Item | Value |
---|---|
geneid | 79668 |
ensemblid | ENSG00000151883.20 |
hgncid | 26124 |
symbol | PARP8 |
name | poly(ADP-ribose) polymerase family member 8 |
refseq_nuc | NM_024615.4 |
refseq_prot | NP_078891.2 |
ensembl_nuc | ENST00000281631.10 |
ensembl_prot | ENSP00000281631.4 |
mane_status | MANE Select |
chr | chr5 |
start | 50666637 |
end | 50846519 |
strand | + |
ver | v1.2 |
region | chr5:50666637-50846519 |
region5000 | chr5:50661637-50851519 |
regionname0 | PARP8_chr5_50666637_50846519 |
regionname5000 | PARP8_chr5_50661637_50851519 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 854 | 320 | 92 | 55 | 121 | 8 | 42 | 94 | PARP8_chr5_50661637_50851519 | PARP8 | MGMCS others(849): Show |
chr5 | 50661637 | 50851519 |
a0002 | 0/0 | 854 | 6 | 0 | 0 | 6 | 0 | 0 | 6 | PARP8_chr5_50661637_50851519 | PARP8 | MGMCS others(849): Show |
chr5 | 50661637 | 50851519 |
a0003 | 0/0 | 854 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | MGMCS others(849): Show |
chr5 | 50661637 | 50851519 |
a0004 | 0/0 | 854 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | MGMCS others(849): Show |
chr5 | 50661637 | 50851519 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2562 | 147 | 62 | 24 | 39 | 5 | 15 | PARP8_chr5_50661637_50851519 | PARP8 | ATGGG others(2557): Show |
chr5 | 50661637 | 50851519 | ||
a0001c0002 | 0/0 | 2562 | 111 | 14 | 20 | 56 | 3 | 18 | PARP8_chr5_50661637_50851519 | PARP8 | ATGGG others(2557): Show |
chr5 | 50661637 | 50851519 | ||
a0001c0003 | 0/0 | 2562 | 47 | 5 | 10 | 24 | 0 | 8 | PARP8_chr5_50661637_50851519 | PARP8 | ATGGG others(2557): Show |
chr5 | 50661637 | 50851519 | ||
a0001c0004 | 0/0 | 2562 | 7 | 6 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | ATGGG others(2557): Show |
chr5 | 50661637 | 50851519 | ||
a0001c0006 | 0/0 | 2562 | 2 | 0 | 0 | 2 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | ATGGG others(2557): Show |
chr5 | 50661637 | 50851519 | ||
a0001c0007 | 0/0 | 2562 | 2 | 2 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | ATGGG others(2557): Show |
chr5 | 50661637 | 50851519 | ||
a0001c0010 | 0/0 | 2562 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | ATGGG others(2557): Show |
chr5 | 50661637 | 50851519 | ||
a0001c0011 | 0/0 | 2562 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | ATGGG others(2557): Show |
chr5 | 50661637 | 50851519 | ||
a0001c0012 | 0/0 | 2562 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | ATGGG others(2557): Show |
chr5 | 50661637 | 50851519 | ||
a0001c0013 | 0/0 | 2562 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | ATGGG others(2557): Show |
chr5 | 50661637 | 50851519 | ||
a0002c0005 | 0/0 | 2562 | 6 | 0 | 0 | 6 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | ATGGG others(2557): Show |
chr5 | 50661637 | 50851519 | ||
a0003c0009 | 0/0 | 2562 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | ATGGG others(2557): Show |
chr5 | 50661637 | 50851519 | ||
a0004c0008 | 0/0 | 2562 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | ATGGG others(2557): Show |
chr5 | 50661637 | 50851519 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 7478 | 41 | 4 | 6 | 24 | 3 | 4 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7473): Show |
chr5 | 50661637 | 50851519 |
a0001c0001t0002 | 0/0 | 7478 | 8 | 7 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7473): Show |
chr5 | 50661637 | 50851519 |
a0001c0001t0004 | 1/0 | 7475 | 23 | 5 | 9 | 0 | 2 | 6 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7470): Show |
chr5 | 50661637 | 50851519 |
a0001c0001t0005 | 0/0 | 7478 | 15 | 7 | 0 | 8 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7473): Show |
chr5 | 50661637 | 50851519 |
a0001c0001t0006 | 0/0 | 7480 | 16 | 14 | 2 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7475): Show |
chr5 | 50661637 | 50851519 |
a0001c0001t0007 | 0/0 | 7478 | 8 | 2 | 4 | 0 | 0 | 2 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7473): Show |
chr5 | 50661637 | 50851519 |
a0001c0001t0008 | 0/0 | 7478 | 8 | 8 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7473): Show |
chr5 | 50661637 | 50851519 |
a0001c0001t0012 | 0/0 | 7478 | 3 | 0 | 0 | 0 | 0 | 3 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7473): Show |
chr5 | 50661637 | 50851519 |
a0001c0001t0013 | 0/0 | 7481 | 2 | 2 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7476): Show |
chr5 | 50661637 | 50851519 |
a0001c0001t0014 | 0/0 | 7479 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7474): Show |
chr5 | 50661637 | 50851519 |
a0001c0001t0015 | 0/0 | 7478 | 2 | 0 | 0 | 2 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7473): Show |
chr5 | 50661637 | 50851519 |
a0001c0001t0016 | 0/0 | 7478 | 2 | 0 | 0 | 2 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7473): Show |
chr5 | 50661637 | 50851519 |
a0001c0001t0017 | 0/0 | 7478 | 2 | 2 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7473): Show |
chr5 | 50661637 | 50851519 |
a0001c0001t0019 | 0/0 | 7480 | 2 | 2 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7475): Show |
chr5 | 50661637 | 50851519 |
a0001c0001t0021 | 0/0 | 7475 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7470): Show |
chr5 | 50661637 | 50851519 |
a0001c0001t0022 | 0/0 | 7475 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7470): Show |
chr5 | 50661637 | 50851519 |
a0001c0001t0024 | 0/0 | 7475 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7470): Show |
chr5 | 50661637 | 50851519 |
a0001c0001t0025 | 0/0 | 7479 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7474): Show |
chr5 | 50661637 | 50851519 |
a0001c0001t0027 | 0/0 | 7490 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7485): Show |
chr5 | 50661637 | 50851519 |
a0001c0001t0030 | 0/0 | 7478 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7473): Show |
chr5 | 50661637 | 50851519 |
a0001c0001t0031 | 0/0 | 7480 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7475): Show |
chr5 | 50661637 | 50851519 |
a0001c0001t0032 | 0/0 | 7478 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7473): Show |
chr5 | 50661637 | 50851519 |
a0001c0001t0033 | 0/0 | 7478 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7473): Show |
chr5 | 50661637 | 50851519 |
a0001c0001t0034 | 0/0 | 7478 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7473): Show |
chr5 | 50661637 | 50851519 |
a0001c0001t0037 | 0/0 | 7478 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7473): Show |
chr5 | 50661637 | 50851519 |
a0001c0001t0047 | 0/0 | 7478 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7473): Show |
chr5 | 50661637 | 50851519 |
a0001c0001t0048 | 0/1 | 7479 | 1 | 0 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7474): Show |
chr5 | 50661637 | 50851519 |
a0001c0001t0049 | 0/0 | 7479 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7474): Show |
chr5 | 50661637 | 50851519 |
a0001c0002t0002 | 0/0 | 7478 | 47 | 12 | 11 | 18 | 0 | 6 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7473): Show |
chr5 | 50661637 | 50851519 |
a0001c0002t0003 | 0/0 | 7478 | 48 | 1 | 9 | 26 | 3 | 9 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7473): Show |
chr5 | 50661637 | 50851519 |
a0001c0002t0005 | 0/0 | 7478 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7473): Show |
chr5 | 50661637 | 50851519 |
a0001c0002t0009 | 0/0 | 7478 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7473): Show |
chr5 | 50661637 | 50851519 |
a0001c0002t0018 | 0/0 | 7479 | 2 | 0 | 0 | 2 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7474): Show |
chr5 | 50661637 | 50851519 |
a0001c0002t0023 | 0/0 | 7475 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7470): Show |
chr5 | 50661637 | 50851519 |
a0001c0002t0026 | 0/0 | 7479 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7474): Show |
chr5 | 50661637 | 50851519 |
a0001c0002t0039 | 0/0 | 7478 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7473): Show |
chr5 | 50661637 | 50851519 |
a0001c0002t0040 | 0/0 | 7478 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7473): Show |
chr5 | 50661637 | 50851519 |
a0001c0002t0041 | 0/0 | 7478 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7473): Show |
chr5 | 50661637 | 50851519 |
a0001c0002t0042 | 0/0 | 7478 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7473): Show |
chr5 | 50661637 | 50851519 |
a0001c0002t0043 | 0/0 | 7465 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7460): Show |
chr5 | 50661637 | 50851519 |
a0001c0002t0044 | 0/0 | 7478 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7473): Show |
chr5 | 50661637 | 50851519 |
a0001c0002t0045 | 0/0 | 7478 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7473): Show |
chr5 | 50661637 | 50851519 |
a0001c0002t0046 | 0/0 | 7478 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7473): Show |
chr5 | 50661637 | 50851519 |
a0001c0002t0050 | 0/0 | 7478 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7473): Show |
chr5 | 50661637 | 50851519 |
a0001c0002t0051 | 0/0 | 7478 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7473): Show |
chr5 | 50661637 | 50851519 |
a0001c0003t0001 | 0/0 | 7478 | 37 | 1 | 7 | 24 | 0 | 5 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7473): Show |
chr5 | 50661637 | 50851519 |
a0001c0003t0010 | 0/0 | 7480 | 5 | 1 | 2 | 0 | 0 | 2 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7475): Show |
chr5 | 50661637 | 50851519 |
a0001c0003t0011 | 0/0 | 7478 | 3 | 3 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7473): Show |
chr5 | 50661637 | 50851519 |
a0001c0003t0014 | 0/0 | 7479 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7474): Show |
chr5 | 50661637 | 50851519 |
a0001c0003t0035 | 0/0 | 7478 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7473): Show |
chr5 | 50661637 | 50851519 |
a0001c0004t0005 | 0/0 | 7478 | 7 | 6 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7473): Show |
chr5 | 50661637 | 50851519 |
a0001c0006t0004 | 0/0 | 7475 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7470): Show |
chr5 | 50661637 | 50851519 |
a0001c0006t0020 | 0/0 | 7476 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7471): Show |
chr5 | 50661637 | 50851519 |
a0001c0007t0028 | 0/0 | 7478 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7473): Show |
chr5 | 50661637 | 50851519 |
a0001c0007t0029 | 0/0 | 7478 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7473): Show |
chr5 | 50661637 | 50851519 |
a0001c0010t0036 | 0/0 | 7478 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7473): Show |
chr5 | 50661637 | 50851519 |
a0001c0011t0004 | 0/0 | 7475 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7470): Show |
chr5 | 50661637 | 50851519 |
a0001c0012t0038 | 0/0 | 7478 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7473): Show |
chr5 | 50661637 | 50851519 |
a0001c0013t0005 | 0/0 | 7478 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7473): Show |
chr5 | 50661637 | 50851519 |
a0002c0005t0002 | 0/0 | 7478 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7473): Show |
chr5 | 50661637 | 50851519 |
a0002c0005t0009 | 0/0 | 7478 | 5 | 0 | 0 | 5 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7473): Show |
chr5 | 50661637 | 50851519 |
a0003c0009t0001 | 0/0 | 7478 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7473): Show |
chr5 | 50661637 | 50851519 |
a0004c0008t0003 | 0/0 | 7478 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | GTGGA others(7473): Show |
chr5 | 50661637 | 50851519 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0004g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0004g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0004g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0004g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0004g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0004g0043 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0004g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0004g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0004g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0005g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0005g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0005g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0005g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0005g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0005g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0005g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0005g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0005g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0005g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0005g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0006g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0006g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0006g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0006g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0006g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0006g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0006g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0006g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0006g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0006g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0006g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0006g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0006g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0006g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0006g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0006g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0007g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0007g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0007g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0007g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0007g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0007g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0007g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0007g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0008g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0008g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0008g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0008g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0008g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0008g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0008g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0008g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0012g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0012g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0012g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0013g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0013g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0014g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0015g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0015g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0016g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0016g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0017g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0017g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0019g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0021g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0022g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0024g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0025g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0027g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0030g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0031g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0032g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0033g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0034g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0037g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0047g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0048g0288 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0001t0049g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0005g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0009g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0018g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0018g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0023g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0026g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0039g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0040g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0041g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0042g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0043g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0044g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0045g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0046g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0050g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0002t0051g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0010g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0010g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0010g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0010g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0010g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0011g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0011g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0011g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0014g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0003t0035g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0004t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0004t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0004t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0004t0005g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0004t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0004t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0004t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0006t0004g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0006t0020g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0007t0028g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0007t0029g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0010t0036g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0011t0004g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0012t0038g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0001c0013t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0002c0005t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0002c0005t0009g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0002c0005t0009g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0002c0005t0009g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0002c0005t0009g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0002c0005t0009g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0003c0009t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
a0004c0008t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0275 | EUR | GBR | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG00099 | hp2 | a0001 | c0001 | t0004 | g0033 | EUR | GBR | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG00438 | hp1 | a0001 | c0002 | t0002 | g0083 | EAS | CHS | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | CHS | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG00544 | hp1 | a0001 | c0001 | t0034 | g0298 | EAS | CHS | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG00544 | hp2 | a0001 | c0002 | t0002 | g0159 | EAS | CHS | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG00558 | hp1 | a0001 | c0001 | t0016 | g0283 | EAS | CHS | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG00558 | hp2 | a0001 | c0002 | t0003 | g0073 | EAS | CHS | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG00597 | hp1 | a0001 | c0002 | t0018 | g0138 | EAS | CHS | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG00597 | hp2 | a0001 | c0002 | t0002 | g0072 | EAS | CHS | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG00609 | hp1 | a0001 | c0002 | t0002 | g0114 | EAS | CHS | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG00609 | hp2 | a0001 | c0002 | t0003 | g0087 | EAS | CHS | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG00639 | hp1 | a0001 | c0002 | t0002 | g0075 | AMR | PUR | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG00639 | hp2 | a0001 | c0002 | t0002 | g0173 | AMR | PUR | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG00642 | hp1 | a0001 | c0001 | t0007 | g0190 | AMR | PUR | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG00642 | hp2 | a0001 | c0002 | t0002 | g0178 | AMR | PUR | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG00673 | hp1 | a0001 | c0003 | t0001 | g0248 | EAS | CHS | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | CHS | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG00733 | hp1 | a0001 | c0001 | t0004 | g0039 | AMR | PUR | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG00733 | hp2 | a0001 | c0001 | t0007 | g0188 | AMR | PUR | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG00738 | hp1 | a0001 | c0003 | t0001 | g0218 | AMR | PUR | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | PUR | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01069 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01071 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01071 | hp2 | a0001 | c0002 | t0002 | g0065 | AMR | PUR | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01074 | hp1 | a0001 | c0002 | t0003 | g0095 | AMR | PUR | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01074 | hp2 | a0001 | c0001 | t0007 | g0186 | AMR | PUR | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01081 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01109 | hp1 | a0001 | c0002 | t0003 | g0096 | AMR | PUR | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01109 | hp2 | a0001 | c0004 | t0005 | g0029 | AMR | PUR | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01167 | hp1 | a0001 | c0001 | t0007 | g0181 | AMR | PUR | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01167 | hp2 | a0001 | c0001 | t0006 | g0196 | AMR | PUR | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01168 | hp1 | a0001 | c0002 | t0002 | g0078 | AMR | PUR | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01169 | hp1 | a0001 | c0002 | t0002 | g0077 | AMR | PUR | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01169 | hp2 | a0001 | c0001 | t0006 | g0197 | AMR | PUR | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | PUR | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01192 | hp2 | a0001 | c0001 | t0025 | g0315 | AMR | PUR | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01243 | hp1 | a0001 | c0003 | t0035 | g0219 | AMR | PUR | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01243 | hp2 | a0001 | c0001 | t0004 | g0042 | AMR | PUR | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01255 | hp1 | a0001 | c0002 | t0003 | g0124 | AMR | CLM | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01255 | hp2 | a0001 | c0003 | t0010 | g0231 | AMR | CLM | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01257 | hp1 | a0003 | c0009 | t0001 | g0286 | AMR | CLM | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01257 | hp2 | a0001 | c0002 | t0003 | g0108 | AMR | CLM | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01261 | hp1 | a0001 | c0003 | t0001 | g0209 | AMR | CLM | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01261 | hp2 | a0001 | c0001 | t0004 | g0056 | AMR | CLM | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01346 | hp1 | a0001 | c0002 | t0003 | g0175 | AMR | CLM | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01346 | hp2 | a0001 | c0001 | t0021 | g0318 | AMR | CLM | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01361 | hp1 | a0001 | c0002 | t0002 | g0076 | AMR | CLM | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | CLM | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01433 | hp1 | a0001 | c0002 | t0002 | g0109 | AMR | CLM | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01433 | hp2 | a0001 | c0003 | t0001 | g0249 | AMR | CLM | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0300 | EUR | IBS | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01515 | hp2 | a0001 | c0002 | t0003 | g0080 | EUR | IBS | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01516 | hp1 | a0001 | c0002 | t0003 | g0123 | EUR | IBS | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01516 | hp2 | a0001 | c0001 | t0004 | g0052 | EUR | IBS | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01884 | hp1 | a0001 | c0001 | t0005 | g0019 | AFR | ACB | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01884 | hp2 | a0001 | c0001 | t0008 | g0313 | AFR | ACB | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01891 | hp1 | a0001 | c0010 | t0036 | g0321 | AFR | ACB | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01891 | hp2 | a0001 | c0001 | t0017 | g0171 | AFR | ACB | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01934 | hp1 | a0001 | c0001 | t0004 | g0048 | AMR | PEL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01934 | hp2 | a0001 | c0003 | t0001 | g0215 | AMR | PEL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01943 | hp1 | a0001 | c0002 | t0003 | g0003 | AMR | PEL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01943 | hp2 | a0001 | c0003 | t0001 | g0250 | AMR | PEL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01952 | hp1 | a0001 | c0002 | t0002 | g0165 | AMR | PEL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01952 | hp2 | a0001 | c0003 | t0010 | g0255 | AMR | PEL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PEL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG01975 | hp2 | a0001 | c0001 | t0004 | g0049 | AMR | PEL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02027 | hp1 | a0004 | c0008 | t0003 | g0137 | EAS | KHV | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02027 | hp2 | a0001 | c0002 | t0002 | g0086 | EAS | KHV | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02055 | hp1 | a0001 | c0003 | t0011 | g0225 | AFR | ACB | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02055 | hp2 | a0001 | c0002 | t0002 | g0102 | AFR | ACB | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02056 | hp2 | a0001 | c0003 | t0001 | g0220 | EAS | KHV | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02074 | hp1 | a0001 | c0002 | t0002 | g0161 | EAS | KHV | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02074 | hp2 | a0001 | c0003 | t0001 | g0238 | EAS | KHV | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02080 | hp1 | a0001 | c0002 | t0005 | g0071 | EAS | KHV | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02129 | hp1 | a0001 | c0001 | t0047 | g0295 | EAS | KHV | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02129 | hp2 | a0001 | c0002 | t0002 | g0082 | EAS | KHV | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | KHV | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02132 | hp2 | a0001 | c0002 | t0003 | g0319 | EAS | KHV | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02145 | hp1 | a0001 | c0001 | t0013 | g0192 | AFR | ACB | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02145 | hp2 | a0001 | c0001 | t0007 | g0184 | AFR | ACB | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02148 | hp1 | a0001 | c0002 | t0003 | g0070 | AMR | PEL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02148 | hp2 | a0001 | c0003 | t0001 | g0217 | AMR | PEL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02155 | hp1 | a0001 | c0002 | t0002 | g0176 | EAS | CDX | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02155 | hp2 | a0001 | c0003 | t0001 | g0253 | EAS | CDX | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | CDX | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02165 | hp2 | a0001 | c0002 | t0003 | g0128 | EAS | CDX | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02257 | hp1 | a0001 | c0001 | t0030 | g0005 | AFR | ACB | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02257 | hp2 | a0001 | c0002 | t0002 | g0105 | AFR | ACB | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02258 | hp2 | a0001 | c0001 | t0006 | g0193 | AFR | ACB | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02273 | hp1 | a0001 | c0002 | t0003 | g0069 | AMR | PEL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02273 | hp2 | a0001 | c0002 | t0002 | g0088 | AMR | PEL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02280 | hp1 | a0001 | c0001 | t0006 | g0201 | AFR | ACB | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | ACB | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02293 | hp1 | a0001 | c0002 | t0002 | g0081 | AMR | PEL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02293 | hp2 | a0001 | c0001 | t0004 | g0038 | AMR | PEL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02300 | hp1 | a0001 | c0003 | t0001 | g0216 | AMR | PEL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02300 | hp2 | a0001 | c0002 | t0003 | g0003 | AMR | PEL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02451 | hp1 | a0001 | c0004 | t0005 | g0030 | AFR | ACB | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02451 | hp2 | a0001 | c0001 | t0006 | g0202 | AFR | ACB | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02572 | hp1 | a0001 | c0001 | t0008 | g0310 | AFR | GWD | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02572 | hp2 | a0001 | c0007 | t0029 | g0006 | AFR | GWD | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02602 | hp1 | a0001 | c0001 | t0004 | g0034 | SAS | PJL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02602 | hp2 | a0001 | c0002 | t0003 | g0125 | SAS | PJL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02615 | hp2 | a0001 | c0001 | t0004 | g0054 | AFR | GWD | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02622 | hp1 | a0001 | c0002 | t0002 | g0111 | AFR | GWD | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02622 | hp2 | a0001 | c0001 | t0033 | g0257 | AFR | GWD | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02630 | hp1 | a0001 | c0001 | t0008 | g0316 | AFR | GWD | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02630 | hp2 | a0001 | c0001 | t0006 | g0191 | AFR | GWD | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02683 | hp1 | a0001 | c0001 | t0004 | g0050 | SAS | PJL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02683 | hp2 | a0001 | c0002 | t0039 | g0152 | SAS | PJL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02698 | hp1 | a0001 | c0002 | t0002 | g0074 | SAS | PJL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02698 | hp2 | a0001 | c0002 | t0003 | g0127 | SAS | PJL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0166 | AFR | GWD | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02717 | hp2 | a0001 | c0002 | t0003 | g0113 | AFR | GWD | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02723 | hp1 | a0001 | c0001 | t0024 | g0051 | AFR | GWD | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02723 | hp2 | a0001 | c0001 | t0008 | g0311 | AFR | GWD | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02735 | hp1 | a0001 | c0001 | t0004 | g0041 | SAS | PJL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02735 | hp2 | a0001 | c0002 | t0003 | g0100 | SAS | PJL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02809 | hp1 | a0001 | c0001 | t0008 | g0299 | AFR | GWD | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02809 | hp2 | a0001 | c0001 | t0032 | g0183 | AFR | GWD | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02886 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | GWD | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0035 | AFR | GWD | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02895 | hp1 | a0001 | c0001 | t0006 | g0194 | AFR | GWD | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02895 | hp2 | a0001 | c0002 | t0002 | g0157 | AFR | GWD | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02897 | hp1 | a0001 | c0001 | t0006 | g0195 | AFR | GWD | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02897 | hp2 | a0001 | c0002 | t0002 | g0110 | AFR | GWD | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02922 | hp1 | a0001 | c0002 | t0002 | g0106 | AFR | ESN | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02922 | hp2 | a0001 | c0001 | t0049 | g0020 | AFR | ESN | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02965 | hp1 | a0001 | c0001 | t0006 | g0199 | AFR | ESN | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02965 | hp2 | a0001 | c0001 | t0008 | g0312 | AFR | ESN | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02970 | hp1 | a0001 | c0001 | t0031 | g0306 | AFR | ESN | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02970 | hp2 | a0001 | c0001 | t0022 | g0047 | AFR | ESN | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02976 | hp1 | a0001 | c0002 | t0002 | g0107 | AFR | ESN | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02976 | hp2 | a0001 | c0001 | t0007 | g0182 | AFR | ESN | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03017 | hp1 | a0001 | c0003 | t0010 | g0251 | SAS | PJL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03017 | hp2 | a0001 | c0002 | t0046 | g0141 | SAS | PJL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03041 | hp1 | a0001 | c0003 | t0011 | g0223 | AFR | GWD | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03041 | hp2 | a0001 | c0001 | t0004 | g0053 | AFR | GWD | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03098 | hp1 | a0001 | c0001 | t0005 | g0018 | AFR | MSL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03098 | hp2 | a0001 | c0004 | t0005 | g0027 | AFR | MSL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03130 | hp1 | a0001 | c0004 | t0005 | g0057 | AFR | ESN | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03130 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | ESN | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03139 | hp1 | a0001 | c0002 | t0002 | g0101 | AFR | ESN | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03139 | hp2 | a0001 | c0001 | t0019 | g0004 | AFR | ESN | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03195 | hp1 | a0001 | c0001 | t0017 | g0170 | AFR | ESN | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03195 | hp2 | a0001 | c0001 | t0006 | g0200 | AFR | ESN | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03209 | hp1 | a0001 | c0001 | t0006 | g0203 | AFR | MSL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03209 | hp2 | a0001 | c0001 | t0037 | g0009 | AFR | MSL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03225 | hp2 | a0001 | c0001 | t0019 | g0004 | AFR | MSL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03239 | hp1 | a0001 | c0002 | t0002 | g0151 | SAS | PJL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03453 | hp1 | a0001 | c0001 | t0005 | g0017 | AFR | MSL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03453 | hp2 | a0001 | c0001 | t0006 | g0205 | AFR | MSL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | MSL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03486 | hp2 | a0001 | c0001 | t0006 | g0208 | AFR | MSL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03490 | hp1 | a0001 | c0002 | t0003 | g0098 | SAS | PJL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03490 | hp2 | a0001 | c0003 | t0001 | g0240 | SAS | PJL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03491 | hp1 | a0001 | c0001 | t0012 | g0280 | SAS | PJL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03491 | hp2 | a0001 | c0002 | t0003 | g0099 | SAS | PJL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03492 | hp1 | a0001 | c0002 | t0003 | g0126 | SAS | PJL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03492 | hp2 | a0001 | c0001 | t0012 | g0281 | SAS | PJL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0155 | AFR | ESN | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03516 | hp2 | a0001 | c0001 | t0008 | g0314 | AFR | ESN | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0167 | AFR | GWD | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03540 | hp2 | a0001 | c0002 | t0041 | g0172 | AFR | GWD | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0169 | AFR | MSL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03579 | hp2 | a0001 | c0013 | t0005 | g0032 | AFR | MSL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03654 | hp1 | a0001 | c0002 | t0051 | g0143 | SAS | PJL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03654 | hp2 | a0001 | c0001 | t0004 | g0040 | SAS | PJL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03669 | hp2 | a0001 | c0001 | t0004 | g0046 | SAS | PJL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03704 | hp1 | a0001 | c0001 | t0012 | g0309 | SAS | PJL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03704 | hp2 | a0001 | c0003 | t0001 | g0242 | SAS | PJL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03710 | hp1 | a0001 | c0002 | t0002 | g0149 | SAS | PJL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03710 | hp2 | a0001 | c0003 | t0001 | g0247 | SAS | PJL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0307 | SAS | BEB | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03831 | hp2 | a0001 | c0002 | t0002 | g0150 | SAS | BEB | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03834 | hp1 | a0001 | c0003 | t0001 | g0239 | SAS | BEB | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03834 | hp2 | a0001 | c0002 | t0003 | g0158 | SAS | BEB | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03942 | hp1 | a0001 | c0001 | t0007 | g0189 | SAS | BEB | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03942 | hp2 | a0001 | c0003 | t0001 | g0243 | SAS | BEB | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG04115 | hp1 | a0001 | c0002 | t0002 | g0148 | SAS | STU | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG04115 | hp2 | a0001 | c0001 | t0007 | g0187 | SAS | STU | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG04199 | hp1 | a0001 | c0002 | t0002 | g0145 | SAS | STU | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG04199 | hp2 | a0001 | c0003 | t0014 | g0241 | SAS | STU | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG04204 | hp1 | a0001 | c0011 | t0004 | g0044 | SAS | STU | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG04204 | hp2 | a0001 | c0002 | t0003 | g0079 | SAS | STU | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG04228 | hp1 | a0001 | c0003 | t0010 | g0254 | SAS | STU | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG04228 | hp2 | a0001 | c0002 | t0003 | g0174 | SAS | STU | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18522 | hp1 | a0001 | c0002 | t0002 | g0103 | AFR | YRI | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18522 | hp2 | a0001 | c0003 | t0011 | g0224 | AFR | YRI | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0168 | AFR | YRI | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18906 | hp2 | a0001 | c0001 | t0006 | g0207 | AFR | YRI | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18940 | hp1 | a0001 | c0006 | t0020 | g0045 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18942 | hp1 | a0002 | c0005 | t0009 | g0271 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18942 | hp2 | a0001 | c0002 | t0002 | g0091 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18944 | hp1 | a0001 | c0001 | t0005 | g0023 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18944 | hp2 | a0001 | c0002 | t0003 | g0142 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18945 | hp1 | a0001 | c0003 | t0001 | g0212 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18946 | hp1 | a0001 | c0002 | t0045 | g0117 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18946 | hp2 | a0001 | c0003 | t0001 | g0221 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18947 | hp1 | a0001 | c0002 | t0003 | g0160 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18947 | hp2 | a0001 | c0003 | t0001 | g0229 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18948 | hp2 | a0001 | c0003 | t0001 | g0211 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18950 | hp1 | a0001 | c0002 | t0003 | g0130 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18950 | hp2 | a0001 | c0003 | t0001 | g0226 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18951 | hp1 | a0001 | c0002 | t0040 | g0164 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18954 | hp1 | a0001 | c0002 | t0003 | g0122 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18954 | hp2 | a0001 | c0003 | t0001 | g0234 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18957 | hp1 | a0001 | c0001 | t0005 | g0022 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18957 | hp2 | a0001 | c0002 | t0002 | g0162 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18960 | hp1 | a0001 | c0002 | t0003 | g0132 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18961 | hp2 | a0001 | c0002 | t0023 | g0094 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18962 | hp2 | a0001 | c0002 | t0003 | g0116 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18964 | hp1 | a0001 | c0003 | t0001 | g0227 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18964 | hp2 | a0001 | c0002 | t0003 | g0112 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18968 | hp1 | a0001 | c0003 | t0001 | g0244 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18968 | hp2 | a0001 | c0002 | t0003 | g0140 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18970 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18970 | hp2 | a0001 | c0003 | t0001 | g0233 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18972 | hp1 | a0001 | c0002 | t0003 | g0131 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18972 | hp2 | a0001 | c0003 | t0001 | g0245 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18974 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18977 | hp1 | a0001 | c0002 | t0050 | g0177 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18977 | hp2 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18978 | hp2 | a0001 | c0002 | t0026 | g0133 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18980 | hp2 | a0001 | c0002 | t0002 | g0084 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18984 | hp1 | a0001 | c0003 | t0001 | g0214 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18984 | hp2 | a0001 | c0002 | t0003 | g0121 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18985 | hp1 | a0001 | c0002 | t0003 | g0097 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18986 | hp1 | a0001 | c0002 | t0002 | g0090 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18986 | hp2 | a0001 | c0003 | t0001 | g0213 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18987 | hp1 | a0002 | c0005 | t0002 | g0276 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18987 | hp2 | a0001 | c0002 | t0009 | g0089 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18988 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18990 | hp1 | a0001 | c0003 | t0001 | g0230 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18990 | hp2 | a0001 | c0002 | t0002 | g0163 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18991 | hp1 | a0001 | c0002 | t0003 | g0154 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18991 | hp2 | a0001 | c0001 | t0005 | g0021 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18992 | hp1 | a0001 | c0001 | t0015 | g0059 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18992 | hp2 | a0001 | c0002 | t0003 | g0120 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18994 | hp1 | a0001 | c0001 | t0014 | g0260 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18994 | hp2 | a0001 | c0002 | t0002 | g0085 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18997 | hp1 | a0001 | c0003 | t0001 | g0235 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA18997 | hp2 | a0001 | c0002 | t0043 | g0135 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA19001 | hp1 | a0001 | c0002 | t0003 | g0118 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA19003 | hp1 | a0001 | c0001 | t0015 | g0060 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA19003 | hp2 | a0001 | c0002 | t0002 | g0147 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA19006 | hp2 | a0001 | c0002 | t0018 | g0134 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA19007 | hp1 | a0001 | c0002 | t0002 | g0092 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA19007 | hp2 | a0001 | c0002 | t0003 | g0139 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA19010 | hp2 | a0001 | c0001 | t0005 | g0014 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA19030 | hp1 | a0001 | c0007 | t0028 | g0007 | AFR | LWK | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA19030 | hp2 | a0001 | c0001 | t0013 | g0204 | AFR | LWK | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA19043 | hp1 | a0001 | c0004 | t0005 | g0028 | AFR | LWK | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA19043 | hp2 | a0001 | c0001 | t0004 | g0036 | AFR | LWK | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA19055 | hp1 | a0001 | c0003 | t0001 | g0228 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA19055 | hp2 | a0001 | c0002 | t0003 | g0179 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA19062 | hp1 | a0002 | c0005 | t0009 | g0277 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA19062 | hp2 | a0001 | c0003 | t0001 | g0222 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA19063 | hp1 | a0002 | c0005 | t0009 | g0287 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA19063 | hp2 | a0001 | c0001 | t0005 | g0024 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA19064 | hp1 | a0001 | c0002 | t0042 | g0153 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA19064 | hp2 | a0001 | c0001 | t0016 | g0301 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA19065 | hp1 | a0001 | c0002 | t0002 | g0093 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA19065 | hp2 | a0001 | c0002 | t0003 | g0119 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA19068 | hp2 | a0001 | c0003 | t0001 | g0210 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA19078 | hp1 | a0001 | c0006 | t0004 | g0322 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA19078 | hp2 | a0001 | c0002 | t0002 | g0144 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA19081 | hp1 | a0002 | c0005 | t0009 | g0278 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA19081 | hp2 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA19083 | hp1 | a0001 | c0001 | t0005 | g0015 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA19083 | hp2 | a0002 | c0005 | t0009 | g0270 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA19086 | hp1 | a0001 | c0003 | t0001 | g0236 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA19086 | hp2 | a0001 | c0002 | t0003 | g0156 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA19088 | hp2 | a0001 | c0003 | t0001 | g0246 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA19090 | hp1 | a0001 | c0003 | t0001 | g0237 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA19090 | hp2 | a0001 | c0002 | t0003 | g0129 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA19091 | hp1 | a0001 | c0002 | t0044 | g0136 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA19240 | hp1 | a0001 | c0012 | t0038 | g0008 | AFR | YRI | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0066 | AFR | YRI | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA20129 | hp1 | a0001 | c0002 | t0002 | g0146 | AFR | ASW | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA20129 | hp2 | a0001 | c0002 | t0002 | g0104 | AFR | ASW | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA20805 | hp1 | a0001 | c0002 | t0003 | g0115 | EUR | TSI | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0269 | EUR | TSI | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA20905 | hp1 | a0001 | c0001 | t0004 | g0037 | SAS | GIH | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0302 | SAS | GIH | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02109 | hp1 | a0001 | c0001 | t0006 | g0198 | AFR | ACB | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02109 | hp2 | a0001 | c0004 | t0005 | g0031 | AFR | ACB | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02486 | hp1 | a0001 | c0003 | t0001 | g0252 | AFR | ACB | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG02486 | hp2 | a0001 | c0001 | t0005 | g0025 | AFR | ACB | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03471 | hp1 | a0001 | c0002 | t0002 | g0320 | AFR | MSL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0055 | AFR | MSL | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG06807 | hp1 | a0001 | c0001 | t0027 | g0185 | AFR | USA | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
HG06807 | hp2 | a0001 | c0003 | t0010 | g0232 | AFR | USA | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA20300 | hp1 | a0001 | c0001 | t0006 | g0206 | AFR | USA | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA20300 | hp2 | a0001 | c0001 | t0005 | g0016 | AFR | USA | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA21309 | hp1 | a0001 | c0001 | t0008 | g0258 | AFR | LWK | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
NA21309 | hp2 | a0001 | c0004 | t0005 | g0026 | AFR | LWK | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
homoSapiens | chm13v2 | a0001 | c0001 | t0048 | g0288 | REF | REF | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0043 | REF | REF | PARP8_chr5_50661637_50851519 | PARP8 | chr5 | 50661637 | 50851519 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:50778594 | C | A | 1 | a0004 | 1 | HG02027.hp1 | missense_variant | MODERATE | c.614C>A | p.Thr205Lys | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/26 | 1073/7475 | 614/2565 | 205/854 | chr5 | 50778594 | |||
chr5:50794329 | G | A | 1 | a0002 | 6 | NA18942.hp1 NA18987.hp1 NA19062.hp1 others(3): Show |
missense_variant | MODERATE | c.860G>A | p.Arg287His | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 11/26 | 1319/7475 | 860/2565 | 287/854 | chr5 | 50794329 | |||
chr5:50795328 | G | A | 1 | a0003 | 1 | HG01257.hp1 | missense_variant | MODERATE | c.1339G>A | p.Glu447Lys | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 12/26 | 1798/7475 | 1339/2565 | 447/854 | chr5 | 50795328 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:50761895 | G | A | 2 | a0001c0002 a0004c0008 |
112 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(109): Show |
synonymous_variant | LOW | c.420G>A | p.Gly140Gly | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 6/26 | 879/7475 | 420/2565 | 140/854 | chr5 | 50761895 | |||
chr5:50761895 | G | T | 1 | a0001c0003 | 47 | HG00673.hp1 HG00738.hp1 HG01243.hp1 others(44): Show |
synonymous_variant | LOW | c.420G>T | p.Gly140Gly | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 6/26 | 879/7475 | 420/2565 | 140/854 | chr5 | 50761895 | |||
chr5:50794270 | C | T | 1 | a0001c0013 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.801C>T | p.His267His | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 11/26 | 1260/7475 | 801/2565 | 267/854 | chr5 | 50794270 | |||
chr5:50795177 | G | A | 1 | a0001c0006 | 2 | NA18940.hp1 NA19078.hp1 |
synonymous_variant | LOW | c.1188G>A | p.Glu396Glu | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 12/26 | 1647/7475 | 1188/2565 | 396/854 | chr5 | 50795177 | |||
chr5:50795318 | G | A | 1 | a0001c0007 | 2 | HG02572.hp2 NA19030.hp1 |
synonymous_variant | LOW | c.1329G>A | p.Glu443Glu | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 12/26 | 1788/7475 | 1329/2565 | 443/854 | chr5 | 50795318 | |||
chr5:50795336 | C | T | 2 | a0001c0004 a0001c0013 |
8 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(5): Show |
synonymous_variant | LOW | c.1347C>T | p.Asn449Asn | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 12/26 | 1806/7475 | 1347/2565 | 449/854 | chr5 | 50795336 | |||
chr5:50824913 | A | G | 1 | a0001c0012 | 1 | NA19240.hp1 | synonymous_variant | LOW | c.1866A>G | p.Pro622Pro | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 18/26 | 2325/7475 | 1866/2565 | 622/854 | chr5 | 50824913 | |||
chr5:50832845 | T | C | 1 | a0001c0010 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.2298T>C | p.Asn766Asn | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 23/26 | 2757/7475 | 2298/2565 | 766/854 | chr5 | 50832845 | |||
chr5:50842065 | T | G | 1 | a0001c0011 | 1 | HG04204.hp1 | synonymous_variant | LOW | c.2562T>G | p.Gly854Gly | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 3021/7475 | 2562/2565 | 854/854 | chr5 | 50842065 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:50666703 | C | CAT | 1 | a0001c0003t0010 | 5 | HG01255.hp2 HG01952.hp2 HG03017.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-393_-392insAT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 1/26 | 392 | chr5 | 50666703 | ||||||
chr5:50666722 | C | G | 1 | a0001c0002t0051 | 1 | HG03654.hp1 | 5_prime_UTR_variant | MODIFIER | c.-374C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 1/26 | 374 | chr5 | 50666722 | ||||||
chr5:50666903 | C | CCCT | 48 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(45): Show |
290 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(287): Show |
5_prime_UTR_variant | MODIFIER | c.-178_-176dupTCC | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 1/26 | 175 | INFO_REALIGN_3_PRIME | chr5 | 50666903 | |||||
chr5:50666909 | T | TCCTCCTC others(8): Show |
1 | a0001c0001t0027 | 1 | HG06807.hp1 | 5_prime_UTR_variant | MODIFIER | c.-176_-175insTCCCCC others(9): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 1/26 | 175 | INFO_REALIGN_3_PRIME | chr5 | 50666909 | |||||
chr5:50666918 | T | TCCTC | 5 | a0001c0001t0013 a0001c0001t0014 a0001c0001t0025 others(2): Show |
6 | HG01192.hp2 HG02145.hp1 HG04199.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-176_-175insTCCC | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 1/26 | 175 | INFO_REALIGN_3_PRIME | chr5 | 50666918 | |||||
chr5:50666992 | C | T | 1 | a0001c0002t0050 | 1 | NA18977.hp1 | 5_prime_UTR_variant | MODIFIER | c.-104C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 1/26 | 104 | chr5 | 50666992 | ||||||
chr5:50667036 | G | C | 3 | a0001c0001t0030 a0001c0007t0028 a0001c0007t0029 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-60G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 1/26 | chr5 | 50667036 | |||||||
chr5:50842550 | C | T | 1 | a0001c0001t0049 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*482C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 482 | chr5 | 50842550 | ||||||
chr5:50842554 | A | G | 1 | a0001c0001t0019 | 2 | HG03139.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*486A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 486 | chr5 | 50842554 | ||||||
chr5:50843197 | A | G | 1 | a0001c0001t0024 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1129A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 1129 | chr5 | 50843197 | ||||||
chr5:50843331 | A | G | 1 | a0001c0001t0047 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1263A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 1263 | chr5 | 50843331 | ||||||
chr5:50843373 | T | TA | 4 | a0001c0001t0006 a0001c0001t0013 a0001c0001t0019 others(1): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1314dupA | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 1315 | INFO_REALIGN_3_PRIME | chr5 | 50843373 | |||||
chr5:50843406 | G | T | 4 | a0001c0001t0006 a0001c0001t0013 a0001c0001t0019 others(1): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1338G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 1338 | chr5 | 50843406 | ||||||
chr5:50843452 | A | G | 8 | a0001c0002t0003 a0001c0002t0018 a0001c0002t0026 others(5): Show |
56 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*1384A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 1384 | chr5 | 50843452 | ||||||
chr5:50843524 | A | T | 19 | a0001c0001t0002 a0001c0001t0017 a0001c0002t0002 others(16): Show |
121 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*1456A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 1456 | chr5 | 50843524 | ||||||
chr5:50843609 | T | C | 1 | a0001c0002t0039 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1541T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 1541 | chr5 | 50843609 | ||||||
chr5:50843654 | G | A | 1 | a0001c0006t0020 | 1 | NA18940.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1586G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 1586 | chr5 | 50843654 | ||||||
chr5:50844045 | G | T | 1 | a0001c0002t0042 | 1 | NA19064.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1977G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 1977 | chr5 | 50844045 | ||||||
chr5:50844111 | G | A | 2 | a0001c0002t0009 a0002c0005t0009 |
6 | NA18942.hp1 NA18987.hp2 NA19062.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2043G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 2043 | chr5 | 50844111 | ||||||
chr5:50844161 | A | G | 1 | a0001c0001t0030 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2093A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 2093 | chr5 | 50844161 | ||||||
chr5:50844189 | A | G | 1 | a0001c0001t0012 | 3 | HG03491.hp1 HG03492.hp2 HG03704.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2121A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 2121 | chr5 | 50844189 | ||||||
chr5:50844215 | A | G | 1 | a0001c0012t0038 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2147A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 2147 | chr5 | 50844215 | ||||||
chr5:50844337 | G | A | 1 | a0001c0001t0030 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2269G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 2269 | chr5 | 50844337 | ||||||
chr5:50844371 | G | A | 45 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(42): Show |
268 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(265): Show |
3_prime_UTR_variant | MODIFIER | c.*2303G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 2303 | chr5 | 50844371 | ||||||
chr5:50844371 | G | T | 1 | a0001c0001t0037 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2303G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 2303 | chr5 | 50844371 | ||||||
chr5:50844622 | A | G | 37 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0008 others(34): Show |
235 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(232): Show |
3_prime_UTR_variant | MODIFIER | c.*2554A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 2554 | chr5 | 50844622 | ||||||
chr5:50844646 | T | C | 1 | a0001c0001t0022 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2578T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 2578 | chr5 | 50844646 | ||||||
chr5:50844782 | C | T | 36 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0008 others(33): Show |
234 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(231): Show |
3_prime_UTR_variant | MODIFIER | c.*2714C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 2714 | chr5 | 50844782 | ||||||
chr5:50844823 | G | A | 1 | a0001c0001t0017 | 2 | HG01891.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2755G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 2755 | chr5 | 50844823 | ||||||
chr5:50844931 | A | G | 4 | a0001c0001t0007 a0001c0001t0021 a0001c0001t0027 others(1): Show |
11 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2863A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 2863 | chr5 | 50844931 | ||||||
chr5:50844972 | G | A | 3 | a0001c0001t0008 a0001c0001t0025 a0001c0001t0033 |
10 | HG01192.hp2 HG01884.hp2 HG02572.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2904G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 2904 | chr5 | 50844972 | ||||||
chr5:50844987 | G | GT | 7 | a0001c0001t0006 a0001c0001t0013 a0001c0001t0019 others(4): Show |
25 | HG00597.hp1 HG01167.hp2 HG01169.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2930dupT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 2931 | INFO_REALIGN_3_PRIME | chr5 | 50844987 | |||||
chr5:50845385 | C | T | 1 | a0001c0002t0046 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3317C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 3317 | chr5 | 50845385 | ||||||
chr5:50845386 | G | A | 2 | a0001c0007t0028 a0001c0007t0029 |
2 | HG02572.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3318G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 3318 | chr5 | 50845386 | ||||||
chr5:50845450 | A | G | 1 | a0001c0001t0031 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3382A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 3382 | chr5 | 50845450 | ||||||
chr5:50845624 | A | C | 1 | a0001c0003t0035 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3556A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 3556 | chr5 | 50845624 | ||||||
chr5:50845736 | A | T | 1 | a0001c0002t0041 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3668A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 3668 | chr5 | 50845736 | ||||||
chr5:50845790 | C | T | 1 | a0001c0003t0011 | 3 | HG02055.hp1 HG03041.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3722C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 3722 | chr5 | 50845790 | ||||||
chr5:50845802 | T | A | 1 | a0001c0001t0016 | 2 | HG00558.hp1 NA19064.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3734T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 3734 | chr5 | 50845802 | ||||||
chr5:50845865 | C | T | 1 | a0001c0007t0029 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3797C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 3797 | chr5 | 50845865 | ||||||
chr5:50845922 | C | A | 1 | a0001c0001t0033 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3854C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 3854 | chr5 | 50845922 | ||||||
chr5:50845941 | G | T | 1 | a0001c0010t0036 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3873G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 3873 | chr5 | 50845941 | ||||||
chr5:50846049 | C | T | 1 | a0001c0002t0045 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3981C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 3981 | chr5 | 50846049 | ||||||
chr5:50846056 | A | G | 1 | a0001c0001t0015 | 2 | NA18992.hp1 NA19003.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3988A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 3988 | chr5 | 50846056 | ||||||
chr5:50846062 | T | G | 1 | a0001c0002t0043 | 1 | NA18997.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3994T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 3994 | chr5 | 50846062 | ||||||
chr5:50846063 | T | G | 1 | a0001c0002t0043 | 1 | NA18997.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3995T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 3995 | chr5 | 50846063 | ||||||
chr5:50846067 | C | G | 1 | a0001c0002t0043 | 1 | NA18997.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3999C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 3999 | chr5 | 50846067 | ||||||
chr5:50846068 | A | T | 1 | a0001c0002t0043 | 1 | NA18997.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4000A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 4000 | chr5 | 50846068 | ||||||
chr5:50846074 | C | A | 1 | a0001c0002t0043 | 1 | NA18997.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4006C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 4006 | chr5 | 50846074 | ||||||
chr5:50846076 | G | A | 1 | a0001c0002t0043 | 1 | NA18997.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4008G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 4008 | chr5 | 50846076 | ||||||
chr5:50846080 | G | T | 1 | a0001c0002t0043 | 1 | NA18997.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4012G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 4012 | chr5 | 50846080 | ||||||
chr5:50846081 | T | C | 1 | a0001c0002t0043 | 1 | NA18997.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4013T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 4013 | chr5 | 50846081 | ||||||
chr5:50846090 | A | C | 1 | a0001c0002t0043 | 1 | NA18997.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4022A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 4022 | chr5 | 50846090 | ||||||
chr5:50846119 | TTTAATGT others(6): Show |
T | 1 | a0001c0002t0043 | 1 | NA18997.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4052_*4064delTTAA others(9): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 4052 | chr5 | 50846119 | ||||||
chr5:50846139 | A | G | 1 | a0001c0001t0015 | 2 | NA18992.hp1 NA19003.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4071A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 4071 | chr5 | 50846139 | ||||||
chr5:50846144 | C | T | 1 | a0001c0002t0040 | 1 | NA18951.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4076C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 4076 | chr5 | 50846144 | ||||||
chr5:50846145 | G | A | 1 | a0001c0002t0044 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4077G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 4077 | chr5 | 50846145 | ||||||
chr5:50846191 | T | G | 55 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(52): Show |
298 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(295): Show |
3_prime_UTR_variant | MODIFIER | c.*4123T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 4123 | chr5 | 50846191 | ||||||
chr5:50846356 | A | G | 1 | a0001c0001t0034 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4288A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 4288 | chr5 | 50846356 | ||||||
chr5:50846437 | C | G | 1 | a0001c0001t0049 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4369C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 26/26 | 4369 | chr5 | 50846437 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:50667267 | G | GGGTGGAG others(10): Show |
1 | a0001c0006t0004g0322 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.91+82_91+98dupGGTG others(13): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 50667267 | ||||||
chr5:50667375 | C | T | 1 | a0001c0010t0036g0321 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.91+189C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 1/25 | chr5 | 50667375 | |||||||
chr5:50667401 | C | T | 265 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(262): Show |
269 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(266): Show |
intron_variant | MODIFIER | c.91+215C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 1/25 | chr5 | 50667401 | |||||||
chr5:50667520 | G | GCGGCGGC others(21): Show |
3 | a0001c0001t0030g0005 a0001c0007t0028g0007 a0001c0007t0029g0006 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.91+356_91+357insGG others(26): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 50667520 | ||||||
chr5:50667563 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.91+377G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 1/25 | chr5 | 50667563 | |||||||
chr5:50667584 | C | T | 1 | a0001c0002t0002g0320 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.91+398C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 1/25 | chr5 | 50667584 | |||||||
chr5:50667703 | A | G | 1 | a0001c0010t0036g0321 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.92-368A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 1/25 | chr5 | 50667703 | |||||||
chr5:50667707 | C | G | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.92-364C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 1/25 | chr5 | 50667707 | |||||||
chr5:50667814 | C | T | 1 | a0001c0002t0003g0319 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.92-257C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 1/25 | chr5 | 50667814 | |||||||
chr5:50667824 | T | G | 294 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(291): Show |
298 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(295): Show |
intron_variant | MODIFIER | c.92-247T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 1/25 | chr5 | 50667824 | |||||||
chr5:50667992 | G | A | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.92-79G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 1/25 | chr5 | 50667992 | |||||||
chr5:50668381 | G | A | 4 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(1): Show |
4 | HG02056.hp1 NA18974.hp2 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.146+256G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50668381 | |||||||
chr5:50668454 | G | A | 1 | a0001c0002t0002g0065 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.146+329G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50668454 | |||||||
chr5:50668927 | C | A | 19 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0012 others(16): Show |
19 | HG01884.hp1 HG01891.hp1 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.146+802C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50668927 | |||||||
chr5:50668973 | A | G | 1 | a0001c0001t0021g0318 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.146+848A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50668973 | |||||||
chr5:50669024 | G | A | 3 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 |
3 | HG03098.hp2 NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.146+899G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50669024 | |||||||
chr5:50669071 | T | C | 119 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(116): Show |
122 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.146+946T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50669071 | |||||||
chr5:50669099 | A | G | 1 | a0001c0002t0003g0179 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.146+974A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50669099 | |||||||
chr5:50669332 | C | T | 1 | a0001c0001t0005g0025 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.146+1207C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50669332 | |||||||
chr5:50669532 | A | G | 1 | a0001c0001t0001g0317 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.146+1407A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50669532 | |||||||
chr5:50669670 | G | C | 1 | a0001c0001t0001g0180 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.146+1545G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50669670 | |||||||
chr5:50669698 | T | C | 11 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0001t0007g0184 others(8): Show |
11 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.146+1573T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50669698 | |||||||
chr5:50669720 | A | G | 1 | a0001c0006t0004g0322 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.146+1595A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50669720 | |||||||
chr5:50669721 | T | A | 1 | a0001c0006t0004g0322 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.146+1596T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50669721 | |||||||
chr5:50669722 | A | T | 1 | a0001c0006t0004g0322 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.146+1597A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50669722 | |||||||
chr5:50669763 | T | G | 30 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(27): Show |
31 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.146+1638T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50669763 | |||||||
chr5:50669841 | C | G | 1 | a0001c0004t0005g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.146+1716C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50669841 | |||||||
chr5:50669867 | A | G | 7 | a0001c0001t0008g0310 a0001c0001t0008g0311 a0001c0001t0008g0312 others(4): Show |
7 | HG01192.hp2 HG01884.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.146+1742A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50669867 | |||||||
chr5:50669872 | G | A | 1 | a0001c0012t0038g0008 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.146+1747G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50669872 | |||||||
chr5:50669938 | C | A | 5 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(2): Show |
5 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.146+1813C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50669938 | |||||||
chr5:50669947 | A | G | 1 | a0001c0002t0002g0178 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.146+1822A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50669947 | |||||||
chr5:50669997 | A | G | 1 | a0001c0012t0038g0008 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.146+1872A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50669997 | |||||||
chr5:50670472 | A | T | 265 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(262): Show |
269 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(266): Show |
intron_variant | MODIFIER | c.146+2347A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50670472 | |||||||
chr5:50670512 | T | G | 1 | a0001c0006t0004g0322 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.146+2387T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50670512 | |||||||
chr5:50670513 | G | C | 1 | a0001c0006t0004g0322 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.146+2388G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50670513 | |||||||
chr5:50670726 | A | G | 1 | a0001c0012t0038g0008 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.146+2601A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50670726 | |||||||
chr5:50670776 | C | T | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.146+2651C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50670776 | |||||||
chr5:50670789 | A | G | 1 | a0001c0001t0021g0318 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.146+2664A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50670789 | |||||||
chr5:50670931 | G | A | 47 | a0001c0003t0001g0209 a0001c0003t0001g0210 a0001c0003t0001g0211 others(44): Show |
47 | HG00673.hp1 HG00738.hp1 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.146+2806G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50670931 | |||||||
chr5:50671020 | A | G | 1 | a0001c0001t0012g0309 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.146+2895A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50671020 | |||||||
chr5:50671061 | C | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG02056.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.146+2936C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50671061 | |||||||
chr5:50671325 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.146+3200G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50671325 | |||||||
chr5:50671348 | G | A | 19 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(16): Show |
20 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.146+3223G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50671348 | |||||||
chr5:50671401 | C | T | 2 | a0001c0001t0001g0307 a0001c0001t0001g0308 |
2 | HG01361.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.146+3276C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50671401 | |||||||
chr5:50671457 | G | A | 295 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(292): Show |
299 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(296): Show |
intron_variant | MODIFIER | c.146+3332G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50671457 | |||||||
chr5:50671461 | A | T | 293 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(290): Show |
297 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(294): Show |
intron_variant | MODIFIER | c.146+3336A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50671461 | |||||||
chr5:50671504 | TA | T | 299 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(296): Show |
303 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(300): Show |
intron_variant | MODIFIER | c.146+3391delA | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50671504 | ||||||
chr5:50671543 | C | T | 4 | a0001c0001t0007g0187 a0001c0001t0007g0188 a0001c0001t0007g0189 others(1): Show |
4 | HG00642.hp1 HG00733.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.146+3418C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50671543 | |||||||
chr5:50671743 | A | T | 1 | a0001c0001t0015g0060 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.146+3618A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50671743 | |||||||
chr5:50671974 | G | A | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.146+3849G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50671974 | |||||||
chr5:50671988 | C | T | 4 | a0001c0001t0005g0021 a0001c0001t0005g0022 a0001c0001t0005g0023 others(1): Show |
4 | NA18944.hp1 NA18957.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.146+3863C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50671988 | |||||||
chr5:50671991 | G | A | 113 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(110): Show |
113 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.146+3866G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50671991 | |||||||
chr5:50672070 | G | C | 1 | a0001c0001t0005g0021 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.146+3945G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50672070 | |||||||
chr5:50672134 | C | T | 1 | a0001c0002t0050g0177 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.146+4009C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50672134 | |||||||
chr5:50672203 | T | C | 3 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 |
3 | HG01192.hp1 HG02280.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.146+4078T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50672203 | |||||||
chr5:50672290 | A | G | 2 | a0001c0001t0001g0305 a0001c0001t0031g0306 |
2 | HG00738.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.146+4165A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50672290 | |||||||
chr5:50672555 | C | T | 1 | a0001c0001t0021g0318 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.146+4430C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50672555 | |||||||
chr5:50672557 | G | C | 1 | a0001c0001t0021g0318 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.146+4432G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50672557 | |||||||
chr5:50672728 | C | T | 1 | a0001c0001t0004g0052 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.146+4603C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50672728 | |||||||
chr5:50672821 | T | C | 1 | a0001c0001t0001g0058 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.146+4696T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50672821 | |||||||
chr5:50673087 | A | G | 1 | a0001c0002t0002g0176 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.146+4962A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50673087 | |||||||
chr5:50673306 | A | G | 2 | a0001c0001t0006g0207 a0001c0001t0006g0208 |
2 | HG03486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.146+5181A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50673306 | |||||||
chr5:50673412 | A | G | 2 | a0001c0002t0003g0174 a0001c0002t0003g0175 |
2 | HG01346.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.146+5287A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50673412 | |||||||
chr5:50673431 | C | T | 12 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0001t0007g0184 others(9): Show |
12 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.146+5306C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50673431 | |||||||
chr5:50673474 | T | G | 2 | a0001c0002t0003g0069 a0001c0002t0003g0070 |
2 | HG02148.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.146+5349T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50673474 | |||||||
chr5:50673491 | A | G | 1 | a0001c0002t0002g0173 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.146+5366A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50673491 | |||||||
chr5:50673805 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.146+5680C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50673805 | |||||||
chr5:50674344 | T | G | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.146+6219T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50674344 | |||||||
chr5:50674428 | C | G | 1 | a0001c0012t0038g0008 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.146+6303C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50674428 | |||||||
chr5:50674449 | C | G | 1 | a0001c0002t0041g0172 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.146+6324C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50674449 | |||||||
chr5:50674662 | T | G | 113 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(110): Show |
113 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.146+6537T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50674662 | |||||||
chr5:50674688 | G | C | 1 | a0001c0002t0005g0071 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.146+6563G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50674688 | |||||||
chr5:50674804 | G | A | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.146+6679G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50674804 | |||||||
chr5:50674828 | C | T | 6 | a0001c0001t0002g0166 a0001c0001t0002g0167 a0001c0001t0002g0168 others(3): Show |
6 | HG01891.hp2 HG02717.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.146+6703C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50674828 | |||||||
chr5:50674920 | A | G | 1 | a0001c0001t0007g0186 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.146+6795A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50674920 | |||||||
chr5:50674926 | G | A | 1 | a0001c0001t0006g0191 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.146+6801G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50674926 | |||||||
chr5:50674997 | A | G | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.146+6872A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50674997 | |||||||
chr5:50675242 | A | G | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.146+7117A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50675242 | |||||||
chr5:50675257 | A | G | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.146+7132A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50675257 | |||||||
chr5:50675379 | G | A | 1 | a0001c0001t0007g0181 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.146+7254G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50675379 | |||||||
chr5:50675481 | A | G | 1 | a0001c0001t0019g0004 | 2 | HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.146+7356A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50675481 | |||||||
chr5:50675608 | C | T | 1 | a0001c0007t0028g0007 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.146+7483C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50675608 | |||||||
chr5:50675645 | T | C | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.146+7520T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50675645 | |||||||
chr5:50675792 | GA | G | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.146+7676delA | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50675792 | ||||||
chr5:50675842 | A | T | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.146+7717A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50675842 | |||||||
chr5:50676075 | T | C | 295 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(292): Show |
299 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(296): Show |
intron_variant | MODIFIER | c.146+7950T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50676075 | |||||||
chr5:50676076 | G | A | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.146+7951G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50676076 | |||||||
chr5:50676103 | T | A | 119 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(116): Show |
122 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.146+7978T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50676103 | |||||||
chr5:50676106 | A | G | 1 | a0001c0001t0001g0304 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.146+7981A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50676106 | |||||||
chr5:50676493 | C | A | 1 | a0001c0010t0036g0321 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.146+8368C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50676493 | |||||||
chr5:50676524 | T | C | 2 | a0001c0001t0008g0258 a0001c0001t0033g0257 |
2 | HG02622.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.146+8399T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50676524 | |||||||
chr5:50676600 | G | A | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.146+8475G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50676600 | |||||||
chr5:50676640 | A | G | 11 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0001t0007g0184 others(8): Show |
11 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.146+8515A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50676640 | |||||||
chr5:50676811 | T | C | 12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(9): Show |
12 | HG01884.hp1 HG03098.hp1 HG03453.hp1 others(9): Show |
intron_variant | MODIFIER | c.146+8686T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50676811 | |||||||
chr5:50676853 | T | TTAA | 12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(9): Show |
12 | HG01884.hp1 HG03098.hp1 HG03453.hp1 others(9): Show |
intron_variant | MODIFIER | c.146+8729_146+8731d others(5): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50676853 | ||||||
chr5:50677058 | A | G | 1 | a0001c0001t0001g0303 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.146+8933A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50677058 | |||||||
chr5:50677127 | C | A | 1 | a0001c0002t0002g0072 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.146+9002C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50677127 | |||||||
chr5:50677302 | C | T | 1 | a0001c0001t0004g0050 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.146+9177C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50677302 | |||||||
chr5:50677314 | C | CA | 11 | a0001c0001t0004g0053 a0001c0001t0004g0054 a0001c0001t0004g0055 others(8): Show |
12 | HG01891.hp1 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.146+9207dupA | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50677314 | ||||||
chr5:50677314 | CA | C | 226 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(223): Show |
229 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(226): Show |
intron_variant | MODIFIER | c.146+9207delA | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50677314 | ||||||
chr5:50677316 | A | G | 2 | a0001c0003t0010g0254 a0001c0003t0010g0255 |
2 | HG01952.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.146+9191A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50677316 | |||||||
chr5:50677395 | T | G | 1 | a0001c0001t0004g0033 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.146+9270T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50677395 | |||||||
chr5:50677494 | G | A | 1 | a0001c0001t0019g0004 | 2 | HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.146+9369G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50677494 | |||||||
chr5:50677548 | G | A | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.146+9423G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50677548 | |||||||
chr5:50677559 | G | T | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.146+9434G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50677559 | |||||||
chr5:50677740 | A | C | 1 | a0001c0001t0001g0302 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.146+9615A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50677740 | |||||||
chr5:50677750 | C | T | 1 | a0001c0002t0002g0173 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.146+9625C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50677750 | |||||||
chr5:50677848 | G | A | 12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(9): Show |
12 | HG01884.hp1 HG03098.hp1 HG03453.hp1 others(9): Show |
intron_variant | MODIFIER | c.146+9723G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50677848 | |||||||
chr5:50677924 | T | TAA | 19 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(16): Show |
20 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.146+9810_146+9811d others(4): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50677924 | ||||||
chr5:50678198 | C | T | 295 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(292): Show |
299 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(296): Show |
intron_variant | MODIFIER | c.146+10073C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50678198 | |||||||
chr5:50678342 | G | T | 3 | a0001c0001t0004g0001 a0001c0001t0004g0048 a0001c0001t0004g0049 |
5 | HG01069.hp2 HG01071.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.146+10217G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50678342 | |||||||
chr5:50678344 | G | C | 1 | a0001c0001t0004g0048 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.146+10219G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50678344 | |||||||
chr5:50678693 | G | C | 1 | a0001c0003t0001g0209 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.146+10568G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50678693 | |||||||
chr5:50678771 | G | C | 113 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(110): Show |
116 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.146+10646G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50678771 | |||||||
chr5:50678890 | C | T | 2 | a0001c0002t0002g0074 a0001c0002t0002g0178 |
2 | HG00642.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.146+10765C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50678890 | |||||||
chr5:50678905 | A | G | 1 | a0001c0004t0005g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.146+10780A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50678905 | |||||||
chr5:50678932 | G | GA | 4 | a0001c0002t0002g0075 a0001c0002t0002g0076 a0001c0002t0002g0077 others(1): Show |
4 | HG00639.hp1 HG01168.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.146+10814dupA | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50678932 | ||||||
chr5:50678985 | A | G | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.146+10860A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50678985 | |||||||
chr5:50679026 | A | G | 1 | a0001c0002t0003g0160 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.146+10901A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50679026 | |||||||
chr5:50679082 | G | A | 2 | a0001c0001t0008g0258 a0001c0001t0033g0257 |
2 | HG02622.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.146+10957G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50679082 | |||||||
chr5:50679139 | C | T | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.146+11014C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50679139 | |||||||
chr5:50679155 | C | T | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.146+11030C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50679155 | |||||||
chr5:50679185 | T | C | 1 | a0001c0001t0005g0012 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.146+11060T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50679185 | |||||||
chr5:50679370 | G | T | 1 | a0001c0002t0002g0159 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.146+11245G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50679370 | |||||||
chr5:50679441 | T | A | 1 | a0001c0002t0003g0079 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.146+11316T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50679441 | |||||||
chr5:50679441 | T | G | 118 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(115): Show |
121 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.146+11316T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50679441 | |||||||
chr5:50679505 | T | C | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.146+11380T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50679505 | |||||||
chr5:50679856 | C | T | 1 | a0001c0001t0001g0062 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.146+11731C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50679856 | |||||||
chr5:50679917 | C | T | 1 | a0001c0003t0001g0253 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.146+11792C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50679917 | |||||||
chr5:50679960 | C | G | 66 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(63): Show |
66 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.146+11835C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50679960 | |||||||
chr5:50679985 | A | G | 1 | a0001c0003t0001g0252 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.146+11860A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50679985 | |||||||
chr5:50680011 | C | T | 1 | a0001c0002t0003g0070 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.146+11886C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50680011 | |||||||
chr5:50680129 | G | T | 1 | a0001c0001t0004g0046 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.146+12004G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50680129 | |||||||
chr5:50680238 | C | T | 12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(9): Show |
12 | HG01884.hp1 HG03098.hp1 HG03453.hp1 others(9): Show |
intron_variant | MODIFIER | c.146+12113C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50680238 | |||||||
chr5:50680255 | T | G | 65 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(62): Show |
65 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.146+12130T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50680255 | |||||||
chr5:50680459 | T | A | 1 | a0001c0010t0036g0321 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.146+12334T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50680459 | |||||||
chr5:50680508 | C | T | 1 | a0001c0001t0012g0309 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.146+12383C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50680508 | |||||||
chr5:50680780 | A | G | 2 | a0001c0010t0036g0321 a0001c0012t0038g0008 |
2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.146+12655A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50680780 | |||||||
chr5:50680827 | T | A | 3 | a0001c0001t0030g0005 a0001c0007t0028g0007 a0001c0007t0029g0006 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.146+12702T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50680827 | |||||||
chr5:50680887 | A | G | 1 | a0001c0001t0001g0305 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.146+12762A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50680887 | |||||||
chr5:50681001 | A | T | 1 | a0001c0001t0006g0205 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.146+12876A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50681001 | |||||||
chr5:50681003 | G | A | 265 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(262): Show |
269 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(266): Show |
intron_variant | MODIFIER | c.146+12878G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50681003 | |||||||
chr5:50681068 | C | T | 282 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(279): Show |
286 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(283): Show |
intron_variant | MODIFIER | c.146+12943C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50681068 | |||||||
chr5:50681161 | A | G | 1 | a0001c0007t0029g0006 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.146+13036A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50681161 | |||||||
chr5:50681195 | T | G | 1 | a0001c0004t0005g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.146+13070T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50681195 | |||||||
chr5:50681337 | G | T | 1 | a0001c0013t0005g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.146+13212G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50681337 | |||||||
chr5:50681618 | TC | T | 3 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 |
3 | HG02258.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.146+13495delC | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50681618 | ||||||
chr5:50681872 | G | C | 1 | a0001c0010t0036g0321 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.146+13747G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50681872 | |||||||
chr5:50681910 | G | C | 1 | a0001c0001t0004g0033 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.146+13785G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50681910 | |||||||
chr5:50681951 | C | T | 1 | a0001c0012t0038g0008 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.146+13826C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50681951 | |||||||
chr5:50681952 | G | A | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.146+13827G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50681952 | |||||||
chr5:50682104 | C | G | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.146+13979C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50682104 | |||||||
chr5:50682382 | A | C | 1 | a0001c0001t0016g0301 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.146+14257A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50682382 | |||||||
chr5:50682424 | T | A | 1 | a0001c0002t0003g0080 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.146+14299T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50682424 | |||||||
chr5:50682425 | A | AT | 3 | a0001c0001t0030g0005 a0001c0007t0028g0007 a0001c0007t0029g0006 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.146+14300_146+1430 others(5): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50682425 | |||||||
chr5:50682450 | GT | G | 31 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(28): Show |
32 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.146+14326delT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50682450 | |||||||
chr5:50682788 | C | T | 265 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(262): Show |
269 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(266): Show |
intron_variant | MODIFIER | c.146+14663C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50682788 | |||||||
chr5:50682940 | TG | T | 265 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(262): Show |
269 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(266): Show |
intron_variant | MODIFIER | c.146+14819delG | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50682940 | ||||||
chr5:50682942 | G | A | 1 | a0001c0010t0036g0321 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.146+14817G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50682942 | |||||||
chr5:50682976 | G | T | 1 | a0001c0002t0003g0160 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.146+14851G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50682976 | |||||||
chr5:50682999 | G | A | 119 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(116): Show |
122 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.146+14874G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50682999 | |||||||
chr5:50683024 | G | C | 11 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0001t0007g0184 others(8): Show |
11 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.146+14899G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50683024 | |||||||
chr5:50683123 | T | G | 265 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(262): Show |
269 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(266): Show |
intron_variant | MODIFIER | c.146+14998T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50683123 | |||||||
chr5:50683137 | G | T | 1 | a0001c0004t0005g0028 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.146+15012G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50683137 | |||||||
chr5:50683632 | A | ATT | 232 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(229): Show |
235 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(232): Show |
intron_variant | MODIFIER | c.146+15511_146+1551 others(6): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50683632 | ||||||
chr5:50683759 | G | A | 6 | a0001c0001t0002g0166 a0001c0001t0002g0167 a0001c0001t0002g0168 others(3): Show |
6 | HG01891.hp2 HG02717.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.146+15634G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50683759 | |||||||
chr5:50683784 | A | G | 3 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 |
3 | HG01192.hp1 HG02280.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.146+15659A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50683784 | |||||||
chr5:50683898 | A | G | 1 | a0001c0002t0003g0158 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.146+15773A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50683898 | |||||||
chr5:50684088 | A | T | 1 | a0001c0002t0002g0157 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.146+15963A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50684088 | |||||||
chr5:50684103 | GAACAGTT others(6): Show |
G | 2 | a0001c0010t0036g0321 a0001c0012t0038g0008 |
2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.146+15984_146+1599 others(17): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50684103 | ||||||
chr5:50684150 | C | T | 8 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0048 others(5): Show |
10 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.146+16025C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50684150 | |||||||
chr5:50684223 | G | T | 295 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(292): Show |
299 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(296): Show |
intron_variant | MODIFIER | c.146+16098G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50684223 | |||||||
chr5:50684367 | G | A | 1 | a0001c0001t0002g0166 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.146+16242G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50684367 | |||||||
chr5:50684444 | G | GA | 268 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(265): Show |
272 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(269): Show |
intron_variant | MODIFIER | c.146+16322dupA | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50684444 | ||||||
chr5:50684451 | G | C | 232 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(229): Show |
235 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(232): Show |
intron_variant | MODIFIER | c.146+16326G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50684451 | |||||||
chr5:50684515 | A | T | 1 | a0001c0001t0027g0185 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.146+16390A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50684515 | |||||||
chr5:50684556 | A | G | 1 | a0001c0003t0010g0251 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.146+16431A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50684556 | |||||||
chr5:50684587 | T | C | 319 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(316): Show |
325 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(322): Show |
intron_variant | MODIFIER | c.146+16462T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50684587 | |||||||
chr5:50684589 | A | G | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.146+16464A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50684589 | |||||||
chr5:50684706 | G | C | 1 | a0001c0001t0004g0034 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.146+16581G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50684706 | |||||||
chr5:50684743 | G | C | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.146+16618G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50684743 | |||||||
chr5:50684766 | C | G | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.146+16641C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50684766 | |||||||
chr5:50684842 | G | A | 2 | a0001c0001t0006g0196 a0001c0001t0006g0197 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.146+16717G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50684842 | |||||||
chr5:50684910 | G | T | 11 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0001t0007g0184 others(8): Show |
11 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.146+16785G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50684910 | |||||||
chr5:50684920 | G | A | 1 | a0001c0004t0005g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.146+16795G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50684920 | |||||||
chr5:50685043 | A | G | 1 | a0001c0007t0029g0006 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.146+16918A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50685043 | |||||||
chr5:50685076 | A | T | 4 | a0001c0001t0007g0182 a0001c0001t0007g0184 a0001c0001t0027g0185 others(1): Show |
4 | HG02145.hp2 HG02809.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.146+16951A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50685076 | |||||||
chr5:50685089 | C | T | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.146+16964C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50685089 | |||||||
chr5:50685155 | A | G | 1 | a0001c0003t0001g0250 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.146+17030A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50685155 | |||||||
chr5:50685209 | C | T | 1 | a0001c0001t0007g0184 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.146+17084C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50685209 | |||||||
chr5:50685466 | A | G | 47 | a0001c0003t0001g0209 a0001c0003t0001g0210 a0001c0003t0001g0211 others(44): Show |
47 | HG00673.hp1 HG00738.hp1 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.146+17341A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50685466 | |||||||
chr5:50685558 | T | C | 1 | a0001c0001t0004g0053 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.146+17433T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50685558 | |||||||
chr5:50685698 | G | A | 3 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 |
3 | HG01192.hp1 HG02280.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.146+17573G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50685698 | |||||||
chr5:50685972 | A | C | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.146+17847A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50685972 | |||||||
chr5:50685986 | G | T | 1 | a0001c0010t0036g0321 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.146+17861G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50685986 | |||||||
chr5:50686085 | C | T | 1 | a0001c0002t0003g0156 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.146+17960C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50686085 | |||||||
chr5:50686177 | C | T | 31 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(28): Show |
32 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.146+18052C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50686177 | |||||||
chr5:50686178 | G | A | 12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(9): Show |
12 | HG01884.hp1 HG03098.hp1 HG03453.hp1 others(9): Show |
intron_variant | MODIFIER | c.146+18053G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50686178 | |||||||
chr5:50686223 | T | A | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.146+18098T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50686223 | |||||||
chr5:50686396 | G | T | 1 | a0001c0001t0001g0305 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.146+18271G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50686396 | |||||||
chr5:50686663 | T | C | 20 | a0001c0002t0002g0081 a0001c0002t0002g0082 a0001c0002t0002g0083 others(17): Show |
20 | HG00438.hp1 HG00609.hp2 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.146+18538T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50686663 | |||||||
chr5:50686866 | G | A | 6 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(3): Show |
6 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.146+18741G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50686866 | |||||||
chr5:50686892 | T | A | 109 | a0001c0002t0002g0065 a0001c0002t0002g0072 a0001c0002t0002g0074 others(106): Show |
112 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.146+18767T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50686892 | |||||||
chr5:50687050 | A | G | 1 | a0001c0001t0001g0300 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.146+18925A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50687050 | |||||||
chr5:50687058 | G | A | 1 | a0001c0001t0004g0046 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.146+18933G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50687058 | |||||||
chr5:50687081 | T | A | 9 | a0001c0003t0001g0210 a0001c0003t0001g0211 a0001c0003t0001g0212 others(6): Show |
9 | HG01934.hp2 HG01943.hp2 HG02148.hp2 others(6): Show |
intron_variant | MODIFIER | c.146+18956T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50687081 | |||||||
chr5:50687299 | T | C | 2 | a0001c0002t0002g0072 a0001c0002t0023g0094 |
2 | HG00597.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.146+19174T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50687299 | |||||||
chr5:50687303 | G | C | 119 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(116): Show |
122 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.146+19178G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50687303 | |||||||
chr5:50687306 | C | T | 1 | a0001c0001t0006g0191 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.146+19181C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50687306 | |||||||
chr5:50687314 | G | C | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.146+19189G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50687314 | |||||||
chr5:50687390 | A | G | 3 | a0001c0001t0030g0005 a0001c0007t0028g0007 a0001c0007t0029g0006 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.146+19265A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50687390 | |||||||
chr5:50687409 | A | G | 6 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(3): Show |
6 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.146+19284A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50687409 | |||||||
chr5:50687491 | G | A | 1 | a0001c0001t0001g0305 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.146+19366G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50687491 | |||||||
chr5:50687644 | G | A | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.146+19519G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50687644 | |||||||
chr5:50687661 | G | A | 2 | a0001c0002t0003g0095 a0001c0002t0003g0096 |
2 | HG01074.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.146+19536G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50687661 | |||||||
chr5:50687743 | C | T | 4 | a0001c0001t0004g0053 a0001c0001t0004g0054 a0001c0001t0004g0055 others(1): Show |
4 | HG01261.hp2 HG02615.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.146+19618C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50687743 | |||||||
chr5:50687797 | C | G | 3 | a0001c0001t0005g0017 a0001c0001t0005g0018 a0001c0001t0005g0019 |
3 | HG01884.hp1 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.146+19672C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50687797 | |||||||
chr5:50687867 | T | C | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.146+19742T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50687867 | |||||||
chr5:50687898 | A | T | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.146+19773A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50687898 | |||||||
chr5:50688039 | A | T | 12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(9): Show |
12 | HG01884.hp1 HG03098.hp1 HG03453.hp1 others(9): Show |
intron_variant | MODIFIER | c.146+19914A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50688039 | |||||||
chr5:50688091 | T | C | 3 | a0001c0001t0030g0005 a0001c0007t0028g0007 a0001c0007t0029g0006 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.146+19966T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50688091 | |||||||
chr5:50688196 | C | T | 1 | a0001c0001t0004g0042 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.146+20071C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50688196 | |||||||
chr5:50688332 | GCAACAC | G | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.146+20208_146+2021 others(10): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50688332 | |||||||
chr5:50688387 | C | A | 1 | a0001c0001t0006g0198 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.146+20262C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50688387 | |||||||
chr5:50688456 | A | G | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.146+20331A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50688456 | |||||||
chr5:50688505 | G | T | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.146+20380G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50688505 | |||||||
chr5:50688507 | G | T | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.146+20382G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50688507 | |||||||
chr5:50688509 | A | G | 1 | a0001c0001t0001g0259 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.146+20384A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50688509 | |||||||
chr5:50688518 | T | C | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.146+20393T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50688518 | |||||||
chr5:50688631 | T | C | 265 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(262): Show |
269 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(266): Show |
intron_variant | MODIFIER | c.146+20506T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50688631 | |||||||
chr5:50688709 | C | T | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.146+20584C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50688709 | |||||||
chr5:50688880 | C | T | 6 | a0001c0001t0031g0306 a0001c0002t0002g0090 a0001c0002t0002g0091 others(3): Show |
6 | HG02970.hp1 NA18942.hp2 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.146+20755C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50688880 | |||||||
chr5:50688881 | G | A | 1 | a0001c0001t0002g0066 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.146+20756G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50688881 | |||||||
chr5:50689018 | AT | A | 19 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(16): Show |
19 | HG01192.hp1 HG01884.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.146+20905delT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50689018 | ||||||
chr5:50689030 | T | G | 1 | a0001c0001t0005g0024 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.146+20905T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50689030 | |||||||
chr5:50689031 | G | A | 1 | a0001c0001t0005g0024 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.146+20906G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50689031 | |||||||
chr5:50689032 | A | AT | 19 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(16): Show |
21 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.146+20925dupT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50689032 | ||||||
chr5:50689032 | A | T | 1 | a0001c0001t0005g0024 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.146+20907A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50689032 | |||||||
chr5:50689032 | AT | A | 157 | a0001c0001t0001g0305 a0001c0001t0008g0299 a0001c0001t0049g0020 others(154): Show |
160 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(157): Show |
intron_variant | MODIFIER | c.146+20925delT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50689032 | ||||||
chr5:50689032 | ATT | A | 68 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(65): Show |
68 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.146+20924_146+2092 others(6): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50689032 | ||||||
chr5:50689142 | C | T | 1 | a0001c0001t0004g0052 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.146+21017C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50689142 | |||||||
chr5:50689148 | T | C | 11 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0001t0007g0184 others(8): Show |
11 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.146+21023T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50689148 | |||||||
chr5:50689192 | A | G | 11 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0001t0007g0184 others(8): Show |
11 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.146+21067A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50689192 | |||||||
chr5:50689199 | G | A | 12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(9): Show |
12 | HG01884.hp1 HG03098.hp1 HG03453.hp1 others(9): Show |
intron_variant | MODIFIER | c.146+21074G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50689199 | |||||||
chr5:50689383 | T | G | 2 | a0001c0003t0001g0218 a0001c0003t0035g0219 |
2 | HG00738.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.146+21258T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50689383 | |||||||
chr5:50689639 | T | C | 1 | a0001c0012t0038g0008 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.146+21514T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50689639 | |||||||
chr5:50689647 | A | G | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.146+21522A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50689647 | |||||||
chr5:50689691 | C | T | 113 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(110): Show |
113 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.146+21566C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50689691 | |||||||
chr5:50689711 | G | A | 1 | a0001c0001t0022g0047 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.146+21586G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50689711 | |||||||
chr5:50689720 | G | A | 2 | a0001c0001t0004g0037 a0001c0001t0004g0052 |
2 | HG01516.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.146+21595G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50689720 | |||||||
chr5:50689818 | A | G | 119 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(116): Show |
122 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.146+21693A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50689818 | |||||||
chr5:50689925 | T | G | 3 | a0001c0001t0030g0005 a0001c0007t0028g0007 a0001c0007t0029g0006 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.146+21800T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50689925 | |||||||
chr5:50690017 | T | C | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.146+21892T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50690017 | |||||||
chr5:50690021 | A | G | 12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(9): Show |
12 | HG01884.hp1 HG03098.hp1 HG03453.hp1 others(9): Show |
intron_variant | MODIFIER | c.146+21896A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50690021 | |||||||
chr5:50690063 | C | T | 3 | a0001c0001t0030g0005 a0001c0007t0028g0007 a0001c0007t0029g0006 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.146+21938C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50690063 | |||||||
chr5:50690206 | A | G | 1 | a0001c0006t0020g0045 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.146+22081A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50690206 | |||||||
chr5:50690667 | A | G | 2 | a0001c0001t0004g0035 a0001c0001t0004g0036 |
2 | HG02886.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.146+22542A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50690667 | |||||||
chr5:50690891 | G | C | 3 | a0001c0003t0001g0220 a0001c0003t0001g0221 a0001c0003t0001g0222 |
3 | HG02056.hp2 NA18946.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.146+22766G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50690891 | |||||||
chr5:50691032 | G | T | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.146+22907G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50691032 | |||||||
chr5:50691384 | C | G | 1 | a0001c0002t0003g0079 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.146+23259C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50691384 | |||||||
chr5:50691491 | T | C | 9 | a0001c0002t0002g0101 a0001c0002t0002g0102 a0001c0002t0002g0103 others(6): Show |
9 | HG02055.hp2 HG02257.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.146+23366T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50691491 | |||||||
chr5:50691583 | G | A | 3 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 |
3 | HG01192.hp1 HG02280.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.146+23458G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50691583 | |||||||
chr5:50691645 | C | T | 1 | a0001c0007t0028g0007 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.146+23520C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50691645 | |||||||
chr5:50691647 | T | C | 319 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(316): Show |
325 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(322): Show |
intron_variant | MODIFIER | c.146+23522T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50691647 | |||||||
chr5:50691674 | C | T | 1 | a0001c0001t0006g0208 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.146+23549C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50691674 | |||||||
chr5:50691878 | A | T | 1 | a0001c0012t0038g0008 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.146+23753A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50691878 | |||||||
chr5:50692022 | G | A | 285 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(282): Show |
289 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(286): Show |
intron_variant | MODIFIER | c.146+23897G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50692022 | |||||||
chr5:50692157 | T | A | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.146+24032T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50692157 | |||||||
chr5:50692165 | C | A | 1 | a0001c0001t0013g0192 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.146+24040C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50692165 | |||||||
chr5:50692186 | C | T | 44 | a0001c0001t0030g0005 a0001c0003t0001g0209 a0001c0003t0001g0210 others(41): Show |
44 | HG00673.hp1 HG00738.hp1 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.146+24061C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50692186 | |||||||
chr5:50692187 | G | A | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.146+24062G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50692187 | |||||||
chr5:50692218 | A | G | 1 | a0001c0004t0005g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.146+24093A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50692218 | |||||||
chr5:50692349 | G | A | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.146+24224G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50692349 | |||||||
chr5:50692628 | C | G | 1 | a0001c0007t0028g0007 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.146+24503C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50692628 | |||||||
chr5:50692759 | G | T | 296 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(293): Show |
300 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(297): Show |
intron_variant | MODIFIER | c.146+24634G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50692759 | |||||||
chr5:50692832 | G | T | 3 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 |
3 | HG03098.hp2 NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.146+24707G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50692832 | |||||||
chr5:50693000 | A | G | 1 | a0001c0001t0001g0305 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.146+24875A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50693000 | |||||||
chr5:50693037 | A | G | 2 | a0001c0003t0001g0218 a0001c0003t0035g0219 |
2 | HG00738.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.146+24912A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50693037 | |||||||
chr5:50693039 | A | G | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.146+24914A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50693039 | |||||||
chr5:50693156 | T | A | 113 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(110): Show |
113 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.146+25031T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50693156 | |||||||
chr5:50693179 | T | C | 1 | a0001c0004t0005g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.146+25054T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50693179 | |||||||
chr5:50693437 | A | G | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.146+25312A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50693437 | |||||||
chr5:50693573 | TAAAG | T | 3 | a0001c0002t0002g0088 a0001c0002t0003g0069 a0001c0002t0003g0070 |
3 | HG02148.hp1 HG02273.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.146+25453_146+2545 others(8): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50693573 | ||||||
chr5:50693593 | A | G | 1 | a0001c0001t0012g0309 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.146+25468A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50693593 | |||||||
chr5:50693667 | A | T | 1 | a0001c0001t0016g0301 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.146+25542A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50693667 | |||||||
chr5:50693768 | G | A | 3 | a0001c0004t0005g0029 a0001c0004t0005g0030 a0001c0004t0005g0031 |
3 | HG01109.hp2 HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.146+25643G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50693768 | |||||||
chr5:50693836 | T | C | 4 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(1): Show |
4 | HG02486.hp2 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.146+25711T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50693836 | |||||||
chr5:50693867 | A | G | 119 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(116): Show |
122 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.146+25742A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50693867 | |||||||
chr5:50693899 | T | G | 11 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0001t0007g0184 others(8): Show |
11 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.146+25774T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50693899 | |||||||
chr5:50694058 | C | T | 1 | a0001c0003t0011g0225 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.146+25933C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50694058 | |||||||
chr5:50694379 | GATTATTA others(15): Show |
G | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.146+26258_146+2627 others(26): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50694379 | ||||||
chr5:50694461 | G | C | 1 | a0001c0010t0036g0321 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.146+26336G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50694461 | |||||||
chr5:50694505 | G | A | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.146+26380G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50694505 | |||||||
chr5:50694619 | G | C | 1 | a0001c0003t0001g0211 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.146+26494G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50694619 | |||||||
chr5:50694749 | A | G | 1 | a0001c0002t0003g0319 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.146+26624A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50694749 | |||||||
chr5:50694812 | G | A | 2 | a0001c0003t0001g0226 a0001c0003t0001g0227 |
2 | NA18950.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.146+26687G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50694812 | |||||||
chr5:50695006 | C | T | 2 | a0001c0003t0001g0209 a0001c0003t0001g0249 |
2 | HG01261.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.146+26881C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50695006 | |||||||
chr5:50695041 | C | T | 295 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(292): Show |
299 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(296): Show |
intron_variant | MODIFIER | c.146+26916C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50695041 | |||||||
chr5:50695262 | G | C | 1 | a0001c0002t0003g0108 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.146+27137G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50695262 | |||||||
chr5:50695316 | T | C | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.146+27191T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50695316 | |||||||
chr5:50695324 | T | G | 4 | a0001c0001t0004g0037 a0001c0001t0004g0038 a0001c0001t0004g0046 others(1): Show |
4 | HG01516.hp2 HG02293.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.146+27199T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50695324 | |||||||
chr5:50695363 | A | G | 1 | a0001c0001t0022g0047 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.146+27238A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50695363 | |||||||
chr5:50695378 | A | G | 1 | a0001c0001t0034g0298 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.146+27253A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50695378 | |||||||
chr5:50695424 | T | C | 1 | a0001c0001t0019g0004 | 2 | HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.146+27299T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50695424 | |||||||
chr5:50695487 | G | A | 4 | a0001c0003t0001g0249 a0001c0003t0011g0223 a0001c0003t0011g0224 others(1): Show |
4 | HG01433.hp2 HG02055.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.146+27362G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50695487 | |||||||
chr5:50695687 | TC | T | 119 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(116): Show |
122 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.146+27563delC | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50695687 | |||||||
chr5:50695727 | G | A | 273 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(270): Show |
277 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(274): Show |
intron_variant | MODIFIER | c.146+27602G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50695727 | |||||||
chr5:50695899 | T | C | 1 | a0001c0003t0011g0225 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.146+27774T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50695899 | |||||||
chr5:50695905 | T | C | 2 | a0001c0002t0002g0101 a0001c0002t0002g0102 |
2 | HG02055.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.146+27780T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50695905 | |||||||
chr5:50696221 | T | C | 1 | a0001c0002t0003g0073 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.146+28096T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50696221 | |||||||
chr5:50696488 | A | G | 1 | a0001c0003t0001g0248 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.146+28363A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50696488 | |||||||
chr5:50696596 | A | G | 265 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(262): Show |
269 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(266): Show |
intron_variant | MODIFIER | c.146+28471A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50696596 | |||||||
chr5:50696717 | C | A | 265 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(262): Show |
269 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(266): Show |
intron_variant | MODIFIER | c.146+28592C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50696717 | |||||||
chr5:50696734 | T | A | 2 | a0001c0001t0004g0035 a0001c0001t0004g0036 |
2 | HG02886.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.146+28609T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50696734 | |||||||
chr5:50696899 | C | T | 1 | a0001c0001t0024g0051 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.146+28774C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50696899 | |||||||
chr5:50696908 | G | C | 6 | a0001c0001t0002g0166 a0001c0001t0002g0167 a0001c0001t0002g0168 others(3): Show |
6 | HG01891.hp2 HG02717.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.146+28783G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50696908 | |||||||
chr5:50696991 | G | A | 4 | a0001c0002t0002g0109 a0001c0002t0002g0110 a0001c0002t0002g0111 others(1): Show |
4 | HG01433.hp1 HG02622.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.146+28866G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50696991 | |||||||
chr5:50697497 | C | T | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.146+29372C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50697497 | |||||||
chr5:50697498 | G | A | 11 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0001t0007g0184 others(8): Show |
11 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.146+29373G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50697498 | |||||||
chr5:50697648 | T | C | 119 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(116): Show |
122 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.146+29523T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50697648 | |||||||
chr5:50698017 | T | G | 55 | a0001c0002t0002g0081 a0001c0002t0002g0088 a0001c0002t0002g0114 others(52): Show |
58 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.146+29892T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50698017 | |||||||
chr5:50698181 | T | C | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.146+30056T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50698181 | |||||||
chr5:50698218 | A | T | 1 | a0001c0001t0007g0181 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.146+30093A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50698218 | |||||||
chr5:50698342 | G | A | 1 | a0001c0001t0014g0260 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.146+30217G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50698342 | |||||||
chr5:50698360 | A | G | 2 | a0001c0003t0001g0218 a0001c0003t0035g0219 |
2 | HG00738.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.146+30235A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50698360 | |||||||
chr5:50698478 | C | T | 1 | a0001c0002t0003g0142 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.146+30353C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50698478 | |||||||
chr5:50698532 | G | A | 3 | a0001c0004t0005g0029 a0001c0004t0005g0030 a0001c0004t0005g0031 |
3 | HG01109.hp2 HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.146+30407G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50698532 | |||||||
chr5:50698686 | C | T | 1 | a0001c0001t0001g0297 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.146+30561C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50698686 | |||||||
chr5:50698701 | G | C | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.146+30576G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50698701 | |||||||
chr5:50698836 | A | G | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.146+30711A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50698836 | |||||||
chr5:50699145 | C | T | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.146+31020C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50699145 | |||||||
chr5:50699177 | A | C | 1 | a0001c0004t0005g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.146+31052A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50699177 | |||||||
chr5:50699226 | T | C | 3 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 |
3 | HG03098.hp2 NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.146+31101T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50699226 | |||||||
chr5:50699248 | A | G | 1 | a0001c0001t0032g0183 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.146+31123A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50699248 | |||||||
chr5:50699329 | G | A | 6 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(3): Show |
6 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.146+31204G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50699329 | |||||||
chr5:50699428 | C | T | 1 | a0001c0001t0004g0050 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.146+31303C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50699428 | |||||||
chr5:50699446 | T | G | 1 | a0001c0001t0002g0067 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.146+31321T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50699446 | |||||||
chr5:50699526 | T | A | 1 | a0001c0001t0002g0066 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.146+31401T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50699526 | |||||||
chr5:50699633 | A | C | 1 | a0001c0010t0036g0321 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.146+31508A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50699633 | |||||||
chr5:50699892 | G | A | 1 | a0001c0001t0001g0261 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.146+31767G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50699892 | |||||||
chr5:50699972 | G | A | 1 | a0001c0012t0038g0008 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.146+31847G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50699972 | |||||||
chr5:50700043 | A | G | 11 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(8): Show |
11 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.146+31918A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50700043 | |||||||
chr5:50700222 | G | A | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.146+32097G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50700222 | |||||||
chr5:50700302 | G | A | 2 | a0001c0003t0001g0210 a0001c0003t0001g0211 |
2 | NA18948.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.146+32177G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50700302 | |||||||
chr5:50700499 | A | G | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.146+32374A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50700499 | |||||||
chr5:50700706 | A | G | 1 | a0001c0001t0004g0042 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.146+32581A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50700706 | |||||||
chr5:50700847 | T | C | 2 | a0001c0001t0001g0262 a0001c0001t0001g0263 |
2 | HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.146+32722T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50700847 | |||||||
chr5:50700885 | G | A | 1 | a0001c0003t0001g0252 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.146+32760G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50700885 | |||||||
chr5:50701565 | G | A | 1 | a0001c0001t0002g0155 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.146+33440G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50701565 | |||||||
chr5:50702256 | A | C | 1 | a0001c0002t0003g0079 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.146+34131A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50702256 | |||||||
chr5:50702401 | A | G | 2 | a0001c0002t0042g0153 a0001c0004t0005g0057 |
2 | HG03130.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.146+34276A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50702401 | |||||||
chr5:50702499 | T | C | 1 | a0001c0013t0005g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.146+34374T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50702499 | |||||||
chr5:50702574 | T | A | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.146+34449T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50702574 | |||||||
chr5:50702575 | C | T | 2 | a0001c0001t0001g0296 a0001c0001t0047g0295 |
2 | HG02129.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.146+34450C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50702575 | |||||||
chr5:50702652 | T | C | 2 | a0001c0002t0002g0109 a0001c0002t0002g0110 |
2 | HG01433.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.146+34527T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50702652 | |||||||
chr5:50702835 | G | A | 1 | a0001c0002t0003g0174 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.146+34710G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50702835 | |||||||
chr5:50702872 | G | T | 1 | a0001c0001t0007g0186 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.146+34747G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50702872 | |||||||
chr5:50703215 | C | T | 1 | a0001c0001t0006g0198 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.146+35090C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50703215 | |||||||
chr5:50703261 | C | T | 1 | a0001c0002t0003g0073 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.146+35136C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50703261 | |||||||
chr5:50703291 | C | T | 119 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(116): Show |
122 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.146+35166C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50703291 | |||||||
chr5:50703299 | C | CA | 21 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(18): Show |
21 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.146+35190dupA | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50703299 | ||||||
chr5:50703299 | CA | C | 108 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(105): Show |
108 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.146+35190delA | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50703299 | ||||||
chr5:50703299 | CAA | C | 6 | a0001c0001t0008g0311 a0001c0001t0008g0312 a0001c0001t0008g0313 others(3): Show |
6 | HG01192.hp2 HG01884.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.146+35189_146+3519 others(6): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50703299 | ||||||
chr5:50703618 | C | A | 4 | a0001c0002t0002g0109 a0001c0002t0002g0110 a0001c0002t0002g0111 others(1): Show |
4 | HG01433.hp1 HG02622.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.146+35493C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50703618 | |||||||
chr5:50703635 | G | A | 1 | a0001c0001t0021g0318 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.146+35510G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50703635 | |||||||
chr5:50703768 | A | C | 1 | a0001c0002t0003g0139 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.146+35643A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50703768 | |||||||
chr5:50703771 | TGTG | T | 3 | a0001c0002t0002g0109 a0001c0002t0002g0110 a0001c0002t0002g0157 |
3 | HG01433.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.146+35650_146+3565 others(7): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50703771 | ||||||
chr5:50703875 | C | G | 282 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(279): Show |
286 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(283): Show |
intron_variant | MODIFIER | c.146+35750C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50703875 | |||||||
chr5:50703904 | T | A | 1 | a0001c0002t0002g0157 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.146+35779T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50703904 | |||||||
chr5:50703964 | C | A | 1 | a0001c0001t0015g0060 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.146+35839C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50703964 | |||||||
chr5:50704258 | C | T | 2 | a0001c0003t0011g0223 a0001c0003t0011g0225 |
2 | HG02055.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.146+36133C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50704258 | |||||||
chr5:50704380 | A | G | 52 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(49): Show |
52 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.146+36255A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50704380 | |||||||
chr5:50704539 | G | T | 1 | a0001c0004t0005g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.146+36414G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50704539 | |||||||
chr5:50704642 | T | C | 1 | a0001c0004t0005g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.146+36517T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50704642 | |||||||
chr5:50704701 | G | A | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.146+36576G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50704701 | |||||||
chr5:50704795 | G | A | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.146+36670G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50704795 | |||||||
chr5:50705018 | C | T | 1 | a0001c0002t0018g0138 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.146+36893C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50705018 | |||||||
chr5:50705626 | G | A | 282 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(279): Show |
286 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(283): Show |
intron_variant | MODIFIER | c.146+37501G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50705626 | |||||||
chr5:50705673 | T | C | 1 | a0001c0003t0001g0250 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.146+37548T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50705673 | |||||||
chr5:50705827 | C | T | 2 | a0001c0001t0001g0262 a0001c0001t0001g0263 |
2 | HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.146+37702C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50705827 | |||||||
chr5:50706095 | A | G | 1 | a0004c0008t0003g0137 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.146+37970A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50706095 | |||||||
chr5:50706151 | G | C | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.146+38026G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50706151 | |||||||
chr5:50706355 | C | T | 282 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(279): Show |
286 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(283): Show |
intron_variant | MODIFIER | c.146+38230C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50706355 | |||||||
chr5:50706624 | T | C | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.146+38499T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50706624 | |||||||
chr5:50706797 | C | G | 5 | a0001c0002t0002g0090 a0001c0002t0002g0091 a0001c0002t0002g0092 others(2): Show |
5 | NA18942.hp2 NA18986.hp1 NA18987.hp2 others(2): Show |
intron_variant | MODIFIER | c.146+38672C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50706797 | |||||||
chr5:50706841 | C | A | 3 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 |
3 | HG01192.hp1 HG02280.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.146+38716C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50706841 | |||||||
chr5:50706866 | A | G | 3 | a0001c0001t0030g0005 a0001c0007t0028g0007 a0001c0007t0029g0006 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.146+38741A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50706866 | |||||||
chr5:50706948 | A | G | 1 | a0001c0012t0038g0008 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.146+38823A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50706948 | |||||||
chr5:50706962 | A | G | 2 | a0001c0001t0004g0035 a0001c0001t0004g0036 |
2 | HG02886.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.146+38837A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50706962 | |||||||
chr5:50707022 | T | A | 1 | a0001c0001t0002g0166 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.146+38897T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50707022 | |||||||
chr5:50707157 | C | T | 1 | a0001c0001t0021g0318 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.146+39032C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50707157 | |||||||
chr5:50707207 | C | T | 6 | a0001c0002t0002g0161 a0001c0002t0002g0162 a0001c0002t0002g0163 others(3): Show |
6 | HG00639.hp2 HG01952.hp1 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.146+39082C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50707207 | |||||||
chr5:50707627 | C | CAG | 92 | a0001c0001t0001g0256 a0001c0001t0001g0259 a0001c0001t0001g0261 others(89): Show |
92 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.146+39538_146+3953 others(6): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50707627 | ||||||
chr5:50707627 | C | CAGAG | 20 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(17): Show |
20 | HG02056.hp1 HG02486.hp1 HG02809.hp1 others(17): Show |
intron_variant | MODIFIER | c.146+39536_146+3953 others(8): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50707627 | ||||||
chr5:50707627 | C | CAGAGAG | 6 | a0001c0001t0001g0292 a0001c0001t0001g0293 a0001c0001t0001g0294 others(3): Show |
6 | HG01975.hp1 HG03710.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.146+39534_146+3953 others(10): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50707627 | ||||||
chr5:50707627 | CAG | C | 37 | a0001c0001t0001g0180 a0001c0001t0001g0264 a0001c0001t0004g0001 others(34): Show |
40 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.146+39538_146+3953 others(6): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50707627 | ||||||
chr5:50707627 | CAGAG | C | 26 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(23): Show |
26 | HG01167.hp2 HG01169.hp2 HG02080.hp1 others(23): Show |
intron_variant | MODIFIER | c.146+39536_146+3953 others(8): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50707627 | ||||||
chr5:50707627 | CAGAGAG | C | 129 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(126): Show |
132 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.146+39534_146+3953 others(10): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50707627 | ||||||
chr5:50707635 | G | A | 3 | a0001c0004t0005g0029 a0001c0004t0005g0030 a0001c0004t0005g0031 |
3 | HG01109.hp2 HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.146+39510G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50707635 | |||||||
chr5:50707636 | A | T | 3 | a0001c0004t0005g0029 a0001c0004t0005g0030 a0001c0004t0005g0031 |
3 | HG01109.hp2 HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.146+39511A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50707636 | |||||||
chr5:50707639 | G | C | 1 | a0001c0002t0003g0112 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.146+39514G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50707639 | |||||||
chr5:50707665 | A | G | 1 | a0001c0003t0011g0223 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.146+39540A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50707665 | |||||||
chr5:50707843 | G | T | 299 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(296): Show |
303 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(300): Show |
intron_variant | MODIFIER | c.146+39718G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50707843 | |||||||
chr5:50707883 | A | G | 1 | a0001c0001t0005g0025 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.146+39758A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50707883 | |||||||
chr5:50707944 | C | T | 3 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0003c0009t0001g0286 |
3 | HG01257.hp1 HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.146+39819C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50707944 | |||||||
chr5:50708125 | T | A | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.146+40000T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50708125 | |||||||
chr5:50708491 | G | A | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.146+40366G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50708491 | |||||||
chr5:50708672 | CACATTGA others(48): Show |
C | 7 | a0001c0001t0002g0155 a0001c0001t0002g0166 a0001c0001t0002g0167 others(4): Show |
7 | HG01891.hp2 HG02717.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.146+40550_146+4060 others(59): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50708672 | ||||||
chr5:50708767 | A | T | 1 | a0001c0002t0002g0147 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.146+40642A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50708767 | |||||||
chr5:50708808 | T | C | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.146+40683T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50708808 | |||||||
chr5:50708974 | CAG | C | 119 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(116): Show |
122 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.146+40850_146+4085 others(6): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50708974 | |||||||
chr5:50709139 | C | T | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.147-41012C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50709139 | |||||||
chr5:50709361 | T | G | 43 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(40): Show |
43 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.147-40790T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50709361 | |||||||
chr5:50709473 | G | C | 1 | a0001c0004t0005g0029 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.147-40678G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50709473 | |||||||
chr5:50709663 | A | G | 1 | a0001c0002t0041g0172 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.147-40488A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50709663 | |||||||
chr5:50709692 | T | G | 295 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(292): Show |
299 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(296): Show |
intron_variant | MODIFIER | c.147-40459T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50709692 | |||||||
chr5:50709706 | C | T | 11 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0001t0007g0184 others(8): Show |
11 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.147-40445C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50709706 | |||||||
chr5:50709754 | A | G | 1 | a0001c0002t0002g0093 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.147-40397A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50709754 | |||||||
chr5:50709805 | C | T | 3 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 |
3 | HG03098.hp2 NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.147-40346C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50709805 | |||||||
chr5:50709844 | A | AGT | 13 | a0001c0001t0006g0199 a0001c0001t0006g0206 a0001c0001t0007g0188 others(10): Show |
13 | HG00642.hp1 HG00733.hp2 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.147-40276_147-4027 others(6): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50709844 | ||||||
chr5:50709844 | A | AGTGT | 12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(9): Show |
12 | HG03130.hp1 HG04115.hp2 NA18944.hp1 others(9): Show |
intron_variant | MODIFIER | c.147-40278_147-4027 others(8): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50709844 | ||||||
chr5:50709844 | A | AGTGTGT | 3 | a0001c0001t0005g0017 a0001c0001t0005g0018 a0001c0001t0005g0019 |
3 | HG01884.hp1 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.147-40280_147-4027 others(10): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50709844 | ||||||
chr5:50709844 | AGT | A | 197 | a0001c0001t0001g0058 a0001c0001t0001g0063 a0001c0001t0001g0064 others(194): Show |
200 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(197): Show |
intron_variant | MODIFIER | c.147-40276_147-4027 others(6): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50709844 | ||||||
chr5:50709844 | AGTGT | A | 25 | a0001c0001t0001g0294 a0001c0001t0004g0053 a0001c0001t0004g0054 others(22): Show |
25 | HG01109.hp2 HG01261.hp2 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.147-40278_147-4027 others(8): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50709844 | ||||||
chr5:50709844 | AGTGTGT | A | 3 | a0001c0001t0001g0282 a0001c0002t0003g0139 a0001c0002t0023g0094 |
3 | NA18951.hp2 NA18961.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.147-40280_147-4027 others(10): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50709844 | ||||||
chr5:50709880 | T | G | 4 | a0001c0001t0007g0182 a0001c0001t0007g0184 a0001c0001t0027g0185 others(1): Show |
4 | HG02145.hp2 HG02809.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.147-40271T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50709880 | |||||||
chr5:50709922 | G | GTA | 7 | a0001c0001t0015g0059 a0001c0001t0015g0060 a0001c0001t0024g0051 others(4): Show |
7 | HG02723.hp1 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.147-40196_147-4019 others(6): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50709922 | ||||||
chr5:50709922 | G | GTATATAT others(3): Show |
1 | a0001c0001t0006g0203 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.147-40204_147-4019 others(14): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50709922 | ||||||
chr5:50709922 | GTA | G | 38 | a0001c0001t0002g0155 a0001c0001t0004g0033 a0001c0001t0004g0035 others(35): Show |
38 | HG00099.hp2 HG00733.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.147-40196_147-4019 others(6): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50709922 | ||||||
chr5:50709922 | GTATA | G | 34 | a0001c0001t0004g0039 a0001c0001t0004g0040 a0001c0001t0004g0041 others(31): Show |
35 | HG00673.hp1 HG00733.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.147-40198_147-4019 others(8): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50709922 | ||||||
chr5:50709922 | GTATATA | G | 40 | a0001c0001t0001g0266 a0001c0001t0001g0291 a0001c0001t0001g0293 others(37): Show |
40 | HG00738.hp2 HG01192.hp2 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.147-40200_147-4019 others(10): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50709922 | ||||||
chr5:50709922 | GTATATAT others(1): Show |
G | 55 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(52): Show |
55 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.147-40202_147-4019 others(12): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50709922 | ||||||
chr5:50709922 | GTATATAT others(3): Show |
G | 7 | a0001c0001t0001g0259 a0001c0001t0004g0054 a0001c0001t0004g0055 others(4): Show |
7 | HG01261.hp2 HG02109.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.147-40204_147-4019 others(14): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50709922 | ||||||
chr5:50709922 | GTATATAT others(5): Show |
G | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.147-40206_147-4019 others(16): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50709922 | ||||||
chr5:50709924 | A | G | 1 | a0001c0002t0003g0096 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.147-40227A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50709924 | |||||||
chr5:50709926 | A | G | 5 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(2): Show |
5 | NA18977.hp2 NA19010.hp2 NA19081.hp2 others(2): Show |
intron_variant | MODIFIER | c.147-40225A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50709926 | |||||||
chr5:50709930 | A | G | 4 | a0001c0001t0005g0021 a0001c0001t0005g0022 a0001c0001t0005g0023 others(1): Show |
4 | NA18944.hp1 NA18957.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.147-40221A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50709930 | |||||||
chr5:50709932 | A | G | 3 | a0001c0001t0005g0017 a0001c0001t0005g0018 a0001c0001t0005g0019 |
3 | HG01884.hp1 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.147-40219A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50709932 | |||||||
chr5:50709951 | T | C | 1 | a0001c0002t0002g0076 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.147-40200T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50709951 | |||||||
chr5:50709951 | T | TAC | 4 | a0001c0002t0002g0075 a0001c0002t0002g0077 a0001c0002t0002g0078 others(1): Show |
4 | HG00639.hp1 HG01168.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.147-40199_147-4019 others(6): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50709951 | ||||||
chr5:50709953 | T | C | 20 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(17): Show |
20 | HG00639.hp1 HG00642.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.147-40198T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50709953 | |||||||
chr5:50709953 | T | TAC | 30 | a0001c0001t0002g0167 a0001c0002t0002g0065 a0001c0002t0002g0072 others(27): Show |
30 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.147-40197_147-4019 others(6): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50709953 | ||||||
chr5:50709955 | T | C | 52 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(49): Show |
52 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.147-40196T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50709955 | |||||||
chr5:50709955 | T | TACAC | 12 | a0001c0001t0002g0168 a0001c0001t0002g0169 a0001c0002t0002g0103 others(9): Show |
13 | HG01943.hp1 HG02300.hp2 HG02683.hp2 others(10): Show |
intron_variant | MODIFIER | c.147-40194_147-4019 others(8): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50709955 | ||||||
chr5:50709955 | T | TATACAC | 12 | a0001c0002t0002g0101 a0001c0002t0002g0102 a0001c0002t0002g0105 others(9): Show |
12 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(9): Show |
intron_variant | MODIFIER | c.147-40195_147-4019 others(10): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50709955 | ||||||
chr5:50709955 | T | TATATACA others(1): Show |
27 | a0001c0002t0002g0107 a0001c0002t0002g0320 a0001c0002t0003g0002 others(24): Show |
29 | HG01074.hp1 HG01109.hp1 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.147-40195_147-4019 others(12): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50709955 | ||||||
chr5:50709955 | T | TATATATA others(3): Show |
13 | a0001c0002t0002g0081 a0001c0002t0002g0088 a0001c0002t0003g0069 others(10): Show |
13 | HG02165.hp2 HG02273.hp1 HG02273.hp2 others(10): Show |
intron_variant | MODIFIER | c.147-40195_147-4019 others(14): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50709955 | ||||||
chr5:50709955 | T | TATATATA others(5): Show |
3 | a0001c0002t0003g0154 a0001c0002t0003g0175 a0004c0008t0003g0137 |
3 | HG01346.hp1 HG02027.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.147-40195_147-4019 others(16): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50709955 | ||||||
chr5:50709955 | T | TATATATA others(7): Show |
3 | a0001c0002t0003g0139 a0001c0002t0003g0179 a0001c0002t0018g0134 |
3 | NA19006.hp2 NA19007.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.147-40195_147-4019 others(18): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50709955 | ||||||
chr5:50709955 | T | TATATATA others(9): Show |
1 | a0001c0002t0043g0135 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.147-40195_147-4019 others(20): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50709955 | ||||||
chr5:50709961 | TACATATA others(5): Show |
T | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.147-40186_147-4017 others(16): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50709961 | ||||||
chr5:50709963 | CAT | C | 6 | a0001c0001t0001g0259 a0001c0001t0001g0267 a0001c0001t0001g0269 others(3): Show |
6 | HG00099.hp1 HG01069.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.147-40182_147-4018 others(6): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50709963 | ||||||
chr5:50710130 | G | C | 2 | a0001c0001t0001g0256 a0001c0001t0001g0282 |
2 | NA18951.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.147-40021G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50710130 | |||||||
chr5:50710134 | A | G | 1 | a0001c0012t0038g0008 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.147-40017A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50710134 | |||||||
chr5:50710343 | C | T | 18 | a0001c0003t0001g0220 a0001c0003t0001g0221 a0001c0003t0001g0222 others(15): Show |
18 | HG00673.hp1 HG02056.hp2 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.147-39808C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50710343 | |||||||
chr5:50710396 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.147-39755G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50710396 | |||||||
chr5:50710525 | A | G | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.147-39626A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50710525 | |||||||
chr5:50710623 | G | A | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.147-39528G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50710623 | |||||||
chr5:50710626 | C | T | 9 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(6): Show |
9 | NA18944.hp1 NA18957.hp1 NA18977.hp2 others(6): Show |
intron_variant | MODIFIER | c.147-39525C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50710626 | |||||||
chr5:50710649 | A | G | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.147-39502A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50710649 | |||||||
chr5:50710724 | A | C | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.147-39427A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50710724 | |||||||
chr5:50710820 | A | G | 2 | a0001c0002t0003g0099 a0001c0002t0003g0100 |
2 | HG02735.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.147-39331A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50710820 | |||||||
chr5:50710825 | T | A | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.147-39326T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50710825 | |||||||
chr5:50711121 | A | G | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.147-39030A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50711121 | |||||||
chr5:50711181 | C | A | 7 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(4): Show |
7 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.147-38970C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50711181 | |||||||
chr5:50711219 | T | A | 1 | a0002c0005t0009g0287 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.147-38932T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50711219 | |||||||
chr5:50711265 | A | G | 1 | a0001c0002t0003g0112 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.147-38886A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50711265 | |||||||
chr5:50711416 | C | T | 1 | a0001c0002t0003g0112 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.147-38735C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50711416 | |||||||
chr5:50711509 | G | A | 2 | a0001c0001t0013g0192 a0001c0001t0013g0204 |
2 | HG02145.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.147-38642G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50711509 | |||||||
chr5:50711639 | C | T | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.147-38512C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50711639 | |||||||
chr5:50711646 | G | A | 1 | a0001c0001t0031g0306 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.147-38505G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50711646 | |||||||
chr5:50711702 | C | T | 1 | a0001c0002t0002g0092 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.147-38449C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50711702 | |||||||
chr5:50711743 | C | T | 2 | a0001c0002t0002g0074 a0001c0002t0002g0178 |
2 | HG00642.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.147-38408C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50711743 | |||||||
chr5:50711767 | T | C | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.147-38384T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50711767 | |||||||
chr5:50712077 | A | C | 113 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(110): Show |
113 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.147-38074A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50712077 | |||||||
chr5:50712120 | G | A | 1 | a0001c0001t0004g0050 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.147-38031G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50712120 | |||||||
chr5:50712180 | A | C | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.147-37971A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50712180 | |||||||
chr5:50712278 | T | C | 2 | a0001c0001t0001g0307 a0001c0001t0001g0308 |
2 | HG01361.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.147-37873T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50712278 | |||||||
chr5:50712326 | A | T | 12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(9): Show |
12 | HG01884.hp1 HG03098.hp1 HG03453.hp1 others(9): Show |
intron_variant | MODIFIER | c.147-37825A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50712326 | |||||||
chr5:50712332 | A | T | 295 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(292): Show |
299 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(296): Show |
intron_variant | MODIFIER | c.147-37819A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50712332 | |||||||
chr5:50712461 | G | A | 3 | a0001c0001t0030g0005 a0001c0007t0028g0007 a0001c0007t0029g0006 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.147-37690G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50712461 | |||||||
chr5:50712553 | T | A | 3 | a0001c0001t0007g0182 a0001c0001t0007g0184 a0001c0001t0027g0185 |
3 | HG02145.hp2 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.147-37598T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50712553 | |||||||
chr5:50712599 | G | C | 2 | a0001c0002t0002g0074 a0001c0002t0002g0178 |
2 | HG00642.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.147-37552G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50712599 | |||||||
chr5:50712721 | C | T | 3 | a0001c0001t0030g0005 a0001c0007t0028g0007 a0001c0007t0029g0006 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.147-37430C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50712721 | |||||||
chr5:50712745 | G | A | 1 | a0001c0007t0029g0006 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.147-37406G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50712745 | |||||||
chr5:50712846 | T | G | 1 | a0001c0001t0016g0283 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.147-37305T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50712846 | |||||||
chr5:50712917 | T | A | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.147-37234T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50712917 | |||||||
chr5:50713156 | T | C | 11 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0001t0007g0184 others(8): Show |
11 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.147-36995T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50713156 | |||||||
chr5:50713229 | T | A | 3 | a0001c0001t0030g0005 a0001c0007t0028g0007 a0001c0007t0029g0006 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.147-36922T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50713229 | |||||||
chr5:50713234 | A | ATAT | 4 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(1): Show |
4 | HG01192.hp1 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.147-36897_147-3689 others(7): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50713234 | ||||||
chr5:50713234 | ATAT | A | 7 | a0001c0001t0002g0166 a0001c0001t0002g0167 a0001c0001t0002g0168 others(4): Show |
7 | HG01891.hp2 HG02717.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.147-36897_147-3689 others(7): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50713234 | ||||||
chr5:50713262 | A | G | 1 | a0001c0002t0003g0154 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.147-36889A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50713262 | |||||||
chr5:50713305 | A | C | 5 | a0001c0002t0002g0090 a0001c0002t0002g0091 a0001c0002t0002g0092 others(2): Show |
5 | NA18942.hp2 NA18986.hp1 NA18987.hp2 others(2): Show |
intron_variant | MODIFIER | c.147-36846A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50713305 | |||||||
chr5:50713337 | C | T | 11 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0001t0007g0184 others(8): Show |
11 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.147-36814C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50713337 | |||||||
chr5:50713487 | C | A | 1 | a0001c0007t0029g0006 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.147-36664C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50713487 | |||||||
chr5:50713500 | C | T | 4 | a0001c0002t0003g0098 a0001c0002t0003g0125 a0001c0002t0003g0126 others(1): Show |
4 | HG02602.hp2 HG02698.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.147-36651C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50713500 | |||||||
chr5:50713521 | G | A | 2 | a0001c0001t0004g0039 a0001c0001t0004g0040 |
2 | HG00733.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.147-36630G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50713521 | |||||||
chr5:50713594 | A | C | 19 | a0001c0003t0001g0220 a0001c0003t0001g0221 a0001c0003t0001g0222 others(16): Show |
19 | HG00673.hp1 HG02056.hp2 HG02074.hp2 others(16): Show |
intron_variant | MODIFIER | c.147-36557A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50713594 | |||||||
chr5:50713616 | C | T | 2 | a0001c0002t0003g0156 a0001c0002t0018g0134 |
2 | NA19006.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.147-36535C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50713616 | |||||||
chr5:50713821 | A | G | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.147-36330A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50713821 | |||||||
chr5:50713839 | G | A | 1 | a0001c0001t0004g0038 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.147-36312G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50713839 | |||||||
chr5:50713842 | C | T | 8 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0048 others(5): Show |
10 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.147-36309C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50713842 | |||||||
chr5:50713939 | T | G | 1 | a0001c0002t0002g0157 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.147-36212T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50713939 | |||||||
chr5:50713983 | G | A | 4 | a0001c0001t0005g0021 a0001c0001t0005g0022 a0001c0001t0005g0023 others(1): Show |
4 | NA18944.hp1 NA18957.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.147-36168G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50713983 | |||||||
chr5:50714034 | A | G | 1 | a0001c0002t0003g0175 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.147-36117A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50714034 | |||||||
chr5:50714084 | C | CT | 11 | a0001c0001t0006g0207 a0001c0001t0007g0182 a0001c0001t0007g0184 others(8): Show |
11 | HG01192.hp2 HG02145.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.147-36052dupT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50714084 | ||||||
chr5:50714100 | C | T | 3 | a0001c0001t0030g0005 a0001c0007t0028g0007 a0001c0007t0029g0006 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.147-36051C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50714100 | |||||||
chr5:50714252 | C | A | 3 | a0001c0004t0005g0029 a0001c0004t0005g0030 a0001c0004t0005g0031 |
3 | HG01109.hp2 HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.147-35899C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50714252 | |||||||
chr5:50714407 | A | T | 1 | a0001c0004t0005g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.147-35744A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50714407 | |||||||
chr5:50714502 | C | T | 10 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0001t0007g0184 others(7): Show |
10 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.147-35649C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50714502 | |||||||
chr5:50714633 | G | C | 1 | a0001c0004t0005g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.147-35518G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50714633 | |||||||
chr5:50714755 | C | T | 1 | a0001c0001t0021g0318 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.147-35396C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50714755 | |||||||
chr5:50714788 | C | T | 2 | a0001c0001t0004g0038 a0001c0001t0004g0046 |
2 | HG02293.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.147-35363C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50714788 | |||||||
chr5:50714815 | G | T | 3 | a0001c0001t0005g0017 a0001c0001t0005g0018 a0001c0001t0005g0019 |
3 | HG01884.hp1 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.147-35336G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50714815 | |||||||
chr5:50715011 | CT | C | 8 | a0001c0002t0002g0101 a0001c0002t0002g0102 a0001c0002t0002g0103 others(5): Show |
8 | HG02055.hp2 HG02257.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.147-35132delT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50715011 | ||||||
chr5:50715019 | T | C | 1 | a0001c0001t0001g0305 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.147-35132T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50715019 | |||||||
chr5:50715073 | G | A | 1 | a0001c0002t0046g0141 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.147-35078G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50715073 | |||||||
chr5:50715194 | C | T | 4 | a0001c0001t0005g0021 a0001c0001t0005g0022 a0001c0001t0005g0023 others(1): Show |
4 | NA18944.hp1 NA18957.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.147-34957C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50715194 | |||||||
chr5:50715496 | GTA | G | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.147-34653_147-3465 others(6): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50715496 | ||||||
chr5:50715540 | A | T | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.147-34611A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50715540 | |||||||
chr5:50715714 | A | G | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.147-34437A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50715714 | |||||||
chr5:50715740 | T | C | 3 | a0001c0001t0007g0182 a0001c0001t0007g0184 a0001c0001t0027g0185 |
3 | HG02145.hp2 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.147-34411T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50715740 | |||||||
chr5:50715861 | T | A | 296 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(293): Show |
300 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(297): Show |
intron_variant | MODIFIER | c.147-34290T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50715861 | |||||||
chr5:50715891 | G | A | 1 | a0001c0002t0003g0108 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.147-34260G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50715891 | |||||||
chr5:50715914 | G | T | 1 | a0001c0002t0002g0145 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.147-34237G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50715914 | |||||||
chr5:50716050 | C | T | 3 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 |
3 | HG03098.hp2 NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.147-34101C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50716050 | |||||||
chr5:50716068 | C | A | 6 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(3): Show |
6 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.147-34083C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50716068 | |||||||
chr5:50716100 | T | A | 1 | a0001c0001t0006g0202 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.147-34051T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50716100 | |||||||
chr5:50716185 | A | G | 11 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0001t0007g0184 others(8): Show |
11 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.147-33966A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50716185 | |||||||
chr5:50716228 | G | A | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.147-33923G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50716228 | |||||||
chr5:50716267 | C | T | 1 | a0001c0007t0028g0007 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.147-33884C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50716267 | |||||||
chr5:50716268 | G | A | 1 | a0001c0010t0036g0321 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.147-33883G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50716268 | |||||||
chr5:50716379 | T | C | 1 | a0001c0002t0002g0147 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.147-33772T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50716379 | |||||||
chr5:50716385 | G | A | 1 | a0003c0009t0001g0286 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.147-33766G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50716385 | |||||||
chr5:50716489 | G | A | 65 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(62): Show |
65 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.147-33662G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50716489 | |||||||
chr5:50716503 | G | A | 1 | a0001c0007t0029g0006 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.147-33648G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50716503 | |||||||
chr5:50716628 | T | A | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.147-33523T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50716628 | |||||||
chr5:50716633 | T | A | 1 | a0001c0001t0001g0307 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.147-33518T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50716633 | |||||||
chr5:50716779 | G | A | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.147-33372G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50716779 | |||||||
chr5:50716859 | CTG | C | 10 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(7): Show |
10 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.147-33288_147-3328 others(6): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50716859 | ||||||
chr5:50717199 | A | G | 7 | a0001c0001t0002g0155 a0001c0001t0002g0166 a0001c0001t0002g0167 others(4): Show |
7 | HG01891.hp2 HG02717.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.147-32952A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50717199 | |||||||
chr5:50717214 | G | A | 1 | a0001c0002t0003g0175 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.147-32937G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50717214 | |||||||
chr5:50717326 | A | C | 4 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(1): Show |
4 | HG02056.hp1 NA18974.hp2 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.147-32825A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50717326 | |||||||
chr5:50717379 | T | C | 1 | a0001c0001t0021g0318 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.147-32772T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50717379 | |||||||
chr5:50717439 | C | T | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.147-32712C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50717439 | |||||||
chr5:50717509 | A | G | 295 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(292): Show |
299 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(296): Show |
intron_variant | MODIFIER | c.147-32642A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50717509 | |||||||
chr5:50717529 | G | T | 1 | a0001c0001t0008g0258 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.147-32622G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50717529 | |||||||
chr5:50717548 | C | T | 1 | a0001c0003t0001g0247 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.147-32603C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50717548 | |||||||
chr5:50717549 | G | A | 1 | a0001c0001t0004g0052 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.147-32602G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50717549 | |||||||
chr5:50717591 | G | A | 1 | a0001c0013t0005g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.147-32560G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50717591 | |||||||
chr5:50717870 | G | A | 1 | a0001c0002t0002g0147 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.147-32281G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50717870 | |||||||
chr5:50718005 | G | A | 1 | a0001c0001t0006g0201 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.147-32146G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50718005 | |||||||
chr5:50718376 | A | G | 6 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(3): Show |
6 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.147-31775A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50718376 | |||||||
chr5:50718473 | A | G | 1 | a0001c0003t0001g0252 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.147-31678A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50718473 | |||||||
chr5:50718545 | C | T | 2 | a0001c0002t0002g0147 a0001c0002t0050g0177 |
2 | NA18977.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.147-31606C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50718545 | |||||||
chr5:50718607 | A | G | 2 | a0001c0002t0003g0156 a0001c0002t0018g0134 |
2 | NA19006.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.147-31544A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50718607 | |||||||
chr5:50718662 | A | G | 1 | a0001c0001t0001g0263 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.147-31489A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50718662 | |||||||
chr5:50718743 | C | T | 1 | a0001c0001t0007g0181 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.147-31408C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50718743 | |||||||
chr5:50718761 | A | G | 1 | a0001c0002t0003g0115 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.147-31390A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50718761 | |||||||
chr5:50718840 | A | G | 109 | a0001c0002t0002g0065 a0001c0002t0002g0072 a0001c0002t0002g0074 others(106): Show |
112 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.147-31311A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50718840 | |||||||
chr5:50718892 | C | G | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.147-31259C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50718892 | |||||||
chr5:50718932 | A | G | 1 | a0001c0010t0036g0321 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.147-31219A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50718932 | |||||||
chr5:50719028 | C | T | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.147-31123C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50719028 | |||||||
chr5:50719330 | ATATAATC others(14): Show |
A | 1 | a0001c0002t0003g0108 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.147-30819_147-3079 others(25): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50719330 | ||||||
chr5:50719332 | A | G | 1 | a0001c0004t0005g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.147-30819A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50719332 | |||||||
chr5:50719362 | T | C | 11 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0001t0007g0184 others(8): Show |
11 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.147-30789T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50719362 | |||||||
chr5:50719557 | T | C | 11 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0001t0007g0184 others(8): Show |
11 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.147-30594T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50719557 | |||||||
chr5:50719600 | T | C | 7 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(4): Show |
7 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.147-30551T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50719600 | |||||||
chr5:50719697 | C | T | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.147-30454C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50719697 | |||||||
chr5:50719737 | T | G | 1 | a0001c0001t0004g0034 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.147-30414T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50719737 | |||||||
chr5:50719751 | T | C | 5 | a0001c0002t0003g0116 a0001c0002t0003g0128 a0001c0002t0003g0129 others(2): Show |
5 | HG02132.hp2 HG02165.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.147-30400T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50719751 | |||||||
chr5:50719795 | A | T | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.147-30356A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50719795 | |||||||
chr5:50719816 | T | C | 11 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0001t0007g0184 others(8): Show |
11 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.147-30335T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50719816 | |||||||
chr5:50720100 | T | C | 1 | a0001c0002t0002g0111 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.147-30051T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50720100 | |||||||
chr5:50720215 | C | T | 1 | a0001c0002t0043g0135 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.147-29936C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50720215 | |||||||
chr5:50720282 | G | A | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.147-29869G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50720282 | |||||||
chr5:50720740 | A | G | 1 | a0001c0012t0038g0008 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.147-29411A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50720740 | |||||||
chr5:50720741 | T | TACCATCC others(1): Show |
282 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(279): Show |
286 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(283): Show |
intron_variant | MODIFIER | c.147-29408_147-2940 others(12): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50720741 | ||||||
chr5:50720750 | C | T | 1 | a0001c0002t0002g0144 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.147-29401C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50720750 | |||||||
chr5:50720837 | C | T | 1 | a0001c0001t0004g0040 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.147-29314C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50720837 | |||||||
chr5:50721082 | G | GT | 16 | a0001c0001t0002g0169 a0001c0001t0005g0011 a0001c0001t0005g0017 others(13): Show |
16 | HG00738.hp1 HG01255.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.147-29055dupT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50721082 | ||||||
chr5:50721160 | A | C | 1 | a0001c0002t0002g0147 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.147-28991A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50721160 | |||||||
chr5:50721450 | AT | A | 7 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(4): Show |
7 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.147-28698delT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50721450 | ||||||
chr5:50721483 | G | A | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.147-28668G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50721483 | |||||||
chr5:50721535 | A | G | 6 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(3): Show |
6 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.147-28616A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50721535 | |||||||
chr5:50721536 | A | G | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.147-28615A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50721536 | |||||||
chr5:50721557 | A | T | 6 | a0001c0001t0007g0181 a0001c0001t0007g0186 a0001c0001t0007g0187 others(3): Show |
6 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.147-28594A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50721557 | |||||||
chr5:50721663 | G | T | 4 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(1): Show |
4 | HG02486.hp2 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.147-28488G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50721663 | |||||||
chr5:50721727 | A | G | 1 | a0001c0003t0001g0210 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.147-28424A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50721727 | |||||||
chr5:50721890 | A | G | 47 | a0001c0003t0001g0209 a0001c0003t0001g0210 a0001c0003t0001g0211 others(44): Show |
47 | HG00673.hp1 HG00738.hp1 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.147-28261A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50721890 | |||||||
chr5:50722118 | G | A | 1 | a0001c0002t0002g0148 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.147-28033G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50722118 | |||||||
chr5:50722232 | C | T | 1 | a0001c0002t0005g0071 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.147-27919C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50722232 | |||||||
chr5:50722233 | G | A | 1 | a0001c0003t0001g0233 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.147-27918G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50722233 | |||||||
chr5:50722328 | T | C | 1 | a0001c0002t0002g0093 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.147-27823T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50722328 | |||||||
chr5:50722370 | G | A | 1 | a0001c0002t0003g0108 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.147-27781G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50722370 | |||||||
chr5:50722511 | A | G | 4 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(1): Show |
4 | HG02486.hp2 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.147-27640A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50722511 | |||||||
chr5:50722714 | C | T | 268 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(265): Show |
272 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(269): Show |
intron_variant | MODIFIER | c.147-27437C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50722714 | |||||||
chr5:50722740 | A | T | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.147-27411A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50722740 | |||||||
chr5:50722779 | C | A | 1 | a0001c0003t0001g0246 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.147-27372C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50722779 | |||||||
chr5:50722812 | G | A | 1 | a0001c0010t0036g0321 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.147-27339G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50722812 | |||||||
chr5:50722990 | G | A | 1 | a0001c0001t0008g0299 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.147-27161G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50722990 | |||||||
chr5:50723177 | A | T | 1 | a0001c0013t0005g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.147-26974A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50723177 | |||||||
chr5:50723222 | A | G | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.147-26929A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50723222 | |||||||
chr5:50723564 | A | G | 1 | a0001c0001t0004g0041 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.147-26587A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50723564 | |||||||
chr5:50723856 | C | T | 1 | a0001c0002t0003g0079 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.147-26295C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50723856 | |||||||
chr5:50723926 | G | C | 1 | a0001c0007t0028g0007 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.147-26225G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50723926 | |||||||
chr5:50724021 | T | G | 1 | a0001c0002t0002g0176 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.147-26130T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50724021 | |||||||
chr5:50724387 | G | A | 295 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(292): Show |
299 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(296): Show |
intron_variant | MODIFIER | c.147-25764G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50724387 | |||||||
chr5:50724572 | T | A | 2 | a0001c0003t0001g0228 a0001c0003t0001g0229 |
2 | NA18947.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.147-25579T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50724572 | |||||||
chr5:50724697 | T | C | 1 | a0001c0002t0003g0154 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.147-25454T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50724697 | |||||||
chr5:50724739 | G | GTT | 12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(9): Show |
12 | HG01884.hp1 HG03098.hp1 HG03453.hp1 others(9): Show |
intron_variant | MODIFIER | c.147-25404_147-2540 others(6): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50724739 | ||||||
chr5:50724945 | G | A | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.147-25206G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50724945 | |||||||
chr5:50725077 | GTA | G | 293 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(290): Show |
297 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(294): Show |
intron_variant | MODIFIER | c.147-25059_147-2505 others(6): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50725077 | ||||||
chr5:50725150 | G | GTA | 21 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(18): Show |
22 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.147-24986_147-2498 others(6): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50725150 | ||||||
chr5:50725152 | A | G | 16 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0012 others(13): Show |
16 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(13): Show |
intron_variant | MODIFIER | c.147-24999A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50725152 | |||||||
chr5:50725165 | T | A | 1 | a0001c0002t0002g0173 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.147-24986T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50725165 | |||||||
chr5:50725228 | T | G | 9 | a0001c0003t0001g0210 a0001c0003t0001g0211 a0001c0003t0001g0212 others(6): Show |
9 | HG01934.hp2 HG01943.hp2 HG02148.hp2 others(6): Show |
intron_variant | MODIFIER | c.147-24923T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50725228 | |||||||
chr5:50725392 | A | G | 2 | a0001c0001t0001g0284 a0001c0001t0001g0285 |
2 | NA18945.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.147-24759A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50725392 | |||||||
chr5:50725461 | T | G | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.147-24690T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50725461 | |||||||
chr5:50725648 | A | G | 3 | a0001c0001t0007g0182 a0001c0001t0007g0184 a0001c0001t0027g0185 |
3 | HG02145.hp2 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.147-24503A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50725648 | |||||||
chr5:50725954 | C | T | 4 | a0001c0003t0001g0252 a0001c0003t0011g0223 a0001c0003t0011g0224 others(1): Show |
4 | HG02055.hp1 HG02486.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.147-24197C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50725954 | |||||||
chr5:50725961 | G | A | 112 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(109): Show |
112 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.147-24190G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50725961 | |||||||
chr5:50726123 | T | A | 2 | a0001c0001t0006g0191 a0001c0001t0006g0206 |
2 | HG02630.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.147-24028T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50726123 | |||||||
chr5:50726124 | A | T | 7 | a0001c0001t0002g0166 a0001c0001t0002g0167 a0001c0001t0002g0168 others(4): Show |
7 | HG01891.hp2 HG02717.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.147-24027A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50726124 | |||||||
chr5:50726218 | A | G | 1 | a0001c0004t0005g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.147-23933A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50726218 | |||||||
chr5:50726244 | T | C | 6 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(3): Show |
6 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.147-23907T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50726244 | |||||||
chr5:50726569 | C | T | 1 | a0001c0013t0005g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.147-23582C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50726569 | |||||||
chr5:50726627 | G | A | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.147-23524G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50726627 | |||||||
chr5:50726806 | C | A | 12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(9): Show |
12 | HG01884.hp1 HG03098.hp1 HG03453.hp1 others(9): Show |
intron_variant | MODIFIER | c.147-23345C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50726806 | |||||||
chr5:50727101 | T | G | 1 | a0001c0001t0017g0170 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.147-23050T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50727101 | |||||||
chr5:50727172 | C | T | 1 | a0001c0003t0001g0243 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.147-22979C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50727172 | |||||||
chr5:50727336 | C | T | 265 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(262): Show |
269 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(266): Show |
intron_variant | MODIFIER | c.147-22815C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50727336 | |||||||
chr5:50727337 | G | A | 1 | a0001c0002t0051g0143 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.147-22814G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50727337 | |||||||
chr5:50727337 | G | T | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.147-22814G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50727337 | |||||||
chr5:50727433 | T | G | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.147-22718T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50727433 | |||||||
chr5:50727540 | C | A | 109 | a0001c0002t0002g0065 a0001c0002t0002g0072 a0001c0002t0002g0074 others(106): Show |
112 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.147-22611C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50727540 | |||||||
chr5:50727622 | A | G | 3 | a0001c0001t0005g0017 a0001c0001t0005g0018 a0001c0001t0005g0019 |
3 | HG01884.hp1 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.147-22529A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50727622 | |||||||
chr5:50727645 | G | A | 2 | a0001c0001t0004g0041 a0001c0001t0004g0049 |
2 | HG01975.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.147-22506G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50727645 | |||||||
chr5:50727654 | G | A | 1 | a0001c0002t0005g0071 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.147-22497G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50727654 | |||||||
chr5:50727683 | G | C | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.147-22468G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50727683 | |||||||
chr5:50727758 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.147-22393G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50727758 | |||||||
chr5:50728183 | A | G | 3 | a0001c0001t0030g0005 a0001c0007t0028g0007 a0001c0007t0029g0006 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.147-21968A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50728183 | |||||||
chr5:50728279 | T | G | 1 | a0001c0001t0008g0311 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.147-21872T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50728279 | |||||||
chr5:50728428 | T | A | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.147-21723T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50728428 | |||||||
chr5:50728452 | G | A | 5 | a0001c0002t0002g0101 a0001c0002t0002g0102 a0001c0002t0002g0103 others(2): Show |
5 | HG02055.hp2 HG02257.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.147-21699G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50728452 | |||||||
chr5:50728465 | C | T | 1 | a0001c0001t0016g0283 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.147-21686C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50728465 | |||||||
chr5:50728751 | T | A | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.147-21400T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50728751 | |||||||
chr5:50728799 | A | G | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.147-21352A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50728799 | |||||||
chr5:50728834 | A | G | 111 | a0001c0001t0005g0023 a0001c0002t0002g0065 a0001c0002t0002g0072 others(108): Show |
114 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.147-21317A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50728834 | |||||||
chr5:50728847 | G | C | 1 | a0001c0001t0005g0010 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.147-21304G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50728847 | |||||||
chr5:50728847 | G | T | 1 | a0001c0012t0038g0008 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.147-21304G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50728847 | |||||||
chr5:50728870 | A | G | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.147-21281A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50728870 | |||||||
chr5:50728899 | C | T | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.147-21252C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50728899 | |||||||
chr5:50728923 | A | C | 113 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(110): Show |
113 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.147-21228A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50728923 | |||||||
chr5:50729065 | G | A | 295 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(292): Show |
299 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(296): Show |
intron_variant | MODIFIER | c.147-21086G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50729065 | |||||||
chr5:50729254 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.147-20897G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50729254 | |||||||
chr5:50729310 | A | G | 1 | a0001c0012t0038g0008 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.147-20841A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50729310 | |||||||
chr5:50729618 | T | A | 1 | a0001c0001t0001g0305 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.147-20533T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50729618 | |||||||
chr5:50729670 | C | A | 1 | a0001c0007t0028g0007 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.147-20481C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50729670 | |||||||
chr5:50729856 | G | C | 111 | a0001c0001t0005g0023 a0001c0002t0002g0065 a0001c0002t0002g0072 others(108): Show |
114 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.147-20295G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50729856 | |||||||
chr5:50730020 | C | T | 3 | a0001c0001t0030g0005 a0001c0007t0028g0007 a0001c0007t0029g0006 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.147-20131C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50730020 | |||||||
chr5:50730075 | A | G | 1 | a0001c0002t0002g0159 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.147-20076A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50730075 | |||||||
chr5:50730173 | A | C | 7 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(4): Show |
7 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.147-19978A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50730173 | |||||||
chr5:50730219 | C | CTATAACT others(219): Show |
1 | a0001c0004t0005g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.147-19931_147-1993 others(230): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50730219 | ||||||
chr5:50730221 | G | T | 1 | a0001c0004t0005g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.147-19930G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50730221 | |||||||
chr5:50730348 | C | G | 1 | a0001c0003t0001g0253 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.147-19803C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50730348 | |||||||
chr5:50730461 | G | A | 3 | a0001c0001t0030g0005 a0001c0007t0028g0007 a0001c0007t0029g0006 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.147-19690G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50730461 | |||||||
chr5:50730599 | C | T | 11 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0001t0007g0184 others(8): Show |
11 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.147-19552C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50730599 | |||||||
chr5:50730605 | C | T | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.147-19546C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50730605 | |||||||
chr5:50730631 | C | T | 119 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(116): Show |
122 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.147-19520C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50730631 | |||||||
chr5:50730635 | T | C | 1 | a0001c0003t0011g0223 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.147-19516T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50730635 | |||||||
chr5:50730866 | A | C | 2 | a0001c0002t0003g0069 a0001c0002t0003g0070 |
2 | HG02148.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.147-19285A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50730866 | |||||||
chr5:50730896 | T | A | 1 | a0001c0001t0001g0282 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.147-19255T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50730896 | |||||||
chr5:50730980 | G | C | 10 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0001t0007g0184 others(7): Show |
10 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.147-19171G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50730980 | |||||||
chr5:50731094 | A | T | 120 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(117): Show |
123 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.147-19057A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50731094 | |||||||
chr5:50731212 | C | G | 2 | a0001c0002t0002g0107 a0001c0002t0002g0320 |
2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.147-18939C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50731212 | |||||||
chr5:50731293 | C | A | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.147-18858C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50731293 | |||||||
chr5:50731305 | A | C | 5 | a0001c0002t0003g0116 a0001c0002t0003g0128 a0001c0002t0003g0129 others(2): Show |
5 | HG02132.hp2 HG02165.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.147-18846A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50731305 | |||||||
chr5:50731534 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.147-18617G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50731534 | |||||||
chr5:50731578 | C | T | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.147-18573C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50731578 | |||||||
chr5:50731879 | A | G | 1 | a0001c0001t0021g0318 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.147-18272A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50731879 | |||||||
chr5:50731906 | C | T | 3 | a0001c0001t0030g0005 a0001c0007t0028g0007 a0001c0007t0029g0006 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.147-18245C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50731906 | |||||||
chr5:50731909 | A | T | 1 | a0001c0007t0029g0006 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.147-18242A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50731909 | |||||||
chr5:50732169 | A | T | 1 | a0001c0007t0029g0006 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.147-17982A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50732169 | |||||||
chr5:50732187 | TA | T | 10 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(7): Show |
10 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.147-17963delA | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50732187 | |||||||
chr5:50732264 | A | G | 5 | a0001c0003t0010g0231 a0001c0003t0010g0232 a0001c0003t0010g0251 others(2): Show |
5 | HG01255.hp2 HG01952.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.147-17887A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50732264 | |||||||
chr5:50732269 | G | A | 66 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(63): Show |
66 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.147-17882G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50732269 | |||||||
chr5:50732272 | A | G | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.147-17879A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50732272 | |||||||
chr5:50732324 | T | C | 2 | a0001c0002t0002g0074 a0001c0002t0002g0178 |
2 | HG00642.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.147-17827T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50732324 | |||||||
chr5:50732361 | A | G | 319 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(316): Show |
325 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(322): Show |
intron_variant | MODIFIER | c.147-17790A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50732361 | |||||||
chr5:50732640 | A | G | 234 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(231): Show |
237 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(234): Show |
intron_variant | MODIFIER | c.147-17511A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50732640 | |||||||
chr5:50732681 | C | T | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.147-17470C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50732681 | |||||||
chr5:50732700 | G | T | 46 | a0001c0003t0001g0209 a0001c0003t0001g0210 a0001c0003t0001g0211 others(43): Show |
46 | HG00673.hp1 HG00738.hp1 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.147-17451G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50732700 | |||||||
chr5:50732766 | C | T | 3 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 |
3 | HG03098.hp2 NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.147-17385C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50732766 | |||||||
chr5:50732776 | G | A | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.147-17375G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50732776 | |||||||
chr5:50732780 | G | A | 1 | a0001c0002t0002g0093 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.147-17371G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50732780 | |||||||
chr5:50732826 | G | T | 1 | a0001c0001t0004g0033 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.147-17325G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50732826 | |||||||
chr5:50732929 | G | A | 1 | a0001c0001t0014g0260 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.147-17222G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50732929 | |||||||
chr5:50732946 | G | C | 1 | a0001c0001t0001g0305 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.147-17205G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50732946 | |||||||
chr5:50733248 | C | T | 2 | a0001c0002t0003g0069 a0001c0002t0003g0070 |
2 | HG02148.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.147-16903C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50733248 | |||||||
chr5:50733250 | C | T | 1 | a0001c0002t0003g0115 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.147-16901C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50733250 | |||||||
chr5:50733258 | C | T | 1 | a0001c0002t0002g0165 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.147-16893C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50733258 | |||||||
chr5:50733299 | C | A | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.147-16852C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50733299 | |||||||
chr5:50733872 | C | G | 282 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(279): Show |
286 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(283): Show |
intron_variant | MODIFIER | c.147-16279C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50733872 | |||||||
chr5:50733965 | C | A | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.147-16186C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50733965 | |||||||
chr5:50733982 | G | A | 1 | a0001c0003t0001g0212 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.147-16169G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50733982 | |||||||
chr5:50734125 | G | A | 1 | a0001c0004t0005g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.147-16026G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50734125 | |||||||
chr5:50734424 | G | A | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.147-15727G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50734424 | |||||||
chr5:50734445 | A | T | 1 | a0001c0002t0040g0164 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.147-15706A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50734445 | |||||||
chr5:50734549 | A | G | 12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(9): Show |
12 | HG01884.hp1 HG03098.hp1 HG03453.hp1 others(9): Show |
intron_variant | MODIFIER | c.147-15602A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50734549 | |||||||
chr5:50734647 | T | C | 1 | a0001c0001t0037g0009 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.147-15504T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50734647 | |||||||
chr5:50734698 | T | C | 1 | a0001c0002t0003g0115 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.147-15453T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50734698 | |||||||
chr5:50734894 | G | A | 1 | a0001c0001t0004g0056 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.147-15257G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50734894 | |||||||
chr5:50734957 | A | C | 146 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(143): Show |
147 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.147-15194A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50734957 | |||||||
chr5:50735034 | C | T | 2 | a0001c0002t0002g0159 a0001c0002t0003g0080 |
2 | HG00544.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.147-15117C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50735034 | |||||||
chr5:50735059 | G | T | 1 | a0001c0001t0008g0310 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.147-15092G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50735059 | |||||||
chr5:50735110 | A | G | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.147-15041A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50735110 | |||||||
chr5:50735118 | A | G | 1 | a0001c0001t0001g0292 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.147-15033A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50735118 | |||||||
chr5:50735475 | G | T | 6 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(3): Show |
6 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.147-14676G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50735475 | |||||||
chr5:50735644 | G | C | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.147-14507G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50735644 | |||||||
chr5:50735731 | G | T | 1 | a0001c0001t0007g0181 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.147-14420G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50735731 | |||||||
chr5:50735911 | A | C | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.147-14240A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50735911 | |||||||
chr5:50735931 | G | A | 12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(9): Show |
12 | HG01884.hp1 HG03098.hp1 HG03453.hp1 others(9): Show |
intron_variant | MODIFIER | c.147-14220G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50735931 | |||||||
chr5:50735956 | T | TC | 71 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(68): Show |
71 | HG00099.hp2 HG00738.hp1 HG01167.hp2 others(68): Show |
intron_variant | MODIFIER | c.147-14184dupC | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50735956 | ||||||
chr5:50735956 | T | TCC | 41 | a0001c0001t0001g0063 a0001c0001t0001g0256 a0001c0001t0001g0259 others(38): Show |
42 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.147-14185_147-1418 others(6): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50735956 | ||||||
chr5:50735956 | TC | T | 24 | a0001c0001t0001g0305 a0001c0001t0002g0067 a0001c0001t0002g0068 others(21): Show |
24 | HG00738.hp2 HG01109.hp2 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.147-14184delC | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50735956 | ||||||
chr5:50735984 | A | T | 1 | a0001c0001t0004g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.147-14167A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50735984 | |||||||
chr5:50735998 | G | A | 1 | a0001c0001t0002g0155 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.147-14153G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50735998 | |||||||
chr5:50736059 | G | A | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.147-14092G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50736059 | |||||||
chr5:50736086 | A | G | 1 | a0001c0001t0004g0038 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.147-14065A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50736086 | |||||||
chr5:50736304 | C | A | 1 | a0001c0002t0045g0117 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.147-13847C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50736304 | |||||||
chr5:50736378 | G | A | 4 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(1): Show |
4 | NA18977.hp2 NA19010.hp2 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.147-13773G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50736378 | |||||||
chr5:50736413 | A | G | 11 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0001t0007g0184 others(8): Show |
11 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.147-13738A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50736413 | |||||||
chr5:50736451 | G | A | 122 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(119): Show |
125 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(122): Show |
intron_variant | MODIFIER | c.147-13700G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50736451 | |||||||
chr5:50736471 | A | G | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.147-13680A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50736471 | |||||||
chr5:50736743 | G | T | 1 | a0001c0001t0021g0318 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.147-13408G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50736743 | |||||||
chr5:50736903 | A | C | 12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(9): Show |
12 | HG01884.hp1 HG03098.hp1 HG03453.hp1 others(9): Show |
intron_variant | MODIFIER | c.147-13248A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50736903 | |||||||
chr5:50736928 | A | T | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.147-13223A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50736928 | |||||||
chr5:50737118 | T | A | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.147-13033T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50737118 | |||||||
chr5:50737119 | C | T | 11 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0001t0007g0184 others(8): Show |
11 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.147-13032C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50737119 | |||||||
chr5:50737414 | G | GTAC | 11 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0001t0007g0184 others(8): Show |
11 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.147-12735_147-1273 others(7): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50737414 | ||||||
chr5:50737420 | A | C | 234 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(231): Show |
237 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(234): Show |
intron_variant | MODIFIER | c.147-12731A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50737420 | |||||||
chr5:50737463 | G | C | 1 | a0001c0001t0019g0004 | 2 | HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.147-12688G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50737463 | |||||||
chr5:50737548 | C | A | 3 | a0001c0001t0030g0005 a0001c0007t0028g0007 a0001c0007t0029g0006 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.147-12603C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50737548 | |||||||
chr5:50737680 | T | C | 1 | a0001c0002t0003g0179 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.147-12471T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50737680 | |||||||
chr5:50737692 | G | A | 268 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(265): Show |
272 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(269): Show |
intron_variant | MODIFIER | c.147-12459G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50737692 | |||||||
chr5:50737833 | T | G | 1 | a0001c0001t0001g0305 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.147-12318T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50737833 | |||||||
chr5:50737848 | T | C | 1 | a0001c0001t0002g0155 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.147-12303T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50737848 | |||||||
chr5:50737971 | T | G | 10 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(7): Show |
10 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.147-12180T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50737971 | |||||||
chr5:50738130 | G | A | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.147-12021G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50738130 | |||||||
chr5:50738302 | C | G | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.147-11849C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50738302 | |||||||
chr5:50738309 | G | A | 47 | a0001c0003t0001g0209 a0001c0003t0001g0210 a0001c0003t0001g0211 others(44): Show |
47 | HG00673.hp1 HG00738.hp1 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.147-11842G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50738309 | |||||||
chr5:50738655 | G | A | 1 | a0001c0003t0001g0233 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.147-11496G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50738655 | |||||||
chr5:50738715 | T | TA | 81 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(78): Show |
81 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.147-11419dupA | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50738715 | ||||||
chr5:50738715 | TA | T | 103 | a0001c0001t0004g0037 a0001c0001t0006g0195 a0001c0001t0006g0199 others(100): Show |
106 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.147-11419delA | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50738715 | ||||||
chr5:50739210 | C | T | 7 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(4): Show |
7 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.147-10941C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50739210 | |||||||
chr5:50739224 | C | T | 2 | a0001c0001t0004g0035 a0001c0001t0004g0036 |
2 | HG02886.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.147-10927C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50739224 | |||||||
chr5:50739243 | T | C | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.147-10908T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50739243 | |||||||
chr5:50739262 | T | A | 65 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(62): Show |
65 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.147-10889T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50739262 | |||||||
chr5:50739362 | CT | C | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.147-10785delT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50739362 | ||||||
chr5:50739458 | G | A | 1 | a0001c0001t0001g0317 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.147-10693G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50739458 | |||||||
chr5:50739468 | A | G | 1 | a0001c0004t0005g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.147-10683A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50739468 | |||||||
chr5:50739519 | A | T | 1 | a0001c0001t0001g0259 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.147-10632A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50739519 | |||||||
chr5:50739611 | A | G | 1 | a0001c0003t0001g0217 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.147-10540A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50739611 | |||||||
chr5:50739709 | CAT | C | 100 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(97): Show |
103 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.147-10419_147-1041 others(6): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50739709 | ||||||
chr5:50739709 | CATAT | C | 54 | a0001c0001t0002g0066 a0001c0001t0002g0155 a0001c0001t0002g0166 others(51): Show |
54 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.147-10421_147-1041 others(8): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50739709 | ||||||
chr5:50739727 | TATA | T | 6 | a0001c0001t0001g0269 a0001c0001t0002g0067 a0001c0001t0002g0068 others(3): Show |
6 | HG01192.hp1 HG02280.hp2 NA18987.hp2 others(3): Show |
intron_variant | MODIFIER | c.147-10423_147-1042 others(7): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50739727 | |||||||
chr5:50739728 | A | AT | 4 | a0001c0003t0001g0214 a0001c0003t0001g0229 a0001c0003t0001g0236 others(1): Show |
4 | NA18947.hp2 NA18972.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.147-10422dupT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50739728 | ||||||
chr5:50739729 | TA | T | 9 | a0001c0001t0001g0305 a0001c0001t0001g0307 a0001c0002t0003g0070 others(6): Show |
9 | HG00738.hp2 HG02055.hp1 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.147-10421delA | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50739729 | |||||||
chr5:50739729 | TATA | T | 19 | a0001c0001t0001g0058 a0001c0001t0001g0304 a0001c0001t0008g0312 others(16): Show |
19 | HG00438.hp1 HG00609.hp1 HG00609.hp2 others(16): Show |
intron_variant | MODIFIER | c.147-10421_147-1041 others(7): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50739729 | |||||||
chr5:50739730 | A | AT | 4 | a0002c0005t0002g0276 a0002c0005t0009g0270 a0002c0005t0009g0271 others(1): Show |
4 | NA18942.hp1 NA18987.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.147-10420dupT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50739730 | ||||||
chr5:50739730 | A | T | 64 | a0001c0001t0001g0259 a0001c0001t0001g0262 a0001c0001t0001g0263 others(61): Show |
64 | HG00099.hp1 HG00673.hp1 HG00738.hp1 others(61): Show |
intron_variant | MODIFIER | c.147-10421A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50739730 | |||||||
chr5:50739732 | A | T | 209 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(206): Show |
212 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(209): Show |
intron_variant | MODIFIER | c.147-10419A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50739732 | |||||||
chr5:50739732 | AT | A | 11 | a0001c0001t0004g0001 a0001c0001t0004g0035 a0001c0001t0004g0036 others(8): Show |
12 | HG00642.hp1 HG01069.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.147-10398delT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50739732 | ||||||
chr5:50739732 | ATT | A | 18 | a0001c0001t0004g0053 a0001c0001t0004g0054 a0001c0001t0004g0056 others(15): Show |
18 | HG01261.hp2 HG01884.hp1 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.147-10399_147-1039 others(6): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50739732 | ||||||
chr5:50739734 | T | A | 8 | a0001c0001t0007g0188 a0001c0001t0015g0060 a0001c0004t0005g0027 others(5): Show |
8 | HG00733.hp2 HG01109.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.147-10417T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50739734 | |||||||
chr5:50739735 | T | A | 5 | a0001c0001t0015g0059 a0001c0001t0021g0318 a0001c0001t0049g0020 others(2): Show |
5 | HG01346.hp2 HG02922.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.147-10416T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50739735 | |||||||
chr5:50739736 | T | A | 18 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(15): Show |
18 | HG01109.hp2 HG01884.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.147-10415T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50739736 | |||||||
chr5:50739737 | T | A | 1 | a0001c0004t0005g0026 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.147-10414T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50739737 | |||||||
chr5:50739738 | T | A | 10 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(7): Show |
10 | HG01884.hp1 HG03098.hp1 HG03453.hp1 others(7): Show |
intron_variant | MODIFIER | c.147-10413T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50739738 | |||||||
chr5:50739944 | T | A | 1 | a0001c0001t0013g0204 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.147-10207T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50739944 | |||||||
chr5:50740037 | C | T | 1 | a0001c0002t0003g0080 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.147-10114C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50740037 | |||||||
chr5:50740044 | C | T | 1 | a0001c0001t0002g0066 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.147-10107C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50740044 | |||||||
chr5:50740076 | C | A | 113 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(110): Show |
113 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.147-10075C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50740076 | |||||||
chr5:50740089 | T | C | 4 | a0001c0001t0004g0053 a0001c0001t0004g0054 a0001c0001t0004g0055 others(1): Show |
4 | HG01261.hp2 HG02615.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.147-10062T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50740089 | |||||||
chr5:50740216 | A | G | 4 | a0001c0001t0004g0037 a0001c0001t0004g0038 a0001c0001t0004g0046 others(1): Show |
4 | HG01516.hp2 HG02293.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.147-9935A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50740216 | |||||||
chr5:50740391 | T | G | 1 | a0001c0004t0005g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.147-9760T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50740391 | |||||||
chr5:50740417 | TTGGAGCA others(12): Show |
T | 1 | a0001c0012t0038g0008 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.147-9713_147-9695d others(21): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50740417 | ||||||
chr5:50740667 | G | A | 1 | a0001c0003t0001g0233 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.147-9484G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50740667 | |||||||
chr5:50740817 | G | GA | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.147-9320dupA | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50740817 | ||||||
chr5:50740817 | GA | G | 130 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(127): Show |
130 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.147-9320delA | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50740817 | ||||||
chr5:50740817 | GAA | G | 6 | a0001c0003t0001g0239 a0001c0003t0001g0240 a0001c0003t0001g0242 others(3): Show |
6 | HG03490.hp2 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.147-9321_147-9320d others(4): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50740817 | ||||||
chr5:50740983 | T | C | 1 | a0001c0004t0005g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.147-9168T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50740983 | |||||||
chr5:50741008 | A | G | 1 | a0001c0001t0024g0051 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.147-9143A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50741008 | |||||||
chr5:50741021 | G | A | 1 | a0001c0002t0002g0157 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.147-9130G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50741021 | |||||||
chr5:50741040 | A | G | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.147-9111A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50741040 | |||||||
chr5:50741059 | A | C | 1 | a0001c0004t0005g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.147-9092A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50741059 | |||||||
chr5:50741285 | A | C | 1 | a0001c0007t0029g0006 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.147-8866A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50741285 | |||||||
chr5:50741305 | G | A | 4 | a0001c0003t0001g0252 a0001c0003t0011g0223 a0001c0003t0011g0224 others(1): Show |
4 | HG02055.hp1 HG02486.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.147-8846G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50741305 | |||||||
chr5:50741547 | C | T | 299 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(296): Show |
303 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(300): Show |
intron_variant | MODIFIER | c.147-8604C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50741547 | |||||||
chr5:50741617 | A | G | 121 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(118): Show |
124 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.147-8534A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50741617 | |||||||
chr5:50741761 | T | G | 1 | a0001c0012t0038g0008 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.147-8390T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50741761 | |||||||
chr5:50741814 | CT | C | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.147-8323delT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50741814 | ||||||
chr5:50741870 | C | T | 1 | a0001c0001t0008g0312 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.147-8281C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50741870 | |||||||
chr5:50741933 | C | G | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.147-8218C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50741933 | |||||||
chr5:50742052 | C | T | 121 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(118): Show |
124 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.147-8099C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50742052 | |||||||
chr5:50742162 | G | T | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.147-7989G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50742162 | |||||||
chr5:50742528 | A | G | 47 | a0001c0003t0001g0209 a0001c0003t0001g0210 a0001c0003t0001g0211 others(44): Show |
47 | HG00673.hp1 HG00738.hp1 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.147-7623A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50742528 | |||||||
chr5:50742598 | T | C | 1 | a0001c0002t0003g0129 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.147-7553T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50742598 | |||||||
chr5:50742743 | C | T | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.147-7408C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50742743 | |||||||
chr5:50742745 | C | T | 1 | a0001c0002t0002g0173 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.147-7406C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50742745 | |||||||
chr5:50742870 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.147-7281G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50742870 | |||||||
chr5:50742936 | T | A | 146 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(143): Show |
147 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.147-7215T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50742936 | |||||||
chr5:50743064 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.147-7087G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50743064 | |||||||
chr5:50743126 | G | A | 1 | a0001c0001t0001g0269 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.147-7025G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50743126 | |||||||
chr5:50743246 | G | A | 24 | a0001c0003t0001g0209 a0001c0003t0001g0210 a0001c0003t0001g0211 others(21): Show |
24 | HG00738.hp1 HG01243.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.147-6905G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50743246 | |||||||
chr5:50743325 | G | A | 18 | a0001c0003t0001g0220 a0001c0003t0001g0221 a0001c0003t0001g0222 others(15): Show |
18 | HG00673.hp1 HG02056.hp2 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.147-6826G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50743325 | |||||||
chr5:50743397 | G | T | 1 | a0001c0010t0036g0321 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.147-6754G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50743397 | |||||||
chr5:50743531 | A | G | 2 | a0001c0003t0001g0209 a0001c0003t0001g0249 |
2 | HG01261.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.147-6620A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50743531 | |||||||
chr5:50743745 | C | CATAA | 21 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(18): Show |
22 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.147-6384_147-6381d others(6): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50743745 | ||||||
chr5:50743762 | ATAAAT | A | 3 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0304 |
3 | NA18948.hp1 NA18960.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.147-6388_147-6384d others(7): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50743762 | |||||||
chr5:50743909 | A | G | 18 | a0001c0003t0001g0220 a0001c0003t0001g0221 a0001c0003t0001g0222 others(15): Show |
18 | HG00673.hp1 HG02056.hp2 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.147-6242A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50743909 | |||||||
chr5:50743933 | G | T | 1 | a0001c0002t0002g0178 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.147-6218G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50743933 | |||||||
chr5:50744299 | G | A | 1 | a0001c0002t0002g0082 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.147-5852G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50744299 | |||||||
chr5:50744361 | G | C | 4 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(1): Show |
4 | NA18977.hp2 NA19010.hp2 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.147-5790G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50744361 | |||||||
chr5:50744475 | G | A | 1 | a0001c0013t0005g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.147-5676G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50744475 | |||||||
chr5:50744653 | G | A | 1 | a0001c0010t0036g0321 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.147-5498G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50744653 | |||||||
chr5:50744807 | C | A | 3 | a0001c0001t0005g0017 a0001c0001t0005g0018 a0001c0001t0005g0019 |
3 | HG01884.hp1 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.147-5344C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50744807 | |||||||
chr5:50744836 | C | T | 1 | a0001c0007t0029g0006 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.147-5315C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50744836 | |||||||
chr5:50744944 | T | C | 282 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(279): Show |
286 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(283): Show |
intron_variant | MODIFIER | c.147-5207T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50744944 | |||||||
chr5:50744989 | A | G | 2 | a0001c0001t0004g0039 a0001c0001t0004g0040 |
2 | HG00733.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.147-5162A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50744989 | |||||||
chr5:50745038 | TCA | T | 3 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 |
3 | HG03098.hp2 NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.147-5110_147-5109d others(4): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50745038 | ||||||
chr5:50745129 | A | T | 1 | a0001c0002t0002g0082 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.147-5022A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50745129 | |||||||
chr5:50745207 | A | G | 6 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(3): Show |
6 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.147-4944A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50745207 | |||||||
chr5:50745493 | T | A | 12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(9): Show |
12 | HG01884.hp1 HG03098.hp1 HG03453.hp1 others(9): Show |
intron_variant | MODIFIER | c.147-4658T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50745493 | |||||||
chr5:50745563 | T | C | 1 | a0001c0002t0002g0075 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.147-4588T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50745563 | |||||||
chr5:50745575 | T | C | 1 | a0003c0009t0001g0286 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.147-4576T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50745575 | |||||||
chr5:50745806 | T | G | 1 | a0001c0001t0021g0318 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.147-4345T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50745806 | |||||||
chr5:50745984 | T | C | 1 | a0001c0001t0002g0155 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.147-4167T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50745984 | |||||||
chr5:50746108 | A | G | 1 | a0001c0001t0001g0305 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.147-4043A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50746108 | |||||||
chr5:50746375 | G | A | 12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(9): Show |
12 | HG01884.hp1 HG03098.hp1 HG03453.hp1 others(9): Show |
intron_variant | MODIFIER | c.147-3776G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50746375 | |||||||
chr5:50746446 | C | T | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.147-3705C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50746446 | |||||||
chr5:50746459 | A | G | 1 | a0001c0001t0008g0313 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.147-3692A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50746459 | |||||||
chr5:50746506 | T | C | 1 | a0001c0001t0001g0272 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.147-3645T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50746506 | |||||||
chr5:50746560 | A | G | 1 | a0001c0010t0036g0321 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.147-3591A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50746560 | |||||||
chr5:50746642 | A | G | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.147-3509A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50746642 | |||||||
chr5:50746670 | A | T | 1 | a0001c0003t0001g0248 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.147-3481A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50746670 | |||||||
chr5:50746729 | C | A | 3 | a0001c0001t0004g0001 a0001c0001t0004g0048 a0001c0001t0004g0049 |
5 | HG01069.hp2 HG01071.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.147-3422C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50746729 | |||||||
chr5:50746802 | A | C | 1 | a0001c0002t0002g0072 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.147-3349A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50746802 | |||||||
chr5:50746818 | G | A | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.147-3333G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50746818 | |||||||
chr5:50746918 | A | T | 1 | a0001c0007t0029g0006 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.147-3233A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50746918 | |||||||
chr5:50747044 | T | C | 11 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0001t0007g0184 others(8): Show |
11 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.147-3107T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50747044 | |||||||
chr5:50747131 | T | C | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.147-3020T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50747131 | |||||||
chr5:50747138 | A | G | 284 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(281): Show |
288 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(285): Show |
intron_variant | MODIFIER | c.147-3013A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50747138 | |||||||
chr5:50747138 | A | T | 11 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0001t0007g0184 others(8): Show |
11 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.147-3013A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50747138 | |||||||
chr5:50747141 | G | GTTT | 21 | a0001c0003t0001g0209 a0001c0003t0001g0210 a0001c0003t0001g0211 others(18): Show |
21 | HG00738.hp1 HG01255.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.147-3004_147-3002d others(5): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50747141 | ||||||
chr5:50747141 | G | T | 1 | a0001c0001t0004g0041 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.147-3010G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50747141 | |||||||
chr5:50747149 | TG | T | 67 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0155 others(64): Show |
67 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.147-3001delG | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50747149 | |||||||
chr5:50747150 | G | T | 221 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(218): Show |
227 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(224): Show |
intron_variant | MODIFIER | c.147-3001G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50747150 | |||||||
chr5:50747152 | T | G | 1 | a0001c0001t0002g0068 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.147-2999T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50747152 | |||||||
chr5:50747153 | T | G | 231 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(228): Show |
235 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(232): Show |
intron_variant | MODIFIER | c.147-2998T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50747153 | |||||||
chr5:50747154 | G | GT | 14 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(11): Show |
14 | HG01109.hp1 HG02486.hp2 HG02886.hp1 others(11): Show |
intron_variant | MODIFIER | c.147-2994dupT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50747154 | ||||||
chr5:50747154 | G | T | 263 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(260): Show |
267 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(264): Show |
intron_variant | MODIFIER | c.147-2997G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50747154 | |||||||
chr5:50747155 | T | G | 21 | a0001c0003t0001g0209 a0001c0003t0001g0210 a0001c0003t0001g0211 others(18): Show |
21 | HG00738.hp1 HG01255.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.147-2996T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50747155 | |||||||
chr5:50747158 | G | GTT | 5 | a0001c0001t0001g0292 a0001c0001t0001g0305 a0002c0005t0002g0276 others(2): Show |
5 | HG00738.hp2 HG01975.hp1 NA18987.hp1 others(2): Show |
intron_variant | MODIFIER | c.147-2990_147-2989d others(4): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50747158 | ||||||
chr5:50747158 | G | T | 29 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(26): Show |
29 | HG00738.hp1 HG01192.hp1 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.147-2993G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50747158 | |||||||
chr5:50747163 | G | GT | 14 | a0001c0001t0001g0307 a0001c0001t0001g0308 a0001c0001t0005g0010 others(11): Show |
14 | HG01074.hp2 HG01361.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.147-2971dupT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50747163 | ||||||
chr5:50747163 | G | GTT | 54 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(51): Show |
54 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.147-2972_147-2971d others(4): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50747163 | ||||||
chr5:50747163 | G | GTTT | 31 | a0001c0001t0001g0063 a0001c0001t0001g0259 a0001c0001t0001g0262 others(28): Show |
31 | HG00673.hp1 HG01069.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.147-2973_147-2971d others(5): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50747163 | ||||||
chr5:50747163 | G | T | 40 | a0001c0001t0001g0292 a0001c0001t0001g0305 a0001c0001t0002g0066 others(37): Show |
40 | HG00738.hp1 HG00738.hp2 HG01192.hp1 others(37): Show |
intron_variant | MODIFIER | c.147-2988G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50747163 | |||||||
chr5:50747168 | T | G | 48 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(45): Show |
52 | HG00597.hp1 HG00639.hp1 HG01109.hp2 others(49): Show |
intron_variant | MODIFIER | c.147-2983T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50747168 | |||||||
chr5:50747170 | T | G | 12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(9): Show |
12 | HG01884.hp1 HG03098.hp1 HG03453.hp1 others(9): Show |
intron_variant | MODIFIER | c.147-2981T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50747170 | |||||||
chr5:50747281 | G | A | 1 | a0001c0001t0002g0169 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.147-2870G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50747281 | |||||||
chr5:50747392 | A | G | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.147-2759A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50747392 | |||||||
chr5:50747413 | A | G | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.147-2738A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50747413 | |||||||
chr5:50747761 | C | CT | 54 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0155 others(51): Show |
54 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.147-2361dupT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50747761 | ||||||
chr5:50747761 | C | CTT | 20 | a0001c0001t0002g0166 a0001c0001t0002g0168 a0001c0001t0004g0053 others(17): Show |
20 | HG01261.hp2 HG01346.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.147-2362_147-2361d others(4): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50747761 | ||||||
chr5:50747761 | CT | C | 30 | a0001c0001t0001g0064 a0001c0001t0001g0256 a0001c0001t0001g0262 others(27): Show |
30 | HG00099.hp1 HG00673.hp1 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.147-2361delT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50747761 | ||||||
chr5:50747761 | CTT | C | 48 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(45): Show |
48 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.147-2362_147-2361d others(4): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50747761 | ||||||
chr5:50747761 | CTTTTTTT others(1): Show |
C | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.147-2368_147-2361d others(10): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50747761 | ||||||
chr5:50747761 | CTTTTTTT others(5): Show |
C | 1 | a0001c0002t0003g0131 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.147-2372_147-2361d others(14): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50747761 | ||||||
chr5:50747761 | CTTTTTTT others(9): Show |
C | 12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(9): Show |
12 | HG01884.hp1 HG03098.hp1 HG03453.hp1 others(9): Show |
intron_variant | MODIFIER | c.147-2376_147-2361d others(18): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50747761 | ||||||
chr5:50747761 | CTTTTTTT others(11): Show |
C | 3 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 |
3 | HG03098.hp2 NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.147-2378_147-2361d others(20): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50747761 | ||||||
chr5:50747777 | T | G | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.147-2374T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50747777 | |||||||
chr5:50747803 | C | A | 4 | a0001c0001t0004g0034 a0001c0001t0004g0039 a0001c0001t0004g0040 others(1): Show |
4 | HG00733.hp1 HG02602.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.147-2348C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50747803 | |||||||
chr5:50747818 | G | A | 113 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(110): Show |
113 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.147-2333G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50747818 | |||||||
chr5:50747821 | A | G | 1 | a0001c0001t0001g0268 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.147-2330A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50747821 | |||||||
chr5:50747927 | C | T | 7 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(4): Show |
7 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.147-2224C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50747927 | |||||||
chr5:50747959 | A | G | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.147-2192A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50747959 | |||||||
chr5:50747976 | A | G | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.147-2175A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50747976 | |||||||
chr5:50748021 | A | G | 65 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(62): Show |
65 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.147-2130A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50748021 | |||||||
chr5:50748193 | T | TTG | 125 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(122): Show |
128 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(125): Show |
intron_variant | MODIFIER | c.147-1940_147-1939d others(4): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50748193 | ||||||
chr5:50748193 | TTG | T | 151 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(148): Show |
152 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(149): Show |
intron_variant | MODIFIER | c.147-1940_147-1939d others(4): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50748193 | ||||||
chr5:50748277 | C | T | 1 | a0002c0005t0009g0271 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.147-1874C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50748277 | |||||||
chr5:50748278 | A | G | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.147-1873A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50748278 | |||||||
chr5:50748491 | G | A | 1 | a0001c0001t0007g0187 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.147-1660G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50748491 | |||||||
chr5:50748788 | G | C | 121 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(118): Show |
124 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.147-1363G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50748788 | |||||||
chr5:50748896 | C | A | 1 | a0001c0001t0024g0051 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.147-1255C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50748896 | |||||||
chr5:50748931 | T | G | 1 | a0003c0009t0001g0286 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.147-1220T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50748931 | |||||||
chr5:50749039 | C | G | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.147-1112C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50749039 | |||||||
chr5:50749197 | T | C | 8 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0048 others(5): Show |
10 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.147-954T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50749197 | |||||||
chr5:50749450 | T | TA | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.147-695dupA | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50749450 | ||||||
chr5:50749450 | TA | T | 5 | a0001c0001t0007g0186 a0001c0001t0007g0187 a0001c0001t0007g0188 others(2): Show |
5 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.147-695delA | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50749450 | ||||||
chr5:50749487 | G | C | 1 | a0001c0002t0002g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.147-664G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50749487 | |||||||
chr5:50749499 | A | G | 1 | a0001c0002t0002g0150 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.147-652A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50749499 | |||||||
chr5:50749530 | G | A | 1 | a0001c0012t0038g0008 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.147-621G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50749530 | |||||||
chr5:50749567 | A | G | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.147-584A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50749567 | |||||||
chr5:50749991 | C | T | 43 | a0001c0003t0001g0209 a0001c0003t0001g0210 a0001c0003t0001g0211 others(40): Show |
43 | HG00673.hp1 HG00738.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.147-160C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50749991 | |||||||
chr5:50750126 | CT | C | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.147-19delT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 50750126 | ||||||
chr5:50750133 | G | T | 155 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(152): Show |
159 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(156): Show |
intron_variant | MODIFIER | c.147-18G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 2/25 | chr5 | 50750133 | |||||||
chr5:50750220 | G | A | 2 | a0001c0001t0030g0005 a0001c0007t0029g0006 |
2 | HG02257.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.184+32G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50750220 | |||||||
chr5:50750239 | T | G | 1 | a0001c0001t0001g0256 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.184+51T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50750239 | |||||||
chr5:50750297 | G | A | 11 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0001t0007g0184 others(8): Show |
11 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.184+109G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50750297 | |||||||
chr5:50750305 | A | G | 265 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(262): Show |
269 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(266): Show |
intron_variant | MODIFIER | c.184+117A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50750305 | |||||||
chr5:50750372 | G | A | 2 | a0001c0006t0004g0322 a0001c0006t0020g0045 |
2 | NA18940.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.184+184G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50750372 | |||||||
chr5:50750395 | T | C | 1 | a0001c0004t0005g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.184+207T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50750395 | |||||||
chr5:50750642 | T | G | 31 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(28): Show |
32 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.184+454T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50750642 | |||||||
chr5:50750663 | A | T | 1 | a0001c0002t0003g0128 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.184+475A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50750663 | |||||||
chr5:50750673 | G | T | 1 | a0001c0002t0003g0120 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.184+485G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50750673 | |||||||
chr5:50750783 | A | C | 1 | a0001c0004t0005g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.184+595A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50750783 | |||||||
chr5:50750919 | G | GA | 109 | a0001c0002t0002g0065 a0001c0002t0002g0072 a0001c0002t0002g0074 others(106): Show |
112 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.184+736dupA | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50750919 | ||||||
chr5:50750964 | A | G | 8 | a0001c0001t0001g0261 a0001c0001t0001g0266 a0002c0005t0002g0276 others(5): Show |
8 | NA18942.hp1 NA18978.hp1 NA18987.hp1 others(5): Show |
intron_variant | MODIFIER | c.184+776A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50750964 | |||||||
chr5:50751103 | TTA | T | 265 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(262): Show |
269 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(266): Show |
intron_variant | MODIFIER | c.184+916_184+917del others(2): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50751103 | |||||||
chr5:50751106 | A | G | 265 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(262): Show |
269 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(266): Show |
intron_variant | MODIFIER | c.184+918A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50751106 | |||||||
chr5:50751180 | G | A | 1 | a0001c0001t0007g0186 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.184+992G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50751180 | |||||||
chr5:50751278 | C | T | 1 | a0001c0002t0002g0091 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.184+1090C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50751278 | |||||||
chr5:50751280 | G | A | 3 | a0001c0001t0007g0182 a0001c0001t0007g0184 a0001c0001t0027g0185 |
3 | HG02145.hp2 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.184+1092G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50751280 | |||||||
chr5:50751372 | T | C | 1 | a0001c0001t0004g0052 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.184+1184T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50751372 | |||||||
chr5:50751431 | G | A | 2 | a0001c0002t0003g0069 a0001c0002t0003g0070 |
2 | HG02148.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.184+1243G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50751431 | |||||||
chr5:50751574 | A | T | 1 | a0001c0002t0002g0110 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.184+1386A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50751574 | |||||||
chr5:50751599 | T | C | 2 | a0001c0001t0001g0256 a0001c0001t0001g0282 |
2 | NA18951.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.184+1411T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50751599 | |||||||
chr5:50751791 | C | A | 1 | a0001c0012t0038g0008 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.184+1603C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50751791 | |||||||
chr5:50751840 | T | C | 1 | a0001c0001t0016g0283 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.184+1652T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50751840 | |||||||
chr5:50751857 | C | T | 2 | a0001c0002t0003g0095 a0001c0002t0003g0096 |
2 | HG01074.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.184+1669C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50751857 | |||||||
chr5:50751878 | C | A | 1 | a0001c0001t0002g0155 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.184+1690C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50751878 | |||||||
chr5:50751898 | G | C | 1 | a0001c0002t0050g0177 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.184+1710G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50751898 | |||||||
chr5:50752032 | C | A | 1 | a0001c0001t0001g0305 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.184+1844C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50752032 | |||||||
chr5:50752115 | G | A | 1 | a0001c0007t0029g0006 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.184+1927G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50752115 | |||||||
chr5:50752124 | T | A | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.184+1936T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50752124 | |||||||
chr5:50752125 | A | T | 260 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(257): Show |
264 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(261): Show |
intron_variant | MODIFIER | c.184+1937A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50752125 | |||||||
chr5:50752313 | C | T | 1 | a0001c0002t0003g0073 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.184+2125C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50752313 | |||||||
chr5:50752598 | C | T | 3 | a0001c0001t0030g0005 a0001c0007t0028g0007 a0001c0007t0029g0006 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.184+2410C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50752598 | |||||||
chr5:50752797 | A | G | 2 | a0001c0003t0001g0221 a0001c0003t0001g0222 |
2 | NA18946.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.184+2609A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50752797 | |||||||
chr5:50752987 | G | A | 1 | a0001c0002t0003g0079 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.184+2799G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50752987 | |||||||
chr5:50752988 | C | A | 113 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(110): Show |
113 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.184+2800C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50752988 | |||||||
chr5:50753079 | G | A | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.184+2891G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50753079 | |||||||
chr5:50753256 | C | T | 6 | a0001c0002t0002g0065 a0001c0002t0002g0148 a0001c0002t0002g0149 others(3): Show |
6 | HG01071.hp2 HG02683.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.184+3068C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50753256 | |||||||
chr5:50753376 | C | A | 1 | a0001c0002t0002g0157 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.184+3188C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50753376 | |||||||
chr5:50753458 | A | G | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.184+3270A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50753458 | |||||||
chr5:50753544 | G | A | 1 | a0001c0007t0028g0007 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.184+3356G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50753544 | |||||||
chr5:50753626 | T | G | 1 | a0001c0001t0001g0256 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.184+3438T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50753626 | |||||||
chr5:50753740 | A | C | 1 | a0001c0001t0001g0256 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.184+3552A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50753740 | |||||||
chr5:50753834 | G | T | 1 | a0001c0002t0003g0080 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.184+3646G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50753834 | |||||||
chr5:50753873 | C | A | 1 | a0001c0004t0005g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.184+3685C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50753873 | |||||||
chr5:50754048 | A | G | 7 | a0001c0001t0002g0155 a0001c0001t0002g0166 a0001c0001t0002g0167 others(4): Show |
7 | HG01891.hp2 HG02717.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.184+3860A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50754048 | |||||||
chr5:50754116 | C | CAT | 19 | a0001c0001t0005g0013 a0001c0001t0007g0186 a0001c0001t0007g0188 others(16): Show |
19 | HG00544.hp2 HG00639.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.184+3962_184+3963d others(4): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754116 | ||||||
chr5:50754116 | C | CATAT | 10 | a0001c0001t0002g0068 a0001c0001t0005g0014 a0001c0001t0005g0015 others(7): Show |
10 | HG00597.hp2 HG00639.hp1 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.184+3960_184+3963d others(6): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754116 | ||||||
chr5:50754116 | C | CATATAT | 15 | a0001c0001t0001g0180 a0001c0001t0002g0067 a0001c0001t0005g0016 others(12): Show |
15 | HG01071.hp2 HG02056.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.184+3958_184+3963d others(8): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754116 | ||||||
chr5:50754116 | C | CATATATA others(1): Show |
14 | a0001c0001t0005g0024 a0001c0001t0006g0199 a0001c0001t0016g0283 others(11): Show |
14 | HG00558.hp1 HG01243.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.184+3956_184+3963d others(10): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754116 | ||||||
chr5:50754116 | C | CATATATA others(3): Show |
12 | a0001c0001t0005g0017 a0001c0001t0006g0196 a0001c0001t0008g0310 others(9): Show |
12 | HG00609.hp1 HG01167.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.184+3954_184+3963d others(12): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754116 | ||||||
chr5:50754116 | C | CATATATA others(5): Show |
14 | a0001c0001t0001g0267 a0001c0001t0001g0302 a0001c0001t0005g0018 others(11): Show |
14 | HG01069.hp1 HG01169.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.184+3952_184+3963d others(14): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754116 | ||||||
chr5:50754116 | C | CATATATA others(7): Show |
12 | a0001c0001t0001g0300 a0001c0001t0006g0198 a0001c0001t0006g0203 others(9): Show |
12 | HG00438.hp1 HG00738.hp1 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.184+3950_184+3963d others(16): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754116 | ||||||
chr5:50754116 | C | CATATATA others(9): Show |
21 | a0001c0001t0001g0272 a0001c0001t0001g0307 a0001c0001t0001g0308 others(18): Show |
22 | HG01255.hp2 HG01361.hp2 HG01934.hp2 others(19): Show |
intron_variant | MODIFIER | c.184+3948_184+3963d others(18): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754116 | ||||||
chr5:50754116 | C | CATATATA others(11): Show |
17 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0264 others(14): Show |
17 | HG00438.hp2 HG01257.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.184+3946_184+3963d others(20): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754116 | ||||||
chr5:50754116 | C | CATATATA others(13): Show |
8 | a0001c0001t0001g0269 a0001c0001t0001g0293 a0001c0001t0001g0296 others(5): Show |
8 | HG01261.hp1 HG02132.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.184+3944_184+3963d others(22): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754116 | ||||||
chr5:50754116 | C | CATATATA others(15): Show |
8 | a0001c0001t0001g0062 a0001c0001t0001g0274 a0001c0001t0001g0282 others(5): Show |
8 | HG00738.hp2 HG01081.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.184+3942_184+3963d others(24): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754116 | ||||||
chr5:50754116 | C | CATATATA others(17): Show |
6 | a0001c0001t0001g0061 a0001c0001t0001g0289 a0001c0001t0001g0291 others(3): Show |
6 | HG03704.hp1 NA18948.hp1 NA19006.hp1 others(3): Show |
intron_variant | MODIFIER | c.184+3940_184+3963d others(26): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754116 | ||||||
chr5:50754116 | C | CATATATA others(19): Show |
5 | a0001c0001t0001g0294 a0001c0001t0001g0297 a0001c0001t0047g0295 others(2): Show |
5 | HG02055.hp1 HG02129.hp1 NA18940.hp2 others(2): Show |
intron_variant | MODIFIER | c.184+3938_184+3963d others(28): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754116 | ||||||
chr5:50754116 | C | CATATATA others(21): Show |
4 | a0001c0001t0001g0261 a0001c0001t0001g0290 a0001c0001t0001g0303 others(1): Show |
4 | HG02155.hp2 NA18960.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.184+3936_184+3963d others(30): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754116 | ||||||
chr5:50754116 | C | CATATATA others(23): Show |
2 | a0001c0001t0001g0266 a0001c0003t0001g0216 |
2 | HG02300.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.184+3934_184+3963d others(32): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754116 | ||||||
chr5:50754116 | C | CATATATA others(27): Show |
1 | a0001c0001t0005g0019 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.184+3930_184+3963d others(36): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754116 | ||||||
chr5:50754118 | T | TATATATA others(16): Show |
1 | a0001c0001t0001g0256 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.184+3931_184+3953d others(25): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754118 | ||||||
chr5:50754124 | T | TATATATA others(15): Show |
1 | a0001c0001t0001g0268 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.184+3957_184+3958i others(24): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754124 | ||||||
chr5:50754134 | TATATATA others(19): Show |
T | 3 | a0001c0002t0003g0099 a0001c0002t0003g0100 a0001c0002t0003g0123 |
3 | HG01516.hp1 HG02735.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.184+3948_184+3973d others(28): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754134 | ||||||
chr5:50754134 | TATATATA others(21): Show |
T | 4 | a0001c0002t0002g0109 a0001c0002t0002g0110 a0001c0002t0002g0111 others(1): Show |
4 | HG01433.hp1 HG02622.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.184+3948_184+3975d others(30): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754134 | ||||||
chr5:50754136 | TATATATA others(19): Show |
T | 50 | a0001c0002t0003g0002 a0001c0002t0003g0003 a0001c0002t0003g0069 others(47): Show |
53 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.184+3950_184+3975d others(28): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754136 | ||||||
chr5:50754138 | T | C | 1 | a0001c0003t0001g0252 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.184+3950T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50754138 | |||||||
chr5:50754140 | T | C | 1 | a0001c0003t0001g0242 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.184+3952T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50754140 | |||||||
chr5:50754142 | TATATATA others(3): Show |
T | 2 | a0001c0001t0007g0181 a0001c0003t0001g0252 |
2 | HG01167.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.184+3956_184+3965d others(12): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754142 | ||||||
chr5:50754144 | T | C | 2 | a0002c0005t0009g0270 a0002c0005t0009g0287 |
2 | NA19063.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.184+3956T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50754144 | |||||||
chr5:50754144 | T | TATATATA others(21): Show |
2 | a0001c0003t0001g0228 a0001c0003t0001g0229 |
2 | NA18947.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.184+3963_184+3964i others(30): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754144 | ||||||
chr5:50754144 | TATATATA others(5): Show |
T | 1 | a0001c0003t0001g0242 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.184+3958_184+3969d others(14): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754144 | ||||||
chr5:50754146 | T | TATATATA others(7): Show |
2 | a0001c0001t0001g0263 a0001c0001t0008g0311 |
2 | HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.184+3963_184+3964i others(16): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754146 | ||||||
chr5:50754146 | T | TATATATA others(13): Show |
1 | a0001c0001t0001g0262 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.184+3963_184+3964i others(22): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754146 | ||||||
chr5:50754148 | T | C | 3 | a0001c0001t0001g0058 a0001c0001t0008g0299 a0001c0012t0038g0008 |
3 | HG02809.hp1 HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.184+3960T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50754148 | |||||||
chr5:50754148 | T | TATATATA others(9): Show |
1 | a0001c0001t0006g0208 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.184+3963_184+3964i others(18): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754148 | ||||||
chr5:50754148 | T | TATATATA others(11): Show |
1 | a0001c0001t0006g0207 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.184+3963_184+3964i others(20): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754148 | ||||||
chr5:50754150 | T | C | 9 | a0001c0001t0004g0001 a0001c0001t0004g0037 a0001c0001t0004g0046 others(6): Show |
9 | HG01081.hp2 HG01516.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.184+3962T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50754150 | |||||||
chr5:50754150 | T | TAC | 6 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0040 others(3): Show |
7 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.184+3992_184+3993d others(4): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754150 | ||||||
chr5:50754150 | T | TATAC | 3 | a0001c0001t0004g0035 a0001c0001t0004g0048 a0001c0001t0004g0049 |
3 | HG01934.hp1 HG01975.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.184+3963_184+3964i others(6): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754150 | ||||||
chr5:50754150 | T | TATACAC | 3 | a0001c0001t0004g0038 a0001c0001t0004g0054 a0001c0001t0007g0182 |
3 | HG02293.hp2 HG02615.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.184+3963_184+3964i others(8): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754150 | ||||||
chr5:50754150 | T | TATATACA others(9): Show |
1 | a0001c0001t0005g0010 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.184+3963_184+3964i others(18): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754150 | ||||||
chr5:50754150 | T | TATATATA others(3): Show |
1 | a0001c0001t0004g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.184+3963_184+3964i others(12): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754150 | ||||||
chr5:50754150 | T | TATATATA others(7): Show |
1 | a0001c0001t0037g0009 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.184+3963_184+3964i others(16): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754150 | ||||||
chr5:50754150 | T | TATATATA others(13): Show |
2 | a0001c0001t0005g0011 a0001c0001t0005g0025 |
2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.184+3963_184+3964i others(22): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754150 | ||||||
chr5:50754150 | T | TATATATA others(11): Show |
1 | a0001c0004t0005g0026 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.184+3963_184+3964i others(20): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754150 | ||||||
chr5:50754150 | T | TATATATA others(9): Show |
1 | a0001c0001t0004g0055 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.184+3963_184+3964i others(18): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754150 | ||||||
chr5:50754150 | T | TATATATA others(19): Show |
1 | a0001c0004t0005g0029 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.184+3963_184+3964i others(28): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754150 | ||||||
chr5:50754150 | T | TATATATA others(13): Show |
1 | a0001c0001t0025g0315 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.184+3963_184+3964i others(22): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754150 | ||||||
chr5:50754150 | T | TATATATA others(9): Show |
1 | a0001c0001t0001g0273 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.184+3963_184+3964i others(18): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754150 | ||||||
chr5:50754150 | T | TATATATA others(15): Show |
1 | a0001c0004t0005g0027 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.184+3963_184+3964i others(24): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754150 | ||||||
chr5:50754150 | T | TATATATA others(15): Show |
2 | a0001c0001t0008g0312 a0001c0001t0008g0313 |
2 | HG01884.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.184+3963_184+3964i others(24): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754150 | ||||||
chr5:50754150 | T | TATATATA others(11): Show |
2 | a0001c0001t0008g0258 a0001c0001t0034g0298 |
2 | HG00544.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.184+3963_184+3964i others(20): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754150 | ||||||
chr5:50754150 | T | TATATATA others(17): Show |
3 | a0001c0001t0008g0314 a0001c0001t0008g0316 a0001c0001t0033g0257 |
3 | HG02622.hp2 HG02630.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.184+3963_184+3964i others(26): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754150 | ||||||
chr5:50754150 | T | TATATATA others(13): Show |
2 | a0001c0001t0001g0265 a0002c0005t0009g0271 |
2 | HG00673.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.184+3963_184+3964i others(22): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754150 | ||||||
chr5:50754150 | T | TATATATA others(25): Show |
1 | a0001c0004t0005g0031 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.184+3963_184+3964i others(34): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754150 | ||||||
chr5:50754150 | T | TATATATA others(21): Show |
1 | a0001c0004t0005g0028 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.184+3963_184+3964i others(30): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754150 | ||||||
chr5:50754150 | T | TATATATA others(17): Show |
1 | a0001c0001t0004g0042 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.184+3963_184+3964i others(26): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754150 | ||||||
chr5:50754150 | T | TATATATA others(19): Show |
1 | a0001c0001t0001g0259 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.184+3963_184+3964i others(28): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754150 | ||||||
chr5:50754150 | T | TATATATA others(31): Show |
1 | a0001c0004t0005g0030 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.184+3963_184+3964i others(40): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754150 | ||||||
chr5:50754150 | T | TATATATA others(27): Show |
1 | a0001c0001t0001g0292 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.184+3963_184+3964i others(36): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754150 | ||||||
chr5:50754152 | C | T | 164 | a0001c0001t0001g0058 a0001c0001t0001g0272 a0001c0001t0001g0282 others(161): Show |
165 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(162): Show |
intron_variant | MODIFIER | c.184+3964C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50754152 | |||||||
chr5:50754154 | C | CATATACA others(3): Show |
1 | a0001c0001t0008g0310 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.184+3967_184+3968i others(12): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754154 | ||||||
chr5:50754154 | C | T | 181 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(178): Show |
181 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(178): Show |
intron_variant | MODIFIER | c.184+3966C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50754154 | |||||||
chr5:50754156 | C | T | 159 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(156): Show |
160 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.184+3968C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50754156 | |||||||
chr5:50754158 | C | T | 91 | a0001c0001t0001g0272 a0001c0001t0001g0282 a0001c0001t0001g0292 others(88): Show |
91 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.184+3970C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50754158 | |||||||
chr5:50754160 | C | T | 86 | a0001c0001t0001g0272 a0001c0001t0002g0066 a0001c0001t0002g0067 others(83): Show |
86 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.184+3972C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50754160 | |||||||
chr5:50754162 | C | T | 25 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(22): Show |
25 | HG00673.hp1 HG01192.hp1 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.184+3974C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50754162 | |||||||
chr5:50754164 | C | T | 2 | a0001c0001t0002g0067 a0001c0001t0002g0068 |
2 | HG01192.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.184+3976C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50754164 | |||||||
chr5:50754176 | CACACATA others(1): Show |
C | 4 | a0001c0001t0001g0317 a0001c0001t0021g0318 a0002c0005t0009g0270 others(1): Show |
4 | HG01346.hp2 NA18962.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.184+3990_184+3997d others(10): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754176 | ||||||
chr5:50754180 | CAT | C | 11 | a0001c0001t0002g0066 a0001c0001t0002g0166 a0001c0001t0002g0167 others(8): Show |
11 | HG00642.hp2 HG01891.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.184+4003_184+4004d others(4): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754180 | ||||||
chr5:50754180 | CATAT | C | 3 | a0001c0001t0007g0181 a0001c0003t0001g0242 a0001c0003t0001g0252 |
3 | HG01167.hp1 HG02486.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.184+4001_184+4004d others(6): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50754180 | ||||||
chr5:50754182 | T | C | 272 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(269): Show |
276 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(273): Show |
intron_variant | MODIFIER | c.184+3994T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50754182 | |||||||
chr5:50754184 | T | C | 142 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(139): Show |
143 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.184+3996T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50754184 | |||||||
chr5:50754186 | T | C | 1 | a0001c0001t0001g0256 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.184+3998T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50754186 | |||||||
chr5:50754230 | C | T | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.184+4042C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50754230 | |||||||
chr5:50754308 | A | G | 1 | a0001c0001t0007g0181 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.184+4120A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50754308 | |||||||
chr5:50754324 | C | T | 1 | a0001c0001t0001g0302 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.184+4136C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50754324 | |||||||
chr5:50754461 | G | C | 1 | a0001c0007t0028g0007 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.184+4273G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50754461 | |||||||
chr5:50754495 | C | G | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.184+4307C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50754495 | |||||||
chr5:50754496 | C | G | 11 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0001t0007g0184 others(8): Show |
11 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.184+4308C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50754496 | |||||||
chr5:50754555 | T | G | 1 | a0001c0004t0005g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.184+4367T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50754555 | |||||||
chr5:50754625 | A | G | 1 | a0001c0001t0022g0047 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.184+4437A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50754625 | |||||||
chr5:50754646 | G | A | 7 | a0001c0001t0002g0155 a0001c0001t0002g0166 a0001c0001t0002g0167 others(4): Show |
7 | HG01891.hp2 HG02717.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.184+4458G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50754646 | |||||||
chr5:50754829 | A | G | 1 | a0001c0010t0036g0321 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.184+4641A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50754829 | |||||||
chr5:50754888 | A | G | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.184+4700A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50754888 | |||||||
chr5:50754965 | G | T | 1 | a0001c0001t0001g0256 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.185-4678G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50754965 | |||||||
chr5:50754977 | G | C | 117 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(114): Show |
120 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.185-4666G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50754977 | |||||||
chr5:50755045 | C | T | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.185-4598C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50755045 | |||||||
chr5:50755082 | C | A | 2 | a0001c0001t0007g0188 a0001c0001t0007g0189 |
2 | HG00733.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.185-4561C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50755082 | |||||||
chr5:50755257 | T | G | 1 | a0001c0001t0001g0256 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.185-4386T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50755257 | |||||||
chr5:50755423 | T | A | 1 | a0001c0001t0005g0021 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.185-4220T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50755423 | |||||||
chr5:50755486 | G | A | 113 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(110): Show |
113 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.185-4157G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50755486 | |||||||
chr5:50755516 | C | T | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.185-4127C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50755516 | |||||||
chr5:50755592 | T | G | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.185-4051T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50755592 | |||||||
chr5:50755724 | A | C | 12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(9): Show |
12 | HG01884.hp1 HG03098.hp1 HG03453.hp1 others(9): Show |
intron_variant | MODIFIER | c.185-3919A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50755724 | |||||||
chr5:50755888 | G | A | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.185-3755G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50755888 | |||||||
chr5:50755891 | C | T | 1 | a0001c0001t0021g0318 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.185-3752C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50755891 | |||||||
chr5:50756069 | G | A | 295 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(292): Show |
299 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(296): Show |
intron_variant | MODIFIER | c.185-3574G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50756069 | |||||||
chr5:50756132 | G | A | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.185-3511G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50756132 | |||||||
chr5:50756221 | G | A | 1 | a0001c0002t0041g0172 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.185-3422G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50756221 | |||||||
chr5:50756227 | G | T | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.185-3416G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50756227 | |||||||
chr5:50756325 | A | G | 3 | a0001c0001t0030g0005 a0001c0007t0028g0007 a0001c0007t0029g0006 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.185-3318A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50756325 | |||||||
chr5:50756330 | G | A | 3 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 |
3 | HG01192.hp1 HG02280.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.185-3313G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50756330 | |||||||
chr5:50756346 | G | A | 1 | a0001c0003t0001g0247 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.185-3297G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50756346 | |||||||
chr5:50756354 | C | G | 1 | a0001c0001t0001g0305 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.185-3289C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50756354 | |||||||
chr5:50756507 | A | G | 3 | a0001c0001t0006g0196 a0001c0001t0006g0197 a0001c0001t0006g0198 |
3 | HG01167.hp2 HG01169.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.185-3136A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50756507 | |||||||
chr5:50756544 | C | G | 1 | a0001c0002t0003g0080 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.185-3099C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50756544 | |||||||
chr5:50756662 | T | C | 9 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(6): Show |
9 | NA18944.hp1 NA18957.hp1 NA18977.hp2 others(6): Show |
intron_variant | MODIFIER | c.185-2981T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50756662 | |||||||
chr5:50756667 | T | G | 282 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(279): Show |
286 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(283): Show |
intron_variant | MODIFIER | c.185-2976T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50756667 | |||||||
chr5:50756716 | C | T | 5 | a0001c0001t0007g0186 a0001c0001t0007g0187 a0001c0001t0007g0188 others(2): Show |
5 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.185-2927C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50756716 | |||||||
chr5:50756850 | C | T | 4 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(1): Show |
4 | HG02486.hp2 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.185-2793C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50756850 | |||||||
chr5:50756876 | A | G | 1 | a0001c0004t0005g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.185-2767A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50756876 | |||||||
chr5:50756966 | T | C | 271 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(268): Show |
275 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(272): Show |
intron_variant | MODIFIER | c.185-2677T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50756966 | |||||||
chr5:50756994 | G | A | 1 | a0001c0001t0007g0189 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.185-2649G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50756994 | |||||||
chr5:50757054 | C | A | 282 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(279): Show |
286 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(283): Show |
intron_variant | MODIFIER | c.185-2589C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50757054 | |||||||
chr5:50757169 | G | T | 1 | a0001c0003t0001g0249 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.185-2474G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50757169 | |||||||
chr5:50757181 | G | A | 295 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(292): Show |
299 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(296): Show |
intron_variant | MODIFIER | c.185-2462G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50757181 | |||||||
chr5:50757421 | A | G | 1 | a0001c0002t0002g0091 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.185-2222A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50757421 | |||||||
chr5:50757481 | C | T | 1 | a0001c0012t0038g0008 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.185-2162C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50757481 | |||||||
chr5:50757666 | C | T | 1 | a0001c0002t0018g0134 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.185-1977C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50757666 | |||||||
chr5:50757710 | T | C | 269 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(266): Show |
273 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(270): Show |
intron_variant | MODIFIER | c.185-1933T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50757710 | |||||||
chr5:50757827 | G | A | 1 | a0001c0002t0003g0123 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.185-1816G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50757827 | |||||||
chr5:50757832 | T | C | 2 | a0001c0002t0003g0069 a0001c0002t0003g0070 |
2 | HG02148.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.185-1811T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50757832 | |||||||
chr5:50758029 | G | T | 40 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(37): Show |
40 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.185-1614G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50758029 | |||||||
chr5:50758032 | T | C | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.185-1611T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50758032 | |||||||
chr5:50758260 | A | G | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.185-1383A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50758260 | |||||||
chr5:50758329 | T | C | 2 | a0001c0001t0012g0280 a0001c0001t0012g0281 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.185-1314T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50758329 | |||||||
chr5:50758415 | C | A | 1 | a0001c0002t0043g0135 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.185-1228C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50758415 | |||||||
chr5:50758487 | T | G | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG02056.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.185-1156T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50758487 | |||||||
chr5:50758519 | A | G | 1 | a0001c0001t0002g0155 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.185-1124A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50758519 | |||||||
chr5:50758581 | C | T | 9 | a0001c0003t0001g0210 a0001c0003t0001g0211 a0001c0003t0001g0212 others(6): Show |
9 | HG01934.hp2 HG01943.hp2 HG02148.hp2 others(6): Show |
intron_variant | MODIFIER | c.185-1062C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50758581 | |||||||
chr5:50758620 | C | T | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.185-1023C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50758620 | |||||||
chr5:50758630 | A | G | 12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(9): Show |
12 | HG01884.hp1 HG03098.hp1 HG03453.hp1 others(9): Show |
intron_variant | MODIFIER | c.185-1013A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50758630 | |||||||
chr5:50758772 | A | C | 3 | a0001c0001t0030g0005 a0001c0007t0028g0007 a0001c0007t0029g0006 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.185-871A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50758772 | |||||||
chr5:50759119 | A | G | 1 | a0001c0010t0036g0321 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.185-524A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50759119 | |||||||
chr5:50759153 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG02056.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.185-490G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50759153 | |||||||
chr5:50759296 | T | C | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.185-347T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50759296 | |||||||
chr5:50759471 | C | T | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.185-172C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | chr5 | 50759471 | |||||||
chr5:50759622 | C | CT | 68 | a0001c0001t0001g0062 a0001c0001t0001g0267 a0001c0001t0001g0284 others(65): Show |
69 | HG00642.hp1 HG00733.hp2 HG00738.hp1 others(66): Show |
splice_region_variant&intron_variant | LOW | c.185-5dupT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50759622 | ||||||
chr5:50759622 | C | CTT | 116 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(113): Show |
119 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(116): Show |
splice_region_variant&intron_variant | LOW | c.185-6_185-5dupTT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 50759622 | ||||||
chr5:50759859 | A | G | 1 | a0001c0001t0002g0155 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.274+127A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 4/25 | chr5 | 50759859 | |||||||
chr5:50760093 | A | T | 1 | a0001c0002t0003g0142 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.275-199A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 4/25 | chr5 | 50760093 | |||||||
chr5:50760239 | G | A | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.275-53G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 4/25 | chr5 | 50760239 | |||||||
chr5:50760423 | G | A | 1 | a0001c0001t0007g0181 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.345+61G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 5/25 | chr5 | 50760423 | |||||||
chr5:50760532 | A | G | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.345+170A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 5/25 | chr5 | 50760532 | |||||||
chr5:50760601 | A | G | 119 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(116): Show |
122 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.345+239A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 5/25 | chr5 | 50760601 | |||||||
chr5:50760680 | C | T | 1 | a0001c0002t0003g0179 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.345+318C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 5/25 | chr5 | 50760680 | |||||||
chr5:50760691 | A | C | 2 | a0001c0002t0002g0081 a0001c0002t0002g0088 |
2 | HG02273.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.345+329A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 5/25 | chr5 | 50760691 | |||||||
chr5:50760989 | T | C | 2 | a0001c0002t0003g0095 a0001c0002t0003g0096 |
2 | HG01074.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.345+627T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 5/25 | chr5 | 50760989 | |||||||
chr5:50761059 | T | A | 1 | a0001c0002t0002g0163 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.345+697T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 5/25 | chr5 | 50761059 | |||||||
chr5:50761159 | A | G | 1 | a0001c0001t0006g0201 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.346-662A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 5/25 | chr5 | 50761159 | |||||||
chr5:50761248 | A | G | 1 | a0001c0004t0005g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.346-573A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 5/25 | chr5 | 50761248 | |||||||
chr5:50761316 | T | C | 4 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(1): Show |
4 | HG02486.hp2 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.346-505T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 5/25 | chr5 | 50761316 | |||||||
chr5:50761376 | T | A | 1 | a0001c0003t0001g0217 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.346-445T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 5/25 | chr5 | 50761376 | |||||||
chr5:50761396 | T | G | 2 | a0001c0001t0001g0058 a0001c0001t0008g0299 |
2 | HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.346-425T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 5/25 | chr5 | 50761396 | |||||||
chr5:50761437 | G | A | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.346-384G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 5/25 | chr5 | 50761437 | |||||||
chr5:50762064 | T | G | 1 | a0001c0001t0006g0198 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.423+166T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 6/25 | chr5 | 50762064 | |||||||
chr5:50762115 | T | C | 3 | a0001c0002t0003g0118 a0001c0002t0018g0138 a0001c0002t0045g0117 |
3 | HG00597.hp1 NA18946.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.423+217T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 6/25 | chr5 | 50762115 | |||||||
chr5:50762209 | T | C | 62 | a0001c0002t0002g0101 a0001c0002t0002g0102 a0001c0002t0002g0103 others(59): Show |
65 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.423+311T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 6/25 | chr5 | 50762209 | |||||||
chr5:50762302 | T | C | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.423+404T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 6/25 | chr5 | 50762302 | |||||||
chr5:50762368 | A | G | 1 | a0001c0001t0002g0066 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.423+470A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 6/25 | chr5 | 50762368 | |||||||
chr5:50762409 | C | T | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.423+511C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 6/25 | chr5 | 50762409 | |||||||
chr5:50762474 | G | A | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.423+576G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 6/25 | chr5 | 50762474 | |||||||
chr5:50762595 | A | C | 1 | a0001c0002t0003g0080 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.424-553A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 6/25 | chr5 | 50762595 | |||||||
chr5:50762665 | T | C | 43 | a0001c0003t0001g0209 a0001c0003t0001g0210 a0001c0003t0001g0211 others(40): Show |
43 | HG00673.hp1 HG00738.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.424-483T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 6/25 | chr5 | 50762665 | |||||||
chr5:50762699 | C | T | 39 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(36): Show |
41 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.424-449C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 6/25 | chr5 | 50762699 | |||||||
chr5:50762752 | C | T | 1 | a0001c0001t0021g0318 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.424-396C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 6/25 | chr5 | 50762752 | |||||||
chr5:50762850 | C | A | 201 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(198): Show |
204 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(201): Show |
intron_variant | MODIFIER | c.424-298C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 6/25 | chr5 | 50762850 | |||||||
chr5:50762928 | C | G | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.424-220C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 6/25 | chr5 | 50762928 | |||||||
chr5:50763459 | T | C | 1 | a0001c0001t0002g0155 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.518+217T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50763459 | |||||||
chr5:50763497 | G | A | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.518+255G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50763497 | |||||||
chr5:50763633 | T | TA | 12 | a0001c0001t0001g0296 a0001c0001t0015g0059 a0001c0001t0015g0060 others(9): Show |
12 | HG01109.hp2 HG02109.hp2 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.518+404dupA | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 50763633 | ||||||
chr5:50763702 | C | T | 1 | a0001c0004t0005g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.518+460C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50763702 | |||||||
chr5:50763712 | AT | A | 24 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(21): Show |
26 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.518+473delT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 50763712 | ||||||
chr5:50763733 | T | C | 23 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(20): Show |
24 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.518+491T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50763733 | |||||||
chr5:50763754 | C | A | 15 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(12): Show |
15 | HG01884.hp1 HG02257.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.518+512C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50763754 | |||||||
chr5:50763789 | T | C | 2 | a0001c0002t0002g0147 a0001c0002t0050g0177 |
2 | NA18977.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.518+547T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50763789 | |||||||
chr5:50763844 | G | C | 3 | a0001c0003t0011g0223 a0001c0003t0011g0224 a0001c0003t0011g0225 |
3 | HG02055.hp1 HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.518+602G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50763844 | |||||||
chr5:50764007 | C | A | 3 | a0001c0001t0030g0005 a0001c0007t0028g0007 a0001c0007t0029g0006 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.518+765C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50764007 | |||||||
chr5:50764257 | C | G | 1 | a0001c0010t0036g0321 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.518+1015C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50764257 | |||||||
chr5:50764556 | C | T | 1 | a0001c0002t0003g0160 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.518+1314C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50764556 | |||||||
chr5:50764755 | A | G | 1 | a0001c0001t0022g0047 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.518+1513A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50764755 | |||||||
chr5:50764813 | C | CT | 104 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(101): Show |
104 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.518+1585dupT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 50764813 | ||||||
chr5:50764813 | CT | C | 10 | a0001c0002t0003g0115 a0001c0002t0003g0121 a0001c0004t0005g0026 others(7): Show |
10 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.518+1585delT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 50764813 | ||||||
chr5:50764896 | T | A | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.518+1654T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50764896 | |||||||
chr5:50764921 | T | A | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.518+1679T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50764921 | |||||||
chr5:50765065 | C | T | 1 | a0001c0012t0038g0008 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.518+1823C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50765065 | |||||||
chr5:50765137 | G | A | 37 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(34): Show |
39 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.518+1895G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50765137 | |||||||
chr5:50765191 | G | A | 1 | a0001c0003t0001g0237 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.518+1949G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50765191 | |||||||
chr5:50765214 | A | G | 11 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0001t0007g0184 others(8): Show |
11 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.518+1972A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50765214 | |||||||
chr5:50765262 | C | CA | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.518+2031dupA | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 50765262 | ||||||
chr5:50765329 | G | C | 1 | a0001c0002t0023g0094 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.518+2087G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50765329 | |||||||
chr5:50765583 | C | G | 40 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(37): Show |
42 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.518+2341C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50765583 | |||||||
chr5:50765981 | T | C | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.518+2739T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50765981 | |||||||
chr5:50765983 | AT | A | 50 | a0001c0001t0015g0059 a0001c0001t0015g0060 a0001c0002t0018g0138 others(47): Show |
50 | HG00597.hp1 HG00673.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.518+2752delT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 50765983 | ||||||
chr5:50766002 | C | T | 2 | a0001c0003t0001g0234 a0001c0003t0001g0236 |
2 | NA18954.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.518+2760C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50766002 | |||||||
chr5:50766065 | T | C | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.518+2823T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50766065 | |||||||
chr5:50766069 | C | A | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.518+2827C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50766069 | |||||||
chr5:50766085 | G | C | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.518+2843G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50766085 | |||||||
chr5:50766107 | T | C | 1 | a0001c0001t0006g0207 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.518+2865T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50766107 | |||||||
chr5:50766143 | G | A | 1 | a0001c0004t0005g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.518+2901G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50766143 | |||||||
chr5:50766153 | A | G | 37 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(34): Show |
39 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.518+2911A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50766153 | |||||||
chr5:50766199 | A | C | 2 | a0001c0002t0002g0074 a0001c0002t0002g0178 |
2 | HG00642.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.518+2957A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50766199 | |||||||
chr5:50766293 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.518+3051G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50766293 | |||||||
chr5:50766351 | G | A | 1 | a0001c0002t0002g0104 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.518+3109G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50766351 | |||||||
chr5:50766666 | CTG | C | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.518+3426_518+3427d others(4): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 50766666 | ||||||
chr5:50766676 | G | A | 1 | a0001c0004t0005g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.518+3434G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50766676 | |||||||
chr5:50766767 | G | A | 1 | a0001c0001t0004g0038 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.518+3525G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50766767 | |||||||
chr5:50766777 | C | T | 113 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(110): Show |
113 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.518+3535C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50766777 | |||||||
chr5:50766778 | G | A | 1 | a0001c0001t0021g0318 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.518+3536G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50766778 | |||||||
chr5:50766812 | G | A | 4 | a0001c0002t0002g0109 a0001c0002t0002g0110 a0001c0002t0002g0111 others(1): Show |
4 | HG01433.hp1 HG02622.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.518+3570G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50766812 | |||||||
chr5:50767028 | T | C | 1 | a0001c0001t0004g0042 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.518+3786T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50767028 | |||||||
chr5:50767201 | G | T | 201 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(198): Show |
204 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(201): Show |
intron_variant | MODIFIER | c.518+3959G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50767201 | |||||||
chr5:50767296 | A | G | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.518+4054A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50767296 | |||||||
chr5:50767346 | C | T | 3 | a0001c0001t0007g0182 a0001c0001t0007g0184 a0001c0001t0027g0185 |
3 | HG02145.hp2 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.518+4104C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50767346 | |||||||
chr5:50767521 | G | A | 9 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(6): Show |
9 | NA18944.hp1 NA18957.hp1 NA18977.hp2 others(6): Show |
intron_variant | MODIFIER | c.518+4279G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50767521 | |||||||
chr5:50767566 | C | A | 1 | a0001c0003t0001g0211 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.518+4324C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50767566 | |||||||
chr5:50767785 | C | T | 8 | a0001c0002t0003g0112 a0001c0002t0003g0116 a0001c0002t0003g0128 others(5): Show |
8 | HG02132.hp2 HG02165.hp2 NA18950.hp1 others(5): Show |
intron_variant | MODIFIER | c.518+4543C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50767785 | |||||||
chr5:50767788 | C | T | 1 | a0001c0002t0002g0091 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.518+4546C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50767788 | |||||||
chr5:50767858 | A | G | 4 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(1): Show |
4 | HG02486.hp2 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.518+4616A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50767858 | |||||||
chr5:50767974 | T | C | 2 | a0001c0001t0006g0200 a0001c0001t0006g0201 |
2 | HG02280.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.518+4732T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50767974 | |||||||
chr5:50768011 | A | ATG | 35 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(32): Show |
37 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.518+4791_518+4792d others(4): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 50768011 | ||||||
chr5:50768458 | C | T | 65 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(62): Show |
65 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.518+5216C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50768458 | |||||||
chr5:50768489 | C | T | 1 | a0001c0001t0004g0052 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.518+5247C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50768489 | |||||||
chr5:50768511 | G | A | 66 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(63): Show |
66 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.518+5269G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50768511 | |||||||
chr5:50768553 | T | C | 200 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(197): Show |
203 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(200): Show |
intron_variant | MODIFIER | c.518+5311T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50768553 | |||||||
chr5:50768825 | T | G | 2 | a0001c0002t0003g0174 a0001c0002t0003g0175 |
2 | HG01346.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.518+5583T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50768825 | |||||||
chr5:50769162 | G | A | 4 | a0001c0001t0004g0053 a0001c0001t0004g0054 a0001c0001t0004g0055 others(1): Show |
4 | HG01261.hp2 HG02615.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.518+5920G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50769162 | |||||||
chr5:50769248 | G | A | 55 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(52): Show |
57 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.518+6006G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50769248 | |||||||
chr5:50769278 | A | AT | 13 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(10): Show |
13 | HG01884.hp1 HG03098.hp1 HG03453.hp1 others(10): Show |
intron_variant | MODIFIER | c.518+6047dupT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 50769278 | ||||||
chr5:50769278 | AT | A | 15 | a0001c0001t0006g0196 a0001c0001t0006g0197 a0001c0001t0006g0198 others(12): Show |
15 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.518+6047delT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 50769278 | ||||||
chr5:50769317 | G | A | 7 | a0001c0001t0002g0155 a0001c0001t0002g0166 a0001c0001t0002g0167 others(4): Show |
7 | HG01891.hp2 HG02717.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.518+6075G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50769317 | |||||||
chr5:50769399 | T | A | 1 | a0001c0001t0013g0192 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.518+6157T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50769399 | |||||||
chr5:50769399 | T | C | 22 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(19): Show |
22 | HG01192.hp1 HG01884.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.518+6157T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50769399 | |||||||
chr5:50769483 | G | A | 1 | a0001c0001t0004g0035 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.518+6241G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50769483 | |||||||
chr5:50769487 | C | T | 54 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(51): Show |
56 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.518+6245C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50769487 | |||||||
chr5:50769499 | C | T | 112 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(109): Show |
112 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.518+6257C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50769499 | |||||||
chr5:50769559 | C | G | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.518+6317C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50769559 | |||||||
chr5:50769582 | G | T | 15 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(12): Show |
15 | HG01109.hp2 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.518+6340G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50769582 | |||||||
chr5:50769642 | G | A | 55 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(52): Show |
57 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.518+6400G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50769642 | |||||||
chr5:50769784 | G | A | 1 | a0001c0001t0004g0038 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.518+6542G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50769784 | |||||||
chr5:50769938 | T | C | 1 | a0001c0012t0038g0008 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.518+6696T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50769938 | |||||||
chr5:50770046 | T | C | 1 | a0001c0003t0001g0247 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.518+6804T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50770046 | |||||||
chr5:50770049 | C | T | 3 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 |
3 | HG03098.hp2 NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.518+6807C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50770049 | |||||||
chr5:50770215 | G | C | 113 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(110): Show |
113 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.518+6973G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50770215 | |||||||
chr5:50770254 | T | C | 3 | a0001c0002t0002g0090 a0001c0002t0002g0092 a0001c0002t0009g0089 |
3 | NA18986.hp1 NA18987.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.518+7012T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50770254 | |||||||
chr5:50770313 | C | T | 3 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 |
3 | HG03098.hp2 NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.518+7071C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50770313 | |||||||
chr5:50770478 | A | T | 4 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(1): Show |
4 | HG02486.hp2 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.518+7236A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50770478 | |||||||
chr5:50770495 | A | G | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.518+7253A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50770495 | |||||||
chr5:50770621 | G | A | 296 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(293): Show |
302 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(299): Show |
intron_variant | MODIFIER | c.518+7379G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50770621 | |||||||
chr5:50770657 | G | A | 2 | a0001c0003t0001g0244 a0001c0003t0001g0245 |
2 | NA18968.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.519-7412G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50770657 | |||||||
chr5:50770677 | A | G | 3 | a0001c0001t0030g0005 a0001c0007t0028g0007 a0001c0007t0029g0006 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.519-7392A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50770677 | |||||||
chr5:50770683 | G | A | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.519-7386G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50770683 | |||||||
chr5:50770692 | C | A | 4 | a0001c0003t0001g0252 a0001c0003t0011g0223 a0001c0003t0011g0224 others(1): Show |
4 | HG02055.hp1 HG02486.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.519-7377C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50770692 | |||||||
chr5:50770709 | G | T | 4 | a0001c0001t0007g0182 a0001c0001t0007g0184 a0001c0001t0027g0185 others(1): Show |
4 | HG02145.hp2 HG02809.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.519-7360G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50770709 | |||||||
chr5:50770719 | G | A | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.519-7350G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50770719 | |||||||
chr5:50770720 | A | C | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.519-7349A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50770720 | |||||||
chr5:50770721 | A | G | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.519-7348A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50770721 | |||||||
chr5:50770724 | C | A | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.519-7345C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50770724 | |||||||
chr5:50770724 | C | CAAAA | 6 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(3): Show |
6 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.519-7345_519-7344i others(6): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50770724 | |||||||
chr5:50770724 | C | CGAAA | 80 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(77): Show |
83 | HG00099.hp2 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.519-7342_519-7341i others(6): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 50770724 | ||||||
chr5:50770903 | A | G | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.519-7166A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50770903 | |||||||
chr5:50770912 | C | T | 3 | a0001c0001t0030g0005 a0001c0007t0028g0007 a0001c0007t0029g0006 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.519-7157C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50770912 | |||||||
chr5:50770921 | G | T | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.519-7148G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50770921 | |||||||
chr5:50770931 | T | G | 1 | a0001c0001t0001g0275 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.519-7138T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50770931 | |||||||
chr5:50770934 | T | C | 3 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 |
3 | HG01192.hp1 HG02280.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.519-7135T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50770934 | |||||||
chr5:50770959 | T | C | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.519-7110T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50770959 | |||||||
chr5:50770985 | T | C | 55 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(52): Show |
57 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.519-7084T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50770985 | |||||||
chr5:50771013 | A | G | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.519-7056A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50771013 | |||||||
chr5:50771103 | C | A | 5 | a0001c0001t0005g0010 a0001c0002t0003g0073 a0001c0002t0003g0120 others(2): Show |
5 | HG00558.hp2 HG01891.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.519-6966C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50771103 | |||||||
chr5:50771103 | CTA | C | 5 | a0001c0001t0030g0005 a0001c0004t0005g0029 a0001c0004t0005g0030 others(2): Show |
5 | HG01109.hp2 HG02109.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.519-6953_519-6952d others(4): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 50771103 | ||||||
chr5:50771105 | A | C | 246 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(243): Show |
249 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(246): Show |
intron_variant | MODIFIER | c.519-6964A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50771105 | |||||||
chr5:50771107 | A | C | 50 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(47): Show |
53 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.519-6962A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50771107 | |||||||
chr5:50771133 | A | G | 2 | a0001c0001t0007g0184 a0001c0001t0027g0185 |
2 | HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.519-6936A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50771133 | |||||||
chr5:50771185 | G | A | 1 | a0001c0007t0028g0007 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.519-6884G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50771185 | |||||||
chr5:50771255 | G | A | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.519-6814G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50771255 | |||||||
chr5:50771619 | T | A | 6 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(3): Show |
6 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.519-6450T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50771619 | |||||||
chr5:50771669 | C | CGATA | 88 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(85): Show |
91 | HG00099.hp2 HG00642.hp1 HG00733.hp1 others(88): Show |
intron_variant | MODIFIER | c.519-6397_519-6394d others(6): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 50771669 | ||||||
chr5:50771740 | CATA | C | 4 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(1): Show |
4 | HG02486.hp2 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.519-6323_519-6321d others(5): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 50771740 | ||||||
chr5:50771976 | A | G | 1 | a0001c0003t0001g0214 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.519-6093A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50771976 | |||||||
chr5:50772027 | C | T | 1 | a0001c0001t0002g0066 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.519-6042C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50772027 | |||||||
chr5:50772116 | C | T | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.519-5953C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50772116 | |||||||
chr5:50772158 | A | G | 2 | a0002c0005t0009g0270 a0002c0005t0009g0287 |
2 | NA19063.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.519-5911A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50772158 | |||||||
chr5:50772196 | T | A | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.519-5873T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50772196 | |||||||
chr5:50772203 | G | A | 2 | a0001c0001t0004g0039 a0001c0001t0004g0040 |
2 | HG00733.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.519-5866G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50772203 | |||||||
chr5:50772276 | G | T | 1 | a0001c0001t0001g0305 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.519-5793G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50772276 | |||||||
chr5:50772385 | G | T | 1 | a0001c0011t0004g0044 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.519-5684G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50772385 | |||||||
chr5:50772411 | A | T | 86 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(83): Show |
89 | HG00099.hp2 HG00642.hp1 HG00733.hp1 others(86): Show |
intron_variant | MODIFIER | c.519-5658A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50772411 | |||||||
chr5:50772667 | C | T | 1 | a0001c0001t0001g0284 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.519-5402C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50772667 | |||||||
chr5:50772674 | T | A | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.519-5395T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50772674 | |||||||
chr5:50772679 | C | CTTTTAT | 6 | a0001c0001t0002g0166 a0001c0001t0002g0167 a0001c0001t0002g0168 others(3): Show |
6 | HG01891.hp2 HG02717.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.519-5361_519-5356d others(8): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 50772679 | ||||||
chr5:50772679 | CTTTTATT others(5): Show |
C | 3 | a0001c0001t0001g0305 a0001c0001t0015g0059 a0001c0001t0015g0060 |
3 | HG00738.hp2 NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.519-5367_519-5356d others(14): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 50772679 | ||||||
chr5:50772785 | C | T | 1 | a0001c0013t0005g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.519-5284C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50772785 | |||||||
chr5:50772791 | G | A | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.519-5278G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50772791 | |||||||
chr5:50772857 | T | G | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.519-5212T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50772857 | |||||||
chr5:50772931 | C | T | 1 | a0001c0001t0022g0047 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.519-5138C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50772931 | |||||||
chr5:50772932 | A | G | 1 | a0001c0001t0022g0047 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.519-5137A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50772932 | |||||||
chr5:50773146 | C | T | 6 | a0001c0002t0002g0065 a0001c0002t0002g0148 a0001c0002t0002g0149 others(3): Show |
6 | HG01071.hp2 HG02683.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.519-4923C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50773146 | |||||||
chr5:50773366 | A | T | 8 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0048 others(5): Show |
10 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.519-4703A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50773366 | |||||||
chr5:50773546 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.519-4523C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50773546 | |||||||
chr5:50773595 | T | C | 1 | a0001c0002t0003g0097 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.519-4474T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50773595 | |||||||
chr5:50773631 | A | G | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.519-4438A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50773631 | |||||||
chr5:50773745 | G | C | 1 | a0001c0001t0001g0062 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.519-4324G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50773745 | |||||||
chr5:50773787 | C | A | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.519-4282C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50773787 | |||||||
chr5:50773832 | A | AT | 26 | a0001c0001t0004g0052 a0001c0001t0006g0191 a0001c0001t0006g0193 others(23): Show |
27 | HG01167.hp2 HG01169.hp2 HG01516.hp2 others(24): Show |
intron_variant | MODIFIER | c.519-4219dupT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 50773832 | ||||||
chr5:50773832 | A | ATT | 9 | a0001c0001t0007g0184 a0001c0001t0007g0186 a0001c0001t0007g0187 others(6): Show |
9 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.519-4220_519-4219d others(4): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 50773832 | ||||||
chr5:50773832 | A | T | 1 | a0001c0007t0028g0007 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.519-4237A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50773832 | |||||||
chr5:50773832 | AT | A | 70 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(67): Show |
70 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.519-4219delT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 50773832 | ||||||
chr5:50773835 | T | A | 1 | a0001c0007t0029g0006 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.519-4234T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50773835 | |||||||
chr5:50773849 | T | G | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.519-4220T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50773849 | |||||||
chr5:50773933 | A | G | 37 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(34): Show |
39 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.519-4136A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50773933 | |||||||
chr5:50773984 | G | A | 2 | a0001c0003t0001g0209 a0001c0003t0001g0249 |
2 | HG01261.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.519-4085G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50773984 | |||||||
chr5:50773992 | A | G | 3 | a0001c0001t0030g0005 a0001c0007t0028g0007 a0001c0007t0029g0006 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.519-4077A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50773992 | |||||||
chr5:50774236 | C | G | 1 | a0001c0002t0003g0108 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.519-3833C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50774236 | |||||||
chr5:50774251 | C | T | 8 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(5): Show |
8 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.519-3818C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50774251 | |||||||
chr5:50774263 | G | A | 1 | a0001c0002t0003g0139 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.519-3806G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50774263 | |||||||
chr5:50774322 | A | G | 8 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(5): Show |
8 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.519-3747A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50774322 | |||||||
chr5:50774337 | C | T | 1 | a0001c0001t0001g0305 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.519-3732C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50774337 | |||||||
chr5:50774344 | C | T | 6 | a0001c0001t0001g0259 a0001c0001t0001g0267 a0001c0001t0001g0269 others(3): Show |
6 | HG00099.hp1 HG01069.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.519-3725C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50774344 | |||||||
chr5:50774414 | C | T | 1 | a0001c0001t0021g0318 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.519-3655C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50774414 | |||||||
chr5:50774427 | G | T | 37 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(34): Show |
39 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.519-3642G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50774427 | |||||||
chr5:50774451 | C | T | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.519-3618C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50774451 | |||||||
chr5:50774455 | C | T | 1 | a0001c0001t0006g0208 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.519-3614C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50774455 | |||||||
chr5:50774492 | C | A | 1 | a0001c0004t0005g0026 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.519-3577C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50774492 | |||||||
chr5:50774501 | G | A | 1 | a0001c0012t0038g0008 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.519-3568G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50774501 | |||||||
chr5:50774503 | G | A | 1 | a0001c0002t0041g0172 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.519-3566G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50774503 | |||||||
chr5:50774520 | C | T | 1 | a0001c0001t0006g0203 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.519-3549C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50774520 | |||||||
chr5:50774540 | G | T | 2 | a0001c0001t0017g0170 a0001c0001t0017g0171 |
2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.519-3529G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50774540 | |||||||
chr5:50774578 | C | T | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.519-3491C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50774578 | |||||||
chr5:50774601 | C | T | 6 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(3): Show |
6 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.519-3468C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50774601 | |||||||
chr5:50774602 | G | A | 1 | a0001c0003t0010g0232 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.519-3467G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50774602 | |||||||
chr5:50774642 | T | C | 55 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(52): Show |
57 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.519-3427T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50774642 | |||||||
chr5:50774689 | C | T | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.519-3380C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50774689 | |||||||
chr5:50774707 | C | T | 2 | a0001c0001t0004g0038 a0001c0001t0004g0046 |
2 | HG02293.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.519-3362C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50774707 | |||||||
chr5:50774734 | A | G | 1 | a0001c0002t0003g0130 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.519-3335A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50774734 | |||||||
chr5:50774882 | C | T | 1 | a0001c0002t0003g0087 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.519-3187C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50774882 | |||||||
chr5:50774927 | GGCTGGGC others(109): Show |
G | 1 | a0001c0001t0004g0040 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.519-3123_519-3008d others(2): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 50774927 | ||||||
chr5:50774960 | G | T | 1 | a0001c0004t0005g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.519-3109G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50774960 | |||||||
chr5:50774963 | C | T | 23 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(20): Show |
23 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.519-3106C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50774963 | |||||||
chr5:50774981 | C | T | 1 | a0001c0001t0006g0203 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.519-3088C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50774981 | |||||||
chr5:50774996 | G | C | 1 | a0002c0005t0009g0278 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.519-3073G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50774996 | |||||||
chr5:50775002 | C | T | 1 | a0001c0001t0006g0200 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.519-3067C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50775002 | |||||||
chr5:50775012 | G | A | 36 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(33): Show |
38 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.519-3057G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50775012 | |||||||
chr5:50775018 | C | T | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.519-3051C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50775018 | |||||||
chr5:50775034 | T | C | 54 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(51): Show |
56 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.519-3035T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50775034 | |||||||
chr5:50775111 | C | T | 1 | a0001c0001t0002g0169 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.519-2958C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50775111 | |||||||
chr5:50775233 | C | T | 1 | a0001c0002t0002g0147 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.519-2836C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50775233 | |||||||
chr5:50775338 | C | T | 7 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(4): Show |
7 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.519-2731C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50775338 | |||||||
chr5:50775366 | C | A | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.519-2703C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50775366 | |||||||
chr5:50775420 | C | T | 113 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(110): Show |
113 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.519-2649C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50775420 | |||||||
chr5:50775495 | C | T | 4 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(1): Show |
4 | HG01192.hp1 HG02280.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.519-2574C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50775495 | |||||||
chr5:50775520 | G | A | 55 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(52): Show |
57 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.519-2549G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50775520 | |||||||
chr5:50775521 | G | A | 11 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0001t0007g0184 others(8): Show |
11 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.519-2548G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50775521 | |||||||
chr5:50775531 | G | A | 1 | a0001c0001t0032g0183 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.519-2538G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50775531 | |||||||
chr5:50775615 | C | T | 1 | a0001c0001t0007g0181 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.519-2454C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50775615 | |||||||
chr5:50775653 | A | G | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.519-2416A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50775653 | |||||||
chr5:50775668 | G | T | 7 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(4): Show |
7 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.519-2401G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50775668 | |||||||
chr5:50775731 | A | G | 199 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(196): Show |
202 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(199): Show |
intron_variant | MODIFIER | c.519-2338A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50775731 | |||||||
chr5:50775789 | T | G | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.519-2280T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50775789 | |||||||
chr5:50775824 | G | A | 5 | a0001c0002t0002g0105 a0001c0002t0003g0098 a0001c0002t0003g0125 others(2): Show |
5 | HG02257.hp2 HG02602.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.519-2245G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50775824 | |||||||
chr5:50775824 | G | T | 1 | a0001c0001t0001g0317 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.519-2245G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50775824 | |||||||
chr5:50775872 | T | C | 43 | a0001c0003t0001g0209 a0001c0003t0001g0210 a0001c0003t0001g0211 others(40): Show |
43 | HG00673.hp1 HG00738.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.519-2197T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50775872 | |||||||
chr5:50776363 | T | C | 1 | a0001c0001t0001g0294 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.519-1706T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50776363 | |||||||
chr5:50776575 | G | A | 4 | a0001c0001t0030g0005 a0001c0007t0028g0007 a0001c0007t0029g0006 others(1): Show |
4 | HG02257.hp1 HG02572.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.519-1494G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50776575 | |||||||
chr5:50776577 | A | C | 37 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(34): Show |
39 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.519-1492A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50776577 | |||||||
chr5:50776605 | A | G | 1 | a0001c0001t0002g0066 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.519-1464A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50776605 | |||||||
chr5:50777002 | A | G | 3 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 |
3 | HG02258.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.519-1067A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50777002 | |||||||
chr5:50777026 | T | C | 113 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(110): Show |
113 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.519-1043T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50777026 | |||||||
chr5:50777114 | T | A | 3 | a0001c0001t0030g0005 a0001c0007t0028g0007 a0001c0007t0029g0006 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.519-955T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50777114 | |||||||
chr5:50777140 | G | A | 1 | a0001c0002t0005g0071 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.519-929G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50777140 | |||||||
chr5:50777244 | C | T | 31 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(28): Show |
32 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.519-825C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50777244 | |||||||
chr5:50777382 | TAAG | T | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.519-684_519-682del others(3): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 50777382 | ||||||
chr5:50777705 | T | C | 5 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(2): Show |
5 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.519-364T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 7/25 | chr5 | 50777705 | |||||||
chr5:50778430 | T | A | 1 | a0001c0001t0007g0182 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.580-130T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 8/25 | chr5 | 50778430 | |||||||
chr5:50778472 | G | T | 1 | a0001c0001t0021g0318 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.580-88G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 8/25 | chr5 | 50778472 | |||||||
chr5:50778497 | GT | G | 7 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0002t0002g0101 others(4): Show |
7 | HG02055.hp2 HG02056.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.580-53delT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr5 | 50778497 | ||||||
chr5:50778697 | G | A | 10 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(7): Show |
10 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.670+47G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50778697 | |||||||
chr5:50778728 | T | A | 1 | a0001c0001t0007g0181 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.670+78T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50778728 | |||||||
chr5:50778885 | A | G | 11 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0001t0007g0184 others(8): Show |
11 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.670+235A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50778885 | |||||||
chr5:50778921 | A | G | 1 | a0001c0001t0004g0034 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.670+271A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50778921 | |||||||
chr5:50778947 | T | A | 3 | a0001c0001t0005g0017 a0001c0001t0005g0018 a0001c0001t0005g0019 |
3 | HG01884.hp1 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.670+297T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50778947 | |||||||
chr5:50779077 | G | T | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.670+427G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50779077 | |||||||
chr5:50779124 | T | C | 1 | a0001c0003t0011g0223 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.670+474T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50779124 | |||||||
chr5:50779149 | G | T | 4 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(1): Show |
4 | HG02486.hp2 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.670+499G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50779149 | |||||||
chr5:50779175 | CCACACAT others(3): Show |
C | 1 | a0001c0003t0001g0233 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.670+542_670+551del others(10): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr5 | 50779175 | ||||||
chr5:50779243 | G | A | 1 | a0001c0002t0003g0070 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.670+593G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50779243 | |||||||
chr5:50779270 | T | C | 52 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(49): Show |
54 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.670+620T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50779270 | |||||||
chr5:50779516 | C | T | 1 | a0001c0013t0005g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.670+866C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50779516 | |||||||
chr5:50779544 | T | G | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.670+894T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50779544 | |||||||
chr5:50779820 | G | A | 65 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(62): Show |
65 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.670+1170G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50779820 | |||||||
chr5:50779851 | C | A | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.670+1201C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50779851 | |||||||
chr5:50779907 | A | AAATT | 49 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(46): Show |
51 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(48): Show |
intron_variant | MODIFIER | c.670+1261_670+1264d others(6): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr5 | 50779907 | ||||||
chr5:50779954 | G | C | 1 | a0001c0012t0038g0008 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.670+1304G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50779954 | |||||||
chr5:50780027 | G | A | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.670+1377G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50780027 | |||||||
chr5:50780210 | T | A | 1 | a0001c0002t0003g0070 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.670+1560T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50780210 | |||||||
chr5:50780235 | G | A | 8 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(5): Show |
8 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.670+1585G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50780235 | |||||||
chr5:50780278 | GCTAA | G | 8 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(5): Show |
8 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.670+1631_670+1634d others(6): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr5 | 50780278 | ||||||
chr5:50780351 | G | T | 1 | a0001c0002t0041g0172 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.670+1701G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50780351 | |||||||
chr5:50780470 | C | A | 2 | a0001c0001t0001g0262 a0001c0001t0001g0263 |
2 | HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.670+1820C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50780470 | |||||||
chr5:50780532 | C | G | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.670+1882C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50780532 | |||||||
chr5:50780557 | G | A | 3 | a0001c0001t0007g0181 a0001c0001t0015g0059 a0001c0001t0015g0060 |
3 | HG01167.hp1 NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.670+1907G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50780557 | |||||||
chr5:50780637 | C | A | 1 | a0001c0002t0003g0156 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.670+1987C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50780637 | |||||||
chr5:50780905 | G | A | 3 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 |
3 | HG01192.hp1 HG02280.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.670+2255G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50780905 | |||||||
chr5:50781001 | T | C | 1 | a0001c0004t0005g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.670+2351T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50781001 | |||||||
chr5:50781052 | A | G | 12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(9): Show |
12 | HG01884.hp1 HG03098.hp1 HG03453.hp1 others(9): Show |
intron_variant | MODIFIER | c.670+2402A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50781052 | |||||||
chr5:50781188 | G | A | 1 | a0001c0002t0002g0093 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.670+2538G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50781188 | |||||||
chr5:50781291 | A | G | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.670+2641A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50781291 | |||||||
chr5:50781310 | G | GA | 3 | a0001c0002t0002g0081 a0001c0002t0002g0165 a0001c0002t0002g0173 |
3 | HG00639.hp2 HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.670+2662dupA | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr5 | 50781310 | ||||||
chr5:50781566 | A | G | 37 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(34): Show |
39 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.670+2916A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50781566 | |||||||
chr5:50781658 | A | G | 6 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(3): Show |
6 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.670+3008A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50781658 | |||||||
chr5:50781709 | T | A | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.670+3059T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50781709 | |||||||
chr5:50781797 | T | C | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.670+3147T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50781797 | |||||||
chr5:50781800 | A | G | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.670+3150A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50781800 | |||||||
chr5:50781824 | C | T | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.670+3174C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50781824 | |||||||
chr5:50781836 | A | G | 1 | a0001c0002t0003g0119 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.670+3186A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50781836 | |||||||
chr5:50781858 | A | G | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.670+3208A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50781858 | |||||||
chr5:50781882 | C | A | 1 | a0001c0003t0001g0212 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.670+3232C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50781882 | |||||||
chr5:50781986 | G | T | 11 | a0001c0002t0003g0073 a0001c0002t0003g0097 a0001c0002t0003g0120 others(8): Show |
11 | HG00558.hp2 NA18944.hp2 NA18960.hp1 others(8): Show |
intron_variant | MODIFIER | c.670+3336G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50781986 | |||||||
chr5:50782015 | A | G | 1 | a0001c0001t0001g0282 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.670+3365A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50782015 | |||||||
chr5:50782059 | G | A | 1 | a0001c0003t0001g0247 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.670+3409G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50782059 | |||||||
chr5:50782154 | T | C | 1 | a0001c0003t0001g0222 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.670+3504T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50782154 | |||||||
chr5:50782165 | T | C | 25 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(22): Show |
27 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.670+3515T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50782165 | |||||||
chr5:50782471 | G | A | 1 | a0001c0002t0003g0142 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.670+3821G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50782471 | |||||||
chr5:50782519 | A | C | 1 | a0001c0003t0001g0253 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.670+3869A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50782519 | |||||||
chr5:50782590 | G | A | 1 | a0001c0002t0003g0115 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.670+3940G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50782590 | |||||||
chr5:50782612 | G | A | 1 | a0001c0001t0006g0193 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.670+3962G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50782612 | |||||||
chr5:50782648 | C | T | 1 | a0001c0002t0002g0091 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.670+3998C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50782648 | |||||||
chr5:50782736 | C | G | 1 | a0001c0001t0047g0295 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.670+4086C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50782736 | |||||||
chr5:50782741 | C | T | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.670+4091C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50782741 | |||||||
chr5:50782966 | G | T | 1 | a0001c0001t0004g0033 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.670+4316G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50782966 | |||||||
chr5:50783161 | G | A | 4 | a0001c0001t0005g0021 a0001c0001t0005g0022 a0001c0001t0005g0023 others(1): Show |
4 | NA18944.hp1 NA18957.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.670+4511G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50783161 | |||||||
chr5:50783200 | A | G | 55 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(52): Show |
57 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.670+4550A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50783200 | |||||||
chr5:50783203 | G | C | 1 | a0001c0002t0002g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.670+4553G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50783203 | |||||||
chr5:50783508 | A | T | 3 | a0002c0005t0002g0276 a0002c0005t0009g0277 a0002c0005t0009g0278 |
3 | NA18987.hp1 NA19062.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.670+4858A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50783508 | |||||||
chr5:50783539 | A | G | 21 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(18): Show |
22 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.670+4889A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50783539 | |||||||
chr5:50783721 | G | T | 1 | a0001c0001t0004g0046 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.671-4802G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50783721 | |||||||
chr5:50783769 | A | C | 19 | a0001c0002t0043g0135 a0001c0003t0001g0220 a0001c0003t0001g0221 others(16): Show |
19 | HG00673.hp1 HG02056.hp2 HG02074.hp2 others(16): Show |
intron_variant | MODIFIER | c.671-4754A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50783769 | |||||||
chr5:50783867 | G | A | 1 | a0001c0001t0015g0059 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.671-4656G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50783867 | |||||||
chr5:50783938 | A | G | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.671-4585A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50783938 | |||||||
chr5:50784016 | T | C | 1 | a0001c0001t0004g0054 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.671-4507T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50784016 | |||||||
chr5:50784029 | T | C | 1 | a0001c0002t0003g0120 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.671-4494T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50784029 | |||||||
chr5:50784161 | A | G | 1 | a0001c0002t0018g0138 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.671-4362A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50784161 | |||||||
chr5:50784252 | A | G | 4 | a0001c0001t0007g0182 a0001c0001t0007g0184 a0001c0001t0027g0185 others(1): Show |
4 | HG02145.hp2 HG02809.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.671-4271A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50784252 | |||||||
chr5:50784486 | C | A | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.671-4037C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50784486 | |||||||
chr5:50784711 | C | T | 1 | a0001c0001t0031g0306 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.671-3812C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50784711 | |||||||
chr5:50785337 | A | G | 4 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(1): Show |
4 | HG02486.hp2 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.671-3186A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50785337 | |||||||
chr5:50785370 | A | G | 3 | a0001c0001t0030g0005 a0001c0007t0028g0007 a0001c0007t0029g0006 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.671-3153A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50785370 | |||||||
chr5:50785499 | G | A | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.671-3024G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50785499 | |||||||
chr5:50785538 | C | G | 1 | a0001c0002t0002g0173 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.671-2985C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50785538 | |||||||
chr5:50785710 | T | G | 1 | a0001c0003t0001g0214 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.671-2813T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50785710 | |||||||
chr5:50785804 | C | A | 6 | a0001c0001t0002g0166 a0001c0001t0002g0167 a0001c0001t0002g0168 others(3): Show |
6 | HG01891.hp2 HG02717.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.671-2719C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50785804 | |||||||
chr5:50786075 | C | T | 3 | a0001c0004t0005g0029 a0001c0004t0005g0030 a0001c0004t0005g0031 |
3 | HG01109.hp2 HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.671-2448C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50786075 | |||||||
chr5:50786109 | TA | T | 9 | a0001c0002t0002g0101 a0001c0002t0002g0102 a0001c0002t0002g0103 others(6): Show |
9 | HG02055.hp2 HG02257.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.671-2412delA | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr5 | 50786109 | ||||||
chr5:50786131 | G | A | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.671-2392G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50786131 | |||||||
chr5:50786222 | C | A | 1 | a0001c0001t0002g0155 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.671-2301C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50786222 | |||||||
chr5:50786531 | A | AT | 10 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(7): Show |
10 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.671-1977dupT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr5 | 50786531 | ||||||
chr5:50786531 | AT | A | 15 | a0001c0001t0001g0292 a0001c0001t0007g0182 a0001c0001t0049g0020 others(12): Show |
15 | HG00639.hp1 HG01109.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.671-1977delT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr5 | 50786531 | ||||||
chr5:50786631 | G | A | 19 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(16): Show |
20 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.671-1892G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50786631 | |||||||
chr5:50786695 | G | C | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.671-1828G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50786695 | |||||||
chr5:50786937 | G | A | 2 | a0001c0002t0002g0104 a0001c0002t0002g0144 |
2 | NA19078.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.671-1586G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50786937 | |||||||
chr5:50786943 | A | C | 1 | a0001c0004t0005g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.671-1580A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50786943 | |||||||
chr5:50786978 | A | G | 1 | a0001c0001t0006g0198 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.671-1545A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50786978 | |||||||
chr5:50787139 | C | T | 7 | a0001c0001t0008g0310 a0001c0001t0008g0311 a0001c0001t0008g0312 others(4): Show |
7 | HG01192.hp2 HG01884.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.671-1384C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50787139 | |||||||
chr5:50787140 | C | T | 1 | a0001c0001t0032g0183 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.671-1383C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50787140 | |||||||
chr5:50787142 | G | A | 7 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(4): Show |
7 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.671-1381G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50787142 | |||||||
chr5:50787196 | C | T | 2 | a0001c0003t0011g0223 a0001c0003t0011g0225 |
2 | HG02055.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.671-1327C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50787196 | |||||||
chr5:50787415 | C | T | 1 | a0001c0007t0028g0007 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.671-1108C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50787415 | |||||||
chr5:50787685 | T | G | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.671-838T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50787685 | |||||||
chr5:50787884 | A | AACATATA others(40): Show |
1 | a0001c0002t0002g0157 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.671-628_671-582dup others(47): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr5 | 50787884 | ||||||
chr5:50787887 | ATATATAT others(13): Show |
A | 1 | a0001c0001t0004g0033 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.671-624_671-605del others(20): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr5 | 50787887 | ||||||
chr5:50788167 | A | ATATTATA others(35): Show |
5 | a0001c0001t0013g0192 a0001c0001t0013g0204 a0001c0002t0002g0148 others(2): Show |
5 | HG01952.hp1 HG02145.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.671-343_671-302dup others(42): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr5 | 50788167 | ||||||
chr5:50788184 | A | G | 1 | a0001c0010t0036g0321 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.671-339A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50788184 | |||||||
chr5:50788191 | ATT | A | 48 | a0001c0002t0043g0135 a0001c0003t0001g0209 a0001c0003t0001g0210 others(45): Show |
48 | HG00673.hp1 HG00738.hp1 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.671-331_671-330del others(2): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50788191 | |||||||
chr5:50788241 | G | GTATAATG others(38): Show |
6 | a0001c0002t0003g0002 a0001c0002t0003g0003 a0001c0002t0003g0119 others(3): Show |
9 | HG01943.hp1 HG02300.hp2 HG03834.hp2 others(6): Show |
intron_variant | MODIFIER | c.671-250_671-206dup others(45): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr5 | 50788241 | ||||||
chr5:50788275 | T | C | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.671-248T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50788275 | |||||||
chr5:50788291 | A | ATGTATTA others(17): Show |
1 | a0001c0012t0038g0008 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.671-227_671-226ins others(24): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr5 | 50788291 | ||||||
chr5:50788320 | T | C | 1 | a0001c0001t0001g0305 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.671-203T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 9/25 | chr5 | 50788320 | |||||||
chr5:50788626 | A | G | 4 | a0001c0001t0004g0053 a0001c0001t0004g0054 a0001c0001t0004g0055 others(1): Show |
4 | HG01261.hp2 HG02615.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.737+37A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50788626 | |||||||
chr5:50788674 | C | CCTT | 214 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(211): Show |
217 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(214): Show |
intron_variant | MODIFIER | c.737+87_737+88insTC others(1): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr5 | 50788674 | ||||||
chr5:50788890 | C | T | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.737+301C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50788890 | |||||||
chr5:50788948 | A | G | 1 | a0001c0001t0004g0038 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.737+359A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50788948 | |||||||
chr5:50789104 | G | A | 3 | a0001c0001t0030g0005 a0001c0007t0028g0007 a0001c0007t0029g0006 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.737+515G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50789104 | |||||||
chr5:50789236 | A | G | 1 | a0001c0001t0002g0066 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.737+647A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50789236 | |||||||
chr5:50789326 | AGAGAACA others(2): Show |
A | 3 | a0001c0001t0030g0005 a0001c0007t0028g0007 a0001c0007t0029g0006 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.737+740_737+748del others(9): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr5 | 50789326 | ||||||
chr5:50789431 | C | T | 1 | a0001c0001t0005g0010 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.737+842C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50789431 | |||||||
chr5:50789480 | AAAT | A | 11 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0001t0007g0184 others(8): Show |
11 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.737+895_737+897del others(3): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr5 | 50789480 | ||||||
chr5:50789510 | C | T | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.737+921C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50789510 | |||||||
chr5:50789537 | A | G | 4 | a0001c0003t0001g0252 a0001c0003t0011g0223 a0001c0003t0011g0224 others(1): Show |
4 | HG02055.hp1 HG02486.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.737+948A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50789537 | |||||||
chr5:50789551 | A | G | 1 | a0001c0010t0036g0321 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.737+962A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50789551 | |||||||
chr5:50789643 | G | T | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.737+1054G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50789643 | |||||||
chr5:50789821 | A | C | 3 | a0001c0002t0002g0084 a0001c0002t0002g0085 a0001c0002t0002g0114 |
3 | HG00609.hp1 NA18980.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.737+1232A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50789821 | |||||||
chr5:50789909 | A | G | 114 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(111): Show |
114 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.737+1320A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50789909 | |||||||
chr5:50790010 | A | C | 3 | a0001c0001t0030g0005 a0001c0007t0028g0007 a0001c0007t0029g0006 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.737+1421A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50790010 | |||||||
chr5:50790058 | C | T | 1 | a0001c0002t0003g0160 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.737+1469C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50790058 | |||||||
chr5:50790147 | C | T | 48 | a0001c0002t0043g0135 a0001c0003t0001g0209 a0001c0003t0001g0210 others(45): Show |
48 | HG00673.hp1 HG00738.hp1 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.737+1558C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50790147 | |||||||
chr5:50790220 | A | G | 55 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(52): Show |
57 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.737+1631A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50790220 | |||||||
chr5:50790358 | C | T | 4 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(1): Show |
4 | HG02486.hp2 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.737+1769C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50790358 | |||||||
chr5:50790790 | G | A | 8 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(5): Show |
8 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.737+2201G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50790790 | |||||||
chr5:50790999 | C | T | 1 | a0001c0001t0004g0049 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.737+2410C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50790999 | |||||||
chr5:50791192 | G | A | 2 | a0001c0001t0001g0284 a0001c0001t0001g0285 |
2 | NA18945.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.737+2603G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50791192 | |||||||
chr5:50791274 | A | G | 1 | a0001c0010t0036g0321 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.737+2685A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50791274 | |||||||
chr5:50791382 | A | G | 55 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(52): Show |
57 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.737+2793A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50791382 | |||||||
chr5:50791632 | G | T | 114 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(111): Show |
114 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.738-2575G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50791632 | |||||||
chr5:50791693 | GTATGACT others(1): Show |
G | 37 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(34): Show |
39 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.738-2509_738-2502d others(10): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr5 | 50791693 | ||||||
chr5:50791898 | T | G | 1 | a0001c0001t0022g0047 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.738-2309T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50791898 | |||||||
chr5:50791962 | T | C | 8 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(5): Show |
8 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.738-2245T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50791962 | |||||||
chr5:50792017 | T | G | 12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(9): Show |
12 | HG01884.hp1 HG03098.hp1 HG03453.hp1 others(9): Show |
intron_variant | MODIFIER | c.738-2190T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50792017 | |||||||
chr5:50792101 | C | T | 3 | a0001c0001t0005g0017 a0001c0001t0005g0018 a0001c0001t0005g0019 |
3 | HG01884.hp1 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.738-2106C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50792101 | |||||||
chr5:50792161 | A | G | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.738-2046A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50792161 | |||||||
chr5:50792183 | C | T | 1 | a0001c0002t0002g0084 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.738-2024C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50792183 | |||||||
chr5:50792400 | T | G | 37 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(34): Show |
39 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.738-1807T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50792400 | |||||||
chr5:50792405 | G | C | 1 | a0001c0012t0038g0008 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.738-1802G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50792405 | |||||||
chr5:50792479 | G | GT | 45 | a0001c0002t0002g0065 a0001c0002t0002g0072 a0001c0002t0002g0074 others(42): Show |
45 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.738-1717dupT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr5 | 50792479 | ||||||
chr5:50792483 | T | G | 55 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(52): Show |
57 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.738-1724T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50792483 | |||||||
chr5:50792529 | G | T | 1 | a0001c0002t0002g0161 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.738-1678G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50792529 | |||||||
chr5:50792671 | A | T | 1 | a0001c0002t0003g0160 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.738-1536A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50792671 | |||||||
chr5:50793016 | G | A | 114 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(111): Show |
114 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.738-1191G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50793016 | |||||||
chr5:50793309 | A | G | 1 | a0001c0007t0028g0007 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.738-898A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50793309 | |||||||
chr5:50793421 | T | G | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.738-786T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50793421 | |||||||
chr5:50793484 | G | A | 1 | a0001c0001t0016g0283 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.738-723G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50793484 | |||||||
chr5:50793686 | T | C | 5 | a0001c0001t0007g0186 a0001c0001t0007g0187 a0001c0001t0007g0188 others(2): Show |
5 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.738-521T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50793686 | |||||||
chr5:50793767 | T | C | 1 | a0001c0002t0003g0087 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.738-440T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50793767 | |||||||
chr5:50793817 | G | A | 270 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(267): Show |
273 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(270): Show |
intron_variant | MODIFIER | c.738-390G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50793817 | |||||||
chr5:50793842 | T | A | 116 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(113): Show |
116 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.738-365T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50793842 | |||||||
chr5:50793889 | G | A | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.738-318G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50793889 | |||||||
chr5:50794038 | A | G | 116 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(113): Show |
116 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.738-169A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50794038 | |||||||
chr5:50794085 | G | A | 88 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(85): Show |
91 | HG00099.hp2 HG00642.hp1 HG00733.hp1 others(88): Show |
intron_variant | MODIFIER | c.738-122G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | chr5 | 50794085 | |||||||
chr5:50794104 | GT | G | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.738-100delT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr5 | 50794104 | ||||||
chr5:50794336 | G | A | 1 | a0001c0001t0001g0293 | 1 | NA18961.hp1 | splice_region_variant&intron_variant | LOW | c.863+4G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 11/25 | chr5 | 50794336 | |||||||
chr5:50794551 | CAT | C | 37 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(34): Show |
39 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.863+220_863+221del others(2): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 11/25 | chr5 | 50794551 | |||||||
chr5:50794554 | T | G | 37 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(34): Show |
39 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.863+222T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 11/25 | chr5 | 50794554 | |||||||
chr5:50794625 | G | C | 1 | a0001c0012t0038g0008 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.864-228G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 11/25 | chr5 | 50794625 | |||||||
chr5:50794629 | G | A | 1 | a0001c0001t0001g0305 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.864-224G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 11/25 | chr5 | 50794629 | |||||||
chr5:50795530 | T | C | 2 | a0001c0003t0001g0210 a0001c0003t0001g0211 |
2 | NA18948.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1428+113T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 12/25 | chr5 | 50795530 | |||||||
chr5:50795532 | T | G | 2 | a0001c0003t0001g0209 a0001c0003t0001g0249 |
2 | HG01261.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1428+115T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 12/25 | chr5 | 50795532 | |||||||
chr5:50795544 | C | A | 1 | a0001c0001t0004g0050 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1428+127C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 12/25 | chr5 | 50795544 | |||||||
chr5:50795722 | T | A | 2 | a0001c0003t0001g0209 a0001c0003t0001g0249 |
2 | HG01261.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1428+305T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 12/25 | chr5 | 50795722 | |||||||
chr5:50795793 | G | C | 8 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(5): Show |
8 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1428+376G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 12/25 | chr5 | 50795793 | |||||||
chr5:50795906 | T | C | 1 | a0001c0001t0008g0299 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1428+489T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 12/25 | chr5 | 50795906 | |||||||
chr5:50796003 | T | A | 37 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(34): Show |
39 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.1428+586T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 12/25 | chr5 | 50796003 | |||||||
chr5:50796068 | G | A | 1 | a0001c0001t0024g0051 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1428+651G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 12/25 | chr5 | 50796068 | |||||||
chr5:50796403 | A | T | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1429-579A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 12/25 | chr5 | 50796403 | |||||||
chr5:50796499 | T | A | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1429-483T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 12/25 | chr5 | 50796499 | |||||||
chr5:50796598 | A | G | 1 | a0001c0002t0002g0176 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1429-384A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 12/25 | chr5 | 50796598 | |||||||
chr5:50796783 | G | A | 5 | a0001c0001t0007g0186 a0001c0001t0007g0187 a0001c0001t0007g0188 others(2): Show |
5 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1429-199G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 12/25 | chr5 | 50796783 | |||||||
chr5:50796789 | G | T | 1 | a0001c0002t0002g0162 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1429-193G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 12/25 | chr5 | 50796789 | |||||||
chr5:50796815 | A | G | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1429-167A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 12/25 | chr5 | 50796815 | |||||||
chr5:50796951 | T | G | 3 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 |
3 | HG02258.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1429-31T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 12/25 | chr5 | 50796951 | |||||||
chr5:50797079 | G | A | 1 | a0001c0001t0021g0318 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1479+47G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 13/25 | chr5 | 50797079 | |||||||
chr5:50797259 | G | A | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1575+26G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50797259 | |||||||
chr5:50797273 | T | C | 9 | a0001c0002t0002g0101 a0001c0002t0002g0102 a0001c0002t0002g0103 others(6): Show |
9 | HG02055.hp2 HG02257.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.1575+40T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50797273 | |||||||
chr5:50797370 | T | C | 4 | a0001c0002t0002g0075 a0001c0002t0002g0076 a0001c0002t0002g0077 others(1): Show |
4 | HG00639.hp1 HG01168.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.1575+137T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50797370 | |||||||
chr5:50797469 | C | A | 3 | a0001c0003t0011g0223 a0001c0003t0011g0224 a0001c0003t0011g0225 |
3 | HG02055.hp1 HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1575+236C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50797469 | |||||||
chr5:50797478 | A | G | 1 | a0001c0002t0003g0115 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1575+245A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50797478 | |||||||
chr5:50797490 | C | T | 1 | a0001c0003t0001g0239 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1575+257C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50797490 | |||||||
chr5:50797733 | A | C | 7 | a0001c0001t0002g0155 a0001c0001t0002g0166 a0001c0001t0002g0167 others(4): Show |
7 | HG01891.hp2 HG02717.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.1575+500A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50797733 | |||||||
chr5:50797754 | T | A | 3 | a0001c0001t0005g0017 a0001c0001t0005g0018 a0001c0001t0005g0019 |
3 | HG01884.hp1 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1575+521T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50797754 | |||||||
chr5:50797810 | A | G | 1 | a0001c0013t0005g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1575+577A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50797810 | |||||||
chr5:50797819 | A | G | 1 | a0001c0003t0001g0212 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1575+586A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50797819 | |||||||
chr5:50798212 | G | A | 1 | a0001c0001t0004g0055 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1575+979G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50798212 | |||||||
chr5:50798325 | C | A | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1575+1092C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50798325 | |||||||
chr5:50798342 | C | A | 1 | a0001c0002t0003g0122 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1575+1109C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50798342 | |||||||
chr5:50798424 | G | GT | 13 | a0001c0001t0001g0264 a0001c0001t0008g0258 a0001c0001t0008g0299 others(10): Show |
13 | HG01192.hp2 HG01884.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.1575+1205dupT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr5 | 50798424 | ||||||
chr5:50798442 | A | G | 1 | a0001c0001t0005g0012 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1575+1209A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50798442 | |||||||
chr5:50798581 | C | T | 4 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(1): Show |
4 | HG02486.hp2 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1575+1348C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50798581 | |||||||
chr5:50798664 | C | T | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1575+1431C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50798664 | |||||||
chr5:50798674 | G | A | 1 | a0001c0002t0002g0091 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1575+1441G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50798674 | |||||||
chr5:50798730 | C | T | 1 | a0001c0001t0015g0060 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1575+1497C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50798730 | |||||||
chr5:50798731 | G | A | 6 | a0001c0001t0002g0166 a0001c0001t0002g0167 a0001c0001t0002g0168 others(3): Show |
6 | HG01891.hp2 HG02717.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1575+1498G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50798731 | |||||||
chr5:50798735 | C | G | 1 | a0001c0002t0003g0130 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1575+1502C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50798735 | |||||||
chr5:50798848 | G | A | 1 | a0001c0001t0007g0190 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1575+1615G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50798848 | |||||||
chr5:50798858 | C | T | 3 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 |
3 | HG03098.hp2 NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1575+1625C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50798858 | |||||||
chr5:50798864 | C | T | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1575+1631C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50798864 | |||||||
chr5:50798975 | T | C | 55 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(52): Show |
57 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.1575+1742T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50798975 | |||||||
chr5:50798992 | T | C | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1575+1759T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50798992 | |||||||
chr5:50799166 | A | G | 8 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(5): Show |
8 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1575+1933A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50799166 | |||||||
chr5:50799253 | G | A | 12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(9): Show |
12 | HG01884.hp1 HG03098.hp1 HG03453.hp1 others(9): Show |
intron_variant | MODIFIER | c.1575+2020G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50799253 | |||||||
chr5:50799352 | C | T | 6 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(3): Show |
6 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1575+2119C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50799352 | |||||||
chr5:50799552 | C | G | 2 | a0001c0001t0001g0268 a0001c0001t0001g0274 |
2 | HG01081.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.1575+2319C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50799552 | |||||||
chr5:50799681 | C | T | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1575+2448C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50799681 | |||||||
chr5:50799760 | C | T | 1 | a0001c0012t0038g0008 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1575+2527C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50799760 | |||||||
chr5:50799940 | C | A | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1575+2707C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50799940 | |||||||
chr5:50799993 | A | G | 1 | a0001c0001t0008g0311 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1575+2760A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50799993 | |||||||
chr5:50800006 | C | T | 3 | a0001c0001t0030g0005 a0001c0007t0028g0007 a0001c0007t0029g0006 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1575+2773C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50800006 | |||||||
chr5:50800080 | A | G | 92 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(89): Show |
95 | HG00099.hp2 HG00642.hp1 HG00733.hp1 others(92): Show |
intron_variant | MODIFIER | c.1575+2847A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50800080 | |||||||
chr5:50800128 | G | A | 25 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(22): Show |
27 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.1575+2895G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50800128 | |||||||
chr5:50800361 | A | G | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1575+3128A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50800361 | |||||||
chr5:50800475 | CAAGAA | C | 6 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(3): Show |
6 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1575+3249_1575+325 others(9): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr5 | 50800475 | ||||||
chr5:50800654 | T | A | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1575+3421T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50800654 | |||||||
chr5:50800756 | A | AT | 52 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(49): Show |
52 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.1575+3540dupT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr5 | 50800756 | ||||||
chr5:50800756 | AT | A | 8 | a0001c0001t0001g0292 a0001c0001t0004g0049 a0001c0001t0015g0059 others(5): Show |
8 | HG01975.hp1 HG01975.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1575+3540delT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr5 | 50800756 | ||||||
chr5:50801112 | T | TTA | 22 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(19): Show |
22 | HG00438.hp2 HG00544.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.1575+3893_1575+389 others(6): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr5 | 50801112 | ||||||
chr5:50801224 | C | G | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1575+3991C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50801224 | |||||||
chr5:50801283 | G | A | 1 | a0001c0002t0042g0153 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1575+4050G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50801283 | |||||||
chr5:50801345 | C | A | 2 | a0001c0002t0003g0099 a0001c0002t0003g0100 |
2 | HG02735.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.1575+4112C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50801345 | |||||||
chr5:50801394 | A | G | 1 | a0001c0010t0036g0321 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1575+4161A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50801394 | |||||||
chr5:50801714 | G | C | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1575+4481G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50801714 | |||||||
chr5:50801798 | G | A | 55 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(52): Show |
57 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.1575+4565G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50801798 | |||||||
chr5:50802024 | G | A | 2 | a0001c0001t0006g0207 a0001c0001t0006g0208 |
2 | HG03486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1575+4791G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50802024 | |||||||
chr5:50802390 | C | T | 12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(9): Show |
12 | HG01884.hp1 HG03098.hp1 HG03453.hp1 others(9): Show |
intron_variant | MODIFIER | c.1575+5157C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50802390 | |||||||
chr5:50802574 | C | T | 6 | a0001c0001t0002g0166 a0001c0001t0002g0167 a0001c0001t0002g0168 others(3): Show |
6 | HG01891.hp2 HG02717.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1575+5341C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50802574 | |||||||
chr5:50802577 | G | A | 1 | a0001c0002t0002g0103 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1575+5344G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50802577 | |||||||
chr5:50802679 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1575+5446G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50802679 | |||||||
chr5:50802693 | A | C | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1575+5460A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50802693 | |||||||
chr5:50802763 | G | A | 1 | a0001c0001t0001g0279 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1575+5530G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50802763 | |||||||
chr5:50802796 | A | G | 25 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(22): Show |
27 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.1575+5563A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50802796 | |||||||
chr5:50802849 | A | T | 21 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(18): Show |
23 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.1575+5616A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50802849 | |||||||
chr5:50802888 | A | G | 1 | a0003c0009t0001g0286 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1575+5655A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50802888 | |||||||
chr5:50802965 | A | G | 1 | a0001c0002t0003g0319 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1575+5732A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50802965 | |||||||
chr5:50803085 | C | T | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1575+5852C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50803085 | |||||||
chr5:50803143 | A | G | 1 | a0002c0005t0009g0287 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1575+5910A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50803143 | |||||||
chr5:50803184 | T | C | 3 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 |
3 | HG01192.hp1 HG02280.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1575+5951T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50803184 | |||||||
chr5:50803239 | T | C | 9 | a0001c0003t0001g0210 a0001c0003t0001g0211 a0001c0003t0001g0212 others(6): Show |
9 | HG01934.hp2 HG01943.hp2 HG02148.hp2 others(6): Show |
intron_variant | MODIFIER | c.1575+6006T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50803239 | |||||||
chr5:50803242 | C | T | 1 | a0001c0001t0006g0199 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1575+6009C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50803242 | |||||||
chr5:50803307 | C | T | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1575+6074C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50803307 | |||||||
chr5:50803498 | T | G | 1 | a0001c0001t0019g0004 | 2 | HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1575+6265T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50803498 | |||||||
chr5:50803636 | T | C | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1575+6403T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50803636 | |||||||
chr5:50803673 | G | T | 4 | a0001c0001t0004g0053 a0001c0001t0004g0054 a0001c0001t0004g0055 others(1): Show |
4 | HG01261.hp2 HG02615.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1575+6440G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50803673 | |||||||
chr5:50803776 | A | T | 1 | a0001c0001t0004g0041 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1575+6543A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50803776 | |||||||
chr5:50803787 | A | G | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1575+6554A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50803787 | |||||||
chr5:50803938 | A | G | 1 | a0001c0002t0046g0141 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1575+6705A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50803938 | |||||||
chr5:50803980 | G | A | 64 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(61): Show |
67 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(64): Show |
intron_variant | MODIFIER | c.1575+6747G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50803980 | |||||||
chr5:50804024 | T | G | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1575+6791T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50804024 | |||||||
chr5:50804114 | A | G | 2 | a0001c0001t0004g0035 a0001c0001t0004g0036 |
2 | HG02886.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1575+6881A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50804114 | |||||||
chr5:50804200 | C | T | 1 | a0001c0001t0021g0318 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1575+6967C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50804200 | |||||||
chr5:50804339 | C | T | 8 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(5): Show |
8 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1575+7106C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50804339 | |||||||
chr5:50804369 | G | T | 1 | a0001c0004t0005g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1575+7136G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50804369 | |||||||
chr5:50804371 | G | A | 11 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0001t0007g0184 others(8): Show |
11 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.1575+7138G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50804371 | |||||||
chr5:50804449 | C | T | 57 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(54): Show |
60 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.1575+7216C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50804449 | |||||||
chr5:50804476 | G | A | 12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(9): Show |
12 | HG01884.hp1 HG03098.hp1 HG03453.hp1 others(9): Show |
intron_variant | MODIFIER | c.1575+7243G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50804476 | |||||||
chr5:50804509 | T | C | 1 | a0001c0001t0004g0038 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1575+7276T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50804509 | |||||||
chr5:50804588 | T | C | 3 | a0001c0001t0007g0182 a0001c0001t0007g0184 a0001c0001t0027g0185 |
3 | HG02145.hp2 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1575+7355T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50804588 | |||||||
chr5:50804729 | T | G | 1 | a0001c0001t0016g0283 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1575+7496T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50804729 | |||||||
chr5:50804781 | G | A | 11 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0001t0007g0184 others(8): Show |
11 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.1575+7548G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50804781 | |||||||
chr5:50804882 | C | T | 6 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(3): Show |
6 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1575+7649C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50804882 | |||||||
chr5:50804976 | G | A | 1 | a0001c0001t0007g0181 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1575+7743G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50804976 | |||||||
chr5:50804994 | G | C | 7 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(4): Show |
7 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1575+7761G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50804994 | |||||||
chr5:50805244 | A | C | 1 | a0001c0007t0029g0006 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1575+8011A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50805244 | |||||||
chr5:50805379 | A | G | 2 | a0001c0003t0011g0223 a0001c0003t0011g0225 |
2 | HG02055.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1575+8146A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50805379 | |||||||
chr5:50805643 | CA | C | 72 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(69): Show |
75 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.1575+8414delA | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr5 | 50805643 | ||||||
chr5:50805646 | A | G | 1 | a0001c0001t0019g0004 | 2 | HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1575+8413A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50805646 | |||||||
chr5:50805737 | T | A | 1 | a0001c0001t0001g0062 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1575+8504T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50805737 | |||||||
chr5:50805769 | A | G | 1 | a0001c0002t0003g0087 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1575+8536A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50805769 | |||||||
chr5:50805823 | T | C | 4 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(1): Show |
4 | HG02486.hp2 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1575+8590T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50805823 | |||||||
chr5:50805883 | G | A | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1575+8650G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50805883 | |||||||
chr5:50806273 | G | A | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1575+9040G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50806273 | |||||||
chr5:50806460 | T | C | 1 | a0001c0002t0002g0162 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1576-8972T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50806460 | |||||||
chr5:50806723 | A | G | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1576-8709A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50806723 | |||||||
chr5:50806748 | T | C | 11 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0001t0007g0184 others(8): Show |
11 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.1576-8684T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50806748 | |||||||
chr5:50806828 | G | A | 12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(9): Show |
12 | HG01884.hp1 HG03098.hp1 HG03453.hp1 others(9): Show |
intron_variant | MODIFIER | c.1576-8604G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50806828 | |||||||
chr5:50806933 | T | A | 3 | a0001c0001t0030g0005 a0001c0007t0028g0007 a0001c0007t0029g0006 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1576-8499T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50806933 | |||||||
chr5:50806953 | T | C | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1576-8479T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50806953 | |||||||
chr5:50807031 | T | C | 3 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 |
3 | HG01192.hp1 HG02280.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1576-8401T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50807031 | |||||||
chr5:50807676 | T | C | 1 | a0001c0001t0024g0051 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1576-7756T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50807676 | |||||||
chr5:50807784 | C | T | 201 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(198): Show |
204 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(201): Show |
intron_variant | MODIFIER | c.1576-7648C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50807784 | |||||||
chr5:50807984 | G | A | 113 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(110): Show |
113 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.1576-7448G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50807984 | |||||||
chr5:50808044 | A | C | 6 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(3): Show |
6 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1576-7388A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50808044 | |||||||
chr5:50808051 | G | T | 1 | a0001c0001t0004g0034 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1576-7381G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50808051 | |||||||
chr5:50808081 | C | G | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1576-7351C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50808081 | |||||||
chr5:50808165 | G | A | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1576-7267G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50808165 | |||||||
chr5:50808221 | A | C | 3 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 |
3 | HG01192.hp1 HG02280.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1576-7211A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50808221 | |||||||
chr5:50808286 | A | G | 2 | a0001c0001t0012g0280 a0001c0001t0012g0281 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1576-7146A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50808286 | |||||||
chr5:50808384 | G | A | 12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(9): Show |
12 | HG01884.hp1 HG03098.hp1 HG03453.hp1 others(9): Show |
intron_variant | MODIFIER | c.1576-7048G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50808384 | |||||||
chr5:50808414 | C | G | 1 | a0001c0012t0038g0008 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1576-7018C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50808414 | |||||||
chr5:50808437 | G | A | 1 | a0001c0001t0002g0155 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1576-6995G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50808437 | |||||||
chr5:50808537 | A | G | 267 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(264): Show |
270 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(267): Show |
intron_variant | MODIFIER | c.1576-6895A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50808537 | |||||||
chr5:50808595 | A | G | 1 | a0001c0006t0004g0322 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1576-6837A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50808595 | |||||||
chr5:50808611 | G | A | 1 | a0001c0001t0007g0182 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1576-6821G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50808611 | |||||||
chr5:50808933 | A | G | 25 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(22): Show |
27 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.1576-6499A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50808933 | |||||||
chr5:50809005 | T | G | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1576-6427T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50809005 | |||||||
chr5:50809024 | TA | T | 114 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(111): Show |
114 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.1576-6399delA | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr5 | 50809024 | ||||||
chr5:50809063 | C | T | 1 | a0001c0002t0003g0128 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1576-6369C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50809063 | |||||||
chr5:50809306 | G | T | 4 | a0001c0001t0007g0182 a0001c0001t0007g0184 a0001c0001t0027g0185 others(1): Show |
4 | HG02145.hp2 HG02809.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1576-6126G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50809306 | |||||||
chr5:50809352 | A | G | 1 | a0001c0001t0007g0184 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1576-6080A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50809352 | |||||||
chr5:50809355 | G | A | 6 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(3): Show |
6 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1576-6077G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50809355 | |||||||
chr5:50809365 | T | C | 25 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(22): Show |
27 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.1576-6067T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50809365 | |||||||
chr5:50809460 | A | G | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1576-5972A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50809460 | |||||||
chr5:50809603 | G | T | 1 | a0001c0002t0002g0091 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1576-5829G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50809603 | |||||||
chr5:50809654 | G | T | 1 | a0001c0002t0002g0082 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1576-5778G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50809654 | |||||||
chr5:50809668 | G | T | 1 | a0001c0007t0028g0007 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1576-5764G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50809668 | |||||||
chr5:50809684 | C | G | 31 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(28): Show |
32 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.1576-5748C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50809684 | |||||||
chr5:50809731 | T | C | 1 | a0001c0003t0001g0239 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1576-5701T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50809731 | |||||||
chr5:50809868 | A | T | 31 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(28): Show |
32 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.1576-5564A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50809868 | |||||||
chr5:50809919 | G | A | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1576-5513G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50809919 | |||||||
chr5:50810261 | A | G | 9 | a0001c0002t0002g0101 a0001c0002t0002g0102 a0001c0002t0002g0103 others(6): Show |
9 | HG02055.hp2 HG02257.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.1576-5171A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50810261 | |||||||
chr5:50810574 | T | G | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1576-4858T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50810574 | |||||||
chr5:50810605 | G | A | 211 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(208): Show |
214 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(211): Show |
intron_variant | MODIFIER | c.1576-4827G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50810605 | |||||||
chr5:50810617 | A | G | 1 | a0001c0004t0005g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1576-4815A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50810617 | |||||||
chr5:50810812 | A | G | 9 | a0001c0002t0002g0101 a0001c0002t0002g0102 a0001c0002t0002g0103 others(6): Show |
9 | HG02055.hp2 HG02257.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.1576-4620A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50810812 | |||||||
chr5:50810951 | C | T | 5 | a0001c0002t0009g0089 a0002c0005t0009g0270 a0002c0005t0009g0277 others(2): Show |
5 | NA18987.hp2 NA19062.hp1 NA19063.hp1 others(2): Show |
intron_variant | MODIFIER | c.1576-4481C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50810951 | |||||||
chr5:50811066 | A | T | 8 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(5): Show |
8 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1576-4366A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50811066 | |||||||
chr5:50811177 | A | G | 1 | a0001c0001t0008g0316 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1576-4255A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50811177 | |||||||
chr5:50811184 | C | G | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1576-4248C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50811184 | |||||||
chr5:50811369 | G | T | 1 | a0001c0001t0007g0181 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1576-4063G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50811369 | |||||||
chr5:50811414 | C | T | 47 | a0001c0003t0001g0209 a0001c0003t0001g0210 a0001c0003t0001g0211 others(44): Show |
47 | HG00673.hp1 HG00738.hp1 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.1576-4018C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50811414 | |||||||
chr5:50811415 | G | A | 47 | a0001c0003t0001g0209 a0001c0003t0001g0210 a0001c0003t0001g0211 others(44): Show |
47 | HG00673.hp1 HG00738.hp1 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.1576-4017G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50811415 | |||||||
chr5:50811556 | C | T | 12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(9): Show |
12 | HG01884.hp1 HG03098.hp1 HG03453.hp1 others(9): Show |
intron_variant | MODIFIER | c.1576-3876C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50811556 | |||||||
chr5:50811595 | GT | G | 9 | a0001c0001t0008g0258 a0001c0001t0008g0310 a0001c0001t0008g0311 others(6): Show |
9 | HG01192.hp2 HG01884.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1576-3827delT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr5 | 50811595 | ||||||
chr5:50811596 | T | G | 1 | a0001c0001t0001g0305 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1576-3836T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50811596 | |||||||
chr5:50811809 | A | G | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1576-3623A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50811809 | |||||||
chr5:50811833 | G | A | 1 | a0001c0001t0001g0317 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1576-3599G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50811833 | |||||||
chr5:50811957 | A | G | 1 | a0001c0001t0012g0309 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1576-3475A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50811957 | |||||||
chr5:50812073 | G | A | 11 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0001t0007g0184 others(8): Show |
11 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.1576-3359G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50812073 | |||||||
chr5:50812107 | A | T | 1 | a0001c0001t0024g0051 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1576-3325A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50812107 | |||||||
chr5:50812369 | C | T | 1 | a0001c0012t0038g0008 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1576-3063C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50812369 | |||||||
chr5:50812371 | G | T | 1 | a0001c0012t0038g0008 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1576-3061G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50812371 | |||||||
chr5:50812411 | G | A | 64 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(61): Show |
67 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(64): Show |
intron_variant | MODIFIER | c.1576-3021G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50812411 | |||||||
chr5:50812420 | G | A | 11 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0001t0007g0184 others(8): Show |
11 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.1576-3012G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50812420 | |||||||
chr5:50812423 | C | T | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1576-3009C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50812423 | |||||||
chr5:50812543 | T | C | 6 | a0001c0002t0009g0089 a0002c0005t0009g0270 a0002c0005t0009g0271 others(3): Show |
6 | NA18942.hp1 NA18987.hp2 NA19062.hp1 others(3): Show |
intron_variant | MODIFIER | c.1576-2889T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50812543 | |||||||
chr5:50812711 | GT | G | 25 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(22): Show |
27 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.1576-2716delT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr5 | 50812711 | ||||||
chr5:50812718 | T | C | 2 | a0001c0001t0001g0291 a0001c0001t0001g0293 |
2 | NA18961.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1576-2714T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50812718 | |||||||
chr5:50812875 | G | C | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1576-2557G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50812875 | |||||||
chr5:50812955 | C | A | 1 | a0001c0007t0028g0007 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1576-2477C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50812955 | |||||||
chr5:50812986 | G | C | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1576-2446G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50812986 | |||||||
chr5:50813096 | G | A | 2 | a0001c0002t0002g0074 a0001c0002t0002g0178 |
2 | HG00642.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1576-2336G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50813096 | |||||||
chr5:50813131 | A | C | 1 | a0001c0001t0008g0311 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1576-2301A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50813131 | |||||||
chr5:50813147 | C | G | 6 | a0001c0002t0009g0089 a0002c0005t0009g0270 a0002c0005t0009g0271 others(3): Show |
6 | NA18942.hp1 NA18987.hp2 NA19062.hp1 others(3): Show |
intron_variant | MODIFIER | c.1576-2285C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50813147 | |||||||
chr5:50813160 | T | C | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1576-2272T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50813160 | |||||||
chr5:50813203 | A | T | 277 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(274): Show |
283 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(280): Show |
intron_variant | MODIFIER | c.1576-2229A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50813203 | |||||||
chr5:50813225 | C | G | 277 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(274): Show |
283 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(280): Show |
intron_variant | MODIFIER | c.1576-2207C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50813225 | |||||||
chr5:50813250 | G | T | 11 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0001t0007g0184 others(8): Show |
11 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.1576-2182G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50813250 | |||||||
chr5:50813267 | G | A | 1 | a0001c0002t0002g0111 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1576-2165G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50813267 | |||||||
chr5:50813278 | G | C | 1 | a0001c0010t0036g0321 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1576-2154G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50813278 | |||||||
chr5:50813394 | GTC | G | 53 | a0001c0002t0003g0002 a0001c0002t0003g0003 a0001c0002t0003g0069 others(50): Show |
56 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.1576-2036_1576-203 others(6): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr5 | 50813394 | ||||||
chr5:50813501 | A | G | 1 | a0001c0002t0003g0080 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1576-1931A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50813501 | |||||||
chr5:50813633 | A | G | 1 | a0001c0007t0029g0006 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1576-1799A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50813633 | |||||||
chr5:50813667 | T | C | 1 | a0001c0001t0001g0305 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1576-1765T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50813667 | |||||||
chr5:50813707 | A | G | 1 | a0001c0001t0007g0181 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1576-1725A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50813707 | |||||||
chr5:50813732 | C | T | 47 | a0001c0003t0001g0209 a0001c0003t0001g0210 a0001c0003t0001g0211 others(44): Show |
47 | HG00673.hp1 HG00738.hp1 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.1576-1700C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50813732 | |||||||
chr5:50813813 | G | C | 3 | a0001c0001t0006g0196 a0001c0001t0006g0197 a0001c0001t0006g0198 |
3 | HG01167.hp2 HG01169.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1576-1619G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50813813 | |||||||
chr5:50813816 | T | C | 1 | a0001c0002t0002g0178 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1576-1616T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50813816 | |||||||
chr5:50813826 | C | T | 24 | a0001c0003t0001g0209 a0001c0003t0001g0210 a0001c0003t0001g0211 others(21): Show |
24 | HG00738.hp1 HG01243.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.1576-1606C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50813826 | |||||||
chr5:50813865 | T | G | 1 | a0001c0001t0001g0282 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1576-1567T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50813865 | |||||||
chr5:50813918 | A | G | 1 | a0001c0001t0007g0181 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1576-1514A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50813918 | |||||||
chr5:50813949 | A | G | 1 | a0001c0001t0001g0261 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1576-1483A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50813949 | |||||||
chr5:50814021 | A | G | 3 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 |
3 | HG01192.hp1 HG02280.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1576-1411A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50814021 | |||||||
chr5:50814113 | G | A | 1 | a0001c0001t0005g0024 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1576-1319G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50814113 | |||||||
chr5:50814173 | A | G | 1 | a0001c0001t0004g0055 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1576-1259A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50814173 | |||||||
chr5:50814298 | G | A | 12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(9): Show |
12 | HG01884.hp1 HG03098.hp1 HG03453.hp1 others(9): Show |
intron_variant | MODIFIER | c.1576-1134G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50814298 | |||||||
chr5:50814314 | A | G | 1 | a0001c0002t0003g0158 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1576-1118A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50814314 | |||||||
chr5:50814339 | GTTGAAA | G | 6 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(3): Show |
6 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1576-1087_1576-108 others(10): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr5 | 50814339 | ||||||
chr5:50814761 | A | G | 1 | a0001c0002t0003g0079 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1576-671A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50814761 | |||||||
chr5:50814912 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1576-520G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50814912 | |||||||
chr5:50814917 | G | A | 12 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0001t0007g0184 others(9): Show |
12 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.1576-515G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50814917 | |||||||
chr5:50815124 | G | A | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1576-308G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50815124 | |||||||
chr5:50815261 | C | T | 7 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1576-171C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50815261 | |||||||
chr5:50815269 | T | A | 3 | a0001c0001t0005g0017 a0001c0001t0005g0018 a0001c0001t0005g0019 |
3 | HG01884.hp1 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1576-163T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50815269 | |||||||
chr5:50815292 | C | T | 8 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(5): Show |
8 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1576-140C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 14/25 | chr5 | 50815292 | |||||||
chr5:50815699 | T | C | 2 | a0001c0001t0007g0184 a0001c0001t0027g0185 |
2 | HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1668+175T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50815699 | |||||||
chr5:50815709 | G | A | 1 | a0001c0001t0008g0311 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1668+185G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50815709 | |||||||
chr5:50815801 | A | G | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1668+277A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50815801 | |||||||
chr5:50815810 | C | G | 1 | a0001c0001t0005g0010 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1668+286C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50815810 | |||||||
chr5:50815823 | T | G | 8 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(5): Show |
8 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1668+299T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50815823 | |||||||
chr5:50815840 | T | C | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1668+316T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50815840 | |||||||
chr5:50815991 | AT | A | 21 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(18): Show |
22 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1668+477delT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr5 | 50815991 | ||||||
chr5:50816088 | G | C | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1668+564G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50816088 | |||||||
chr5:50816210 | A | G | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1668+686A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50816210 | |||||||
chr5:50816277 | G | T | 3 | a0001c0001t0030g0005 a0001c0007t0028g0007 a0001c0007t0029g0006 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1668+753G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50816277 | |||||||
chr5:50816334 | A | C | 4 | a0001c0002t0002g0109 a0001c0002t0002g0110 a0001c0002t0002g0111 others(1): Show |
4 | HG01433.hp1 HG02622.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1668+810A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50816334 | |||||||
chr5:50816334 | A | G | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1668+810A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50816334 | |||||||
chr5:50816495 | A | G | 1 | a0001c0004t0005g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1668+971A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50816495 | |||||||
chr5:50816513 | C | A | 1 | a0001c0001t0016g0301 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1668+989C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50816513 | |||||||
chr5:50816709 | C | G | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1668+1185C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50816709 | |||||||
chr5:50816742 | C | T | 3 | a0001c0001t0030g0005 a0001c0007t0028g0007 a0001c0007t0029g0006 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1668+1218C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50816742 | |||||||
chr5:50816759 | A | G | 1 | a0001c0002t0005g0071 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1668+1235A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50816759 | |||||||
chr5:50816842 | C | G | 2 | a0001c0001t0001g0262 a0001c0001t0001g0263 |
2 | HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1668+1318C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50816842 | |||||||
chr5:50817013 | T | C | 6 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(3): Show |
6 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1668+1489T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50817013 | |||||||
chr5:50817236 | A | G | 1 | a0001c0012t0038g0008 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1668+1712A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50817236 | |||||||
chr5:50817292 | G | A | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1668+1768G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50817292 | |||||||
chr5:50817322 | G | T | 1 | a0001c0002t0002g0147 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1668+1798G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50817322 | |||||||
chr5:50817676 | A | G | 1 | a0001c0010t0036g0321 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1668+2152A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50817676 | |||||||
chr5:50817819 | T | A | 1 | a0001c0012t0038g0008 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1668+2295T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50817819 | |||||||
chr5:50817826 | C | T | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1668+2302C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50817826 | |||||||
chr5:50817827 | G | A | 1 | a0001c0010t0036g0321 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1668+2303G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50817827 | |||||||
chr5:50817853 | G | T | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1668+2329G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50817853 | |||||||
chr5:50817860 | T | G | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1668+2336T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50817860 | |||||||
chr5:50818037 | C | T | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1668+2513C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50818037 | |||||||
chr5:50818097 | T | G | 1 | a0001c0001t0001g0180 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1668+2573T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50818097 | |||||||
chr5:50818120 | A | T | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1668+2596A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50818120 | |||||||
chr5:50818123 | C | G | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1668+2599C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50818123 | |||||||
chr5:50818150 | T | C | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1668+2626T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50818150 | |||||||
chr5:50818175 | A | AG | 12 | a0001c0001t0001g0266 a0001c0001t0001g0290 a0001c0001t0001g0305 others(9): Show |
12 | HG00738.hp2 HG01934.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1668+2652dupG | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr5 | 50818175 | ||||||
chr5:50818176 | GC | G | 34 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(31): Show |
34 | HG01167.hp1 HG01192.hp1 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.1668+2665delC | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr5 | 50818176 | ||||||
chr5:50818177 | C | G | 147 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(144): Show |
149 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.1668+2653C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50818177 | |||||||
chr5:50818178 | C | G | 29 | a0001c0001t0001g0266 a0001c0001t0001g0290 a0001c0001t0001g0305 others(26): Show |
29 | HG00738.hp2 HG01167.hp1 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.1668+2654C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50818178 | |||||||
chr5:50818179 | C | G | 114 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(111): Show |
114 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.1668+2655C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50818179 | |||||||
chr5:50818182 | C | CG | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1668+2658_1668+265 others(5): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50818182 | |||||||
chr5:50818185 | C | A | 1 | a0001c0002t0003g0073 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1668+2661C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50818185 | |||||||
chr5:50818189 | C | A | 3 | a0001c0001t0001g0267 a0001c0001t0001g0300 a0001c0001t0004g0042 |
3 | HG01069.hp1 HG01243.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1668+2665C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50818189 | |||||||
chr5:50818190 | A | C | 3 | a0001c0002t0002g0077 a0001c0007t0028g0007 a0001c0007t0029g0006 |
3 | HG01169.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1668+2666A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50818190 | |||||||
chr5:50818226 | T | TTTTTCTT others(3): Show |
88 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(85): Show |
91 | HG00099.hp2 HG00642.hp1 HG00733.hp1 others(88): Show |
intron_variant | MODIFIER | c.1668+2710_1668+271 others(14): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr5 | 50818226 | ||||||
chr5:50818247 | C | T | 37 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(34): Show |
39 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.1668+2723C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50818247 | |||||||
chr5:50818310 | C | G | 11 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0001t0007g0184 others(8): Show |
11 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.1668+2786C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50818310 | |||||||
chr5:50818347 | G | C | 10 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(7): Show |
10 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1668+2823G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50818347 | |||||||
chr5:50818431 | T | C | 12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(9): Show |
12 | HG01884.hp1 HG03098.hp1 HG03453.hp1 others(9): Show |
intron_variant | MODIFIER | c.1669-2782T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50818431 | |||||||
chr5:50818587 | C | T | 113 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(110): Show |
113 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.1669-2626C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50818587 | |||||||
chr5:50818677 | C | G | 4 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(1): Show |
4 | HG02486.hp2 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1669-2536C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50818677 | |||||||
chr5:50818786 | A | C | 8 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(5): Show |
8 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1669-2427A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50818786 | |||||||
chr5:50818828 | G | A | 3 | a0001c0001t0007g0182 a0001c0001t0007g0184 a0001c0001t0027g0185 |
3 | HG02145.hp2 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1669-2385G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50818828 | |||||||
chr5:50818907 | C | T | 1 | a0001c0003t0001g0253 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1669-2306C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50818907 | |||||||
chr5:50818913 | G | C | 2 | a0001c0002t0003g0174 a0001c0002t0003g0175 |
2 | HG01346.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1669-2300G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50818913 | |||||||
chr5:50819018 | A | G | 49 | a0001c0001t0004g0034 a0001c0001t0004g0035 a0001c0001t0004g0036 others(46): Show |
50 | HG00733.hp1 HG01167.hp2 HG01169.hp2 others(47): Show |
intron_variant | MODIFIER | c.1669-2195A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50819018 | |||||||
chr5:50819110 | G | A | 1 | a0001c0001t0001g0279 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1669-2103G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50819110 | |||||||
chr5:50819125 | T | C | 1 | a0001c0010t0036g0321 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1669-2088T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50819125 | |||||||
chr5:50819292 | G | T | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1669-1921G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50819292 | |||||||
chr5:50819358 | AGTGAGAG others(13): Show |
A | 1 | a0001c0013t0005g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1669-1852_1669-183 others(24): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr5 | 50819358 | ||||||
chr5:50819427 | C | CT | 31 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(28): Show |
31 | HG00099.hp2 HG00438.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1669-1756dupT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr5 | 50819427 | ||||||
chr5:50819427 | C | CTT | 12 | a0001c0001t0004g0001 a0001c0001t0004g0035 a0001c0001t0004g0036 others(9): Show |
13 | HG01071.hp1 HG01081.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.1669-1757_1669-175 others(6): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr5 | 50819427 | ||||||
chr5:50819427 | C | CTTT | 13 | a0001c0001t0004g0048 a0001c0001t0006g0193 a0001c0001t0006g0195 others(10): Show |
14 | HG01167.hp2 HG01169.hp2 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.1669-1758_1669-175 others(7): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr5 | 50819427 | ||||||
chr5:50819427 | CT | C | 66 | a0001c0001t0001g0064 a0001c0001t0001g0180 a0001c0001t0001g0264 others(63): Show |
66 | HG00673.hp1 HG00738.hp1 HG00738.hp2 others(63): Show |
intron_variant | MODIFIER | c.1669-1756delT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr5 | 50819427 | ||||||
chr5:50819427 | CTT | C | 63 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(60): Show |
63 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.1669-1757_1669-175 others(6): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr5 | 50819427 | ||||||
chr5:50819427 | CTTT | C | 11 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0274 others(8): Show |
11 | HG01081.hp1 HG01109.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.1669-1758_1669-175 others(7): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr5 | 50819427 | ||||||
chr5:50819427 | CTTTTTTT others(4): Show |
C | 1 | a0001c0007t0028g0007 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1669-1766_1669-175 others(15): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr5 | 50819427 | ||||||
chr5:50819427 | CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0031g0306 a0001c0007t0029g0006 |
2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1669-1767_1669-175 others(16): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr5 | 50819427 | ||||||
chr5:50819427 | CTTTTTTT others(11): Show |
C | 1 | a0001c0001t0008g0258 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1669-1773_1669-175 others(22): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr5 | 50819427 | ||||||
chr5:50819550 | C | T | 8 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(5): Show |
8 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1669-1663C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50819550 | |||||||
chr5:50819691 | T | A | 3 | a0001c0002t0009g0089 a0002c0005t0009g0277 a0002c0005t0009g0278 |
3 | NA18987.hp2 NA19062.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1669-1522T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50819691 | |||||||
chr5:50819737 | G | A | 1 | a0001c0001t0006g0201 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1669-1476G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50819737 | |||||||
chr5:50819737 | G | T | 6 | a0001c0002t0009g0089 a0002c0005t0009g0270 a0002c0005t0009g0271 others(3): Show |
6 | NA18942.hp1 NA18987.hp2 NA19062.hp1 others(3): Show |
intron_variant | MODIFIER | c.1669-1476G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50819737 | |||||||
chr5:50819750 | A | G | 1 | a0001c0002t0002g0091 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1669-1463A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50819750 | |||||||
chr5:50820053 | G | T | 4 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(1): Show |
4 | HG02486.hp2 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1669-1160G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50820053 | |||||||
chr5:50820094 | G | A | 4 | a0001c0001t0007g0182 a0001c0001t0007g0184 a0001c0001t0027g0185 others(1): Show |
4 | HG02145.hp2 HG02809.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1669-1119G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50820094 | |||||||
chr5:50820227 | C | T | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1669-986C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50820227 | |||||||
chr5:50820375 | A | ACT | 3 | a0001c0001t0030g0005 a0001c0007t0028g0007 a0001c0007t0029g0006 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1669-835_1669-834d others(4): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr5 | 50820375 | ||||||
chr5:50820462 | A | G | 1 | a0001c0012t0038g0008 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1669-751A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50820462 | |||||||
chr5:50820469 | T | C | 6 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(3): Show |
6 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1669-744T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50820469 | |||||||
chr5:50820622 | T | C | 47 | a0001c0003t0001g0209 a0001c0003t0001g0210 a0001c0003t0001g0211 others(44): Show |
47 | HG00673.hp1 HG00738.hp1 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.1669-591T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50820622 | |||||||
chr5:50820711 | C | A | 1 | a0001c0001t0001g0305 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1669-502C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50820711 | |||||||
chr5:50820797 | C | A | 2 | a0001c0001t0001g0262 a0001c0001t0001g0263 |
2 | HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1669-416C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50820797 | |||||||
chr5:50820839 | A | C | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1669-374A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50820839 | |||||||
chr5:50820878 | A | G | 1 | a0001c0001t0008g0311 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1669-335A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50820878 | |||||||
chr5:50820914 | G | A | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1669-299G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 15/25 | chr5 | 50820914 | |||||||
chr5:50821384 | A | G | 1 | a0001c0001t0007g0181 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1794+46A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 16/25 | chr5 | 50821384 | |||||||
chr5:50821447 | A | T | 4 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0303 others(1): Show |
4 | NA18948.hp1 NA18960.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.1794+109A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 16/25 | chr5 | 50821447 | |||||||
chr5:50821540 | G | A | 1 | a0001c0001t0004g0034 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1794+202G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 16/25 | chr5 | 50821540 | |||||||
chr5:50821562 | C | G | 2 | a0001c0002t0002g0101 a0001c0002t0002g0102 |
2 | HG02055.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1794+224C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 16/25 | chr5 | 50821562 | |||||||
chr5:50821668 | A | C | 1 | a0003c0009t0001g0286 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1794+330A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 16/25 | chr5 | 50821668 | |||||||
chr5:50821766 | A | G | 7 | a0001c0002t0002g0082 a0001c0002t0002g0083 a0001c0002t0002g0084 others(4): Show |
7 | HG00438.hp1 HG00609.hp1 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.1794+428A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 16/25 | chr5 | 50821766 | |||||||
chr5:50821803 | T | C | 1 | a0001c0002t0002g0111 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1794+465T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 16/25 | chr5 | 50821803 | |||||||
chr5:50821948 | C | T | 2 | a0001c0002t0002g0074 a0001c0002t0002g0178 |
2 | HG00642.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1795-387C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 16/25 | chr5 | 50821948 | |||||||
chr5:50821983 | G | T | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1795-352G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 16/25 | chr5 | 50821983 | |||||||
chr5:50822102 | G | A | 3 | a0001c0003t0001g0237 a0001c0003t0001g0238 a0001c0003t0001g0246 |
3 | HG02074.hp2 NA19088.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1795-233G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 16/25 | chr5 | 50822102 | |||||||
chr5:50822112 | A | G | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1795-223A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 16/25 | chr5 | 50822112 | |||||||
chr5:50822183 | T | C | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1795-152T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 16/25 | chr5 | 50822183 | |||||||
chr5:50822266 | A | G | 8 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(5): Show |
8 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1795-69A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 16/25 | chr5 | 50822266 | |||||||
chr5:50822297 | C | A | 4 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(1): Show |
4 | HG02056.hp1 NA18974.hp2 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.1795-38C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 16/25 | chr5 | 50822297 | |||||||
chr5:50822412 | A | G | 1 | a0001c0001t0002g0155 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1860+12A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 17/25 | chr5 | 50822412 | |||||||
chr5:50822416 | G | A | 11 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0001t0007g0184 others(8): Show |
11 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.1860+16G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 17/25 | chr5 | 50822416 | |||||||
chr5:50822620 | C | T | 1 | a0001c0012t0038g0008 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1860+220C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 17/25 | chr5 | 50822620 | |||||||
chr5:50822723 | G | A | 4 | a0001c0003t0001g0234 a0001c0003t0001g0235 a0001c0003t0001g0236 others(1): Show |
4 | HG00673.hp1 NA18954.hp2 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1860+323G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 17/25 | chr5 | 50822723 | |||||||
chr5:50822828 | G | T | 1 | a0001c0001t0001g0064 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1860+428G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 17/25 | chr5 | 50822828 | |||||||
chr5:50822835 | G | A | 1 | a0001c0002t0002g0088 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1860+435G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 17/25 | chr5 | 50822835 | |||||||
chr5:50822938 | C | A | 1 | a0001c0012t0038g0008 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1860+538C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 17/25 | chr5 | 50822938 | |||||||
chr5:50822952 | A | G | 11 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0001t0007g0184 others(8): Show |
11 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.1860+552A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 17/25 | chr5 | 50822952 | |||||||
chr5:50823062 | T | C | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1860+662T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 17/25 | chr5 | 50823062 | |||||||
chr5:50823074 | C | T | 3 | a0001c0001t0004g0034 a0001c0001t0004g0039 a0001c0001t0004g0040 |
3 | HG00733.hp1 HG02602.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1860+674C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 17/25 | chr5 | 50823074 | |||||||
chr5:50823078 | CATT | C | 3 | a0001c0004t0005g0029 a0001c0004t0005g0030 a0001c0004t0005g0031 |
3 | HG01109.hp2 HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1860+681_1860+683d others(5): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr5 | 50823078 | ||||||
chr5:50823125 | T | C | 202 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(199): Show |
205 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(202): Show |
intron_variant | MODIFIER | c.1860+725T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 17/25 | chr5 | 50823125 | |||||||
chr5:50823326 | G | T | 47 | a0001c0003t0001g0209 a0001c0003t0001g0210 a0001c0003t0001g0211 others(44): Show |
47 | HG00673.hp1 HG00738.hp1 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.1860+926G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 17/25 | chr5 | 50823326 | |||||||
chr5:50823461 | C | T | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1860+1061C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 17/25 | chr5 | 50823461 | |||||||
chr5:50823581 | G | C | 1 | a0001c0012t0038g0008 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1860+1181G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 17/25 | chr5 | 50823581 | |||||||
chr5:50823708 | C | T | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1861-1200C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 17/25 | chr5 | 50823708 | |||||||
chr5:50823739 | A | G | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1861-1169A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 17/25 | chr5 | 50823739 | |||||||
chr5:50823905 | G | A | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1861-1003G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 17/25 | chr5 | 50823905 | |||||||
chr5:50824039 | A | G | 9 | a0001c0002t0002g0101 a0001c0002t0002g0102 a0001c0002t0002g0103 others(6): Show |
9 | HG02055.hp2 HG02257.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.1861-869A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 17/25 | chr5 | 50824039 | |||||||
chr5:50824075 | A | G | 41 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(38): Show |
43 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.1861-833A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 17/25 | chr5 | 50824075 | |||||||
chr5:50824219 | A | C | 5 | a0001c0001t0007g0186 a0001c0001t0007g0187 a0001c0001t0007g0188 others(2): Show |
5 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1861-689A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 17/25 | chr5 | 50824219 | |||||||
chr5:50824433 | C | T | 1 | a0001c0010t0036g0321 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1861-475C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 17/25 | chr5 | 50824433 | |||||||
chr5:50824467 | A | T | 2 | a0002c0005t0009g0270 a0002c0005t0009g0287 |
2 | NA19063.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.1861-441A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 17/25 | chr5 | 50824467 | |||||||
chr5:50824512 | A | G | 1 | a0001c0002t0003g0154 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1861-396A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 17/25 | chr5 | 50824512 | |||||||
chr5:50824585 | C | CA | 36 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(33): Show |
38 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.1861-322dupA | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr5 | 50824585 | ||||||
chr5:50824637 | G | C | 36 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(33): Show |
38 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.1861-271G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 17/25 | chr5 | 50824637 | |||||||
chr5:50824796 | AAAT | A | 3 | a0001c0001t0030g0005 a0001c0007t0028g0007 a0001c0007t0029g0006 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1861-111_1861-109d others(5): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 17/25 | chr5 | 50824796 | |||||||
chr5:50824828 | G | A | 1 | a0001c0001t0001g0304 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1861-80G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 17/25 | chr5 | 50824828 | |||||||
chr5:50825038 | A | G | 6 | a0001c0001t0002g0166 a0001c0001t0002g0167 a0001c0001t0002g0168 others(3): Show |
6 | HG01891.hp2 HG02717.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1928+63A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 18/25 | chr5 | 50825038 | |||||||
chr5:50825051 | A | T | 2 | a0001c0001t0004g0039 a0001c0001t0004g0040 |
2 | HG00733.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1928+76A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 18/25 | chr5 | 50825051 | |||||||
chr5:50825145 | C | T | 1 | a0001c0003t0011g0224 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1928+170C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 18/25 | chr5 | 50825145 | |||||||
chr5:50825267 | G | C | 1 | a0001c0002t0002g0157 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1928+292G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 18/25 | chr5 | 50825267 | |||||||
chr5:50825322 | A | C | 1 | a0001c0010t0036g0321 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1928+347A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 18/25 | chr5 | 50825322 | |||||||
chr5:50825437 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1928+462C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 18/25 | chr5 | 50825437 | |||||||
chr5:50825469 | A | C | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1928+494A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 18/25 | chr5 | 50825469 | |||||||
chr5:50825789 | C | T | 201 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(198): Show |
204 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(201): Show |
intron_variant | MODIFIER | c.1928+814C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 18/25 | chr5 | 50825789 | |||||||
chr5:50825814 | G | C | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1928+839G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 18/25 | chr5 | 50825814 | |||||||
chr5:50826102 | G | A | 1 | a0001c0001t0008g0299 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1929-653G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 18/25 | chr5 | 50826102 | |||||||
chr5:50826333 | GA | G | 13 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0001t0007g0184 others(10): Show |
13 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.1929-414delA | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr5 | 50826333 | ||||||
chr5:50826489 | G | T | 1 | a0001c0002t0003g0179 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1929-266G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 18/25 | chr5 | 50826489 | |||||||
chr5:50826502 | T | C | 12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(9): Show |
12 | HG01884.hp1 HG03098.hp1 HG03453.hp1 others(9): Show |
intron_variant | MODIFIER | c.1929-253T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 18/25 | chr5 | 50826502 | |||||||
chr5:50826531 | C | A | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1929-224C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 18/25 | chr5 | 50826531 | |||||||
chr5:50826601 | A | G | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1929-154A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 18/25 | chr5 | 50826601 | |||||||
chr5:50826734 | A | T | 1 | a0001c0002t0003g0087 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1929-21A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 18/25 | chr5 | 50826734 | |||||||
chr5:50826811 | G | GT | 11 | a0001c0002t0003g0002 a0001c0002t0003g0003 a0001c0002t0003g0118 others(8): Show |
14 | HG00597.hp1 HG01943.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.1977+22dupT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr5 | 50826811 | ||||||
chr5:50826811 | GT | G | 78 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(75): Show |
81 | HG00099.hp2 HG00642.hp1 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.1977+22delT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr5 | 50826811 | ||||||
chr5:50826811 | GTT | G | 8 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(5): Show |
8 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1977+21_1977+22del others(2): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr5 | 50826811 | ||||||
chr5:50826827 | C | A | 1 | a0001c0001t0021g0318 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1977+24C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 19/25 | chr5 | 50826827 | |||||||
chr5:50827116 | A | G | 55 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(52): Show |
57 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.1977+313A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 19/25 | chr5 | 50827116 | |||||||
chr5:50827135 | T | G | 1 | a0001c0001t0001g0256 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1977+332T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 19/25 | chr5 | 50827135 | |||||||
chr5:50827156 | C | A | 4 | a0001c0002t0002g0109 a0001c0002t0002g0110 a0001c0002t0002g0111 others(1): Show |
4 | HG01433.hp1 HG02622.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1977+353C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 19/25 | chr5 | 50827156 | |||||||
chr5:50827180 | C | T | 10 | a0001c0002t0003g0002 a0001c0002t0003g0003 a0001c0002t0003g0118 others(7): Show |
13 | HG00597.hp1 HG01943.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.1977+377C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 19/25 | chr5 | 50827180 | |||||||
chr5:50827237 | A | G | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1977+434A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 19/25 | chr5 | 50827237 | |||||||
chr5:50827380 | A | C | 1 | a0004c0008t0003g0137 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1978-564A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 19/25 | chr5 | 50827380 | |||||||
chr5:50827461 | T | C | 1 | a0001c0012t0038g0008 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1978-483T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 19/25 | chr5 | 50827461 | |||||||
chr5:50827652 | C | T | 8 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(5): Show |
8 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1978-292C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 19/25 | chr5 | 50827652 | |||||||
chr5:50827700 | G | A | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1978-244G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 19/25 | chr5 | 50827700 | |||||||
chr5:50827752 | C | T | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1978-192C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 19/25 | chr5 | 50827752 | |||||||
chr5:50827777 | G | A | 30 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(27): Show |
31 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.1978-167G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 19/25 | chr5 | 50827777 | |||||||
chr5:50827778 | T | C | 4 | a0001c0002t0002g0081 a0001c0002t0002g0088 a0001c0002t0002g0165 others(1): Show |
4 | HG00639.hp2 HG01952.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.1978-166T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 19/25 | chr5 | 50827778 | |||||||
chr5:50827819 | G | T | 1 | a0001c0010t0036g0321 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1978-125G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 19/25 | chr5 | 50827819 | |||||||
chr5:50827866 | A | G | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1978-78A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 19/25 | chr5 | 50827866 | |||||||
chr5:50827893 | A | AATAT | 4 | a0001c0002t0002g0161 a0001c0002t0002g0162 a0001c0002t0002g0163 others(1): Show |
4 | HG02074.hp1 NA18951.hp1 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.1978-48_1978-45dup others(4): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr5 | 50827893 | ||||||
chr5:50828256 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2091-56C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 20/25 | chr5 | 50828256 | |||||||
chr5:50828432 | G | A | 1 | a0001c0003t0001g0230 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2163+48G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 21/25 | chr5 | 50828432 | |||||||
chr5:50828434 | G | A | 1 | a0001c0004t0005g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2163+50G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 21/25 | chr5 | 50828434 | |||||||
chr5:50828660 | G | A | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2163+276G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 21/25 | chr5 | 50828660 | |||||||
chr5:50828663 | T | G | 1 | a0001c0003t0001g0243 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2163+279T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 21/25 | chr5 | 50828663 | |||||||
chr5:50828729 | T | TTA | 13 | a0001c0001t0001g0272 a0001c0001t0021g0318 a0001c0001t0049g0020 others(10): Show |
13 | HG01346.hp2 HG02055.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.2163+363_2163+364d others(4): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 50828729 | ||||||
chr5:50828729 | T | TTATA | 13 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(10): Show |
13 | HG01884.hp1 HG03098.hp1 HG03453.hp1 others(10): Show |
intron_variant | MODIFIER | c.2163+361_2163+364d others(6): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 50828729 | ||||||
chr5:50828729 | T | TTATATA | 22 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(19): Show |
24 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.2163+359_2163+364d others(8): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 50828729 | ||||||
chr5:50828731 | A | T | 1 | a0001c0001t0006g0206 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2163+347A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 21/25 | chr5 | 50828731 | |||||||
chr5:50828905 | AAAAAG | A | 12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(9): Show |
12 | HG01884.hp1 HG03098.hp1 HG03453.hp1 others(9): Show |
intron_variant | MODIFIER | c.2163+533_2163+537d others(7): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 50828905 | ||||||
chr5:50829072 | G | A | 1 | a0001c0002t0003g0079 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2163+688G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 21/25 | chr5 | 50829072 | |||||||
chr5:50829264 | G | A | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.2164-628G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 21/25 | chr5 | 50829264 | |||||||
chr5:50829291 | C | A | 1 | a0001c0003t0001g0245 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2164-601C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 21/25 | chr5 | 50829291 | |||||||
chr5:50829411 | A | G | 3 | a0001c0001t0030g0005 a0001c0007t0028g0007 a0001c0007t0029g0006 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2164-481A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 21/25 | chr5 | 50829411 | |||||||
chr5:50829583 | C | T | 65 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(62): Show |
65 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.2164-309C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 21/25 | chr5 | 50829583 | |||||||
chr5:50829600 | G | A | 1 | a0001c0001t0008g0299 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2164-292G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 21/25 | chr5 | 50829600 | |||||||
chr5:50829729 | A | C | 1 | a0001c0004t0005g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2164-163A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 21/25 | chr5 | 50829729 | |||||||
chr5:50830016 | T | C | 1 | a0001c0001t0004g0053 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2233+55T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 22/25 | chr5 | 50830016 | |||||||
chr5:50830067 | T | C | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.2233+106T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 22/25 | chr5 | 50830067 | |||||||
chr5:50830277 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2233+316A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 22/25 | chr5 | 50830277 | |||||||
chr5:50830435 | G | C | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2233+474G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 22/25 | chr5 | 50830435 | |||||||
chr5:50830622 | C | A | 6 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(3): Show |
6 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2233+661C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 22/25 | chr5 | 50830622 | |||||||
chr5:50830661 | T | C | 1 | a0001c0001t0002g0066 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2233+700T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 22/25 | chr5 | 50830661 | |||||||
chr5:50830662 | T | A | 1 | a0001c0001t0002g0066 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2233+701T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 22/25 | chr5 | 50830662 | |||||||
chr5:50830819 | C | CGT | 142 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(139): Show |
143 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.2233+886_2233+887d others(4): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr5 | 50830819 | ||||||
chr5:50830819 | C | CGTGT | 5 | a0001c0001t0001g0282 a0001c0001t0008g0313 a0001c0001t0013g0192 others(2): Show |
5 | HG01884.hp2 HG02145.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.2233+884_2233+887d others(6): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr5 | 50830819 | ||||||
chr5:50830819 | CGT | C | 50 | a0001c0001t0002g0168 a0001c0001t0005g0010 a0001c0001t0005g0011 others(47): Show |
50 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2233+886_2233+887d others(4): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr5 | 50830819 | ||||||
chr5:50830819 | CGTGT | C | 29 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(26): Show |
31 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.2233+884_2233+887d others(6): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr5 | 50830819 | ||||||
chr5:50830819 | CGTGTGT | C | 14 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(11): Show |
14 | HG01361.hp1 HG01884.hp1 HG03098.hp1 others(11): Show |
intron_variant | MODIFIER | c.2233+882_2233+887d others(8): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr5 | 50830819 | ||||||
chr5:50830905 | T | G | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2233+944T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 22/25 | chr5 | 50830905 | |||||||
chr5:50831103 | T | C | 1 | a0001c0001t0007g0181 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2233+1142T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 22/25 | chr5 | 50831103 | |||||||
chr5:50831273 | C | T | 4 | a0001c0001t0004g0053 a0001c0001t0004g0054 a0001c0001t0004g0055 others(1): Show |
4 | HG01261.hp2 HG02615.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2233+1312C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 22/25 | chr5 | 50831273 | |||||||
chr5:50831402 | A | G | 1 | a0001c0002t0003g0079 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2234-1379A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 22/25 | chr5 | 50831402 | |||||||
chr5:50831428 | G | A | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.2234-1353G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 22/25 | chr5 | 50831428 | |||||||
chr5:50831455 | A | T | 113 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(110): Show |
113 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.2234-1326A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 22/25 | chr5 | 50831455 | |||||||
chr5:50831664 | A | T | 1 | a0001c0012t0038g0008 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2234-1117A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 22/25 | chr5 | 50831664 | |||||||
chr5:50831766 | T | C | 6 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(3): Show |
6 | HG01891.hp1 HG02486.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2234-1015T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 22/25 | chr5 | 50831766 | |||||||
chr5:50831771 | A | G | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2234-1010A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 22/25 | chr5 | 50831771 | |||||||
chr5:50831858 | A | T | 3 | a0001c0003t0011g0223 a0001c0003t0011g0224 a0001c0003t0011g0225 |
3 | HG02055.hp1 HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2234-923A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 22/25 | chr5 | 50831858 | |||||||
chr5:50832188 | C | G | 25 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(22): Show |
27 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.2234-593C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 22/25 | chr5 | 50832188 | |||||||
chr5:50832475 | A | G | 4 | a0001c0001t0005g0021 a0001c0001t0005g0022 a0001c0001t0005g0023 others(1): Show |
4 | NA18944.hp1 NA18957.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.2234-306A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 22/25 | chr5 | 50832475 | |||||||
chr5:50832736 | T | A | 11 | a0001c0002t0003g0073 a0001c0002t0003g0097 a0001c0002t0003g0120 others(8): Show |
11 | HG00558.hp2 NA18944.hp2 NA18960.hp1 others(8): Show |
intron_variant | MODIFIER | c.2234-45T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 22/25 | chr5 | 50832736 | |||||||
chr5:50832952 | A | T | 1 | a0001c0001t0004g0046 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2307+98A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 23/25 | chr5 | 50832952 | |||||||
chr5:50833254 | G | A | 2 | a0001c0001t0001g0267 a0001c0001t0001g0300 |
2 | HG01069.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.2307+400G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 23/25 | chr5 | 50833254 | |||||||
chr5:50833327 | C | T | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2307+473C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 23/25 | chr5 | 50833327 | |||||||
chr5:50833427 | G | A | 2 | a0001c0003t0001g0228 a0001c0003t0001g0229 |
2 | NA18947.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.2308-552G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 23/25 | chr5 | 50833427 | |||||||
chr5:50833459 | T | C | 1 | a0001c0010t0036g0321 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2308-520T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 23/25 | chr5 | 50833459 | |||||||
chr5:50833512 | G | GA | 7 | a0001c0002t0002g0161 a0001c0002t0002g0162 a0001c0002t0002g0163 others(4): Show |
7 | HG02074.hp1 HG02572.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.2308-454dupA | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr5 | 50833512 | ||||||
chr5:50833542 | T | C | 1 | a0001c0002t0003g0073 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2308-437T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 23/25 | chr5 | 50833542 | |||||||
chr5:50833714 | G | A | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2308-265G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 23/25 | chr5 | 50833714 | |||||||
chr5:50833778 | A | G | 1 | a0001c0002t0041g0172 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2308-201A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 23/25 | chr5 | 50833778 | |||||||
chr5:50833799 | T | C | 1 | a0001c0001t0022g0047 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2308-180T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 23/25 | chr5 | 50833799 | |||||||
chr5:50833885 | G | A | 1 | a0001c0002t0005g0071 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2308-94G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 23/25 | chr5 | 50833885 | |||||||
chr5:50833891 | T | G | 8 | a0001c0004t0005g0026 a0001c0004t0005g0027 a0001c0004t0005g0028 others(5): Show |
8 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.2308-88T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 23/25 | chr5 | 50833891 | |||||||
chr5:50833911 | A | G | 21 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(18): Show |
21 | HG01109.hp2 HG01884.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.2308-68A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 23/25 | chr5 | 50833911 | |||||||
chr5:50834319 | C | T | 3 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 |
3 | HG01192.hp1 HG02280.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2377+271C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 24/25 | chr5 | 50834319 | |||||||
chr5:50834332 | T | C | 2 | a0001c0002t0002g0074 a0001c0002t0002g0178 |
2 | HG00642.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.2377+284T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 24/25 | chr5 | 50834332 | |||||||
chr5:50834423 | A | G | 1 | a0001c0013t0005g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2377+375A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 24/25 | chr5 | 50834423 | |||||||
chr5:50834619 | C | T | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.2378-312C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 24/25 | chr5 | 50834619 | |||||||
chr5:50834725 | G | T | 3 | a0001c0001t0030g0005 a0001c0007t0028g0007 a0001c0007t0029g0006 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2378-206G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 24/25 | chr5 | 50834725 | |||||||
chr5:50835024 | A | G | 1 | a0001c0001t0004g0052 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2462+9A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50835024 | |||||||
chr5:50835084 | T | A | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2462+69T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50835084 | |||||||
chr5:50835203 | A | T | 3 | a0001c0001t0030g0005 a0001c0007t0028g0007 a0001c0007t0029g0006 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2462+188A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50835203 | |||||||
chr5:50835251 | A | C | 1 | a0001c0002t0002g0157 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2462+236A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50835251 | |||||||
chr5:50835268 | C | A | 1 | a0001c0001t0008g0310 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2462+253C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50835268 | |||||||
chr5:50835309 | G | A | 47 | a0001c0003t0001g0209 a0001c0003t0001g0210 a0001c0003t0001g0211 others(44): Show |
47 | HG00673.hp1 HG00738.hp1 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.2462+294G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50835309 | |||||||
chr5:50835404 | G | A | 3 | a0001c0001t0030g0005 a0001c0007t0028g0007 a0001c0007t0029g0006 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2462+389G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50835404 | |||||||
chr5:50835438 | G | C | 2 | a0001c0003t0001g0209 a0001c0003t0001g0249 |
2 | HG01261.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.2462+423G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50835438 | |||||||
chr5:50835648 | T | C | 2 | a0001c0001t0007g0184 a0001c0001t0027g0185 |
2 | HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2462+633T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50835648 | |||||||
chr5:50835769 | G | GT | 8 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0025 others(5): Show |
8 | HG02109.hp1 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.2462+763dupT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 50835769 | ||||||
chr5:50835770 | T | G | 1 | a0001c0002t0003g0129 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2462+755T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50835770 | |||||||
chr5:50836026 | C | T | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.2462+1011C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50836026 | |||||||
chr5:50836377 | G | C | 1 | a0001c0003t0001g0212 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2462+1362G>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50836377 | |||||||
chr5:50836390 | G | A | 13 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(10): Show |
13 | HG01884.hp1 HG02080.hp1 HG03098.hp1 others(10): Show |
intron_variant | MODIFIER | c.2462+1375G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50836390 | |||||||
chr5:50836416 | A | G | 1 | a0001c0001t0001g0305 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2462+1401A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50836416 | |||||||
chr5:50836439 | G | A | 3 | a0001c0001t0004g0054 a0001c0001t0004g0055 a0001c0001t0004g0056 |
3 | HG01261.hp2 HG02615.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2462+1424G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50836439 | |||||||
chr5:50836563 | A | G | 1 | a0001c0001t0007g0181 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2462+1548A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50836563 | |||||||
chr5:50836672 | T | A | 113 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(110): Show |
113 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.2462+1657T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50836672 | |||||||
chr5:50836723 | G | A | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2462+1708G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50836723 | |||||||
chr5:50836778 | A | G | 1 | a0001c0002t0002g0083 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2462+1763A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50836778 | |||||||
chr5:50837000 | A | AT | 21 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(18): Show |
21 | HG01109.hp2 HG01884.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.2462+1990dupT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 50837000 | ||||||
chr5:50837017 | T | A | 1 | a0001c0001t0049g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2462+2002T>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50837017 | |||||||
chr5:50837192 | C | T | 2 | a0001c0001t0004g0035 a0001c0001t0004g0036 |
2 | HG02886.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2462+2177C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50837192 | |||||||
chr5:50837195 | G | A | 294 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(291): Show |
298 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(295): Show |
intron_variant | MODIFIER | c.2462+2180G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50837195 | |||||||
chr5:50837510 | G | A | 46 | a0001c0003t0001g0209 a0001c0003t0001g0210 a0001c0003t0001g0211 others(43): Show |
46 | HG00673.hp1 HG00738.hp1 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.2462+2495G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50837510 | |||||||
chr5:50837542 | A | G | 43 | a0001c0002t0002g0065 a0001c0002t0002g0072 a0001c0002t0002g0074 others(40): Show |
43 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.2462+2527A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50837542 | |||||||
chr5:50837564 | T | C | 3 | a0001c0001t0030g0005 a0001c0007t0028g0007 a0001c0007t0029g0006 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2462+2549T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50837564 | |||||||
chr5:50837675 | A | T | 3 | a0001c0001t0030g0005 a0001c0007t0028g0007 a0001c0007t0029g0006 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2462+2660A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50837675 | |||||||
chr5:50837780 | A | C | 1 | a0001c0001t0006g0206 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2462+2765A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50837780 | |||||||
chr5:50837849 | A | G | 1 | a0001c0001t0002g0155 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2462+2834A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50837849 | |||||||
chr5:50837882 | A | T | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2462+2867A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50837882 | |||||||
chr5:50837919 | C | G | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.2462+2904C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50837919 | |||||||
chr5:50837935 | T | G | 1 | a0001c0003t0001g0218 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2462+2920T>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50837935 | |||||||
chr5:50838008 | AT | A | 18 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0034 others(15): Show |
20 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.2462+2994delT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50838008 | |||||||
chr5:50838131 | T | C | 2 | a0001c0001t0015g0059 a0001c0001t0015g0060 |
2 | NA18992.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.2462+3116T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50838131 | |||||||
chr5:50838444 | C | T | 20 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(17): Show |
20 | HG01109.hp2 HG01884.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.2462+3429C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50838444 | |||||||
chr5:50838473 | A | T | 1 | a0001c0001t0032g0183 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2462+3458A>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50838473 | |||||||
chr5:50838552 | C | CT | 13 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(10): Show |
13 | HG01884.hp1 HG02080.hp1 HG03098.hp1 others(10): Show |
intron_variant | MODIFIER | c.2463-3410dupT | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 50838552 | ||||||
chr5:50838579 | G | A | 1 | a0001c0001t0001g0305 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2463-3387G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50838579 | |||||||
chr5:50838630 | G | A | 2 | a0001c0002t0003g0095 a0001c0002t0003g0096 |
2 | HG01074.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.2463-3336G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50838630 | |||||||
chr5:50838670 | T | C | 2 | a0001c0002t0003g0087 a0001c0002t0003g0128 |
2 | HG00609.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.2463-3296T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50838670 | |||||||
chr5:50838885 | A | G | 3 | a0001c0004t0005g0029 a0001c0004t0005g0030 a0001c0004t0005g0031 |
3 | HG01109.hp2 HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2463-3081A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50838885 | |||||||
chr5:50838893 | C | T | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2463-3073C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50838893 | |||||||
chr5:50839487 | G | T | 319 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(316): Show |
325 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(322): Show |
intron_variant | MODIFIER | c.2463-2479G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50839487 | |||||||
chr5:50839599 | G | T | 6 | a0001c0003t0001g0239 a0001c0003t0001g0240 a0001c0003t0001g0242 others(3): Show |
6 | HG03490.hp2 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.2463-2367G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50839599 | |||||||
chr5:50839666 | T | TTC | 208 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0284 others(205): Show |
212 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(209): Show |
intron_variant | MODIFIER | c.2463-2276_2463-227 others(6): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 50839666 | ||||||
chr5:50839666 | T | TTCTC | 14 | a0001c0001t0002g0068 a0001c0001t0015g0059 a0001c0001t0015g0060 others(11): Show |
14 | HG00597.hp2 HG01109.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.2463-2278_2463-227 others(8): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 50839666 | ||||||
chr5:50839666 | T | TTCTCTC | 59 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(56): Show |
59 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.2463-2280_2463-227 others(10): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 50839666 | ||||||
chr5:50839666 | TTC | T | 8 | a0001c0001t0005g0017 a0001c0001t0005g0018 a0001c0001t0005g0019 others(5): Show |
8 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.2463-2276_2463-227 others(6): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 50839666 | ||||||
chr5:50839796 | A | C | 1 | a0001c0010t0036g0321 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2463-2170A>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50839796 | |||||||
chr5:50839857 | G | A | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2463-2109G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50839857 | |||||||
chr5:50839957 | A | G | 10 | a0001c0002t0003g0002 a0001c0002t0003g0003 a0001c0002t0003g0118 others(7): Show |
13 | HG00597.hp1 HG01943.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.2463-2009A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50839957 | |||||||
chr5:50840083 | A | G | 9 | a0001c0003t0001g0210 a0001c0003t0001g0211 a0001c0003t0001g0212 others(6): Show |
9 | HG01934.hp2 HG01943.hp2 HG02148.hp2 others(6): Show |
intron_variant | MODIFIER | c.2463-1883A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50840083 | |||||||
chr5:50840154 | TAA | T | 10 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0001t0007g0184 others(7): Show |
10 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.2463-1811_2463-181 others(6): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50840154 | |||||||
chr5:50840218 | C | T | 1 | a0001c0002t0003g0115 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2463-1748C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50840218 | |||||||
chr5:50840396 | A | G | 1 | a0001c0001t0001g0279 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2463-1570A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50840396 | |||||||
chr5:50840615 | G | A | 2 | a0001c0007t0028g0007 a0001c0007t0029g0006 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2463-1351G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50840615 | |||||||
chr5:50840797 | T | C | 43 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(40): Show |
43 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.2463-1169T>C | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50840797 | |||||||
chr5:50840811 | G | A | 20 | a0001c0001t0006g0191 a0001c0001t0006g0193 a0001c0001t0006g0194 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.2463-1155G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50840811 | |||||||
chr5:50840816 | C | A | 1 | a0001c0002t0043g0135 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.2463-1150C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50840816 | |||||||
chr5:50840913 | C | T | 1 | a0001c0002t0002g0159 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2463-1053C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50840913 | |||||||
chr5:50841029 | C | G | 1 | a0001c0002t0003g0179 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.2463-937C>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50841029 | |||||||
chr5:50841312 | G | T | 1 | a0001c0001t0001g0308 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2463-654G>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50841312 | |||||||
chr5:50841318 | A | G | 66 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(63): Show |
66 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.2463-648A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50841318 | |||||||
chr5:50841405 | C | A | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2463-561C>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50841405 | |||||||
chr5:50841420 | A | G | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2463-546A>G | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50841420 | |||||||
chr5:50841446 | A | AT | 3 | a0001c0001t0030g0005 a0001c0007t0028g0007 a0001c0007t0029g0006 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2463-520_2463-519i others(3): Show |
PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50841446 | |||||||
chr5:50841742 | T | TA | 24 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(21): Show |
24 | HG01109.hp2 HG01884.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.2463-212dupA | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 50841742 | ||||||
chr5:50841742 | TA | T | 108 | a0001c0001t0006g0194 a0001c0002t0002g0065 a0001c0002t0002g0072 others(105): Show |
111 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.2463-212delA | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 50841742 | ||||||
chr5:50841808 | G | A | 1 | a0001c0001t0021g0318 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2463-158G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50841808 | |||||||
chr5:50841867 | C | T | 1 | a0001c0001t0001g0317 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2463-99C>T | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50841867 | |||||||
chr5:50841873 | G | A | 1 | a0001c0001t0030g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2463-93G>A | PARP8 | ENSG00000151883.20 | transcript | ENST00000281631.10 | protein_coding | 25/25 | chr5 | 50841873 |