631 | A | G | 1 | a0002c0001t0002g0157 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-136-10477T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115101631 | |||||||
chr9:115101632 | T | C | 74 | a0001c0002t0001g0134 a0001c0002t0001g0138 a0001c0002t0001g0141 others(71): Show |
75 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.-136-10478A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115101632 | |||||||
chr9:115101644 | C | T | 3 | a0016c0022t0004g0252 a0016c0022t0004g0261 a0042c0063t0012g0149 |
3 | HG02647.hp1 HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-136-10490G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115101644 | |||||||
chr9:115101675 | A | T | 9 | a0009c0092t0002g0093 a0012c0012t0006g0057 a0012c0012t0006g0058 others(6): Show |
9 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.-136-10521T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115101675 | |||||||
chr9:115101676 | A | G | 2 | a0004c0018t0004g0224 a0006c0007t0005g0204 |
2 | HG02145.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-136-10522T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115101676 | |||||||
chr9:115101805 | A | C | 354 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(351): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.-136-10651T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115101805 | |||||||
chr9:115101870 | G | T | 354 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(351): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.-136-10716C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115101870 | |||||||
chr9:115102068 | T | C | 1 | a0002c0001t0002g0100 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-136-10914A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115102068 | |||||||
chr9:115102078 | C | T | 1 | a0001c0002t0001g0128 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-136-10924G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115102078 | |||||||
chr9:115102207 | A | G | 1 | a0003c0013t0001g0282 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-136-11053T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115102207 | |||||||
chr9:115102330 | C | T | 215 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(212): Show |
217 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.-136-11176G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115102330 | |||||||
chr9:115102398 | A | G | 214 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(211): Show |
216 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.-136-11244T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115102398 | |||||||
chr9:115102646 | G | T | 20 | a0001c0009t0001g0244 a0003c0003t0001g0229 a0003c0003t0001g0239 others(17): Show |
21 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.-136-11492C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115102646 | |||||||
chr9:115102706 | A | G | 2 | a0001c0009t0001g0101 a0040c0088t0002g0097 |
2 | HG02602.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.-136-11552T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115102706 | |||||||
chr9:115102927 | G | A | 7 | a0004c0051t0004g0342 a0005c0034t0002g0197 a0005c0034t0002g0198 others(4): Show |
7 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136-11773C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115102927 | |||||||
chr9:115102996 | C | G | 132 | a0001c0002t0001g0128 a0001c0002t0001g0267 a0001c0002t0001g0268 others(129): Show |
133 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.-136-11842G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115102996 | |||||||
chr9:115103097 | G | A | 145 | a0001c0002t0001g0128 a0001c0002t0001g0267 a0001c0002t0001g0268 others(142): Show |
146 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.-136-11943C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115103097 | |||||||
chr9:115103200 | T | C | 1 | a0006c0007t0005g0324 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-136-12046A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115103200 | |||||||
chr9:115103217 | G | A | 1 | a0005c0062t0026g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-136-12063C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115103217 | |||||||
chr9:115103224 | C | T | 2 | a0010c0008t0003g0027 a0010c0008t0003g0032 |
2 | NA19010.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.-136-12070G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115103224 | |||||||
chr9:115103227 | T | C | 2 | a0005c0034t0002g0197 a0005c0034t0002g0198 |
2 | HG01109.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.-136-12073A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115103227 | |||||||
chr9:115103363 | A | G | 354 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(351): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.-136-12209T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115103363 | |||||||
chr9:115103383 | T | A | 2 | a0002c0001t0002g0167 a0009c0031t0001g0166 |
2 | NA19002.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.-136-12229A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115103383 | |||||||
chr9:115103547 | A | G | 169 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(166): Show |
170 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.-136-12393T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115103547 | |||||||
chr9:115103549 | A | G | 13 | a0003c0003t0001g0344 a0003c0003t0004g0337 a0005c0037t0004g0271 others(10): Show |
13 | HG02109.hp2 HG02258.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136-12395T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115103549 | |||||||
chr9:115103666 | G | A | 7 | a0003c0027t0002g0214 a0003c0027t0002g0215 a0003c0027t0002g0218 others(4): Show |
7 | HG02895.hp1 HG02897.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-136-12512C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115103666 | |||||||
chr9:115103952 | G | A | 1 | a0002c0001t0002g0168 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-136-12798C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115103952 | |||||||
chr9:115103957 | A | G | 46 | a0002c0001t0007g0018 a0007c0006t0003g0028 a0007c0006t0003g0052 others(43): Show |
47 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.-136-12803T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115103957 | |||||||
chr9:115103966 | A | G | 1 | a0002c0001t0002g0082 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-136-12812T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115103966 | |||||||
chr9:115103967 | GATCC | G | 38 | a0001c0009t0001g0123 a0001c0009t0002g0117 a0001c0009t0010g0105 others(35): Show |
39 | HG00099.hp2 HG00140.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.-136-12817_-136-12 others(10): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115103967 | |||||||
chr9:115103976 | A | G | 1 | a0008c0005t0001g0102 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-136-12822T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115103976 | |||||||
chr9:115104039 | A | G | 8 | a0003c0035t0004g0150 a0003c0035t0004g0151 a0005c0061t0002g0257 others(5): Show |
8 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-136-12885T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115104039 | |||||||
chr9:115104145 | A | G | 169 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(166): Show |
170 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.-136-12991T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115104145 | |||||||
chr9:115104433 | G | A | 1 | a0004c0004t0002g0325 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-136-13279C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115104433 | |||||||
chr9:115104467 | A | G | 1 | a0007c0006t0017g0012 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-136-13313T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115104467 | |||||||
chr9:115104667 | C | T | 132 | a0001c0002t0001g0192 a0001c0009t0001g0123 a0001c0009t0001g0155 others(129): Show |
135 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.-137+13315G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115104667 | |||||||
chr9:115104699 | T | C | 1 | a0037c0064t0014g0343 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-137+13283A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115104699 | |||||||
chr9:115104809 | G | C | 1 | a0002c0001t0002g0168 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-137+13173C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115104809 | |||||||
chr9:115104894 | C | T | 1 | a0005c0103t0012g0091 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-137+13088G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115104894 | |||||||
chr9:115105113 | A | T | 3 | a0001c0002t0001g0134 a0001c0002t0013g0135 a0002c0020t0002g0148 |
3 | HG02071.hp1 NA18747.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.-137+12869T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115105113 | |||||||
chr9:115105228 | C | T | 8 | a0003c0035t0004g0150 a0003c0035t0004g0151 a0005c0061t0002g0257 others(5): Show |
8 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-137+12754G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115105228 | |||||||
chr9:115105270 | C | G | 1 | a0003c0035t0004g0150 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-137+12712G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115105270 | |||||||
chr9:115105298 | G | T | 6 | a0016c0022t0004g0252 a0016c0022t0004g0261 a0026c0046t0004g0339 others(3): Show |
6 | HG02145.hp1 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-137+12684C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115105298 | |||||||
chr9:115105679 | G | T | 133 | a0001c0002t0001g0192 a0001c0009t0001g0123 a0001c0009t0001g0155 others(130): Show |
136 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.-137+12303C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115105679 | |||||||
chr9:115105740 | G | C | 6 | a0003c0003t0004g0337 a0005c0037t0004g0271 a0005c0067t0002g0359 others(3): Show |
6 | HG02109.hp2 HG02280.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-137+12242C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115105740 | |||||||
chr9:115105844 | T | C | 1 | a0001c0009t0001g0244 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-137+12138A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115105844 | |||||||
chr9:115105948 | G | A | 1 | a0047c0060t0014g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-137+12034C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115105948 | |||||||
chr9:115106040 | T | C | 214 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(211): Show |
216 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.-137+11942A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115106040 | |||||||
chr9:115106063 | G | C | 8 | a0003c0027t0002g0214 a0003c0027t0002g0215 a0003c0027t0002g0218 others(5): Show |
8 | HG02895.hp1 HG02897.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.-137+11919C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115106063 | |||||||
chr9:115106064 | A | G | 9 | a0003c0003t0001g0279 a0003c0003t0019g0273 a0003c0003t0019g0360 others(6): Show |
9 | HG01081.hp1 HG01175.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.-137+11918T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115106064 | |||||||
chr9:115106130 | T | G | 3 | a0022c0033t0001g0126 a0022c0033t0001g0127 a0022c0033t0001g0338 |
3 | HG01884.hp2 HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-137+11852A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115106130 | |||||||
chr9:115106419 | A | C | 24 | a0001c0002t0001g0134 a0001c0002t0001g0138 a0001c0002t0001g0141 others(21): Show |
24 | HG02071.hp1 HG02071.hp2 HG02080.hp2 others(21): Show |
intron_variant | MODIFIER | c.-137+11563T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115106419 | |||||||
chr9:115106863 | G | C | 1 | a0008c0005t0002g0187 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-137+11119C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115106863 | |||||||
chr9:115106897 | A | G | 24 | a0001c0002t0001g0134 a0001c0002t0001g0138 a0001c0002t0001g0141 others(21): Show |
24 | HG02071.hp1 HG02071.hp2 HG02080.hp2 others(21): Show |
intron_variant | MODIFIER | c.-137+11085T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115106897 | |||||||
chr9:115106954 | G | A | 4 | a0003c0003t0001g0229 a0003c0003t0001g0239 a0003c0003t0001g0240 others(1): Show |
4 | HG00609.hp1 NA18953.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.-137+11028C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115106954 | |||||||
chr9:115107077 | AT | A | 35 | a0001c0009t0001g0244 a0003c0003t0001g0229 a0003c0003t0001g0239 others(32): Show |
36 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.-137+10904delA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115107077 | |||||||
chr9:115107138 | T | G | 67 | a0001c0002t0001g0134 a0001c0002t0001g0138 a0001c0002t0001g0141 others(64): Show |
68 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.-137+10844A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115107138 | |||||||
chr9:115107278 | T | C | 4 | a0015c0021t0004g0129 a0015c0021t0004g0254 a0015c0021t0004g0255 others(1): Show |
4 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-137+10704A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115107278 | |||||||
chr9:115107392 | A | G | 15 | a0001c0002t0001g0192 a0001c0009t0010g0163 a0001c0011t0001g0161 others(12): Show |
15 | HG02040.hp2 HG02080.hp1 HG02083.hp1 others(12): Show |
intron_variant | MODIFIER | c.-137+10590T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115107392 | |||||||
chr9:115107405 | T | G | 169 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(166): Show |
170 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.-137+10577A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115107405 | |||||||
chr9:115107591 | C | T | 8 | a0003c0035t0004g0150 a0003c0035t0004g0151 a0005c0061t0002g0257 others(5): Show |
8 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-137+10391G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115107591 | |||||||
chr9:115107651 | C | T | 132 | a0001c0002t0001g0128 a0001c0002t0001g0267 a0001c0002t0001g0268 others(129): Show |
133 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.-137+10331G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115107651 | |||||||
chr9:115107804 | A | G | 2 | a0028c0036t0002g0202 a0028c0036t0002g0203 |
2 | HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-137+10178T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115107804 | |||||||
chr9:115107861 | A | T | 1 | a0004c0051t0004g0342 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-137+10121T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115107861 | |||||||
chr9:115107951 | C | T | 132 | a0001c0002t0001g0128 a0001c0002t0001g0267 a0001c0002t0001g0268 others(129): Show |
133 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.-137+10031G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115107951 | |||||||
chr9:115107964 | G | A | 1 | a0001c0009t0001g0188 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-137+10018C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115107964 | |||||||
chr9:115108079 | A | G | 3 | a0022c0033t0001g0126 a0022c0033t0001g0127 a0022c0033t0001g0338 |
3 | HG01884.hp2 HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-137+9903T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115108079 | |||||||
chr9:115108240 | C | T | 2 | a0005c0034t0002g0197 a0005c0034t0002g0198 |
2 | HG01109.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.-137+9742G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115108240 | |||||||
chr9:115108494 | G | T | 8 | a0009c0092t0002g0093 a0012c0012t0006g0057 a0012c0012t0006g0058 others(5): Show |
8 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-137+9488C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115108494 | |||||||
chr9:115108500 | T | G | 2 | a0015c0021t0004g0129 a0015c0021t0004g0256 |
2 | HG01891.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-137+9482A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115108500 | |||||||
chr9:115108549 | T | A | 1 | a0001c0009t0001g0123 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-137+9433A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115108549 | |||||||
chr9:115108561 | C | T | 1 | a0004c0004t0002g0278 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-137+9421G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115108561 | |||||||
chr9:115108656 | G | T | 5 | a0001c0002t0001g0267 a0001c0002t0001g0268 a0001c0002t0001g0275 others(2): Show |
5 | HG01069.hp1 HG01074.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.-137+9326C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115108656 | |||||||
chr9:115108705 | C | A | 8 | a0003c0035t0004g0150 a0003c0035t0004g0151 a0005c0061t0002g0257 others(5): Show |
8 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-137+9277G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115108705 | |||||||
chr9:115109149 | A | G | 1 | a0002c0001t0002g0100 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-137+8833T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115109149 | |||||||
chr9:115109458 | A | G | 1 | a0001c0002t0001g0268 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-137+8524T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115109458 | |||||||
chr9:115109790 | C | T | 1 | a0004c0004t0002g0233 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-137+8192G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115109790 | |||||||
chr9:115109799 | T | G | 7 | a0005c0103t0012g0091 a0016c0022t0004g0252 a0016c0022t0004g0261 others(4): Show |
7 | HG02145.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-137+8183A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115109799 | |||||||
chr9:115109897 | A | T | 2 | a0001c0009t0001g0155 a0001c0009t0001g0160 |
2 | NA18939.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.-137+8085T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115109897 | |||||||
chr9:115109978 | T | A | 24 | a0001c0002t0001g0134 a0001c0002t0001g0138 a0001c0002t0001g0141 others(21): Show |
24 | HG02071.hp1 HG02071.hp2 HG02080.hp2 others(21): Show |
intron_variant | MODIFIER | c.-137+8004A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115109978 | |||||||
chr9:115110004 | T | C | 15 | a0003c0077t0004g0356 a0014c0016t0006g0069 a0014c0016t0006g0071 others(12): Show |
15 | HG00642.hp2 HG00741.hp2 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.-137+7978A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115110004 | |||||||
chr9:115110110 | C | A | 2 | a0010c0008t0003g0027 a0010c0008t0003g0032 |
2 | NA19010.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.-137+7872G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115110110 | |||||||
chr9:115110123 | G | A | 8 | a0003c0035t0004g0150 a0003c0035t0004g0151 a0005c0061t0002g0257 others(5): Show |
8 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-137+7859C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115110123 | |||||||
chr9:115110284 | C | T | 4 | a0004c0045t0002g0230 a0004c0045t0002g0231 a0006c0015t0002g0241 others(1): Show |
4 | HG00741.hp1 HG01358.hp2 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.-137+7698G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115110284 | |||||||
chr9:115110417 | GGTTGCTG others(18): Show |
G | 7 | a0005c0103t0012g0091 a0016c0022t0004g0252 a0016c0022t0004g0261 others(4): Show |
7 | HG02145.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-137+7540_-137+756 others(29): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115110417 | |||||||
chr9:115110421 | G | T | 8 | a0003c0035t0004g0150 a0003c0035t0004g0151 a0005c0061t0002g0257 others(5): Show |
8 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-137+7561C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115110421 | |||||||
chr9:115110500 | G | A | 1 | a0021c0028t0012g0260 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-137+7482C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115110500 | |||||||
chr9:115110564 | A | G | 19 | a0001c0009t0001g0244 a0003c0003t0001g0229 a0003c0003t0001g0239 others(16): Show |
20 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.-137+7418T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115110564 | |||||||
chr9:115110737 | G | A | 1 | a0001c0002t0008g0144 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-137+7245C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115110737 | |||||||
chr9:115110754 | G | C | 1 | a0004c0050t0014g0345 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-137+7228C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115110754 | |||||||
chr9:115110878 | A | AT | 8 | a0005c0034t0002g0197 a0005c0034t0002g0198 a0009c0044t0001g0335 others(5): Show |
8 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.-137+7103dupA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115110878 | |||||||
chr9:115110878 | AT | A | 280 | a0001c0002t0001g0128 a0001c0002t0001g0192 a0001c0002t0001g0267 others(277): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.-137+7103delA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115110878 | |||||||
chr9:115110878 | ATT | A | 6 | a0001c0009t0015g0124 a0001c0009t0015g0350 a0002c0001t0002g0158 others(3): Show |
6 | HG00738.hp2 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-137+7102_-137+710 others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115110878 | |||||||
chr9:115110948 | C | T | 1 | a0002c0001t0002g0098 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-137+7034G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115110948 | |||||||
chr9:115110958 | C | T | 1 | a0003c0013t0001g0272 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-137+7024G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115110958 | |||||||
chr9:115110966 | G | A | 6 | a0007c0006t0003g0052 a0007c0006t0007g0001 a0007c0006t0007g0051 others(3): Show |
7 | NA18947.hp2 NA18975.hp1 NA19000.hp1 others(4): Show |
intron_variant | MODIFIER | c.-137+7016C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115110966 | |||||||
chr9:115111046 | A | T | 1 | a0011c0010t0001g0064 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-137+6936T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111046 | |||||||
chr9:115111071 | G | A | 1 | a0001c0002t0001g0327 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-137+6911C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111071 | |||||||
chr9:115111072 | G | A | 138 | a0001c0002t0001g0128 a0001c0002t0001g0267 a0001c0002t0001g0268 others(135): Show |
139 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-137+6910C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111072 | |||||||
chr9:115111104 | T | C | 3 | a0003c0035t0004g0150 a0003c0035t0004g0151 a0005c0061t0002g0257 |
3 | HG02559.hp2 HG02895.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-137+6878A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111104 | |||||||
chr9:115111160 | C | T | 2 | a0003c0035t0004g0150 a0003c0035t0004g0151 |
2 | HG02559.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-137+6822G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111160 | |||||||
chr9:115111215 | G | A | 8 | a0003c0035t0004g0150 a0003c0035t0004g0151 a0005c0061t0002g0257 others(5): Show |
8 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-137+6767C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111215 | |||||||
chr9:115111221 | T | C | 1 | a0005c0061t0002g0257 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-137+6761A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111221 | |||||||
chr9:115111249 | G | A | 7 | a0004c0051t0004g0342 a0005c0034t0002g0197 a0005c0034t0002g0198 others(4): Show |
7 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-137+6733C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111249 | |||||||
chr9:115111385 | T | TTC | 14 | a0001c0009t0001g0244 a0003c0003t0001g0239 a0003c0003t0001g0240 others(11): Show |
15 | HG00609.hp1 HG00621.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-137+6595_-137+659 others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111385 | |||||||
chr9:115111399 | C | CT | 114 | a0001c0002t0001g0128 a0001c0002t0001g0267 a0001c0002t0001g0275 others(111): Show |
115 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.-137+6582dupA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111399 | |||||||
chr9:115111399 | C | CTCTCTTT others(8): Show |
1 | a0002c0098t0002g0147 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-137+6582_-137+658 others(19): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111399 | |||||||
chr9:115111399 | C | CTCTCTTT others(10): Show |
2 | a0002c0020t0001g0145 a0009c0099t0001g0146 |
2 | HG02071.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.-137+6582_-137+658 others(21): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111399 | |||||||
chr9:115111399 | C | CTCTCTTT others(11): Show |
5 | a0001c0002t0003g0007 a0001c0002t0013g0135 a0001c0024t0003g0008 others(2): Show |
5 | NA18747.hp2 NA18992.hp2 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.-137+6582_-137+658 others(22): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111399 | |||||||
chr9:115111399 | C | CTCTCTTT others(12): Show |
5 | a0001c0002t0001g0134 a0001c0002t0001g0141 a0001c0002t0001g0142 others(2): Show |
5 | HG02071.hp1 HG02698.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.-137+6582_-137+658 others(23): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111399 | |||||||
chr9:115111399 | C | CTCTCTTT others(13): Show |
4 | a0001c0002t0001g0138 a0001c0002t0008g0139 a0009c0044t0001g0140 others(1): Show |
4 | HG02080.hp2 NA18948.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.-137+6582_-137+658 others(24): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111399 | |||||||
chr9:115111399 | C | CTCTCTTT others(14): Show |
2 | a0001c0002t0008g0136 a0001c0002t0008g0137 |
2 | NA18999.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.-137+6582_-137+658 others(25): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111399 | |||||||
chr9:115111399 | C | CTCTTTTT others(8): Show |
4 | a0005c0061t0002g0257 a0015c0021t0004g0254 a0015c0021t0004g0255 others(1): Show |
4 | HG02572.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-137+6582_-137+658 others(19): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111399 | |||||||
chr9:115111399 | C | CTCTTTTT others(9): Show |
1 | a0015c0021t0004g0129 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-137+6582_-137+658 others(20): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111399 | |||||||
chr9:115111399 | C | CTCTTTTT others(14): Show |
1 | a0003c0077t0004g0356 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-137+6582_-137+658 others(25): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111399 | |||||||
chr9:115111399 | C | CTT | 10 | a0001c0002t0001g0268 a0003c0003t0001g0199 a0004c0004t0001g0269 others(7): Show |
10 | HG01433.hp2 HG01952.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-137+6581_-137+658 others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111399 | |||||||
chr9:115111399 | C | CTTTTTTT others(4): Show |
2 | a0020c0025t0001g0348 a0020c0025t0001g0349 |
2 | HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-137+6572_-137+658 others(15): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111399 | |||||||
chr9:115111399 | C | CTTTTTTT others(5): Show |
1 | a0020c0025t0001g0347 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-137+6571_-137+658 others(16): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111399 | |||||||
chr9:115111399 | C | CTTTTTTT others(8): Show |
1 | a0005c0062t0026g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-137+6568_-137+658 others(19): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111399 | |||||||
chr9:115111399 | CT | C | 42 | a0002c0001t0002g0195 a0002c0001t0007g0018 a0003c0003t0001g0332 others(39): Show |
43 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(40): Show |
intron_variant | MODIFIER | c.-137+6582delA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111399 | |||||||
chr9:115111399 | CTT | C | 84 | a0001c0009t0001g0101 a0001c0009t0001g0123 a0001c0009t0001g0155 others(81): Show |
86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.-137+6581_-137+658 others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111399 | |||||||
chr9:115111399 | CTTT | C | 14 | a0001c0002t0001g0192 a0001c0024t0001g0133 a0002c0001t0002g0125 others(11): Show |
14 | HG01099.hp2 HG02040.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-137+6580_-137+658 others(7): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111399 | |||||||
chr9:115111399 | CTTTTTTT | C | 6 | a0005c0017t0001g0081 a0005c0017t0002g0076 a0005c0017t0002g0078 others(3): Show |
6 | HG01346.hp2 HG03017.hp1 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.-137+6576_-137+658 others(11): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111399 | |||||||
chr9:115111399 | CTTTTTTT others(1): Show |
C | 7 | a0004c0051t0004g0342 a0005c0034t0002g0197 a0005c0034t0002g0198 others(4): Show |
7 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-137+6575_-137+658 others(12): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111399 | |||||||
chr9:115111399 | CTTTTTTT others(3): Show |
C | 1 | a0005c0103t0012g0091 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-137+6573_-137+658 others(14): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111399 | |||||||
chr9:115111399 | CTTTTTTT others(7): Show |
C | 1 | a0047c0060t0014g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-137+6569_-137+658 others(18): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111399 | |||||||
chr9:115111400 | T | TC | 5 | a0004c0050t0014g0345 a0006c0015t0002g0241 a0024c0083t0001g0056 others(2): Show |
5 | HG01109.hp1 HG02922.hp2 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.-137+6581_-137+658 others(5): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111400 | |||||||
chr9:115111402 | T | C | 1 | a0037c0064t0014g0343 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-137+6580A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111402 | |||||||
chr9:115111403 | T | C | 2 | a0003c0035t0004g0150 a0003c0035t0004g0151 |
2 | HG02559.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-137+6579A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111403 | |||||||
chr9:115111404 | T | C | 5 | a0001c0024t0001g0133 a0002c0020t0002g0065 a0002c0020t0002g0249 others(2): Show |
5 | HG02257.hp1 NA18995.hp1 NA19068.hp2 others(2): Show |
intron_variant | MODIFIER | c.-137+6578A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111404 | |||||||
chr9:115111405 | T | C | 3 | a0003c0035t0004g0150 a0003c0035t0004g0151 a0031c0053t0018g0245 |
3 | HG00323.hp1 HG02559.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-137+6577A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111405 | |||||||
chr9:115111406 | T | C | 4 | a0001c0024t0001g0133 a0002c0020t0002g0065 a0002c0020t0002g0249 others(1): Show |
4 | NA18995.hp1 NA19068.hp2 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.-137+6576A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111406 | |||||||
chr9:115111429 | A | T | 32 | a0001c0002t0001g0134 a0001c0002t0001g0138 a0001c0002t0001g0141 others(29): Show |
32 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.-137+6553T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111429 | |||||||
chr9:115111431 | G | A | 45 | a0001c0009t0001g0244 a0003c0003t0001g0229 a0003c0003t0001g0239 others(42): Show |
46 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.-137+6551C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111431 | |||||||
chr9:115111434 | A | C | 8 | a0003c0035t0004g0150 a0003c0035t0004g0151 a0005c0061t0002g0257 others(5): Show |
8 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-137+6548T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111434 | |||||||
chr9:115111495 | G | A | 32 | a0001c0002t0001g0134 a0001c0002t0001g0138 a0001c0002t0001g0141 others(29): Show |
32 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.-137+6487C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111495 | |||||||
chr9:115111570 | G | C | 1 | a0003c0003t0001g0344 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-137+6412C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111570 | |||||||
chr9:115111599 | C | T | 1 | a0001c0002t0001g0267 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-137+6383G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111599 | |||||||
chr9:115111628 | C | T | 2 | a0026c0046t0004g0339 a0026c0046t0004g0340 |
2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-137+6354G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111628 | |||||||
chr9:115111688 | A | G | 89 | a0001c0002t0001g0192 a0001c0009t0001g0101 a0001c0009t0001g0123 others(86): Show |
91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.-137+6294T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111688 | |||||||
chr9:115111821 | T | A | 1 | a0002c0001t0002g0195 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-137+6161A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111821 | |||||||
chr9:115111938 | A | C | 1 | a0013c0029t0003g0010 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-137+6044T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111938 | |||||||
chr9:115111976 | T | A | 1 | a0008c0005t0001g0196 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-137+6006A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111976 | |||||||
chr9:115112094 | G | C | 3 | a0025c0038t0005g0353 a0025c0038t0005g0354 a0027c0071t0001g0355 |
3 | HG02572.hp2 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-137+5888C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115112094 | |||||||
chr9:115112154 | T | A | 28 | a0001c0009t0001g0244 a0003c0003t0001g0229 a0003c0003t0001g0239 others(25): Show |
29 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.-137+5828A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115112154 | |||||||
chr9:115112245 | C | T | 1 | a0005c0062t0026g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-137+5737G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115112245 | |||||||
chr9:115112261 | G | C | 1 | a0047c0060t0014g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-137+5721C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115112261 | |||||||
chr9:115112326 | C | A | 4 | a0004c0004t0002g0220 a0004c0004t0002g0223 a0006c0007t0005g0221 others(1): Show |
4 | NA18944.hp1 NA18954.hp2 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.-137+5656G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115112326 | |||||||
chr9:115112338 | A | G | 1 | a0003c0003t0004g0337 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-137+5644T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115112338 | |||||||
chr9:115112369 | A | G | 1 | a0009c0092t0002g0093 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-137+5613T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115112369 | |||||||
chr9:115112433 | A | G | 3 | a0022c0033t0001g0126 a0022c0033t0001g0127 a0022c0033t0001g0338 |
3 | HG01884.hp2 HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-137+5549T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115112433 | |||||||
chr9:115112498 | T | A | 19 | a0001c0009t0001g0244 a0003c0003t0001g0229 a0003c0003t0001g0239 others(16): Show |
20 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.-137+5484A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115112498 | |||||||
chr9:115112541 | G | A | 2 | a0003c0035t0004g0150 a0003c0035t0004g0151 |
2 | HG02559.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-137+5441C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115112541 | |||||||
chr9:115112550 | A | G | 1 | a0004c0075t0004g0266 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-137+5432T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115112550 | |||||||
chr9:115112555 | C | T | 1 | a0002c0096t0002g0156 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-137+5427G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115112555 | |||||||
chr9:115112634 | C | T | 8 | a0003c0035t0004g0150 a0003c0035t0004g0151 a0005c0061t0002g0257 others(5): Show |
8 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-137+5348G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115112634 | |||||||
chr9:115112722 | TG | T | 4 | a0001c0011t0001g0095 a0002c0001t0002g0002 a0002c0001t0002g0094 others(1): Show |
5 | NA19065.hp1 NA19066.hp2 NA19067.hp2 others(2): Show |
intron_variant | MODIFIER | c.-137+5259delC | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115112722 | |||||||
chr9:115112729 | G | A | 1 | a0010c0008t0003g0034 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-137+5253C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115112729 | |||||||
chr9:115112766 | C | A | 1 | a0005c0034t0002g0198 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-137+5216G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115112766 | |||||||
chr9:115112851 | T | C | 204 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(201): Show |
206 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.-137+5131A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115112851 | |||||||
chr9:115112879 | C | T | 1 | a0001c0009t0001g0155 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-137+5103G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115112879 | |||||||
chr9:115112989 | T | A | 1 | a0002c0001t0002g0125 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-137+4993A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115112989 | |||||||
chr9:115112997 | G | A | 2 | a0001c0009t0001g0244 a0031c0053t0018g0245 |
2 | HG00323.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-137+4985C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115112997 | |||||||
chr9:115113120 | G | A | 4 | a0004c0051t0004g0342 a0022c0033t0001g0126 a0022c0033t0001g0127 others(1): Show |
4 | HG01884.hp2 HG01891.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-137+4862C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115113120 | |||||||
chr9:115113166 | GC | G | 130 | a0001c0002t0001g0128 a0001c0002t0001g0267 a0001c0002t0001g0268 others(127): Show |
131 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.-137+4815delG | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115113166 | |||||||
chr9:115113168 | T | A | 130 | a0001c0002t0001g0128 a0001c0002t0001g0267 a0001c0002t0001g0268 others(127): Show |
131 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.-137+4814A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115113168 | |||||||
chr9:115113402 | T | C | 135 | a0001c0002t0001g0192 a0001c0009t0001g0101 a0001c0009t0001g0123 others(132): Show |
138 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.-137+4580A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115113402 | |||||||
chr9:115113409 | A | C | 135 | a0001c0002t0001g0192 a0001c0009t0001g0101 a0001c0009t0001g0123 others(132): Show |
138 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.-137+4573T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115113409 | |||||||
chr9:115113468 | C | T | 36 | a0001c0009t0001g0244 a0003c0003t0001g0229 a0003c0003t0001g0239 others(33): Show |
37 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.-137+4514G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115113468 | |||||||
chr9:115113498 | C | G | 8 | a0014c0016t0006g0069 a0014c0016t0006g0071 a0014c0016t0006g0072 others(5): Show |
8 | HG00642.hp2 HG00741.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.-137+4484G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115113498 | |||||||
chr9:115113622 | T | C | 1 | a0004c0018t0004g0224 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-137+4360A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115113622 | |||||||
chr9:115113713 | A | T | 8 | a0003c0035t0004g0150 a0003c0035t0004g0151 a0005c0061t0002g0257 others(5): Show |
8 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-137+4269T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115113713 | |||||||
chr9:115113726 | G | A | 2 | a0005c0034t0002g0197 a0005c0034t0002g0198 |
2 | HG01109.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.-137+4256C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115113726 | |||||||
chr9:115113801 | G | A | 17 | a0004c0051t0004g0342 a0005c0034t0002g0197 a0005c0034t0002g0198 others(14): Show |
17 | HG00642.hp2 HG00741.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.-137+4181C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115113801 | |||||||
chr9:115113999 | C | T | 3 | a0022c0033t0001g0126 a0022c0033t0001g0127 a0022c0033t0001g0338 |
3 | HG01884.hp2 HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-137+3983G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115113999 | |||||||
chr9:115114161 | C | G | 1 | a0002c0001t0002g0154 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-137+3821G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115114161 | |||||||
chr9:115114171 | A | G | 7 | a0003c0003t0001g0344 a0011c0010t0001g0064 a0011c0010t0001g0227 others(4): Show |
7 | HG02258.hp1 HG02615.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.-137+3811T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115114171 | |||||||
chr9:115114341 | T | C | 1 | a0011c0010t0001g0225 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-137+3641A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115114341 | |||||||
chr9:115114356 | C | T | 45 | a0002c0001t0007g0018 a0007c0006t0003g0028 a0007c0006t0003g0052 others(42): Show |
46 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.-137+3626G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115114356 | |||||||
chr9:115114365 | C | T | 1 | a0002c0001t0002g0092 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-137+3617G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115114365 | |||||||
chr9:115114411 | G | A | 1 | a0036c0104t0028g0341 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-137+3571C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115114411 | |||||||
chr9:115114549 | G | A | 1 | a0007c0006t0007g0035 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-137+3433C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115114549 | |||||||
chr9:115114694 | A | G | 1 | a0001c0011t0008g0153 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-137+3288T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115114694 | |||||||
chr9:115114784 | T | C | 8 | a0014c0016t0006g0069 a0014c0016t0006g0071 a0014c0016t0006g0072 others(5): Show |
8 | HG00642.hp2 HG00741.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.-137+3198A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115114784 | |||||||
chr9:115114836 | T | C | 2 | a0004c0004t0002g0333 a0004c0018t0004g0334 |
2 | HG02698.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.-137+3146A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115114836 | |||||||
chr9:115114923 | A | ACACATAG others(4): Show |
354 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(351): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.-137+3058_-137+305 others(15): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115114923 | |||||||
chr9:115114933 | CT | C | 8 | a0003c0035t0004g0150 a0003c0035t0004g0151 a0005c0061t0002g0257 others(5): Show |
8 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-137+3048delA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115114933 | |||||||
chr9:115114965 | G | A | 1 | a0004c0018t0004g0226 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-137+3017C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115114965 | |||||||
chr9:115114971 | T | G | 13 | a0003c0035t0004g0150 a0003c0035t0004g0151 a0003c0077t0004g0356 others(10): Show |
13 | HG01192.hp1 HG01243.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.-137+3011A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115114971 | |||||||
chr9:115115046 | G | T | 1 | a0003c0077t0004g0356 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-137+2936C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115115046 | |||||||
chr9:115115047 | C | T | 2 | a0016c0022t0004g0130 a0016c0022t0004g0131 |
2 | HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-137+2935G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115115047 | |||||||
chr9:115115048 | G | A | 1 | a0048c0057t0014g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-137+2934C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115115048 | |||||||
chr9:115115101 | A | G | 7 | a0005c0103t0012g0091 a0016c0022t0004g0252 a0016c0022t0004g0261 others(4): Show |
7 | HG02145.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-137+2881T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115115101 | |||||||
chr9:115115108 | TAG | T | 22 | a0001c0002t0001g0134 a0001c0002t0001g0138 a0001c0002t0001g0141 others(19): Show |
22 | HG02071.hp1 HG02080.hp2 HG02698.hp2 others(19): Show |
intron_variant | MODIFIER | c.-137+2872_-137+287 others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115115108 | |||||||
chr9:115115207 | C | T | 8 | a0008c0005t0001g0083 a0008c0005t0001g0085 a0008c0005t0001g0086 others(5): Show |
8 | HG00140.hp2 HG00738.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.-137+2775G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115115207 | |||||||
chr9:115115232 | T | A | 19 | a0007c0006t0003g0052 a0007c0006t0007g0001 a0007c0006t0007g0006 others(16): Show |
20 | HG00408.hp1 HG00558.hp2 NA18947.hp2 others(17): Show |
intron_variant | MODIFIER | c.-137+2750A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115115232 | |||||||
chr9:115115478 | T | C | 8 | a0003c0035t0004g0150 a0003c0035t0004g0151 a0005c0061t0002g0257 others(5): Show |
8 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-137+2504A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115115478 | |||||||
chr9:115115862 | C | T | 53 | a0003c0003t0001g0199 a0003c0003t0001g0207 a0003c0003t0001g0208 others(50): Show |
53 | HG01346.hp2 HG01884.hp1 HG01884.hp2 others(50): Show |
intron_variant | MODIFIER | c.-137+2120G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115115862 | |||||||
chr9:115115887 | G | A | 2 | a0016c0022t0004g0130 a0016c0022t0004g0131 |
2 | HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-137+2095C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115115887 | |||||||
chr9:115115909 | T | C | 21 | a0001c0002t0001g0134 a0001c0002t0001g0138 a0001c0002t0001g0141 others(18): Show |
21 | HG02071.hp1 HG02071.hp2 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.-137+2073A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115115909 | |||||||
chr9:115116055 | T | A | 215 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(212): Show |
217 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.-137+1927A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115116055 | |||||||
chr9:115116191 | T | G | 208 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(205): Show |
210 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.-137+1791A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115116191 | |||||||
chr9:115116232 | G | C | 1 | a0003c0003t0001g0336 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-137+1750C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115116232 | |||||||
chr9:115116422 | G | A | 1 | a0003c0003t0004g0337 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-137+1560C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115116422 | |||||||
chr9:115116632 | G | A | 96 | a0001c0002t0001g0128 a0001c0009t0001g0101 a0001c0009t0001g0123 others(93): Show |
97 | HG00099.hp2 HG00140.hp2 HG00642.hp2 others(94): Show |
intron_variant | MODIFIER | c.-137+1350C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115116632 | |||||||
chr9:115116860 | A | G | 13 | a0003c0003t0001g0344 a0004c0050t0014g0345 a0004c0051t0004g0342 others(10): Show |
13 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.-137+1122T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115116860 | |||||||
chr9:115116879 | G | A | 3 | a0001c0002t0001g0134 a0001c0002t0013g0135 a0002c0020t0002g0148 |
3 | HG02071.hp1 NA18747.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.-137+1103C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115116879 | |||||||
chr9:115116933 | C | A | 274 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(271): Show |
278 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.-137+1049G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115116933 | |||||||
chr9:115117061 | C | T | 6 | a0005c0067t0002g0359 a0016c0022t0004g0261 a0021c0028t0012g0258 others(3): Show |
6 | HG01496.hp1 HG02280.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-137+921G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115117061 | |||||||
chr9:115117135 | A | G | 178 | a0001c0002t0001g0134 a0001c0002t0001g0192 a0001c0002t0003g0007 others(175): Show |
181 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.-137+847T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115117135 | |||||||
chr9:115117174 | C | G | 8 | a0005c0017t0001g0081 a0005c0017t0002g0076 a0005c0017t0002g0078 others(5): Show |
8 | HG01346.hp2 HG02922.hp1 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.-137+808G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115117174 | |||||||
chr9:115117231 | C | T | 1 | a0005c0017t0002g0076 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-137+751G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115117231 | |||||||
chr9:115117285 | G | C | 1 | a0002c0020t0002g0148 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-137+697C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115117285 | |||||||
chr9:115117340 | C | T | 3 | a0003c0035t0004g0150 a0003c0035t0004g0151 a0042c0063t0012g0149 |
3 | HG02559.hp2 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-137+642G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115117340 | |||||||
chr9:115117418 | G | A | 2 | a0016c0022t0004g0130 a0016c0022t0004g0131 |
2 | HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-137+564C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115117418 | |||||||
chr9:115117489 | T | C | 3 | a0005c0067t0002g0359 a0006c0007t0005g0357 a0043c0047t0001g0358 |
3 | HG02280.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-137+493A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115117489 | |||||||
chr9:115117574 | C | G | 1 | a0007c0006t0007g0006 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-137+408G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115117574 | |||||||
chr9:115117689 | G | A | 65 | a0001c0002t0001g0128 a0001c0009t0001g0101 a0001c0009t0001g0123 others(62): Show |
66 | HG00099.hp2 HG00140.hp2 HG00738.hp2 others(63): Show |
intron_variant | MODIFIER | c.-137+293C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115117689 | |||||||
chr9:115117699 | A | T | 1 | a0003c0003t0019g0360 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-137+283T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115117699 | |||||||
chr9:115117848 | C | CT | 75 | a0001c0002t0001g0128 a0001c0009t0001g0101 a0001c0009t0001g0123 others(72): Show |
76 | HG00099.hp2 HG00140.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.-137+133dupA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115117848 | |||||||
chr9:115117852 | T | A | 1 | a0003c0003t0019g0360 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-137+130A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115117852 | |||||||
chr9:115117861 | C | A | 1 | a0005c0023t0018g0361 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-137+121G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115117861 | |||||||
chr9:115117870 | A | G | 92 | a0001c0002t0001g0128 a0001c0002t0001g0134 a0001c0002t0001g0138 others(89): Show |
93 | HG00099.hp2 HG00140.hp2 HG00642.hp2 others(90): Show |
intron_variant | MODIFIER | c.-137+112T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115117870 | |||||||
chr9:115117878 | C | G | 8 | a0011c0010t0001g0064 a0012c0012t0006g0057 a0012c0012t0006g0058 others(5): Show |
8 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-137+104G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115117878 | |||||||
chr9:115117942 | A | G | 2 | a0024c0082t0004g0055 a0024c0083t0001g0056 |
2 | HG01109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-137+40T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115117942 |