Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55008 |
| ensemblid | ENSG00000138642.16 |
| hgncid | 26072 |
| symbol | HERC6 |
| name | HECT and RLD domain containing E3 ubiquitin protein ligase family member 6 |
| refseq_nuc | NM_017912.4 |
| refseq_prot | NP_060382.3 |
| ensembl_nuc | ENST00000264346.12 |
| ensembl_prot | ENSP00000264346.8 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 88378852 |
| end | 88443097 |
| strand | + |
| ver | v1.2 |
| region | chr4:88378852-88443097 |
| region5000 | chr4:88373852-88448097 |
| regionname0 | HERC6_chr4_88378852_88443097 |
| regionname5000 | HERC6_chr4_88373852_88448097 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 1022 | 72 | 21 | 11 | 24 | 1 | 15 | 18 | HERC6_chr4_88373852_88448097 | HERC6 | MYFCW others(1017): Show |
chr4 | 88373852 | 88448097 |
| a0002 | 1/1 | 1022 | 59 | 7 | 10 | 19 | 8 | 13 | 15 | HERC6_chr4_88373852_88448097 | HERC6 | MYFCW others(1017): Show |
chr4 | 88373852 | 88448097 |
| a0003 | 0/0 | 1022 | 9 | 0 | 2 | 7 | 0 | 0 | 5 | HERC6_chr4_88373852_88448097 | HERC6 | MYFCW others(1017): Show |
chr4 | 88373852 | 88448097 |
| a0004 | 0/0 | 1022 | 7 | 4 | 0 | 2 | 0 | 1 | 2 | HERC6_chr4_88373852_88448097 | HERC6 | MYFCW others(1017): Show |
chr4 | 88373852 | 88448097 |
| a0005 | 0/0 | 1022 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | MYFCW others(1017): Show |
chr4 | 88373852 | 88448097 |
| a0006 | 0/0 | 1022 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | MYFCW others(1017): Show |
chr4 | 88373852 | 88448097 |
| a0007 | 0/0 | 1022 | 3 | 0 | 0 | 0 | 1 | 2 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | MYFCW others(1017): Show |
chr4 | 88373852 | 88448097 |
| a0008 | 0/0 | 1022 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | MYFCW others(1017): Show |
chr4 | 88373852 | 88448097 |
| a0009 | 0/0 | 1020 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | MYFCW others(1015): Show |
chr4 | 88373852 | 88448097 |
| a0010 | 0/0 | 1022 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | MYFCW others(1017): Show |
chr4 | 88373852 | 88448097 |
| a0011 | 0/0 | 1022 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | MYFCW others(1017): Show |
chr4 | 88373852 | 88448097 |
| a0012 | 0/0 | 1022 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | MYFCW others(1017): Show |
chr4 | 88373852 | 88448097 |
| a0013 | 0/0 | 1022 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | MYFCW others(1017): Show |
chr4 | 88373852 | 88448097 |
| a0014 | 0/0 | 1022 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | MYFCW others(1017): Show |
chr4 | 88373852 | 88448097 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 3066 | 66 | 20 | 9 | 23 | 0 | 14 | HERC6_chr4_88373852_88448097 | HERC6 | ATGTA others(3061): Show |
chr4 | 88373852 | 88448097 | ||
| a0001c0008 | 0/0 | 3066 | 4 | 1 | 1 | 0 | 1 | 1 | HERC6_chr4_88373852_88448097 | HERC6 | ATGTA others(3061): Show |
chr4 | 88373852 | 88448097 | ||
| a0001c0015 | 0/0 | 3066 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | ATGTA others(3061): Show |
chr4 | 88373852 | 88448097 | ||
| a0001c0019 | 0/0 | 3066 | 1 | 0 | 1 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | ATGTA others(3061): Show |
chr4 | 88373852 | 88448097 | ||
| a0002c0002 | 1/1 | 3066 | 54 | 7 | 8 | 18 | 7 | 12 | HERC6_chr4_88373852_88448097 | HERC6 | ATGTA others(3061): Show |
chr4 | 88373852 | 88448097 | ||
| a0002c0005 | 0/0 | 3066 | 5 | 0 | 2 | 1 | 1 | 1 | HERC6_chr4_88373852_88448097 | HERC6 | ATGTA others(3061): Show |
chr4 | 88373852 | 88448097 | ||
| a0003c0003 | 0/0 | 3066 | 7 | 0 | 0 | 7 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | ATGTA others(3061): Show |
chr4 | 88373852 | 88448097 | ||
| a0003c0016 | 0/0 | 3066 | 1 | 0 | 1 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | ATGTA others(3061): Show |
chr4 | 88373852 | 88448097 | ||
| a0003c0021 | 0/0 | 3066 | 1 | 0 | 1 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | ATGTA others(3061): Show |
chr4 | 88373852 | 88448097 | ||
| a0004c0004 | 0/0 | 3066 | 6 | 3 | 0 | 2 | 0 | 1 | HERC6_chr4_88373852_88448097 | HERC6 | ATGTA others(3061): Show |
chr4 | 88373852 | 88448097 | ||
| a0004c0017 | 0/0 | 3066 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | ATGTA others(3061): Show |
chr4 | 88373852 | 88448097 | ||
| a0005c0007 | 0/0 | 3066 | 5 | 4 | 1 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | ATGTA others(3061): Show |
chr4 | 88373852 | 88448097 | ||
| a0006c0006 | 0/0 | 3066 | 5 | 5 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | ATGTA others(3061): Show |
chr4 | 88373852 | 88448097 | ||
| a0007c0011 | 0/0 | 3066 | 3 | 0 | 0 | 0 | 1 | 2 | HERC6_chr4_88373852_88448097 | HERC6 | ATGTA others(3061): Show |
chr4 | 88373852 | 88448097 | ||
| a0008c0009 | 0/0 | 3066 | 3 | 3 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | ATGTA others(3061): Show |
chr4 | 88373852 | 88448097 | ||
| a0009c0010 | 0/0 | 3066 | 3 | 3 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | ATGTA others(3061): Show |
chr4 | 88373852 | 88448097 | ||
| a0010c0014 | 0/0 | 3066 | 2 | 0 | 1 | 0 | 0 | 1 | HERC6_chr4_88373852_88448097 | HERC6 | ATGTA others(3061): Show |
chr4 | 88373852 | 88448097 | ||
| a0011c0012 | 0/0 | 3066 | 2 | 2 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | ATGTA others(3061): Show |
chr4 | 88373852 | 88448097 | ||
| a0012c0013 | 0/0 | 3066 | 2 | 2 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | ATGTA others(3061): Show |
chr4 | 88373852 | 88448097 | ||
| a0013c0020 | 0/0 | 3066 | 1 | 0 | 1 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | ATGTA others(3061): Show |
chr4 | 88373852 | 88448097 | ||
| a0014c0018 | 0/0 | 3066 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | ATGTA others(3061): Show |
chr4 | 88373852 | 88448097 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3776 | 63 | 17 | 9 | 23 | 0 | 14 | HERC6_chr4_88373852_88448097 | HERC6 | ACCAG others(3771): Show |
chr4 | 88373852 | 88448097 |
| a0001c0001t0003 | 0/0 | 3776 | 3 | 3 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | ACCAG others(3771): Show |
chr4 | 88373852 | 88448097 |
| a0001c0008t0001 | 0/0 | 3776 | 4 | 1 | 1 | 0 | 1 | 1 | HERC6_chr4_88373852_88448097 | HERC6 | ACCAG others(3771): Show |
chr4 | 88373852 | 88448097 |
| a0001c0015t0001 | 0/0 | 3776 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | ACCAG others(3771): Show |
chr4 | 88373852 | 88448097 |
| a0001c0019t0001 | 0/0 | 3776 | 1 | 0 | 1 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | ACCAG others(3771): Show |
chr4 | 88373852 | 88448097 |
| a0002c0002t0001 | 1/1 | 3776 | 54 | 7 | 8 | 18 | 7 | 12 | HERC6_chr4_88373852_88448097 | HERC6 | ACCAG others(3771): Show |
chr4 | 88373852 | 88448097 |
| a0002c0005t0001 | 0/0 | 3776 | 5 | 0 | 2 | 1 | 1 | 1 | HERC6_chr4_88373852_88448097 | HERC6 | ACCAG others(3771): Show |
chr4 | 88373852 | 88448097 |
| a0003c0003t0001 | 0/0 | 3776 | 7 | 0 | 0 | 7 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | ACCAG others(3771): Show |
chr4 | 88373852 | 88448097 |
| a0003c0016t0001 | 0/0 | 3776 | 1 | 0 | 1 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | ACCAG others(3771): Show |
chr4 | 88373852 | 88448097 |
| a0003c0021t0001 | 0/0 | 3776 | 1 | 0 | 1 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | ACCAG others(3771): Show |
chr4 | 88373852 | 88448097 |
| a0004c0004t0001 | 0/0 | 3776 | 6 | 3 | 0 | 2 | 0 | 1 | HERC6_chr4_88373852_88448097 | HERC6 | ACCAG others(3771): Show |
chr4 | 88373852 | 88448097 |
| a0004c0017t0001 | 0/0 | 3776 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | ACCAG others(3771): Show |
chr4 | 88373852 | 88448097 |
| a0005c0007t0001 | 0/0 | 3776 | 5 | 4 | 1 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | ACCAG others(3771): Show |
chr4 | 88373852 | 88448097 |
| a0006c0006t0001 | 0/0 | 3776 | 5 | 5 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | ACCAG others(3771): Show |
chr4 | 88373852 | 88448097 |
| a0007c0011t0001 | 0/0 | 3776 | 3 | 0 | 0 | 0 | 1 | 2 | HERC6_chr4_88373852_88448097 | HERC6 | ACCAG others(3771): Show |
chr4 | 88373852 | 88448097 |
| a0008c0009t0001 | 0/0 | 3776 | 3 | 3 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | ACCAG others(3771): Show |
chr4 | 88373852 | 88448097 |
| a0009c0010t0002 | 0/0 | 3744 | 3 | 3 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | ACCAG others(3739): Show |
chr4 | 88373852 | 88448097 |
| a0010c0014t0001 | 0/0 | 3776 | 1 | 0 | 1 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | ACCAG others(3771): Show |
chr4 | 88373852 | 88448097 |
| a0010c0014t0004 | 0/0 | 3776 | 1 | 0 | 0 | 0 | 0 | 1 | HERC6_chr4_88373852_88448097 | HERC6 | ACCAG others(3771): Show |
chr4 | 88373852 | 88448097 |
| a0011c0012t0001 | 0/0 | 3776 | 2 | 2 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | ACCAG others(3771): Show |
chr4 | 88373852 | 88448097 |
| a0012c0013t0001 | 0/0 | 3776 | 2 | 2 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | ACCAG others(3771): Show |
chr4 | 88373852 | 88448097 |
| a0013c0020t0001 | 0/0 | 3776 | 1 | 0 | 1 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | ACCAG others(3771): Show |
chr4 | 88373852 | 88448097 |
| a0014c0018t0001 | 0/0 | 3776 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | ACCAG others(3771): Show |
chr4 | 88373852 | 88448097 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0008t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0008t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0008t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0008t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0015t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0001c0019t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0018 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0054 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0005t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0005t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0005t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0005t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0002c0005t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0003c0003t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0003c0003t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0003c0003t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0003c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0003c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0003c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0003c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0003c0016t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0003c0021t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0004c0004t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0004c0004t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0004c0004t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0004c0004t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0004c0004t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0004c0004t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0004c0017t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0005c0007t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0005c0007t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0005c0007t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0005c0007t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0005c0007t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0006c0006t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0006c0006t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0006c0006t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0006c0006t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0006c0006t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0007c0011t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0007c0011t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0007c0011t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0008c0009t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0008c0009t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0008c0009t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0009c0010t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0009c0010t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0009c0010t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0010c0014t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0010c0014t0004g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0011c0012t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0011c0012t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0012c0013t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0012c0013t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0013c0020t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| a0014c0018t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0002 | c0005 | t0001 | g0059 | EUR | GBR | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0105 | EUR | GBR | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0016 | EUR | FIN | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0104 | EUR | FIN | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0008 | EUR | FIN | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0040 | EUR | FIN | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG00639 | hp1 | a0005 | c0007 | t0001 | g0092 | AMR | PUR | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG00639 | hp2 | a0002 | c0005 | t0001 | g0068 | AMR | PUR | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG00735 | hp1 | a0013 | c0020 | t0001 | g0051 | AMR | PUR | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG01167 | hp1 | a0001 | c0008 | t0001 | g0057 | AMR | PUR | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG01168 | hp2 | a0010 | c0014 | t0001 | g0020 | AMR | PUR | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0080 | AMR | PUR | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0037 | AMR | CLM | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0042 | AMR | CLM | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0165 | AMR | CLM | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | CLM | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0025 | AMR | CLM | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG01346 | hp2 | a0001 | c0019 | t0001 | g0063 | AMR | CLM | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG01496 | hp1 | a0003 | c0021 | t0001 | g0128 | AMR | CLM | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG01496 | hp2 | a0002 | c0005 | t0001 | g0060 | AMR | CLM | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG01516 | hp1 | a0001 | c0008 | t0001 | g0058 | EUR | IBS | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG01516 | hp2 | a0007 | c0011 | t0001 | g0124 | EUR | IBS | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG01884 | hp2 | a0014 | c0018 | t0001 | g0066 | AFR | ACB | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0041 | AFR | ACB | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0114 | AMR | PEL | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG01978 | hp2 | a0003 | c0016 | t0001 | g0171 | AMR | PEL | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0036 | EAS | KHV | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0043 | EAS | KHV | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0148 | EAS | CDX | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG02165 | hp2 | a0003 | c0003 | t0001 | g0147 | EAS | CDX | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0121 | AFR | ACB | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0117 | AFR | ACB | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG02258 | hp2 | a0011 | c0012 | t0001 | g0052 | AFR | ACB | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0134 | AMR | PEL | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG02451 | hp1 | a0005 | c0007 | t0001 | g0096 | AFR | ACB | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG02451 | hp2 | a0004 | c0004 | t0001 | g0161 | AFR | ACB | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG02523 | hp1 | a0003 | c0003 | t0001 | g0029 | EAS | KHV | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG02647 | hp2 | a0005 | c0007 | t0001 | g0003 | AFR | GWD | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0098 | AFR | GWD | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG02735 | hp1 | a0002 | c0005 | t0001 | g0062 | SAS | PJL | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0108 | SAS | PJL | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG02809 | hp2 | a0008 | c0009 | t0001 | g0050 | AFR | GWD | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG02896 | hp1 | a0006 | c0006 | t0001 | g0072 | AFR | GWD | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0095 | AFR | GWD | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG02897 | hp1 | a0006 | c0006 | t0001 | g0073 | AFR | GWD | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG02922 | hp1 | a0001 | c0008 | t0001 | g0069 | AFR | ESN | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG02922 | hp2 | a0006 | c0006 | t0001 | g0032 | AFR | ESN | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0081 | AFR | ESN | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG02965 | hp2 | a0011 | c0012 | t0001 | g0053 | AFR | ESN | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG03139 | hp1 | a0005 | c0007 | t0001 | g0093 | AFR | ESN | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ESN | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG03195 | hp2 | a0009 | c0010 | t0002 | g0120 | AFR | ESN | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG03209 | hp1 | a0012 | c0013 | t0001 | g0149 | AFR | MSL | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG03209 | hp2 | a0005 | c0007 | t0001 | g0090 | AFR | MSL | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG03225 | hp1 | a0012 | c0013 | t0001 | g0157 | AFR | MSL | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG03225 | hp2 | a0004 | c0017 | t0001 | g0067 | AFR | MSL | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG03239 | hp2 | a0010 | c0014 | t0004 | g0079 | SAS | PJL | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0107 | SAS | PJL | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0028 | SAS | PJL | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ESN | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG03516 | hp2 | a0006 | c0006 | t0001 | g0071 | AFR | ESN | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0127 | SAS | PJL | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | STU | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | STU | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG03831 | hp1 | a0004 | c0004 | t0001 | g0129 | SAS | BEB | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG03831 | hp2 | a0001 | c0008 | t0001 | g0061 | SAS | BEB | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0170 | SAS | BEB | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | BEB | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG03942 | hp2 | a0007 | c0011 | t0001 | g0125 | SAS | BEB | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0013 | SAS | STU | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0026 | SAS | STU | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0049 | SAS | BEB | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | STU | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | STU | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA18522 | hp1 | a0004 | c0004 | t0001 | g0144 | AFR | YRI | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | YRI | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CHB | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0110 | EAS | CHB | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHB | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CHB | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA18906 | hp1 | a0008 | c0009 | t0001 | g0074 | AFR | YRI | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA18906 | hp2 | a0009 | c0010 | t0002 | g0006 | AFR | YRI | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0103 | EAS | JPT | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA18948 | hp1 | a0004 | c0004 | t0001 | g0010 | EAS | JPT | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0132 | EAS | JPT | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA18957 | hp1 | a0001 | c0015 | t0001 | g0024 | EAS | JPT | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA18966 | hp1 | a0003 | c0003 | t0001 | g0014 | EAS | JPT | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA18970 | hp1 | a0003 | c0003 | t0001 | g0035 | EAS | JPT | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0166 | EAS | JPT | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA18971 | hp2 | a0003 | c0003 | t0001 | g0021 | EAS | JPT | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0160 | EAS | JPT | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA19003 | hp1 | a0004 | c0004 | t0001 | g0115 | EAS | JPT | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA19003 | hp2 | a0003 | c0003 | t0001 | g0048 | EAS | JPT | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0130 | EAS | JPT | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA19007 | hp1 | a0003 | c0003 | t0001 | g0158 | EAS | JPT | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA19043 | hp1 | a0004 | c0004 | t0001 | g0005 | AFR | LWK | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | LWK | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA19064 | hp1 | a0002 | c0005 | t0001 | g0064 | EAS | JPT | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0033 | EUR | TSI | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0045 | EUR | TSI | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | GIH | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA20905 | hp2 | a0007 | c0011 | t0001 | g0143 | SAS | GIH | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG02486 | hp2 | a0008 | c0009 | t0001 | g0047 | AFR | ACB | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0083 | AFR | ACB | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG02559 | hp2 | a0009 | c0010 | t0002 | g0119 | AFR | ACB | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0082 | AFR | USA | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| HG06807 | hp2 | a0006 | c0006 | t0001 | g0070 | AFR | USA | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0126 | AFR | USA | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0089 | AFR | USA | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0054 | REF | REF | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0018 | REF | REF | HERC6_chr4_88373852_88448097 | HERC6 | chr4 | 88373852 | 88448097 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:88378949 | A | G | 1 | a0007 | 3 | HG01516.hp2 HG03942.hp2 NA20905.hp2 |
missense_variant | MODERATE | c.28A>G | p.Arg10Gly | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/23 | 98/3776 | 28/3069 | 10/1022 | chr4 | 88378949 | |||
| chr4:88385507 | T | C | 5 | a0006 a0007 a0008 others(2): Show |
14 | HG00735.hp1 HG01516.hp2 HG02258.hp2 others(11): Show |
missense_variant | MODERATE | c.368T>C | p.Met123Thr | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/23 | 438/3776 | 368/3069 | 123/1022 | chr4 | 88385507 | |||
| chr4:88390810 | T | C | 2 | a0003 a0010 |
11 | HG01168.hp2 HG01496.hp1 HG01978.hp2 others(8): Show |
missense_variant | MODERATE | c.595T>C | p.Cys199Arg | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 4/23 | 665/3776 | 595/3069 | 199/1022 | chr4 | 88390810 | |||
| chr4:88390842 | T | A | 4 | a0004 a0008 a0009 others(1): Show |
14 | HG01884.hp2 HG02451.hp2 HG02486.hp2 others(11): Show |
missense_variant | MODERATE | c.627T>A | p.Ser209Arg | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 4/23 | 697/3776 | 627/3069 | 209/1022 | chr4 | 88390842 | |||
| chr4:88398144 | T | C | 10 | a0001 a0003 a0004 others(7): Show |
109 | HG00639.hp1 HG00735.hp2 HG01071.hp1 others(106): Show |
missense_variant&splice_region_variant | MODERATE | c.1027T>C | p.Phe343Leu | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 8/23 | 1097/3776 | 1027/3069 | 343/1022 | chr4 | 88398144 | |||
| chr4:88423879 | G | A | 1 | a0012 | 2 | HG03209.hp1 HG03225.hp1 |
missense_variant | MODERATE | c.1733G>A | p.Arg578Gln | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 14/23 | 1803/3776 | 1733/3069 | 578/1022 | chr4 | 88423879 | |||
| chr4:88424608 | C | T | 3 | a0005 a0011 a0014 |
8 | HG00639.hp1 HG01884.hp2 HG02258.hp2 others(5): Show |
missense_variant | MODERATE | c.1841C>T | p.Thr614Ile | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 15/23 | 1911/3776 | 1841/3069 | 614/1022 | chr4 | 88424608 | |||
| chr4:88436931 | C | A | 1 | a0009 | 3 | HG02559.hp2 HG03195.hp2 NA18906.hp2 |
missense_variant | MODERATE | c.2444C>A | p.Ala815Asp | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 19/23 | 2514/3776 | 2444/3069 | 815/1022 | chr4 | 88436931 | |||
| chr4:88442360 | C | A | 1 | a0009 | 3 | HG02559.hp2 HG03195.hp2 NA18906.hp2 |
missense_variant | MODERATE | c.2969C>A | p.Ser990Tyr | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 23/23 | 3039/3776 | 2969/3069 | 990/1022 | chr4 | 88442360 | |||
| chr4:88442452 | C | T | 1 | a0009 | 3 | HG02559.hp2 HG03195.hp2 NA18906.hp2 |
stop_gained | HIGH | c.3061C>T | p.Gln1021* | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 23/23 | 3131/3776 | 3061/3069 | 1021/1022 | chr4 | 88442452 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:88378972 | G | A | 1 | a0001c0015 | 1 | NA18957.hp1 | synonymous_variant | LOW | c.51G>A | p.Thr17Thr | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/23 | 121/3776 | 51/3069 | 17/1022 | chr4 | 88378972 | |||
| chr4:88378975 | G | A | 1 | a0003c0016 | 1 | HG01978.hp2 | synonymous_variant | LOW | c.54G>A | p.Ala18Ala | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/23 | 124/3776 | 54/3069 | 18/1022 | chr4 | 88378975 | |||
| chr4:88379089 | C | A | 5 | a0001c0008 a0001c0019 a0002c0005 others(2): Show |
12 | HG00140.hp1 HG00639.hp2 HG01167.hp1 others(9): Show |
synonymous_variant | LOW | c.168C>A | p.Gly56Gly | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/23 | 238/3776 | 168/3069 | 56/1022 | chr4 | 88379089 | |||
| chr4:88390731 | G | A | 1 | a0012c0013 | 2 | HG03209.hp1 HG03225.hp1 |
synonymous_variant | LOW | c.516G>A | p.Pro172Pro | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 4/23 | 586/3776 | 516/3069 | 172/1022 | chr4 | 88390731 | |||
| chr4:88439925 | A | G | 1 | a0001c0019 | 1 | HG01346.hp2 | synonymous_variant | LOW | c.2607A>G | p.Lys869Lys | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 21/23 | 2677/3776 | 2607/3069 | 869/1022 | chr4 | 88439925 | |||
| chr4:88440171 | C | T | 1 | a0003c0021 | 1 | HG01496.hp1 | synonymous_variant | LOW | c.2763C>T | p.Tyr921Tyr | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 22/23 | 2833/3776 | 2763/3069 | 921/1022 | chr4 | 88440171 | |||
| chr4:88442262 | T | C | 1 | a0009c0010 | 3 | HG02559.hp2 HG03195.hp2 NA18906.hp2 |
synonymous_variant | LOW | c.2871T>C | p.His957His | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 23/23 | 2941/3776 | 2871/3069 | 957/1022 | chr4 | 88442262 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:88378888 | G | A | 1 | a0010c0014t0004 | 1 | HG03239.hp2 | 5_prime_UTR_variant | MODIFIER | c.-34G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/23 | 34 | chr4 | 88378888 | ||||||
| chr4:88442568 | G | A | 1 | a0009c0010t0002 | 3 | HG02559.hp2 HG03195.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*108G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 23/23 | 108 | chr4 | 88442568 | ||||||
| chr4:88442814 | T | C | 1 | a0001c0001t0003 | 3 | HG02559.hp1 HG02965.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*354T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 23/23 | 354 | chr4 | 88442814 | ||||||
| chr4:88443026 | CCTGTGGA others(25): Show |
C | 1 | a0009c0010t0002 | 3 | HG02559.hp2 HG03195.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*570_*601delTGGAAT others(26): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 23/23 | 570 | INFO_REALIGN_3_PRIME | chr4 | 88443026 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:88379133 | C | G | 1 | a0014c0018t0001g0066 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.199+13C>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379133 | |||||||
| chr4:88379207 | G | A | 4 | a0001c0001t0001g0004 a0004c0004t0001g0005 a0005c0007t0001g0003 others(1): Show |
4 | HG02647.hp2 HG02809.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.199+87G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379207 | |||||||
| chr4:88379268 | G | A | 2 | a0001c0001t0001g0004 a0005c0007t0001g0003 |
2 | HG02647.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.199+148G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379268 | |||||||
| chr4:88379490 | G | T | 4 | a0001c0001t0001g0004 a0004c0004t0001g0005 a0005c0007t0001g0003 others(1): Show |
4 | HG02647.hp2 HG02809.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.199+370G>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379490 | |||||||
| chr4:88379522 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.199+402C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379522 | |||||||
| chr4:88379581 | A | G | 126 | a0001c0001t0001g0004 a0001c0001t0001g0055 a0001c0001t0001g0056 others(123): Show |
126 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.199+461A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379581 | |||||||
| chr4:88379623 | A | AAT | 25 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(22): Show |
25 | HG01168.hp1 HG01169.hp2 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.199+515_199+516dup others(2): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379623 | ||||||
| chr4:88379625 | T | A | 4 | a0008c0009t0001g0050 a0011c0012t0001g0052 a0011c0012t0001g0053 others(1): Show |
4 | HG00735.hp1 HG02258.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.199+505T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379625 | |||||||
| chr4:88379637 | A | T | 5 | a0003c0016t0001g0171 a0008c0009t0001g0050 a0011c0012t0001g0052 others(2): Show |
5 | HG00735.hp1 HG01978.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.199+517A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379637 | |||||||
| chr4:88379639 | A | T | 1 | a0002c0002t0001g0049 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.199+519A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379639 | |||||||
| chr4:88379649 | T | A | 15 | a0001c0001t0001g0056 a0001c0001t0001g0131 a0001c0001t0001g0139 others(12): Show |
15 | HG01496.hp1 HG02040.hp1 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.199+529T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379649 | |||||||
| chr4:88379685 | C | CAAATATA others(10): Show |
3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0004c0004t0001g0144 |
3 | HG02895.hp2 HG02897.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.199+574_199+575ins others(17): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379685 | ||||||
| chr4:88379685 | C | T | 2 | a0004c0004t0001g0005 a0009c0010t0002g0006 |
2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.199+565C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379685 | |||||||
| chr4:88379686 | A | G | 1 | a0003c0003t0001g0048 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.199+566A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379686 | |||||||
| chr4:88379687 | A | AAT | 34 | a0001c0001t0001g0056 a0001c0001t0001g0078 a0001c0001t0001g0094 others(31): Show |
34 | HG00280.hp2 HG00735.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.199+573_199+574dup others(2): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379687 | ||||||
| chr4:88379687 | A | AATATAAT others(87): Show |
13 | a0001c0001t0001g0150 a0001c0001t0001g0155 a0001c0001t0001g0159 others(10): Show |
13 | HG01168.hp1 HG01169.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.199+572_199+573ins others(94): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379687 | ||||||
| chr4:88379687 | A | AATATAAT others(119): Show |
1 | a0002c0002t0001g0170 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.199+572_199+573ins others(126): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379687 | ||||||
| chr4:88379687 | A | AATATATA others(12): Show |
2 | a0001c0001t0001g0172 a0009c0010t0002g0006 |
2 | HG01891.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.199+574_199+575ins others(19): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379687 | ||||||
| chr4:88379687 | A | AATATATA others(27): Show |
18 | a0001c0001t0001g0065 a0001c0001t0001g0075 a0001c0001t0001g0076 others(15): Show |
18 | HG00140.hp1 HG00639.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.199+574_199+575ins others(34): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379687 | ||||||
| chr4:88379687 | A | AATATATA others(59): Show |
38 | a0001c0001t0001g0004 a0001c0001t0001g0084 a0001c0001t0001g0085 others(35): Show |
38 | HG00140.hp2 HG00639.hp1 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.199+574_199+575ins others(66): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379687 | ||||||
| chr4:88379687 | A | AATATATA others(91): Show |
2 | a0002c0002t0001g0126 a0002c0002t0001g0127 |
2 | HG03654.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.199+574_199+575ins others(98): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379687 | ||||||
| chr4:88379687 | A | AATATATA others(187): Show |
3 | a0002c0002t0001g0130 a0002c0002t0001g0136 a0004c0004t0001g0129 |
3 | HG03831.hp1 NA18966.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.199+574_199+575ins others(194): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379687 | ||||||
| chr4:88379687 | AAT | A | 12 | a0001c0001t0001g0055 a0001c0001t0001g0151 a0001c0001t0001g0152 others(9): Show |
12 | HG01978.hp2 HG02165.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.199+573_199+574del others(2): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379687 | ||||||
| chr4:88379702 | A | AAT | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0004c0004t0001g0144 |
3 | HG02895.hp2 HG02897.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.199+588_199+589dup others(2): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379702 | ||||||
| chr4:88379728 | T | C | 1 | a0001c0008t0001g0057 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.199+608T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379728 | |||||||
| chr4:88379733 | A | AAATATAT others(17): Show |
1 | a0007c0011t0001g0143 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.199+622_199+623ins others(24): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379733 | ||||||
| chr4:88379742 | A | AATATATA others(29): Show |
2 | a0001c0001t0001g0009 a0002c0002t0001g0001 |
3 | HG03491.hp2 HG03492.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.199+702_199+737dup others(36): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379742 | ||||||
| chr4:88379742 | A | ATATATAA others(61): Show |
1 | a0013c0020t0001g0051 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.199+622_199+623ins others(68): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379742 | |||||||
| chr4:88379742 | A | ATATATAA others(170): Show |
1 | a0008c0009t0001g0050 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.199+622_199+623ins others(177): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379742 | |||||||
| chr4:88379742 | A | ATATATAA others(169): Show |
3 | a0006c0006t0001g0072 a0011c0012t0001g0052 a0011c0012t0001g0053 |
3 | HG02258.hp2 HG02896.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.199+622_199+623ins others(176): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379742 | |||||||
| chr4:88379742 | A | ATATATAA others(241): Show |
1 | a0006c0006t0001g0070 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.199+622_199+623ins others(248): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379742 | |||||||
| chr4:88379742 | A | ATATATAA others(277): Show |
1 | a0006c0006t0001g0071 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.199+622_199+623ins others(284): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379742 | |||||||
| chr4:88379742 | A | ATATATAA others(89): Show |
3 | a0001c0001t0001g0078 a0002c0002t0001g0080 a0010c0014t0004g0079 |
3 | HG00735.hp2 HG01192.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.199+622_199+623ins others(96): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379742 | |||||||
| chr4:88379742 | A | ATATATAA others(93): Show |
6 | a0001c0001t0001g0094 a0001c0001t0001g0097 a0001c0001t0003g0081 others(3): Show |
6 | HG02451.hp1 HG02723.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.199+622_199+623ins others(100): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379742 | |||||||
| chr4:88379742 | A | ATATATAA others(129): Show |
3 | a0001c0001t0003g0083 a0002c0002t0001g0104 a0002c0002t0001g0114 |
3 | HG00280.hp2 HG01978.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.199+622_199+623ins others(136): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379742 | |||||||
| chr4:88379742 | A | ATATATAA others(142): Show |
10 | a0001c0001t0001g0055 a0001c0001t0001g0151 a0001c0001t0001g0152 others(7): Show |
10 | HG01978.hp2 HG02165.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.199+622_199+623ins others(149): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379742 | |||||||
| chr4:88379742 | A | ATATATAA others(178): Show |
1 | a0002c0002t0001g0160 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.199+622_199+623ins others(185): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379742 | |||||||
| chr4:88379742 | A | ATATATAA others(174): Show |
1 | a0001c0001t0001g0169 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.199+622_199+623ins others(181): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379742 | |||||||
| chr4:88379742 | A | ATATATAA others(328): Show |
1 | a0003c0021t0001g0128 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.199+622_199+623ins others(335): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379742 | |||||||
| chr4:88379742 | A | ATATATAA others(329): Show |
4 | a0001c0001t0001g0131 a0002c0002t0001g0132 a0002c0002t0001g0133 others(1): Show |
4 | HG02300.hp2 HG03239.hp1 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.199+622_199+623ins others(336): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379742 | |||||||
| chr4:88379742 | A | ATATATAA others(365): Show |
1 | a0002c0002t0001g0135 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.199+622_199+623ins others(372): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379742 | |||||||
| chr4:88379742 | A | ATATATAA others(361): Show |
3 | a0001c0001t0001g0139 a0002c0002t0001g0137 a0002c0002t0001g0138 |
3 | HG02040.hp1 NA18962.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.199+622_199+623ins others(368): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379742 | |||||||
| chr4:88379742 | A | ATATATAA others(433): Show |
1 | a0001c0001t0001g0140 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.199+622_199+623ins others(440): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379742 | |||||||
| chr4:88379742 | A | ATATATAA others(278): Show |
1 | a0001c0001t0001g0141 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.199+622_199+623ins others(285): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379742 | |||||||
| chr4:88379742 | A | ATATATAA others(350): Show |
1 | a0001c0001t0001g0142 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.199+622_199+623ins others(357): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379742 | |||||||
| chr4:88379751 | C | T | 1 | a0007c0011t0001g0143 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.199+631C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379751 | |||||||
| chr4:88379776 | T | TATATATA others(10): Show |
8 | a0001c0001t0001g0150 a0001c0001t0001g0155 a0001c0001t0001g0159 others(5): Show |
8 | HG01168.hp1 HG01169.hp2 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.199+667_199+683dup others(17): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379776 | ||||||
| chr4:88379786 | A | G | 1 | a0004c0004t0001g0005 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.199+666A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379786 | |||||||
| chr4:88379787 | C | CATATAAA others(133): Show |
1 | a0003c0003t0001g0158 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.199+683_199+684ins others(140): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379787 | ||||||
| chr4:88379787 | C | CATATAAA others(10): Show |
3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0004c0004t0001g0144 |
3 | HG02895.hp2 HG02897.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.199+683_199+699dup others(17): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379787 | ||||||
| chr4:88379804 | T | C | 5 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0002c0002t0001g0165 others(2): Show |
5 | HG01257.hp1 HG02523.hp2 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.199+684T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379804 | |||||||
| chr4:88379812 | T | TATATATA others(97): Show |
1 | a0002c0002t0001g0165 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.199+699_199+700ins others(104): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379812 | ||||||
| chr4:88379812 | T | TATATATA others(97): Show |
3 | a0001c0001t0001g0167 a0002c0002t0001g0166 a0002c0002t0001g0170 |
3 | HG02523.hp2 HG03927.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.199+699_199+700ins others(104): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379812 | ||||||
| chr4:88379812 | T | TATATATA others(131): Show |
1 | a0001c0001t0001g0168 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.199+699_199+700ins others(138): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379812 | ||||||
| chr4:88379823 | C | T | 7 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0002c0002t0001g0165 others(4): Show |
7 | HG01257.hp1 HG02523.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.199+703C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379823 | |||||||
| chr4:88379823 | CAT | C | 8 | a0001c0001t0001g0065 a0001c0008t0001g0058 a0001c0008t0001g0061 others(5): Show |
8 | HG00140.hp1 HG01346.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.199+707_199+708del others(2): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379823 | ||||||
| chr4:88379846 | AAT | A | 11 | a0001c0001t0001g0055 a0001c0001t0001g0151 a0001c0001t0001g0152 others(8): Show |
11 | HG01978.hp2 HG02165.hp2 HG03209.hp1 others(8): Show |
intron_variant | MODIFIER | c.199+736_199+737del others(2): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379846 | ||||||
| chr4:88379848 | T | TATATATA others(25): Show |
1 | a0007c0011t0001g0125 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.199+735_199+736ins others(32): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379848 | ||||||
| chr4:88379848 | T | TATATATA others(8): Show |
1 | a0004c0004t0001g0005 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.199+735_199+736ins others(15): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379848 | ||||||
| chr4:88379858 | G | A | 124 | a0001c0001t0001g0055 a0001c0001t0001g0065 a0001c0001t0001g0075 others(121): Show |
124 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.199+738G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379858 | |||||||
| chr4:88379859 | C | T | 12 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0167 others(9): Show |
12 | HG01257.hp1 HG02523.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.199+739C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379859 | |||||||
| chr4:88379882 | AAT | A | 6 | a0001c0001t0001g0150 a0001c0001t0001g0155 a0001c0001t0001g0159 others(3): Show |
6 | HG02165.hp1 HG03225.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.199+772_199+773del others(2): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379882 | ||||||
| chr4:88379884 | T | TATATAAT others(6): Show |
2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.199+769_199+770ins others(13): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379884 | ||||||
| chr4:88379884 | T | TATATATA others(8): Show |
2 | a0007c0011t0001g0124 a0007c0011t0001g0143 |
2 | HG01516.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.199+771_199+772ins others(15): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379884 | ||||||
| chr4:88379884 | T | TATATATA others(114): Show |
4 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(1): Show |
4 | HG01168.hp1 HG01169.hp2 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.199+771_199+772ins others(121): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379884 | ||||||
| chr4:88379884 | T | TATATATA others(25): Show |
1 | a0008c0009t0001g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.199+771_199+772ins others(32): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379884 | ||||||
| chr4:88379884 | T | TATATATA others(82): Show |
5 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0002c0002t0001g0121 others(2): Show |
5 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.199+774_199+775ins others(89): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379884 | ||||||
| chr4:88379884 | T | TATATATA others(217): Show |
1 | a0001c0001t0001g0172 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.199+791_199+792ins others(224): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379884 | ||||||
| chr4:88379892 | T | A | 11 | a0001c0001t0001g0055 a0001c0001t0001g0151 a0001c0001t0001g0152 others(8): Show |
11 | HG01978.hp2 HG02165.hp2 HG03209.hp1 others(8): Show |
intron_variant | MODIFIER | c.199+772T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379892 | |||||||
| chr4:88379893 | A | C | 1 | a0003c0003t0001g0147 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.199+773A>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379893 | |||||||
| chr4:88379893 | A | T | 10 | a0001c0001t0001g0055 a0001c0001t0001g0151 a0001c0001t0001g0152 others(7): Show |
10 | HG01978.hp2 HG03209.hp1 HG03516.hp2 others(7): Show |
intron_variant | MODIFIER | c.199+773A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379893 | |||||||
| chr4:88379895 | T | C | 80 | a0001c0001t0001g0078 a0001c0001t0001g0084 a0001c0001t0001g0085 others(77): Show |
80 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.199+775T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379895 | |||||||
| chr4:88379899 | T | A | 11 | a0001c0001t0001g0055 a0001c0001t0001g0151 a0001c0001t0001g0152 others(8): Show |
11 | HG01978.hp2 HG02165.hp2 HG03209.hp1 others(8): Show |
intron_variant | MODIFIER | c.199+779T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379899 | |||||||
| chr4:88379901 | A | AAT | 3 | a0002c0002t0001g0046 a0002c0002t0001g0160 a0008c0009t0001g0047 |
3 | HG02486.hp2 NA18970.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.199+789_199+790dup others(2): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379901 | ||||||
| chr4:88379901 | A | AATATATA others(173): Show |
1 | a0004c0004t0001g0129 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.199+807_199+808ins others(180): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379901 | ||||||
| chr4:88379901 | A | AATATATA others(209): Show |
1 | a0002c0002t0001g0130 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.199+807_199+808ins others(216): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379901 | ||||||
| chr4:88379901 | A | ATATATAT others(153): Show |
1 | a0008c0009t0001g0074 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.199+781_199+782ins others(160): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379901 | |||||||
| chr4:88379901 | A | T | 11 | a0001c0001t0001g0055 a0001c0001t0001g0151 a0001c0001t0001g0152 others(8): Show |
11 | HG01978.hp2 HG02165.hp2 HG03209.hp1 others(8): Show |
intron_variant | MODIFIER | c.199+781A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379901 | |||||||
| chr4:88379912 | T | TATATAAA others(12): Show |
17 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(14): Show |
17 | HG00639.hp1 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.199+807_199+808ins others(19): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379912 | ||||||
| chr4:88379912 | T | TATATAAA others(48): Show |
11 | a0001c0001t0001g0106 a0001c0001t0001g0109 a0001c0001t0001g0111 others(8): Show |
11 | HG00140.hp2 HG02735.hp2 HG03490.hp2 others(8): Show |
intron_variant | MODIFIER | c.199+807_199+808ins others(55): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379912 | ||||||
| chr4:88379912 | T | TATATAAA others(84): Show |
2 | a0001c0001t0001g0118 a0002c0002t0001g0117 |
2 | HG02257.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.199+807_199+808ins others(91): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379912 | ||||||
| chr4:88379912 | T | TATATAAA others(120): Show |
1 | a0002c0002t0001g0136 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.199+807_199+808ins others(127): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379912 | ||||||
| chr4:88379918 | A | AAT | 4 | a0001c0001t0001g0099 a0002c0002t0001g0045 a0006c0006t0001g0071 others(1): Show |
4 | HG03041.hp1 HG03516.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.199+806_199+807dup others(2): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379918 | ||||||
| chr4:88379918 | A | AATATATA others(408): Show |
1 | a0006c0006t0001g0073 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.199+807_199+808ins others(415): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379918 | ||||||
| chr4:88379928 | A | T | 14 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0001g0097 others(11): Show |
14 | HG00280.hp2 HG00735.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.199+808A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379928 | |||||||
| chr4:88379929 | T | A | 14 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0001g0097 others(11): Show |
14 | HG00280.hp2 HG00735.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.199+809T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379929 | |||||||
| chr4:88379929 | T | C | 2 | a0001c0001t0001g0099 a0013c0020t0001g0051 |
2 | HG00735.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.199+809T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379929 | |||||||
| chr4:88379931 | T | C | 11 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0001g0097 others(8): Show |
11 | HG00280.hp2 HG00735.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.199+811T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379931 | |||||||
| chr4:88379935 | A | T | 14 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0001g0097 others(11): Show |
14 | HG00280.hp2 HG00735.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.199+815A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379935 | |||||||
| chr4:88379935 | AAT | A | 5 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0002c0002t0001g0170 others(2): Show |
5 | HG01496.hp1 HG02523.hp2 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.199+825_199+826del others(2): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379935 | ||||||
| chr4:88379937 | T | A | 14 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0001g0097 others(11): Show |
14 | HG00280.hp2 HG00735.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.199+817T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379937 | |||||||
| chr4:88379937 | T | TATATATA others(8): Show |
4 | a0002c0002t0001g0045 a0002c0002t0001g0165 a0002c0002t0001g0166 others(1): Show |
4 | HG01257.hp1 HG02896.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.199+824_199+825ins others(15): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379937 | ||||||
| chr4:88379937 | T | TATATATA others(169): Show |
1 | a0009c0010t0002g0006 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.199+824_199+825ins others(176): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379937 | ||||||
| chr4:88379937 | T | TATATATA others(97): Show |
2 | a0001c0001t0001g0004 a0005c0007t0001g0003 |
2 | HG02647.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.199+824_199+825ins others(104): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379937 | ||||||
| chr4:88379937 | T | TATATATA others(80): Show |
1 | a0013c0020t0001g0051 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.199+824_199+825ins others(87): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379937 | ||||||
| chr4:88379937 | T | TATATATA others(99): Show |
1 | a0001c0001t0001g0065 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.199+824_199+825ins others(106): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379937 | ||||||
| chr4:88379945 | T | A | 3 | a0001c0001t0001g0099 a0001c0001t0003g0083 a0007c0011t0001g0125 |
3 | HG02559.hp1 HG03041.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.199+825T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379945 | |||||||
| chr4:88379946 | A | T | 3 | a0001c0001t0001g0099 a0001c0001t0003g0083 a0007c0011t0001g0125 |
3 | HG02559.hp1 HG03041.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.199+826A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379946 | |||||||
| chr4:88379948 | T | C | 31 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(28): Show |
31 | HG00140.hp2 HG00639.hp1 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.199+828T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379948 | |||||||
| chr4:88379952 | T | A | 3 | a0001c0001t0001g0099 a0001c0001t0003g0083 a0007c0011t0001g0125 |
3 | HG02559.hp1 HG03041.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.199+832T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379952 | |||||||
| chr4:88379954 | A | AAT | 19 | a0001c0001t0001g0065 a0001c0008t0001g0057 a0001c0008t0001g0061 others(16): Show |
19 | HG00140.hp1 HG00639.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.199+842_199+843dup others(2): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379954 | ||||||
| chr4:88379954 | A | AATATATA others(12): Show |
2 | a0001c0001t0001g0075 a0001c0001t0001g0076 |
2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.199+842_199+860dup others(19): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379954 | ||||||
| chr4:88379954 | A | AATATATA others(48): Show |
1 | a0007c0011t0001g0124 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.199+860_199+861ins others(55): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379954 | ||||||
| chr4:88379954 | A | AATATATA others(31): Show |
1 | a0014c0018t0001g0066 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.199+843_199+844ins others(38): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379954 | ||||||
| chr4:88379954 | A | T | 3 | a0001c0001t0001g0099 a0001c0001t0003g0083 a0007c0011t0001g0125 |
3 | HG02559.hp1 HG03041.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.199+834A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379954 | |||||||
| chr4:88379954 | AATATATA others(29): Show |
A | 1 | a0001c0001t0001g0012 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.199+878_199+913del others(36): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379954 | ||||||
| chr4:88379965 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.199+845T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379965 | |||||||
| chr4:88379971 | A | AAT | 11 | a0001c0001t0001g0004 a0001c0001t0001g0077 a0001c0001t0001g0159 others(8): Show |
11 | HG01168.hp1 HG01169.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.199+859_199+860dup others(2): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379971 | ||||||
| chr4:88379971 | A | AATATATA others(84): Show |
8 | a0001c0001t0001g0131 a0001c0001t0001g0139 a0001c0001t0001g0140 others(5): Show |
8 | HG02040.hp1 HG02132.hp2 HG03239.hp1 others(5): Show |
intron_variant | MODIFIER | c.199+860_199+861ins others(91): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379971 | ||||||
| chr4:88379971 | AATATATA others(12): Show |
A | 2 | a0001c0001t0001g0011 a0004c0004t0001g0010 |
2 | HG03654.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.199+878_199+896del others(19): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379971 | ||||||
| chr4:88379981 | A | T | 11 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(8): Show |
11 | HG03225.hp1 HG03688.hp1 HG03704.hp1 others(8): Show |
intron_variant | MODIFIER | c.199+861A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379981 | |||||||
| chr4:88379982 | T | A | 11 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(8): Show |
11 | HG03225.hp1 HG03688.hp1 HG03704.hp1 others(8): Show |
intron_variant | MODIFIER | c.199+862T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379982 | |||||||
| chr4:88379984 | T | C | 6 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(3): Show |
6 | HG03688.hp1 HG03704.hp2 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.199+864T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379984 | |||||||
| chr4:88379988 | A | T | 11 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(8): Show |
11 | HG03225.hp1 HG03688.hp1 HG03704.hp1 others(8): Show |
intron_variant | MODIFIER | c.199+868A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379988 | |||||||
| chr4:88379988 | AAT | A | 7 | a0001c0001t0001g0055 a0001c0001t0001g0151 a0001c0001t0001g0152 others(4): Show |
7 | HG02165.hp1 NA18939.hp2 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.199+878_199+879del others(2): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379988 | ||||||
| chr4:88379990 | T | A | 11 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(8): Show |
11 | HG03225.hp1 HG03688.hp1 HG03704.hp1 others(8): Show |
intron_variant | MODIFIER | c.199+870T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379990 | |||||||
| chr4:88379990 | T | TATATATA others(8): Show |
2 | a0001c0001t0001g0154 a0003c0016t0001g0171 |
2 | HG01978.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.199+877_199+878ins others(15): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379990 | ||||||
| chr4:88379990 | T | TATATATA others(59): Show |
2 | a0001c0001t0001g0159 a0003c0003t0001g0147 |
2 | HG02165.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.199+877_199+878ins others(66): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379990 | ||||||
| chr4:88379990 | T | TATATATA others(184): Show |
1 | a0012c0013t0001g0149 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.199+877_199+878ins others(191): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379990 | ||||||
| chr4:88379990 | T | TATATATA others(44): Show |
1 | a0001c0001t0001g0156 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.199+877_199+878ins others(51): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379990 | ||||||
| chr4:88379990 | T | TATATATA others(81): Show |
1 | a0002c0002t0001g0160 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.199+877_199+878ins others(88): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379990 | ||||||
| chr4:88379990 | T | TATATATA others(27): Show |
2 | a0002c0002t0001g0134 a0004c0004t0001g0161 |
2 | HG02300.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.199+877_199+878ins others(34): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379990 | ||||||
| chr4:88379990 | T | TATATATA others(82): Show |
1 | a0001c0001t0001g0077 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.199+877_199+878ins others(89): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379990 | ||||||
| chr4:88379990 | TATATATA others(10): Show |
T | 1 | a0002c0002t0001g0044 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.199+914_199+930del others(17): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88379990 | ||||||
| chr4:88379998 | T | A | 35 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(32): Show |
35 | HG00140.hp2 HG00639.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.199+878T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379998 | |||||||
| chr4:88379999 | A | T | 35 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(32): Show |
35 | HG00140.hp2 HG00639.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.199+879A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88379999 | |||||||
| chr4:88380001 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.199+881T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380001 | |||||||
| chr4:88380005 | T | A | 35 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(32): Show |
35 | HG00140.hp2 HG00639.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.199+885T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380005 | |||||||
| chr4:88380007 | A | AAT | 14 | a0001c0001t0001g0154 a0001c0001t0001g0156 a0001c0001t0001g0159 others(11): Show |
14 | HG01516.hp2 HG01978.hp2 HG02165.hp2 others(11): Show |
intron_variant | MODIFIER | c.199+895_199+896dup others(2): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380007 | ||||||
| chr4:88380007 | A | AATATATA others(12): Show |
3 | a0001c0019t0001g0063 a0002c0005t0001g0064 a0002c0005t0001g0068 |
3 | HG00639.hp2 HG01346.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.199+895_199+913dup others(19): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380007 | ||||||
| chr4:88380007 | A | AATATATA others(48): Show |
1 | a0001c0008t0001g0069 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.199+913_199+914ins others(55): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380007 | ||||||
| chr4:88380007 | A | T | 35 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(32): Show |
35 | HG00140.hp2 HG00639.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.199+887A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380007 | |||||||
| chr4:88380024 | A | AAT | 15 | a0001c0001t0001g0142 a0001c0001t0001g0172 a0001c0008t0001g0057 others(12): Show |
15 | HG00735.hp1 HG01167.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.199+912_199+913dup others(2): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380024 | ||||||
| chr4:88380026 | T | TATATATA others(10): Show |
1 | a0002c0005t0001g0059 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.199+913_199+914ins others(17): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380026 | ||||||
| chr4:88380034 | A | T | 8 | a0001c0001t0001g0004 a0001c0001t0001g0122 a0001c0001t0001g0123 others(5): Show |
8 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.199+914A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380034 | |||||||
| chr4:88380035 | T | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0122 a0001c0001t0001g0123 others(5): Show |
8 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.199+915T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380035 | |||||||
| chr4:88380041 | A | AATATATA others(152): Show |
1 | a0001c0008t0001g0061 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.199+930_199+931ins others(159): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380041 | ||||||
| chr4:88380041 | A | T | 8 | a0001c0001t0001g0004 a0001c0001t0001g0122 a0001c0001t0001g0123 others(5): Show |
8 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.199+921A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380041 | |||||||
| chr4:88380041 | AAT | A | 3 | a0001c0001t0001g0099 a0001c0001t0001g0150 a0006c0006t0001g0070 |
3 | HG03041.hp1 HG03704.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.199+931_199+932del others(2): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380041 | ||||||
| chr4:88380043 | T | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0122 a0001c0001t0001g0123 others(5): Show |
8 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.199+923T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380043 | |||||||
| chr4:88380043 | T | TATATATA others(8): Show |
2 | a0002c0002t0001g0135 a0004c0017t0001g0067 |
2 | HG03225.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.199+930_199+931ins others(15): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380043 | ||||||
| chr4:88380043 | T | TATATATA others(27): Show |
1 | a0004c0004t0001g0005 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.199+930_199+931ins others(34): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380043 | ||||||
| chr4:88380043 | T | TATATATA others(44): Show |
1 | a0001c0008t0001g0057 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.199+930_199+931ins others(51): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380043 | ||||||
| chr4:88380043 | T | TATATATA others(152): Show |
2 | a0001c0008t0001g0058 a0002c0005t0001g0060 |
2 | HG01496.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.199+930_199+931ins others(159): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380043 | ||||||
| chr4:88380043 | T | TATATATA others(150): Show |
1 | a0002c0005t0001g0062 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.199+930_199+931ins others(157): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380043 | ||||||
| chr4:88380045 | T | TATATAAT others(114): Show |
1 | a0001c0001t0001g0155 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.199+930_199+931ins others(121): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380045 | ||||||
| chr4:88380051 | T | A | 39 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0084 others(36): Show |
39 | HG00140.hp2 HG00639.hp1 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.199+931T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380051 | |||||||
| chr4:88380052 | A | T | 39 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0084 others(36): Show |
39 | HG00140.hp2 HG00639.hp1 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.199+932A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380052 | |||||||
| chr4:88380058 | T | A | 39 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0084 others(36): Show |
39 | HG00140.hp2 HG00639.hp1 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.199+938T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380058 | |||||||
| chr4:88380060 | A | AAT | 10 | a0001c0001t0001g0077 a0001c0001t0001g0155 a0001c0008t0001g0057 others(7): Show |
10 | HG01167.hp1 HG02258.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.199+948_199+949dup others(2): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380060 | ||||||
| chr4:88380060 | A | AATATATA others(12): Show |
1 | a0001c0001t0001g0118 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.199+948_199+966dup others(19): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380060 | ||||||
| chr4:88380060 | A | AATATATA others(29): Show |
1 | a0002c0002t0001g0043 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.199+984_199+1019du others(37): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380060 | ||||||
| chr4:88380060 | A | AATATATA others(65): Show |
5 | a0001c0001t0001g0055 a0001c0001t0001g0151 a0001c0001t0001g0152 others(2): Show |
5 | HG02165.hp1 NA18939.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.199+966_199+967ins others(72): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380060 | ||||||
| chr4:88380060 | A | AATATATA others(77): Show |
3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0004c0004t0001g0144 |
3 | HG02895.hp2 HG02897.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.199+949_199+950ins others(84): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380060 | ||||||
| chr4:88380060 | A | T | 40 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0084 others(37): Show |
40 | HG00140.hp2 HG00639.hp1 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.199+940A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380060 | |||||||
| chr4:88380077 | A | AAT | 18 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(15): Show |
18 | HG00735.hp1 HG01884.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.199+965_199+966dup others(2): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380077 | ||||||
| chr4:88380077 | A | AATATATA others(67): Show |
7 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0002c0002t0001g0080 others(4): Show |
7 | HG00280.hp2 HG00735.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.199+966_199+967ins others(74): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380077 | ||||||
| chr4:88380085 | T | TATAATAT others(68): Show |
1 | a0014c0018t0001g0066 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.199+966_199+967ins others(75): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380085 | ||||||
| chr4:88380087 | A | T | 2 | a0003c0003t0001g0158 a0006c0006t0001g0071 |
2 | HG03516.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.199+967A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380087 | |||||||
| chr4:88380088 | T | A | 2 | a0003c0003t0001g0158 a0006c0006t0001g0071 |
2 | HG03516.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.199+968T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380088 | |||||||
| chr4:88380092 | T | C | 1 | a0002c0002t0001g0104 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.199+972T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380092 | |||||||
| chr4:88380094 | A | T | 3 | a0003c0003t0001g0158 a0006c0006t0001g0071 a0007c0011t0001g0124 |
3 | HG01516.hp2 HG03516.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.199+974A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380094 | |||||||
| chr4:88380096 | T | A | 3 | a0003c0003t0001g0158 a0006c0006t0001g0071 a0007c0011t0001g0124 |
3 | HG01516.hp2 HG03516.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.199+976T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380096 | |||||||
| chr4:88380096 | T | TATATATA others(8): Show |
1 | a0007c0011t0001g0125 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.199+983_199+984ins others(15): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380096 | ||||||
| chr4:88380096 | T | TATATATA others(99): Show |
1 | a0007c0011t0001g0143 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.199+983_199+984ins others(106): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380096 | ||||||
| chr4:88380096 | T | TATATATA others(99): Show |
1 | a0012c0013t0001g0157 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.199+983_199+984ins others(106): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380096 | ||||||
| chr4:88380096 | T | TATATATA others(27): Show |
1 | a0002c0002t0001g0013 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.199+1020_199+1053d others(36): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380096 | ||||||
| chr4:88380096 | TATATATA others(10): Show |
T | 5 | a0001c0001t0001g0011 a0001c0001t0001g0038 a0001c0001t0001g0039 others(2): Show |
5 | HG01256.hp1 HG03654.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.199+1037_199+1053d others(19): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380096 | ||||||
| chr4:88380104 | T | A | 2 | a0001c0001t0001g0100 a0005c0007t0001g0003 |
2 | HG02647.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.199+984T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380104 | |||||||
| chr4:88380105 | A | T | 2 | a0001c0001t0001g0100 a0005c0007t0001g0003 |
2 | HG02647.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.199+985A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380105 | |||||||
| chr4:88380111 | T | A | 2 | a0001c0001t0001g0100 a0005c0007t0001g0003 |
2 | HG02647.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.199+991T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380111 | |||||||
| chr4:88380113 | A | AAT | 2 | a0002c0002t0001g0121 a0009c0010t0002g0006 |
2 | HG02257.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.199+1001_199+1002d others(4): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380113 | ||||||
| chr4:88380113 | A | AATATATA others(14): Show |
2 | a0001c0001t0003g0081 a0001c0001t0003g0082 |
2 | HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.199+1002_199+1003i others(23): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380113 | ||||||
| chr4:88380113 | A | T | 2 | a0001c0001t0001g0100 a0005c0007t0001g0003 |
2 | HG02647.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.199+993A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380113 | |||||||
| chr4:88380128 | T | A | 1 | a0009c0010t0002g0006 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.199+1008T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380128 | |||||||
| chr4:88380130 | A | AAT | 60 | a0001c0001t0001g0055 a0001c0001t0001g0065 a0001c0001t0001g0099 others(57): Show |
60 | HG00140.hp1 HG00639.hp2 HG01168.hp1 others(57): Show |
intron_variant | MODIFIER | c.199+1018_199+1019d others(4): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380130 | ||||||
| chr4:88380130 | A | T | 1 | a0009c0010t0002g0006 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.199+1010A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380130 | |||||||
| chr4:88380139 | A | C | 1 | a0013c0020t0001g0051 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.199+1019A>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380139 | |||||||
| chr4:88380140 | A | G | 3 | a0002c0002t0001g0040 a0002c0002t0001g0041 a0002c0002t0001g0042 |
3 | HG00323.hp2 HG01256.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.199+1020A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380140 | |||||||
| chr4:88380145 | T | A | 1 | a0002c0002t0001g0046 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.199+1025T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380145 | |||||||
| chr4:88380147 | A | AAT | 25 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(22): Show |
25 | HG00140.hp2 HG00639.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.199+1035_199+1036d others(4): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380147 | ||||||
| chr4:88380147 | A | T | 1 | a0004c0004t0001g0115 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.199+1027A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380147 | |||||||
| chr4:88380157 | A | T | 2 | a0004c0017t0001g0067 a0006c0006t0001g0070 |
2 | HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.199+1037A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380157 | |||||||
| chr4:88380158 | T | A | 2 | a0004c0017t0001g0067 a0006c0006t0001g0070 |
2 | HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.199+1038T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380158 | |||||||
| chr4:88380164 | A | T | 2 | a0004c0017t0001g0067 a0006c0006t0001g0070 |
2 | HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.199+1044A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380164 | |||||||
| chr4:88380164 | AAT | A | 9 | a0001c0001t0001g0099 a0001c0001t0001g0101 a0001c0001t0001g0102 others(6): Show |
9 | HG01257.hp1 HG01884.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.199+1054_199+1055d others(4): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380164 | ||||||
| chr4:88380166 | T | A | 1 | a0006c0006t0001g0070 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.199+1046T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380166 | |||||||
| chr4:88380174 | T | A | 10 | a0001c0008t0001g0057 a0001c0008t0001g0058 a0001c0008t0001g0061 others(7): Show |
10 | HG00140.hp1 HG00639.hp2 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.199+1054T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380174 | |||||||
| chr4:88380175 | A | AATATATA others(73): Show |
2 | a0001c0001t0003g0083 a0009c0010t0002g0119 |
2 | HG02559.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.199+1072_199+1073i others(82): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380175 | ||||||
| chr4:88380175 | A | AATATATA others(55): Show |
1 | a0001c0001t0001g0094 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.199+1072_199+1073i others(64): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380175 | ||||||
| chr4:88380177 | TATATAAA others(10): Show |
T | 1 | a0002c0002t0001g0036 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.199+1080_199+1096d others(19): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380177 | ||||||
| chr4:88380183 | A | AATATATA others(4): Show |
3 | a0007c0011t0001g0124 a0007c0011t0001g0125 a0007c0011t0001g0143 |
3 | HG01516.hp2 HG03942.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.199+1072_199+1073i others(13): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380183 | ||||||
| chr4:88380187 | T | TATATAAT others(6): Show |
1 | a0001c0001t0001g0172 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.199+1072_199+1073i others(15): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380187 | ||||||
| chr4:88380193 | T | A | 59 | a0001c0001t0001g0004 a0001c0001t0001g0055 a0001c0001t0001g0065 others(56): Show |
59 | HG00280.hp2 HG00735.hp2 HG01168.hp1 others(56): Show |
intron_variant | MODIFIER | c.199+1073T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380193 | |||||||
| chr4:88380194 | A | AAT | 12 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(9): Show |
12 | HG00735.hp1 HG01257.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.199+1078_199+1079d others(4): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380194 | ||||||
| chr4:88380194 | A | AATATATA others(80): Show |
1 | a0002c0005t0001g0068 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.199+1079_199+1080i others(89): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380194 | ||||||
| chr4:88380194 | A | AATATATA others(65): Show |
1 | a0001c0019t0001g0063 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.199+1079_199+1080i others(74): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380194 | ||||||
| chr4:88380194 | A | AATATATA others(82): Show |
3 | a0001c0008t0001g0058 a0002c0005t0001g0059 a0002c0005t0001g0060 |
3 | HG00140.hp1 HG01496.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.199+1079_199+1080i others(91): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380194 | ||||||
| chr4:88380194 | A | ATATAAAT others(189): Show |
1 | a0008c0009t0001g0074 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.199+1074_199+1075i others(198): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380194 | |||||||
| chr4:88380194 | A | T | 59 | a0001c0001t0001g0004 a0001c0001t0001g0055 a0001c0001t0001g0065 others(56): Show |
59 | HG00280.hp2 HG00735.hp2 HG01168.hp1 others(56): Show |
intron_variant | MODIFIER | c.199+1074A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380194 | |||||||
| chr4:88380198 | T | G | 1 | a0003c0003t0001g0158 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.199+1078T>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380198 | |||||||
| chr4:88380200 | A | T | 44 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(41): Show |
44 | HG00140.hp2 HG00639.hp1 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.199+1080A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380200 | |||||||
| chr4:88380202 | T | A | 41 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(38): Show |
41 | HG00140.hp2 HG00639.hp1 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.199+1082T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380202 | |||||||
| chr4:88380210 | T | A | 6 | a0001c0001t0001g0142 a0001c0008t0001g0057 a0001c0008t0001g0061 others(3): Show |
6 | HG01167.hp1 HG02735.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.199+1090T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380210 | |||||||
| chr4:88380211 | A | T | 2 | a0001c0001t0001g0142 a0009c0010t0002g0120 |
2 | HG03195.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.199+1091A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380211 | |||||||
| chr4:88380215 | T | TAA | 2 | a0001c0001t0001g0142 a0009c0010t0002g0120 |
2 | HG03195.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.199+1096_199+1097i others(4): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380215 | ||||||
| chr4:88380219 | A | AAT | 82 | a0001c0001t0001g0055 a0001c0001t0001g0065 a0001c0001t0001g0075 others(79): Show |
82 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.199+1105_199+1106d others(4): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380219 | ||||||
| chr4:88380219 | A | AATAT | 15 | a0001c0001t0001g0094 a0001c0001t0001g0099 a0001c0001t0001g0102 others(12): Show |
15 | HG01167.hp1 HG02559.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.199+1103_199+1106d others(6): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380219 | ||||||
| chr4:88380219 | A | AATATATA others(14): Show |
2 | a0001c0001t0001g0004 a0006c0006t0001g0073 |
2 | HG02809.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.199+1106_199+1107i others(23): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380219 | ||||||
| chr4:88380219 | A | AATATATA others(24): Show |
1 | a0002c0002t0001g0095 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.199+1106_199+1107i others(33): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380219 | ||||||
| chr4:88380219 | A | AATATATA others(43): Show |
1 | a0001c0001t0001g0123 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.199+1106_199+1107i others(52): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380219 | ||||||
| chr4:88380219 | A | AATATATA others(60): Show |
7 | a0001c0001t0001g0078 a0001c0001t0001g0122 a0001c0001t0003g0081 others(4): Show |
7 | HG00735.hp2 HG01192.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.199+1106_199+1107i others(69): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380219 | ||||||
| chr4:88380219 | A | AATATATA others(94): Show |
2 | a0002c0002t0001g0104 a0002c0002t0001g0114 |
2 | HG00280.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.199+1106_199+1107i others(103): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380219 | ||||||
| chr4:88380219 | A | AATATATA others(46): Show |
1 | a0004c0004t0001g0005 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.199+1106_199+1107i others(55): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380219 | ||||||
| chr4:88380219 | A | AATATATA others(317): Show |
1 | a0013c0020t0001g0051 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.199+1106_199+1107i others(326): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380219 | ||||||
| chr4:88380219 | A | AATATATA others(266): Show |
1 | a0006c0006t0001g0072 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.199+1106_199+1107i others(275): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380219 | ||||||
| chr4:88380219 | A | AATATATA others(341): Show |
1 | a0011c0012t0001g0052 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.199+1106_199+1107i others(350): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380219 | ||||||
| chr4:88380219 | A | AATATATA others(379): Show |
1 | a0008c0009t0001g0050 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.199+1106_199+1107i others(388): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380219 | ||||||
| chr4:88380219 | A | T | 6 | a0001c0001t0001g0142 a0002c0005t0001g0064 a0007c0011t0001g0124 others(3): Show |
6 | HG01516.hp2 HG03195.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.199+1099A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380219 | |||||||
| chr4:88380225 | T | A | 3 | a0007c0011t0001g0124 a0007c0011t0001g0125 a0007c0011t0001g0143 |
3 | HG01516.hp2 HG03942.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.199+1105T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380225 | |||||||
| chr4:88380227 | A | T | 1 | a0002c0002t0001g0098 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.199+1107A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380227 | |||||||
| chr4:88380228 | T | A | 1 | a0002c0002t0001g0098 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.199+1108T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380228 | |||||||
| chr4:88380234 | A | AAT | 30 | a0001c0001t0001g0065 a0001c0001t0001g0077 a0001c0001t0001g0131 others(27): Show |
30 | HG01168.hp1 HG01169.hp2 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.199+1122_199+1123d others(4): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380234 | ||||||
| chr4:88380234 | A | AATATATA others(27): Show |
1 | a0005c0007t0001g0003 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.199+1123_199+1124i others(36): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380234 | ||||||
| chr4:88380244 | ATAT | A | 3 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0006c0006t0001g0071 |
3 | HG01884.hp1 HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.199+1125_199+1127d others(5): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380244 | |||||||
| chr4:88380247 | T | A | 2 | a0001c0001t0001g0004 a0004c0004t0001g0005 |
2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.199+1127T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380247 | |||||||
| chr4:88380251 | A | AAT | 58 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(55): Show |
58 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.199+1137_199+1138d others(4): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380251 | ||||||
| chr4:88380251 | A | AATAT | 55 | a0001c0001t0001g0055 a0001c0001t0001g0084 a0001c0001t0001g0085 others(52): Show |
55 | HG00140.hp2 HG00639.hp1 HG01167.hp2 others(52): Show |
intron_variant | MODIFIER | c.199+1135_199+1138d others(6): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380251 | ||||||
| chr4:88380251 | A | AATATATA others(7): Show |
1 | a0009c0010t0002g0120 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.199+1138_199+1139i others(16): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380251 | ||||||
| chr4:88380251 | A | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0075 a0001c0001t0001g0076 others(2): Show |
5 | HG01884.hp1 HG02258.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.199+1131A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380251 | |||||||
| chr4:88380264 | T | A | 1 | a0001c0001t0001g0065 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.199+1144T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380264 | |||||||
| chr4:88380266 | A | AAT | 19 | a0001c0001t0001g0101 a0001c0001t0001g0116 a0001c0001t0001g0118 others(16): Show |
19 | HG01168.hp1 HG01169.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.199+1154_199+1155d others(4): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380266 | ||||||
| chr4:88380283 | A | AAT | 30 | a0001c0001t0001g0004 a0001c0001t0001g0065 a0001c0001t0001g0084 others(27): Show |
30 | HG00140.hp1 HG01167.hp2 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.199+1169_199+1170d others(4): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380283 | ||||||
| chr4:88380283 | A | AATAT | 26 | a0001c0001t0001g0088 a0001c0001t0001g0091 a0001c0001t0001g0097 others(23): Show |
26 | HG00140.hp2 HG00639.hp1 HG02257.hp2 others(23): Show |
intron_variant | MODIFIER | c.199+1167_199+1170d others(6): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380283 | ||||||
| chr4:88380283 | A | AATATATA others(106): Show |
1 | a0001c0001t0001g0172 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.199+1187_199+1188i others(115): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380283 | ||||||
| chr4:88380283 | A | T | 1 | a0001c0001t0001g0077 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.199+1163A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380283 | |||||||
| chr4:88380283 | AATATATA others(12): Show |
A | 1 | a0008c0009t0001g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.199+1214_199+1232d others(21): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380283 | ||||||
| chr4:88380289 | T | TATATAAT others(221): Show |
1 | a0001c0001t0001g0150 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.199+1170_199+1171i others(230): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380289 | ||||||
| chr4:88380290 | A | AT | 27 | a0001c0001t0001g0055 a0001c0001t0001g0099 a0001c0001t0001g0102 others(24): Show |
27 | HG01167.hp1 HG01257.hp1 HG01978.hp2 others(24): Show |
intron_variant | MODIFIER | c.199+1170_199+1171i others(3): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380290 | |||||||
| chr4:88380290 | A | ATAATATA others(5): Show |
1 | a0001c0001t0001g0116 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.199+1170_199+1171i others(14): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380290 | |||||||
| chr4:88380291 | A | T | 10 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0100 others(7): Show |
10 | HG00639.hp2 HG01168.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.199+1171A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380291 | |||||||
| chr4:88380292 | T | A | 10 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0100 others(7): Show |
10 | HG00639.hp2 HG01168.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.199+1172T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380292 | |||||||
| chr4:88380292 | T | TA | 27 | a0001c0001t0001g0055 a0001c0001t0001g0099 a0001c0001t0001g0102 others(24): Show |
27 | HG01167.hp1 HG01257.hp1 HG01978.hp2 others(24): Show |
intron_variant | MODIFIER | c.199+1173dupA | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380292 | ||||||
| chr4:88380298 | A | T | 36 | a0001c0001t0001g0055 a0001c0001t0001g0075 a0001c0001t0001g0076 others(33): Show |
36 | HG00639.hp2 HG01167.hp1 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.199+1178A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380298 | |||||||
| chr4:88380298 | AAT | A | 19 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0122 others(16): Show |
19 | HG00280.hp2 HG00735.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.199+1188_199+1189d others(4): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380298 | ||||||
| chr4:88380300 | T | A | 36 | a0001c0001t0001g0055 a0001c0001t0001g0075 a0001c0001t0001g0076 others(33): Show |
36 | HG00639.hp2 HG01167.hp1 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.199+1180T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380300 | |||||||
| chr4:88380300 | T | TATATATA others(8): Show |
2 | a0001c0008t0001g0061 a0002c0005t0001g0062 |
2 | HG02735.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.199+1187_199+1188i others(17): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380300 | ||||||
| chr4:88380302 | T | A | 1 | a0014c0018t0001g0066 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.199+1182T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380302 | |||||||
| chr4:88380302 | T | TATA | 2 | a0001c0001t0001g0004 a0001c0001t0001g0065 |
2 | HG02809.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.199+1183_199+1185d others(5): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380302 | ||||||
| chr4:88380302 | T | TATATA | 22 | a0001c0001t0001g0088 a0001c0001t0001g0091 a0001c0001t0001g0097 others(19): Show |
22 | HG00140.hp2 HG00639.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.199+1183_199+1187d others(7): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380302 | ||||||
| chr4:88380307 | A | AATATAT | 4 | a0001c0001t0001g0094 a0004c0004t0001g0005 a0005c0007t0001g0003 others(1): Show |
4 | HG02647.hp2 HG02723.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.199+1187_199+1188i others(8): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380307 | |||||||
| chr4:88380308 | T | A | 7 | a0001c0001t0001g0094 a0004c0004t0001g0005 a0005c0007t0001g0003 others(4): Show |
7 | HG01516.hp2 HG02647.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.199+1188T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380308 | |||||||
| chr4:88380309 | A | AAAT | 24 | a0001c0001t0001g0004 a0001c0001t0001g0065 a0001c0001t0001g0088 others(21): Show |
24 | HG00140.hp2 HG00639.hp1 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.199+1190_199+1191i others(5): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380309 | ||||||
| chr4:88380309 | A | T | 3 | a0007c0011t0001g0124 a0007c0011t0001g0125 a0007c0011t0001g0143 |
3 | HG01516.hp2 HG03942.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.199+1189A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380309 | |||||||
| chr4:88380311 | T | A | 2 | a0006c0006t0001g0072 a0006c0006t0001g0073 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.199+1191T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380311 | |||||||
| chr4:88380315 | T | A | 3 | a0007c0011t0001g0124 a0007c0011t0001g0125 a0007c0011t0001g0143 |
3 | HG01516.hp2 HG03942.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.199+1195T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380315 | |||||||
| chr4:88380316 | A | ATATAT | 3 | a0007c0011t0001g0124 a0007c0011t0001g0125 a0007c0011t0001g0143 |
3 | HG01516.hp2 HG03942.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.199+1196_199+1197i others(7): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380316 | |||||||
| chr4:88380317 | A | ATAT | 2 | a0001c0001t0001g0004 a0001c0001t0001g0065 |
2 | HG02809.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.199+1197_199+1198i others(5): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380317 | |||||||
| chr4:88380317 | A | ATATAT | 4 | a0001c0001t0001g0094 a0004c0004t0001g0005 a0005c0007t0001g0003 others(1): Show |
4 | HG02647.hp2 HG02723.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.199+1197_199+1198i others(7): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380317 | |||||||
| chr4:88380317 | A | T | 2 | a0006c0006t0001g0072 a0006c0006t0001g0073 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.199+1197A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380317 | |||||||
| chr4:88380317 | AAT | A | 23 | a0001c0001t0001g0116 a0001c0001t0001g0118 a0001c0001t0001g0131 others(20): Show |
23 | HG01167.hp1 HG01496.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.199+1207_199+1208d others(4): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380317 | ||||||
| chr4:88380317 | AATAT | A | 13 | a0001c0001t0001g0078 a0001c0001t0001g0122 a0001c0001t0001g0123 others(10): Show |
13 | HG00280.hp2 HG00735.hp2 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.199+1205_199+1208d others(6): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380317 | ||||||
| chr4:88380319 | T | A | 6 | a0001c0001t0001g0094 a0004c0004t0001g0005 a0005c0007t0001g0003 others(3): Show |
6 | HG02647.hp2 HG02723.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.199+1199T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380319 | |||||||
| chr4:88380319 | T | TATATAAT others(6): Show |
2 | a0001c0001t0001g0075 a0001c0001t0001g0076 |
2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.199+1204_199+1205i others(15): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380319 | ||||||
| chr4:88380319 | T | TATATATA others(59): Show |
1 | a0002c0005t0001g0064 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.199+1206_199+1207i others(68): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380319 | ||||||
| chr4:88380321 | T | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0065 |
2 | HG02809.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.199+1201T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380321 | |||||||
| chr4:88380321 | T | TATATA | 6 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.199+1202_199+1206d others(7): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380321 | ||||||
| chr4:88380321 | T | TATATAAT others(40): Show |
4 | a0001c0008t0001g0058 a0001c0019t0001g0063 a0002c0005t0001g0059 others(1): Show |
4 | HG00140.hp1 HG01346.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.199+1206_199+1207i others(49): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380321 | ||||||
| chr4:88380328 | A | AAAT | 6 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.199+1209_199+1210i others(5): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380328 | ||||||
| chr4:88380336 | A | AAT | 2 | a0006c0006t0001g0072 a0006c0006t0001g0073 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.199+1226_199+1227d others(4): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380336 | ||||||
| chr4:88380336 | AAT | A | 4 | a0001c0001t0001g0004 a0002c0005t0001g0068 a0004c0017t0001g0067 others(1): Show |
4 | HG00639.hp2 HG02647.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.199+1226_199+1227d others(4): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380336 | ||||||
| chr4:88380342 | T | A | 1 | a0001c0001t0001g0116 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.199+1222T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380342 | |||||||
| chr4:88380346 | T | A | 76 | a0001c0001t0001g0055 a0001c0001t0001g0065 a0001c0001t0001g0075 others(73): Show |
76 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.199+1226T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380346 | |||||||
| chr4:88380347 | A | AATATAAA others(12): Show |
1 | a0003c0003t0001g0014 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.199+1245_199+1263d others(21): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380347 | ||||||
| chr4:88380347 | A | T | 76 | a0001c0001t0001g0055 a0001c0001t0001g0065 a0001c0001t0001g0075 others(73): Show |
76 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.199+1227A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380347 | |||||||
| chr4:88380353 | A | T | 35 | a0001c0001t0001g0004 a0001c0001t0001g0084 a0001c0001t0001g0085 others(32): Show |
35 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.199+1233A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380353 | |||||||
| chr4:88380353 | AATATATA others(14): Show |
A | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0004c0004t0001g0144 |
3 | HG02895.hp2 HG02897.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.199+1287_199+1307d others(23): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380353 | ||||||
| chr4:88380355 | T | A | 35 | a0001c0001t0001g0004 a0001c0001t0001g0084 a0001c0001t0001g0085 others(32): Show |
35 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.199+1235T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380355 | |||||||
| chr4:88380365 | A | T | 3 | a0007c0011t0001g0124 a0007c0011t0001g0125 a0013c0020t0001g0051 |
3 | HG00735.hp1 HG01516.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.199+1245A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380365 | |||||||
| chr4:88380366 | T | A | 3 | a0007c0011t0001g0124 a0007c0011t0001g0125 a0013c0020t0001g0051 |
3 | HG00735.hp1 HG01516.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.199+1246T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380366 | |||||||
| chr4:88380368 | TATAA | T | 23 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0078 others(20): Show |
23 | HG00140.hp1 HG00280.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.199+1252_199+1255d others(6): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380368 | ||||||
| chr4:88380372 | AAT | A | 7 | a0001c0001t0001g0004 a0004c0004t0001g0005 a0005c0007t0001g0003 others(4): Show |
7 | HG00735.hp1 HG01516.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.199+1264_199+1265d others(4): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380372 | ||||||
| chr4:88380374 | T | A | 23 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0078 others(20): Show |
23 | HG00140.hp1 HG00280.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.199+1254T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380374 | |||||||
| chr4:88380374 | T | TATATATA others(188): Show |
1 | a0001c0001t0001g0118 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.199+1261_199+1262i others(197): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380374 | ||||||
| chr4:88380374 | T | TATATATA others(89): Show |
2 | a0001c0001t0001g0116 a0005c0007t0001g0092 |
2 | HG00639.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.199+1261_199+1262i others(98): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380374 | ||||||
| chr4:88380374 | T | TATATATA others(57): Show |
2 | a0002c0005t0001g0068 a0004c0017t0001g0067 |
2 | HG00639.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.199+1261_199+1262i others(66): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380374 | ||||||
| chr4:88380374 | T | TATATATA others(205): Show |
3 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0002c0002t0001g0103 |
3 | HG03704.hp2 NA18612.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.199+1261_199+1262i others(214): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380374 | ||||||
| chr4:88380374 | T | TATATATA others(106): Show |
2 | a0002c0002t0001g0105 a0005c0007t0001g0093 |
2 | HG00140.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.199+1261_199+1262i others(115): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380374 | ||||||
| chr4:88380374 | T | TATATATA others(57): Show |
1 | a0002c0005t0001g0064 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.199+1261_199+1262i others(66): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380374 | ||||||
| chr4:88380374 | T | TATATATA others(123): Show |
14 | a0001c0001t0001g0088 a0001c0001t0001g0097 a0001c0001t0001g0106 others(11): Show |
14 | HG02257.hp2 HG02451.hp1 HG02735.hp2 others(11): Show |
intron_variant | MODIFIER | c.199+1261_199+1262i others(132): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380374 | ||||||
| chr4:88380374 | T | TATATATA others(106): Show |
5 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0002c0002t0001g0110 others(2): Show |
5 | NA18612.hp2 NA18747.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.199+1261_199+1262i others(115): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380374 | ||||||
| chr4:88380374 | T | TATATATA others(108): Show |
1 | a0001c0001t0001g0077 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.199+1261_199+1262i others(117): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380374 | ||||||
| chr4:88380374 | T | TATATATA others(91): Show |
4 | a0001c0001t0001g0091 a0001c0008t0001g0057 a0001c0008t0001g0061 others(1): Show |
4 | HG01167.hp1 HG02735.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.199+1261_199+1262i others(100): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380374 | ||||||
| chr4:88380374 | T | TATATATA others(159): Show |
1 | a0001c0001t0001g0099 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.199+1261_199+1262i others(168): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380374 | ||||||
| chr4:88380374 | T | TATATATA others(241): Show |
1 | a0001c0001t0001g0131 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.199+1261_199+1262i others(250): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380374 | ||||||
| chr4:88380374 | T | TATATATA others(385): Show |
1 | a0001c0001t0001g0142 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.199+1261_199+1262i others(394): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380374 | ||||||
| chr4:88380374 | T | TATATATA others(421): Show |
1 | a0001c0001t0001g0139 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.199+1261_199+1262i others(430): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380374 | ||||||
| chr4:88380374 | T | TATATATA others(8): Show |
4 | a0001c0001t0001g0065 a0001c0001t0001g0172 a0007c0011t0001g0143 others(1): Show |
4 | HG01891.hp1 HG02895.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.199+1263_199+1264i others(17): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380374 | ||||||
| chr4:88380374 | T | TATATATA others(142): Show |
4 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.199+1263_199+1264i others(151): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380374 | ||||||
| chr4:88380374 | T | TATATATA others(110): Show |
1 | a0001c0001t0001g0101 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.199+1263_199+1264i others(119): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380374 | ||||||
| chr4:88380374 | T | TATATATA others(141): Show |
1 | a0002c0002t0001g0098 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.199+1263_199+1264i others(150): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380374 | ||||||
| chr4:88380374 | T | TATATATA others(260): Show |
1 | a0002c0002t0001g0134 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.199+1263_199+1264i others(269): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380374 | ||||||
| chr4:88380374 | T | TATATATA others(332): Show |
1 | a0002c0002t0001g0130 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.199+1263_199+1264i others(341): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380374 | ||||||
| chr4:88380374 | T | TATATATA others(368): Show |
2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | HG02132.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.199+1263_199+1264i others(377): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380374 | ||||||
| chr4:88380374 | T | TATATATA others(402): Show |
1 | a0003c0021t0001g0128 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.199+1263_199+1264i others(411): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380374 | ||||||
| chr4:88380374 | T | TATATATA others(476): Show |
5 | a0002c0002t0001g0132 a0002c0002t0001g0133 a0002c0002t0001g0135 others(2): Show |
5 | NA18951.hp2 NA18959.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.199+1263_199+1264i others(485): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380374 | ||||||
| chr4:88380374 | T | TATATATA others(584): Show |
1 | a0002c0002t0001g0136 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.199+1263_199+1264i others(593): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380374 | ||||||
| chr4:88380374 | T | TATATATA others(347): Show |
1 | a0011c0012t0001g0053 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.199+1263_199+1264i others(356): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380374 | ||||||
| chr4:88380374 | T | TATATATA others(405): Show |
1 | a0004c0004t0001g0129 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.199+1263_199+1264i others(414): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380374 | ||||||
| chr4:88380376 | T | TATAAATA others(97): Show |
9 | a0001c0001t0001g0055 a0001c0001t0001g0151 a0001c0001t0001g0152 others(6): Show |
9 | HG01257.hp1 HG02165.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.199+1259_199+1260i others(106): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380376 | ||||||
| chr4:88380376 | T | TATATAAT others(137): Show |
1 | a0001c0001t0001g0169 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.199+1261_199+1262i others(146): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380376 | ||||||
| chr4:88380376 | T | TATATAAT others(133): Show |
6 | a0001c0001t0001g0156 a0001c0001t0001g0167 a0001c0001t0001g0168 others(3): Show |
6 | HG01978.hp2 HG02451.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.199+1261_199+1262i others(142): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380376 | ||||||
| chr4:88380376 | T | TATATAAT others(152): Show |
1 | a0001c0001t0001g0154 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.199+1261_199+1262i others(161): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380376 | ||||||
| chr4:88380376 | T | TATATAAT others(169): Show |
4 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(1): Show |
4 | HG01168.hp1 HG01169.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.199+1261_199+1262i others(178): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380376 | ||||||
| chr4:88380376 | T | TATATAAT others(106): Show |
1 | a0002c0002t0001g0170 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.199+1261_199+1262i others(115): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380376 | ||||||
| chr4:88380376 | T | TATATATA others(6): Show |
1 | a0001c0001t0001g0150 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.199+1263_199+1264i others(15): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380376 | ||||||
| chr4:88380376 | T | TATATATA others(152): Show |
3 | a0001c0001t0001g0159 a0003c0003t0001g0158 a0012c0013t0001g0157 |
3 | HG03225.hp1 NA18999.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.199+1263_199+1264i others(161): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380376 | ||||||
| chr4:88380377 | ATATATAT others(13): Show |
A | 1 | a0014c0018t0001g0066 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.199+1258_199+1277d others(22): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380377 | |||||||
| chr4:88380383 | ATAATATA others(13): Show |
A | 1 | a0011c0012t0001g0052 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.199+1264_199+1283d others(22): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380383 | |||||||
| chr4:88380392 | AAATATAT others(13): Show |
A | 1 | a0008c0009t0001g0050 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.199+1275_199+1294d others(22): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380392 | ||||||
| chr4:88380393 | AAT | A | 2 | a0004c0004t0001g0010 a0008c0009t0001g0074 |
2 | NA18906.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.199+1285_199+1286d others(4): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380393 | ||||||
| chr4:88380397 | TATATATA others(10): Show |
T | 1 | a0001c0001t0001g0094 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.199+1287_199+1303d others(19): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88380397 | ||||||
| chr4:88380412 | T | G | 1 | a0001c0001t0001g0150 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.199+1292T>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380412 | |||||||
| chr4:88380431 | A | G | 3 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 |
3 | HG01884.hp1 HG02258.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.199+1311A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380431 | |||||||
| chr4:88380496 | A | C | 1 | a0008c0009t0001g0050 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.199+1376A>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380496 | |||||||
| chr4:88380522 | C | T | 125 | a0001c0001t0001g0004 a0001c0001t0001g0055 a0001c0001t0001g0065 others(122): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.199+1402C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380522 | |||||||
| chr4:88380632 | G | C | 1 | a0002c0002t0001g0165 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.199+1512G>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380632 | |||||||
| chr4:88380646 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.199+1526G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380646 | |||||||
| chr4:88380791 | A | G | 1 | a0002c0002t0001g0165 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.199+1671A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380791 | |||||||
| chr4:88380794 | C | G | 26 | a0001c0001t0001g0055 a0001c0001t0001g0150 a0001c0001t0001g0151 others(23): Show |
26 | HG01168.hp1 HG01169.hp2 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.199+1674C>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380794 | |||||||
| chr4:88380794 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.199+1674C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380794 | |||||||
| chr4:88380949 | A | G | 1 | a0002c0002t0001g0127 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.199+1829A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88380949 | |||||||
| chr4:88381231 | C | A | 1 | a0004c0004t0001g0144 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.200-1990C>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88381231 | |||||||
| chr4:88381231 | C | T | 2 | a0004c0004t0001g0005 a0009c0010t0002g0006 |
2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.200-1990C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88381231 | |||||||
| chr4:88381234 | C | T | 1 | a0004c0004t0001g0144 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.200-1987C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88381234 | |||||||
| chr4:88381554 | C | CT | 5 | a0001c0001t0001g0009 a0003c0003t0001g0035 a0003c0003t0001g0048 others(2): Show |
5 | HG03516.hp2 HG03688.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.200-1645dupT | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88381554 | ||||||
| chr4:88381554 | CT | C | 35 | a0001c0001t0001g0004 a0001c0001t0001g0055 a0001c0001t0001g0101 others(32): Show |
35 | HG00323.hp2 HG01168.hp1 HG01169.hp2 others(32): Show |
intron_variant | MODIFIER | c.200-1645delT | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88381554 | ||||||
| chr4:88381554 | CTT | C | 81 | a0001c0001t0001g0065 a0001c0001t0001g0075 a0001c0001t0001g0076 others(78): Show |
81 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.200-1646_200-1645d others(4): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88381554 | ||||||
| chr4:88381554 | CTTT | C | 9 | a0001c0001t0001g0084 a0001c0008t0001g0057 a0002c0005t0001g0060 others(6): Show |
9 | HG00639.hp1 HG01167.hp1 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.200-1647_200-1645d others(5): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88381554 | ||||||
| chr4:88381660 | C | T | 13 | a0001c0001t0001g0091 a0001c0001t0001g0094 a0001c0001t0001g0097 others(10): Show |
13 | HG02257.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.200-1561C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88381660 | |||||||
| chr4:88381667 | T | G | 1 | a0007c0011t0001g0124 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.200-1554T>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88381667 | |||||||
| chr4:88381791 | C | T | 7 | a0006c0006t0001g0072 a0006c0006t0001g0073 a0008c0009t0001g0050 others(4): Show |
7 | HG00735.hp1 HG02258.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.200-1430C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88381791 | |||||||
| chr4:88381906 | T | C | 1 | a0002c0005t0001g0060 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.200-1315T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88381906 | |||||||
| chr4:88381953 | A | C | 3 | a0007c0011t0001g0124 a0007c0011t0001g0125 a0007c0011t0001g0143 |
3 | HG01516.hp2 HG03942.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.200-1268A>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88381953 | |||||||
| chr4:88382575 | C | T | 1 | a0004c0004t0001g0005 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.200-646C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88382575 | |||||||
| chr4:88382707 | G | C | 1 | a0004c0004t0001g0005 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.200-514G>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88382707 | |||||||
| chr4:88383110 | G | C | 4 | a0001c0001t0001g0004 a0004c0004t0001g0005 a0005c0007t0001g0003 others(1): Show |
4 | HG02647.hp2 HG02809.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.200-111G>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88383110 | |||||||
| chr4:88383190 | G | T | 1 | a0002c0002t0001g0166 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.200-31G>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88383190 | |||||||
| chr4:88383198 | G | A | 1 | a0007c0011t0001g0143 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.200-23G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 1/22 | chr4 | 88383198 | |||||||
| chr4:88383405 | A | G | 1 | a0005c0007t0001g0003 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.359+25A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 2/22 | chr4 | 88383405 | |||||||
| chr4:88383515 | T | C | 1 | a0008c0009t0001g0074 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.359+135T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 2/22 | chr4 | 88383515 | |||||||
| chr4:88383526 | A | G | 12 | a0001c0008t0001g0057 a0001c0008t0001g0058 a0001c0008t0001g0061 others(9): Show |
12 | HG00140.hp1 HG00639.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.359+146A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 2/22 | chr4 | 88383526 | |||||||
| chr4:88383620 | G | A | 49 | a0001c0001t0001g0078 a0001c0001t0001g0084 a0001c0001t0001g0085 others(46): Show |
49 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.359+240G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 2/22 | chr4 | 88383620 | |||||||
| chr4:88383697 | A | G | 1 | a0002c0002t0001g0134 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.359+317A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 2/22 | chr4 | 88383697 | |||||||
| chr4:88383720 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.359+340C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 2/22 | chr4 | 88383720 | |||||||
| chr4:88383724 | A | G | 25 | a0001c0001t0001g0055 a0001c0001t0001g0150 a0001c0001t0001g0151 others(22): Show |
25 | HG01168.hp1 HG01169.hp2 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.359+344A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 2/22 | chr4 | 88383724 | |||||||
| chr4:88383763 | C | CA | 13 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0017 others(10): Show |
13 | HG00280.hp1 HG00735.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.359+413dupA | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr4 | 88383763 | ||||||
| chr4:88383763 | C | CAA | 7 | a0001c0019t0001g0063 a0002c0005t0001g0060 a0002c0005t0001g0062 others(4): Show |
7 | HG00639.hp2 HG01346.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.359+412_359+413dup others(2): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr4 | 88383763 | ||||||
| chr4:88383763 | CA | C | 57 | a0001c0001t0001g0034 a0001c0001t0001g0084 a0001c0001t0001g0085 others(54): Show |
57 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.359+413delA | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr4 | 88383763 | ||||||
| chr4:88383763 | CAA | C | 18 | a0001c0001t0001g0055 a0001c0001t0001g0065 a0001c0001t0001g0100 others(15): Show |
18 | HG01516.hp2 HG02132.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.359+412_359+413del others(2): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr4 | 88383763 | ||||||
| chr4:88383763 | CAAA | C | 11 | a0001c0001t0001g0131 a0001c0001t0001g0139 a0001c0001t0001g0140 others(8): Show |
11 | HG01496.hp1 HG02040.hp1 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.359+411_359+413del others(3): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr4 | 88383763 | ||||||
| chr4:88383763 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0004 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.359+402_359+413del others(12): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr4 | 88383763 | ||||||
| chr4:88383910 | A | G | 25 | a0001c0001t0001g0055 a0001c0001t0001g0150 a0001c0001t0001g0151 others(22): Show |
25 | HG01168.hp1 HG01169.hp2 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.359+530A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 2/22 | chr4 | 88383910 | |||||||
| chr4:88383924 | A | C | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0004c0004t0001g0144 |
3 | HG02895.hp2 HG02897.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.359+544A>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 2/22 | chr4 | 88383924 | |||||||
| chr4:88384077 | A | C | 1 | a0002c0002t0001g0170 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.359+697A>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 2/22 | chr4 | 88384077 | |||||||
| chr4:88384116 | G | A | 4 | a0008c0009t0001g0050 a0011c0012t0001g0052 a0011c0012t0001g0053 others(1): Show |
4 | HG00735.hp1 HG02258.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.359+736G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 2/22 | chr4 | 88384116 | |||||||
| chr4:88384132 | T | C | 12 | a0001c0008t0001g0057 a0001c0008t0001g0058 a0001c0008t0001g0061 others(9): Show |
12 | HG00140.hp1 HG00639.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.359+752T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 2/22 | chr4 | 88384132 | |||||||
| chr4:88384333 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.359+953C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 2/22 | chr4 | 88384333 | |||||||
| chr4:88384879 | C | G | 4 | a0008c0009t0001g0050 a0011c0012t0001g0052 a0011c0012t0001g0053 others(1): Show |
4 | HG00735.hp1 HG02258.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.360-620C>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 2/22 | chr4 | 88384879 | |||||||
| chr4:88384880 | G | A | 3 | a0002c0002t0001g0107 a0006c0006t0001g0072 a0006c0006t0001g0073 |
3 | HG02896.hp1 HG02897.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.360-619G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 2/22 | chr4 | 88384880 | |||||||
| chr4:88384929 | A | T | 49 | a0001c0001t0001g0078 a0001c0001t0001g0084 a0001c0001t0001g0085 others(46): Show |
49 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.360-570A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 2/22 | chr4 | 88384929 | |||||||
| chr4:88384977 | C | T | 1 | a0002c0002t0001g0033 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.360-522C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 2/22 | chr4 | 88384977 | |||||||
| chr4:88385024 | GA | G | 65 | a0001c0001t0001g0055 a0001c0001t0001g0131 a0001c0001t0001g0139 others(62): Show |
65 | HG00140.hp1 HG00639.hp2 HG01167.hp1 others(62): Show |
intron_variant | MODIFIER | c.360-464delA | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr4 | 88385024 | ||||||
| chr4:88385354 | A | G | 168 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(165): Show |
170 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.360-145A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 2/22 | chr4 | 88385354 | |||||||
| chr4:88385359 | A | C | 15 | a0001c0001t0001g0131 a0001c0001t0001g0139 a0001c0001t0001g0140 others(12): Show |
15 | HG01496.hp1 HG02040.hp1 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.360-140A>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 2/22 | chr4 | 88385359 | |||||||
| chr4:88385971 | A | T | 1 | a0002c0002t0001g0160 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.436+396A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | chr4 | 88385971 | |||||||
| chr4:88386199 | C | CT | 6 | a0001c0001t0001g0031 a0001c0001t0001g0056 a0001c0001t0001g0145 others(3): Show |
6 | HG02895.hp2 HG02897.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.436+641dupT | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 88386199 | ||||||
| chr4:88386199 | CT | C | 7 | a0001c0001t0001g0106 a0001c0001t0001g0163 a0002c0002t0001g0108 others(4): Show |
7 | HG01168.hp1 HG02257.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.436+641delT | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 88386199 | ||||||
| chr4:88386204 | T | C | 1 | a0008c0009t0001g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.436+629T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | chr4 | 88386204 | |||||||
| chr4:88386336 | G | A | 3 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0002c0002t0001g0046 |
3 | NA18747.hp1 NA18951.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.436+761G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | chr4 | 88386336 | |||||||
| chr4:88386372 | A | T | 39 | a0001c0001t0001g0055 a0001c0001t0001g0131 a0001c0001t0001g0139 others(36): Show |
39 | HG01168.hp1 HG01169.hp2 HG01257.hp1 others(36): Show |
intron_variant | MODIFIER | c.436+797A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | chr4 | 88386372 | |||||||
| chr4:88386405 | T | C | 2 | a0006c0006t0001g0070 a0006c0006t0001g0071 |
2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.436+830T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | chr4 | 88386405 | |||||||
| chr4:88386506 | C | T | 4 | a0001c0001t0001g0004 a0004c0004t0001g0005 a0005c0007t0001g0003 others(1): Show |
4 | HG02647.hp2 HG02809.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.436+931C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | chr4 | 88386506 | |||||||
| chr4:88386639 | T | A | 7 | a0006c0006t0001g0072 a0006c0006t0001g0073 a0008c0009t0001g0050 others(4): Show |
7 | HG00735.hp1 HG02258.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.436+1064T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | chr4 | 88386639 | |||||||
| chr4:88386639 | T | G | 1 | a0002c0002t0001g0160 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.436+1064T>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | chr4 | 88386639 | |||||||
| chr4:88386706 | G | A | 1 | a0001c0001t0001g0151 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.436+1131G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | chr4 | 88386706 | |||||||
| chr4:88387119 | G | A | 1 | a0013c0020t0001g0051 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.436+1544G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | chr4 | 88387119 | |||||||
| chr4:88387185 | C | G | 1 | a0008c0009t0001g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.436+1610C>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | chr4 | 88387185 | |||||||
| chr4:88387194 | T | A | 4 | a0002c0002t0001g0037 a0007c0011t0001g0124 a0007c0011t0001g0125 others(1): Show |
4 | HG01256.hp1 HG01516.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.436+1619T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | chr4 | 88387194 | |||||||
| chr4:88387438 | T | C | 1 | a0008c0009t0001g0074 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.436+1863T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | chr4 | 88387438 | |||||||
| chr4:88387463 | A | G | 1 | a0004c0017t0001g0067 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.436+1888A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | chr4 | 88387463 | |||||||
| chr4:88387574 | C | T | 1 | a0004c0004t0001g0129 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.436+1999C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | chr4 | 88387574 | |||||||
| chr4:88387673 | T | C | 2 | a0006c0006t0001g0032 a0008c0009t0001g0047 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.436+2098T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | chr4 | 88387673 | |||||||
| chr4:88387955 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.436+2380A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | chr4 | 88387955 | |||||||
| chr4:88388138 | AT | A | 24 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(21): Show |
24 | HG00639.hp1 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.437-2504delT | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 88388138 | ||||||
| chr4:88388220 | G | A | 2 | a0006c0006t0001g0032 a0008c0009t0001g0047 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.437-2432G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | chr4 | 88388220 | |||||||
| chr4:88388278 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.437-2374C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | chr4 | 88388278 | |||||||
| chr4:88388359 | T | C | 10 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(7): Show |
10 | HG00735.hp1 HG01884.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.437-2293T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | chr4 | 88388359 | |||||||
| chr4:88388407 | C | T | 14 | a0001c0019t0001g0063 a0002c0002t0001g0132 a0002c0002t0001g0133 others(11): Show |
14 | HG00140.hp1 HG00639.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.437-2245C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | chr4 | 88388407 | |||||||
| chr4:88388446 | G | A | 1 | a0002c0002t0001g0036 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.437-2206G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | chr4 | 88388446 | |||||||
| chr4:88388481 | G | A | 37 | a0001c0001t0001g0012 a0001c0001t0001g0055 a0001c0001t0001g0078 others(34): Show |
37 | HG00735.hp2 HG01071.hp1 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.437-2171G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | chr4 | 88388481 | |||||||
| chr4:88388482 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.437-2170C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | chr4 | 88388482 | |||||||
| chr4:88388512 | T | A | 2 | a0006c0006t0001g0072 a0006c0006t0001g0073 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.437-2140T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | chr4 | 88388512 | |||||||
| chr4:88388549 | CA | C | 26 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(23): Show |
26 | HG00639.hp1 HG01169.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.437-2083delA | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 88388549 | ||||||
| chr4:88388549 | CAAA | C | 22 | a0001c0001t0001g0088 a0001c0001t0001g0145 a0001c0001t0001g0146 others(19): Show |
22 | HG00140.hp1 HG00639.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.437-2085_437-2083d others(5): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 88388549 | ||||||
| chr4:88388549 | CAAAA | C | 34 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0055 others(31): Show |
34 | HG00735.hp1 HG01071.hp1 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.437-2086_437-2083d others(6): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 88388549 | ||||||
| chr4:88388549 | CAAAAA | C | 16 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(13): Show |
16 | HG00735.hp2 HG01192.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.437-2087_437-2083d others(7): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 88388549 | ||||||
| chr4:88389215 | A | G | 8 | a0001c0001t0001g0017 a0001c0001t0001g0078 a0001c0008t0001g0058 others(5): Show |
8 | HG00735.hp2 HG01516.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.437-1437A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | chr4 | 88389215 | |||||||
| chr4:88389235 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.437-1417G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | chr4 | 88389235 | |||||||
| chr4:88389601 | G | C | 2 | a0001c0001t0001g0019 a0001c0001t0001g0034 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.437-1051G>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | chr4 | 88389601 | |||||||
| chr4:88389684 | C | T | 24 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0027 others(21): Show |
26 | HG01168.hp1 HG01169.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.437-968C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | chr4 | 88389684 | |||||||
| chr4:88389707 | TC | T | 49 | a0001c0001t0001g0009 a0001c0001t0001g0038 a0001c0001t0001g0065 others(46): Show |
49 | HG00280.hp2 HG00323.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.437-944delC | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | chr4 | 88389707 | |||||||
| chr4:88389715 | T | G | 2 | a0001c0001t0001g0156 a0002c0005t0001g0064 |
2 | NA19004.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.437-937T>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | chr4 | 88389715 | |||||||
| chr4:88389748 | T | C | 25 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0022 others(22): Show |
25 | HG00735.hp2 HG01071.hp1 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.437-904T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | chr4 | 88389748 | |||||||
| chr4:88389829 | G | A | 1 | a0001c0008t0001g0069 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.437-823G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | chr4 | 88389829 | |||||||
| chr4:88389880 | G | A | 62 | a0001c0001t0001g0017 a0001c0001t0001g0031 a0001c0001t0001g0039 others(59): Show |
62 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.437-772G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | chr4 | 88389880 | |||||||
| chr4:88390177 | C | A | 1 | a0009c0010t0002g0119 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.437-475C>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | chr4 | 88390177 | |||||||
| chr4:88390177 | C | CA | 25 | a0001c0001t0001g0009 a0001c0001t0001g0065 a0001c0001t0001g0075 others(22): Show |
25 | HG01168.hp1 HG01169.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.437-451dupA | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 88390177 | ||||||
| chr4:88390177 | C | CAA | 37 | a0001c0001t0001g0031 a0001c0001t0001g0039 a0002c0002t0001g0007 others(34): Show |
37 | HG00140.hp2 HG00280.hp1 HG01256.hp2 others(34): Show |
intron_variant | MODIFIER | c.437-452_437-451dup others(2): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 88390177 | ||||||
| chr4:88390177 | CA | C | 26 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0015 others(23): Show |
26 | HG01071.hp1 HG01071.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.437-451delA | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | 88390177 | ||||||
| chr4:88390194 | A | G | 1 | a0002c0002t0001g0095 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.437-458A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | chr4 | 88390194 | |||||||
| chr4:88390198 | A | G | 11 | a0001c0001t0001g0101 a0001c0001t0001g0131 a0002c0002t0001g0043 others(8): Show |
11 | HG01496.hp1 HG02132.hp1 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.437-454A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | chr4 | 88390198 | |||||||
| chr4:88390249 | G | C | 25 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0022 others(22): Show |
25 | HG00735.hp2 HG01071.hp1 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.437-403G>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | chr4 | 88390249 | |||||||
| chr4:88390264 | G | T | 72 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0019 others(69): Show |
73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.437-388G>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | chr4 | 88390264 | |||||||
| chr4:88390349 | T | C | 1 | a0002c0002t0001g0160 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.437-303T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | chr4 | 88390349 | |||||||
| chr4:88390388 | G | A | 38 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0019 others(35): Show |
38 | HG00140.hp2 HG00280.hp1 HG01256.hp2 others(35): Show |
intron_variant | MODIFIER | c.437-264G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | chr4 | 88390388 | |||||||
| chr4:88390645 | G | A | 3 | a0001c0001t0001g0065 a0001c0001t0001g0075 a0001c0001t0001g0169 |
3 | HG02258.hp1 HG02895.hp1 NA19043.hp2 |
splice_region_variant&intron_variant | LOW | c.437-7G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 3/22 | chr4 | 88390645 | |||||||
| chr4:88391035 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.664+156G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 4/22 | chr4 | 88391035 | |||||||
| chr4:88391293 | A | G | 1 | a0001c0001t0001g0159 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.664+414A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 4/22 | chr4 | 88391293 | |||||||
| chr4:88391378 | G | A | 63 | a0001c0001t0001g0038 a0001c0001t0001g0084 a0001c0001t0001g0086 others(60): Show |
63 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.664+499G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 4/22 | chr4 | 88391378 | |||||||
| chr4:88391435 | A | G | 27 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0015 others(24): Show |
27 | HG00735.hp2 HG01071.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.664+556A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 4/22 | chr4 | 88391435 | |||||||
| chr4:88391557 | C | T | 1 | a0002c0002t0001g0126 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.664+678C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 4/22 | chr4 | 88391557 | |||||||
| chr4:88391891 | C | T | 39 | a0001c0001t0001g0084 a0001c0001t0001g0086 a0001c0001t0001g0087 others(36): Show |
39 | HG00140.hp2 HG00280.hp1 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.664+1012C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 4/22 | chr4 | 88391891 | |||||||
| chr4:88391935 | C | G | 2 | a0001c0001t0001g0122 a0008c0009t0001g0074 |
2 | HG02486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.664+1056C>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 4/22 | chr4 | 88391935 | |||||||
| chr4:88391996 | T | TTCTCCCT others(12): Show |
1 | a0002c0005t0001g0060 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.664+1147_664+1165d others(21): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr4 | 88391996 | ||||||
| chr4:88392057 | T | C | 40 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0015 others(37): Show |
40 | HG00735.hp2 HG01071.hp1 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.664+1178T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 4/22 | chr4 | 88392057 | |||||||
| chr4:88392106 | C | T | 2 | a0006c0006t0001g0072 a0006c0006t0001g0073 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.664+1227C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 4/22 | chr4 | 88392106 | |||||||
| chr4:88392383 | T | C | 3 | a0001c0001t0001g0094 a0001c0001t0001g0122 a0008c0009t0001g0074 |
3 | HG02486.hp1 HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.665-1105T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 4/22 | chr4 | 88392383 | |||||||
| chr4:88392419 | C | T | 5 | a0001c0001t0001g0065 a0001c0001t0001g0075 a0001c0001t0001g0169 others(2): Show |
5 | HG02258.hp1 HG02895.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.665-1069C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 4/22 | chr4 | 88392419 | |||||||
| chr4:88392460 | G | A | 2 | a0012c0013t0001g0149 a0012c0013t0001g0157 |
2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.665-1028G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 4/22 | chr4 | 88392460 | |||||||
| chr4:88392466 | A | G | 11 | a0004c0004t0001g0005 a0004c0004t0001g0129 a0004c0004t0001g0144 others(8): Show |
11 | HG01884.hp2 HG02451.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.665-1022A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 4/22 | chr4 | 88392466 | |||||||
| chr4:88392830 | A | G | 44 | a0001c0001t0001g0084 a0001c0001t0001g0086 a0001c0001t0001g0087 others(41): Show |
44 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.665-658A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 4/22 | chr4 | 88392830 | |||||||
| chr4:88392872 | C | G | 2 | a0001c0001t0001g0122 a0008c0009t0001g0074 |
2 | HG02486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.665-616C>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 4/22 | chr4 | 88392872 | |||||||
| chr4:88393158 | T | C | 32 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0015 others(29): Show |
32 | HG00735.hp2 HG01071.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.665-330T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 4/22 | chr4 | 88393158 | |||||||
| chr4:88393304 | TA | T | 21 | a0001c0001t0001g0088 a0001c0001t0001g0145 a0001c0001t0001g0146 others(18): Show |
21 | HG01884.hp2 HG02165.hp2 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.665-174delA | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr4 | 88393304 | ||||||
| chr4:88393447 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.665-41T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 4/22 | chr4 | 88393447 | |||||||
| chr4:88393460 | C | G | 1 | a0001c0001t0001g0162 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.665-28C>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 4/22 | chr4 | 88393460 | |||||||
| chr4:88393483 | A | G | 1 | a0010c0014t0004g0079 | 1 | HG03239.hp2 | splice_region_variant&intron_variant | LOW | c.665-5A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 4/22 | chr4 | 88393483 | |||||||
| chr4:88393792 | A | G | 12 | a0001c0001t0001g0084 a0001c0001t0001g0086 a0001c0001t0001g0087 others(9): Show |
12 | HG00639.hp1 HG01167.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.759+210A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 5/22 | chr4 | 88393792 | |||||||
| chr4:88393830 | A | G | 1 | a0003c0003t0001g0014 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.759+248A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 5/22 | chr4 | 88393830 | |||||||
| chr4:88393980 | T | G | 30 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0015 others(27): Show |
30 | HG00735.hp2 HG01071.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.759+398T>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 5/22 | chr4 | 88393980 | |||||||
| chr4:88394245 | C | A | 26 | a0001c0001t0001g0099 a0002c0002t0001g0016 a0002c0002t0001g0030 others(23): Show |
26 | HG00140.hp2 HG00280.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.759+663C>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 5/22 | chr4 | 88394245 | |||||||
| chr4:88394256 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.759+674C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 5/22 | chr4 | 88394256 | |||||||
| chr4:88394285 | C | T | 4 | a0001c0001t0001g0094 a0001c0001t0001g0122 a0002c0002t0001g0112 others(1): Show |
4 | HG02486.hp1 HG02723.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.759+703C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 5/22 | chr4 | 88394285 | |||||||
| chr4:88394290 | T | C | 1 | a0002c0002t0001g0112 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.759+708T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 5/22 | chr4 | 88394290 | |||||||
| chr4:88394462 | G | C | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.759+880G>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 5/22 | chr4 | 88394462 | |||||||
| chr4:88394474 | C | CA | 17 | a0001c0001t0001g0056 a0001c0001t0001g0085 a0001c0001t0001g0086 others(14): Show |
17 | HG00639.hp1 HG01192.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.759+913dupA | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | 88394474 | ||||||
| chr4:88394474 | C | CAA | 19 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0015 others(16): Show |
19 | HG01071.hp1 HG01071.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.759+912_759+913dup others(2): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | 88394474 | ||||||
| chr4:88394474 | C | CAAA | 8 | a0001c0001t0001g0023 a0001c0001t0001g0055 a0001c0001t0001g0078 others(5): Show |
8 | HG00735.hp2 HG01891.hp1 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.759+911_759+913dup others(3): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | 88394474 | ||||||
| chr4:88394474 | CA | C | 5 | a0001c0001t0001g0077 a0001c0001t0001g0097 a0002c0002t0001g0148 others(2): Show |
5 | HG02165.hp1 HG02922.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.759+913delA | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | 88394474 | ||||||
| chr4:88394528 | A | AATT | 40 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(37): Show |
40 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.759+974_759+976dup others(3): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | 88394528 | ||||||
| chr4:88394528 | AATT | A | 11 | a0001c0001t0001g0065 a0001c0001t0001g0075 a0001c0001t0001g0077 others(8): Show |
11 | HG02258.hp1 HG02486.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.759+974_759+976del others(3): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | 88394528 | ||||||
| chr4:88394550 | A | T | 1 | a0001c0001t0001g0172 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.759+968A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 5/22 | chr4 | 88394550 | |||||||
| chr4:88395057 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.760-958T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 5/22 | chr4 | 88395057 | |||||||
| chr4:88395077 | A | G | 45 | a0001c0001t0001g0084 a0001c0001t0001g0086 a0001c0001t0001g0087 others(42): Show |
45 | HG00639.hp1 HG01167.hp1 HG01167.hp2 others(42): Show |
intron_variant | MODIFIER | c.760-938A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 5/22 | chr4 | 88395077 | |||||||
| chr4:88395312 | T | C | 1 | a0003c0003t0001g0048 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.760-703T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 5/22 | chr4 | 88395312 | |||||||
| chr4:88395313 | C | T | 1 | a0003c0003t0001g0048 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.760-702C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 5/22 | chr4 | 88395313 | |||||||
| chr4:88395314 | A | C | 1 | a0003c0003t0001g0048 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.760-701A>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 5/22 | chr4 | 88395314 | |||||||
| chr4:88395339 | T | C | 2 | a0002c0002t0001g0117 a0010c0014t0001g0020 |
2 | HG01168.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.760-676T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 5/22 | chr4 | 88395339 | |||||||
| chr4:88395357 | A | G | 33 | a0001c0001t0001g0099 a0002c0002t0001g0028 a0002c0002t0001g0030 others(30): Show |
33 | HG01256.hp2 HG01891.hp2 HG02040.hp2 others(30): Show |
intron_variant | MODIFIER | c.760-658A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 5/22 | chr4 | 88395357 | |||||||
| chr4:88395614 | A | G | 28 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0015 others(25): Show |
28 | HG00735.hp2 HG01071.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.760-401A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 5/22 | chr4 | 88395614 | |||||||
| chr4:88395696 | T | A | 28 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0015 others(25): Show |
28 | HG00735.hp2 HG01071.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.760-319T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 5/22 | chr4 | 88395696 | |||||||
| chr4:88395697 | A | T | 7 | a0001c0001t0001g0065 a0001c0001t0001g0075 a0001c0001t0001g0077 others(4): Show |
7 | HG02258.hp1 HG02895.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.760-318A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 5/22 | chr4 | 88395697 | |||||||
| chr4:88395713 | T | G | 106 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0015 others(103): Show |
106 | HG00639.hp1 HG00735.hp2 HG01071.hp1 others(103): Show |
intron_variant | MODIFIER | c.760-302T>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 5/22 | chr4 | 88395713 | |||||||
| chr4:88396177 | G | T | 3 | a0001c0001t0001g0065 a0001c0001t0001g0075 a0001c0001t0001g0169 |
3 | HG02258.hp1 HG02895.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.887+35G>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 6/22 | chr4 | 88396177 | |||||||
| chr4:88396306 | A | G | 1 | a0002c0002t0001g0025 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.887+164A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 6/22 | chr4 | 88396306 | |||||||
| chr4:88396703 | C | G | 5 | a0001c0001t0001g0065 a0001c0001t0001g0075 a0001c0001t0001g0169 others(2): Show |
5 | HG02258.hp1 HG02895.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.888-148C>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 6/22 | chr4 | 88396703 | |||||||
| chr4:88396716 | T | C | 28 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0015 others(25): Show |
28 | HG00735.hp2 HG01071.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.888-135T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 6/22 | chr4 | 88396716 | |||||||
| chr4:88397120 | A | AT | 12 | a0001c0001t0001g0084 a0001c0001t0001g0086 a0001c0001t0001g0087 others(9): Show |
12 | HG00639.hp1 HG01167.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.1024+142dupT | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | 88397120 | ||||||
| chr4:88397300 | T | C | 6 | a0001c0001t0001g0084 a0001c0001t0001g0086 a0001c0001t0001g0087 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1024+313T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 7/22 | chr4 | 88397300 | |||||||
| chr4:88397301 | G | A | 6 | a0001c0001t0001g0084 a0001c0001t0001g0086 a0001c0001t0001g0087 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1024+314G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 7/22 | chr4 | 88397301 | |||||||
| chr4:88397303 | G | C | 104 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0012 others(101): Show |
104 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(101): Show |
intron_variant | MODIFIER | c.1024+316G>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 7/22 | chr4 | 88397303 | |||||||
| chr4:88397456 | A | G | 3 | a0001c0001t0001g0077 a0001c0001t0001g0097 a0006c0006t0001g0032 |
3 | HG02922.hp2 HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1024+469A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 7/22 | chr4 | 88397456 | |||||||
| chr4:88397652 | G | A | 2 | a0001c0001t0001g0100 a0004c0017t0001g0067 |
2 | HG03225.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1025-490G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 7/22 | chr4 | 88397652 | |||||||
| chr4:88397654 | C | A | 1 | a0004c0004t0001g0144 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1025-488C>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 7/22 | chr4 | 88397654 | |||||||
| chr4:88397672 | T | C | 110 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0012 others(107): Show |
110 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.1025-470T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 7/22 | chr4 | 88397672 | |||||||
| chr4:88398078 | A | G | 13 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(10): Show |
13 | HG00639.hp1 HG01167.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.1025-64A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 7/22 | chr4 | 88398078 | |||||||
| chr4:88398266 | C | T | 3 | a0001c0008t0001g0061 a0002c0002t0001g0016 a0002c0002t0001g0105 |
3 | HG00140.hp2 HG00280.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1092+57C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 8/22 | chr4 | 88398266 | |||||||
| chr4:88398582 | C | G | 29 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0039 others(26): Show |
29 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.1092+373C>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 8/22 | chr4 | 88398582 | |||||||
| chr4:88398694 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1092+485G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 8/22 | chr4 | 88398694 | |||||||
| chr4:88398810 | A | G | 76 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0017 others(73): Show |
77 | HG00280.hp1 HG00639.hp1 HG01167.hp1 others(74): Show |
intron_variant | MODIFIER | c.1092+601A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 8/22 | chr4 | 88398810 | |||||||
| chr4:88398841 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1092+632C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 8/22 | chr4 | 88398841 | |||||||
| chr4:88398853 | C | G | 2 | a0003c0003t0001g0029 a0003c0003t0001g0147 |
2 | HG02165.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.1092+644C>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 8/22 | chr4 | 88398853 | |||||||
| chr4:88398892 | G | A | 1 | a0002c0002t0001g0098 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1092+683G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 8/22 | chr4 | 88398892 | |||||||
| chr4:88399052 | G | A | 1 | a0008c0009t0001g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1092+843G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 8/22 | chr4 | 88399052 | |||||||
| chr4:88399179 | G | A | 1 | a0001c0008t0001g0069 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1092+970G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 8/22 | chr4 | 88399179 | |||||||
| chr4:88399254 | A | G | 35 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0022 others(32): Show |
35 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.1092+1045A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 8/22 | chr4 | 88399254 | |||||||
| chr4:88399493 | C | T | 1 | a0012c0013t0001g0149 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1092+1284C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 8/22 | chr4 | 88399493 | |||||||
| chr4:88399731 | T | C | 4 | a0001c0001t0001g0111 a0001c0001t0001g0167 a0002c0002t0001g0103 others(1): Show |
4 | HG02523.hp2 NA18747.hp2 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.1092+1522T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 8/22 | chr4 | 88399731 | |||||||
| chr4:88399746 | C | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0004c0004t0001g0129 |
3 | HG03490.hp1 HG03492.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1092+1537C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 8/22 | chr4 | 88399746 | |||||||
| chr4:88400393 | C | T | 1 | a0002c0002t0001g0114 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1092+2184C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 8/22 | chr4 | 88400393 | |||||||
| chr4:88400615 | G | C | 103 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(100): Show |
104 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.1092+2406G>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 8/22 | chr4 | 88400615 | |||||||
| chr4:88400618 | A | G | 5 | a0004c0017t0001g0067 a0008c0009t0001g0050 a0009c0010t0002g0006 others(2): Show |
5 | HG02559.hp2 HG02809.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1092+2409A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 8/22 | chr4 | 88400618 | |||||||
| chr4:88400731 | G | A | 103 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(100): Show |
104 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.1092+2522G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 8/22 | chr4 | 88400731 | |||||||
| chr4:88400891 | G | A | 1 | a0007c0011t0001g0125 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1092+2682G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 8/22 | chr4 | 88400891 | |||||||
| chr4:88401014 | C | G | 103 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(100): Show |
104 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.1092+2805C>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 8/22 | chr4 | 88401014 | |||||||
| chr4:88401428 | G | T | 1 | a0002c0002t0001g0107 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1092+3219G>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 8/22 | chr4 | 88401428 | |||||||
| chr4:88401490 | CA | C | 7 | a0001c0001t0001g0150 a0001c0001t0001g0168 a0002c0002t0001g0132 others(4): Show |
7 | HG01257.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1092+3298delA | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr4 | 88401490 | ||||||
| chr4:88401503 | A | G | 2 | a0006c0006t0001g0070 a0006c0006t0001g0071 |
2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1092+3294A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 8/22 | chr4 | 88401503 | |||||||
| chr4:88401585 | G | T | 1 | a0001c0001t0001g0169 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1093-3291G>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 8/22 | chr4 | 88401585 | |||||||
| chr4:88401771 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1093-3105G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 8/22 | chr4 | 88401771 | |||||||
| chr4:88401934 | T | G | 1 | a0007c0011t0001g0143 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1093-2942T>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 8/22 | chr4 | 88401934 | |||||||
| chr4:88401975 | G | C | 9 | a0001c0001t0001g0075 a0001c0001t0001g0088 a0001c0001t0001g0113 others(6): Show |
9 | HG01496.hp1 HG02258.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.1093-2901G>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 8/22 | chr4 | 88401975 | |||||||
| chr4:88402062 | T | C | 92 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(89): Show |
93 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.1093-2814T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 8/22 | chr4 | 88402062 | |||||||
| chr4:88402511 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1093-2365G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 8/22 | chr4 | 88402511 | |||||||
| chr4:88402747 | A | G | 1 | a0002c0002t0001g0001 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1093-2129A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 8/22 | chr4 | 88402747 | |||||||
| chr4:88402748 | T | G | 2 | a0006c0006t0001g0072 a0006c0006t0001g0073 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1093-2128T>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 8/22 | chr4 | 88402748 | |||||||
| chr4:88402817 | T | C | 2 | a0001c0001t0001g0075 a0001c0001t0001g0088 |
2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1093-2059T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 8/22 | chr4 | 88402817 | |||||||
| chr4:88402942 | C | T | 11 | a0001c0001t0001g0169 a0004c0017t0001g0067 a0005c0007t0001g0090 others(8): Show |
11 | HG01884.hp2 HG02451.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1093-1934C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 8/22 | chr4 | 88402942 | |||||||
| chr4:88403471 | T | G | 1 | a0001c0001t0001g0169 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1093-1405T>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 8/22 | chr4 | 88403471 | |||||||
| chr4:88403569 | G | A | 8 | a0001c0001t0001g0169 a0004c0017t0001g0067 a0006c0006t0001g0072 others(5): Show |
8 | HG02559.hp2 HG02809.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1093-1307G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 8/22 | chr4 | 88403569 | |||||||
| chr4:88403725 | G | A | 1 | a0001c0001t0001g0027 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1093-1151G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 8/22 | chr4 | 88403725 | |||||||
| chr4:88403872 | T | A | 100 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(97): Show |
101 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.1093-1004T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 8/22 | chr4 | 88403872 | |||||||
| chr4:88404042 | G | A | 8 | a0001c0001t0001g0169 a0004c0017t0001g0067 a0006c0006t0001g0072 others(5): Show |
8 | HG02559.hp2 HG02809.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1093-834G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 8/22 | chr4 | 88404042 | |||||||
| chr4:88404193 | CT | C | 32 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0022 others(29): Show |
32 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.1093-667delT | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr4 | 88404193 | ||||||
| chr4:88404431 | C | T | 1 | a0004c0004t0001g0144 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1093-445C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 8/22 | chr4 | 88404431 | |||||||
| chr4:88404567 | G | T | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1093-309G>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 8/22 | chr4 | 88404567 | |||||||
| chr4:88404682 | G | T | 1 | a0002c0002t0001g0117 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1093-194G>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 8/22 | chr4 | 88404682 | |||||||
| chr4:88404869 | C | A | 1 | a0001c0001t0001g0039 | 1 | NA18951.hp1 | splice_region_variant&intron_variant | LOW | c.1093-7C>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 8/22 | chr4 | 88404869 | |||||||
| chr4:88405306 | T | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0102 |
2 | NA18612.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1215-248T>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 9/22 | chr4 | 88405306 | |||||||
| chr4:88405317 | C | G | 3 | a0001c0001t0001g0084 a0001c0001t0001g0086 a0001c0001t0001g0087 |
3 | HG01167.hp2 HG01169.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1215-237C>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 9/22 | chr4 | 88405317 | |||||||
| chr4:88405456 | T | G | 7 | a0004c0017t0001g0067 a0008c0009t0001g0050 a0009c0010t0002g0006 others(4): Show |
7 | HG02559.hp2 HG02809.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.1215-98T>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 9/22 | chr4 | 88405456 | |||||||
| chr4:88405881 | A | T | 3 | a0001c0001t0001g0141 a0001c0001t0001g0151 a0001c0001t0001g0154 |
3 | HG02132.hp2 NA18948.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1274+268A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 10/22 | chr4 | 88405881 | |||||||
| chr4:88406020 | G | C | 1 | a0004c0004t0001g0144 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1274+407G>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 10/22 | chr4 | 88406020 | |||||||
| chr4:88406143 | A | G | 1 | a0004c0004t0001g0005 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1274+530A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 10/22 | chr4 | 88406143 | |||||||
| chr4:88406803 | G | A | 2 | a0002c0002t0001g0046 a0002c0002t0001g0160 |
2 | NA18970.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1274+1190G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 10/22 | chr4 | 88406803 | |||||||
| chr4:88406890 | G | T | 1 | a0002c0002t0001g0108 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1274+1277G>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 10/22 | chr4 | 88406890 | |||||||
| chr4:88406892 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1274+1279G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 10/22 | chr4 | 88406892 | |||||||
| chr4:88406946 | A | G | 2 | a0012c0013t0001g0149 a0012c0013t0001g0157 |
2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1274+1333A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 10/22 | chr4 | 88406946 | |||||||
| chr4:88407048 | C | T | 2 | a0012c0013t0001g0149 a0012c0013t0001g0157 |
2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1274+1435C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 10/22 | chr4 | 88407048 | |||||||
| chr4:88407160 | C | T | 1 | a0002c0002t0001g0117 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1275-1364C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 10/22 | chr4 | 88407160 | |||||||
| chr4:88407381 | TTTTG | T | 5 | a0004c0017t0001g0067 a0008c0009t0001g0050 a0009c0010t0002g0006 others(2): Show |
5 | HG02559.hp2 HG02809.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1275-1126_1275-112 others(8): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | 88407381 | ||||||
| chr4:88408425 | T | C | 2 | a0012c0013t0001g0149 a0012c0013t0001g0157 |
2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1275-99T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 10/22 | chr4 | 88408425 | |||||||
| chr4:88409137 | A | G | 40 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0022 others(37): Show |
40 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.1368+520A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 11/22 | chr4 | 88409137 | |||||||
| chr4:88409892 | C | T | 3 | a0002c0002t0001g0028 a0002c0002t0001g0148 a0002c0002t0001g0166 |
3 | HG02165.hp1 HG03491.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1368+1275C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 11/22 | chr4 | 88409892 | |||||||
| chr4:88409898 | G | C | 27 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0027 others(24): Show |
28 | HG00280.hp1 HG01168.hp1 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.1368+1281G>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 11/22 | chr4 | 88409898 | |||||||
| chr4:88410079 | C | G | 27 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0027 others(24): Show |
28 | HG00280.hp1 HG01168.hp1 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.1368+1462C>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 11/22 | chr4 | 88410079 | |||||||
| chr4:88410531 | C | T | 1 | a0009c0010t0002g0006 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1368+1914C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 11/22 | chr4 | 88410531 | |||||||
| chr4:88410731 | G | C | 2 | a0001c0001t0001g0140 a0001c0001t0001g0155 |
2 | NA18941.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1368+2114G>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 11/22 | chr4 | 88410731 | |||||||
| chr4:88411646 | G | A | 5 | a0004c0017t0001g0067 a0008c0009t0001g0050 a0009c0010t0002g0006 others(2): Show |
5 | HG02559.hp2 HG02809.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1369-1431G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 11/22 | chr4 | 88411646 | |||||||
| chr4:88412299 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1369-778G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 11/22 | chr4 | 88412299 | |||||||
| chr4:88412393 | C | T | 1 | a0002c0002t0001g0108 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1369-684C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 11/22 | chr4 | 88412393 | |||||||
| chr4:88413431 | T | C | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1558+165T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 12/22 | chr4 | 88413431 | |||||||
| chr4:88413715 | G | A | 5 | a0004c0017t0001g0067 a0008c0009t0001g0050 a0009c0010t0002g0006 others(2): Show |
5 | HG02559.hp2 HG02809.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1558+449G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 12/22 | chr4 | 88413715 | |||||||
| chr4:88414248 | A | C | 1 | a0001c0001t0001g0153 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1558+982A>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 12/22 | chr4 | 88414248 | |||||||
| chr4:88414288 | T | C | 35 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0027 others(32): Show |
36 | HG00280.hp1 HG01168.hp1 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.1558+1022T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 12/22 | chr4 | 88414288 | |||||||
| chr4:88414299 | C | T | 1 | a0002c0002t0001g0001 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1558+1033C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 12/22 | chr4 | 88414299 | |||||||
| chr4:88414310 | AT | A | 108 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(105): Show |
109 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.1558+1057delT | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | 88414310 | ||||||
| chr4:88414515 | C | T | 117 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(114): Show |
118 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.1558+1249C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 12/22 | chr4 | 88414515 | |||||||
| chr4:88414563 | T | C | 7 | a0004c0017t0001g0067 a0008c0009t0001g0050 a0009c0010t0002g0006 others(4): Show |
7 | HG02559.hp2 HG02809.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.1558+1297T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 12/22 | chr4 | 88414563 | |||||||
| chr4:88414701 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1558+1435C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 12/22 | chr4 | 88414701 | |||||||
| chr4:88414883 | T | C | 1 | a0007c0011t0001g0143 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1558+1617T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 12/22 | chr4 | 88414883 | |||||||
| chr4:88415589 | A | G | 2 | a0012c0013t0001g0149 a0012c0013t0001g0157 |
2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1559-1836A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 12/22 | chr4 | 88415589 | |||||||
| chr4:88416247 | G | A | 10 | a0002c0002t0001g0036 a0002c0002t0001g0110 a0002c0002t0001g0112 others(7): Show |
10 | HG02040.hp2 HG02300.hp2 NA18612.hp2 others(7): Show |
intron_variant | MODIFIER | c.1559-1178G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 12/22 | chr4 | 88416247 | |||||||
| chr4:88416446 | T | A | 116 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(113): Show |
117 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.1559-979T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 12/22 | chr4 | 88416446 | |||||||
| chr4:88416463 | G | A | 1 | a0001c0001t0001g0039 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1559-962G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 12/22 | chr4 | 88416463 | |||||||
| chr4:88416530 | A | G | 1 | a0001c0008t0001g0069 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1559-895A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 12/22 | chr4 | 88416530 | |||||||
| chr4:88417947 | TA | T | 109 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(106): Show |
110 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.1713+382delA | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 88417947 | ||||||
| chr4:88418366 | C | G | 1 | a0001c0001t0001g0078 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1713+787C>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 13/22 | chr4 | 88418366 | |||||||
| chr4:88418391 | G | A | 7 | a0001c0001t0001g0113 a0002c0002t0001g0033 a0003c0003t0001g0021 others(4): Show |
7 | HG01496.hp1 NA18962.hp2 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1713+812G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 13/22 | chr4 | 88418391 | |||||||
| chr4:88418459 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1713+880C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 13/22 | chr4 | 88418459 | |||||||
| chr4:88418491 | T | G | 1 | a0001c0015t0001g0024 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1713+912T>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 13/22 | chr4 | 88418491 | |||||||
| chr4:88418640 | C | A | 1 | a0001c0001t0001g0085 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1713+1061C>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 13/22 | chr4 | 88418640 | |||||||
| chr4:88418709 | CAT | C | 3 | a0001c0001t0001g0084 a0001c0001t0001g0086 a0001c0001t0001g0087 |
3 | HG01167.hp2 HG01169.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1713+1131_1713+113 others(6): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 13/22 | chr4 | 88418709 | |||||||
| chr4:88418785 | G | A | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1713+1206G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 13/22 | chr4 | 88418785 | |||||||
| chr4:88419375 | A | G | 2 | a0006c0006t0001g0072 a0006c0006t0001g0073 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1713+1796A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 13/22 | chr4 | 88419375 | |||||||
| chr4:88419546 | CT | C | 7 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0078 others(4): Show |
7 | HG00735.hp2 HG02040.hp1 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.1713+1969delT | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 88419546 | ||||||
| chr4:88419608 | G | A | 1 | a0005c0007t0001g0096 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1713+2029G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 13/22 | chr4 | 88419608 | |||||||
| chr4:88420161 | T | A | 5 | a0004c0017t0001g0067 a0008c0009t0001g0050 a0009c0010t0002g0006 others(2): Show |
5 | HG02559.hp2 HG02809.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1713+2582T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 13/22 | chr4 | 88420161 | |||||||
| chr4:88420322 | T | C | 2 | a0012c0013t0001g0149 a0012c0013t0001g0157 |
2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1713+2743T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 13/22 | chr4 | 88420322 | |||||||
| chr4:88420662 | A | G | 1 | a0004c0004t0001g0144 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1713+3083A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 13/22 | chr4 | 88420662 | |||||||
| chr4:88420699 | G | A | 1 | a0002c0002t0001g0033 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1713+3120G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 13/22 | chr4 | 88420699 | |||||||
| chr4:88420736 | A | G | 16 | a0001c0001t0001g0004 a0001c0001t0001g0076 a0001c0001t0001g0077 others(13): Show |
16 | HG00639.hp1 HG01167.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1714-3124A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 13/22 | chr4 | 88420736 | |||||||
| chr4:88420749 | T | C | 3 | a0005c0007t0001g0090 a0005c0007t0001g0096 a0014c0018t0001g0066 |
3 | HG01884.hp2 HG02451.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1714-3111T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 13/22 | chr4 | 88420749 | |||||||
| chr4:88420850 | C | A | 164 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(161): Show |
166 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1714-3010C>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 13/22 | chr4 | 88420850 | |||||||
| chr4:88420851 | A | C | 164 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(161): Show |
166 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1714-3009A>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 13/22 | chr4 | 88420851 | |||||||
| chr4:88420992 | C | T | 2 | a0001c0001t0001g0168 a0002c0002t0001g0130 |
2 | NA18939.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1714-2868C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 13/22 | chr4 | 88420992 | |||||||
| chr4:88421006 | A | C | 1 | a0002c0002t0001g0095 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1714-2854A>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 13/22 | chr4 | 88421006 | |||||||
| chr4:88421237 | A | G | 1 | a0002c0002t0001g0117 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1714-2623A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 13/22 | chr4 | 88421237 | |||||||
| chr4:88421241 | C | T | 5 | a0004c0017t0001g0067 a0008c0009t0001g0050 a0009c0010t0002g0006 others(2): Show |
5 | HG02559.hp2 HG02809.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1714-2619C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 13/22 | chr4 | 88421241 | |||||||
| chr4:88421436 | TTTTTC | T | 7 | a0001c0001t0001g0084 a0001c0001t0001g0086 a0001c0001t0003g0081 others(4): Show |
7 | HG00280.hp2 HG01167.hp2 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.1714-2409_1714-240 others(9): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 88421436 | ||||||
| chr4:88421451 | C | CT | 35 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0027 others(32): Show |
36 | HG00280.hp1 HG01168.hp1 HG01346.hp2 others(33): Show |
intron_variant | MODIFIER | c.1714-2395dupT | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 88421451 | ||||||
| chr4:88421456 | T | C | 2 | a0002c0002t0001g0089 a0002c0002t0001g0121 |
2 | HG02257.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1714-2404T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 13/22 | chr4 | 88421456 | |||||||
| chr4:88421484 | G | A | 5 | a0002c0002t0001g0132 a0002c0002t0001g0133 a0002c0002t0001g0135 others(2): Show |
5 | NA18951.hp2 NA18959.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.1714-2376G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 13/22 | chr4 | 88421484 | |||||||
| chr4:88421533 | C | T | 4 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0085 others(1): Show |
4 | HG02647.hp1 HG03490.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.1714-2327C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 13/22 | chr4 | 88421533 | |||||||
| chr4:88421764 | C | T | 5 | a0004c0017t0001g0067 a0008c0009t0001g0050 a0009c0010t0002g0006 others(2): Show |
5 | HG02559.hp2 HG02809.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1714-2096C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 13/22 | chr4 | 88421764 | |||||||
| chr4:88421824 | T | C | 106 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(103): Show |
107 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.1714-2036T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 13/22 | chr4 | 88421824 | |||||||
| chr4:88422041 | C | T | 5 | a0004c0017t0001g0067 a0008c0009t0001g0050 a0009c0010t0002g0006 others(2): Show |
5 | HG02559.hp2 HG02809.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1714-1819C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 13/22 | chr4 | 88422041 | |||||||
| chr4:88422079 | G | A | 1 | a0001c0001t0001g0038 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1714-1781G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 13/22 | chr4 | 88422079 | |||||||
| chr4:88422602 | C | CATA | 106 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(103): Show |
107 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.1714-1256_1714-125 others(7): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 88422602 | ||||||
| chr4:88422714 | G | A | 3 | a0009c0010t0002g0006 a0009c0010t0002g0119 a0009c0010t0002g0120 |
3 | HG02559.hp2 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1714-1146G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 13/22 | chr4 | 88422714 | |||||||
| chr4:88422832 | T | C | 1 | a0003c0003t0001g0147 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1714-1028T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 13/22 | chr4 | 88422832 | |||||||
| chr4:88424322 | A | G | 3 | a0001c0001t0001g0075 a0001c0001t0001g0088 a0001c0001t0001g0169 |
3 | HG02258.hp1 HG03041.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1828-273A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 14/22 | chr4 | 88424322 | |||||||
| chr4:88424324 | C | G | 2 | a0001c0001t0001g0118 a0001c0019t0001g0063 |
2 | HG01346.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1828-271C>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 14/22 | chr4 | 88424324 | |||||||
| chr4:88424338 | T | C | 1 | a0001c0001t0001g0168 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1828-257T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 14/22 | chr4 | 88424338 | |||||||
| chr4:88424883 | G | A | 1 | a0001c0001t0001g0031 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1935+181G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 15/22 | chr4 | 88424883 | |||||||
| chr4:88424935 | C | T | 101 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(98): Show |
102 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1935+233C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 15/22 | chr4 | 88424935 | |||||||
| chr4:88425339 | C | G | 5 | a0004c0017t0001g0067 a0008c0009t0001g0050 a0009c0010t0002g0006 others(2): Show |
5 | HG02559.hp2 HG02809.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1935+637C>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 15/22 | chr4 | 88425339 | |||||||
| chr4:88425340 | G | A | 29 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0022 others(26): Show |
29 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.1935+638G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 15/22 | chr4 | 88425340 | |||||||
| chr4:88425575 | C | T | 5 | a0004c0017t0001g0067 a0008c0009t0001g0050 a0009c0010t0002g0006 others(2): Show |
5 | HG02559.hp2 HG02809.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1935+873C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 15/22 | chr4 | 88425575 | |||||||
| chr4:88425794 | CT | C | 35 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0027 others(32): Show |
36 | HG00280.hp1 HG01168.hp1 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.1935+1101delT | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr4 | 88425794 | ||||||
| chr4:88426021 | G | A | 2 | a0005c0007t0001g0092 a0005c0007t0001g0093 |
2 | HG00639.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1935+1319G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 15/22 | chr4 | 88426021 | |||||||
| chr4:88426387 | C | T | 1 | a0010c0014t0001g0020 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1935+1685C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 15/22 | chr4 | 88426387 | |||||||
| chr4:88426467 | T | TTAG | 2 | a0001c0001t0001g0022 a0001c0001t0001g0023 |
2 | HG03927.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1935+1767_1935+176 others(7): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr4 | 88426467 | ||||||
| chr4:88426545 | T | C | 1 | a0010c0014t0001g0020 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1935+1843T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 15/22 | chr4 | 88426545 | |||||||
| chr4:88427044 | A | G | 3 | a0002c0002t0001g0028 a0002c0002t0001g0148 a0002c0002t0001g0166 |
3 | HG02165.hp1 HG03491.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1936-1536A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 15/22 | chr4 | 88427044 | |||||||
| chr4:88427052 | G | A | 28 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0022 others(25): Show |
28 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.1936-1528G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 15/22 | chr4 | 88427052 | |||||||
| chr4:88428036 | A | G | 1 | a0002c0002t0001g0042 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1936-544A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 15/22 | chr4 | 88428036 | |||||||
| chr4:88428950 | T | A | 2 | a0006c0006t0001g0072 a0006c0006t0001g0073 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2106+200T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 16/22 | chr4 | 88428950 | |||||||
| chr4:88429156 | G | T | 1 | a0001c0001t0001g0094 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2106+406G>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 16/22 | chr4 | 88429156 | |||||||
| chr4:88429200 | C | T | 1 | a0008c0009t0001g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2106+450C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 16/22 | chr4 | 88429200 | |||||||
| chr4:88429837 | G | A | 5 | a0004c0017t0001g0067 a0008c0009t0001g0050 a0009c0010t0002g0006 others(2): Show |
5 | HG02559.hp2 HG02809.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2106+1087G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 16/22 | chr4 | 88429837 | |||||||
| chr4:88430359 | A | C | 1 | a0001c0001t0001g0152 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2107-803A>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 16/22 | chr4 | 88430359 | |||||||
| chr4:88430569 | C | CAAAT | 50 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0017 others(47): Show |
50 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.2107-553_2107-550d others(6): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr4 | 88430569 | ||||||
| chr4:88430569 | C | CAAATAAA others(1): Show |
11 | a0001c0001t0001g0039 a0001c0001t0001g0075 a0001c0001t0001g0084 others(8): Show |
11 | HG01167.hp2 HG01192.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.2107-557_2107-550d others(10): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr4 | 88430569 | ||||||
| chr4:88430569 | C | CAAATAAA others(5): Show |
2 | a0001c0019t0001g0063 a0004c0017t0001g0067 |
2 | HG01346.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2107-561_2107-550d others(14): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr4 | 88430569 | ||||||
| chr4:88430569 | CAAAT | C | 2 | a0001c0001t0001g0123 a0002c0002t0001g0033 |
2 | HG03516.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2107-553_2107-550d others(6): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr4 | 88430569 | ||||||
| chr4:88430569 | CAAATAAA others(1): Show |
C | 2 | a0001c0001t0001g0076 a0001c0001t0001g0099 |
2 | HG01884.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2107-557_2107-550d others(10): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr4 | 88430569 | ||||||
| chr4:88430569 | CAAATAAA others(9): Show |
C | 1 | a0002c0002t0001g0095 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2107-565_2107-550d others(18): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr4 | 88430569 | ||||||
| chr4:88430612 | A | ATAAATAA others(1): Show |
4 | a0001c0001t0001g0094 a0001c0001t0001g0122 a0001c0008t0001g0057 others(1): Show |
4 | HG01167.hp1 HG02486.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2107-550_2107-549i others(10): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 16/22 | chr4 | 88430612 | |||||||
| chr4:88430689 | A | G | 1 | a0002c0002t0001g0121 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2107-473A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 16/22 | chr4 | 88430689 | |||||||
| chr4:88431123 | T | C | 2 | a0001c0001t0001g0085 a0012c0013t0001g0149 |
2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2107-39T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 16/22 | chr4 | 88431123 | |||||||
| chr4:88431380 | T | C | 1 | a0002c0002t0001g0049 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2250+75T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 17/22 | chr4 | 88431380 | |||||||
| chr4:88431725 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2250+420C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 17/22 | chr4 | 88431725 | |||||||
| chr4:88432033 | A | C | 1 | a0014c0018t0001g0066 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2250+728A>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 17/22 | chr4 | 88432033 | |||||||
| chr4:88432298 | C | T | 1 | a0004c0004t0001g0144 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2250+993C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 17/22 | chr4 | 88432298 | |||||||
| chr4:88432486 | G | A | 2 | a0001c0001t0001g0076 a0001c0001t0001g0099 |
2 | HG01884.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2250+1181G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 17/22 | chr4 | 88432486 | |||||||
| chr4:88432599 | C | T | 3 | a0009c0010t0002g0006 a0009c0010t0002g0119 a0009c0010t0002g0120 |
3 | HG02559.hp2 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2250+1294C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 17/22 | chr4 | 88432599 | |||||||
| chr4:88433256 | G | A | 1 | a0002c0002t0001g0098 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2250+1951G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 17/22 | chr4 | 88433256 | |||||||
| chr4:88433276 | C | T | 1 | a0001c0008t0001g0061 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2250+1971C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 17/22 | chr4 | 88433276 | |||||||
| chr4:88433786 | C | T | 1 | a0008c0009t0001g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2251-1939C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 17/22 | chr4 | 88433786 | |||||||
| chr4:88433951 | T | C | 101 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(98): Show |
101 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.2251-1774T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 17/22 | chr4 | 88433951 | |||||||
| chr4:88433954 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2251-1771T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 17/22 | chr4 | 88433954 | |||||||
| chr4:88434497 | G | A | 3 | a0001c0001t0001g0077 a0001c0001t0001g0097 a0006c0006t0001g0032 |
3 | HG02922.hp2 HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2251-1228G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 17/22 | chr4 | 88434497 | |||||||
| chr4:88434765 | C | CA | 28 | a0001c0001t0001g0084 a0001c0001t0001g0086 a0001c0001t0001g0100 others(25): Show |
28 | HG01167.hp2 HG01192.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.2251-945dupA | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr4 | 88434765 | ||||||
| chr4:88434765 | C | CAA | 24 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0015 others(21): Show |
24 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.2251-946_2251-945d others(4): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr4 | 88434765 | ||||||
| chr4:88434888 | G | C | 2 | a0001c0001t0001g0085 a0012c0013t0001g0149 |
2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2251-837G>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 17/22 | chr4 | 88434888 | |||||||
| chr4:88435531 | A | G | 1 | a0002c0002t0001g0104 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2251-194A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 17/22 | chr4 | 88435531 | |||||||
| chr4:88436392 | C | T | 1 | a0004c0004t0001g0161 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2417+501C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 18/22 | chr4 | 88436392 | |||||||
| chr4:88436408 | G | A | 3 | a0009c0010t0002g0006 a0009c0010t0002g0119 a0009c0010t0002g0120 |
3 | HG02559.hp2 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2418-497G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 18/22 | chr4 | 88436408 | |||||||
| chr4:88436453 | T | C | 3 | a0009c0010t0002g0006 a0009c0010t0002g0119 a0009c0010t0002g0120 |
3 | HG02559.hp2 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2418-452T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 18/22 | chr4 | 88436453 | |||||||
| chr4:88436486 | T | G | 1 | a0002c0002t0001g0013 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2418-419T>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 18/22 | chr4 | 88436486 | |||||||
| chr4:88436749 | C | T | 3 | a0009c0010t0002g0006 a0009c0010t0002g0119 a0009c0010t0002g0120 |
3 | HG02559.hp2 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2418-156C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 18/22 | chr4 | 88436749 | |||||||
| chr4:88436835 | C | T | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2418-70C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 18/22 | chr4 | 88436835 | |||||||
| chr4:88437060 | C | G | 1 | a0007c0011t0001g0143 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2484+89C>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 19/22 | chr4 | 88437060 | |||||||
| chr4:88437103 | T | C | 3 | a0009c0010t0002g0006 a0009c0010t0002g0119 a0009c0010t0002g0120 |
3 | HG02559.hp2 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2484+132T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 19/22 | chr4 | 88437103 | |||||||
| chr4:88437128 | T | C | 3 | a0009c0010t0002g0006 a0009c0010t0002g0119 a0009c0010t0002g0120 |
3 | HG02559.hp2 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2484+157T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 19/22 | chr4 | 88437128 | |||||||
| chr4:88437194 | T | C | 3 | a0009c0010t0002g0006 a0009c0010t0002g0119 a0009c0010t0002g0120 |
3 | HG02559.hp2 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2484+223T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 19/22 | chr4 | 88437194 | |||||||
| chr4:88437897 | G | C | 1 | a0002c0002t0001g0132 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2555+116G>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 20/22 | chr4 | 88437897 | |||||||
| chr4:88438011 | T | A | 3 | a0009c0010t0002g0006 a0009c0010t0002g0119 a0009c0010t0002g0120 |
3 | HG02559.hp2 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2555+230T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 20/22 | chr4 | 88438011 | |||||||
| chr4:88438025 | A | C | 168 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(165): Show |
170 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.2555+244A>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 20/22 | chr4 | 88438025 | |||||||
| chr4:88438051 | A | C | 1 | a0002c0002t0001g0170 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2555+270A>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 20/22 | chr4 | 88438051 | |||||||
| chr4:88438082 | C | T | 1 | a0002c0005t0001g0060 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2555+301C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 20/22 | chr4 | 88438082 | |||||||
| chr4:88438125 | C | CA | 15 | a0001c0001t0001g0031 a0001c0001t0001g0118 a0001c0001t0001g0123 others(12): Show |
15 | HG01891.hp1 HG01978.hp2 HG02897.hp2 others(12): Show |
intron_variant | MODIFIER | c.2555+367dupA | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | 88438125 | ||||||
| chr4:88438125 | CA | C | 7 | a0001c0001t0001g0101 a0001c0001t0001g0169 a0001c0008t0001g0069 others(4): Show |
7 | HG02896.hp1 HG02897.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2555+367delA | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | 88438125 | ||||||
| chr4:88438687 | T | C | 1 | a0001c0001t0001g0031 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2555+906T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 20/22 | chr4 | 88438687 | |||||||
| chr4:88438785 | T | C | 1 | a0002c0002t0001g0046 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2555+1004T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 20/22 | chr4 | 88438785 | |||||||
| chr4:88438863 | G | A | 2 | a0006c0006t0001g0072 a0006c0006t0001g0073 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2556-1011G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 20/22 | chr4 | 88438863 | |||||||
| chr4:88439001 | G | A | 2 | a0006c0006t0001g0072 a0006c0006t0001g0073 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2556-873G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 20/22 | chr4 | 88439001 | |||||||
| chr4:88439119 | A | AC | 2 | a0001c0001t0003g0081 a0001c0001t0003g0083 |
2 | HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2556-755_2556-754i others(3): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 20/22 | chr4 | 88439119 | |||||||
| chr4:88439121 | G | T | 2 | a0001c0001t0003g0081 a0001c0001t0003g0083 |
2 | HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2556-753G>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 20/22 | chr4 | 88439121 | |||||||
| chr4:88439122 | G | C | 2 | a0001c0001t0003g0081 a0001c0001t0003g0083 |
2 | HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2556-752G>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 20/22 | chr4 | 88439122 | |||||||
| chr4:88439123 | A | T | 2 | a0001c0001t0003g0081 a0001c0001t0003g0083 |
2 | HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2556-751A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 20/22 | chr4 | 88439123 | |||||||
| chr4:88439124 | T | A | 2 | a0001c0001t0003g0081 a0001c0001t0003g0083 |
2 | HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2556-750T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 20/22 | chr4 | 88439124 | |||||||
| chr4:88439125 | G | C | 2 | a0001c0001t0003g0081 a0001c0001t0003g0083 |
2 | HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2556-749G>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 20/22 | chr4 | 88439125 | |||||||
| chr4:88439126 | G | C | 2 | a0001c0001t0003g0081 a0001c0001t0003g0083 |
2 | HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2556-748G>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 20/22 | chr4 | 88439126 | |||||||
| chr4:88439127 | T | A | 2 | a0001c0001t0003g0081 a0001c0001t0003g0083 |
2 | HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2556-747T>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 20/22 | chr4 | 88439127 | |||||||
| chr4:88439252 | C | T | 3 | a0009c0010t0002g0006 a0009c0010t0002g0119 a0009c0010t0002g0120 |
3 | HG02559.hp2 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2556-622C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 20/22 | chr4 | 88439252 | |||||||
| chr4:88439288 | C | T | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0012c0013t0001g0157 |
3 | HG02895.hp2 HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2556-586C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 20/22 | chr4 | 88439288 | |||||||
| chr4:88439362 | AGAAAG | A | 4 | a0001c0001t0001g0075 a0001c0001t0001g0088 a0001c0001t0001g0169 others(1): Show |
4 | HG02258.hp1 HG03041.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.2556-506_2556-502d others(7): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | 88439362 | ||||||
| chr4:88439371 | AG | A | 3 | a0009c0010t0002g0006 a0009c0010t0002g0119 a0009c0010t0002g0120 |
3 | HG02559.hp2 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2556-502delG | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 20/22 | chr4 | 88439371 | |||||||
| chr4:88439379 | A | G | 3 | a0009c0010t0002g0006 a0009c0010t0002g0119 a0009c0010t0002g0120 |
3 | HG02559.hp2 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2556-495A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 20/22 | chr4 | 88439379 | |||||||
| chr4:88439382 | G | A | 3 | a0009c0010t0002g0006 a0009c0010t0002g0119 a0009c0010t0002g0120 |
3 | HG02559.hp2 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2556-492G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 20/22 | chr4 | 88439382 | |||||||
| chr4:88439383 | A | G | 3 | a0009c0010t0002g0006 a0009c0010t0002g0119 a0009c0010t0002g0120 |
3 | HG02559.hp2 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2556-491A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 20/22 | chr4 | 88439383 | |||||||
| chr4:88439395 | AAAGGGAA others(2): Show |
A | 3 | a0009c0010t0002g0006 a0009c0010t0002g0119 a0009c0010t0002g0120 |
3 | HG02559.hp2 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2556-478_2556-470d others(11): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 20/22 | chr4 | 88439395 | |||||||
| chr4:88439408 | AGG | A | 3 | a0009c0010t0002g0006 a0009c0010t0002g0119 a0009c0010t0002g0120 |
3 | HG02559.hp2 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2556-464_2556-463d others(4): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | 88439408 | ||||||
| chr4:88439416 | G | A | 3 | a0009c0010t0002g0006 a0009c0010t0002g0119 a0009c0010t0002g0120 |
3 | HG02559.hp2 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2556-458G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 20/22 | chr4 | 88439416 | |||||||
| chr4:88439417 | G | A | 3 | a0009c0010t0002g0006 a0009c0010t0002g0119 a0009c0010t0002g0120 |
3 | HG02559.hp2 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2556-457G>A | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 20/22 | chr4 | 88439417 | |||||||
| chr4:88439727 | G | C | 1 | a0003c0016t0001g0171 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2556-147G>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 20/22 | chr4 | 88439727 | |||||||
| chr4:88439767 | A | G | 1 | a0007c0011t0001g0143 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2556-107A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 20/22 | chr4 | 88439767 | |||||||
| chr4:88439779 | C | CAATAGA | 9 | a0001c0001t0001g0084 a0001c0001t0001g0086 a0001c0001t0001g0087 others(6): Show |
9 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.2556-89_2556-84dup others(6): Show |
HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | 88439779 | ||||||
| chr4:88439837 | C | T | 1 | a0009c0010t0002g0119 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2556-37C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 20/22 | chr4 | 88439837 | |||||||
| chr4:88439842 | C | CT | 5 | a0001c0001t0001g0139 a0001c0001t0001g0155 a0002c0002t0001g0036 others(2): Show |
5 | HG02040.hp1 HG02040.hp2 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.2556-13dupT | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | 88439842 | ||||||
| chr4:88439842 | CT | C | 6 | a0001c0001t0001g0084 a0001c0001t0001g0154 a0003c0003t0001g0048 others(3): Show |
6 | HG01167.hp2 HG02451.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.2556-13delT | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | 88439842 | ||||||
| chr4:88440101 | A | G | 1 | a0001c0001t0001g0142 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2739+44A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 21/22 | chr4 | 88440101 | |||||||
| chr4:88440607 | C | T | 3 | a0009c0010t0002g0006 a0009c0010t0002g0119 a0009c0010t0002g0120 |
3 | HG02559.hp2 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2842+357C>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 22/22 | chr4 | 88440607 | |||||||
| chr4:88440677 | T | C | 1 | a0014c0018t0001g0066 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2842+427T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 22/22 | chr4 | 88440677 | |||||||
| chr4:88440822 | T | G | 1 | a0002c0002t0001g0133 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2842+572T>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 22/22 | chr4 | 88440822 | |||||||
| chr4:88441152 | A | G | 4 | a0001c0001t0001g0056 a0001c0001t0001g0141 a0001c0001t0001g0163 others(1): Show |
4 | HG01168.hp1 HG01169.hp2 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2842+902A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 22/22 | chr4 | 88441152 | |||||||
| chr4:88441604 | A | G | 15 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0034 others(12): Show |
15 | HG01167.hp1 HG01884.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.2843-630A>G | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 22/22 | chr4 | 88441604 | |||||||
| chr4:88441617 | T | C | 3 | a0009c0010t0002g0006 a0009c0010t0002g0119 a0009c0010t0002g0120 |
3 | HG02559.hp2 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2843-617T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 22/22 | chr4 | 88441617 | |||||||
| chr4:88441836 | T | C | 1 | a0008c0009t0001g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2843-398T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 22/22 | chr4 | 88441836 | |||||||
| chr4:88441959 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2843-275T>C | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 22/22 | chr4 | 88441959 | |||||||
| chr4:88442162 | A | T | 1 | a0004c0004t0001g0144 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2843-72A>T | HERC6 | ENSG00000138642.16 | transcript | ENST00000264346.12 | protein_coding | 22/22 | chr4 | 88442162 |