Item | Value |
---|---|
geneid | 64282 |
ensemblid | ENSG00000121274.14 |
hgncid | 30758 |
symbol | TENT4B |
name | terminal nucleotidyltransferase 4B |
refseq_nuc | NM_001365324.3 |
refseq_prot | NP_001352253.1 |
ensembl_nuc | ENST00000561678.7 |
ensembl_prot | ENSP00000455837.3 |
mane_status | MANE Select |
chr | chr16 |
start | 50153306 |
end | 50235310 |
strand | + |
ver | v1.2 |
region | chr16:50153306-50235310 |
region5000 | chr16:50148306-50240310 |
regionname0 | TENT4B_chr16_50153306_50235310 |
regionname5000 | TENT4B_chr16_50148306_50240310 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 713 | 306 | 88 | 59 | 117 | 12 | 28 | 83 | TENT4B_chr16_50148306_50240310 | TENT4B | MDPRI others(708): Show |
chr16 | 50148306 | 50240310 |
a0002 | 0/0 | 713 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | TENT4B_chr16_50148306_50240310 | TENT4B | MDPRI others(708): Show |
chr16 | 50148306 | 50240310 |
a0003 | 0/0 | 713 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | MDPRI others(708): Show |
chr16 | 50148306 | 50240310 |
a0004 | 0/0 | 713 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TENT4B_chr16_50148306_50240310 | TENT4B | MDPRI others(708): Show |
chr16 | 50148306 | 50240310 |
a0005 | 0/0 | 717 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TENT4B_chr16_50148306_50240310 | TENT4B | MDPRI others(712): Show |
chr16 | 50148306 | 50240310 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2139 | 282 | 76 | 58 | 107 | 12 | 27 | TENT4B_chr16_50148306_50240310 | TENT4B | ATGGA others(2134): Show |
chr16 | 50148306 | 50240310 | ||
a0001c0002 | 0/0 | 2139 | 11 | 0 | 1 | 10 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | ATGGA others(2134): Show |
chr16 | 50148306 | 50240310 | ||
a0001c0003 | 0/0 | 2139 | 8 | 8 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | ATGGA others(2134): Show |
chr16 | 50148306 | 50240310 | ||
a0001c0005 | 0/0 | 2139 | 2 | 2 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | ATGGA others(2134): Show |
chr16 | 50148306 | 50240310 | ||
a0001c0009 | 0/0 | 2139 | 1 | 0 | 0 | 0 | 0 | 1 | TENT4B_chr16_50148306_50240310 | TENT4B | ATGGA others(2134): Show |
chr16 | 50148306 | 50240310 | ||
a0001c0010 | 0/0 | 2139 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | ATGGA others(2134): Show |
chr16 | 50148306 | 50240310 | ||
a0001c0011 | 0/0 | 2139 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | ATGGA others(2134): Show |
chr16 | 50148306 | 50240310 | ||
a0002c0004 | 0/0 | 2139 | 3 | 0 | 0 | 3 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | ATGGA others(2134): Show |
chr16 | 50148306 | 50240310 | ||
a0003c0007 | 0/0 | 2139 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | ATGGA others(2134): Show |
chr16 | 50148306 | 50240310 | ||
a0004c0008 | 0/0 | 2139 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | ATGGA others(2134): Show |
chr16 | 50148306 | 50240310 | ||
a0005c0006 | 0/0 | 2151 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | ATGGA others(2146): Show |
chr16 | 50148306 | 50240310 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 8440 | 82 | 16 | 13 | 42 | 3 | 8 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8435): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0002 | 0/0 | 8439 | 77 | 9 | 18 | 39 | 4 | 7 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8434): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0003 | 0/0 | 8440 | 17 | 1 | 1 | 12 | 0 | 3 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8435): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0004 | 0/0 | 8443 | 11 | 2 | 5 | 1 | 0 | 3 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8438): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0005 | 0/0 | 8442 | 10 | 0 | 7 | 0 | 2 | 1 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8437): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0007 | 0/0 | 8442 | 5 | 5 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8437): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0008 | 0/0 | 8439 | 4 | 4 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8434): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0009 | 0/0 | 8440 | 4 | 4 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8435): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0010 | 0/0 | 8439 | 4 | 4 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8434): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0011 | 0/0 | 8436 | 3 | 3 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8431): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0012 | 0/0 | 8447 | 3 | 3 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8442): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0013 | 0/0 | 8441 | 3 | 0 | 0 | 3 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8436): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0014 | 0/0 | 8439 | 3 | 0 | 0 | 3 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8434): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0015 | 0/0 | 8439 | 3 | 0 | 2 | 0 | 0 | 1 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8434): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0016 | 0/0 | 8444 | 3 | 0 | 2 | 0 | 1 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8439): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0017 | 0/0 | 8442 | 3 | 0 | 2 | 0 | 0 | 1 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8437): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0018 | 0/0 | 8442 | 3 | 2 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8437): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0019 | 0/0 | 8442 | 3 | 2 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8437): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0020 | 1/0 | 8440 | 3 | 1 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8435): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0021 | 0/0 | 8439 | 2 | 0 | 1 | 0 | 0 | 1 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8434): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0022 | 0/0 | 8439 | 2 | 2 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8434): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0023 | 0/0 | 8438 | 2 | 1 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8433): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0024 | 0/0 | 8441 | 2 | 2 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8436): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0025 | 0/0 | 8439 | 1 | 0 | 0 | 0 | 1 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8434): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0026 | 0/0 | 8455 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8450): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0027 | 0/1 | 8439 | 1 | 0 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8434): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0028 | 0/0 | 8446 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8441): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0031 | 0/0 | 8439 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8434): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0033 | 0/0 | 8439 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8434): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0034 | 0/0 | 8441 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8436): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0035 | 0/0 | 8441 | 1 | 0 | 0 | 0 | 0 | 1 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8436): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0036 | 0/0 | 8439 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8434): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0037 | 0/0 | 8440 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8435): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0038 | 0/0 | 8439 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8434): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0040 | 0/0 | 8439 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8434): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0041 | 0/0 | 8439 | 1 | 0 | 0 | 0 | 0 | 1 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8434): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0042 | 0/0 | 8439 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8434): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0043 | 0/0 | 8440 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8435): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0044 | 0/0 | 8439 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8434): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0045 | 0/0 | 8440 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8435): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0046 | 0/0 | 8440 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8435): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0047 | 0/0 | 8440 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8435): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0048 | 0/0 | 8440 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8435): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0050 | 0/0 | 8440 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8435): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0051 | 0/0 | 8442 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8437): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0052 | 0/0 | 8441 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8436): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0053 | 0/0 | 8441 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8436): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0054 | 0/0 | 8440 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8435): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0055 | 0/0 | 8442 | 1 | 0 | 0 | 0 | 1 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8437): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0056 | 0/0 | 8440 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8435): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0057 | 0/0 | 8440 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8435): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0058 | 0/0 | 8439 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8434): Show |
chr16 | 50148306 | 50240310 |
a0001c0001t0059 | 0/0 | 8440 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8435): Show |
chr16 | 50148306 | 50240310 |
a0001c0002t0002 | 0/0 | 8439 | 9 | 0 | 1 | 8 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8434): Show |
chr16 | 50148306 | 50240310 |
a0001c0002t0032 | 0/0 | 8440 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8435): Show |
chr16 | 50148306 | 50240310 |
a0001c0002t0039 | 0/0 | 8439 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8434): Show |
chr16 | 50148306 | 50240310 |
a0001c0003t0006 | 0/0 | 8441 | 6 | 6 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8436): Show |
chr16 | 50148306 | 50240310 |
a0001c0003t0029 | 0/0 | 8444 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8439): Show |
chr16 | 50148306 | 50240310 |
a0001c0003t0060 | 0/0 | 8441 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8436): Show |
chr16 | 50148306 | 50240310 |
a0001c0005t0001 | 0/0 | 8440 | 2 | 2 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8435): Show |
chr16 | 50148306 | 50240310 |
a0001c0009t0049 | 0/0 | 8438 | 1 | 0 | 0 | 0 | 0 | 1 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8433): Show |
chr16 | 50148306 | 50240310 |
a0001c0010t0001 | 0/0 | 8440 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8435): Show |
chr16 | 50148306 | 50240310 |
a0001c0011t0030 | 0/0 | 8440 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8435): Show |
chr16 | 50148306 | 50240310 |
a0002c0004t0001 | 0/0 | 8440 | 3 | 0 | 0 | 3 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8435): Show |
chr16 | 50148306 | 50240310 |
a0003c0007t0002 | 0/0 | 8439 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8434): Show |
chr16 | 50148306 | 50240310 |
a0004c0008t0001 | 0/0 | 8440 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8435): Show |
chr16 | 50148306 | 50240310 |
a0005c0006t0003 | 0/0 | 8452 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | CTTCT others(8447): Show |
chr16 | 50148306 | 50240310 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0003g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0004g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0004g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0004g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0004g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0004g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0004g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0004g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0004g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0004g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0005g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0005g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0005g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0005g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0005g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0005g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0005g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0005g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0005g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0005g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0007g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0007g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0007g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0007g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0007g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0008g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0008g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0008g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0008g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0009g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0009g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0009g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0009g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0010g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0010g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0010g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0010g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0011g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0011g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0011g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0012g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0012g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0012g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0013g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0013g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0013g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0014g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0014g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0014g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0015g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0015g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0015g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0016g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0016g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0016g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0017g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0017g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0017g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0018g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0018g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0018g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0019g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0019g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0019g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0020g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0020g0209 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0020g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0021g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0021g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0022g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0022g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0023g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0023g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0024g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0024g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0025g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0026g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0027g0162 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0028g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0031g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0033g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0034g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0035g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0036g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0037g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0038g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0040g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0041g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0042g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0043g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0044g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0045g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0046g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0047g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0048g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0050g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0051g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0052g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0053g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0054g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0055g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0056g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0057g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0058g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0001t0059g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0002t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0002t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0002t0032g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0002t0039g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0003t0006g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0003t0006g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0003t0006g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0003t0006g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0003t0006g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0003t0006g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0003t0029g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0003t0060g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0005t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0005t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0009t0049g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0010t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0001c0011t0030g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0002c0004t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0002c0004t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0002c0004t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0003c0007t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0004c0008t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
a0005c0006t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0055 | g0168 | EUR | GBR | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG00099 | hp2 | a0001 | c0001 | t0005 | g0091 | EUR | GBR | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG00323 | hp1 | a0001 | c0001 | t0025 | g0066 | EUR | FIN | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG00323 | hp2 | a0001 | c0001 | t0005 | g0089 | EUR | FIN | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | CHS | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | CHS | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG00544 | hp1 | a0001 | c0002 | t0032 | g0123 | EAS | CHS | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG00544 | hp2 | a0001 | c0001 | t0020 | g0305 | EAS | CHS | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG00597 | hp1 | a0001 | c0001 | t0003 | g0099 | EAS | CHS | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | CHS | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | CHS | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG00609 | hp2 | a0001 | c0002 | t0002 | g0117 | EAS | CHS | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG00639 | hp1 | a0001 | c0002 | t0002 | g0130 | AMR | PUR | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG00639 | hp2 | a0001 | c0001 | t0004 | g0298 | AMR | PUR | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | CHS | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | CHS | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG00738 | hp1 | a0001 | c0001 | t0015 | g0067 | AMR | PUR | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG00738 | hp2 | a0001 | c0001 | t0034 | g0087 | AMR | PUR | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG00741 | hp1 | a0001 | c0001 | t0005 | g0120 | AMR | PUR | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG00741 | hp2 | a0001 | c0001 | t0016 | g0189 | AMR | PUR | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01070 | hp2 | a0001 | c0001 | t0017 | g0136 | AMR | PUR | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01071 | hp1 | a0001 | c0001 | t0017 | g0137 | AMR | PUR | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01071 | hp2 | a0001 | c0001 | t0005 | g0118 | AMR | PUR | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01081 | hp1 | a0001 | c0001 | t0004 | g0190 | AMR | PUR | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0116 | AMR | PUR | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0112 | AMR | PUR | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01106 | hp1 | a0001 | c0001 | t0015 | g0059 | AMR | PUR | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01109 | hp1 | a0001 | c0001 | t0019 | g0138 | AMR | PUR | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01109 | hp2 | a0001 | c0001 | t0038 | g0156 | AMR | PUR | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01167 | hp1 | a0001 | c0001 | t0018 | g0179 | AMR | PUR | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01167 | hp2 | a0001 | c0001 | t0023 | g0140 | AMR | PUR | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01168 | hp1 | a0001 | c0001 | t0005 | g0041 | AMR | PUR | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | PUR | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01169 | hp1 | a0001 | c0001 | t0005 | g0042 | AMR | PUR | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0163 | AMR | PUR | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0052 | AMR | PUR | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0176 | AMR | PUR | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01243 | hp2 | a0001 | c0001 | t0016 | g0188 | AMR | PUR | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01255 | hp1 | a0001 | c0001 | t0005 | g0088 | AMR | CLM | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | CLM | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01256 | hp1 | a0001 | c0001 | t0004 | g0267 | AMR | CLM | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0147 | AMR | CLM | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01261 | hp1 | a0001 | c0001 | t0005 | g0092 | AMR | CLM | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | CLM | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | CLM | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | CLM | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0040 | AMR | CLM | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01433 | hp1 | a0001 | c0001 | t0004 | g0303 | AMR | CLM | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01433 | hp2 | a0003 | c0007 | t0002 | g0090 | AMR | CLM | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0277 | EUR | IBS | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0146 | EUR | IBS | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0080 | EUR | IBS | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0278 | EUR | IBS | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0280 | EUR | IBS | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0055 | EUR | IBS | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | ACB | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01891 | hp2 | a0001 | c0001 | t0024 | g0015 | AFR | ACB | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0104 | AMR | PEL | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01934 | hp1 | a0001 | c0001 | t0047 | g0249 | AMR | PEL | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0181 | AMR | PEL | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0075 | AMR | PEL | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PEL | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01978 | hp2 | a0001 | c0001 | t0040 | g0107 | AMR | PEL | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01981 | hp1 | a0001 | c0001 | t0005 | g0132 | AMR | PEL | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0108 | AMR | PEL | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0102 | AMR | PEL | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | PEL | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02027 | hp1 | a0001 | c0001 | t0042 | g0135 | EAS | KHV | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02027 | hp2 | a0001 | c0001 | t0043 | g0048 | EAS | KHV | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02055 | hp1 | a0001 | c0001 | t0011 | g0141 | AFR | ACB | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02055 | hp2 | a0001 | c0001 | t0007 | g0024 | AFR | ACB | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | KHV | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | KHV | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | KHV | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02074 | hp2 | a0001 | c0001 | t0056 | g0260 | EAS | KHV | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | KHV | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0097 | EAS | KHV | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | KHV | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | KHV | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02145 | hp1 | a0001 | c0001 | t0028 | g0198 | AFR | ACB | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02145 | hp2 | a0001 | c0001 | t0010 | g0006 | AFR | ACB | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0109 | AMR | PEL | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CDX | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02165 | hp2 | a0001 | c0002 | t0002 | g0057 | EAS | CDX | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02257 | hp1 | a0001 | c0001 | t0007 | g0023 | AFR | ACB | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02258 | hp1 | a0001 | c0001 | t0009 | g0167 | AFR | ACB | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02258 | hp2 | a0001 | c0001 | t0023 | g0073 | AFR | ACB | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02280 | hp1 | a0001 | c0001 | t0011 | g0054 | AFR | ACB | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02280 | hp2 | a0001 | c0001 | t0024 | g0016 | AFR | ACB | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0105 | AMR | PEL | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02300 | hp2 | a0001 | c0001 | t0004 | g0293 | AMR | PEL | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | ACB | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02451 | hp2 | a0001 | c0001 | t0057 | g0011 | AFR | ACB | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02523 | hp1 | a0001 | c0002 | t0002 | g0121 | EAS | KHV | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02523 | hp2 | a0001 | c0001 | t0004 | g0284 | EAS | KHV | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02572 | hp1 | a0001 | c0001 | t0010 | g0007 | AFR | GWD | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | GWD | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02615 | hp1 | a0001 | c0001 | t0010 | g0009 | AFR | GWD | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02615 | hp2 | a0001 | c0005 | t0001 | g0230 | AFR | GWD | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0154 | AFR | GWD | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02630 | hp1 | a0001 | c0003 | t0060 | g0207 | AFR | GWD | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02630 | hp2 | a0001 | c0001 | t0019 | g0095 | AFR | GWD | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02647 | hp1 | a0001 | c0001 | t0018 | g0182 | AFR | GWD | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0139 | SAS | PJL | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0071 | SAS | PJL | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02717 | hp2 | a0001 | c0001 | t0004 | g0304 | AFR | GWD | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02723 | hp1 | a0001 | c0001 | t0026 | g0017 | AFR | GWD | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02723 | hp2 | a0001 | c0001 | t0012 | g0196 | AFR | GWD | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02809 | hp1 | a0001 | c0001 | t0018 | g0183 | AFR | GWD | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | GWD | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0178 | AFR | GWD | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02886 | hp1 | a0001 | c0011 | t0030 | g0208 | AFR | GWD | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02886 | hp2 | a0001 | c0001 | t0059 | g0245 | AFR | GWD | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02895 | hp1 | a0001 | c0001 | t0053 | g0308 | AFR | GWD | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0072 | AFR | GWD | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02896 | hp2 | a0001 | c0001 | t0009 | g0044 | AFR | GWD | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02897 | hp1 | a0001 | c0001 | t0009 | g0043 | AFR | GWD | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02922 | hp1 | a0001 | c0001 | t0008 | g0149 | AFR | ESN | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02922 | hp2 | a0001 | c0001 | t0019 | g0094 | AFR | ESN | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ESN | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02965 | hp2 | a0001 | c0001 | t0008 | g0119 | AFR | ESN | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | ESN | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02976 | hp2 | a0001 | c0003 | t0006 | g0191 | AFR | ESN | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0128 | SAS | PJL | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG03041 | hp1 | a0001 | c0001 | t0012 | g0195 | AFR | GWD | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0310 | AFR | GWD | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0172 | AFR | ESN | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG03195 | hp1 | a0001 | c0001 | t0044 | g0053 | AFR | ESN | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG03195 | hp2 | a0001 | c0001 | t0007 | g0026 | AFR | ESN | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG03209 | hp1 | a0001 | c0005 | t0001 | g0224 | AFR | MSL | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG03209 | hp2 | a0001 | c0001 | t0046 | g0212 | AFR | MSL | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG03225 | hp1 | a0001 | c0001 | t0008 | g0122 | AFR | MSL | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG03225 | hp2 | a0001 | c0001 | t0004 | g0199 | AFR | MSL | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG03239 | hp2 | a0001 | c0001 | t0035 | g0065 | SAS | PJL | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG03453 | hp1 | a0001 | c0001 | t0050 | g0034 | AFR | MSL | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG03453 | hp2 | a0001 | c0001 | t0007 | g0014 | AFR | MSL | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG03486 | hp1 | a0001 | c0001 | t0031 | g0153 | AFR | MSL | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG03486 | hp2 | a0001 | c0001 | t0012 | g0197 | AFR | MSL | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG03491 | hp1 | a0001 | c0001 | t0004 | g0292 | SAS | PJL | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | PJL | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0184 | SAS | PJL | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG03516 | hp1 | a0001 | c0001 | t0022 | g0020 | AFR | ESN | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG03516 | hp2 | a0001 | c0003 | t0006 | g0206 | AFR | ESN | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG03579 | hp1 | a0001 | c0003 | t0006 | g0192 | AFR | MSL | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG03579 | hp2 | a0001 | c0001 | t0008 | g0166 | AFR | MSL | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG03654 | hp1 | a0001 | c0009 | t0049 | g0077 | SAS | PJL | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG03669 | hp1 | a0001 | c0001 | t0015 | g0068 | SAS | PJL | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0309 | SAS | PJL | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0171 | SAS | PJL | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0101 | SAS | BEB | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG03831 | hp2 | a0001 | c0001 | t0004 | g0268 | SAS | BEB | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | BEB | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0133 | SAS | BEB | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG03942 | hp1 | a0001 | c0001 | t0005 | g0180 | SAS | BEB | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG03942 | hp2 | a0001 | c0001 | t0017 | g0186 | SAS | BEB | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG04115 | hp1 | a0001 | c0001 | t0004 | g0300 | SAS | STU | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0029 | SAS | STU | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG04228 | hp1 | a0001 | c0001 | t0041 | g0177 | SAS | STU | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0307 | SAS | STU | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | YRI | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18522 | hp2 | a0001 | c0001 | t0052 | g0013 | AFR | YRI | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | CHB | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18612 | hp2 | a0001 | c0001 | t0036 | g0127 | EAS | CHB | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | CHB | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | CHB | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18906 | hp1 | a0001 | c0001 | t0011 | g0142 | AFR | YRI | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18906 | hp2 | a0001 | c0001 | t0009 | g0033 | AFR | YRI | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18942 | hp2 | a0001 | c0001 | t0014 | g0151 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18943 | hp2 | a0001 | c0002 | t0002 | g0111 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18960 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18969 | hp1 | a0001 | c0002 | t0002 | g0115 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18969 | hp2 | a0004 | c0008 | t0001 | g0251 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18971 | hp1 | a0001 | c0001 | t0013 | g0083 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18972 | hp1 | a0002 | c0004 | t0001 | g0283 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18983 | hp1 | a0001 | c0002 | t0002 | g0114 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18992 | hp1 | a0002 | c0004 | t0001 | g0282 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18992 | hp2 | a0001 | c0002 | t0002 | g0113 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA19002 | hp1 | a0001 | c0001 | t0014 | g0110 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA19002 | hp2 | a0002 | c0004 | t0001 | g0281 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA19005 | hp1 | a0001 | c0002 | t0039 | g0079 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA19009 | hp2 | a0001 | c0001 | t0045 | g0231 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA19012 | hp2 | a0005 | c0006 | t0003 | g0045 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA19030 | hp1 | a0001 | c0001 | t0020 | g0203 | AFR | LWK | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA19030 | hp2 | a0001 | c0003 | t0006 | g0002 | AFR | LWK | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | LWK | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA19043 | hp2 | a0001 | c0001 | t0022 | g0021 | AFR | LWK | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA19057 | hp1 | a0001 | c0001 | t0033 | g0158 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA19065 | hp2 | a0001 | c0001 | t0013 | g0143 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA19067 | hp2 | a0001 | c0001 | t0013 | g0200 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA19068 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA19079 | hp2 | a0001 | c0001 | t0014 | g0152 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | YRI | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA19240 | hp2 | a0001 | c0003 | t0006 | g0205 | AFR | YRI | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA20129 | hp1 | a0001 | c0010 | t0001 | g0214 | AFR | ASW | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0106 | AFR | ASW | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA20752 | hp1 | a0001 | c0001 | t0016 | g0187 | EUR | TSI | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0185 | EUR | TSI | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | GIH | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA20905 | hp2 | a0001 | c0001 | t0021 | g0037 | SAS | GIH | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01123 | hp1 | a0001 | c0001 | t0021 | g0124 | AMR | CLM | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0155 | AMR | CLM | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02109 | hp1 | a0001 | c0001 | t0058 | g0175 | AFR | ACB | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02109 | hp2 | a0001 | c0001 | t0051 | g0025 | AFR | ACB | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02486 | hp2 | a0001 | c0001 | t0048 | g0081 | AFR | ACB | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02559 | hp1 | a0001 | c0001 | t0010 | g0008 | AFR | ACB | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG02559 | hp2 | a0001 | c0003 | t0029 | g0194 | AFR | ACB | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG06807 | hp1 | a0001 | c0001 | t0037 | g0027 | AFR | USA | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
HG06807 | hp2 | a0001 | c0003 | t0006 | g0204 | AFR | USA | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA20300 | hp1 | a0001 | c0001 | t0054 | g0010 | AFR | USA | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0301 | AFR | USA | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA21309 | hp1 | a0001 | c0001 | t0007 | g0022 | AFR | LWK | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | LWK | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
homoSapiens | chm13v2 | a0001 | c0001 | t0027 | g0162 | REF | REF | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
homoSapiens | grch38p0 | a0001 | c0001 | t0020 | g0209 | REF | REF | TENT4B_chr16_50148306_50240310 | TENT4B | chr16 | 50148306 | 50240310 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:50153744 | C | CAGCGGCG others(5): Show |
1 | a0005 | 1 | NA19012.hp2 | disruptive_inframe_insertion | MODERATE | c.134_145dupCGAGCGGC others(4): Show |
p.Ala45_Gly48dup | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/12 | 462/8440 | 146/2142 | 49/713 | INFO_REALIGN_3_PRIME | chr16 | 50153744 | ||
chr16:50153985 | G | A | 1 | a0003 | 1 | HG01433.hp2 | missense_variant | MODERATE | c.364G>A | p.Ala122Thr | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/12 | 680/8440 | 364/2142 | 122/713 | chr16 | 50153985 | |||
chr16:50154175 | C | T | 1 | a0002 | 3 | NA18972.hp1 NA18992.hp1 NA19002.hp2 |
missense_variant | MODERATE | c.554C>T | p.Ala185Val | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/12 | 870/8440 | 554/2142 | 185/713 | chr16 | 50154175 | |||
chr16:50223196 | G | C | 1 | a0004 | 1 | NA18969.hp2 | missense_variant | MODERATE | c.1190G>C | p.Cys397Ser | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 7/12 | 1506/8440 | 1190/2142 | 397/713 | chr16 | 50223196 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:50153945 | G | A | 1 | a0001c0003 | 8 | HG02559.hp2 HG02630.hp1 HG02976.hp2 others(5): Show |
synonymous_variant | LOW | c.324G>A | p.Thr108Thr | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/12 | 640/8440 | 324/2142 | 108/713 | chr16 | 50153945 | |||
chr16:50154098 | C | T | 1 | a0001c0011 | 1 | HG02886.hp1 | synonymous_variant | LOW | c.477C>T | p.Asn159Asn | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/12 | 793/8440 | 477/2142 | 159/713 | chr16 | 50154098 | |||
chr16:50154116 | C | T | 1 | a0001c0002 | 11 | HG00544.hp1 HG00609.hp2 HG00639.hp1 others(8): Show |
synonymous_variant | LOW | c.495C>T | p.Asn165Asn | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/12 | 811/8440 | 495/2142 | 165/713 | chr16 | 50154116 | |||
chr16:50225180 | A | G | 1 | a0001c0010 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.1695A>G | p.Gly565Gly | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 10/12 | 2011/8440 | 1695/2142 | 565/713 | chr16 | 50225180 | |||
chr16:50227844 | C | T | 1 | a0002c0004 | 3 | NA18972.hp1 NA18992.hp1 NA19002.hp2 |
synonymous_variant | LOW | c.1806C>T | p.Ser602Ser | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 11/12 | 2122/8440 | 1806/2142 | 602/713 | chr16 | 50227844 | |||
chr16:50227913 | G | T | 1 | a0001c0009 | 1 | HG03654.hp1 | synonymous_variant | LOW | c.1875G>T | p.Ser625Ser | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 11/12 | 2191/8440 | 1875/2142 | 625/713 | chr16 | 50227913 | |||
chr16:50227988 | C | T | 1 | a0001c0005 | 2 | HG02615.hp2 HG03209.hp1 |
synonymous_variant | LOW | c.1950C>T | p.Ser650Ser | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 11/12 | 2266/8440 | 1950/2142 | 650/713 | chr16 | 50227988 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:50153312 | T | C | 1 | a0001c0001t0025 | 1 | HG00323.hp1 | 5_prime_UTR_variant | MODIFIER | c.-310T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/12 | 310 | chr16 | 50153312 | ||||||
chr16:50153367 | C | T | 1 | a0001c0003t0060 | 1 | HG02630.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-255C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/12 | chr16 | 50153367 | |||||||
chr16:50153412 | A | G | 1 | a0001c0001t0059 | 1 | HG02886.hp2 | 5_prime_UTR_variant | MODIFIER | c.-210A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/12 | 210 | chr16 | 50153412 | ||||||
chr16:50153488 | G | GAGC | 3 | a0001c0001t0004 a0001c0001t0005 a0001c0003t0029 |
22 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(19): Show |
5_prime_UTR_variant | MODIFIER | c.-115_-113dupAGC | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/12 | 112 | INFO_REALIGN_3_PRIME | chr16 | 50153488 | |||||
chr16:50153488 | G | GAGCAGC | 2 | a0001c0001t0012 a0001c0001t0028 |
4 | HG02145.hp1 HG02723.hp2 HG03041.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-118_-113dupAGCAGC | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/12 | 112 | INFO_REALIGN_3_PRIME | chr16 | 50153488 | |||||
chr16:50153488 | G | GAGCAGCA others(8): Show |
1 | a0001c0001t0026 | 1 | HG02723.hp1 | 5_prime_UTR_variant | MODIFIER | c.-127_-113dupAGCAGC others(9): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/12 | 112 | INFO_REALIGN_3_PRIME | chr16 | 50153488 | |||||
chr16:50153498 | A | G | 1 | a0001c0001t0058 | 1 | HG02109.hp1 | 5_prime_UTR_variant | MODIFIER | c.-124A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/12 | 124 | chr16 | 50153498 | ||||||
chr16:50153501 | A | G | 2 | a0001c0001t0056 a0001c0001t0057 |
2 | HG02074.hp2 HG02451.hp2 |
5_prime_UTR_variant | MODIFIER | c.-121A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/12 | 121 | chr16 | 50153501 | ||||||
chr16:50153507 | AGCG | A | 1 | a0001c0001t0011 | 3 | HG02055.hp1 HG02280.hp1 NA18906.hp1 |
5_prime_UTR_variant | MODIFIER | c.-112_-110delGGC | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/12 | 110 | INFO_REALIGN_3_PRIME | chr16 | 50153507 | |||||
chr16:50153510 | G | A | 65 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(62): Show |
305 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(302): Show |
5_prime_UTR_variant | MODIFIER | c.-112G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/12 | 112 | chr16 | 50153510 | ||||||
chr16:50153522 | A | G | 1 | a0001c0001t0010 | 4 | HG02145.hp2 HG02559.hp1 HG02572.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-100A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/12 | 100 | chr16 | 50153522 | ||||||
chr16:50229851 | G | A | 64 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(61): Show |
297 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(294): Show |
3_prime_UTR_variant | MODIFIER | c.*523G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 523 | chr16 | 50229851 | ||||||
chr16:50229928 | T | TC | 3 | a0001c0003t0006 a0001c0003t0029 a0001c0003t0060 |
8 | HG02559.hp2 HG02630.hp1 HG02976.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*601dupC | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 602 | INFO_REALIGN_3_PRIME | chr16 | 50229928 | |||||
chr16:50230023 | A | G | 1 | a0001c0001t0055 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*695A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 695 | chr16 | 50230023 | ||||||
chr16:50230031 | G | T | 11 | a0001c0001t0007 a0001c0001t0017 a0001c0001t0018 others(8): Show |
22 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*703G>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 703 | chr16 | 50230031 | ||||||
chr16:50230102 | G | A | 1 | a0001c0011t0030 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*774G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 774 | chr16 | 50230102 | ||||||
chr16:50230138 | C | T | 2 | a0001c0001t0009 a0001c0001t0050 |
5 | HG02258.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*810C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 810 | chr16 | 50230138 | ||||||
chr16:50230143 | T | C | 1 | a0001c0001t0017 | 3 | HG01070.hp2 HG01071.hp1 HG03942.hp2 |
3_prime_UTR_variant | MODIFIER | c.*815T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 815 | chr16 | 50230143 | ||||||
chr16:50230148 | T | C | 1 | a0001c0001t0031 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*820T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 820 | chr16 | 50230148 | ||||||
chr16:50230184 | G | A | 1 | a0001c0001t0055 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*856G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 856 | chr16 | 50230184 | ||||||
chr16:50230278 | T | C | 1 | a0001c0011t0030 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*950T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 950 | chr16 | 50230278 | ||||||
chr16:50230300 | G | GA | 31 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(28): Show |
155 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*989dupA | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 990 | INFO_REALIGN_3_PRIME | chr16 | 50230300 | |||||
chr16:50230300 | G | GAA | 7 | a0001c0001t0007 a0001c0001t0017 a0001c0001t0018 others(4): Show |
17 | HG00099.hp1 HG00544.hp1 HG01070.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*988_*989dupAA | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 990 | INFO_REALIGN_3_PRIME | chr16 | 50230300 | |||||
chr16:50230497 | T | C | 1 | a0001c0001t0051 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1169T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 1169 | chr16 | 50230497 | ||||||
chr16:50230877 | G | T | 1 | a0001c0001t0044 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1549G>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 1549 | chr16 | 50230877 | ||||||
chr16:50231042 | C | CTTTA | 1 | a0001c0001t0016 | 3 | HG00741.hp2 HG01243.hp2 NA20752.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1715_*1716insTTAT | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 1716 | INFO_REALIGN_3_PRIME | chr16 | 50231042 | |||||
chr16:50231860 | T | C | 1 | a0001c0001t0022 | 2 | HG03516.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2532T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 2532 | chr16 | 50231860 | ||||||
chr16:50231907 | C | T | 49 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(46): Show |
189 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(186): Show |
3_prime_UTR_variant | MODIFIER | c.*2579C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 2579 | chr16 | 50231907 | ||||||
chr16:50231951 | G | T | 46 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(43): Show |
184 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*2623G>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 2623 | chr16 | 50231951 | ||||||
chr16:50232056 | A | G | 1 | a0001c0001t0050 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2728A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 2728 | chr16 | 50232056 | ||||||
chr16:50232074 | G | A | 1 | a0001c0001t0033 | 1 | NA19057.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2746G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 2746 | chr16 | 50232074 | ||||||
chr16:50232363 | C | A | 3 | a0001c0001t0021 a0001c0001t0034 a0001c0001t0035 |
4 | HG00738.hp2 HG01123.hp1 HG03239.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3035C>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 3035 | chr16 | 50232363 | ||||||
chr16:50232812 | A | G | 1 | a0001c0001t0024 | 2 | HG01891.hp2 HG02280.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3484A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 3484 | chr16 | 50232812 | ||||||
chr16:50232937 | A | G | 1 | a0001c0001t0008 | 4 | HG02922.hp1 HG02965.hp2 HG03225.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3609A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 3609 | chr16 | 50232937 | ||||||
chr16:50232980 | T | C | 1 | a0001c0001t0014 | 3 | NA18942.hp2 NA19002.hp1 NA19079.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3652T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 3652 | chr16 | 50232980 | ||||||
chr16:50233102 | C | G | 1 | a0001c0001t0047 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3774C>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 3774 | chr16 | 50233102 | ||||||
chr16:50233142 | G | T | 3 | a0001c0001t0015 a0001c0001t0025 a0001c0009t0049 |
5 | HG00323.hp1 HG00738.hp1 HG01106.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3814G>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 3814 | chr16 | 50233142 | ||||||
chr16:50233358 | T | G | 3 | a0001c0001t0017 a0001c0001t0018 a0001c0001t0055 |
7 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4030T>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 4030 | chr16 | 50233358 | ||||||
chr16:50233468 | A | G | 1 | a0001c0001t0048 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4140A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 4140 | chr16 | 50233468 | ||||||
chr16:50233520 | G | A | 1 | a0001c0001t0036 | 1 | NA18612.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4192G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 4192 | chr16 | 50233520 | ||||||
chr16:50233532 | A | C | 1 | a0001c0001t0046 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4204A>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 4204 | chr16 | 50233532 | ||||||
chr16:50233539 | A | G | 1 | a0001c0001t0043 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4211A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 4211 | chr16 | 50233539 | ||||||
chr16:50233599 | C | G | 6 | a0001c0001t0017 a0001c0001t0018 a0001c0001t0019 others(3): Show |
13 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*4271C>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 4271 | chr16 | 50233599 | ||||||
chr16:50233654 | A | G | 1 | a0001c0001t0052 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4326A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 4326 | chr16 | 50233654 | ||||||
chr16:50233692 | TA | T | 23 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0008 others(20): Show |
127 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*4372delA | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 4372 | INFO_REALIGN_3_PRIME | chr16 | 50233692 | |||||
chr16:50233693 | A | T | 1 | a0001c0001t0024 | 2 | HG01891.hp2 HG02280.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4365A>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 4365 | chr16 | 50233693 | ||||||
chr16:50233701 | T | G | 1 | a0001c0001t0038 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4373T>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 4373 | chr16 | 50233701 | ||||||
chr16:50233703 | T | G | 1 | a0001c0001t0038 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4375T>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 4375 | chr16 | 50233703 | ||||||
chr16:50233786 | A | C | 1 | a0001c0001t0026 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4458A>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 4458 | chr16 | 50233786 | ||||||
chr16:50234364 | TG | T | 29 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(26): Show |
153 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(150): Show |
3_prime_UTR_variant | MODIFIER | c.*5038delG | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 5038 | INFO_REALIGN_3_PRIME | chr16 | 50234364 | |||||
chr16:50234609 | T | C | 1 | a0001c0002t0039 | 1 | NA19005.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5281T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 5281 | chr16 | 50234609 | ||||||
chr16:50234637 | T | G | 1 | a0001c0001t0040 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5309T>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 5309 | chr16 | 50234637 | ||||||
chr16:50234639 | A | T | 1 | a0001c0001t0010 | 4 | HG02145.hp2 HG02559.hp1 HG02572.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5311A>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 5311 | chr16 | 50234639 | ||||||
chr16:50234720 | A | T | 1 | a0001c0001t0042 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5392A>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 5392 | chr16 | 50234720 | ||||||
chr16:50234753 | T | C | 1 | a0001c0001t0037 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5425T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 5425 | chr16 | 50234753 | ||||||
chr16:50234835 | G | C | 1 | a0001c0001t0041 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5507G>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 5507 | chr16 | 50234835 | ||||||
chr16:50234853 | G | A | 1 | a0001c0001t0010 | 4 | HG02145.hp2 HG02559.hp1 HG02572.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5525G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 5525 | chr16 | 50234853 | ||||||
chr16:50234906 | G | T | 47 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(44): Show |
187 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(184): Show |
3_prime_UTR_variant | MODIFIER | c.*5578G>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 5578 | chr16 | 50234906 | ||||||
chr16:50235006 | C | T | 1 | a0001c0001t0052 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5678C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 5678 | chr16 | 50235006 | ||||||
chr16:50235066 | T | C | 1 | a0001c0001t0045 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5738T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 5738 | chr16 | 50235066 | ||||||
chr16:50235204 | T | G | 1 | a0001c0001t0034 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5876T>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 5876 | chr16 | 50235204 | ||||||
chr16:50235251 | G | A | 1 | a0001c0001t0026 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5923G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 12/12 | 5923 | chr16 | 50235251 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:50154380 | TGTTGCAC others(3): Show |
T | 1 | a0001c0003t0006g0002 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.638+123_638+132del others(10): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50154380 | ||||||
chr16:50154414 | C | A | 1 | a0001c0001t0003g0003 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.638+155C>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50154414 | |||||||
chr16:50154529 | C | T | 1 | a0001c0001t0001g0311 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.638+270C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50154529 | |||||||
chr16:50154539 | C | T | 1 | a0001c0001t0002g0310 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.638+280C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50154539 | |||||||
chr16:50154653 | G | C | 2 | a0001c0001t0002g0004 a0001c0001t0002g0005 |
2 | HG02129.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.638+394G>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50154653 | |||||||
chr16:50154662 | G | T | 1 | a0001c0001t0001g0309 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.638+403G>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50154662 | |||||||
chr16:50154667 | G | A | 4 | a0001c0001t0010g0006 a0001c0001t0010g0007 a0001c0001t0010g0008 others(1): Show |
4 | HG02145.hp2 HG02559.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.638+408G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50154667 | |||||||
chr16:50154727 | C | G | 1 | a0001c0001t0053g0308 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.638+468C>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50154727 | |||||||
chr16:50154845 | A | G | 1 | a0001c0001t0001g0307 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.638+586A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50154845 | |||||||
chr16:50154872 | G | A | 186 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(183): Show |
187 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.638+613G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50154872 | |||||||
chr16:50155018 | G | A | 3 | a0001c0001t0016g0187 a0001c0001t0016g0188 a0001c0001t0016g0189 |
3 | HG00741.hp2 HG01243.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.638+759G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50155018 | |||||||
chr16:50155207 | T | C | 2 | a0001c0001t0054g0010 a0001c0001t0057g0011 |
2 | HG02451.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.638+948T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50155207 | |||||||
chr16:50155268 | C | CATGGGTG others(7): Show |
1 | a0001c0001t0004g0190 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.638+1009_638+1010i others(16): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50155268 | |||||||
chr16:50155268 | C | CGTGTGTG others(3): Show |
1 | a0001c0001t0017g0186 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.638+1012_638+1013i others(12): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50155268 | ||||||
chr16:50155272 | G | GGGGTGTG others(1): Show |
6 | a0001c0001t0001g0193 a0001c0001t0012g0195 a0001c0001t0012g0196 others(3): Show |
6 | HG02145.hp1 HG02148.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.638+1014_638+1015i others(10): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50155272 | ||||||
chr16:50155272 | G | GGGGTGTG others(17): Show |
1 | a0001c0001t0004g0199 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.638+1014_638+1015i others(26): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50155272 | ||||||
chr16:50155272 | G | GGT | 19 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0213 others(16): Show |
19 | HG02055.hp2 HG02109.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.638+1052_638+1053d others(4): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50155272 | ||||||
chr16:50155272 | G | GGTGT | 14 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(11): Show |
14 | HG01070.hp1 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.638+1050_638+1053d others(6): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50155272 | ||||||
chr16:50155272 | G | GGTGTGT | 71 | a0001c0001t0001g0084 a0001c0001t0001g0222 a0001c0001t0001g0223 others(68): Show |
72 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.638+1048_638+1053d others(8): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50155272 | ||||||
chr16:50155272 | G | GGTGTGTG others(1): Show |
79 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(76): Show |
79 | HG00544.hp1 HG00597.hp1 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.638+1046_638+1053d others(10): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50155272 | ||||||
chr16:50155272 | G | GGTGTGTG others(3): Show |
47 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(44): Show |
47 | HG00423.hp2 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.638+1044_638+1053d others(12): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50155272 | ||||||
chr16:50155272 | G | GGTGTGTG others(5): Show |
13 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0287 others(10): Show |
13 | HG00673.hp1 HG01099.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.638+1042_638+1053d others(14): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50155272 | ||||||
chr16:50155272 | G | GGTGTGTG others(7): Show |
14 | a0001c0001t0001g0294 a0001c0001t0001g0295 a0001c0001t0001g0296 others(11): Show |
14 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(11): Show |
intron_variant | MODIFIER | c.638+1040_638+1053d others(16): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50155272 | ||||||
chr16:50155272 | G | GGTGTGTG others(9): Show |
4 | a0001c0001t0001g0299 a0001c0001t0002g0176 a0001c0001t0041g0177 others(1): Show |
4 | HG01243.hp1 HG02109.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.638+1038_638+1053d others(18): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50155272 | ||||||
chr16:50155272 | G | GGTGTGTG others(11): Show |
5 | a0001c0001t0002g0181 a0001c0001t0003g0178 a0001c0001t0004g0300 others(2): Show |
5 | HG01167.hp1 HG01934.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.638+1036_638+1053d others(20): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50155272 | ||||||
chr16:50155272 | G | GGTGTGTG others(13): Show |
3 | a0001c0001t0001g0301 a0001c0001t0001g0302 a0001c0001t0004g0303 |
3 | HG01433.hp1 HG02976.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.638+1034_638+1053d others(22): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50155272 | ||||||
chr16:50155272 | G | GGTGTGTG others(17): Show |
1 | a0001c0001t0004g0304 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.638+1030_638+1053d others(26): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50155272 | ||||||
chr16:50155272 | G | GGTGTGTG others(21): Show |
2 | a0001c0001t0018g0182 a0001c0001t0018g0183 |
2 | HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.638+1026_638+1053d others(30): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50155272 | ||||||
chr16:50155272 | G | GTGTGTGT others(4): Show |
1 | a0001c0001t0020g0305 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.638+1013_638+1014i others(13): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50155272 | |||||||
chr16:50155272 | G | GTGTGTGT others(12): Show |
1 | a0001c0001t0001g0306 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.638+1013_638+1014i others(21): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50155272 | |||||||
chr16:50155272 | G | T | 4 | a0001c0001t0002g0184 a0001c0001t0002g0185 a0001c0001t0004g0190 others(1): Show |
4 | HG01081.hp1 HG03492.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.638+1013G>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50155272 | |||||||
chr16:50155272 | GGTGTGTG others(1): Show |
G | 3 | a0001c0002t0002g0012 a0001c0003t0006g0002 a0001c0003t0006g0191 |
3 | HG02976.hp2 NA18960.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.638+1046_638+1053d others(10): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50155272 | ||||||
chr16:50155274 | T | G | 1 | a0001c0003t0006g0192 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.638+1015T>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50155274 | |||||||
chr16:50155282 | T | G | 2 | a0001c0003t0006g0002 a0001c0003t0006g0191 |
2 | HG02976.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.638+1023T>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50155282 | |||||||
chr16:50155618 | T | C | 1 | a0001c0001t0003g0178 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.638+1359T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50155618 | |||||||
chr16:50156339 | A | G | 158 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(155): Show |
159 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.638+2080A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50156339 | |||||||
chr16:50156345 | AT | A | 300 | a0001c0001t0001g0084 a0001c0001t0001g0193 a0001c0001t0001g0201 others(297): Show |
301 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.638+2102delT | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50156345 | ||||||
chr16:50156422 | G | A | 1 | a0001c0001t0001g0222 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.638+2163G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50156422 | |||||||
chr16:50156469 | C | T | 9 | a0001c0001t0004g0190 a0001c0001t0004g0267 a0001c0001t0004g0268 others(6): Show |
9 | HG00639.hp2 HG01081.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.638+2210C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50156469 | |||||||
chr16:50156472 | G | A | 20 | a0001c0001t0002g0050 a0001c0001t0002g0098 a0001c0001t0003g0003 others(17): Show |
20 | HG00597.hp1 HG00609.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.638+2213G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50156472 | |||||||
chr16:50156489 | C | T | 1 | a0001c0001t0028g0198 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.638+2230C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50156489 | |||||||
chr16:50156602 | C | G | 1 | a0001c0001t0026g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.638+2343C>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50156602 | |||||||
chr16:50156729 | A | G | 1 | a0001c0001t0002g0161 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.638+2470A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50156729 | |||||||
chr16:50156756 | G | A | 1 | a0001c0001t0044g0053 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.638+2497G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50156756 | |||||||
chr16:50156795 | A | G | 2 | a0001c0001t0024g0015 a0001c0001t0024g0016 |
2 | HG01891.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.638+2536A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50156795 | |||||||
chr16:50156924 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.638+2665G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50156924 | |||||||
chr16:50156940 | T | C | 2 | a0001c0001t0002g0163 a0001c0001t0023g0140 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.638+2681T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50156940 | |||||||
chr16:50156979 | T | C | 1 | a0001c0001t0052g0013 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.638+2720T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50156979 | |||||||
chr16:50157024 | A | G | 10 | a0001c0001t0017g0136 a0001c0001t0017g0137 a0001c0001t0017g0186 others(7): Show |
10 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.638+2765A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50157024 | |||||||
chr16:50157047 | T | C | 1 | a0001c0001t0001g0210 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.638+2788T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50157047 | |||||||
chr16:50157064 | A | G | 9 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0213 others(6): Show |
9 | HG02257.hp2 HG02486.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.638+2805A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50157064 | |||||||
chr16:50157230 | A | G | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.638+2971A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50157230 | |||||||
chr16:50157267 | C | A | 22 | a0001c0001t0007g0014 a0001c0001t0007g0022 a0001c0001t0007g0023 others(19): Show |
22 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.638+3008C>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50157267 | |||||||
chr16:50157564 | C | T | 1 | a0001c0001t0055g0168 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.638+3305C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50157564 | |||||||
chr16:50157623 | G | A | 98 | a0001c0001t0001g0193 a0001c0001t0001g0201 a0001c0001t0001g0202 others(95): Show |
98 | HG00423.hp2 HG00544.hp2 HG00673.hp2 others(95): Show |
intron_variant | MODIFIER | c.638+3364G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50157623 | |||||||
chr16:50157922 | T | C | 192 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(189): Show |
193 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.638+3663T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50157922 | |||||||
chr16:50157938 | G | T | 22 | a0001c0001t0007g0014 a0001c0001t0007g0022 a0001c0001t0007g0023 others(19): Show |
22 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.638+3679G>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50157938 | |||||||
chr16:50158043 | G | A | 5 | a0001c0001t0009g0033 a0001c0001t0009g0043 a0001c0001t0009g0044 others(2): Show |
5 | HG02258.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.638+3784G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50158043 | |||||||
chr16:50158232 | G | A | 159 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(156): Show |
160 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.638+3973G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50158232 | |||||||
chr16:50158259 | G | A | 3 | a0001c0001t0011g0054 a0001c0001t0011g0141 a0001c0001t0011g0142 |
3 | HG02055.hp1 HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.638+4000G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50158259 | |||||||
chr16:50158284 | A | C | 4 | a0001c0001t0010g0006 a0001c0001t0010g0007 a0001c0001t0010g0008 others(1): Show |
4 | HG02145.hp2 HG02559.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.638+4025A>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50158284 | |||||||
chr16:50158290 | T | C | 1 | a0001c0001t0004g0292 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.638+4031T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50158290 | |||||||
chr16:50158301 | G | C | 2 | a0001c0001t0009g0043 a0001c0001t0009g0044 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.638+4042G>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50158301 | |||||||
chr16:50158602 | T | A | 3 | a0001c0001t0003g0096 a0001c0001t0003g0097 a0005c0006t0003g0045 |
3 | HG02083.hp2 NA18747.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.638+4343T>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50158602 | |||||||
chr16:50159025 | C | A | 1 | a0001c0001t0003g0139 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.638+4766C>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50159025 | |||||||
chr16:50159062 | G | A | 10 | a0001c0001t0001g0193 a0001c0001t0001g0238 a0001c0001t0001g0239 others(7): Show |
10 | HG01261.hp2 HG01361.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.638+4803G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50159062 | |||||||
chr16:50159246 | G | GT | 33 | a0001c0001t0001g0193 a0001c0001t0001g0232 a0001c0001t0001g0233 others(30): Show |
33 | HG00423.hp2 HG00673.hp2 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.638+5003dupT | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50159246 | ||||||
chr16:50159246 | GT | G | 133 | a0001c0001t0001g0084 a0001c0001t0001g0244 a0001c0001t0002g0001 others(130): Show |
134 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.638+5003delT | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50159246 | ||||||
chr16:50159455 | G | C | 10 | a0001c0001t0017g0136 a0001c0001t0017g0137 a0001c0001t0017g0186 others(7): Show |
10 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.638+5196G>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50159455 | |||||||
chr16:50159769 | C | T | 5 | a0001c0001t0007g0014 a0001c0001t0007g0023 a0001c0001t0007g0024 others(2): Show |
5 | HG02055.hp2 HG02109.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.638+5510C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50159769 | |||||||
chr16:50159860 | G | A | 1 | a0001c0001t0059g0245 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.638+5601G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50159860 | |||||||
chr16:50159904 | G | T | 1 | a0001c0001t0026g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.638+5645G>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50159904 | |||||||
chr16:50159960 | G | A | 2 | a0001c0001t0004g0199 a0001c0001t0004g0304 |
2 | HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.638+5701G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50159960 | |||||||
chr16:50160040 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.638+5781C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50160040 | |||||||
chr16:50160048 | C | T | 3 | a0001c0001t0010g0007 a0001c0001t0010g0008 a0001c0001t0010g0009 |
3 | HG02559.hp1 HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.638+5789C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50160048 | |||||||
chr16:50160088 | G | A | 10 | a0001c0001t0002g0102 a0001c0001t0002g0103 a0001c0001t0002g0104 others(7): Show |
10 | HG01928.hp2 HG01978.hp2 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.638+5829G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50160088 | |||||||
chr16:50160195 | G | C | 1 | a0001c0001t0002g0093 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.638+5936G>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50160195 | |||||||
chr16:50160318 | T | C | 1 | a0001c0001t0026g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.638+6059T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50160318 | |||||||
chr16:50160706 | G | A | 4 | a0001c0001t0010g0006 a0001c0001t0010g0007 a0001c0001t0010g0008 others(1): Show |
4 | HG02145.hp2 HG02559.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.638+6447G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50160706 | |||||||
chr16:50160915 | C | T | 2 | a0001c0001t0001g0265 a0001c0001t0001g0266 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.638+6656C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50160915 | |||||||
chr16:50160924 | A | G | 14 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(11): Show |
14 | HG02074.hp2 HG02080.hp1 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.638+6665A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50160924 | |||||||
chr16:50160927 | G | C | 2 | a0001c0001t0002g0108 a0001c0001t0002g0109 |
2 | HG01981.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.638+6668G>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50160927 | |||||||
chr16:50161145 | T | G | 1 | a0001c0001t0002g0184 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.638+6886T>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50161145 | |||||||
chr16:50161164 | C | T | 1 | a0001c0001t0059g0245 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.638+6905C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50161164 | |||||||
chr16:50161229 | T | C | 8 | a0001c0001t0007g0014 a0001c0001t0007g0022 a0001c0001t0007g0023 others(5): Show |
8 | HG02055.hp2 HG02109.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.638+6970T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50161229 | |||||||
chr16:50161350 | A | G | 1 | a0001c0001t0002g0134 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.638+7091A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50161350 | |||||||
chr16:50161569 | G | A | 1 | a0001c0001t0014g0110 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.638+7310G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50161569 | |||||||
chr16:50161768 | A | G | 7 | a0001c0001t0005g0041 a0001c0001t0005g0042 a0001c0001t0005g0088 others(4): Show |
7 | HG00099.hp2 HG00323.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.638+7509A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50161768 | |||||||
chr16:50161787 | C | T | 1 | a0001c0001t0002g0040 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.638+7528C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50161787 | |||||||
chr16:50161849 | A | G | 1 | a0001c0001t0052g0013 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.638+7590A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50161849 | |||||||
chr16:50161861 | G | A | 22 | a0001c0001t0007g0014 a0001c0001t0007g0022 a0001c0001t0007g0023 others(19): Show |
22 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.638+7602G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50161861 | |||||||
chr16:50161990 | C | A | 2 | a0001c0001t0002g0036 a0001c0001t0002g0146 |
2 | HG01070.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.638+7731C>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50161990 | |||||||
chr16:50162620 | A | G | 1 | a0001c0001t0034g0087 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.638+8361A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50162620 | |||||||
chr16:50162657 | A | G | 13 | a0001c0001t0017g0136 a0001c0001t0017g0137 a0001c0001t0017g0186 others(10): Show |
13 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.638+8398A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50162657 | |||||||
chr16:50162705 | G | A | 1 | a0001c0001t0001g0246 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.638+8446G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50162705 | |||||||
chr16:50162928 | T | G | 1 | a0001c0011t0030g0208 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.638+8669T>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50162928 | |||||||
chr16:50163030 | G | A | 1 | a0001c0002t0002g0111 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.638+8771G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50163030 | |||||||
chr16:50163380 | A | G | 4 | a0001c0001t0012g0195 a0001c0001t0012g0196 a0001c0001t0012g0197 others(1): Show |
4 | HG02145.hp1 HG02723.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.638+9121A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50163380 | |||||||
chr16:50163417 | C | CT | 9 | a0001c0001t0001g0291 a0001c0001t0001g0307 a0001c0001t0002g0039 others(6): Show |
9 | HG00544.hp2 HG01175.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.638+9176dupT | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50163417 | ||||||
chr16:50163417 | CT | C | 15 | a0001c0001t0001g0247 a0001c0001t0001g0275 a0001c0001t0001g0276 others(12): Show |
15 | HG00423.hp2 HG01099.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.638+9176delT | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50163417 | ||||||
chr16:50163456 | C | T | 1 | a0001c0001t0001g0247 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.638+9197C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50163456 | |||||||
chr16:50163561 | G | A | 22 | a0001c0001t0007g0014 a0001c0001t0007g0022 a0001c0001t0007g0023 others(19): Show |
22 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.638+9302G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50163561 | |||||||
chr16:50163766 | A | G | 159 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(156): Show |
160 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.638+9507A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50163766 | |||||||
chr16:50163896 | G | A | 2 | a0001c0001t0054g0010 a0001c0001t0057g0011 |
2 | HG02451.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.638+9637G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50163896 | |||||||
chr16:50163947 | CG | C | 3 | a0001c0001t0016g0187 a0001c0001t0016g0188 a0001c0001t0016g0189 |
3 | HG00741.hp2 HG01243.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.638+9691delG | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50163947 | ||||||
chr16:50163956 | G | A | 1 | a0001c0001t0026g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.638+9697G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50163956 | |||||||
chr16:50163984 | C | T | 159 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(156): Show |
160 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.638+9725C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50163984 | |||||||
chr16:50163991 | C | G | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.638+9732C>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50163991 | |||||||
chr16:50164001 | T | C | 1 | a0001c0001t0001g0269 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.638+9742T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50164001 | |||||||
chr16:50164173 | T | G | 1 | a0001c0001t0026g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.638+9914T>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50164173 | |||||||
chr16:50164204 | C | T | 5 | a0001c0001t0009g0033 a0001c0001t0009g0043 a0001c0001t0009g0044 others(2): Show |
5 | HG02258.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.638+9945C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50164204 | |||||||
chr16:50164311 | TTTG | T | 159 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(156): Show |
160 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.638+10064_638+1006 others(7): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50164311 | ||||||
chr16:50164340 | C | A | 159 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(156): Show |
160 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.638+10081C>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50164340 | |||||||
chr16:50164413 | A | T | 5 | a0001c0001t0009g0033 a0001c0001t0009g0043 a0001c0001t0009g0044 others(2): Show |
5 | HG02258.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.638+10154A>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50164413 | |||||||
chr16:50164726 | A | T | 1 | a0001c0001t0003g0052 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.638+10467A>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50164726 | |||||||
chr16:50164861 | G | C | 1 | a0001c0001t0020g0203 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.638+10602G>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50164861 | |||||||
chr16:50164901 | A | G | 2 | a0001c0001t0054g0010 a0001c0001t0057g0011 |
2 | HG02451.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.638+10642A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50164901 | |||||||
chr16:50164901 | A | T | 1 | a0001c0001t0010g0009 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.638+10642A>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50164901 | |||||||
chr16:50165058 | AT | A | 158 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(155): Show |
159 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.638+10814delT | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50165058 | ||||||
chr16:50165059 | T | A | 3 | a0001c0001t0001g0241 a0001c0003t0006g0204 a0001c0003t0060g0207 |
3 | HG01978.hp1 HG02630.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.638+10800T>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50165059 | |||||||
chr16:50165219 | T | C | 1 | a0001c0001t0054g0010 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.638+10960T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50165219 | |||||||
chr16:50165368 | G | T | 1 | a0001c0001t0020g0203 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.638+11109G>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50165368 | |||||||
chr16:50165424 | T | C | 1 | a0001c0001t0002g0148 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.638+11165T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50165424 | |||||||
chr16:50165495 | AT | A | 159 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(156): Show |
160 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.638+11237delT | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50165495 | |||||||
chr16:50165522 | A | G | 2 | a0001c0001t0024g0015 a0001c0001t0024g0016 |
2 | HG01891.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.638+11263A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50165522 | |||||||
chr16:50165547 | C | T | 1 | a0001c0001t0007g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.638+11288C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50165547 | |||||||
chr16:50165570 | T | C | 8 | a0001c0003t0006g0002 a0001c0003t0006g0191 a0001c0003t0006g0192 others(5): Show |
8 | HG02559.hp2 HG02630.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.638+11311T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50165570 | |||||||
chr16:50165587 | C | T | 3 | a0002c0004t0001g0281 a0002c0004t0001g0282 a0002c0004t0001g0283 |
3 | NA18972.hp1 NA18992.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.638+11328C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50165587 | |||||||
chr16:50165660 | T | C | 1 | a0001c0001t0001g0273 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.638+11401T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50165660 | |||||||
chr16:50165673 | A | G | 5 | a0001c0001t0009g0033 a0001c0001t0009g0043 a0001c0001t0009g0044 others(2): Show |
5 | HG02258.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.638+11414A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50165673 | |||||||
chr16:50165917 | A | G | 1 | a0001c0001t0022g0021 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.638+11658A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50165917 | |||||||
chr16:50165932 | A | T | 1 | a0001c0001t0053g0308 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.638+11673A>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50165932 | |||||||
chr16:50166080 | C | CT | 12 | a0001c0001t0002g0086 a0001c0001t0002g0134 a0001c0001t0002g0145 others(9): Show |
12 | HG02071.hp2 HG02258.hp1 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.638+11841dupT | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50166080 | ||||||
chr16:50166080 | CT | C | 116 | a0001c0001t0001g0193 a0001c0001t0001g0201 a0001c0001t0001g0202 others(113): Show |
116 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(113): Show |
intron_variant | MODIFIER | c.638+11841delT | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50166080 | ||||||
chr16:50166094 | T | G | 1 | a0001c0001t0020g0305 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.638+11835T>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50166094 | |||||||
chr16:50166095 | T | G | 1 | a0001c0001t0001g0248 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.638+11836T>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50166095 | |||||||
chr16:50166108 | A | G | 1 | a0001c0001t0008g0166 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.638+11849A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50166108 | |||||||
chr16:50166176 | A | G | 297 | a0001c0001t0001g0084 a0001c0001t0001g0193 a0001c0001t0001g0201 others(294): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.638+11917A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50166176 | |||||||
chr16:50166285 | A | G | 1 | a0001c0001t0026g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.638+12026A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50166285 | |||||||
chr16:50166378 | C | T | 1 | a0001c0001t0014g0110 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.638+12119C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50166378 | |||||||
chr16:50166388 | A | T | 1 | a0001c0001t0007g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.638+12129A>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50166388 | |||||||
chr16:50166521 | A | G | 1 | a0001c0001t0002g0160 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.638+12262A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50166521 | |||||||
chr16:50166602 | A | G | 5 | a0001c0001t0007g0014 a0001c0001t0007g0023 a0001c0001t0007g0024 others(2): Show |
5 | HG02055.hp2 HG02109.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.638+12343A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50166602 | |||||||
chr16:50166780 | AT | A | 164 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(161): Show |
165 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.638+12543delT | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50166780 | ||||||
chr16:50166780 | ATT | A | 9 | a0001c0001t0002g0055 a0001c0001t0002g0112 a0001c0001t0003g0046 others(6): Show |
9 | HG01099.hp1 HG01167.hp1 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.638+12542_638+1254 others(6): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50166780 | ||||||
chr16:50166780 | ATTTTTTT | A | 104 | a0001c0001t0001g0193 a0001c0001t0001g0201 a0001c0001t0001g0202 others(101): Show |
104 | HG00423.hp2 HG00544.hp2 HG00673.hp2 others(101): Show |
intron_variant | MODIFIER | c.638+12537_638+1254 others(11): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50166780 | ||||||
chr16:50166813 | A | G | 1 | a0001c0001t0002g0085 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.638+12554A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50166813 | |||||||
chr16:50166869 | A | G | 1 | a0001c0003t0029g0194 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.638+12610A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50166869 | |||||||
chr16:50166873 | G | A | 3 | a0001c0001t0012g0195 a0001c0001t0012g0196 a0001c0001t0012g0197 |
3 | HG02723.hp2 HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.638+12614G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50166873 | |||||||
chr16:50167180 | A | G | 4 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0219 others(1): Show |
4 | HG02056.hp2 HG02083.hp1 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.638+12921A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50167180 | |||||||
chr16:50167385 | G | GTTT | 21 | a0001c0001t0007g0014 a0001c0001t0007g0022 a0001c0001t0007g0023 others(18): Show |
21 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.638+13136_638+1313 others(7): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50167385 | ||||||
chr16:50167666 | T | TTTG | 183 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(180): Show |
184 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.638+13417_638+1341 others(7): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50167666 | ||||||
chr16:50167696 | C | T | 1 | a0001c0001t0003g0028 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.638+13437C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50167696 | |||||||
chr16:50167780 | C | G | 1 | a0001c0001t0002g0001 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.638+13521C>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50167780 | |||||||
chr16:50167958 | G | C | 1 | a0001c0001t0002g0056 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.638+13699G>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50167958 | |||||||
chr16:50168083 | G | A | 1 | a0001c0001t0026g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.638+13824G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50168083 | |||||||
chr16:50168093 | A | G | 8 | a0001c0001t0007g0014 a0001c0001t0007g0022 a0001c0001t0007g0023 others(5): Show |
8 | HG02055.hp2 HG02109.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.638+13834A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50168093 | |||||||
chr16:50168123 | AG | A | 127 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(124): Show |
128 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.638+13865delG | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50168123 | |||||||
chr16:50168124 | G | A | 1 | a0001c0001t0002g0039 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.638+13865G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50168124 | |||||||
chr16:50168467 | A | AT | 15 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0272 others(12): Show |
15 | HG00639.hp1 HG02135.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.638+14226dupT | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50168467 | ||||||
chr16:50168467 | A | ATT | 95 | a0001c0001t0001g0193 a0001c0001t0001g0201 a0001c0001t0001g0202 others(92): Show |
95 | HG00423.hp2 HG00544.hp2 HG00673.hp2 others(92): Show |
intron_variant | MODIFIER | c.638+14225_638+1422 others(6): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50168467 | ||||||
chr16:50168467 | A | ATTT | 8 | a0001c0003t0006g0002 a0001c0003t0006g0191 a0001c0003t0006g0192 others(5): Show |
8 | HG02559.hp2 HG02630.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.638+14224_638+1422 others(7): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50168467 | ||||||
chr16:50168576 | A | C | 9 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0213 others(6): Show |
9 | HG02257.hp2 HG02486.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.638+14317A>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50168576 | |||||||
chr16:50168650 | A | C | 1 | a0001c0001t0002g0176 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.638+14391A>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50168650 | |||||||
chr16:50168677 | G | A | 1 | a0001c0003t0029g0194 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.638+14418G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50168677 | |||||||
chr16:50168966 | A | G | 132 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(129): Show |
133 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.638+14707A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50168966 | |||||||
chr16:50168974 | C | A | 1 | a0001c0001t0002g0134 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.638+14715C>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50168974 | |||||||
chr16:50169083 | A | G | 3 | a0001c0001t0001g0084 a0001c0001t0002g0038 a0001c0001t0013g0083 |
3 | NA18971.hp1 NA19007.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.638+14824A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50169083 | |||||||
chr16:50169249 | C | T | 1 | a0001c0001t0002g0032 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.638+14990C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50169249 | |||||||
chr16:50169260 | G | A | 296 | a0001c0001t0001g0084 a0001c0001t0001g0193 a0001c0001t0001g0201 others(293): Show |
297 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.638+15001G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50169260 | |||||||
chr16:50169299 | C | T | 1 | a0001c0001t0053g0308 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.638+15040C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50169299 | |||||||
chr16:50169387 | G | GT | 10 | a0001c0001t0001g0285 a0001c0001t0002g0129 a0001c0001t0002g0133 others(7): Show |
10 | HG01934.hp2 HG02027.hp1 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.638+15154dupT | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50169387 | ||||||
chr16:50169387 | GT | G | 89 | a0001c0001t0001g0201 a0001c0001t0001g0215 a0001c0001t0001g0216 others(86): Show |
89 | HG00099.hp1 HG00597.hp2 HG00741.hp2 others(86): Show |
intron_variant | MODIFIER | c.638+15154delT | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50169387 | ||||||
chr16:50169387 | GTT | G | 72 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0213 others(69): Show |
73 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.638+15153_638+1515 others(6): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50169387 | ||||||
chr16:50169387 | GTTT | G | 61 | a0001c0001t0001g0084 a0001c0001t0001g0221 a0001c0001t0002g0029 others(58): Show |
61 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.638+15152_638+1515 others(7): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50169387 | ||||||
chr16:50169387 | GTTTTTTT | G | 9 | a0001c0001t0004g0190 a0001c0001t0004g0199 a0001c0001t0004g0267 others(6): Show |
9 | HG00639.hp2 HG01081.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.638+15148_638+1515 others(11): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50169387 | ||||||
chr16:50169387 | GTTTTTTT others(3): Show |
G | 5 | a0001c0001t0012g0195 a0001c0001t0012g0196 a0001c0001t0012g0197 others(2): Show |
5 | HG02145.hp1 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.638+15145_638+1515 others(14): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50169387 | ||||||
chr16:50169558 | G | C | 297 | a0001c0001t0001g0084 a0001c0001t0001g0193 a0001c0001t0001g0201 others(294): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.638+15299G>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50169558 | |||||||
chr16:50169599 | G | C | 297 | a0001c0001t0001g0084 a0001c0001t0001g0193 a0001c0001t0001g0201 others(294): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.638+15340G>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50169599 | |||||||
chr16:50169903 | G | T | 1 | a0001c0001t0053g0308 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.638+15644G>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50169903 | |||||||
chr16:50169914 | G | A | 1 | a0001c0001t0002g0029 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.638+15655G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50169914 | |||||||
chr16:50170107 | A | G | 1 | a0001c0001t0001g0259 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.638+15848A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50170107 | |||||||
chr16:50170132 | A | G | 1 | a0001c0001t0004g0268 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.638+15873A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50170132 | |||||||
chr16:50170282 | G | C | 1 | a0001c0001t0004g0303 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.638+16023G>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50170282 | |||||||
chr16:50170296 | G | A | 25 | a0001c0001t0002g0071 a0001c0001t0002g0102 a0001c0001t0002g0103 others(22): Show |
25 | HG00597.hp2 HG01123.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.638+16037G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50170296 | |||||||
chr16:50170444 | A | T | 1 | a0001c0001t0004g0190 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.638+16185A>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50170444 | |||||||
chr16:50170518 | G | A | 5 | a0001c0001t0012g0195 a0001c0001t0012g0196 a0001c0001t0012g0197 others(2): Show |
5 | HG02145.hp1 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.638+16259G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50170518 | |||||||
chr16:50170579 | C | G | 1 | a0001c0001t0026g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.638+16320C>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50170579 | |||||||
chr16:50170614 | GTTCCTGG others(6): Show |
G | 1 | a0001c0001t0031g0153 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.638+16356_638+1636 others(17): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50170614 | |||||||
chr16:50170632 | A | T | 1 | a0001c0001t0031g0153 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.638+16373A>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50170632 | |||||||
chr16:50170813 | C | T | 2 | a0001c0001t0054g0010 a0001c0001t0057g0011 |
2 | HG02451.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.638+16554C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50170813 | |||||||
chr16:50170858 | G | A | 1 | a0001c0001t0053g0308 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.638+16599G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50170858 | |||||||
chr16:50170916 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.638+16657C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50170916 | |||||||
chr16:50170960 | G | GT | 140 | a0001c0001t0001g0084 a0001c0001t0001g0202 a0001c0001t0002g0001 others(137): Show |
141 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.638+16714dupT | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50170960 | ||||||
chr16:50171172 | A | G | 1 | a0001c0001t0004g0303 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.638+16913A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50171172 | |||||||
chr16:50171187 | G | A | 1 | a0001c0001t0005g0132 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.638+16928G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50171187 | |||||||
chr16:50171197 | T | G | 1 | a0001c0001t0004g0300 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.638+16938T>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50171197 | |||||||
chr16:50171502 | G | A | 3 | a0001c0001t0011g0054 a0001c0001t0011g0141 a0001c0001t0011g0142 |
3 | HG02055.hp1 HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.638+17243G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50171502 | |||||||
chr16:50171502 | G | T | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.638+17243G>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50171502 | |||||||
chr16:50171547 | A | C | 1 | a0001c0001t0004g0292 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.638+17288A>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50171547 | |||||||
chr16:50171556 | C | T | 8 | a0001c0003t0006g0002 a0001c0003t0006g0191 a0001c0003t0006g0192 others(5): Show |
8 | HG02559.hp2 HG02630.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.638+17297C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50171556 | |||||||
chr16:50171577 | CCAAGGCA others(4): Show |
C | 158 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(155): Show |
159 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.638+17320_638+1733 others(15): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50171577 | ||||||
chr16:50171636 | T | C | 1 | a0001c0001t0002g0173 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.638+17377T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50171636 | |||||||
chr16:50172097 | C | T | 1 | a0001c0001t0002g0157 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.638+17838C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50172097 | |||||||
chr16:50172227 | T | C | 1 | a0001c0003t0029g0194 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.638+17968T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50172227 | |||||||
chr16:50172295 | C | T | 298 | a0001c0001t0001g0084 a0001c0001t0001g0193 a0001c0001t0001g0201 others(295): Show |
299 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.638+18036C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50172295 | |||||||
chr16:50172419 | A | G | 13 | a0001c0001t0017g0136 a0001c0001t0017g0137 a0001c0001t0017g0186 others(10): Show |
13 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.638+18160A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50172419 | |||||||
chr16:50172497 | A | G | 1 | a0001c0001t0002g0070 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.638+18238A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50172497 | |||||||
chr16:50172508 | C | CT | 142 | a0001c0001t0001g0084 a0001c0001t0001g0295 a0001c0001t0002g0001 others(139): Show |
143 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.638+18265dupT | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50172508 | ||||||
chr16:50172508 | C | CTT | 8 | a0001c0001t0002g0169 a0001c0001t0002g0171 a0001c0001t0010g0006 others(5): Show |
8 | HG02129.hp1 HG02145.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.638+18264_638+1826 others(6): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50172508 | ||||||
chr16:50172508 | CT | C | 12 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0009g0033 others(9): Show |
12 | HG02258.hp1 HG02886.hp1 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.638+18265delT | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50172508 | ||||||
chr16:50172508 | CTT | C | 127 | a0001c0001t0001g0193 a0001c0001t0001g0201 a0001c0001t0001g0202 others(124): Show |
127 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.638+18264_638+1826 others(6): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50172508 | ||||||
chr16:50172561 | A | G | 1 | a0001c0001t0001g0248 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.638+18302A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50172561 | |||||||
chr16:50172677 | A | C | 3 | a0001c0001t0001g0222 a0001c0001t0001g0250 a0004c0008t0001g0251 |
3 | NA18941.hp1 NA18945.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.638+18418A>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50172677 | |||||||
chr16:50172824 | A | G | 1 | a0001c0001t0008g0122 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.638+18565A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50172824 | |||||||
chr16:50172980 | G | A | 11 | a0001c0001t0004g0190 a0001c0001t0004g0199 a0001c0001t0004g0267 others(8): Show |
11 | HG00639.hp2 HG01081.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.638+18721G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50172980 | |||||||
chr16:50173005 | A | G | 1 | a0001c0011t0030g0208 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.638+18746A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50173005 | |||||||
chr16:50173121 | T | A | 1 | a0001c0001t0002g0072 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.638+18862T>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50173121 | |||||||
chr16:50173146 | A | G | 1 | a0001c0001t0053g0308 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.638+18887A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50173146 | |||||||
chr16:50173351 | G | A | 2 | a0001c0001t0002g0126 a0001c0001t0002g0165 |
2 | HG00673.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.638+19092G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50173351 | |||||||
chr16:50173444 | C | T | 3 | a0001c0001t0002g0055 a0001c0001t0002g0080 a0001c0001t0002g0157 |
3 | HG01346.hp2 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.638+19185C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50173444 | |||||||
chr16:50173730 | A | G | 1 | a0001c0001t0002g0157 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.638+19471A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50173730 | |||||||
chr16:50173797 | G | T | 1 | a0001c0001t0002g0071 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.638+19538G>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50173797 | |||||||
chr16:50173820 | G | A | 297 | a0001c0001t0001g0084 a0001c0001t0001g0193 a0001c0001t0001g0201 others(294): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.638+19561G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50173820 | |||||||
chr16:50173978 | G | A | 1 | a0001c0001t0003g0178 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.638+19719G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50173978 | |||||||
chr16:50174071 | A | G | 1 | a0001c0001t0014g0110 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.638+19812A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50174071 | |||||||
chr16:50174166 | C | T | 1 | a0001c0002t0002g0114 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.638+19907C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50174166 | |||||||
chr16:50174249 | C | A | 20 | a0001c0001t0002g0050 a0001c0001t0002g0098 a0001c0001t0003g0003 others(17): Show |
20 | HG00597.hp1 HG00609.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.638+19990C>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50174249 | |||||||
chr16:50174292 | T | C | 1 | a0001c0001t0003g0178 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.638+20033T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50174292 | |||||||
chr16:50174358 | A | G | 1 | a0001c0001t0001g0218 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.638+20099A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50174358 | |||||||
chr16:50174742 | C | CT | 16 | a0001c0001t0009g0033 a0001c0001t0009g0043 a0001c0001t0009g0044 others(13): Show |
16 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.638+20504dupT | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50174742 | ||||||
chr16:50174742 | CT | C | 254 | a0001c0001t0001g0084 a0001c0001t0001g0193 a0001c0001t0001g0201 others(251): Show |
255 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(252): Show |
intron_variant | MODIFIER | c.638+20504delT | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50174742 | ||||||
chr16:50174742 | CTT | C | 12 | a0001c0001t0001g0222 a0001c0001t0001g0266 a0001c0001t0001g0302 others(9): Show |
12 | HG00099.hp2 HG01106.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.638+20503_638+2050 others(6): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50174742 | ||||||
chr16:50174874 | C | T | 1 | a0001c0001t0026g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.638+20615C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50174874 | |||||||
chr16:50174887 | C | T | 2 | a0001c0001t0001g0265 a0001c0001t0001g0266 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.638+20628C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50174887 | |||||||
chr16:50174999 | C | T | 158 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(155): Show |
159 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.638+20740C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50174999 | |||||||
chr16:50175085 | C | A | 1 | a0001c0001t0054g0010 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.638+20826C>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50175085 | |||||||
chr16:50175163 | T | C | 2 | a0001c0003t0006g0002 a0001c0003t0006g0191 |
2 | HG02976.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.638+20904T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50175163 | |||||||
chr16:50175179 | G | T | 1 | a0001c0001t0001g0236 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.638+20920G>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50175179 | |||||||
chr16:50175359 | C | T | 5 | a0001c0001t0012g0195 a0001c0001t0012g0196 a0001c0001t0012g0197 others(2): Show |
5 | HG02145.hp1 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.638+21100C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50175359 | |||||||
chr16:50175461 | A | G | 1 | a0001c0011t0030g0208 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.638+21202A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50175461 | |||||||
chr16:50175511 | A | C | 5 | a0001c0001t0012g0195 a0001c0001t0012g0196 a0001c0001t0012g0197 others(2): Show |
5 | HG02145.hp1 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.638+21252A>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50175511 | |||||||
chr16:50175547 | C | T | 1 | a0001c0001t0053g0308 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.638+21288C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50175547 | |||||||
chr16:50176092 | C | CT | 31 | a0001c0001t0001g0227 a0001c0001t0001g0229 a0001c0001t0002g0050 others(28): Show |
31 | HG00597.hp1 HG00609.hp1 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.638+21847dupT | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50176092 | ||||||
chr16:50176140 | G | T | 1 | a0001c0001t0001g0243 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.638+21881G>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50176140 | |||||||
chr16:50176149 | T | A | 1 | a0001c0001t0059g0245 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.638+21890T>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50176149 | |||||||
chr16:50176354 | C | T | 17 | a0001c0001t0001g0218 a0001c0001t0001g0247 a0001c0001t0001g0254 others(14): Show |
17 | HG00544.hp2 HG02074.hp2 HG02080.hp1 others(14): Show |
intron_variant | MODIFIER | c.638+22095C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50176354 | |||||||
chr16:50176494 | C | CT | 6 | a0001c0001t0004g0199 a0001c0001t0004g0284 a0001c0001t0004g0303 others(3): Show |
6 | HG01433.hp1 HG02523.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.638+22265dupT | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50176494 | ||||||
chr16:50176494 | CT | C | 125 | a0001c0001t0001g0193 a0001c0001t0001g0201 a0001c0001t0001g0211 others(122): Show |
125 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.638+22265delT | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50176494 | ||||||
chr16:50176494 | CTT | C | 132 | a0001c0001t0001g0084 a0001c0001t0001g0234 a0001c0001t0001g0255 others(129): Show |
133 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.638+22264_638+2226 others(6): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50176494 | ||||||
chr16:50176494 | CTTT | C | 7 | a0001c0001t0002g0055 a0001c0001t0002g0116 a0001c0001t0002g0145 others(4): Show |
7 | HG01081.hp2 HG01517.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.638+22263_638+2226 others(7): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50176494 | ||||||
chr16:50176494 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0004g0268 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.638+22254_638+2226 others(16): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50176494 | ||||||
chr16:50176578 | C | A | 2 | a0001c0001t0007g0023 a0001c0001t0007g0024 |
2 | HG02055.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.638+22319C>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50176578 | |||||||
chr16:50176612 | T | A | 1 | a0001c0001t0002g0036 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.638+22353T>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50176612 | |||||||
chr16:50176625 | G | A | 7 | a0001c0001t0005g0041 a0001c0001t0005g0042 a0001c0001t0005g0088 others(4): Show |
7 | HG00099.hp2 HG00323.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.638+22366G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50176625 | |||||||
chr16:50176770 | G | A | 1 | a0001c0001t0052g0013 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.638+22511G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50176770 | |||||||
chr16:50176924 | T | G | 2 | a0001c0001t0022g0020 a0001c0001t0022g0021 |
2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.638+22665T>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50176924 | |||||||
chr16:50176929 | G | A | 1 | a0001c0001t0020g0203 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.638+22670G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50176929 | |||||||
chr16:50177041 | C | T | 3 | a0001c0001t0011g0054 a0001c0001t0011g0141 a0001c0001t0011g0142 |
3 | HG02055.hp1 HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.638+22782C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50177041 | |||||||
chr16:50177098 | G | A | 1 | a0001c0001t0002g0061 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.638+22839G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50177098 | |||||||
chr16:50177143 | C | T | 3 | a0001c0001t0014g0110 a0001c0001t0014g0151 a0001c0001t0014g0152 |
3 | NA18942.hp2 NA19002.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.638+22884C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50177143 | |||||||
chr16:50177201 | C | T | 41 | a0001c0001t0002g0036 a0001c0001t0002g0071 a0001c0001t0002g0102 others(38): Show |
41 | HG00597.hp2 HG00673.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.638+22942C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50177201 | |||||||
chr16:50177209 | G | T | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.638+22950G>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50177209 | |||||||
chr16:50177303 | C | G | 3 | a0001c0001t0002g0060 a0001c0001t0002g0112 a0001c0001t0002g0116 |
3 | HG01081.hp2 HG01099.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.638+23044C>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50177303 | |||||||
chr16:50177790 | T | C | 159 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(156): Show |
160 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.638+23531T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50177790 | |||||||
chr16:50178033 | T | G | 160 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(157): Show |
161 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.638+23774T>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50178033 | |||||||
chr16:50178142 | C | CT | 123 | a0001c0001t0001g0084 a0001c0001t0002g0005 a0001c0001t0002g0019 others(120): Show |
123 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.638+23904dupT | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50178142 | ||||||
chr16:50178142 | CT | C | 30 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0266 others(27): Show |
30 | HG00597.hp1 HG00609.hp1 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.638+23904delT | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50178142 | ||||||
chr16:50178415 | G | C | 1 | a0001c0001t0002g0086 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.638+24156G>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50178415 | |||||||
chr16:50178610 | A | C | 1 | a0001c0001t0026g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.638+24351A>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50178610 | |||||||
chr16:50178638 | G | T | 1 | a0001c0001t0002g0056 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.638+24379G>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50178638 | |||||||
chr16:50178656 | T | C | 27 | a0001c0001t0007g0014 a0001c0001t0007g0022 a0001c0001t0007g0023 others(24): Show |
27 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.638+24397T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50178656 | |||||||
chr16:50178678 | T | G | 38 | a0001c0001t0001g0193 a0001c0001t0001g0222 a0001c0001t0001g0232 others(35): Show |
38 | HG00423.hp2 HG00673.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.638+24419T>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50178678 | |||||||
chr16:50179191 | C | T | 1 | a0001c0001t0004g0284 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.638+24932C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50179191 | |||||||
chr16:50179257 | G | A | 6 | a0001c0001t0017g0136 a0001c0001t0017g0137 a0001c0001t0017g0186 others(3): Show |
6 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.638+24998G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50179257 | |||||||
chr16:50179458 | G | A | 27 | a0001c0001t0007g0014 a0001c0001t0007g0022 a0001c0001t0007g0023 others(24): Show |
27 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.638+25199G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50179458 | |||||||
chr16:50179554 | A | G | 1 | a0001c0001t0026g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.638+25295A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50179554 | |||||||
chr16:50179903 | T | C | 5 | a0001c0001t0009g0033 a0001c0001t0009g0043 a0001c0001t0009g0044 others(2): Show |
5 | HG02258.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.638+25644T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50179903 | |||||||
chr16:50179936 | T | C | 1 | a0001c0001t0023g0073 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.638+25677T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50179936 | |||||||
chr16:50180111 | C | CT | 187 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(184): Show |
188 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.638+25862dupT | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50180111 | ||||||
chr16:50180166 | C | T | 2 | a0001c0001t0002g0161 a0001c0001t0002g0170 |
2 | HG00423.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.638+25907C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50180166 | |||||||
chr16:50180172 | C | T | 159 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(156): Show |
160 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.638+25913C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50180172 | |||||||
chr16:50180194 | C | T | 1 | a0001c0001t0048g0081 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.638+25935C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50180194 | |||||||
chr16:50180324 | C | T | 4 | a0001c0001t0012g0195 a0001c0001t0012g0196 a0001c0001t0012g0197 others(1): Show |
4 | HG02145.hp1 HG02723.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.638+26065C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50180324 | |||||||
chr16:50180383 | A | G | 2 | a0001c0001t0002g0004 a0001c0001t0002g0005 |
2 | HG02129.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.638+26124A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50180383 | |||||||
chr16:50180568 | G | T | 1 | a0001c0001t0001g0226 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.638+26309G>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50180568 | |||||||
chr16:50180624 | G | A | 8 | a0001c0003t0006g0002 a0001c0003t0006g0191 a0001c0003t0006g0192 others(5): Show |
8 | HG02559.hp2 HG02630.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.638+26365G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50180624 | |||||||
chr16:50180695 | C | T | 4 | a0001c0001t0010g0006 a0001c0001t0010g0007 a0001c0001t0010g0008 others(1): Show |
4 | HG02145.hp2 HG02559.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.638+26436C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50180695 | |||||||
chr16:50180708 | C | CA | 131 | a0001c0001t0001g0084 a0001c0001t0001g0234 a0001c0001t0001g0294 others(128): Show |
132 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.638+26466dupA | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50180708 | ||||||
chr16:50180775 | A | G | 2 | a0001c0001t0007g0023 a0001c0001t0007g0024 |
2 | HG02055.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.638+26516A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50180775 | |||||||
chr16:50180936 | T | C | 187 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(184): Show |
188 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.638+26677T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50180936 | |||||||
chr16:50181044 | A | G | 1 | a0001c0001t0004g0298 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.638+26785A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50181044 | |||||||
chr16:50181137 | A | G | 1 | a0001c0001t0003g0178 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.638+26878A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50181137 | |||||||
chr16:50181249 | G | T | 1 | a0001c0001t0020g0203 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.638+26990G>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50181249 | |||||||
chr16:50181327 | C | CT | 23 | a0001c0001t0002g0050 a0001c0001t0002g0093 a0001c0001t0002g0098 others(20): Show |
23 | HG00597.hp1 HG00609.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.638+27082dupT | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50181327 | ||||||
chr16:50181341 | T | C | 1 | a0001c0001t0026g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.638+27082T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50181341 | |||||||
chr16:50181433 | A | G | 1 | a0001c0001t0020g0203 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.638+27174A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50181433 | |||||||
chr16:50181464 | A | AT | 13 | a0001c0001t0001g0263 a0001c0001t0002g0055 a0001c0001t0002g0080 others(10): Show |
13 | HG01516.hp1 HG01517.hp2 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.638+27226dupT | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50181464 | ||||||
chr16:50181464 | AT | A | 50 | a0001c0001t0001g0211 a0001c0001t0001g0272 a0001c0001t0001g0274 others(47): Show |
50 | HG00099.hp1 HG00639.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.638+27226delT | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50181464 | ||||||
chr16:50181817 | G | A | 2 | a0001c0001t0054g0010 a0001c0001t0057g0011 |
2 | HG02451.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.638+27558G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50181817 | |||||||
chr16:50181896 | A | G | 1 | a0001c0001t0052g0013 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.638+27637A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50181896 | |||||||
chr16:50182175 | G | A | 2 | a0001c0001t0002g0064 a0001c0001t0003g0078 |
2 | NA18975.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.638+27916G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50182175 | |||||||
chr16:50182186 | G | A | 5 | a0001c0001t0009g0033 a0001c0001t0009g0043 a0001c0001t0009g0044 others(2): Show |
5 | HG02258.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.638+27927G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50182186 | |||||||
chr16:50182311 | C | T | 1 | a0001c0001t0052g0013 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.638+28052C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50182311 | |||||||
chr16:50182588 | A | G | 4 | a0001c0001t0010g0006 a0001c0001t0010g0007 a0001c0001t0010g0008 others(1): Show |
4 | HG02145.hp2 HG02559.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.638+28329A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50182588 | |||||||
chr16:50182785 | A | T | 2 | a0001c0001t0001g0270 a0001c0001t0001g0295 |
2 | NA18967.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.638+28526A>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50182785 | |||||||
chr16:50182891 | C | CT | 11 | a0001c0001t0001g0210 a0001c0001t0004g0190 a0001c0001t0012g0195 others(8): Show |
11 | HG01081.hp1 HG01109.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.639-28401dupT | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50182891 | ||||||
chr16:50182891 | C | CTT | 22 | a0001c0001t0002g0098 a0001c0001t0003g0018 a0001c0001t0003g0035 others(19): Show |
22 | HG00597.hp1 HG00639.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.639-28402_639-2840 others(6): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50182891 | ||||||
chr16:50182891 | C | CTTT | 17 | a0001c0001t0001g0296 a0001c0001t0001g0301 a0001c0001t0002g0050 others(14): Show |
17 | HG00609.hp1 HG00741.hp2 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.639-28403_639-2840 others(7): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50182891 | ||||||
chr16:50182891 | C | CTTTT | 14 | a0001c0001t0001g0227 a0001c0001t0001g0257 a0001c0001t0001g0271 others(11): Show |
14 | HG01106.hp2 HG01167.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.639-28404_639-2840 others(8): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50182891 | ||||||
chr16:50182891 | C | CTTTTTT | 31 | a0001c0001t0001g0193 a0001c0001t0001g0201 a0001c0001t0001g0211 others(28): Show |
31 | HG00423.hp2 HG00673.hp2 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.639-28406_639-2840 others(10): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50182891 | ||||||
chr16:50182891 | C | CTTTTTTT | 16 | a0001c0001t0001g0202 a0001c0001t0001g0220 a0001c0001t0001g0221 others(13): Show |
16 | HG01516.hp1 HG01517.hp2 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.639-28407_639-2840 others(11): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50182891 | ||||||
chr16:50182891 | C | CTTTTTTT others(1): Show |
42 | a0001c0001t0001g0243 a0001c0001t0001g0287 a0001c0001t0001g0295 others(39): Show |
42 | HG00609.hp2 HG00673.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.639-28408_639-2840 others(12): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50182891 | ||||||
chr16:50182891 | C | CTTTTTTT others(2): Show |
31 | a0001c0001t0002g0001 a0001c0001t0002g0102 a0001c0001t0002g0103 others(28): Show |
32 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.639-28409_639-2840 others(13): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50182891 | ||||||
chr16:50182891 | C | CTTTTTTT others(3): Show |
15 | a0001c0001t0002g0104 a0001c0001t0002g0105 a0001c0001t0002g0106 others(12): Show |
15 | HG00597.hp2 HG01099.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.639-28410_639-2840 others(14): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50182891 | ||||||
chr16:50182891 | C | CTTTTTTT others(4): Show |
6 | a0001c0001t0001g0255 a0001c0001t0002g0076 a0001c0001t0002g0154 others(3): Show |
6 | HG00738.hp2 HG01123.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.639-28411_639-2840 others(15): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50182891 | ||||||
chr16:50182891 | C | CTTTTTTT others(5): Show |
3 | a0001c0001t0005g0120 a0001c0001t0014g0152 a0001c0001t0036g0127 |
3 | HG00741.hp1 NA18612.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.639-28412_639-2840 others(16): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50182891 | ||||||
chr16:50182891 | C | CTTTTTTT others(7): Show |
2 | a0001c0001t0025g0066 a0001c0002t0002g0121 |
2 | HG00323.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.639-28414_639-2840 others(18): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50182891 | ||||||
chr16:50182891 | C | CTTTTTTT others(8): Show |
6 | a0001c0001t0002g0038 a0001c0001t0002g0085 a0001c0001t0002g0145 others(3): Show |
6 | HG01071.hp2 HG01106.hp1 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.639-28415_639-2840 others(19): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50182891 | ||||||
chr16:50182891 | C | CTTTTTTT others(9): Show |
3 | a0001c0001t0001g0084 a0001c0001t0002g0040 a0001c0001t0002g0161 |
3 | HG01361.hp2 NA19007.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.639-28416_639-2840 others(20): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50182891 | ||||||
chr16:50182891 | C | CTTTTTTT others(10): Show |
3 | a0001c0001t0002g0056 a0001c0001t0002g0086 a0001c0001t0002g0170 |
3 | HG00423.hp1 NA18985.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.639-28417_639-2840 others(21): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50182891 | ||||||
chr16:50182891 | C | CTTTTTTT others(11): Show |
2 | a0001c0001t0002g0071 a0001c0001t0015g0067 |
2 | HG00738.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.639-28418_639-2840 others(22): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50182891 | ||||||
chr16:50182891 | C | CTTTTTTT others(12): Show |
1 | a0001c0001t0002g0070 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.639-28419_639-2840 others(23): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50182891 | ||||||
chr16:50182891 | C | CTTTTTTT others(13): Show |
1 | a0001c0009t0049g0077 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.639-28420_639-2840 others(24): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50182891 | ||||||
chr16:50182891 | C | CTTTTTTT others(15): Show |
5 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0131 others(2): Show |
5 | HG03942.hp1 NA18945.hp1 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.639-28422_639-2840 others(26): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50182891 | ||||||
chr16:50182891 | C | CTTTTTTT others(19): Show |
1 | a0001c0001t0015g0068 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.639-28426_639-2840 others(30): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50182891 | ||||||
chr16:50182891 | C | CTTTTTTT others(20): Show |
1 | a0001c0001t0002g0069 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.639-28427_639-2840 others(31): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50182891 | ||||||
chr16:50182891 | C | CTTTTTTT others(21): Show |
2 | a0001c0001t0002g0039 a0001c0001t0002g0064 |
2 | NA18975.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.639-28428_639-2840 others(32): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50182891 | ||||||
chr16:50182891 | C | CTTTTTTT others(25): Show |
1 | a0001c0001t0002g0082 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.639-28401_639-2840 others(36): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50182891 | ||||||
chr16:50182891 | C | CTTTTTTT others(29): Show |
1 | a0001c0001t0003g0078 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.639-28401_639-2840 others(40): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50182891 | ||||||
chr16:50182891 | CTTTTTTT others(3): Show |
C | 4 | a0001c0001t0002g0074 a0001c0001t0007g0024 a0001c0001t0043g0048 others(1): Show |
4 | HG02027.hp2 HG02055.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.639-28410_639-2840 others(14): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50182891 | ||||||
chr16:50182891 | CTTTTTTT others(4): Show |
C | 7 | a0001c0001t0007g0014 a0001c0001t0007g0022 a0001c0001t0007g0023 others(4): Show |
7 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.639-28411_639-2840 others(15): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50182891 | ||||||
chr16:50182891 | CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0002g0036 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.639-28416_639-2840 others(20): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50182891 | ||||||
chr16:50182891 | CTTTTTTT others(13): Show |
C | 1 | a0001c0001t0020g0203 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.639-28420_639-2840 others(24): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50182891 | ||||||
chr16:50182989 | G | C | 1 | a0001c0001t0043g0048 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.639-28334G>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50182989 | |||||||
chr16:50183026 | A | T | 1 | a0001c0001t0004g0190 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.639-28297A>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50183026 | |||||||
chr16:50183036 | T | A | 1 | a0001c0005t0001g0224 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.639-28287T>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50183036 | |||||||
chr16:50183113 | G | A | 20 | a0001c0001t0002g0050 a0001c0001t0002g0098 a0001c0001t0003g0003 others(17): Show |
20 | HG00597.hp1 HG00609.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.639-28210G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50183113 | |||||||
chr16:50183258 | G | A | 11 | a0001c0001t0004g0190 a0001c0001t0004g0199 a0001c0001t0004g0267 others(8): Show |
11 | HG00639.hp2 HG01081.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.639-28065G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50183258 | |||||||
chr16:50183376 | G | A | 20 | a0001c0001t0002g0050 a0001c0001t0002g0098 a0001c0001t0003g0003 others(17): Show |
20 | HG00597.hp1 HG00609.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.639-27947G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50183376 | |||||||
chr16:50183479 | G | A | 186 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(183): Show |
187 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.639-27844G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50183479 | |||||||
chr16:50183521 | CT | C | 162 | a0001c0001t0001g0084 a0001c0001t0001g0272 a0001c0001t0002g0001 others(159): Show |
163 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.639-27786delT | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50183521 | ||||||
chr16:50183521 | CTT | C | 21 | a0001c0001t0002g0146 a0001c0001t0007g0014 a0001c0001t0007g0022 others(18): Show |
21 | HG00738.hp1 HG00738.hp2 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.639-27787_639-2778 others(6): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50183521 | ||||||
chr16:50183698 | C | A | 185 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(182): Show |
186 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.639-27625C>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50183698 | |||||||
chr16:50184007 | A | G | 2 | a0001c0001t0002g0004 a0001c0001t0002g0005 |
2 | HG02129.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.639-27316A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50184007 | |||||||
chr16:50184541 | C | A | 158 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(155): Show |
159 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.639-26782C>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50184541 | |||||||
chr16:50184621 | G | C | 1 | a0001c0001t0026g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.639-26702G>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50184621 | |||||||
chr16:50184637 | A | G | 5 | a0001c0001t0002g0029 a0001c0001t0002g0060 a0001c0001t0002g0061 others(2): Show |
5 | HG01081.hp2 HG01099.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.639-26686A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50184637 | |||||||
chr16:50184682 | A | AG | 5 | a0001c0001t0007g0014 a0001c0001t0007g0023 a0001c0001t0007g0024 others(2): Show |
5 | HG02055.hp2 HG02109.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.639-26640dupG | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50184682 | ||||||
chr16:50184687 | A | T | 1 | a0001c0001t0007g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.639-26636A>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50184687 | |||||||
chr16:50184721 | A | ATTTTG | 5 | a0001c0001t0002g0155 a0001c0001t0021g0037 a0001c0001t0021g0124 others(2): Show |
5 | HG00738.hp2 HG01123.hp1 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.639-26588_639-2658 others(9): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50184721 | ||||||
chr16:50184742 | G | T | 1 | a0001c0001t0026g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.639-26581G>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50184742 | |||||||
chr16:50184751 | G | A | 1 | a0001c0001t0002g0098 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.639-26572G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50184751 | |||||||
chr16:50184808 | T | G | 1 | a0001c0002t0002g0012 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.639-26515T>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50184808 | |||||||
chr16:50184929 | T | G | 1 | a0001c0001t0001g0252 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.639-26394T>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50184929 | |||||||
chr16:50184949 | A | G | 5 | a0001c0001t0009g0033 a0001c0001t0009g0043 a0001c0001t0009g0044 others(2): Show |
5 | HG02258.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.639-26374A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50184949 | |||||||
chr16:50184964 | C | T | 2 | a0001c0001t0022g0020 a0001c0001t0022g0021 |
2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.639-26359C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50184964 | |||||||
chr16:50185244 | G | C | 1 | a0001c0001t0001g0229 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.639-26079G>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50185244 | |||||||
chr16:50185481 | A | G | 1 | a0001c0001t0001g0243 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.639-25842A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50185481 | |||||||
chr16:50185512 | A | G | 10 | a0001c0001t0017g0136 a0001c0001t0017g0137 a0001c0001t0017g0186 others(7): Show |
10 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.639-25811A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50185512 | |||||||
chr16:50185538 | A | G | 159 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(156): Show |
160 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.639-25785A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50185538 | |||||||
chr16:50185594 | T | A | 6 | a0001c0001t0005g0041 a0001c0001t0005g0042 a0001c0001t0005g0088 others(3): Show |
6 | HG00099.hp2 HG00323.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.639-25729T>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50185594 | |||||||
chr16:50185696 | T | C | 4 | a0001c0001t0010g0006 a0001c0001t0010g0007 a0001c0001t0010g0008 others(1): Show |
4 | HG02145.hp2 HG02559.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.639-25627T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50185696 | |||||||
chr16:50185738 | CTCTTT | C | 14 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0039 others(11): Show |
14 | NA18941.hp2 NA18945.hp1 NA18951.hp2 others(11): Show |
intron_variant | MODIFIER | c.639-25580_639-2557 others(9): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50185738 | ||||||
chr16:50185853 | C | T | 1 | a0001c0001t0026g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.639-25470C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50185853 | |||||||
chr16:50186390 | G | T | 158 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(155): Show |
159 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.639-24933G>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50186390 | |||||||
chr16:50186395 | T | C | 1 | a0001c0001t0002g0032 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.639-24928T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50186395 | |||||||
chr16:50186634 | A | G | 4 | a0001c0001t0008g0119 a0001c0001t0008g0122 a0001c0001t0008g0149 others(1): Show |
4 | HG02922.hp1 HG02965.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.639-24689A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50186634 | |||||||
chr16:50186709 | A | G | 1 | a0001c0001t0022g0021 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.639-24614A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50186709 | |||||||
chr16:50186925 | T | G | 11 | a0001c0001t0004g0190 a0001c0001t0004g0199 a0001c0001t0004g0267 others(8): Show |
11 | HG00639.hp2 HG01081.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.639-24398T>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50186925 | |||||||
chr16:50187211 | T | C | 5 | a0001c0001t0012g0195 a0001c0001t0012g0196 a0001c0001t0012g0197 others(2): Show |
5 | HG02145.hp1 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.639-24112T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50187211 | |||||||
chr16:50187353 | C | T | 27 | a0001c0001t0007g0014 a0001c0001t0007g0022 a0001c0001t0007g0023 others(24): Show |
27 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.639-23970C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50187353 | |||||||
chr16:50187545 | T | G | 5 | a0001c0001t0009g0033 a0001c0001t0009g0043 a0001c0001t0009g0044 others(2): Show |
5 | HG02258.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.639-23778T>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50187545 | |||||||
chr16:50187569 | C | T | 8 | a0001c0003t0006g0002 a0001c0003t0006g0191 a0001c0003t0006g0192 others(5): Show |
8 | HG02559.hp2 HG02630.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.639-23754C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50187569 | |||||||
chr16:50187944 | T | C | 2 | a0001c0005t0001g0224 a0001c0005t0001g0230 |
2 | HG02615.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.639-23379T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50187944 | |||||||
chr16:50188182 | T | G | 159 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(156): Show |
160 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.639-23141T>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50188182 | |||||||
chr16:50188210 | T | C | 159 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(156): Show |
160 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.639-23113T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50188210 | |||||||
chr16:50188283 | A | G | 5 | a0001c0001t0009g0033 a0001c0001t0009g0043 a0001c0001t0009g0044 others(2): Show |
5 | HG02258.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.639-23040A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50188283 | |||||||
chr16:50188312 | A | G | 5 | a0001c0001t0009g0033 a0001c0001t0009g0043 a0001c0001t0009g0044 others(2): Show |
5 | HG02258.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.639-23011A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50188312 | |||||||
chr16:50188383 | G | A | 1 | a0001c0001t0005g0180 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.639-22940G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50188383 | |||||||
chr16:50188389 | G | A | 1 | a0001c0001t0026g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.639-22934G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50188389 | |||||||
chr16:50188403 | A | G | 1 | a0001c0001t0052g0013 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.639-22920A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50188403 | |||||||
chr16:50188415 | T | C | 298 | a0001c0001t0001g0084 a0001c0001t0001g0193 a0001c0001t0001g0201 others(295): Show |
299 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.639-22908T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50188415 | |||||||
chr16:50188709 | G | T | 1 | a0001c0001t0048g0081 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.639-22614G>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50188709 | |||||||
chr16:50189015 | G | C | 159 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(156): Show |
160 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.639-22308G>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50189015 | |||||||
chr16:50189089 | C | T | 2 | a0001c0001t0009g0043 a0001c0001t0009g0044 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.639-22234C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50189089 | |||||||
chr16:50189114 | G | A | 1 | a0001c0001t0037g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.639-22209G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50189114 | |||||||
chr16:50189340 | T | C | 1 | a0001c0001t0007g0023 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.639-21983T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50189340 | |||||||
chr16:50189363 | G | A | 10 | a0001c0001t0017g0136 a0001c0001t0017g0137 a0001c0001t0017g0186 others(7): Show |
10 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.639-21960G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50189363 | |||||||
chr16:50189547 | C | A | 4 | a0001c0001t0002g0074 a0001c0001t0002g0086 a0001c0001t0002g0161 others(1): Show |
4 | HG00423.hp1 NA18966.hp2 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.639-21776C>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50189547 | |||||||
chr16:50189655 | G | A | 1 | a0001c0002t0002g0121 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.639-21668G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50189655 | |||||||
chr16:50189733 | C | CCGATAAT others(4650): Show |
2 | a0001c0001t0001g0228 a0001c0001t0013g0200 |
2 | NA18963.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.639-21589_639-2158 others(4661): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50189733 | ||||||
chr16:50189734 | CA | C | 112 | a0001c0001t0001g0193 a0001c0001t0001g0201 a0001c0001t0001g0202 others(109): Show |
113 | HG00423.hp2 HG00544.hp2 HG00673.hp2 others(110): Show |
intron_variant | MODIFIER | c.639-21588delA | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50189734 | |||||||
chr16:50189735 | A | C | 2 | a0001c0001t0001g0228 a0001c0001t0013g0200 |
2 | NA18963.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.639-21588A>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50189735 | |||||||
chr16:50189809 | G | C | 1 | a0001c0001t0001g0244 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.639-21514G>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50189809 | |||||||
chr16:50189834 | GTCAGGAG others(23): Show |
G | 1 | a0001c0001t0026g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.639-21480_639-2145 others(34): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50189834 | ||||||
chr16:50190075 | C | CA | 11 | a0001c0001t0001g0256 a0001c0001t0001g0270 a0001c0001t0012g0195 others(8): Show |
11 | HG02145.hp1 HG02451.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.639-21230dupA | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50190075 | ||||||
chr16:50190075 | CA | C | 6 | a0001c0001t0001g0277 a0001c0001t0001g0285 a0001c0001t0017g0136 others(3): Show |
6 | HG01070.hp2 HG01167.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.639-21230delA | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50190075 | ||||||
chr16:50190087 | AAAAAAAC | A | 153 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(150): Show |
153 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.639-21232_639-2122 others(11): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50190087 | ||||||
chr16:50190146 | A | G | 8 | a0001c0001t0007g0014 a0001c0001t0007g0022 a0001c0001t0007g0023 others(5): Show |
8 | HG02055.hp2 HG02109.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.639-21177A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50190146 | |||||||
chr16:50190193 | A | G | 17 | a0001c0001t0001g0218 a0001c0001t0001g0247 a0001c0001t0001g0254 others(14): Show |
17 | HG00544.hp2 HG02074.hp2 HG02080.hp1 others(14): Show |
intron_variant | MODIFIER | c.639-21130A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50190193 | |||||||
chr16:50190312 | G | A | 2 | a0001c0001t0001g0225 a0001c0001t0047g0249 |
2 | HG01934.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.639-21011G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50190312 | |||||||
chr16:50190472 | A | G | 159 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(156): Show |
160 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.639-20851A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50190472 | |||||||
chr16:50190564 | C | T | 187 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(184): Show |
188 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.639-20759C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50190564 | |||||||
chr16:50190628 | G | A | 3 | a0001c0001t0015g0067 a0001c0001t0015g0068 a0001c0009t0049g0077 |
3 | HG00738.hp1 HG03654.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.639-20695G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50190628 | |||||||
chr16:50190696 | A | G | 5 | a0001c0001t0012g0195 a0001c0001t0012g0196 a0001c0001t0012g0197 others(2): Show |
5 | HG02145.hp1 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.639-20627A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50190696 | |||||||
chr16:50190748 | A | G | 1 | a0001c0001t0012g0197 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.639-20575A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50190748 | |||||||
chr16:50190812 | C | T | 159 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(156): Show |
160 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.639-20511C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50190812 | |||||||
chr16:50190834 | A | T | 1 | a0001c0001t0001g0295 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.639-20489A>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50190834 | |||||||
chr16:50190959 | A | C | 10 | a0001c0001t0017g0136 a0001c0001t0017g0137 a0001c0001t0017g0186 others(7): Show |
10 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.639-20364A>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50190959 | |||||||
chr16:50191020 | C | A | 159 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(156): Show |
160 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.639-20303C>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50191020 | |||||||
chr16:50191142 | A | G | 2 | a0001c0001t0022g0020 a0001c0001t0022g0021 |
2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.639-20181A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50191142 | |||||||
chr16:50191174 | T | C | 1 | a0001c0001t0003g0028 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.639-20149T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50191174 | |||||||
chr16:50191194 | T | C | 159 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(156): Show |
160 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.639-20129T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50191194 | |||||||
chr16:50191483 | A | G | 1 | a0001c0001t0003g0028 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.639-19840A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50191483 | |||||||
chr16:50191542 | C | T | 1 | a0001c0001t0020g0203 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.639-19781C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50191542 | |||||||
chr16:50191638 | G | A | 6 | a0001c0002t0002g0111 a0001c0002t0002g0115 a0001c0002t0002g0117 others(3): Show |
6 | HG00544.hp1 HG00609.hp2 HG00639.hp1 others(3): Show |
intron_variant | MODIFIER | c.639-19685G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50191638 | |||||||
chr16:50191640 | C | A | 1 | a0001c0001t0017g0186 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.639-19683C>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50191640 | |||||||
chr16:50191711 | C | G | 159 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(156): Show |
160 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.639-19612C>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50191711 | |||||||
chr16:50191775 | C | T | 1 | a0001c0001t0031g0153 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.639-19548C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50191775 | |||||||
chr16:50192100 | C | T | 131 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(128): Show |
132 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.639-19223C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50192100 | |||||||
chr16:50192226 | C | CT | 8 | a0001c0001t0007g0014 a0001c0001t0007g0022 a0001c0001t0007g0023 others(5): Show |
8 | HG02055.hp2 HG02109.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.639-19096dupT | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50192226 | ||||||
chr16:50192232 | C | CA | 27 | a0001c0001t0001g0216 a0001c0001t0001g0226 a0001c0001t0007g0014 others(24): Show |
27 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.639-19074dupA | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50192232 | ||||||
chr16:50192232 | CA | C | 163 | a0001c0001t0001g0084 a0001c0001t0001g0234 a0001c0001t0002g0001 others(160): Show |
164 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.639-19074delA | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50192232 | ||||||
chr16:50192251 | C | G | 1 | a0001c0001t0015g0068 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.639-19072C>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50192251 | |||||||
chr16:50192429 | A | T | 1 | a0001c0001t0052g0013 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.639-18894A>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50192429 | |||||||
chr16:50192766 | CT | C | 158 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(155): Show |
159 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.639-18553delT | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50192766 | ||||||
chr16:50192864 | T | C | 1 | a0001c0001t0037g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.639-18459T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50192864 | |||||||
chr16:50192879 | T | A | 1 | a0001c0001t0004g0284 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.639-18444T>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50192879 | |||||||
chr16:50192902 | T | C | 159 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(156): Show |
160 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.639-18421T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50192902 | |||||||
chr16:50193331 | G | GT | 144 | a0001c0001t0001g0193 a0001c0001t0001g0201 a0001c0001t0001g0210 others(141): Show |
144 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(141): Show |
intron_variant | MODIFIER | c.639-17970dupT | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50193331 | ||||||
chr16:50193331 | G | GTT | 36 | a0001c0001t0001g0202 a0001c0001t0001g0213 a0001c0001t0001g0221 others(33): Show |
36 | HG00639.hp2 HG01081.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.639-17971_639-1797 others(6): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50193331 | ||||||
chr16:50193400 | C | T | 1 | a0001c0011t0030g0208 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.639-17923C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50193400 | |||||||
chr16:50193401 | G | A | 1 | a0001c0001t0007g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.639-17922G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50193401 | |||||||
chr16:50193424 | G | T | 1 | a0001c0001t0002g0072 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.639-17899G>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50193424 | |||||||
chr16:50193427 | T | C | 1 | a0001c0001t0002g0072 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.639-17896T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50193427 | |||||||
chr16:50193462 | C | T | 1 | a0001c0001t0037g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.639-17861C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50193462 | |||||||
chr16:50193481 | G | A | 5 | a0001c0001t0009g0033 a0001c0001t0009g0043 a0001c0001t0009g0044 others(2): Show |
5 | HG02258.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.639-17842G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50193481 | |||||||
chr16:50193498 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.639-17825C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50193498 | |||||||
chr16:50193629 | C | T | 1 | a0001c0001t0002g0039 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.639-17694C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50193629 | |||||||
chr16:50193634 | G | A | 1 | a0001c0001t0008g0119 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.639-17689G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50193634 | |||||||
chr16:50193817 | C | A | 2 | a0001c0001t0022g0020 a0001c0001t0022g0021 |
2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.639-17506C>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50193817 | |||||||
chr16:50193837 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.639-17486G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50193837 | |||||||
chr16:50193979 | G | A | 158 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(155): Show |
159 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.639-17344G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50193979 | |||||||
chr16:50194075 | G | T | 158 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(155): Show |
159 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.639-17248G>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50194075 | |||||||
chr16:50194174 | C | T | 5 | a0001c0001t0009g0033 a0001c0001t0009g0043 a0001c0001t0009g0044 others(2): Show |
5 | HG02258.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.639-17149C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50194174 | |||||||
chr16:50194216 | C | CT | 166 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(163): Show |
167 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.639-17094dupT | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50194216 | ||||||
chr16:50194277 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.639-17046G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50194277 | |||||||
chr16:50194483 | G | A | 1 | a0001c0001t0003g0139 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.639-16840G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50194483 | |||||||
chr16:50194505 | A | G | 1 | a0001c0001t0038g0156 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.639-16818A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50194505 | |||||||
chr16:50194522 | C | A | 1 | a0001c0001t0009g0033 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.639-16801C>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50194522 | |||||||
chr16:50194744 | A | AT | 93 | a0001c0001t0001g0193 a0001c0001t0001g0201 a0001c0001t0001g0210 others(90): Show |
93 | HG00423.hp2 HG00544.hp2 HG00673.hp2 others(90): Show |
intron_variant | MODIFIER | c.639-16557dupT | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50194744 | ||||||
chr16:50194744 | AT | A | 180 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(177): Show |
181 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.639-16557delT | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50194744 | ||||||
chr16:50194772 | G | A | 158 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(155): Show |
159 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.639-16551G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50194772 | |||||||
chr16:50194810 | G | A | 4 | a0001c0001t0010g0006 a0001c0001t0010g0007 a0001c0001t0010g0008 others(1): Show |
4 | HG02145.hp2 HG02559.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.639-16513G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50194810 | |||||||
chr16:50194874 | A | G | 191 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(188): Show |
192 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.639-16449A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50194874 | |||||||
chr16:50194933 | T | C | 11 | a0001c0001t0004g0190 a0001c0001t0004g0199 a0001c0001t0004g0267 others(8): Show |
11 | HG00639.hp2 HG01081.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.639-16390T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50194933 | |||||||
chr16:50194939 | C | T | 10 | a0001c0001t0017g0136 a0001c0001t0017g0137 a0001c0001t0017g0186 others(7): Show |
10 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.639-16384C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50194939 | |||||||
chr16:50194950 | C | T | 1 | a0001c0001t0002g0181 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.639-16373C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50194950 | |||||||
chr16:50194951 | G | A | 2 | a0001c0001t0001g0225 a0001c0001t0047g0249 |
2 | HG01934.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.639-16372G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50194951 | |||||||
chr16:50194967 | T | C | 1 | a0001c0001t0002g0036 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.639-16356T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50194967 | |||||||
chr16:50194995 | T | C | 158 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(155): Show |
159 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.639-16328T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50194995 | |||||||
chr16:50195068 | T | G | 5 | a0001c0001t0009g0033 a0001c0001t0009g0043 a0001c0001t0009g0044 others(2): Show |
5 | HG02258.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.639-16255T>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50195068 | |||||||
chr16:50195329 | C | T | 1 | a0001c0001t0003g0028 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.639-15994C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50195329 | |||||||
chr16:50195361 | C | T | 1 | a0001c0001t0034g0087 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.639-15962C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50195361 | |||||||
chr16:50195397 | A | G | 11 | a0001c0001t0004g0190 a0001c0001t0004g0199 a0001c0001t0004g0267 others(8): Show |
11 | HG00639.hp2 HG01081.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.639-15926A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50195397 | |||||||
chr16:50195559 | T | G | 1 | a0001c0001t0026g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.639-15764T>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50195559 | |||||||
chr16:50196005 | A | G | 20 | a0001c0001t0002g0050 a0001c0001t0002g0098 a0001c0001t0003g0003 others(17): Show |
20 | HG00597.hp1 HG00609.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.639-15318A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50196005 | |||||||
chr16:50196167 | C | A | 1 | a0001c0001t0002g0070 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.639-15156C>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50196167 | |||||||
chr16:50196228 | A | G | 1 | a0001c0001t0002g0126 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.639-15095A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50196228 | |||||||
chr16:50196272 | A | G | 158 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(155): Show |
159 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.639-15051A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50196272 | |||||||
chr16:50196351 | T | TG | 131 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(128): Show |
132 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.639-14971dupG | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50196351 | ||||||
chr16:50196434 | G | A | 1 | a0001c0001t0002g0040 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.639-14889G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50196434 | |||||||
chr16:50196469 | G | A | 1 | a0001c0001t0002g0029 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.639-14854G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50196469 | |||||||
chr16:50196488 | T | TATC | 39 | a0001c0001t0001g0193 a0001c0001t0001g0220 a0001c0001t0001g0225 others(36): Show |
39 | HG01081.hp1 HG01099.hp2 HG01255.hp2 others(36): Show |
intron_variant | MODIFIER | c.639-14798_639-1479 others(7): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50196488 | ||||||
chr16:50196488 | T | TATCATC | 48 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0210 others(45): Show |
48 | HG01106.hp2 HG01175.hp1 HG01261.hp2 others(45): Show |
intron_variant | MODIFIER | c.639-14801_639-1479 others(10): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50196488 | ||||||
chr16:50196488 | T | TATCATCA others(2): Show |
7 | a0001c0001t0001g0234 a0001c0001t0001g0250 a0001c0001t0001g0278 others(4): Show |
7 | HG00741.hp2 HG01243.hp2 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.639-14804_639-1479 others(13): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50196488 | ||||||
chr16:50196488 | T | TATCATCA others(5): Show |
1 | a0001c0001t0001g0222 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.639-14807_639-1479 others(16): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50196488 | ||||||
chr16:50196488 | TATC | T | 162 | a0001c0001t0001g0084 a0001c0001t0001g0218 a0001c0001t0001g0247 others(159): Show |
163 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.639-14798_639-1479 others(7): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50196488 | ||||||
chr16:50196488 | TATCATCA others(14): Show |
T | 5 | a0001c0001t0009g0033 a0001c0001t0009g0043 a0001c0001t0009g0044 others(2): Show |
5 | HG02258.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.639-14816_639-1479 others(25): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50196488 | ||||||
chr16:50196745 | G | A | 1 | a0001c0003t0029g0194 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.639-14578G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50196745 | |||||||
chr16:50196763 | C | CA | 11 | a0001c0001t0017g0136 a0001c0001t0017g0137 a0001c0001t0017g0186 others(8): Show |
11 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.639-14546dupA | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50196763 | ||||||
chr16:50196763 | CA | C | 173 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(170): Show |
174 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.639-14546delA | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50196763 | ||||||
chr16:50196832 | G | A | 3 | a0002c0004t0001g0281 a0002c0004t0001g0282 a0002c0004t0001g0283 |
3 | NA18972.hp1 NA18992.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.639-14491G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50196832 | |||||||
chr16:50196935 | C | CA | 7 | a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(4): Show |
7 | HG01891.hp2 HG02280.hp2 NA18941.hp2 others(4): Show |
intron_variant | MODIFIER | c.639-14375dupA | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50196935 | ||||||
chr16:50196935 | CA | C | 8 | a0001c0001t0007g0014 a0001c0001t0007g0022 a0001c0001t0007g0023 others(5): Show |
8 | HG02055.hp2 HG02109.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.639-14375delA | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50196935 | ||||||
chr16:50197107 | T | TA | 7 | a0001c0001t0001g0257 a0001c0001t0001g0272 a0001c0001t0001g0291 others(4): Show |
7 | HG02145.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.639-14206dupA | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50197107 | ||||||
chr16:50197125 | C | CA | 16 | a0001c0001t0002g0098 a0001c0001t0003g0018 a0001c0001t0003g0047 others(13): Show |
16 | HG00639.hp2 HG01081.hp1 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.639-14188dupA | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50197125 | ||||||
chr16:50197298 | T | G | 3 | a0001c0001t0016g0187 a0001c0001t0016g0188 a0001c0001t0016g0189 |
3 | HG00741.hp2 HG01243.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.639-14025T>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50197298 | |||||||
chr16:50197385 | T | C | 93 | a0001c0001t0001g0193 a0001c0001t0001g0201 a0001c0001t0001g0202 others(90): Show |
93 | HG00423.hp2 HG00544.hp2 HG00673.hp2 others(90): Show |
intron_variant | MODIFIER | c.639-13938T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50197385 | |||||||
chr16:50197462 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.639-13861T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50197462 | |||||||
chr16:50197742 | G | C | 1 | a0001c0001t0002g0040 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.639-13581G>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50197742 | |||||||
chr16:50197780 | C | T | 1 | a0001c0001t0001g0244 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.639-13543C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50197780 | |||||||
chr16:50197798 | C | T | 5 | a0001c0001t0002g0001 a0001c0001t0002g0075 a0001c0001t0002g0134 others(2): Show |
6 | HG01943.hp2 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.639-13525C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50197798 | |||||||
chr16:50197990 | G | A | 1 | a0001c0001t0001g0294 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.639-13333G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50197990 | |||||||
chr16:50198119 | T | TA | 176 | a0001c0001t0001g0084 a0001c0001t0001g0286 a0001c0001t0002g0001 others(173): Show |
177 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.639-13188dupA | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50198119 | ||||||
chr16:50198119 | T | TAA | 11 | a0001c0001t0007g0022 a0001c0001t0007g0023 a0001c0001t0007g0024 others(8): Show |
11 | HG02055.hp2 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.639-13189_639-1318 others(6): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50198119 | ||||||
chr16:50198119 | T | TTA | 3 | a0001c0001t0010g0006 a0001c0001t0010g0008 a0001c0001t0010g0009 |
3 | HG02145.hp2 HG02559.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.639-13204_639-1320 others(6): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50198119 | |||||||
chr16:50198373 | C | T | 2 | a0001c0001t0002g0019 a0001c0001t0002g0076 |
2 | HG02080.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.639-12950C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50198373 | |||||||
chr16:50198378 | C | A | 1 | a0001c0001t0014g0151 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.639-12945C>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50198378 | |||||||
chr16:50198417 | TA | T | 49 | a0001c0001t0002g0050 a0001c0001t0002g0064 a0001c0001t0002g0098 others(46): Show |
49 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.639-12890delA | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50198417 | ||||||
chr16:50198417 | TAA | T | 129 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(126): Show |
130 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.639-12891_639-1289 others(6): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50198417 | ||||||
chr16:50198439 | A | G | 6 | a0001c0001t0002g0030 a0001c0001t0010g0006 a0001c0001t0010g0007 others(3): Show |
6 | HG02145.hp2 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.639-12884A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50198439 | |||||||
chr16:50198561 | T | A | 7 | a0001c0001t0001g0271 a0001c0001t0001g0296 a0001c0001t0001g0297 others(4): Show |
7 | HG01106.hp2 HG01891.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.639-12762T>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50198561 | |||||||
chr16:50198634 | G | A | 1 | a0001c0001t0001g0246 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.639-12689G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50198634 | |||||||
chr16:50198769 | T | C | 2 | a0001c0001t0024g0015 a0001c0001t0024g0016 |
2 | HG01891.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.639-12554T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50198769 | |||||||
chr16:50198770 | G | A | 186 | a0001c0001t0001g0084 a0001c0001t0001g0258 a0001c0001t0002g0001 others(183): Show |
187 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.639-12553G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50198770 | |||||||
chr16:50198897 | A | G | 1 | a0001c0001t0001g0223 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.639-12426A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50198897 | |||||||
chr16:50198909 | T | A | 1 | a0001c0001t0001g0263 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.639-12414T>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50198909 | |||||||
chr16:50199272 | G | C | 185 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(182): Show |
186 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.639-12051G>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50199272 | |||||||
chr16:50199386 | A | C | 1 | a0001c0001t0001g0246 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.639-11937A>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50199386 | |||||||
chr16:50199457 | A | C | 1 | a0001c0001t0014g0151 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.639-11866A>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50199457 | |||||||
chr16:50199829 | T | A | 1 | a0001c0001t0055g0168 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.639-11494T>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50199829 | |||||||
chr16:50199915 | G | T | 1 | a0001c0001t0020g0203 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.639-11408G>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50199915 | |||||||
chr16:50199935 | G | C | 1 | a0001c0002t0002g0130 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.639-11388G>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50199935 | |||||||
chr16:50200081 | G | A | 1 | a0001c0001t0026g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.639-11242G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50200081 | |||||||
chr16:50200163 | C | T | 1 | a0001c0001t0026g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.639-11160C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50200163 | |||||||
chr16:50200226 | C | T | 2 | a0001c0001t0009g0043 a0001c0001t0009g0044 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.639-11097C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50200226 | |||||||
chr16:50200227 | G | A | 1 | a0001c0001t0003g0003 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.639-11096G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50200227 | |||||||
chr16:50200365 | T | TA | 10 | a0001c0001t0017g0136 a0001c0001t0017g0137 a0001c0001t0017g0186 others(7): Show |
10 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.639-10947dupA | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50200365 | ||||||
chr16:50200802 | T | TA | 5 | a0001c0001t0012g0195 a0001c0001t0012g0196 a0001c0001t0012g0197 others(2): Show |
5 | HG02145.hp1 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.639-10521_639-1052 others(5): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50200802 | |||||||
chr16:50200803 | T | A | 28 | a0001c0001t0007g0014 a0001c0001t0007g0022 a0001c0001t0007g0023 others(25): Show |
28 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.639-10520T>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50200803 | |||||||
chr16:50200881 | A | C | 1 | a0001c0001t0007g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.639-10442A>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50200881 | |||||||
chr16:50200921 | C | T | 2 | a0001c0003t0006g0204 a0001c0003t0060g0207 |
2 | HG02630.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.639-10402C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50200921 | |||||||
chr16:50200992 | G | A | 1 | a0001c0001t0004g0267 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.639-10331G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50200992 | |||||||
chr16:50201146 | A | G | 1 | a0001c0001t0016g0187 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.639-10177A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50201146 | |||||||
chr16:50201265 | G | A | 1 | a0001c0001t0003g0139 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.639-10058G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50201265 | |||||||
chr16:50201272 | C | T | 2 | a0001c0001t0005g0041 a0001c0001t0005g0042 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.639-10051C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50201272 | |||||||
chr16:50201273 | A | G | 158 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(155): Show |
159 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.639-10050A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50201273 | |||||||
chr16:50201274 | C | T | 1 | a0001c0001t0001g0222 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.639-10049C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50201274 | |||||||
chr16:50201398 | G | A | 1 | a0001c0001t0002g0125 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.639-9925G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50201398 | |||||||
chr16:50201406 | G | A | 5 | a0001c0001t0009g0033 a0001c0001t0009g0043 a0001c0001t0009g0044 others(2): Show |
5 | HG02258.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.639-9917G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50201406 | |||||||
chr16:50201459 | C | G | 2 | a0001c0001t0002g0126 a0001c0001t0002g0165 |
2 | HG00673.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.639-9864C>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50201459 | |||||||
chr16:50201486 | G | A | 1 | a0001c0001t0026g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.639-9837G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50201486 | |||||||
chr16:50201493 | C | T | 1 | a0001c0001t0026g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.639-9830C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50201493 | |||||||
chr16:50201507 | A | T | 99 | a0001c0001t0001g0193 a0001c0001t0001g0201 a0001c0001t0001g0202 others(96): Show |
99 | HG00423.hp2 HG00544.hp2 HG00673.hp2 others(96): Show |
intron_variant | MODIFIER | c.639-9816A>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50201507 | |||||||
chr16:50201813 | A | C | 183 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(180): Show |
184 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.639-9510A>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50201813 | |||||||
chr16:50201830 | T | TA | 9 | a0001c0001t0017g0136 a0001c0001t0017g0137 a0001c0001t0017g0186 others(6): Show |
9 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.639-9474dupA | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50201830 | ||||||
chr16:50201830 | TAA | T | 136 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(133): Show |
137 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.639-9475_639-9474d others(4): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50201830 | ||||||
chr16:50201830 | TAAA | T | 19 | a0001c0001t0002g0050 a0001c0001t0002g0098 a0001c0001t0003g0003 others(16): Show |
19 | HG00597.hp1 HG00609.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.639-9476_639-9474d others(5): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50201830 | ||||||
chr16:50201863 | A | G | 1 | a0001c0001t0026g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.639-9460A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50201863 | |||||||
chr16:50201964 | G | A | 1 | a0001c0001t0026g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.639-9359G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50201964 | |||||||
chr16:50202001 | A | G | 22 | a0001c0001t0007g0014 a0001c0001t0007g0022 a0001c0001t0007g0023 others(19): Show |
22 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.639-9322A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50202001 | |||||||
chr16:50202859 | A | G | 1 | a0001c0001t0007g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.639-8464A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50202859 | |||||||
chr16:50203121 | T | C | 1 | a0001c0002t0002g0057 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.639-8202T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50203121 | |||||||
chr16:50203230 | G | A | 1 | a0001c0001t0051g0025 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.639-8093G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50203230 | |||||||
chr16:50203351 | G | A | 297 | a0001c0001t0001g0084 a0001c0001t0001g0193 a0001c0001t0001g0201 others(294): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.639-7972G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50203351 | |||||||
chr16:50203366 | A | T | 99 | a0001c0001t0001g0193 a0001c0001t0001g0201 a0001c0001t0001g0202 others(96): Show |
99 | HG00423.hp2 HG00544.hp2 HG00673.hp2 others(96): Show |
intron_variant | MODIFIER | c.639-7957A>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50203366 | |||||||
chr16:50203419 | C | T | 5 | a0001c0001t0009g0033 a0001c0001t0009g0043 a0001c0001t0009g0044 others(2): Show |
5 | HG02258.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.639-7904C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50203419 | |||||||
chr16:50203522 | T | G | 3 | a0001c0001t0018g0179 a0001c0001t0018g0182 a0001c0001t0018g0183 |
3 | HG01167.hp1 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.639-7801T>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50203522 | |||||||
chr16:50203568 | C | T | 1 | a0001c0001t0003g0101 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.639-7755C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50203568 | |||||||
chr16:50203616 | A | G | 1 | a0001c0001t0002g0071 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.639-7707A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50203616 | |||||||
chr16:50203702 | C | T | 10 | a0001c0001t0017g0136 a0001c0001t0017g0137 a0001c0001t0017g0186 others(7): Show |
10 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.639-7621C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50203702 | |||||||
chr16:50203879 | G | A | 13 | a0001c0001t0017g0136 a0001c0001t0017g0137 a0001c0001t0017g0186 others(10): Show |
13 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.639-7444G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50203879 | |||||||
chr16:50204027 | G | A | 183 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(180): Show |
184 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.639-7296G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50204027 | |||||||
chr16:50204177 | G | T | 1 | a0001c0001t0048g0081 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.639-7146G>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50204177 | |||||||
chr16:50204284 | G | C | 1 | a0001c0001t0002g0108 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.639-7039G>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50204284 | |||||||
chr16:50204424 | G | A | 1 | a0001c0001t0026g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.639-6899G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50204424 | |||||||
chr16:50204432 | A | T | 6 | a0001c0001t0002g0040 a0001c0001t0015g0059 a0001c0001t0015g0067 others(3): Show |
6 | HG00323.hp1 HG00738.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.639-6891A>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50204432 | |||||||
chr16:50204460 | C | G | 1 | a0001c0011t0030g0208 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.639-6863C>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50204460 | |||||||
chr16:50204512 | T | C | 1 | a0001c0001t0024g0016 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.639-6811T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50204512 | |||||||
chr16:50204616 | G | A | 1 | a0001c0001t0048g0081 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.639-6707G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50204616 | |||||||
chr16:50204865 | CTT | C | 156 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(153): Show |
157 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.639-6456_639-6455d others(4): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50204865 | ||||||
chr16:50204895 | C | T | 3 | a0001c0001t0018g0179 a0001c0001t0018g0182 a0001c0001t0018g0183 |
3 | HG01167.hp1 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.639-6428C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50204895 | |||||||
chr16:50205256 | A | G | 1 | a0001c0001t0004g0298 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.639-6067A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50205256 | |||||||
chr16:50205280 | G | A | 3 | a0001c0001t0024g0015 a0001c0001t0024g0016 a0001c0001t0053g0308 |
3 | HG01891.hp2 HG02280.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.639-6043G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50205280 | |||||||
chr16:50205290 | A | C | 1 | a0001c0001t0026g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.639-6033A>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50205290 | |||||||
chr16:50205365 | T | A | 5 | a0001c0001t0001g0258 a0001c0001t0002g0171 a0001c0001t0014g0110 others(2): Show |
5 | HG03704.hp2 NA18942.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.639-5958T>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50205365 | |||||||
chr16:50205558 | C | CTTTTTTT others(6): Show |
1 | a0001c0003t0006g0205 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.639-5727_639-5715d others(15): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50205558 | ||||||
chr16:50205558 | C | CTTTTTTT others(7): Show |
1 | a0001c0003t0006g0206 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.639-5728_639-5715d others(16): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50205558 | ||||||
chr16:50205558 | CTTTTTTT others(2): Show |
C | 7 | a0001c0001t0001g0213 a0001c0001t0001g0216 a0001c0001t0001g0233 others(4): Show |
7 | HG02257.hp2 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.639-5723_639-5715d others(11): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50205558 | ||||||
chr16:50205558 | CTTTTTTT others(3): Show |
C | 6 | a0001c0001t0001g0210 a0001c0001t0001g0215 a0001c0001t0001g0221 others(3): Show |
6 | HG01243.hp2 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.639-5724_639-5715d others(12): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50205558 | ||||||
chr16:50205558 | CTTTTTTT others(4): Show |
C | 7 | a0001c0001t0001g0211 a0001c0001t0001g0264 a0001c0001t0018g0182 others(4): Show |
7 | HG01109.hp1 HG02071.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.639-5725_639-5715d others(13): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50205558 | ||||||
chr16:50205558 | CTTTTTTT others(5): Show |
C | 23 | a0001c0001t0001g0202 a0001c0001t0001g0219 a0001c0001t0001g0227 others(20): Show |
23 | HG00741.hp2 HG01106.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.639-5726_639-5715d others(14): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50205558 | ||||||
chr16:50205558 | CTTTTTTT others(6): Show |
C | 33 | a0001c0001t0001g0193 a0001c0001t0001g0201 a0001c0001t0001g0218 others(30): Show |
33 | HG00423.hp2 HG00544.hp2 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.639-5727_639-5715d others(15): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50205558 | ||||||
chr16:50205558 | CTTTTTTT others(7): Show |
C | 37 | a0001c0001t0001g0220 a0001c0001t0001g0222 a0001c0001t0001g0225 others(34): Show |
37 | HG00099.hp1 HG01099.hp2 HG01255.hp2 others(34): Show |
intron_variant | MODIFIER | c.639-5728_639-5715d others(16): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50205558 | ||||||
chr16:50205558 | CTTTTTTT others(8): Show |
C | 2 | a0001c0001t0001g0285 a0001c0001t0005g0180 |
2 | HG03942.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.639-5729_639-5715d others(17): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50205558 | ||||||
chr16:50205558 | CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0002g0074 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.639-5730_639-5715d others(18): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50205558 | ||||||
chr16:50205558 | CTTTTTTT others(11): Show |
C | 3 | a0001c0001t0001g0084 a0001c0001t0002g0076 a0001c0001t0002g0170 |
3 | HG00423.hp1 HG02080.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.639-5732_639-5715d others(20): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50205558 | ||||||
chr16:50205558 | CTTTTTTT others(12): Show |
C | 36 | a0001c0001t0002g0004 a0001c0001t0002g0030 a0001c0001t0002g0038 others(33): Show |
36 | HG00738.hp1 HG00738.hp2 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.639-5733_639-5715d others(21): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50205558 | ||||||
chr16:50205558 | CTTTTTTT others(13): Show |
C | 99 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0019 others(96): Show |
100 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.639-5734_639-5715d others(22): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50205558 | ||||||
chr16:50205558 | CTTTTTTT others(14): Show |
C | 17 | a0001c0001t0002g0050 a0001c0001t0002g0098 a0001c0001t0003g0003 others(14): Show |
17 | HG00323.hp2 HG00609.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.639-5735_639-5715d others(23): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50205558 | ||||||
chr16:50205558 | CTTTTTTT others(15): Show |
C | 9 | a0001c0001t0004g0190 a0001c0001t0004g0199 a0001c0001t0004g0267 others(6): Show |
9 | HG00639.hp2 HG01081.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.639-5736_639-5715d others(24): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50205558 | ||||||
chr16:50205558 | CTTTTTTT others(16): Show |
C | 2 | a0001c0001t0004g0284 a0001c0001t0020g0203 |
2 | HG02523.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.639-5737_639-5715d others(25): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50205558 | ||||||
chr16:50205558 | CTTTTTTT others(21): Show |
C | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.639-5742_639-5715d others(30): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50205558 | ||||||
chr16:50205558 | CTTTTTTT others(22): Show |
C | 5 | a0001c0001t0001g0236 a0001c0001t0012g0196 a0001c0001t0012g0197 others(2): Show |
5 | HG02109.hp2 HG02145.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.639-5743_639-5715d others(31): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50205558 | ||||||
chr16:50205558 | CTTTTTTT others(23): Show |
C | 2 | a0001c0001t0001g0311 a0001c0001t0012g0195 |
2 | HG03041.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.639-5744_639-5715d others(32): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50205558 | ||||||
chr16:50205558 | CTTTTTTT others(24): Show |
C | 4 | a0001c0001t0024g0015 a0001c0001t0024g0016 a0001c0001t0048g0081 others(1): Show |
4 | HG01891.hp2 HG02280.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.639-5745_639-5715d others(33): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50205558 | ||||||
chr16:50205666 | C | T | 1 | a0001c0003t0006g0204 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.639-5657C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50205666 | |||||||
chr16:50206354 | A | AT | 8 | a0001c0001t0001g0223 a0001c0001t0001g0270 a0001c0001t0001g0271 others(5): Show |
8 | HG01106.hp2 HG01175.hp1 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.639-4947dupT | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50206354 | ||||||
chr16:50206354 | AT | A | 155 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(152): Show |
156 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.639-4947delT | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50206354 | ||||||
chr16:50206354 | ATT | A | 27 | a0001c0001t0002g0031 a0001c0001t0002g0040 a0001c0001t0005g0089 others(24): Show |
27 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.639-4948_639-4947d others(4): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50206354 | ||||||
chr16:50206452 | C | T | 1 | a0001c0001t0051g0025 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.639-4871C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50206452 | |||||||
chr16:50206654 | C | T | 2 | a0001c0001t0028g0198 a0001c0001t0057g0011 |
2 | HG02145.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.639-4669C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50206654 | |||||||
chr16:50206724 | T | C | 1 | a0001c0001t0026g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.639-4599T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50206724 | |||||||
chr16:50206909 | G | GT | 306 | a0001c0001t0001g0084 a0001c0001t0001g0193 a0001c0001t0001g0201 others(303): Show |
307 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.639-4402dupT | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50206909 | ||||||
chr16:50206955 | T | A | 5 | a0001c0001t0009g0033 a0001c0001t0009g0043 a0001c0001t0009g0044 others(2): Show |
5 | HG02258.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.639-4368T>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50206955 | |||||||
chr16:50206958 | G | A | 5 | a0001c0001t0012g0195 a0001c0001t0012g0196 a0001c0001t0012g0197 others(2): Show |
5 | HG02145.hp1 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.639-4365G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50206958 | |||||||
chr16:50207123 | C | T | 183 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(180): Show |
184 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.639-4200C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50207123 | |||||||
chr16:50207130 | T | C | 3 | a0001c0001t0011g0054 a0001c0001t0011g0141 a0001c0001t0011g0142 |
3 | HG02055.hp1 HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.639-4193T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50207130 | |||||||
chr16:50207250 | C | T | 21 | a0001c0001t0007g0014 a0001c0001t0007g0022 a0001c0001t0007g0023 others(18): Show |
21 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.639-4073C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50207250 | |||||||
chr16:50207275 | G | A | 106 | a0001c0001t0001g0193 a0001c0001t0001g0201 a0001c0001t0001g0202 others(103): Show |
106 | HG00423.hp2 HG00544.hp2 HG00673.hp2 others(103): Show |
intron_variant | MODIFIER | c.639-4048G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50207275 | |||||||
chr16:50207326 | C | T | 1 | a0001c0001t0003g0178 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.639-3997C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50207326 | |||||||
chr16:50207329 | G | A | 1 | a0001c0001t0003g0178 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.639-3994G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50207329 | |||||||
chr16:50207430 | G | A | 1 | a0001c0001t0021g0037 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.639-3893G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50207430 | |||||||
chr16:50207463 | G | A | 3 | a0001c0001t0011g0054 a0001c0001t0011g0141 a0001c0001t0011g0142 |
3 | HG02055.hp1 HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.639-3860G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50207463 | |||||||
chr16:50207821 | G | C | 1 | a0001c0001t0014g0151 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.639-3502G>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50207821 | |||||||
chr16:50207964 | T | G | 2 | a0001c0001t0002g0036 a0001c0001t0002g0146 |
2 | HG01070.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.639-3359T>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50207964 | |||||||
chr16:50208029 | A | T | 5 | a0001c0001t0002g0001 a0001c0001t0002g0075 a0001c0001t0002g0134 others(2): Show |
6 | HG01943.hp2 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.639-3294A>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50208029 | |||||||
chr16:50208113 | C | G | 8 | a0001c0003t0006g0002 a0001c0003t0006g0191 a0001c0003t0006g0192 others(5): Show |
8 | HG02559.hp2 HG02630.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.639-3210C>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50208113 | |||||||
chr16:50208292 | C | T | 150 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(147): Show |
151 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.639-3031C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50208292 | |||||||
chr16:50208492 | ACAAGGTG others(33): Show |
A | 4 | a0001c0001t0010g0006 a0001c0001t0010g0007 a0001c0001t0010g0008 others(1): Show |
4 | HG02145.hp2 HG02559.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.639-2830_639-2791d others(42): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50208492 | |||||||
chr16:50208495 | A | G | 1 | a0001c0001t0013g0200 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.639-2828A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50208495 | |||||||
chr16:50208667 | A | G | 1 | a0001c0001t0022g0021 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.639-2656A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50208667 | |||||||
chr16:50208866 | G | T | 2 | a0001c0001t0005g0089 a0001c0001t0005g0092 |
2 | HG00323.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.639-2457G>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50208866 | |||||||
chr16:50208891 | C | A | 96 | a0001c0001t0001g0193 a0001c0001t0001g0201 a0001c0001t0001g0202 others(93): Show |
96 | HG00423.hp2 HG00544.hp2 HG00673.hp2 others(93): Show |
intron_variant | MODIFIER | c.639-2432C>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50208891 | |||||||
chr16:50209023 | G | A | 130 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(127): Show |
131 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.639-2300G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50209023 | |||||||
chr16:50209128 | G | C | 1 | a0001c0001t0052g0013 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.639-2195G>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50209128 | |||||||
chr16:50209270 | C | T | 2 | a0001c0001t0022g0020 a0001c0001t0022g0021 |
2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.639-2053C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50209270 | |||||||
chr16:50209310 | A | G | 1 | a0001c0001t0001g0222 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.639-2013A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50209310 | |||||||
chr16:50209355 | A | G | 1 | a0001c0001t0052g0013 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.639-1968A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50209355 | |||||||
chr16:50209463 | A | G | 130 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(127): Show |
131 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.639-1860A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50209463 | |||||||
chr16:50209504 | C | G | 8 | a0001c0003t0006g0002 a0001c0003t0006g0191 a0001c0003t0006g0192 others(5): Show |
8 | HG02559.hp2 HG02630.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.639-1819C>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50209504 | |||||||
chr16:50209546 | C | G | 1 | a0001c0001t0002g0072 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.639-1777C>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50209546 | |||||||
chr16:50209583 | T | C | 1 | a0001c0001t0001g0289 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.639-1740T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50209583 | |||||||
chr16:50209599 | C | T | 2 | a0001c0003t0006g0204 a0001c0003t0060g0207 |
2 | HG02630.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.639-1724C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50209599 | |||||||
chr16:50209802 | C | A | 4 | a0001c0001t0012g0195 a0001c0001t0012g0196 a0001c0001t0012g0197 others(1): Show |
4 | HG02145.hp1 HG02723.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.639-1521C>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50209802 | |||||||
chr16:50209913 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.639-1410C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50209913 | |||||||
chr16:50209917 | A | G | 4 | a0001c0001t0004g0267 a0001c0001t0004g0293 a0001c0001t0004g0298 others(1): Show |
4 | HG00639.hp2 HG01256.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.639-1406A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50209917 | |||||||
chr16:50209945 | G | C | 297 | a0001c0001t0001g0084 a0001c0001t0001g0193 a0001c0001t0001g0201 others(294): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.639-1378G>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50209945 | |||||||
chr16:50210087 | T | C | 1 | a0001c0001t0057g0011 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.639-1236T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50210087 | |||||||
chr16:50210103 | G | C | 1 | a0001c0001t0026g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.639-1220G>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50210103 | |||||||
chr16:50210193 | G | A | 1 | a0001c0001t0048g0081 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.639-1130G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50210193 | |||||||
chr16:50210309 | C | A | 1 | a0001c0001t0011g0054 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.639-1014C>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50210309 | |||||||
chr16:50210369 | CCCTTGAA others(5): Show |
C | 1 | a0001c0001t0001g0233 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.639-949_639-938del others(12): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50210369 | ||||||
chr16:50210395 | C | T | 1 | a0001c0001t0048g0081 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.639-928C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50210395 | |||||||
chr16:50210802 | G | A | 2 | a0001c0001t0002g0163 a0001c0001t0023g0140 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.639-521G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50210802 | |||||||
chr16:50211204 | A | T | 8 | a0001c0003t0006g0002 a0001c0003t0006g0191 a0001c0003t0006g0192 others(5): Show |
8 | HG02559.hp2 HG02630.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.639-119A>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 1/11 | chr16 | 50211204 | |||||||
chr16:50211601 | A | T | 1 | a0001c0001t0001g0247 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.762+155A>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 2/11 | chr16 | 50211601 | |||||||
chr16:50211827 | T | C | 1 | a0001c0001t0020g0203 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.762+381T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 2/11 | chr16 | 50211827 | |||||||
chr16:50212415 | C | T | 1 | a0001c0001t0004g0284 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.762+969C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 2/11 | chr16 | 50212415 | |||||||
chr16:50212604 | C | T | 1 | a0001c0001t0002g0310 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.762+1158C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 2/11 | chr16 | 50212604 | |||||||
chr16:50212646 | G | A | 4 | a0001c0001t0002g0060 a0001c0001t0002g0061 a0001c0001t0002g0112 others(1): Show |
4 | HG01081.hp2 HG01099.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.762+1200G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 2/11 | chr16 | 50212646 | |||||||
chr16:50212751 | A | T | 297 | a0001c0001t0001g0084 a0001c0001t0001g0193 a0001c0001t0001g0201 others(294): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.762+1305A>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 2/11 | chr16 | 50212751 | |||||||
chr16:50212889 | C | T | 1 | a0001c0001t0005g0120 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.763-1332C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 2/11 | chr16 | 50212889 | |||||||
chr16:50213104 | G | C | 3 | a0001c0001t0001g0222 a0001c0001t0001g0250 a0004c0008t0001g0251 |
3 | NA18941.hp1 NA18945.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.763-1117G>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 2/11 | chr16 | 50213104 | |||||||
chr16:50213204 | G | A | 1 | a0001c0001t0009g0033 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.763-1017G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 2/11 | chr16 | 50213204 | |||||||
chr16:50213684 | TC | T | 3 | a0002c0004t0001g0281 a0002c0004t0001g0282 a0002c0004t0001g0283 |
3 | NA18972.hp1 NA18992.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.763-535delC | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 50213684 | ||||||
chr16:50213689 | A | G | 1 | a0001c0001t0051g0025 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.763-532A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 2/11 | chr16 | 50213689 | |||||||
chr16:50213695 | C | A | 3 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0002g0145 |
3 | HG02300.hp1 NA19090.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.763-526C>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 2/11 | chr16 | 50213695 | |||||||
chr16:50213706 | T | G | 3 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0002g0145 |
3 | HG02300.hp1 NA19090.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.763-515T>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 2/11 | chr16 | 50213706 | |||||||
chr16:50213769 | T | G | 22 | a0001c0001t0007g0014 a0001c0001t0007g0022 a0001c0001t0007g0023 others(19): Show |
22 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.763-452T>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 2/11 | chr16 | 50213769 | |||||||
chr16:50213858 | T | G | 2 | a0001c0001t0002g0019 a0001c0001t0002g0076 |
2 | HG02080.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.763-363T>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 2/11 | chr16 | 50213858 | |||||||
chr16:50213953 | C | A | 2 | a0001c0001t0001g0236 a0001c0001t0001g0311 |
2 | NA18985.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.763-268C>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 2/11 | chr16 | 50213953 | |||||||
chr16:50214108 | A | G | 8 | a0001c0001t0007g0014 a0001c0001t0007g0022 a0001c0001t0007g0023 others(5): Show |
8 | HG02055.hp2 HG02109.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.763-113A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 2/11 | chr16 | 50214108 | |||||||
chr16:50214339 | G | T | 5 | a0001c0001t0009g0033 a0001c0001t0009g0043 a0001c0001t0009g0044 others(2): Show |
5 | HG02258.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.809+72G>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 3/11 | chr16 | 50214339 | |||||||
chr16:50214341 | G | A | 1 | a0001c0001t0002g0061 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.809+74G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 3/11 | chr16 | 50214341 | |||||||
chr16:50214580 | C | T | 2 | a0001c0001t0002g0055 a0001c0001t0002g0080 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.809+313C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 3/11 | chr16 | 50214580 | |||||||
chr16:50214605 | G | A | 2 | a0001c0001t0001g0232 a0001c0001t0001g0235 |
2 | HG00673.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.809+338G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 3/11 | chr16 | 50214605 | |||||||
chr16:50214608 | A | G | 1 | a0001c0001t0003g0139 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.809+341A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 3/11 | chr16 | 50214608 | |||||||
chr16:50214797 | A | G | 1 | a0001c0001t0002g0174 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.809+530A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 3/11 | chr16 | 50214797 | |||||||
chr16:50214887 | A | G | 2 | a0001c0001t0022g0020 a0001c0001t0022g0021 |
2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.809+620A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 3/11 | chr16 | 50214887 | |||||||
chr16:50214954 | C | T | 4 | a0001c0001t0004g0267 a0001c0001t0004g0293 a0001c0001t0004g0298 others(1): Show |
4 | HG00639.hp2 HG01256.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.809+687C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 3/11 | chr16 | 50214954 | |||||||
chr16:50215111 | C | T | 1 | a0001c0001t0026g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.809+844C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 3/11 | chr16 | 50215111 | |||||||
chr16:50215169 | C | G | 14 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0039 others(11): Show |
14 | NA18941.hp2 NA18945.hp1 NA18951.hp2 others(11): Show |
intron_variant | MODIFIER | c.809+902C>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 3/11 | chr16 | 50215169 | |||||||
chr16:50215192 | G | A | 10 | a0001c0001t0017g0136 a0001c0001t0017g0137 a0001c0001t0017g0186 others(7): Show |
10 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.810-883G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 3/11 | chr16 | 50215192 | |||||||
chr16:50215210 | G | A | 2 | a0001c0001t0022g0021 a0001c0001t0053g0308 |
2 | HG02895.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.810-865G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 3/11 | chr16 | 50215210 | |||||||
chr16:50215239 | A | G | 2 | a0001c0001t0024g0015 a0001c0001t0024g0016 |
2 | HG01891.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.810-836A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 3/11 | chr16 | 50215239 | |||||||
chr16:50215515 | A | G | 4 | a0001c0001t0010g0006 a0001c0001t0010g0007 a0001c0001t0010g0008 others(1): Show |
4 | HG02145.hp2 HG02559.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.810-560A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 3/11 | chr16 | 50215515 | |||||||
chr16:50215518 | G | C | 6 | a0001c0001t0007g0014 a0001c0001t0007g0022 a0001c0001t0007g0023 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.810-557G>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 3/11 | chr16 | 50215518 | |||||||
chr16:50215618 | A | G | 13 | a0001c0001t0017g0136 a0001c0001t0017g0137 a0001c0001t0017g0186 others(10): Show |
13 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.810-457A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 3/11 | chr16 | 50215618 | |||||||
chr16:50215768 | C | T | 13 | a0001c0001t0017g0136 a0001c0001t0017g0137 a0001c0001t0017g0186 others(10): Show |
13 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.810-307C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 3/11 | chr16 | 50215768 | |||||||
chr16:50215827 | A | C | 1 | a0001c0001t0059g0245 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.810-248A>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 3/11 | chr16 | 50215827 | |||||||
chr16:50215876 | A | T | 5 | a0001c0001t0009g0033 a0001c0001t0009g0043 a0001c0001t0009g0044 others(2): Show |
5 | HG02258.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.810-199A>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 3/11 | chr16 | 50215876 | |||||||
chr16:50216056 | A | G | 2 | a0001c0001t0024g0015 a0001c0001t0024g0016 |
2 | HG01891.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.810-19A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 3/11 | chr16 | 50216056 | |||||||
chr16:50216056 | A | T | 2 | a0001c0001t0001g0236 a0001c0001t0001g0311 |
2 | NA18985.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.810-19A>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 3/11 | chr16 | 50216056 | |||||||
chr16:50216215 | A | G | 1 | a0001c0001t0026g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.930+20A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 4/11 | chr16 | 50216215 | |||||||
chr16:50216301 | T | C | 1 | a0001c0001t0002g0030 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.930+106T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 4/11 | chr16 | 50216301 | |||||||
chr16:50216322 | G | A | 27 | a0001c0001t0007g0014 a0001c0001t0007g0022 a0001c0001t0007g0023 others(24): Show |
27 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.930+127G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 4/11 | chr16 | 50216322 | |||||||
chr16:50216448 | T | C | 3 | a0001c0001t0019g0094 a0001c0001t0019g0095 a0001c0001t0019g0138 |
3 | HG01109.hp1 HG02630.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.930+253T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 4/11 | chr16 | 50216448 | |||||||
chr16:50216511 | C | T | 1 | a0001c0003t0006g0002 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.930+316C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 4/11 | chr16 | 50216511 | |||||||
chr16:50216544 | T | C | 1 | a0001c0001t0020g0203 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.930+349T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 4/11 | chr16 | 50216544 | |||||||
chr16:50216675 | TTTTG | T | 155 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(152): Show |
156 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.930+488_930+491del others(4): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr16 | 50216675 | ||||||
chr16:50216780 | G | A | 1 | a0001c0001t0002g0036 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.930+585G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 4/11 | chr16 | 50216780 | |||||||
chr16:50216781 | T | C | 1 | a0001c0001t0002g0036 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.930+586T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 4/11 | chr16 | 50216781 | |||||||
chr16:50216782 | G | A | 1 | a0001c0001t0002g0036 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.930+587G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 4/11 | chr16 | 50216782 | |||||||
chr16:50216823 | T | TA | 154 | a0001c0001t0001g0193 a0001c0001t0001g0201 a0001c0001t0001g0202 others(151): Show |
154 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(151): Show |
intron_variant | MODIFIER | c.930+634dupA | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr16 | 50216823 | ||||||
chr16:50217039 | T | C | 3 | a0001c0001t0001g0222 a0001c0001t0001g0250 a0004c0008t0001g0251 |
3 | NA18941.hp1 NA18945.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.931-517T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 4/11 | chr16 | 50217039 | |||||||
chr16:50217679 | G | A | 131 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(128): Show |
132 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.1038+16G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | chr16 | 50217679 | |||||||
chr16:50217760 | G | GTCTCTCT others(1): Show |
3 | a0001c0003t0006g0192 a0001c0003t0006g0205 a0001c0003t0006g0206 |
3 | HG03516.hp2 HG03579.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1038+105_1038+112d others(10): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr16 | 50217760 | ||||||
chr16:50217760 | G | GTCTCTCT others(3): Show |
114 | a0001c0001t0001g0193 a0001c0001t0001g0201 a0001c0001t0001g0202 others(111): Show |
114 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(111): Show |
intron_variant | MODIFIER | c.1038+103_1038+112d others(12): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr16 | 50217760 | ||||||
chr16:50217760 | G | GTCTCTCT others(5): Show |
27 | a0001c0001t0001g0218 a0001c0001t0001g0274 a0001c0001t0002g0050 others(24): Show |
27 | HG00597.hp1 HG00609.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.1038+101_1038+112d others(14): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr16 | 50217760 | ||||||
chr16:50217760 | G | GTCTCTCT others(13): Show |
14 | a0001c0001t0002g0032 a0001c0001t0002g0058 a0001c0001t0002g0134 others(11): Show |
14 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1038+112_1038+113i others(22): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr16 | 50217760 | ||||||
chr16:50217760 | G | GTCTCTCT others(15): Show |
2 | a0001c0001t0007g0022 a0001c0001t0050g0034 |
2 | HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1038+112_1038+113i others(24): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr16 | 50217760 | ||||||
chr16:50217760 | G | GTCTCTCT others(17): Show |
1 | a0001c0001t0054g0010 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1038+112_1038+113i others(26): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr16 | 50217760 | ||||||
chr16:50217760 | G | GTCTCTCT others(21): Show |
13 | a0001c0001t0017g0136 a0001c0001t0017g0137 a0001c0001t0017g0186 others(10): Show |
13 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.1038+112_1038+113i others(30): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr16 | 50217760 | ||||||
chr16:50217760 | G | GTCTCTCT others(21): Show |
1 | a0001c0001t0057g0011 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1038+112_1038+113i others(30): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr16 | 50217760 | ||||||
chr16:50217940 | A | AT | 15 | a0001c0001t0001g0290 a0001c0001t0004g0300 a0001c0001t0007g0024 others(12): Show |
15 | HG02055.hp2 HG02258.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1038+293dupT | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr16 | 50217940 | ||||||
chr16:50218087 | CT | C | 3 | a0001c0001t0024g0015 a0001c0001t0024g0016 a0001c0001t0053g0308 |
3 | HG01891.hp2 HG02280.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1038+427delT | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr16 | 50218087 | ||||||
chr16:50218102 | C | T | 22 | a0001c0001t0007g0014 a0001c0001t0007g0022 a0001c0001t0007g0023 others(19): Show |
22 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1038+439C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | chr16 | 50218102 | |||||||
chr16:50218291 | A | G | 157 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0004 others(154): Show |
158 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.1038+628A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | chr16 | 50218291 | |||||||
chr16:50218324 | A | G | 98 | a0001c0001t0001g0193 a0001c0001t0001g0201 a0001c0001t0001g0202 others(95): Show |
98 | HG00423.hp2 HG00544.hp2 HG00673.hp2 others(95): Show |
intron_variant | MODIFIER | c.1038+661A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | chr16 | 50218324 | |||||||
chr16:50218497 | G | A | 1 | a0001c0001t0028g0198 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1038+834G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | chr16 | 50218497 | |||||||
chr16:50218512 | C | T | 4 | a0001c0001t0010g0006 a0001c0001t0010g0007 a0001c0001t0010g0008 others(1): Show |
4 | HG02145.hp2 HG02559.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1038+849C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | chr16 | 50218512 | |||||||
chr16:50218841 | A | G | 1 | a0001c0001t0048g0081 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1038+1178A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | chr16 | 50218841 | |||||||
chr16:50218926 | T | G | 11 | a0001c0001t0004g0190 a0001c0001t0004g0199 a0001c0001t0004g0267 others(8): Show |
11 | HG00639.hp2 HG01081.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.1038+1263T>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | chr16 | 50218926 | |||||||
chr16:50218946 | C | T | 1 | a0001c0009t0049g0077 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1038+1283C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | chr16 | 50218946 | |||||||
chr16:50219085 | A | G | 1 | a0001c0001t0052g0013 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1038+1422A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | chr16 | 50219085 | |||||||
chr16:50219093 | G | GGT | 5 | a0001c0001t0002g0098 a0001c0001t0003g0018 a0001c0001t0003g0047 others(2): Show |
5 | NA18942.hp1 NA18951.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.1038+1445_1038+144 others(6): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr16 | 50219093 | ||||||
chr16:50219093 | G | GGTGTGT | 4 | a0001c0001t0010g0006 a0001c0001t0010g0007 a0001c0001t0010g0008 others(1): Show |
4 | HG02145.hp2 HG02559.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1038+1441_1038+144 others(10): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr16 | 50219093 | ||||||
chr16:50219263 | T | C | 1 | a0001c0001t0002g0061 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1038+1600T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | chr16 | 50219263 | |||||||
chr16:50219322 | T | G | 1 | a0001c0001t0041g0177 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1038+1659T>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | chr16 | 50219322 | |||||||
chr16:50219452 | G | A | 1 | a0001c0001t0026g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1038+1789G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | chr16 | 50219452 | |||||||
chr16:50219477 | T | C | 4 | a0001c0001t0012g0195 a0001c0001t0012g0196 a0001c0001t0012g0197 others(1): Show |
4 | HG02145.hp1 HG02723.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1038+1814T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | chr16 | 50219477 | |||||||
chr16:50219700 | C | G | 1 | a0001c0001t0002g0004 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1038+2037C>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | chr16 | 50219700 | |||||||
chr16:50219727 | TTC | T | 4 | a0001c0001t0002g0060 a0001c0001t0002g0061 a0001c0001t0002g0112 others(1): Show |
4 | HG01081.hp2 HG01099.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.1038+2070_1038+207 others(6): Show |
TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr16 | 50219727 | ||||||
chr16:50219812 | G | C | 2 | a0001c0001t0002g0036 a0001c0001t0002g0146 |
2 | HG01070.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1038+2149G>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | chr16 | 50219812 | |||||||
chr16:50219993 | AT | A | 296 | a0001c0001t0001g0084 a0001c0001t0001g0193 a0001c0001t0001g0201 others(293): Show |
297 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.1039-2300delT | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr16 | 50219993 | ||||||
chr16:50219994 | T | A | 1 | a0001c0002t0032g0123 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1039-2312T>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | chr16 | 50219994 | |||||||
chr16:50220230 | C | T | 1 | a0001c0001t0044g0053 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1039-2076C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | chr16 | 50220230 | |||||||
chr16:50220283 | C | T | 1 | a0001c0001t0001g0226 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1039-2023C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | chr16 | 50220283 | |||||||
chr16:50220525 | A | G | 20 | a0001c0001t0002g0050 a0001c0001t0002g0098 a0001c0001t0003g0003 others(17): Show |
20 | HG00597.hp1 HG00609.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.1039-1781A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | chr16 | 50220525 | |||||||
chr16:50220685 | C | G | 84 | a0001c0001t0001g0193 a0001c0001t0001g0201 a0001c0001t0001g0202 others(81): Show |
84 | HG00423.hp2 HG00544.hp2 HG00673.hp2 others(81): Show |
intron_variant | MODIFIER | c.1039-1621C>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | chr16 | 50220685 | |||||||
chr16:50220743 | G | A | 8 | a0001c0001t0007g0014 a0001c0001t0007g0022 a0001c0001t0007g0023 others(5): Show |
8 | HG02055.hp2 HG02109.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1039-1563G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | chr16 | 50220743 | |||||||
chr16:50220988 | A | G | 1 | a0001c0001t0002g0019 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1039-1318A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | chr16 | 50220988 | |||||||
chr16:50221211 | G | C | 148 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0019 others(145): Show |
149 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.1039-1095G>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | chr16 | 50221211 | |||||||
chr16:50221342 | C | T | 1 | a0001c0001t0020g0203 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1039-964C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | chr16 | 50221342 | |||||||
chr16:50221826 | C | T | 13 | a0001c0001t0017g0136 a0001c0001t0017g0137 a0001c0001t0017g0186 others(10): Show |
13 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.1039-480C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | chr16 | 50221826 | |||||||
chr16:50221923 | C | T | 1 | a0001c0001t0016g0187 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1039-383C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | chr16 | 50221923 | |||||||
chr16:50221998 | C | T | 3 | a0001c0001t0002g0060 a0001c0001t0002g0112 a0001c0001t0002g0116 |
3 | HG01081.hp2 HG01099.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.1039-308C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | chr16 | 50221998 | |||||||
chr16:50222017 | G | T | 27 | a0001c0001t0007g0014 a0001c0001t0007g0022 a0001c0001t0007g0023 others(24): Show |
27 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1039-289G>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | chr16 | 50222017 | |||||||
chr16:50222040 | C | A | 5 | a0001c0001t0012g0195 a0001c0001t0012g0196 a0001c0001t0012g0197 others(2): Show |
5 | HG02145.hp1 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1039-266C>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | chr16 | 50222040 | |||||||
chr16:50222065 | C | T | 1 | a0001c0001t0004g0303 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1039-241C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | chr16 | 50222065 | |||||||
chr16:50222118 | G | T | 1 | a0001c0001t0003g0049 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1039-188G>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | chr16 | 50222118 | |||||||
chr16:50222145 | A | G | 11 | a0001c0001t0004g0190 a0001c0001t0004g0199 a0001c0001t0004g0267 others(8): Show |
11 | HG00639.hp2 HG01081.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.1039-161A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 5/11 | chr16 | 50222145 | |||||||
chr16:50222683 | A | T | 1 | a0001c0001t0041g0177 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1167+249A>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 6/11 | chr16 | 50222683 | |||||||
chr16:50222696 | A | G | 3 | a0001c0001t0005g0118 a0001c0001t0005g0120 a0001c0001t0005g0132 |
3 | HG00741.hp1 HG01071.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1167+262A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 6/11 | chr16 | 50222696 | |||||||
chr16:50222700 | G | A | 1 | a0001c0001t0052g0013 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1167+266G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 6/11 | chr16 | 50222700 | |||||||
chr16:50222703 | C | T | 1 | a0001c0001t0003g0049 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1167+269C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 6/11 | chr16 | 50222703 | |||||||
chr16:50222951 | G | A | 1 | a0001c0001t0026g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1168-223G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 6/11 | chr16 | 50222951 | |||||||
chr16:50223003 | T | C | 1 | a0001c0001t0004g0298 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1168-171T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 6/11 | chr16 | 50223003 | |||||||
chr16:50223094 | G | A | 1 | a0001c0001t0002g0126 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1168-80G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 6/11 | chr16 | 50223094 | |||||||
chr16:50223098 | T | G | 3 | a0002c0004t0001g0281 a0002c0004t0001g0282 a0002c0004t0001g0283 |
3 | NA18972.hp1 NA18992.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1168-76T>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 6/11 | chr16 | 50223098 | |||||||
chr16:50223481 | G | A | 5 | a0001c0001t0002g0001 a0001c0001t0002g0075 a0001c0001t0002g0134 others(2): Show |
6 | HG01943.hp2 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1381+94G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 7/11 | chr16 | 50223481 | |||||||
chr16:50224254 | A | G | 1 | a0001c0001t0026g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1382-403A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 7/11 | chr16 | 50224254 | |||||||
chr16:50224434 | G | A | 1 | a0001c0001t0003g0035 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1382-223G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 7/11 | chr16 | 50224434 | |||||||
chr16:50224586 | A | G | 1 | a0001c0001t0001g0279 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1382-71A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 7/11 | chr16 | 50224586 | |||||||
chr16:50225302 | C | T | 1 | a0001c0001t0003g0178 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1800+17C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 10/11 | chr16 | 50225302 | |||||||
chr16:50225572 | A | G | 100 | a0001c0001t0001g0084 a0001c0001t0001g0193 a0001c0001t0001g0201 others(97): Show |
100 | HG00423.hp2 HG00544.hp2 HG00673.hp2 others(97): Show |
intron_variant | MODIFIER | c.1800+287A>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 10/11 | chr16 | 50225572 | |||||||
chr16:50225665 | G | A | 189 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(186): Show |
190 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.1800+380G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 10/11 | chr16 | 50225665 | |||||||
chr16:50225731 | G | A | 1 | a0001c0001t0010g0007 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1800+446G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 10/11 | chr16 | 50225731 | |||||||
chr16:50226086 | G | C | 1 | a0001c0011t0030g0208 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1800+801G>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 10/11 | chr16 | 50226086 | |||||||
chr16:50226089 | T | G | 1 | a0001c0001t0052g0013 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1800+804T>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 10/11 | chr16 | 50226089 | |||||||
chr16:50226213 | C | T | 1 | a0001c0001t0001g0275 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1800+928C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 10/11 | chr16 | 50226213 | |||||||
chr16:50226471 | G | A | 9 | a0001c0001t0004g0190 a0001c0001t0004g0267 a0001c0001t0004g0268 others(6): Show |
9 | HG00639.hp2 HG01081.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.1800+1186G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 10/11 | chr16 | 50226471 | |||||||
chr16:50226494 | C | T | 1 | a0001c0001t0002g0075 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1800+1209C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 10/11 | chr16 | 50226494 | |||||||
chr16:50226525 | G | A | 1 | a0001c0001t0002g0164 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1800+1240G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 10/11 | chr16 | 50226525 | |||||||
chr16:50226668 | G | A | 1 | a0001c0001t0004g0292 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1801-1171G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 10/11 | chr16 | 50226668 | |||||||
chr16:50226719 | T | A | 5 | a0001c0001t0009g0033 a0001c0001t0009g0043 a0001c0001t0009g0044 others(2): Show |
5 | HG02258.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1801-1120T>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 10/11 | chr16 | 50226719 | |||||||
chr16:50226734 | G | A | 8 | a0001c0001t0007g0014 a0001c0001t0007g0022 a0001c0001t0007g0023 others(5): Show |
8 | HG02055.hp2 HG02109.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1801-1105G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 10/11 | chr16 | 50226734 | |||||||
chr16:50226787 | G | A | 100 | a0001c0001t0001g0084 a0001c0001t0001g0193 a0001c0001t0001g0201 others(97): Show |
100 | HG00423.hp2 HG00544.hp2 HG00673.hp2 others(97): Show |
intron_variant | MODIFIER | c.1801-1052G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 10/11 | chr16 | 50226787 | |||||||
chr16:50226794 | T | G | 1 | a0001c0001t0003g0003 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1801-1045T>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 10/11 | chr16 | 50226794 | |||||||
chr16:50227170 | G | A | 297 | a0001c0001t0001g0084 a0001c0001t0001g0193 a0001c0001t0001g0201 others(294): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.1801-669G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 10/11 | chr16 | 50227170 | |||||||
chr16:50227182 | G | A | 1 | a0001c0001t0002g0133 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1801-657G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 10/11 | chr16 | 50227182 | |||||||
chr16:50227318 | G | A | 1 | a0001c0001t0002g0032 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1801-521G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 10/11 | chr16 | 50227318 | |||||||
chr16:50227392 | C | T | 1 | a0001c0001t0026g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1801-447C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 10/11 | chr16 | 50227392 | |||||||
chr16:50227466 | G | A | 2 | a0001c0001t0005g0041 a0001c0001t0005g0042 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1801-373G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 10/11 | chr16 | 50227466 | |||||||
chr16:50228017 | G | A | 1 | a0001c0001t0043g0048 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1965+14G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 11/11 | chr16 | 50228017 | |||||||
chr16:50228062 | C | G | 5 | a0001c0001t0009g0033 a0001c0001t0009g0043 a0001c0001t0009g0044 others(2): Show |
5 | HG02258.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1965+59C>G | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 11/11 | chr16 | 50228062 | |||||||
chr16:50228100 | G | A | 1 | a0001c0001t0002g0171 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1965+97G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 11/11 | chr16 | 50228100 | |||||||
chr16:50228315 | A | C | 1 | a0001c0001t0001g0263 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1965+312A>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 11/11 | chr16 | 50228315 | |||||||
chr16:50228485 | T | C | 1 | a0001c0001t0003g0178 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1965+482T>C | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 11/11 | chr16 | 50228485 | |||||||
chr16:50228613 | GC | G | 154 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(151): Show |
155 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.1966-538delC | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 11/11 | chr16 | 50228613 | |||||||
chr16:50228656 | C | T | 1 | a0001c0001t0007g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1966-496C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 11/11 | chr16 | 50228656 | |||||||
chr16:50228678 | G | A | 1 | a0001c0001t0001g0294 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1966-474G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 11/11 | chr16 | 50228678 | |||||||
chr16:50228686 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1966-466C>T | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 11/11 | chr16 | 50228686 | |||||||
chr16:50228713 | G | A | 1 | a0001c0001t0034g0087 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1966-439G>A | TENT4B | ENSG00000121274.14 | transcript | ENST00000561678.7 | protein_coding | 11/11 | chr16 | 50228713 |