Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5195 |
| ensemblid | ENSG00000142655.13 |
| hgncid | 8856 |
| symbol | PEX14 |
| name | peroxisomal biogenesis factor 14 |
| refseq_nuc | NM_004565.3 |
| refseq_prot | NP_004556.1 |
| ensembl_nuc | ENST00000356607.9 |
| ensembl_prot | ENSP00000349016.4 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 10474950 |
| end | 10630758 |
| strand | + |
| ver | v1.2 |
| region | chr1:10474950-10630758 |
| region5000 | chr1:10469950-10635758 |
| regionname0 | PEX14_chr1_10474950_10630758 |
| regionname5000 | PEX14_chr1_10469950_10635758 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 377 | 243 | 71 | 46 | 89 | 10 | 25 | 57 | PEX14_chr1_10469950_10635758 | PEX14 | MASSE others(372): Show |
chr1 | 10469950 | 10635758 |
| a0002 | 0/0 | 377 | 9 | 8 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | MASSE others(372): Show |
chr1 | 10469950 | 10635758 |
| a0003 | 0/0 | 377 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | MASSE others(372): Show |
chr1 | 10469950 | 10635758 |
| a0004 | 0/0 | 377 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | MASSE others(372): Show |
chr1 | 10469950 | 10635758 |
| a0005 | 0/0 | 377 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PEX14_chr1_10469950_10635758 | PEX14 | MASSE others(372): Show |
chr1 | 10469950 | 10635758 |
| a0006 | 0/0 | 377 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | MASSE others(372): Show |
chr1 | 10469950 | 10635758 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1131 | 141 | 52 | 21 | 51 | 4 | 12 | PEX14_chr1_10469950_10635758 | PEX14 | ATGGC others(1126): Show |
chr1 | 10469950 | 10635758 | ||
| a0001c0002 | 0/0 | 1131 | 44 | 3 | 16 | 18 | 3 | 4 | PEX14_chr1_10469950_10635758 | PEX14 | ATGGC others(1126): Show |
chr1 | 10469950 | 10635758 | ||
| a0001c0003 | 0/0 | 1131 | 23 | 6 | 1 | 12 | 1 | 3 | PEX14_chr1_10469950_10635758 | PEX14 | ATGGC others(1126): Show |
chr1 | 10469950 | 10635758 | ||
| a0001c0004 | 0/1 | 1131 | 16 | 2 | 5 | 3 | 2 | 3 | PEX14_chr1_10469950_10635758 | PEX14 | ATGGC others(1126): Show |
chr1 | 10469950 | 10635758 | ||
| a0001c0006 | 0/0 | 1131 | 5 | 5 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | ATGGC others(1126): Show |
chr1 | 10469950 | 10635758 | ||
| a0001c0007 | 0/0 | 1131 | 4 | 0 | 1 | 1 | 0 | 2 | PEX14_chr1_10469950_10635758 | PEX14 | ATGGC others(1126): Show |
chr1 | 10469950 | 10635758 | ||
| a0001c0008 | 0/0 | 1131 | 3 | 1 | 1 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | ATGGC others(1126): Show |
chr1 | 10469950 | 10635758 | ||
| a0001c0009 | 0/0 | 1131 | 2 | 0 | 0 | 2 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | ATGGC others(1126): Show |
chr1 | 10469950 | 10635758 | ||
| a0001c0012 | 0/0 | 1131 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | ATGGC others(1126): Show |
chr1 | 10469950 | 10635758 | ||
| a0001c0014 | 0/0 | 1131 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | ATGGC others(1126): Show |
chr1 | 10469950 | 10635758 | ||
| a0001c0015 | 0/0 | 1131 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | ATGGC others(1126): Show |
chr1 | 10469950 | 10635758 | ||
| a0001c0016 | 0/0 | 1131 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | ATGGC others(1126): Show |
chr1 | 10469950 | 10635758 | ||
| a0001c0017 | 0/0 | 1131 | 1 | 0 | 0 | 0 | 0 | 1 | PEX14_chr1_10469950_10635758 | PEX14 | ATGGC others(1126): Show |
chr1 | 10469950 | 10635758 | ||
| a0002c0005 | 0/0 | 1131 | 9 | 8 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | ATGGC others(1126): Show |
chr1 | 10469950 | 10635758 | ||
| a0003c0011 | 0/0 | 1131 | 2 | 0 | 1 | 0 | 0 | 1 | PEX14_chr1_10469950_10635758 | PEX14 | ATGGC others(1126): Show |
chr1 | 10469950 | 10635758 | ||
| a0004c0010 | 0/0 | 1131 | 2 | 2 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | ATGGC others(1126): Show |
chr1 | 10469950 | 10635758 | ||
| a0005c0018 | 0/0 | 1131 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | ATGGC others(1126): Show |
chr1 | 10469950 | 10635758 | ||
| a0006c0013 | 0/0 | 1131 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | ATGGC others(1126): Show |
chr1 | 10469950 | 10635758 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1922 | 137 | 51 | 20 | 50 | 4 | 11 | PEX14_chr1_10469950_10635758 | PEX14 | AGTCA others(1917): Show |
chr1 | 10469950 | 10635758 |
| a0001c0001t0002 | 0/0 | 1922 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | AGTCA others(1917): Show |
chr1 | 10469950 | 10635758 |
| a0001c0001t0003 | 0/0 | 1922 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | AGTCA others(1917): Show |
chr1 | 10469950 | 10635758 |
| a0001c0001t0004 | 0/0 | 1922 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | AGTCA others(1917): Show |
chr1 | 10469950 | 10635758 |
| a0001c0001t0006 | 0/0 | 1922 | 1 | 0 | 0 | 0 | 0 | 1 | PEX14_chr1_10469950_10635758 | PEX14 | AGTCA others(1917): Show |
chr1 | 10469950 | 10635758 |
| a0001c0002t0001 | 0/0 | 1922 | 43 | 3 | 16 | 17 | 3 | 4 | PEX14_chr1_10469950_10635758 | PEX14 | AGTCA others(1917): Show |
chr1 | 10469950 | 10635758 |
| a0001c0002t0005 | 0/0 | 1922 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | AGTCA others(1917): Show |
chr1 | 10469950 | 10635758 |
| a0001c0003t0001 | 0/0 | 1922 | 23 | 6 | 1 | 12 | 1 | 3 | PEX14_chr1_10469950_10635758 | PEX14 | AGTCA others(1917): Show |
chr1 | 10469950 | 10635758 |
| a0001c0004t0001 | 0/1 | 1922 | 16 | 2 | 5 | 3 | 2 | 3 | PEX14_chr1_10469950_10635758 | PEX14 | AGTCA others(1917): Show |
chr1 | 10469950 | 10635758 |
| a0001c0006t0001 | 0/0 | 1922 | 5 | 5 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | AGTCA others(1917): Show |
chr1 | 10469950 | 10635758 |
| a0001c0007t0001 | 0/0 | 1922 | 4 | 0 | 1 | 1 | 0 | 2 | PEX14_chr1_10469950_10635758 | PEX14 | AGTCA others(1917): Show |
chr1 | 10469950 | 10635758 |
| a0001c0008t0001 | 0/0 | 1922 | 3 | 1 | 1 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | AGTCA others(1917): Show |
chr1 | 10469950 | 10635758 |
| a0001c0009t0001 | 0/0 | 1922 | 2 | 0 | 0 | 2 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | AGTCA others(1917): Show |
chr1 | 10469950 | 10635758 |
| a0001c0012t0001 | 0/0 | 1922 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | AGTCA others(1917): Show |
chr1 | 10469950 | 10635758 |
| a0001c0014t0001 | 0/0 | 1922 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | AGTCA others(1917): Show |
chr1 | 10469950 | 10635758 |
| a0001c0015t0001 | 0/0 | 1922 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | AGTCA others(1917): Show |
chr1 | 10469950 | 10635758 |
| a0001c0016t0001 | 0/0 | 1922 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | AGTCA others(1917): Show |
chr1 | 10469950 | 10635758 |
| a0001c0017t0001 | 0/0 | 1922 | 1 | 0 | 0 | 0 | 0 | 1 | PEX14_chr1_10469950_10635758 | PEX14 | AGTCA others(1917): Show |
chr1 | 10469950 | 10635758 |
| a0002c0005t0001 | 0/0 | 1922 | 9 | 8 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | AGTCA others(1917): Show |
chr1 | 10469950 | 10635758 |
| a0003c0011t0001 | 0/0 | 1922 | 2 | 0 | 1 | 0 | 0 | 1 | PEX14_chr1_10469950_10635758 | PEX14 | AGTCA others(1917): Show |
chr1 | 10469950 | 10635758 |
| a0004c0010t0001 | 0/0 | 1922 | 2 | 2 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | AGTCA others(1917): Show |
chr1 | 10469950 | 10635758 |
| a0005c0018t0001 | 0/0 | 1922 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | AGTCA others(1917): Show |
chr1 | 10469950 | 10635758 |
| a0006c0013t0001 | 0/0 | 1922 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | AGTCA others(1917): Show |
chr1 | 10469950 | 10635758 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0177 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0004g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0001t0006g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0002t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0002t0005g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0003t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0003t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0003t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0003t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0003t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0003t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0003t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0003t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0003t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0003t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0003t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0004t0001g0004 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0004t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0004t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0004t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0004t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0004t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0004t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0004t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0004t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0004t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0004t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0004t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0004t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0004t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0004t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0004t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0006t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0006t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0006t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0006t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0006t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0007t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0007t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0007t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0007t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0008t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0008t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0008t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0009t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0009t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0012t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0014t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0015t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0016t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0001c0017t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0002c0005t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0002c0005t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0002c0005t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0002c0005t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0002c0005t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0002c0005t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0002c0005t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0002c0005t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0002c0005t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0003c0011t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0003c0011t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0004c0010t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0004c0010t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0005c0018t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| a0006c0013t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG00099 | hp2 | a0001 | c0003 | t0001 | g0085 | EUR | GBR | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0068 | EUR | FIN | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0188 | EUR | FIN | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG00408 | hp1 | a0001 | c0003 | t0001 | g0151 | EAS | CHS | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0201 | EAS | CHS | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG00423 | hp1 | a0001 | c0003 | t0001 | g0025 | EAS | CHS | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | CHS | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG00544 | hp2 | a0001 | c0003 | t0001 | g0027 | EAS | CHS | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0199 | EAS | CHS | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG00558 | hp2 | a0001 | c0003 | t0001 | g0222 | EAS | CHS | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0223 | EAS | CHS | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0168 | EAS | CHS | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG00733 | hp2 | a0001 | c0004 | t0001 | g0046 | AMR | PUR | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0215 | AMR | PUR | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0023 | AMR | PUR | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG00741 | hp2 | a0001 | c0004 | t0001 | g0053 | AMR | PUR | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01069 | hp2 | a0001 | c0004 | t0001 | g0090 | AMR | PUR | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0178 | AMR | PUR | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0186 | AMR | PUR | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01109 | hp2 | a0003 | c0011 | t0001 | g0191 | AMR | PUR | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01167 | hp1 | a0002 | c0005 | t0001 | g0172 | AMR | PUR | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0183 | AMR | PUR | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0175 | AMR | PUR | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01175 | hp2 | a0001 | c0004 | t0001 | g0166 | AMR | PUR | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01255 | hp2 | a0001 | c0008 | t0001 | g0182 | AMR | CLM | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0198 | AMR | CLM | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01358 | hp2 | a0001 | c0004 | t0001 | g0147 | AMR | CLM | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0185 | AMR | CLM | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0033 | AMR | CLM | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0067 | EUR | IBS | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0204 | EUR | IBS | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01517 | hp1 | a0001 | c0004 | t0001 | g0079 | EUR | IBS | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0205 | EUR | IBS | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01884 | hp1 | a0002 | c0005 | t0001 | g0230 | AFR | ACB | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0253 | AFR | ACB | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01891 | hp2 | a0001 | c0014 | t0001 | g0251 | AFR | ACB | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01928 | hp1 | a0001 | c0007 | t0001 | g0187 | AMR | PEL | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0197 | AMR | PEL | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01934 | hp1 | a0001 | c0016 | t0001 | g0070 | AMR | PEL | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0184 | AMR | PEL | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0190 | AMR | PEL | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0208 | AMR | PEL | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0214 | AMR | PEL | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG01981 | hp2 | a0001 | c0003 | t0001 | g0238 | AMR | PEL | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02056 | hp1 | a0001 | c0007 | t0001 | g0211 | EAS | KHV | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0169 | EAS | KHV | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02080 | hp1 | a0001 | c0009 | t0001 | g0062 | EAS | KHV | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0195 | EAS | KHV | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0170 | EAS | KHV | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02155 | hp1 | a0001 | c0003 | t0001 | g0078 | EAS | CDX | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0167 | EAS | CDX | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0163 | EAS | CDX | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | CDX | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02258 | hp1 | a0001 | c0008 | t0001 | g0192 | AFR | ACB | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0216 | AMR | PEL | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02451 | hp2 | a0001 | c0003 | t0001 | g0102 | AFR | ACB | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02622 | hp1 | a0002 | c0005 | t0001 | g0228 | AFR | GWD | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02630 | hp2 | a0004 | c0010 | t0001 | g0123 | AFR | GWD | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02717 | hp1 | a0001 | c0006 | t0001 | g0119 | AFR | GWD | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0179 | AFR | GWD | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02723 | hp1 | a0001 | c0003 | t0001 | g0132 | AFR | GWD | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0176 | SAS | PJL | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02809 | hp1 | a0002 | c0005 | t0001 | g0218 | AFR | GWD | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02886 | hp1 | a0001 | c0003 | t0001 | g0133 | AFR | GWD | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02896 | hp2 | a0002 | c0005 | t0001 | g0013 | AFR | GWD | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | ESN | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02970 | hp2 | a0002 | c0005 | t0001 | g0173 | AFR | ESN | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ESN | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | MSL | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0181 | AFR | ESN | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG03139 | hp1 | a0001 | c0006 | t0001 | g0087 | AFR | ESN | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | MSL | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | MSL | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG03225 | hp1 | a0001 | c0015 | t0001 | g0255 | AFR | MSL | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG03225 | hp2 | a0001 | c0003 | t0001 | g0088 | AFR | MSL | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG03453 | hp2 | a0002 | c0005 | t0001 | g0233 | AFR | MSL | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG03486 | hp1 | a0001 | c0006 | t0001 | g0236 | AFR | MSL | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG03486 | hp2 | a0002 | c0005 | t0001 | g0207 | AFR | MSL | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0196 | SAS | PJL | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG03492 | hp2 | a0001 | c0003 | t0001 | g0135 | SAS | PJL | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG03516 | hp1 | a0001 | c0006 | t0001 | g0086 | AFR | ESN | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ESN | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG03540 | hp2 | a0001 | c0003 | t0001 | g0105 | AFR | GWD | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | MSL | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG03654 | hp1 | a0001 | c0001 | t0006 | g0010 | SAS | PJL | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG03669 | hp2 | a0001 | c0007 | t0001 | g0189 | SAS | PJL | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | BEB | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | BEB | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | BEB | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0254 | SAS | BEB | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG03942 | hp1 | a0001 | c0004 | t0001 | g0152 | SAS | BEB | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG03942 | hp2 | a0001 | c0004 | t0001 | g0024 | SAS | BEB | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG04115 | hp1 | a0001 | c0004 | t0001 | g0060 | SAS | STU | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0217 | SAS | STU | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG04199 | hp1 | a0003 | c0011 | t0001 | g0107 | SAS | STU | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG04199 | hp2 | a0001 | c0007 | t0001 | g0203 | SAS | STU | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG04204 | hp1 | a0001 | c0003 | t0001 | g0083 | SAS | STU | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | STU | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | YRI | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | CHB | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CHB | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA18939 | hp2 | a0001 | c0003 | t0001 | g0066 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA18942 | hp1 | a0005 | c0018 | t0001 | g0171 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA18944 | hp1 | a0001 | c0002 | t0005 | g0200 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA18947 | hp1 | a0001 | c0003 | t0001 | g0028 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA18947 | hp2 | a0001 | c0008 | t0001 | g0213 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA18963 | hp2 | a0001 | c0012 | t0001 | g0055 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA18964 | hp1 | a0001 | c0003 | t0001 | g0103 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA18966 | hp1 | a0001 | c0003 | t0001 | g0041 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0202 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA18982 | hp1 | a0001 | c0003 | t0001 | g0149 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA18982 | hp2 | a0001 | c0003 | t0001 | g0057 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA18995 | hp1 | a0001 | c0003 | t0001 | g0026 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0224 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA19000 | hp1 | a0001 | c0004 | t0001 | g0162 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA19004 | hp1 | a0001 | c0009 | t0001 | g0063 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA19012 | hp1 | a0001 | c0004 | t0001 | g0042 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA19030 | hp1 | a0001 | c0004 | t0001 | g0209 | AFR | LWK | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0108 | AFR | LWK | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA19043 | hp1 | a0001 | c0006 | t0001 | g0124 | AFR | LWK | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | LWK | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA19070 | hp1 | a0001 | c0004 | t0001 | g0038 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0077 | AFR | YRI | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | YRI | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA20129 | hp1 | a0001 | c0004 | t0001 | g0074 | AFR | ASW | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA20129 | hp2 | a0006 | c0013 | t0001 | g0206 | AFR | ASW | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA20752 | hp1 | a0001 | c0004 | t0001 | g0148 | EUR | TSI | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0073 | EUR | TSI | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA20905 | hp1 | a0001 | c0003 | t0001 | g0158 | SAS | GIH | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA20905 | hp2 | a0001 | c0017 | t0001 | g0130 | SAS | GIH | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02559 | hp1 | a0002 | c0005 | t0001 | g0127 | AFR | ACB | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG03471 | hp1 | a0004 | c0010 | t0001 | g0098 | AFR | MSL | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | USA | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | USA | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | LWK | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | LWK | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| homoSapiens | chm13v2 | a0001 | c0004 | t0001 | g0004 | REF | REF | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0177 | REF | REF | PEX14_chr1_10469950_10635758 | PEX14 | chr1 | 10469950 | 10635758 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:10599276 | T | G | 1 | a0005 | 1 | NA18942.hp1 | missense_variant | MODERATE | c.208T>G | p.Ser70Ala | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/9 | 225/1922 | 208/1134 | 70/377 | chr1 | 10599276 | |||
| chr1:10618408 | G | C | 1 | a0006 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.375G>C | p.Gln125His | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/9 | 392/1922 | 375/1134 | 125/377 | chr1 | 10618408 | |||
| chr1:10623034 | C | G | 1 | a0003 | 2 | HG01109.hp2 HG04199.hp1 |
missense_variant | MODERATE | c.400C>G | p.Leu134Val | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 6/9 | 417/1922 | 400/1134 | 134/377 | chr1 | 10623034 | |||
| chr1:10623109 | G | A | 1 | a0002 | 9 | HG01167.hp1 HG01884.hp1 HG02559.hp1 others(6): Show |
missense_variant | MODERATE | c.475G>A | p.Val159Met | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 6/9 | 492/1922 | 475/1134 | 159/377 | chr1 | 10623109 | |||
| chr1:10629812 | G | A | 1 | a0004 | 2 | HG02630.hp2 HG03471.hp1 |
missense_variant | MODERATE | c.959G>A | p.Arg320Lys | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 9/9 | 976/1922 | 959/1134 | 320/377 | chr1 | 10629812 | |||
| chr1:10629846 | T | G | 1 | a0005 | 1 | NA18942.hp1 | missense_variant | MODERATE | c.993T>G | p.Asp331Glu | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 9/9 | 1010/1922 | 993/1134 | 331/377 | chr1 | 10629846 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:10495315 | G | A | 2 | a0001c0009 a0001c0012 |
3 | HG02080.hp1 NA18963.hp2 NA19004.hp1 |
synonymous_variant | LOW | c.78G>A | p.Glu26Glu | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/9 | 95/1922 | 78/1134 | 26/377 | chr1 | 10495315 | |||
| chr1:10536284 | C | T | 5 | a0001c0002 a0001c0007 a0001c0008 others(2): Show |
54 | HG00280.hp2 HG00408.hp2 HG00558.hp1 others(51): Show |
synonymous_variant | LOW | c.156C>T | p.Phe52Phe | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/9 | 173/1922 | 156/1134 | 52/377 | chr1 | 10536284 | |||
| chr1:10624356 | G | A | 1 | a0001c0014 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.504G>A | p.Thr168Thr | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 7/9 | 521/1922 | 504/1134 | 168/377 | chr1 | 10624356 | |||
| chr1:10624365 | C | A | 1 | a0001c0006 | 5 | HG02717.hp1 HG03139.hp1 HG03486.hp1 others(2): Show |
synonymous_variant | LOW | c.513C>A | p.Ala171Ala | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 7/9 | 530/1922 | 513/1134 | 171/377 | chr1 | 10624365 | |||
| chr1:10624419 | C | T | 1 | a0001c0017 | 1 | NA20905.hp2 | synonymous_variant | LOW | c.567C>T | p.His189His | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 7/9 | 584/1922 | 567/1134 | 189/377 | chr1 | 10624419 | |||
| chr1:10629648 | A | G | 1 | a0001c0016 | 1 | HG01934.hp1 | synonymous_variant | LOW | c.795A>G | p.Ser265Ser | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 9/9 | 812/1922 | 795/1134 | 265/377 | chr1 | 10629648 | |||
| chr1:10629726 | C | T | 1 | a0001c0015 | 1 | HG03225.hp1 | synonymous_variant | LOW | c.873C>T | p.His291His | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 9/9 | 890/1922 | 873/1134 | 291/377 | chr1 | 10629726 | |||
| chr1:10629867 | C | T | 3 | a0001c0003 a0001c0007 a0001c0012 |
28 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(25): Show |
synonymous_variant | LOW | c.1014C>T | p.Asp338Asp | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 9/9 | 1031/1922 | 1014/1134 | 338/377 | chr1 | 10629867 | |||
| chr1:10629885 | G | T | 2 | a0001c0004 a0001c0008 |
18 | HG00733.hp2 HG00741.hp2 HG01069.hp2 others(15): Show |
synonymous_variant | LOW | c.1032G>T | p.Gly344Gly | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 9/9 | 1049/1922 | 1032/1134 | 344/377 | chr1 | 10629885 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:10630182 | C | T | 1 | a0001c0001t0006 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*195C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 9/9 | 195 | chr1 | 10630182 | ||||||
| chr1:10630240 | G | A | 1 | a0001c0001t0002 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*253G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 9/9 | 253 | chr1 | 10630240 | ||||||
| chr1:10630296 | C | T | 1 | a0001c0002t0005 | 1 | NA18944.hp1 | 3_prime_UTR_variant | MODIFIER | c.*309C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 9/9 | 309 | chr1 | 10630296 | ||||||
| chr1:10630354 | G | T | 1 | a0001c0001t0004 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*367G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 9/9 | 367 | chr1 | 10630354 | ||||||
| chr1:10630429 | C | T | 1 | a0001c0001t0003 | 1 | NA18950.hp1 | 3_prime_UTR_variant | MODIFIER | c.*442C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 9/9 | 442 | chr1 | 10630429 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:10475212 | G | T | 3 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0015t0001g0255 |
3 | HG03209.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.36+210G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10475212 | |||||||
| chr1:10475235 | C | T | 1 | a0001c0002t0001g0254 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.36+233C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10475235 | |||||||
| chr1:10475236 | G | C | 1 | a0001c0002t0001g0254 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.36+234G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10475236 | |||||||
| chr1:10475416 | C | T | 5 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0252 others(2): Show |
5 | HG01891.hp1 HG01891.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.36+414C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10475416 | |||||||
| chr1:10475472 | G | C | 2 | a0001c0001t0001g0002 a0001c0001t0001g0003 |
2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.36+470G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10475472 | |||||||
| chr1:10475535 | A | C | 1 | a0001c0001t0001g0248 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.36+533A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10475535 | |||||||
| chr1:10475753 | G | A | 8 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(5): Show |
8 | HG00099.hp1 HG01099.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.36+751G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10475753 | |||||||
| chr1:10475767 | G | A | 7 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(4): Show |
7 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.36+765G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10475767 | |||||||
| chr1:10475798 | C | T | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.36+796C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10475798 | |||||||
| chr1:10475946 | A | G | 6 | a0001c0001t0001g0245 a0001c0001t0001g0249 a0001c0001t0001g0250 others(3): Show |
6 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.36+944A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10475946 | |||||||
| chr1:10475982 | A | C | 6 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0241 others(3): Show |
6 | HG00673.hp1 NA18939.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.36+980A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10475982 | |||||||
| chr1:10476448 | G | C | 1 | a0001c0001t0001g0020 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.36+1446G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10476448 | |||||||
| chr1:10476524 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.36+1522G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10476524 | |||||||
| chr1:10476578 | G | A | 84 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(81): Show |
84 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.36+1576G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10476578 | |||||||
| chr1:10476590 | C | G | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.36+1588C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10476590 | |||||||
| chr1:10476602 | C | T | 2 | a0001c0002t0001g0237 a0001c0003t0001g0238 |
2 | HG01981.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.36+1600C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10476602 | |||||||
| chr1:10476737 | C | T | 20 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(17): Show |
20 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.36+1735C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10476737 | |||||||
| chr1:10476787 | G | A | 20 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(17): Show |
20 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.36+1785G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10476787 | |||||||
| chr1:10476942 | G | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(1): Show |
4 | HG02280.hp1 HG02630.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.36+1940G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10476942 | |||||||
| chr1:10476967 | C | G | 1 | a0001c0001t0001g0225 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.36+1965C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10476967 | |||||||
| chr1:10477019 | G | A | 20 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(17): Show |
20 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.36+2017G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10477019 | |||||||
| chr1:10477033 | C | A | 157 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(154): Show |
157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.36+2031C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10477033 | |||||||
| chr1:10477075 | C | CT | 23 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(20): Show |
23 | HG00558.hp2 HG00609.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.36+2086dupT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 10477075 | ||||||
| chr1:10477144 | C | G | 13 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0226 others(10): Show |
13 | HG01884.hp1 HG02055.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.36+2142C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10477144 | |||||||
| chr1:10477195 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.36+2193C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10477195 | |||||||
| chr1:10477196 | T | G | 1 | a0001c0001t0001g0096 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.36+2194T>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10477196 | |||||||
| chr1:10477197 | A | C | 1 | a0001c0001t0001g0114 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.36+2195A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10477197 | |||||||
| chr1:10477199 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.36+2197T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10477199 | |||||||
| chr1:10477363 | C | A | 44 | a0001c0001t0001g0020 a0001c0001t0001g0131 a0001c0001t0001g0134 others(41): Show |
44 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.36+2361C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10477363 | |||||||
| chr1:10477380 | C | G | 129 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(126): Show |
129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.36+2378C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10477380 | |||||||
| chr1:10477782 | C | T | 7 | a0001c0001t0001g0112 a0001c0001t0001g0245 a0001c0001t0001g0249 others(4): Show |
7 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.36+2780C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10477782 | |||||||
| chr1:10477849 | C | G | 22 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(19): Show |
22 | HG00609.hp2 HG00673.hp1 HG01981.hp2 others(19): Show |
intron_variant | MODIFIER | c.36+2847C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10477849 | |||||||
| chr1:10477875 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.36+2873T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10477875 | |||||||
| chr1:10477926 | T | C | 4 | a0001c0002t0001g0167 a0001c0002t0001g0168 a0001c0002t0001g0169 others(1): Show |
4 | HG00673.hp2 HG02071.hp2 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.36+2924T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10477926 | |||||||
| chr1:10477980 | C | T | 13 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0226 others(10): Show |
13 | HG01884.hp1 HG02055.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.36+2978C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10477980 | |||||||
| chr1:10478090 | A | G | 30 | a0001c0001t0001g0020 a0001c0001t0001g0138 a0001c0001t0001g0139 others(27): Show |
30 | HG00408.hp1 HG00544.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.36+3088A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10478090 | |||||||
| chr1:10478168 | C | T | 13 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0226 others(10): Show |
13 | HG01884.hp1 HG02055.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.36+3166C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10478168 | |||||||
| chr1:10478252 | A | C | 1 | a0002c0005t0001g0218 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.36+3250A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10478252 | |||||||
| chr1:10478449 | T | A | 20 | a0001c0001t0001g0097 a0001c0001t0001g0115 a0001c0001t0001g0116 others(17): Show |
20 | HG01109.hp1 HG01884.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.36+3447T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10478449 | |||||||
| chr1:10478785 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.36+3783G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10478785 | |||||||
| chr1:10478894 | T | C | 201 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(198): Show |
201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.36+3892T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10478894 | |||||||
| chr1:10478973 | G | A | 1 | a0001c0017t0001g0130 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.36+3971G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10478973 | |||||||
| chr1:10478994 | G | A | 1 | a0004c0010t0001g0098 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.36+3992G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10478994 | |||||||
| chr1:10479285 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.36+4283G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10479285 | |||||||
| chr1:10479285 | G | C | 1 | a0005c0018t0001g0171 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.36+4283G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10479285 | |||||||
| chr1:10479446 | C | A | 20 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(17): Show |
20 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.36+4444C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10479446 | |||||||
| chr1:10479486 | C | T | 201 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(198): Show |
201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.36+4484C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10479486 | |||||||
| chr1:10479776 | A | G | 22 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(19): Show |
22 | HG00609.hp2 HG00673.hp1 HG01981.hp2 others(19): Show |
intron_variant | MODIFIER | c.36+4774A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10479776 | |||||||
| chr1:10479836 | A | G | 6 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(3): Show |
6 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.36+4834A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10479836 | |||||||
| chr1:10479861 | G | A | 7 | a0001c0001t0001g0112 a0001c0001t0001g0245 a0001c0001t0001g0249 others(4): Show |
7 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.36+4859G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10479861 | |||||||
| chr1:10480079 | G | A | 3 | a0002c0005t0001g0172 a0002c0005t0001g0173 a0002c0005t0001g0218 |
3 | HG01167.hp1 HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.36+5077G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10480079 | |||||||
| chr1:10480150 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.36+5148G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10480150 | |||||||
| chr1:10480183 | G | T | 13 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0226 others(10): Show |
13 | HG01884.hp1 HG02055.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.36+5181G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10480183 | |||||||
| chr1:10480199 | TG | T | 21 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(18): Show |
21 | HG00609.hp2 HG00673.hp1 HG01981.hp2 others(18): Show |
intron_variant | MODIFIER | c.36+5198delG | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10480199 | |||||||
| chr1:10480200 | GT | G | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(173): Show |
176 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.36+5210delT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 10480200 | ||||||
| chr1:10480201 | T | A | 21 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(18): Show |
21 | HG00609.hp2 HG00673.hp1 HG01981.hp2 others(18): Show |
intron_variant | MODIFIER | c.36+5199T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10480201 | |||||||
| chr1:10480202 | T | A | 1 | a0001c0001t0001g0244 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.36+5200T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10480202 | |||||||
| chr1:10480209 | T | G | 1 | a0002c0005t0001g0172 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.36+5207T>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10480209 | |||||||
| chr1:10480232 | A | G | 1 | a0004c0010t0001g0098 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.36+5230A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10480232 | |||||||
| chr1:10480387 | C | CT | 67 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(64): Show |
68 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.36+5409dupT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 10480387 | ||||||
| chr1:10480387 | C | CTT | 5 | a0001c0001t0001g0016 a0001c0001t0001g0095 a0001c0002t0001g0215 others(2): Show |
5 | HG00735.hp1 HG02280.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.36+5408_36+5409dup others(2): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 10480387 | ||||||
| chr1:10480387 | CT | C | 27 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0001c0001t0001g0100 others(24): Show |
27 | HG00673.hp1 HG01256.hp1 HG01981.hp2 others(24): Show |
intron_variant | MODIFIER | c.36+5409delT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 10480387 | ||||||
| chr1:10480387 | CTTTTTT | C | 64 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(61): Show |
64 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.36+5404_36+5409del others(6): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 10480387 | ||||||
| chr1:10480568 | G | A | 1 | a0001c0017t0001g0130 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.36+5566G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10480568 | |||||||
| chr1:10480620 | G | T | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.36+5618G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10480620 | |||||||
| chr1:10480829 | CTCTCTCT others(5): Show |
C | 1 | a0001c0001t0001g0180 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.36+5839_36+5850del others(12): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 10480829 | ||||||
| chr1:10480841 | TTC | T | 46 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(43): Show |
47 | HG00280.hp2 HG00673.hp1 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.36+5857_36+5858del others(2): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 10480841 | ||||||
| chr1:10480859 | C | A | 8 | a0001c0001t0001g0113 a0001c0001t0001g0219 a0001c0001t0001g0220 others(5): Show |
8 | HG00558.hp2 HG00609.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.36+5857C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10480859 | |||||||
| chr1:10480859 | CTA | C | 30 | a0001c0001t0001g0097 a0001c0001t0001g0106 a0001c0001t0001g0109 others(27): Show |
30 | HG00609.hp2 HG01109.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.36+5867_36+5868del others(2): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 10480859 | ||||||
| chr1:10480861 | A | C | 78 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(75): Show |
78 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.36+5859A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10480861 | |||||||
| chr1:10480863 | A | C | 31 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(28): Show |
31 | HG00280.hp1 HG00621.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.36+5861A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10480863 | |||||||
| chr1:10480867 | A | AT | 4 | a0001c0001t0001g0064 a0001c0001t0001g0092 a0001c0001t0001g0093 others(1): Show |
4 | HG01081.hp2 HG01168.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.36+5866dupT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 10480867 | ||||||
| chr1:10480868 | TA | T | 3 | a0001c0001t0001g0065 a0001c0001t0001g0113 a0001c0003t0001g0066 |
3 | HG00621.hp2 HG03453.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.36+5867delA | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10480868 | |||||||
| chr1:10480869 | A | T | 82 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.36+5867A>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10480869 | |||||||
| chr1:10480869 | AT | A | 14 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0020 others(11): Show |
14 | HG01884.hp1 HG02055.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.36+5878delT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 10480869 | ||||||
| chr1:10480869 | ATT | A | 10 | a0001c0001t0001g0017 a0001c0001t0001g0112 a0001c0001t0001g0245 others(7): Show |
10 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.36+5877_36+5878del others(2): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 10480869 | ||||||
| chr1:10480871 | T | A | 8 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(5): Show |
8 | HG01167.hp1 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.36+5869T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10480871 | |||||||
| chr1:10480872 | T | A | 13 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0226 others(10): Show |
13 | HG01884.hp1 HG02055.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.36+5870T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10480872 | |||||||
| chr1:10480873 | T | A | 8 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(5): Show |
8 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.36+5871T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10480873 | |||||||
| chr1:10480874 | T | A | 13 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0226 others(10): Show |
13 | HG01884.hp1 HG02055.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.36+5872T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10480874 | |||||||
| chr1:10480876 | T | A | 1 | a0001c0001t0001g0227 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.36+5874T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10480876 | |||||||
| chr1:10481117 | CT | C | 27 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0099 others(24): Show |
27 | HG00609.hp2 HG00673.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.36+6127delT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 10481117 | ||||||
| chr1:10481140 | C | CT | 31 | a0001c0001t0001g0020 a0001c0001t0001g0137 a0001c0001t0001g0138 others(28): Show |
31 | HG00408.hp1 HG00544.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.36+6149dupT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 10481140 | ||||||
| chr1:10481236 | C | T | 129 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(126): Show |
129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.36+6234C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10481236 | |||||||
| chr1:10481623 | G | T | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0128 |
3 | HG02559.hp2 HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.36+6621G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10481623 | |||||||
| chr1:10481767 | G | C | 85 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(82): Show |
85 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.36+6765G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10481767 | |||||||
| chr1:10481823 | CT | C | 177 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(174): Show |
177 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.36+6839delT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 10481823 | ||||||
| chr1:10481892 | C | T | 1 | a0002c0005t0001g0127 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.36+6890C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10481892 | |||||||
| chr1:10481928 | C | T | 22 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(19): Show |
22 | HG00609.hp2 HG00673.hp1 HG01981.hp2 others(19): Show |
intron_variant | MODIFIER | c.36+6926C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10481928 | |||||||
| chr1:10482014 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.36+7012G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10482014 | |||||||
| chr1:10482289 | T | C | 1 | a0001c0004t0001g0024 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.36+7287T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10482289 | |||||||
| chr1:10482291 | G | T | 1 | a0001c0002t0001g0179 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.36+7289G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10482291 | |||||||
| chr1:10482338 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.36+7336C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10482338 | |||||||
| chr1:10482437 | C | CT | 7 | a0001c0002t0001g0170 a0001c0002t0001g0178 a0001c0002t0001g0210 others(4): Show |
7 | HG01099.hp1 HG01981.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.36+7451dupT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 10482437 | ||||||
| chr1:10482477 | C | T | 1 | a0004c0010t0001g0098 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.36+7475C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10482477 | |||||||
| chr1:10482505 | C | G | 1 | a0001c0003t0001g0238 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.36+7503C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10482505 | |||||||
| chr1:10482527 | G | A | 21 | a0001c0002t0001g0001 a0001c0002t0001g0167 a0001c0002t0001g0168 others(18): Show |
22 | HG00280.hp2 HG00673.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.36+7525G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10482527 | |||||||
| chr1:10482552 | G | A | 31 | a0001c0001t0001g0020 a0001c0001t0001g0137 a0001c0001t0001g0138 others(28): Show |
31 | HG00408.hp1 HG00544.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.36+7550G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10482552 | |||||||
| chr1:10482594 | C | T | 1 | a0002c0005t0001g0218 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.36+7592C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10482594 | |||||||
| chr1:10482654 | G | A | 21 | a0001c0001t0001g0097 a0001c0001t0001g0115 a0001c0001t0001g0116 others(18): Show |
21 | HG01109.hp1 HG01884.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.36+7652G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10482654 | |||||||
| chr1:10482657 | G | A | 201 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(198): Show |
201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.36+7655G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10482657 | |||||||
| chr1:10482712 | A | G | 3 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0015t0001g0255 |
3 | HG03209.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.36+7710A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10482712 | |||||||
| chr1:10482721 | C | T | 1 | a0001c0008t0001g0192 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.36+7719C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10482721 | |||||||
| chr1:10482722 | G | A | 4 | a0001c0001t0001g0174 a0002c0005t0001g0172 a0002c0005t0001g0173 others(1): Show |
4 | HG01167.hp1 HG02809.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.36+7720G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10482722 | |||||||
| chr1:10482797 | C | T | 2 | a0001c0001t0001g0109 a0001c0003t0001g0108 |
2 | HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.36+7795C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10482797 | |||||||
| chr1:10482863 | G | T | 85 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(82): Show |
85 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.36+7861G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10482863 | |||||||
| chr1:10482883 | T | A | 44 | a0001c0001t0001g0020 a0001c0001t0001g0131 a0001c0001t0001g0134 others(41): Show |
44 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.36+7881T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10482883 | |||||||
| chr1:10483029 | C | G | 2 | a0001c0009t0001g0062 a0001c0009t0001g0063 |
2 | HG02080.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.36+8027C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10483029 | |||||||
| chr1:10483266 | C | T | 1 | a0001c0017t0001g0130 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.36+8264C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10483266 | |||||||
| chr1:10483274 | G | C | 1 | a0001c0001t0001g0246 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.36+8272G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10483274 | |||||||
| chr1:10483420 | G | A | 13 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0226 others(10): Show |
13 | HG01884.hp1 HG02055.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.36+8418G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10483420 | |||||||
| chr1:10483496 | CAGTAGAG others(2434): Show |
C | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.36+8514_37-9318del | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 10483496 | ||||||
| chr1:10483607 | G | A | 13 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0226 others(10): Show |
13 | HG01884.hp1 HG02055.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.36+8605G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10483607 | |||||||
| chr1:10483678 | A | G | 1 | a0001c0003t0001g0041 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.36+8676A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10483678 | |||||||
| chr1:10483760 | A | AC | 151 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(148): Show |
151 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.36+8761dupC | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 10483760 | ||||||
| chr1:10483779 | A | G | 58 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(55): Show |
58 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.36+8777A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10483779 | |||||||
| chr1:10483931 | A | AATTC | 142 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(139): Show |
142 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.36+8932_36+8933ins others(4): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 10483931 | ||||||
| chr1:10484001 | T | C | 22 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(19): Show |
22 | HG00609.hp2 HG00673.hp1 HG01981.hp2 others(19): Show |
intron_variant | MODIFIER | c.36+8999T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10484001 | |||||||
| chr1:10484028 | C | CT | 18 | a0001c0001t0001g0003 a0001c0001t0001g0089 a0001c0001t0001g0092 others(15): Show |
18 | HG01081.hp2 HG01168.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.36+9043dupT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 10484028 | ||||||
| chr1:10484028 | CT | C | 13 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(10): Show |
13 | HG01099.hp1 HG02109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.36+9043delT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 10484028 | ||||||
| chr1:10484149 | C | T | 5 | a0001c0001t0001g0118 a0001c0001t0001g0121 a0001c0001t0001g0248 others(2): Show |
5 | HG02559.hp1 HG02717.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.36+9147C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10484149 | |||||||
| chr1:10484177 | A | AC | 85 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(82): Show |
85 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.36+9177dupC | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 10484177 | ||||||
| chr1:10484291 | G | A | 1 | a0001c0002t0001g0186 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.36+9289G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10484291 | |||||||
| chr1:10484294 | T | C | 6 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(3): Show |
6 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.36+9292T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10484294 | |||||||
| chr1:10484330 | G | T | 1 | a0001c0001t0001g0112 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.36+9328G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10484330 | |||||||
| chr1:10484331 | T | C | 203 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(200): Show |
203 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.36+9329T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10484331 | |||||||
| chr1:10484332 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.36+9330C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10484332 | |||||||
| chr1:10484384 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.36+9382G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10484384 | |||||||
| chr1:10484418 | C | T | 1 | a0001c0003t0001g0025 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.36+9416C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10484418 | |||||||
| chr1:10484422 | C | T | 1 | a0001c0003t0001g0057 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.36+9420C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10484422 | |||||||
| chr1:10484490 | G | A | 199 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(196): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.36+9488G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10484490 | |||||||
| chr1:10484668 | A | G | 171 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(168): Show |
171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.36+9666A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10484668 | |||||||
| chr1:10484826 | G | A | 4 | a0001c0002t0001g0167 a0001c0002t0001g0168 a0001c0002t0001g0169 others(1): Show |
4 | HG00673.hp2 HG02071.hp2 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.36+9824G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10484826 | |||||||
| chr1:10484931 | C | A | 83 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(80): Show |
83 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.36+9929C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10484931 | |||||||
| chr1:10484948 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.36+9946C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10484948 | |||||||
| chr1:10485021 | A | C | 1 | a0006c0013t0001g0206 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.36+10019A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10485021 | |||||||
| chr1:10485145 | C | T | 2 | a0001c0001t0001g0067 a0001c0001t0001g0075 |
2 | HG01175.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.37-10129C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10485145 | |||||||
| chr1:10485299 | G | GT | 21 | a0001c0001t0001g0045 a0001c0001t0001g0071 a0001c0001t0001g0112 others(18): Show |
21 | HG00673.hp2 HG01106.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.37-9951dupT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 10485299 | ||||||
| chr1:10485299 | G | GTT | 5 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0245 others(2): Show |
5 | HG02109.hp2 HG02630.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.37-9952_37-9951dup others(2): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 10485299 | ||||||
| chr1:10485299 | GT | G | 36 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0056 others(33): Show |
36 | HG00609.hp2 HG01167.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.37-9951delT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 10485299 | ||||||
| chr1:10485384 | A | C | 6 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0003t0001g0083 others(3): Show |
6 | HG02647.hp1 HG02735.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.37-9890A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10485384 | |||||||
| chr1:10485482 | A | C | 1 | a0001c0001t0001g0226 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.37-9792A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10485482 | |||||||
| chr1:10485503 | G | A | 1 | a0001c0002t0005g0200 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.37-9771G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10485503 | |||||||
| chr1:10485504 | C | T | 2 | a0001c0001t0001g0049 a0001c0004t0001g0053 |
2 | HG00741.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.37-9770C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10485504 | |||||||
| chr1:10485533 | G | A | 199 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(196): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.37-9741G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10485533 | |||||||
| chr1:10485688 | A | G | 1 | a0004c0010t0001g0098 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.37-9586A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10485688 | |||||||
| chr1:10485758 | G | GT | 15 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0054 others(12): Show |
15 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.37-9501dupT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 10485758 | ||||||
| chr1:10485842 | G | A | 1 | a0004c0010t0001g0098 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.37-9432G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10485842 | |||||||
| chr1:10485881 | T | A | 7 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(4): Show |
7 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.37-9393T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10485881 | |||||||
| chr1:10485882 | A | G | 7 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(4): Show |
7 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.37-9392A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10485882 | |||||||
| chr1:10485988 | C | T | 20 | a0001c0001t0001g0097 a0001c0001t0001g0115 a0001c0001t0001g0116 others(17): Show |
20 | HG01109.hp1 HG01884.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.37-9286C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10485988 | |||||||
| chr1:10486061 | A | G | 1 | a0003c0011t0001g0107 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.37-9213A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10486061 | |||||||
| chr1:10486184 | G | A | 22 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(19): Show |
22 | HG00609.hp2 HG00673.hp1 HG01981.hp2 others(19): Show |
intron_variant | MODIFIER | c.37-9090G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10486184 | |||||||
| chr1:10486203 | A | G | 1 | a0002c0005t0001g0173 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.37-9071A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10486203 | |||||||
| chr1:10486360 | G | GT | 10 | a0001c0001t0001g0020 a0001c0001t0001g0061 a0001c0001t0001g0073 others(7): Show |
10 | HG01109.hp2 HG01175.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.37-8894dupT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 10486360 | ||||||
| chr1:10486360 | GT | G | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0076 others(8): Show |
11 | HG01081.hp1 HG01255.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.37-8894delT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 10486360 | ||||||
| chr1:10486500 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.37-8774C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10486500 | |||||||
| chr1:10486616 | A | G | 1 | a0001c0001t0001g0112 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.37-8658A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10486616 | |||||||
| chr1:10486689 | C | CT | 155 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(152): Show |
155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.37-8569dupT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 10486689 | ||||||
| chr1:10486689 | C | CTT | 12 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(9): Show |
12 | HG01884.hp1 HG02055.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.37-8570_37-8569dup others(2): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 10486689 | ||||||
| chr1:10486689 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.37-8585C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10486689 | |||||||
| chr1:10486751 | G | C | 13 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0226 others(10): Show |
13 | HG01884.hp1 HG02055.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.37-8523G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10486751 | |||||||
| chr1:10486862 | T | C | 1 | a0004c0010t0001g0098 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.37-8412T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10486862 | |||||||
| chr1:10487206 | C | T | 193 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(190): Show |
193 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.37-8068C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10487206 | |||||||
| chr1:10487329 | G | GT | 29 | a0001c0001t0001g0097 a0001c0001t0001g0115 a0001c0001t0001g0116 others(26): Show |
29 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.37-7932dupT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 10487329 | ||||||
| chr1:10487427 | G | C | 30 | a0001c0001t0001g0097 a0001c0001t0001g0115 a0001c0001t0001g0116 others(27): Show |
30 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.37-7847G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10487427 | |||||||
| chr1:10487481 | C | CT | 117 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(114): Show |
117 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.37-7771dupT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 10487481 | ||||||
| chr1:10487481 | C | CTT | 7 | a0001c0001t0001g0017 a0001c0001t0001g0059 a0001c0001t0001g0075 others(4): Show |
7 | HG01069.hp2 HG01070.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.37-7772_37-7771dup others(2): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 10487481 | ||||||
| chr1:10487481 | C | CTTT | 17 | a0001c0001t0001g0080 a0001c0001t0001g0106 a0001c0001t0001g0109 others(14): Show |
17 | HG00609.hp2 HG00673.hp1 HG01981.hp2 others(14): Show |
intron_variant | MODIFIER | c.37-7773_37-7771dup others(3): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 10487481 | ||||||
| chr1:10487481 | CT | C | 9 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0229 others(6): Show |
9 | HG01168.hp1 HG01255.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.37-7771delT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 10487481 | ||||||
| chr1:10487481 | CTTTTTTT others(3): Show |
C | 1 | a0001c0002t0001g0193 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.37-7780_37-7771del others(10): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 10487481 | ||||||
| chr1:10487629 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.37-7645C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10487629 | |||||||
| chr1:10487630 | G | A | 160 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(157): Show |
160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.37-7644G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10487630 | |||||||
| chr1:10488012 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.37-7262C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10488012 | |||||||
| chr1:10488075 | C | G | 1 | a0001c0001t0001g0019 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.37-7199C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10488075 | |||||||
| chr1:10488100 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.37-7174A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10488100 | |||||||
| chr1:10488168 | G | C | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.37-7106G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10488168 | |||||||
| chr1:10488242 | C | T | 1 | a0001c0007t0001g0189 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.37-7032C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10488242 | |||||||
| chr1:10488338 | G | T | 1 | a0001c0002t0001g0217 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.37-6936G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10488338 | |||||||
| chr1:10488437 | G | A | 7 | a0001c0001t0001g0131 a0001c0001t0001g0134 a0001c0001t0001g0136 others(4): Show |
7 | HG00741.hp1 HG02129.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.37-6837G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10488437 | |||||||
| chr1:10488490 | G | A | 1 | a0001c0001t0001g0018 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.37-6784G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10488490 | |||||||
| chr1:10488621 | T | C | 1 | a0001c0001t0001g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.37-6653T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10488621 | |||||||
| chr1:10488936 | T | C | 3 | a0002c0005t0001g0172 a0002c0005t0001g0173 a0002c0005t0001g0218 |
3 | HG01167.hp1 HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.37-6338T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10488936 | |||||||
| chr1:10489043 | C | T | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.37-6231C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10489043 | |||||||
| chr1:10489228 | G | A | 27 | a0001c0001t0001g0097 a0001c0001t0001g0115 a0001c0001t0001g0116 others(24): Show |
27 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.37-6046G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10489228 | |||||||
| chr1:10489323 | A | G | 84 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(81): Show |
84 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.37-5951A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10489323 | |||||||
| chr1:10489571 | C | A | 199 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(196): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.37-5703C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10489571 | |||||||
| chr1:10489692 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.37-5582C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10489692 | |||||||
| chr1:10489770 | C | T | 13 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0226 others(10): Show |
13 | HG01884.hp1 HG02055.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.37-5504C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10489770 | |||||||
| chr1:10489791 | G | C | 203 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(200): Show |
203 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.37-5483G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10489791 | |||||||
| chr1:10490097 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.37-5177G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10490097 | |||||||
| chr1:10490295 | C | T | 72 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(69): Show |
72 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.37-4979C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10490295 | |||||||
| chr1:10490450 | C | T | 6 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(3): Show |
6 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.37-4824C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10490450 | |||||||
| chr1:10490511 | C | T | 2 | a0001c0001t0001g0249 a0001c0001t0001g0250 |
2 | HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.37-4763C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10490511 | |||||||
| chr1:10490523 | C | T | 3 | a0002c0005t0001g0172 a0002c0005t0001g0173 a0002c0005t0001g0218 |
3 | HG01167.hp1 HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.37-4751C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10490523 | |||||||
| chr1:10490654 | C | G | 5 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0002c0005t0001g0172 others(2): Show |
5 | HG01167.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.37-4620C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10490654 | |||||||
| chr1:10490700 | C | CT | 6 | a0001c0001t0001g0072 a0001c0001t0001g0164 a0001c0001t0003g0058 others(3): Show |
6 | HG02451.hp2 HG03942.hp2 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.37-4555dupT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 10490700 | ||||||
| chr1:10490700 | CT | C | 11 | a0001c0001t0001g0019 a0001c0001t0001g0067 a0001c0001t0001g0231 others(8): Show |
11 | HG01167.hp1 HG01167.hp2 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.37-4555delT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 10490700 | ||||||
| chr1:10490820 | A | G | 204 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(201): Show |
204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.37-4454A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10490820 | |||||||
| chr1:10490924 | G | A | 1 | a0001c0002t0001g0237 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.37-4350G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10490924 | |||||||
| chr1:10490997 | GT | G | 9 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(6): Show |
9 | HG01099.hp1 NA18942.hp2 NA18964.hp2 others(6): Show |
intron_variant | MODIFIER | c.37-4261delT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 10490997 | ||||||
| chr1:10491146 | C | T | 13 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0226 others(10): Show |
13 | HG01884.hp1 HG02055.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.37-4128C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10491146 | |||||||
| chr1:10491190 | G | A | 4 | a0001c0003t0001g0025 a0001c0003t0001g0026 a0001c0003t0001g0027 others(1): Show |
4 | HG00423.hp1 HG00544.hp2 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.37-4084G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10491190 | |||||||
| chr1:10491484 | G | GAGCCTCC others(6): Show |
6 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0002c0005t0001g0172 others(3): Show |
6 | HG01167.hp1 HG02622.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.37-3782_37-3781ins others(13): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 10491484 | ||||||
| chr1:10491674 | CT | C | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(203): Show |
207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.37-3577delT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 10491674 | ||||||
| chr1:10491674 | CTT | C | 10 | a0001c0001t0001g0040 a0001c0001t0001g0082 a0001c0001t0001g0141 others(7): Show |
10 | HG01070.hp1 HG01167.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.37-3578_37-3577del others(2): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 10491674 | ||||||
| chr1:10491706 | A | G | 201 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(198): Show |
201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.37-3568A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10491706 | |||||||
| chr1:10491706 | A | T | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.37-3568A>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10491706 | |||||||
| chr1:10491733 | T | C | 2 | a0002c0005t0001g0173 a0002c0005t0001g0218 |
2 | HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.37-3541T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10491733 | |||||||
| chr1:10491880 | G | A | 1 | a0001c0002t0001g0237 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.37-3394G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10491880 | |||||||
| chr1:10492037 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.37-3237C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10492037 | |||||||
| chr1:10492114 | A | G | 6 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0250 others(3): Show |
6 | HG01167.hp1 HG02622.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.37-3160A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10492114 | |||||||
| chr1:10492349 | G | T | 1 | a0001c0001t0001g0018 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.37-2925G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10492349 | |||||||
| chr1:10492472 | A | G | 1 | a0001c0001t0001g0019 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.37-2802A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10492472 | |||||||
| chr1:10492500 | A | G | 27 | a0001c0001t0001g0097 a0001c0001t0001g0115 a0001c0001t0001g0116 others(24): Show |
27 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.37-2774A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10492500 | |||||||
| chr1:10492529 | T | G | 2 | a0001c0001t0001g0118 a0001c0006t0001g0119 |
2 | HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.37-2745T>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10492529 | |||||||
| chr1:10492661 | C | T | 44 | a0001c0001t0001g0020 a0001c0001t0001g0131 a0001c0001t0001g0134 others(41): Show |
44 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.37-2613C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10492661 | |||||||
| chr1:10493091 | C | T | 20 | a0001c0001t0001g0097 a0001c0001t0001g0115 a0001c0001t0001g0116 others(17): Show |
20 | HG01109.hp1 HG01884.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.37-2183C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10493091 | |||||||
| chr1:10493255 | G | A | 3 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 |
3 | HG01081.hp2 HG01168.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.37-2019G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10493255 | |||||||
| chr1:10493257 | C | T | 4 | a0001c0001t0001g0180 a0001c0004t0001g0209 a0002c0005t0001g0207 others(1): Show |
4 | HG03139.hp2 HG03486.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.37-2017C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10493257 | |||||||
| chr1:10493874 | T | C | 1 | a0001c0001t0001g0252 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.37-1400T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10493874 | |||||||
| chr1:10493962 | G | T | 2 | a0001c0001t0001g0002 a0001c0001t0001g0003 |
2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.37-1312G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10493962 | |||||||
| chr1:10494031 | G | A | 2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | NA18950.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.37-1243G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10494031 | |||||||
| chr1:10494068 | C | T | 3 | a0001c0003t0001g0088 a0001c0006t0001g0086 a0001c0006t0001g0087 |
3 | HG03139.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.37-1206C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10494068 | |||||||
| chr1:10494082 | C | A | 1 | a0001c0001t0001g0089 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.37-1192C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10494082 | |||||||
| chr1:10494217 | G | A | 1 | a0001c0001t0001g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.37-1057G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10494217 | |||||||
| chr1:10494305 | G | A | 13 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0226 others(10): Show |
13 | HG01884.hp1 HG02055.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.37-969G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10494305 | |||||||
| chr1:10494448 | A | G | 201 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(198): Show |
201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.37-826A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10494448 | |||||||
| chr1:10494652 | G | T | 164 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(161): Show |
164 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.37-622G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10494652 | |||||||
| chr1:10494737 | T | C | 174 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(171): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.37-537T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10494737 | |||||||
| chr1:10495200 | C | T | 164 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(161): Show |
164 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.37-74C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 1/8 | chr1 | 10495200 | |||||||
| chr1:10495373 | G | A | 1 | a0001c0001t0001g0034 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.84+52G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10495373 | |||||||
| chr1:10495429 | G | A | 1 | a0001c0002t0001g0184 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.84+108G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10495429 | |||||||
| chr1:10495605 | C | T | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.84+284C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10495605 | |||||||
| chr1:10496039 | C | T | 1 | a0004c0010t0001g0098 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.84+718C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10496039 | |||||||
| chr1:10496040 | G | A | 132 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(129): Show |
132 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.84+719G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10496040 | |||||||
| chr1:10496119 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.84+798G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10496119 | |||||||
| chr1:10496121 | G | A | 27 | a0001c0001t0001g0097 a0001c0001t0001g0115 a0001c0001t0001g0116 others(24): Show |
27 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.84+800G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10496121 | |||||||
| chr1:10496132 | A | C | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.84+811A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10496132 | |||||||
| chr1:10496133 | C | T | 1 | a0001c0001t0003g0058 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.84+812C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10496133 | |||||||
| chr1:10496329 | C | T | 6 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 others(3): Show |
6 | HG00558.hp2 HG00609.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.84+1008C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10496329 | |||||||
| chr1:10496390 | G | T | 192 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(189): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.84+1069G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10496390 | |||||||
| chr1:10496428 | T | C | 173 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(170): Show |
173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.84+1107T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10496428 | |||||||
| chr1:10496738 | CTGTACTG others(10): Show |
C | 1 | a0001c0001t0001g0139 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.84+1421_84+1437del others(17): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10496738 | ||||||
| chr1:10496776 | A | C | 2 | a0001c0002t0001g0188 a0001c0006t0001g0236 |
2 | HG00280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.84+1455A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10496776 | |||||||
| chr1:10496902 | T | G | 3 | a0002c0005t0001g0172 a0002c0005t0001g0173 a0002c0005t0001g0218 |
3 | HG01167.hp1 HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.84+1581T>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10496902 | |||||||
| chr1:10496949 | A | G | 1 | a0001c0001t0001g0018 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.84+1628A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10496949 | |||||||
| chr1:10497194 | T | C | 173 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(170): Show |
173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.84+1873T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10497194 | |||||||
| chr1:10497266 | C | T | 27 | a0001c0001t0001g0097 a0001c0001t0001g0115 a0001c0001t0001g0116 others(24): Show |
27 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.84+1945C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10497266 | |||||||
| chr1:10497278 | T | G | 1 | a0001c0001t0001g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.84+1957T>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10497278 | |||||||
| chr1:10497395 | G | A | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.84+2074G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10497395 | |||||||
| chr1:10497487 | A | G | 171 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(168): Show |
171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.84+2166A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10497487 | |||||||
| chr1:10497577 | C | T | 2 | a0001c0002t0001g0204 a0001c0002t0001g0205 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.84+2256C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10497577 | |||||||
| chr1:10497850 | T | G | 1 | a0001c0001t0001g0111 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.84+2529T>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10497850 | |||||||
| chr1:10498037 | T | G | 1 | a0001c0002t0001g0179 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.84+2716T>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10498037 | |||||||
| chr1:10498153 | G | A | 34 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(31): Show |
34 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.84+2832G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10498153 | |||||||
| chr1:10498280 | T | TAAAAC | 30 | a0001c0001t0001g0120 a0001c0001t0001g0144 a0001c0001t0001g0145 others(27): Show |
30 | HG00280.hp2 HG00544.hp1 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.84+2994_84+2998dup others(5): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10498280 | ||||||
| chr1:10498280 | T | TAAAACAA others(3): Show |
2 | a0001c0002t0001g0001 a0001c0002t0001g0210 |
3 | HG01256.hp2 HG01258.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.84+2989_84+2998dup others(10): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10498280 | ||||||
| chr1:10498280 | TAAAAC | T | 123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(120): Show |
123 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.84+2994_84+2998del others(5): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10498280 | ||||||
| chr1:10498280 | TAAAACAA others(3): Show |
T | 4 | a0001c0001t0001g0017 a0001c0001t0001g0097 a0001c0001t0001g0246 others(1): Show |
4 | HG02451.hp1 HG02622.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.84+2989_84+2998del others(10): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10498280 | ||||||
| chr1:10498280 | TAAAACAA others(13): Show |
T | 7 | a0001c0001t0001g0174 a0001c0001t0001g0245 a0001c0001t0001g0249 others(4): Show |
7 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.84+2979_84+2998del others(20): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10498280 | ||||||
| chr1:10498342 | C | T | 3 | a0001c0001t0001g0174 a0001c0001t0001g0252 a0001c0001t0002g0253 |
3 | HG01891.hp1 HG02723.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.84+3021C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10498342 | |||||||
| chr1:10498580 | G | A | 2 | a0001c0001t0001g0100 a0001c0003t0001g0102 |
2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.84+3259G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10498580 | |||||||
| chr1:10498663 | G | A | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.84+3342G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10498663 | |||||||
| chr1:10498781 | C | T | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.84+3460C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10498781 | |||||||
| chr1:10498825 | C | T | 6 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(3): Show |
6 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.84+3504C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10498825 | |||||||
| chr1:10499078 | T | C | 3 | a0001c0003t0001g0088 a0001c0006t0001g0086 a0001c0006t0001g0087 |
3 | HG03139.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.84+3757T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10499078 | |||||||
| chr1:10499266 | G | C | 1 | a0004c0010t0001g0098 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.84+3945G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10499266 | |||||||
| chr1:10499291 | G | C | 1 | a0002c0005t0001g0228 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.84+3970G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10499291 | |||||||
| chr1:10499445 | AT | A | 84 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(81): Show |
85 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.84+4145delT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10499445 | ||||||
| chr1:10499445 | ATT | A | 135 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.84+4144_84+4145del others(2): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10499445 | ||||||
| chr1:10499445 | ATTT | A | 6 | a0001c0001t0001g0040 a0001c0001t0001g0138 a0001c0001t0001g0246 others(3): Show |
6 | HG00558.hp2 HG01256.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.84+4143_84+4145del others(3): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10499445 | ||||||
| chr1:10499501 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.84+4180T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10499501 | |||||||
| chr1:10499541 | C | T | 88 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(85): Show |
88 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.84+4220C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10499541 | |||||||
| chr1:10499616 | T | G | 14 | a0001c0001t0001g0097 a0001c0001t0001g0115 a0001c0001t0001g0116 others(11): Show |
14 | HG02258.hp2 HG02451.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.84+4295T>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10499616 | |||||||
| chr1:10499654 | G | A | 1 | a0001c0001t0001g0005 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.84+4333G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10499654 | |||||||
| chr1:10499798 | C | T | 1 | a0004c0010t0001g0098 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.84+4477C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10499798 | |||||||
| chr1:10499904 | A | G | 2 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.84+4583A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10499904 | |||||||
| chr1:10499936 | A | C | 1 | a0001c0001t0001g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.84+4615A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10499936 | |||||||
| chr1:10500091 | G | A | 7 | a0001c0001t0001g0174 a0001c0001t0001g0245 a0001c0001t0001g0249 others(4): Show |
7 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.84+4770G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10500091 | |||||||
| chr1:10500157 | CTG | C | 139 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(136): Show |
139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.84+4839_84+4840del others(2): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10500157 | ||||||
| chr1:10500188 | A | C | 1 | a0001c0001t0001g0056 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.84+4867A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10500188 | |||||||
| chr1:10500241 | T | TA | 15 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0226 others(12): Show |
15 | HG01884.hp1 HG02055.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.84+4935dupA | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10500241 | ||||||
| chr1:10500241 | TA | T | 5 | a0001c0001t0001g0099 a0001c0001t0001g0101 a0001c0001t0001g0110 others(2): Show |
5 | HG02280.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.84+4935delA | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10500241 | ||||||
| chr1:10500373 | C | CA | 39 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0081 others(36): Show |
39 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.84+5081dupA | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10500373 | ||||||
| chr1:10500373 | C | CAA | 13 | a0001c0001t0001g0020 a0001c0001t0001g0131 a0001c0001t0001g0134 others(10): Show |
13 | HG00741.hp1 HG01358.hp2 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.84+5080_84+5081dup others(2): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10500373 | ||||||
| chr1:10500373 | CA | C | 19 | a0001c0001t0001g0061 a0001c0001t0001g0097 a0001c0001t0001g0112 others(16): Show |
20 | HG01256.hp2 HG01258.hp1 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.84+5081delA | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10500373 | ||||||
| chr1:10500373 | CAA | C | 58 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(55): Show |
58 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.84+5080_84+5081del others(2): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10500373 | ||||||
| chr1:10500373 | CAAAA | C | 13 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(10): Show |
13 | HG01433.hp1 HG01433.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.84+5078_84+5081del others(4): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10500373 | ||||||
| chr1:10500373 | CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0001g0052 a0001c0001t0001g0064 |
2 | NA18999.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.84+5072_84+5081del others(10): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10500373 | ||||||
| chr1:10500373 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0059 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.84+5071_84+5081del others(11): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10500373 | ||||||
| chr1:10500382 | A | G | 1 | a0001c0004t0001g0209 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.84+5061A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10500382 | |||||||
| chr1:10500675 | A | G | 1 | a0001c0001t0003g0058 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.84+5354A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10500675 | |||||||
| chr1:10500703 | T | G | 5 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(2): Show |
5 | HG02280.hp1 HG02630.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.84+5382T>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10500703 | |||||||
| chr1:10500723 | C | T | 1 | a0004c0010t0001g0098 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.84+5402C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10500723 | |||||||
| chr1:10500849 | G | T | 1 | a0001c0001t0001g0244 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.84+5528G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10500849 | |||||||
| chr1:10500931 | A | G | 43 | a0001c0001t0001g0020 a0001c0001t0001g0131 a0001c0001t0001g0134 others(40): Show |
43 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.84+5610A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10500931 | |||||||
| chr1:10501225 | A | G | 56 | a0001c0001t0001g0117 a0001c0001t0001g0180 a0001c0002t0001g0001 others(53): Show |
57 | HG00280.hp2 HG00408.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.84+5904A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10501225 | |||||||
| chr1:10501280 | C | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG01081.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.84+5959C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10501280 | |||||||
| chr1:10501290 | G | GTTTATT | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(144): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.84+5990_84+5995dup others(6): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10501290 | ||||||
| chr1:10501322 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.84+6001G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10501322 | |||||||
| chr1:10501368 | G | T | 3 | a0001c0001t0001g0099 a0001c0001t0001g0101 a0001c0001t0001g0110 |
3 | HG02280.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.84+6047G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10501368 | |||||||
| chr1:10501406 | T | C | 205 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(202): Show |
206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.84+6085T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10501406 | |||||||
| chr1:10501431 | G | A | 1 | a0001c0003t0001g0149 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.84+6110G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10501431 | |||||||
| chr1:10501451 | G | A | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.84+6130G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10501451 | |||||||
| chr1:10501451 | G | T | 1 | a0001c0003t0001g0103 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.84+6130G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10501451 | |||||||
| chr1:10501502 | C | T | 31 | a0001c0001t0001g0020 a0001c0001t0001g0137 a0001c0001t0001g0138 others(28): Show |
31 | HG00408.hp1 HG00544.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.84+6181C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10501502 | |||||||
| chr1:10501528 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.84+6207C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10501528 | |||||||
| chr1:10501547 | C | T | 116 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(113): Show |
116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.84+6226C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10501547 | |||||||
| chr1:10501866 | C | T | 69 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(66): Show |
70 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.84+6545C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10501866 | |||||||
| chr1:10501882 | G | T | 1 | a0001c0002t0001g0175 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.84+6561G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10501882 | |||||||
| chr1:10501897 | T | C | 69 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(66): Show |
70 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.84+6576T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10501897 | |||||||
| chr1:10502013 | A | G | 5 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0229 others(2): Show |
5 | HG01884.hp1 HG02622.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.84+6692A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10502013 | |||||||
| chr1:10502040 | A | G | 1 | a0001c0001t0001g0018 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.84+6719A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10502040 | |||||||
| chr1:10502106 | C | T | 43 | a0001c0001t0001g0020 a0001c0001t0001g0131 a0001c0001t0001g0134 others(40): Show |
43 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.84+6785C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10502106 | |||||||
| chr1:10502115 | C | G | 7 | a0001c0001t0001g0174 a0001c0001t0001g0245 a0001c0001t0001g0249 others(4): Show |
7 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.84+6794C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10502115 | |||||||
| chr1:10502458 | C | T | 1 | a0001c0002t0001g0254 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.84+7137C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10502458 | |||||||
| chr1:10502620 | G | A | 2 | a0001c0001t0001g0241 a0001c0001t0001g0242 |
2 | NA18970.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.84+7299G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10502620 | |||||||
| chr1:10502796 | CT | C | 10 | a0001c0001t0001g0117 a0001c0001t0001g0159 a0001c0001t0001g0246 others(7): Show |
10 | HG01167.hp1 HG02258.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.84+7492delT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10502796 | ||||||
| chr1:10502796 | CTT | C | 63 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(60): Show |
64 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.84+7491_84+7492del others(2): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10502796 | ||||||
| chr1:10502820 | A | G | 1 | a0004c0010t0001g0098 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.84+7499A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10502820 | |||||||
| chr1:10502897 | A | T | 1 | a0001c0001t0001g0032 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.84+7576A>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10502897 | |||||||
| chr1:10502939 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.84+7618C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10502939 | |||||||
| chr1:10503021 | G | A | 2 | a0001c0002t0001g0193 a0001c0002t0001g0195 |
2 | HG02080.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.84+7700G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10503021 | |||||||
| chr1:10503189 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.84+7868T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10503189 | |||||||
| chr1:10503281 | C | CA | 13 | a0001c0001t0001g0097 a0001c0001t0001g0115 a0001c0001t0001g0126 others(10): Show |
13 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.84+7985dupA | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10503281 | ||||||
| chr1:10503281 | CA | C | 23 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0020 others(20): Show |
23 | HG00673.hp1 HG01106.hp1 HG01517.hp1 others(20): Show |
intron_variant | MODIFIER | c.84+7985delA | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10503281 | ||||||
| chr1:10503281 | CAA | C | 105 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(102): Show |
105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.84+7984_84+7985del others(2): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10503281 | ||||||
| chr1:10503300 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.84+7979A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10503300 | |||||||
| chr1:10503300 | AAAAAAAG | A | 63 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(60): Show |
64 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.84+7983_84+7989del others(7): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10503300 | ||||||
| chr1:10503302 | A | G | 1 | a0001c0001t0001g0019 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.84+7981A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10503302 | |||||||
| chr1:10503303 | A | G | 1 | a0001c0001t0001g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.84+7982A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10503303 | |||||||
| chr1:10503303 | AAAAGAAA others(5): Show |
A | 3 | a0002c0005t0001g0172 a0002c0005t0001g0173 a0002c0005t0001g0218 |
3 | HG01167.hp1 HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.84+7986_84+7997del others(12): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10503303 | ||||||
| chr1:10503316 | A | G | 3 | a0002c0005t0001g0172 a0002c0005t0001g0173 a0002c0005t0001g0218 |
3 | HG01167.hp1 HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.84+7995A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10503316 | |||||||
| chr1:10503392 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.84+8071C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10503392 | |||||||
| chr1:10503435 | A | G | 69 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(66): Show |
70 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.84+8114A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10503435 | |||||||
| chr1:10503552 | A | G | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.84+8231A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10503552 | |||||||
| chr1:10503568 | G | T | 2 | a0001c0001t0001g0100 a0001c0003t0001g0102 |
2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.84+8247G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10503568 | |||||||
| chr1:10503614 | G | C | 148 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(145): Show |
148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.84+8293G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10503614 | |||||||
| chr1:10503624 | C | T | 56 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(53): Show |
57 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.84+8303C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10503624 | |||||||
| chr1:10503660 | G | A | 51 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(48): Show |
52 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.84+8339G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10503660 | |||||||
| chr1:10503667 | G | A | 13 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0226 others(10): Show |
13 | HG01884.hp1 HG02055.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.84+8346G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10503667 | |||||||
| chr1:10503721 | C | G | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.84+8400C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10503721 | |||||||
| chr1:10503788 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.84+8467C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10503788 | |||||||
| chr1:10503847 | C | A | 1 | a0001c0001t0001g0112 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.84+8526C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10503847 | |||||||
| chr1:10503878 | C | T | 82 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.84+8557C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10503878 | |||||||
| chr1:10503885 | C | G | 2 | a0001c0001t0001g0112 a0004c0010t0001g0098 |
2 | HG03471.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.84+8564C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10503885 | |||||||
| chr1:10503985 | C | T | 1 | a0001c0001t0001g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.84+8664C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10503985 | |||||||
| chr1:10504064 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.84+8743T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10504064 | |||||||
| chr1:10504129 | C | T | 1 | a0001c0001t0001g0052 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.84+8808C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10504129 | |||||||
| chr1:10504400 | T | C | 1 | a0004c0010t0001g0098 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.84+9079T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10504400 | |||||||
| chr1:10504618 | G | A | 164 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(161): Show |
164 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.84+9297G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10504618 | |||||||
| chr1:10504717 | TTTTCC | T | 42 | a0001c0001t0001g0020 a0001c0001t0001g0117 a0001c0001t0001g0131 others(39): Show |
42 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.84+9416_84+9420del others(5): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10504717 | ||||||
| chr1:10504772 | C | T | 21 | a0001c0001t0001g0106 a0001c0001t0001g0109 a0001c0001t0001g0111 others(18): Show |
21 | HG00609.hp2 HG00673.hp1 HG01981.hp2 others(18): Show |
intron_variant | MODIFIER | c.84+9451C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10504772 | |||||||
| chr1:10504852 | T | C | 95 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(92): Show |
95 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.84+9531T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10504852 | |||||||
| chr1:10504905 | T | G | 240 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(237): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.84+9584T>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10504905 | |||||||
| chr1:10504920 | A | G | 1 | a0004c0010t0001g0098 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.84+9599A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10504920 | |||||||
| chr1:10504966 | G | A | 1 | a0001c0001t0001g0005 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.84+9645G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10504966 | |||||||
| chr1:10505286 | C | T | 29 | a0001c0001t0001g0020 a0001c0001t0001g0137 a0001c0001t0001g0138 others(26): Show |
29 | HG00408.hp1 HG00544.hp1 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.84+9965C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10505286 | |||||||
| chr1:10505308 | A | G | 6 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(3): Show |
6 | HG01167.hp1 HG02280.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.84+9987A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10505308 | |||||||
| chr1:10505315 | G | A | 164 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(161): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.84+9994G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10505315 | |||||||
| chr1:10505385 | G | A | 1 | a0003c0011t0001g0107 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.84+10064G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10505385 | |||||||
| chr1:10505431 | C | T | 78 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(75): Show |
78 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.84+10110C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10505431 | |||||||
| chr1:10505577 | C | T | 240 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(237): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.84+10256C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10505577 | |||||||
| chr1:10505636 | C | T | 1 | a0001c0001t0001g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.84+10315C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10505636 | |||||||
| chr1:10505667 | C | T | 5 | a0001c0001t0001g0018 a0001c0001t0001g0249 a0001c0001t0001g0252 others(2): Show |
5 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.84+10346C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10505667 | |||||||
| chr1:10505684 | A | AT | 148 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(145): Show |
148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.84+10377dupT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10505684 | ||||||
| chr1:10505857 | T | C | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.84+10536T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10505857 | |||||||
| chr1:10505890 | A | C | 76 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(73): Show |
76 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.84+10569A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10505890 | |||||||
| chr1:10506038 | C | A | 144 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(141): Show |
145 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.84+10717C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10506038 | |||||||
| chr1:10506091 | T | C | 147 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(144): Show |
148 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.84+10770T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10506091 | |||||||
| chr1:10506158 | A | G | 64 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(61): Show |
65 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.84+10837A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10506158 | |||||||
| chr1:10506215 | C | T | 73 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(70): Show |
74 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.84+10894C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10506215 | |||||||
| chr1:10506428 | G | A | 2 | a0001c0001t0001g0082 a0001c0003t0001g0083 |
2 | HG02735.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.84+11107G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10506428 | |||||||
| chr1:10506439 | C | T | 1 | a0006c0013t0001g0206 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.84+11118C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10506439 | |||||||
| chr1:10506465 | C | T | 67 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(64): Show |
68 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.84+11144C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10506465 | |||||||
| chr1:10506504 | C | T | 3 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0015t0001g0255 |
3 | HG03209.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.84+11183C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10506504 | |||||||
| chr1:10506520 | G | A | 5 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0115 others(2): Show |
5 | HG02109.hp1 HG02559.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.84+11199G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10506520 | |||||||
| chr1:10506611 | A | G | 196 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(193): Show |
197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.84+11290A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10506611 | |||||||
| chr1:10506613 | T | C | 3 | a0001c0001t0001g0249 a0001c0001t0001g0252 a0001c0001t0002g0253 |
3 | HG01891.hp1 HG02723.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.84+11292T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10506613 | |||||||
| chr1:10506771 | C | T | 6 | a0001c0001t0001g0049 a0001c0001t0001g0080 a0001c0001t0001g0091 others(3): Show |
6 | HG00099.hp2 HG01069.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.84+11450C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10506771 | |||||||
| chr1:10506940 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.84+11619T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10506940 | |||||||
| chr1:10506958 | G | T | 1 | a0001c0001t0001g0084 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.84+11637G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10506958 | |||||||
| chr1:10507001 | C | T | 120 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(117): Show |
120 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.84+11680C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10507001 | |||||||
| chr1:10507011 | C | G | 6 | a0001c0001t0001g0120 a0001c0001t0001g0226 a0001c0001t0001g0227 others(3): Show |
6 | HG01884.hp1 HG02622.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.84+11690C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10507011 | |||||||
| chr1:10507065 | G | A | 122 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(119): Show |
122 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.84+11744G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10507065 | |||||||
| chr1:10507151 | C | A | 72 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(69): Show |
72 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.84+11830C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10507151 | |||||||
| chr1:10507191 | C | T | 1 | a0001c0012t0001g0055 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.84+11870C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10507191 | |||||||
| chr1:10507326 | G | A | 2 | a0001c0001t0001g0100 a0001c0003t0001g0102 |
2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.84+12005G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10507326 | |||||||
| chr1:10507355 | C | T | 6 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0241 others(3): Show |
6 | HG00673.hp1 NA18939.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.84+12034C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10507355 | |||||||
| chr1:10507402 | A | G | 1 | a0001c0001t0001g0112 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.84+12081A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10507402 | |||||||
| chr1:10507455 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.84+12134C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10507455 | |||||||
| chr1:10507456 | G | A | 4 | a0001c0001t0001g0249 a0001c0001t0001g0252 a0001c0001t0002g0253 others(1): Show |
4 | HG01891.hp1 HG02723.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.84+12135G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10507456 | |||||||
| chr1:10507601 | C | T | 196 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(193): Show |
197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.84+12280C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10507601 | |||||||
| chr1:10507654 | C | G | 1 | a0001c0001t0001g0052 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.84+12333C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10507654 | |||||||
| chr1:10507654 | C | T | 74 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(71): Show |
74 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.84+12333C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10507654 | |||||||
| chr1:10507743 | G | A | 5 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0115 others(2): Show |
5 | HG02109.hp1 HG02559.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.84+12422G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10507743 | |||||||
| chr1:10507763 | A | T | 5 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0115 others(2): Show |
5 | HG02109.hp1 HG02559.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.84+12442A>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10507763 | |||||||
| chr1:10508220 | T | G | 67 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(64): Show |
68 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.84+12899T>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10508220 | |||||||
| chr1:10508261 | C | T | 3 | a0001c0001t0001g0249 a0001c0001t0001g0252 a0001c0001t0002g0253 |
3 | HG01891.hp1 HG02723.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.84+12940C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10508261 | |||||||
| chr1:10508405 | C | T | 8 | a0001c0001t0001g0120 a0001c0001t0001g0226 a0001c0001t0001g0227 others(5): Show |
8 | HG01884.hp1 HG02622.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.84+13084C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10508405 | |||||||
| chr1:10508439 | C | T | 1 | a0001c0004t0001g0024 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.84+13118C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10508439 | |||||||
| chr1:10508579 | C | A | 2 | a0001c0001t0001g0100 a0001c0003t0001g0102 |
2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.84+13258C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10508579 | |||||||
| chr1:10508579 | C | G | 8 | a0001c0001t0001g0120 a0001c0001t0001g0226 a0001c0001t0001g0227 others(5): Show |
8 | HG01884.hp1 HG02622.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.84+13258C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10508579 | |||||||
| chr1:10508581 | C | G | 4 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0234 others(1): Show |
4 | HG02055.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.84+13260C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10508581 | |||||||
| chr1:10508734 | T | A | 1 | a0001c0001t0001g0139 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.84+13413T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10508734 | |||||||
| chr1:10508859 | A | G | 1 | a0001c0004t0001g0060 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.84+13538A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10508859 | |||||||
| chr1:10508860 | T | C | 1 | a0001c0002t0001g0185 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.84+13539T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10508860 | |||||||
| chr1:10508943 | C | CT | 67 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(64): Show |
68 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.84+13633dupT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10508943 | ||||||
| chr1:10508968 | G | T | 2 | a0001c0002t0001g0204 a0001c0002t0001g0205 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.84+13647G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10508968 | |||||||
| chr1:10509055 | G | A | 7 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0100 others(4): Show |
7 | HG02109.hp1 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.84+13734G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10509055 | |||||||
| chr1:10509056 | C | G | 4 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(1): Show |
4 | HG00099.hp1 HG02738.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.84+13735C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10509056 | |||||||
| chr1:10509066 | A | G | 1 | a0001c0001t0001g0249 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.84+13745A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10509066 | |||||||
| chr1:10509093 | C | T | 4 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0234 others(1): Show |
4 | HG02055.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.84+13772C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10509093 | |||||||
| chr1:10509142 | G | C | 1 | a0001c0016t0001g0070 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.84+13821G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10509142 | |||||||
| chr1:10509201 | G | A | 66 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(63): Show |
67 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.84+13880G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10509201 | |||||||
| chr1:10509274 | C | A | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.84+13953C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10509274 | |||||||
| chr1:10509599 | C | T | 1 | a0001c0002t0001g0163 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.84+14278C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10509599 | |||||||
| chr1:10509715 | T | A | 3 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0015t0001g0255 |
3 | HG03209.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.84+14394T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10509715 | |||||||
| chr1:10509873 | C | T | 33 | a0001c0001t0001g0019 a0001c0001t0001g0092 a0001c0001t0001g0093 others(30): Show |
33 | HG00609.hp2 HG00673.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.84+14552C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10509873 | |||||||
| chr1:10509884 | T | C | 5 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0115 others(2): Show |
5 | HG02109.hp1 HG02559.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.84+14563T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10509884 | |||||||
| chr1:10509928 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.84+14607A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10509928 | |||||||
| chr1:10509941 | T | C | 5 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0115 others(2): Show |
5 | HG02109.hp1 HG02559.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.84+14620T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10509941 | |||||||
| chr1:10510167 | C | T | 1 | a0001c0004t0001g0162 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.84+14846C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10510167 | |||||||
| chr1:10510172 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.84+14851C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10510172 | |||||||
| chr1:10510350 | T | C | 1 | a0001c0001t0001g0139 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.84+15029T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10510350 | |||||||
| chr1:10510433 | C | T | 2 | a0001c0001t0001g0100 a0001c0003t0001g0102 |
2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.84+15112C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10510433 | |||||||
| chr1:10510504 | C | T | 5 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0115 others(2): Show |
5 | HG02109.hp1 HG02559.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.84+15183C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10510504 | |||||||
| chr1:10510664 | G | A | 25 | a0001c0002t0001g0033 a0001c0002t0001g0104 a0001c0002t0001g0163 others(22): Show |
25 | HG00408.hp2 HG00558.hp1 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.84+15343G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10510664 | |||||||
| chr1:10510771 | T | C | 1 | a0001c0004t0001g0079 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.84+15450T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10510771 | |||||||
| chr1:10510824 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.84+15503C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10510824 | |||||||
| chr1:10510883 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.84+15562C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10510883 | |||||||
| chr1:10510987 | T | C | 5 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0115 others(2): Show |
5 | HG02109.hp1 HG02559.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.84+15666T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10510987 | |||||||
| chr1:10511085 | GCAGAGCT | G | 55 | a0001c0001t0001g0089 a0001c0001t0001g0180 a0001c0002t0001g0001 others(52): Show |
56 | HG00280.hp2 HG00408.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.84+15765_84+15771d others(9): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10511085 | |||||||
| chr1:10511225 | G | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 |
3 | HG02280.hp1 HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.84+15904G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10511225 | |||||||
| chr1:10511484 | G | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0018 |
2 | HG02109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.84+16163G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10511484 | |||||||
| chr1:10511614 | G | A | 5 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0115 others(2): Show |
5 | HG02109.hp1 HG02559.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.84+16293G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10511614 | |||||||
| chr1:10511648 | G | A | 1 | a0001c0002t0001g0237 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.84+16327G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10511648 | |||||||
| chr1:10511659 | T | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 |
3 | HG02280.hp1 HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.84+16338T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10511659 | |||||||
| chr1:10511668 | C | T | 5 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0115 others(2): Show |
5 | HG02109.hp1 HG02559.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.84+16347C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10511668 | |||||||
| chr1:10511735 | T | C | 1 | a0001c0001t0001g0073 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.84+16414T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10511735 | |||||||
| chr1:10511784 | C | A | 38 | a0001c0001t0001g0019 a0001c0001t0001g0092 a0001c0001t0001g0093 others(35): Show |
38 | HG00609.hp2 HG00673.hp1 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.84+16463C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10511784 | |||||||
| chr1:10511788 | G | C | 3 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 |
3 | HG02280.hp1 HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.84+16467G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10511788 | |||||||
| chr1:10511880 | T | A | 1 | a0001c0014t0001g0251 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.84+16559T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10511880 | |||||||
| chr1:10511941 | T | C | 1 | a0001c0016t0001g0070 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.84+16620T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10511941 | |||||||
| chr1:10512021 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.84+16700A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10512021 | |||||||
| chr1:10512085 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.84+16764G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10512085 | |||||||
| chr1:10512346 | G | A | 5 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0115 others(2): Show |
5 | HG02109.hp1 HG02559.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.84+17025G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10512346 | |||||||
| chr1:10512466 | G | A | 3 | a0001c0001t0001g0109 a0001c0001t0001g0114 a0001c0003t0001g0108 |
3 | HG03130.hp2 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.84+17145G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10512466 | |||||||
| chr1:10512483 | G | A | 6 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0241 others(3): Show |
6 | HG00673.hp1 NA18939.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.84+17162G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10512483 | |||||||
| chr1:10512639 | T | A | 2 | a0001c0014t0001g0251 a0004c0010t0001g0098 |
2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.84+17318T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10512639 | |||||||
| chr1:10512650 | A | G | 1 | a0001c0001t0001g0139 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.84+17329A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10512650 | |||||||
| chr1:10512692 | C | CT | 5 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0115 others(2): Show |
5 | HG02109.hp1 HG02559.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.84+17382dupT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10512692 | ||||||
| chr1:10512734 | C | G | 1 | a0001c0001t0001g0106 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.84+17413C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10512734 | |||||||
| chr1:10512791 | C | G | 1 | a0001c0003t0001g0222 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.84+17470C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10512791 | |||||||
| chr1:10512849 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.84+17528C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10512849 | |||||||
| chr1:10512910 | G | T | 23 | a0001c0002t0001g0001 a0001c0002t0001g0077 a0001c0002t0001g0167 others(20): Show |
24 | HG00280.hp2 HG00673.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.84+17589G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10512910 | |||||||
| chr1:10512924 | C | T | 2 | a0001c0001t0001g0100 a0001c0003t0001g0102 |
2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.84+17603C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10512924 | |||||||
| chr1:10512929 | C | G | 2 | a0001c0001t0001g0100 a0001c0003t0001g0102 |
2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.84+17608C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10512929 | |||||||
| chr1:10512986 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.84+17665C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10512986 | |||||||
| chr1:10513159 | A | G | 3 | a0001c0001t0001g0249 a0001c0001t0001g0252 a0001c0001t0002g0253 |
3 | HG01891.hp1 HG02723.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.84+17838A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10513159 | |||||||
| chr1:10513239 | GT | G | 82 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.84+17923delT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10513239 | ||||||
| chr1:10513247 | C | T | 2 | a0001c0001t0001g0003 a0002c0005t0001g0207 |
2 | HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.84+17926C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10513247 | |||||||
| chr1:10513629 | T | C | 5 | a0001c0001t0001g0003 a0001c0001t0001g0113 a0001c0001t0001g0246 others(2): Show |
5 | HG02622.hp2 HG02976.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.84+18308T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10513629 | |||||||
| chr1:10513733 | G | T | 2 | a0001c0014t0001g0251 a0004c0010t0001g0098 |
2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.84+18412G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10513733 | |||||||
| chr1:10513785 | A | G | 3 | a0001c0001t0001g0113 a0001c0001t0001g0246 a0001c0001t0001g0247 |
3 | HG02622.hp2 HG02976.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.84+18464A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10513785 | |||||||
| chr1:10513810 | G | A | 82 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.84+18489G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10513810 | |||||||
| chr1:10513812 | G | C | 2 | a0001c0001t0001g0100 a0001c0003t0001g0102 |
2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.84+18491G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10513812 | |||||||
| chr1:10514100 | G | C | 2 | a0001c0001t0001g0100 a0001c0003t0001g0102 |
2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.84+18779G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10514100 | |||||||
| chr1:10514128 | GA | G | 131 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(128): Show |
131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.84+18813delA | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10514128 | ||||||
| chr1:10514156 | C | CTCTG | 3 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0015t0001g0255 |
3 | HG03209.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.84+18836_84+18837i others(6): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10514156 | ||||||
| chr1:10514156 | C | CTG | 62 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0020 others(59): Show |
62 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.84+18877_84+18878d others(4): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10514156 | ||||||
| chr1:10514156 | C | CTGTG | 47 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0021 others(44): Show |
47 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.84+18875_84+18878d others(6): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10514156 | ||||||
| chr1:10514156 | C | CTGTGTG | 10 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0044 others(7): Show |
10 | HG00099.hp1 HG00423.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.84+18873_84+18878d others(8): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10514156 | ||||||
| chr1:10514156 | CTG | C | 52 | a0001c0001t0001g0012 a0001c0001t0001g0099 a0001c0001t0001g0100 others(49): Show |
52 | HG00280.hp2 HG00558.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.84+18877_84+18878d others(4): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10514156 | ||||||
| chr1:10514156 | CTGTG | C | 9 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0241 others(6): Show |
9 | HG01358.hp2 HG01891.hp1 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.84+18875_84+18878d others(6): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10514156 | ||||||
| chr1:10514156 | CTGTGTG | C | 32 | a0001c0001t0001g0003 a0001c0001t0001g0092 a0001c0001t0001g0093 others(29): Show |
32 | HG00609.hp2 HG00673.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.84+18873_84+18878d others(8): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10514156 | ||||||
| chr1:10514156 | CTGTGTGT others(1): Show |
C | 4 | a0001c0001t0001g0019 a0001c0001t0001g0106 a0001c0001t0001g0117 others(1): Show |
4 | HG02258.hp2 HG02622.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.84+18871_84+18878d others(10): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10514156 | ||||||
| chr1:10514156 | CTGTGTGT others(13): Show |
C | 1 | a0001c0001t0001g0032 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.84+18859_84+18878d others(22): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10514156 | ||||||
| chr1:10514160 | G | C | 5 | a0001c0001t0001g0099 a0001c0001t0001g0101 a0001c0001t0001g0110 others(2): Show |
5 | HG02280.hp2 HG02723.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.84+18839G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10514160 | |||||||
| chr1:10514162 | G | C | 5 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0249 others(2): Show |
5 | HG01891.hp1 HG03516.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.84+18841G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10514162 | |||||||
| chr1:10514164 | G | C | 32 | a0001c0001t0001g0003 a0001c0001t0001g0092 a0001c0001t0001g0093 others(29): Show |
32 | HG00609.hp2 HG00673.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.84+18843G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10514164 | |||||||
| chr1:10514166 | G | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0106 a0001c0001t0001g0247 |
3 | HG02622.hp2 HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.84+18845G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10514166 | |||||||
| chr1:10514286 | G | A | 3 | a0001c0001t0001g0249 a0001c0001t0001g0252 a0001c0001t0002g0253 |
3 | HG01891.hp1 HG02723.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.84+18965G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10514286 | |||||||
| chr1:10514430 | T | G | 1 | a0001c0002t0001g0215 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.84+19109T>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10514430 | |||||||
| chr1:10514519 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.84+19198C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10514519 | |||||||
| chr1:10514532 | A | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 |
3 | HG02280.hp1 HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.84+19211A>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10514532 | |||||||
| chr1:10514547 | C | T | 2 | a0001c0002t0001g0185 a0003c0011t0001g0191 |
2 | HG01109.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.84+19226C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10514547 | |||||||
| chr1:10514620 | C | T | 7 | a0001c0001t0001g0049 a0001c0001t0001g0080 a0001c0001t0001g0084 others(4): Show |
7 | HG00099.hp2 HG01069.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.84+19299C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10514620 | |||||||
| chr1:10514631 | A | G | 3 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 |
3 | HG02280.hp1 HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.84+19310A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10514631 | |||||||
| chr1:10514984 | C | T | 2 | a0001c0014t0001g0251 a0004c0010t0001g0098 |
2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.84+19663C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10514984 | |||||||
| chr1:10515002 | G | A | 1 | a0001c0002t0001g0188 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.84+19681G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10515002 | |||||||
| chr1:10515176 | AAG | A | 4 | a0001c0002t0001g0167 a0001c0002t0001g0168 a0001c0002t0001g0169 others(1): Show |
4 | HG00673.hp2 HG02071.hp2 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.84+19859_84+19860d others(4): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10515176 | ||||||
| chr1:10515182 | A | T | 5 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0115 others(2): Show |
5 | HG02109.hp1 HG02559.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.84+19861A>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10515182 | |||||||
| chr1:10515493 | C | T | 1 | a0001c0003t0001g0149 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.84+20172C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10515493 | |||||||
| chr1:10515666 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.84+20345A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10515666 | |||||||
| chr1:10516197 | T | A | 1 | a0001c0007t0001g0189 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.85-20016T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10516197 | |||||||
| chr1:10516318 | T | C | 1 | a0001c0004t0001g0042 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.85-19895T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10516318 | |||||||
| chr1:10516420 | G | A | 1 | a0001c0003t0001g0102 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.85-19793G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10516420 | |||||||
| chr1:10516452 | G | T | 1 | a0001c0001t0002g0253 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.85-19761G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10516452 | |||||||
| chr1:10516489 | C | T | 1 | a0001c0008t0001g0182 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.85-19724C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10516489 | |||||||
| chr1:10516544 | G | A | 1 | a0001c0001t0001g0243 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.85-19669G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10516544 | |||||||
| chr1:10516631 | C | G | 1 | a0001c0004t0001g0053 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.85-19582C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10516631 | |||||||
| chr1:10516827 | A | G | 6 | a0001c0001t0001g0120 a0001c0001t0001g0226 a0001c0001t0001g0227 others(3): Show |
6 | HG01884.hp1 HG02622.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.85-19386A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10516827 | |||||||
| chr1:10517162 | G | A | 1 | a0001c0001t0001g0005 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.85-19051G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10517162 | |||||||
| chr1:10517217 | A | G | 86 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(83): Show |
86 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.85-18996A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10517217 | |||||||
| chr1:10517218 | A | AACTCT | 86 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(83): Show |
86 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.85-18995_85-18994i others(7): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10517218 | |||||||
| chr1:10517219 | G | C | 86 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(83): Show |
86 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.85-18994G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10517219 | |||||||
| chr1:10517230 | T | G | 2 | a0001c0001t0001g0252 a0001c0001t0002g0253 |
2 | HG01891.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.85-18983T>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10517230 | |||||||
| chr1:10517654 | C | CT | 94 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(91): Show |
94 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.85-18547dupT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10517654 | ||||||
| chr1:10517683 | A | G | 87 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(84): Show |
87 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.85-18530A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10517683 | |||||||
| chr1:10517690 | A | AT | 7 | a0001c0001t0001g0121 a0001c0001t0001g0159 a0001c0001t0001g0165 others(4): Show |
7 | HG02622.hp2 HG02976.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.85-18509dupT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10517690 | ||||||
| chr1:10517690 | AT | A | 88 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(85): Show |
88 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.85-18509delT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10517690 | ||||||
| chr1:10517706 | A | G | 6 | a0001c0001t0001g0003 a0001c0001t0001g0100 a0001c0003t0001g0102 others(3): Show |
6 | HG01891.hp2 HG02451.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.85-18507A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10517706 | |||||||
| chr1:10517747 | G | A | 1 | a0001c0002t0001g0179 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.85-18466G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10517747 | |||||||
| chr1:10517791 | C | T | 2 | a0001c0001t0001g0100 a0001c0003t0001g0102 |
2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.85-18422C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10517791 | |||||||
| chr1:10518143 | C | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0018 |
2 | HG02109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.85-18070C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10518143 | |||||||
| chr1:10518529 | G | A | 1 | a0001c0001t0001g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.85-17684G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10518529 | |||||||
| chr1:10518549 | G | A | 124 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(121): Show |
124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.85-17664G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10518549 | |||||||
| chr1:10518734 | T | C | 83 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(80): Show |
83 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.85-17479T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10518734 | |||||||
| chr1:10518892 | G | T | 3 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0015t0001g0255 |
3 | HG03209.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.85-17321G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10518892 | |||||||
| chr1:10518914 | A | G | 1 | a0001c0002t0001g0168 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.85-17299A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10518914 | |||||||
| chr1:10519061 | T | C | 1 | a0001c0001t0001g0052 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.85-17152T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10519061 | |||||||
| chr1:10519488 | G | T | 52 | a0001c0001t0001g0117 a0001c0002t0001g0001 a0001c0002t0001g0033 others(49): Show |
53 | HG00280.hp2 HG00408.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.85-16725G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10519488 | |||||||
| chr1:10519562 | A | G | 2 | a0001c0001t0001g0100 a0001c0003t0001g0102 |
2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.85-16651A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10519562 | |||||||
| chr1:10519586 | G | A | 9 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(6): Show |
9 | HG01891.hp2 HG02109.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.85-16627G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10519586 | |||||||
| chr1:10519593 | G | C | 190 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(187): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.85-16620G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10519593 | |||||||
| chr1:10519663 | A | G | 3 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0015t0001g0255 |
3 | HG03209.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.85-16550A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10519663 | |||||||
| chr1:10519751 | T | C | 48 | a0001c0001t0001g0020 a0001c0001t0001g0050 a0001c0001t0001g0131 others(45): Show |
48 | HG00408.hp1 HG00544.hp1 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.85-16462T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10519751 | |||||||
| chr1:10519888 | G | A | 1 | a0001c0002t0001g0077 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.85-16325G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10519888 | |||||||
| chr1:10520088 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.85-16125C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10520088 | |||||||
| chr1:10520145 | C | CTTT | 3 | a0001c0001t0001g0089 a0001c0001t0001g0180 a0006c0013t0001g0206 |
3 | HG02055.hp2 HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.85-16066_85-16065i others(5): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10520145 | ||||||
| chr1:10520148 | C | CT | 51 | a0001c0001t0001g0020 a0001c0001t0001g0050 a0001c0001t0001g0115 others(48): Show |
51 | HG00408.hp1 HG00544.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.85-16051dupT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10520148 | ||||||
| chr1:10520148 | C | CTTTTTTT others(1): Show |
21 | a0001c0001t0001g0019 a0001c0001t0001g0092 a0001c0001t0001g0093 others(18): Show |
21 | HG00609.hp2 HG01081.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.85-16058_85-16051d others(10): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10520148 | ||||||
| chr1:10520148 | C | CTTTTTTT others(2): Show |
7 | a0001c0001t0001g0106 a0001c0001t0001g0227 a0001c0001t0001g0229 others(4): Show |
7 | HG01884.hp1 HG02622.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.85-16059_85-16051d others(11): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10520148 | ||||||
| chr1:10520148 | C | CTTTTTTT others(3): Show |
2 | a0001c0001t0001g0120 a0001c0006t0001g0236 |
2 | HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.85-16060_85-16051d others(12): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10520148 | ||||||
| chr1:10520148 | C | CTTTTTTT others(5): Show |
3 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0015t0001g0255 |
3 | HG03209.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.85-16062_85-16051d others(14): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10520148 | ||||||
| chr1:10520148 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0001g0117 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.85-16063_85-16051d others(15): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10520148 | ||||||
| chr1:10520148 | C | CTTTTTTT others(8): Show |
2 | a0001c0001t0001g0100 a0001c0003t0001g0102 |
2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.85-16057_85-16043d others(17): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10520148 | ||||||
| chr1:10520148 | C | CTTTTTTT others(8): Show |
1 | a0001c0002t0001g0163 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.85-16051_85-16050i others(17): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10520148 | ||||||
| chr1:10520148 | C | CTTTTTTT others(9): Show |
21 | a0001c0002t0001g0033 a0001c0002t0001g0178 a0001c0002t0001g0179 others(18): Show |
21 | HG00408.hp2 HG00558.hp1 HG00609.hp1 others(18): Show |
intron_variant | MODIFIER | c.85-16051_85-16050i others(18): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10520148 | ||||||
| chr1:10520148 | C | CTTTTTTT others(10): Show |
6 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0002t0001g0104 others(3): Show |
6 | HG02080.hp2 HG02109.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.85-16051_85-16050i others(19): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10520148 | ||||||
| chr1:10520148 | C | CTTTTTTT others(11): Show |
1 | a0001c0007t0001g0211 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.85-16051_85-16050i others(20): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10520148 | ||||||
| chr1:10520148 | C | T | 3 | a0001c0001t0001g0089 a0001c0001t0001g0180 a0006c0013t0001g0206 |
3 | HG02055.hp2 HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.85-16065C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10520148 | |||||||
| chr1:10520151 | T | C | 4 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0249 others(1): Show |
4 | HG01891.hp1 HG02622.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.85-16062T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10520151 | |||||||
| chr1:10520153 | T | TTTTTTTT others(9): Show |
22 | a0001c0002t0001g0001 a0001c0002t0001g0077 a0001c0002t0001g0167 others(19): Show |
23 | HG00280.hp2 HG00735.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.85-16051_85-16050i others(18): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10520153 | ||||||
| chr1:10520153 | T | TTTTTTTT others(10): Show |
1 | a0001c0002t0001g0168 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.85-16051_85-16050i others(19): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10520153 | ||||||
| chr1:10520155 | T | TTTTTTTT others(9): Show |
1 | a0001c0002t0001g0214 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.85-16051_85-16050i others(18): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10520155 | ||||||
| chr1:10520161 | TTG | T | 8 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0082 others(5): Show |
8 | HG01070.hp2 HG02622.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.85-16050_85-16049d others(4): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10520161 | ||||||
| chr1:10520162 | TG | T | 77 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(74): Show |
77 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.85-16050delG | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10520162 | |||||||
| chr1:10520163 | G | T | 47 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(44): Show |
47 | HG00609.hp2 HG01081.hp2 HG01167.hp1 others(44): Show |
intron_variant | MODIFIER | c.85-16050G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10520163 | |||||||
| chr1:10520218 | C | G | 138 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(135): Show |
138 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.85-15995C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10520218 | |||||||
| chr1:10520261 | C | T | 2 | a0001c0001t0001g0137 a0001c0001t0001g0157 |
2 | HG02738.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.85-15952C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10520261 | |||||||
| chr1:10520559 | C | T | 1 | a0001c0002t0001g0033 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.85-15654C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10520559 | |||||||
| chr1:10520719 | G | C | 2 | a0002c0005t0001g0173 a0002c0005t0001g0218 |
2 | HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.85-15494G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10520719 | |||||||
| chr1:10520828 | A | C | 1 | a0001c0001t0001g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.85-15385A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10520828 | |||||||
| chr1:10520834 | C | T | 51 | a0001c0002t0001g0001 a0001c0002t0001g0033 a0001c0002t0001g0077 others(48): Show |
52 | HG00280.hp2 HG00408.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.85-15379C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10520834 | |||||||
| chr1:10520972 | C | T | 5 | a0001c0001t0001g0100 a0001c0001t0001g0256 a0001c0001t0001g0257 others(2): Show |
5 | HG02451.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.85-15241C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10520972 | |||||||
| chr1:10520978 | C | CT | 115 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.85-15220dupT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10520978 | ||||||
| chr1:10520978 | C | CTT | 69 | a0001c0001t0001g0003 a0001c0001t0001g0106 a0001c0001t0001g0113 others(66): Show |
70 | HG00280.hp2 HG00408.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.85-15221_85-15220d others(4): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10520978 | ||||||
| chr1:10520994 | A | T | 52 | a0001c0001t0001g0117 a0001c0002t0001g0001 a0001c0002t0001g0033 others(49): Show |
53 | HG00280.hp2 HG00408.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.85-15219A>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10520994 | |||||||
| chr1:10521143 | T | C | 33 | a0001c0001t0001g0019 a0001c0001t0001g0092 a0001c0001t0001g0093 others(30): Show |
33 | HG00609.hp2 HG01081.hp2 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.85-15070T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10521143 | |||||||
| chr1:10521293 | A | C | 1 | a0001c0001t0001g0089 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.85-14920A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10521293 | |||||||
| chr1:10521295 | T | A | 1 | a0001c0001t0001g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.85-14918T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10521295 | |||||||
| chr1:10521457 | A | G | 6 | a0001c0001t0001g0049 a0001c0001t0001g0080 a0001c0001t0001g0091 others(3): Show |
6 | HG00099.hp2 HG01069.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.85-14756A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10521457 | |||||||
| chr1:10521601 | G | A | 52 | a0001c0001t0001g0117 a0001c0002t0001g0001 a0001c0002t0001g0033 others(49): Show |
53 | HG00280.hp2 HG00408.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.85-14612G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10521601 | |||||||
| chr1:10521990 | T | C | 190 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(187): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.85-14223T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10521990 | |||||||
| chr1:10522055 | C | T | 1 | a0001c0001t0003g0058 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.85-14158C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10522055 | |||||||
| chr1:10522070 | C | T | 45 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0092 others(42): Show |
45 | HG00609.hp2 HG01081.hp2 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.85-14143C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10522070 | |||||||
| chr1:10522388 | A | C | 2 | a0001c0001t0001g0003 a0002c0005t0001g0207 |
2 | HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.85-13825A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10522388 | |||||||
| chr1:10522444 | A | C | 1 | a0001c0001t0001g0141 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.85-13769A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10522444 | |||||||
| chr1:10522848 | G | C | 1 | a0001c0001t0001g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.85-13365G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10522848 | |||||||
| chr1:10523112 | T | C | 3 | a0001c0001t0001g0048 a0001c0002t0001g0185 a0003c0011t0001g0191 |
3 | HG00423.hp2 HG01109.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.85-13101T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10523112 | |||||||
| chr1:10523176 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.85-13037C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10523176 | |||||||
| chr1:10523215 | A | G | 3 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0015t0001g0255 |
3 | HG03209.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.85-12998A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10523215 | |||||||
| chr1:10523366 | T | C | 3 | a0001c0001t0001g0113 a0001c0001t0001g0246 a0001c0001t0001g0247 |
3 | HG02622.hp2 HG02976.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.85-12847T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10523366 | |||||||
| chr1:10523424 | C | T | 1 | a0001c0001t0001g0140 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.85-12789C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10523424 | |||||||
| chr1:10523474 | A | G | 190 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(187): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.85-12739A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10523474 | |||||||
| chr1:10523628 | T | TA | 5 | a0001c0001t0001g0100 a0001c0001t0001g0249 a0001c0001t0002g0253 others(2): Show |
5 | HG01891.hp1 HG01981.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.85-12570dupA | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10523628 | ||||||
| chr1:10523628 | TA | T | 112 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(109): Show |
112 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.85-12570delA | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10523628 | ||||||
| chr1:10523637 | A | G | 2 | a0001c0014t0001g0251 a0004c0010t0001g0098 |
2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.85-12576A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10523637 | |||||||
| chr1:10523679 | G | T | 21 | a0001c0001t0001g0019 a0001c0001t0001g0092 a0001c0001t0001g0093 others(18): Show |
21 | HG00609.hp2 HG01081.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.85-12534G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10523679 | |||||||
| chr1:10523825 | T | TA | 20 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(17): Show |
20 | HG01167.hp1 HG01891.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.85-12366dupA | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10523825 | ||||||
| chr1:10523825 | TA | T | 6 | a0001c0001t0001g0101 a0001c0001t0001g0126 a0001c0001t0001g0141 others(3): Show |
6 | HG01070.hp1 HG01884.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.85-12366delA | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10523825 | ||||||
| chr1:10523825 | TAA | T | 135 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(132): Show |
136 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.85-12367_85-12366d others(4): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10523825 | ||||||
| chr1:10523966 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.85-12247A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10523966 | |||||||
| chr1:10524289 | T | C | 48 | a0001c0001t0001g0020 a0001c0001t0001g0050 a0001c0001t0001g0131 others(45): Show |
48 | HG00408.hp1 HG00544.hp1 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.85-11924T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10524289 | |||||||
| chr1:10524615 | G | A | 190 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(187): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.85-11598G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10524615 | |||||||
| chr1:10524653 | G | A | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.85-11560G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10524653 | |||||||
| chr1:10524677 | T | TTTGA | 33 | a0001c0001t0001g0019 a0001c0001t0001g0092 a0001c0001t0001g0093 others(30): Show |
33 | HG00609.hp2 HG01081.hp2 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.85-11509_85-11506d others(6): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10524677 | ||||||
| chr1:10524681 | A | T | 145 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(142): Show |
146 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.85-11532A>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10524681 | |||||||
| chr1:10524752 | A | G | 1 | a0001c0001t0001g0140 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.85-11461A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10524752 | |||||||
| chr1:10524753 | G | T | 1 | a0001c0002t0001g0199 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.85-11460G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10524753 | |||||||
| chr1:10524989 | C | T | 145 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(142): Show |
146 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.85-11224C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10524989 | |||||||
| chr1:10525082 | A | T | 33 | a0001c0001t0001g0019 a0001c0001t0001g0092 a0001c0001t0001g0093 others(30): Show |
33 | HG00609.hp2 HG01081.hp2 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.85-11131A>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10525082 | |||||||
| chr1:10525258 | A | G | 33 | a0001c0001t0001g0019 a0001c0001t0001g0092 a0001c0001t0001g0093 others(30): Show |
33 | HG00609.hp2 HG01081.hp2 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.85-10955A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10525258 | |||||||
| chr1:10525320 | T | TA | 32 | a0001c0001t0001g0020 a0001c0001t0001g0050 a0001c0001t0001g0137 others(29): Show |
32 | HG00408.hp1 HG00544.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.85-10880dupA | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10525320 | ||||||
| chr1:10525427 | A | G | 1 | a0001c0001t0001g0239 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.85-10786A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10525427 | |||||||
| chr1:10525470 | C | A | 46 | a0001c0001t0001g0020 a0001c0001t0001g0050 a0001c0001t0001g0131 others(43): Show |
46 | HG00408.hp1 HG00544.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.85-10743C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10525470 | |||||||
| chr1:10525903 | C | T | 5 | a0001c0001t0001g0100 a0001c0001t0001g0256 a0001c0001t0001g0257 others(2): Show |
5 | HG02451.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.85-10310C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10525903 | |||||||
| chr1:10526038 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.85-10175C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10526038 | |||||||
| chr1:10526167 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.85-10046G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10526167 | |||||||
| chr1:10526200 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.85-10013G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10526200 | |||||||
| chr1:10526221 | A | AT | 69 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(66): Show |
70 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.85-9974dupT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10526221 | ||||||
| chr1:10526343 | C | G | 1 | a0001c0006t0001g0236 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.85-9870C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10526343 | |||||||
| chr1:10526376 | A | G | 243 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(240): Show |
244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.85-9837A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10526376 | |||||||
| chr1:10526420 | T | C | 3 | a0001c0001t0001g0113 a0001c0001t0001g0246 a0001c0001t0001g0247 |
3 | HG02622.hp2 HG02976.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.85-9793T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10526420 | |||||||
| chr1:10526458 | A | G | 5 | a0001c0001t0001g0003 a0001c0001t0001g0117 a0001c0014t0001g0251 others(2): Show |
5 | HG01891.hp2 HG02258.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.85-9755A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10526458 | |||||||
| chr1:10526744 | T | A | 187 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(184): Show |
188 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.85-9469T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10526744 | |||||||
| chr1:10526783 | C | G | 4 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0234 others(1): Show |
4 | HG02055.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.85-9430C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10526783 | |||||||
| chr1:10526825 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.85-9388G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10526825 | |||||||
| chr1:10526940 | C | T | 1 | a0001c0002t0001g0175 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.85-9273C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10526940 | |||||||
| chr1:10526941 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.85-9272G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10526941 | |||||||
| chr1:10527028 | A | G | 1 | a0001c0003t0001g0041 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.85-9185A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10527028 | |||||||
| chr1:10527107 | A | G | 19 | a0001c0001t0001g0019 a0001c0001t0001g0092 a0001c0001t0001g0093 others(16): Show |
19 | HG00609.hp2 HG01081.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.85-9106A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10527107 | |||||||
| chr1:10527211 | C | CA | 13 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0043 others(10): Show |
13 | HG01891.hp2 HG02258.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.85-8987dupA | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10527211 | ||||||
| chr1:10527211 | C | CAA | 55 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0115 others(52): Show |
56 | HG00280.hp2 HG00558.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.85-8988_85-8987dup others(2): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10527211 | ||||||
| chr1:10527211 | C | CAAA | 80 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(77): Show |
80 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.85-8989_85-8987dup others(3): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10527211 | ||||||
| chr1:10527211 | C | CAAAA | 6 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0003g0058 others(3): Show |
6 | HG02080.hp1 HG02300.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.85-8990_85-8987dup others(4): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10527211 | ||||||
| chr1:10527227 | G | A | 1 | a0001c0001t0001g0043 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.85-8986G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10527227 | |||||||
| chr1:10527258 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.85-8955G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10527258 | |||||||
| chr1:10527362 | C | T | 31 | a0001c0001t0001g0019 a0001c0001t0001g0092 a0001c0001t0001g0093 others(28): Show |
31 | HG00609.hp2 HG01081.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.85-8851C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10527362 | |||||||
| chr1:10527515 | C | CA | 51 | a0001c0002t0001g0001 a0001c0002t0001g0033 a0001c0002t0001g0077 others(48): Show |
52 | HG00280.hp2 HG00408.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.85-8683dupA | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10527515 | ||||||
| chr1:10527737 | G | A | 137 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(134): Show |
138 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.85-8476G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10527737 | |||||||
| chr1:10527784 | A | G | 136 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(133): Show |
137 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.85-8429A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10527784 | |||||||
| chr1:10527853 | T | C | 2 | a0001c0001t0001g0226 a0001c0001t0001g0229 |
2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.85-8360T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10527853 | |||||||
| chr1:10528779 | C | T | 6 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0241 others(3): Show |
6 | HG00673.hp1 NA18939.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.85-7434C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10528779 | |||||||
| chr1:10528893 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.85-7320C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10528893 | |||||||
| chr1:10529148 | T | C | 1 | a0001c0001t0001g0245 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.85-7065T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10529148 | |||||||
| chr1:10529240 | T | C | 3 | a0001c0001t0001g0089 a0001c0001t0001g0180 a0006c0013t0001g0206 |
3 | HG02055.hp2 HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.85-6973T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10529240 | |||||||
| chr1:10529248 | C | T | 5 | a0001c0001t0001g0019 a0002c0005t0001g0127 a0002c0005t0001g0172 others(2): Show |
5 | HG01167.hp1 HG02559.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.85-6965C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10529248 | |||||||
| chr1:10529293 | C | T | 2 | a0001c0014t0001g0251 a0004c0010t0001g0098 |
2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.85-6920C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10529293 | |||||||
| chr1:10529401 | A | T | 5 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0115 others(2): Show |
5 | HG02109.hp1 HG02559.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.85-6812A>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10529401 | |||||||
| chr1:10529779 | A | G | 83 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(80): Show |
83 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.85-6434A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10529779 | |||||||
| chr1:10529784 | T | C | 3 | a0001c0001t0001g0003 a0001c0001t0001g0117 a0002c0005t0001g0207 |
3 | HG02258.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.85-6429T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10529784 | |||||||
| chr1:10529810 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.85-6403G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10529810 | |||||||
| chr1:10529868 | G | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 |
3 | HG02280.hp1 HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.85-6345G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10529868 | |||||||
| chr1:10529878 | T | C | 2 | a0001c0014t0001g0251 a0004c0010t0001g0098 |
2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.85-6335T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10529878 | |||||||
| chr1:10530314 | G | GT | 3 | a0001c0001t0001g0099 a0001c0001t0001g0101 a0001c0001t0001g0110 |
3 | HG02280.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.85-5898dupT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10530314 | ||||||
| chr1:10530663 | C | T | 8 | a0001c0002t0001g0033 a0001c0002t0001g0197 a0001c0002t0001g0198 others(5): Show |
8 | HG00408.hp2 HG00558.hp1 HG00609.hp1 others(5): Show |
intron_variant | MODIFIER | c.85-5550C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10530663 | |||||||
| chr1:10530895 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.85-5318C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10530895 | |||||||
| chr1:10531010 | C | T | 31 | a0001c0001t0001g0019 a0001c0001t0001g0092 a0001c0001t0001g0093 others(28): Show |
31 | HG00609.hp2 HG01081.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.85-5203C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10531010 | |||||||
| chr1:10531047 | T | C | 31 | a0001c0001t0001g0019 a0001c0001t0001g0092 a0001c0001t0001g0093 others(28): Show |
31 | HG00609.hp2 HG01081.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.85-5166T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10531047 | |||||||
| chr1:10531121 | T | C | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.85-5092T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10531121 | |||||||
| chr1:10531176 | G | A | 1 | a0001c0002t0001g0188 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.85-5037G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10531176 | |||||||
| chr1:10531212 | C | A | 2 | a0001c0001t0001g0241 a0001c0001t0001g0242 |
2 | NA18970.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.85-5001C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10531212 | |||||||
| chr1:10531421 | T | G | 1 | a0001c0004t0001g0147 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.85-4792T>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10531421 | |||||||
| chr1:10531494 | G | A | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG00733.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.85-4719G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10531494 | |||||||
| chr1:10531875 | C | T | 3 | a0001c0001t0001g0089 a0001c0001t0001g0180 a0006c0013t0001g0206 |
3 | HG02055.hp2 HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.85-4338C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10531875 | |||||||
| chr1:10531935 | T | C | 5 | a0001c0001t0001g0003 a0001c0001t0001g0117 a0001c0014t0001g0251 others(2): Show |
5 | HG01891.hp2 HG02258.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.85-4278T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10531935 | |||||||
| chr1:10531975 | A | G | 3 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 |
3 | HG02280.hp1 HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.85-4238A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10531975 | |||||||
| chr1:10532174 | C | G | 13 | a0001c0001t0001g0020 a0001c0001t0001g0137 a0001c0001t0001g0138 others(10): Show |
13 | HG00733.hp1 HG01070.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.85-4039C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10532174 | |||||||
| chr1:10532560 | A | G | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.85-3653A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10532560 | |||||||
| chr1:10532634 | A | G | 1 | a0001c0001t0001g0250 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.85-3579A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10532634 | |||||||
| chr1:10532883 | A | G | 3 | a0001c0001t0001g0003 a0001c0001t0001g0117 a0002c0005t0001g0207 |
3 | HG02258.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.85-3330A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10532883 | |||||||
| chr1:10533172 | C | G | 1 | a0002c0005t0001g0173 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.85-3041C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10533172 | |||||||
| chr1:10533189 | G | A | 1 | a0002c0005t0001g0173 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.85-3024G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10533189 | |||||||
| chr1:10533239 | G | T | 28 | a0001c0002t0001g0033 a0001c0002t0001g0104 a0001c0002t0001g0163 others(25): Show |
28 | HG00408.hp2 HG00558.hp1 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.85-2974G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10533239 | |||||||
| chr1:10533484 | T | A | 143 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(140): Show |
144 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.85-2729T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10533484 | |||||||
| chr1:10533490 | C | A | 8 | a0001c0001t0001g0120 a0001c0001t0001g0226 a0001c0001t0001g0227 others(5): Show |
8 | HG01884.hp1 HG02622.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.85-2723C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10533490 | |||||||
| chr1:10533565 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.85-2648C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10533565 | |||||||
| chr1:10533598 | C | G | 1 | a0001c0001t0001g0249 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.85-2615C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10533598 | |||||||
| chr1:10533847 | A | G | 6 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0241 others(3): Show |
6 | HG00673.hp1 NA18939.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.85-2366A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10533847 | |||||||
| chr1:10534341 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.85-1872C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10534341 | |||||||
| chr1:10534347 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.85-1866C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10534347 | |||||||
| chr1:10534352 | G | T | 1 | a0005c0018t0001g0171 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.85-1861G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10534352 | |||||||
| chr1:10534390 | C | T | 3 | a0001c0001t0001g0109 a0001c0001t0001g0114 a0001c0003t0001g0108 |
3 | HG03130.hp2 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.85-1823C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10534390 | |||||||
| chr1:10534455 | A | G | 19 | a0001c0001t0001g0019 a0001c0001t0001g0092 a0001c0001t0001g0093 others(16): Show |
19 | HG00609.hp2 HG01081.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.85-1758A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10534455 | |||||||
| chr1:10534733 | A | G | 53 | a0001c0002t0001g0001 a0001c0002t0001g0033 a0001c0002t0001g0077 others(50): Show |
54 | HG00280.hp2 HG00408.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.85-1480A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10534733 | |||||||
| chr1:10534828 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.85-1385C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10534828 | |||||||
| chr1:10534963 | T | C | 2 | a0001c0002t0001g0193 a0001c0002t0001g0195 |
2 | HG02080.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.85-1250T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10534963 | |||||||
| chr1:10535154 | T | C | 193 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(190): Show |
194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.85-1059T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10535154 | |||||||
| chr1:10535238 | G | A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0117 a0001c0014t0001g0251 others(2): Show |
5 | HG01891.hp2 HG02258.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.85-975G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10535238 | |||||||
| chr1:10535402 | A | G | 1 | a0001c0003t0001g0133 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.85-811A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10535402 | |||||||
| chr1:10535512 | C | T | 1 | a0006c0013t0001g0206 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.85-701C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10535512 | |||||||
| chr1:10535531 | C | T | 1 | a0001c0006t0001g0087 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.85-682C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10535531 | |||||||
| chr1:10535776 | C | CGT | 81 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(78): Show |
81 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.85-421_85-420dupTG | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 10535776 | ||||||
| chr1:10535790 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.85-423T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10535790 | |||||||
| chr1:10535873 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.85-340G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10535873 | |||||||
| chr1:10535925 | A | G | 2 | a0001c0001t0001g0137 a0001c0001t0001g0157 |
2 | HG02738.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.85-288A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10535925 | |||||||
| chr1:10535965 | C | T | 53 | a0001c0001t0001g0017 a0001c0002t0001g0001 a0001c0002t0001g0033 others(50): Show |
54 | HG00280.hp2 HG00408.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.85-248C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10535965 | |||||||
| chr1:10535969 | G | A | 4 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0002g0253 others(1): Show |
4 | HG01891.hp1 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.85-244G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10535969 | |||||||
| chr1:10536106 | A | G | 1 | a0001c0001t0001g0244 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.85-107A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 2/8 | chr1 | 10536106 | |||||||
| chr1:10536331 | A | G | 239 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(236): Show |
240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.169+34A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10536331 | |||||||
| chr1:10536365 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.169+68C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10536365 | |||||||
| chr1:10536473 | A | G | 234 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(231): Show |
235 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.169+176A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10536473 | |||||||
| chr1:10536565 | G | A | 55 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(52): Show |
55 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.169+268G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10536565 | |||||||
| chr1:10536567 | C | T | 55 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(52): Show |
55 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.169+270C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10536567 | |||||||
| chr1:10536772 | C | T | 1 | a0001c0003t0001g0103 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.169+475C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10536772 | |||||||
| chr1:10536797 | T | G | 1 | a0001c0004t0001g0024 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.169+500T>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10536797 | |||||||
| chr1:10536829 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.169+532A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10536829 | |||||||
| chr1:10536955 | A | G | 3 | a0001c0001t0001g0037 a0001c0001t0001g0039 a0001c0004t0001g0038 |
3 | NA18942.hp2 NA18964.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.169+658A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10536955 | |||||||
| chr1:10536967 | A | G | 85 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(82): Show |
85 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.169+670A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10536967 | |||||||
| chr1:10536996 | T | G | 239 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(236): Show |
240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.169+699T>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10536996 | |||||||
| chr1:10537011 | T | C | 35 | a0001c0001t0001g0019 a0001c0001t0001g0092 a0001c0001t0001g0093 others(32): Show |
35 | HG00609.hp2 HG01081.hp2 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.169+714T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10537011 | |||||||
| chr1:10537066 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.169+769G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10537066 | |||||||
| chr1:10537146 | C | T | 5 | a0001c0001t0001g0003 a0001c0001t0001g0117 a0001c0014t0001g0251 others(2): Show |
5 | HG01891.hp2 HG02258.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+849C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10537146 | |||||||
| chr1:10537160 | A | C | 55 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(52): Show |
55 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.169+863A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10537160 | |||||||
| chr1:10537287 | G | A | 3 | a0001c0001t0001g0099 a0001c0001t0001g0101 a0001c0001t0001g0110 |
3 | HG02280.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.169+990G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10537287 | |||||||
| chr1:10537312 | C | T | 2 | a0001c0001t0001g0100 a0001c0003t0001g0102 |
2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.169+1015C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10537312 | |||||||
| chr1:10537341 | A | AACCCCCC others(5): Show |
2 | a0001c0014t0001g0251 a0004c0010t0001g0098 |
2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.169+1044_169+1045i others(14): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10537341 | |||||||
| chr1:10537341 | A | ACCC | 23 | a0001c0001t0001g0051 a0001c0001t0001g0073 a0001c0001t0001g0082 others(20): Show |
23 | HG00280.hp2 HG00408.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.169+1054_169+1056d others(5): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10537341 | ||||||
| chr1:10537341 | A | ACCCC | 87 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(84): Show |
88 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.169+1053_169+1056d others(6): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10537341 | ||||||
| chr1:10537341 | A | ACCCCC | 36 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(33): Show |
36 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.169+1052_169+1056d others(7): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10537341 | ||||||
| chr1:10537341 | A | ACCCCCC | 22 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0031 others(19): Show |
22 | HG01099.hp1 HG01099.hp2 HG01168.hp2 others(19): Show |
intron_variant | MODIFIER | c.169+1051_169+1056d others(8): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10537341 | ||||||
| chr1:10537341 | A | ACCCCCCC | 16 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0092 others(13): Show |
16 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(13): Show |
intron_variant | MODIFIER | c.169+1050_169+1056d others(9): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10537341 | ||||||
| chr1:10537341 | A | ACCCCCCC others(3): Show |
7 | a0001c0001t0001g0180 a0001c0001t0001g0239 a0001c0001t0001g0242 others(4): Show |
7 | HG01167.hp1 HG03139.hp2 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.169+1047_169+1056d others(12): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10537341 | ||||||
| chr1:10537341 | A | ACCCCCCC others(4): Show |
3 | a0001c0001t0001g0116 a0001c0003t0001g0103 a0002c0005t0001g0127 |
3 | HG02559.hp1 NA18964.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.169+1046_169+1056d others(13): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10537341 | ||||||
| chr1:10537341 | A | ACCCCCCC others(5): Show |
2 | a0001c0001t0001g0089 a0001c0001t0001g0244 |
2 | HG02055.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.169+1045_169+1056d others(14): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10537341 | ||||||
| chr1:10537341 | A | ACCCCCCC others(6): Show |
1 | a0001c0001t0001g0115 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.169+1056_169+1057i others(15): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10537341 | ||||||
| chr1:10537494 | C | T | 53 | a0001c0002t0001g0001 a0001c0002t0001g0033 a0001c0002t0001g0077 others(50): Show |
54 | HG00280.hp2 HG00408.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.169+1197C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10537494 | |||||||
| chr1:10537657 | G | T | 1 | a0001c0006t0001g0124 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.169+1360G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10537657 | |||||||
| chr1:10537934 | C | CTG | 21 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(18): Show |
21 | HG01109.hp1 HG01884.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.169+1638_169+1639i others(4): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10537934 | ||||||
| chr1:10537935 | T | TG | 234 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(231): Show |
235 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.169+1638_169+1639i others(3): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10537935 | |||||||
| chr1:10538116 | G | A | 31 | a0001c0001t0001g0019 a0001c0001t0001g0092 a0001c0001t0001g0093 others(28): Show |
31 | HG00609.hp2 HG01081.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.169+1819G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10538116 | |||||||
| chr1:10538154 | A | G | 1 | a0002c0005t0001g0218 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.169+1857A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10538154 | |||||||
| chr1:10538159 | G | A | 53 | a0001c0002t0001g0001 a0001c0002t0001g0033 a0001c0002t0001g0077 others(50): Show |
54 | HG00280.hp2 HG00408.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.169+1862G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10538159 | |||||||
| chr1:10538841 | G | A | 1 | a0001c0004t0001g0148 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.169+2544G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10538841 | |||||||
| chr1:10539156 | T | G | 244 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(241): Show |
245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.169+2859T>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10539156 | |||||||
| chr1:10539163 | G | A | 3 | a0001c0003t0001g0103 a0001c0003t0001g0238 a0001c0012t0001g0055 |
3 | HG01981.hp2 NA18963.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.169+2866G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10539163 | |||||||
| chr1:10539263 | G | C | 1 | a0001c0001t0001g0012 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.169+2966G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10539263 | |||||||
| chr1:10539297 | T | C | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.169+3000T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10539297 | |||||||
| chr1:10539506 | C | T | 4 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0002g0253 others(1): Show |
4 | HG01891.hp1 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.169+3209C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10539506 | |||||||
| chr1:10539586 | CAT | C | 138 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(135): Show |
139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.169+3291_169+3292d others(4): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10539586 | ||||||
| chr1:10539600 | A | G | 2 | a0001c0001t0001g0081 a0001c0001t0001g0174 |
2 | HG02647.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.169+3303A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10539600 | |||||||
| chr1:10539785 | G | A | 239 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(236): Show |
240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.169+3488G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10539785 | |||||||
| chr1:10539814 | A | C | 1 | a0001c0004t0001g0209 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.169+3517A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10539814 | |||||||
| chr1:10540227 | G | A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0117 a0001c0014t0001g0251 others(2): Show |
5 | HG01891.hp2 HG02258.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+3930G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10540227 | |||||||
| chr1:10540339 | C | T | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0128 |
3 | HG02559.hp2 HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.169+4042C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10540339 | |||||||
| chr1:10540548 | TTG | T | 54 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(51): Show |
54 | HG00280.hp1 HG00423.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.169+4254_169+4255d others(4): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10540548 | ||||||
| chr1:10540601 | G | GA | 101 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0029 others(98): Show |
102 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.169+4314dupA | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10540601 | ||||||
| chr1:10540928 | C | A | 1 | a0001c0006t0001g0236 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.169+4631C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10540928 | |||||||
| chr1:10541075 | G | A | 6 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0241 others(3): Show |
6 | HG00673.hp1 NA18939.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.169+4778G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10541075 | |||||||
| chr1:10541340 | GT | G | 4 | a0001c0004t0001g0046 a0001c0004t0001g0053 a0001c0004t0001g0079 others(1): Show |
4 | HG00733.hp2 HG00741.hp2 HG01069.hp2 others(1): Show |
intron_variant | MODIFIER | c.169+5047delT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10541340 | ||||||
| chr1:10541409 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.169+5112C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10541409 | |||||||
| chr1:10541644 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.169+5347C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10541644 | |||||||
| chr1:10541704 | G | A | 51 | a0001c0001t0001g0020 a0001c0001t0001g0050 a0001c0001t0001g0131 others(48): Show |
51 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.169+5407G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10541704 | |||||||
| chr1:10542080 | T | TA | 239 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(236): Show |
240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.169+5792dupA | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10542080 | ||||||
| chr1:10542090 | T | A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0117 a0001c0014t0001g0251 others(2): Show |
5 | HG01891.hp2 HG02258.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+5793T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10542090 | |||||||
| chr1:10542228 | A | T | 1 | a0001c0001t0001g0032 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.169+5931A>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10542228 | |||||||
| chr1:10542519 | C | T | 242 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(239): Show |
243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.169+6222C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10542519 | |||||||
| chr1:10542543 | C | T | 1 | a0001c0003t0001g0102 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.169+6246C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10542543 | |||||||
| chr1:10542701 | C | T | 141 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(138): Show |
142 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.169+6404C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10542701 | |||||||
| chr1:10542727 | C | CTCCA | 52 | a0001c0001t0001g0020 a0001c0001t0001g0050 a0001c0001t0001g0112 others(49): Show |
52 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.169+6431_169+6434d others(6): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10542727 | ||||||
| chr1:10542853 | A | G | 2 | a0001c0003t0001g0238 a0001c0012t0001g0055 |
2 | HG01981.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.169+6556A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10542853 | |||||||
| chr1:10543284 | G | C | 4 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0002g0253 others(1): Show |
4 | HG01891.hp1 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.169+6987G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10543284 | |||||||
| chr1:10543290 | G | A | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0128 |
3 | HG02559.hp2 HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.169+6993G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10543290 | |||||||
| chr1:10543293 | C | T | 31 | a0001c0001t0001g0019 a0001c0001t0001g0092 a0001c0001t0001g0093 others(28): Show |
31 | HG00609.hp2 HG01081.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.169+6996C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10543293 | |||||||
| chr1:10543329 | T | C | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.169+7032T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10543329 | |||||||
| chr1:10543388 | C | G | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.169+7091C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10543388 | |||||||
| chr1:10543464 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.169+7167G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10543464 | |||||||
| chr1:10543659 | T | C | 67 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(64): Show |
68 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.169+7362T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10543659 | |||||||
| chr1:10543835 | A | G | 144 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(141): Show |
145 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.169+7538A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10543835 | |||||||
| chr1:10543867 | T | C | 35 | a0001c0001t0001g0019 a0001c0001t0001g0092 a0001c0001t0001g0093 others(32): Show |
35 | HG00609.hp2 HG01081.hp2 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.169+7570T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10543867 | |||||||
| chr1:10543930 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.169+7633A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10543930 | |||||||
| chr1:10544009 | C | T | 19 | a0001c0001t0001g0019 a0001c0001t0001g0092 a0001c0001t0001g0093 others(16): Show |
19 | HG00609.hp2 HG01081.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.169+7712C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10544009 | |||||||
| chr1:10544017 | G | A | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.169+7720G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10544017 | |||||||
| chr1:10544108 | A | G | 1 | a0001c0001t0001g0140 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.169+7811A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10544108 | |||||||
| chr1:10544142 | A | C | 1 | a0001c0002t0001g0217 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.169+7845A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10544142 | |||||||
| chr1:10544292 | A | G | 5 | a0001c0001t0001g0003 a0001c0001t0001g0117 a0001c0014t0001g0251 others(2): Show |
5 | HG01891.hp2 HG02258.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+7995A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10544292 | |||||||
| chr1:10544482 | G | A | 144 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(141): Show |
145 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.169+8185G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10544482 | |||||||
| chr1:10544563 | T | G | 1 | a0001c0002t0001g0179 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.169+8266T>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10544563 | |||||||
| chr1:10544615 | C | T | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.169+8318C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10544615 | |||||||
| chr1:10544657 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.169+8360C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10544657 | |||||||
| chr1:10544754 | CT | C | 144 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(141): Show |
145 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.169+8468delT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10544754 | ||||||
| chr1:10544855 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.169+8558C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10544855 | |||||||
| chr1:10545134 | C | T | 2 | a0001c0001t0001g0100 a0001c0003t0001g0102 |
2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.169+8837C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10545134 | |||||||
| chr1:10545739 | C | A | 70 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(67): Show |
70 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.169+9442C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10545739 | |||||||
| chr1:10545795 | A | G | 3 | a0001c0001t0001g0113 a0001c0001t0001g0246 a0001c0001t0001g0247 |
3 | HG02622.hp2 HG02976.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.169+9498A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10545795 | |||||||
| chr1:10545814 | C | T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(1): Show |
4 | HG02280.hp1 HG02630.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.169+9517C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10545814 | |||||||
| chr1:10545946 | G | A | 242 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(239): Show |
243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.169+9649G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10545946 | |||||||
| chr1:10545949 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.169+9652G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10545949 | |||||||
| chr1:10546133 | A | G | 2 | a0001c0001t0001g0100 a0001c0003t0001g0102 |
2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.169+9836A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10546133 | |||||||
| chr1:10546419 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.169+10122G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10546419 | |||||||
| chr1:10546550 | C | T | 35 | a0001c0001t0001g0019 a0001c0001t0001g0049 a0001c0001t0001g0080 others(32): Show |
35 | HG00099.hp2 HG00609.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.169+10253C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10546550 | |||||||
| chr1:10546563 | C | CA | 99 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0017 others(96): Show |
99 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.169+10287dupA | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10546563 | ||||||
| chr1:10546563 | C | CAA | 13 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0106 others(10): Show |
13 | HG02055.hp1 HG02109.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.169+10286_169+1028 others(6): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10546563 | ||||||
| chr1:10546595 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.169+10298G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10546595 | |||||||
| chr1:10546609 | A | G | 1 | a0001c0001t0001g0220 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.169+10312A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10546609 | |||||||
| chr1:10546615 | C | G | 1 | a0001c0001t0001g0136 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.169+10318C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10546615 | |||||||
| chr1:10546704 | GA | G | 5 | a0001c0001t0001g0018 a0001c0001t0001g0113 a0001c0002t0001g0168 others(2): Show |
5 | HG00673.hp2 HG02109.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.169+10422delA | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10546704 | ||||||
| chr1:10546730 | G | A | 76 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(73): Show |
76 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.169+10433G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10546730 | |||||||
| chr1:10546737 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.169+10440T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10546737 | |||||||
| chr1:10546878 | C | A | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0128 |
3 | HG02559.hp2 HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.169+10581C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10546878 | |||||||
| chr1:10546939 | G | T | 148 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(145): Show |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.169+10642G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10546939 | |||||||
| chr1:10547171 | C | T | 240 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(237): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.169+10874C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10547171 | |||||||
| chr1:10547333 | G | A | 1 | a0001c0001t0001g0029 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.169+11036G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10547333 | |||||||
| chr1:10547337 | C | T | 136 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(133): Show |
137 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.169+11040C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10547337 | |||||||
| chr1:10547394 | T | C | 69 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0050 others(66): Show |
69 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.169+11097T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10547394 | |||||||
| chr1:10547405 | A | G | 2 | a0001c0001t0001g0100 a0001c0003t0001g0102 |
2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.169+11108A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10547405 | |||||||
| chr1:10547477 | G | A | 3 | a0001c0001t0001g0113 a0001c0001t0001g0246 a0001c0001t0001g0247 |
3 | HG02622.hp2 HG02976.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.169+11180G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10547477 | |||||||
| chr1:10547486 | G | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0022 |
2 | HG01081.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.169+11189G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10547486 | |||||||
| chr1:10547838 | C | T | 12 | a0001c0001t0001g0049 a0001c0001t0001g0080 a0001c0001t0001g0091 others(9): Show |
12 | HG00099.hp2 HG01069.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.169+11541C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10547838 | |||||||
| chr1:10547885 | G | A | 1 | a0001c0004t0001g0209 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.169+11588G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10547885 | |||||||
| chr1:10547940 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.169+11643G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10547940 | |||||||
| chr1:10547954 | G | A | 14 | a0001c0001t0001g0003 a0001c0001t0001g0099 a0001c0001t0001g0101 others(11): Show |
14 | HG01891.hp2 HG02055.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.169+11657G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10547954 | |||||||
| chr1:10548148 | C | T | 1 | a0005c0018t0001g0171 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.169+11851C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10548148 | |||||||
| chr1:10548151 | A | G | 1 | a0001c0001t0001g0100 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.169+11854A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10548151 | |||||||
| chr1:10548200 | G | C | 22 | a0001c0001t0001g0019 a0001c0001t0001g0092 a0001c0001t0001g0093 others(19): Show |
22 | HG00609.hp2 HG01081.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.169+11903G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10548200 | |||||||
| chr1:10548341 | A | G | 12 | a0001c0001t0001g0049 a0001c0001t0001g0080 a0001c0001t0001g0091 others(9): Show |
12 | HG00099.hp2 HG01069.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.169+12044A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10548341 | |||||||
| chr1:10548394 | T | G | 1 | a0001c0003t0001g0222 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.169+12097T>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10548394 | |||||||
| chr1:10548526 | T | C | 64 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(61): Show |
64 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.169+12229T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10548526 | |||||||
| chr1:10548539 | T | C | 155 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(152): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.169+12242T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10548539 | |||||||
| chr1:10548686 | G | C | 1 | a0001c0001t0001g0084 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.169+12389G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10548686 | |||||||
| chr1:10548764 | A | G | 2 | a0001c0001t0001g0245 a0001c0003t0001g0105 |
2 | HG02109.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.169+12467A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10548764 | |||||||
| chr1:10549033 | C | T | 155 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(152): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.169+12736C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10549033 | |||||||
| chr1:10549043 | A | C | 2 | a0001c0001t0001g0241 a0001c0001t0001g0242 |
2 | NA18970.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.169+12746A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10549043 | |||||||
| chr1:10549232 | A | G | 2 | a0001c0001t0001g0017 a0001c0001t0001g0018 |
2 | HG02109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.169+12935A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10549232 | |||||||
| chr1:10549338 | C | T | 85 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(82): Show |
85 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.169+13041C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10549338 | |||||||
| chr1:10549403 | C | T | 155 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(152): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.169+13106C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10549403 | |||||||
| chr1:10549448 | G | A | 64 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(61): Show |
64 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.169+13151G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10549448 | |||||||
| chr1:10549775 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.169+13478G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10549775 | |||||||
| chr1:10549820 | G | T | 12 | a0001c0001t0001g0049 a0001c0001t0001g0080 a0001c0001t0001g0091 others(9): Show |
12 | HG00099.hp2 HG01069.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.169+13523G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10549820 | |||||||
| chr1:10549916 | G | T | 56 | a0001c0001t0001g0089 a0001c0001t0001g0180 a0001c0002t0001g0001 others(53): Show |
57 | HG00280.hp2 HG00408.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.169+13619G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10549916 | |||||||
| chr1:10549956 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.169+13659C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10549956 | |||||||
| chr1:10550072 | G | A | 52 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(49): Show |
52 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.169+13775G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10550072 | |||||||
| chr1:10550100 | A | C | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0128 |
3 | HG02559.hp2 HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.169+13803A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10550100 | |||||||
| chr1:10550484 | T | G | 1 | a0001c0001t0001g0112 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.169+14187T>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10550484 | |||||||
| chr1:10550623 | C | T | 12 | a0001c0001t0001g0049 a0001c0001t0001g0080 a0001c0001t0001g0091 others(9): Show |
12 | HG00099.hp2 HG01069.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.169+14326C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10550623 | |||||||
| chr1:10550641 | A | G | 4 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0002g0253 others(1): Show |
4 | HG01891.hp1 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.169+14344A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10550641 | |||||||
| chr1:10550819 | G | A | 155 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(152): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.169+14522G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10550819 | |||||||
| chr1:10550977 | T | G | 4 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0002g0253 others(1): Show |
4 | HG01891.hp1 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.169+14680T>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10550977 | |||||||
| chr1:10551346 | T | C | 75 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(72): Show |
75 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.169+15049T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10551346 | |||||||
| chr1:10551360 | G | A | 76 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(73): Show |
76 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.169+15063G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10551360 | |||||||
| chr1:10551537 | A | T | 155 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(152): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.169+15240A>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10551537 | |||||||
| chr1:10551647 | T | C | 1 | a0001c0001t0001g0106 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.169+15350T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10551647 | |||||||
| chr1:10551779 | A | C | 1 | a0001c0002t0001g0196 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.169+15482A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10551779 | |||||||
| chr1:10551780 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.169+15483A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10551780 | |||||||
| chr1:10552018 | G | A | 155 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(152): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.169+15721G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10552018 | |||||||
| chr1:10552047 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.169+15750C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10552047 | |||||||
| chr1:10552071 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.169+15774C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10552071 | |||||||
| chr1:10552101 | A | T | 12 | a0001c0001t0001g0049 a0001c0001t0001g0080 a0001c0001t0001g0091 others(9): Show |
12 | HG00099.hp2 HG01069.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.169+15804A>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10552101 | |||||||
| chr1:10552215 | G | A | 2 | a0001c0014t0001g0251 a0004c0010t0001g0098 |
2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.169+15918G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10552215 | |||||||
| chr1:10552303 | A | G | 240 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(237): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.169+16006A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10552303 | |||||||
| chr1:10552357 | G | A | 4 | a0001c0003t0001g0088 a0001c0006t0001g0086 a0001c0006t0001g0087 others(1): Show |
4 | HG02896.hp2 HG03139.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.169+16060G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10552357 | |||||||
| chr1:10552441 | CA | C | 6 | a0001c0001t0001g0032 a0001c0001t0001g0227 a0001c0001t0001g0231 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.169+16154delA | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10552441 | ||||||
| chr1:10552579 | A | C | 155 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(152): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.169+16282A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10552579 | |||||||
| chr1:10552729 | T | C | 2 | a0001c0001t0001g0082 a0001c0003t0001g0083 |
2 | HG02735.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.169+16432T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10552729 | |||||||
| chr1:10552753 | T | C | 155 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(152): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.169+16456T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10552753 | |||||||
| chr1:10552763 | G | C | 52 | a0001c0002t0001g0001 a0001c0002t0001g0033 a0001c0002t0001g0077 others(49): Show |
53 | HG00280.hp2 HG00408.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.169+16466G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10552763 | |||||||
| chr1:10553059 | C | A | 1 | a0001c0001t0001g0134 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.169+16762C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10553059 | |||||||
| chr1:10553110 | G | A | 75 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(72): Show |
75 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.169+16813G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10553110 | |||||||
| chr1:10553235 | G | A | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0128 |
3 | HG02559.hp2 HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.169+16938G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10553235 | |||||||
| chr1:10553287 | T | G | 85 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(82): Show |
85 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.169+16990T>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10553287 | |||||||
| chr1:10553294 | T | C | 23 | a0001c0002t0001g0001 a0001c0002t0001g0167 a0001c0002t0001g0168 others(20): Show |
24 | HG00280.hp2 HG00673.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.169+16997T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10553294 | |||||||
| chr1:10553344 | G | A | 3 | a0001c0001t0001g0089 a0001c0001t0001g0180 a0006c0013t0001g0206 |
3 | HG02055.hp2 HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.169+17047G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10553344 | |||||||
| chr1:10553440 | T | C | 70 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(67): Show |
70 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.169+17143T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10553440 | |||||||
| chr1:10553503 | A | G | 155 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(152): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.169+17206A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10553503 | |||||||
| chr1:10553554 | G | A | 5 | a0001c0002t0001g0175 a0001c0002t0001g0183 a0001c0002t0001g0185 others(2): Show |
5 | HG00735.hp1 HG01109.hp2 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.169+17257G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10553554 | |||||||
| chr1:10553603 | C | T | 75 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(72): Show |
75 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.169+17306C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10553603 | |||||||
| chr1:10553640 | GCTTCTCC others(3): Show |
G | 79 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(76): Show |
79 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.169+17345_169+1735 others(14): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10553640 | ||||||
| chr1:10553683 | G | A | 1 | a0001c0004t0001g0148 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.169+17386G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10553683 | |||||||
| chr1:10553863 | C | T | 3 | a0001c0001t0001g0113 a0001c0001t0001g0246 a0001c0001t0001g0247 |
3 | HG02622.hp2 HG02976.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.169+17566C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10553863 | |||||||
| chr1:10553977 | A | G | 2 | a0001c0002t0001g0167 a0001c0002t0001g0168 |
2 | HG00673.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.169+17680A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10553977 | |||||||
| chr1:10554056 | G | A | 7 | a0001c0001t0001g0120 a0001c0001t0001g0226 a0001c0001t0001g0229 others(4): Show |
7 | HG01884.hp1 HG02622.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.169+17759G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10554056 | |||||||
| chr1:10554133 | C | CA | 8 | a0001c0001t0001g0097 a0001c0001t0001g0120 a0001c0001t0001g0226 others(5): Show |
8 | HG02451.hp1 HG02622.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.169+17857dupA | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10554133 | ||||||
| chr1:10554133 | CA | C | 126 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0011 others(123): Show |
126 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.169+17857delA | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10554133 | ||||||
| chr1:10554133 | CAA | C | 74 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(71): Show |
75 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.169+17856_169+1785 others(6): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10554133 | ||||||
| chr1:10554133 | CAAA | C | 16 | a0001c0001t0001g0003 a0001c0001t0001g0099 a0001c0001t0001g0101 others(13): Show |
16 | HG01891.hp2 HG02055.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.169+17855_169+1785 others(7): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10554133 | ||||||
| chr1:10554149 | A | T | 2 | a0001c0006t0001g0124 a0004c0010t0001g0123 |
2 | HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.169+17852A>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10554149 | |||||||
| chr1:10554176 | C | T | 85 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(82): Show |
85 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.169+17879C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10554176 | |||||||
| chr1:10554303 | C | CA | 93 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(90): Show |
94 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.169+18022dupA | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10554303 | ||||||
| chr1:10554303 | C | CAA | 113 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(110): Show |
113 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.169+18021_169+1802 others(6): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10554303 | ||||||
| chr1:10554359 | TAAAGGGC others(8): Show |
T | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0128 |
3 | HG02559.hp2 HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.169+18081_169+1809 others(19): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10554359 | ||||||
| chr1:10554383 | G | A | 2 | a0001c0001t0001g0145 a0001c0001t0001g0154 |
2 | HG02040.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.169+18086G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10554383 | |||||||
| chr1:10554415 | G | C | 244 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(241): Show |
245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.169+18118G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10554415 | |||||||
| chr1:10554444 | C | G | 1 | a0001c0001t0001g0065 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.169+18147C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10554444 | |||||||
| chr1:10554490 | G | A | 1 | a0001c0002t0001g0188 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.169+18193G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10554490 | |||||||
| chr1:10554505 | G | A | 1 | a0001c0004t0001g0079 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.169+18208G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10554505 | |||||||
| chr1:10554720 | C | CT | 78 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(75): Show |
78 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.169+18433dupT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10554720 | ||||||
| chr1:10554747 | A | G | 53 | a0001c0002t0001g0001 a0001c0002t0001g0033 a0001c0002t0001g0077 others(50): Show |
54 | HG00280.hp2 HG00408.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.169+18450A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10554747 | |||||||
| chr1:10554757 | A | G | 2 | a0001c0001t0001g0100 a0001c0003t0001g0102 |
2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.169+18460A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10554757 | |||||||
| chr1:10554774 | C | T | 7 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(4): Show |
7 | NA18942.hp2 NA18964.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.169+18477C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10554774 | |||||||
| chr1:10554861 | C | G | 4 | a0001c0001t0001g0099 a0001c0001t0001g0101 a0001c0001t0001g0110 others(1): Show |
4 | HG02280.hp2 HG02965.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.169+18564C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10554861 | |||||||
| chr1:10554862 | G | A | 1 | a0002c0005t0001g0233 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.169+18565G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10554862 | |||||||
| chr1:10555132 | C | A | 155 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(152): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.169+18835C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10555132 | |||||||
| chr1:10555422 | A | T | 2 | a0001c0001t0001g0100 a0001c0003t0001g0102 |
2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.169+19125A>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10555422 | |||||||
| chr1:10555642 | A | AGT | 56 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0020 others(53): Show |
56 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.169+19369_169+1937 others(6): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10555642 | ||||||
| chr1:10555642 | A | AGTGT | 82 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(79): Show |
82 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.169+19367_169+1937 others(8): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10555642 | ||||||
| chr1:10555642 | A | AGTGTGT | 22 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0048 others(19): Show |
22 | HG00423.hp2 HG01891.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.169+19365_169+1937 others(10): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10555642 | ||||||
| chr1:10555642 | A | AGTGTGTG others(1): Show |
29 | a0001c0001t0001g0019 a0001c0001t0001g0106 a0001c0001t0001g0109 others(26): Show |
30 | HG00099.hp2 HG00609.hp2 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.169+19363_169+1937 others(12): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10555642 | ||||||
| chr1:10555642 | A | AGTGTGTG others(3): Show |
40 | a0001c0001t0001g0049 a0001c0001t0001g0080 a0001c0001t0001g0091 others(37): Show |
40 | HG00408.hp2 HG00558.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.169+19361_169+1937 others(14): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10555642 | ||||||
| chr1:10555642 | A | AGTGTGTG others(5): Show |
3 | a0001c0002t0001g0179 a0001c0002t0001g0197 a0001c0003t0001g0103 |
3 | HG01928.hp2 HG02717.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.169+19359_169+1937 others(16): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10555642 | ||||||
| chr1:10555642 | A | AGTGTGTG others(7): Show |
1 | a0001c0001t0001g0247 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.169+19357_169+1937 others(18): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10555642 | ||||||
| chr1:10555642 | AGTGTGTG others(1): Show |
A | 3 | a0001c0001t0001g0089 a0001c0001t0001g0180 a0006c0013t0001g0206 |
3 | HG02055.hp2 HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.169+19363_169+1937 others(12): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10555642 | ||||||
| chr1:10555718 | T | C | 155 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(152): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.169+19421T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10555718 | |||||||
| chr1:10555782 | G | A | 2 | a0001c0001t0001g0100 a0001c0003t0001g0102 |
2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.169+19485G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10555782 | |||||||
| chr1:10555925 | G | A | 2 | a0001c0002t0001g0176 a0001c0002t0001g0186 |
2 | HG01106.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.169+19628G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10555925 | |||||||
| chr1:10556104 | G | A | 14 | a0001c0001t0001g0003 a0001c0001t0001g0099 a0001c0001t0001g0101 others(11): Show |
14 | HG01891.hp2 HG02055.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.169+19807G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10556104 | |||||||
| chr1:10556171 | G | A | 153 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(150): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.169+19874G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10556171 | |||||||
| chr1:10556374 | A | T | 5 | a0001c0001t0001g0106 a0001c0001t0001g0245 a0001c0001t0001g0246 others(2): Show |
5 | HG02109.hp2 HG02622.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.169+20077A>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10556374 | |||||||
| chr1:10556409 | G | A | 3 | a0001c0001t0001g0131 a0001c0003t0001g0135 a0001c0017t0001g0130 |
3 | HG03492.hp2 HG03654.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.169+20112G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10556409 | |||||||
| chr1:10556427 | C | T | 156 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(153): Show |
157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.169+20130C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10556427 | |||||||
| chr1:10556448 | C | A | 54 | a0001c0002t0001g0001 a0001c0002t0001g0033 a0001c0002t0001g0077 others(51): Show |
55 | HG00280.hp2 HG00408.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.169+20151C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10556448 | |||||||
| chr1:10556542 | G | T | 1 | a0001c0001t0001g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.169+20245G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10556542 | |||||||
| chr1:10556717 | A | AG | 30 | a0001c0001t0001g0019 a0001c0001t0001g0049 a0001c0001t0001g0080 others(27): Show |
30 | HG00099.hp2 HG00609.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.169+20421dupG | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10556717 | ||||||
| chr1:10556977 | G | A | 53 | a0001c0002t0001g0001 a0001c0002t0001g0033 a0001c0002t0001g0077 others(50): Show |
54 | HG00280.hp2 HG00408.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.169+20680G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10556977 | |||||||
| chr1:10556999 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.169+20702G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10556999 | |||||||
| chr1:10557134 | A | G | 15 | a0001c0001t0001g0003 a0001c0001t0001g0099 a0001c0001t0001g0101 others(12): Show |
15 | HG01891.hp2 HG02055.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.169+20837A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10557134 | |||||||
| chr1:10557215 | A | T | 155 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(152): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.169+20918A>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10557215 | |||||||
| chr1:10557222 | T | C | 1 | a0001c0001t0001g0250 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.169+20925T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10557222 | |||||||
| chr1:10557294 | C | G | 18 | a0001c0001t0001g0019 a0001c0001t0001g0092 a0001c0001t0001g0093 others(15): Show |
18 | HG00609.hp2 HG01081.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.169+20997C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10557294 | |||||||
| chr1:10557302 | T | C | 79 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(76): Show |
79 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.169+21005T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10557302 | |||||||
| chr1:10557323 | C | T | 1 | a0001c0004t0001g0147 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.169+21026C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10557323 | |||||||
| chr1:10557534 | T | C | 155 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(152): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.169+21237T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10557534 | |||||||
| chr1:10557729 | G | A | 1 | a0001c0001t0001g0036 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.169+21432G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10557729 | |||||||
| chr1:10557834 | CT | C | 143 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(140): Show |
144 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.169+21552delT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10557834 | ||||||
| chr1:10557849 | T | A | 151 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(148): Show |
152 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.169+21552T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10557849 | |||||||
| chr1:10557867 | T | C | 23 | a0001c0002t0001g0001 a0001c0002t0001g0167 a0001c0002t0001g0168 others(20): Show |
24 | HG00280.hp2 HG00673.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.169+21570T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10557867 | |||||||
| chr1:10557998 | T | C | 244 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(241): Show |
245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.169+21701T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10557998 | |||||||
| chr1:10558002 | T | C | 1 | a0001c0004t0001g0209 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.169+21705T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10558002 | |||||||
| chr1:10558052 | A | G | 53 | a0001c0002t0001g0001 a0001c0002t0001g0033 a0001c0002t0001g0077 others(50): Show |
54 | HG00280.hp2 HG00408.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.169+21755A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10558052 | |||||||
| chr1:10558309 | G | T | 242 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(239): Show |
243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.169+22012G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10558309 | |||||||
| chr1:10558487 | C | T | 1 | a0001c0002t0001g0169 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.169+22190C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10558487 | |||||||
| chr1:10558540 | G | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(1): Show |
4 | HG02280.hp1 HG02630.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.169+22243G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10558540 | |||||||
| chr1:10558601 | G | A | 2 | a0001c0003t0001g0238 a0001c0012t0001g0055 |
2 | HG01981.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.169+22304G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10558601 | |||||||
| chr1:10558716 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.169+22419G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10558716 | |||||||
| chr1:10558736 | C | CAAA | 18 | a0001c0001t0001g0019 a0001c0001t0001g0092 a0001c0001t0001g0093 others(15): Show |
18 | HG00609.hp2 HG01081.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.169+22457_169+2245 others(7): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10558736 | ||||||
| chr1:10558736 | CA | C | 122 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(119): Show |
122 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.169+22459delA | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10558736 | ||||||
| chr1:10558736 | CAA | C | 5 | a0001c0001t0001g0076 a0001c0001t0001g0080 a0001c0001t0001g0113 others(2): Show |
5 | HG02976.hp2 HG03453.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+22458_169+2245 others(6): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10558736 | ||||||
| chr1:10558736 | CAAAAAAA others(4): Show |
C | 15 | a0001c0001t0001g0003 a0001c0001t0001g0099 a0001c0001t0001g0101 others(12): Show |
15 | HG01891.hp2 HG02055.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.169+22449_169+2245 others(15): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10558736 | ||||||
| chr1:10558747 | A | G | 52 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(49): Show |
52 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.169+22450A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10558747 | |||||||
| chr1:10558814 | T | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0015 |
2 | HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.169+22517T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10558814 | |||||||
| chr1:10558934 | A | T | 155 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(152): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.169+22637A>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10558934 | |||||||
| chr1:10558937 | C | A | 155 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(152): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.169+22640C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10558937 | |||||||
| chr1:10559309 | C | A | 1 | a0001c0002t0001g0224 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.169+23012C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10559309 | |||||||
| chr1:10559445 | A | T | 2 | a0001c0001t0001g0145 a0001c0001t0001g0154 |
2 | HG02040.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.169+23148A>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10559445 | |||||||
| chr1:10559583 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0118 |
2 | HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.169+23286G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10559583 | |||||||
| chr1:10559606 | C | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0117 a0002c0005t0001g0207 |
3 | HG02258.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.169+23309C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10559606 | |||||||
| chr1:10559908 | G | C | 156 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(153): Show |
157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.169+23611G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10559908 | |||||||
| chr1:10559937 | G | T | 15 | a0001c0001t0001g0049 a0001c0001t0001g0080 a0001c0001t0001g0091 others(12): Show |
15 | HG00099.hp2 HG01069.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.169+23640G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10559937 | |||||||
| chr1:10560051 | T | C | 244 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(241): Show |
245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.169+23754T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10560051 | |||||||
| chr1:10560066 | T | C | 156 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(153): Show |
157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.169+23769T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10560066 | |||||||
| chr1:10560080 | G | A | 1 | a0002c0005t0001g0127 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.169+23783G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10560080 | |||||||
| chr1:10560150 | C | T | 2 | a0001c0001t0001g0100 a0001c0003t0001g0102 |
2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.169+23853C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10560150 | |||||||
| chr1:10560182 | C | T | 84 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
84 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.169+23885C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10560182 | |||||||
| chr1:10560213 | A | G | 156 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(153): Show |
157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.169+23916A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10560213 | |||||||
| chr1:10560644 | C | T | 248 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(245): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.169+24347C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10560644 | |||||||
| chr1:10560662 | T | C | 141 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(138): Show |
142 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.169+24365T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10560662 | |||||||
| chr1:10560716 | A | C | 141 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(138): Show |
142 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.169+24419A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10560716 | |||||||
| chr1:10560718 | C | CT | 30 | a0001c0001t0001g0019 a0001c0001t0001g0049 a0001c0001t0001g0091 others(27): Show |
30 | HG00099.hp2 HG00609.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.169+24438dupT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10560718 | ||||||
| chr1:10560718 | C | CTT | 20 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0092 others(17): Show |
20 | HG01192.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.169+24437_169+2443 others(6): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10560718 | ||||||
| chr1:10560718 | C | CTTTT | 44 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0020 others(41): Show |
44 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.169+24435_169+2443 others(8): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10560718 | ||||||
| chr1:10560719 | T | C | 1 | a0001c0002t0001g0254 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.169+24422T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10560719 | |||||||
| chr1:10560961 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.169+24664C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10560961 | |||||||
| chr1:10560993 | A | G | 47 | a0001c0001t0001g0020 a0001c0001t0001g0050 a0001c0001t0001g0112 others(44): Show |
47 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.169+24696A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10560993 | |||||||
| chr1:10561004 | A | G | 64 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(61): Show |
65 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.169+24707A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10561004 | |||||||
| chr1:10561093 | G | A | 240 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(237): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.169+24796G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10561093 | |||||||
| chr1:10561220 | C | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(1): Show |
4 | HG02280.hp1 HG02630.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.169+24923C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10561220 | |||||||
| chr1:10561228 | C | A | 1 | a0001c0001t0001g0112 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.169+24931C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10561228 | |||||||
| chr1:10561306 | G | A | 141 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(138): Show |
142 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.169+25009G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10561306 | |||||||
| chr1:10561848 | C | T | 3 | a0001c0001t0001g0113 a0001c0001t0001g0246 a0001c0001t0001g0247 |
3 | HG02622.hp2 HG02976.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.169+25551C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10561848 | |||||||
| chr1:10561909 | A | C | 18 | a0001c0001t0001g0019 a0001c0001t0001g0092 a0001c0001t0001g0093 others(15): Show |
18 | HG00609.hp2 HG01081.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.169+25612A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10561909 | |||||||
| chr1:10561950 | C | T | 3 | a0001c0001t0001g0140 a0001c0001t0003g0058 a0001c0003t0001g0057 |
3 | NA18950.hp1 NA18979.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.169+25653C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10561950 | |||||||
| chr1:10562016 | A | G | 3 | a0001c0001t0001g0089 a0001c0001t0001g0180 a0006c0013t0001g0206 |
3 | HG02055.hp2 HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.169+25719A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10562016 | |||||||
| chr1:10562133 | C | T | 3 | a0001c0001t0001g0089 a0001c0001t0001g0180 a0006c0013t0001g0206 |
3 | HG02055.hp2 HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.169+25836C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10562133 | |||||||
| chr1:10562248 | C | T | 15 | a0001c0001t0001g0003 a0001c0001t0001g0099 a0001c0001t0001g0101 others(12): Show |
15 | HG01891.hp2 HG02055.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.169+25951C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10562248 | |||||||
| chr1:10562317 | A | G | 46 | a0001c0001t0001g0020 a0001c0001t0001g0050 a0001c0001t0001g0131 others(43): Show |
46 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.169+26020A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10562317 | |||||||
| chr1:10562324 | A | C | 2 | a0001c0001t0001g0100 a0001c0003t0001g0102 |
2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.169+26027A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10562324 | |||||||
| chr1:10562341 | T | G | 4 | a0002c0005t0001g0127 a0002c0005t0001g0172 a0002c0005t0001g0173 others(1): Show |
4 | HG01167.hp1 HG02559.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.169+26044T>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10562341 | |||||||
| chr1:10562617 | G | A | 242 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(239): Show |
243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.169+26320G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10562617 | |||||||
| chr1:10562746 | C | T | 242 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(239): Show |
243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.169+26449C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10562746 | |||||||
| chr1:10562858 | T | C | 141 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(138): Show |
142 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.169+26561T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10562858 | |||||||
| chr1:10562861 | A | C | 1 | a0001c0001t0001g0112 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.169+26564A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10562861 | |||||||
| chr1:10562914 | C | CT | 139 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(136): Show |
140 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.169+26621dupT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10562914 | ||||||
| chr1:10562919 | C | T | 141 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(138): Show |
142 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.169+26622C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10562919 | |||||||
| chr1:10562968 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.169+26671A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10562968 | |||||||
| chr1:10563014 | C | G | 1 | a0001c0006t0001g0086 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.169+26717C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10563014 | |||||||
| chr1:10563078 | AT | A | 7 | a0001c0001t0001g0017 a0001c0001t0001g0097 a0001c0001t0001g0121 others(4): Show |
7 | HG02451.hp1 HG02717.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.169+26800delT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10563078 | ||||||
| chr1:10563078 | ATT | A | 82 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0015 others(79): Show |
82 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.169+26799_169+2680 others(6): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10563078 | ||||||
| chr1:10563078 | ATTT | A | 157 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(154): Show |
158 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.169+26798_169+2680 others(7): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10563078 | ||||||
| chr1:10563119 | T | C | 84 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
84 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.169+26822T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10563119 | |||||||
| chr1:10563153 | C | T | 1 | a0002c0005t0001g0127 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.169+26856C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10563153 | |||||||
| chr1:10563182 | T | C | 141 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(138): Show |
142 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.169+26885T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10563182 | |||||||
| chr1:10563328 | G | A | 3 | a0001c0001t0001g0009 a0001c0001t0001g0056 a0001c0001t0006g0010 |
3 | HG01433.hp2 HG03654.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.169+27031G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10563328 | |||||||
| chr1:10563338 | G | A | 2 | a0001c0001t0001g0145 a0001c0001t0001g0154 |
2 | HG02040.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.169+27041G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10563338 | |||||||
| chr1:10563574 | G | A | 1 | a0001c0002t0001g0179 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.169+27277G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10563574 | |||||||
| chr1:10563619 | C | A | 1 | a0001c0001t0001g0076 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.169+27322C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10563619 | |||||||
| chr1:10563630 | A | C | 1 | a0001c0001t0001g0076 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.169+27333A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10563630 | |||||||
| chr1:10563647 | G | A | 1 | a0001c0003t0001g0083 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.169+27350G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10563647 | |||||||
| chr1:10563651 | G | A | 12 | a0001c0001t0001g0049 a0001c0001t0001g0080 a0001c0001t0001g0091 others(9): Show |
12 | HG00099.hp2 HG01069.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.169+27354G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10563651 | |||||||
| chr1:10563729 | G | A | 18 | a0001c0001t0001g0019 a0001c0001t0001g0092 a0001c0001t0001g0093 others(15): Show |
18 | HG00609.hp2 HG01081.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.169+27432G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10563729 | |||||||
| chr1:10563772 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.169+27475C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10563772 | |||||||
| chr1:10563780 | C | G | 3 | a0001c0001t0001g0003 a0001c0001t0001g0117 a0002c0005t0001g0207 |
3 | HG02258.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.169+27483C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10563780 | |||||||
| chr1:10563784 | T | C | 225 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(222): Show |
226 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.169+27487T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10563784 | |||||||
| chr1:10563861 | A | G | 244 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(241): Show |
245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.169+27564A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10563861 | |||||||
| chr1:10563917 | G | GA | 206 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(203): Show |
207 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.169+27631dupA | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10563917 | ||||||
| chr1:10563954 | A | G | 1 | a0001c0016t0001g0070 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.169+27657A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10563954 | |||||||
| chr1:10564000 | CAT | C | 51 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(48): Show |
51 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.169+27704_169+2770 others(6): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10564000 | |||||||
| chr1:10564129 | T | G | 1 | a0001c0001t0001g0180 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.169+27832T>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10564129 | |||||||
| chr1:10564149 | C | T | 1 | a0001c0002t0001g0254 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.169+27852C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10564149 | |||||||
| chr1:10564183 | C | CTT | 248 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(245): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.169+27887_169+2788 others(6): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10564183 | ||||||
| chr1:10564258 | A | G | 141 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(138): Show |
142 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.169+27961A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10564258 | |||||||
| chr1:10564411 | A | G | 141 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(138): Show |
142 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.169+28114A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10564411 | |||||||
| chr1:10564430 | A | AT | 27 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0106 others(24): Show |
27 | HG00609.hp2 HG00673.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.169+28148dupT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10564430 | ||||||
| chr1:10564595 | CT | C | 41 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(38): Show |
41 | HG00099.hp2 HG00280.hp2 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.169+28316delT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10564595 | ||||||
| chr1:10564595 | CTT | C | 178 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
179 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.169+28315_169+2831 others(6): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10564595 | ||||||
| chr1:10564659 | C | G | 1 | a0001c0003t0001g0149 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.169+28362C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10564659 | |||||||
| chr1:10564864 | T | A | 1 | a0001c0001t0001g0157 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.169+28567T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10564864 | |||||||
| chr1:10564904 | C | CT | 180 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(177): Show |
181 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.169+28624dupT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10564904 | ||||||
| chr1:10564904 | C | CTT | 27 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0094 others(24): Show |
27 | HG01070.hp1 HG01167.hp1 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.169+28623_169+2862 others(6): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10564904 | ||||||
| chr1:10564904 | C | CTTT | 13 | a0001c0001t0001g0019 a0001c0001t0001g0092 a0001c0001t0001g0093 others(10): Show |
13 | HG00609.hp2 HG01081.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.169+28622_169+2862 others(7): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10564904 | ||||||
| chr1:10565039 | G | T | 4 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0002g0253 others(1): Show |
4 | HG01891.hp1 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.169+28742G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10565039 | |||||||
| chr1:10565064 | C | A | 1 | a0001c0001t0001g0121 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.169+28767C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10565064 | |||||||
| chr1:10565124 | G | A | 2 | a0001c0001t0001g0100 a0001c0003t0001g0102 |
2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.169+28827G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10565124 | |||||||
| chr1:10565135 | C | G | 2 | a0001c0007t0001g0203 a0003c0011t0001g0107 |
2 | HG04199.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.169+28838C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10565135 | |||||||
| chr1:10565154 | G | A | 2 | a0001c0014t0001g0251 a0004c0010t0001g0098 |
2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.169+28857G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10565154 | |||||||
| chr1:10565163 | A | G | 1 | a0001c0004t0001g0209 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.169+28866A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10565163 | |||||||
| chr1:10565193 | C | T | 2 | a0001c0001t0001g0231 a0001c0001t0001g0232 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.169+28896C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10565193 | |||||||
| chr1:10565194 | G | T | 3 | a0001c0001t0001g0113 a0001c0001t0001g0246 a0001c0001t0001g0247 |
3 | HG02622.hp2 HG02976.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.169+28897G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10565194 | |||||||
| chr1:10565228 | A | C | 1 | a0001c0004t0001g0209 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.169+28931A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10565228 | |||||||
| chr1:10565348 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.169+29051G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10565348 | |||||||
| chr1:10565404 | GTATAGCC others(3): Show |
G | 12 | a0001c0001t0001g0049 a0001c0001t0001g0080 a0001c0001t0001g0091 others(9): Show |
12 | HG00099.hp2 HG01069.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.169+29111_169+2912 others(14): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10565404 | ||||||
| chr1:10565438 | A | T | 84 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
84 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.169+29141A>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10565438 | |||||||
| chr1:10565550 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.169+29253T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10565550 | |||||||
| chr1:10565597 | C | T | 12 | a0001c0001t0001g0049 a0001c0001t0001g0080 a0001c0001t0001g0091 others(9): Show |
12 | HG00099.hp2 HG01069.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.169+29300C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10565597 | |||||||
| chr1:10565660 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.169+29363T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10565660 | |||||||
| chr1:10565981 | A | G | 1 | a0001c0002t0001g0193 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.169+29684A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10565981 | |||||||
| chr1:10566073 | T | A | 1 | a0001c0001t0001g0003 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.169+29776T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10566073 | |||||||
| chr1:10566230 | G | T | 141 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(138): Show |
142 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.169+29933G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10566230 | |||||||
| chr1:10566493 | CT | C | 141 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(138): Show |
142 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.169+30208delT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10566493 | ||||||
| chr1:10566536 | T | C | 2 | a0001c0001t0001g0100 a0001c0003t0001g0102 |
2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.169+30239T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10566536 | |||||||
| chr1:10566580 | T | C | 242 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(239): Show |
243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.169+30283T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10566580 | |||||||
| chr1:10566865 | G | C | 141 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(138): Show |
142 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.169+30568G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10566865 | |||||||
| chr1:10567117 | A | C | 1 | a0001c0003t0001g0041 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.169+30820A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10567117 | |||||||
| chr1:10567148 | C | A | 2 | a0001c0001t0001g0081 a0001c0001t0001g0174 |
2 | HG02647.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.169+30851C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10567148 | |||||||
| chr1:10567361 | A | G | 2 | a0001c0001t0001g0100 a0001c0003t0001g0102 |
2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.169+31064A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10567361 | |||||||
| chr1:10567485 | G | T | 51 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(48): Show |
51 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.169+31188G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10567485 | |||||||
| chr1:10567562 | C | T | 150 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(147): Show |
151 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.169+31265C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10567562 | |||||||
| chr1:10567644 | A | G | 51 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(48): Show |
51 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.169+31347A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10567644 | |||||||
| chr1:10567848 | C | T | 18 | a0001c0001t0001g0019 a0001c0001t0001g0092 a0001c0001t0001g0093 others(15): Show |
18 | HG00609.hp2 HG01081.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.170-31390C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10567848 | |||||||
| chr1:10568069 | C | T | 1 | a0001c0001t0001g0032 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.170-31169C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10568069 | |||||||
| chr1:10568190 | C | G | 9 | a0001c0001t0001g0099 a0001c0001t0001g0101 a0001c0001t0001g0110 others(6): Show |
9 | HG01891.hp2 HG02280.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.170-31048C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10568190 | |||||||
| chr1:10568293 | G | A | 141 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(138): Show |
142 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.170-30945G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10568293 | |||||||
| chr1:10568323 | T | TC | 16 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0097 others(13): Show |
16 | HG00609.hp2 HG01981.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.170-30900dupC | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10568323 | ||||||
| chr1:10568323 | TC | T | 32 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0020 others(29): Show |
32 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.170-30900delC | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10568323 | ||||||
| chr1:10568323 | TCC | T | 31 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0035 others(28): Show |
31 | HG01167.hp1 HG02027.hp1 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.170-30901_170-3090 others(6): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10568323 | ||||||
| chr1:10568323 | TCCC | T | 76 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(73): Show |
76 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.170-30902_170-3090 others(7): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10568323 | ||||||
| chr1:10568323 | TCCCC | T | 61 | a0001c0001t0001g0067 a0001c0001t0001g0115 a0001c0001t0001g0116 others(58): Show |
62 | HG00280.hp2 HG00408.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.170-30903_170-3090 others(8): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10568323 | ||||||
| chr1:10568326 | C | T | 12 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0045 others(9): Show |
12 | HG02027.hp1 HG02055.hp2 HG02738.hp1 others(9): Show |
intron_variant | MODIFIER | c.170-30912C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10568326 | |||||||
| chr1:10568327 | C | T | 68 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(65): Show |
68 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.170-30911C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10568327 | |||||||
| chr1:10568328 | C | T | 61 | a0001c0001t0001g0067 a0001c0001t0001g0115 a0001c0001t0001g0116 others(58): Show |
62 | HG00280.hp2 HG00408.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.170-30910C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10568328 | |||||||
| chr1:10568338 | C | A | 3 | a0001c0001t0001g0089 a0001c0001t0001g0180 a0006c0013t0001g0206 |
3 | HG02055.hp2 HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.170-30900C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10568338 | |||||||
| chr1:10568338 | C | G | 1 | a0001c0001t0001g0048 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.170-30900C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10568338 | |||||||
| chr1:10568406 | A | G | 1 | a0001c0002t0001g0176 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.170-30832A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10568406 | |||||||
| chr1:10568419 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.170-30819G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10568419 | |||||||
| chr1:10568825 | C | T | 141 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(138): Show |
142 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.170-30413C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10568825 | |||||||
| chr1:10568970 | C | T | 7 | a0001c0001t0001g0120 a0001c0001t0001g0226 a0001c0001t0001g0229 others(4): Show |
7 | HG01884.hp1 HG02622.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.170-30268C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10568970 | |||||||
| chr1:10569076 | C | A | 141 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(138): Show |
142 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.170-30162C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10569076 | |||||||
| chr1:10569222 | C | T | 2 | a0001c0001t0001g0159 a0001c0001t0001g0165 |
2 | NA18992.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.170-30016C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10569222 | |||||||
| chr1:10569254 | T | C | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0128 |
3 | HG02559.hp2 HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.170-29984T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10569254 | |||||||
| chr1:10569378 | C | T | 15 | a0001c0001t0001g0003 a0001c0001t0001g0099 a0001c0001t0001g0101 others(12): Show |
15 | HG01891.hp2 HG02055.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.170-29860C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10569378 | |||||||
| chr1:10569433 | C | T | 3 | a0001c0001t0001g0106 a0001c0001t0001g0245 a0001c0003t0001g0105 |
3 | HG02109.hp2 HG03540.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.170-29805C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10569433 | |||||||
| chr1:10569441 | C | T | 1 | a0001c0001t0001g0064 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.170-29797C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10569441 | |||||||
| chr1:10569505 | G | A | 141 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(138): Show |
142 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.170-29733G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10569505 | |||||||
| chr1:10569600 | A | G | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0128 |
3 | HG02559.hp2 HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.170-29638A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10569600 | |||||||
| chr1:10569715 | G | T | 2 | a0001c0002t0001g0176 a0001c0002t0001g0186 |
2 | HG01106.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.170-29523G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10569715 | |||||||
| chr1:10569761 | T | C | 2 | a0001c0002t0001g0204 a0001c0002t0001g0205 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.170-29477T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10569761 | |||||||
| chr1:10569790 | T | C | 242 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(239): Show |
243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.170-29448T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10569790 | |||||||
| chr1:10569811 | C | G | 1 | a0001c0002t0001g0217 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.170-29427C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10569811 | |||||||
| chr1:10569875 | C | T | 18 | a0001c0001t0001g0019 a0001c0001t0001g0092 a0001c0001t0001g0093 others(15): Show |
18 | HG00609.hp2 HG01081.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.170-29363C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10569875 | |||||||
| chr1:10570073 | C | G | 15 | a0001c0001t0001g0003 a0001c0001t0001g0099 a0001c0001t0001g0101 others(12): Show |
15 | HG01891.hp2 HG02055.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.170-29165C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10570073 | |||||||
| chr1:10570230 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.170-29008T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10570230 | |||||||
| chr1:10570243 | A | G | 242 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(239): Show |
243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.170-28995A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10570243 | |||||||
| chr1:10570481 | C | T | 12 | a0001c0001t0001g0049 a0001c0001t0001g0080 a0001c0001t0001g0091 others(9): Show |
12 | HG00099.hp2 HG01069.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.170-28757C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10570481 | |||||||
| chr1:10570607 | C | G | 2 | a0001c0001t0001g0138 a0001c0004t0001g0060 |
2 | HG01256.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.170-28631C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10570607 | |||||||
| chr1:10570609 | G | A | 15 | a0001c0001t0001g0003 a0001c0001t0001g0099 a0001c0001t0001g0101 others(12): Show |
15 | HG01891.hp2 HG02055.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.170-28629G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10570609 | |||||||
| chr1:10570725 | T | A | 1 | a0001c0001t0001g0221 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.170-28513T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10570725 | |||||||
| chr1:10570848 | G | GTTTGTTT | 71 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(68): Show |
71 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.170-28387_170-2838 others(11): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10570848 | ||||||
| chr1:10570848 | G | GTTTTTTT | 41 | a0001c0001t0001g0089 a0001c0001t0001g0116 a0001c0001t0001g0252 others(38): Show |
42 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.170-28379_170-2837 others(11): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10570848 | ||||||
| chr1:10570848 | G | GTTTTTTT others(1): Show |
14 | a0001c0001t0001g0115 a0001c0001t0001g0128 a0001c0001t0001g0249 others(11): Show |
14 | HG00558.hp1 HG00673.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.170-28380_170-2837 others(12): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10570848 | ||||||
| chr1:10570848 | G | GTTTTTTT others(3): Show |
2 | a0001c0001t0002g0253 a0001c0015t0001g0255 |
2 | HG01891.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.170-28382_170-2837 others(14): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10570848 | ||||||
| chr1:10570848 | GT | G | 18 | a0001c0001t0001g0019 a0001c0001t0001g0092 a0001c0001t0001g0093 others(15): Show |
18 | HG00609.hp2 HG01081.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.170-28373delT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10570848 | ||||||
| chr1:10570909 | G | A | 141 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(138): Show |
142 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.170-28329G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10570909 | |||||||
| chr1:10571015 | G | GT | 32 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0089 others(29): Show |
32 | HG00609.hp2 HG00673.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.170-28201dupT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10571015 | ||||||
| chr1:10571015 | G | GTT | 7 | a0001c0001t0001g0109 a0001c0003t0001g0103 a0001c0003t0001g0108 others(4): Show |
7 | HG01981.hp2 HG02559.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.170-28202_170-2820 others(6): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10571015 | ||||||
| chr1:10571015 | GT | G | 143 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(140): Show |
144 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.170-28201delT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10571015 | ||||||
| chr1:10571116 | C | T | 13 | a0001c0001t0001g0050 a0001c0001t0001g0139 a0001c0001t0001g0142 others(10): Show |
13 | HG00408.hp1 HG00544.hp1 HG02165.hp2 others(10): Show |
intron_variant | MODIFIER | c.170-28122C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10571116 | |||||||
| chr1:10571180 | C | T | 65 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(62): Show |
65 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.170-28058C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10571180 | |||||||
| chr1:10571327 | TA | T | 17 | a0001c0001t0001g0049 a0001c0001t0001g0080 a0001c0001t0001g0091 others(14): Show |
17 | HG00099.hp2 HG01069.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.170-27902delA | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10571327 | ||||||
| chr1:10571373 | G | A | 1 | a0001c0002t0001g0237 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.170-27865G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10571373 | |||||||
| chr1:10571393 | G | A | 5 | a0001c0001t0001g0100 a0001c0001t0001g0113 a0001c0001t0001g0246 others(2): Show |
5 | HG02451.hp2 HG02622.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.170-27845G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10571393 | |||||||
| chr1:10571398 | C | G | 244 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(241): Show |
245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.170-27840C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10571398 | |||||||
| chr1:10571448 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.170-27790G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10571448 | |||||||
| chr1:10571595 | G | T | 2 | a0001c0001t0001g0145 a0001c0001t0001g0154 |
2 | HG02040.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.170-27643G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10571595 | |||||||
| chr1:10571679 | G | C | 1 | a0001c0004t0001g0209 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.170-27559G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10571679 | |||||||
| chr1:10571682 | G | A | 141 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(138): Show |
142 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.170-27556G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10571682 | |||||||
| chr1:10571707 | G | T | 18 | a0001c0001t0001g0019 a0001c0001t0001g0092 a0001c0001t0001g0093 others(15): Show |
18 | HG00609.hp2 HG01081.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.170-27531G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10571707 | |||||||
| chr1:10571754 | A | C | 141 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(138): Show |
142 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.170-27484A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10571754 | |||||||
| chr1:10571758 | G | A | 141 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(138): Show |
142 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.170-27480G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10571758 | |||||||
| chr1:10571922 | A | C | 1 | a0001c0001t0001g0032 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.170-27316A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10571922 | |||||||
| chr1:10571960 | T | G | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.170-27278T>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10571960 | |||||||
| chr1:10572131 | T | C | 1 | a0001c0002t0001g0077 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.170-27107T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10572131 | |||||||
| chr1:10572178 | C | T | 56 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0128 others(53): Show |
57 | HG00280.hp2 HG00408.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.170-27060C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10572178 | |||||||
| chr1:10572303 | G | A | 248 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(245): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.170-26935G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10572303 | |||||||
| chr1:10572464 | G | A | 15 | a0001c0001t0001g0003 a0001c0001t0001g0099 a0001c0001t0001g0101 others(12): Show |
15 | HG01891.hp2 HG02055.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.170-26774G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10572464 | |||||||
| chr1:10572558 | A | G | 51 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(48): Show |
51 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.170-26680A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10572558 | |||||||
| chr1:10572590 | G | A | 141 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(138): Show |
142 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.170-26648G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10572590 | |||||||
| chr1:10572599 | A | G | 15 | a0001c0001t0001g0003 a0001c0001t0001g0099 a0001c0001t0001g0101 others(12): Show |
15 | HG01891.hp2 HG02055.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.170-26639A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10572599 | |||||||
| chr1:10572623 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.170-26615C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10572623 | |||||||
| chr1:10572680 | GC | G | 140 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(137): Show |
141 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.170-26550delC | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10572680 | ||||||
| chr1:10572689 | A | C | 12 | a0001c0001t0001g0049 a0001c0001t0001g0080 a0001c0001t0001g0091 others(9): Show |
12 | HG00099.hp2 HG01069.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.170-26549A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10572689 | |||||||
| chr1:10572794 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.170-26444C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10572794 | |||||||
| chr1:10572815 | C | T | 5 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0073 others(2): Show |
5 | HG01175.hp1 HG01358.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.170-26423C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10572815 | |||||||
| chr1:10572828 | G | T | 5 | a0001c0001t0001g0049 a0001c0001t0001g0080 a0001c0001t0001g0091 others(2): Show |
5 | HG00099.hp2 HG01069.hp1 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.170-26410G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10572828 | |||||||
| chr1:10572883 | A | G | 1 | a0001c0002t0001g0195 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.170-26355A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10572883 | |||||||
| chr1:10572898 | C | T | 5 | a0001c0001t0001g0100 a0001c0001t0001g0113 a0001c0001t0001g0246 others(2): Show |
5 | HG02451.hp2 HG02622.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.170-26340C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10572898 | |||||||
| chr1:10572933 | C | T | 3 | a0001c0001t0001g0089 a0001c0001t0001g0180 a0006c0013t0001g0206 |
3 | HG02055.hp2 HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.170-26305C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10572933 | |||||||
| chr1:10573188 | G | A | 131 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(128): Show |
131 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.170-26050G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10573188 | |||||||
| chr1:10573216 | G | A | 141 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(138): Show |
142 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.170-26022G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10573216 | |||||||
| chr1:10573364 | A | C | 80 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(77): Show |
80 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.170-25874A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10573364 | |||||||
| chr1:10573396 | G | A | 141 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(138): Show |
142 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.170-25842G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10573396 | |||||||
| chr1:10573432 | A | G | 27 | a0001c0001t0001g0020 a0001c0001t0001g0050 a0001c0001t0001g0137 others(24): Show |
27 | HG00408.hp1 HG00544.hp1 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.170-25806A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10573432 | |||||||
| chr1:10573465 | C | G | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0128 |
3 | HG02559.hp2 HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.170-25773C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10573465 | |||||||
| chr1:10573486 | C | A | 141 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(138): Show |
142 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.170-25752C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10573486 | |||||||
| chr1:10573515 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0018 |
2 | HG02109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.170-25723C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10573515 | |||||||
| chr1:10573569 | G | GAATGGCG others(3): Show |
1 | a0001c0001t0001g0065 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.170-25667_170-2565 others(14): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10573569 | ||||||
| chr1:10573594 | G | A | 46 | a0001c0001t0001g0020 a0001c0001t0001g0050 a0001c0001t0001g0131 others(43): Show |
46 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.170-25644G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10573594 | |||||||
| chr1:10573788 | T | C | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.170-25450T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10573788 | |||||||
| chr1:10573829 | G | A | 12 | a0001c0001t0001g0049 a0001c0001t0001g0080 a0001c0001t0001g0091 others(9): Show |
12 | HG00099.hp2 HG01069.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.170-25409G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10573829 | |||||||
| chr1:10573965 | G | A | 3 | a0001c0001t0001g0099 a0001c0001t0001g0101 a0001c0001t0001g0110 |
3 | HG02280.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.170-25273G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10573965 | |||||||
| chr1:10574017 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.170-25221G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10574017 | |||||||
| chr1:10574114 | T | C | 159 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(156): Show |
160 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.170-25124T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10574114 | |||||||
| chr1:10574138 | A | C | 5 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(2): Show |
5 | HG02280.hp1 HG02630.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.170-25100A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10574138 | |||||||
| chr1:10574138 | A | T | 46 | a0001c0001t0001g0020 a0001c0001t0001g0050 a0001c0001t0001g0131 others(43): Show |
46 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.170-25100A>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10574138 | |||||||
| chr1:10574509 | T | G | 15 | a0001c0001t0001g0003 a0001c0001t0001g0099 a0001c0001t0001g0101 others(12): Show |
15 | HG01891.hp2 HG02055.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.170-24729T>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10574509 | |||||||
| chr1:10574539 | C | G | 1 | a0001c0001t0002g0253 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.170-24699C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10574539 | |||||||
| chr1:10574637 | A | G | 1 | a0001c0001t0001g0220 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.170-24601A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10574637 | |||||||
| chr1:10574724 | T | A | 1 | a0001c0003t0001g0105 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.170-24514T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10574724 | |||||||
| chr1:10574729 | G | A | 4 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0002g0253 others(1): Show |
4 | HG01891.hp1 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.170-24509G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10574729 | |||||||
| chr1:10575064 | G | A | 46 | a0001c0001t0001g0020 a0001c0001t0001g0050 a0001c0001t0001g0131 others(43): Show |
46 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.170-24174G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10575064 | |||||||
| chr1:10575074 | T | TA | 71 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(68): Show |
72 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.170-24152dupA | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10575074 | ||||||
| chr1:10575202 | A | G | 6 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0256 others(3): Show |
6 | HG01891.hp1 HG02109.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.170-24036A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10575202 | |||||||
| chr1:10575271 | C | T | 71 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(68): Show |
71 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.170-23967C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10575271 | |||||||
| chr1:10575305 | C | T | 51 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(48): Show |
51 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.170-23933C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10575305 | |||||||
| chr1:10575599 | T | C | 39 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(36): Show |
39 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.170-23639T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10575599 | |||||||
| chr1:10575816 | G | A | 1 | a0001c0002t0001g0212 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.170-23422G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10575816 | |||||||
| chr1:10575944 | C | T | 3 | a0001c0001t0001g0106 a0001c0001t0001g0245 a0001c0003t0001g0105 |
3 | HG02109.hp2 HG03540.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.170-23294C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10575944 | |||||||
| chr1:10576386 | G | A | 141 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(138): Show |
142 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.170-22852G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10576386 | |||||||
| chr1:10576402 | G | A | 141 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(138): Show |
142 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.170-22836G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10576402 | |||||||
| chr1:10576494 | C | T | 2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | NA18950.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.170-22744C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10576494 | |||||||
| chr1:10576551 | GAAATGGT others(7432): Show |
G | 2 | a0001c0001t0001g0145 a0001c0001t0001g0154 |
2 | HG02040.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.170-22680_170-1524 others(4): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10576551 | ||||||
| chr1:10576759 | C | CT | 59 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(56): Show |
59 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.170-22463dupT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10576759 | ||||||
| chr1:10576759 | C | CTT | 6 | a0001c0001t0001g0045 a0001c0004t0001g0046 a0001c0004t0001g0053 others(3): Show |
6 | HG00733.hp2 HG00741.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.170-22464_170-2246 others(6): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10576759 | ||||||
| chr1:10576759 | CT | C | 9 | a0001c0001t0001g0101 a0001c0001t0001g0227 a0001c0001t0001g0231 others(6): Show |
9 | HG00558.hp2 HG01515.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.170-22463delT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10576759 | ||||||
| chr1:10576791 | C | T | 1 | a0001c0004t0001g0209 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.170-22447C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10576791 | |||||||
| chr1:10576796 | C | T | 51 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(48): Show |
51 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.170-22442C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10576796 | |||||||
| chr1:10576817 | C | T | 12 | a0001c0001t0001g0049 a0001c0001t0001g0080 a0001c0001t0001g0091 others(9): Show |
12 | HG00099.hp2 HG01069.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.170-22421C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10576817 | |||||||
| chr1:10576818 | G | A | 1 | a0001c0004t0001g0209 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.170-22420G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10576818 | |||||||
| chr1:10576881 | C | G | 1 | a0001c0001t0001g0252 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.170-22357C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10576881 | |||||||
| chr1:10576898 | A | T | 139 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(136): Show |
140 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.170-22340A>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10576898 | |||||||
| chr1:10577021 | C | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0117 a0002c0005t0001g0207 |
3 | HG02258.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.170-22217C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577021 | |||||||
| chr1:10577161 | A | G | 2 | a0001c0001t0001g0146 a0001c0001t0001g0153 |
2 | HG02027.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.170-22077A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577161 | |||||||
| chr1:10577189 | C | CAGG | 139 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(136): Show |
140 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.170-22047_170-2204 others(7): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577189 | ||||||
| chr1:10577213 | A | G | 3 | a0001c0001t0001g0003 a0001c0001t0001g0117 a0002c0005t0001g0207 |
3 | HG02258.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.170-22025A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577213 | |||||||
| chr1:10577217 | C | T | 5 | a0001c0002t0001g0194 a0001c0002t0001g0196 a0001c0002t0001g0224 others(2): Show |
5 | HG03490.hp2 NA18942.hp1 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.170-22021C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577217 | |||||||
| chr1:10577279 | C | T | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0128 |
3 | HG02559.hp2 HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.170-21959C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577279 | |||||||
| chr1:10577408 | A | C | 1 | a0001c0001t0001g0002 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.170-21830A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577408 | |||||||
| chr1:10577409 | C | A | 5 | a0001c0001t0001g0036 a0001c0003t0001g0025 a0001c0004t0001g0162 others(2): Show |
5 | HG00423.hp1 HG03471.hp1 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.170-21829C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577409 | |||||||
| chr1:10577410 | C | A | 4 | a0001c0001t0001g0002 a0001c0001t0001g0121 a0001c0001t0001g0142 others(1): Show |
4 | HG03098.hp2 NA18522.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.170-21828C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577410 | |||||||
| chr1:10577410 | C | CA | 70 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(67): Show |
70 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.170-21816dupA | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577410 | ||||||
| chr1:10577410 | C | CAA | 21 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0099 others(18): Show |
21 | HG01167.hp1 HG01891.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.170-21817_170-2181 others(6): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577410 | ||||||
| chr1:10577410 | C | CAAA | 83 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0030 others(80): Show |
84 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.170-21818_170-2181 others(7): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577410 | ||||||
| chr1:10577410 | C | CAAAA | 53 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(50): Show |
53 | HG00099.hp1 HG00423.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.170-21819_170-2181 others(8): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577410 | ||||||
| chr1:10577410 | C | CAAAAA | 15 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0051 others(12): Show |
15 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.170-21820_170-2181 others(9): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577410 | ||||||
| chr1:10577410 | C | CCAAA | 3 | a0001c0003t0001g0025 a0001c0012t0001g0055 a0004c0010t0001g0098 |
3 | HG00423.hp1 HG03471.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.170-21828_170-2182 others(8): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577410 | |||||||
| chr1:10577460 | T | C | 12 | a0001c0001t0001g0049 a0001c0001t0001g0080 a0001c0001t0001g0091 others(9): Show |
12 | HG00099.hp2 HG01069.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.170-21778T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577460 | |||||||
| chr1:10577529 | C | CATATATA others(7): Show |
1 | a0001c0001t0001g0092 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.170-21688_170-2167 others(18): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577529 | ||||||
| chr1:10577535 | T | TATATATA others(22): Show |
1 | a0001c0001t0001g0109 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.170-21679_170-2167 others(33): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577535 | ||||||
| chr1:10577537 | T | TATATATA others(20): Show |
1 | a0001c0001t0001g0114 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.170-21679_170-2167 others(31): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577537 | ||||||
| chr1:10577544 | ATATATAT others(22): Show |
A | 1 | a0001c0001t0001g0097 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.170-21692_170-2166 others(33): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577544 | ||||||
| chr1:10577544 | ATATATAT others(30): Show |
A | 1 | a0001c0001t0001g0252 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.170-21692_170-2165 others(41): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577544 | ||||||
| chr1:10577545 | T | TATATATA others(10): Show |
1 | a0001c0003t0001g0108 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.170-21681_170-2168 others(21): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577545 | ||||||
| chr1:10577546 | ATATATAT others(13): Show |
A | 1 | a0001c0001t0001g0021 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.170-21690_170-2167 others(24): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577546 | ||||||
| chr1:10577546 | ATATATAT others(14): Show |
A | 1 | a0001c0001t0001g0022 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.170-21690_170-2167 others(25): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577546 | ||||||
| chr1:10577546 | ATATATAT others(15): Show |
A | 2 | a0001c0001t0004g0023 a0001c0016t0001g0070 |
2 | HG00735.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.170-21690_170-2166 others(26): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577546 | ||||||
| chr1:10577546 | ATATATAT others(16): Show |
A | 2 | a0001c0001t0001g0071 a0001c0004t0001g0074 |
2 | HG01358.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.170-21690_170-2166 others(27): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577546 | ||||||
| chr1:10577546 | ATATATAT others(27): Show |
A | 3 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0002g0253 |
3 | HG01891.hp1 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.170-21690_170-2165 others(38): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577546 | ||||||
| chr1:10577546 | ATATATAT others(28): Show |
A | 1 | a0001c0015t0001g0255 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.170-21690_170-2165 others(39): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577546 | ||||||
| chr1:10577548 | ATATATAT others(10): Show |
A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0146 |
2 | HG00280.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.170-21688_170-2167 others(21): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577548 | ||||||
| chr1:10577548 | ATATATAT others(12): Show |
A | 2 | a0001c0001t0001g0073 a0001c0001t0001g0153 |
2 | HG02056.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.170-21688_170-2167 others(23): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577548 | ||||||
| chr1:10577548 | ATATATAT others(14): Show |
A | 1 | a0001c0001t0001g0067 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.170-21688_170-2166 others(25): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577548 | ||||||
| chr1:10577548 | ATATATAT others(16): Show |
A | 1 | a0001c0001t0001g0144 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.170-21688_170-2166 others(27): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577548 | ||||||
| chr1:10577548 | ATATATAT others(17): Show |
A | 5 | a0001c0001t0001g0050 a0001c0001t0001g0142 a0001c0001t0001g0160 others(2): Show |
5 | HG01358.hp2 HG02165.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.170-21688_170-2166 others(28): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577548 | ||||||
| chr1:10577548 | ATATATAT others(18): Show |
A | 7 | a0001c0001t0001g0106 a0001c0001t0001g0141 a0001c0001t0001g0143 others(4): Show |
7 | HG00408.hp1 HG01070.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.170-21688_170-2166 others(29): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577548 | ||||||
| chr1:10577548 | ATATATAT others(19): Show |
A | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG00733.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.170-21688_170-2166 others(30): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577548 | ||||||
| chr1:10577548 | ATATATAT others(20): Show |
A | 2 | a0001c0001t0001g0239 a0001c0003t0001g0132 |
2 | HG02723.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.170-21688_170-2166 others(31): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577548 | ||||||
| chr1:10577548 | ATATATAT others(21): Show |
A | 2 | a0001c0001t0001g0136 a0001c0001t0001g0244 |
2 | HG02129.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.170-21688_170-2166 others(32): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577548 | ||||||
| chr1:10577548 | ATATATAT others(22): Show |
A | 1 | a0001c0001t0001g0134 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.170-21688_170-2166 others(33): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577548 | ||||||
| chr1:10577548 | ATATATAT others(28): Show |
A | 1 | a0001c0001t0001g0096 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.170-21688_170-2165 others(39): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577548 | ||||||
| chr1:10577550 | ATATATAT others(8): Show |
A | 1 | a0004c0010t0001g0098 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.170-21686_170-2167 others(19): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577550 | ||||||
| chr1:10577550 | ATATATAT others(10): Show |
A | 1 | a0001c0014t0001g0251 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.170-21686_170-2167 others(21): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577550 | ||||||
| chr1:10577550 | ATATATAT others(15): Show |
A | 3 | a0001c0001t0001g0075 a0001c0003t0001g0105 a0001c0004t0001g0162 |
3 | HG01175.hp1 HG03540.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.170-21686_170-2166 others(26): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577550 | ||||||
| chr1:10577550 | ATATATAT others(17): Show |
A | 4 | a0001c0001t0001g0020 a0001c0001t0001g0139 a0001c0001t0001g0245 others(1): Show |
4 | HG02109.hp2 HG03831.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.170-21686_170-2166 others(28): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577550 | ||||||
| chr1:10577550 | ATATATAT others(18): Show |
A | 4 | a0001c0001t0001g0137 a0001c0001t0001g0157 a0001c0003t0001g0149 others(1): Show |
4 | HG02738.hp2 HG03942.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.170-21686_170-2166 others(29): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577550 | ||||||
| chr1:10577550 | ATATATAT others(19): Show |
A | 3 | a0001c0001t0001g0138 a0001c0001t0001g0241 a0001c0001t0001g0242 |
3 | HG01256.hp1 NA18970.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.170-21686_170-2166 others(30): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577550 | ||||||
| chr1:10577550 | ATATATAT others(20): Show |
A | 2 | a0001c0003t0001g0133 a0001c0017t0001g0130 |
2 | HG02886.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.170-21686_170-2166 others(31): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577550 | ||||||
| chr1:10577550 | ATATATAT others(21): Show |
A | 5 | a0001c0001t0001g0131 a0001c0001t0001g0220 a0001c0003t0001g0041 others(2): Show |
5 | HG00558.hp2 HG03492.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.170-21686_170-2165 others(32): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577550 | ||||||
| chr1:10577550 | ATATATAT others(22): Show |
A | 1 | a0001c0001t0001g0225 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.170-21686_170-2165 others(33): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577550 | ||||||
| chr1:10577550 | ATATATAT others(29): Show |
A | 1 | a0001c0002t0001g0186 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.170-21686_170-2165 others(40): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577550 | ||||||
| chr1:10577550 | ATATATAT others(30): Show |
A | 6 | a0001c0002t0001g0175 a0001c0002t0001g0176 a0001c0002t0001g0181 others(3): Show |
6 | HG00280.hp2 HG01168.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.170-21686_170-2165 others(41): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577550 | ||||||
| chr1:10577551 | TATATATA others(4): Show |
T | 1 | a0001c0003t0001g0028 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.170-21686_170-2167 others(15): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577551 | |||||||
| chr1:10577552 | A | ATTTTTTT others(9): Show |
1 | a0001c0001t0001g0051 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.170-21685_170-2168 others(20): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577552 | ||||||
| chr1:10577552 | ATATATAT others(4): Show |
A | 1 | a0001c0001t0001g0072 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.170-21684_170-2167 others(15): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577552 | ||||||
| chr1:10577552 | ATATATAT others(16): Show |
A | 1 | a0001c0001t0001g0240 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.170-21684_170-2166 others(27): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577552 | ||||||
| chr1:10577552 | ATATATAT others(18): Show |
A | 2 | a0001c0001t0001g0159 a0001c0001t0001g0243 |
2 | NA18939.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.170-21684_170-2166 others(29): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577552 | ||||||
| chr1:10577552 | ATATATAT others(19): Show |
A | 1 | a0001c0001t0001g0219 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.170-21684_170-2165 others(30): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577552 | ||||||
| chr1:10577552 | ATATATAT others(22): Show |
A | 1 | a0001c0001t0001g0221 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.170-21684_170-2165 others(33): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577552 | ||||||
| chr1:10577552 | ATATATAT others(25): Show |
A | 4 | a0001c0001t0001g0054 a0001c0001t0001g0140 a0001c0001t0003g0058 others(1): Show |
4 | NA18950.hp1 NA18979.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.170-21684_170-2165 others(36): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577552 | ||||||
| chr1:10577552 | ATATATAT others(28): Show |
A | 5 | a0001c0002t0001g0183 a0001c0002t0001g0185 a0001c0002t0001g0194 others(2): Show |
5 | HG00735.hp1 HG01109.hp2 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.170-21684_170-2165 others(39): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577552 | ||||||
| chr1:10577552 | ATATATAT others(29): Show |
A | 4 | a0001c0002t0001g0196 a0001c0002t0001g0224 a0001c0002t0005g0200 others(1): Show |
4 | HG03490.hp2 NA18942.hp1 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.170-21684_170-2164 others(40): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577552 | ||||||
| chr1:10577554 | A | G | 2 | a0001c0001t0001g0100 a0001c0003t0001g0102 |
2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.170-21684A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577554 | |||||||
| chr1:10577554 | A | T | 1 | a0001c0001t0001g0051 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.170-21684A>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577554 | |||||||
| chr1:10577554 | ATATATAT others(3): Show |
A | 7 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0227 others(4): Show |
7 | HG01099.hp2 HG02055.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.170-21682_170-2167 others(14): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577554 | ||||||
| chr1:10577554 | ATATATAT others(5): Show |
A | 4 | a0001c0001t0001g0044 a0001c0001t0001g0069 a0001c0004t0001g0042 others(1): Show |
4 | HG00621.hp1 NA18747.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.170-21682_170-2167 others(16): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577554 | ||||||
| chr1:10577554 | ATATATAT others(6): Show |
A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0052 a0002c0005t0001g0207 |
3 | HG03486.hp2 HG03540.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.170-21682_170-2167 others(17): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577554 | ||||||
| chr1:10577554 | ATATATAT others(16): Show |
A | 1 | a0001c0001t0001g0165 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.170-21682_170-2166 others(27): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577554 | ||||||
| chr1:10577554 | ATATATAT others(21): Show |
A | 1 | a0001c0001t0001g0065 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.170-21682_170-2165 others(32): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577554 | ||||||
| chr1:10577554 | ATATATAT others(24): Show |
A | 1 | a0001c0001t0001g0039 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.170-21682_170-2165 others(35): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577554 | ||||||
| chr1:10577554 | ATATATAT others(25): Show |
A | 4 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(1): Show |
4 | NA18969.hp2 NA18971.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.170-21682_170-2165 others(36): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577554 | ||||||
| chr1:10577554 | ATATATAT others(26): Show |
A | 2 | a0001c0001t0001g0120 a0002c0005t0001g0228 |
2 | HG02622.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.170-21682_170-2165 others(37): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577554 | ||||||
| chr1:10577554 | ATATATAT others(27): Show |
A | 1 | a0001c0001t0001g0235 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.170-21682_170-2164 others(38): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577554 | ||||||
| chr1:10577556 | A | ATTTTTTT others(14): Show |
1 | a0001c0001t0001g0012 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.170-21681_170-2168 others(25): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577556 | ||||||
| chr1:10577556 | A | G | 6 | a0001c0001t0001g0049 a0001c0001t0001g0080 a0001c0001t0001g0091 others(3): Show |
6 | HG00099.hp2 HG01069.hp1 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.170-21682A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577556 | |||||||
| chr1:10577556 | A | T | 2 | a0001c0001t0001g0051 a0001c0004t0001g0024 |
2 | HG01433.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.170-21682A>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577556 | |||||||
| chr1:10577556 | ATATATAT others(3): Show |
A | 1 | a0001c0001t0001g0064 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.170-21680_170-2167 others(14): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577556 | ||||||
| chr1:10577556 | ATATATAT others(4): Show |
A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0117 |
2 | HG02258.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.170-21680_170-2167 others(15): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577556 | ||||||
| chr1:10577556 | ATATATAT others(5): Show |
A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0006t0001g0087 |
3 | HG03139.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.170-21680_170-2166 others(16): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577556 | ||||||
| chr1:10577556 | ATATATAT others(6): Show |
A | 1 | a0001c0001t0001g0008 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.170-21680_170-2166 others(17): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577556 | ||||||
| chr1:10577556 | ATATATAT others(7): Show |
A | 1 | a0002c0005t0001g0013 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.170-21680_170-2166 others(18): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577556 | ||||||
| chr1:10577556 | ATATATAT others(14): Show |
A | 1 | a0001c0001t0001g0045 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.170-21680_170-2166 others(25): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577556 | ||||||
| chr1:10577556 | ATATATAT others(23): Show |
A | 4 | a0001c0004t0001g0046 a0001c0004t0001g0053 a0001c0004t0001g0079 others(1): Show |
4 | HG00733.hp2 HG00741.hp2 HG01069.hp2 others(1): Show |
intron_variant | MODIFIER | c.170-21680_170-2165 others(34): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577556 | ||||||
| chr1:10577556 | ATATATAT others(25): Show |
A | 2 | a0001c0001t0001g0037 a0001c0004t0001g0038 |
2 | NA18942.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.170-21680_170-2164 others(36): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577556 | ||||||
| chr1:10577558 | A | G | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.170-21680A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577558 | |||||||
| chr1:10577558 | A | T | 4 | a0001c0001t0001g0012 a0001c0001t0001g0051 a0001c0004t0001g0024 others(1): Show |
4 | HG01106.hp1 HG01433.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.170-21680A>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577558 | |||||||
| chr1:10577558 | ATATATTT others(3): Show |
A | 1 | a0001c0001t0001g0059 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.170-21678_170-2166 others(14): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577558 | ||||||
| chr1:10577558 | ATATATTT others(6): Show |
A | 1 | a0001c0001t0001g0081 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.170-21678_170-2166 others(17): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577558 | ||||||
| chr1:10577558 | ATATATTT others(8): Show |
A | 2 | a0001c0001t0001g0048 a0001c0006t0001g0086 |
2 | HG00423.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.170-21678_170-2166 others(19): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577558 | ||||||
| chr1:10577558 | ATATATTT others(15): Show |
A | 1 | a0001c0001t0001g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.170-21678_170-2165 others(26): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577558 | ||||||
| chr1:10577558 | ATATATTT others(17): Show |
A | 1 | a0001c0009t0001g0063 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.170-21678_170-2165 others(28): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577558 | ||||||
| chr1:10577558 | ATATATTT others(23): Show |
A | 2 | a0001c0001t0001g0040 a0001c0001t0001g0047 |
2 | NA18948.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.170-21678_170-2164 others(34): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577558 | ||||||
| chr1:10577560 | A | G | 2 | a0001c0006t0001g0236 a0002c0005t0001g0230 |
2 | HG01884.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.170-21678A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577560 | |||||||
| chr1:10577560 | A | T | 4 | a0001c0001t0001g0012 a0001c0001t0001g0051 a0001c0004t0001g0024 others(1): Show |
4 | HG01106.hp1 HG01433.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.170-21678A>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577560 | |||||||
| chr1:10577560 | ATATTTTT others(3): Show |
A | 1 | a0001c0001t0006g0010 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.170-21676_170-2166 others(14): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577560 | ||||||
| chr1:10577560 | ATATTTTT others(4): Show |
A | 1 | a0001c0001t0001g0084 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.170-21676_170-2166 others(15): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577560 | ||||||
| chr1:10577560 | ATATTTTT others(6): Show |
A | 1 | a0001c0001t0001g0174 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.170-21676_170-2166 others(17): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577560 | ||||||
| chr1:10577560 | ATATTTTT others(12): Show |
A | 1 | a0001c0001t0001g0115 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.170-21676_170-2165 others(23): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577560 | ||||||
| chr1:10577560 | ATATTTTT others(16): Show |
A | 1 | a0001c0002t0001g0214 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.170-21676_170-2165 others(27): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577560 | ||||||
| chr1:10577562 | A | T | 5 | a0001c0001t0001g0012 a0001c0001t0001g0051 a0001c0004t0001g0024 others(2): Show |
5 | HG01106.hp1 HG01433.hp1 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.170-21676A>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577562 | |||||||
| chr1:10577562 | ATT | A | 5 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0002t0001g0205 others(2): Show |
5 | HG00609.hp1 HG01081.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.170-21629_170-2162 others(6): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577562 | ||||||
| chr1:10577562 | ATTT | A | 7 | a0001c0002t0001g0168 a0001c0002t0001g0169 a0001c0002t0001g0170 others(4): Show |
7 | HG00558.hp1 HG00673.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.170-21630_170-2162 others(7): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577562 | ||||||
| chr1:10577562 | ATTTT | A | 7 | a0001c0001t0001g0002 a0001c0001t0001g0089 a0001c0001t0001g0126 others(4): Show |
7 | HG01099.hp1 HG01884.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.170-21631_170-2162 others(8): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577562 | ||||||
| chr1:10577562 | ATTTTTT | A | 5 | a0001c0001t0001g0061 a0001c0001t0001g0248 a0001c0002t0001g0190 others(2): Show |
5 | HG01978.hp1 HG02027.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.170-21633_170-2162 others(10): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577562 | ||||||
| chr1:10577562 | ATTTTTTT | A | 7 | a0001c0001t0001g0080 a0001c0001t0001g0095 a0001c0001t0001g0121 others(4): Show |
7 | HG01884.hp1 HG02486.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.170-21634_170-2162 others(11): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577562 | ||||||
| chr1:10577562 | ATTTTTTT others(1): Show |
A | 7 | a0001c0001t0001g0030 a0001c0001t0001g0049 a0001c0001t0001g0091 others(4): Show |
7 | HG00099.hp2 HG01069.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.170-21635_170-2162 others(12): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577562 | ||||||
| chr1:10577562 | ATTTTTTT others(2): Show |
A | 10 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0029 others(7): Show |
10 | HG00609.hp2 HG01928.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.170-21636_170-2162 others(13): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577562 | ||||||
| chr1:10577562 | ATTTTTTT others(3): Show |
A | 3 | a0001c0001t0001g0056 a0001c0002t0001g0237 a0001c0003t0001g0027 |
3 | HG00544.hp2 HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.170-21637_170-2162 others(14): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577562 | ||||||
| chr1:10577562 | ATTTTTTT others(4): Show |
A | 3 | a0001c0001t0001g0017 a0001c0001t0001g0032 a0001c0003t0001g0026 |
3 | HG03579.hp1 NA18992.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.170-21638_170-2162 others(15): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577562 | ||||||
| chr1:10577562 | ATTTTTTT others(5): Show |
A | 6 | a0001c0001t0001g0009 a0001c0001t0001g0100 a0001c0001t0001g0246 others(3): Show |
6 | HG01433.hp2 HG02451.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.170-21639_170-2162 others(16): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577562 | ||||||
| chr1:10577562 | ATTTTTTT others(6): Show |
A | 2 | a0001c0003t0001g0025 a0001c0003t0001g0083 |
2 | HG00423.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.170-21640_170-2162 others(17): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577562 | ||||||
| chr1:10577562 | ATTTTTTT others(7): Show |
A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0113 |
2 | HG02280.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.170-21641_170-2162 others(18): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577562 | ||||||
| chr1:10577562 | ATTTTTTT others(8): Show |
A | 1 | a0001c0002t0001g0001 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.170-21642_170-2162 others(19): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577562 | ||||||
| chr1:10577562 | ATTTTTTT others(11): Show |
A | 2 | a0001c0001t0001g0116 a0001c0001t0001g0118 |
2 | HG02970.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.170-21645_170-2162 others(22): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577562 | ||||||
| chr1:10577562 | ATTTTTTT others(12): Show |
A | 3 | a0001c0001t0001g0014 a0001c0002t0001g0033 a0001c0002t0001g0198 |
3 | HG01258.hp2 HG01496.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.170-21646_170-2162 others(23): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577562 | ||||||
| chr1:10577562 | ATTTTTTT others(13): Show |
A | 2 | a0001c0001t0001g0015 a0001c0002t0001g0197 |
2 | HG01928.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.170-21647_170-2162 others(24): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577562 | ||||||
| chr1:10577562 | ATTTTTTT others(14): Show |
A | 2 | a0001c0002t0001g0202 a0001c0002t0001g0208 |
2 | HG01978.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.170-21648_170-2162 others(25): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577562 | ||||||
| chr1:10577562 | ATTTTTTT others(15): Show |
A | 1 | a0001c0002t0001g0195 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.170-21649_170-2162 others(26): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577562 | ||||||
| chr1:10577562 | ATTTTTTT others(19): Show |
A | 1 | a0001c0001t0001g0112 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.170-21653_170-2162 others(30): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577562 | ||||||
| chr1:10577563 | T | TA | 3 | a0001c0001t0001g0109 a0001c0001t0001g0114 a0002c0005t0001g0127 |
3 | HG02559.hp1 HG03130.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.170-21675_170-2167 others(5): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577563 | |||||||
| chr1:10577563 | T | TATATATA others(6): Show |
1 | a0001c0012t0001g0055 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.170-21675_170-2167 others(17): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577563 | |||||||
| chr1:10577564 | T | A | 5 | a0001c0001t0001g0092 a0001c0001t0001g0249 a0001c0002t0001g0216 others(2): Show |
5 | HG01192.hp2 HG02300.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.170-21674T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577564 | |||||||
| chr1:10577565 | T | A | 9 | a0001c0001t0001g0109 a0001c0001t0001g0114 a0001c0003t0001g0103 others(6): Show |
9 | HG01167.hp1 HG02559.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.170-21673T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577565 | |||||||
| chr1:10577566 | T | A | 10 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(7): Show |
10 | HG00609.hp1 HG01081.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.170-21672T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577566 | |||||||
| chr1:10577567 | T | A | 15 | a0001c0001t0001g0109 a0001c0001t0001g0114 a0001c0002t0001g0168 others(12): Show |
15 | HG00558.hp1 HG00673.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.170-21671T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577567 | |||||||
| chr1:10577568 | T | A | 14 | a0001c0001t0001g0089 a0001c0001t0001g0092 a0001c0001t0001g0093 others(11): Show |
14 | HG00609.hp1 HG01081.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.170-21670T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577568 | |||||||
| chr1:10577568 | T | G | 2 | a0001c0001t0001g0226 a0001c0001t0001g0229 |
2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.170-21670T>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577568 | |||||||
| chr1:10577569 | T | A | 19 | a0001c0001t0001g0031 a0001c0001t0001g0109 a0001c0001t0001g0114 others(16): Show |
19 | HG00408.hp2 HG00558.hp1 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.170-21669T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577569 | |||||||
| chr1:10577570 | T | A | 21 | a0001c0001t0001g0061 a0001c0001t0001g0089 a0001c0001t0001g0092 others(18): Show |
21 | HG00609.hp1 HG01081.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.170-21668T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577570 | |||||||
| chr1:10577571 | T | A | 25 | a0001c0001t0001g0031 a0001c0001t0001g0080 a0001c0001t0001g0095 others(22): Show |
25 | HG00408.hp2 HG00558.hp1 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.170-21667T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577571 | |||||||
| chr1:10577572 | T | A | 28 | a0001c0001t0001g0030 a0001c0001t0001g0049 a0001c0001t0001g0061 others(25): Show |
28 | HG00099.hp2 HG00609.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.170-21666T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577572 | |||||||
| chr1:10577573 | T | A | 35 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0029 others(32): Show |
35 | HG00408.hp2 HG00558.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.170-21665T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577573 | |||||||
| chr1:10577574 | T | A | 29 | a0001c0001t0001g0030 a0001c0001t0001g0049 a0001c0001t0001g0061 others(26): Show |
29 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.170-21664T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577574 | |||||||
| chr1:10577575 | T | A | 34 | a0001c0001t0001g0017 a0001c0001t0001g0029 a0001c0001t0001g0031 others(31): Show |
34 | HG00408.hp2 HG00558.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.170-21663T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577575 | |||||||
| chr1:10577576 | T | A | 31 | a0001c0001t0001g0030 a0001c0001t0001g0049 a0001c0001t0001g0061 others(28): Show |
31 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.170-21662T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577576 | |||||||
| chr1:10577577 | T | A | 33 | a0001c0001t0001g0017 a0001c0001t0001g0029 a0001c0001t0001g0031 others(30): Show |
33 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.170-21661T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577577 | |||||||
| chr1:10577578 | T | A | 33 | a0001c0001t0001g0016 a0001c0001t0001g0030 a0001c0001t0001g0049 others(30): Show |
33 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.170-21660T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577578 | |||||||
| chr1:10577579 | T | A | 29 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0032 others(26): Show |
30 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.170-21659T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577579 | |||||||
| chr1:10577580 | T | A | 31 | a0001c0001t0001g0016 a0001c0001t0001g0030 a0001c0001t0001g0049 others(28): Show |
31 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.170-21658T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577580 | |||||||
| chr1:10577581 | T | A | 29 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0032 others(26): Show |
30 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.170-21657T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577581 | |||||||
| chr1:10577582 | T | A | 31 | a0001c0001t0001g0016 a0001c0001t0001g0030 a0001c0001t0001g0049 others(28): Show |
31 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.170-21656T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577582 | |||||||
| chr1:10577583 | T | A | 31 | a0001c0001t0001g0014 a0001c0001t0001g0029 a0001c0001t0001g0031 others(28): Show |
32 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.170-21655T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577583 | |||||||
| chr1:10577584 | T | A | 32 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0030 others(29): Show |
32 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.170-21654T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577584 | |||||||
| chr1:10577585 | T | A | 31 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0032 others(28): Show |
32 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.170-21653T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577585 | |||||||
| chr1:10577586 | T | A | 28 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0030 others(25): Show |
28 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.170-21652T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577586 | |||||||
| chr1:10577587 | T | A | 23 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0080 others(20): Show |
23 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.170-21651T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577587 | |||||||
| chr1:10577587 | T | G | 5 | a0001c0001t0001g0099 a0001c0001t0001g0101 a0001c0001t0001g0110 others(2): Show |
5 | HG02280.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.170-21651T>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577587 | |||||||
| chr1:10577588 | T | A | 21 | a0001c0001t0001g0016 a0001c0001t0001g0049 a0001c0001t0001g0061 others(18): Show |
21 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(18): Show |
intron_variant | MODIFIER | c.170-21650T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577588 | |||||||
| chr1:10577588 | T | G | 7 | a0001c0001t0001g0003 a0001c0001t0001g0117 a0001c0001t0001g0227 others(4): Show |
7 | HG02055.hp1 HG02258.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.170-21650T>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577588 | |||||||
| chr1:10577589 | T | A | 11 | a0001c0001t0001g0080 a0001c0001t0001g0095 a0001c0002t0001g0167 others(8): Show |
11 | HG00423.hp1 HG00673.hp2 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.170-21649T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577589 | |||||||
| chr1:10577590 | T | A | 7 | a0001c0001t0001g0049 a0001c0001t0001g0061 a0001c0001t0001g0091 others(4): Show |
7 | HG00099.hp2 HG01069.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.170-21648T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577590 | |||||||
| chr1:10577591 | T | A | 2 | a0001c0002t0001g0179 a0001c0003t0001g0108 |
2 | HG02717.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.170-21647T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577591 | |||||||
| chr1:10577592 | T | A | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.170-21646T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577592 | |||||||
| chr1:10577592 | T | G | 6 | a0001c0001t0001g0099 a0001c0001t0001g0101 a0001c0001t0001g0110 others(3): Show |
6 | HG02280.hp2 HG02965.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.170-21646T>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577592 | |||||||
| chr1:10577593 | T | A | 1 | a0001c0003t0001g0108 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.170-21645T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577593 | |||||||
| chr1:10577593 | T | G | 9 | a0001c0001t0001g0003 a0001c0001t0001g0117 a0001c0001t0001g0227 others(6): Show |
9 | HG01891.hp2 HG02055.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.170-21645T>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577593 | |||||||
| chr1:10577595 | T | A | 1 | a0001c0003t0001g0108 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.170-21643T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577595 | |||||||
| chr1:10577597 | T | A | 1 | a0001c0003t0001g0108 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.170-21641T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577597 | |||||||
| chr1:10577610 | T | G | 3 | a0001c0001t0001g0065 a0001c0001t0001g0069 a0001c0001t0001g0072 |
3 | HG00621.hp1 HG00621.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.170-21628T>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577610 | |||||||
| chr1:10577652 | C | T | 70 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(67): Show |
71 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.170-21586C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577652 | |||||||
| chr1:10577762 | G | A | 1 | a0001c0003t0001g0222 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.170-21476G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577762 | |||||||
| chr1:10577784 | T | TA | 51 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(48): Show |
51 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.170-21453dupA | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10577784 | ||||||
| chr1:10577794 | G | A | 1 | a0001c0007t0001g0189 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.170-21444G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577794 | |||||||
| chr1:10577827 | T | G | 1 | a0001c0001t0001g0226 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.170-21411T>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10577827 | |||||||
| chr1:10578080 | A | G | 3 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 |
3 | HG01081.hp2 HG01168.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.170-21158A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10578080 | |||||||
| chr1:10578145 | G | A | 38 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0092 others(35): Show |
38 | HG00609.hp2 HG01081.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.170-21093G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10578145 | |||||||
| chr1:10578547 | C | T | 85 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(82): Show |
86 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.170-20691C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10578547 | |||||||
| chr1:10578592 | T | C | 1 | a0001c0004t0001g0166 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.170-20646T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10578592 | |||||||
| chr1:10578684 | A | T | 242 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(239): Show |
243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.170-20554A>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10578684 | |||||||
| chr1:10579050 | TTAAAG | T | 70 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(67): Show |
70 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.170-20184_170-2018 others(9): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10579050 | ||||||
| chr1:10579221 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.170-20017C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10579221 | |||||||
| chr1:10579441 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.170-19797C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10579441 | |||||||
| chr1:10579514 | G | A | 2 | a0001c0001t0001g0049 a0001c0001t0001g0091 |
2 | HG01069.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.170-19724G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10579514 | |||||||
| chr1:10579593 | C | T | 17 | a0001c0001t0001g0019 a0001c0001t0001g0092 a0001c0001t0001g0093 others(14): Show |
17 | HG01081.hp2 HG01167.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.170-19645C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10579593 | |||||||
| chr1:10579654 | G | A | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0128 |
3 | HG02559.hp2 HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.170-19584G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10579654 | |||||||
| chr1:10579864 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.170-19374C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10579864 | |||||||
| chr1:10580276 | A | G | 224 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(221): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.170-18962A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10580276 | |||||||
| chr1:10580381 | C | T | 106 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(103): Show |
106 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.170-18857C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10580381 | |||||||
| chr1:10580398 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.170-18840T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10580398 | |||||||
| chr1:10580435 | G | C | 1 | a0001c0001t0001g0106 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.170-18803G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10580435 | |||||||
| chr1:10580635 | A | G | 1 | a0001c0001t0001g0239 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.170-18603A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10580635 | |||||||
| chr1:10580845 | A | G | 1 | a0001c0001t0001g0005 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.170-18393A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10580845 | |||||||
| chr1:10580876 | C | G | 109 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(106): Show |
109 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.170-18362C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10580876 | |||||||
| chr1:10580973 | A | T | 2 | a0001c0009t0001g0062 a0001c0009t0001g0063 |
2 | HG02080.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.170-18265A>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10580973 | |||||||
| chr1:10581088 | A | G | 1 | a0002c0005t0001g0233 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.170-18150A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10581088 | |||||||
| chr1:10581305 | C | CT | 22 | a0001c0001t0001g0019 a0001c0001t0001g0047 a0001c0001t0001g0092 others(19): Show |
22 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(19): Show |
intron_variant | MODIFIER | c.170-17914dupT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10581305 | ||||||
| chr1:10581305 | C | CTT | 8 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(5): Show |
8 | HG01070.hp2 HG01081.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.170-17915_170-1791 others(6): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10581305 | ||||||
| chr1:10581305 | C | CTTT | 23 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(20): Show |
23 | HG00099.hp2 HG01069.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.170-17916_170-1791 others(7): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10581305 | ||||||
| chr1:10581345 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.170-17893C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10581345 | |||||||
| chr1:10581446 | C | T | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0128 |
3 | HG02559.hp2 HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.170-17792C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10581446 | |||||||
| chr1:10581454 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.170-17784C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10581454 | |||||||
| chr1:10581685 | T | A | 13 | a0001c0001t0001g0050 a0001c0001t0001g0139 a0001c0001t0001g0142 others(10): Show |
13 | HG00408.hp1 HG00544.hp1 HG02165.hp2 others(10): Show |
intron_variant | MODIFIER | c.170-17553T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10581685 | |||||||
| chr1:10581746 | TTAATTTA | T | 51 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(48): Show |
51 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.170-17481_170-1747 others(11): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10581746 | ||||||
| chr1:10582011 | GATTAA | G | 212 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(209): Show |
213 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.170-17218_170-1721 others(9): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10582011 | ||||||
| chr1:10582177 | CT | C | 6 | a0001c0001t0001g0227 a0001c0001t0001g0231 a0001c0001t0001g0232 others(3): Show |
6 | HG01168.hp1 HG02055.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.170-17050delT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10582177 | ||||||
| chr1:10582449 | A | G | 37 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(34): Show |
37 | HG00099.hp2 HG01069.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.170-16789A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10582449 | |||||||
| chr1:10582605 | G | A | 1 | a0001c0003t0001g0132 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.170-16633G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10582605 | |||||||
| chr1:10582736 | G | T | 233 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(230): Show |
234 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.170-16502G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10582736 | |||||||
| chr1:10582826 | C | T | 9 | a0001c0001t0001g0131 a0001c0001t0001g0134 a0001c0001t0001g0136 others(6): Show |
9 | HG00741.hp1 HG01109.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.170-16412C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10582826 | |||||||
| chr1:10582878 | C | T | 1 | a0001c0001t0001g0242 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.170-16360C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10582878 | |||||||
| chr1:10583140 | G | A | 45 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(42): Show |
46 | HG00423.hp1 HG00544.hp2 HG01099.hp1 others(43): Show |
intron_variant | MODIFIER | c.170-16098G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10583140 | |||||||
| chr1:10583150 | G | T | 1 | a0001c0003t0001g0083 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.170-16088G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10583150 | |||||||
| chr1:10583172 | T | C | 2 | a0001c0002t0001g0104 a0001c0002t0001g0237 |
2 | NA18959.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.170-16066T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10583172 | |||||||
| chr1:10583192 | A | G | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.170-16046A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10583192 | |||||||
| chr1:10583224 | C | CT | 7 | a0001c0001t0001g0099 a0001c0001t0001g0101 a0001c0001t0001g0110 others(4): Show |
7 | HG02109.hp2 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.170-16001dupT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10583224 | ||||||
| chr1:10583224 | CT | C | 29 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0018 others(26): Show |
29 | HG00609.hp1 HG00741.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.170-16001delT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10583224 | ||||||
| chr1:10583351 | C | T | 1 | a0001c0002t0001g0175 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.170-15887C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10583351 | |||||||
| chr1:10583376 | C | T | 3 | a0001c0001t0001g0109 a0001c0003t0001g0105 a0001c0003t0001g0108 |
3 | HG03540.hp2 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.170-15862C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10583376 | |||||||
| chr1:10583383 | C | CT | 66 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0032 others(63): Show |
66 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.170-15836dupT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10583383 | ||||||
| chr1:10583383 | C | CTT | 6 | a0001c0001t0001g0020 a0001c0001t0001g0144 a0001c0001t0001g0146 others(3): Show |
6 | HG00544.hp1 HG02027.hp2 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.170-15837_170-1583 others(6): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10583383 | ||||||
| chr1:10583383 | CT | C | 7 | a0001c0001t0001g0002 a0001c0001t0001g0049 a0001c0001t0001g0113 others(4): Show |
7 | HG01069.hp1 HG02055.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.170-15836delT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10583383 | ||||||
| chr1:10583384 | T | C | 3 | a0001c0001t0001g0056 a0001c0001t0001g0082 a0001c0001t0006g0010 |
3 | HG02735.hp1 HG03654.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.170-15854T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10583384 | |||||||
| chr1:10583392 | T | TC | 6 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0002c0005t0001g0127 others(3): Show |
6 | HG01167.hp1 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.170-15846_170-1584 others(5): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10583392 | |||||||
| chr1:10583402 | T | A | 3 | a0001c0001t0001g0226 a0001c0002t0001g0217 a0004c0010t0001g0098 |
3 | HG02965.hp2 HG03471.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.170-15836T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10583402 | |||||||
| chr1:10583403 | A | T | 10 | a0001c0001t0001g0019 a0001c0001t0001g0084 a0001c0001t0001g0111 others(7): Show |
10 | HG00609.hp2 HG01255.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.170-15835A>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10583403 | |||||||
| chr1:10583404 | A | T | 8 | a0001c0001t0001g0019 a0001c0001t0001g0111 a0001c0003t0001g0028 others(5): Show |
8 | HG00609.hp2 HG01255.hp2 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.170-15834A>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10583404 | |||||||
| chr1:10583410 | TG | T | 20 | a0001c0001t0001g0003 a0001c0001t0001g0089 a0001c0001t0001g0099 others(17): Show |
20 | HG00741.hp1 HG02055.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.170-15827delG | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10583410 | |||||||
| chr1:10583412 | A | G | 1 | a0001c0002t0001g0196 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.170-15826A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10583412 | |||||||
| chr1:10583617 | C | T | 236 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(233): Show |
237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.170-15621C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10583617 | |||||||
| chr1:10583620 | T | G | 7 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(4): Show |
7 | HG01891.hp2 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.170-15618T>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10583620 | |||||||
| chr1:10583662 | A | T | 39 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0011 others(36): Show |
40 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.170-15576A>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10583662 | |||||||
| chr1:10583667 | T | TAAGTC | 193 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(190): Show |
194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.170-15571_170-1557 others(9): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10583667 | |||||||
| chr1:10583772 | C | T | 106 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0021 others(103): Show |
106 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.170-15466C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10583772 | |||||||
| chr1:10583831 | G | A | 1 | a0001c0004t0001g0147 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.170-15407G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10583831 | |||||||
| chr1:10583913 | G | A | 3 | a0002c0005t0001g0013 a0002c0005t0001g0172 a0002c0005t0001g0173 |
3 | HG01167.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.170-15325G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10583913 | |||||||
| chr1:10584092 | G | A | 30 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0030 others(27): Show |
30 | HG00558.hp1 HG00609.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.170-15146G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10584092 | |||||||
| chr1:10584111 | T | C | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.170-15127T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10584111 | |||||||
| chr1:10584284 | A | G | 2 | a0001c0001t0001g0089 a0001c0001t0001g0180 |
2 | HG02055.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.170-14954A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10584284 | |||||||
| chr1:10584294 | G | A | 89 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(86): Show |
89 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.170-14944G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10584294 | |||||||
| chr1:10584341 | C | T | 33 | a0001c0001t0001g0019 a0001c0001t0001g0092 a0001c0001t0001g0093 others(30): Show |
33 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.170-14897C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10584341 | |||||||
| chr1:10584437 | T | C | 31 | a0001c0001t0001g0019 a0001c0001t0001g0093 a0001c0001t0001g0094 others(28): Show |
31 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.170-14801T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10584437 | |||||||
| chr1:10584460 | C | T | 2 | a0001c0002t0001g0201 a0001c0002t0001g0223 |
2 | HG00408.hp2 HG00609.hp1 |
intron_variant | MODIFIER | c.170-14778C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10584460 | |||||||
| chr1:10584531 | T | A | 1 | a0001c0007t0001g0189 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.170-14707T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10584531 | |||||||
| chr1:10584616 | C | A | 1 | a0004c0010t0001g0123 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.170-14622C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10584616 | |||||||
| chr1:10584995 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.170-14243G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10584995 | |||||||
| chr1:10585070 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.170-14168G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10585070 | |||||||
| chr1:10585258 | T | C | 1 | a0001c0002t0001g0224 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.170-13980T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10585258 | |||||||
| chr1:10585323 | C | A | 1 | a0001c0001t0001g0029 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.170-13915C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10585323 | |||||||
| chr1:10585408 | C | G | 1 | a0001c0002t0001g0001 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.170-13830C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10585408 | |||||||
| chr1:10585565 | C | T | 245 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(242): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.170-13673C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10585565 | |||||||
| chr1:10585594 | C | T | 1 | a0001c0003t0001g0085 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.170-13644C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10585594 | |||||||
| chr1:10585599 | G | C | 93 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(90): Show |
93 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.170-13639G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10585599 | |||||||
| chr1:10585677 | C | T | 37 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0030 others(34): Show |
37 | HG00558.hp1 HG00609.hp2 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.170-13561C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10585677 | |||||||
| chr1:10585737 | T | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0219 |
2 | HG00621.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.170-13501T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10585737 | |||||||
| chr1:10585764 | T | C | 241 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(238): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.170-13474T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10585764 | |||||||
| chr1:10585786 | C | T | 2 | a0001c0002t0001g0210 a0001c0008t0001g0213 |
2 | NA18947.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.170-13452C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10585786 | |||||||
| chr1:10585868 | C | G | 6 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(3): Show |
6 | NA18942.hp2 NA18964.hp2 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.170-13370C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10585868 | |||||||
| chr1:10585891 | G | A | 9 | a0001c0001t0001g0003 a0001c0001t0001g0049 a0001c0001t0001g0080 others(6): Show |
9 | HG00099.hp2 HG01069.hp1 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.170-13347G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10585891 | |||||||
| chr1:10585967 | A | T | 1 | a0001c0001t0001g0089 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.170-13271A>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10585967 | |||||||
| chr1:10586234 | G | A | 9 | a0001c0001t0001g0003 a0001c0001t0001g0049 a0001c0001t0001g0080 others(6): Show |
9 | HG00099.hp2 HG01069.hp1 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.170-13004G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10586234 | |||||||
| chr1:10586519 | C | T | 5 | a0001c0001t0001g0049 a0001c0001t0001g0080 a0001c0001t0001g0091 others(2): Show |
5 | HG00099.hp2 HG01069.hp1 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.170-12719C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10586519 | |||||||
| chr1:10586599 | C | CATAATGT others(1): Show |
30 | a0001c0001t0001g0017 a0001c0001t0001g0030 a0001c0001t0001g0061 others(27): Show |
30 | HG00558.hp1 HG00609.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.170-12638_170-1263 others(12): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10586599 | ||||||
| chr1:10586628 | C | CT | 67 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 others(64): Show |
67 | HG00280.hp1 HG00423.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.170-12581dupT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10586628 | ||||||
| chr1:10586628 | C | CTT | 16 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0021 others(13): Show |
16 | HG00544.hp1 HG00735.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.170-12582_170-1258 others(6): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10586628 | ||||||
| chr1:10586628 | CT | C | 6 | a0001c0001t0001g0018 a0001c0001t0001g0049 a0001c0001t0001g0100 others(3): Show |
6 | HG01069.hp1 HG01517.hp2 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.170-12581delT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10586628 | ||||||
| chr1:10586628 | CTTTTTTT others(3): Show |
C | 31 | a0001c0001t0001g0017 a0001c0001t0001g0030 a0001c0001t0001g0061 others(28): Show |
31 | HG00558.hp1 HG00609.hp2 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.170-12590_170-1258 others(14): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10586628 | ||||||
| chr1:10586628 | CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0001g0089 a0001c0001t0001g0180 |
2 | HG02055.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.170-12593_170-1258 others(17): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10586628 | ||||||
| chr1:10586628 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0227 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.170-12594_170-1258 others(18): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10586628 | ||||||
| chr1:10586628 | CTTTTTTT others(8): Show |
C | 30 | a0001c0001t0001g0019 a0001c0001t0001g0093 a0001c0001t0001g0094 others(27): Show |
30 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.170-12595_170-1258 others(19): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10586628 | ||||||
| chr1:10586663 | G | A | 37 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0030 others(34): Show |
37 | HG00558.hp1 HG00609.hp2 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.170-12575G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10586663 | |||||||
| chr1:10586901 | A | C | 1 | a0001c0001t0001g0250 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.170-12337A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10586901 | |||||||
| chr1:10586933 | G | A | 5 | a0001c0001t0001g0015 a0001c0001t0001g0226 a0001c0001t0001g0229 others(2): Show |
5 | HG02055.hp1 HG02630.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.170-12305G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10586933 | |||||||
| chr1:10586952 | A | C | 1 | a0001c0002t0001g0169 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.170-12286A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10586952 | |||||||
| chr1:10587082 | C | T | 1 | a0001c0003t0001g0083 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.170-12156C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10587082 | |||||||
| chr1:10587223 | G | A | 37 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0030 others(34): Show |
37 | HG00558.hp1 HG00609.hp2 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.170-12015G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10587223 | |||||||
| chr1:10587238 | C | T | 2 | a0001c0001t0001g0256 a0001c0015t0001g0255 |
2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.170-12000C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10587238 | |||||||
| chr1:10587239 | G | A | 1 | a0001c0001t0001g0161 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.170-11999G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10587239 | |||||||
| chr1:10587440 | G | C | 1 | a0001c0001t0001g0043 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.170-11798G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10587440 | |||||||
| chr1:10587867 | C | T | 37 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0030 others(34): Show |
37 | HG00558.hp1 HG00609.hp2 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.170-11371C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10587867 | |||||||
| chr1:10587895 | C | CTTTT | 16 | a0001c0001t0001g0089 a0001c0001t0001g0093 a0001c0001t0001g0094 others(13): Show |
16 | HG00408.hp1 HG00544.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.170-11321_170-1131 others(8): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10587895 | ||||||
| chr1:10587895 | CT | C | 161 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(158): Show |
162 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.170-11318delT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10587895 | ||||||
| chr1:10587895 | CTT | C | 14 | a0001c0001t0001g0031 a0001c0001t0001g0120 a0001c0001t0001g0136 others(11): Show |
14 | HG01496.hp1 HG01517.hp1 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.170-11319_170-1131 others(6): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10587895 | ||||||
| chr1:10587916 | T | A | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0002g0253 |
3 | HG01891.hp1 HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.170-11322T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10587916 | |||||||
| chr1:10587917 | T | A | 33 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0030 others(30): Show |
33 | HG00558.hp1 HG00609.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.170-11321T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10587917 | |||||||
| chr1:10587918 | T | A | 40 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0030 others(37): Show |
40 | HG00558.hp1 HG00609.hp2 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.170-11320T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10587918 | |||||||
| chr1:10587919 | T | A | 54 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0020 others(51): Show |
54 | HG00280.hp2 HG00558.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.170-11319T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10587919 | |||||||
| chr1:10587920 | T | A | 193 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(190): Show |
194 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.170-11318T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10587920 | |||||||
| chr1:10587920 | T | TAA | 5 | a0001c0001t0001g0003 a0001c0001t0001g0080 a0001c0001t0001g0091 others(2): Show |
5 | HG00099.hp2 HG01070.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.170-11309_170-1130 others(6): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10587920 | ||||||
| chr1:10587920 | T | TTTTA | 9 | a0001c0001t0001g0019 a0001c0001t0001g0246 a0001c0002t0001g0179 others(6): Show |
9 | HG01167.hp1 HG02559.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.170-11318_170-1131 others(8): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10587920 | |||||||
| chr1:10587921 | A | T | 1 | a0001c0008t0001g0182 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.170-11317A>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10587921 | |||||||
| chr1:10587966 | C | T | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.170-11272C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10587966 | |||||||
| chr1:10588043 | TG | T | 3 | a0001c0001t0001g0018 a0001c0014t0001g0251 a0004c0010t0001g0098 |
3 | HG01891.hp2 HG02109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.170-11194delG | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10588043 | |||||||
| chr1:10588173 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.170-11065T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10588173 | |||||||
| chr1:10588188 | C | T | 1 | a0001c0002t0001g0001 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.170-11050C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10588188 | |||||||
| chr1:10588219 | CA | C | 37 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0030 others(34): Show |
37 | HG00558.hp1 HG00609.hp2 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.170-11008delA | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10588219 | ||||||
| chr1:10588332 | G | A | 1 | a0001c0001t0001g0018 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.170-10906G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10588332 | |||||||
| chr1:10588443 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.170-10795G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10588443 | |||||||
| chr1:10588469 | T | A | 1 | a0001c0002t0001g0077 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.170-10769T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10588469 | |||||||
| chr1:10588593 | G | A | 1 | a0001c0002t0001g0077 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.170-10645G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10588593 | |||||||
| chr1:10588735 | A | G | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.170-10503A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10588735 | |||||||
| chr1:10588748 | G | A | 241 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(238): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.170-10490G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10588748 | |||||||
| chr1:10588758 | G | A | 30 | a0001c0001t0001g0019 a0001c0001t0001g0093 a0001c0001t0001g0094 others(27): Show |
30 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.170-10480G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10588758 | |||||||
| chr1:10588804 | C | T | 1 | a0002c0005t0001g0230 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.170-10434C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10588804 | |||||||
| chr1:10588953 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.170-10285G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10588953 | |||||||
| chr1:10589138 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.170-10100A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10589138 | |||||||
| chr1:10589166 | G | A | 37 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0030 others(34): Show |
37 | HG00558.hp1 HG00609.hp2 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.170-10072G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10589166 | |||||||
| chr1:10589310 | G | A | 5 | a0001c0001t0001g0049 a0001c0001t0001g0080 a0001c0001t0001g0091 others(2): Show |
5 | HG00099.hp2 HG01069.hp1 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.170-9928G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10589310 | |||||||
| chr1:10589390 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.170-9848C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10589390 | |||||||
| chr1:10589450 | T | C | 37 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0030 others(34): Show |
37 | HG00558.hp1 HG00609.hp2 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.170-9788T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10589450 | |||||||
| chr1:10589561 | TTTTG | T | 162 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(159): Show |
163 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.170-9647_170-9644d others(6): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10589561 | ||||||
| chr1:10589561 | TTTTGTTT others(1): Show |
T | 8 | a0001c0001t0001g0015 a0001c0001t0001g0089 a0001c0001t0001g0100 others(5): Show |
8 | HG02055.hp1 HG02055.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.170-9651_170-9644d others(10): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10589561 | ||||||
| chr1:10589561 | TTTTGTTT others(9): Show |
T | 32 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0030 others(29): Show |
32 | HG00558.hp1 HG00609.hp2 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.170-9659_170-9644d others(18): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10589561 | ||||||
| chr1:10589843 | C | G | 2 | a0001c0002t0001g0168 a0001c0004t0001g0038 |
2 | HG00673.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.170-9395C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10589843 | |||||||
| chr1:10589875 | C | G | 3 | a0001c0001t0001g0120 a0002c0005t0001g0228 a0002c0005t0001g0230 |
3 | HG01884.hp1 HG02622.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.170-9363C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10589875 | |||||||
| chr1:10589908 | C | A | 39 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0017 others(36): Show |
39 | HG00558.hp1 HG00609.hp2 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.170-9330C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10589908 | |||||||
| chr1:10589919 | A | G | 39 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0017 others(36): Show |
39 | HG00558.hp1 HG00609.hp2 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.170-9319A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10589919 | |||||||
| chr1:10590011 | C | T | 39 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0017 others(36): Show |
39 | HG00558.hp1 HG00609.hp2 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.170-9227C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10590011 | |||||||
| chr1:10590068 | G | A | 39 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0017 others(36): Show |
39 | HG00558.hp1 HG00609.hp2 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.170-9170G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10590068 | |||||||
| chr1:10590144 | G | A | 30 | a0001c0001t0001g0019 a0001c0001t0001g0093 a0001c0001t0001g0094 others(27): Show |
30 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.170-9094G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10590144 | |||||||
| chr1:10590194 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.170-9044C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10590194 | |||||||
| chr1:10590287 | C | T | 29 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0021 others(26): Show |
29 | HG00280.hp1 HG00733.hp2 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.170-8951C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10590287 | |||||||
| chr1:10590291 | G | A | 2 | a0001c0001t0001g0100 a0001c0001t0001g0247 |
2 | HG02622.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.170-8947G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10590291 | |||||||
| chr1:10590325 | T | C | 247 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(244): Show |
248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.170-8913T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10590325 | |||||||
| chr1:10590452 | T | C | 245 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(242): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.170-8786T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10590452 | |||||||
| chr1:10590538 | A | C | 1 | a0001c0001t0001g0145 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.170-8700A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10590538 | |||||||
| chr1:10590600 | T | C | 2 | a0001c0002t0001g0163 a0001c0002t0001g0212 |
2 | HG02165.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.170-8638T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10590600 | |||||||
| chr1:10590917 | C | T | 19 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0049 others(16): Show |
19 | HG00099.hp2 HG00673.hp1 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.170-8321C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10590917 | |||||||
| chr1:10591091 | A | G | 2 | a0001c0001t0001g0021 a0001c0001t0001g0022 |
2 | HG01081.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.170-8147A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10591091 | |||||||
| chr1:10591313 | GTTAGA | G | 9 | a0001c0001t0001g0015 a0001c0001t0001g0226 a0001c0001t0001g0229 others(6): Show |
9 | HG02055.hp1 HG02630.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.170-7924_170-7920d others(7): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10591313 | |||||||
| chr1:10591320 | A | T | 9 | a0001c0001t0001g0015 a0001c0001t0001g0226 a0001c0001t0001g0229 others(6): Show |
9 | HG02055.hp1 HG02630.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.170-7918A>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10591320 | |||||||
| chr1:10591363 | C | CT | 41 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(38): Show |
41 | HG00558.hp1 HG00609.hp2 HG01099.hp1 others(38): Show |
intron_variant | MODIFIER | c.170-7873dupT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10591363 | ||||||
| chr1:10591403 | C | T | 198 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(195): Show |
199 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.170-7835C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10591403 | |||||||
| chr1:10591532 | T | C | 5 | a0001c0001t0001g0049 a0001c0001t0001g0080 a0001c0001t0001g0091 others(2): Show |
5 | HG00099.hp2 HG01069.hp1 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.170-7706T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10591532 | |||||||
| chr1:10591546 | T | C | 62 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(59): Show |
62 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.170-7692T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10591546 | |||||||
| chr1:10591610 | C | T | 2 | a0001c0001t0001g0003 a0001c0001t0001g0117 |
2 | HG02258.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.170-7628C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10591610 | |||||||
| chr1:10591634 | A | G | 1 | a0001c0001t0001g0056 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.170-7604A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10591634 | |||||||
| chr1:10591635 | C | CTG | 98 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0015 others(95): Show |
99 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.170-7562_170-7561d others(4): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10591635 | ||||||
| chr1:10591635 | C | CTGTG | 79 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(76): Show |
79 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.170-7564_170-7561d others(6): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10591635 | ||||||
| chr1:10591635 | C | CTGTGTG | 10 | a0001c0001t0001g0075 a0001c0001t0001g0095 a0001c0001t0001g0097 others(7): Show |
10 | HG01175.hp1 HG01358.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.170-7566_170-7561d others(8): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10591635 | ||||||
| chr1:10591635 | C | CTGTGTGT others(1): Show |
3 | a0001c0001t0001g0073 a0001c0002t0001g0176 a0001c0015t0001g0255 |
3 | HG02735.hp2 HG03225.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.170-7568_170-7561d others(10): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10591635 | ||||||
| chr1:10591635 | CTG | C | 12 | a0001c0001t0001g0002 a0001c0001t0001g0072 a0001c0001t0001g0100 others(9): Show |
12 | HG01884.hp2 HG01928.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.170-7562_170-7561d others(4): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10591635 | ||||||
| chr1:10591635 | CTGTGTGT others(7): Show |
C | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.170-7574_170-7561d others(16): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10591635 | ||||||
| chr1:10591814 | G | C | 1 | a0001c0004t0001g0147 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.170-7424G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10591814 | |||||||
| chr1:10591870 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.170-7368C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10591870 | |||||||
| chr1:10592025 | CTTTG | C | 214 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(211): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.170-7208_170-7205d others(6): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10592025 | ||||||
| chr1:10592121 | G | A | 1 | a0001c0001t0001g0139 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.170-7117G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10592121 | |||||||
| chr1:10592250 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.170-6988T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10592250 | |||||||
| chr1:10592488 | G | A | 48 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0093 others(45): Show |
48 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.170-6750G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10592488 | |||||||
| chr1:10592548 | G | A | 167 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(164): Show |
168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.170-6690G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10592548 | |||||||
| chr1:10592920 | T | C | 216 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(213): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.170-6318T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10592920 | |||||||
| chr1:10593191 | G | A | 1 | a0001c0001t0001g0044 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.170-6047G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10593191 | |||||||
| chr1:10593281 | T | C | 1 | a0001c0001t0001g0248 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.170-5957T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10593281 | |||||||
| chr1:10593352 | C | T | 6 | a0001c0001t0001g0049 a0001c0001t0001g0080 a0001c0001t0001g0091 others(3): Show |
6 | HG00099.hp2 HG01069.hp1 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.170-5886C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10593352 | |||||||
| chr1:10593565 | T | C | 8 | a0001c0001t0001g0134 a0001c0003t0001g0083 a0001c0003t0001g0102 others(5): Show |
8 | HG00741.hp1 HG02451.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.170-5673T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10593565 | |||||||
| chr1:10593571 | G | T | 67 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(64): Show |
67 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.170-5667G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10593571 | |||||||
| chr1:10593674 | TAGAC | T | 6 | a0002c0005t0001g0013 a0002c0005t0001g0127 a0002c0005t0001g0172 others(3): Show |
6 | HG01167.hp1 HG02559.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.170-5561_170-5558d others(6): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10593674 | ||||||
| chr1:10593689 | G | C | 1 | a0001c0001t0001g0114 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.170-5549G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10593689 | |||||||
| chr1:10593921 | G | A | 1 | a0001c0001t0001g0242 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.170-5317G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10593921 | |||||||
| chr1:10594070 | A | G | 6 | a0001c0001t0001g0221 a0001c0003t0001g0238 a0001c0007t0001g0187 others(3): Show |
6 | HG01928.hp1 HG01981.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.170-5168A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10594070 | |||||||
| chr1:10594115 | C | G | 3 | a0001c0001t0001g0099 a0001c0001t0001g0101 a0001c0001t0001g0257 |
3 | HG02965.hp1 HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.170-5123C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10594115 | |||||||
| chr1:10594118 | CTT | C | 3 | a0001c0001t0001g0018 a0001c0001t0001g0249 a0001c0002t0001g0179 |
3 | HG02109.hp1 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.170-5117_170-5116d others(4): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10594118 | ||||||
| chr1:10594121 | T | C | 3 | a0001c0001t0001g0018 a0001c0001t0001g0249 a0001c0002t0001g0179 |
3 | HG02109.hp1 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.170-5117T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10594121 | |||||||
| chr1:10594312 | A | G | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(194): Show |
198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.170-4926A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10594312 | |||||||
| chr1:10594371 | T | C | 2 | a0001c0003t0001g0135 a0001c0003t0001g0158 |
2 | HG03492.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.170-4867T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10594371 | |||||||
| chr1:10594495 | C | T | 45 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(42): Show |
45 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.170-4743C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10594495 | |||||||
| chr1:10594631 | T | C | 17 | a0001c0001t0001g0141 a0001c0002t0001g0001 a0001c0004t0001g0024 others(14): Show |
18 | HG00733.hp2 HG00741.hp2 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.170-4607T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10594631 | |||||||
| chr1:10594713 | G | A | 2 | a0001c0001t0001g0109 a0001c0002t0001g0181 |
2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.170-4525G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10594713 | |||||||
| chr1:10594780 | G | A | 8 | a0001c0001t0001g0032 a0001c0001t0001g0109 a0001c0002t0001g0001 others(5): Show |
9 | HG00280.hp2 HG01256.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.170-4458G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10594780 | |||||||
| chr1:10594829 | C | CA | 199 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(196): Show |
200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.170-4409_170-4408i others(3): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10594829 | |||||||
| chr1:10595008 | AGGATGTA others(3): Show |
A | 1 | a0001c0001t0001g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.170-4229_170-4220d others(12): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10595008 | |||||||
| chr1:10595019 | C | A | 1 | a0001c0001t0001g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.170-4219C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10595019 | |||||||
| chr1:10595105 | C | T | 1 | a0001c0002t0001g0178 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.170-4133C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10595105 | |||||||
| chr1:10595375 | T | C | 1 | a0001c0001t0001g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.170-3863T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10595375 | |||||||
| chr1:10595460 | T | C | 1 | a0004c0010t0001g0098 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.170-3778T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10595460 | |||||||
| chr1:10595652 | G | A | 8 | a0001c0001t0001g0049 a0001c0001t0001g0080 a0001c0001t0001g0082 others(5): Show |
8 | HG00099.hp2 HG01069.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.170-3586G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10595652 | |||||||
| chr1:10595675 | C | T | 2 | a0001c0001t0001g0029 a0001c0002t0001g0199 |
2 | HG00558.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.170-3563C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10595675 | |||||||
| chr1:10595746 | C | G | 1 | a0001c0006t0001g0124 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.170-3492C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10595746 | |||||||
| chr1:10595856 | G | A | 16 | a0001c0001t0001g0141 a0001c0004t0001g0024 a0001c0004t0001g0042 others(13): Show |
16 | HG00733.hp2 HG00741.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.170-3382G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10595856 | |||||||
| chr1:10595862 | A | AG | 213 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(210): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.170-3376_170-3375i others(3): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10595862 | |||||||
| chr1:10595879 | C | A | 223 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(220): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.170-3359C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10595879 | |||||||
| chr1:10596098 | G | C | 1 | a0001c0001t0003g0058 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.170-3140G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10596098 | |||||||
| chr1:10596197 | A | G | 1 | a0001c0002t0001g0198 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.170-3041A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10596197 | |||||||
| chr1:10596267 | C | T | 46 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(43): Show |
46 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.170-2971C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10596267 | |||||||
| chr1:10596278 | C | T | 7 | a0001c0001t0001g0012 a0001c0001t0001g0021 a0001c0001t0001g0022 others(4): Show |
7 | HG00280.hp1 HG01081.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.170-2960C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10596278 | |||||||
| chr1:10596294 | C | A | 68 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(65): Show |
68 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.170-2944C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10596294 | |||||||
| chr1:10596294 | C | T | 1 | a0001c0002t0001g0176 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.170-2944C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10596294 | |||||||
| chr1:10596470 | G | A | 5 | a0001c0001t0001g0018 a0001c0001t0001g0248 a0001c0001t0001g0249 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.170-2768G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10596470 | |||||||
| chr1:10596607 | G | T | 17 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0003t0001g0025 others(14): Show |
17 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(14): Show |
intron_variant | MODIFIER | c.170-2631G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10596607 | |||||||
| chr1:10596770 | T | C | 5 | a0001c0001t0001g0018 a0001c0001t0001g0248 a0001c0001t0001g0249 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.170-2468T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10596770 | |||||||
| chr1:10597327 | A | G | 6 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0106 others(3): Show |
6 | HG02622.hp2 HG02630.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.170-1911A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10597327 | |||||||
| chr1:10597410 | A | G | 42 | a0001c0001t0001g0002 a0001c0001t0001g0093 a0001c0001t0001g0094 others(39): Show |
42 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.170-1828A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10597410 | |||||||
| chr1:10597528 | C | A | 1 | a0001c0004t0001g0166 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.170-1710C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10597528 | |||||||
| chr1:10597547 | C | T | 9 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0106 others(6): Show |
9 | HG01891.hp1 HG02622.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.170-1691C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10597547 | |||||||
| chr1:10597855 | T | C | 9 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0106 others(6): Show |
9 | HG01891.hp1 HG02622.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.170-1383T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10597855 | |||||||
| chr1:10598081 | G | A | 1 | a0001c0001t0001g0073 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.170-1157G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10598081 | |||||||
| chr1:10598145 | G | A | 7 | a0001c0001t0001g0049 a0001c0001t0001g0080 a0001c0001t0001g0082 others(4): Show |
7 | HG00099.hp2 HG01069.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.170-1093G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10598145 | |||||||
| chr1:10598164 | T | C | 70 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(67): Show |
70 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.170-1074T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10598164 | |||||||
| chr1:10598291 | C | T | 1 | a0001c0001t0001g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.170-947C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10598291 | |||||||
| chr1:10598310 | C | T | 2 | a0001c0001t0001g0003 a0001c0001t0001g0117 |
2 | HG02258.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.170-928C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10598310 | |||||||
| chr1:10598415 | C | T | 1 | a0001c0001t0002g0253 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.170-823C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10598415 | |||||||
| chr1:10598792 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.170-446C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10598792 | |||||||
| chr1:10598876 | CCT | C | 8 | a0001c0001t0001g0049 a0001c0001t0001g0080 a0001c0001t0001g0082 others(5): Show |
8 | HG00099.hp2 HG01069.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.170-359_170-358del others(2): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10598876 | ||||||
| chr1:10598879 | C | CT | 83 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(80): Show |
84 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.170-349dupT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 10598879 | ||||||
| chr1:10598899 | A | G | 2 | a0001c0002t0001g0077 a0001c0002t0001g0217 |
2 | HG04115.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.170-339A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10598899 | |||||||
| chr1:10599095 | C | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0138 |
2 | HG01256.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.170-143C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10599095 | |||||||
| chr1:10599120 | A | G | 2 | a0001c0001t0001g0121 a0001c0001t0001g0246 |
2 | HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.170-118A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 3/8 | chr1 | 10599120 | |||||||
| chr1:10599879 | T | A | 1 | a0001c0002t0001g0254 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.298+513T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10599879 | |||||||
| chr1:10599953 | T | C | 1 | a0001c0003t0001g0085 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.298+587T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10599953 | |||||||
| chr1:10600423 | A | G | 5 | a0001c0001t0001g0018 a0001c0001t0001g0248 a0001c0001t0001g0249 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.298+1057A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10600423 | |||||||
| chr1:10600496 | C | T | 1 | a0001c0001t0001g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.298+1130C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10600496 | |||||||
| chr1:10600811 | T | G | 1 | a0001c0001t0001g0052 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.298+1445T>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10600811 | |||||||
| chr1:10600855 | C | T | 1 | a0001c0002t0001g0179 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.298+1489C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10600855 | |||||||
| chr1:10600993 | G | A | 1 | a0003c0011t0001g0107 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.298+1627G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10600993 | |||||||
| chr1:10601076 | A | G | 1 | a0001c0001t0001g0047 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.298+1710A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10601076 | |||||||
| chr1:10601130 | C | T | 2 | a0001c0001t0001g0003 a0001c0001t0001g0117 |
2 | HG02258.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.298+1764C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10601130 | |||||||
| chr1:10601183 | A | C | 5 | a0001c0001t0001g0018 a0001c0001t0001g0248 a0001c0001t0001g0249 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.298+1817A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10601183 | |||||||
| chr1:10601262 | C | CA | 23 | a0001c0001t0001g0016 a0001c0001t0001g0031 a0001c0001t0001g0054 others(20): Show |
23 | HG00609.hp1 HG00733.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.298+1918dupA | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 10601262 | ||||||
| chr1:10601262 | C | CAAA | 12 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(9): Show |
12 | HG01168.hp2 HG02258.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.298+1916_298+1918d others(5): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 10601262 | ||||||
| chr1:10601262 | C | CAAAA | 34 | a0001c0001t0001g0093 a0001c0001t0001g0097 a0001c0001t0001g0100 others(31): Show |
34 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.298+1915_298+1918d others(6): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 10601262 | ||||||
| chr1:10601262 | C | CAAAAA | 6 | a0001c0001t0001g0002 a0001c0001t0001g0114 a0001c0001t0001g0122 others(3): Show |
6 | HG02615.hp2 HG03130.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+1914_298+1918d others(7): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 10601262 | ||||||
| chr1:10601262 | CA | C | 14 | a0001c0001t0001g0018 a0001c0001t0001g0040 a0001c0001t0001g0043 others(11): Show |
14 | HG00099.hp2 HG01070.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.298+1918delA | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 10601262 | ||||||
| chr1:10601502 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.298+2136C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10601502 | |||||||
| chr1:10601510 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.298+2144C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10601510 | |||||||
| chr1:10601518 | A | T | 1 | a0001c0002t0001g0179 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.298+2152A>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10601518 | |||||||
| chr1:10601519 | T | A | 1 | a0001c0002t0001g0179 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.298+2153T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10601519 | |||||||
| chr1:10601523 | G | C | 1 | a0001c0001t0001g0039 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.298+2157G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10601523 | |||||||
| chr1:10601605 | G | A | 1 | a0001c0001t0001g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.298+2239G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10601605 | |||||||
| chr1:10601694 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.298+2328G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10601694 | |||||||
| chr1:10601843 | G | A | 1 | a0001c0014t0001g0251 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.298+2477G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10601843 | |||||||
| chr1:10602407 | G | C | 17 | a0001c0001t0001g0141 a0001c0004t0001g0024 a0001c0004t0001g0038 others(14): Show |
17 | HG00733.hp2 HG00741.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.298+3041G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10602407 | |||||||
| chr1:10602422 | T | TA | 5 | a0001c0001t0001g0011 a0001c0001t0001g0116 a0001c0001t0001g0180 others(2): Show |
5 | HG02738.hp1 HG03139.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.298+3069dupA | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 10602422 | ||||||
| chr1:10602430 | A | G | 1 | a0001c0001t0001g0052 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.298+3064A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10602430 | |||||||
| chr1:10602821 | G | A | 1 | a0004c0010t0001g0123 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.298+3455G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10602821 | |||||||
| chr1:10602826 | G | C | 1 | a0001c0001t0001g0067 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.298+3460G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10602826 | |||||||
| chr1:10602884 | G | T | 1 | a0001c0001t0001g0089 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.298+3518G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10602884 | |||||||
| chr1:10603468 | C | G | 2 | a0001c0001t0001g0109 a0001c0002t0001g0181 |
2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.298+4102C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10603468 | |||||||
| chr1:10603516 | C | T | 64 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(61): Show |
64 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.298+4150C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10603516 | |||||||
| chr1:10603821 | A | T | 2 | a0001c0001t0001g0003 a0001c0001t0001g0117 |
2 | HG02258.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.298+4455A>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10603821 | |||||||
| chr1:10604004 | A | G | 3 | a0001c0001t0001g0003 a0001c0001t0001g0117 a0001c0002t0001g0179 |
3 | HG02258.hp2 HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.298+4638A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10604004 | |||||||
| chr1:10604122 | G | A | 1 | a0004c0010t0001g0098 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.298+4756G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10604122 | |||||||
| chr1:10604200 | C | T | 1 | a0001c0001t0002g0253 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.298+4834C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10604200 | |||||||
| chr1:10604349 | C | T | 1 | a0001c0003t0001g0025 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.298+4983C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10604349 | |||||||
| chr1:10604462 | T | A | 1 | a0001c0001t0001g0143 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.298+5096T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10604462 | |||||||
| chr1:10604495 | C | T | 3 | a0001c0001t0001g0109 a0001c0001t0001g0134 a0001c0002t0001g0181 |
3 | HG00741.hp1 HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.298+5129C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10604495 | |||||||
| chr1:10604509 | G | A | 41 | a0001c0001t0001g0002 a0001c0001t0001g0093 a0001c0001t0001g0094 others(38): Show |
41 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.298+5143G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10604509 | |||||||
| chr1:10604522 | G | T | 2 | a0001c0001t0004g0023 a0001c0002t0001g0175 |
2 | HG00735.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.298+5156G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10604522 | |||||||
| chr1:10604651 | G | A | 3 | a0001c0002t0001g0185 a0001c0002t0001g0186 a0003c0011t0001g0191 |
3 | HG01106.hp2 HG01109.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.298+5285G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10604651 | |||||||
| chr1:10604666 | T | C | 1 | a0001c0014t0001g0251 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.298+5300T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10604666 | |||||||
| chr1:10604862 | G | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0120 |
3 | HG02280.hp1 HG02897.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.298+5496G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10604862 | |||||||
| chr1:10604876 | G | C | 1 | a0001c0001t0001g0245 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.298+5510G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10604876 | |||||||
| chr1:10604876 | G | T | 1 | a0001c0001t0001g0159 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.298+5510G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10604876 | |||||||
| chr1:10605135 | C | G | 1 | a0001c0001t0001g0112 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.298+5769C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10605135 | |||||||
| chr1:10605307 | G | A | 1 | a0001c0001t0001g0043 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.298+5941G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10605307 | |||||||
| chr1:10605850 | C | T | 8 | a0002c0005t0001g0013 a0002c0005t0001g0127 a0002c0005t0001g0172 others(5): Show |
8 | HG01167.hp1 HG01884.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.298+6484C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10605850 | |||||||
| chr1:10605934 | T | G | 2 | a0001c0001t0001g0019 a0001c0001t0001g0113 |
2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.298+6568T>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10605934 | |||||||
| chr1:10606172 | C | A | 1 | a0001c0001t0001g0054 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.298+6806C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10606172 | |||||||
| chr1:10606316 | G | A | 1 | a0001c0004t0001g0209 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.298+6950G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10606316 | |||||||
| chr1:10606460 | T | G | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(199): Show |
203 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.298+7094T>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10606460 | |||||||
| chr1:10606503 | G | T | 1 | a0001c0001t0001g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.298+7137G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10606503 | |||||||
| chr1:10606530 | A | G | 1 | a0001c0001t0001g0241 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+7164A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10606530 | |||||||
| chr1:10606535 | TG | T | 52 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0049 others(49): Show |
52 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.298+7170delG | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10606535 | |||||||
| chr1:10606589 | C | T | 61 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0018 others(58): Show |
61 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.298+7223C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10606589 | |||||||
| chr1:10606678 | A | G | 142 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(139): Show |
143 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.298+7312A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10606678 | |||||||
| chr1:10606700 | A | G | 3 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0117 |
3 | HG02258.hp2 HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.298+7334A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10606700 | |||||||
| chr1:10607236 | A | G | 1 | a0001c0001t0001g0250 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.298+7870A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10607236 | |||||||
| chr1:10607545 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.298+8179G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10607545 | |||||||
| chr1:10608322 | A | T | 138 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(135): Show |
139 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.298+8956A>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10608322 | |||||||
| chr1:10608335 | T | G | 1 | a0001c0001t0001g0221 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.298+8969T>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10608335 | |||||||
| chr1:10608364 | T | C | 1 | a0001c0001t0001g0035 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.298+8998T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10608364 | |||||||
| chr1:10608657 | C | T | 2 | a0001c0001t0002g0253 a0001c0002t0001g0168 |
2 | HG00673.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.298+9291C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10608657 | |||||||
| chr1:10608674 | GA | G | 195 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(192): Show |
196 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.298+9320delA | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 10608674 | ||||||
| chr1:10608674 | GAA | G | 13 | a0001c0001t0001g0020 a0001c0001t0001g0049 a0001c0001t0001g0080 others(10): Show |
13 | HG01069.hp1 HG01070.hp2 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.298+9319_298+9320d others(4): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 10608674 | ||||||
| chr1:10608740 | A | AT | 7 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(4): Show |
7 | HG00099.hp1 HG01192.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.298+9375dupT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 10608740 | ||||||
| chr1:10608742 | A | T | 213 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(210): Show |
214 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.298+9376A>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10608742 | |||||||
| chr1:10608879 | C | T | 1 | a0001c0009t0001g0063 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.299-9453C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10608879 | |||||||
| chr1:10609041 | C | G | 140 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(137): Show |
141 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.299-9291C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10609041 | |||||||
| chr1:10609453 | A | G | 9 | a0002c0005t0001g0013 a0002c0005t0001g0127 a0002c0005t0001g0172 others(6): Show |
9 | HG01167.hp1 HG01884.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.299-8879A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10609453 | |||||||
| chr1:10609460 | T | A | 54 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0020 others(51): Show |
54 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.299-8872T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10609460 | |||||||
| chr1:10609600 | A | G | 9 | a0002c0005t0001g0013 a0002c0005t0001g0127 a0002c0005t0001g0172 others(6): Show |
9 | HG01167.hp1 HG01884.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.299-8732A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10609600 | |||||||
| chr1:10609673 | T | C | 1 | a0001c0001t0002g0253 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.299-8659T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10609673 | |||||||
| chr1:10609703 | G | A | 1 | a0004c0010t0001g0123 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.299-8629G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10609703 | |||||||
| chr1:10609727 | G | A | 3 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0002t0001g0179 |
3 | HG02717.hp2 HG02886.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.299-8605G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10609727 | |||||||
| chr1:10609767 | C | A | 2 | a0001c0001t0001g0116 a0001c0001t0001g0246 |
2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.299-8565C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10609767 | |||||||
| chr1:10609778 | G | A | 2 | a0001c0001t0001g0003 a0001c0001t0001g0117 |
2 | HG02258.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.299-8554G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10609778 | |||||||
| chr1:10609871 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.299-8461C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10609871 | |||||||
| chr1:10610149 | A | C | 3 | a0001c0001t0001g0014 a0001c0001t0001g0106 a0001c0001t0001g0247 |
3 | HG02622.hp2 HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.299-8183A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10610149 | |||||||
| chr1:10610202 | C | G | 1 | a0001c0001t0006g0010 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.299-8130C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10610202 | |||||||
| chr1:10610368 | TATATACA others(1): Show |
T | 17 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0020 others(14): Show |
17 | HG01256.hp1 HG01884.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.299-7962_299-7955d others(10): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 10610368 | ||||||
| chr1:10610370 | T | C | 26 | a0001c0001t0001g0012 a0001c0001t0001g0021 a0001c0001t0001g0022 others(23): Show |
26 | HG00673.hp1 HG01081.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.299-7962T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10610370 | |||||||
| chr1:10610370 | TATAC | T | 3 | a0001c0001t0001g0113 a0001c0004t0001g0060 a0004c0010t0001g0098 |
3 | HG03453.hp1 HG03471.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.299-7960_299-7957d others(6): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 10610370 | ||||||
| chr1:10610370 | TATACAC | T | 38 | a0001c0001t0001g0018 a0001c0001t0001g0049 a0001c0001t0001g0091 others(35): Show |
38 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.299-7960_299-7955d others(8): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 10610370 | ||||||
| chr1:10610372 | T | C | 147 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(144): Show |
148 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.299-7960T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10610372 | |||||||
| chr1:10610372 | T | TACAC | 4 | a0001c0001t0002g0253 a0001c0003t0001g0102 a0001c0003t0001g0132 others(1): Show |
4 | HG01891.hp1 HG02451.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-7936_299-7933d others(6): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 10610372 | ||||||
| chr1:10610372 | TACACAC | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0116 a0001c0001t0001g0246 |
3 | HG02976.hp2 HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.299-7938_299-7933d others(8): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 10610372 | ||||||
| chr1:10610374 | C | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0161 |
2 | NA18959.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.299-7958C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10610374 | |||||||
| chr1:10610398 | C | CACACACA others(1): Show |
3 | a0001c0001t0001g0059 a0001c0001t0001g0065 a0001c0001t0001g0084 |
3 | HG00621.hp2 HG02615.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.299-7933_299-7932i others(10): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 10610398 | ||||||
| chr1:10610398 | C | CACACAT | 64 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(61): Show |
65 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.299-7933_299-7932i others(8): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 10610398 | ||||||
| chr1:10610398 | C | CACAT | 8 | a0001c0001t0001g0032 a0001c0001t0001g0043 a0001c0001t0001g0075 others(5): Show |
8 | HG01175.hp1 HG02071.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.299-7933_299-7932i others(6): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 10610398 | ||||||
| chr1:10610398 | C | CAT | 46 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(43): Show |
46 | HG00280.hp1 HG00673.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.299-7924_299-7923d others(4): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 10610398 | ||||||
| chr1:10610398 | C | T | 20 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0072 others(17): Show |
20 | HG00673.hp1 HG01081.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.299-7934C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10610398 | |||||||
| chr1:10610400 | T | C | 8 | a0001c0001t0001g0142 a0001c0001t0001g0153 a0001c0002t0001g0163 others(5): Show |
8 | HG02056.hp2 HG02080.hp2 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.299-7932T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10610400 | |||||||
| chr1:10610412 | C | G | 3 | a0001c0001t0001g0003 a0001c0001t0001g0117 a0001c0001t0001g0250 |
3 | HG02258.hp2 HG03098.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.299-7920C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10610412 | |||||||
| chr1:10610424 | G | T | 1 | a0001c0001t0001g0019 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.299-7908G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10610424 | |||||||
| chr1:10610433 | C | G | 1 | a0001c0014t0001g0251 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.299-7899C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10610433 | |||||||
| chr1:10610482 | G | A | 2 | a0001c0001t0001g0003 a0001c0001t0001g0117 |
2 | HG02258.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.299-7850G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10610482 | |||||||
| chr1:10610572 | C | T | 2 | a0001c0001t0001g0003 a0001c0001t0001g0117 |
2 | HG02258.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.299-7760C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10610572 | |||||||
| chr1:10610736 | G | A | 1 | a0001c0001t0001g0005 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.299-7596G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10610736 | |||||||
| chr1:10610855 | C | T | 4 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0002t0001g0179 others(1): Show |
4 | HG02717.hp2 HG02886.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-7477C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10610855 | |||||||
| chr1:10610914 | GTTC | G | 2 | a0001c0001t0001g0131 a0003c0011t0001g0107 |
2 | HG03654.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.299-7410_299-7408d others(5): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 10610914 | ||||||
| chr1:10610943 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.299-7389A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10610943 | |||||||
| chr1:10611028 | CTTGAGGT others(7): Show |
C | 1 | a0001c0001t0001g0059 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.299-7280_299-7267d others(16): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 10611028 | ||||||
| chr1:10611142 | A | G | 1 | a0001c0008t0001g0192 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.299-7190A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10611142 | |||||||
| chr1:10611265 | C | T | 54 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(51): Show |
54 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.299-7067C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10611265 | |||||||
| chr1:10611266 | A | G | 224 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(221): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.299-7066A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10611266 | |||||||
| chr1:10611370 | C | T | 17 | a0001c0004t0001g0024 a0001c0004t0001g0038 a0001c0004t0001g0042 others(14): Show |
17 | HG00733.hp2 HG00741.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.299-6962C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10611370 | |||||||
| chr1:10611378 | G | A | 4 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0002t0001g0179 others(1): Show |
4 | HG02717.hp2 HG02886.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-6954G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10611378 | |||||||
| chr1:10611397 | A | G | 4 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0002t0001g0179 others(1): Show |
4 | HG02717.hp2 HG02886.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-6935A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10611397 | |||||||
| chr1:10611508 | G | A | 13 | a0001c0001t0001g0017 a0001c0001t0001g0145 a0001c0001t0001g0146 others(10): Show |
13 | HG00099.hp2 HG02027.hp2 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.299-6824G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10611508 | |||||||
| chr1:10611651 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.299-6681T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10611651 | |||||||
| chr1:10611883 | A | G | 1 | a0001c0001t0001g0018 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.299-6449A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10611883 | |||||||
| chr1:10612017 | C | T | 3 | a0002c0005t0001g0228 a0002c0005t0001g0230 a0002c0005t0001g0233 |
3 | HG01884.hp1 HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.299-6315C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10612017 | |||||||
| chr1:10612065 | A | G | 1 | a0001c0003t0001g0085 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.299-6267A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10612065 | |||||||
| chr1:10612372 | C | G | 65 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0018 others(62): Show |
65 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.299-5960C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10612372 | |||||||
| chr1:10612560 | C | A | 6 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0243 others(3): Show |
6 | HG01099.hp1 HG01928.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.299-5772C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10612560 | |||||||
| chr1:10612732 | C | G | 1 | a0004c0010t0001g0098 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.299-5600C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10612732 | |||||||
| chr1:10612878 | A | G | 65 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0018 others(62): Show |
65 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.299-5454A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10612878 | |||||||
| chr1:10612924 | G | A | 6 | a0002c0005t0001g0013 a0002c0005t0001g0127 a0002c0005t0001g0172 others(3): Show |
6 | HG01167.hp1 HG02559.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.299-5408G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10612924 | |||||||
| chr1:10613037 | C | T | 137 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(134): Show |
138 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.299-5295C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10613037 | |||||||
| chr1:10613077 | C | T | 1 | a0001c0004t0001g0038 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.299-5255C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10613077 | |||||||
| chr1:10613078 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.299-5254G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10613078 | |||||||
| chr1:10613120 | G | A | 6 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0243 others(3): Show |
6 | HG01099.hp1 HG01928.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.299-5212G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10613120 | |||||||
| chr1:10613137 | G | A | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(199): Show |
203 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.299-5195G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10613137 | |||||||
| chr1:10613339 | A | G | 3 | a0001c0002t0001g0033 a0001c0002t0001g0198 a0001c0002t0001g0208 |
3 | HG01258.hp2 HG01496.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.299-4993A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10613339 | |||||||
| chr1:10613357 | C | G | 1 | a0001c0003t0001g0085 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.299-4975C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10613357 | |||||||
| chr1:10613363 | C | G | 1 | a0001c0003t0001g0238 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.299-4969C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10613363 | |||||||
| chr1:10613496 | A | G | 1 | a0001c0001t0002g0253 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.299-4836A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10613496 | |||||||
| chr1:10613689 | C | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0106 |
2 | HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.299-4643C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10613689 | |||||||
| chr1:10614203 | C | T | 1 | a0001c0001t0001g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.299-4129C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10614203 | |||||||
| chr1:10614297 | G | C | 1 | a0001c0002t0001g0178 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.299-4035G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10614297 | |||||||
| chr1:10614384 | A | C | 1 | a0001c0001t0001g0065 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.299-3948A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10614384 | |||||||
| chr1:10614435 | C | T | 1 | a0001c0001t0004g0023 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.299-3897C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10614435 | |||||||
| chr1:10614444 | C | CTTGGG | 5 | a0001c0001t0001g0019 a0001c0001t0001g0248 a0001c0001t0001g0249 others(2): Show |
5 | HG02717.hp2 HG02886.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-3887_299-3883d others(7): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 10614444 | ||||||
| chr1:10614450 | G | A | 5 | a0001c0001t0001g0019 a0001c0001t0001g0248 a0001c0001t0001g0249 others(2): Show |
5 | HG02717.hp2 HG02886.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-3882G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10614450 | |||||||
| chr1:10614473 | A | G | 1 | a0001c0001t0001g0246 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.299-3859A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10614473 | |||||||
| chr1:10614580 | G | A | 3 | a0001c0001t0001g0129 a0001c0001t0001g0226 a0001c0001t0001g0229 |
3 | HG01109.hp1 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.299-3752G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10614580 | |||||||
| chr1:10614625 | T | C | 12 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0117 others(9): Show |
12 | HG02258.hp2 HG02717.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.299-3707T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10614625 | |||||||
| chr1:10614740 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.299-3592C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10614740 | |||||||
| chr1:10614928 | G | A | 1 | a0001c0017t0001g0130 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.299-3404G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10614928 | |||||||
| chr1:10615040 | G | C | 4 | a0001c0001t0001g0129 a0001c0001t0001g0226 a0001c0001t0001g0229 others(1): Show |
4 | HG01109.hp1 HG02965.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-3292G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10615040 | |||||||
| chr1:10615057 | A | G | 2 | a0001c0001t0001g0246 a0001c0002t0001g0179 |
2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.299-3275A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10615057 | |||||||
| chr1:10615092 | T | C | 1 | a0001c0001t0001g0252 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.299-3240T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10615092 | |||||||
| chr1:10615108 | T | C | 2 | a0001c0001t0001g0092 a0001c0001t0001g0156 |
2 | HG00733.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.299-3224T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10615108 | |||||||
| chr1:10615219 | C | T | 3 | a0001c0001t0001g0248 a0001c0002t0001g0179 a0004c0010t0001g0098 |
3 | HG02717.hp2 HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.299-3113C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10615219 | |||||||
| chr1:10615500 | A | G | 1 | a0001c0002t0001g0179 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.299-2832A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10615500 | |||||||
| chr1:10615773 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.299-2559A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10615773 | |||||||
| chr1:10615813 | C | T | 1 | a0001c0004t0001g0042 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.299-2519C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10615813 | |||||||
| chr1:10615814 | G | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0115 a0001c0001t0001g0117 |
3 | HG02258.hp2 HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.299-2518G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10615814 | |||||||
| chr1:10615868 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.299-2464G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10615868 | |||||||
| chr1:10616079 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.299-2253G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10616079 | |||||||
| chr1:10616261 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.299-2071C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10616261 | |||||||
| chr1:10616366 | T | A | 1 | a0001c0009t0001g0062 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.299-1966T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10616366 | |||||||
| chr1:10616420 | G | A | 1 | a0001c0014t0001g0251 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.299-1912G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10616420 | |||||||
| chr1:10616626 | C | T | 1 | a0001c0001t0001g0225 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.299-1706C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10616626 | |||||||
| chr1:10616716 | T | C | 1 | a0001c0001t0001g0248 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.299-1616T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10616716 | |||||||
| chr1:10616721 | G | A | 1 | a0001c0002t0001g0168 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.299-1611G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10616721 | |||||||
| chr1:10616743 | G | T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0114 a0001c0001t0001g0122 others(5): Show |
8 | HG01884.hp2 HG02615.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.299-1589G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10616743 | |||||||
| chr1:10616746 | T | C | 1 | a0001c0001t0001g0143 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.299-1586T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10616746 | |||||||
| chr1:10616844 | C | T | 2 | a0001c0001t0001g0159 a0001c0001t0001g0243 |
2 | NA18939.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.299-1488C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10616844 | |||||||
| chr1:10616876 | G | A | 1 | a0001c0014t0001g0251 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.299-1456G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10616876 | |||||||
| chr1:10616914 | C | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0115 a0001c0001t0001g0117 |
3 | HG02258.hp2 HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.299-1418C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10616914 | |||||||
| chr1:10616934 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.299-1398T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10616934 | |||||||
| chr1:10617005 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.299-1327A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10617005 | |||||||
| chr1:10617151 | C | T | 1 | a0001c0003t0001g0222 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.299-1181C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10617151 | |||||||
| chr1:10617367 | C | G | 3 | a0001c0001t0001g0099 a0001c0001t0001g0101 a0001c0001t0001g0257 |
3 | HG02965.hp1 HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.299-965C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10617367 | |||||||
| chr1:10617480 | C | T | 7 | a0001c0001t0001g0221 a0001c0002t0001g0170 a0002c0005t0001g0127 others(4): Show |
7 | HG01884.hp1 HG02129.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.299-852C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10617480 | |||||||
| chr1:10617677 | G | A | 1 | a0001c0002t0001g0214 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.299-655G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10617677 | |||||||
| chr1:10617879 | C | T | 1 | a0001c0004t0001g0209 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.299-453C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10617879 | |||||||
| chr1:10618104 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.299-228C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10618104 | |||||||
| chr1:10618214 | T | C | 1 | a0001c0002t0001g0214 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.299-118T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10618214 | |||||||
| chr1:10618237 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.299-95C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10618237 | |||||||
| chr1:10618300 | T | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0115 a0001c0001t0001g0117 |
3 | HG02258.hp2 HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.299-32T>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10618300 | |||||||
| chr1:10618324 | G | A | 1 | a0001c0001t0001g0018 | 1 | HG02109.hp1 | splice_region_variant&intron_variant | LOW | c.299-8G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10618324 | |||||||
| chr1:10618324 | G | T | 1 | a0001c0001t0001g0113 | 1 | HG03453.hp1 | splice_region_variant&intron_variant | LOW | c.299-8G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 4/8 | chr1 | 10618324 | |||||||
| chr1:10618431 | A | T | 42 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0049 others(39): Show |
42 | HG01069.hp1 HG01070.hp2 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.384+14A>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | chr1 | 10618431 | |||||||
| chr1:10618511 | G | T | 1 | a0001c0001t0001g0110 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.384+94G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | chr1 | 10618511 | |||||||
| chr1:10618553 | G | A | 42 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0049 others(39): Show |
42 | HG01069.hp1 HG01070.hp2 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.384+136G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | chr1 | 10618553 | |||||||
| chr1:10618674 | C | T | 6 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0129 others(3): Show |
6 | HG01109.hp1 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.384+257C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | chr1 | 10618674 | |||||||
| chr1:10618747 | T | C | 1 | a0001c0001t0001g0247 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.384+330T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | chr1 | 10618747 | |||||||
| chr1:10618786 | C | T | 44 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0049 others(41): Show |
44 | HG01069.hp1 HG01070.hp2 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.384+369C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | chr1 | 10618786 | |||||||
| chr1:10619315 | A | AT | 30 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0020 others(27): Show |
30 | HG00099.hp2 HG00741.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.384+917dupT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 10619315 | ||||||
| chr1:10619315 | AT | A | 8 | a0001c0001t0001g0101 a0001c0001t0001g0116 a0001c0001t0001g0231 others(5): Show |
8 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(5): Show |
intron_variant | MODIFIER | c.384+917delT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 10619315 | ||||||
| chr1:10619528 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.384+1111C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | chr1 | 10619528 | |||||||
| chr1:10619557 | C | T | 9 | a0001c0001t0001g0002 a0001c0001t0001g0067 a0001c0001t0001g0071 others(6): Show |
9 | HG01358.hp1 HG01515.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.384+1140C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | chr1 | 10619557 | |||||||
| chr1:10619610 | C | T | 1 | a0001c0001t0001g0043 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.384+1193C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | chr1 | 10619610 | |||||||
| chr1:10619657 | C | T | 19 | a0001c0001t0001g0037 a0001c0001t0001g0039 a0001c0001t0001g0076 others(16): Show |
19 | HG00733.hp2 HG00741.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.384+1240C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | chr1 | 10619657 | |||||||
| chr1:10619897 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.384+1480C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | chr1 | 10619897 | |||||||
| chr1:10619932 | G | A | 1 | a0001c0001t0001g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.384+1515G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | chr1 | 10619932 | |||||||
| chr1:10619980 | C | T | 53 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0017 others(50): Show |
53 | HG01069.hp1 HG01070.hp2 HG01099.hp1 others(50): Show |
intron_variant | MODIFIER | c.384+1563C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | chr1 | 10619980 | |||||||
| chr1:10619983 | C | T | 4 | a0001c0001t0001g0081 a0001c0001t0001g0174 a0001c0001t0001g0231 others(1): Show |
4 | HG02647.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.384+1566C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | chr1 | 10619983 | |||||||
| chr1:10620115 | AAAAAAGA others(5): Show |
A | 1 | a0001c0001t0001g0044 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.384+1714_384+1725d others(14): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 10620115 | ||||||
| chr1:10620266 | A | G | 1 | a0001c0001t0001g0052 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.384+1849A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | chr1 | 10620266 | |||||||
| chr1:10620291 | C | CAATAA | 45 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0036 others(42): Show |
45 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.384+1911_384+1915d others(7): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 10620291 | ||||||
| chr1:10620291 | C | CAATAAAA others(3): Show |
1 | a0001c0001t0001g0059 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.384+1906_384+1915d others(12): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 10620291 | ||||||
| chr1:10620291 | C | CAATAAAA others(8): Show |
20 | a0001c0003t0001g0025 a0001c0003t0001g0026 a0001c0003t0001g0027 others(17): Show |
20 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(17): Show |
intron_variant | MODIFIER | c.384+1901_384+1915d others(17): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 10620291 | ||||||
| chr1:10620291 | C | CAATAAAA others(13): Show |
5 | a0001c0003t0001g0057 a0001c0003t0001g0088 a0001c0003t0001g0102 others(2): Show |
5 | HG02451.hp2 HG02723.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.384+1896_384+1915d others(22): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 10620291 | ||||||
| chr1:10620291 | CAATAA | C | 51 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(48): Show |
51 | HG01069.hp1 HG01070.hp2 HG01099.hp1 others(48): Show |
intron_variant | MODIFIER | c.384+1911_384+1915d others(7): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 10620291 | ||||||
| chr1:10620291 | CAATAAAA others(3): Show |
C | 2 | a0001c0001t0001g0017 a0001c0001t0001g0243 |
2 | HG03579.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.384+1906_384+1915d others(12): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 10620291 | ||||||
| chr1:10620291 | CAATAAAA others(18): Show |
C | 2 | a0001c0001t0001g0248 a0001c0002t0001g0179 |
2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.384+1891_384+1915d others(27): Show |
PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 10620291 | ||||||
| chr1:10620611 | A | T | 1 | a0001c0002t0001g0188 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.384+2194A>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | chr1 | 10620611 | |||||||
| chr1:10620761 | T | C | 4 | a0001c0001t0001g0160 a0001c0002t0001g0178 a0001c0002t0001g0197 others(1): Show |
4 | HG01099.hp1 HG01928.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.385-2258T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | chr1 | 10620761 | |||||||
| chr1:10621007 | G | C | 5 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0115 others(2): Show |
5 | HG02258.hp2 HG03209.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.385-2012G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | chr1 | 10621007 | |||||||
| chr1:10621016 | G | A | 2 | a0001c0002t0001g0201 a0001c0002t0001g0223 |
2 | HG00408.hp2 HG00609.hp1 |
intron_variant | MODIFIER | c.385-2003G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | chr1 | 10621016 | |||||||
| chr1:10621209 | A | C | 1 | a0001c0001t0003g0058 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.385-1810A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | chr1 | 10621209 | |||||||
| chr1:10621300 | A | G | 1 | a0001c0001t0001g0221 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.385-1719A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | chr1 | 10621300 | |||||||
| chr1:10621342 | C | CT | 20 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0045 others(17): Show |
20 | HG00621.hp2 HG01099.hp2 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.385-1655dupT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 10621342 | ||||||
| chr1:10621342 | CT | C | 15 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0099 others(12): Show |
15 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.385-1655delT | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 10621342 | ||||||
| chr1:10621395 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.385-1624G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | chr1 | 10621395 | |||||||
| chr1:10621439 | C | T | 1 | a0005c0018t0001g0171 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.385-1580C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | chr1 | 10621439 | |||||||
| chr1:10621496 | G | A | 18 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(15): Show |
18 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.385-1523G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | chr1 | 10621496 | |||||||
| chr1:10621572 | C | T | 3 | a0001c0001t0001g0099 a0001c0001t0001g0101 a0001c0001t0001g0257 |
3 | HG02965.hp1 HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.385-1447C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | chr1 | 10621572 | |||||||
| chr1:10621636 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.385-1383C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | chr1 | 10621636 | |||||||
| chr1:10621718 | A | G | 1 | a0001c0003t0001g0149 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.385-1301A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | chr1 | 10621718 | |||||||
| chr1:10622136 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.385-883T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | chr1 | 10622136 | |||||||
| chr1:10622187 | C | T | 235 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(232): Show |
236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.385-832C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | chr1 | 10622187 | |||||||
| chr1:10622208 | G | C | 1 | a0001c0001t0001g0245 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.385-811G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | chr1 | 10622208 | |||||||
| chr1:10622249 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.385-770C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | chr1 | 10622249 | |||||||
| chr1:10622337 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.385-682C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | chr1 | 10622337 | |||||||
| chr1:10622450 | G | C | 1 | a0001c0001t0001g0100 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.385-569G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | chr1 | 10622450 | |||||||
| chr1:10622595 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.385-424C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | chr1 | 10622595 | |||||||
| chr1:10622624 | C | T | 2 | a0001c0001t0001g0239 a0001c0001t0001g0244 |
2 | NA19055.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.385-395C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | chr1 | 10622624 | |||||||
| chr1:10622800 | C | T | 29 | a0001c0003t0001g0025 a0001c0003t0001g0026 a0001c0003t0001g0027 others(26): Show |
29 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(26): Show |
intron_variant | MODIFIER | c.385-219C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | chr1 | 10622800 | |||||||
| chr1:10622843 | G | A | 2 | a0001c0001t0001g0018 a0001c0014t0001g0251 |
2 | HG01891.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.385-176G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | chr1 | 10622843 | |||||||
| chr1:10622944 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.385-75C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 5/8 | chr1 | 10622944 | |||||||
| chr1:10623185 | C | T | 28 | a0001c0003t0001g0025 a0001c0003t0001g0026 a0001c0003t0001g0027 others(25): Show |
28 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(25): Show |
intron_variant | MODIFIER | c.487+64C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 6/8 | chr1 | 10623185 | |||||||
| chr1:10623215 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.487+94G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 6/8 | chr1 | 10623215 | |||||||
| chr1:10623353 | C | T | 1 | a0001c0004t0001g0209 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.487+232C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 6/8 | chr1 | 10623353 | |||||||
| chr1:10623490 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.487+369G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 6/8 | chr1 | 10623490 | |||||||
| chr1:10623615 | C | T | 5 | a0001c0004t0001g0024 a0001c0004t0001g0046 a0001c0004t0001g0053 others(2): Show |
5 | HG00733.hp2 HG00741.hp2 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.487+494C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 6/8 | chr1 | 10623615 | |||||||
| chr1:10623626 | G | T | 50 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(47): Show |
50 | HG01069.hp1 HG01070.hp2 HG01099.hp1 others(47): Show |
intron_variant | MODIFIER | c.487+505G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 6/8 | chr1 | 10623626 | |||||||
| chr1:10623657 | C | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0115 a0001c0001t0001g0117 |
3 | HG02258.hp2 HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.487+536C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 6/8 | chr1 | 10623657 | |||||||
| chr1:10623694 | G | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG01081.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.487+573G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 6/8 | chr1 | 10623694 | |||||||
| chr1:10623711 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.487+590C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 6/8 | chr1 | 10623711 | |||||||
| chr1:10623754 | A | G | 3 | a0001c0001t0001g0116 a0001c0001t0001g0248 a0001c0002t0001g0179 |
3 | HG02717.hp2 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.488-586A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 6/8 | chr1 | 10623754 | |||||||
| chr1:10623772 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.488-568G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 6/8 | chr1 | 10623772 | |||||||
| chr1:10623799 | G | A | 1 | a0001c0002t0001g0163 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.488-541G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 6/8 | chr1 | 10623799 | |||||||
| chr1:10623889 | A | G | 1 | a0001c0001t0001g0112 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.488-451A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 6/8 | chr1 | 10623889 | |||||||
| chr1:10623980 | C | A | 4 | a0001c0001t0001g0116 a0001c0001t0001g0248 a0001c0002t0001g0179 others(1): Show |
4 | HG02717.hp2 HG02886.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.488-360C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 6/8 | chr1 | 10623980 | |||||||
| chr1:10624041 | C | A | 27 | a0001c0003t0001g0025 a0001c0003t0001g0026 a0001c0003t0001g0027 others(24): Show |
27 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(24): Show |
intron_variant | MODIFIER | c.488-299C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 6/8 | chr1 | 10624041 | |||||||
| chr1:10624122 | T | C | 1 | a0001c0001t0001g0036 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.488-218T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 6/8 | chr1 | 10624122 | |||||||
| chr1:10624134 | A | C | 1 | a0003c0011t0001g0107 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.488-206A>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 6/8 | chr1 | 10624134 | |||||||
| chr1:10624216 | T | C | 1 | a0001c0001t0001g0241 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.488-124T>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 6/8 | chr1 | 10624216 | |||||||
| chr1:10624282 | C | G | 1 | a0001c0001t0001g0061 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.488-58C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 6/8 | chr1 | 10624282 | |||||||
| chr1:10624676 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.585+239C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 7/8 | chr1 | 10624676 | |||||||
| chr1:10624844 | C | G | 1 | a0001c0001t0001g0121 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.585+407C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 7/8 | chr1 | 10624844 | |||||||
| chr1:10624931 | G | A | 1 | a0001c0006t0001g0236 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.585+494G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 7/8 | chr1 | 10624931 | |||||||
| chr1:10625044 | C | T | 28 | a0001c0003t0001g0025 a0001c0003t0001g0026 a0001c0003t0001g0027 others(25): Show |
28 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(25): Show |
intron_variant | MODIFIER | c.585+607C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 7/8 | chr1 | 10625044 | |||||||
| chr1:10625185 | G | A | 2 | a0004c0010t0001g0098 a0004c0010t0001g0123 |
2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.585+748G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 7/8 | chr1 | 10625185 | |||||||
| chr1:10625631 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.585+1194C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 7/8 | chr1 | 10625631 | |||||||
| chr1:10625694 | C | G | 1 | a0001c0001t0001g0229 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.585+1257C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 7/8 | chr1 | 10625694 | |||||||
| chr1:10625719 | T | G | 1 | a0001c0001t0001g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.585+1282T>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 7/8 | chr1 | 10625719 | |||||||
| chr1:10625873 | C | T | 45 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0020 others(42): Show |
45 | HG01069.hp1 HG01070.hp2 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.586-1399C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 7/8 | chr1 | 10625873 | |||||||
| chr1:10625939 | C | G | 1 | a0001c0001t0001g0061 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.586-1333C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 7/8 | chr1 | 10625939 | |||||||
| chr1:10626129 | A | T | 1 | a0001c0001t0001g0019 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.586-1143A>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 7/8 | chr1 | 10626129 | |||||||
| chr1:10626393 | G | T | 2 | a0001c0001t0001g0231 a0001c0001t0001g0232 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.586-879G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 7/8 | chr1 | 10626393 | |||||||
| chr1:10626512 | C | T | 2 | a0001c0001t0001g0018 a0001c0014t0001g0251 |
2 | HG01891.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.586-760C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 7/8 | chr1 | 10626512 | |||||||
| chr1:10626669 | G | A | 1 | a0001c0003t0001g0026 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.586-603G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 7/8 | chr1 | 10626669 | |||||||
| chr1:10626895 | A | T | 3 | a0002c0005t0001g0013 a0002c0005t0001g0173 a0002c0005t0001g0218 |
3 | HG02809.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.586-377A>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 7/8 | chr1 | 10626895 | |||||||
| chr1:10627015 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.586-257C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 7/8 | chr1 | 10627015 | |||||||
| chr1:10627149 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.586-123C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 7/8 | chr1 | 10627149 | |||||||
| chr1:10627171 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.586-101G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 7/8 | chr1 | 10627171 | |||||||
| chr1:10627201 | C | T | 1 | a0001c0004t0001g0038 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.586-71C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 7/8 | chr1 | 10627201 | |||||||
| chr1:10627208 | C | T | 1 | a0001c0001t0001g0005 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.586-64C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 7/8 | chr1 | 10627208 | |||||||
| chr1:10627213 | G | A | 1 | a0001c0003t0001g0238 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.586-59G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 7/8 | chr1 | 10627213 | |||||||
| chr1:10627409 | G | T | 1 | a0001c0001t0001g0249 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.677+46G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 8/8 | chr1 | 10627409 | |||||||
| chr1:10627460 | C | A | 1 | a0001c0002t0001g0077 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.677+97C>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 8/8 | chr1 | 10627460 | |||||||
| chr1:10627618 | G | A | 1 | a0001c0001t0001g0161 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.677+255G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 8/8 | chr1 | 10627618 | |||||||
| chr1:10627669 | G | C | 51 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(48): Show |
51 | HG01069.hp1 HG01070.hp2 HG01099.hp1 others(48): Show |
intron_variant | MODIFIER | c.677+306G>C | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 8/8 | chr1 | 10627669 | |||||||
| chr1:10627670 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.677+307G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 8/8 | chr1 | 10627670 | |||||||
| chr1:10627918 | T | G | 2 | a0001c0001t0001g0059 a0001c0001t0001g0064 |
2 | NA18984.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.677+555T>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 8/8 | chr1 | 10627918 | |||||||
| chr1:10628023 | C | T | 2 | a0001c0003t0001g0135 a0001c0003t0001g0158 |
2 | HG03492.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.677+660C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 8/8 | chr1 | 10628023 | |||||||
| chr1:10628037 | G | A | 3 | a0001c0001t0001g0129 a0001c0001t0001g0226 a0001c0001t0001g0229 |
3 | HG01109.hp1 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.677+674G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 8/8 | chr1 | 10628037 | |||||||
| chr1:10628096 | C | G | 3 | a0001c0001t0001g0003 a0001c0001t0001g0115 a0001c0001t0001g0117 |
3 | HG02258.hp2 HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.677+733C>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 8/8 | chr1 | 10628096 | |||||||
| chr1:10628361 | T | G | 1 | a0001c0001t0003g0058 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.677+998T>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 8/8 | chr1 | 10628361 | |||||||
| chr1:10628561 | A | T | 5 | a0001c0006t0001g0086 a0001c0006t0001g0087 a0001c0006t0001g0119 others(2): Show |
5 | HG02717.hp1 HG03139.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.678-970A>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 8/8 | chr1 | 10628561 | |||||||
| chr1:10628640 | C | T | 1 | a0001c0002t0001g0167 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.678-891C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 8/8 | chr1 | 10628640 | |||||||
| chr1:10628710 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.678-821G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 8/8 | chr1 | 10628710 | |||||||
| chr1:10628866 | G | T | 1 | a0001c0001t0001g0242 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.678-665G>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 8/8 | chr1 | 10628866 | |||||||
| chr1:10628870 | T | G | 2 | a0001c0001t0001g0018 a0001c0014t0001g0251 |
2 | HG01891.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.678-661T>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 8/8 | chr1 | 10628870 | |||||||
| chr1:10628998 | A | G | 1 | a0001c0001t0001g0248 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.678-533A>G | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 8/8 | chr1 | 10628998 | |||||||
| chr1:10629316 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.678-215C>T | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 8/8 | chr1 | 10629316 | |||||||
| chr1:10629486 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.678-45G>A | PEX14 | ENSG00000142655.13 | transcript | ENST00000356607.9 | protein_coding | 8/8 | chr1 | 10629486 |