Item | Value |
---|---|
geneid | 5184 |
ensemblid | ENSG00000124299.16 |
hgncid | 8840 |
symbol | PEPD |
name | peptidase D |
refseq_nuc | NM_000285.4 |
refseq_prot | NP_000276.2 |
ensembl_nuc | ENST00000244137.12 |
ensembl_prot | ENSP00000244137.5 |
mane_status | MANE Select |
chr | chr19 |
start | 33386950 |
end | 33521791 |
strand | - |
ver | v1.2 |
region | chr19:33386950-33521791 |
region5000 | chr19:33381950-33526791 |
regionname0 | PEPD_chr19_33386950_33521791 |
regionname5000 | PEPD_chr19_33381950_33526791 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 493 | 211 | 43 | 47 | 86 | 10 | 23 | 67 | PEPD_chr19_33381950_33526791 | PEPD | MAAAT others(488): Show |
chr19 | 33381950 | 33526791 |
a0002 | 0/0 | 493 | 76 | 29 | 15 | 23 | 5 | 4 | 11 | PEPD_chr19_33381950_33526791 | PEPD | MAAAT others(488): Show |
chr19 | 33381950 | 33526791 |
a0003 | 0/0 | 493 | 13 | 0 | 0 | 12 | 0 | 1 | 9 | PEPD_chr19_33381950_33526791 | PEPD | MAAAT others(488): Show |
chr19 | 33381950 | 33526791 |
a0004 | 0/0 | 493 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | MAAAT others(488): Show |
chr19 | 33381950 | 33526791 |
a0005 | 0/0 | 493 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | PEPD_chr19_33381950_33526791 | PEPD | MAAAT others(488): Show |
chr19 | 33381950 | 33526791 |
a0006 | 0/0 | 493 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | MAAAT others(488): Show |
chr19 | 33381950 | 33526791 |
a0007 | 0/0 | 493 | 2 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | MAAAT others(488): Show |
chr19 | 33381950 | 33526791 |
a0008 | 0/0 | 493 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | MAAAT others(488): Show |
chr19 | 33381950 | 33526791 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1479 | 163 | 40 | 43 | 49 | 9 | 20 | PEPD_chr19_33381950_33526791 | PEPD | ATGGC others(1474): Show |
chr19 | 33381950 | 33526791 | ||
a0001c0003 | 0/0 | 1479 | 43 | 2 | 3 | 34 | 1 | 3 | PEPD_chr19_33381950_33526791 | PEPD | ATGGC others(1474): Show |
chr19 | 33381950 | 33526791 | ||
a0001c0007 | 0/0 | 1479 | 4 | 0 | 1 | 3 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | ATGGC others(1474): Show |
chr19 | 33381950 | 33526791 | ||
a0001c0014 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | ATGGC others(1474): Show |
chr19 | 33381950 | 33526791 | ||
a0002c0002 | 0/0 | 1479 | 74 | 29 | 14 | 22 | 5 | 4 | PEPD_chr19_33381950_33526791 | PEPD | ATGGC others(1474): Show |
chr19 | 33381950 | 33526791 | ||
a0002c0012 | 0/0 | 1479 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | ATGGC others(1474): Show |
chr19 | 33381950 | 33526791 | ||
a0002c0013 | 0/0 | 1479 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | ATGGC others(1474): Show |
chr19 | 33381950 | 33526791 | ||
a0003c0004 | 0/0 | 1479 | 7 | 0 | 0 | 7 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | ATGGC others(1474): Show |
chr19 | 33381950 | 33526791 | ||
a0003c0005 | 0/0 | 1479 | 6 | 0 | 0 | 5 | 0 | 1 | PEPD_chr19_33381950_33526791 | PEPD | ATGGC others(1474): Show |
chr19 | 33381950 | 33526791 | ||
a0004c0006 | 0/0 | 1479 | 6 | 6 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | ATGGC others(1474): Show |
chr19 | 33381950 | 33526791 | ||
a0005c0008 | 0/0 | 1479 | 3 | 0 | 0 | 3 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | ATGGC others(1474): Show |
chr19 | 33381950 | 33526791 | ||
a0006c0010 | 0/0 | 1479 | 2 | 2 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | ATGGC others(1474): Show |
chr19 | 33381950 | 33526791 | ||
a0007c0009 | 0/0 | 1479 | 2 | 1 | 0 | 0 | 1 | 0 | PEPD_chr19_33381950_33526791 | PEPD | ATGGC others(1474): Show |
chr19 | 33381950 | 33526791 | ||
a0008c0011 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | ATGGC others(1474): Show |
chr19 | 33381950 | 33526791 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 1907 | 128 | 40 | 26 | 37 | 6 | 18 | PEPD_chr19_33381950_33526791 | PEPD | GCACT others(1902): Show |
chr19 | 33381950 | 33526791 |
a0001c0001t0003 | 0/1 | 1911 | 23 | 0 | 17 | 0 | 3 | 2 | PEPD_chr19_33381950_33526791 | PEPD | GCACT others(1906): Show |
chr19 | 33381950 | 33526791 |
a0001c0001t0004 | 0/0 | 1907 | 12 | 0 | 0 | 12 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | GCACT others(1902): Show |
chr19 | 33381950 | 33526791 |
a0001c0003t0001 | 0/0 | 1907 | 43 | 2 | 3 | 34 | 1 | 3 | PEPD_chr19_33381950_33526791 | PEPD | GCACT others(1902): Show |
chr19 | 33381950 | 33526791 |
a0001c0007t0001 | 0/0 | 1907 | 4 | 0 | 1 | 3 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | GCACT others(1902): Show |
chr19 | 33381950 | 33526791 |
a0001c0014t0001 | 0/0 | 1907 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | GCACT others(1902): Show |
chr19 | 33381950 | 33526791 |
a0002c0002t0002 | 0/0 | 1912 | 71 | 26 | 14 | 22 | 5 | 4 | PEPD_chr19_33381950_33526791 | PEPD | GCACT others(1907): Show |
chr19 | 33381950 | 33526791 |
a0002c0002t0005 | 0/0 | 1907 | 3 | 3 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | GCACT others(1902): Show |
chr19 | 33381950 | 33526791 |
a0002c0012t0002 | 0/0 | 1912 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | GCACT others(1907): Show |
chr19 | 33381950 | 33526791 |
a0002c0013t0002 | 0/0 | 1912 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | GCACT others(1907): Show |
chr19 | 33381950 | 33526791 |
a0003c0004t0001 | 0/0 | 1907 | 7 | 0 | 0 | 7 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | GCACT others(1902): Show |
chr19 | 33381950 | 33526791 |
a0003c0005t0001 | 0/0 | 1907 | 6 | 0 | 0 | 5 | 0 | 1 | PEPD_chr19_33381950_33526791 | PEPD | GCACT others(1902): Show |
chr19 | 33381950 | 33526791 |
a0004c0006t0001 | 0/0 | 1907 | 6 | 6 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | GCACT others(1902): Show |
chr19 | 33381950 | 33526791 |
a0005c0008t0001 | 0/0 | 1907 | 3 | 0 | 0 | 3 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | GCACT others(1902): Show |
chr19 | 33381950 | 33526791 |
a0006c0010t0002 | 0/0 | 1912 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | GCACT others(1907): Show |
chr19 | 33381950 | 33526791 |
a0006c0010t0005 | 0/0 | 1907 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | GCACT others(1902): Show |
chr19 | 33381950 | 33526791 |
a0007c0009t0001 | 0/0 | 1907 | 2 | 1 | 0 | 0 | 1 | 0 | PEPD_chr19_33381950_33526791 | PEPD | GCACT others(1902): Show |
chr19 | 33381950 | 33526791 |
a0008c0011t0001 | 0/0 | 1907 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | GCACT others(1902): Show |
chr19 | 33381950 | 33526791 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0245 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0003g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0003g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0003g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0003g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0003g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0003g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0003g0287 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0001t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0003t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0003t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0003t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0003t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0003t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0003t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0003t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0003t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0003t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0003t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0003t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0003t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0003t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0003t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0003t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0007t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0007t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0007t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0001c0014t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0005g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0002t0005g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0012t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0002c0013t0002g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0003c0004t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0003c0004t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0003c0004t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0003c0004t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0003c0004t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0003c0004t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0003c0004t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0003c0005t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0003c0005t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0003c0005t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0003c0005t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0003c0005t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0003c0005t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0004c0006t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0004c0006t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0004c0006t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0004c0006t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0004c0006t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0004c0006t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0005c0008t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0005c0008t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0005c0008t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0006c0010t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0006c0010t0005g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0007c0009t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0007c0009t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
a0008c0011t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0002 | g0047 | EUR | GBR | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0284 | EUR | GBR | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG00140 | hp2 | a0002 | c0002 | t0002 | g0009 | EUR | GBR | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0277 | EUR | FIN | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0105 | EUR | FIN | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG00323 | hp1 | a0001 | c0003 | t0001 | g0217 | EUR | FIN | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0106 | EUR | FIN | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG00408 | hp1 | a0002 | c0002 | t0002 | g0158 | EAS | CHS | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG00408 | hp2 | a0002 | c0002 | t0002 | g0149 | EAS | CHS | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG00438 | hp1 | a0001 | c0003 | t0001 | g0200 | EAS | CHS | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG00438 | hp2 | a0002 | c0002 | t0002 | g0146 | EAS | CHS | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG00544 | hp1 | a0002 | c0002 | t0002 | g0214 | EAS | CHS | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG00544 | hp2 | a0001 | c0001 | t0004 | g0142 | EAS | CHS | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG00558 | hp1 | a0001 | c0003 | t0001 | g0222 | EAS | CHS | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG00558 | hp2 | a0002 | c0002 | t0002 | g0150 | EAS | CHS | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG00597 | hp1 | a0002 | c0002 | t0002 | g0219 | EAS | CHS | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG00609 | hp2 | a0002 | c0002 | t0002 | g0083 | EAS | CHS | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG00621 | hp2 | a0002 | c0002 | t0002 | g0118 | EAS | CHS | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0183 | AMR | PUR | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0273 | AMR | PUR | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG00733 | hp2 | a0001 | c0001 | t0003 | g0045 | AMR | PUR | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01070 | hp2 | a0002 | c0002 | t0002 | g0012 | AMR | PUR | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01074 | hp1 | a0002 | c0013 | t0002 | g0011 | AMR | PUR | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0073 | AMR | PUR | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01081 | hp2 | a0002 | c0002 | t0002 | g0072 | AMR | PUR | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0274 | AMR | PUR | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0275 | AMR | PUR | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01109 | hp1 | a0002 | c0002 | t0002 | g0260 | AMR | PUR | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01109 | hp2 | a0002 | c0002 | t0002 | g0013 | AMR | PUR | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01168 | hp1 | a0001 | c0007 | t0001 | g0242 | AMR | PUR | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01175 | hp1 | a0002 | c0002 | t0002 | g0068 | AMR | PUR | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0285 | AMR | PUR | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01192 | hp2 | a0001 | c0003 | t0001 | g0250 | AMR | PUR | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01243 | hp2 | a0001 | c0003 | t0001 | g0253 | AMR | PUR | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01257 | hp1 | a0002 | c0002 | t0002 | g0046 | AMR | CLM | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01257 | hp2 | a0002 | c0002 | t0002 | g0026 | AMR | CLM | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0276 | AMR | CLM | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0182 | AMR | CLM | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01358 | hp1 | a0001 | c0003 | t0001 | g0252 | AMR | CLM | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | CLM | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01433 | hp2 | a0002 | c0002 | t0002 | g0257 | AMR | CLM | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01496 | hp1 | a0002 | c0002 | t0002 | g0010 | AMR | CLM | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01496 | hp2 | a0002 | c0002 | t0002 | g0129 | AMR | CLM | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01515 | hp1 | a0002 | c0002 | t0002 | g0008 | EUR | IBS | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01516 | hp1 | a0002 | c0002 | t0002 | g0201 | EUR | IBS | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0286 | EUR | IBS | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01517 | hp1 | a0002 | c0002 | t0002 | g0202 | EUR | IBS | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01884 | hp1 | a0002 | c0002 | t0002 | g0241 | AFR | ACB | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | ACB | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01928 | hp2 | a0002 | c0002 | t0002 | g0014 | AMR | PEL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0187 | AMR | PEL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01943 | hp1 | a0001 | c0001 | t0003 | g0188 | AMR | PEL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | PEL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PEL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0184 | AMR | PEL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02040 | hp2 | a0001 | c0003 | t0001 | g0231 | EAS | KHV | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | ACB | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02055 | hp2 | a0002 | c0002 | t0002 | g0006 | AFR | ACB | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02056 | hp2 | a0003 | c0004 | t0001 | g0070 | EAS | KHV | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02071 | hp1 | a0002 | c0002 | t0002 | g0189 | EAS | KHV | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02071 | hp2 | a0001 | c0003 | t0001 | g0220 | EAS | KHV | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02074 | hp1 | a0002 | c0002 | t0002 | g0159 | EAS | KHV | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02083 | hp2 | a0003 | c0004 | t0001 | g0079 | EAS | KHV | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02129 | hp1 | a0002 | c0012 | t0002 | g0135 | EAS | KHV | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02135 | hp1 | a0001 | c0003 | t0001 | g0007 | EAS | KHV | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02148 | hp1 | a0002 | c0002 | t0002 | g0234 | AMR | PEL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0181 | AMR | PEL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | CDX | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02155 | hp2 | a0002 | c0002 | t0002 | g0117 | EAS | CDX | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02165 | hp1 | a0001 | c0003 | t0001 | g0221 | EAS | CDX | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | CDX | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02257 | hp1 | a0002 | c0002 | t0002 | g0307 | AFR | ACB | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02257 | hp2 | a0002 | c0002 | t0002 | g0299 | AFR | ACB | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02258 | hp1 | a0002 | c0002 | t0005 | g0298 | AFR | ACB | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | ACB | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02280 | hp2 | a0002 | c0002 | t0002 | g0258 | AFR | ACB | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02293 | hp2 | a0002 | c0002 | t0002 | g0256 | AMR | PEL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02300 | hp1 | a0002 | c0002 | t0002 | g0044 | AMR | PEL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0179 | AMR | PEL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02451 | hp1 | a0002 | c0002 | t0002 | g0029 | AFR | ACB | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02451 | hp2 | a0002 | c0002 | t0002 | g0290 | AFR | ACB | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02523 | hp1 | a0003 | c0004 | t0001 | g0084 | EAS | KHV | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02602 | hp1 | a0001 | c0003 | t0001 | g0246 | SAS | PJL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02615 | hp2 | a0002 | c0002 | t0002 | g0031 | AFR | GWD | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | GWD | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0087 | SAS | PJL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02698 | hp2 | a0001 | c0003 | t0001 | g0108 | SAS | PJL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02738 | hp2 | a0002 | c0002 | t0002 | g0038 | SAS | PJL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02809 | hp1 | a0004 | c0006 | t0001 | g0301 | AFR | GWD | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | GWD | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02818 | hp1 | a0004 | c0006 | t0001 | g0296 | AFR | GWD | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02895 | hp1 | a0004 | c0006 | t0001 | g0302 | AFR | GWD | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02895 | hp2 | a0002 | c0002 | t0002 | g0033 | AFR | GWD | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02897 | hp2 | a0004 | c0006 | t0001 | g0300 | AFR | GWD | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02922 | hp2 | a0008 | c0011 | t0001 | g0270 | AFR | ESN | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ESN | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02970 | hp2 | a0002 | c0002 | t0002 | g0032 | AFR | ESN | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02976 | hp1 | a0002 | c0002 | t0002 | g0171 | AFR | ESN | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG03041 | hp1 | a0004 | c0006 | t0001 | g0303 | AFR | GWD | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG03041 | hp2 | a0002 | c0002 | t0002 | g0172 | AFR | GWD | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG03098 | hp2 | a0002 | c0002 | t0002 | g0035 | AFR | MSL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | ESN | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG03195 | hp1 | a0002 | c0002 | t0002 | g0175 | AFR | ESN | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG03209 | hp1 | a0002 | c0002 | t0002 | g0034 | AFR | MSL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG03225 | hp1 | a0002 | c0002 | t0002 | g0174 | AFR | MSL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | MSL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG03453 | hp2 | a0006 | c0010 | t0005 | g0168 | AFR | MSL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | MSL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG03486 | hp2 | a0002 | c0002 | t0002 | g0128 | AFR | MSL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0283 | SAS | PJL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG03516 | hp1 | a0002 | c0002 | t0002 | g0259 | AFR | ESN | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG03516 | hp2 | a0002 | c0002 | t0002 | g0122 | AFR | ESN | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | MSL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG03579 | hp2 | a0004 | c0006 | t0001 | g0297 | AFR | MSL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG03669 | hp1 | a0002 | c0002 | t0002 | g0036 | SAS | PJL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG03669 | hp2 | a0002 | c0002 | t0002 | g0090 | SAS | PJL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG03704 | hp1 | a0001 | c0003 | t0001 | g0211 | SAS | PJL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0281 | SAS | PJL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | BEB | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | BEB | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | BEB | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG03834 | hp2 | a0002 | c0002 | t0002 | g0304 | SAS | BEB | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | BEB | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0280 | SAS | BEB | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG03942 | hp1 | a0003 | c0005 | t0001 | g0244 | SAS | BEB | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | BEB | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | STU | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | STU | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | STU | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | STU | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | YRI | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18522 | hp2 | a0002 | c0002 | t0002 | g0169 | AFR | YRI | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18906 | hp1 | a0002 | c0002 | t0002 | g0262 | AFR | YRI | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | YRI | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18940 | hp1 | a0001 | c0003 | t0001 | g0113 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18940 | hp2 | a0001 | c0001 | t0004 | g0074 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18942 | hp1 | a0001 | c0003 | t0001 | g0115 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18942 | hp2 | a0003 | c0005 | t0001 | g0016 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18943 | hp1 | a0001 | c0003 | t0001 | g0225 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18943 | hp2 | a0001 | c0001 | t0004 | g0080 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18944 | hp2 | a0003 | c0005 | t0001 | g0015 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18945 | hp1 | a0001 | c0003 | t0001 | g0194 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18950 | hp2 | a0001 | c0003 | t0001 | g0209 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18951 | hp1 | a0001 | c0003 | t0001 | g0193 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18951 | hp2 | a0003 | c0004 | t0001 | g0095 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18952 | hp1 | a0001 | c0001 | t0004 | g0190 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18954 | hp1 | a0002 | c0002 | t0002 | g0218 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18957 | hp2 | a0001 | c0003 | t0001 | g0167 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18959 | hp1 | a0001 | c0003 | t0001 | g0143 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18964 | hp1 | a0001 | c0007 | t0001 | g0005 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18967 | hp2 | a0001 | c0003 | t0001 | g0144 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18968 | hp1 | a0001 | c0003 | t0001 | g0232 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18968 | hp2 | a0003 | c0004 | t0001 | g0096 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18969 | hp1 | a0005 | c0008 | t0001 | g0248 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18969 | hp2 | a0002 | c0002 | t0002 | g0233 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18970 | hp2 | a0002 | c0002 | t0002 | g0164 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18971 | hp1 | a0001 | c0003 | t0001 | g0227 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18971 | hp2 | a0001 | c0001 | t0004 | g0065 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18973 | hp1 | a0003 | c0004 | t0001 | g0210 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18973 | hp2 | a0001 | c0003 | t0001 | g0198 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18975 | hp1 | a0001 | c0001 | t0004 | g0063 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18975 | hp2 | a0001 | c0003 | t0001 | g0239 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18979 | hp1 | a0001 | c0001 | t0004 | g0069 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18979 | hp2 | a0001 | c0003 | t0001 | g0238 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18981 | hp1 | a0001 | c0003 | t0001 | g0255 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18981 | hp2 | a0001 | c0001 | t0004 | g0066 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18983 | hp1 | a0003 | c0005 | t0001 | g0243 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18983 | hp2 | a0003 | c0004 | t0001 | g0097 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18984 | hp1 | a0001 | c0003 | t0001 | g0215 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18984 | hp2 | a0001 | c0001 | t0004 | g0076 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18989 | hp1 | a0002 | c0002 | t0002 | g0213 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18990 | hp1 | a0002 | c0002 | t0002 | g0236 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18991 | hp1 | a0001 | c0001 | t0004 | g0064 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18991 | hp2 | a0001 | c0003 | t0001 | g0226 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18998 | hp1 | a0001 | c0003 | t0001 | g0161 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18998 | hp2 | a0002 | c0002 | t0002 | g0088 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA19005 | hp1 | a0002 | c0002 | t0002 | g0235 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA19007 | hp1 | a0001 | c0003 | t0001 | g0223 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA19007 | hp2 | a0002 | c0002 | t0002 | g0078 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA19009 | hp2 | a0001 | c0003 | t0001 | g0195 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA19010 | hp1 | a0001 | c0003 | t0001 | g0196 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA19012 | hp1 | a0001 | c0003 | t0001 | g0199 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA19012 | hp2 | a0001 | c0003 | t0001 | g0147 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA19030 | hp1 | a0002 | c0002 | t0002 | g0292 | AFR | LWK | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | LWK | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | LWK | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA19043 | hp2 | a0002 | c0002 | t0002 | g0291 | AFR | LWK | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA19057 | hp1 | a0001 | c0007 | t0001 | g0212 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA19057 | hp2 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA19060 | hp1 | a0001 | c0003 | t0001 | g0240 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA19060 | hp2 | a0001 | c0007 | t0001 | g0005 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA19065 | hp1 | a0003 | c0005 | t0001 | g0025 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA19066 | hp2 | a0001 | c0003 | t0001 | g0224 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA19068 | hp1 | a0005 | c0008 | t0001 | g0249 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA19079 | hp1 | a0001 | c0001 | t0004 | g0077 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA19079 | hp2 | a0002 | c0002 | t0002 | g0228 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA19082 | hp1 | a0002 | c0002 | t0002 | g0085 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA19084 | hp1 | a0005 | c0008 | t0001 | g0247 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA19085 | hp1 | a0001 | c0003 | t0001 | g0151 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA19085 | hp2 | a0001 | c0003 | t0001 | g0160 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA19088 | hp2 | a0003 | c0005 | t0001 | g0017 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA19090 | hp1 | a0002 | c0002 | t0002 | g0086 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA19240 | hp1 | a0002 | c0002 | t0005 | g0208 | AFR | YRI | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | YRI | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA20129 | hp1 | a0002 | c0002 | t0002 | g0030 | AFR | ASW | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | ASW | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0230 | EUR | TSI | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA20752 | hp2 | a0007 | c0009 | t0001 | g0185 | EUR | TSI | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02559 | hp1 | a0001 | c0014 | t0001 | g0263 | AFR | ACB | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG02559 | hp2 | a0001 | c0003 | t0001 | g0251 | AFR | ACB | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG03471 | hp2 | a0007 | c0009 | t0001 | g0186 | AFR | MSL | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG06807 | hp1 | a0001 | c0003 | t0001 | g0254 | AFR | USA | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
HG06807 | hp2 | a0006 | c0010 | t0002 | g0166 | AFR | USA | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA18955 | hp2 | a0001 | c0003 | t0001 | g0197 | EAS | JPT | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA20300 | hp1 | a0002 | c0002 | t0002 | g0028 | AFR | USA | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | USA | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA21309 | hp1 | a0002 | c0002 | t0002 | g0081 | AFR | LWK | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
NA21309 | hp2 | a0002 | c0002 | t0005 | g0091 | AFR | LWK | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0287 | REF | REF | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0245 | REF | REF | PEPD_chr19_33381950_33526791 | PEPD | chr19 | 33381950 | 33526791 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:33387931 | G | A | 2 | a0002 a0006 |
78 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(75): Show |
missense_variant | MODERATE | c.1303C>T | p.Leu435Phe | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 14/15 | 1334/1907 | 1303/1482 | 435/493 | chr19 | 33387931 | |||
chr19:33387940 | C | T | 1 | a0007 | 2 | HG03471.hp2 NA20752.hp2 |
missense_variant | MODERATE | c.1294G>A | p.Ala432Thr | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 14/15 | 1325/1907 | 1294/1482 | 432/493 | chr19 | 33387940 | |||
chr19:33388071 | C | T | 1 | a0003 | 13 | HG02056.hp2 HG02083.hp2 HG02523.hp1 others(10): Show |
missense_variant | MODERATE | c.1163G>A | p.Arg388His | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 14/15 | 1194/1907 | 1163/1482 | 388/493 | chr19 | 33388071 | |||
chr19:33401747 | C | T | 1 | a0005 | 3 | NA18969.hp1 NA19068.hp1 NA19084.hp1 |
missense_variant | MODERATE | c.941G>A | p.Arg314His | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/15 | 972/1907 | 941/1482 | 314/493 | chr19 | 33401747 | |||
chr19:33478046 | C | T | 1 | a0008 | 1 | HG02922.hp2 | missense_variant&splice_region_variant | MODERATE | c.548G>A | p.Cys183Tyr | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/15 | 579/1907 | 548/1482 | 183/493 | chr19 | 33478046 | |||
chr19:33478085 | T | A | 2 | a0004 a0006 |
8 | HG02809.hp1 HG02818.hp1 HG02895.hp1 others(5): Show |
missense_variant | MODERATE | c.509A>T | p.Glu170Val | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/15 | 540/1907 | 509/1482 | 170/493 | chr19 | 33478085 | |||
chr19:33490057 | G | A | 1 | a0006 | 2 | HG03453.hp2 HG06807.hp2 |
missense_variant&splice_region_variant | MODERATE | c.442C>T | p.Arg148Cys | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/15 | 473/1907 | 442/1482 | 148/493 | chr19 | 33490057 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:33391316 | G | A | 1 | a0001c0003 | 43 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(40): Show |
synonymous_variant | LOW | c.1131C>T | p.His377His | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/15 | 1162/1907 | 1131/1482 | 377/493 | chr19 | 33391316 | |||
chr19:33401854 | G | A | 1 | a0002c0013 | 1 | HG01074.hp1 | synonymous_variant | LOW | c.834C>T | p.Gly278Gly | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/15 | 865/1907 | 834/1482 | 278/493 | chr19 | 33401854 | |||
chr19:33463006 | A | G | 4 | a0001c0007 a0002c0012 a0003c0005 others(1): Show |
14 | HG01168.hp1 HG02129.hp1 HG03942.hp1 others(11): Show |
synonymous_variant | LOW | c.660T>C | p.Tyr220Tyr | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/15 | 691/1907 | 660/1482 | 220/493 | chr19 | 33463006 | |||
chr19:33490007 | G | A | 1 | a0001c0014 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.492C>T | p.Asp164Asp | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/15 | 523/1907 | 492/1482 | 164/493 | chr19 | 33490007 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:33387006 | G | GAAAGT | 4 | a0002c0002t0002 a0002c0012t0002 a0002c0013t0002 others(1): Show |
74 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*333_*337dupACTTT | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 15/15 | 337 | chr19 | 33387006 | ||||||
chr19:33387133 | A | G | 6 | a0002c0002t0002 a0002c0002t0005 a0002c0012t0002 others(3): Show |
78 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*211T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 15/15 | 211 | chr19 | 33387133 | ||||||
chr19:33387165 | G | GTAAT | 1 | a0001c0001t0003 | 22 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*175_*178dupATTA | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 15/15 | 178 | chr19 | 33387165 | ||||||
chr19:33387291 | G | A | 1 | a0001c0001t0004 | 12 | HG00544.hp2 NA18940.hp2 NA18943.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*53C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 15/15 | 53 | chr19 | 33387291 | ||||||
chr19:33387292 | A | G | 4 | a0002c0002t0002 a0002c0012t0002 a0002c0013t0002 others(1): Show |
74 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*52T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 15/15 | 52 | chr19 | 33387292 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:33387753 | G | C | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | NA18945.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1344+137C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 14/14 | chr19 | 33387753 | |||||||
chr19:33387760 | C | T | 12 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0052 others(9): Show |
12 | HG01070.hp1 HG01071.hp2 HG02293.hp1 others(9): Show |
intron_variant | MODIFIER | c.1344+130G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 14/14 | chr19 | 33387760 | |||||||
chr19:33387826 | G | A | 1 | a0002c0002t0002g0083 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1344+64C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 14/14 | chr19 | 33387826 | |||||||
chr19:33388191 | A | G | 1 | a0002c0002t0002g0241 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1153-110T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33388191 | |||||||
chr19:33388243 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1153-162G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33388243 | |||||||
chr19:33388298 | A | G | 4 | a0001c0003t0001g0250 a0001c0003t0001g0251 a0001c0003t0001g0252 others(1): Show |
4 | HG01192.hp2 HG01243.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153-217T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33388298 | |||||||
chr19:33388299 | C | T | 4 | a0001c0003t0001g0250 a0001c0003t0001g0251 a0001c0003t0001g0252 others(1): Show |
4 | HG01192.hp2 HG01243.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153-218G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33388299 | |||||||
chr19:33388300 | ACTAC | A | 4 | a0001c0003t0001g0250 a0001c0003t0001g0251 a0001c0003t0001g0252 others(1): Show |
4 | HG01192.hp2 HG01243.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153-223_1153-220d others(6): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33388300 | |||||||
chr19:33388389 | G | A | 1 | a0001c0001t0001g0293 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1153-308C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33388389 | |||||||
chr19:33388546 | G | A | 3 | a0001c0001t0001g0004 a0001c0001t0001g0154 a0001c0001t0001g0157 |
4 | HG00597.hp2 NA18944.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153-465C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33388546 | |||||||
chr19:33388577 | A | G | 303 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(300): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.1153-496T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33388577 | |||||||
chr19:33388625 | G | A | 9 | a0002c0002t0002g0028 a0002c0002t0002g0128 a0002c0002t0002g0169 others(6): Show |
9 | HG01109.hp1 HG02451.hp2 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.1153-544C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33388625 | |||||||
chr19:33388852 | AGCTGAGG others(13): Show |
A | 28 | a0001c0001t0001g0002 a0001c0001t0001g0043 a0001c0001t0001g0067 others(25): Show |
29 | HG00099.hp2 HG00544.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.1153-791_1153-772d others(22): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33388852 | |||||||
chr19:33388947 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1153-866G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33388947 | |||||||
chr19:33388962 | C | T | 1 | a0002c0002t0002g0169 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1153-881G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33388962 | |||||||
chr19:33388974 | G | C | 1 | a0001c0001t0001g0018 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1153-893C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33388974 | |||||||
chr19:33389026 | C | T | 1 | a0003c0004t0001g0096 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1153-945G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33389026 | |||||||
chr19:33389094 | C | G | 68 | a0002c0002t0002g0006 a0002c0002t0002g0008 a0002c0002t0002g0009 others(65): Show |
68 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.1153-1013G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33389094 | |||||||
chr19:33389275 | C | T | 1 | a0002c0002t0002g0072 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1153-1194G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33389275 | |||||||
chr19:33389376 | C | T | 1 | a0001c0003t0001g0251 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1153-1295G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33389376 | |||||||
chr19:33389442 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1153-1361G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33389442 | |||||||
chr19:33389443 | A | G | 108 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0027 others(105): Show |
111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.1153-1362T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33389443 | |||||||
chr19:33389460 | AC | A | 20 | a0001c0001t0003g0001 a0001c0001t0003g0045 a0001c0001t0003g0073 others(17): Show |
22 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.1153-1380delG | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33389460 | |||||||
chr19:33389497 | T | TC | 77 | a0002c0002t0002g0006 a0002c0002t0002g0008 a0002c0002t0002g0009 others(74): Show |
77 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.1153-1417dupG | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33389497 | |||||||
chr19:33389647 | C | T | 7 | a0002c0002t0002g0122 a0002c0002t0002g0258 a0002c0002t0002g0259 others(4): Show |
7 | HG02257.hp2 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1153-1566G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33389647 | |||||||
chr19:33389679 | A | G | 8 | a0002c0002t0002g0029 a0002c0002t0002g0030 a0002c0002t0002g0031 others(5): Show |
8 | HG02257.hp1 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1153-1598T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33389679 | |||||||
chr19:33389873 | T | C | 1 | a0006c0010t0005g0168 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1152+1422A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33389873 | |||||||
chr19:33389878 | A | G | 20 | a0001c0001t0003g0001 a0001c0001t0003g0045 a0001c0001t0003g0073 others(17): Show |
22 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.1152+1417T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33389878 | |||||||
chr19:33389891 | G | A | 1 | a0002c0002t0002g0260 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1152+1404C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33389891 | |||||||
chr19:33389918 | C | T | 17 | a0001c0001t0001g0022 a0001c0001t0001g0050 a0001c0001t0001g0051 others(14): Show |
17 | HG02630.hp1 HG02809.hp1 HG02818.hp1 others(14): Show |
intron_variant | MODIFIER | c.1152+1377G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33389918 | |||||||
chr19:33389919 | G | A | 1 | a0006c0010t0005g0168 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1152+1376C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33389919 | |||||||
chr19:33389973 | G | A | 2 | a0002c0002t0002g0122 a0002c0002t0002g0259 |
2 | HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1152+1322C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33389973 | |||||||
chr19:33390016 | A | T | 29 | a0001c0001t0001g0002 a0001c0001t0001g0043 a0001c0001t0001g0067 others(26): Show |
30 | HG00099.hp2 HG00544.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.1152+1279T>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33390016 | |||||||
chr19:33390021 | C | T | 2 | a0001c0001t0001g0293 a0002c0002t0002g0128 |
2 | HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1152+1274G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33390021 | |||||||
chr19:33390222 | G | T | 4 | a0001c0001t0001g0089 a0001c0001t0001g0098 a0001c0001t0001g0107 others(1): Show |
4 | HG01175.hp2 HG01243.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.1152+1073C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33390222 | |||||||
chr19:33390242 | G | GA | 4 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0230 others(1): Show |
4 | HG03831.hp1 NA18945.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.1152+1052dupT | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33390242 | |||||||
chr19:33390488 | C | G | 1 | a0002c0002t0002g0299 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1152+807G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33390488 | |||||||
chr19:33390540 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1152+755C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33390540 | |||||||
chr19:33390584 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1152+711C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33390584 | |||||||
chr19:33390611 | GC | G | 20 | a0001c0001t0003g0001 a0001c0001t0003g0045 a0001c0001t0003g0073 others(17): Show |
22 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.1152+683delG | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33390611 | |||||||
chr19:33390672 | C | T | 3 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0308 |
3 | HG02055.hp1 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1152+623G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33390672 | |||||||
chr19:33390725 | C | G | 2 | a0002c0002t0002g0122 a0002c0002t0002g0259 |
2 | HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1152+570G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33390725 | |||||||
chr19:33390741 | C | G | 61 | a0001c0001t0001g0293 a0002c0002t0002g0006 a0002c0002t0002g0008 others(58): Show |
61 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.1152+554G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33390741 | |||||||
chr19:33390744 | G | T | 61 | a0001c0001t0001g0293 a0002c0002t0002g0006 a0002c0002t0002g0008 others(58): Show |
61 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.1152+551C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33390744 | |||||||
chr19:33390762 | A | T | 1 | a0001c0001t0001g0173 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1152+533T>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33390762 | |||||||
chr19:33390899 | A | C | 1 | a0001c0001t0001g0293 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1152+396T>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33390899 | |||||||
chr19:33390951 | T | C | 61 | a0001c0001t0001g0293 a0002c0002t0002g0006 a0002c0002t0002g0008 others(58): Show |
61 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.1152+344A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33390951 | |||||||
chr19:33390974 | C | T | 1 | a0003c0005t0001g0017 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1152+321G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33390974 | |||||||
chr19:33391027 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1152+268G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33391027 | |||||||
chr19:33391058 | G | T | 61 | a0001c0001t0001g0293 a0002c0002t0002g0006 a0002c0002t0002g0008 others(58): Show |
61 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.1152+237C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33391058 | |||||||
chr19:33391274 | G | A | 4 | a0002c0002t0002g0122 a0002c0002t0002g0258 a0002c0002t0002g0259 others(1): Show |
4 | HG02257.hp2 HG02280.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1152+21C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 13/14 | chr19 | 33391274 | |||||||
chr19:33391552 | T | C | 61 | a0001c0001t0001g0293 a0002c0002t0002g0006 a0002c0002t0002g0008 others(58): Show |
61 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.968-73A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33391552 | |||||||
chr19:33391653 | C | T | 1 | a0002c0002t0005g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.968-174G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33391653 | |||||||
chr19:33391668 | T | A | 1 | a0003c0005t0001g0015 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.968-189A>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33391668 | |||||||
chr19:33391692 | G | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG00642.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.968-213C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33391692 | |||||||
chr19:33391720 | T | C | 61 | a0001c0001t0001g0293 a0002c0002t0002g0006 a0002c0002t0002g0008 others(58): Show |
61 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.968-241A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33391720 | |||||||
chr19:33391746 | A | G | 151 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0027 others(148): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.968-267T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33391746 | |||||||
chr19:33391806 | A | G | 62 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0002c0002t0002g0006 others(59): Show |
62 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.968-327T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33391806 | |||||||
chr19:33391864 | G | A | 1 | a0002c0002t0002g0262 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.968-385C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33391864 | |||||||
chr19:33391888 | A | G | 3 | a0001c0003t0001g0167 a0001c0003t0001g0224 a0001c0003t0001g0226 |
3 | NA18957.hp2 NA18991.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.968-409T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33391888 | |||||||
chr19:33391890 | A | G | 1 | a0002c0002t0002g0128 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.968-411T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33391890 | |||||||
chr19:33392025 | A | T | 62 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0002c0002t0002g0006 others(59): Show |
62 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.968-546T>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33392025 | |||||||
chr19:33392091 | G | A | 1 | a0001c0001t0001g0040 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.968-612C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33392091 | |||||||
chr19:33392111 | G | A | 1 | a0002c0002t0002g0213 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.968-632C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33392111 | |||||||
chr19:33392134 | G | T | 155 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0043 others(152): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.968-655C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33392134 | |||||||
chr19:33392142 | T | A | 2 | a0001c0001t0001g0266 a0001c0001t0001g0269 |
2 | HG01891.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.968-663A>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33392142 | |||||||
chr19:33392153 | G | GC | 62 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0002c0002t0002g0006 others(59): Show |
62 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.968-675dupG | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33392153 | |||||||
chr19:33392192 | C | T | 3 | a0002c0002t0005g0091 a0002c0002t0005g0208 a0002c0002t0005g0298 |
3 | HG02258.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.968-713G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33392192 | |||||||
chr19:33392255 | G | T | 2 | a0001c0001t0001g0293 a0001c0001t0001g0294 |
2 | HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.968-776C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33392255 | |||||||
chr19:33392291 | G | C | 150 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0043 others(147): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.968-812C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33392291 | |||||||
chr19:33392339 | C | T | 2 | a0001c0001t0001g0293 a0001c0001t0001g0294 |
2 | HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.968-860G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33392339 | |||||||
chr19:33392342 | C | T | 56 | a0002c0002t0002g0006 a0002c0002t0002g0008 a0002c0002t0002g0009 others(53): Show |
56 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.968-863G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33392342 | |||||||
chr19:33392349 | G | A | 1 | a0001c0001t0001g0018 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.968-870C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33392349 | |||||||
chr19:33392485 | G | C | 1 | a0002c0002t0002g0259 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.968-1006C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33392485 | |||||||
chr19:33392592 | G | A | 3 | a0005c0008t0001g0247 a0005c0008t0001g0248 a0005c0008t0001g0249 |
3 | NA18969.hp1 NA19068.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.968-1113C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33392592 | |||||||
chr19:33392691 | A | G | 8 | a0001c0001t0004g0063 a0001c0001t0004g0064 a0001c0001t0004g0065 others(5): Show |
8 | NA18940.hp2 NA18952.hp1 NA18971.hp2 others(5): Show |
intron_variant | MODIFIER | c.968-1212T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33392691 | |||||||
chr19:33392698 | G | A | 5 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0002c0002t0005g0091 others(2): Show |
5 | HG02258.hp1 HG02630.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.968-1219C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33392698 | |||||||
chr19:33392718 | C | T | 1 | a0002c0002t0002g0085 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.968-1239G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33392718 | |||||||
chr19:33392805 | C | T | 27 | a0001c0001t0001g0022 a0001c0001t0001g0050 a0001c0001t0001g0051 others(24): Show |
27 | HG01884.hp2 HG02258.hp2 HG02486.hp2 others(24): Show |
intron_variant | MODIFIER | c.968-1326G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33392805 | |||||||
chr19:33392816 | T | A | 1 | a0001c0001t0001g0206 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.968-1337A>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33392816 | |||||||
chr19:33392816 | T | C | 1 | a0006c0010t0005g0168 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.968-1337A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33392816 | |||||||
chr19:33392872 | C | A | 1 | a0001c0003t0001g0007 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.968-1393G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33392872 | |||||||
chr19:33392915 | TA | T | 74 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0002c0002t0002g0006 others(71): Show |
74 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.968-1437delT | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33392915 | |||||||
chr19:33392970 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.968-1491G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33392970 | |||||||
chr19:33392971 | G | A | 55 | a0002c0002t0002g0006 a0002c0002t0002g0008 a0002c0002t0002g0009 others(52): Show |
55 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.968-1492C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33392971 | |||||||
chr19:33393017 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.968-1538G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33393017 | |||||||
chr19:33393077 | A | AC | 13 | a0002c0002t0002g0044 a0002c0002t0002g0046 a0002c0002t0002g0047 others(10): Show |
13 | HG00099.hp1 HG01081.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.968-1599dupG | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33393077 | |||||||
chr19:33393159 | G | A | 55 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0043 others(52): Show |
56 | HG00099.hp2 HG00621.hp1 HG01074.hp2 others(53): Show |
intron_variant | MODIFIER | c.968-1680C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33393159 | |||||||
chr19:33393160 | TCCCGGGG others(99): Show |
T | 1 | a0001c0001t0001g0293 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.968-1787_968-1682d others(2): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33393160 | |||||||
chr19:33393164 | G | A | 3 | a0002c0002t0005g0091 a0002c0002t0005g0208 a0002c0002t0005g0298 |
3 | HG02258.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.968-1685C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33393164 | |||||||
chr19:33393197 | CGGGGTCT others(34): Show |
C | 1 | a0001c0001t0001g0294 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.968-1759_968-1719d others(43): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33393197 | |||||||
chr19:33393198 | G | A | 13 | a0002c0002t0002g0044 a0002c0002t0002g0046 a0002c0002t0002g0047 others(10): Show |
13 | HG00099.hp1 HG01081.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.968-1719C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33393198 | |||||||
chr19:33393215 | G | A | 2 | a0001c0001t0001g0141 a0002c0002t0002g0128 |
2 | HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.968-1736C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33393215 | |||||||
chr19:33393217 | C | G | 77 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0141 others(74): Show |
77 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.968-1738G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33393217 | |||||||
chr19:33393229 | CCCGGGGT | C | 74 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0141 others(71): Show |
74 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.968-1757_968-1751d others(9): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33393229 | |||||||
chr19:33393231 | CGGGGTCT | C | 75 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0022 others(72): Show |
78 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.968-1759_968-1753d others(9): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33393231 | |||||||
chr19:33393239 | G | A | 25 | a0001c0001t0001g0022 a0001c0001t0001g0050 a0001c0001t0001g0051 others(22): Show |
25 | HG01884.hp2 HG02258.hp2 HG02486.hp2 others(22): Show |
intron_variant | MODIFIER | c.968-1760C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33393239 | |||||||
chr19:33393265 | G | A | 78 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0141 others(75): Show |
78 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.968-1786C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33393265 | |||||||
chr19:33393276 | T | TGGGGTCT others(17): Show |
4 | a0001c0001t0001g0265 a0001c0001t0001g0288 a0001c0001t0001g0289 others(1): Show |
4 | HG02258.hp2 HG02897.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.968-1821_968-1798d others(26): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33393276 | |||||||
chr19:33393325 | G | A | 1 | a0001c0007t0001g0242 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.968-1846C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33393325 | |||||||
chr19:33393435 | A | G | 79 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0141 others(76): Show |
79 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.968-1956T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33393435 | |||||||
chr19:33393487 | G | GCCTCCGT others(32): Show |
7 | a0001c0001t0001g0022 a0001c0001t0001g0052 a0001c0001t0001g0053 others(4): Show |
7 | HG02630.hp1 HG02896.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.968-2047_968-2009d others(41): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33393487 | |||||||
chr19:33393487 | GCCTCCGT others(32): Show |
G | 5 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0288 others(2): Show |
5 | HG02258.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.968-2047_968-2009d others(41): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33393487 | |||||||
chr19:33393493 | G | A | 1 | a0001c0001t0003g0284 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.968-2014C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33393493 | |||||||
chr19:33393505 | T | G | 22 | a0001c0001t0001g0018 a0001c0001t0001g0278 a0001c0001t0001g0279 others(19): Show |
24 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.968-2026A>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33393505 | |||||||
chr19:33393514 | TCAAACAG others(36): Show |
T | 10 | a0001c0001t0001g0141 a0002c0002t0002g0028 a0002c0002t0002g0128 others(7): Show |
10 | HG01109.hp1 HG02451.hp2 HG03195.hp1 others(7): Show |
intron_variant | MODIFIER | c.968-2078_968-2036d others(45): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33393514 | |||||||
chr19:33393526 | A | G | 51 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0230 others(48): Show |
51 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.968-2047T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33393526 | |||||||
chr19:33393531 | C | T | 4 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0230 others(1): Show |
4 | HG03831.hp1 NA18945.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.968-2052G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33393531 | |||||||
chr19:33393553 | TCAAA | T | 71 | a0001c0001t0001g0018 a0001c0001t0001g0123 a0001c0001t0001g0133 others(68): Show |
71 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.968-2078_968-2075d others(6): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33393553 | |||||||
chr19:33393585 | G | A | 1 | a0002c0002t0002g0299 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.968-2106C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33393585 | |||||||
chr19:33393591 | T | C | 65 | a0001c0001t0001g0018 a0001c0001t0001g0048 a0001c0001t0001g0133 others(62): Show |
65 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.968-2112A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33393591 | |||||||
chr19:33393602 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.968-2123C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33393602 | |||||||
chr19:33393638 | G | A | 13 | a0001c0001t0001g0141 a0001c0001t0001g0267 a0001c0001t0001g0268 others(10): Show |
13 | HG01109.hp1 HG01884.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.968-2159C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33393638 | |||||||
chr19:33393711 | T | A | 1 | a0001c0003t0001g0108 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.968-2232A>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33393711 | |||||||
chr19:33394006 | T | G | 8 | a0001c0001t0001g0294 a0001c0001t0001g0305 a0001c0001t0001g0306 others(5): Show |
8 | HG02055.hp1 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.968-2527A>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33394006 | |||||||
chr19:33394163 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.968-2684C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33394163 | |||||||
chr19:33394212 | C | T | 29 | a0001c0001t0001g0082 a0001c0001t0001g0133 a0001c0001t0001g0134 others(26): Show |
31 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.968-2733G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33394212 | |||||||
chr19:33394364 | C | A | 1 | a0001c0001t0001g0289 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.968-2885G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33394364 | |||||||
chr19:33394364 | CG | C | 4 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0230 others(1): Show |
4 | HG03831.hp1 NA18945.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.968-2886delC | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33394364 | |||||||
chr19:33394376 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.968-2897G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33394376 | |||||||
chr19:33394412 | T | C | 45 | a0001c0001t0001g0022 a0001c0001t0001g0048 a0001c0001t0001g0050 others(42): Show |
45 | HG00099.hp1 HG00642.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.968-2933A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33394412 | |||||||
chr19:33394419 | G | A | 1 | a0003c0005t0001g0015 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.968-2940C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33394419 | |||||||
chr19:33394521 | T | C | 1 | a0001c0001t0001g0294 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.968-3042A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33394521 | |||||||
chr19:33394548 | A | T | 1 | a0002c0002t0002g0241 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.968-3069T>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33394548 | |||||||
chr19:33394572 | C | T | 1 | a0001c0001t0001g0116 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.968-3093G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33394572 | |||||||
chr19:33394595 | G | T | 1 | a0001c0001t0001g0132 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.968-3116C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33394595 | |||||||
chr19:33394711 | T | C | 1 | a0002c0002t0002g0046 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.968-3232A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33394711 | |||||||
chr19:33394747 | G | A | 1 | a0001c0003t0001g0217 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.968-3268C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33394747 | |||||||
chr19:33394824 | C | T | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0308 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.968-3345G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33394824 | |||||||
chr19:33394874 | G | A | 2 | a0001c0001t0001g0018 a0002c0002t0002g0171 |
2 | HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.968-3395C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33394874 | |||||||
chr19:33394999 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.968-3520G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33394999 | |||||||
chr19:33395135 | C | T | 1 | a0002c0002t0002g0258 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.968-3656G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33395135 | |||||||
chr19:33395148 | G | A | 4 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0230 others(1): Show |
4 | HG03831.hp1 NA18945.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.968-3669C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33395148 | |||||||
chr19:33395197 | T | G | 1 | a0002c0002t0002g0241 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.968-3718A>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33395197 | |||||||
chr19:33395198 | C | G | 1 | a0002c0002t0002g0241 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.968-3719G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33395198 | |||||||
chr19:33395229 | T | C | 1 | a0005c0008t0001g0247 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.968-3750A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33395229 | |||||||
chr19:33395283 | C | T | 1 | a0002c0002t0002g0299 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.968-3804G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33395283 | |||||||
chr19:33395415 | T | C | 10 | a0001c0001t0001g0027 a0001c0001t0001g0176 a0002c0002t0002g0028 others(7): Show |
10 | HG01891.hp1 HG02451.hp2 HG03195.hp1 others(7): Show |
intron_variant | MODIFIER | c.968-3936A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33395415 | |||||||
chr19:33395435 | T | C | 52 | a0001c0001t0001g0170 a0001c0001t0001g0173 a0001c0001t0001g0207 others(49): Show |
52 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.968-3956A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33395435 | |||||||
chr19:33395448 | C | T | 110 | a0001c0001t0001g0027 a0001c0001t0001g0075 a0001c0001t0001g0092 others(107): Show |
110 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.968-3969G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33395448 | |||||||
chr19:33395558 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.968-4079C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33395558 | |||||||
chr19:33395597 | C | T | 2 | a0001c0001t0001g0266 a0001c0001t0001g0269 |
2 | HG01891.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.968-4118G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33395597 | |||||||
chr19:33395739 | A | G | 17 | a0001c0001t0001g0018 a0001c0001t0001g0293 a0001c0001t0001g0294 others(14): Show |
17 | HG00099.hp1 HG00733.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.968-4260T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33395739 | |||||||
chr19:33395787 | T | C | 8 | a0001c0001t0003g0045 a0002c0002t0002g0044 a0002c0002t0002g0046 others(5): Show |
8 | HG00099.hp1 HG00733.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.968-4308A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33395787 | |||||||
chr19:33395790 | C | T | 7 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0308 others(4): Show |
7 | HG02055.hp1 HG02257.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.968-4311G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33395790 | |||||||
chr19:33395794 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.968-4315G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33395794 | |||||||
chr19:33395807 | T | A | 177 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0040 others(174): Show |
179 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.968-4328A>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33395807 | |||||||
chr19:33395848 | C | T | 4 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0230 others(1): Show |
4 | HG03831.hp1 NA18945.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.968-4369G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33395848 | |||||||
chr19:33396051 | T | C | 4 | a0001c0001t0001g0266 a0001c0001t0001g0269 a0002c0002t0002g0259 others(1): Show |
4 | HG01109.hp1 HG01891.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.968-4572A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33396051 | |||||||
chr19:33396056 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.968-4577G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33396056 | |||||||
chr19:33396133 | G | A | 111 | a0001c0001t0001g0022 a0001c0001t0001g0040 a0001c0001t0001g0041 others(108): Show |
113 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.968-4654C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33396133 | |||||||
chr19:33396146 | G | A | 5 | a0001c0001t0001g0266 a0001c0001t0001g0269 a0002c0002t0002g0259 others(2): Show |
5 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.968-4667C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33396146 | |||||||
chr19:33396254 | A | C | 133 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0040 others(130): Show |
135 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.968-4775T>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33396254 | |||||||
chr19:33396369 | A | G | 124 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0027 others(121): Show |
126 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.968-4890T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33396369 | |||||||
chr19:33396370 | G | A | 1 | a0002c0002t0005g0298 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.968-4891C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33396370 | |||||||
chr19:33396406 | C | T | 4 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0230 others(1): Show |
4 | HG03831.hp1 NA18945.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.968-4927G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33396406 | |||||||
chr19:33396499 | T | C | 192 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0040 others(189): Show |
194 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.968-5020A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33396499 | |||||||
chr19:33396507 | C | G | 1 | a0002c0002t0002g0129 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.968-5028G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33396507 | |||||||
chr19:33396631 | GC | G | 65 | a0001c0001t0001g0170 a0001c0001t0001g0173 a0001c0001t0001g0207 others(62): Show |
65 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.967+5089delG | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33396631 | |||||||
chr19:33396696 | A | G | 1 | a0001c0001t0001g0294 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.967+5025T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33396696 | |||||||
chr19:33397148 | T | C | 183 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0040 others(180): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.967+4573A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33397148 | |||||||
chr19:33397178 | G | A | 5 | a0002c0002t0002g0008 a0002c0002t0002g0009 a0002c0002t0002g0010 others(2): Show |
5 | HG00140.hp2 HG01496.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.967+4543C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33397178 | |||||||
chr19:33397181 | G | A | 1 | a0003c0004t0001g0084 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.967+4540C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33397181 | |||||||
chr19:33397416 | G | A | 2 | a0001c0001t0001g0132 a0001c0001t0001g0261 |
2 | HG01934.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.967+4305C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33397416 | |||||||
chr19:33397456 | C | T | 1 | a0007c0009t0001g0186 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.967+4265G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33397456 | |||||||
chr19:33397554 | G | A | 180 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0040 others(177): Show |
182 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.967+4167C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33397554 | |||||||
chr19:33397633 | C | T | 52 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(49): Show |
52 | HG00140.hp2 HG00544.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.967+4088G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33397633 | |||||||
chr19:33397665 | G | C | 3 | a0002c0002t0002g0258 a0006c0010t0002g0166 a0006c0010t0005g0168 |
3 | HG02280.hp2 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.967+4056C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33397665 | |||||||
chr19:33397682 | A | G | 183 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0040 others(180): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.967+4039T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33397682 | |||||||
chr19:33397763 | T | G | 186 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0040 others(183): Show |
188 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.967+3958A>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33397763 | |||||||
chr19:33397798 | G | A | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0308 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.967+3923C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33397798 | |||||||
chr19:33397815 | C | G | 2 | a0002c0002t0005g0208 a0002c0002t0005g0298 |
2 | HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.967+3906G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33397815 | |||||||
chr19:33398094 | G | A | 183 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0040 others(180): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.967+3627C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33398094 | |||||||
chr19:33398253 | T | C | 2 | a0001c0001t0001g0293 a0001c0001t0001g0294 |
2 | HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.967+3468A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33398253 | |||||||
chr19:33398261 | C | T | 6 | a0001c0001t0001g0176 a0002c0002t0002g0028 a0002c0002t0002g0122 others(3): Show |
6 | HG01891.hp1 HG03195.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.967+3460G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33398261 | |||||||
chr19:33398294 | G | A | 10 | a0002c0002t0002g0026 a0002c0002t0002g0029 a0002c0002t0002g0030 others(7): Show |
10 | HG01257.hp2 HG02451.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.967+3427C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33398294 | |||||||
chr19:33398309 | C | T | 63 | a0001c0001t0001g0170 a0001c0001t0001g0173 a0001c0001t0001g0207 others(60): Show |
63 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.967+3412G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33398309 | |||||||
chr19:33398362 | G | A | 1 | a0001c0003t0001g0232 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.967+3359C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33398362 | |||||||
chr19:33398463 | A | G | 183 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0040 others(180): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.967+3258T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33398463 | |||||||
chr19:33398503 | C | A | 6 | a0004c0006t0001g0296 a0004c0006t0001g0297 a0004c0006t0001g0300 others(3): Show |
6 | HG02809.hp1 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.967+3218G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33398503 | |||||||
chr19:33398687 | A | G | 190 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0040 others(187): Show |
192 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.967+3034T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33398687 | |||||||
chr19:33398802 | A | G | 3 | a0002c0002t0002g0258 a0006c0010t0002g0166 a0006c0010t0005g0168 |
3 | HG02280.hp2 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.967+2919T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33398802 | |||||||
chr19:33398915 | G | A | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0308 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.967+2806C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33398915 | |||||||
chr19:33399084 | A | G | 1 | a0002c0002t0002g0174 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.967+2637T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33399084 | |||||||
chr19:33399085 | G | A | 9 | a0001c0001t0003g0045 a0002c0002t0002g0044 a0002c0002t0002g0046 others(6): Show |
9 | HG00099.hp1 HG00733.hp2 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.967+2636C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33399085 | |||||||
chr19:33399098 | C | T | 48 | a0001c0001t0001g0075 a0001c0001t0001g0092 a0001c0001t0001g0093 others(45): Show |
48 | HG00140.hp2 HG00544.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.967+2623G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33399098 | |||||||
chr19:33399110 | T | A | 1 | a0002c0002t0002g0171 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.967+2611A>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33399110 | |||||||
chr19:33399115 | A | C | 1 | a0001c0001t0001g0138 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.967+2606T>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33399115 | |||||||
chr19:33399260 | G | A | 2 | a0006c0010t0002g0166 a0006c0010t0005g0168 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.967+2461C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33399260 | |||||||
chr19:33399264 | G | C | 37 | a0001c0003t0001g0108 a0001c0003t0001g0143 a0001c0003t0001g0144 others(34): Show |
37 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.967+2457C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33399264 | |||||||
chr19:33399276 | C | G | 3 | a0003c0004t0001g0095 a0003c0004t0001g0096 a0003c0004t0001g0097 |
3 | NA18951.hp2 NA18968.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.967+2445G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33399276 | |||||||
chr19:33399322 | T | C | 12 | a0001c0001t0001g0027 a0001c0001t0001g0176 a0002c0002t0002g0028 others(9): Show |
12 | HG01891.hp1 HG02451.hp2 HG03195.hp1 others(9): Show |
intron_variant | MODIFIER | c.967+2399A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33399322 | |||||||
chr19:33399389 | T | G | 52 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(49): Show |
52 | HG00140.hp2 HG00544.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.967+2332A>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33399389 | |||||||
chr19:33399454 | G | A | 1 | a0001c0001t0001g0294 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.967+2267C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33399454 | |||||||
chr19:33399622 | TGGCTGAG | T | 7 | a0001c0001t0001g0004 a0001c0001t0001g0154 a0001c0001t0001g0155 others(4): Show |
8 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(5): Show |
intron_variant | MODIFIER | c.967+2092_967+2098d others(9): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33399622 | |||||||
chr19:33399644 | A | AG | 12 | a0001c0001t0001g0266 a0001c0001t0001g0269 a0001c0001t0001g0305 others(9): Show |
12 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.967+2076_967+2077i others(3): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33399644 | |||||||
chr19:33399914 | G | C | 1 | a0001c0001t0001g0121 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.967+1807C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33399914 | |||||||
chr19:33399932 | C | G | 146 | a0001c0001t0001g0027 a0001c0001t0001g0040 a0001c0001t0001g0041 others(143): Show |
146 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.967+1789G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33399932 | |||||||
chr19:33399997 | C | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 |
3 | HG01071.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.967+1724G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33399997 | |||||||
chr19:33400025 | A | C | 17 | a0001c0001t0001g0176 a0001c0001t0001g0305 a0001c0001t0001g0306 others(14): Show |
17 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.967+1696T>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33400025 | |||||||
chr19:33400065 | C | T | 2 | a0002c0002t0002g0213 a0002c0002t0002g0214 |
2 | HG00544.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.967+1656G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33400065 | |||||||
chr19:33400092 | C | T | 5 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0308 others(2): Show |
5 | HG02055.hp1 HG02257.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.967+1629G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33400092 | |||||||
chr19:33400107 | A | T | 63 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(60): Show |
65 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.967+1614T>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33400107 | |||||||
chr19:33400138 | C | T | 1 | a0002c0002t0002g0085 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.967+1583G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33400138 | |||||||
chr19:33400289 | G | A | 75 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(72): Show |
75 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.967+1432C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33400289 | |||||||
chr19:33400307 | G | A | 2 | a0002c0002t0002g0158 a0002c0002t0002g0159 |
2 | HG00408.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.967+1414C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33400307 | |||||||
chr19:33400522 | A | G | 1 | a0002c0002t0002g0257 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.967+1199T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33400522 | |||||||
chr19:33400632 | T | C | 4 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(1): Show |
4 | HG01099.hp2 HG02257.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.967+1089A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33400632 | |||||||
chr19:33400861 | C | CAGGT | 4 | a0001c0001t0001g0266 a0001c0001t0001g0269 a0002c0002t0002g0259 others(1): Show |
4 | HG01109.hp1 HG01891.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.967+859_967+860ins others(4): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33400861 | |||||||
chr19:33400862 | C | G | 4 | a0001c0001t0001g0266 a0001c0001t0001g0269 a0002c0002t0002g0259 others(1): Show |
4 | HG01109.hp1 HG01891.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.967+859G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33400862 | |||||||
chr19:33400864 | C | T | 4 | a0001c0001t0001g0266 a0001c0001t0001g0269 a0002c0002t0002g0259 others(1): Show |
4 | HG01109.hp1 HG01891.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.967+857G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33400864 | |||||||
chr19:33400865 | T | A | 4 | a0001c0001t0001g0266 a0001c0001t0001g0269 a0002c0002t0002g0259 others(1): Show |
4 | HG01109.hp1 HG01891.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.967+856A>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33400865 | |||||||
chr19:33401033 | G | A | 52 | a0001c0001t0001g0170 a0001c0001t0001g0173 a0001c0001t0001g0207 others(49): Show |
52 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.967+688C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33401033 | |||||||
chr19:33401262 | G | A | 2 | a0002c0002t0002g0233 a0002c0002t0002g0235 |
2 | NA18969.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.967+459C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33401262 | |||||||
chr19:33401339 | G | A | 2 | a0001c0001t0001g0099 a0001c0001t0001g0101 |
2 | NA18953.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.967+382C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33401339 | |||||||
chr19:33401449 | C | T | 1 | a0002c0002t0002g0149 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.967+272G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33401449 | |||||||
chr19:33401503 | C | T | 168 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0040 others(165): Show |
168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.967+218G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33401503 | |||||||
chr19:33401575 | C | T | 50 | a0001c0001t0001g0027 a0001c0001t0001g0075 a0001c0001t0001g0092 others(47): Show |
50 | HG00140.hp2 HG00544.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.967+146G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33401575 | |||||||
chr19:33401671 | G | A | 1 | a0002c0002t0002g0171 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.967+50C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 12/14 | chr19 | 33401671 | |||||||
chr19:33401913 | C | T | 3 | a0002c0002t0002g0258 a0006c0010t0002g0166 a0006c0010t0005g0168 |
3 | HG02280.hp2 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.819-44G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33401913 | |||||||
chr19:33401991 | T | A | 1 | a0002c0002t0002g0241 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.819-122A>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33401991 | |||||||
chr19:33402102 | A | G | 150 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0040 others(147): Show |
150 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.819-233T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33402102 | |||||||
chr19:33402252 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.819-383C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33402252 | |||||||
chr19:33402284 | C | A | 4 | a0001c0001t0001g0266 a0001c0001t0001g0269 a0002c0002t0002g0259 others(1): Show |
4 | HG01109.hp1 HG01891.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.819-415G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33402284 | |||||||
chr19:33402390 | C | T | 1 | a0002c0002t0002g0258 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.819-521G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33402390 | |||||||
chr19:33402468 | G | A | 2 | a0001c0001t0001g0141 a0002c0002t0002g0128 |
2 | HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.819-599C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33402468 | |||||||
chr19:33402545 | T | C | 150 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0040 others(147): Show |
150 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.819-676A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33402545 | |||||||
chr19:33403093 | C | T | 1 | a0001c0001t0001g0018 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.819-1224G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33403093 | |||||||
chr19:33403137 | G | A | 147 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0040 others(144): Show |
147 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.819-1268C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33403137 | |||||||
chr19:33403186 | G | A | 4 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(1): Show |
4 | HG01099.hp2 HG02257.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.819-1317C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33403186 | |||||||
chr19:33403288 | C | T | 2 | a0002c0002t0002g0072 a0002c0002t0002g0090 |
2 | HG01081.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.819-1419G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33403288 | |||||||
chr19:33403415 | T | C | 8 | a0001c0001t0001g0004 a0001c0001t0001g0154 a0001c0001t0001g0155 others(5): Show |
9 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(6): Show |
intron_variant | MODIFIER | c.819-1546A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33403415 | |||||||
chr19:33403565 | T | C | 4 | a0001c0001t0001g0266 a0001c0001t0001g0269 a0002c0002t0002g0259 others(1): Show |
4 | HG01109.hp1 HG01891.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.819-1696A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33403565 | |||||||
chr19:33403663 | A | C | 1 | a0002c0002t0002g0146 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.819-1794T>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33403663 | |||||||
chr19:33403709 | G | A | 89 | a0001c0001t0001g0022 a0001c0001t0001g0048 a0001c0001t0001g0050 others(86): Show |
89 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.819-1840C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33403709 | |||||||
chr19:33403734 | G | C | 3 | a0002c0002t0005g0091 a0002c0002t0005g0208 a0002c0002t0005g0298 |
3 | HG02258.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.819-1865C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33403734 | |||||||
chr19:33403748 | A | C | 1 | a0001c0001t0001g0155 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.819-1879T>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33403748 | |||||||
chr19:33403782 | A | G | 4 | a0001c0001t0003g0045 a0002c0002t0002g0044 a0002c0002t0002g0046 others(1): Show |
4 | HG00099.hp1 HG00733.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.819-1913T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33403782 | |||||||
chr19:33403940 | C | T | 195 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0027 others(192): Show |
197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.819-2071G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33403940 | |||||||
chr19:33404074 | G | A | 9 | a0001c0001t0003g0045 a0002c0002t0002g0044 a0002c0002t0002g0046 others(6): Show |
9 | HG00099.hp1 HG00733.hp2 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.819-2205C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33404074 | |||||||
chr19:33404104 | C | T | 1 | a0002c0002t0002g0032 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.819-2235G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33404104 | |||||||
chr19:33404105 | G | A | 4 | a0001c0001t0001g0266 a0001c0001t0001g0269 a0002c0002t0002g0259 others(1): Show |
4 | HG01109.hp1 HG01891.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.819-2236C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33404105 | |||||||
chr19:33404106 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.819-2237C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33404106 | |||||||
chr19:33404407 | C | T | 49 | a0001c0001t0001g0027 a0001c0001t0001g0075 a0001c0001t0001g0092 others(46): Show |
49 | HG00140.hp2 HG00544.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.819-2538G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33404407 | |||||||
chr19:33404408 | G | A | 23 | a0001c0001t0001g0018 a0001c0001t0001g0082 a0001c0001t0001g0278 others(20): Show |
25 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.819-2539C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33404408 | |||||||
chr19:33404444 | A | G | 3 | a0002c0002t0002g0258 a0006c0010t0002g0166 a0006c0010t0005g0168 |
3 | HG02280.hp2 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.819-2575T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33404444 | |||||||
chr19:33404457 | A | C | 1 | a0001c0003t0001g0007 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.819-2588T>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33404457 | |||||||
chr19:33404457 | AAAC | A | 167 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0040 others(164): Show |
167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.819-2591_819-2589d others(5): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33404457 | |||||||
chr19:33404509 | G | A | 1 | a0002c0002t0002g0262 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.819-2640C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33404509 | |||||||
chr19:33404734 | C | T | 1 | a0002c0002t0002g0047 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.819-2865G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33404734 | |||||||
chr19:33404818 | T | TA | 100 | a0001c0001t0001g0022 a0001c0001t0001g0048 a0001c0001t0001g0050 others(97): Show |
100 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.819-2950dupT | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33404818 | |||||||
chr19:33404913 | C | T | 2 | a0001c0001t0001g0230 a0001c0001t0001g0237 |
2 | HG03831.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.819-3044G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33404913 | |||||||
chr19:33405010 | G | A | 1 | a0002c0002t0002g0259 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.819-3141C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33405010 | |||||||
chr19:33405093 | C | G | 1 | a0002c0002t0002g0044 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.819-3224G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33405093 | |||||||
chr19:33405161 | G | A | 2 | a0002c0002t0002g0028 a0002c0002t0002g0175 |
2 | HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.819-3292C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33405161 | |||||||
chr19:33405243 | C | T | 23 | a0001c0001t0001g0018 a0001c0001t0001g0082 a0001c0001t0001g0278 others(20): Show |
25 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.819-3374G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33405243 | |||||||
chr19:33405289 | G | A | 143 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0040 others(140): Show |
143 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.819-3420C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33405289 | |||||||
chr19:33405320 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.819-3451A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33405320 | |||||||
chr19:33405389 | G | A | 2 | a0001c0001t0001g0230 a0001c0001t0001g0237 |
2 | HG03831.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.819-3520C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33405389 | |||||||
chr19:33405526 | A | C | 194 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0027 others(191): Show |
196 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.819-3657T>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33405526 | |||||||
chr19:33405550 | C | T | 22 | a0001c0001t0001g0082 a0001c0001t0001g0278 a0001c0001t0001g0279 others(19): Show |
24 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.819-3681G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33405550 | |||||||
chr19:33405562 | G | A | 1 | a0002c0002t0002g0241 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.819-3693C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33405562 | |||||||
chr19:33405652 | G | A | 6 | a0001c0001t0001g0176 a0002c0002t0002g0028 a0002c0002t0002g0122 others(3): Show |
6 | HG01891.hp1 HG03195.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.819-3783C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33405652 | |||||||
chr19:33405773 | T | A | 1 | a0001c0001t0001g0294 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.819-3904A>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33405773 | |||||||
chr19:33405818 | C | T | 1 | a0001c0001t0003g0281 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.819-3949G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33405818 | |||||||
chr19:33406090 | C | T | 1 | a0001c0003t0001g0255 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.819-4221G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33406090 | |||||||
chr19:33406106 | A | G | 1 | a0001c0003t0001g0254 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.819-4237T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33406106 | |||||||
chr19:33406122 | C | T | 10 | a0001c0001t0001g0176 a0002c0002t0002g0028 a0002c0002t0002g0122 others(7): Show |
10 | HG01891.hp1 HG02451.hp2 HG03195.hp1 others(7): Show |
intron_variant | MODIFIER | c.819-4253G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33406122 | |||||||
chr19:33406126 | C | A | 1 | a0001c0003t0001g0226 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.819-4257G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33406126 | |||||||
chr19:33406243 | A | G | 100 | a0001c0001t0001g0022 a0001c0001t0001g0048 a0001c0001t0001g0050 others(97): Show |
100 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.819-4374T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33406243 | |||||||
chr19:33406261 | G | T | 17 | a0001c0001t0001g0176 a0001c0001t0001g0305 a0001c0001t0001g0306 others(14): Show |
17 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.819-4392C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33406261 | |||||||
chr19:33406296 | C | T | 3 | a0002c0002t0002g0258 a0006c0010t0002g0166 a0006c0010t0005g0168 |
3 | HG02280.hp2 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.819-4427G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33406296 | |||||||
chr19:33406317 | A | G | 39 | a0001c0001t0001g0027 a0001c0001t0001g0075 a0001c0001t0001g0092 others(36): Show |
39 | HG00140.hp2 HG00609.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.819-4448T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33406317 | |||||||
chr19:33406346 | A | G | 1 | a0001c0001t0001g0264 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.819-4477T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33406346 | |||||||
chr19:33406572 | A | C | 152 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0040 others(149): Show |
152 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.819-4703T>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33406572 | |||||||
chr19:33406740 | T | C | 1 | a0002c0002t0002g0175 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.819-4871A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33406740 | |||||||
chr19:33406744 | C | T | 2 | a0001c0001t0001g0022 a0001c0001t0001g0052 |
2 | HG02630.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.819-4875G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33406744 | |||||||
chr19:33406749 | C | T | 1 | a0001c0003t0001g0255 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.819-4880G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33406749 | |||||||
chr19:33406763 | C | G | 23 | a0001c0001t0001g0018 a0001c0001t0001g0082 a0001c0001t0001g0278 others(20): Show |
25 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.819-4894G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33406763 | |||||||
chr19:33406807 | C | T | 23 | a0001c0001t0001g0018 a0001c0001t0001g0082 a0001c0001t0001g0278 others(20): Show |
25 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.818+4865G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33406807 | |||||||
chr19:33406841 | T | C | 21 | a0001c0003t0001g0167 a0001c0003t0001g0193 a0001c0003t0001g0194 others(18): Show |
21 | HG00438.hp1 HG00558.hp1 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.818+4831A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33406841 | |||||||
chr19:33406884 | G | A | 3 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0013t0002g0011 |
3 | HG01074.hp1 HG01109.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.818+4788C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33406884 | |||||||
chr19:33406917 | G | A | 28 | a0001c0001t0001g0022 a0001c0001t0001g0048 a0001c0001t0001g0050 others(25): Show |
28 | HG01884.hp2 HG02258.hp2 HG02486.hp2 others(25): Show |
intron_variant | MODIFIER | c.818+4755C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33406917 | |||||||
chr19:33406937 | C | G | 22 | a0001c0001t0001g0082 a0001c0001t0001g0278 a0001c0001t0001g0279 others(19): Show |
24 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.818+4735G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33406937 | |||||||
chr19:33407028 | T | G | 80 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0048 others(77): Show |
82 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.818+4644A>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33407028 | |||||||
chr19:33407120 | C | T | 1 | a0001c0003t0001g0199 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.818+4552G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33407120 | |||||||
chr19:33407159 | A | C | 2 | a0002c0002t0002g0171 a0002c0002t0002g0241 |
2 | HG01884.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.818+4513T>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33407159 | |||||||
chr19:33407297 | T | C | 1 | a0001c0003t0001g0197 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.818+4375A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33407297 | |||||||
chr19:33407339 | G | A | 2 | a0001c0001t0001g0266 a0001c0001t0001g0269 |
2 | HG01891.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.818+4333C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33407339 | |||||||
chr19:33407380 | T | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 |
3 | HG01071.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.818+4292A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33407380 | |||||||
chr19:33407443 | G | A | 2 | a0002c0002t0002g0028 a0002c0002t0002g0175 |
2 | HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.818+4229C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33407443 | |||||||
chr19:33407599 | T | C | 1 | a0001c0001t0001g0111 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.818+4073A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33407599 | |||||||
chr19:33407626 | T | G | 1 | a0001c0001t0001g0294 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.818+4046A>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33407626 | |||||||
chr19:33407782 | G | A | 1 | a0001c0001t0003g0045 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.818+3890C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33407782 | |||||||
chr19:33407864 | C | T | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0308 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.818+3808G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33407864 | |||||||
chr19:33407880 | G | A | 2 | a0002c0002t0002g0233 a0002c0002t0002g0235 |
2 | NA18969.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.818+3792C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33407880 | |||||||
chr19:33407919 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.818+3753C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33407919 | |||||||
chr19:33408159 | G | A | 168 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0040 others(165): Show |
170 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.818+3513C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33408159 | |||||||
chr19:33408187 | G | T | 8 | a0001c0001t0001g0018 a0001c0001t0001g0133 a0001c0001t0001g0134 others(5): Show |
8 | HG02055.hp1 HG02257.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.818+3485C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33408187 | |||||||
chr19:33408192 | G | A | 8 | a0001c0001t0001g0018 a0001c0001t0001g0133 a0001c0001t0001g0134 others(5): Show |
8 | HG02055.hp1 HG02257.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.818+3480C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33408192 | |||||||
chr19:33408240 | T | C | 1 | a0002c0002t0002g0171 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.818+3432A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33408240 | |||||||
chr19:33408331 | G | A | 3 | a0002c0002t0005g0091 a0002c0002t0005g0208 a0002c0002t0005g0298 |
3 | HG02258.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.818+3341C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33408331 | |||||||
chr19:33408343 | G | A | 1 | a0001c0001t0001g0294 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.818+3329C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33408343 | |||||||
chr19:33408429 | T | C | 1 | a0002c0002t0002g0304 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.818+3243A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33408429 | |||||||
chr19:33408460 | T | C | 1 | a0001c0003t0001g0161 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.818+3212A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33408460 | |||||||
chr19:33408488 | G | T | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0308 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.818+3184C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33408488 | |||||||
chr19:33408806 | C | G | 5 | a0004c0006t0001g0296 a0004c0006t0001g0297 a0004c0006t0001g0300 others(2): Show |
5 | HG02809.hp1 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.818+2866G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33408806 | |||||||
chr19:33408826 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.818+2846G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33408826 | |||||||
chr19:33408840 | G | A | 11 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(8): Show |
11 | HG01099.hp2 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.818+2832C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33408840 | |||||||
chr19:33408872 | C | T | 38 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(35): Show |
38 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(35): Show |
intron_variant | MODIFIER | c.818+2800G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33408872 | |||||||
chr19:33409003 | A | C | 28 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(25): Show |
28 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(25): Show |
intron_variant | MODIFIER | c.818+2669T>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33409003 | |||||||
chr19:33409099 | G | A | 1 | a0001c0001t0001g0294 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.818+2573C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33409099 | |||||||
chr19:33409105 | C | T | 1 | a0001c0001t0001g0294 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.818+2567G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33409105 | |||||||
chr19:33409162 | T | C | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0308 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.818+2510A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33409162 | |||||||
chr19:33409228 | G | A | 1 | a0001c0001t0001g0003 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.818+2444C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33409228 | |||||||
chr19:33409260 | G | T | 13 | a0001c0001t0001g0170 a0001c0001t0001g0173 a0002c0012t0002g0135 others(10): Show |
13 | HG02129.hp1 HG02280.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.818+2412C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33409260 | |||||||
chr19:33409351 | C | G | 199 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0040 others(196): Show |
201 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.818+2321G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33409351 | |||||||
chr19:33409362 | T | C | 12 | a0001c0001t0001g0176 a0002c0002t0002g0028 a0002c0002t0002g0122 others(9): Show |
12 | HG01109.hp1 HG01891.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.818+2310A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33409362 | |||||||
chr19:33409597 | C | A | 2 | a0001c0001t0004g0039 a0001c0001t0004g0080 |
2 | NA18943.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.818+2075G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33409597 | |||||||
chr19:33409652 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.818+2020C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33409652 | |||||||
chr19:33409700 | G | A | 1 | a0008c0011t0001g0270 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.818+1972C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33409700 | |||||||
chr19:33409743 | C | T | 1 | a0002c0002t0002g0030 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.818+1929G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33409743 | |||||||
chr19:33409803 | C | T | 38 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(35): Show |
38 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(35): Show |
intron_variant | MODIFIER | c.818+1869G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33409803 | |||||||
chr19:33409857 | T | G | 30 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(27): Show |
30 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(27): Show |
intron_variant | MODIFIER | c.818+1815A>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33409857 | |||||||
chr19:33409901 | C | T | 38 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(35): Show |
38 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(35): Show |
intron_variant | MODIFIER | c.818+1771G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33409901 | |||||||
chr19:33410070 | G | A | 1 | a0002c0002t0005g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.818+1602C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33410070 | |||||||
chr19:33410102 | G | C | 1 | a0001c0001t0001g0082 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.818+1570C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33410102 | |||||||
chr19:33410109 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.818+1563G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33410109 | |||||||
chr19:33410128 | A | G | 17 | a0001c0001t0001g0176 a0002c0002t0002g0028 a0002c0002t0002g0122 others(14): Show |
17 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.818+1544T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33410128 | |||||||
chr19:33410185 | T | C | 4 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0230 others(1): Show |
4 | HG03831.hp1 NA18945.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.818+1487A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33410185 | |||||||
chr19:33410274 | T | C | 104 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0040 others(101): Show |
104 | HG00140.hp2 HG00609.hp2 HG00642.hp2 others(101): Show |
intron_variant | MODIFIER | c.818+1398A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33410274 | |||||||
chr19:33410336 | G | A | 1 | a0002c0002t0002g0257 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.818+1336C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33410336 | |||||||
chr19:33410512 | C | T | 3 | a0002c0002t0002g0028 a0002c0002t0002g0169 a0002c0002t0002g0175 |
3 | HG03195.hp1 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.818+1160G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33410512 | |||||||
chr19:33410528 | T | C | 2 | a0006c0010t0002g0166 a0006c0010t0005g0168 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.818+1144A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33410528 | |||||||
chr19:33410549 | C | G | 1 | a0001c0003t0001g0223 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.818+1123G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33410549 | |||||||
chr19:33410577 | G | A | 2 | a0002c0002t0005g0208 a0002c0002t0005g0298 |
2 | HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.818+1095C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33410577 | |||||||
chr19:33410638 | G | A | 3 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0295 |
3 | HG01123.hp1 HG01928.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.818+1034C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33410638 | |||||||
chr19:33410640 | G | A | 1 | a0001c0003t0001g0161 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.818+1032C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33410640 | |||||||
chr19:33410644 | C | T | 43 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0075 others(40): Show |
43 | HG00140.hp2 HG00609.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.818+1028G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33410644 | |||||||
chr19:33410653 | C | CA | 11 | a0001c0001t0001g0027 a0002c0002t0002g0026 a0002c0002t0002g0029 others(8): Show |
11 | HG01257.hp2 HG02451.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.818+1018dupT | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33410653 | |||||||
chr19:33410731 | G | C | 3 | a0003c0004t0001g0095 a0003c0004t0001g0096 a0003c0004t0001g0097 |
3 | NA18951.hp2 NA18968.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.818+941C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33410731 | |||||||
chr19:33410769 | T | C | 1 | a0001c0001t0001g0261 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.818+903A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33410769 | |||||||
chr19:33410770 | A | C | 1 | a0001c0001t0001g0261 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.818+902T>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33410770 | |||||||
chr19:33410771 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.818+901C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33410771 | |||||||
chr19:33410807 | AG | A | 29 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(26): Show |
29 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(26): Show |
intron_variant | MODIFIER | c.818+864delC | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33410807 | |||||||
chr19:33410983 | G | A | 8 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0230 others(5): Show |
8 | HG02055.hp1 HG02257.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.818+689C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33410983 | |||||||
chr19:33411016 | C | T | 23 | a0001c0001t0001g0082 a0001c0001t0001g0261 a0001c0001t0001g0278 others(20): Show |
25 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.818+656G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33411016 | |||||||
chr19:33411021 | G | A | 3 | a0003c0004t0001g0095 a0003c0004t0001g0096 a0003c0004t0001g0097 |
3 | NA18951.hp2 NA18968.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.818+651C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33411021 | |||||||
chr19:33411268 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.818+404G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33411268 | |||||||
chr19:33411269 | G | A | 3 | a0002c0002t0005g0091 a0002c0002t0005g0208 a0002c0002t0005g0298 |
3 | HG02258.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.818+403C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33411269 | |||||||
chr19:33411326 | C | T | 4 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0230 others(1): Show |
4 | HG03831.hp1 NA18945.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.818+346G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33411326 | |||||||
chr19:33411406 | T | G | 1 | a0001c0003t0001g0246 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.818+266A>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33411406 | |||||||
chr19:33411513 | G | A | 2 | a0001c0001t0001g0267 a0001c0001t0001g0268 |
2 | HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.818+159C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 11/14 | chr19 | 33411513 | |||||||
chr19:33411867 | C | G | 7 | a0002c0002t0002g0029 a0002c0002t0002g0030 a0002c0002t0002g0031 others(4): Show |
7 | HG02451.hp1 HG02615.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.741-118G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 10/14 | chr19 | 33411867 | |||||||
chr19:33411903 | A | G | 103 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0040 others(100): Show |
103 | HG00140.hp2 HG00609.hp2 HG00642.hp2 others(100): Show |
intron_variant | MODIFIER | c.741-154T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 10/14 | chr19 | 33411903 | |||||||
chr19:33411958 | C | T | 29 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(26): Show |
29 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(26): Show |
intron_variant | MODIFIER | c.741-209G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 10/14 | chr19 | 33411958 | |||||||
chr19:33412021 | G | T | 3 | a0003c0004t0001g0070 a0003c0004t0001g0079 a0003c0004t0001g0084 |
3 | HG02056.hp2 HG02083.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.741-272C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 10/14 | chr19 | 33412021 | |||||||
chr19:33412102 | G | T | 1 | a0001c0001t0001g0131 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.741-353C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 10/14 | chr19 | 33412102 | |||||||
chr19:33412279 | G | A | 43 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0075 others(40): Show |
43 | HG00140.hp2 HG00609.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.741-530C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 10/14 | chr19 | 33412279 | |||||||
chr19:33412282 | G | A | 4 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0230 others(1): Show |
4 | HG03831.hp1 NA18945.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.741-533C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 10/14 | chr19 | 33412282 | |||||||
chr19:33412283 | A | G | 103 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0040 others(100): Show |
103 | HG00140.hp2 HG00609.hp2 HG00642.hp2 others(100): Show |
intron_variant | MODIFIER | c.741-534T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 10/14 | chr19 | 33412283 | |||||||
chr19:33412318 | G | C | 1 | a0002c0002t0002g0304 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.741-569C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 10/14 | chr19 | 33412318 | |||||||
chr19:33412430 | C | G | 2 | a0001c0001t0001g0170 a0001c0001t0001g0173 |
2 | HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.741-681G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 10/14 | chr19 | 33412430 | |||||||
chr19:33412446 | C | A | 31 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(28): Show |
31 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(28): Show |
intron_variant | MODIFIER | c.741-697G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 10/14 | chr19 | 33412446 | |||||||
chr19:33412496 | A | G | 39 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(36): Show |
39 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(36): Show |
intron_variant | MODIFIER | c.741-747T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 10/14 | chr19 | 33412496 | |||||||
chr19:33412615 | C | G | 2 | a0001c0001t0001g0170 a0001c0001t0001g0173 |
2 | HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.741-866G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 10/14 | chr19 | 33412615 | |||||||
chr19:33412683 | G | A | 39 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(36): Show |
39 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(36): Show |
intron_variant | MODIFIER | c.740+892C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 10/14 | chr19 | 33412683 | |||||||
chr19:33412762 | G | A | 5 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0003g0273 others(2): Show |
5 | HG00733.hp1 HG01099.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.740+813C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 10/14 | chr19 | 33412762 | |||||||
chr19:33412856 | G | T | 2 | a0007c0009t0001g0185 a0007c0009t0001g0186 |
2 | HG03471.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.740+719C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 10/14 | chr19 | 33412856 | |||||||
chr19:33412908 | G | C | 8 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0230 others(5): Show |
8 | HG02055.hp1 HG02257.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.740+667C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 10/14 | chr19 | 33412908 | |||||||
chr19:33412982 | G | C | 43 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0075 others(40): Show |
43 | HG00140.hp2 HG00609.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.740+593C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 10/14 | chr19 | 33412982 | |||||||
chr19:33412991 | C | A | 43 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0075 others(40): Show |
43 | HG00140.hp2 HG00609.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.740+584G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 10/14 | chr19 | 33412991 | |||||||
chr19:33412997 | C | A | 43 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0075 others(40): Show |
43 | HG00140.hp2 HG00609.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.740+578G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 10/14 | chr19 | 33412997 | |||||||
chr19:33413034 | C | A | 1 | a0001c0003t0001g0246 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.740+541G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 10/14 | chr19 | 33413034 | |||||||
chr19:33413207 | T | G | 1 | a0001c0001t0004g0142 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.740+368A>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 10/14 | chr19 | 33413207 | |||||||
chr19:33413407 | C | T | 1 | a0001c0014t0001g0263 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.740+168G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 10/14 | chr19 | 33413407 | |||||||
chr19:33413410 | G | T | 29 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(26): Show |
29 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(26): Show |
intron_variant | MODIFIER | c.740+165C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 10/14 | chr19 | 33413410 | |||||||
chr19:33413448 | G | A | 28 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(25): Show |
28 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(25): Show |
intron_variant | MODIFIER | c.740+127C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 10/14 | chr19 | 33413448 | |||||||
chr19:33413543 | C | A | 3 | a0002c0002t0002g0026 a0002c0002t0002g0036 a0002c0002t0002g0038 |
3 | HG01257.hp2 HG02738.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.740+32G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 10/14 | chr19 | 33413543 | |||||||
chr19:33413799 | C | T | 1 | a0002c0002t0002g0241 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.672-156G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33413799 | |||||||
chr19:33413813 | G | T | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0308 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.672-170C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33413813 | |||||||
chr19:33413878 | G | A | 8 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0230 others(5): Show |
8 | HG02055.hp1 HG02257.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.672-235C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33413878 | |||||||
chr19:33413923 | G | A | 42 | a0001c0001t0001g0027 a0001c0001t0001g0075 a0001c0001t0001g0092 others(39): Show |
42 | HG00140.hp2 HG00609.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.672-280C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33413923 | |||||||
chr19:33413955 | T | C | 30 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(27): Show |
30 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(27): Show |
intron_variant | MODIFIER | c.672-312A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33413955 | |||||||
chr19:33413970 | C | T | 1 | a0002c0002t0005g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.672-327G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33413970 | |||||||
chr19:33414066 | CCCA | C | 7 | a0001c0003t0001g0167 a0001c0003t0001g0223 a0001c0003t0001g0224 others(4): Show |
7 | NA18943.hp1 NA18957.hp2 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.672-426_672-424del others(3): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33414066 | |||||||
chr19:33414072 | C | G | 1 | a0001c0003t0001g0246 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.672-429G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33414072 | |||||||
chr19:33414083 | G | A | 6 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0133 others(3): Show |
6 | HG02602.hp2 HG03831.hp1 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.672-440C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33414083 | |||||||
chr19:33414130 | A | G | 44 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0048 others(41): Show |
44 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(41): Show |
intron_variant | MODIFIER | c.672-487T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33414130 | |||||||
chr19:33414183 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.672-540C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33414183 | |||||||
chr19:33414215 | G | A | 1 | a0002c0002t0002g0290 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.672-572C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33414215 | |||||||
chr19:33414362 | G | A | 1 | a0001c0001t0003g0274 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.672-719C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33414362 | |||||||
chr19:33414415 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.672-772C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33414415 | |||||||
chr19:33414449 | C | T | 3 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 |
3 | HG01099.hp2 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.672-806G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33414449 | |||||||
chr19:33414575 | C | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG00642.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.672-932G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33414575 | |||||||
chr19:33414614 | C | T | 1 | a0002c0002t0005g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.672-971G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33414614 | |||||||
chr19:33414615 | G | A | 59 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0133 others(56): Show |
59 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.672-972C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33414615 | |||||||
chr19:33414620 | G | A | 1 | a0001c0001t0001g0003 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.672-977C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33414620 | |||||||
chr19:33414624 | G | A | 54 | a0001c0001t0001g0170 a0001c0001t0001g0173 a0001c0001t0001g0216 others(51): Show |
54 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.672-981C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33414624 | |||||||
chr19:33414776 | C | T | 1 | a0003c0004t0001g0210 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.672-1133G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33414776 | |||||||
chr19:33414977 | G | C | 4 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(1): Show |
4 | HG01099.hp2 HG02257.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.672-1334C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33414977 | |||||||
chr19:33415063 | G | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0133 others(1): Show |
4 | HG02602.hp2 HG03942.hp2 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.672-1420C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33415063 | |||||||
chr19:33415078 | C | T | 10 | a0002c0002t0002g0026 a0002c0002t0002g0029 a0002c0002t0002g0030 others(7): Show |
10 | HG01257.hp2 HG02451.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.672-1435G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33415078 | |||||||
chr19:33415079 | A | G | 103 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0040 others(100): Show |
105 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.672-1436T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33415079 | |||||||
chr19:33415196 | A | G | 108 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0040 others(105): Show |
110 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.672-1553T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33415196 | |||||||
chr19:33415204 | C | T | 100 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0040 others(97): Show |
102 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.672-1561G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33415204 | |||||||
chr19:33415209 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.672-1566G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33415209 | |||||||
chr19:33415217 | T | C | 173 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0024 others(170): Show |
175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.672-1574A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33415217 | |||||||
chr19:33415285 | C | T | 11 | a0001c0001t0001g0261 a0001c0001t0003g0001 a0001c0001t0003g0179 others(8): Show |
13 | HG00639.hp2 HG00642.hp1 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.672-1642G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33415285 | |||||||
chr19:33415286 | G | A | 2 | a0006c0010t0002g0166 a0006c0010t0005g0168 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.672-1643C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33415286 | |||||||
chr19:33415290 | TG | T | 10 | a0001c0001t0003g0045 a0002c0002t0002g0044 a0002c0002t0002g0046 others(7): Show |
10 | HG00099.hp1 HG00733.hp2 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.672-1648delC | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33415290 | |||||||
chr19:33415305 | C | T | 1 | a0002c0002t0002g0258 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.672-1662G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33415305 | |||||||
chr19:33415326 | G | A | 1 | a0002c0002t0002g0258 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.672-1683C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33415326 | |||||||
chr19:33415456 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.672-1813C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33415456 | |||||||
chr19:33415464 | G | A | 1 | a0002c0002t0002g0241 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.672-1821C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33415464 | |||||||
chr19:33415478 | C | A | 1 | a0001c0001t0001g0018 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.672-1835G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33415478 | |||||||
chr19:33415479 | C | T | 1 | a0001c0003t0001g0254 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.672-1836G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33415479 | |||||||
chr19:33415574 | GCT | G | 3 | a0002c0002t0005g0091 a0002c0002t0005g0208 a0002c0002t0005g0298 |
3 | HG02258.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.672-1933_672-1932d others(4): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33415574 | |||||||
chr19:33415730 | C | A | 54 | a0001c0001t0001g0207 a0001c0001t0001g0216 a0001c0001t0001g0305 others(51): Show |
54 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.672-2087G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33415730 | |||||||
chr19:33415738 | G | A | 1 | a0008c0011t0001g0270 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.672-2095C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33415738 | |||||||
chr19:33415747 | G | A | 32 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(29): Show |
32 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(29): Show |
intron_variant | MODIFIER | c.672-2104C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33415747 | |||||||
chr19:33415766 | G | A | 31 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(28): Show |
31 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(28): Show |
intron_variant | MODIFIER | c.672-2123C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33415766 | |||||||
chr19:33415858 | A | G | 104 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0040 others(101): Show |
106 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.672-2215T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33415858 | |||||||
chr19:33415978 | G | A | 72 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0040 others(69): Show |
74 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.672-2335C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33415978 | |||||||
chr19:33416010 | C | T | 7 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0288 others(4): Show |
7 | HG02258.hp2 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.672-2367G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33416010 | |||||||
chr19:33416049 | CAG | C | 3 | a0001c0001t0001g0004 a0001c0001t0001g0154 a0001c0001t0001g0157 |
4 | HG00597.hp2 NA18944.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.672-2408_672-2407d others(4): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33416049 | |||||||
chr19:33416079 | C | T | 4 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0133 others(1): Show |
4 | HG02602.hp2 HG03942.hp2 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.672-2436G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33416079 | |||||||
chr19:33416141 | C | T | 1 | a0001c0001t0001g0229 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.672-2498G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33416141 | |||||||
chr19:33416152 | C | T | 15 | a0001c0001t0001g0082 a0001c0001t0001g0278 a0001c0001t0001g0279 others(12): Show |
15 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.672-2509G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33416152 | |||||||
chr19:33416156 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.672-2513G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33416156 | |||||||
chr19:33416195 | G | A | 66 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0075 others(63): Show |
68 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.672-2552C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33416195 | |||||||
chr19:33416236 | G | A | 1 | a0001c0001t0003g0284 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.672-2593C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33416236 | |||||||
chr19:33416487 | T | C | 3 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 |
3 | HG01099.hp2 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.672-2844A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33416487 | |||||||
chr19:33416489 | G | A | 1 | a0001c0003t0001g0221 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.672-2846C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33416489 | |||||||
chr19:33416535 | C | G | 1 | a0001c0001t0001g0294 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.672-2892G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33416535 | |||||||
chr19:33416590 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.672-2947G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33416590 | |||||||
chr19:33416630 | T | C | 162 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0024 others(159): Show |
164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.672-2987A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33416630 | |||||||
chr19:33416743 | A | T | 2 | a0002c0002t0002g0149 a0002c0002t0002g0150 |
2 | HG00408.hp2 HG00558.hp2 |
intron_variant | MODIFIER | c.672-3100T>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33416743 | |||||||
chr19:33416762 | C | T | 3 | a0002c0002t0005g0091 a0002c0002t0005g0208 a0002c0002t0005g0298 |
3 | HG02258.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.672-3119G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33416762 | |||||||
chr19:33416904 | C | T | 1 | a0002c0002t0002g0085 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.672-3261G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33416904 | |||||||
chr19:33416912 | G | A | 4 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(1): Show |
4 | HG01099.hp2 HG02257.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.672-3269C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33416912 | |||||||
chr19:33416965 | C | T | 1 | a0002c0002t0002g0009 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.672-3322G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33416965 | |||||||
chr19:33417113 | G | A | 1 | a0002c0002t0002g0172 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.672-3470C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33417113 | |||||||
chr19:33417166 | G | A | 18 | a0001c0001t0001g0082 a0001c0001t0001g0278 a0001c0001t0001g0279 others(15): Show |
18 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.672-3523C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33417166 | |||||||
chr19:33417177 | C | T | 2 | a0006c0010t0002g0166 a0006c0010t0005g0168 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.672-3534G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33417177 | |||||||
chr19:33417178 | G | A | 2 | a0001c0001t0001g0082 a0001c0001t0003g0087 |
2 | HG02698.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.672-3535C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33417178 | |||||||
chr19:33417218 | C | A | 4 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(1): Show |
4 | HG01099.hp2 HG02257.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.672-3575G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33417218 | |||||||
chr19:33417245 | C | T | 1 | a0001c0001t0001g0027 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.672-3602G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33417245 | |||||||
chr19:33417454 | C | T | 48 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0075 others(45): Show |
50 | HG00140.hp2 HG00609.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.672-3811G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33417454 | |||||||
chr19:33417587 | C | T | 47 | a0001c0001t0001g0216 a0001c0003t0001g0108 a0001c0003t0001g0143 others(44): Show |
47 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.672-3944G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33417587 | |||||||
chr19:33417589 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.672-3946G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33417589 | |||||||
chr19:33417591 | C | T | 8 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(5): Show |
8 | HG01099.hp2 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.672-3948G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33417591 | |||||||
chr19:33417593 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.672-3950C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33417593 | |||||||
chr19:33417811 | A | C | 74 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0040 others(71): Show |
76 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.672-4168T>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33417811 | |||||||
chr19:33417829 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.672-4186T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33417829 | |||||||
chr19:33417843 | C | T | 2 | a0001c0001t0001g0141 a0002c0002t0002g0128 |
2 | HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.672-4200G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33417843 | |||||||
chr19:33417893 | C | T | 30 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(27): Show |
30 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(27): Show |
intron_variant | MODIFIER | c.672-4250G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33417893 | |||||||
chr19:33417980 | C | T | 1 | a0002c0002t0005g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.672-4337G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33417980 | |||||||
chr19:33417981 | G | A | 30 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(27): Show |
30 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(27): Show |
intron_variant | MODIFIER | c.672-4338C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33417981 | |||||||
chr19:33418014 | G | A | 1 | a0001c0001t0004g0069 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.672-4371C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33418014 | |||||||
chr19:33418057 | C | T | 1 | a0002c0002t0002g0033 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.672-4414G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33418057 | |||||||
chr19:33418093 | G | A | 12 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0003g0045 others(9): Show |
12 | HG00099.hp1 HG00733.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.672-4450C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33418093 | |||||||
chr19:33418303 | A | T | 1 | a0001c0001t0004g0064 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.672-4660T>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33418303 | |||||||
chr19:33418326 | A | T | 1 | a0001c0001t0004g0064 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.672-4683T>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33418326 | |||||||
chr19:33418552 | C | G | 15 | a0001c0001t0001g0082 a0001c0001t0001g0278 a0001c0001t0001g0279 others(12): Show |
15 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.672-4909G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33418552 | |||||||
chr19:33418606 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.672-4963G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33418606 | |||||||
chr19:33418609 | C | T | 30 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(27): Show |
30 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(27): Show |
intron_variant | MODIFIER | c.672-4966G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33418609 | |||||||
chr19:33418717 | G | A | 1 | a0002c0002t0002g0262 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.672-5074C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33418717 | |||||||
chr19:33418721 | T | G | 1 | a0001c0001t0004g0064 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.672-5078A>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33418721 | |||||||
chr19:33418739 | C | T | 32 | a0001c0001t0001g0027 a0001c0001t0001g0075 a0002c0002t0002g0008 others(29): Show |
32 | HG00140.hp2 HG00609.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.672-5096G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33418739 | |||||||
chr19:33418792 | G | A | 30 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(27): Show |
30 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(27): Show |
intron_variant | MODIFIER | c.672-5149C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33418792 | |||||||
chr19:33418801 | C | T | 1 | a0002c0002t0005g0298 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.672-5158G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33418801 | |||||||
chr19:33418804 | T | G | 172 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0024 others(169): Show |
174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.672-5161A>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33418804 | |||||||
chr19:33418864 | G | A | 15 | a0001c0001t0001g0082 a0001c0001t0001g0278 a0001c0001t0001g0279 others(12): Show |
15 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.672-5221C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33418864 | |||||||
chr19:33418945 | C | T | 121 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0040 others(118): Show |
123 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.672-5302G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33418945 | |||||||
chr19:33419006 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.672-5363G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33419006 | |||||||
chr19:33419120 | C | G | 46 | a0001c0001t0001g0216 a0001c0003t0001g0143 a0001c0003t0001g0144 others(43): Show |
46 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.672-5477G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33419120 | |||||||
chr19:33419199 | A | G | 1 | a0001c0001t0001g0269 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.672-5556T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33419199 | |||||||
chr19:33419242 | T | C | 153 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0040 others(150): Show |
155 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.672-5599A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33419242 | |||||||
chr19:33419243 | G | A | 5 | a0001c0003t0001g0250 a0001c0003t0001g0251 a0001c0003t0001g0252 others(2): Show |
5 | HG01192.hp2 HG01243.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.672-5600C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33419243 | |||||||
chr19:33419293 | G | A | 1 | a0002c0002t0005g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.672-5650C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33419293 | |||||||
chr19:33419294 | G | C | 1 | a0001c0001t0004g0064 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.672-5651C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33419294 | |||||||
chr19:33419295 | C | G | 1 | a0001c0001t0004g0064 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.672-5652G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33419295 | |||||||
chr19:33419327 | T | A | 1 | a0001c0001t0004g0064 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.672-5684A>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33419327 | |||||||
chr19:33419331 | A | T | 2 | a0001c0001t0001g0141 a0002c0002t0002g0128 |
2 | HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.672-5688T>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33419331 | |||||||
chr19:33419344 | T | G | 1 | a0001c0001t0004g0064 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.672-5701A>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33419344 | |||||||
chr19:33419395 | A | C | 1 | a0001c0001t0001g0119 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.672-5752T>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33419395 | |||||||
chr19:33419407 | T | G | 32 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(29): Show |
32 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(29): Show |
intron_variant | MODIFIER | c.672-5764A>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33419407 | |||||||
chr19:33419447 | T | C | 1 | a0004c0006t0001g0301 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.672-5804A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33419447 | |||||||
chr19:33419560 | G | T | 3 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 |
3 | HG02630.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.672-5917C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33419560 | |||||||
chr19:33419581 | C | T | 30 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(27): Show |
30 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(27): Show |
intron_variant | MODIFIER | c.672-5938G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33419581 | |||||||
chr19:33419620 | G | C | 1 | a0001c0001t0004g0064 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.672-5977C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33419620 | |||||||
chr19:33419621 | C | T | 1 | a0001c0001t0004g0064 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.672-5978G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33419621 | |||||||
chr19:33419622 | T | G | 1 | a0001c0001t0004g0064 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.672-5979A>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33419622 | |||||||
chr19:33419633 | T | C | 153 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0040 others(150): Show |
155 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.672-5990A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33419633 | |||||||
chr19:33419673 | G | A | 1 | a0001c0001t0004g0064 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.672-6030C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33419673 | |||||||
chr19:33419674 | A | G | 1 | a0001c0001t0004g0064 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.672-6031T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33419674 | |||||||
chr19:33419733 | G | C | 1 | a0001c0001t0001g0294 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.672-6090C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33419733 | |||||||
chr19:33419759 | G | A | 1 | a0001c0003t0001g0194 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.672-6116C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33419759 | |||||||
chr19:33419834 | C | T | 153 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0040 others(150): Show |
155 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.672-6191G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33419834 | |||||||
chr19:33419900 | A | G | 1 | a0001c0001t0004g0064 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.672-6257T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33419900 | |||||||
chr19:33419901 | T | A | 1 | a0001c0001t0004g0064 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.672-6258A>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33419901 | |||||||
chr19:33419902 | C | T | 1 | a0001c0001t0004g0064 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.672-6259G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33419902 | |||||||
chr19:33419907 | A | G | 1 | a0001c0001t0001g0003 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.672-6264T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33419907 | |||||||
chr19:33419925 | C | T | 55 | a0001c0001t0001g0207 a0001c0001t0001g0216 a0001c0001t0001g0230 others(52): Show |
55 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.672-6282G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33419925 | |||||||
chr19:33420191 | T | C | 4 | a0001c0001t0001g0119 a0001c0001t0001g0126 a0001c0001t0001g0136 others(1): Show |
4 | HG00639.hp1 HG01361.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.672-6548A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33420191 | |||||||
chr19:33420328 | T | G | 1 | a0001c0001t0001g0264 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.672-6685A>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33420328 | |||||||
chr19:33420358 | A | AT | 100 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0040 others(97): Show |
100 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.672-6716dupA | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33420358 | |||||||
chr19:33420429 | G | T | 56 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0040 others(53): Show |
58 | HG00140.hp2 HG00609.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.672-6786C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33420429 | |||||||
chr19:33420433 | T | C | 1 | a0002c0002t0002g0150 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.672-6790A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33420433 | |||||||
chr19:33420475 | C | T | 15 | a0001c0001t0001g0082 a0001c0001t0001g0272 a0001c0001t0001g0278 others(12): Show |
15 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.672-6832G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33420475 | |||||||
chr19:33420589 | C | T | 2 | a0001c0001t0001g0266 a0001c0001t0001g0269 |
2 | HG01891.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.672-6946G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33420589 | |||||||
chr19:33420595 | G | T | 2 | a0006c0010t0002g0166 a0006c0010t0005g0168 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.672-6952C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33420595 | |||||||
chr19:33420610 | G | A | 2 | a0002c0002t0002g0149 a0002c0002t0002g0150 |
2 | HG00408.hp2 HG00558.hp2 |
intron_variant | MODIFIER | c.672-6967C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33420610 | |||||||
chr19:33420637 | G | A | 2 | a0001c0001t0001g0294 a0002c0002t0002g0241 |
2 | HG01884.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.672-6994C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33420637 | |||||||
chr19:33420651 | G | A | 1 | a0002c0002t0002g0006 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.672-7008C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33420651 | |||||||
chr19:33420702 | A | AAAAT | 99 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0040 others(96): Show |
99 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.672-7063_672-7060d others(6): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33420702 | |||||||
chr19:33420702 | A | AAAATAAA others(5): Show |
15 | a0001c0001t0001g0082 a0001c0001t0001g0272 a0001c0001t0001g0278 others(12): Show |
15 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.672-7071_672-7060d others(14): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33420702 | |||||||
chr19:33420702 | A | AAAATAAA others(9): Show |
1 | a0002c0002t0002g0258 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.672-7075_672-7060d others(18): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33420702 | |||||||
chr19:33420702 | AAAATAAA others(5): Show |
A | 11 | a0001c0001t0001g0261 a0001c0001t0003g0001 a0001c0001t0003g0179 others(8): Show |
13 | HG00639.hp2 HG00642.hp1 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.672-7071_672-7060d others(14): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33420702 | |||||||
chr19:33420733 | G | T | 4 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0133 others(1): Show |
4 | HG02602.hp2 HG03942.hp2 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.672-7090C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33420733 | |||||||
chr19:33420746 | T | TA | 32 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(29): Show |
32 | HG01175.hp1 HG01884.hp2 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.672-7104dupT | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33420746 | |||||||
chr19:33420799 | T | C | 190 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0024 others(187): Show |
193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.672-7156A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33420799 | |||||||
chr19:33420972 | C | T | 4 | a0002c0002t0002g0008 a0002c0002t0002g0009 a0002c0002t0002g0201 others(1): Show |
4 | HG00140.hp2 HG01515.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.672-7329G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33420972 | |||||||
chr19:33420973 | G | A | 1 | a0002c0002t0002g0129 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.672-7330C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33420973 | |||||||
chr19:33420974 | T | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0133 others(1): Show |
4 | HG02602.hp2 HG03942.hp2 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.672-7331A>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33420974 | |||||||
chr19:33421009 | G | A | 55 | a0001c0001t0001g0207 a0001c0001t0001g0216 a0001c0001t0001g0230 others(52): Show |
55 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.672-7366C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33421009 | |||||||
chr19:33421262 | A | T | 1 | a0001c0001t0001g0116 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.672-7619T>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33421262 | |||||||
chr19:33421290 | C | T | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0308 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.672-7647G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33421290 | |||||||
chr19:33421333 | C | T | 1 | a0002c0002t0002g0236 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.672-7690G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33421333 | |||||||
chr19:33421392 | G | A | 12 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0003g0045 others(9): Show |
12 | HG00099.hp1 HG00733.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.672-7749C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33421392 | |||||||
chr19:33421498 | T | C | 42 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(39): Show |
42 | HG00099.hp1 HG00733.hp2 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.672-7855A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33421498 | |||||||
chr19:33421533 | C | T | 2 | a0001c0001t0001g0170 a0001c0001t0001g0173 |
2 | HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.672-7890G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33421533 | |||||||
chr19:33421691 | C | T | 1 | a0001c0001t0003g0281 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.672-8048G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33421691 | |||||||
chr19:33421779 | G | T | 109 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0040 others(106): Show |
111 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.672-8136C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33421779 | |||||||
chr19:33422048 | G | A | 1 | a0001c0001t0001g0018 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.672-8405C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33422048 | |||||||
chr19:33422131 | T | C | 2 | a0001c0001t0001g0289 a0001c0001t0001g0293 |
2 | HG02258.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.672-8488A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33422131 | |||||||
chr19:33422174 | T | C | 1 | a0002c0002t0002g0175 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.672-8531A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33422174 | |||||||
chr19:33422198 | A | G | 44 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(41): Show |
44 | HG00099.hp1 HG00733.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.672-8555T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33422198 | |||||||
chr19:33422423 | C | CCTAT | 153 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0040 others(150): Show |
155 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.672-8784_672-8781d others(6): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33422423 | |||||||
chr19:33422459 | CATCT | C | 45 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(42): Show |
45 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.672-8820_672-8817d others(6): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33422459 | |||||||
chr19:33422538 | C | A | 30 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(27): Show |
30 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(27): Show |
intron_variant | MODIFIER | c.672-8895G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33422538 | |||||||
chr19:33422559 | CATCA | C | 4 | a0001c0001t0001g0119 a0001c0001t0001g0126 a0001c0001t0001g0136 others(1): Show |
4 | HG00639.hp1 HG01361.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.672-8920_672-8917d others(6): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33422559 | |||||||
chr19:33422627 | C | CATCT | 149 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0040 others(146): Show |
151 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.672-8988_672-8985d others(6): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33422627 | |||||||
chr19:33422648 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.672-9005G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33422648 | |||||||
chr19:33422789 | CCTCT | C | 23 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0052 others(20): Show |
23 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.672-9150_672-9147d others(6): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33422789 | |||||||
chr19:33422790 | C | A | 28 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(25): Show |
28 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(25): Show |
intron_variant | MODIFIER | c.672-9147G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33422790 | |||||||
chr19:33422797 | T | C | 31 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(28): Show |
31 | HG01099.hp2 HG01884.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.672-9154A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33422797 | |||||||
chr19:33422809 | C | CTTCTAT | 9 | a0001c0001t0001g0056 a0001c0001t0001g0058 a0001c0001t0001g0264 others(6): Show |
9 | HG01891.hp2 HG02258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.672-9167_672-9166i others(8): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33422809 | |||||||
chr19:33422809 | C | CTTCTATA others(3): Show |
9 | a0001c0001t0001g0041 a0001c0001t0001g0134 a0001c0001t0001g0267 others(6): Show |
9 | HG01884.hp2 HG02280.hp2 HG02698.hp1 others(6): Show |
intron_variant | MODIFIER | c.672-9167_672-9166i others(12): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33422809 | |||||||
chr19:33422809 | C | CTTCTATA others(7): Show |
13 | a0001c0001t0001g0040 a0001c0001t0001g0042 a0001c0001t0001g0048 others(10): Show |
13 | HG01099.hp2 HG02615.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.672-9167_672-9166i others(16): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33422809 | |||||||
chr19:33422813 | C | T | 31 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(28): Show |
31 | HG01099.hp2 HG01884.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.672-9170G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33422813 | |||||||
chr19:33422814 | T | A | 31 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(28): Show |
31 | HG01099.hp2 HG01884.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.672-9171A>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33422814 | |||||||
chr19:33422818 | A | ATATCTAT others(1): Show |
3 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0133 |
3 | HG02602.hp2 HG03942.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.672-9183_672-9176d others(10): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33422818 | |||||||
chr19:33422818 | A | ATATCTAT others(9): Show |
1 | a0001c0001t0001g0207 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.672-9191_672-9176d others(18): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33422818 | |||||||
chr19:33422818 | A | ATATCTAT others(13): Show |
15 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0308 others(12): Show |
15 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(12): Show |
intron_variant | MODIFIER | c.672-9195_672-9176d others(22): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33422818 | |||||||
chr19:33422818 | A | ATATCTAT others(17): Show |
44 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0055 others(41): Show |
44 | HG00323.hp1 HG00597.hp1 HG01192.hp2 others(41): Show |
intron_variant | MODIFIER | c.672-9176_672-9175i others(26): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33422818 | |||||||
chr19:33422818 | A | ATATCTAT others(21): Show |
16 | a0001c0001t0001g0216 a0001c0001t0003g0045 a0001c0003t0001g0209 others(13): Show |
16 | HG00099.hp1 HG00733.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.672-9176_672-9175i others(30): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33422818 | |||||||
chr19:33422818 | A | ATATCTAT others(25): Show |
1 | a0001c0003t0001g0240 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.672-9176_672-9175i others(34): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33422818 | |||||||
chr19:33422818 | A | ATC | 31 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(28): Show |
31 | HG01099.hp2 HG01884.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.672-9176_672-9175i others(4): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33422818 | |||||||
chr19:33422818 | ATATC | A | 20 | a0001c0001t0001g0062 a0001c0001t0001g0170 a0001c0001t0001g0173 others(17): Show |
21 | HG01891.hp1 HG02129.hp1 HG02165.hp2 others(18): Show |
intron_variant | MODIFIER | c.672-9179_672-9176d others(6): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33422818 | |||||||
chr19:33422818 | ATATCTAT others(1): Show |
A | 44 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0075 others(41): Show |
46 | HG00140.hp2 HG00609.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.672-9183_672-9176d others(10): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33422818 | |||||||
chr19:33422835 | TATCC | T | 43 | a0001c0001t0001g0003 a0001c0001t0001g0061 a0001c0001t0001g0092 others(40): Show |
44 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.672-9196_672-9193d others(6): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33422835 | |||||||
chr19:33422839 | C | T | 8 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0082 others(5): Show |
8 | HG02280.hp2 HG02602.hp2 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.672-9196G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33422839 | |||||||
chr19:33423067 | T | C | 1 | a0001c0003t0001g0232 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.672-9424A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33423067 | |||||||
chr19:33423095 | T | TCATC | 40 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(37): Show |
40 | HG01884.hp2 HG01891.hp2 HG02486.hp2 others(37): Show |
intron_variant | MODIFIER | c.672-9456_672-9453d others(6): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33423095 | |||||||
chr19:33423095 | T | TCATCCAT others(1): Show |
20 | a0001c0001t0001g0082 a0001c0001t0001g0272 a0001c0001t0001g0278 others(17): Show |
20 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.672-9460_672-9453d others(10): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33423095 | |||||||
chr19:33423095 | T | TCATCCAT others(5): Show |
48 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(45): Show |
50 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.672-9464_672-9453d others(14): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33423095 | |||||||
chr19:33423095 | T | TCATCCAT others(9): Show |
41 | a0001c0001t0001g0027 a0001c0001t0001g0216 a0001c0001t0001g0230 others(38): Show |
41 | HG00140.hp2 HG00323.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.672-9468_672-9453d others(18): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33423095 | |||||||
chr19:33423095 | T | TCATCCAT others(13): Show |
7 | a0001c0001t0001g0018 a0001c0003t0001g0239 a0001c0003t0001g0240 others(4): Show |
7 | HG00597.hp1 HG01358.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.672-9472_672-9453d others(22): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33423095 | |||||||
chr19:33423095 | T | TCATCCAT others(17): Show |
12 | a0001c0003t0001g0143 a0001c0003t0001g0144 a0001c0003t0001g0151 others(9): Show |
12 | HG00544.hp1 HG01257.hp2 HG02148.hp1 others(9): Show |
intron_variant | MODIFIER | c.672-9476_672-9453d others(26): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33423095 | |||||||
chr19:33423095 | TCATCCAT others(5): Show |
T | 1 | a0002c0002t0002g0258 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.672-9464_672-9453d others(14): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33423095 | |||||||
chr19:33423105 | A | C | 4 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0133 others(1): Show |
4 | HG02602.hp2 HG03942.hp2 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.672-9462T>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33423105 | |||||||
chr19:33423233 | G | A | 1 | a0002c0002t0002g0032 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.672-9590C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33423233 | |||||||
chr19:33423259 | A | T | 141 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0040 others(138): Show |
143 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.672-9616T>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33423259 | |||||||
chr19:33423362 | A | G | 4 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(1): Show |
4 | HG01099.hp2 HG02257.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.672-9719T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33423362 | |||||||
chr19:33423379 | C | G | 12 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0003g0045 others(9): Show |
12 | HG00099.hp1 HG00733.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.672-9736G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33423379 | |||||||
chr19:33423511 | A | G | 12 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0003g0045 others(9): Show |
12 | HG00099.hp1 HG00733.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.672-9868T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33423511 | |||||||
chr19:33423534 | G | A | 55 | a0001c0001t0001g0207 a0001c0001t0001g0216 a0001c0001t0001g0230 others(52): Show |
55 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.672-9891C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33423534 | |||||||
chr19:33423599 | T | C | 1 | a0002c0002t0002g0068 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.672-9956A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33423599 | |||||||
chr19:33423664 | C | T | 28 | a0001c0001t0001g0002 a0001c0001t0001g0043 a0001c0001t0001g0067 others(25): Show |
29 | HG00099.hp2 HG00621.hp1 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.672-10021G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33423664 | |||||||
chr19:33423819 | G | T | 1 | a0001c0001t0001g0003 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.672-10176C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33423819 | |||||||
chr19:33424038 | A | G | 157 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0040 others(154): Show |
159 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.672-10395T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33424038 | |||||||
chr19:33424089 | C | G | 12 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0003g0045 others(9): Show |
12 | HG00099.hp1 HG00733.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.672-10446G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33424089 | |||||||
chr19:33424178 | T | C | 146 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0040 others(143): Show |
148 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.672-10535A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33424178 | |||||||
chr19:33424370 | G | A | 13 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0003g0045 others(10): Show |
13 | HG00099.hp1 HG00733.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.672-10727C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33424370 | |||||||
chr19:33424454 | A | G | 148 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0040 others(145): Show |
150 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.672-10811T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33424454 | |||||||
chr19:33424500 | C | G | 4 | a0002c0002t0002g0171 a0002c0002t0005g0091 a0002c0002t0005g0208 others(1): Show |
4 | HG02258.hp1 HG02976.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.672-10857G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33424500 | |||||||
chr19:33424543 | C | G | 1 | a0002c0002t0002g0078 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.672-10900G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33424543 | |||||||
chr19:33424610 | C | T | 1 | a0002c0002t0002g0085 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.672-10967G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33424610 | |||||||
chr19:33424615 | G | A | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00099.hp1 HG00733.hp2 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.672-10972C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33424615 | |||||||
chr19:33424662 | A | G | 1 | a0001c0001t0001g0282 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.672-11019T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33424662 | |||||||
chr19:33424727 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.672-11084C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33424727 | |||||||
chr19:33424865 | C | T | 41 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(38): Show |
41 | HG00099.hp1 HG00733.hp2 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.672-11222G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33424865 | |||||||
chr19:33424930 | C | A | 35 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(32): Show |
35 | HG00099.hp1 HG00733.hp2 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.672-11287G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33424930 | |||||||
chr19:33424994 | AAACAAAC | A | 64 | a0001c0001t0001g0043 a0001c0001t0001g0191 a0001c0001t0001g0192 others(61): Show |
64 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.672-11358_672-1135 others(11): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33424994 | |||||||
chr19:33425105 | C | T | 17 | a0001c0001t0001g0082 a0001c0001t0001g0272 a0001c0001t0001g0279 others(14): Show |
17 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.672-11462G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33425105 | |||||||
chr19:33425276 | G | A | 1 | a0002c0002t0002g0010 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.672-11633C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33425276 | |||||||
chr19:33425297 | A | AAAAC | 120 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0040 others(117): Show |
120 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.672-11658_672-1165 others(8): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33425297 | |||||||
chr19:33425297 | A | AAAACAAA others(1): Show |
3 | a0001c0001t0001g0052 a0001c0003t0001g0246 a0002c0002t0002g0258 |
3 | HG02280.hp2 HG02602.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.672-11662_672-1165 others(12): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33425297 | |||||||
chr19:33425297 | A | AAAACAAA others(5): Show |
41 | a0001c0001t0001g0004 a0001c0001t0001g0048 a0001c0001t0001g0050 others(38): Show |
42 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.672-11666_672-1165 others(16): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33425297 | |||||||
chr19:33425297 | A | AAAACAAA others(9): Show |
7 | a0001c0001t0001g0049 a0001c0001t0001g0053 a0001c0001t0001g0054 others(4): Show |
7 | HG02615.hp1 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.672-11670_672-1165 others(20): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33425297 | |||||||
chr19:33425327 | G | T | 1 | a0002c0002t0002g0072 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.672-11684C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33425327 | |||||||
chr19:33425365 | C | T | 43 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(40): Show |
43 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.672-11722G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33425365 | |||||||
chr19:33425383 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.672-11740G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33425383 | |||||||
chr19:33425417 | C | T | 1 | a0007c0009t0001g0185 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.672-11774G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33425417 | |||||||
chr19:33425426 | G | A | 118 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0040 others(115): Show |
118 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.672-11783C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33425426 | |||||||
chr19:33425464 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.672-11821A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33425464 | |||||||
chr19:33425483 | A | G | 43 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(40): Show |
43 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.672-11840T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33425483 | |||||||
chr19:33425526 | C | T | 1 | a0002c0002t0002g0026 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.672-11883G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33425526 | |||||||
chr19:33425599 | C | T | 43 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(40): Show |
43 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.672-11956G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33425599 | |||||||
chr19:33426593 | C | T | 1 | a0001c0001t0003g0277 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.672-12950G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33426593 | |||||||
chr19:33426729 | G | A | 11 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(8): Show |
11 | HG01099.hp2 HG02257.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.672-13086C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33426729 | |||||||
chr19:33426826 | G | A | 2 | a0001c0001t0001g0082 a0001c0001t0003g0087 |
2 | HG02698.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.672-13183C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33426826 | |||||||
chr19:33426880 | G | A | 1 | a0002c0012t0002g0135 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.672-13237C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33426880 | |||||||
chr19:33426893 | C | T | 64 | a0001c0001t0001g0043 a0001c0001t0001g0191 a0001c0001t0001g0192 others(61): Show |
64 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.672-13250G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33426893 | |||||||
chr19:33426905 | G | A | 69 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0043 others(66): Show |
69 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.672-13262C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33426905 | |||||||
chr19:33426911 | A | G | 1 | a0002c0002t0002g0258 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.672-13268T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33426911 | |||||||
chr19:33426937 | C | A | 1 | a0001c0001t0001g0018 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.672-13294G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33426937 | |||||||
chr19:33426938 | A | G | 123 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0024 others(120): Show |
123 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.672-13295T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33426938 | |||||||
chr19:33426957 | C | A | 1 | a0002c0002t0002g0258 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.672-13314G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33426957 | |||||||
chr19:33426997 | G | A | 15 | a0001c0007t0001g0005 a0001c0007t0001g0212 a0001c0007t0001g0242 others(12): Show |
16 | HG01109.hp1 HG01168.hp1 HG02129.hp1 others(13): Show |
intron_variant | MODIFIER | c.672-13354C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33426997 | |||||||
chr19:33427008 | G | A | 24 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0037 others(21): Show |
24 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.672-13365C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33427008 | |||||||
chr19:33427127 | T | C | 1 | a0002c0002t0005g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.672-13484A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33427127 | |||||||
chr19:33427153 | G | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.672-13510C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33427153 | |||||||
chr19:33427166 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.672-13523G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33427166 | |||||||
chr19:33427252 | G | GTCGTGGC others(10): Show |
3 | a0002c0002t0005g0091 a0002c0002t0005g0208 a0002c0002t0005g0298 |
3 | HG02258.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.672-13626_672-1361 others(21): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33427252 | |||||||
chr19:33427408 | C | T | 65 | a0001c0001t0001g0043 a0001c0001t0001g0094 a0001c0001t0001g0191 others(62): Show |
65 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.672-13765G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33427408 | |||||||
chr19:33427517 | A | G | 163 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0024 others(160): Show |
163 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.672-13874T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33427517 | |||||||
chr19:33427663 | T | G | 212 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0024 others(209): Show |
215 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.672-14020A>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33427663 | |||||||
chr19:33427683 | A | G | 11 | a0001c0001t0001g0037 a0002c0002t0002g0026 a0002c0002t0002g0029 others(8): Show |
11 | HG01257.hp2 HG02293.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.672-14040T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33427683 | |||||||
chr19:33427689 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.672-14046G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33427689 | |||||||
chr19:33427736 | A | ATG | 163 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0024 others(160): Show |
163 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.672-14094_672-1409 others(6): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33427736 | |||||||
chr19:33427821 | C | T | 13 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0266 others(10): Show |
13 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.672-14178G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33427821 | |||||||
chr19:33427881 | T | C | 97 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0037 others(94): Show |
97 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.672-14238A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33427881 | |||||||
chr19:33427938 | G | A | 2 | a0006c0010t0002g0166 a0006c0010t0005g0168 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.672-14295C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33427938 | |||||||
chr19:33428016 | T | C | 1 | a0002c0002t0002g0299 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.672-14373A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33428016 | |||||||
chr19:33428062 | G | T | 1 | a0001c0001t0001g0207 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.672-14419C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33428062 | |||||||
chr19:33428161 | C | T | 3 | a0002c0002t0005g0091 a0002c0002t0005g0208 a0002c0002t0005g0298 |
3 | HG02258.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.672-14518G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33428161 | |||||||
chr19:33428184 | T | C | 64 | a0001c0001t0001g0043 a0001c0001t0001g0191 a0001c0001t0001g0192 others(61): Show |
64 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.672-14541A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33428184 | |||||||
chr19:33428539 | C | T | 64 | a0001c0001t0001g0043 a0001c0001t0001g0191 a0001c0001t0001g0192 others(61): Show |
64 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.672-14896G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33428539 | |||||||
chr19:33428540 | AC | A | 24 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0037 others(21): Show |
24 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.672-14898delG | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33428540 | |||||||
chr19:33428580 | G | C | 212 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0024 others(209): Show |
215 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.672-14937C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33428580 | |||||||
chr19:33428597 | T | C | 1 | a0002c0002t0002g0258 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.672-14954A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33428597 | |||||||
chr19:33428731 | T | C | 1 | a0002c0002t0002g0241 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.672-15088A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33428731 | |||||||
chr19:33428837 | G | A | 3 | a0002c0002t0005g0091 a0002c0002t0005g0208 a0002c0002t0005g0298 |
3 | HG02258.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.672-15194C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33428837 | |||||||
chr19:33428969 | T | A | 2 | a0001c0001t0001g0271 a0008c0011t0001g0270 |
2 | HG01884.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.672-15326A>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33428969 | |||||||
chr19:33428971 | T | C | 64 | a0001c0001t0001g0043 a0001c0001t0001g0191 a0001c0001t0001g0192 others(61): Show |
64 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.672-15328A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33428971 | |||||||
chr19:33429059 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.672-15416G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33429059 | |||||||
chr19:33429161 | G | C | 2 | a0001c0001t0001g0170 a0001c0001t0001g0173 |
2 | HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.672-15518C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33429161 | |||||||
chr19:33429252 | C | T | 63 | a0001c0001t0001g0043 a0001c0001t0001g0191 a0001c0001t0001g0192 others(60): Show |
63 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.672-15609G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33429252 | |||||||
chr19:33429410 | G | A | 1 | a0002c0002t0005g0298 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.672-15767C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33429410 | |||||||
chr19:33429512 | A | G | 1 | a0002c0002t0002g0044 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.672-15869T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33429512 | |||||||
chr19:33429733 | A | G | 74 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(71): Show |
74 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.672-16090T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33429733 | |||||||
chr19:33429815 | A | C | 181 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0024 others(178): Show |
181 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.672-16172T>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33429815 | |||||||
chr19:33429883 | G | A | 1 | a0002c0002t0002g0258 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.672-16240C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33429883 | |||||||
chr19:33429913 | G | A | 1 | a0001c0003t0001g0215 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.672-16270C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33429913 | |||||||
chr19:33430020 | G | T | 2 | a0002c0002t0005g0208 a0002c0002t0005g0298 |
2 | HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.672-16377C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33430020 | |||||||
chr19:33430334 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.672-16691G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33430334 | |||||||
chr19:33430357 | A | C | 181 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0024 others(178): Show |
181 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.672-16714T>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33430357 | |||||||
chr19:33430361 | G | A | 7 | a0001c0001t0001g0004 a0001c0001t0001g0154 a0001c0001t0001g0155 others(4): Show |
8 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(5): Show |
intron_variant | MODIFIER | c.672-16718C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33430361 | |||||||
chr19:33430462 | T | C | 185 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0024 others(182): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.672-16819A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33430462 | |||||||
chr19:33430463 | G | A | 1 | a0001c0003t0001g0211 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.672-16820C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33430463 | |||||||
chr19:33430482 | G | A | 63 | a0001c0001t0001g0043 a0001c0001t0001g0191 a0001c0001t0001g0192 others(60): Show |
63 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.672-16839C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33430482 | |||||||
chr19:33430582 | G | GT | 4 | a0001c0001t0001g0133 a0001c0003t0001g0197 a0002c0002t0002g0026 others(1): Show |
4 | HG01257.hp2 HG02738.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.672-16940dupA | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33430582 | |||||||
chr19:33430636 | A | C | 67 | a0001c0001t0001g0043 a0001c0001t0001g0191 a0001c0001t0001g0192 others(64): Show |
67 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.672-16993T>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33430636 | |||||||
chr19:33430823 | G | A | 12 | a0001c0001t0001g0180 a0001c0001t0001g0261 a0001c0001t0003g0001 others(9): Show |
14 | HG00639.hp2 HG00642.hp1 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.672-17180C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33430823 | |||||||
chr19:33430856 | G | A | 1 | a0001c0001t0003g0188 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.672-17213C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33430856 | |||||||
chr19:33431017 | G | A | 3 | a0002c0002t0005g0091 a0002c0002t0005g0208 a0002c0002t0005g0298 |
3 | HG02258.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.672-17374C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33431017 | |||||||
chr19:33431180 | A | G | 14 | a0001c0001t0003g0284 a0001c0007t0001g0005 a0001c0007t0001g0212 others(11): Show |
15 | HG00140.hp1 HG01168.hp1 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.672-17537T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33431180 | |||||||
chr19:33431180 | AAGGG | A | 11 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(8): Show |
11 | HG01099.hp2 HG02257.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.672-17541_672-1753 others(8): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33431180 | |||||||
chr19:33431190 | G | A | 60 | a0001c0001t0001g0043 a0001c0001t0001g0191 a0001c0001t0001g0192 others(57): Show |
60 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.672-17547C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33431190 | |||||||
chr19:33431210 | GGGAGGGA others(1): Show |
G | 3 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0293 |
3 | HG02258.hp2 HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.672-17575_672-1756 others(12): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33431210 | |||||||
chr19:33431355 | T | C | 15 | a0001c0007t0001g0005 a0001c0007t0001g0212 a0001c0007t0001g0242 others(12): Show |
16 | HG01109.hp1 HG01168.hp1 HG02129.hp1 others(13): Show |
intron_variant | MODIFIER | c.672-17712A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33431355 | |||||||
chr19:33431461 | C | T | 1 | a0002c0002t0002g0171 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.672-17818G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33431461 | |||||||
chr19:33431663 | G | A | 13 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(10): Show |
13 | HG01099.hp2 HG02257.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.672-18020C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33431663 | |||||||
chr19:33431836 | T | C | 1 | a0001c0001t0003g0184 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.672-18193A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33431836 | |||||||
chr19:33431883 | C | G | 1 | a0001c0001t0001g0288 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.672-18240G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33431883 | |||||||
chr19:33431992 | C | CA | 65 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(62): Show |
65 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.672-18350dupT | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33431992 | |||||||
chr19:33431992 | C | CAA | 22 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(19): Show |
22 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.672-18351_672-1835 others(6): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33431992 | |||||||
chr19:33431992 | C | CAAAAAAA others(3): Show |
4 | a0001c0001t0001g0018 a0001c0001t0001g0207 a0001c0001t0001g0283 others(1): Show |
4 | HG01123.hp2 HG02280.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.672-18359_672-1835 others(14): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33431992 | |||||||
chr19:33431992 | C | CAAAAAAA others(4): Show |
17 | a0001c0001t0001g0082 a0001c0001t0001g0272 a0001c0001t0001g0278 others(14): Show |
17 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.672-18360_672-1835 others(15): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33431992 | |||||||
chr19:33431992 | C | CAAAAAAA others(5): Show |
11 | a0001c0001t0001g0037 a0001c0003t0001g0108 a0002c0002t0002g0026 others(8): Show |
11 | HG01257.hp2 HG02293.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.672-18361_672-1835 others(16): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33431992 | |||||||
chr19:33431992 | C | CAAAAAAA others(6): Show |
2 | a0001c0001t0001g0027 a0002c0002t0002g0038 |
2 | HG02738.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.672-18362_672-1835 others(17): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33431992 | |||||||
chr19:33431992 | C | CAAAAAAA others(13): Show |
1 | a0001c0003t0001g0167 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.672-18350_672-1834 others(24): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33431992 | |||||||
chr19:33431992 | C | CAAAAAAA others(14): Show |
22 | a0001c0001t0001g0043 a0001c0001t0001g0191 a0001c0001t0001g0192 others(19): Show |
22 | HG00323.hp1 HG00544.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.672-18350_672-1834 others(25): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33431992 | |||||||
chr19:33431992 | C | CAAAAAAA others(15): Show |
25 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0206 others(22): Show |
25 | HG00438.hp1 HG01358.hp1 HG02071.hp1 others(22): Show |
intron_variant | MODIFIER | c.672-18350_672-1834 others(26): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33431992 | |||||||
chr19:33431992 | C | CAAAAAAA others(16): Show |
10 | a0001c0001t0001g0305 a0001c0001t0001g0308 a0001c0003t0001g0151 others(7): Show |
10 | HG00597.hp1 HG02055.hp1 HG02148.hp1 others(7): Show |
intron_variant | MODIFIER | c.672-18350_672-1834 others(27): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33431992 | |||||||
chr19:33431992 | C | CAAAAAAA others(17): Show |
1 | a0001c0003t0001g0246 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.672-18350_672-1834 others(28): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33431992 | |||||||
chr19:33431992 | C | CAAAAAAA others(18): Show |
2 | a0001c0003t0001g0222 a0001c0003t0001g0251 |
2 | HG00558.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.672-18350_672-1834 others(29): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33431992 | |||||||
chr19:33431992 | C | CAAAAAAA others(19): Show |
1 | a0001c0003t0001g0193 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.672-18350_672-1834 others(30): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33431992 | |||||||
chr19:33431992 | CA | C | 15 | a0001c0001t0001g0020 a0001c0001t0001g0145 a0001c0001t0001g0180 others(12): Show |
17 | HG00639.hp2 HG00642.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.672-18350delT | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33431992 | |||||||
chr19:33432010 | A | AAAAAAAA others(14): Show |
1 | a0002c0002t0005g0298 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.672-18368_672-1836 others(25): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33432010 | |||||||
chr19:33432010 | A | AAAAAAAA others(13): Show |
1 | a0002c0002t0005g0208 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.672-18368_672-1836 others(24): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33432010 | |||||||
chr19:33432054 | T | C | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | NA18945.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.672-18411A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33432054 | |||||||
chr19:33432138 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.672-18495A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33432138 | |||||||
chr19:33432277 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.672-18634A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33432277 | |||||||
chr19:33432354 | G | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.672-18711C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33432354 | |||||||
chr19:33432418 | G | A | 1 | a0002c0002t0002g0036 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.672-18775C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33432418 | |||||||
chr19:33432528 | T | C | 13 | a0001c0007t0001g0005 a0001c0007t0001g0212 a0001c0007t0001g0242 others(10): Show |
14 | HG01168.hp1 HG02129.hp1 HG03942.hp1 others(11): Show |
intron_variant | MODIFIER | c.672-18885A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33432528 | |||||||
chr19:33432576 | T | C | 43 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(40): Show |
43 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.672-18933A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33432576 | |||||||
chr19:33432695 | C | A | 1 | a0001c0001t0001g0180 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.672-19052G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33432695 | |||||||
chr19:33432707 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.672-19064G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33432707 | |||||||
chr19:33432708 | G | A | 43 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(40): Show |
43 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.672-19065C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33432708 | |||||||
chr19:33432863 | C | T | 1 | a0003c0005t0001g0243 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.672-19220G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33432863 | |||||||
chr19:33432870 | G | C | 3 | a0001c0001t0001g0137 a0001c0001t0001g0140 a0001c0001t0001g0163 |
3 | HG01070.hp1 HG01071.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.672-19227C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33432870 | |||||||
chr19:33432947 | C | T | 12 | a0001c0001t0001g0027 a0001c0001t0001g0037 a0002c0002t0002g0026 others(9): Show |
12 | HG01257.hp2 HG02293.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.672-19304G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33432947 | |||||||
chr19:33432985 | A | G | 3 | a0002c0002t0005g0091 a0002c0002t0005g0208 a0002c0002t0005g0298 |
3 | HG02258.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.672-19342T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33432985 | |||||||
chr19:33432991 | A | T | 1 | a0001c0003t0001g0211 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.672-19348T>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33432991 | |||||||
chr19:33433097 | C | T | 1 | a0002c0002t0002g0083 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.672-19454G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33433097 | |||||||
chr19:33433297 | T | C | 18 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0054 others(15): Show |
18 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.672-19654A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33433297 | |||||||
chr19:33433399 | G | A | 1 | a0001c0001t0001g0178 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.672-19756C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33433399 | |||||||
chr19:33433547 | G | C | 12 | a0001c0001t0001g0180 a0001c0001t0001g0261 a0001c0001t0003g0001 others(9): Show |
14 | HG00639.hp2 HG00642.hp1 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.672-19904C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33433547 | |||||||
chr19:33433642 | A | G | 42 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0037 others(39): Show |
42 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(39): Show |
intron_variant | MODIFIER | c.672-19999T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33433642 | |||||||
chr19:33433848 | G | T | 1 | a0003c0005t0001g0015 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.672-20205C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33433848 | |||||||
chr19:33433986 | C | T | 2 | a0001c0003t0001g0194 a0001c0003t0001g0198 |
2 | NA18945.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.672-20343G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33433986 | |||||||
chr19:33434569 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.672-20926G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33434569 | |||||||
chr19:33434627 | G | A | 60 | a0001c0001t0001g0043 a0001c0001t0001g0191 a0001c0001t0001g0192 others(57): Show |
60 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.672-20984C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33434627 | |||||||
chr19:33434682 | C | T | 41 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0037 others(38): Show |
41 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(38): Show |
intron_variant | MODIFIER | c.672-21039G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33434682 | |||||||
chr19:33434703 | G | A | 1 | a0002c0002t0002g0290 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.672-21060C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33434703 | |||||||
chr19:33434836 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.672-21193G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33434836 | |||||||
chr19:33434848 | G | A | 3 | a0002c0002t0005g0091 a0002c0002t0005g0208 a0002c0002t0005g0298 |
3 | HG02258.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.672-21205C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33434848 | |||||||
chr19:33434858 | C | G | 1 | a0003c0004t0001g0084 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.672-21215G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33434858 | |||||||
chr19:33434902 | G | A | 3 | a0002c0002t0005g0091 a0002c0002t0005g0208 a0002c0002t0005g0298 |
3 | HG02258.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.672-21259C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33434902 | |||||||
chr19:33434983 | A | G | 1 | a0002c0002t0002g0292 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.672-21340T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33434983 | |||||||
chr19:33435039 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.672-21396C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33435039 | |||||||
chr19:33435106 | T | C | 185 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0024 others(182): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.672-21463A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33435106 | |||||||
chr19:33435107 | G | A | 134 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(131): Show |
134 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.672-21464C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33435107 | |||||||
chr19:33435181 | G | A | 1 | a0001c0003t0001g0108 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.672-21538C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33435181 | |||||||
chr19:33435235 | G | A | 3 | a0002c0002t0005g0091 a0002c0002t0005g0208 a0002c0002t0005g0298 |
3 | HG02258.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.672-21592C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33435235 | |||||||
chr19:33435357 | T | C | 2 | a0002c0002t0002g0259 a0002c0002t0002g0260 |
2 | HG01109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.672-21714A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33435357 | |||||||
chr19:33435496 | C | T | 125 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0049 others(122): Show |
125 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.672-21853G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33435496 | |||||||
chr19:33435648 | A | T | 2 | a0001c0003t0001g0209 a0001c0003t0001g0232 |
2 | NA18950.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.672-22005T>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33435648 | |||||||
chr19:33435744 | T | G | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.672-22101A>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33435744 | |||||||
chr19:33435751 | A | T | 1 | a0001c0003t0001g0246 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.672-22108T>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33435751 | |||||||
chr19:33435792 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.672-22149G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33435792 | |||||||
chr19:33435804 | G | A | 1 | a0001c0001t0004g0064 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.672-22161C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33435804 | |||||||
chr19:33435850 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.672-22207C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33435850 | |||||||
chr19:33435951 | G | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.672-22308C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33435951 | |||||||
chr19:33436085 | G | C | 64 | a0001c0001t0001g0043 a0001c0001t0001g0191 a0001c0001t0001g0192 others(61): Show |
64 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.672-22442C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33436085 | |||||||
chr19:33436094 | A | G | 44 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0024 others(41): Show |
44 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(41): Show |
intron_variant | MODIFIER | c.672-22451T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33436094 | |||||||
chr19:33436210 | AAGAGGG | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0002c0002t0002g0009 others(1): Show |
4 | HG00140.hp2 HG02602.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.672-22573_672-2256 others(10): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33436210 | |||||||
chr19:33436222 | G | A | 2 | a0001c0001t0003g0045 a0002c0002t0002g0047 |
2 | HG00099.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.672-22579C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33436222 | |||||||
chr19:33436344 | C | T | 1 | a0002c0002t0002g0169 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.672-22701G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33436344 | |||||||
chr19:33436367 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.672-22724G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33436367 | |||||||
chr19:33436375 | G | A | 1 | a0001c0001t0003g0087 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.672-22732C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33436375 | |||||||
chr19:33436398 | G | T | 2 | a0001c0003t0001g0220 a0002c0002t0002g0189 |
2 | HG02071.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.672-22755C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33436398 | |||||||
chr19:33436423 | C | T | 15 | a0001c0007t0001g0005 a0001c0007t0001g0212 a0001c0007t0001g0242 others(12): Show |
16 | HG01109.hp1 HG01168.hp1 HG02129.hp1 others(13): Show |
intron_variant | MODIFIER | c.672-22780G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33436423 | |||||||
chr19:33436438 | C | T | 12 | a0001c0001t0001g0027 a0001c0001t0001g0037 a0002c0002t0002g0026 others(9): Show |
12 | HG01257.hp2 HG02293.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.672-22795G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33436438 | |||||||
chr19:33436491 | G | T | 1 | a0002c0002t0002g0078 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.672-22848C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33436491 | |||||||
chr19:33436516 | G | A | 1 | a0002c0002t0002g0236 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.672-22873C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33436516 | |||||||
chr19:33436565 | G | T | 32 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0037 others(29): Show |
32 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.672-22922C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33436565 | |||||||
chr19:33436648 | C | T | 2 | a0001c0001t0001g0137 a0001c0001t0001g0140 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.672-23005G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33436648 | |||||||
chr19:33436785 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.672-23142A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33436785 | |||||||
chr19:33436810 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.672-23167C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33436810 | |||||||
chr19:33436836 | T | C | 10 | a0002c0002t0002g0006 a0002c0002t0002g0008 a0002c0002t0002g0009 others(7): Show |
10 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.672-23193A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33436836 | |||||||
chr19:33436976 | A | G | 1 | a0001c0001t0001g0295 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.672-23333T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33436976 | |||||||
chr19:33437019 | G | A | 6 | a0002c0002t0002g0030 a0002c0002t0002g0031 a0002c0002t0002g0032 others(3): Show |
6 | HG02615.hp2 HG02895.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.672-23376C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33437019 | |||||||
chr19:33437095 | T | C | 23 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(20): Show |
23 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.672-23452A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33437095 | |||||||
chr19:33437100 | G | C | 47 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0048 others(44): Show |
47 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.672-23457C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33437100 | |||||||
chr19:33437161 | C | T | 1 | a0002c0002t0002g0068 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.672-23518G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33437161 | |||||||
chr19:33437415 | G | A | 42 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(39): Show |
42 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.672-23772C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33437415 | |||||||
chr19:33437441 | G | A | 2 | a0002c0002t0002g0259 a0002c0002t0002g0260 |
2 | HG01109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.672-23798C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33437441 | |||||||
chr19:33437723 | A | T | 1 | a0002c0002t0002g0174 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.672-24080T>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33437723 | |||||||
chr19:33437768 | C | T | 3 | a0002c0002t0005g0091 a0002c0002t0005g0208 a0002c0002t0005g0298 |
3 | HG02258.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.672-24125G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33437768 | |||||||
chr19:33437829 | A | G | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.672-24186T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33437829 | |||||||
chr19:33437837 | T | C | 64 | a0001c0001t0001g0043 a0001c0001t0001g0191 a0001c0001t0001g0192 others(61): Show |
64 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.672-24194A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33437837 | |||||||
chr19:33437850 | G | A | 2 | a0001c0003t0001g0194 a0001c0003t0001g0198 |
2 | NA18945.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.672-24207C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33437850 | |||||||
chr19:33438078 | T | C | 1 | a0002c0002t0002g0014 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.672-24435A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33438078 | |||||||
chr19:33438127 | G | C | 1 | a0002c0002t0005g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.672-24484C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33438127 | |||||||
chr19:33438166 | C | T | 1 | a0003c0005t0001g0017 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.672-24523G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33438166 | |||||||
chr19:33438188 | T | C | 184 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0024 others(181): Show |
184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.672-24545A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33438188 | |||||||
chr19:33438243 | C | T | 12 | a0001c0001t0001g0180 a0001c0001t0001g0261 a0001c0001t0003g0001 others(9): Show |
14 | HG00639.hp2 HG00642.hp1 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.672-24600G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33438243 | |||||||
chr19:33438409 | C | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.671+24586G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33438409 | |||||||
chr19:33438438 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.671+24557C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33438438 | |||||||
chr19:33438449 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.671+24546G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33438449 | |||||||
chr19:33438597 | A | G | 32 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0037 others(29): Show |
32 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.671+24398T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33438597 | |||||||
chr19:33438723 | C | T | 3 | a0001c0001t0001g0102 a0001c0001t0001g0105 a0001c0001t0001g0106 |
3 | HG00280.hp2 HG00323.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.671+24272G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33438723 | |||||||
chr19:33438837 | A | C | 3 | a0002c0002t0005g0091 a0002c0002t0005g0208 a0002c0002t0005g0298 |
3 | HG02258.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.671+24158T>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33438837 | |||||||
chr19:33438932 | T | C | 185 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0024 others(182): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.671+24063A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33438932 | |||||||
chr19:33438957 | T | C | 3 | a0002c0002t0005g0091 a0002c0002t0005g0208 a0002c0002t0005g0298 |
3 | HG02258.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.671+24038A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33438957 | |||||||
chr19:33439041 | A | C | 2 | a0002c0002t0005g0208 a0002c0002t0005g0298 |
2 | HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.671+23954T>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33439041 | |||||||
chr19:33439081 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.671+23914C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33439081 | |||||||
chr19:33439130 | T | G | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.671+23865A>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33439130 | |||||||
chr19:33439136 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.671+23859G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33439136 | |||||||
chr19:33439157 | C | T | 1 | a0002c0002t0002g0081 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.671+23838G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33439157 | |||||||
chr19:33439280 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.671+23715A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33439280 | |||||||
chr19:33439323 | G | C | 10 | a0002c0002t0002g0006 a0002c0002t0002g0008 a0002c0002t0002g0009 others(7): Show |
10 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.671+23672C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33439323 | |||||||
chr19:33439430 | A | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.671+23565T>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33439430 | |||||||
chr19:33439436 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.671+23559C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33439436 | |||||||
chr19:33439438 | C | T | 5 | a0001c0001t0001g0272 a0001c0001t0003g0275 a0001c0001t0003g0284 others(2): Show |
5 | HG00140.hp1 HG01106.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.671+23557G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33439438 | |||||||
chr19:33439461 | C | T | 1 | a0002c0002t0002g0174 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.671+23534G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33439461 | |||||||
chr19:33439472 | G | A | 1 | a0002c0002t0002g0013 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.671+23523C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33439472 | |||||||
chr19:33439564 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.671+23431C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33439564 | |||||||
chr19:33439744 | G | A | 1 | a0001c0001t0001g0267 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.671+23251C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33439744 | |||||||
chr19:33439756 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.671+23239C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33439756 | |||||||
chr19:33439778 | T | C | 2 | a0001c0001t0001g0170 a0001c0001t0001g0173 |
2 | HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.671+23217A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33439778 | |||||||
chr19:33439886 | G | A | 1 | a0001c0001t0003g0275 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.671+23109C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33439886 | |||||||
chr19:33439981 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.671+23014C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33439981 | |||||||
chr19:33440102 | C | T | 3 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 |
3 | HG00621.hp1 NA18953.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.671+22893G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33440102 | |||||||
chr19:33440320 | T | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.671+22675A>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33440320 | |||||||
chr19:33440594 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.671+22401G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33440594 | |||||||
chr19:33440699 | G | T | 2 | a0006c0010t0002g0166 a0006c0010t0005g0168 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.671+22296C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33440699 | |||||||
chr19:33440828 | A | C | 2 | a0002c0002t0002g0259 a0002c0002t0002g0260 |
2 | HG01109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.671+22167T>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33440828 | |||||||
chr19:33440897 | C | G | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.671+22098G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33440897 | |||||||
chr19:33440915 | G | A | 10 | a0002c0002t0002g0006 a0002c0002t0002g0008 a0002c0002t0002g0009 others(7): Show |
10 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.671+22080C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33440915 | |||||||
chr19:33441159 | C | T | 2 | a0001c0003t0001g0209 a0001c0003t0001g0232 |
2 | NA18950.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.671+21836G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33441159 | |||||||
chr19:33441215 | C | G | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.671+21780G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33441215 | |||||||
chr19:33441233 | G | GAAACACG others(31): Show |
1 | a0001c0001t0001g0099 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.671+21724_671+2176 others(42): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33441233 | |||||||
chr19:33441409 | T | C | 185 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0024 others(182): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.671+21586A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33441409 | |||||||
chr19:33441422 | C | G | 3 | a0002c0002t0005g0091 a0002c0002t0005g0208 a0002c0002t0005g0298 |
3 | HG02258.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.671+21573G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33441422 | |||||||
chr19:33441439 | G | A | 1 | a0003c0005t0001g0015 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.671+21556C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33441439 | |||||||
chr19:33441491 | C | T | 3 | a0002c0002t0005g0091 a0002c0002t0005g0208 a0002c0002t0005g0298 |
3 | HG02258.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.671+21504G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33441491 | |||||||
chr19:33441518 | C | G | 19 | a0001c0001t0001g0082 a0001c0001t0001g0272 a0001c0001t0001g0278 others(16): Show |
19 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.671+21477G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33441518 | |||||||
chr19:33441568 | G | C | 10 | a0002c0002t0002g0006 a0002c0002t0002g0008 a0002c0002t0002g0009 others(7): Show |
10 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.671+21427C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33441568 | |||||||
chr19:33441696 | C | T | 3 | a0001c0001t0001g0137 a0001c0001t0001g0140 a0001c0001t0001g0163 |
3 | HG01070.hp1 HG01071.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.671+21299G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33441696 | |||||||
chr19:33441835 | C | T | 4 | a0001c0001t0001g0089 a0001c0001t0001g0098 a0001c0001t0001g0107 others(1): Show |
4 | HG01175.hp2 HG01243.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.671+21160G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33441835 | |||||||
chr19:33442069 | G | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.671+20926C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33442069 | |||||||
chr19:33442165 | G | A | 1 | a0001c0003t0001g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.671+20830C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33442165 | |||||||
chr19:33442230 | C | T | 1 | a0001c0001t0001g0018 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.671+20765G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33442230 | |||||||
chr19:33442244 | T | C | 2 | a0002c0002t0002g0149 a0002c0002t0002g0150 |
2 | HG00408.hp2 HG00558.hp2 |
intron_variant | MODIFIER | c.671+20751A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33442244 | |||||||
chr19:33442256 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.671+20739G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33442256 | |||||||
chr19:33442406 | CA | C | 93 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0040 others(90): Show |
93 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.671+20588delT | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33442406 | |||||||
chr19:33442429 | G | A | 1 | a0003c0005t0001g0017 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.671+20566C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33442429 | |||||||
chr19:33442542 | T | A | 12 | a0001c0001t0001g0180 a0001c0001t0001g0261 a0001c0001t0003g0001 others(9): Show |
14 | HG00639.hp2 HG00642.hp1 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.671+20453A>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33442542 | |||||||
chr19:33442543 | A | AC | 42 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0037 others(39): Show |
42 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(39): Show |
intron_variant | MODIFIER | c.671+20451_671+2045 others(5): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33442543 | |||||||
chr19:33442543 | A | T | 134 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(131): Show |
134 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.671+20452T>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33442543 | |||||||
chr19:33442544 | A | C | 3 | a0002c0002t0005g0091 a0002c0002t0005g0208 a0002c0002t0005g0298 |
3 | HG02258.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.671+20451T>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33442544 | |||||||
chr19:33442546 | AT | A | 12 | a0001c0001t0001g0271 a0001c0001t0004g0039 a0001c0003t0001g0167 others(9): Show |
12 | HG00323.hp1 HG01257.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.671+20448delA | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33442546 | |||||||
chr19:33442547 | T | A | 196 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0024 others(193): Show |
199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.671+20448A>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33442547 | |||||||
chr19:33442565 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.671+20430G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33442565 | |||||||
chr19:33442641 | A | G | 208 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0024 others(205): Show |
211 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.671+20354T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33442641 | |||||||
chr19:33442652 | T | A | 1 | a0002c0002t0002g0258 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.671+20343A>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33442652 | |||||||
chr19:33442747 | A | C | 13 | a0001c0007t0001g0005 a0001c0007t0001g0212 a0001c0007t0001g0242 others(10): Show |
14 | HG01168.hp1 HG02129.hp1 HG03942.hp1 others(11): Show |
intron_variant | MODIFIER | c.671+20248T>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33442747 | |||||||
chr19:33442875 | G | A | 1 | a0001c0003t0001g0007 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.671+20120C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33442875 | |||||||
chr19:33442889 | G | A | 1 | a0002c0002t0002g0083 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.671+20106C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33442889 | |||||||
chr19:33442994 | G | A | 1 | a0002c0002t0002g0299 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.671+20001C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33442994 | |||||||
chr19:33443102 | G | A | 1 | a0001c0003t0001g0252 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.671+19893C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33443102 | |||||||
chr19:33443175 | C | T | 1 | a0001c0003t0001g0143 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.671+19820G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33443175 | |||||||
chr19:33443225 | C | T | 1 | a0001c0003t0001g0231 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.671+19770G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33443225 | |||||||
chr19:33443622 | G | A | 1 | a0002c0002t0002g0081 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.671+19373C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33443622 | |||||||
chr19:33443777 | C | T | 44 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(41): Show |
44 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.671+19218G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33443777 | |||||||
chr19:33443934 | C | T | 16 | a0001c0001t0001g0180 a0001c0001t0001g0261 a0001c0001t0003g0001 others(13): Show |
18 | HG00639.hp2 HG00642.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.671+19061G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33443934 | |||||||
chr19:33443980 | G | GCA | 3 | a0001c0001t0001g0170 a0001c0001t0001g0173 a0002c0002t0002g0046 |
3 | HG01257.hp1 HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.671+19013_671+1901 others(6): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33443980 | |||||||
chr19:33443982 | A | G | 11 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(8): Show |
11 | HG01099.hp2 HG02257.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.671+19013T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33443982 | |||||||
chr19:33444059 | G | A | 2 | a0002c0002t0002g0259 a0002c0002t0002g0260 |
2 | HG01109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.671+18936C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33444059 | |||||||
chr19:33444074 | C | T | 10 | a0002c0002t0002g0006 a0002c0002t0002g0008 a0002c0002t0002g0009 others(7): Show |
10 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.671+18921G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33444074 | |||||||
chr19:33444077 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.671+18918C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33444077 | |||||||
chr19:33444196 | C | T | 184 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(181): Show |
187 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.671+18799G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33444196 | |||||||
chr19:33444207 | C | G | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.671+18788G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33444207 | |||||||
chr19:33444239 | AAGGCTGG others(16): Show |
A | 44 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(41): Show |
44 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.671+18733_671+1875 others(27): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33444239 | |||||||
chr19:33444358 | A | T | 15 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0002c0002t0002g0006 others(12): Show |
15 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.671+18637T>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33444358 | |||||||
chr19:33444424 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.671+18571C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33444424 | |||||||
chr19:33444691 | C | A | 1 | a0001c0001t0001g0022 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.671+18304G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33444691 | |||||||
chr19:33444695 | C | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.671+18300G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33444695 | |||||||
chr19:33444695 | C | G | 2 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.671+18300G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33444695 | |||||||
chr19:33444769 | T | C | 80 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(77): Show |
80 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.671+18226A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33444769 | |||||||
chr19:33444888 | GACA | G | 12 | a0001c0001t0001g0180 a0001c0001t0001g0261 a0001c0001t0003g0001 others(9): Show |
14 | HG00639.hp2 HG00642.hp1 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.671+18104_671+1810 others(7): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33444888 | |||||||
chr19:33444905 | G | A | 3 | a0002c0002t0005g0091 a0002c0002t0005g0208 a0002c0002t0005g0298 |
3 | HG02258.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.671+18090C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33444905 | |||||||
chr19:33445152 | C | T | 2 | a0002c0002t0002g0028 a0002c0002t0002g0175 |
2 | HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.671+17843G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33445152 | |||||||
chr19:33445244 | C | G | 1 | a0001c0001t0001g0075 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.671+17751G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33445244 | |||||||
chr19:33445439 | T | C | 1 | a0001c0001t0004g0039 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.671+17556A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33445439 | |||||||
chr19:33445538 | A | G | 2 | a0002c0002t0002g0259 a0002c0002t0002g0260 |
2 | HG01109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.671+17457T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33445538 | |||||||
chr19:33445558 | C | T | 1 | a0005c0008t0001g0247 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.671+17437G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33445558 | |||||||
chr19:33445581 | C | G | 1 | a0001c0001t0001g0103 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.671+17414G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33445581 | |||||||
chr19:33445612 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.671+17383G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33445612 | |||||||
chr19:33445733 | G | A | 1 | a0001c0003t0001g0215 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.671+17262C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33445733 | |||||||
chr19:33445846 | G | A | 15 | a0001c0007t0001g0005 a0001c0007t0001g0212 a0001c0007t0001g0242 others(12): Show |
16 | HG01109.hp1 HG01168.hp1 HG02129.hp1 others(13): Show |
intron_variant | MODIFIER | c.671+17149C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33445846 | |||||||
chr19:33445850 | T | A | 1 | a0001c0001t0004g0080 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.671+17145A>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33445850 | |||||||
chr19:33445888 | C | G | 12 | a0001c0001t0001g0180 a0001c0001t0001g0261 a0001c0001t0003g0001 others(9): Show |
14 | HG00639.hp2 HG00642.hp1 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.671+17107G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33445888 | |||||||
chr19:33445898 | C | T | 1 | a0001c0001t0003g0182 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.671+17097G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33445898 | |||||||
chr19:33445982 | C | T | 27 | a0001c0001t0001g0180 a0001c0001t0001g0261 a0001c0001t0003g0001 others(24): Show |
30 | HG00639.hp2 HG00642.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.671+17013G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33445982 | |||||||
chr19:33446024 | C | T | 47 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(44): Show |
47 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.671+16971G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33446024 | |||||||
chr19:33446221 | C | T | 22 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(19): Show |
22 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.671+16774G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33446221 | |||||||
chr19:33446354 | T | C | 13 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(10): Show |
13 | HG01099.hp2 HG02257.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.671+16641A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33446354 | |||||||
chr19:33446371 | C | T | 80 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(77): Show |
80 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.671+16624G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33446371 | |||||||
chr19:33446416 | G | A | 27 | a0001c0001t0001g0180 a0001c0001t0001g0261 a0001c0001t0003g0001 others(24): Show |
30 | HG00639.hp2 HG00642.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.671+16579C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33446416 | |||||||
chr19:33446484 | G | A | 5 | a0002c0002t0002g0030 a0002c0002t0002g0031 a0002c0002t0002g0033 others(2): Show |
5 | HG02615.hp2 HG02895.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.671+16511C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33446484 | |||||||
chr19:33446571 | C | T | 12 | a0001c0001t0001g0027 a0001c0001t0001g0037 a0002c0002t0002g0026 others(9): Show |
12 | HG01257.hp2 HG02293.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.671+16424G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33446571 | |||||||
chr19:33446639 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.671+16356C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33446639 | |||||||
chr19:33446704 | C | T | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0308 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.671+16291G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33446704 | |||||||
chr19:33446794 | G | A | 1 | a0002c0002t0002g0228 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.671+16201C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33446794 | |||||||
chr19:33446807 | C | T | 36 | a0001c0001t0001g0082 a0001c0001t0001g0170 a0001c0001t0001g0173 others(33): Show |
36 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.671+16188G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33446807 | |||||||
chr19:33446874 | C | T | 2 | a0001c0001t0001g0141 a0002c0002t0002g0128 |
2 | HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.671+16121G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33446874 | |||||||
chr19:33446992 | G | C | 1 | a0002c0002t0002g0292 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.671+16003C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33446992 | |||||||
chr19:33447199 | G | A | 7 | a0002c0002t0002g0029 a0002c0002t0002g0030 a0002c0002t0002g0031 others(4): Show |
7 | HG02451.hp1 HG02615.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.671+15796C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33447199 | |||||||
chr19:33447341 | G | A | 2 | a0002c0002t0005g0208 a0002c0002t0005g0298 |
2 | HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.671+15654C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33447341 | |||||||
chr19:33447864 | T | G | 3 | a0002c0002t0005g0091 a0002c0002t0005g0208 a0002c0002t0005g0298 |
3 | HG02258.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.671+15131A>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33447864 | |||||||
chr19:33447894 | C | T | 183 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(180): Show |
186 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.671+15101G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33447894 | |||||||
chr19:33447911 | C | T | 3 | a0001c0001t0001g0004 a0001c0001t0001g0154 a0001c0001t0001g0157 |
4 | HG00597.hp2 NA18944.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.671+15084G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33447911 | |||||||
chr19:33447933 | C | T | 3 | a0001c0001t0001g0280 a0001c0001t0001g0282 a0001c0001t0001g0283 |
3 | HG01106.hp1 HG03491.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.671+15062G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33447933 | |||||||
chr19:33447953 | C | T | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG02165.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.671+15042G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33447953 | |||||||
chr19:33447986 | A | G | 10 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(7): Show |
10 | HG01099.hp2 HG02257.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.671+15009T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33447986 | |||||||
chr19:33448284 | A | G | 13 | a0001c0007t0001g0005 a0001c0007t0001g0212 a0001c0007t0001g0242 others(10): Show |
14 | HG01168.hp1 HG02129.hp1 HG03942.hp1 others(11): Show |
intron_variant | MODIFIER | c.671+14711T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33448284 | |||||||
chr19:33448292 | C | T | 1 | a0002c0002t0002g0169 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.671+14703G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33448292 | |||||||
chr19:33448415 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.671+14580C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33448415 | |||||||
chr19:33448529 | C | CT | 10 | a0002c0002t0002g0006 a0002c0002t0002g0008 a0002c0002t0002g0009 others(7): Show |
10 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.671+14465dupA | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33448529 | |||||||
chr19:33448688 | C | T | 5 | a0001c0001t0001g0280 a0001c0001t0001g0282 a0001c0001t0001g0283 others(2): Show |
5 | HG00733.hp1 HG01099.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.671+14307G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33448688 | |||||||
chr19:33448699 | C | T | 3 | a0001c0001t0001g0112 a0001c0003t0001g0113 a0001c0003t0001g0115 |
3 | NA18940.hp1 NA18942.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.671+14296G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33448699 | |||||||
chr19:33448708 | G | A | 60 | a0001c0001t0001g0043 a0001c0001t0001g0191 a0001c0001t0001g0192 others(57): Show |
60 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.671+14287C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33448708 | |||||||
chr19:33448777 | T | A | 1 | a0001c0001t0001g0268 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.671+14218A>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33448777 | |||||||
chr19:33448778 | C | G | 1 | a0001c0001t0001g0268 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.671+14217G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33448778 | |||||||
chr19:33448841 | T | G | 1 | a0002c0002t0002g0258 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.671+14154A>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33448841 | |||||||
chr19:33448891 | G | C | 19 | a0001c0001t0001g0082 a0001c0001t0001g0272 a0001c0001t0001g0278 others(16): Show |
19 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.671+14104C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33448891 | |||||||
chr19:33448921 | T | A | 2 | a0002c0002t0005g0208 a0002c0002t0005g0298 |
2 | HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.671+14074A>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33448921 | |||||||
chr19:33449000 | A | G | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.671+13995T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33449000 | |||||||
chr19:33449172 | C | T | 3 | a0001c0001t0001g0002 a0001c0001t0001g0109 a0001c0001t0001g0110 |
4 | HG00099.hp2 HG01074.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.671+13823G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33449172 | |||||||
chr19:33449324 | C | G | 10 | a0002c0002t0002g0006 a0002c0002t0002g0008 a0002c0002t0002g0009 others(7): Show |
10 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.671+13671G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33449324 | |||||||
chr19:33449354 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.671+13641C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33449354 | |||||||
chr19:33449473 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.671+13522G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33449473 | |||||||
chr19:33449600 | A | G | 10 | a0002c0002t0002g0006 a0002c0002t0002g0008 a0002c0002t0002g0009 others(7): Show |
10 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.671+13395T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33449600 | |||||||
chr19:33449647 | G | A | 1 | a0002c0002t0002g0171 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.671+13348C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33449647 | |||||||
chr19:33449705 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.671+13290A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33449705 | |||||||
chr19:33449756 | GCGGTGTC | G | 186 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0040 others(183): Show |
189 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.671+13232_671+1323 others(11): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33449756 | |||||||
chr19:33449824 | G | A | 3 | a0002c0002t0005g0091 a0002c0002t0005g0208 a0002c0002t0005g0298 |
3 | HG02258.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.671+13171C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33449824 | |||||||
chr19:33449878 | T | A | 2 | a0001c0001t0001g0230 a0001c0001t0001g0237 |
2 | HG03831.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.671+13117A>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33449878 | |||||||
chr19:33449880 | T | G | 2 | a0001c0001t0001g0230 a0001c0001t0001g0237 |
2 | HG03831.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.671+13115A>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33449880 | |||||||
chr19:33449979 | T | C | 1 | a0006c0010t0002g0166 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.671+13016A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33449979 | |||||||
chr19:33450149 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.671+12846G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33450149 | |||||||
chr19:33450190 | C | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.671+12805G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33450190 | |||||||
chr19:33450220 | G | A | 3 | a0001c0003t0001g0143 a0001c0003t0001g0144 a0001c0003t0001g0151 |
3 | NA18959.hp1 NA18967.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.671+12775C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33450220 | |||||||
chr19:33450379 | T | G | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.671+12616A>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33450379 | |||||||
chr19:33450390 | G | A | 1 | a0002c0002t0002g0036 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.671+12605C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33450390 | |||||||
chr19:33450598 | C | G | 129 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0040 others(126): Show |
132 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.671+12397G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33450598 | |||||||
chr19:33450657 | C | T | 1 | a0001c0001t0003g0286 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.671+12338G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33450657 | |||||||
chr19:33450786 | G | A | 12 | a0001c0001t0001g0180 a0001c0001t0001g0261 a0001c0001t0003g0001 others(9): Show |
14 | HG00639.hp2 HG00642.hp1 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.671+12209C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33450786 | |||||||
chr19:33450805 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.671+12190C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33450805 | |||||||
chr19:33450812 | G | A | 1 | a0001c0001t0003g0188 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.671+12183C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33450812 | |||||||
chr19:33451042 | A | C | 1 | a0002c0002t0002g0036 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.671+11953T>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33451042 | |||||||
chr19:33451057 | C | T | 5 | a0004c0006t0001g0296 a0004c0006t0001g0297 a0004c0006t0001g0300 others(2): Show |
5 | HG02809.hp1 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.671+11938G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33451057 | |||||||
chr19:33451058 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.671+11937C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33451058 | |||||||
chr19:33451069 | C | T | 1 | a0002c0002t0002g0241 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.671+11926G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33451069 | |||||||
chr19:33451192 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.671+11803A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33451192 | |||||||
chr19:33451205 | C | G | 1 | a0001c0001t0003g0284 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.671+11790G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33451205 | |||||||
chr19:33451226 | A | G | 3 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0013t0002g0011 |
3 | HG01074.hp1 HG01109.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.671+11769T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33451226 | |||||||
chr19:33451314 | G | A | 129 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0040 others(126): Show |
132 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.671+11681C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33451314 | |||||||
chr19:33451622 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.671+11373G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33451622 | |||||||
chr19:33451660 | C | T | 36 | a0001c0001t0001g0082 a0001c0001t0001g0170 a0001c0001t0001g0173 others(33): Show |
36 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.671+11335G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33451660 | |||||||
chr19:33451712 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.671+11283A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33451712 | |||||||
chr19:33451743 | T | C | 1 | a0001c0001t0001g0261 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.671+11252A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33451743 | |||||||
chr19:33451753 | A | G | 1 | a0001c0001t0001g0279 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.671+11242T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33451753 | |||||||
chr19:33451932 | C | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.671+11063G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33451932 | |||||||
chr19:33452102 | C | T | 1 | a0002c0002t0002g0008 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.671+10893G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33452102 | |||||||
chr19:33452165 | T | C | 12 | a0001c0001t0001g0180 a0001c0001t0001g0261 a0001c0001t0003g0001 others(9): Show |
14 | HG00639.hp2 HG00642.hp1 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.671+10830A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33452165 | |||||||
chr19:33452175 | A | C | 36 | a0001c0001t0001g0082 a0001c0001t0001g0170 a0001c0001t0001g0173 others(33): Show |
36 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.671+10820T>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33452175 | |||||||
chr19:33452251 | G | T | 1 | a0001c0001t0003g0286 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.671+10744C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33452251 | |||||||
chr19:33452591 | G | A | 44 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(41): Show |
44 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.671+10404C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33452591 | |||||||
chr19:33452778 | T | C | 44 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(41): Show |
44 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.671+10217A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33452778 | |||||||
chr19:33453005 | C | G | 16 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0266 others(13): Show |
16 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.671+9990G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33453005 | |||||||
chr19:33453050 | G | A | 13 | a0001c0007t0001g0005 a0001c0007t0001g0212 a0001c0007t0001g0242 others(10): Show |
14 | HG01168.hp1 HG02129.hp1 HG03942.hp1 others(11): Show |
intron_variant | MODIFIER | c.671+9945C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33453050 | |||||||
chr19:33453059 | C | T | 10 | a0002c0002t0002g0006 a0002c0002t0002g0008 a0002c0002t0002g0009 others(7): Show |
10 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.671+9936G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33453059 | |||||||
chr19:33453080 | G | A | 95 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(92): Show |
95 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.671+9915C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33453080 | |||||||
chr19:33453313 | T | TAAAAAAA others(5): Show |
1 | a0001c0001t0001g0279 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.671+9681_671+9682i others(14): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33453313 | |||||||
chr19:33453317 | A | AAAAAAAA others(6): Show |
1 | a0001c0001t0003g0281 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.671+9677_671+9678i others(15): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33453317 | |||||||
chr19:33453317 | A | AAAAAAAA others(5): Show |
11 | a0001c0001t0001g0272 a0001c0001t0001g0278 a0001c0001t0003g0073 others(8): Show |
11 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(8): Show |
intron_variant | MODIFIER | c.671+9677_671+9678i others(14): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33453317 | |||||||
chr19:33453317 | A | AAAAAAAA others(5): Show |
5 | a0001c0001t0001g0082 a0001c0001t0001g0280 a0001c0001t0001g0282 others(2): Show |
5 | HG01106.hp1 HG02698.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.671+9677_671+9678i others(14): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33453317 | |||||||
chr19:33453317 | A | AAAAAAAA others(9): Show |
1 | a0002c0002t0005g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.671+9677_671+9678i others(18): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33453317 | |||||||
chr19:33453317 | A | AAAAAAAT others(8): Show |
1 | a0002c0002t0002g0258 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.671+9677_671+9678i others(17): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33453317 | |||||||
chr19:33453317 | A | AAAATAAA others(1): Show |
27 | a0001c0001t0001g0180 a0001c0001t0001g0261 a0001c0001t0003g0001 others(24): Show |
30 | HG00639.hp2 HG01109.hp1 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.671+9670_671+9677d others(10): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33453317 | |||||||
chr19:33453317 | A | AAAATAAA others(5): Show |
3 | a0001c0001t0001g0170 a0001c0001t0001g0173 a0001c0001t0003g0183 |
3 | HG00642.hp1 HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.671+9666_671+9677d others(14): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33453317 | |||||||
chr19:33453317 | A | AAAATAAA others(9): Show |
39 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0054 others(36): Show |
39 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.671+9662_671+9677d others(18): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33453317 | |||||||
chr19:33453317 | A | AAAATAAA others(13): Show |
34 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(31): Show |
34 | HG01099.hp2 HG01891.hp2 HG02257.hp1 others(31): Show |
intron_variant | MODIFIER | c.671+9658_671+9677d others(22): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33453317 | |||||||
chr19:33453317 | A | AAAATAAA others(17): Show |
6 | a0001c0001t0001g0048 a0001c0001t0001g0288 a0001c0001t0001g0293 others(3): Show |
6 | HG02055.hp1 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.671+9654_671+9677d others(26): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33453317 | |||||||
chr19:33453441 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.671+9554G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33453441 | |||||||
chr19:33453454 | T | C | 2 | a0001c0001t0001g0294 a0002c0002t0002g0241 |
2 | HG01884.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.671+9541A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33453454 | |||||||
chr19:33453518 | T | C | 27 | a0001c0001t0001g0180 a0001c0001t0001g0261 a0001c0001t0003g0001 others(24): Show |
30 | HG00639.hp2 HG00642.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.671+9477A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33453518 | |||||||
chr19:33453870 | T | C | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0308 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.671+9125A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33453870 | |||||||
chr19:33453981 | G | A | 124 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(121): Show |
127 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.671+9014C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33453981 | |||||||
chr19:33453990 | C | T | 12 | a0001c0001t0001g0180 a0001c0001t0001g0261 a0001c0001t0003g0001 others(9): Show |
14 | HG00639.hp2 HG00642.hp1 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.671+9005G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33453990 | |||||||
chr19:33454143 | T | G | 1 | a0001c0001t0001g0288 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.671+8852A>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33454143 | |||||||
chr19:33454248 | A | C | 1 | a0001c0003t0001g0198 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.671+8747T>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33454248 | |||||||
chr19:33454333 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.671+8662C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33454333 | |||||||
chr19:33454372 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.671+8623A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33454372 | |||||||
chr19:33454502 | T | C | 1 | a0002c0002t0002g0228 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.671+8493A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33454502 | |||||||
chr19:33454577 | C | T | 1 | a0001c0001t0003g0281 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.671+8418G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33454577 | |||||||
chr19:33454747 | A | G | 1 | a0002c0002t0002g0175 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.671+8248T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33454747 | |||||||
chr19:33454901 | C | A | 1 | a0001c0001t0004g0074 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.671+8094G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33454901 | |||||||
chr19:33454903 | C | G | 1 | a0001c0001t0004g0074 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.671+8092G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33454903 | |||||||
chr19:33454912 | A | T | 1 | a0001c0001t0004g0074 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.671+8083T>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33454912 | |||||||
chr19:33455118 | A | G | 129 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0040 others(126): Show |
132 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.671+7877T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33455118 | |||||||
chr19:33455208 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.671+7787A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33455208 | |||||||
chr19:33455264 | A | G | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0308 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.671+7731T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33455264 | |||||||
chr19:33455295 | C | T | 1 | a0002c0002t0002g0038 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.671+7700G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33455295 | |||||||
chr19:33455460 | T | C | 57 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(54): Show |
57 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.671+7535A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33455460 | |||||||
chr19:33455487 | G | T | 1 | a0001c0001t0004g0074 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.671+7508C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33455487 | |||||||
chr19:33455488 | G | A | 1 | a0001c0001t0004g0074 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.671+7507C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33455488 | |||||||
chr19:33455489 | T | G | 1 | a0001c0001t0004g0074 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.671+7506A>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33455489 | |||||||
chr19:33455491 | T | G | 1 | a0001c0001t0004g0074 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.671+7504A>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33455491 | |||||||
chr19:33455492 | T | A | 1 | a0001c0001t0004g0074 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.671+7503A>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33455492 | |||||||
chr19:33455496 | C | T | 1 | a0001c0001t0004g0074 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.671+7499G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33455496 | |||||||
chr19:33455535 | C | T | 13 | a0001c0007t0001g0005 a0001c0007t0001g0212 a0001c0007t0001g0242 others(10): Show |
14 | HG01168.hp1 HG02129.hp1 HG03942.hp1 others(11): Show |
intron_variant | MODIFIER | c.671+7460G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33455535 | |||||||
chr19:33455643 | T | C | 129 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0040 others(126): Show |
132 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.671+7352A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33455643 | |||||||
chr19:33455678 | A | AT | 129 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(126): Show |
132 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.671+7316dupA | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33455678 | |||||||
chr19:33455678 | A | ATT | 14 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(11): Show |
14 | HG01099.hp2 HG01952.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.671+7315_671+7316d others(4): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33455678 | |||||||
chr19:33455678 | AT | A | 51 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0043 others(48): Show |
51 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.671+7316delA | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33455678 | |||||||
chr19:33455987 | C | T | 124 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(121): Show |
127 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.671+7008G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33455987 | |||||||
chr19:33455988 | G | A | 1 | a0002c0002t0002g0118 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.671+7007C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33455988 | |||||||
chr19:33456191 | G | A | 2 | a0001c0001t0001g0191 a0001c0001t0001g0192 |
2 | NA18970.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.671+6804C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33456191 | |||||||
chr19:33456271 | T | C | 3 | a0002c0002t0005g0091 a0002c0002t0005g0208 a0002c0002t0005g0298 |
3 | HG02258.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.671+6724A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33456271 | |||||||
chr19:33456303 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.671+6692G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33456303 | |||||||
chr19:33456354 | T | C | 129 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0040 others(126): Show |
132 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.671+6641A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33456354 | |||||||
chr19:33456410 | A | G | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.671+6585T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33456410 | |||||||
chr19:33456572 | G | C | 1 | a0001c0001t0001g0055 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.671+6423C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33456572 | |||||||
chr19:33456653 | G | A | 1 | a0001c0003t0001g0007 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.671+6342C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33456653 | |||||||
chr19:33456820 | C | T | 129 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0040 others(126): Show |
132 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.671+6175G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33456820 | |||||||
chr19:33456932 | C | G | 2 | a0002c0002t0002g0259 a0002c0002t0002g0260 |
2 | HG01109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.671+6063G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33456932 | |||||||
chr19:33457043 | C | T | 15 | a0001c0007t0001g0005 a0001c0007t0001g0212 a0001c0007t0001g0242 others(12): Show |
16 | HG01109.hp1 HG01168.hp1 HG02129.hp1 others(13): Show |
intron_variant | MODIFIER | c.671+5952G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33457043 | |||||||
chr19:33457213 | C | A | 2 | a0006c0010t0002g0166 a0006c0010t0005g0168 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.671+5782G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33457213 | |||||||
chr19:33457386 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.671+5609C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33457386 | |||||||
chr19:33457398 | C | T | 3 | a0002c0002t0005g0091 a0002c0002t0005g0208 a0002c0002t0005g0298 |
3 | HG02258.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.671+5597G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33457398 | |||||||
chr19:33457410 | G | A | 27 | a0001c0001t0001g0180 a0001c0001t0001g0261 a0001c0001t0003g0001 others(24): Show |
30 | HG00639.hp2 HG00642.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.671+5585C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33457410 | |||||||
chr19:33457424 | T | G | 27 | a0001c0001t0001g0180 a0001c0001t0001g0261 a0001c0001t0003g0001 others(24): Show |
30 | HG00639.hp2 HG00642.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.671+5571A>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33457424 | |||||||
chr19:33457689 | T | G | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG00642.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.671+5306A>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33457689 | |||||||
chr19:33457701 | G | A | 3 | a0002c0002t0005g0091 a0002c0002t0005g0208 a0002c0002t0005g0298 |
3 | HG02258.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.671+5294C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33457701 | |||||||
chr19:33457813 | A | G | 1 | a0002c0002t0005g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.671+5182T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33457813 | |||||||
chr19:33457853 | G | A | 126 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0040 others(123): Show |
129 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.671+5142C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33457853 | |||||||
chr19:33457858 | C | CAAAAACA others(3): Show |
139 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0040 others(136): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.671+5136_671+5137i others(12): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33457858 | |||||||
chr19:33457899 | C | G | 11 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(8): Show |
11 | HG01099.hp2 HG02257.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.671+5096G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33457899 | |||||||
chr19:33457934 | C | T | 126 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0040 others(123): Show |
129 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.671+5061G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33457934 | |||||||
chr19:33457984 | T | C | 34 | a0001c0001t0001g0082 a0001c0001t0001g0264 a0001c0001t0001g0265 others(31): Show |
34 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.671+5011A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33457984 | |||||||
chr19:33457996 | C | G | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | NA18954.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.671+4999G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33457996 | |||||||
chr19:33458152 | G | C | 27 | a0001c0001t0001g0180 a0001c0001t0001g0261 a0001c0001t0003g0001 others(24): Show |
30 | HG00639.hp2 HG00642.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.671+4843C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33458152 | |||||||
chr19:33458238 | T | G | 36 | a0001c0001t0001g0082 a0001c0001t0001g0170 a0001c0001t0001g0173 others(33): Show |
36 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.671+4757A>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33458238 | |||||||
chr19:33458388 | G | C | 1 | a0001c0003t0001g0167 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.671+4607C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33458388 | |||||||
chr19:33458466 | T | G | 126 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0040 others(123): Show |
129 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.671+4529A>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33458466 | |||||||
chr19:33458475 | T | C | 10 | a0002c0002t0002g0006 a0002c0002t0002g0008 a0002c0002t0002g0009 others(7): Show |
10 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.671+4520A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33458475 | |||||||
chr19:33458476 | G | A | 5 | a0002c0002t0002g0008 a0002c0002t0002g0009 a0002c0002t0002g0010 others(2): Show |
5 | HG00140.hp2 HG01496.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.671+4519C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33458476 | |||||||
chr19:33458544 | T | G | 1 | a0002c0002t0002g0228 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.671+4451A>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33458544 | |||||||
chr19:33458551 | GGGTGTGT others(22): Show |
G | 126 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0040 others(123): Show |
129 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.671+4415_671+4443d others(31): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33458551 | |||||||
chr19:33458610 | G | A | 1 | a0002c0002t0002g0044 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.671+4385C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33458610 | |||||||
chr19:33458643 | T | G | 2 | a0001c0001t0001g0294 a0002c0002t0002g0241 |
2 | HG01884.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.671+4352A>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33458643 | |||||||
chr19:33458644 | G | T | 124 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(121): Show |
127 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.671+4351C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33458644 | |||||||
chr19:33458646 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.671+4349C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33458646 | |||||||
chr19:33458703 | G | T | 1 | a0002c0002t0002g0262 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.671+4292C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33458703 | |||||||
chr19:33458800 | A | AGGGCATG others(932): Show |
4 | a0001c0001t0001g0037 a0002c0002t0002g0026 a0002c0002t0002g0036 others(1): Show |
4 | HG01257.hp2 HG02293.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.671+4194_671+4195i others(941): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33458800 | |||||||
chr19:33458800 | A | AGGGCATG others(932): Show |
19 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0173 others(16): Show |
19 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.671+4194_671+4195i others(941): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33458800 | |||||||
chr19:33458800 | A | AGGGCATG others(934): Show |
1 | a0001c0001t0001g0191 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.671+4194_671+4195i others(943): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33458800 | |||||||
chr19:33458800 | A | AGGGCATG others(934): Show |
1 | a0001c0001t0001g0126 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.671+4194_671+4195i others(943): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33458800 | |||||||
chr19:33458800 | A | AGGGCATG others(932): Show |
3 | a0002c0002t0005g0091 a0002c0002t0005g0208 a0002c0002t0005g0298 |
3 | HG02258.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.671+4194_671+4195i others(941): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33458800 | |||||||
chr19:33458800 | A | ATGGCATG others(918): Show |
13 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(10): Show |
13 | HG01099.hp2 HG02257.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.671+4194_671+4195i others(927): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33458800 | |||||||
chr19:33458800 | A | ATGGCATG others(932): Show |
2 | a0001c0001t0001g0306 a0001c0001t0001g0308 |
2 | HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.671+4194_671+4195i others(941): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33458800 | |||||||
chr19:33458800 | A | ATGGCATG others(925): Show |
1 | a0001c0001t0001g0180 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.671+4194_671+4195i others(934): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33458800 | |||||||
chr19:33458800 | A | ATGGCATG others(925): Show |
11 | a0001c0001t0001g0261 a0001c0001t0003g0001 a0001c0001t0003g0179 others(8): Show |
13 | HG00639.hp2 HG00642.hp1 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.671+4194_671+4195i others(934): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33458800 | |||||||
chr19:33458800 | A | ATGGCATG others(932): Show |
80 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(77): Show |
80 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.671+4194_671+4195i others(941): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33458800 | |||||||
chr19:33458800 | A | ATGGCATG others(932): Show |
1 | a0001c0001t0001g0272 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.671+4194_671+4195i others(941): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33458800 | |||||||
chr19:33458800 | A | ATGGCATG others(922): Show |
2 | a0002c0002t0002g0259 a0002c0002t0002g0260 |
2 | HG01109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.671+4194_671+4195i others(931): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33458800 | |||||||
chr19:33458800 | A | ATGGCATG others(925): Show |
13 | a0001c0007t0001g0005 a0001c0007t0001g0212 a0001c0007t0001g0242 others(10): Show |
14 | HG01168.hp1 HG02129.hp1 HG03942.hp1 others(11): Show |
intron_variant | MODIFIER | c.671+4194_671+4195i others(934): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33458800 | |||||||
chr19:33458800 | A | ATGGCATG others(932): Show |
2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.671+4194_671+4195i others(941): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33458800 | |||||||
chr19:33459074 | G | A | 1 | a0002c0002t0005g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.671+3921C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33459074 | |||||||
chr19:33459205 | C | T | 1 | a0001c0003t0001g0246 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.671+3790G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33459205 | |||||||
chr19:33459371 | C | T | 44 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(41): Show |
44 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.671+3624G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33459371 | |||||||
chr19:33459486 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.671+3509C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33459486 | |||||||
chr19:33459491 | G | A | 18 | a0001c0001t0001g0082 a0001c0001t0001g0272 a0001c0001t0001g0278 others(15): Show |
18 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.671+3504C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33459491 | |||||||
chr19:33459629 | G | A | 1 | a0003c0005t0001g0015 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.671+3366C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33459629 | |||||||
chr19:33459664 | G | A | 9 | a0001c0001t0001g0104 a0001c0001t0001g0120 a0001c0001t0001g0145 others(6): Show |
9 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+3331C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33459664 | |||||||
chr19:33459673 | C | CT | 94 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0040 others(91): Show |
94 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.671+3321dupA | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33459673 | |||||||
chr19:33459673 | C | CTT | 27 | a0001c0001t0001g0180 a0001c0001t0001g0261 a0001c0001t0003g0001 others(24): Show |
30 | HG00639.hp2 HG00642.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.671+3320_671+3321d others(4): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33459673 | |||||||
chr19:33459863 | T | C | 3 | a0005c0008t0001g0247 a0005c0008t0001g0248 a0005c0008t0001g0249 |
3 | NA18969.hp1 NA19068.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.671+3132A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33459863 | |||||||
chr19:33460220 | A | G | 128 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0040 others(125): Show |
131 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.671+2775T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33460220 | |||||||
chr19:33460284 | C | T | 1 | a0001c0001t0001g0018 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.671+2711G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33460284 | |||||||
chr19:33460360 | C | T | 2 | a0001c0001t0003g0273 a0001c0001t0003g0274 |
2 | HG00733.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.671+2635G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33460360 | |||||||
chr19:33460378 | A | G | 2 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.671+2617T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33460378 | |||||||
chr19:33460693 | A | G | 125 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0040 others(122): Show |
128 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.671+2302T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33460693 | |||||||
chr19:33460729 | C | T | 1 | a0001c0001t0003g0087 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.671+2266G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33460729 | |||||||
chr19:33460786 | C | T | 125 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0040 others(122): Show |
128 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.671+2209G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33460786 | |||||||
chr19:33460876 | G | A | 1 | a0001c0001t0001g0018 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.671+2119C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33460876 | |||||||
chr19:33460902 | G | A | 27 | a0001c0001t0001g0180 a0001c0001t0001g0261 a0001c0001t0003g0001 others(24): Show |
30 | HG00639.hp2 HG00642.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.671+2093C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33460902 | |||||||
chr19:33460922 | G | C | 1 | a0002c0002t0002g0258 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.671+2073C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33460922 | |||||||
chr19:33461048 | T | C | 138 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0040 others(135): Show |
141 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.671+1947A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33461048 | |||||||
chr19:33461183 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.671+1812A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33461183 | |||||||
chr19:33461291 | C | T | 128 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0040 others(125): Show |
131 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.671+1704G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33461291 | |||||||
chr19:33461353 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.671+1642C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33461353 | |||||||
chr19:33461439 | C | T | 7 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0308 others(4): Show |
7 | HG02055.hp1 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.671+1556G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33461439 | |||||||
chr19:33461442 | T | C | 128 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0040 others(125): Show |
131 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.671+1553A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33461442 | |||||||
chr19:33461450 | G | A | 23 | a0001c0001t0001g0043 a0001c0001t0001g0191 a0001c0001t0001g0192 others(20): Show |
23 | HG00438.hp1 HG00558.hp1 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.671+1545C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33461450 | |||||||
chr19:33461482 | T | C | 125 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(122): Show |
128 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.671+1513A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33461482 | |||||||
chr19:33461549 | C | T | 3 | a0002c0002t0005g0091 a0002c0002t0005g0208 a0002c0002t0005g0298 |
3 | HG02258.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.671+1446G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33461549 | |||||||
chr19:33461567 | G | A | 3 | a0001c0001t0001g0002 a0001c0001t0001g0109 a0001c0001t0001g0110 |
4 | HG00099.hp2 HG01074.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.671+1428C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33461567 | |||||||
chr19:33461673 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.671+1322A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33461673 | |||||||
chr19:33461729 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.671+1266C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33461729 | |||||||
chr19:33461734 | G | A | 1 | a0003c0005t0001g0015 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.671+1261C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33461734 | |||||||
chr19:33461806 | G | A | 1 | a0002c0002t0002g0258 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.671+1189C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33461806 | |||||||
chr19:33461818 | C | T | 123 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(120): Show |
126 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.671+1177G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33461818 | |||||||
chr19:33461869 | G | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.671+1126C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33461869 | |||||||
chr19:33462075 | C | T | 5 | a0001c0001t0001g0272 a0001c0001t0003g0275 a0001c0001t0003g0284 others(2): Show |
5 | HG00140.hp1 HG01106.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.671+920G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33462075 | |||||||
chr19:33462136 | A | C | 1 | a0001c0001t0001g0024 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.671+859T>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33462136 | |||||||
chr19:33462137 | G | A | 1 | a0001c0001t0001g0024 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.671+858C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33462137 | |||||||
chr19:33462177 | G | C | 1 | a0003c0004t0001g0070 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.671+818C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33462177 | |||||||
chr19:33462282 | C | T | 123 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(120): Show |
126 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.671+713G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33462282 | |||||||
chr19:33462313 | GTGGTACC others(5): Show |
G | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.671+670_671+681del others(12): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33462313 | |||||||
chr19:33462448 | T | G | 96 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(93): Show |
96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.671+547A>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33462448 | |||||||
chr19:33462523 | C | G | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.671+472G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33462523 | |||||||
chr19:33462592 | T | A | 7 | a0001c0001t0001g0004 a0001c0001t0001g0154 a0001c0001t0001g0155 others(4): Show |
8 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(5): Show |
intron_variant | MODIFIER | c.671+403A>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33462592 | |||||||
chr19:33462689 | T | C | 1 | a0001c0003t0001g0217 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.671+306A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33462689 | |||||||
chr19:33462837 | A | G | 129 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0040 others(126): Show |
132 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.671+158T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33462837 | |||||||
chr19:33462893 | C | T | 1 | a0003c0004t0001g0096 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.671+102G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33462893 | |||||||
chr19:33462894 | G | A | 44 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(41): Show |
44 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.671+101C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33462894 | |||||||
chr19:33462925 | T | C | 59 | a0001c0001t0001g0043 a0001c0001t0001g0191 a0001c0001t0001g0192 others(56): Show |
59 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.671+70A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 9/14 | chr19 | 33462925 | |||||||
chr19:33463096 | C | A | 1 | a0002c0002t0002g0128 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.625-55G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 8/14 | chr19 | 33463096 | |||||||
chr19:33463417 | C | T | 1 | a0001c0003t0001g0239 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.625-376G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 8/14 | chr19 | 33463417 | |||||||
chr19:33463547 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.624+440A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 8/14 | chr19 | 33463547 | |||||||
chr19:33463682 | T | G | 35 | a0001c0001t0001g0180 a0001c0001t0001g0261 a0001c0001t0003g0001 others(32): Show |
38 | HG00639.hp2 HG00642.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.624+305A>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 8/14 | chr19 | 33463682 | |||||||
chr19:33463753 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.624+234G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 8/14 | chr19 | 33463753 | |||||||
chr19:33463811 | C | T | 12 | a0001c0001t0001g0180 a0001c0001t0001g0261 a0001c0001t0003g0001 others(9): Show |
14 | HG00639.hp2 HG00642.hp1 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.624+176G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 8/14 | chr19 | 33463811 | |||||||
chr19:33463867 | T | A | 44 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(41): Show |
44 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.624+120A>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 8/14 | chr19 | 33463867 | |||||||
chr19:33463972 | C | T | 1 | a0002c0002t0002g0038 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.624+15G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 8/14 | chr19 | 33463972 | |||||||
chr19:33464294 | C | G | 9 | a0001c0001t0001g0261 a0001c0001t0003g0001 a0001c0001t0003g0179 others(6): Show |
11 | HG00639.hp2 HG00642.hp1 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.549-232G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33464294 | |||||||
chr19:33464429 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.549-367C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33464429 | |||||||
chr19:33464578 | G | A | 1 | a0001c0007t0001g0242 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.549-516C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33464578 | |||||||
chr19:33464579 | T | C | 35 | a0001c0001t0001g0180 a0001c0001t0001g0261 a0001c0001t0003g0001 others(32): Show |
38 | HG00639.hp2 HG00642.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.549-517A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33464579 | |||||||
chr19:33464663 | G | A | 3 | a0002c0002t0005g0091 a0002c0002t0005g0208 a0002c0002t0005g0298 |
3 | HG02258.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.549-601C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33464663 | |||||||
chr19:33464760 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.549-698A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33464760 | |||||||
chr19:33464914 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.549-852G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33464914 | |||||||
chr19:33465006 | G | A | 3 | a0002c0002t0002g0290 a0002c0002t0002g0291 a0002c0002t0002g0292 |
3 | HG02451.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.549-944C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33465006 | |||||||
chr19:33465246 | T | C | 13 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(10): Show |
13 | HG01099.hp2 HG02257.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.549-1184A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33465246 | |||||||
chr19:33465474 | C | T | 8 | a0001c0001t0001g0004 a0001c0001t0001g0154 a0001c0001t0001g0155 others(5): Show |
9 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(6): Show |
intron_variant | MODIFIER | c.549-1412G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33465474 | |||||||
chr19:33465731 | G | A | 5 | a0004c0006t0001g0296 a0004c0006t0001g0297 a0004c0006t0001g0300 others(2): Show |
5 | HG02809.hp1 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.549-1669C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33465731 | |||||||
chr19:33465786 | C | T | 3 | a0002c0002t0005g0091 a0002c0002t0005g0208 a0002c0002t0005g0298 |
3 | HG02258.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.549-1724G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33465786 | |||||||
chr19:33466118 | T | C | 12 | a0001c0001t0001g0180 a0001c0001t0001g0261 a0001c0001t0003g0001 others(9): Show |
14 | HG00639.hp2 HG00642.hp1 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.549-2056A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33466118 | |||||||
chr19:33466317 | A | G | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.549-2255T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33466317 | |||||||
chr19:33466320 | T | C | 1 | a0002c0002t0002g0010 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.549-2258A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33466320 | |||||||
chr19:33466494 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.549-2432G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33466494 | |||||||
chr19:33466535 | A | G | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.549-2473T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33466535 | |||||||
chr19:33466644 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.549-2582A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33466644 | |||||||
chr19:33466665 | C | T | 4 | a0001c0001t0001g0176 a0002c0002t0002g0028 a0002c0002t0002g0174 others(1): Show |
4 | HG01891.hp1 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.549-2603G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33466665 | |||||||
chr19:33466757 | GA | G | 12 | a0001c0001t0001g0178 a0001c0001t0001g0264 a0001c0001t0001g0265 others(9): Show |
12 | HG01074.hp1 HG01891.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.549-2696delT | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33466757 | |||||||
chr19:33466769 | A | G | 1 | a0002c0002t0002g0122 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.549-2707T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33466769 | |||||||
chr19:33466769 | AGAAAT | A | 50 | a0001c0001t0001g0043 a0001c0001t0001g0191 a0001c0001t0001g0192 others(47): Show |
50 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.549-2712_549-2708d others(7): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33466769 | |||||||
chr19:33466774 | T | A | 2 | a0001c0001t0001g0216 a0001c0003t0001g0195 |
2 | HG02155.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.549-2712A>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33466774 | |||||||
chr19:33466779 | A | T | 4 | a0001c0003t0001g0195 a0001c0003t0001g0196 a0001c0003t0001g0197 others(1): Show |
4 | NA18955.hp2 NA18979.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.549-2717T>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33466779 | |||||||
chr19:33466781 | T | A | 1 | a0001c0001t0001g0170 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.549-2719A>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33466781 | |||||||
chr19:33467030 | G | A | 3 | a0003c0004t0001g0095 a0003c0004t0001g0096 a0003c0004t0001g0097 |
3 | NA18951.hp2 NA18968.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.549-2968C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33467030 | |||||||
chr19:33467073 | T | C | 129 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0040 others(126): Show |
132 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.549-3011A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33467073 | |||||||
chr19:33467090 | G | A | 1 | a0001c0001t0001g0295 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.549-3028C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33467090 | |||||||
chr19:33467156 | CA | C | 13 | a0001c0001t0001g0049 a0001c0003t0001g0232 a0001c0007t0001g0212 others(10): Show |
13 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.549-3095delT | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33467156 | |||||||
chr19:33467156 | CAA | C | 126 | a0001c0001t0001g0023 a0001c0001t0001g0040 a0001c0001t0001g0041 others(123): Show |
129 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.549-3096_549-3095d others(4): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33467156 | |||||||
chr19:33467173 | A | G | 1 | a0001c0001t0001g0024 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.549-3111T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33467173 | |||||||
chr19:33467249 | T | TG | 19 | a0001c0001t0001g0082 a0001c0001t0001g0272 a0001c0001t0001g0278 others(16): Show |
19 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.549-3188dupC | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33467249 | |||||||
chr19:33467315 | G | A | 2 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.549-3253C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33467315 | |||||||
chr19:33467323 | T | C | 1 | a0002c0002t0005g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.549-3261A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33467323 | |||||||
chr19:33467348 | C | CT | 15 | a0001c0007t0001g0005 a0001c0007t0001g0212 a0001c0007t0001g0242 others(12): Show |
16 | HG01109.hp1 HG01168.hp1 HG02129.hp1 others(13): Show |
intron_variant | MODIFIER | c.549-3287dupA | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33467348 | |||||||
chr19:33467348 | C | CTT | 12 | a0001c0001t0001g0180 a0001c0001t0001g0261 a0001c0001t0003g0001 others(9): Show |
14 | HG00639.hp2 HG00642.hp1 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.549-3288_549-3287d others(4): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33467348 | |||||||
chr19:33467430 | C | T | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG00642.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.549-3368G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33467430 | |||||||
chr19:33467475 | G | A | 2 | a0002c0002t0002g0256 a0002c0002t0002g0257 |
2 | HG01433.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.549-3413C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33467475 | |||||||
chr19:33467550 | T | A | 44 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(41): Show |
44 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.549-3488A>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33467550 | |||||||
chr19:33467721 | G | A | 1 | a0003c0005t0001g0016 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.549-3659C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33467721 | |||||||
chr19:33467962 | C | T | 3 | a0001c0001t0001g0141 a0002c0002t0002g0122 a0002c0002t0002g0128 |
3 | HG03486.hp2 HG03516.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.549-3900G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33467962 | |||||||
chr19:33467990 | C | T | 27 | a0001c0001t0001g0180 a0001c0001t0001g0261 a0001c0001t0003g0001 others(24): Show |
30 | HG00639.hp2 HG00642.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.549-3928G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33467990 | |||||||
chr19:33468066 | T | C | 44 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(41): Show |
44 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.549-4004A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33468066 | |||||||
chr19:33468138 | G | C | 1 | a0001c0001t0001g0114 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.549-4076C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33468138 | |||||||
chr19:33468236 | T | C | 129 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0040 others(126): Show |
132 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.549-4174A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33468236 | |||||||
chr19:33468384 | C | T | 2 | a0001c0001t0003g0273 a0001c0001t0003g0274 |
2 | HG00733.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.549-4322G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33468384 | |||||||
chr19:33468525 | G | A | 3 | a0001c0001t0001g0098 a0001c0001t0001g0107 a0001c0001t0001g0131 |
3 | HG01175.hp2 HG01255.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.549-4463C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33468525 | |||||||
chr19:33468533 | G | A | 1 | a0001c0001t0001g0018 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.549-4471C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33468533 | |||||||
chr19:33468601 | C | T | 15 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0266 others(12): Show |
15 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.549-4539G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33468601 | |||||||
chr19:33468627 | G | A | 23 | a0001c0001t0001g0043 a0001c0001t0001g0191 a0001c0001t0001g0192 others(20): Show |
23 | HG00438.hp1 HG00558.hp1 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.549-4565C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33468627 | |||||||
chr19:33468679 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.549-4617G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33468679 | |||||||
chr19:33468698 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.549-4636G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33468698 | |||||||
chr19:33468724 | G | A | 1 | a0002c0002t0005g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.549-4662C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33468724 | |||||||
chr19:33468782 | T | A | 2 | a0001c0001t0001g0294 a0002c0002t0002g0241 |
2 | HG01884.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.549-4720A>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33468782 | |||||||
chr19:33468971 | C | T | 10 | a0002c0002t0002g0006 a0002c0002t0002g0008 a0002c0002t0002g0009 others(7): Show |
10 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.549-4909G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33468971 | |||||||
chr19:33469159 | G | A | 5 | a0001c0001t0001g0265 a0001c0001t0001g0288 a0001c0001t0001g0289 others(2): Show |
5 | HG02258.hp2 HG02630.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.549-5097C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33469159 | |||||||
chr19:33469248 | C | A | 13 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(10): Show |
13 | HG01099.hp2 HG02257.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.549-5186G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33469248 | |||||||
chr19:33469280 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.549-5218G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33469280 | |||||||
chr19:33469451 | C | T | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0308 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.549-5389G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33469451 | |||||||
chr19:33469490 | T | C | 21 | a0001c0001t0001g0082 a0001c0001t0001g0170 a0001c0001t0001g0173 others(18): Show |
21 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.549-5428A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33469490 | |||||||
chr19:33469540 | CA | C | 4 | a0001c0001t0001g0019 a0001c0001t0001g0137 a0001c0001t0001g0140 others(1): Show |
4 | HG01070.hp1 HG01071.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.549-5479delT | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33469540 | |||||||
chr19:33469652 | C | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.549-5590G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33469652 | |||||||
chr19:33469887 | C | T | 15 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0266 others(12): Show |
15 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.549-5825G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33469887 | |||||||
chr19:33469912 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.549-5850C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33469912 | |||||||
chr19:33470289 | G | A | 3 | a0001c0001t0004g0076 a0002c0002t0002g0086 a0002c0002t0002g0164 |
3 | NA18970.hp2 NA18984.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.549-6227C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33470289 | |||||||
chr19:33470400 | T | C | 129 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0040 others(126): Show |
132 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.549-6338A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33470400 | |||||||
chr19:33470496 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.549-6434G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33470496 | |||||||
chr19:33470514 | C | A | 2 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.549-6452G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33470514 | |||||||
chr19:33470638 | G | A | 3 | a0002c0002t0005g0091 a0002c0002t0005g0208 a0002c0002t0005g0298 |
3 | HG02258.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.549-6576C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33470638 | |||||||
chr19:33470644 | C | T | 124 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(121): Show |
127 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.549-6582G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33470644 | |||||||
chr19:33470679 | T | A | 10 | a0002c0002t0002g0006 a0002c0002t0002g0008 a0002c0002t0002g0009 others(7): Show |
10 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.549-6617A>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33470679 | |||||||
chr19:33470744 | C | T | 1 | a0002c0002t0002g0174 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.549-6682G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33470744 | |||||||
chr19:33471012 | T | A | 2 | a0001c0001t0001g0191 a0001c0001t0001g0192 |
2 | NA18970.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.549-6950A>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33471012 | |||||||
chr19:33471073 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.548+6973G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33471073 | |||||||
chr19:33471172 | C | G | 1 | a0002c0002t0002g0258 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.548+6874G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33471172 | |||||||
chr19:33471195 | G | C | 1 | a0002c0002t0002g0236 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.548+6851C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33471195 | |||||||
chr19:33471222 | T | C | 12 | a0001c0001t0001g0180 a0001c0001t0001g0261 a0001c0001t0003g0001 others(9): Show |
14 | HG00639.hp2 HG00642.hp1 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.548+6824A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33471222 | |||||||
chr19:33471266 | G | A | 129 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0040 others(126): Show |
132 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.548+6780C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33471266 | |||||||
chr19:33471300 | G | A | 1 | a0001c0003t0001g0200 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.548+6746C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33471300 | |||||||
chr19:33471424 | G | A | 36 | a0001c0001t0001g0082 a0001c0001t0001g0170 a0001c0001t0001g0173 others(33): Show |
36 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.548+6622C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33471424 | |||||||
chr19:33471451 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.548+6595T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33471451 | |||||||
chr19:33471460 | G | A | 2 | a0002c0002t0002g0034 a0002c0002t0002g0035 |
2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.548+6586C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33471460 | |||||||
chr19:33471521 | G | A | 1 | a0002c0002t0002g0081 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.548+6525C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33471521 | |||||||
chr19:33471590 | T | A | 3 | a0002c0002t0005g0091 a0002c0002t0005g0208 a0002c0002t0005g0298 |
3 | HG02258.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.548+6456A>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33471590 | |||||||
chr19:33471658 | C | A | 1 | a0002c0002t0002g0081 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.548+6388G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33471658 | |||||||
chr19:33471671 | A | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.548+6375T>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33471671 | |||||||
chr19:33471801 | C | T | 1 | a0003c0005t0001g0243 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.548+6245G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33471801 | |||||||
chr19:33471836 | C | T | 1 | a0004c0006t0001g0303 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.548+6210G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33471836 | |||||||
chr19:33471856 | A | T | 1 | a0001c0001t0001g0279 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.548+6190T>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33471856 | |||||||
chr19:33471912 | G | A | 1 | a0002c0002t0002g0299 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.548+6134C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33471912 | |||||||
chr19:33472017 | C | T | 1 | a0001c0001t0001g0018 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.548+6029G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33472017 | |||||||
chr19:33472117 | A | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.548+5929T>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33472117 | |||||||
chr19:33472161 | CA | C | 9 | a0001c0001t0001g0082 a0001c0001t0001g0305 a0001c0001t0001g0306 others(6): Show |
9 | HG02055.hp1 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.548+5884delT | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33472161 | |||||||
chr19:33472161 | CAA | C | 120 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0040 others(117): Show |
123 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.548+5883_548+5884d others(4): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33472161 | |||||||
chr19:33472175 | A | C | 1 | a0001c0001t0001g0024 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.548+5871T>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33472175 | |||||||
chr19:33472366 | T | C | 5 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(2): Show |
5 | HG01099.hp2 HG02257.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.548+5680A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33472366 | |||||||
chr19:33472435 | C | T | 1 | a0001c0003t0001g0196 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.548+5611G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33472435 | |||||||
chr19:33472452 | A | G | 3 | a0001c0003t0001g0220 a0002c0002t0002g0218 a0002c0002t0002g0219 |
3 | HG00597.hp1 HG02071.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.548+5594T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33472452 | |||||||
chr19:33472538 | A | T | 140 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0024 others(137): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.548+5508T>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33472538 | |||||||
chr19:33472664 | A | G | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.548+5382T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33472664 | |||||||
chr19:33472808 | A | C | 3 | a0002c0002t0005g0091 a0002c0002t0005g0208 a0002c0002t0005g0298 |
3 | HG02258.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.548+5238T>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33472808 | |||||||
chr19:33472860 | C | T | 84 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(81): Show |
84 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.548+5186G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33472860 | |||||||
chr19:33473098 | C | T | 12 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(9): Show |
12 | HG01099.hp2 HG02257.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.548+4948G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33473098 | |||||||
chr19:33473156 | C | T | 1 | a0001c0001t0001g0289 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.548+4890G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33473156 | |||||||
chr19:33473269 | G | A | 1 | a0002c0002t0002g0008 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.548+4777C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33473269 | |||||||
chr19:33473274 | A | G | 4 | a0002c0002t0005g0091 a0002c0002t0005g0208 a0002c0002t0005g0298 others(1): Show |
4 | HG02258.hp1 HG06807.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.548+4772T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33473274 | |||||||
chr19:33473275 | T | C | 129 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0040 others(126): Show |
132 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.548+4771A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33473275 | |||||||
chr19:33473378 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.548+4668G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33473378 | |||||||
chr19:33473450 | T | C | 10 | a0002c0002t0002g0006 a0002c0002t0002g0008 a0002c0002t0002g0009 others(7): Show |
10 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.548+4596A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33473450 | |||||||
chr19:33473535 | AAC | A | 10 | a0002c0002t0002g0006 a0002c0002t0002g0008 a0002c0002t0002g0009 others(7): Show |
10 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.548+4509_548+4510d others(4): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33473535 | |||||||
chr19:33473546 | G | A | 44 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(41): Show |
44 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.548+4500C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33473546 | |||||||
chr19:33473569 | G | A | 13 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0266 others(10): Show |
13 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.548+4477C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33473569 | |||||||
chr19:33473585 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.548+4461G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33473585 | |||||||
chr19:33473602 | C | T | 1 | a0001c0001t0003g0087 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.548+4444G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33473602 | |||||||
chr19:33473611 | G | A | 1 | a0002c0002t0002g0044 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.548+4435C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33473611 | |||||||
chr19:33473627 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.548+4419G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33473627 | |||||||
chr19:33473880 | C | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.548+4166G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33473880 | |||||||
chr19:33474003 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.548+4043G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33474003 | |||||||
chr19:33474072 | A | G | 1 | a0002c0002t0002g0258 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.548+3974T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33474072 | |||||||
chr19:33474432 | C | A | 2 | a0001c0001t0001g0170 a0001c0001t0001g0173 |
2 | HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.548+3614G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33474432 | |||||||
chr19:33474507 | A | G | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.548+3539T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33474507 | |||||||
chr19:33474606 | C | T | 10 | a0002c0002t0002g0006 a0002c0002t0002g0008 a0002c0002t0002g0009 others(7): Show |
10 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.548+3440G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33474606 | |||||||
chr19:33474662 | T | C | 126 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0040 others(123): Show |
129 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.548+3384A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33474662 | |||||||
chr19:33474858 | G | C | 1 | a0001c0001t0001g0022 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.548+3188C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33474858 | |||||||
chr19:33474895 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.548+3151C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33474895 | |||||||
chr19:33474910 | G | A | 124 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(121): Show |
127 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.548+3136C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33474910 | |||||||
chr19:33474981 | TAAAAAAA others(3): Show |
T | 19 | a0001c0001t0001g0082 a0001c0001t0001g0272 a0001c0001t0001g0278 others(16): Show |
19 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.548+3055_548+3064d others(12): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33474981 | |||||||
chr19:33474993 | A | G | 44 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(41): Show |
44 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.548+3053T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33474993 | |||||||
chr19:33475166 | G | C | 10 | a0002c0002t0002g0006 a0002c0002t0002g0008 a0002c0002t0002g0009 others(7): Show |
10 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.548+2880C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33475166 | |||||||
chr19:33475170 | A | G | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG02165.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.548+2876T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33475170 | |||||||
chr19:33475191 | T | C | 12 | a0001c0003t0001g0209 a0001c0003t0001g0220 a0001c0003t0001g0232 others(9): Show |
12 | HG00544.hp1 HG00597.hp1 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.548+2855A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33475191 | |||||||
chr19:33475288 | G | C | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0308 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.548+2758C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33475288 | |||||||
chr19:33475348 | G | A | 1 | a0006c0010t0005g0168 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.548+2698C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33475348 | |||||||
chr19:33475547 | T | C | 60 | a0001c0001t0001g0043 a0001c0001t0001g0191 a0001c0001t0001g0192 others(57): Show |
60 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.548+2499A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33475547 | |||||||
chr19:33475562 | C | T | 13 | a0001c0001t0001g0027 a0001c0001t0001g0037 a0001c0001t0001g0127 others(10): Show |
13 | HG01257.hp2 HG02293.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.548+2484G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33475562 | |||||||
chr19:33475576 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.548+2470G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33475576 | |||||||
chr19:33475724 | C | T | 1 | a0002c0002t0002g0149 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.548+2322G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33475724 | |||||||
chr19:33475733 | T | C | 1 | a0001c0001t0001g0178 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.548+2313A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33475733 | |||||||
chr19:33475735 | G | A | 84 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(81): Show |
84 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.548+2311C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33475735 | |||||||
chr19:33475755 | C | T | 44 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(41): Show |
44 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.548+2291G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33475755 | |||||||
chr19:33476020 | A | C | 139 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0040 others(136): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.548+2026T>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33476020 | |||||||
chr19:33476038 | T | C | 7 | a0002c0002t0002g0299 a0004c0006t0001g0296 a0004c0006t0001g0297 others(4): Show |
7 | HG02257.hp2 HG02809.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.548+2008A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33476038 | |||||||
chr19:33476248 | C | T | 10 | a0002c0002t0002g0006 a0002c0002t0002g0008 a0002c0002t0002g0009 others(7): Show |
10 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.548+1798G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33476248 | |||||||
chr19:33476287 | G | A | 1 | a0002c0002t0005g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.548+1759C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33476287 | |||||||
chr19:33476296 | C | T | 27 | a0001c0001t0001g0180 a0001c0001t0001g0261 a0001c0001t0003g0001 others(24): Show |
30 | HG00639.hp2 HG00642.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.548+1750G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33476296 | |||||||
chr19:33476379 | T | C | 1 | a0002c0002t0002g0299 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.548+1667A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33476379 | |||||||
chr19:33476477 | A | G | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.548+1569T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33476477 | |||||||
chr19:33476482 | C | T | 10 | a0002c0002t0002g0006 a0002c0002t0002g0008 a0002c0002t0002g0009 others(7): Show |
10 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.548+1564G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33476482 | |||||||
chr19:33476543 | C | A | 1 | a0001c0001t0003g0275 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.548+1503G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33476543 | |||||||
chr19:33476724 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.548+1322G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33476724 | |||||||
chr19:33476726 | T | C | 152 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0024 others(149): Show |
155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.548+1320A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33476726 | |||||||
chr19:33476730 | C | T | 56 | a0001c0001t0001g0043 a0001c0001t0001g0191 a0001c0001t0001g0192 others(53): Show |
56 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.548+1316G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33476730 | |||||||
chr19:33476853 | C | T | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0308 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.548+1193G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33476853 | |||||||
chr19:33476888 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.548+1158G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33476888 | |||||||
chr19:33477069 | C | A | 1 | a0001c0001t0003g0276 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.548+977G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33477069 | |||||||
chr19:33477110 | C | T | 5 | a0001c0003t0001g0250 a0001c0003t0001g0251 a0001c0003t0001g0252 others(2): Show |
5 | HG01192.hp2 HG01243.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.548+936G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33477110 | |||||||
chr19:33477229 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.548+817G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33477229 | |||||||
chr19:33477512 | C | G | 129 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0040 others(126): Show |
132 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.548+534G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33477512 | |||||||
chr19:33477623 | T | C | 127 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0040 others(124): Show |
130 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.548+423A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33477623 | |||||||
chr19:33477809 | T | C | 27 | a0001c0001t0001g0180 a0001c0001t0001g0261 a0001c0001t0003g0001 others(24): Show |
30 | HG00639.hp2 HG00642.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.548+237A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33477809 | |||||||
chr19:33477908 | GA | G | 19 | a0001c0001t0001g0082 a0001c0001t0001g0272 a0001c0001t0001g0278 others(16): Show |
19 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.548+137delT | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33477908 | |||||||
chr19:33477959 | G | A | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0308 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.548+87C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 7/14 | chr19 | 33477959 | |||||||
chr19:33478099 | C | T | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | NA18954.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.504-9G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33478099 | |||||||
chr19:33478137 | T | C | 1 | a0001c0001t0004g0076 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.504-47A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33478137 | |||||||
chr19:33478167 | A | G | 1 | a0002c0002t0002g0006 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.504-77T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33478167 | |||||||
chr19:33478237 | T | C | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0308 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.504-147A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33478237 | |||||||
chr19:33478341 | C | G | 2 | a0001c0001t0001g0170 a0001c0001t0001g0173 |
2 | HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.504-251G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33478341 | |||||||
chr19:33478526 | G | C | 126 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0040 others(123): Show |
129 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.504-436C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33478526 | |||||||
chr19:33478554 | G | C | 16 | a0001c0001t0001g0272 a0001c0001t0001g0278 a0001c0001t0001g0279 others(13): Show |
16 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.504-464C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33478554 | |||||||
chr19:33478615 | T | A | 129 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0040 others(126): Show |
132 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.504-525A>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33478615 | |||||||
chr19:33478664 | A | T | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | NA18989.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.504-574T>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33478664 | |||||||
chr19:33478862 | C | T | 3 | a0002c0002t0005g0091 a0002c0002t0005g0208 a0002c0002t0005g0298 |
3 | HG02258.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.504-772G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33478862 | |||||||
chr19:33478909 | C | T | 139 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0040 others(136): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.504-819G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33478909 | |||||||
chr19:33478918 | A | G | 2 | a0002c0002t0002g0028 a0002c0002t0002g0175 |
2 | HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.504-828T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33478918 | |||||||
chr19:33478937 | A | G | 1 | a0001c0001t0001g0216 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.504-847T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33478937 | |||||||
chr19:33478992 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.504-902C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33478992 | |||||||
chr19:33479035 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.504-945G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33479035 | |||||||
chr19:33479036 | G | A | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0308 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.504-946C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33479036 | |||||||
chr19:33479056 | G | A | 10 | a0002c0002t0002g0006 a0002c0002t0002g0008 a0002c0002t0002g0009 others(7): Show |
10 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.504-966C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33479056 | |||||||
chr19:33479069 | T | A | 139 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0040 others(136): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.504-979A>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33479069 | |||||||
chr19:33479231 | G | T | 126 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0040 others(123): Show |
129 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.504-1141C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33479231 | |||||||
chr19:33479236 | T | A | 1 | a0001c0001t0001g0237 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.504-1146A>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33479236 | |||||||
chr19:33479399 | G | A | 1 | a0001c0001t0001g0178 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.504-1309C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33479399 | |||||||
chr19:33479443 | T | C | 1 | a0001c0003t0001g0227 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.504-1353A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33479443 | |||||||
chr19:33479460 | T | C | 3 | a0002c0002t0005g0091 a0002c0002t0005g0208 a0002c0002t0005g0298 |
3 | HG02258.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.504-1370A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33479460 | |||||||
chr19:33479497 | T | TAATC | 3 | a0001c0001t0004g0076 a0002c0002t0002g0086 a0002c0002t0002g0164 |
3 | NA18970.hp2 NA18984.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.504-1408_504-1407i others(6): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33479497 | |||||||
chr19:33479543 | C | T | 293 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0018 others(290): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.504-1453G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33479543 | |||||||
chr19:33479609 | G | C | 126 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0040 others(123): Show |
129 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.504-1519C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33479609 | |||||||
chr19:33479858 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.504-1768A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33479858 | |||||||
chr19:33479886 | C | T | 1 | a0001c0001t0001g0027 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.504-1796G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33479886 | |||||||
chr19:33480083 | C | T | 215 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0024 others(212): Show |
218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.504-1993G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33480083 | |||||||
chr19:33480106 | C | T | 12 | a0001c0001t0001g0180 a0001c0001t0001g0261 a0001c0001t0003g0001 others(9): Show |
14 | HG00639.hp2 HG00642.hp1 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.504-2016G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33480106 | |||||||
chr19:33480185 | T | C | 1 | a0002c0002t0002g0029 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.504-2095A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33480185 | |||||||
chr19:33480207 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.504-2117G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33480207 | |||||||
chr19:33480210 | T | C | 1 | a0001c0001t0003g0073 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.504-2120A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33480210 | |||||||
chr19:33480229 | C | T | 1 | a0003c0004t0001g0095 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.504-2139G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33480229 | |||||||
chr19:33480437 | T | C | 1 | a0002c0002t0002g0030 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.504-2347A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33480437 | |||||||
chr19:33480461 | C | T | 7 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0308 others(4): Show |
7 | HG02055.hp1 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.504-2371G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33480461 | |||||||
chr19:33480524 | C | T | 3 | a0001c0001t0004g0063 a0001c0001t0004g0065 a0003c0005t0001g0025 |
3 | NA18971.hp2 NA18975.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.504-2434G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33480524 | |||||||
chr19:33480525 | G | A | 21 | a0001c0001t0001g0082 a0001c0001t0001g0272 a0001c0001t0001g0278 others(18): Show |
21 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.504-2435C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33480525 | |||||||
chr19:33480545 | G | A | 2 | a0006c0010t0002g0166 a0006c0010t0005g0168 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.504-2455C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33480545 | |||||||
chr19:33480579 | G | A | 1 | a0001c0003t0001g0195 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.504-2489C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33480579 | |||||||
chr19:33480603 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.504-2513A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33480603 | |||||||
chr19:33480623 | C | T | 1 | a0003c0004t0001g0095 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.504-2533G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33480623 | |||||||
chr19:33480667 | C | T | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0308 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.504-2577G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33480667 | |||||||
chr19:33480798 | A | T | 1 | a0002c0002t0002g0228 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.504-2708T>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33480798 | |||||||
chr19:33480813 | C | CGT | 68 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0027 others(65): Show |
69 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.504-2725_504-2724d others(4): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33480813 | |||||||
chr19:33480813 | C | CGTGT | 16 | a0001c0001t0001g0104 a0001c0001t0001g0120 a0001c0001t0001g0145 others(13): Show |
16 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.504-2727_504-2724d others(6): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33480813 | |||||||
chr19:33480813 | C | CGTGTGT | 7 | a0001c0003t0001g0167 a0001c0003t0001g0223 a0001c0003t0001g0224 others(4): Show |
7 | NA18943.hp1 NA18957.hp2 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.504-2729_504-2724d others(8): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33480813 | |||||||
chr19:33480813 | CGT | C | 4 | a0001c0001t0001g0002 a0001c0001t0001g0109 a0001c0001t0001g0110 others(1): Show |
5 | HG00099.hp2 HG01074.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.504-2725_504-2724d others(4): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33480813 | |||||||
chr19:33480827 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.504-2737A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33480827 | |||||||
chr19:33480836 | G | GTA | 21 | a0001c0001t0001g0170 a0001c0001t0001g0173 a0001c0001t0001g0264 others(18): Show |
21 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.504-2747_504-2746i others(4): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33480836 | |||||||
chr19:33480838 | G | A | 21 | a0001c0001t0001g0170 a0001c0001t0001g0173 a0001c0001t0001g0264 others(18): Show |
21 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.504-2748C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33480838 | |||||||
chr19:33480838 | G | GTATA | 19 | a0001c0001t0001g0272 a0001c0001t0001g0278 a0001c0001t0001g0279 others(16): Show |
19 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.504-2749_504-2748i others(6): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33480838 | |||||||
chr19:33480840 | G | A | 40 | a0001c0001t0001g0170 a0001c0001t0001g0173 a0001c0001t0001g0264 others(37): Show |
40 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.504-2750C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33480840 | |||||||
chr19:33480840 | G | GTATA | 13 | a0001c0007t0001g0005 a0001c0007t0001g0212 a0001c0007t0001g0242 others(10): Show |
14 | HG01168.hp1 HG02129.hp1 HG03942.hp1 others(11): Show |
intron_variant | MODIFIER | c.504-2754_504-2751d others(6): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33480840 | |||||||
chr19:33480840 | G | GTGTATAT others(1): Show |
10 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0002c0002t0002g0171 others(7): Show |
10 | HG01099.hp2 HG02257.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.504-2751_504-2750i others(10): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33480840 | |||||||
chr19:33480840 | G | GTGTGTAT others(1): Show |
55 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0040 others(52): Show |
57 | HG00099.hp1 HG00609.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.504-2751_504-2750i others(10): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33480840 | |||||||
chr19:33480840 | G | GTGTGTGT others(3): Show |
4 | a0001c0001t0001g0048 a0001c0001t0001g0051 a0001c0001t0001g0071 others(1): Show |
4 | HG02622.hp2 HG03927.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.504-2751_504-2750i others(12): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33480840 | |||||||
chr19:33480842 | A | G | 11 | a0001c0001t0001g0027 a0001c0001t0001g0037 a0002c0002t0002g0029 others(8): Show |
11 | HG02293.hp1 HG02451.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.504-2752T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33480842 | |||||||
chr19:33480859 | C | T | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0308 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.504-2769G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33480859 | |||||||
chr19:33481017 | G | C | 124 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(121): Show |
127 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.504-2927C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33481017 | |||||||
chr19:33481090 | C | A | 2 | a0002c0002t0002g0028 a0002c0002t0002g0175 |
2 | HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.504-3000G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33481090 | |||||||
chr19:33481229 | GAAAC | G | 15 | a0001c0007t0001g0005 a0001c0007t0001g0212 a0001c0007t0001g0242 others(12): Show |
16 | HG01109.hp1 HG01168.hp1 HG02129.hp1 others(13): Show |
intron_variant | MODIFIER | c.504-3143_504-3140d others(6): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33481229 | |||||||
chr19:33481274 | T | C | 2 | a0002c0002t0002g0259 a0002c0002t0002g0260 |
2 | HG01109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.504-3184A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33481274 | |||||||
chr19:33481337 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.504-3247G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33481337 | |||||||
chr19:33481357 | A | C | 13 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(10): Show |
13 | HG02615.hp1 HG02622.hp2 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.504-3267T>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33481357 | |||||||
chr19:33481359 | G | T | 124 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(121): Show |
127 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.504-3269C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33481359 | |||||||
chr19:33481383 | A | G | 1 | a0001c0001t0001g0216 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.504-3293T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33481383 | |||||||
chr19:33481402 | A | AC | 129 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0040 others(126): Show |
132 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.504-3313dupG | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33481402 | |||||||
chr19:33481422 | C | T | 124 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(121): Show |
127 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.504-3332G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33481422 | |||||||
chr19:33481514 | C | T | 3 | a0002c0002t0002g0290 a0002c0002t0002g0291 a0002c0002t0002g0292 |
3 | HG02451.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.504-3424G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33481514 | |||||||
chr19:33481521 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.504-3431C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33481521 | |||||||
chr19:33481952 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.504-3862G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33481952 | |||||||
chr19:33482031 | A | AAAC | 42 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0040 others(39): Show |
45 | HG00639.hp2 HG00642.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.504-3944_504-3942d others(5): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33482031 | |||||||
chr19:33482031 | A | AAACAAC | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0308 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.504-3947_504-3942d others(8): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33482031 | |||||||
chr19:33482179 | A | T | 16 | a0001c0001t0001g0272 a0001c0001t0001g0278 a0001c0001t0001g0279 others(13): Show |
16 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.504-4089T>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33482179 | |||||||
chr19:33482194 | A | G | 1 | a0003c0004t0001g0097 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.504-4104T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33482194 | |||||||
chr19:33482768 | C | T | 1 | a0002c0002t0002g0169 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.504-4678G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33482768 | |||||||
chr19:33482881 | T | C | 57 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(54): Show |
57 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.504-4791A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33482881 | |||||||
chr19:33482885 | G | C | 96 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(93): Show |
96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.504-4795C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33482885 | |||||||
chr19:33482921 | T | C | 28 | a0001c0001t0001g0018 a0001c0001t0001g0180 a0001c0001t0001g0261 others(25): Show |
31 | HG00639.hp2 HG00642.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.504-4831A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33482921 | |||||||
chr19:33483007 | G | A | 98 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0040 others(95): Show |
98 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.504-4917C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33483007 | |||||||
chr19:33483418 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.504-5328A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33483418 | |||||||
chr19:33483570 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.504-5480C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33483570 | |||||||
chr19:33483668 | G | A | 1 | a0001c0003t0001g0246 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.504-5578C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33483668 | |||||||
chr19:33483674 | T | C | 1 | a0001c0003t0001g0007 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.504-5584A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33483674 | |||||||
chr19:33483930 | C | A | 4 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(1): Show |
4 | HG01099.hp2 HG02257.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.504-5840G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33483930 | |||||||
chr19:33483937 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.504-5847A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33483937 | |||||||
chr19:33483948 | A | G | 57 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(54): Show |
57 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.504-5858T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33483948 | |||||||
chr19:33483954 | T | C | 1 | a0001c0001t0001g0177 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.504-5864A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33483954 | |||||||
chr19:33483961 | C | T | 2 | a0002c0002t0002g0213 a0002c0002t0002g0214 |
2 | HG00544.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.504-5871G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33483961 | |||||||
chr19:33484050 | G | C | 5 | a0001c0001t0001g0272 a0001c0001t0003g0275 a0001c0001t0003g0284 others(2): Show |
5 | HG00140.hp1 HG01106.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.503+5946C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33484050 | |||||||
chr19:33484333 | C | A | 1 | a0003c0004t0001g0097 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.503+5663G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33484333 | |||||||
chr19:33484365 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.503+5631G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33484365 | |||||||
chr19:33484438 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.503+5558A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33484438 | |||||||
chr19:33484439 | G | A | 3 | a0001c0001t0001g0120 a0001c0001t0001g0152 a0001c0001t0001g0153 |
3 | NA18989.hp2 NA19005.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.503+5557C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33484439 | |||||||
chr19:33484670 | G | C | 1 | a0003c0004t0001g0095 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.503+5326C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33484670 | |||||||
chr19:33484761 | G | GAC | 3 | a0001c0001t0001g0170 a0001c0001t0001g0173 a0002c0002t0005g0091 |
3 | HG02280.hp1 HG02622.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.503+5233_503+5234d others(4): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33484761 | |||||||
chr19:33484821 | C | T | 44 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(41): Show |
44 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.503+5175G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33484821 | |||||||
chr19:33484936 | G | A | 3 | a0002c0002t0005g0091 a0002c0002t0005g0208 a0002c0002t0005g0298 |
3 | HG02258.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.503+5060C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33484936 | |||||||
chr19:33484951 | C | T | 12 | a0001c0001t0001g0180 a0001c0001t0001g0261 a0001c0001t0003g0001 others(9): Show |
14 | HG00639.hp2 HG00642.hp1 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.503+5045G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33484951 | |||||||
chr19:33485032 | G | A | 13 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0266 others(10): Show |
13 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.503+4964C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33485032 | |||||||
chr19:33485093 | C | G | 8 | a0004c0006t0001g0296 a0004c0006t0001g0297 a0004c0006t0001g0300 others(5): Show |
8 | HG02809.hp1 HG02818.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.503+4903G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33485093 | |||||||
chr19:33485100 | G | A | 1 | a0001c0001t0001g0279 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.503+4896C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33485100 | |||||||
chr19:33485149 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.503+4847G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33485149 | |||||||
chr19:33485221 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.503+4775G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33485221 | |||||||
chr19:33485259 | C | T | 15 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0266 others(12): Show |
15 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.503+4737G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33485259 | |||||||
chr19:33485265 | AG | A | 8 | a0001c0001t0001g0272 a0001c0001t0003g0073 a0001c0001t0003g0275 others(5): Show |
8 | HG00140.hp1 HG00280.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.503+4730delC | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33485265 | |||||||
chr19:33485355 | T | C | 1 | a0002c0002t0002g0085 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.503+4641A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33485355 | |||||||
chr19:33485388 | G | A | 1 | a0002c0002t0002g0014 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.503+4608C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33485388 | |||||||
chr19:33485475 | A | G | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0308 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.503+4521T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33485475 | |||||||
chr19:33485491 | T | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.503+4505A>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33485491 | |||||||
chr19:33485491 | T | TA | 10 | a0002c0002t0002g0038 a0002c0002t0002g0175 a0004c0006t0001g0296 others(7): Show |
10 | HG02738.hp2 HG02809.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.503+4504dupT | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33485491 | |||||||
chr19:33485491 | T | TAAA | 6 | a0001c0001t0001g0267 a0001c0001t0001g0306 a0001c0001t0001g0308 others(3): Show |
6 | HG02257.hp1 HG02809.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.503+4502_503+4504d others(5): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33485491 | |||||||
chr19:33485491 | T | TAAAA | 53 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(50): Show |
53 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.503+4501_503+4504d others(6): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33485491 | |||||||
chr19:33485491 | T | TAAAAAAA | 13 | a0001c0001t0001g0082 a0001c0001t0001g0272 a0001c0001t0001g0278 others(10): Show |
13 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.503+4498_503+4504d others(9): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33485491 | |||||||
chr19:33485491 | T | TAAAAAAA others(13): Show |
1 | a0002c0002t0002g0258 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.503+4504_503+4505i others(22): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33485491 | |||||||
chr19:33485491 | T | TAAAAAAA others(14): Show |
1 | a0001c0001t0001g0170 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.503+4504_503+4505i others(23): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33485491 | |||||||
chr19:33485491 | T | TAAAAAAA others(25): Show |
1 | a0001c0001t0001g0173 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.503+4504_503+4505i others(34): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33485491 | |||||||
chr19:33485491 | TA | T | 22 | a0001c0001t0001g0111 a0001c0001t0001g0133 a0001c0001t0001g0137 others(19): Show |
22 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.503+4504delT | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33485491 | |||||||
chr19:33485566 | G | A | 13 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(10): Show |
13 | HG01099.hp2 HG02257.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.503+4430C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33485566 | |||||||
chr19:33485649 | A | G | 40 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(37): Show |
43 | HG00639.hp2 HG00642.hp1 HG01099.hp2 others(40): Show |
intron_variant | MODIFIER | c.503+4347T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33485649 | |||||||
chr19:33485733 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.503+4263C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33485733 | |||||||
chr19:33485810 | T | C | 1 | a0002c0002t0002g0171 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.503+4186A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33485810 | |||||||
chr19:33485818 | T | C | 12 | a0001c0001t0001g0180 a0001c0001t0001g0261 a0001c0001t0003g0001 others(9): Show |
14 | HG00639.hp2 HG00642.hp1 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.503+4178A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33485818 | |||||||
chr19:33485917 | TTCTG | T | 85 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0048 others(82): Show |
85 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.503+4075_503+4078d others(6): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33485917 | |||||||
chr19:33485982 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.503+4014C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33485982 | |||||||
chr19:33485992 | C | G | 1 | a0001c0001t0001g0075 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.503+4004G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33485992 | |||||||
chr19:33486105 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.503+3891C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33486105 | |||||||
chr19:33486186 | C | T | 1 | a0002c0002t0002g0172 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.503+3810G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33486186 | |||||||
chr19:33486260 | C | A | 1 | a0001c0003t0001g0108 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.503+3736G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33486260 | |||||||
chr19:33486293 | G | C | 1 | a0001c0001t0001g0116 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.503+3703C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33486293 | |||||||
chr19:33486300 | C | G | 85 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0048 others(82): Show |
85 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.503+3696G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33486300 | |||||||
chr19:33486395 | C | T | 44 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(41): Show |
44 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.503+3601G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33486395 | |||||||
chr19:33486413 | C | T | 41 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(38): Show |
44 | HG00639.hp2 HG00642.hp1 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.503+3583G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33486413 | |||||||
chr19:33486464 | C | T | 10 | a0002c0002t0002g0006 a0002c0002t0002g0008 a0002c0002t0002g0009 others(7): Show |
10 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.503+3532G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33486464 | |||||||
chr19:33486490 | T | C | 153 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0024 others(150): Show |
156 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.503+3506A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33486490 | |||||||
chr19:33486552 | C | A | 1 | a0001c0001t0001g0114 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.503+3444G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33486552 | |||||||
chr19:33486598 | T | C | 44 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(41): Show |
44 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.503+3398A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33486598 | |||||||
chr19:33486776 | CAGGGTCC others(2): Show |
C | 27 | a0001c0001t0001g0180 a0001c0001t0001g0261 a0001c0001t0003g0001 others(24): Show |
30 | HG00639.hp2 HG00642.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.503+3211_503+3219d others(11): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33486776 | |||||||
chr19:33486792 | T | C | 1 | a0001c0003t0001g0253 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.503+3204A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33486792 | |||||||
chr19:33486867 | T | TG | 45 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(42): Show |
45 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.503+3128dupC | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33486867 | |||||||
chr19:33486889 | C | T | 1 | a0002c0002t0002g0013 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.503+3107G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33486889 | |||||||
chr19:33486932 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.503+3064G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33486932 | |||||||
chr19:33487072 | A | T | 1 | a0001c0001t0003g0182 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.503+2924T>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33487072 | |||||||
chr19:33487243 | G | T | 1 | a0002c0002t0002g0010 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.503+2753C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33487243 | |||||||
chr19:33487329 | T | C | 1 | a0001c0001t0001g0294 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.503+2667A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33487329 | |||||||
chr19:33487429 | C | G | 2 | a0002c0002t0002g0259 a0002c0002t0002g0260 |
2 | HG01109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.503+2567G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33487429 | |||||||
chr19:33487493 | G | A | 11 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(8): Show |
11 | HG02615.hp1 HG02622.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.503+2503C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33487493 | |||||||
chr19:33487518 | G | A | 27 | a0001c0001t0001g0180 a0001c0001t0001g0261 a0001c0001t0003g0001 others(24): Show |
30 | HG00639.hp2 HG00642.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.503+2478C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33487518 | |||||||
chr19:33487521 | T | C | 1 | a0001c0001t0001g0155 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.503+2475A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33487521 | |||||||
chr19:33487597 | G | C | 1 | a0002c0002t0002g0078 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.503+2399C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33487597 | |||||||
chr19:33487699 | G | A | 1 | a0002c0002t0002g0174 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.503+2297C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33487699 | |||||||
chr19:33487749 | A | T | 1 | a0001c0001t0003g0181 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.503+2247T>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33487749 | |||||||
chr19:33487780 | A | T | 1 | a0001c0001t0001g0203 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.503+2216T>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33487780 | |||||||
chr19:33487781 | GTTTGCAG others(15): Show |
G | 1 | a0001c0001t0001g0203 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.503+2193_503+2214d others(24): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33487781 | |||||||
chr19:33487817 | A | G | 99 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0040 others(96): Show |
99 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.503+2179T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33487817 | |||||||
chr19:33487833 | G | T | 1 | a0001c0001t0001g0061 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.503+2163C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33487833 | |||||||
chr19:33487835 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.503+2161C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33487835 | |||||||
chr19:33487886 | G | T | 1 | a0001c0003t0001g0211 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.503+2110C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33487886 | |||||||
chr19:33487892 | T | C | 1 | a0002c0002t0002g0171 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.503+2104A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33487892 | |||||||
chr19:33488106 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.503+1890G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33488106 | |||||||
chr19:33488203 | T | G | 1 | a0002c0002t0002g0304 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.503+1793A>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33488203 | |||||||
chr19:33488253 | C | A | 1 | a0001c0003t0001g0007 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.503+1743G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33488253 | |||||||
chr19:33488347 | C | T | 18 | a0001c0001t0001g0082 a0001c0001t0001g0272 a0001c0001t0001g0278 others(15): Show |
18 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.503+1649G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33488347 | |||||||
chr19:33488440 | A | G | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.503+1556T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33488440 | |||||||
chr19:33488487 | G | A | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0308 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.503+1509C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33488487 | |||||||
chr19:33488724 | T | G | 1 | a0001c0001t0001g0018 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.503+1272A>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33488724 | |||||||
chr19:33488809 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.503+1187A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33488809 | |||||||
chr19:33488935 | C | T | 13 | a0001c0007t0001g0005 a0001c0007t0001g0212 a0001c0007t0001g0242 others(10): Show |
14 | HG01168.hp1 HG02129.hp1 HG03942.hp1 others(11): Show |
intron_variant | MODIFIER | c.503+1061G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33488935 | |||||||
chr19:33488958 | G | A | 6 | a0001c0001t0001g0043 a0001c0001t0001g0191 a0001c0001t0001g0192 others(3): Show |
6 | HG02071.hp1 NA18951.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.503+1038C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33488958 | |||||||
chr19:33489063 | G | T | 1 | a0003c0005t0001g0243 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.503+933C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33489063 | |||||||
chr19:33489583 | C | T | 10 | a0002c0002t0002g0006 a0002c0002t0002g0008 a0002c0002t0002g0009 others(7): Show |
10 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.503+413G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33489583 | |||||||
chr19:33489637 | T | A | 1 | a0001c0001t0001g0153 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.503+359A>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 6/14 | chr19 | 33489637 | |||||||
chr19:33490087 | C | T | 13 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(10): Show |
13 | HG01099.hp2 HG02257.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.442-30G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 5/14 | chr19 | 33490087 | |||||||
chr19:33490091 | G | A | 1 | a0001c0001t0003g0274 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.442-34C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 5/14 | chr19 | 33490091 | |||||||
chr19:33490093 | C | T | 1 | a0001c0001t0001g0027 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.442-36G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 5/14 | chr19 | 33490093 | |||||||
chr19:33490148 | G | T | 44 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(41): Show |
44 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.442-91C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 5/14 | chr19 | 33490148 | |||||||
chr19:33490267 | T | C | 1 | a0002c0002t0002g0006 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.442-210A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 5/14 | chr19 | 33490267 | |||||||
chr19:33490460 | C | T | 4 | a0001c0001t0001g0119 a0001c0001t0001g0126 a0001c0001t0001g0136 others(1): Show |
4 | HG00639.hp1 HG01361.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-403G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 5/14 | chr19 | 33490460 | |||||||
chr19:33490536 | G | T | 27 | a0001c0001t0001g0180 a0001c0001t0001g0261 a0001c0001t0003g0001 others(24): Show |
30 | HG00639.hp2 HG00642.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.442-479C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 5/14 | chr19 | 33490536 | |||||||
chr19:33490689 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.442-632A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 5/14 | chr19 | 33490689 | |||||||
chr19:33490817 | C | G | 1 | a0002c0002t0002g0164 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.442-760G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 5/14 | chr19 | 33490817 | |||||||
chr19:33491021 | T | C | 117 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0037 others(114): Show |
120 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(117): Show |
intron_variant | MODIFIER | c.442-964A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 5/14 | chr19 | 33491021 | |||||||
chr19:33491055 | G | A | 1 | a0001c0001t0001g0283 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.442-998C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 5/14 | chr19 | 33491055 | |||||||
chr19:33491095 | A | T | 1 | a0001c0003t0001g0221 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.442-1038T>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 5/14 | chr19 | 33491095 | |||||||
chr19:33491099 | A | T | 2 | a0002c0002t0002g0259 a0002c0002t0002g0260 |
2 | HG01109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.442-1042T>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 5/14 | chr19 | 33491099 | |||||||
chr19:33491174 | G | T | 1 | a0002c0002t0002g0171 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.442-1117C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 5/14 | chr19 | 33491174 | |||||||
chr19:33491344 | G | C | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0308 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-1287C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 5/14 | chr19 | 33491344 | |||||||
chr19:33491349 | C | T | 2 | a0001c0001t0001g0170 a0001c0001t0001g0173 |
2 | HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.442-1292G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 5/14 | chr19 | 33491349 | |||||||
chr19:33491652 | C | T | 3 | a0005c0008t0001g0247 a0005c0008t0001g0248 a0005c0008t0001g0249 |
3 | NA18969.hp1 NA19068.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.442-1595G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 5/14 | chr19 | 33491652 | |||||||
chr19:33491681 | T | C | 34 | a0001c0001t0001g0180 a0001c0001t0001g0261 a0001c0001t0003g0001 others(31): Show |
37 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.441+1609A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 5/14 | chr19 | 33491681 | |||||||
chr19:33491862 | T | C | 1 | a0006c0010t0005g0168 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.441+1428A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 5/14 | chr19 | 33491862 | |||||||
chr19:33492001 | T | A | 25 | a0001c0001t0001g0180 a0001c0001t0001g0261 a0001c0001t0003g0001 others(22): Show |
28 | HG00639.hp2 HG00642.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.441+1289A>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 5/14 | chr19 | 33492001 | |||||||
chr19:33492016 | C | T | 1 | a0002c0002t0002g0258 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.441+1274G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 5/14 | chr19 | 33492016 | |||||||
chr19:33492043 | C | CA | 26 | a0001c0001t0001g0170 a0001c0001t0001g0173 a0001c0001t0001g0266 others(23): Show |
26 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.441+1246dupT | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 5/14 | chr19 | 33492043 | |||||||
chr19:33492043 | CA | C | 18 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0040 others(15): Show |
18 | HG01099.hp2 HG01168.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.441+1246delT | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 5/14 | chr19 | 33492043 | |||||||
chr19:33492043 | CAAAAA | C | 7 | a0002c0002t0002g0299 a0004c0006t0001g0296 a0004c0006t0001g0297 others(4): Show |
7 | HG02257.hp2 HG02809.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+1242_441+1246d others(7): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 5/14 | chr19 | 33492043 | |||||||
chr19:33492103 | C | T | 2 | a0002c0002t0002g0259 a0002c0002t0002g0260 |
2 | HG01109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.441+1187G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 5/14 | chr19 | 33492103 | |||||||
chr19:33492187 | C | A | 2 | a0001c0001t0001g0170 a0001c0001t0001g0173 |
2 | HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.441+1103G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 5/14 | chr19 | 33492187 | |||||||
chr19:33492250 | C | T | 46 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(43): Show |
46 | HG00609.hp2 HG00733.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.441+1040G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 5/14 | chr19 | 33492250 | |||||||
chr19:33492313 | G | A | 1 | a0001c0001t0001g0280 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.441+977C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 5/14 | chr19 | 33492313 | |||||||
chr19:33492513 | C | T | 1 | a0002c0002t0002g0029 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.441+777G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 5/14 | chr19 | 33492513 | |||||||
chr19:33492518 | G | T | 1 | a0001c0001t0001g0018 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.441+772C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 5/14 | chr19 | 33492518 | |||||||
chr19:33492666 | C | A | 1 | a0001c0001t0001g0170 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.441+624G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 5/14 | chr19 | 33492666 | |||||||
chr19:33492749 | T | TG | 15 | a0001c0001t0001g0272 a0001c0001t0001g0278 a0001c0001t0001g0279 others(12): Show |
15 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.441+540dupC | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 5/14 | chr19 | 33492749 | |||||||
chr19:33492887 | T | C | 1 | a0001c0003t0001g0246 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.441+403A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 5/14 | chr19 | 33492887 | |||||||
chr19:33492890 | T | G | 1 | a0001c0001t0001g0075 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.441+400A>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 5/14 | chr19 | 33492890 | |||||||
chr19:33492893 | T | C | 1 | a0001c0001t0001g0308 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.441+397A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 5/14 | chr19 | 33492893 | |||||||
chr19:33493004 | G | A | 2 | a0001c0001t0001g0082 a0001c0001t0003g0087 |
2 | HG02698.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.441+286C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 5/14 | chr19 | 33493004 | |||||||
chr19:33493006 | A | G | 4 | a0001c0003t0001g0220 a0002c0002t0002g0218 a0002c0002t0002g0219 others(1): Show |
4 | HG00597.hp1 HG02071.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.441+284T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 5/14 | chr19 | 33493006 | |||||||
chr19:33493053 | T | C | 2 | a0002c0002t0002g0028 a0002c0002t0002g0175 |
2 | HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.441+237A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 5/14 | chr19 | 33493053 | |||||||
chr19:33493144 | T | C | 84 | a0001c0001t0001g0018 a0001c0001t0001g0040 a0001c0001t0001g0041 others(81): Show |
84 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.441+146A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 5/14 | chr19 | 33493144 | |||||||
chr19:33493229 | C | T | 1 | a0002c0002t0002g0171 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.441+61G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 5/14 | chr19 | 33493229 | |||||||
chr19:33493235 | T | C | 3 | a0003c0005t0001g0015 a0003c0005t0001g0016 a0003c0005t0001g0017 |
3 | NA18942.hp2 NA18944.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.441+55A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 5/14 | chr19 | 33493235 | |||||||
chr19:33493371 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.394-34C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33493371 | |||||||
chr19:33493374 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.394-37G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33493374 | |||||||
chr19:33493492 | C | A | 1 | a0002c0002t0002g0174 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.394-155G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33493492 | |||||||
chr19:33493645 | C | T | 2 | a0001c0001t0001g0170 a0001c0001t0001g0173 |
2 | HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.394-308G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33493645 | |||||||
chr19:33493690 | C | G | 51 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(48): Show |
51 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.394-353G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33493690 | |||||||
chr19:33493692 | C | T | 1 | a0002c0002t0002g0171 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.394-355G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33493692 | |||||||
chr19:33493731 | T | G | 1 | a0001c0001t0001g0103 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.394-394A>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33493731 | |||||||
chr19:33493964 | T | C | 83 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(80): Show |
83 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.394-627A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33493964 | |||||||
chr19:33494195 | T | C | 13 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0266 others(10): Show |
13 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.394-858A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33494195 | |||||||
chr19:33494239 | C | G | 1 | a0002c0002t0002g0259 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.394-902G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33494239 | |||||||
chr19:33494301 | G | A | 24 | a0001c0001t0001g0180 a0001c0001t0001g0261 a0001c0001t0003g0001 others(21): Show |
27 | HG00639.hp2 HG00642.hp1 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.394-964C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33494301 | |||||||
chr19:33494360 | C | G | 2 | a0002c0002t0002g0259 a0002c0002t0002g0260 |
2 | HG01109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.394-1023G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33494360 | |||||||
chr19:33494390 | T | C | 1 | a0001c0001t0001g0282 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.394-1053A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33494390 | |||||||
chr19:33494711 | G | C | 1 | a0001c0001t0001g0018 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.394-1374C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33494711 | |||||||
chr19:33494801 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.394-1464G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33494801 | |||||||
chr19:33494831 | T | C | 15 | a0001c0001t0001g0272 a0001c0001t0001g0278 a0001c0001t0001g0279 others(12): Show |
15 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.394-1494A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33494831 | |||||||
chr19:33494853 | C | T | 3 | a0002c0002t0005g0091 a0002c0002t0005g0208 a0002c0002t0005g0298 |
3 | HG02258.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.394-1516G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33494853 | |||||||
chr19:33494902 | G | A | 37 | a0001c0001t0001g0180 a0001c0001t0001g0261 a0001c0001t0001g0264 others(34): Show |
40 | HG00639.hp2 HG00642.hp1 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.394-1565C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33494902 | |||||||
chr19:33494959 | C | T | 2 | a0002c0002t0002g0256 a0002c0002t0002g0257 |
2 | HG01433.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.394-1622G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33494959 | |||||||
chr19:33495006 | G | A | 11 | a0002c0002t0002g0006 a0002c0002t0002g0008 a0002c0002t0002g0009 others(8): Show |
11 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.394-1669C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33495006 | |||||||
chr19:33495068 | G | A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0305 a0001c0001t0001g0306 others(2): Show |
6 | HG01515.hp2 HG01517.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.394-1731C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33495068 | |||||||
chr19:33495079 | T | G | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0308 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-1742A>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33495079 | |||||||
chr19:33495130 | C | T | 83 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(80): Show |
83 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.394-1793G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33495130 | |||||||
chr19:33495287 | C | T | 1 | a0002c0002t0002g0241 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.394-1950G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33495287 | |||||||
chr19:33495311 | G | C | 1 | a0002c0002t0002g0086 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.394-1974C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33495311 | |||||||
chr19:33495412 | C | T | 3 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0295 |
3 | HG01123.hp1 HG01928.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.394-2075G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33495412 | |||||||
chr19:33495473 | G | A | 54 | a0001c0001t0001g0043 a0001c0001t0001g0191 a0001c0001t0001g0192 others(51): Show |
54 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.394-2136C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33495473 | |||||||
chr19:33495500 | C | CA | 9 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0058 others(6): Show |
9 | HG02630.hp1 HG02970.hp1 HG03831.hp2 others(6): Show |
intron_variant | MODIFIER | c.394-2164dupT | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33495500 | |||||||
chr19:33495500 | CA | C | 6 | a0002c0002t0002g0008 a0002c0002t0002g0009 a0002c0002t0002g0012 others(3): Show |
6 | HG00140.hp2 HG01070.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.394-2164delT | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33495500 | |||||||
chr19:33495575 | G | A | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | NA18945.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.394-2238C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33495575 | |||||||
chr19:33495587 | A | G | 1 | a0006c0010t0002g0166 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.394-2250T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33495587 | |||||||
chr19:33495619 | G | A | 48 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(45): Show |
48 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.394-2282C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33495619 | |||||||
chr19:33495756 | C | A | 69 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(66): Show |
69 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.394-2419G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33495756 | |||||||
chr19:33495844 | C | T | 15 | a0001c0001t0001g0272 a0001c0001t0001g0278 a0001c0001t0001g0279 others(12): Show |
15 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.394-2507G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33495844 | |||||||
chr19:33495881 | T | C | 10 | a0002c0002t0002g0006 a0002c0002t0002g0008 a0002c0002t0002g0009 others(7): Show |
10 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.394-2544A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33495881 | |||||||
chr19:33495987 | CAAAAAAC others(3): Show |
C | 46 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(43): Show |
46 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.394-2660_394-2651d others(12): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33495987 | |||||||
chr19:33496093 | C | T | 1 | a0002c0002t0002g0292 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.394-2756G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33496093 | |||||||
chr19:33496168 | A | G | 67 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0024 others(64): Show |
67 | HG00099.hp1 HG00733.hp2 HG01081.hp1 others(64): Show |
intron_variant | MODIFIER | c.394-2831T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33496168 | |||||||
chr19:33496234 | G | C | 27 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0024 others(24): Show |
27 | HG01099.hp2 HG01257.hp2 HG02257.hp2 others(24): Show |
intron_variant | MODIFIER | c.394-2897C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33496234 | |||||||
chr19:33496271 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.394-2934G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33496271 | |||||||
chr19:33496518 | T | G | 70 | a0001c0001t0001g0042 a0001c0001t0001g0048 a0001c0001t0001g0049 others(67): Show |
70 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.394-3181A>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33496518 | |||||||
chr19:33496572 | C | T | 1 | a0004c0006t0001g0297 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.394-3235G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33496572 | |||||||
chr19:33496601 | T | G | 2 | a0002c0002t0002g0259 a0002c0002t0002g0260 |
2 | HG01109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.394-3264A>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33496601 | |||||||
chr19:33496677 | TCA | T | 14 | a0001c0001t0001g0018 a0001c0001t0001g0037 a0001c0001t0001g0121 others(11): Show |
14 | HG01123.hp2 HG02258.hp1 HG02293.hp1 others(11): Show |
intron_variant | MODIFIER | c.394-3342_394-3341d others(4): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33496677 | |||||||
chr19:33496679 | A | T | 288 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(285): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.394-3342T>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33496679 | |||||||
chr19:33496835 | G | T | 49 | a0001c0001t0001g0043 a0001c0001t0001g0191 a0001c0001t0001g0192 others(46): Show |
49 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.394-3498C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33496835 | |||||||
chr19:33496836 | A | T | 49 | a0001c0001t0001g0043 a0001c0001t0001g0191 a0001c0001t0001g0192 others(46): Show |
49 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.394-3499T>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33496836 | |||||||
chr19:33496838 | G | A | 49 | a0001c0001t0001g0043 a0001c0001t0001g0191 a0001c0001t0001g0192 others(46): Show |
49 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.394-3501C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33496838 | |||||||
chr19:33496865 | C | G | 1 | a0001c0003t0001g0108 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.394-3528G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33496865 | |||||||
chr19:33496897 | G | A | 1 | a0001c0003t0001g0238 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.394-3560C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33496897 | |||||||
chr19:33496949 | C | G | 79 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0018 others(76): Show |
81 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.394-3612G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33496949 | |||||||
chr19:33497056 | G | A | 24 | a0001c0001t0001g0136 a0001c0001t0001g0180 a0001c0001t0001g0261 others(21): Show |
26 | HG00639.hp2 HG00642.hp1 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.394-3719C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33497056 | |||||||
chr19:33497223 | C | T | 14 | a0001c0001t0001g0272 a0001c0001t0001g0278 a0001c0001t0001g0279 others(11): Show |
14 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.393+3715G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33497223 | |||||||
chr19:33497228 | C | T | 1 | a0001c0001t0003g0286 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.393+3710G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33497228 | |||||||
chr19:33497295 | G | A | 1 | a0002c0002t0002g0026 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.393+3643C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33497295 | |||||||
chr19:33497475 | T | C | 2 | a0001c0001t0003g0276 a0001c0001t0003g0277 |
2 | HG00280.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.393+3463A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33497475 | |||||||
chr19:33497576 | C | T | 117 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0024 others(114): Show |
117 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.393+3362G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33497576 | |||||||
chr19:33497606 | GAC | G | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0308 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.393+3330_393+3331d others(4): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33497606 | |||||||
chr19:33497607 | A | G | 1 | a0002c0002t0005g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.393+3331T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33497607 | |||||||
chr19:33497610 | A | T | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0308 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.393+3328T>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33497610 | |||||||
chr19:33497611 | G | T | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0308 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.393+3327C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33497611 | |||||||
chr19:33497612 | C | T | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0308 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.393+3326G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33497612 | |||||||
chr19:33497643 | G | A | 9 | a0002c0002t0002g0008 a0002c0002t0002g0009 a0002c0002t0002g0010 others(6): Show |
9 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.393+3295C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33497643 | |||||||
chr19:33497668 | G | C | 7 | a0001c0001t0001g0089 a0001c0001t0001g0123 a0001c0001t0001g0137 others(4): Show |
7 | HG01070.hp1 HG01071.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.393+3270C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33497668 | |||||||
chr19:33497704 | T | C | 1 | a0004c0006t0001g0303 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.393+3234A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33497704 | |||||||
chr19:33497795 | C | CA | 3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 |
3 | HG02074.hp2 HG02129.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.393+3142dupT | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33497795 | |||||||
chr19:33498033 | G | A | 1 | a0005c0008t0001g0249 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.393+2905C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33498033 | |||||||
chr19:33498068 | C | T | 12 | a0001c0007t0001g0005 a0001c0007t0001g0212 a0001c0007t0001g0242 others(9): Show |
13 | HG01168.hp1 HG03942.hp1 NA18942.hp2 others(10): Show |
intron_variant | MODIFIER | c.393+2870G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33498068 | |||||||
chr19:33498229 | G | C | 52 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(49): Show |
52 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.393+2709C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33498229 | |||||||
chr19:33498270 | A | T | 2 | a0002c0002t0005g0091 a0002c0002t0005g0298 |
2 | HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.393+2668T>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33498270 | |||||||
chr19:33498311 | C | T | 1 | a0001c0001t0004g0063 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.393+2627G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33498311 | |||||||
chr19:33498321 | G | A | 15 | a0001c0001t0001g0027 a0001c0001t0001g0037 a0001c0003t0001g0108 others(12): Show |
15 | HG01257.hp2 HG02293.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.393+2617C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33498321 | |||||||
chr19:33498339 | G | A | 54 | a0001c0001t0001g0043 a0001c0001t0001g0191 a0001c0001t0001g0192 others(51): Show |
54 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.393+2599C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33498339 | |||||||
chr19:33498589 | C | G | 68 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(65): Show |
68 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.393+2349G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33498589 | |||||||
chr19:33498737 | GTCCTGGA others(81): Show |
G | 1 | a0001c0001t0001g0116 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.393+2113_393+2200d others(90): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33498737 | |||||||
chr19:33498844 | G | T | 3 | a0001c0001t0003g0073 a0002c0002t0002g0072 a0002c0002t0002g0090 |
3 | HG01081.hp1 HG01081.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.393+2094C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33498844 | |||||||
chr19:33498901 | C | T | 1 | a0002c0002t0002g0171 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.393+2037G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33498901 | |||||||
chr19:33499013 | A | G | 2 | a0001c0001t0001g0170 a0001c0001t0001g0173 |
2 | HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.393+1925T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33499013 | |||||||
chr19:33499201 | A | G | 15 | a0001c0001t0001g0027 a0001c0001t0001g0037 a0001c0003t0001g0108 others(12): Show |
15 | HG01257.hp2 HG02293.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.393+1737T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33499201 | |||||||
chr19:33499400 | G | A | 2 | a0002c0002t0005g0091 a0002c0002t0005g0298 |
2 | HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.393+1538C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33499400 | |||||||
chr19:33499533 | C | T | 215 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0024 others(212): Show |
218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.393+1405G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33499533 | |||||||
chr19:33499736 | A | C | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | NA18954.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.393+1202T>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33499736 | |||||||
chr19:33499741 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.393+1197T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33499741 | |||||||
chr19:33499744 | G | T | 2 | a0001c0001t0001g0207 a0002c0002t0005g0208 |
2 | HG01123.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.393+1194C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33499744 | |||||||
chr19:33499970 | T | C | 1 | a0002c0002t0002g0012 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.393+968A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33499970 | |||||||
chr19:33500040 | C | T | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0308 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.393+898G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33500040 | |||||||
chr19:33500179 | C | A | 1 | a0001c0001t0001g0141 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.393+759G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33500179 | |||||||
chr19:33500179 | C | T | 2 | a0001c0001t0001g0294 a0002c0002t0002g0241 |
2 | HG01884.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.393+759G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33500179 | |||||||
chr19:33500186 | G | A | 20 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(17): Show |
20 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.393+752C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33500186 | |||||||
chr19:33500344 | G | A | 53 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(50): Show |
53 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.393+594C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33500344 | |||||||
chr19:33500350 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.393+588T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33500350 | |||||||
chr19:33500426 | G | A | 53 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(50): Show |
53 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.393+512C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33500426 | |||||||
chr19:33500586 | G | A | 1 | a0002c0002t0002g0258 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.393+352C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33500586 | |||||||
chr19:33500714 | A | C | 2 | a0001c0001t0001g0170 a0001c0001t0001g0173 |
2 | HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.393+224T>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33500714 | |||||||
chr19:33500716 | T | A | 3 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0013t0002g0011 |
3 | HG01074.hp1 HG01109.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.393+222A>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33500716 | |||||||
chr19:33500747 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.393+191G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33500747 | |||||||
chr19:33500851 | G | A | 1 | a0001c0014t0001g0263 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.393+87C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 4/14 | chr19 | 33500851 | |||||||
chr19:33501136 | C | T | 2 | a0002c0002t0002g0259 a0002c0002t0002g0260 |
2 | HG01109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.330-135G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33501136 | |||||||
chr19:33501190 | C | T | 2 | a0002c0002t0002g0028 a0002c0002t0002g0175 |
2 | HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.330-189G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33501190 | |||||||
chr19:33501201 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.330-200C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33501201 | |||||||
chr19:33501235 | G | A | 1 | a0001c0003t0001g0167 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.330-234C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33501235 | |||||||
chr19:33501589 | G | A | 1 | a0001c0001t0003g0276 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.330-588C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33501589 | |||||||
chr19:33501690 | T | A | 1 | a0001c0003t0001g0115 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.330-689A>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33501690 | |||||||
chr19:33501743 | C | T | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0308 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.330-742G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33501743 | |||||||
chr19:33502416 | T | C | 3 | a0002c0002t0002g0258 a0002c0002t0002g0259 a0002c0002t0002g0260 |
3 | HG01109.hp1 HG02280.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.330-1415A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33502416 | |||||||
chr19:33502914 | C | T | 2 | a0002c0002t0005g0091 a0002c0002t0005g0298 |
2 | HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.330-1913G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33502914 | |||||||
chr19:33502952 | C | CG | 27 | a0001c0001t0001g0024 a0001c0001t0001g0102 a0001c0001t0001g0123 others(24): Show |
27 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.330-1952dupC | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33502952 | |||||||
chr19:33502952 | C | CGG | 64 | a0001c0001t0001g0023 a0001c0001t0001g0040 a0001c0001t0001g0041 others(61): Show |
64 | HG00280.hp1 HG00609.hp2 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.330-1953_330-1952d others(4): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33502952 | |||||||
chr19:33502952 | C | CGGG | 23 | a0001c0001t0001g0018 a0001c0001t0001g0048 a0001c0001t0001g0049 others(20): Show |
23 | HG00140.hp1 HG00140.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.330-1954_330-1952d others(5): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33502952 | |||||||
chr19:33502959 | G | C | 2 | a0001c0003t0001g0239 a0001c0003t0001g0240 |
2 | NA18975.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.330-1958C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33502959 | |||||||
chr19:33502993 | G | A | 12 | a0001c0001t0001g0104 a0001c0001t0001g0120 a0001c0001t0001g0145 others(9): Show |
12 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(9): Show |
intron_variant | MODIFIER | c.330-1992C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33502993 | |||||||
chr19:33503053 | G | A | 7 | a0002c0002t0002g0299 a0004c0006t0001g0296 a0004c0006t0001g0297 others(4): Show |
7 | HG02257.hp2 HG02809.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.330-2052C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33503053 | |||||||
chr19:33503269 | G | A | 1 | a0001c0001t0001g0018 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.330-2268C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33503269 | |||||||
chr19:33503511 | T | C | 117 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0024 others(114): Show |
117 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.330-2510A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33503511 | |||||||
chr19:33503594 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.330-2593G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33503594 | |||||||
chr19:33503600 | C | T | 5 | a0002c0002t0002g0008 a0002c0002t0002g0009 a0002c0002t0002g0010 others(2): Show |
5 | HG00140.hp2 HG01496.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.330-2599G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33503600 | |||||||
chr19:33503663 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.330-2662G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33503663 | |||||||
chr19:33503809 | G | A | 16 | a0001c0001t0001g0272 a0001c0001t0001g0278 a0001c0001t0001g0279 others(13): Show |
16 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.330-2808C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33503809 | |||||||
chr19:33503950 | G | A | 69 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(66): Show |
69 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.330-2949C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33503950 | |||||||
chr19:33504041 | G | A | 13 | a0001c0001t0001g0037 a0002c0002t0002g0026 a0002c0002t0002g0028 others(10): Show |
13 | HG01257.hp2 HG02293.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.330-3040C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33504041 | |||||||
chr19:33504327 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.330-3326G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33504327 | |||||||
chr19:33504447 | G | A | 1 | a0002c0002t0002g0258 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.330-3446C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33504447 | |||||||
chr19:33504485 | C | T | 16 | a0001c0001t0001g0272 a0001c0001t0001g0278 a0001c0001t0001g0279 others(13): Show |
16 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.330-3484G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33504485 | |||||||
chr19:33504512 | C | G | 1 | a0001c0001t0001g0119 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.330-3511G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33504512 | |||||||
chr19:33504891 | C | T | 55 | a0001c0001t0001g0043 a0001c0001t0001g0165 a0001c0001t0001g0191 others(52): Show |
55 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.330-3890G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33504891 | |||||||
chr19:33504912 | C | A | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | NA18989.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.330-3911G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33504912 | |||||||
chr19:33505272 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.330-4271C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33505272 | |||||||
chr19:33505296 | G | C | 4 | a0001c0001t0001g0037 a0002c0002t0002g0026 a0002c0002t0002g0036 others(1): Show |
4 | HG01257.hp2 HG02293.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.330-4295C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33505296 | |||||||
chr19:33505367 | C | G | 1 | a0001c0001t0001g0018 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.330-4366G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33505367 | |||||||
chr19:33505398 | A | G | 142 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0049 others(139): Show |
142 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.330-4397T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33505398 | |||||||
chr19:33505500 | G | A | 34 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(31): Show |
34 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.330-4499C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33505500 | |||||||
chr19:33505536 | G | A | 1 | a0001c0001t0001g0154 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.330-4535C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33505536 | |||||||
chr19:33505543 | A | G | 2 | a0002c0002t0002g0174 a0002c0002t0002g0175 |
2 | HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.330-4542T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33505543 | |||||||
chr19:33505551 | C | G | 1 | a0002c0002t0002g0213 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.330-4550G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33505551 | |||||||
chr19:33505553 | A | G | 95 | a0001c0001t0001g0043 a0001c0001t0001g0061 a0001c0001t0001g0180 others(92): Show |
98 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.330-4552T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33505553 | |||||||
chr19:33505612 | G | A | 3 | a0001c0001t0001g0207 a0001c0003t0001g0246 a0002c0002t0005g0208 |
3 | HG01123.hp2 HG02602.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.330-4611C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33505612 | |||||||
chr19:33505688 | C | A | 1 | a0001c0001t0001g0022 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.330-4687G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33505688 | |||||||
chr19:33505708 | C | T | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0308 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.330-4707G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33505708 | |||||||
chr19:33505722 | G | A | 1 | a0006c0010t0005g0168 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.330-4721C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33505722 | |||||||
chr19:33505797 | CACCCTCA others(105): Show |
C | 17 | a0001c0001t0001g0002 a0001c0001t0001g0094 a0001c0001t0001g0099 others(14): Show |
18 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(15): Show |
intron_variant | MODIFIER | c.330-4908_330-4797d others(2): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33505797 | |||||||
chr19:33505877 | AACACCCT others(13): Show |
A | 1 | a0002c0002t0002g0035 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.330-4896_330-4877d others(22): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33505877 | |||||||
chr19:33505968 | C | A | 2 | a0002c0002t0005g0091 a0002c0002t0005g0298 |
2 | HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.330-4967G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33505968 | |||||||
chr19:33505984 | C | T | 1 | a0008c0011t0001g0270 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.330-4983G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33505984 | |||||||
chr19:33505996 | C | T | 2 | a0002c0002t0002g0259 a0002c0002t0002g0260 |
2 | HG01109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.330-4995G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33505996 | |||||||
chr19:33506125 | C | A | 1 | a0002c0002t0002g0291 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.329+4903G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33506125 | |||||||
chr19:33506164 | C | T | 1 | a0001c0014t0001g0263 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.329+4864G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33506164 | |||||||
chr19:33506209 | C | T | 95 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(92): Show |
98 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.329+4819G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33506209 | |||||||
chr19:33506276 | A | C | 61 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0024 others(58): Show |
61 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.329+4752T>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33506276 | |||||||
chr19:33506334 | C | A | 1 | a0002c0002t0002g0164 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.329+4694G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33506334 | |||||||
chr19:33506344 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.329+4684G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33506344 | |||||||
chr19:33506395 | T | TCA | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0308 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.329+4631_329+4632d others(4): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33506395 | |||||||
chr19:33506436 | CCA | C | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0308 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.329+4590_329+4591d others(4): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33506436 | |||||||
chr19:33506625 | TCA | T | 13 | a0001c0001t0001g0027 a0001c0001t0001g0037 a0002c0002t0002g0026 others(10): Show |
13 | HG01257.hp2 HG02293.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.329+4401_329+4402d others(4): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33506625 | |||||||
chr19:33506870 | C | T | 21 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(18): Show |
21 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.329+4158G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33506870 | |||||||
chr19:33506929 | A | C | 1 | a0001c0001t0001g0116 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.329+4099T>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33506929 | |||||||
chr19:33506933 | A | G | 1 | a0002c0002t0005g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.329+4095T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33506933 | |||||||
chr19:33506992 | C | T | 13 | a0001c0001t0001g0027 a0001c0001t0001g0037 a0002c0002t0002g0026 others(10): Show |
13 | HG01257.hp2 HG02293.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.329+4036G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33506992 | |||||||
chr19:33507097 | C | T | 5 | a0001c0001t0003g0045 a0002c0002t0002g0044 a0002c0002t0002g0046 others(2): Show |
5 | HG00099.hp1 HG00733.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.329+3931G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33507097 | |||||||
chr19:33507193 | A | T | 5 | a0001c0001t0001g0067 a0001c0001t0004g0063 a0001c0001t0004g0064 others(2): Show |
5 | NA18952.hp2 NA18971.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.329+3835T>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33507193 | |||||||
chr19:33507263 | G | A | 2 | a0002c0002t0002g0149 a0002c0002t0002g0150 |
2 | HG00408.hp2 HG00558.hp2 |
intron_variant | MODIFIER | c.329+3765C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33507263 | |||||||
chr19:33507408 | C | A | 1 | a0002c0002t0002g0086 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.329+3620G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33507408 | |||||||
chr19:33507533 | C | T | 1 | a0001c0001t0001g0023 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.329+3495G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33507533 | |||||||
chr19:33507646 | AGTCTGGT others(30): Show |
A | 1 | a0001c0001t0001g0092 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.329+3345_329+3381d others(39): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33507646 | |||||||
chr19:33507890 | C | T | 2 | a0001c0007t0001g0005 a0001c0007t0001g0212 |
3 | NA18964.hp1 NA19057.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.329+3138G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33507890 | |||||||
chr19:33507966 | C | T | 8 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0024 others(5): Show |
8 | HG02055.hp1 HG02257.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.329+3062G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33507966 | |||||||
chr19:33508005 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.329+3023G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33508005 | |||||||
chr19:33508052 | C | T | 1 | a0001c0003t0001g0211 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.329+2976G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33508052 | |||||||
chr19:33508085 | AC | A | 13 | a0001c0001t0001g0027 a0001c0001t0001g0037 a0002c0002t0002g0026 others(10): Show |
13 | HG01257.hp2 HG02293.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.329+2942delG | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33508085 | |||||||
chr19:33508289 | C | G | 1 | a0001c0003t0001g0195 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.329+2739G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33508289 | |||||||
chr19:33508293 | C | T | 15 | a0001c0001t0001g0272 a0001c0001t0001g0278 a0001c0001t0001g0279 others(12): Show |
15 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.329+2735G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33508293 | |||||||
chr19:33508391 | A | G | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0308 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.329+2637T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33508391 | |||||||
chr19:33508441 | C | T | 1 | a0002c0002t0002g0171 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.329+2587G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33508441 | |||||||
chr19:33508452 | C | T | 1 | a0002c0002t0005g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.329+2576G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33508452 | |||||||
chr19:33508586 | G | A | 2 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.329+2442C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33508586 | |||||||
chr19:33508591 | C | T | 17 | a0001c0001t0001g0002 a0001c0001t0001g0094 a0001c0001t0001g0099 others(14): Show |
18 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(15): Show |
intron_variant | MODIFIER | c.329+2437G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33508591 | |||||||
chr19:33508630 | G | A | 8 | a0002c0002t0002g0299 a0002c0002t0005g0298 a0004c0006t0001g0296 others(5): Show |
8 | HG02257.hp2 HG02258.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.329+2398C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33508630 | |||||||
chr19:33508672 | A | T | 1 | a0001c0001t0001g0154 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.329+2356T>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33508672 | |||||||
chr19:33508779 | A | C | 1 | a0001c0001t0001g0107 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.329+2249T>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33508779 | |||||||
chr19:33508815 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.329+2213G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33508815 | |||||||
chr19:33509020 | C | T | 11 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(8): Show |
11 | HG01099.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.329+2008G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33509020 | |||||||
chr19:33509084 | C | T | 15 | a0001c0001t0001g0272 a0001c0001t0001g0278 a0001c0001t0001g0279 others(12): Show |
15 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.329+1944G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33509084 | |||||||
chr19:33509106 | G | A | 52 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(49): Show |
52 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.329+1922C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33509106 | |||||||
chr19:33509112 | C | T | 15 | a0001c0001t0001g0272 a0001c0001t0001g0278 a0001c0001t0001g0279 others(12): Show |
15 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.329+1916G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33509112 | |||||||
chr19:33509119 | C | T | 100 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(97): Show |
103 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.329+1909G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33509119 | |||||||
chr19:33509121 | C | T | 6 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 others(3): Show |
6 | HG02074.hp2 HG02083.hp1 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.329+1907G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33509121 | |||||||
chr19:33509159 | T | C | 1 | a0001c0003t0001g0193 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.329+1869A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33509159 | |||||||
chr19:33509223 | G | A | 1 | a0002c0002t0002g0171 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.329+1805C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33509223 | |||||||
chr19:33509499 | G | A | 1 | a0001c0001t0001g0018 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.329+1529C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33509499 | |||||||
chr19:33509819 | T | C | 100 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(97): Show |
103 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.329+1209A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33509819 | |||||||
chr19:33509898 | C | CAGCCCGA others(30): Show |
1 | a0001c0001t0001g0092 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.329+1093_329+1129d others(39): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33509898 | |||||||
chr19:33510134 | G | A | 3 | a0001c0001t0001g0102 a0001c0001t0001g0105 a0001c0001t0001g0106 |
3 | HG00280.hp2 HG00323.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.329+894C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33510134 | |||||||
chr19:33510238 | G | C | 1 | a0001c0003t0001g0151 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.329+790C>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33510238 | |||||||
chr19:33510296 | T | G | 1 | a0001c0001t0001g0018 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.329+732A>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33510296 | |||||||
chr19:33510317 | G | A | 1 | a0002c0002t0002g0258 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.329+711C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33510317 | |||||||
chr19:33510360 | AGG | A | 15 | a0001c0001t0001g0272 a0001c0001t0001g0278 a0001c0001t0001g0279 others(12): Show |
15 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.329+666_329+667del others(2): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33510360 | |||||||
chr19:33510399 | A | G | 12 | a0001c0001t0001g0180 a0001c0001t0001g0261 a0001c0001t0003g0001 others(9): Show |
14 | HG00639.hp2 HG00642.hp1 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.329+629T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33510399 | |||||||
chr19:33510402 | G | A | 1 | a0001c0003t0001g0254 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.329+626C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33510402 | |||||||
chr19:33510425 | A | C | 3 | a0001c0001t0001g0102 a0001c0001t0001g0105 a0001c0001t0001g0106 |
3 | HG00280.hp2 HG00323.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.329+603T>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33510425 | |||||||
chr19:33510591 | T | C | 3 | a0005c0008t0001g0247 a0005c0008t0001g0248 a0005c0008t0001g0249 |
3 | NA18969.hp1 NA19068.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.329+437A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33510591 | |||||||
chr19:33510980 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.329+48G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 3/14 | chr19 | 33510980 | |||||||
chr19:33511214 | G | A | 1 | a0002c0002t0005g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.202-59C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 2/14 | chr19 | 33511214 | |||||||
chr19:33511508 | G | T | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG02165.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.202-353C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 2/14 | chr19 | 33511508 | |||||||
chr19:33511514 | C | T | 1 | a0003c0004t0001g0210 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.202-359G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 2/14 | chr19 | 33511514 | |||||||
chr19:33512026 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.201+567T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 2/14 | chr19 | 33512026 | |||||||
chr19:33512271 | T | C | 5 | a0001c0003t0001g0250 a0001c0003t0001g0251 a0001c0003t0001g0252 others(2): Show |
5 | HG01192.hp2 HG01243.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.201+322A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 2/14 | chr19 | 33512271 | |||||||
chr19:33512349 | T | C | 116 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(113): Show |
119 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.201+244A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 2/14 | chr19 | 33512349 | |||||||
chr19:33512357 | A | G | 1 | a0001c0003t0001g0194 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.201+236T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 2/14 | chr19 | 33512357 | |||||||
chr19:33512417 | C | T | 1 | a0002c0002t0002g0169 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.201+176G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 2/14 | chr19 | 33512417 | |||||||
chr19:33512451 | T | G | 2 | a0002c0002t0005g0091 a0002c0002t0005g0298 |
2 | HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.201+142A>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 2/14 | chr19 | 33512451 | |||||||
chr19:33512468 | G | A | 9 | a0002c0002t0002g0008 a0002c0002t0002g0009 a0002c0002t0002g0010 others(6): Show |
9 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.201+125C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 2/14 | chr19 | 33512468 | |||||||
chr19:33512806 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.18-30G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33512806 | |||||||
chr19:33512820 | C | G | 6 | a0001c0001t0001g0043 a0001c0001t0001g0191 a0001c0001t0001g0192 others(3): Show |
6 | HG02071.hp1 NA18951.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.18-44G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33512820 | |||||||
chr19:33513040 | A | C | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(209): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.18-264T>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33513040 | |||||||
chr19:33513138 | C | T | 1 | a0001c0001t0003g0179 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.18-362G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33513138 | |||||||
chr19:33513185 | G | T | 1 | a0001c0001t0001g0102 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.18-409C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33513185 | |||||||
chr19:33513211 | T | A | 1 | a0001c0001t0001g0094 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.18-435A>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33513211 | |||||||
chr19:33513365 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.18-589G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33513365 | |||||||
chr19:33513394 | A | G | 1 | a0001c0003t0001g0209 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.18-618T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33513394 | |||||||
chr19:33513407 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.18-631G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33513407 | |||||||
chr19:33513563 | C | G | 3 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 |
3 | HG00621.hp1 NA18953.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.18-787G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33513563 | |||||||
chr19:33513578 | G | A | 1 | a0002c0002t0002g0047 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.18-802C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33513578 | |||||||
chr19:33513606 | C | T | 1 | a0002c0002t0002g0006 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.18-830G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33513606 | |||||||
chr19:33513794 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.18-1018G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33513794 | |||||||
chr19:33513870 | A | ACCCAGCC others(28): Show |
140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(137): Show |
143 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.18-1129_18-1095dup others(35): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33513870 | |||||||
chr19:33514035 | G | A | 52 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(49): Show |
52 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.18-1259C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33514035 | |||||||
chr19:33514040 | G | A | 6 | a0001c0001t0001g0207 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG01123.hp2 HG02055.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.18-1264C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33514040 | |||||||
chr19:33514046 | G | A | 2 | a0001c0001t0001g0289 a0001c0001t0001g0293 |
2 | HG02258.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.18-1270C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33514046 | |||||||
chr19:33514078 | A | T | 198 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(195): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.18-1302T>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33514078 | |||||||
chr19:33514205 | G | T | 1 | a0001c0014t0001g0263 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.18-1429C>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33514205 | |||||||
chr19:33514257 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.18-1481G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33514257 | |||||||
chr19:33514452 | G | A | 1 | a0002c0002t0005g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.18-1676C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33514452 | |||||||
chr19:33514504 | A | G | 39 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0067 others(36): Show |
39 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.18-1728T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33514504 | |||||||
chr19:33514607 | G | A | 1 | a0002c0002t0005g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.18-1831C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33514607 | |||||||
chr19:33514640 | G | A | 39 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0067 others(36): Show |
39 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.18-1864C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33514640 | |||||||
chr19:33514758 | C | T | 201 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(198): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.18-1982G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33514758 | |||||||
chr19:33514876 | C | T | 1 | a0002c0002t0002g0008 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.18-2100G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33514876 | |||||||
chr19:33515019 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.18-2243G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33515019 | |||||||
chr19:33515069 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.18-2293C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33515069 | |||||||
chr19:33515228 | C | T | 4 | a0001c0001t0003g0045 a0002c0002t0002g0044 a0002c0002t0002g0046 others(1): Show |
4 | HG00099.hp1 HG00733.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.18-2452G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33515228 | |||||||
chr19:33515321 | C | T | 1 | a0001c0001t0001g0018 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.18-2545G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33515321 | |||||||
chr19:33515333 | C | G | 1 | a0002c0002t0002g0262 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.18-2557G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33515333 | |||||||
chr19:33515350 | C | T | 3 | a0003c0004t0001g0095 a0003c0004t0001g0096 a0003c0004t0001g0097 |
3 | NA18951.hp2 NA18968.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.18-2574G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33515350 | |||||||
chr19:33515388 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.18-2612G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33515388 | |||||||
chr19:33515474 | C | T | 52 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(49): Show |
52 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.18-2698G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33515474 | |||||||
chr19:33515481 | A | G | 14 | a0001c0001t0001g0043 a0001c0001t0001g0094 a0001c0001t0001g0191 others(11): Show |
14 | HG00438.hp1 HG02071.hp1 HG02523.hp2 others(11): Show |
intron_variant | MODIFIER | c.18-2705T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33515481 | |||||||
chr19:33515571 | C | T | 7 | a0001c0001t0001g0272 a0001c0001t0003g0275 a0001c0001t0003g0276 others(4): Show |
7 | HG00140.hp1 HG00280.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.18-2795G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33515571 | |||||||
chr19:33516070 | C | T | 1 | a0002c0002t0002g0044 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.18-3294G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33516070 | |||||||
chr19:33516073 | A | G | 53 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(50): Show |
53 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.18-3297T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33516073 | |||||||
chr19:33516099 | C | T | 12 | a0001c0001t0001g0180 a0001c0001t0001g0261 a0001c0001t0003g0001 others(9): Show |
14 | HG00639.hp2 HG00642.hp1 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.18-3323G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33516099 | |||||||
chr19:33516125 | T | A | 7 | a0001c0001t0001g0004 a0001c0001t0001g0154 a0001c0001t0001g0155 others(4): Show |
8 | HG00408.hp1 HG00597.hp2 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.18-3349A>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33516125 | |||||||
chr19:33516253 | G | A | 18 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(15): Show |
18 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.18-3477C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33516253 | |||||||
chr19:33516325 | T | C | 1 | a0001c0001t0004g0039 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.18-3549A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33516325 | |||||||
chr19:33516473 | A | G | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG00642.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.18-3697T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33516473 | |||||||
chr19:33516569 | A | G | 53 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(50): Show |
53 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.18-3793T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33516569 | |||||||
chr19:33516649 | T | C | 2 | a0001c0001t0001g0271 a0008c0011t0001g0270 |
2 | HG01884.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.18-3873A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33516649 | |||||||
chr19:33516723 | G | A | 201 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(198): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.18-3947C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33516723 | |||||||
chr19:33516752 | G | A | 1 | a0001c0003t0001g0255 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.18-3976C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33516752 | |||||||
chr19:33516931 | G | A | 8 | a0002c0002t0002g0006 a0002c0002t0002g0008 a0002c0002t0002g0009 others(5): Show |
8 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.18-4155C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33516931 | |||||||
chr19:33517273 | A | G | 15 | a0001c0001t0001g0272 a0001c0001t0001g0278 a0001c0001t0001g0279 others(12): Show |
15 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.17+4471T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33517273 | |||||||
chr19:33517383 | C | A | 1 | a0002c0002t0002g0088 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.17+4361G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33517383 | |||||||
chr19:33517384 | C | A | 4 | a0001c0001t0001g0176 a0002c0002t0002g0169 a0002c0002t0002g0174 others(1): Show |
4 | HG01891.hp1 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.17+4360G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33517384 | |||||||
chr19:33517402 | T | C | 5 | a0001c0001t0001g0272 a0001c0001t0003g0275 a0001c0001t0003g0284 others(2): Show |
5 | HG00140.hp1 HG01106.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.17+4342A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33517402 | |||||||
chr19:33517560 | AAAAAAAC | A | 11 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(8): Show |
11 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.17+4177_17+4183del others(7): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33517560 | |||||||
chr19:33517610 | C | T | 13 | a0001c0001t0001g0027 a0001c0001t0001g0037 a0002c0002t0002g0026 others(10): Show |
13 | HG01257.hp2 HG02293.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.17+4134G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33517610 | |||||||
chr19:33517692 | T | A | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0308 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.17+4052A>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33517692 | |||||||
chr19:33517694 | C | T | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(86): Show |
92 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.17+4050G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33517694 | |||||||
chr19:33517705 | G | A | 13 | a0001c0001t0001g0027 a0001c0001t0001g0037 a0002c0002t0002g0026 others(10): Show |
13 | HG01257.hp2 HG02293.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.17+4039C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33517705 | |||||||
chr19:33517803 | A | C | 50 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0049 others(47): Show |
50 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.17+3941T>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33517803 | |||||||
chr19:33517921 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.17+3823G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33517921 | |||||||
chr19:33517954 | C | CA | 25 | a0001c0001t0001g0272 a0001c0001t0001g0278 a0001c0001t0001g0279 others(22): Show |
25 | HG00140.hp1 HG00280.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.17+3789dupT | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33517954 | |||||||
chr19:33517954 | CA | C | 13 | a0001c0001t0001g0027 a0001c0001t0001g0037 a0002c0002t0002g0026 others(10): Show |
13 | HG01257.hp2 HG02293.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.17+3789delT | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33517954 | |||||||
chr19:33518141 | T | C | 1 | a0002c0002t0002g0006 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.17+3603A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33518141 | |||||||
chr19:33518163 | C | T | 2 | a0001c0003t0001g0160 a0001c0003t0001g0161 |
2 | NA18998.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.17+3581G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33518163 | |||||||
chr19:33518397 | G | A | 1 | a0002c0002t0002g0258 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.17+3347C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33518397 | |||||||
chr19:33518457 | T | C | 1 | a0001c0001t0001g0293 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.17+3287A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33518457 | |||||||
chr19:33518471 | C | T | 11 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(8): Show |
11 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.17+3273G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33518471 | |||||||
chr19:33518486 | T | C | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(203): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.17+3258A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33518486 | |||||||
chr19:33518751 | C | T | 1 | a0001c0001t0001g0018 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.17+2993G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33518751 | |||||||
chr19:33518826 | G | A | 78 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(75): Show |
81 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.17+2918C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33518826 | |||||||
chr19:33518910 | G | A | 1 | a0002c0002t0002g0006 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.17+2834C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33518910 | |||||||
chr19:33519096 | C | A | 2 | a0001c0003t0001g0160 a0001c0003t0001g0161 |
2 | NA18998.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.17+2648G>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33519096 | |||||||
chr19:33519180 | C | T | 1 | a0002c0002t0002g0169 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.17+2564G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33519180 | |||||||
chr19:33519275 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.17+2469C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33519275 | |||||||
chr19:33519283 | A | G | 35 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(32): Show |
35 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.17+2461T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33519283 | |||||||
chr19:33519340 | C | T | 1 | a0002c0002t0005g0298 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.17+2404G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33519340 | |||||||
chr19:33519383 | T | C | 163 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(160): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.17+2361A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33519383 | |||||||
chr19:33519540 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.17+2204C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33519540 | |||||||
chr19:33519622 | C | T | 1 | a0001c0001t0001g0272 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.17+2122G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33519622 | |||||||
chr19:33519628 | G | A | 13 | a0001c0001t0001g0027 a0001c0001t0001g0037 a0002c0002t0002g0026 others(10): Show |
13 | HG01257.hp2 HG02293.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.17+2116C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33519628 | |||||||
chr19:33519755 | C | G | 1 | a0006c0010t0005g0168 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.17+1989G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33519755 | |||||||
chr19:33520020 | T | C | 1 | a0001c0001t0001g0261 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.17+1724A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33520020 | |||||||
chr19:33520060 | G | A | 10 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0266 others(7): Show |
10 | HG01884.hp2 HG01891.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.17+1684C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33520060 | |||||||
chr19:33520064 | C | CA | 19 | a0001c0001t0001g0037 a0001c0001t0001g0165 a0001c0001t0001g0272 others(16): Show |
19 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.17+1679dupT | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33520064 | |||||||
chr19:33520064 | CA | C | 6 | a0001c0001t0004g0039 a0001c0003t0001g0167 a0002c0002t0002g0026 others(3): Show |
6 | HG01257.hp2 HG02818.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.17+1679delT | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33520064 | |||||||
chr19:33520303 | G | A | 6 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0293 others(3): Show |
6 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.17+1441C>T | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33520303 | |||||||
chr19:33520342 | T | G | 141 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(138): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.17+1402A>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33520342 | |||||||
chr19:33520428 | A | G | 163 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(160): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.17+1316T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33520428 | |||||||
chr19:33520468 | T | C | 1 | a0001c0001t0001g0294 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.17+1276A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33520468 | |||||||
chr19:33520591 | T | C | 1 | a0001c0001t0001g0295 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.17+1153A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33520591 | |||||||
chr19:33520680 | T | C | 8 | a0002c0002t0002g0299 a0002c0002t0005g0298 a0004c0006t0001g0296 others(5): Show |
8 | HG02257.hp2 HG02258.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.17+1064A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33520680 | |||||||
chr19:33520788 | T | C | 140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(137): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.17+956A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33520788 | |||||||
chr19:33520816 | CCTT | C | 8 | a0002c0002t0002g0006 a0002c0002t0002g0008 a0002c0002t0002g0009 others(5): Show |
8 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.17+925_17+927delAA others(1): Show |
PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33520816 | |||||||
chr19:33520852 | C | T | 1 | a0003c0005t0001g0025 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.17+892G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33520852 | |||||||
chr19:33520991 | A | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.17+753T>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33520991 | |||||||
chr19:33521151 | C | T | 4 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(1): Show |
4 | HG01071.hp1 HG02630.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.17+593G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33521151 | |||||||
chr19:33521318 | C | G | 1 | a0001c0001t0001g0018 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.17+426G>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33521318 | |||||||
chr19:33521347 | GA | G | 3 | a0003c0005t0001g0015 a0003c0005t0001g0016 a0003c0005t0001g0017 |
3 | NA18942.hp2 NA18944.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.17+396delT | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33521347 | |||||||
chr19:33521375 | T | C | 1 | a0002c0002t0002g0304 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.17+369A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33521375 | |||||||
chr19:33521387 | C | T | 7 | a0002c0002t0002g0008 a0002c0002t0002g0009 a0002c0002t0002g0010 others(4): Show |
7 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.17+357G>A | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33521387 | |||||||
chr19:33521580 | A | G | 1 | a0001c0003t0001g0007 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.17+164T>C | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33521580 | |||||||
chr19:33521634 | T | C | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0308 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.17+110A>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33521634 | |||||||
chr19:33521694 | A | C | 1 | a0002c0002t0002g0006 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.17+50T>G | PEPD | ENSG00000124299.16 | transcript | ENST00000244137.12 | protein_coding | 1/14 | chr19 | 33521694 |