Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 25831 |
| ensemblid | ENSG00000092148.14 |
| hgncid | 20157 |
| symbol | HECTD1 |
| name | HECT domain E3 ubiquitin protein ligase 1 |
| refseq_nuc | NM_015382.4 |
| refseq_prot | NP_056197.3 |
| ensembl_nuc | ENST00000399332.6 |
| ensembl_prot | ENSP00000382269.1 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 31100117 |
| end | 31207793 |
| strand | - |
| ver | v1.2 |
| region | chr14:31100117-31207793 |
| region5000 | chr14:31095117-31212793 |
| regionname0 | HECTD1_chr14_31100117_31207793 |
| regionname5000 | HECTD1_chr14_31095117_31212793 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 2610 | 311 | 81 | 55 | 127 | 12 | 34 | 97 | HECTD1_chr14_31095117_31212793 | HECTD1 | MADVD others(2605): Show |
chr14 | 31095117 | 31212793 |
| a0002 | 0/0 | 2610 | 19 | 0 | 6 | 7 | 2 | 4 | 7 | HECTD1_chr14_31095117_31212793 | HECTD1 | MADVD others(2605): Show |
chr14 | 31095117 | 31212793 |
| a0003 | 0/0 | 2610 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | MADVD others(2605): Show |
chr14 | 31095117 | 31212793 |
| a0004 | 0/0 | 2610 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | MADVD others(2605): Show |
chr14 | 31095117 | 31212793 |
| a0005 | 0/0 | 2610 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | HECTD1_chr14_31095117_31212793 | HECTD1 | MADVD others(2605): Show |
chr14 | 31095117 | 31212793 |
| a0006 | 0/0 | 2610 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | MADVD others(2605): Show |
chr14 | 31095117 | 31212793 |
| a0007 | 0/0 | 2610 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | MADVD others(2605): Show |
chr14 | 31095117 | 31212793 |
| a0008 | 0/0 | 2610 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | MADVD others(2605): Show |
chr14 | 31095117 | 31212793 |
| a0009 | 0/0 | 2610 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | MADVD others(2605): Show |
chr14 | 31095117 | 31212793 |
| a0010 | 0/0 | 2610 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | MADVD others(2605): Show |
chr14 | 31095117 | 31212793 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 7830 | 114 | 25 | 23 | 45 | 6 | 14 | HECTD1_chr14_31095117_31212793 | HECTD1 | ATGGC others(7825): Show |
chr14 | 31095117 | 31212793 | ||
| a0001c0002 | 0/0 | 7830 | 52 | 30 | 3 | 19 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | ATGGC others(7825): Show |
chr14 | 31095117 | 31212793 | ||
| a0001c0003 | 0/0 | 7830 | 37 | 3 | 5 | 17 | 1 | 11 | HECTD1_chr14_31095117_31212793 | HECTD1 | ATGGC others(7825): Show |
chr14 | 31095117 | 31212793 | ||
| a0001c0004 | 0/0 | 7830 | 28 | 14 | 9 | 0 | 0 | 5 | HECTD1_chr14_31095117_31212793 | HECTD1 | ATGGC others(7825): Show |
chr14 | 31095117 | 31212793 | ||
| a0001c0006 | 0/0 | 7830 | 14 | 0 | 4 | 10 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | ATGGC others(7825): Show |
chr14 | 31095117 | 31212793 | ||
| a0001c0007 | 0/1 | 7830 | 14 | 0 | 6 | 0 | 4 | 3 | HECTD1_chr14_31095117_31212793 | HECTD1 | ATGGC others(7825): Show |
chr14 | 31095117 | 31212793 | ||
| a0001c0008 | 0/0 | 7830 | 12 | 0 | 0 | 12 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | ATGGC others(7825): Show |
chr14 | 31095117 | 31212793 | ||
| a0001c0009 | 0/0 | 7830 | 8 | 0 | 0 | 8 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | ATGGC others(7825): Show |
chr14 | 31095117 | 31212793 | ||
| a0001c0010 | 0/0 | 7830 | 5 | 0 | 0 | 4 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | ATGGC others(7825): Show |
chr14 | 31095117 | 31212793 | ||
| a0001c0011 | 0/0 | 7830 | 4 | 4 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | ATGGC others(7825): Show |
chr14 | 31095117 | 31212793 | ||
| a0001c0012 | 0/0 | 7830 | 4 | 0 | 0 | 4 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | ATGGC others(7825): Show |
chr14 | 31095117 | 31212793 | ||
| a0001c0013 | 0/0 | 7830 | 3 | 0 | 1 | 2 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | ATGGC others(7825): Show |
chr14 | 31095117 | 31212793 | ||
| a0001c0017 | 0/0 | 7830 | 2 | 2 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | ATGGC others(7825): Show |
chr14 | 31095117 | 31212793 | ||
| a0001c0018 | 0/0 | 7830 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | ATGGC others(7825): Show |
chr14 | 31095117 | 31212793 | ||
| a0001c0021 | 0/0 | 7830 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | ATGGC others(7825): Show |
chr14 | 31095117 | 31212793 | ||
| a0001c0022 | 0/0 | 7830 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | ATGGC others(7825): Show |
chr14 | 31095117 | 31212793 | ||
| a0001c0023 | 0/0 | 7830 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | ATGGC others(7825): Show |
chr14 | 31095117 | 31212793 | ||
| a0001c0025 | 0/0 | 7830 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | ATGGC others(7825): Show |
chr14 | 31095117 | 31212793 | ||
| a0001c0026 | 0/0 | 7830 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | ATGGC others(7825): Show |
chr14 | 31095117 | 31212793 | ||
| a0001c0029 | 0/0 | 7830 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | ATGGC others(7825): Show |
chr14 | 31095117 | 31212793 | ||
| a0001c0030 | 0/0 | 7830 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | ATGGC others(7825): Show |
chr14 | 31095117 | 31212793 | ||
| a0001c0031 | 0/0 | 7830 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | ATGGC others(7825): Show |
chr14 | 31095117 | 31212793 | ||
| a0001c0033 | 0/0 | 7830 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | ATGGC others(7825): Show |
chr14 | 31095117 | 31212793 | ||
| a0001c0034 | 0/0 | 7830 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | ATGGC others(7825): Show |
chr14 | 31095117 | 31212793 | ||
| a0001c0035 | 0/0 | 7830 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | ATGGC others(7825): Show |
chr14 | 31095117 | 31212793 | ||
| a0001c0036 | 0/0 | 7830 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | ATGGC others(7825): Show |
chr14 | 31095117 | 31212793 | ||
| a0001c0037 | 0/0 | 7830 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | ATGGC others(7825): Show |
chr14 | 31095117 | 31212793 | ||
| a0002c0005 | 0/0 | 7830 | 18 | 0 | 6 | 7 | 1 | 4 | HECTD1_chr14_31095117_31212793 | HECTD1 | ATGGC others(7825): Show |
chr14 | 31095117 | 31212793 | ||
| a0002c0020 | 0/0 | 7830 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | ATGGC others(7825): Show |
chr14 | 31095117 | 31212793 | ||
| a0003c0014 | 0/0 | 7830 | 3 | 3 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | ATGGC others(7825): Show |
chr14 | 31095117 | 31212793 | ||
| a0004c0015 | 0/0 | 7830 | 2 | 0 | 0 | 0 | 0 | 2 | HECTD1_chr14_31095117_31212793 | HECTD1 | ATGGC others(7825): Show |
chr14 | 31095117 | 31212793 | ||
| a0005c0016 | 0/0 | 7830 | 2 | 0 | 0 | 2 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | ATGGC others(7825): Show |
chr14 | 31095117 | 31212793 | ||
| a0006c0024 | 0/0 | 7830 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | ATGGC others(7825): Show |
chr14 | 31095117 | 31212793 | ||
| a0007c0028 | 0/0 | 7830 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | ATGGC others(7825): Show |
chr14 | 31095117 | 31212793 | ||
| a0008c0027 | 0/0 | 7830 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | ATGGC others(7825): Show |
chr14 | 31095117 | 31212793 | ||
| a0009c0019 | 0/0 | 7830 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | ATGGC others(7825): Show |
chr14 | 31095117 | 31212793 | ||
| a0010c0032 | 0/0 | 7830 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | ATGGC others(7825): Show |
chr14 | 31095117 | 31212793 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 9445 | 112 | 25 | 22 | 44 | 6 | 14 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0001c0001t0002 | 0/0 | 9445 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0001c0001t0012 | 0/0 | 9445 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0001c0002t0001 | 0/0 | 9445 | 45 | 26 | 0 | 19 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0001c0002t0006 | 0/0 | 9445 | 3 | 2 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0001c0002t0010 | 0/0 | 9445 | 2 | 1 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0001c0002t0013 | 0/0 | 9445 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0001c0002t0014 | 0/0 | 9445 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0001c0003t0001 | 0/0 | 9445 | 36 | 3 | 5 | 16 | 1 | 11 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0001c0003t0011 | 0/0 | 9445 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0001c0004t0001 | 0/0 | 9445 | 21 | 10 | 8 | 0 | 0 | 3 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0001c0004t0005 | 0/0 | 9445 | 5 | 4 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0001c0004t0008 | 0/0 | 9445 | 2 | 0 | 0 | 0 | 0 | 2 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0001c0006t0001 | 0/0 | 9445 | 3 | 0 | 0 | 3 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0001c0006t0002 | 0/0 | 9445 | 11 | 0 | 4 | 7 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0001c0007t0001 | 0/1 | 9445 | 11 | 0 | 5 | 0 | 2 | 3 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0001c0007t0007 | 0/0 | 9445 | 3 | 0 | 1 | 0 | 2 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0001c0008t0001 | 0/0 | 9445 | 12 | 0 | 0 | 12 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0001c0009t0003 | 0/0 | 9445 | 8 | 0 | 0 | 8 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0001c0010t0004 | 0/0 | 9445 | 5 | 0 | 0 | 4 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0001c0011t0001 | 0/0 | 9445 | 4 | 4 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0001c0012t0001 | 0/0 | 9445 | 4 | 0 | 0 | 4 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0001c0013t0001 | 0/0 | 9445 | 3 | 0 | 1 | 2 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0001c0017t0009 | 0/0 | 9445 | 2 | 2 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0001c0018t0004 | 0/0 | 9445 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0001c0021t0001 | 0/0 | 9445 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0001c0022t0001 | 0/0 | 9445 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0001c0023t0001 | 0/0 | 9445 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0001c0025t0001 | 0/0 | 9445 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0001c0026t0001 | 0/0 | 9445 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0001c0029t0001 | 0/0 | 9445 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0001c0030t0001 | 0/0 | 9445 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0001c0031t0001 | 0/0 | 9445 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0001c0033t0001 | 0/0 | 9445 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0001c0034t0001 | 0/0 | 9445 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0001c0035t0001 | 0/0 | 9445 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0001c0036t0001 | 0/0 | 9445 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0001c0037t0001 | 0/0 | 9445 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0002c0005t0001 | 0/0 | 9445 | 18 | 0 | 6 | 7 | 1 | 4 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0002c0020t0001 | 0/0 | 9445 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0003c0014t0001 | 0/0 | 9445 | 3 | 3 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0004c0015t0001 | 0/0 | 9445 | 2 | 0 | 0 | 0 | 0 | 2 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0005c0016t0001 | 0/0 | 9445 | 2 | 0 | 0 | 2 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0006c0024t0001 | 0/0 | 9445 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0007c0028t0001 | 0/0 | 9445 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0008c0027t0001 | 0/0 | 9445 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0009c0019t0001 | 0/0 | 9445 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| a0010c0032t0001 | 0/0 | 9445 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | GCCTC others(9440): Show |
chr14 | 31095117 | 31212793 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0234 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0012g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0006g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0006g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0006g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0010g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0010g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0013g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0014g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0011g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0005g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0005g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0005g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0005g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0005g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0008g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0008g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0006t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0006t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0006t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0006t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0006t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0006t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0006t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0006t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0006t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0006t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0006t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0006t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0006t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0006t0002g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0007t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0007t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0007t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0007t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0007t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0007t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0007t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0007t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0007t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0007t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0007t0001g0045 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0007t0007g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0007t0007g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0007t0007g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0008t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0008t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0008t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0008t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0008t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0008t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0008t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0008t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0008t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0008t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0008t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0008t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0009t0003g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0009t0003g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0009t0003g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0009t0003g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0009t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0009t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0009t0003g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0009t0003g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0010t0004g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0010t0004g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0010t0004g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0010t0004g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0010t0004g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0011t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0011t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0011t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0011t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0012t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0012t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0012t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0012t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0013t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0013t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0013t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0017t0009g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0017t0009g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0018t0004g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0021t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0022t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0023t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0025t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0026t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0029t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0030t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0031t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0033t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0034t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0035t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0036t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0037t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0002c0005t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0002c0005t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0002c0005t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0002c0005t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0002c0005t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0002c0005t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0002c0005t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0002c0005t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0002c0005t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0002c0005t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0002c0005t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0002c0005t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0002c0005t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0002c0005t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0002c0005t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0002c0005t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0002c0005t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0002c0005t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0002c0020t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0003c0014t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0003c0014t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0003c0014t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0004c0015t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0004c0015t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0005c0016t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0005c0016t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0006c0024t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0007c0028t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0008c0027t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0009c0019t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0010c0032t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0007 | t0001 | g0028 | EUR | GBR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0145 | EUR | GBR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00140 | hp1 | a0001 | c0003 | t0001 | g0292 | EUR | GBR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00140 | hp2 | a0002 | c0005 | t0001 | g0270 | EUR | GBR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0152 | EUR | FIN | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00280 | hp2 | a0002 | c0020 | t0001 | g0278 | EUR | FIN | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00323 | hp1 | a0001 | c0007 | t0007 | g0025 | EUR | FIN | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0241 | EUR | FIN | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00423 | hp2 | a0001 | c0003 | t0001 | g0289 | EAS | CHS | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | CHS | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00544 | hp2 | a0001 | c0008 | t0001 | g0308 | EAS | CHS | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00558 | hp1 | a0001 | c0009 | t0003 | g0006 | EAS | CHS | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00609 | hp2 | a0001 | c0009 | t0003 | g0005 | EAS | CHS | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00621 | hp2 | a0001 | c0035 | t0001 | g0064 | EAS | CHS | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00639 | hp2 | a0001 | c0002 | t0006 | g0023 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00673 | hp1 | a0001 | c0034 | t0001 | g0311 | EAS | CHS | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00733 | hp1 | a0002 | c0005 | t0001 | g0274 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00738 | hp2 | a0001 | c0007 | t0001 | g0039 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00741 | hp2 | a0001 | c0036 | t0001 | g0043 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01069 | hp1 | a0001 | c0007 | t0001 | g0033 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01069 | hp2 | a0001 | c0004 | t0001 | g0067 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01071 | hp2 | a0001 | c0004 | t0001 | g0068 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01074 | hp1 | a0001 | c0007 | t0001 | g0030 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01074 | hp2 | a0001 | c0006 | t0002 | g0210 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01081 | hp2 | a0001 | c0003 | t0001 | g0099 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01099 | hp1 | a0001 | c0013 | t0001 | g0130 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01099 | hp2 | a0001 | c0004 | t0001 | g0037 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01106 | hp1 | a0001 | c0004 | t0005 | g0093 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01109 | hp1 | a0001 | c0029 | t0001 | g0327 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01109 | hp2 | a0001 | c0002 | t0013 | g0339 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01168 | hp2 | a0002 | c0005 | t0001 | g0271 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01175 | hp2 | a0001 | c0003 | t0001 | g0328 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01192 | hp2 | a0001 | c0003 | t0001 | g0299 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01243 | hp1 | a0001 | c0003 | t0001 | g0318 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01243 | hp2 | a0002 | c0005 | t0001 | g0275 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01255 | hp1 | a0001 | c0001 | t0012 | g0178 | AMR | CLM | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01255 | hp2 | a0001 | c0007 | t0001 | g0029 | AMR | CLM | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01256 | hp1 | a0001 | c0007 | t0007 | g0032 | AMR | CLM | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01261 | hp2 | a0001 | c0004 | t0001 | g0065 | AMR | CLM | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01346 | hp2 | a0001 | c0003 | t0001 | g0314 | AMR | CLM | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01358 | hp1 | a0002 | c0005 | t0001 | g0265 | AMR | CLM | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01433 | hp2 | a0001 | c0007 | t0001 | g0036 | AMR | CLM | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | CLM | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01496 | hp2 | a0001 | c0037 | t0001 | g0261 | AMR | CLM | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0235 | EUR | IBS | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01516 | hp2 | a0001 | c0007 | t0007 | g0031 | EUR | IBS | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0106 | AFR | ACB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0113 | AFR | ACB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01891 | hp2 | a0001 | c0004 | t0001 | g0044 | AFR | ACB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01928 | hp1 | a0002 | c0005 | t0001 | g0262 | AMR | PEL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01928 | hp2 | a0001 | c0004 | t0001 | g0078 | AMR | PEL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01943 | hp1 | a0006 | c0024 | t0001 | g0074 | AMR | PEL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01952 | hp1 | a0001 | c0030 | t0001 | g0280 | AMR | PEL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01952 | hp2 | a0001 | c0006 | t0002 | g0329 | AMR | PEL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01975 | hp1 | a0001 | c0004 | t0001 | g0080 | AMR | PEL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01993 | hp2 | a0001 | c0002 | t0010 | g0108 | AMR | PEL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02015 | hp1 | a0001 | c0003 | t0001 | g0290 | EAS | KHV | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0259 | AFR | ACB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02056 | hp2 | a0001 | c0003 | t0001 | g0333 | EAS | KHV | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02071 | hp1 | a0001 | c0023 | t0001 | g0179 | EAS | KHV | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02071 | hp2 | a0001 | c0009 | t0003 | g0007 | EAS | KHV | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02074 | hp1 | a0001 | c0010 | t0004 | g0014 | EAS | KHV | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0079 | EAS | KHV | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02080 | hp1 | a0001 | c0003 | t0001 | g0312 | EAS | KHV | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0063 | EAS | KHV | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | KHV | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02083 | hp2 | a0001 | c0006 | t0001 | g0149 | EAS | KHV | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02129 | hp1 | a0001 | c0003 | t0001 | g0316 | EAS | KHV | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0071 | EAS | KHV | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02145 | hp1 | a0003 | c0014 | t0001 | g0081 | AFR | ACB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02155 | hp1 | a0001 | c0033 | t0001 | g0319 | EAS | CDX | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02155 | hp2 | a0001 | c0009 | t0003 | g0003 | EAS | CDX | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0256 | AFR | ACB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02257 | hp2 | a0001 | c0025 | t0001 | g0092 | AFR | ACB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02258 | hp1 | a0001 | c0002 | t0006 | g0024 | AFR | ACB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02273 | hp1 | a0001 | c0006 | t0002 | g0224 | AMR | PEL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0257 | AFR | ACB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02280 | hp2 | a0001 | c0017 | t0009 | g0020 | AFR | ACB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02300 | hp1 | a0001 | c0006 | t0002 | g0209 | AMR | PEL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02300 | hp2 | a0001 | c0004 | t0001 | g0066 | AMR | PEL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02451 | hp2 | a0007 | c0028 | t0001 | g0070 | AFR | ACB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02572 | hp1 | a0001 | c0021 | t0001 | g0229 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02572 | hp2 | a0001 | c0004 | t0005 | g0095 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02602 | hp1 | a0001 | c0003 | t0001 | g0305 | SAS | PJL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02602 | hp2 | a0002 | c0005 | t0001 | g0263 | SAS | PJL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0251 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0105 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02630 | hp2 | a0001 | c0011 | t0001 | g0049 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0252 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02683 | hp1 | a0001 | c0004 | t0001 | g0088 | SAS | PJL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02698 | hp1 | a0001 | c0003 | t0001 | g0282 | SAS | PJL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02698 | hp2 | a0001 | c0007 | t0001 | g0027 | SAS | PJL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0086 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02809 | hp1 | a0001 | c0011 | t0001 | g0048 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0085 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02818 | hp1 | a0001 | c0002 | t0014 | g0340 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0111 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0104 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0103 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02922 | hp1 | a0001 | c0011 | t0001 | g0047 | AFR | ESN | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ESN | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0254 | AFR | ESN | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02965 | hp2 | a0001 | c0004 | t0001 | g0026 | AFR | ESN | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02970 | hp1 | a0001 | c0017 | t0009 | g0021 | AFR | ESN | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02970 | hp2 | a0001 | c0004 | t0001 | g0001 | AFR | ESN | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03017 | hp2 | a0001 | c0003 | t0001 | g0304 | SAS | PJL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03041 | hp1 | a0001 | c0002 | t0010 | g0107 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03041 | hp2 | a0001 | c0011 | t0001 | g0050 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0102 | AFR | MSL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0255 | AFR | ESN | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03130 | hp2 | a0001 | c0026 | t0001 | g0091 | AFR | ESN | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0250 | AFR | ESN | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | ESN | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0258 | AFR | ESN | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0335 | AFR | ESN | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0337 | AFR | MSL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03209 | hp2 | a0001 | c0004 | t0005 | g0094 | AFR | MSL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | MSL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03225 | hp2 | a0001 | c0004 | t0001 | g0089 | AFR | MSL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03239 | hp1 | a0001 | c0003 | t0001 | g0301 | SAS | PJL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | MSL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0253 | AFR | MSL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | MSL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | MSL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03490 | hp2 | a0004 | c0015 | t0001 | g0161 | SAS | PJL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03492 | hp2 | a0004 | c0015 | t0001 | g0144 | SAS | PJL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03516 | hp1 | a0003 | c0014 | t0001 | g0082 | AFR | ESN | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ESN | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03540 | hp1 | a0001 | c0002 | t0006 | g0022 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03540 | hp2 | a0008 | c0027 | t0001 | g0110 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | MSL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03579 | hp2 | a0001 | c0004 | t0005 | g0096 | AFR | MSL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03654 | hp1 | a0001 | c0003 | t0001 | g0322 | SAS | PJL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03669 | hp1 | a0001 | c0007 | t0001 | g0040 | SAS | PJL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03704 | hp1 | a0001 | c0004 | t0008 | g0012 | SAS | PJL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03704 | hp2 | a0002 | c0005 | t0001 | g0276 | SAS | PJL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03710 | hp2 | a0001 | c0003 | t0001 | g0313 | SAS | PJL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03831 | hp1 | a0002 | c0005 | t0001 | g0273 | SAS | BEB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | BEB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03834 | hp1 | a0001 | c0007 | t0001 | g0041 | SAS | BEB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03834 | hp2 | a0001 | c0003 | t0001 | g0302 | SAS | BEB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03927 | hp2 | a0001 | c0004 | t0001 | g0098 | SAS | BEB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | BEB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03942 | hp2 | a0001 | c0010 | t0004 | g0018 | SAS | BEB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | STU | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG04115 | hp2 | a0001 | c0003 | t0001 | g0324 | SAS | STU | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG04184 | hp1 | a0001 | c0003 | t0001 | g0300 | SAS | BEB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG04184 | hp2 | a0001 | c0004 | t0008 | g0013 | SAS | BEB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | STU | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG04199 | hp2 | a0001 | c0003 | t0001 | g0294 | SAS | STU | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG04204 | hp1 | a0001 | c0004 | t0001 | g0097 | SAS | STU | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG04204 | hp2 | a0002 | c0005 | t0001 | g0264 | SAS | STU | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | CHB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | CHB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18906 | hp1 | a0001 | c0004 | t0001 | g0042 | AFR | YRI | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | YRI | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18939 | hp1 | a0001 | c0003 | t0001 | g0295 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18943 | hp1 | a0001 | c0012 | t0001 | g0060 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18943 | hp2 | a0001 | c0006 | t0002 | g0189 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18946 | hp1 | a0001 | c0008 | t0001 | g0287 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18947 | hp1 | a0001 | c0003 | t0001 | g0321 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18947 | hp2 | a0001 | c0006 | t0002 | g0232 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18948 | hp1 | a0001 | c0003 | t0001 | g0288 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18953 | hp2 | a0001 | c0003 | t0001 | g0303 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18954 | hp2 | a0001 | c0003 | t0001 | g0309 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18956 | hp2 | a0001 | c0008 | t0001 | g0326 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18957 | hp1 | a0001 | c0012 | t0001 | g0055 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18957 | hp2 | a0001 | c0006 | t0001 | g0286 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18961 | hp2 | a0001 | c0022 | t0001 | g0284 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18966 | hp1 | a0001 | c0012 | t0001 | g0056 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18968 | hp1 | a0001 | c0003 | t0001 | g0334 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18968 | hp2 | a0001 | c0012 | t0001 | g0052 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18969 | hp1 | a0001 | c0013 | t0001 | g0182 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18969 | hp2 | a0001 | c0008 | t0001 | g0310 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18970 | hp2 | a0002 | c0005 | t0001 | g0267 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18971 | hp1 | a0001 | c0010 | t0004 | g0015 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18975 | hp1 | a0001 | c0003 | t0011 | g0011 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18977 | hp2 | a0001 | c0008 | t0001 | g0320 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18982 | hp1 | a0001 | c0009 | t0003 | g0010 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18987 | hp1 | a0001 | c0003 | t0001 | g0315 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18987 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18992 | hp1 | a0001 | c0018 | t0004 | g0019 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18994 | hp1 | a0001 | c0003 | t0001 | g0330 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18994 | hp2 | a0001 | c0006 | t0002 | g0231 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18995 | hp1 | a0001 | c0008 | t0001 | g0325 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18999 | hp1 | a0002 | c0005 | t0001 | g0266 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18999 | hp2 | a0001 | c0006 | t0001 | g0323 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19000 | hp2 | a0001 | c0008 | t0001 | g0281 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19001 | hp1 | a0002 | c0005 | t0001 | g0277 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19002 | hp2 | a0001 | c0008 | t0001 | g0331 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19005 | hp2 | a0002 | c0005 | t0001 | g0269 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19006 | hp1 | a0002 | c0005 | t0001 | g0046 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19009 | hp1 | a0001 | c0006 | t0002 | g0192 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19011 | hp2 | a0001 | c0008 | t0001 | g0306 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19012 | hp1 | a0001 | c0013 | t0001 | g0165 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19012 | hp2 | a0001 | c0003 | t0001 | g0296 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19043 | hp1 | a0001 | c0003 | t0001 | g0317 | AFR | LWK | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19043 | hp2 | a0001 | c0004 | t0005 | g0090 | AFR | LWK | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19055 | hp1 | a0001 | c0008 | t0001 | g0283 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19055 | hp2 | a0001 | c0009 | t0003 | g0009 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19057 | hp1 | a0001 | c0010 | t0004 | g0017 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19062 | hp1 | a0001 | c0003 | t0001 | g0332 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19065 | hp1 | a0001 | c0008 | t0001 | g0307 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19065 | hp2 | a0001 | c0006 | t0002 | g0163 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19067 | hp1 | a0009 | c0019 | t0001 | g0211 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19067 | hp2 | a0001 | c0006 | t0002 | g0207 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19068 | hp1 | a0001 | c0008 | t0001 | g0279 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19074 | hp2 | a0001 | c0009 | t0003 | g0008 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19075 | hp2 | a0001 | c0010 | t0004 | g0016 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19076 | hp1 | a0010 | c0032 | t0001 | g0087 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19076 | hp2 | a0001 | c0006 | t0002 | g0125 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19077 | hp2 | a0001 | c0009 | t0003 | g0004 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19078 | hp1 | a0005 | c0016 | t0001 | g0137 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19078 | hp2 | a0002 | c0005 | t0001 | g0272 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19082 | hp1 | a0001 | c0003 | t0001 | g0285 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19082 | hp2 | a0005 | c0016 | t0001 | g0133 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19087 | hp1 | a0002 | c0005 | t0001 | g0260 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | YRI | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0114 | AFR | YRI | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA20129 | hp1 | a0001 | c0003 | t0001 | g0291 | AFR | ASW | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA20129 | hp2 | a0001 | c0003 | t0001 | g0298 | AFR | ASW | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA20752 | hp1 | a0001 | c0007 | t0001 | g0035 | EUR | TSI | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0236 | EUR | TSI | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0173 | EUR | TSI | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA20805 | hp2 | a0001 | c0031 | t0001 | g0293 | EUR | TSI | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | GIH | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA20905 | hp2 | a0001 | c0003 | t0001 | g0297 | SAS | GIH | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01123 | hp1 | a0001 | c0004 | t0001 | g0075 | AMR | CLM | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01123 | hp2 | a0002 | c0005 | t0001 | g0268 | AMR | CLM | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0336 | AFR | ACB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0112 | AFR | ACB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02486 | hp1 | a0001 | c0004 | t0001 | g0038 | AFR | ACB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02486 | hp2 | a0003 | c0014 | t0001 | g0083 | AFR | ACB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02559 | hp1 | a0001 | c0004 | t0001 | g0001 | AFR | ACB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0109 | AFR | ACB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG06807 | hp1 | a0001 | c0004 | t0001 | g0034 | AFR | USA | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0051 | AFR | USA | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA20300 | hp1 | a0001 | c0004 | t0001 | g0073 | AFR | USA | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0338 | AFR | USA | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA21309 | hp1 | a0001 | c0004 | t0001 | g0115 | AFR | LWK | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | LWK | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| homoSapiens | chm13v2 | a0001 | c0007 | t0001 | g0045 | REF | REF | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0234 | REF | REF | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:31105639 | C | T | 1 | a0004 | 2 | HG03490.hp2 HG03492.hp2 |
missense_variant | MODERATE | c.7256G>A | p.Arg2419Lys | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 39/43 | 8055/9445 | 7256/7833 | 2419/2610 | chr14 | 31105639 | |||
| chr14:31113406 | A | T | 1 | a0010 | 1 | NA19076.hp1 | missense_variant | MODERATE | c.5935T>A | p.Leu1979Ile | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 33/43 | 6734/9445 | 5935/7833 | 1979/2610 | chr14 | 31113406 | |||
| chr14:31113962 | G | C | 1 | a0010 | 1 | NA19076.hp1 | missense_variant | MODERATE | c.5771C>G | p.Ala1924Gly | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 32/43 | 6570/9445 | 5771/7833 | 1924/2610 | chr14 | 31113962 | |||
| chr14:31114306 | C | T | 1 | a0002 | 19 | HG00140.hp2 HG00280.hp2 HG00733.hp1 others(16): Show |
missense_variant | MODERATE | c.5653G>A | p.Glu1885Lys | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 31/43 | 6452/9445 | 5653/7833 | 1885/2610 | chr14 | 31114306 | |||
| chr14:31116441 | G | T | 1 | a0009 | 1 | NA19067.hp1 | missense_variant | MODERATE | c.5413C>A | p.Leu1805Ile | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 30/43 | 6212/9445 | 5413/7833 | 1805/2610 | chr14 | 31116441 | |||
| chr14:31127928 | G | C | 1 | a0006 | 1 | HG01943.hp1 | missense_variant | MODERATE | c.4838C>G | p.Ser1613Cys | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/43 | 5637/9445 | 4838/7833 | 1613/2610 | chr14 | 31127928 | |||
| chr14:31129095 | T | C | 1 | a0005 | 2 | NA19078.hp1 NA19082.hp2 |
missense_variant | MODERATE | c.4276A>G | p.Ile1426Val | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 25/43 | 5075/9445 | 4276/7833 | 1426/2610 | chr14 | 31129095 | |||
| chr14:31129200 | C | T | 1 | a0007 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.4171G>A | p.Val1391Met | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 25/43 | 4970/9445 | 4171/7833 | 1391/2610 | chr14 | 31129200 | |||
| chr14:31129209 | C | T | 1 | a0008 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.4162G>A | p.Val1388Met | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 25/43 | 4961/9445 | 4162/7833 | 1388/2610 | chr14 | 31129209 | |||
| chr14:31148762 | C | A | 1 | a0003 | 3 | HG02145.hp1 HG02486.hp2 HG03516.hp1 |
missense_variant | MODERATE | c.2455G>T | p.Gly819Cys | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/43 | 3254/9445 | 2455/7833 | 819/2610 | chr14 | 31148762 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:31101195 | G | A | 1 | a0001c0009 | 8 | HG00558.hp1 HG00609.hp2 HG02071.hp2 others(5): Show |
synonymous_variant | LOW | c.7680C>T | p.Leu2560Leu | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 42/43 | 8479/9445 | 7680/7833 | 2560/2610 | chr14 | 31101195 | |||
| chr14:31102963 | C | T | 1 | a0001c0030 | 1 | HG01952.hp1 | synonymous_variant | LOW | c.7503G>A | p.Glu2501Glu | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 41/43 | 8302/9445 | 7503/7833 | 2501/2610 | chr14 | 31102963 | |||
| chr14:31109556 | C | T | 19 | a0001c0002 a0001c0003 a0001c0008 others(16): Show |
130 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(127): Show |
synonymous_variant | LOW | c.6321G>A | p.Glu2107Glu | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 36/43 | 7120/9445 | 6321/7833 | 2107/2610 | chr14 | 31109556 | |||
| chr14:31109585 | A | G | 1 | a0001c0021 | 1 | HG02572.hp1 | synonymous_variant | LOW | c.6292T>C | p.Leu2098Leu | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 36/43 | 7091/9445 | 6292/7833 | 2098/2610 | chr14 | 31109585 | |||
| chr14:31113320 | T | C | 28 | a0001c0002 a0001c0003 a0001c0004 others(25): Show |
202 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(199): Show |
synonymous_variant | LOW | c.6021A>G | p.Leu2007Leu | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 33/43 | 6820/9445 | 6021/7833 | 2007/2610 | chr14 | 31113320 | |||
| chr14:31113958 | G | A | 1 | a0010c0032 | 1 | NA19076.hp1 | synonymous_variant | LOW | c.5775C>T | p.Phe1925Phe | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 32/43 | 6574/9445 | 5775/7833 | 1925/2610 | chr14 | 31113958 | |||
| chr14:31113961 | A | G | 1 | a0010c0032 | 1 | NA19076.hp1 | synonymous_variant | LOW | c.5772T>C | p.Ala1924Ala | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 32/43 | 6571/9445 | 5772/7833 | 1924/2610 | chr14 | 31113961 | |||
| chr14:31113967 | G | A | 4 | a0001c0008 a0001c0030 a0001c0033 others(1): Show |
15 | HG00544.hp2 HG00673.hp1 HG01952.hp1 others(12): Show |
synonymous_variant | LOW | c.5766C>T | p.Asp1922Asp | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 32/43 | 6565/9445 | 5766/7833 | 1922/2610 | chr14 | 31113967 | |||
| chr14:31116415 | C | T | 1 | a0001c0029 | 1 | HG01109.hp1 | synonymous_variant | LOW | c.5439G>A | p.Pro1813Pro | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 30/43 | 6238/9445 | 5439/7833 | 1813/2610 | chr14 | 31116415 | |||
| chr14:31127870 | T | C | 1 | a0001c0031 | 1 | NA20805.hp2 | synonymous_variant | LOW | c.4896A>G | p.Gln1632Gln | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/43 | 5695/9445 | 4896/7833 | 1632/2610 | chr14 | 31127870 | |||
| chr14:31128835 | T | C | 1 | a0001c0035 | 1 | HG00621.hp2 | synonymous_variant | LOW | c.4536A>G | p.Ala1512Ala | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 25/43 | 5335/9445 | 4536/7833 | 1512/2610 | chr14 | 31128835 | |||
| chr14:31128892 | T | C | 1 | a0001c0017 | 2 | HG02280.hp2 HG02970.hp1 |
synonymous_variant | LOW | c.4479A>G | p.Ser1493Ser | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 25/43 | 5278/9445 | 4479/7833 | 1493/2610 | chr14 | 31128892 | |||
| chr14:31129042 | A | G | 7 | a0001c0003 a0001c0008 a0001c0029 others(4): Show |
54 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(51): Show |
synonymous_variant | LOW | c.4329T>C | p.Ser1443Ser | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 25/43 | 5128/9445 | 4329/7833 | 1443/2610 | chr14 | 31129042 | |||
| chr14:31129297 | T | C | 1 | a0001c0026 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.4074A>G | p.Gln1358Gln | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 25/43 | 4873/9445 | 4074/7833 | 1358/2610 | chr14 | 31129297 | |||
| chr14:31133254 | T | G | 1 | a0001c0018 | 1 | NA18992.hp1 | synonymous_variant | LOW | c.3906A>C | p.Thr1302Thr | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/43 | 4705/9445 | 3906/7833 | 1302/2610 | chr14 | 31133254 | |||
| chr14:31133257 | G | A | 1 | a0001c0033 | 1 | HG02155.hp1 | synonymous_variant | LOW | c.3903C>T | p.Val1301Val | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/43 | 4702/9445 | 3903/7833 | 1301/2610 | chr14 | 31133257 | |||
| chr14:31134904 | G | C | 1 | a0001c0025 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.3546C>G | p.Thr1182Thr | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/43 | 4345/9445 | 3546/7833 | 1182/2610 | chr14 | 31134904 | |||
| chr14:31149087 | A | G | 2 | a0001c0011 a0001c0026 |
5 | HG02630.hp2 HG02809.hp1 HG02922.hp1 others(2): Show |
synonymous_variant | LOW | c.2229T>C | p.Pro743Pro | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 14/43 | 3028/9445 | 2229/7833 | 743/2610 | chr14 | 31149087 | |||
| chr14:31150186 | T | C | 20 | a0001c0002 a0001c0003 a0001c0008 others(17): Show |
131 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(128): Show |
synonymous_variant | LOW | c.1968A>G | p.Gln656Gln | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 13/43 | 2767/9445 | 1968/7833 | 656/2610 | chr14 | 31150186 | |||
| chr14:31157204 | T | C | 2 | a0001c0010 a0001c0018 |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
synonymous_variant | LOW | c.1722A>G | p.Thr574Thr | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 11/43 | 2521/9445 | 1722/7833 | 574/2610 | chr14 | 31157204 | |||
| chr14:31168347 | A | G | 1 | a0001c0013 | 3 | HG01099.hp1 NA18969.hp1 NA19012.hp1 |
synonymous_variant | LOW | c.1573T>C | p.Leu525Leu | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/43 | 2372/9445 | 1573/7833 | 525/2610 | chr14 | 31168347 | |||
| chr14:31168468 | A | G | 1 | a0001c0036 | 1 | HG00741.hp2 | synonymous_variant | LOW | c.1452T>C | p.Asp484Asp | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/43 | 2251/9445 | 1452/7833 | 484/2610 | chr14 | 31168468 | |||
| chr14:31169465 | G | A | 1 | a0001c0023 | 1 | HG02071.hp1 | synonymous_variant | LOW | c.1336C>T | p.Leu446Leu | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 9/43 | 2135/9445 | 1336/7833 | 446/2610 | chr14 | 31169465 | |||
| chr14:31173600 | G | A | 1 | a0001c0034 | 1 | HG00673.hp1 | synonymous_variant | LOW | c.810C>T | p.Ser270Ser | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 5/43 | 1609/9445 | 810/7833 | 270/2610 | chr14 | 31173600 | |||
| chr14:31173651 | T | G | 2 | a0001c0012 a0001c0035 |
5 | HG00621.hp2 NA18943.hp1 NA18957.hp1 others(2): Show |
synonymous_variant | LOW | c.759A>C | p.Ala253Ala | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 5/43 | 1558/9445 | 759/7833 | 253/2610 | chr14 | 31173651 | |||
| chr14:31178035 | G | A | 28 | a0001c0002 a0001c0003 a0001c0004 others(25): Show |
215 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(212): Show |
synonymous_variant | LOW | c.360C>T | p.Ala120Ala | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/43 | 1159/9445 | 360/7833 | 120/2610 | chr14 | 31178035 | |||
| chr14:31178137 | C | T | 2 | a0001c0010 a0001c0018 |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
synonymous_variant | LOW | c.258G>A | p.Ala86Ala | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/43 | 1057/9445 | 258/7833 | 86/2610 | chr14 | 31178137 | |||
| chr14:31178233 | T | C | 2 | a0001c0007 a0001c0036 |
14 | HG00099.hp1 HG00323.hp1 HG00738.hp2 others(11): Show |
synonymous_variant | LOW | c.162A>G | p.Leu54Leu | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/43 | 961/9445 | 162/7833 | 54/2610 | chr14 | 31178233 | |||
| chr14:31178242 | G | A | 2 | a0001c0037 a0002c0005 |
19 | HG00140.hp2 HG00733.hp1 HG01123.hp2 others(16): Show |
synonymous_variant | LOW | c.153C>T | p.Arg51Arg | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/43 | 952/9445 | 153/7833 | 51/2610 | chr14 | 31178242 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:31100179 | C | T | 2 | a0001c0001t0002 a0001c0006t0002 |
12 | HG01074.hp2 HG01952.hp2 HG02083.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*751G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 43/43 | 751 | chr14 | 31100179 | ||||||
| chr14:31100226 | C | T | 2 | a0001c0010t0004 a0001c0018t0004 |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*704G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 43/43 | 704 | chr14 | 31100226 | ||||||
| chr14:31100271 | T | A | 1 | a0001c0002t0010 | 2 | HG01993.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*659A>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 43/43 | 659 | chr14 | 31100271 | ||||||
| chr14:31100525 | T | G | 1 | a0001c0004t0005 | 5 | HG01106.hp1 HG02572.hp2 HG03209.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*405A>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 43/43 | 405 | chr14 | 31100525 | ||||||
| chr14:31100846 | G | A | 1 | a0001c0007t0007 | 3 | HG00323.hp1 HG01256.hp1 HG01516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*84C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 43/43 | 84 | chr14 | 31100846 | ||||||
| chr14:31100928 | G | A | 1 | a0001c0001t0012 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 43/43 | 2 | chr14 | 31100928 | ||||||
| chr14:31207084 | G | T | 1 | a0001c0002t0006 | 3 | HG00639.hp2 HG02258.hp1 HG03540.hp1 |
5_prime_UTR_variant | MODIFIER | c.-90C>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 1/43 | 1148 | chr14 | 31207084 | ||||||
| chr14:31207173 | C | T | 1 | a0001c0017t0009 | 2 | HG02280.hp2 HG02970.hp1 |
5_prime_UTR_variant | MODIFIER | c.-179G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 1/43 | 1237 | chr14 | 31207173 | ||||||
| chr14:31207177 | A | G | 2 | a0001c0010t0004 a0001c0018t0004 |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-183T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 1/43 | 1241 | chr14 | 31207177 | ||||||
| chr14:31207324 | G | A | 1 | a0001c0002t0014 | 1 | HG02818.hp1 | 5_prime_UTR_variant | MODIFIER | c.-330C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 1/43 | 1388 | chr14 | 31207324 | ||||||
| chr14:31207396 | C | T | 1 | a0001c0004t0008 | 2 | HG03704.hp1 HG04184.hp2 |
5_prime_UTR_variant | MODIFIER | c.-402G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 1/43 | 1460 | chr14 | 31207396 | ||||||
| chr14:31207596 | A | C | 1 | a0001c0003t0011 | 1 | NA18975.hp1 | 5_prime_UTR_variant | MODIFIER | c.-602T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 1/43 | 1660 | chr14 | 31207596 | ||||||
| chr14:31207662 | G | A | 2 | a0001c0002t0013 a0001c0002t0014 |
2 | HG01109.hp2 HG02818.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-668C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 1/43 | chr14 | 31207662 | |||||||
| chr14:31207693 | C | T | 1 | a0001c0009t0003 | 8 | HG00558.hp1 HG00609.hp2 HG02071.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-699G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 1/43 | 1757 | chr14 | 31207693 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:31101101 | T | G | 1 | a0001c0001t0001g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.7696-34A>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 42/42 | chr14 | 31101101 | |||||||
| chr14:31101330 | A | G | 1 | a0001c0010t0004g0018 | 1 | HG03942.hp2 | splice_region_variant&intron_variant | LOW | c.7551-6T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 41/42 | chr14 | 31101330 | |||||||
| chr14:31101390 | T | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.7551-66A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 41/42 | chr14 | 31101390 | |||||||
| chr14:31101558 | T | C | 1 | a0001c0002t0006g0024 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.7551-234A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 41/42 | chr14 | 31101558 | |||||||
| chr14:31101564 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.7551-240C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 41/42 | chr14 | 31101564 | |||||||
| chr14:31101598 | G | A | 2 | a0001c0002t0010g0107 a0001c0002t0010g0108 |
2 | HG01993.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.7551-274C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 41/42 | chr14 | 31101598 | |||||||
| chr14:31101661 | G | A | 2 | a0004c0015t0001g0144 a0004c0015t0001g0161 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.7551-337C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 41/42 | chr14 | 31101661 | |||||||
| chr14:31101664 | C | T | 1 | a0010c0032t0001g0087 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.7551-340G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 41/42 | chr14 | 31101664 | |||||||
| chr14:31101841 | G | C | 8 | a0001c0009t0003g0003 a0001c0009t0003g0004 a0001c0009t0003g0005 others(5): Show |
8 | HG00558.hp1 HG00609.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.7551-517C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 41/42 | chr14 | 31101841 | |||||||
| chr14:31101860 | G | A | 3 | a0001c0006t0002g0125 a0001c0006t0002g0163 a0001c0006t0002g0192 |
3 | NA19009.hp1 NA19065.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.7551-536C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 41/42 | chr14 | 31101860 | |||||||
| chr14:31101921 | C | T | 1 | a0001c0002t0001g0336 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.7551-597G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 41/42 | chr14 | 31101921 | |||||||
| chr14:31102036 | C | T | 3 | a0001c0002t0006g0022 a0001c0002t0006g0023 a0001c0002t0006g0024 |
3 | HG00639.hp2 HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.7551-712G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 41/42 | chr14 | 31102036 | |||||||
| chr14:31102120 | T | C | 1 | a0001c0008t0001g0287 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.7550+796A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 41/42 | chr14 | 31102120 | |||||||
| chr14:31102266 | A | G | 2 | a0001c0002t0013g0339 a0001c0002t0014g0340 |
2 | HG01109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.7550+650T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 41/42 | chr14 | 31102266 | |||||||
| chr14:31102424 | G | GCC | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.7550+491_7550+492i others(4): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 41/42 | chr14 | 31102424 | |||||||
| chr14:31102426 | C | CT | 99 | a0001c0001t0001g0100 a0001c0001t0001g0147 a0001c0001t0001g0170 others(96): Show |
100 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.7550+489dupA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 41/42 | chr14 | 31102426 | |||||||
| chr14:31102426 | C | CTT | 7 | a0001c0002t0001g0076 a0001c0002t0001g0102 a0001c0003t0001g0296 others(4): Show |
7 | HG01175.hp2 HG01192.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.7550+488_7550+489d others(4): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 41/42 | chr14 | 31102426 | |||||||
| chr14:31102426 | C | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.7550+490G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 41/42 | chr14 | 31102426 | |||||||
| chr14:31102635 | G | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.7550+281C>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 41/42 | chr14 | 31102635 | |||||||
| chr14:31102663 | C | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0213 |
2 | HG01081.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.7550+253G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 41/42 | chr14 | 31102663 | |||||||
| chr14:31102672 | C | T | 107 | a0001c0001t0001g0205 a0001c0002t0001g0051 a0001c0002t0001g0053 others(104): Show |
107 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.7550+244G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 41/42 | chr14 | 31102672 | |||||||
| chr14:31102676 | C | T | 60 | a0001c0004t0001g0001 a0001c0004t0001g0026 a0001c0004t0001g0034 others(57): Show |
61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.7550+240G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 41/42 | chr14 | 31102676 | |||||||
| chr14:31102719 | C | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.7550+197G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 41/42 | chr14 | 31102719 | |||||||
| chr14:31102721 | C | T | 1 | a0001c0029t0001g0327 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.7550+195G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 41/42 | chr14 | 31102721 | |||||||
| chr14:31102757 | C | A | 5 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(2): Show |
5 | HG02074.hp1 NA18971.hp1 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.7550+159G>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 41/42 | chr14 | 31102757 | |||||||
| chr14:31102906 | T | C | 3 | a0003c0014t0001g0081 a0003c0014t0001g0082 a0003c0014t0001g0083 |
3 | HG02145.hp1 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.7550+10A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 41/42 | chr14 | 31102906 | |||||||
| chr14:31103271 | G | A | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.7400-205C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 40/42 | chr14 | 31103271 | |||||||
| chr14:31103392 | A | C | 1 | a0001c0004t0001g0038 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.7400-326T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 40/42 | chr14 | 31103392 | |||||||
| chr14:31103399 | G | A | 8 | a0001c0009t0003g0003 a0001c0009t0003g0004 a0001c0009t0003g0005 others(5): Show |
8 | HG00558.hp1 HG00609.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.7400-333C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 40/42 | chr14 | 31103399 | |||||||
| chr14:31103459 | G | A | 1 | a0001c0004t0001g0115 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.7400-393C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 40/42 | chr14 | 31103459 | |||||||
| chr14:31103463 | A | G | 1 | a0001c0004t0001g0115 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.7400-397T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 40/42 | chr14 | 31103463 | |||||||
| chr14:31103464 | T | C | 1 | a0001c0004t0001g0115 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.7400-398A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 40/42 | chr14 | 31103464 | |||||||
| chr14:31103474 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.7400-408C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 40/42 | chr14 | 31103474 | |||||||
| chr14:31103557 | A | G | 3 | a0003c0014t0001g0081 a0003c0014t0001g0082 a0003c0014t0001g0083 |
3 | HG02145.hp1 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.7400-491T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 40/42 | chr14 | 31103557 | |||||||
| chr14:31103657 | CAT | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.7400-593_7400-592d others(4): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 40/42 | chr14 | 31103657 | |||||||
| chr14:31103852 | A | G | 2 | a0001c0002t0013g0339 a0001c0002t0014g0340 |
2 | HG01109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.7400-786T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 40/42 | chr14 | 31103852 | |||||||
| chr14:31103860 | GGGAGGCT others(3): Show |
G | 1 | a0001c0002t0001g0336 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.7400-804_7400-795d others(12): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 40/42 | chr14 | 31103860 | |||||||
| chr14:31103864 | G | A | 1 | a0001c0002t0001g0337 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.7400-798C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 40/42 | chr14 | 31103864 | |||||||
| chr14:31104171 | T | C | 2 | a0001c0002t0010g0107 a0001c0002t0010g0108 |
2 | HG01993.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.7400-1105A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 40/42 | chr14 | 31104171 | |||||||
| chr14:31104452 | C | T | 4 | a0001c0002t0001g0051 a0001c0003t0001g0294 a0001c0003t0001g0302 others(1): Show |
4 | HG03834.hp2 HG04115.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.7399+931G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 40/42 | chr14 | 31104452 | |||||||
| chr14:31104526 | C | T | 2 | a0001c0004t0008g0012 a0001c0004t0008g0013 |
2 | HG03704.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.7399+857G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 40/42 | chr14 | 31104526 | |||||||
| chr14:31104619 | T | C | 14 | a0001c0008t0001g0281 a0001c0008t0001g0283 a0001c0008t0001g0287 others(11): Show |
14 | HG00544.hp2 HG00673.hp1 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.7399+764A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 40/42 | chr14 | 31104619 | |||||||
| chr14:31104706 | T | G | 1 | a0001c0010t0004g0018 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.7399+677A>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 40/42 | chr14 | 31104706 | |||||||
| chr14:31104829 | C | G | 3 | a0001c0002t0001g0335 a0001c0002t0001g0336 a0001c0002t0001g0337 |
3 | HG02109.hp1 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.7399+554G>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 40/42 | chr14 | 31104829 | |||||||
| chr14:31104845 | T | A | 200 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0054 others(197): Show |
201 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.7399+538A>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 40/42 | chr14 | 31104845 | |||||||
| chr14:31104999 | C | CT | 30 | a0001c0001t0001g0134 a0001c0001t0001g0138 a0001c0001t0001g0175 others(27): Show |
30 | HG00558.hp1 HG00609.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.7399+383dupA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 40/42 | chr14 | 31104999 | |||||||
| chr14:31105027 | G | A | 8 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(5): Show |
8 | HG02074.hp1 HG02280.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.7399+356C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 40/42 | chr14 | 31105027 | |||||||
| chr14:31105146 | T | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.7399+237A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 40/42 | chr14 | 31105146 | |||||||
| chr14:31105239 | G | A | 6 | a0001c0002t0001g0109 a0001c0002t0001g0111 a0001c0002t0001g0112 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.7399+144C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 40/42 | chr14 | 31105239 | |||||||
| chr14:31105248 | G | A | 1 | a0001c0008t0001g0283 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.7399+135C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 40/42 | chr14 | 31105248 | |||||||
| chr14:31105301 | G | A | 2 | a0001c0017t0009g0020 a0001c0017t0009g0021 |
2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.7399+82C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 40/42 | chr14 | 31105301 | |||||||
| chr14:31105582 | C | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.7305+8G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 39/42 | chr14 | 31105582 | |||||||
| chr14:31105776 | T | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.7227-108A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 38/42 | chr14 | 31105776 | |||||||
| chr14:31105830 | A | T | 1 | a0001c0007t0001g0030 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.7227-162T>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 38/42 | chr14 | 31105830 | |||||||
| chr14:31105879 | C | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.7227-211G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 38/42 | chr14 | 31105879 | |||||||
| chr14:31105911 | C | A | 1 | a0001c0004t0001g0115 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.7227-243G>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 38/42 | chr14 | 31105911 | |||||||
| chr14:31105956 | C | G | 1 | a0001c0001t0001g0198 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.7227-288G>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 38/42 | chr14 | 31105956 | |||||||
| chr14:31106104 | A | T | 1 | a0001c0004t0001g0115 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.7227-436T>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 38/42 | chr14 | 31106104 | |||||||
| chr14:31106204 | G | C | 2 | a0001c0002t0010g0107 a0001c0002t0010g0108 |
2 | HG01993.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.7226+442C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 38/42 | chr14 | 31106204 | |||||||
| chr14:31106232 | A | C | 3 | a0001c0002t0001g0109 a0001c0002t0001g0112 a0001c0002t0001g0113 |
3 | HG01891.hp1 HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.7226+414T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 38/42 | chr14 | 31106232 | |||||||
| chr14:31106266 | T | C | 1 | a0001c0002t0006g0024 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.7226+380A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 38/42 | chr14 | 31106266 | |||||||
| chr14:31106435 | T | G | 1 | a0007c0028t0001g0070 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.7226+211A>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 38/42 | chr14 | 31106435 | |||||||
| chr14:31106611 | T | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.7226+35A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 38/42 | chr14 | 31106611 | |||||||
| chr14:31106636 | T | C | 1 | a0001c0003t0001g0296 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.7226+10A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 38/42 | chr14 | 31106636 | |||||||
| chr14:31107540 | A | G | 1 | a0001c0017t0009g0020 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.6618+27T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 37/42 | chr14 | 31107540 | |||||||
| chr14:31107737 | C | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.6481-33G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 36/42 | chr14 | 31107737 | |||||||
| chr14:31108059 | C | G | 1 | a0001c0006t0002g0232 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.6481-355G>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 36/42 | chr14 | 31108059 | |||||||
| chr14:31108086 | T | C | 2 | a0001c0004t0008g0012 a0001c0004t0008g0013 |
2 | HG03704.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.6481-382A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 36/42 | chr14 | 31108086 | |||||||
| chr14:31108115 | C | CAG | 202 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0054 others(199): Show |
203 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.6481-413_6481-412d others(4): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 36/42 | chr14 | 31108115 | |||||||
| chr14:31108185 | G | A | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.6481-481C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 36/42 | chr14 | 31108185 | |||||||
| chr14:31108193 | G | A | 1 | a0001c0002t0001g0111 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.6481-489C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 36/42 | chr14 | 31108193 | |||||||
| chr14:31108272 | T | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.6481-568A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 36/42 | chr14 | 31108272 | |||||||
| chr14:31108359 | G | C | 23 | a0001c0004t0001g0065 a0001c0004t0001g0066 a0001c0004t0001g0067 others(20): Show |
23 | HG00099.hp1 HG00323.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.6481-655C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 36/42 | chr14 | 31108359 | |||||||
| chr14:31108448 | T | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.6481-744A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 36/42 | chr14 | 31108448 | |||||||
| chr14:31108505 | T | TA | 6 | a0001c0001t0001g0170 a0001c0001t0001g0197 a0001c0001t0001g0198 others(3): Show |
6 | HG00741.hp1 HG01192.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.6481-802dupT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 36/42 | chr14 | 31108505 | |||||||
| chr14:31108636 | A | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.6480+761T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 36/42 | chr14 | 31108636 | |||||||
| chr14:31108661 | T | TA | 10 | a0001c0003t0001g0285 a0001c0004t0005g0095 a0001c0009t0003g0003 others(7): Show |
10 | HG00558.hp1 HG00609.hp2 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.6480+735dupT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 36/42 | chr14 | 31108661 | |||||||
| chr14:31108821 | A | C | 202 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0054 others(199): Show |
203 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.6480+576T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 36/42 | chr14 | 31108821 | |||||||
| chr14:31108988 | C | T | 1 | a0001c0004t0001g0098 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.6480+409G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 36/42 | chr14 | 31108988 | |||||||
| chr14:31109217 | G | A | 10 | a0001c0002t0001g0250 a0001c0002t0001g0251 a0001c0002t0001g0252 others(7): Show |
10 | HG02055.hp1 HG02257.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.6480+180C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 36/42 | chr14 | 31109217 | |||||||
| chr14:31109642 | CT | C | 3 | a0001c0001t0001g0123 a0001c0001t0001g0140 a0001c0001t0001g0237 |
3 | NA18939.hp2 NA18982.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.6279-45delA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 35/42 | chr14 | 31109642 | |||||||
| chr14:31109899 | C | A | 1 | a0001c0002t0001g0109 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.6279-301G>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 35/42 | chr14 | 31109899 | |||||||
| chr14:31110094 | C | T | 1 | a0006c0024t0001g0074 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.6279-496G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 35/42 | chr14 | 31110094 | |||||||
| chr14:31110141 | A | G | 1 | a0001c0002t0006g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.6279-543T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 35/42 | chr14 | 31110141 | |||||||
| chr14:31110426 | G | A | 5 | a0001c0009t0003g0005 a0001c0009t0003g0006 a0001c0009t0003g0007 others(2): Show |
5 | HG00558.hp1 HG00609.hp2 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.6279-828C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 35/42 | chr14 | 31110426 | |||||||
| chr14:31110542 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.6279-944C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 35/42 | chr14 | 31110542 | |||||||
| chr14:31110582 | A | G | 30 | a0001c0004t0001g0001 a0001c0004t0001g0026 a0001c0004t0001g0034 others(27): Show |
31 | HG00099.hp1 HG00323.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.6279-984T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 35/42 | chr14 | 31110582 | |||||||
| chr14:31110775 | A | C | 1 | a0001c0003t0001g0282 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.6279-1177T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 35/42 | chr14 | 31110775 | |||||||
| chr14:31110864 | C | T | 1 | a0001c0003t0001g0314 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.6279-1266G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 35/42 | chr14 | 31110864 | |||||||
| chr14:31110878 | G | A | 2 | a0001c0002t0001g0103 a0001c0002t0001g0104 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.6279-1280C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 35/42 | chr14 | 31110878 | |||||||
| chr14:31110954 | C | CT | 28 | a0001c0002t0001g0053 a0001c0002t0001g0054 a0001c0002t0001g0057 others(25): Show |
28 | HG00621.hp2 HG02074.hp2 HG02080.hp2 others(25): Show |
intron_variant | MODIFIER | c.6279-1357dupA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 35/42 | chr14 | 31110954 | |||||||
| chr14:31110956 | T | C | 8 | a0001c0009t0003g0003 a0001c0009t0003g0004 a0001c0009t0003g0005 others(5): Show |
8 | HG00558.hp1 HG00609.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.6279-1358A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 35/42 | chr14 | 31110956 | |||||||
| chr14:31111008 | G | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.6278+1408C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 35/42 | chr14 | 31111008 | |||||||
| chr14:31111263 | A | T | 1 | a0001c0001t0002g0166 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.6278+1153T>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 35/42 | chr14 | 31111263 | |||||||
| chr14:31111353 | C | T | 4 | a0001c0001t0001g0147 a0001c0001t0001g0240 a0001c0002t0001g0336 others(1): Show |
4 | HG02109.hp1 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.6278+1063G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 35/42 | chr14 | 31111353 | |||||||
| chr14:31111396 | G | A | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.6278+1020C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 35/42 | chr14 | 31111396 | |||||||
| chr14:31111460 | G | A | 1 | a0001c0004t0001g0115 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.6278+956C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 35/42 | chr14 | 31111460 | |||||||
| chr14:31111482 | A | G | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.6278+934T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 35/42 | chr14 | 31111482 | |||||||
| chr14:31111518 | C | T | 3 | a0001c0002t0001g0335 a0001c0002t0001g0336 a0001c0002t0001g0337 |
3 | HG02109.hp1 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.6278+898G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 35/42 | chr14 | 31111518 | |||||||
| chr14:31111637 | C | T | 1 | a0001c0002t0006g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.6278+779G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 35/42 | chr14 | 31111637 | |||||||
| chr14:31111807 | C | T | 2 | a0001c0002t0013g0339 a0001c0002t0014g0340 |
2 | HG01109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.6278+609G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 35/42 | chr14 | 31111807 | |||||||
| chr14:31111912 | C | T | 2 | a0001c0002t0001g0058 a0001c0002t0001g0059 |
2 | NA19080.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.6278+504G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 35/42 | chr14 | 31111912 | |||||||
| chr14:31111982 | AAAAAACA others(5): Show |
A | 3 | a0003c0014t0001g0081 a0003c0014t0001g0082 a0003c0014t0001g0083 |
3 | HG02145.hp1 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.6278+422_6278+433d others(14): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 35/42 | chr14 | 31111982 | |||||||
| chr14:31112017 | C | T | 1 | a0001c0003t0001g0285 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.6278+399G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 35/42 | chr14 | 31112017 | |||||||
| chr14:31112154 | G | A | 1 | a0001c0003t0001g0322 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.6278+262C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 35/42 | chr14 | 31112154 | |||||||
| chr14:31112224 | C | G | 1 | a0001c0002t0001g0335 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.6278+192G>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 35/42 | chr14 | 31112224 | |||||||
| chr14:31112299 | A | G | 1 | a0001c0017t0009g0021 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.6278+117T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 35/42 | chr14 | 31112299 | |||||||
| chr14:31112547 | C | T | 2 | a0001c0007t0001g0033 a0001c0007t0001g0039 |
2 | HG00738.hp2 HG01069.hp1 |
splice_region_variant&intron_variant | LOW | c.6151-4G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 34/42 | chr14 | 31112547 | |||||||
| chr14:31112679 | G | A | 1 | a0002c0005t0001g0262 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.6151-136C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 34/42 | chr14 | 31112679 | |||||||
| chr14:31112712 | C | T | 1 | a0007c0028t0001g0070 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.6151-169G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 34/42 | chr14 | 31112712 | |||||||
| chr14:31112751 | A | T | 6 | a0001c0004t0001g0088 a0001c0004t0001g0089 a0001c0004t0001g0097 others(3): Show |
6 | HG02257.hp2 HG02683.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.6151-208T>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 34/42 | chr14 | 31112751 | |||||||
| chr14:31112765 | G | A | 91 | a0001c0002t0001g0053 a0001c0002t0001g0054 a0001c0002t0001g0057 others(88): Show |
91 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.6151-222C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 34/42 | chr14 | 31112765 | |||||||
| chr14:31112806 | C | T | 9 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(6): Show |
9 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.6151-263G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 34/42 | chr14 | 31112806 | |||||||
| chr14:31112836 | C | G | 61 | a0001c0001t0001g0187 a0001c0001t0001g0244 a0001c0002t0001g0051 others(58): Show |
61 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.6150+268G>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 34/42 | chr14 | 31112836 | |||||||
| chr14:31112846 | A | G | 1 | a0001c0001t0001g0135 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.6150+258T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 34/42 | chr14 | 31112846 | |||||||
| chr14:31112969 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.6150+135C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 34/42 | chr14 | 31112969 | |||||||
| chr14:31113023 | A | C | 3 | a0003c0014t0001g0081 a0003c0014t0001g0082 a0003c0014t0001g0083 |
3 | HG02145.hp1 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.6150+81T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 34/42 | chr14 | 31113023 | |||||||
| chr14:31113648 | A | T | 1 | a0010c0032t0001g0087 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.5857-164T>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 32/42 | chr14 | 31113648 | |||||||
| chr14:31113691 | T | C | 1 | a0001c0004t0008g0013 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.5856+186A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 32/42 | chr14 | 31113691 | |||||||
| chr14:31113701 | T | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.5856+176A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 32/42 | chr14 | 31113701 | |||||||
| chr14:31113783 | C | G | 3 | a0002c0005t0001g0263 a0002c0005t0001g0264 a0002c0020t0001g0278 |
3 | HG00280.hp2 HG02602.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.5856+94G>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 32/42 | chr14 | 31113783 | |||||||
| chr14:31113806 | A | G | 1 | a0010c0032t0001g0087 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.5856+71T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 32/42 | chr14 | 31113806 | |||||||
| chr14:31113807 | G | C | 1 | a0010c0032t0001g0087 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.5856+70C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 32/42 | chr14 | 31113807 | |||||||
| chr14:31113808 | C | T | 1 | a0010c0032t0001g0087 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.5856+69G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 32/42 | chr14 | 31113808 | |||||||
| chr14:31113840 | T | C | 1 | a0001c0002t0001g0336 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.5856+37A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 32/42 | chr14 | 31113840 | |||||||
| chr14:31114205 | C | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.5673+81G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 31/42 | chr14 | 31114205 | |||||||
| chr14:31114476 | T | C | 10 | a0001c0002t0001g0250 a0001c0002t0001g0251 a0001c0002t0001g0252 others(7): Show |
10 | HG02055.hp1 HG02257.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.5619-136A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 30/42 | chr14 | 31114476 | |||||||
| chr14:31114586 | A | C | 1 | a0010c0032t0001g0087 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.5619-246T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 30/42 | chr14 | 31114586 | |||||||
| chr14:31114651 | C | T | 10 | a0001c0002t0001g0250 a0001c0002t0001g0251 a0001c0002t0001g0252 others(7): Show |
10 | HG02055.hp1 HG02257.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.5619-311G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 30/42 | chr14 | 31114651 | |||||||
| chr14:31114656 | G | C | 3 | a0001c0002t0006g0022 a0001c0002t0006g0023 a0001c0002t0006g0024 |
3 | HG00639.hp2 HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.5619-316C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 30/42 | chr14 | 31114656 | |||||||
| chr14:31114663 | T | C | 1 | a0001c0003t0001g0290 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.5619-323A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 30/42 | chr14 | 31114663 | |||||||
| chr14:31114761 | A | C | 3 | a0003c0014t0001g0081 a0003c0014t0001g0082 a0003c0014t0001g0083 |
3 | HG02145.hp1 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.5619-421T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 30/42 | chr14 | 31114761 | |||||||
| chr14:31114862 | T | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.5619-522A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 30/42 | chr14 | 31114862 | |||||||
| chr14:31114913 | A | AATACT | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.5619-574_5619-573i others(7): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 30/42 | chr14 | 31114913 | |||||||
| chr14:31115039 | A | G | 203 | a0001c0001t0001g0116 a0001c0002t0001g0051 a0001c0002t0001g0053 others(200): Show |
204 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.5619-699T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 30/42 | chr14 | 31115039 | |||||||
| chr14:31115177 | A | C | 106 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0054 others(103): Show |
106 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.5619-837T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 30/42 | chr14 | 31115177 | |||||||
| chr14:31115223 | G | A | 1 | a0001c0002t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5619-883C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 30/42 | chr14 | 31115223 | |||||||
| chr14:31115251 | T | C | 2 | a0001c0001t0001g0194 a0009c0019t0001g0211 |
2 | NA18971.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.5619-911A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 30/42 | chr14 | 31115251 | |||||||
| chr14:31115305 | C | T | 4 | a0001c0002t0010g0107 a0001c0002t0010g0108 a0001c0017t0009g0020 others(1): Show |
4 | HG01993.hp2 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.5618+931G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 30/42 | chr14 | 31115305 | |||||||
| chr14:31115338 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.5618+898G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 30/42 | chr14 | 31115338 | |||||||
| chr14:31115479 | C | T | 2 | a0001c0002t0013g0339 a0001c0002t0014g0340 |
2 | HG01109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.5618+757G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 30/42 | chr14 | 31115479 | |||||||
| chr14:31115542 | T | G | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.5618+694A>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 30/42 | chr14 | 31115542 | |||||||
| chr14:31115663 | G | A | 7 | a0001c0002t0010g0107 a0001c0002t0010g0108 a0001c0017t0009g0020 others(4): Show |
7 | HG01993.hp2 HG02145.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.5618+573C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 30/42 | chr14 | 31115663 | |||||||
| chr14:31115692 | T | C | 1 | a0001c0003t0001g0305 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.5618+544A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 30/42 | chr14 | 31115692 | |||||||
| chr14:31115968 | G | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.5618+268C>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 30/42 | chr14 | 31115968 | |||||||
| chr14:31115991 | G | A | 10 | a0001c0002t0001g0250 a0001c0002t0001g0251 a0001c0002t0001g0252 others(7): Show |
10 | HG02055.hp1 HG02257.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.5618+245C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 30/42 | chr14 | 31115991 | |||||||
| chr14:31116083 | T | C | 63 | a0001c0004t0001g0001 a0001c0004t0001g0026 a0001c0004t0001g0034 others(60): Show |
64 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.5618+153A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 30/42 | chr14 | 31116083 | |||||||
| chr14:31116102 | A | G | 7 | a0001c0004t0001g0088 a0001c0004t0001g0089 a0001c0004t0001g0097 others(4): Show |
7 | HG02257.hp2 HG02683.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.5618+134T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 30/42 | chr14 | 31116102 | |||||||
| chr14:31116210 | C | A | 1 | a0001c0001t0001g0145 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.5618+26G>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 30/42 | chr14 | 31116210 | |||||||
| chr14:31116691 | C | T | 83 | a0001c0002t0001g0053 a0001c0002t0001g0054 a0001c0002t0001g0057 others(80): Show |
83 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.5396-233G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 29/42 | chr14 | 31116691 | |||||||
| chr14:31116776 | G | A | 1 | a0001c0006t0002g0224 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.5396-318C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 29/42 | chr14 | 31116776 | |||||||
| chr14:31116808 | T | C | 1 | a0001c0025t0001g0092 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.5396-350A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 29/42 | chr14 | 31116808 | |||||||
| chr14:31116820 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.5396-362C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 29/42 | chr14 | 31116820 | |||||||
| chr14:31117209 | C | A | 5 | a0001c0011t0001g0047 a0001c0011t0001g0048 a0001c0011t0001g0049 others(2): Show |
5 | HG02630.hp2 HG02809.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.5396-751G>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 29/42 | chr14 | 31117209 | |||||||
| chr14:31117320 | C | T | 5 | a0001c0004t0005g0090 a0001c0004t0005g0093 a0001c0004t0005g0094 others(2): Show |
5 | HG01106.hp1 HG02572.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.5396-862G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 29/42 | chr14 | 31117320 | |||||||
| chr14:31117370 | T | A | 1 | a0001c0003t0001g0282 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.5396-912A>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 29/42 | chr14 | 31117370 | |||||||
| chr14:31117440 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.5396-982C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 29/42 | chr14 | 31117440 | |||||||
| chr14:31117477 | C | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.5396-1019G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 29/42 | chr14 | 31117477 | |||||||
| chr14:31117530 | G | T | 1 | a0001c0004t0001g0088 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.5396-1072C>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 29/42 | chr14 | 31117530 | |||||||
| chr14:31117590 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.5396-1132G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 29/42 | chr14 | 31117590 | |||||||
| chr14:31117743 | A | G | 1 | a0001c0004t0001g0044 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.5396-1285T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 29/42 | chr14 | 31117743 | |||||||
| chr14:31117745 | C | T | 1 | a0001c0004t0001g0044 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.5396-1287G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 29/42 | chr14 | 31117745 | |||||||
| chr14:31117780 | G | C | 18 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(15): Show |
18 | HG01891.hp1 HG02074.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.5396-1322C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 29/42 | chr14 | 31117780 | |||||||
| chr14:31118047 | T | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.5396-1589A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 29/42 | chr14 | 31118047 | |||||||
| chr14:31118098 | G | A | 9 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(6): Show |
9 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.5395+1612C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 29/42 | chr14 | 31118098 | |||||||
| chr14:31118156 | C | T | 1 | a0001c0017t0009g0020 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.5395+1554G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 29/42 | chr14 | 31118156 | |||||||
| chr14:31118211 | C | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.5395+1499G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 29/42 | chr14 | 31118211 | |||||||
| chr14:31118228 | A | G | 4 | a0001c0002t0001g0069 a0001c0002t0001g0076 a0001c0002t0001g0077 others(1): Show |
4 | NA18963.hp2 NA18977.hp1 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.5395+1482T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 29/42 | chr14 | 31118228 | |||||||
| chr14:31118294 | C | T | 4 | a0001c0002t0010g0107 a0001c0002t0010g0108 a0001c0017t0009g0020 others(1): Show |
4 | HG01993.hp2 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.5395+1416G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 29/42 | chr14 | 31118294 | |||||||
| chr14:31118615 | C | G | 5 | a0001c0009t0003g0005 a0001c0009t0003g0006 a0001c0009t0003g0007 others(2): Show |
5 | HG00558.hp1 HG00609.hp2 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.5395+1095G>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 29/42 | chr14 | 31118615 | |||||||
| chr14:31118758 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5395+952C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 29/42 | chr14 | 31118758 | |||||||
| chr14:31118793 | C | T | 48 | a0001c0004t0001g0001 a0001c0004t0001g0026 a0001c0004t0001g0034 others(45): Show |
49 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.5395+917G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 29/42 | chr14 | 31118793 | |||||||
| chr14:31118898 | G | GA | 41 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0138 others(38): Show |
41 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.5395+811dupT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 29/42 | chr14 | 31118898 | |||||||
| chr14:31118898 | GA | G | 17 | a0001c0001t0001g0151 a0001c0004t0001g0034 a0001c0004t0001g0073 others(14): Show |
17 | HG00741.hp2 HG01106.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.5395+811delT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 29/42 | chr14 | 31118898 | |||||||
| chr14:31118898 | GAA | G | 52 | a0001c0004t0001g0001 a0001c0004t0001g0026 a0001c0004t0001g0037 others(49): Show |
53 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.5395+810_5395+811d others(4): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 29/42 | chr14 | 31118898 | |||||||
| chr14:31118898 | GAAA | G | 14 | a0001c0002t0001g0076 a0001c0002t0001g0079 a0001c0002t0001g0102 others(11): Show |
14 | HG00621.hp2 HG01109.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.5395+809_5395+811d others(5): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 29/42 | chr14 | 31118898 | |||||||
| chr14:31118898 | GAAAA | G | 55 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0054 others(52): Show |
55 | HG00423.hp2 HG00639.hp2 HG01884.hp1 others(52): Show |
intron_variant | MODIFIER | c.5395+808_5395+811d others(6): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 29/42 | chr14 | 31118898 | |||||||
| chr14:31118898 | GAAAAA | G | 45 | a0001c0002t0006g0022 a0001c0003t0001g0099 a0001c0003t0001g0282 others(42): Show |
45 | HG00140.hp1 HG00544.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.5395+807_5395+811d others(7): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 29/42 | chr14 | 31118898 | |||||||
| chr14:31118898 | GAAAAAAA others(6): Show |
G | 1 | a0001c0001t0001g0177 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.5395+799_5395+811d others(15): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 29/42 | chr14 | 31118898 | |||||||
| chr14:31118898 | GAAAAAAA others(10): Show |
G | 10 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(7): Show |
10 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.5395+795_5395+811d others(19): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 29/42 | chr14 | 31118898 | |||||||
| chr14:31118900 | A | G | 10 | a0001c0004t0001g0034 a0001c0004t0001g0073 a0001c0007t0001g0036 others(7): Show |
10 | HG00741.hp2 HG01243.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.5395+810T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 29/42 | chr14 | 31118900 | |||||||
| chr14:31118901 | A | G | 37 | a0001c0004t0001g0001 a0001c0004t0001g0026 a0001c0004t0001g0037 others(34): Show |
38 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.5395+809T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 29/42 | chr14 | 31118901 | |||||||
| chr14:31118902 | A | G | 2 | a0001c0002t0013g0339 a0001c0007t0007g0032 |
2 | HG01109.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.5395+808T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 29/42 | chr14 | 31118902 | |||||||
| chr14:31118903 | A | G | 1 | a0001c0002t0014g0340 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.5395+807T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 29/42 | chr14 | 31118903 | |||||||
| chr14:31119123 | T | A | 130 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0054 others(127): Show |
130 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.5395+587A>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 29/42 | chr14 | 31119123 | |||||||
| chr14:31119155 | T | C | 1 | a0002c0005t0001g0275 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.5395+555A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 29/42 | chr14 | 31119155 | |||||||
| chr14:31119251 | G | T | 1 | a0001c0003t0001g0330 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.5395+459C>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 29/42 | chr14 | 31119251 | |||||||
| chr14:31119273 | A | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.5395+437T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 29/42 | chr14 | 31119273 | |||||||
| chr14:31119301 | T | C | 4 | a0001c0002t0010g0107 a0001c0002t0010g0108 a0001c0017t0009g0020 others(1): Show |
4 | HG01993.hp2 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.5395+409A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 29/42 | chr14 | 31119301 | |||||||
| chr14:31119519 | T | G | 1 | a0001c0002t0006g0024 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.5395+191A>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 29/42 | chr14 | 31119519 | |||||||
| chr14:31119536 | A | G | 6 | a0001c0002t0001g0069 a0001c0002t0001g0076 a0001c0002t0001g0077 others(3): Show |
6 | HG02074.hp2 NA18963.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.5395+174T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 29/42 | chr14 | 31119536 | |||||||
| chr14:31119616 | T | A | 1 | a0001c0002t0006g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.5395+94A>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 29/42 | chr14 | 31119616 | |||||||
| chr14:31119673 | T | C | 3 | a0001c0002t0001g0335 a0001c0002t0001g0336 a0001c0002t0001g0337 |
3 | HG02109.hp1 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.5395+37A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 29/42 | chr14 | 31119673 | |||||||
| chr14:31119906 | C | A | 1 | a0001c0003t0001g0324 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.5239-40G>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 28/42 | chr14 | 31119906 | |||||||
| chr14:31119916 | T | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.5239-50A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 28/42 | chr14 | 31119916 | |||||||
| chr14:31119923 | A | C | 8 | a0001c0009t0003g0003 a0001c0009t0003g0004 a0001c0009t0003g0005 others(5): Show |
8 | HG00558.hp1 HG00609.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.5239-57T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 28/42 | chr14 | 31119923 | |||||||
| chr14:31120039 | A | G | 50 | a0001c0004t0001g0001 a0001c0004t0001g0026 a0001c0004t0001g0034 others(47): Show |
51 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.5239-173T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 28/42 | chr14 | 31120039 | |||||||
| chr14:31120059 | T | C | 4 | a0001c0002t0010g0107 a0001c0002t0010g0108 a0001c0017t0009g0020 others(1): Show |
4 | HG01993.hp2 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.5239-193A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 28/42 | chr14 | 31120059 | |||||||
| chr14:31120210 | C | G | 3 | a0003c0014t0001g0081 a0003c0014t0001g0082 a0003c0014t0001g0083 |
3 | HG02145.hp1 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.5239-344G>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 28/42 | chr14 | 31120210 | |||||||
| chr14:31120313 | G | A | 1 | a0001c0001t0001g0175 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.5239-447C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 28/42 | chr14 | 31120313 | |||||||
| chr14:31120541 | A | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.5239-675T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 28/42 | chr14 | 31120541 | |||||||
| chr14:31120656 | A | G | 1 | a0001c0025t0001g0092 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.5238+727T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 28/42 | chr14 | 31120656 | |||||||
| chr14:31120739 | T | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.5238+644A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 28/42 | chr14 | 31120739 | |||||||
| chr14:31120830 | T | TAA | 3 | a0001c0001t0001g0141 a0001c0001t0001g0171 a0001c0001t0001g0208 |
3 | HG02145.hp2 HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.5238+551_5238+552d others(4): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 28/42 | chr14 | 31120830 | |||||||
| chr14:31120891 | T | C | 4 | a0001c0002t0010g0107 a0001c0002t0010g0108 a0001c0017t0009g0020 others(1): Show |
4 | HG01993.hp2 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.5238+492A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 28/42 | chr14 | 31120891 | |||||||
| chr14:31120908 | G | A | 1 | a0001c0002t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5238+475C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 28/42 | chr14 | 31120908 | |||||||
| chr14:31121151 | C | T | 10 | a0001c0002t0001g0250 a0001c0002t0001g0251 a0001c0002t0001g0252 others(7): Show |
10 | HG02055.hp1 HG02257.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.5238+232G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 28/42 | chr14 | 31121151 | |||||||
| chr14:31121186 | A | G | 2 | a0001c0002t0013g0339 a0001c0002t0014g0340 |
2 | HG01109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.5238+197T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 28/42 | chr14 | 31121186 | |||||||
| chr14:31121250 | T | C | 1 | a0001c0002t0001g0062 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.5238+133A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 28/42 | chr14 | 31121250 | |||||||
| chr14:31121281 | A | C | 1 | a0001c0002t0001g0335 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.5238+102T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 28/42 | chr14 | 31121281 | |||||||
| chr14:31121283 | C | T | 5 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(2): Show |
5 | HG02074.hp1 NA18971.hp1 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.5238+100G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 28/42 | chr14 | 31121283 | |||||||
| chr14:31121634 | C | G | 3 | a0001c0002t0001g0335 a0001c0002t0001g0336 a0001c0002t0001g0337 |
3 | HG02109.hp1 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.5116-129G>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 27/42 | chr14 | 31121634 | |||||||
| chr14:31121943 | C | T | 5 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(2): Show |
5 | HG02074.hp1 NA18971.hp1 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.5116-438G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 27/42 | chr14 | 31121943 | |||||||
| chr14:31121951 | T | G | 2 | a0001c0012t0001g0056 a0001c0012t0001g0060 |
2 | NA18943.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.5116-446A>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 27/42 | chr14 | 31121951 | |||||||
| chr14:31121962 | G | C | 1 | a0001c0001t0001g0139 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.5116-457C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 27/42 | chr14 | 31121962 | |||||||
| chr14:31121968 | A | AT | 8 | a0001c0009t0003g0003 a0001c0009t0003g0004 a0001c0009t0003g0005 others(5): Show |
8 | HG00558.hp1 HG00609.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.5116-464dupA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 27/42 | chr14 | 31121968 | |||||||
| chr14:31121968 | AT | A | 7 | a0001c0001t0001g0151 a0001c0010t0004g0014 a0001c0010t0004g0015 others(4): Show |
7 | HG02074.hp1 HG03942.hp2 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.5116-464delA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 27/42 | chr14 | 31121968 | |||||||
| chr14:31122148 | T | C | 111 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0054 others(108): Show |
111 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.5116-643A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 27/42 | chr14 | 31122148 | |||||||
| chr14:31122197 | A | T | 131 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0054 others(128): Show |
131 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.5116-692T>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 27/42 | chr14 | 31122197 | |||||||
| chr14:31122229 | G | A | 2 | a0001c0017t0009g0020 a0001c0017t0009g0021 |
2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.5115+685C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 27/42 | chr14 | 31122229 | |||||||
| chr14:31122262 | A | G | 13 | a0001c0002t0001g0250 a0001c0002t0001g0251 a0001c0002t0001g0252 others(10): Show |
13 | HG02055.hp1 HG02109.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.5115+652T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 27/42 | chr14 | 31122262 | |||||||
| chr14:31122263 | C | CGT | 70 | a0001c0001t0001g0186 a0001c0002t0001g0053 a0001c0002t0001g0059 others(67): Show |
70 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.5115+649_5115+650d others(4): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 27/42 | chr14 | 31122263 | |||||||
| chr14:31122263 | C | CGTGT | 3 | a0001c0002t0001g0111 a0001c0003t0001g0312 a0002c0005t0001g0275 |
3 | HG01243.hp2 HG02080.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.5115+647_5115+650d others(6): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 27/42 | chr14 | 31122263 | |||||||
| chr14:31122263 | C | CGTGTGT | 32 | a0001c0003t0001g0291 a0001c0004t0001g0001 a0001c0004t0001g0026 others(29): Show |
33 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.5115+645_5115+650d others(8): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 27/42 | chr14 | 31122263 | |||||||
| chr14:31122263 | C | CGTGTGTG others(1): Show |
19 | a0001c0004t0001g0078 a0001c0010t0004g0018 a0001c0037t0001g0261 others(16): Show |
19 | HG00140.hp2 HG00280.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.5115+643_5115+650d others(10): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 27/42 | chr14 | 31122263 | |||||||
| chr14:31122263 | C | CGTGTGTG others(3): Show |
5 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(2): Show |
5 | HG02074.hp1 NA18971.hp1 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.5115+641_5115+650d others(12): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 27/42 | chr14 | 31122263 | |||||||
| chr14:31122263 | C | T | 13 | a0001c0002t0001g0250 a0001c0002t0001g0251 a0001c0002t0001g0252 others(10): Show |
13 | HG02055.hp1 HG02109.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.5115+651G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 27/42 | chr14 | 31122263 | |||||||
| chr14:31122263 | CGT | C | 3 | a0001c0002t0006g0022 a0001c0002t0006g0023 a0001c0002t0006g0024 |
3 | HG00639.hp2 HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.5115+649_5115+650d others(4): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 27/42 | chr14 | 31122263 | |||||||
| chr14:31122263 | CGTGT | C | 26 | a0001c0002t0001g0054 a0001c0002t0001g0057 a0001c0002t0001g0058 others(23): Show |
26 | HG00621.hp2 HG02074.hp2 HG02080.hp2 others(23): Show |
intron_variant | MODIFIER | c.5115+647_5115+650d others(6): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 27/42 | chr14 | 31122263 | |||||||
| chr14:31122304 | C | T | 3 | a0001c0002t0001g0335 a0001c0002t0001g0336 a0001c0002t0001g0337 |
3 | HG02109.hp1 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.5115+610G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 27/42 | chr14 | 31122304 | |||||||
| chr14:31122316 | G | C | 1 | a0001c0002t0001g0336 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.5115+598C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 27/42 | chr14 | 31122316 | |||||||
| chr14:31122318 | C | T | 3 | a0001c0004t0005g0090 a0001c0004t0005g0094 a0001c0004t0005g0095 |
3 | HG02572.hp2 HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.5115+596G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 27/42 | chr14 | 31122318 | |||||||
| chr14:31122379 | A | ATG | 151 | a0001c0001t0001g0100 a0001c0002t0001g0053 a0001c0002t0001g0054 others(148): Show |
152 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.5115+533_5115+534d others(4): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 27/42 | chr14 | 31122379 | |||||||
| chr14:31122379 | A | ATGTG | 11 | a0001c0002t0006g0022 a0001c0007t0001g0027 a0001c0007t0001g0028 others(8): Show |
11 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(8): Show |
intron_variant | MODIFIER | c.5115+531_5115+534d others(6): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 27/42 | chr14 | 31122379 | |||||||
| chr14:31122379 | ATG | A | 3 | a0001c0002t0001g0335 a0001c0002t0001g0336 a0001c0002t0001g0337 |
3 | HG02109.hp1 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.5115+533_5115+534d others(4): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 27/42 | chr14 | 31122379 | |||||||
| chr14:31122393 | G | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.5115+521C>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 27/42 | chr14 | 31122393 | |||||||
| chr14:31122479 | C | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.5115+435G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 27/42 | chr14 | 31122479 | |||||||
| chr14:31122498 | G | A | 3 | a0003c0014t0001g0081 a0003c0014t0001g0082 a0003c0014t0001g0083 |
3 | HG02145.hp1 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.5115+416C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 27/42 | chr14 | 31122498 | |||||||
| chr14:31122536 | T | C | 200 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0054 others(197): Show |
201 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.5115+378A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 27/42 | chr14 | 31122536 | |||||||
| chr14:31122550 | A | G | 3 | a0001c0002t0001g0335 a0001c0002t0001g0336 a0001c0002t0001g0337 |
3 | HG02109.hp1 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.5115+364T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 27/42 | chr14 | 31122550 | |||||||
| chr14:31122709 | A | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.5115+205T>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 27/42 | chr14 | 31122709 | |||||||
| chr14:31122737 | T | C | 9 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(6): Show |
9 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.5115+177A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 27/42 | chr14 | 31122737 | |||||||
| chr14:31122763 | C | G | 3 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 |
3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.5115+151G>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 27/42 | chr14 | 31122763 | |||||||
| chr14:31122788 | A | G | 2 | a0001c0007t0001g0027 a0001c0007t0001g0028 |
2 | HG00099.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.5115+126T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 27/42 | chr14 | 31122788 | |||||||
| chr14:31123179 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.4982-132G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31123179 | |||||||
| chr14:31123240 | C | T | 3 | a0001c0002t0001g0335 a0001c0002t0001g0336 a0001c0002t0001g0337 |
3 | HG02109.hp1 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.4982-193G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31123240 | |||||||
| chr14:31123335 | C | G | 1 | a0001c0003t0001g0289 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.4982-288G>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31123335 | |||||||
| chr14:31123361 | AATCAGTG others(15): Show |
A | 2 | a0001c0009t0003g0004 a0001c0009t0003g0010 |
2 | NA18982.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.4982-336_4982-315d others(24): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31123361 | |||||||
| chr14:31123374 | C | T | 1 | a0001c0003t0001g0296 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.4982-327G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31123374 | |||||||
| chr14:31123445 | G | A | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.4982-398C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31123445 | |||||||
| chr14:31123562 | G | A | 3 | a0003c0014t0001g0081 a0003c0014t0001g0082 a0003c0014t0001g0083 |
3 | HG02145.hp1 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.4982-515C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31123562 | |||||||
| chr14:31123738 | T | A | 4 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0239 others(1): Show |
4 | HG02055.hp2 HG02647.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.4982-691A>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31123738 | |||||||
| chr14:31123857 | T | G | 5 | a0001c0003t0001g0285 a0001c0003t0001g0288 a0001c0003t0001g0295 others(2): Show |
5 | NA18939.hp1 NA18947.hp1 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.4982-810A>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31123857 | |||||||
| chr14:31123875 | G | A | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.4982-828C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31123875 | |||||||
| chr14:31123889 | T | G | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.4982-842A>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31123889 | |||||||
| chr14:31123967 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4982-920A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31123967 | |||||||
| chr14:31123977 | T | C | 3 | a0001c0006t0002g0207 a0001c0006t0002g0231 a0001c0006t0002g0232 |
3 | NA18947.hp2 NA18994.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.4982-930A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31123977 | |||||||
| chr14:31124139 | T | C | 1 | a0001c0025t0001g0092 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4982-1092A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31124139 | |||||||
| chr14:31124279 | T | C | 3 | a0001c0002t0001g0335 a0001c0002t0001g0336 a0001c0002t0001g0337 |
3 | HG02109.hp1 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.4982-1232A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31124279 | |||||||
| chr14:31124343 | C | T | 3 | a0001c0003t0001g0298 a0001c0003t0001g0305 a0001c0003t0001g0314 |
3 | HG01346.hp2 HG02602.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4982-1296G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31124343 | |||||||
| chr14:31124562 | G | A | 2 | a0001c0002t0010g0107 a0001c0002t0010g0108 |
2 | HG01993.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.4982-1515C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31124562 | |||||||
| chr14:31124774 | A | T | 1 | a0001c0007t0001g0041 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.4982-1727T>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31124774 | |||||||
| chr14:31124806 | TA | T | 3 | a0001c0002t0001g0109 a0001c0002t0001g0112 a0001c0002t0001g0113 |
3 | HG01891.hp1 HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.4982-1760delT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31124806 | |||||||
| chr14:31124809 | AT | A | 179 | a0001c0001t0001g0159 a0001c0002t0001g0051 a0001c0002t0001g0053 others(176): Show |
180 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.4982-1763delA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31124809 | |||||||
| chr14:31124809 | ATT | A | 9 | a0001c0002t0001g0335 a0001c0002t0001g0336 a0001c0002t0001g0337 others(6): Show |
9 | HG02074.hp1 HG02109.hp1 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.4982-1764_4982-176 others(6): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31124809 | |||||||
| chr14:31124838 | C | T | 8 | a0001c0009t0003g0003 a0001c0009t0003g0004 a0001c0009t0003g0005 others(5): Show |
8 | HG00558.hp1 HG00609.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.4982-1791G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31124838 | |||||||
| chr14:31124951 | G | A | 2 | a0001c0002t0010g0107 a0001c0002t0010g0108 |
2 | HG01993.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.4982-1904C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31124951 | |||||||
| chr14:31124961 | C | A | 1 | a0001c0001t0001g0222 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4982-1914G>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31124961 | |||||||
| chr14:31125022 | A | G | 49 | a0001c0004t0001g0001 a0001c0004t0001g0026 a0001c0004t0001g0034 others(46): Show |
50 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.4982-1975T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31125022 | |||||||
| chr14:31125173 | C | CT | 26 | a0001c0001t0001g0138 a0001c0001t0001g0180 a0001c0001t0001g0216 others(23): Show |
26 | HG01071.hp2 HG01109.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.4982-2127dupA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31125173 | |||||||
| chr14:31125173 | CT | C | 12 | a0001c0001t0001g0157 a0001c0001t0001g0235 a0001c0001t0001g0241 others(9): Show |
12 | HG00323.hp2 HG01255.hp2 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.4982-2127delA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31125173 | |||||||
| chr14:31125229 | A | C | 1 | a0001c0023t0001g0179 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.4982-2182T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31125229 | |||||||
| chr14:31125242 | G | T | 130 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0054 others(127): Show |
130 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.4982-2195C>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31125242 | |||||||
| chr14:31125353 | T | C | 12 | a0001c0004t0001g0088 a0001c0004t0001g0089 a0001c0004t0001g0097 others(9): Show |
12 | HG01106.hp1 HG02257.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.4982-2306A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31125353 | |||||||
| chr14:31125381 | C | T | 1 | a0001c0004t0001g0088 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.4982-2334G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31125381 | |||||||
| chr14:31125420 | G | A | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.4981+2365C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31125420 | |||||||
| chr14:31125469 | G | A | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.4981+2316C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31125469 | |||||||
| chr14:31125560 | G | C | 1 | a0001c0001t0001g0195 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4981+2225C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31125560 | |||||||
| chr14:31125789 | A | G | 8 | a0001c0009t0003g0003 a0001c0009t0003g0004 a0001c0009t0003g0005 others(5): Show |
8 | HG00558.hp1 HG00609.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.4981+1996T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31125789 | |||||||
| chr14:31125837 | A | G | 1 | a0001c0002t0001g0051 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.4981+1948T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31125837 | |||||||
| chr14:31125848 | AT | A | 6 | a0001c0002t0001g0103 a0001c0002t0001g0336 a0001c0002t0001g0337 others(3): Show |
6 | HG02109.hp1 HG02897.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.4981+1936delA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31125848 | |||||||
| chr14:31126180 | C | G | 3 | a0001c0001t0001g0132 a0001c0001t0001g0134 a0001c0001t0001g0135 |
3 | HG03927.hp1 NA18953.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.4981+1605G>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31126180 | |||||||
| chr14:31126460 | A | G | 131 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0054 others(128): Show |
131 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.4981+1325T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31126460 | |||||||
| chr14:31126558 | G | A | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.4981+1227C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31126558 | |||||||
| chr14:31126561 | A | G | 1 | a0001c0006t0001g0323 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.4981+1224T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31126561 | |||||||
| chr14:31126681 | T | A | 1 | a0001c0025t0001g0092 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4981+1104A>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31126681 | |||||||
| chr14:31126682 | A | T | 2 | a0001c0017t0009g0020 a0001c0017t0009g0021 |
2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.4981+1103T>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31126682 | |||||||
| chr14:31126748 | T | C | 2 | a0001c0002t0010g0107 a0001c0002t0010g0108 |
2 | HG01993.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.4981+1037A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31126748 | |||||||
| chr14:31126897 | T | C | 1 | a0001c0002t0006g0024 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4981+888A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31126897 | |||||||
| chr14:31126973 | ATT | A | 6 | a0001c0002t0001g0069 a0001c0002t0001g0076 a0001c0002t0001g0077 others(3): Show |
6 | HG02074.hp2 NA18963.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.4981+810_4981+811d others(4): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31126973 | |||||||
| chr14:31126980 | T | C | 2 | a0001c0001t0001g0132 a0001c0001t0001g0135 |
2 | HG03927.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.4981+805A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31126980 | |||||||
| chr14:31126995 | G | T | 5 | a0001c0003t0001g0292 a0001c0003t0001g0299 a0001c0003t0001g0301 others(2): Show |
5 | HG00140.hp1 HG01175.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.4981+790C>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31126995 | |||||||
| chr14:31127038 | C | T | 1 | a0001c0023t0001g0179 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.4981+747G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31127038 | |||||||
| chr14:31127128 | C | G | 9 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(6): Show |
9 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.4981+657G>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31127128 | |||||||
| chr14:31127266 | C | T | 1 | a0001c0001t0001g0338 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4981+519G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31127266 | |||||||
| chr14:31127295 | C | A | 1 | a0001c0001t0001g0153 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.4981+490G>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31127295 | |||||||
| chr14:31127311 | T | A | 34 | a0001c0001t0001g0222 a0001c0002t0001g0053 a0001c0002t0001g0054 others(31): Show |
34 | HG00621.hp2 HG02074.hp2 HG02080.hp2 others(31): Show |
intron_variant | MODIFIER | c.4981+474A>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31127311 | |||||||
| chr14:31127415 | G | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.4981+370C>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31127415 | |||||||
| chr14:31127465 | C | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.4981+320G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31127465 | |||||||
| chr14:31127773 | A | T | 2 | a0001c0002t0013g0339 a0001c0002t0014g0340 |
2 | HG01109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.4981+12T>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31127773 | |||||||
| chr14:31128041 | G | A | 1 | a0009c0019t0001g0211 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.4760-35C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 25/42 | chr14 | 31128041 | |||||||
| chr14:31128120 | A | C | 2 | a0001c0002t0013g0339 a0001c0002t0014g0340 |
2 | HG01109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.4760-114T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 25/42 | chr14 | 31128120 | |||||||
| chr14:31128193 | TATA | T | 7 | a0001c0004t0001g0088 a0001c0004t0001g0089 a0001c0004t0001g0097 others(4): Show |
7 | HG02257.hp2 HG02683.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.4760-190_4760-188d others(5): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 25/42 | chr14 | 31128193 | |||||||
| chr14:31128255 | T | C | 2 | a0001c0009t0003g0007 a0001c0009t0003g0009 |
2 | HG02071.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.4760-249A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 25/42 | chr14 | 31128255 | |||||||
| chr14:31128338 | C | G | 3 | a0001c0001t0001g0141 a0001c0001t0001g0171 a0001c0001t0001g0208 |
3 | HG02145.hp2 HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.4759+274G>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 25/42 | chr14 | 31128338 | |||||||
| chr14:31128426 | C | T | 1 | a0001c0030t0001g0280 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.4759+186G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 25/42 | chr14 | 31128426 | |||||||
| chr14:31129646 | T | C | 1 | a0001c0002t0001g0120 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.3923-198A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31129646 | |||||||
| chr14:31129647 | C | G | 1 | a0001c0001t0001g0243 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3923-199G>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31129647 | |||||||
| chr14:31129788 | T | C | 2 | a0001c0017t0009g0020 a0001c0017t0009g0021 |
2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3923-340A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31129788 | |||||||
| chr14:31129793 | G | C | 1 | a0001c0001t0001g0160 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3923-345C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31129793 | |||||||
| chr14:31130072 | C | T | 130 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0054 others(127): Show |
130 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.3923-624G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31130072 | |||||||
| chr14:31130150 | G | C | 2 | a0001c0017t0009g0020 a0001c0017t0009g0021 |
2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3923-702C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31130150 | |||||||
| chr14:31130361 | T | C | 9 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(6): Show |
9 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.3923-913A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31130361 | |||||||
| chr14:31130478 | C | CA | 7 | a0001c0001t0001g0156 a0001c0002t0001g0051 a0001c0011t0001g0047 others(4): Show |
7 | HG02630.hp2 HG02809.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.3923-1031dupT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31130478 | |||||||
| chr14:31130478 | CA | C | 8 | a0001c0002t0001g0336 a0001c0002t0001g0337 a0001c0010t0004g0014 others(5): Show |
8 | HG02074.hp1 HG02109.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.3923-1031delT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31130478 | |||||||
| chr14:31130629 | T | A | 6 | a0001c0001t0001g0148 a0001c0001t0001g0160 a0001c0001t0001g0185 others(3): Show |
6 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.3923-1181A>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31130629 | |||||||
| chr14:31130635 | G | A | 1 | a0001c0001t0001g0175 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3923-1187C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31130635 | |||||||
| chr14:31130663 | A | G | 3 | a0001c0002t0001g0335 a0001c0002t0001g0336 a0001c0002t0001g0337 |
3 | HG02109.hp1 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.3923-1215T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31130663 | |||||||
| chr14:31130674 | T | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.3923-1226A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31130674 | |||||||
| chr14:31130717 | C | T | 1 | a0001c0002t0001g0335 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3923-1269G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31130717 | |||||||
| chr14:31130918 | G | C | 1 | a0001c0001t0001g0128 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.3923-1470C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31130918 | |||||||
| chr14:31130994 | C | G | 1 | a0001c0002t0001g0058 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.3923-1546G>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31130994 | |||||||
| chr14:31131028 | C | CA | 166 | a0001c0001t0001g0101 a0001c0001t0001g0216 a0001c0001t0001g0218 others(163): Show |
167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.3923-1581dupT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31131028 | |||||||
| chr14:31131044 | T | C | 1 | a0001c0008t0001g0283 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.3923-1596A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31131044 | |||||||
| chr14:31131124 | C | T | 1 | a0001c0008t0001g0308 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.3923-1676G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31131124 | |||||||
| chr14:31131158 | G | T | 1 | a0001c0013t0001g0182 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.3923-1710C>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31131158 | |||||||
| chr14:31131303 | A | C | 1 | a0001c0002t0001g0051 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3923-1855T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31131303 | |||||||
| chr14:31131638 | A | G | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.3922+1600T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31131638 | |||||||
| chr14:31131684 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3922+1554G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31131684 | |||||||
| chr14:31131931 | G | A | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.3922+1307C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31131931 | |||||||
| chr14:31132142 | T | C | 1 | a0001c0004t0001g0115 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3922+1096A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31132142 | |||||||
| chr14:31132175 | C | T | 2 | a0001c0017t0009g0020 a0001c0017t0009g0021 |
2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3922+1063G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31132175 | |||||||
| chr14:31132263 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3922+975G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31132263 | |||||||
| chr14:31132296 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.3922+942C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31132296 | |||||||
| chr14:31132298 | A | G | 2 | a0001c0002t0006g0023 a0001c0002t0006g0024 |
2 | HG00639.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.3922+940T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31132298 | |||||||
| chr14:31132437 | C | CA | 20 | a0001c0001t0001g0123 a0001c0001t0001g0129 a0001c0001t0001g0132 others(17): Show |
20 | HG01884.hp2 HG01943.hp2 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.3922+800dupT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31132437 | |||||||
| chr14:31132437 | CA | C | 178 | a0001c0002t0001g0053 a0001c0002t0001g0057 a0001c0002t0001g0058 others(175): Show |
179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.3922+800delT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31132437 | |||||||
| chr14:31132437 | CAA | C | 6 | a0001c0002t0001g0051 a0001c0011t0001g0047 a0001c0011t0001g0048 others(3): Show |
6 | HG02630.hp2 HG02809.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.3922+799_3922+800d others(4): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31132437 | |||||||
| chr14:31132464 | A | G | 1 | a0001c0001t0001g0151 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.3922+774T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31132464 | |||||||
| chr14:31132578 | A | G | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.3922+660T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31132578 | |||||||
| chr14:31132599 | A | G | 2 | a0001c0001t0001g0126 a0004c0015t0001g0144 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.3922+639T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31132599 | |||||||
| chr14:31132848 | C | T | 199 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0054 others(196): Show |
200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.3922+390G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31132848 | |||||||
| chr14:31132868 | T | G | 7 | a0001c0002t0010g0107 a0001c0002t0010g0108 a0001c0017t0009g0020 others(4): Show |
7 | HG01993.hp2 HG02145.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.3922+370A>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31132868 | |||||||
| chr14:31132905 | G | C | 1 | a0001c0002t0010g0108 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3922+333C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31132905 | |||||||
| chr14:31132916 | A | T | 1 | a0001c0002t0001g0113 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3922+322T>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31132916 | |||||||
| chr14:31132937 | G | C | 2 | a0001c0009t0003g0004 a0001c0009t0003g0010 |
2 | NA18982.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.3922+301C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31132937 | |||||||
| chr14:31133024 | G | A | 3 | a0003c0014t0001g0081 a0003c0014t0001g0082 a0003c0014t0001g0083 |
3 | HG02145.hp1 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3922+214C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31133024 | |||||||
| chr14:31133162 | T | G | 1 | a0001c0034t0001g0311 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.3922+76A>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31133162 | |||||||
| chr14:31133194 | TTAAC | T | 3 | a0001c0002t0001g0335 a0001c0002t0001g0336 a0001c0002t0001g0337 |
3 | HG02109.hp1 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.3922+40_3922+43del others(4): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31133194 | |||||||
| chr14:31133207 | T | G | 1 | a0001c0001t0001g0116 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3922+31A>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31133207 | |||||||
| chr14:31133457 | T | C | 1 | a0001c0002t0006g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3746-43A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 23/42 | chr14 | 31133457 | |||||||
| chr14:31133460 | A | C | 13 | a0001c0007t0001g0027 a0001c0007t0001g0028 a0001c0007t0001g0029 others(10): Show |
13 | HG00099.hp1 HG00323.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.3746-46T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 23/42 | chr14 | 31133460 | |||||||
| chr14:31133808 | A | G | 3 | a0001c0002t0010g0107 a0001c0002t0010g0108 a0001c0017t0009g0021 |
3 | HG01993.hp2 HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3579-133T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31133808 | |||||||
| chr14:31133926 | A | C | 1 | a0001c0001t0001g0212 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.3579-251T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31133926 | |||||||
| chr14:31134042 | T | TAAAAAAA others(2): Show |
10 | a0001c0004t0001g0080 a0001c0007t0007g0025 a0001c0009t0003g0003 others(7): Show |
10 | HG00323.hp1 HG00558.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.3579-376_3579-368d others(11): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134042 | |||||||
| chr14:31134042 | T | TAAAAAAA others(3): Show |
49 | a0001c0004t0001g0001 a0001c0004t0001g0026 a0001c0004t0001g0034 others(46): Show |
50 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.3579-377_3579-368d others(12): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134042 | |||||||
| chr14:31134042 | T | TAAAAAAA others(4): Show |
1 | a0002c0005t0001g0275 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3579-378_3579-368d others(13): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134042 | |||||||
| chr14:31134042 | T | TAAAAAAA others(5): Show |
1 | a0001c0004t0001g0115 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3579-379_3579-368d others(14): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134042 | |||||||
| chr14:31134042 | T | TAAAAAAA others(6): Show |
4 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0017 others(1): Show |
4 | HG02074.hp1 NA18971.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.3579-380_3579-368d others(15): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134042 | |||||||
| chr14:31134042 | T | TAAAAAAA others(7): Show |
4 | a0001c0004t0001g0089 a0001c0004t0008g0012 a0001c0010t0004g0016 others(1): Show |
4 | HG02257.hp2 HG03225.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.3579-368_3579-367i others(16): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134042 | |||||||
| chr14:31134042 | T | TAAAAAAA others(8): Show |
8 | a0001c0002t0013g0339 a0001c0003t0001g0309 a0001c0003t0001g0313 others(5): Show |
8 | HG01109.hp2 HG02683.hp1 HG03516.hp1 others(5): Show |
intron_variant | MODIFIER | c.3579-368_3579-367i others(17): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134042 | |||||||
| chr14:31134042 | T | TAAAAAAA others(9): Show |
46 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(43): Show |
46 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.3579-368_3579-367i others(18): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134042 | |||||||
| chr14:31134042 | T | TAAAAAAA others(10): Show |
18 | a0001c0002t0001g0111 a0001c0002t0001g0112 a0001c0002t0001g0113 others(15): Show |
18 | HG01081.hp2 HG01175.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.3579-368_3579-367i others(19): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134042 | |||||||
| chr14:31134042 | T | TAAAAAAA others(11): Show |
20 | a0001c0002t0001g0054 a0001c0002t0001g0057 a0001c0002t0001g0061 others(17): Show |
20 | HG01243.hp1 HG02056.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.3579-368_3579-367i others(20): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134042 | |||||||
| chr14:31134042 | T | TAAAAAAA others(12): Show |
13 | a0001c0002t0001g0053 a0001c0002t0001g0058 a0001c0002t0001g0059 others(10): Show |
13 | HG00621.hp2 HG02074.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.3579-368_3579-367i others(21): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134042 | |||||||
| chr14:31134042 | T | TAAAAAAA others(13): Show |
5 | a0001c0011t0001g0047 a0001c0011t0001g0048 a0001c0011t0001g0049 others(2): Show |
5 | HG02630.hp2 HG02809.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.3579-368_3579-367i others(22): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134042 | |||||||
| chr14:31134042 | T | TAAAAAAA others(15): Show |
3 | a0001c0002t0001g0051 a0001c0002t0001g0084 a0001c0002t0001g0106 |
3 | HG01884.hp1 HG06807.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.3579-368_3579-367i others(24): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134042 | |||||||
| chr14:31134042 | T | TAAAAAAA others(16): Show |
5 | a0001c0002t0001g0250 a0001c0002t0001g0253 a0001c0002t0001g0255 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.3579-368_3579-367i others(25): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134042 | |||||||
| chr14:31134042 | T | TAAAAAAA others(17): Show |
5 | a0001c0002t0001g0251 a0001c0002t0001g0252 a0001c0002t0001g0254 others(2): Show |
5 | HG02055.hp1 HG02257.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.3579-368_3579-367i others(26): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134042 | |||||||
| chr14:31134042 | T | TAAAAAAA others(21): Show |
1 | a0001c0002t0001g0337 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3579-368_3579-367i others(30): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134042 | |||||||
| chr14:31134042 | T | TAAAAAAA others(24): Show |
1 | a0001c0002t0001g0336 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3579-368_3579-367i others(33): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134042 | |||||||
| chr14:31134042 | T | TAAAAAAA others(30): Show |
1 | a0001c0002t0001g0335 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3579-368_3579-367i others(39): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134042 | |||||||
| chr14:31134042 | T | TAAAAAAA others(36): Show |
1 | a0001c0004t0005g0093 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3579-368_3579-367i others(45): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134042 | |||||||
| chr14:31134042 | T | TAAAAAAA others(40): Show |
1 | a0001c0004t0005g0096 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3579-368_3579-367i others(49): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134042 | |||||||
| chr14:31134056 | G | A | 3 | a0001c0002t0001g0335 a0001c0002t0001g0336 a0001c0002t0001g0337 |
3 | HG02109.hp1 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.3579-381C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134056 | |||||||
| chr14:31134102 | G | A | 1 | a0001c0026t0001g0091 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3579-427C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134102 | |||||||
| chr14:31134182 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3579-507G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134182 | |||||||
| chr14:31134213 | C | A | 1 | a0001c0010t0004g0018 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3579-538G>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134213 | |||||||
| chr14:31134242 | G | A | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.3579-567C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134242 | |||||||
| chr14:31134274 | A | C | 2 | a0001c0002t0010g0107 a0001c0002t0010g0108 |
2 | HG01993.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.3578+598T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134274 | |||||||
| chr14:31134518 | A | ATG | 20 | a0001c0001t0001g0134 a0001c0001t0001g0146 a0001c0001t0001g0199 others(17): Show |
20 | HG00741.hp1 HG01256.hp1 HG01516.hp2 others(17): Show |
intron_variant | MODIFIER | c.3578+352_3578+353d others(4): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134518 | |||||||
| chr14:31134518 | A | ATGTG | 10 | a0001c0001t0001g0132 a0001c0001t0001g0135 a0001c0001t0001g0154 others(7): Show |
10 | HG00323.hp1 HG01261.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.3578+350_3578+353d others(6): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134518 | |||||||
| chr14:31134518 | A | ATGTGTG | 7 | a0001c0001t0001g0227 a0001c0006t0002g0209 a0001c0009t0003g0006 others(4): Show |
7 | HG00558.hp1 HG01243.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.3578+348_3578+353d others(8): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134518 | |||||||
| chr14:31134518 | A | ATGTGTGT others(1): Show |
6 | a0001c0001t0001g0200 a0001c0001t0001g0203 a0001c0004t0001g0115 others(3): Show |
6 | HG00609.hp2 HG01123.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.3578+346_3578+353d others(10): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134518 | |||||||
| chr14:31134518 | A | ATGTGTGT others(3): Show |
6 | a0001c0002t0006g0022 a0001c0002t0006g0024 a0001c0009t0003g0004 others(3): Show |
6 | HG00140.hp2 HG01928.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.3578+344_3578+353d others(12): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134518 | |||||||
| chr14:31134518 | A | ATGTGTGT others(7): Show |
2 | a0001c0009t0003g0008 a0002c0005t0001g0269 |
2 | NA19005.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.3578+340_3578+353d others(16): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134518 | |||||||
| chr14:31134518 | A | ATGTGTGT others(9): Show |
2 | a0002c0005t0001g0272 a0002c0005t0001g0277 |
2 | NA19001.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.3578+338_3578+353d others(18): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134518 | |||||||
| chr14:31134518 | A | ATGTGTGT others(13): Show |
3 | a0002c0005t0001g0046 a0002c0005t0001g0260 a0002c0005t0001g0266 |
3 | NA18999.hp1 NA19006.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.3578+334_3578+353d others(22): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134518 | |||||||
| chr14:31134518 | ATG | A | 6 | a0001c0001t0001g0204 a0001c0002t0006g0023 a0001c0017t0009g0020 others(3): Show |
6 | HG00639.hp2 HG02280.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.3578+352_3578+353d others(4): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134518 | |||||||
| chr14:31134518 | ATGTG | A | 5 | a0001c0001t0001g0124 a0001c0010t0004g0014 a0001c0010t0004g0015 others(2): Show |
5 | HG02074.hp1 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.3578+350_3578+353d others(6): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134518 | |||||||
| chr14:31134518 | ATGTGTG | A | 8 | a0001c0002t0001g0102 a0001c0002t0001g0106 a0001c0004t0001g0042 others(5): Show |
8 | HG01884.hp1 HG02071.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.3578+348_3578+353d others(8): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134518 | |||||||
| chr14:31134518 | ATGTGTGT others(1): Show |
A | 5 | a0001c0002t0001g0054 a0001c0002t0001g0103 a0001c0002t0001g0104 others(2): Show |
5 | HG01099.hp2 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.3578+346_3578+353d others(10): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134518 | |||||||
| chr14:31134518 | ATGTGTGT others(3): Show |
A | 2 | a0001c0002t0001g0058 a0001c0003t0001g0304 |
2 | HG03017.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.3578+344_3578+353d others(12): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134518 | |||||||
| chr14:31134518 | ATGTGTGT others(5): Show |
A | 22 | a0001c0002t0001g0053 a0001c0002t0001g0059 a0001c0002t0001g0061 others(19): Show |
22 | HG00544.hp2 HG00621.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.3578+342_3578+353d others(14): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134518 | |||||||
| chr14:31134518 | ATGTGTGT others(7): Show |
A | 53 | a0001c0002t0001g0057 a0001c0002t0001g0069 a0001c0002t0001g0071 others(50): Show |
53 | HG00140.hp1 HG00423.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.3578+340_3578+353d others(16): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134518 | |||||||
| chr14:31134518 | ATGTGTGT others(9): Show |
A | 4 | a0001c0003t0001g0330 a0001c0008t0001g0306 a0001c0008t0001g0326 others(1): Show |
4 | NA18956.hp2 NA18994.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.3578+338_3578+353d others(18): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134518 | |||||||
| chr14:31134520 | G | A | 4 | a0001c0002t0001g0051 a0001c0011t0001g0047 a0001c0011t0001g0049 others(1): Show |
4 | HG02630.hp2 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.3578+352C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134520 | |||||||
| chr14:31134551 | TGTGTGTG others(11): Show |
T | 2 | a0001c0001t0001g0191 a0001c0001t0001g0219 |
2 | HG00738.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.3578+303_3578+320d others(20): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134551 | |||||||
| chr14:31134551 | TGTGTGTG others(13): Show |
T | 1 | a0001c0002t0001g0336 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3578+301_3578+320d others(22): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134551 | |||||||
| chr14:31134553 | TGTGTGTG others(9): Show |
T | 2 | a0001c0001t0001g0002 a0001c0001t0001g0116 |
3 | HG01071.hp1 HG01993.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3578+303_3578+318d others(18): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134553 | |||||||
| chr14:31134553 | TGTGTGTG others(11): Show |
T | 1 | a0001c0002t0001g0335 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3578+301_3578+318d others(20): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134553 | |||||||
| chr14:31134555 | TGTGTGTG others(7): Show |
T | 1 | a0008c0027t0001g0110 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3578+303_3578+316d others(16): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134555 | |||||||
| chr14:31134557 | TGTGTGTG others(7): Show |
T | 1 | a0001c0002t0001g0337 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3578+301_3578+314d others(16): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134557 | |||||||
| chr14:31134559 | TGTGTGTG others(3): Show |
T | 19 | a0001c0001t0001g0128 a0001c0001t0001g0138 a0001c0001t0001g0139 others(16): Show |
19 | HG00544.hp1 HG00609.hp1 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.3578+303_3578+312d others(12): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134559 | |||||||
| chr14:31134559 | TGTGTGTG others(5): Show |
T | 1 | a0001c0025t0001g0092 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3578+301_3578+312d others(14): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134559 | |||||||
| chr14:31134561 | TGTGTGTG others(1): Show |
T | 20 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0156 others(17): Show |
20 | HG00558.hp2 HG00621.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.3578+303_3578+310d others(10): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134561 | |||||||
| chr14:31134561 | TGTGTGTG others(3): Show |
T | 1 | a0001c0004t0005g0095 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3578+301_3578+310d others(12): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134561 | |||||||
| chr14:31134563 | T | C | 5 | a0001c0002t0010g0107 a0001c0002t0010g0108 a0001c0010t0004g0018 others(2): Show |
5 | HG01993.hp2 HG02280.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.3578+309A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134563 | |||||||
| chr14:31134563 | TGTGTGC | T | 41 | a0001c0001t0001g0100 a0001c0001t0001g0123 a0001c0001t0001g0131 others(38): Show |
41 | HG00423.hp1 HG00639.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.3578+303_3578+308d others(8): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134563 | |||||||
| chr14:31134565 | T | C | 6 | a0001c0002t0001g0106 a0001c0002t0010g0107 a0001c0002t0010g0108 others(3): Show |
6 | HG01884.hp1 HG01993.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.3578+307A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134565 | |||||||
| chr14:31134565 | TGTGC | T | 29 | a0001c0001t0001g0121 a0001c0001t0001g0129 a0001c0001t0001g0141 others(26): Show |
29 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(26): Show |
intron_variant | MODIFIER | c.3578+303_3578+306d others(6): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134565 | |||||||
| chr14:31134567 | T | C | 44 | a0001c0002t0001g0053 a0001c0002t0001g0054 a0001c0002t0001g0057 others(41): Show |
44 | HG00621.hp2 HG01099.hp2 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.3578+305A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134567 | |||||||
| chr14:31134567 | T | TGC | 3 | a0001c0002t0013g0339 a0001c0002t0014g0340 a0002c0005t0001g0274 |
3 | HG00733.hp1 HG01109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.3578+303_3578+304d others(4): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134567 | |||||||
| chr14:31134567 | TGC | T | 23 | a0001c0001t0001g0101 a0001c0001t0001g0155 a0001c0001t0001g0170 others(20): Show |
23 | HG00280.hp2 HG00673.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.3578+303_3578+304d others(4): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134567 | |||||||
| chr14:31134567 | TGCGC | T | 6 | a0001c0004t0001g0066 a0001c0004t0001g0080 a0001c0004t0001g0098 others(3): Show |
6 | HG01943.hp1 HG01975.hp1 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.3578+301_3578+304d others(6): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134567 | |||||||
| chr14:31134568 | G | A | 4 | a0001c0002t0010g0107 a0001c0002t0010g0108 a0001c0017t0009g0020 others(1): Show |
4 | HG01993.hp2 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.3578+304C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134568 | |||||||
| chr14:31134569 | C | T | 44 | a0001c0001t0001g0122 a0001c0001t0001g0132 a0001c0001t0001g0134 others(41): Show |
44 | HG00323.hp1 HG00558.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.3578+303G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134569 | |||||||
| chr14:31134571 | C | T | 9 | a0001c0002t0006g0022 a0001c0004t0001g0065 a0001c0004t0001g0067 others(6): Show |
9 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.3578+301G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134571 | |||||||
| chr14:31134626 | C | G | 4 | a0001c0002t0010g0107 a0001c0002t0010g0108 a0001c0017t0009g0020 others(1): Show |
4 | HG01993.hp2 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.3578+246G>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134626 | |||||||
| chr14:31134655 | T | C | 1 | a0001c0004t0001g0038 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3578+217A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134655 | |||||||
| chr14:31134721 | G | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.3578+151C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134721 | |||||||
| chr14:31134737 | T | G | 9 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(6): Show |
9 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.3578+135A>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134737 | |||||||
| chr14:31134743 | G | C | 5 | a0002c0005t0001g0046 a0002c0005t0001g0266 a0002c0005t0001g0269 others(2): Show |
5 | NA18999.hp1 NA19001.hp1 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.3578+129C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 22/42 | chr14 | 31134743 | |||||||
| chr14:31135657 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3115-42G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 20/42 | chr14 | 31135657 | |||||||
| chr14:31135673 | T | G | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.3115-58A>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 20/42 | chr14 | 31135673 | |||||||
| chr14:31135736 | T | A | 2 | a0001c0006t0001g0286 a0001c0006t0001g0323 |
2 | NA18957.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.3115-121A>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 20/42 | chr14 | 31135736 | |||||||
| chr14:31135742 | G | A | 1 | a0001c0004t0001g0089 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3115-127C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 20/42 | chr14 | 31135742 | |||||||
| chr14:31135856 | A | G | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.3115-241T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 20/42 | chr14 | 31135856 | |||||||
| chr14:31136000 | G | C | 1 | a0001c0004t0001g0042 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3115-385C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 20/42 | chr14 | 31136000 | |||||||
| chr14:31136023 | AAAC | A | 84 | a0001c0001t0001g0128 a0001c0002t0001g0053 a0001c0002t0001g0054 others(81): Show |
84 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.3115-411_3115-409d others(5): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 20/42 | chr14 | 31136023 | |||||||
| chr14:31136023 | AAACAAC | A | 3 | a0001c0002t0001g0335 a0001c0002t0001g0336 a0001c0002t0001g0337 |
3 | HG02109.hp1 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.3115-414_3115-409d others(8): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 20/42 | chr14 | 31136023 | |||||||
| chr14:31136243 | CAAAT | C | 4 | a0001c0001t0001g0157 a0001c0001t0001g0169 a0001c0001t0001g0216 others(1): Show |
4 | NA18961.hp1 NA18983.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.3114+284_3114+287d others(6): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 20/42 | chr14 | 31136243 | |||||||
| chr14:31136799 | C | T | 2 | a0001c0004t0001g0037 a0001c0004t0001g0042 |
2 | HG01099.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2980-134G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31136799 | |||||||
| chr14:31136818 | C | CT | 20 | a0001c0002t0001g0051 a0001c0002t0010g0107 a0001c0002t0010g0108 others(17): Show |
20 | HG00609.hp2 HG01109.hp1 HG01993.hp2 others(17): Show |
intron_variant | MODIFIER | c.2980-154dupA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31136818 | |||||||
| chr14:31136829 | TC | T | 11 | a0001c0002t0001g0106 a0001c0002t0001g0250 a0001c0002t0001g0252 others(8): Show |
11 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.2980-165delG | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31136829 | |||||||
| chr14:31136830 | C | T | 172 | a0001c0001t0001g0128 a0001c0002t0001g0051 a0001c0002t0001g0053 others(169): Show |
173 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.2980-165G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31136830 | |||||||
| chr14:31136834 | T | TG | 9 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(6): Show |
9 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.2980-170_2980-169i others(3): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31136834 | |||||||
| chr14:31136845 | G | A | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.2980-180C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31136845 | |||||||
| chr14:31136890 | C | T | 2 | a0001c0002t0006g0023 a0001c0002t0006g0024 |
2 | HG00639.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.2980-225G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31136890 | |||||||
| chr14:31136915 | G | A | 1 | a0001c0004t0001g0080 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2980-250C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31136915 | |||||||
| chr14:31137034 | G | A | 3 | a0001c0013t0001g0130 a0001c0013t0001g0165 a0001c0013t0001g0182 |
3 | HG01099.hp1 NA18969.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.2980-369C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31137034 | |||||||
| chr14:31137044 | G | T | 2 | a0001c0004t0001g0089 a0001c0025t0001g0092 |
2 | HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2980-379C>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31137044 | |||||||
| chr14:31137065 | A | G | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.2980-400T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31137065 | |||||||
| chr14:31137071 | C | T | 1 | a0001c0010t0004g0018 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2980-406G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31137071 | |||||||
| chr14:31137086 | T | C | 3 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 |
3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2980-421A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31137086 | |||||||
| chr14:31137102 | G | A | 3 | a0001c0003t0001g0298 a0001c0003t0001g0305 a0001c0003t0001g0314 |
3 | HG01346.hp2 HG02602.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2980-437C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31137102 | |||||||
| chr14:31137121 | C | CT | 69 | a0001c0001t0001g0116 a0001c0001t0001g0121 a0001c0001t0001g0128 others(66): Show |
69 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.2980-457dupA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31137121 | |||||||
| chr14:31137121 | C | CTT | 10 | a0001c0001t0001g0153 a0001c0002t0001g0076 a0001c0002t0001g0103 others(7): Show |
10 | HG01928.hp1 HG02897.hp1 HG03209.hp1 others(7): Show |
intron_variant | MODIFIER | c.2980-458_2980-457d others(4): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31137121 | |||||||
| chr14:31137374 | C | G | 1 | a0001c0003t0001g0312 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2980-709G>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31137374 | |||||||
| chr14:31137412 | G | A | 8 | a0001c0009t0003g0003 a0001c0009t0003g0004 a0001c0009t0003g0005 others(5): Show |
8 | HG00558.hp1 HG00609.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.2980-747C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31137412 | |||||||
| chr14:31137421 | C | T | 1 | a0001c0029t0001g0327 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2980-756G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31137421 | |||||||
| chr14:31137449 | C | T | 1 | a0001c0003t0001g0314 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2980-784G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31137449 | |||||||
| chr14:31137458 | T | C | 9 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(6): Show |
9 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.2980-793A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31137458 | |||||||
| chr14:31137467 | C | T | 1 | a0001c0034t0001g0311 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2980-802G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31137467 | |||||||
| chr14:31137535 | C | T | 6 | a0001c0002t0001g0109 a0001c0002t0001g0111 a0001c0002t0001g0112 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2980-870G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31137535 | |||||||
| chr14:31137536 | G | C | 3 | a0003c0014t0001g0081 a0003c0014t0001g0082 a0003c0014t0001g0083 |
3 | HG02145.hp1 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2980-871C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31137536 | |||||||
| chr14:31137566 | T | C | 9 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(6): Show |
9 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.2980-901A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31137566 | |||||||
| chr14:31137587 | CA | C | 12 | a0001c0004t0001g0088 a0001c0004t0001g0089 a0001c0004t0001g0097 others(9): Show |
12 | HG01106.hp1 HG02257.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.2980-923delT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31137587 | |||||||
| chr14:31137646 | G | A | 2 | a0001c0009t0003g0007 a0001c0009t0003g0009 |
2 | HG02071.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.2980-981C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31137646 | |||||||
| chr14:31137697 | G | A | 1 | a0001c0010t0004g0018 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2980-1032C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31137697 | |||||||
| chr14:31137767 | C | A | 2 | a0001c0017t0009g0020 a0001c0017t0009g0021 |
2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2980-1102G>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31137767 | |||||||
| chr14:31138263 | G | C | 3 | a0003c0014t0001g0081 a0003c0014t0001g0082 a0003c0014t0001g0083 |
3 | HG02145.hp1 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2980-1598C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31138263 | |||||||
| chr14:31138396 | C | T | 12 | a0001c0004t0001g0088 a0001c0004t0001g0089 a0001c0004t0001g0097 others(9): Show |
12 | HG01106.hp1 HG02257.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.2979+1496G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31138396 | |||||||
| chr14:31138434 | C | T | 1 | a0001c0004t0001g0089 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2979+1458G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31138434 | |||||||
| chr14:31138443 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2979+1449G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31138443 | |||||||
| chr14:31138583 | T | C | 1 | a0001c0013t0001g0165 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2979+1309A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31138583 | |||||||
| chr14:31138613 | C | T | 5 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(2): Show |
5 | HG02074.hp1 NA18971.hp1 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.2979+1279G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31138613 | |||||||
| chr14:31138745 | C | G | 10 | a0001c0002t0001g0250 a0001c0002t0001g0251 a0001c0002t0001g0252 others(7): Show |
10 | HG02055.hp1 HG02257.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.2979+1147G>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31138745 | |||||||
| chr14:31138928 | T | C | 1 | a0007c0028t0001g0070 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2979+964A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31138928 | |||||||
| chr14:31139041 | G | GAT | 46 | a0001c0001t0001g0123 a0001c0001t0001g0126 a0001c0001t0001g0127 others(43): Show |
46 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.2979+849_2979+850d others(4): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31139041 | |||||||
| chr14:31139041 | GAT | G | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.2979+849_2979+850d others(4): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31139041 | |||||||
| chr14:31139041 | GATATAT | G | 54 | a0001c0003t0001g0099 a0001c0003t0001g0282 a0001c0003t0001g0285 others(51): Show |
54 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.2979+845_2979+850d others(8): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31139041 | |||||||
| chr14:31139289 | C | A | 79 | a0001c0001t0001g0002 a0001c0001t0001g0100 a0001c0001t0001g0101 others(76): Show |
80 | HG00280.hp1 HG00323.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.2979+603G>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31139289 | |||||||
| chr14:31139328 | G | T | 1 | a0001c0002t0001g0106 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2979+564C>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31139328 | |||||||
| chr14:31139340 | T | C | 1 | a0001c0001t0001g0123 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2979+552A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31139340 | |||||||
| chr14:31139362 | A | T | 1 | a0001c0004t0001g0044 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2979+530T>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31139362 | |||||||
| chr14:31139439 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2979+453C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31139439 | |||||||
| chr14:31139509 | T | C | 28 | a0001c0002t0001g0053 a0001c0002t0001g0054 a0001c0002t0001g0057 others(25): Show |
28 | HG00621.hp2 HG02074.hp2 HG02080.hp2 others(25): Show |
intron_variant | MODIFIER | c.2979+383A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31139509 | |||||||
| chr14:31139584 | T | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.2979+308A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31139584 | |||||||
| chr14:31139702 | T | A | 9 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(6): Show |
9 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.2979+190A>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31139702 | |||||||
| chr14:31139704 | G | T | 5 | a0001c0004t0005g0090 a0001c0004t0005g0093 a0001c0004t0005g0094 others(2): Show |
5 | HG01106.hp1 HG02572.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2979+188C>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31139704 | |||||||
| chr14:31139718 | G | A | 10 | a0001c0002t0001g0250 a0001c0002t0001g0251 a0001c0002t0001g0252 others(7): Show |
10 | HG02055.hp1 HG02257.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.2979+174C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31139718 | |||||||
| chr14:31140001 | C | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.2874-4G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 18/42 | chr14 | 31140001 | |||||||
| chr14:31140073 | A | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.2874-76T>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 18/42 | chr14 | 31140073 | |||||||
| chr14:31140075 | T | C | 1 | a0001c0003t0001g0297 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2874-78A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 18/42 | chr14 | 31140075 | |||||||
| chr14:31140174 | G | A | 2 | a0001c0001t0001g0199 a0001c0001t0001g0228 |
2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2874-177C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 18/42 | chr14 | 31140174 | |||||||
| chr14:31140236 | T | C | 1 | a0001c0004t0001g0115 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2874-239A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 18/42 | chr14 | 31140236 | |||||||
| chr14:31140290 | T | C | 4 | a0001c0002t0010g0107 a0001c0002t0010g0108 a0001c0017t0009g0020 others(1): Show |
4 | HG01993.hp2 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2874-293A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 18/42 | chr14 | 31140290 | |||||||
| chr14:31140482 | A | G | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.2874-485T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 18/42 | chr14 | 31140482 | |||||||
| chr14:31140544 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2874-547A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 18/42 | chr14 | 31140544 | |||||||
| chr14:31140590 | TA | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.2874-594delT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 18/42 | chr14 | 31140590 | |||||||
| chr14:31140731 | A | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.2874-734T>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 18/42 | chr14 | 31140731 | |||||||
| chr14:31140750 | G | A | 1 | a0001c0004t0008g0012 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2874-753C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 18/42 | chr14 | 31140750 | |||||||
| chr14:31140885 | G | A | 67 | a0001c0001t0001g0002 a0001c0001t0001g0100 a0001c0001t0001g0101 others(64): Show |
68 | HG00280.hp1 HG00323.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.2874-888C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 18/42 | chr14 | 31140885 | |||||||
| chr14:31140896 | T | G | 11 | a0001c0002t0001g0106 a0001c0002t0001g0250 a0001c0002t0001g0251 others(8): Show |
11 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.2874-899A>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 18/42 | chr14 | 31140896 | |||||||
| chr14:31140919 | T | C | 50 | a0001c0004t0001g0001 a0001c0004t0001g0026 a0001c0004t0001g0034 others(47): Show |
51 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.2874-922A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 18/42 | chr14 | 31140919 | |||||||
| chr14:31140932 | C | CT | 54 | a0001c0003t0001g0099 a0001c0003t0001g0282 a0001c0003t0001g0285 others(51): Show |
54 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.2873+925dupA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 18/42 | chr14 | 31140932 | |||||||
| chr14:31140932 | CT | C | 230 | a0001c0001t0001g0002 a0001c0001t0001g0100 a0001c0001t0001g0101 others(227): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.2873+925delA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 18/42 | chr14 | 31140932 | |||||||
| chr14:31141010 | T | C | 131 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0054 others(128): Show |
131 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.2873+848A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 18/42 | chr14 | 31141010 | |||||||
| chr14:31141056 | T | G | 1 | a0001c0004t0001g0098 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2873+802A>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 18/42 | chr14 | 31141056 | |||||||
| chr14:31141063 | G | A | 1 | a0001c0004t0001g0044 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2873+795C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 18/42 | chr14 | 31141063 | |||||||
| chr14:31141072 | C | T | 10 | a0001c0001t0001g0127 a0001c0001t0001g0151 a0001c0001t0001g0156 others(7): Show |
10 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(7): Show |
intron_variant | MODIFIER | c.2873+786G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 18/42 | chr14 | 31141072 | |||||||
| chr14:31141087 | C | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0213 |
2 | HG01081.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.2873+771G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 18/42 | chr14 | 31141087 | |||||||
| chr14:31141110 | T | TAG | 6 | a0001c0002t0001g0051 a0001c0011t0001g0047 a0001c0011t0001g0048 others(3): Show |
6 | HG02630.hp2 HG02809.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2873+746_2873+747d others(4): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 18/42 | chr14 | 31141110 | |||||||
| chr14:31141161 | G | C | 1 | a0002c0005t0001g0262 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2873+697C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 18/42 | chr14 | 31141161 | |||||||
| chr14:31141232 | T | C | 131 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0054 others(128): Show |
131 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.2873+626A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 18/42 | chr14 | 31141232 | |||||||
| chr14:31141250 | A | G | 1 | a0001c0003t0001g0316 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2873+608T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 18/42 | chr14 | 31141250 | |||||||
| chr14:31141296 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2873+562G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 18/42 | chr14 | 31141296 | |||||||
| chr14:31141323 | T | A | 1 | a0001c0002t0001g0335 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2873+535A>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 18/42 | chr14 | 31141323 | |||||||
| chr14:31141324 | A | T | 7 | a0001c0003t0001g0334 a0001c0010t0004g0014 a0001c0010t0004g0015 others(4): Show |
7 | HG02074.hp1 HG03942.hp2 NA18968.hp1 others(4): Show |
intron_variant | MODIFIER | c.2873+534T>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 18/42 | chr14 | 31141324 | |||||||
| chr14:31141520 | G | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.2873+338C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 18/42 | chr14 | 31141520 | |||||||
| chr14:31141557 | C | T | 1 | a0001c0001t0001g0338 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2873+301G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 18/42 | chr14 | 31141557 | |||||||
| chr14:31141733 | T | C | 50 | a0001c0004t0001g0001 a0001c0004t0001g0026 a0001c0004t0001g0034 others(47): Show |
51 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.2873+125A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 18/42 | chr14 | 31141733 | |||||||
| chr14:31141758 | C | A | 85 | a0001c0002t0001g0053 a0001c0002t0001g0054 a0001c0002t0001g0057 others(82): Show |
85 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.2873+100G>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 18/42 | chr14 | 31141758 | |||||||
| chr14:31141816 | G | A | 15 | a0001c0002t0001g0109 a0001c0002t0001g0111 a0001c0002t0001g0112 others(12): Show |
15 | HG01891.hp1 HG02074.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.2873+42C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 18/42 | chr14 | 31141816 | |||||||
| chr14:31141979 | C | CA | 11 | a0001c0002t0001g0106 a0001c0002t0001g0250 a0001c0002t0001g0251 others(8): Show |
11 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.2779-28dupT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 17/42 | chr14 | 31141979 | |||||||
| chr14:31141999 | A | T | 1 | a0001c0001t0001g0245 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2779-47T>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 17/42 | chr14 | 31141999 | |||||||
| chr14:31142013 | C | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.2779-61G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 17/42 | chr14 | 31142013 | |||||||
| chr14:31142225 | T | C | 1 | a0001c0002t0001g0335 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2779-273A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 17/42 | chr14 | 31142225 | |||||||
| chr14:31142235 | C | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.2779-283G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 17/42 | chr14 | 31142235 | |||||||
| chr14:31142261 | T | C | 2 | a0001c0002t0013g0339 a0001c0002t0014g0340 |
2 | HG01109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2779-309A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 17/42 | chr14 | 31142261 | |||||||
| chr14:31142417 | A | G | 6 | a0001c0002t0001g0109 a0001c0002t0001g0111 a0001c0002t0001g0112 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2779-465T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 17/42 | chr14 | 31142417 | |||||||
| chr14:31142419 | T | C | 1 | a0001c0002t0001g0336 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2779-467A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 17/42 | chr14 | 31142419 | |||||||
| chr14:31142433 | A | AT | 20 | a0001c0001t0001g0176 a0001c0002t0001g0111 a0001c0002t0001g0114 others(17): Show |
20 | HG01074.hp2 HG01952.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.2779-482dupA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 17/42 | chr14 | 31142433 | |||||||
| chr14:31142433 | AT | A | 15 | a0001c0001t0001g0168 a0001c0002t0001g0250 a0001c0002t0001g0251 others(12): Show |
15 | HG01168.hp1 HG01256.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.2779-482delA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 17/42 | chr14 | 31142433 | |||||||
| chr14:31142544 | C | T | 1 | a0001c0001t0001g0245 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2779-592G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 17/42 | chr14 | 31142544 | |||||||
| chr14:31142558 | A | G | 1 | a0001c0001t0001g0205 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2779-606T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 17/42 | chr14 | 31142558 | |||||||
| chr14:31142678 | T | C | 3 | a0003c0014t0001g0081 a0003c0014t0001g0082 a0003c0014t0001g0083 |
3 | HG02145.hp1 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2779-726A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 17/42 | chr14 | 31142678 | |||||||
| chr14:31142731 | G | A | 8 | a0001c0002t0001g0335 a0001c0002t0010g0107 a0001c0002t0010g0108 others(5): Show |
8 | HG01993.hp2 HG02145.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2779-779C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 17/42 | chr14 | 31142731 | |||||||
| chr14:31142863 | G | A | 4 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0239 others(1): Show |
4 | HG02055.hp2 HG02647.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2779-911C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 17/42 | chr14 | 31142863 | |||||||
| chr14:31142961 | A | G | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.2779-1009T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 17/42 | chr14 | 31142961 | |||||||
| chr14:31143055 | ATAAT | A | 3 | a0001c0002t0006g0022 a0001c0002t0006g0023 a0001c0002t0006g0024 |
3 | HG00639.hp2 HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2778+1052_2778+105 others(8): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 17/42 | chr14 | 31143055 | |||||||
| chr14:31143170 | T | C | 1 | a0001c0002t0001g0337 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2778+941A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 17/42 | chr14 | 31143170 | |||||||
| chr14:31143199 | A | C | 1 | a0001c0008t0001g0283 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2778+912T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 17/42 | chr14 | 31143199 | |||||||
| chr14:31143277 | G | T | 1 | a0001c0001t0001g0142 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2778+834C>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 17/42 | chr14 | 31143277 | |||||||
| chr14:31143371 | G | A | 1 | a0001c0004t0001g0089 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2778+740C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 17/42 | chr14 | 31143371 | |||||||
| chr14:31143429 | T | C | 2 | a0001c0004t0001g0001 a0001c0004t0001g0034 |
3 | HG02559.hp1 HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2778+682A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 17/42 | chr14 | 31143429 | |||||||
| chr14:31143569 | G | A | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.2778+542C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 17/42 | chr14 | 31143569 | |||||||
| chr14:31143593 | G | A | 3 | a0001c0001t0001g0126 a0001c0001t0001g0145 a0004c0015t0001g0144 |
3 | HG00099.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2778+518C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 17/42 | chr14 | 31143593 | |||||||
| chr14:31143815 | A | G | 8 | a0001c0009t0003g0003 a0001c0009t0003g0004 a0001c0009t0003g0005 others(5): Show |
8 | HG00558.hp1 HG00609.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.2778+296T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 17/42 | chr14 | 31143815 | |||||||
| chr14:31144332 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2632-75T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 16/42 | chr14 | 31144332 | |||||||
| chr14:31144443 | C | T | 3 | a0003c0014t0001g0081 a0003c0014t0001g0082 a0003c0014t0001g0083 |
3 | HG02145.hp1 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2632-186G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 16/42 | chr14 | 31144443 | |||||||
| chr14:31144666 | C | T | 2 | a0001c0002t0001g0069 a0001c0007t0001g0041 |
2 | HG03834.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.2631+141G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 16/42 | chr14 | 31144666 | |||||||
| chr14:31144716 | C | T | 1 | a0001c0002t0001g0336 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2631+91G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 16/42 | chr14 | 31144716 | |||||||
| chr14:31145167 | T | C | 29 | a0001c0004t0001g0001 a0001c0004t0001g0026 a0001c0004t0001g0034 others(26): Show |
30 | HG00099.hp1 HG00323.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.2497-226A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31145167 | |||||||
| chr14:31145403 | T | G | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.2497-462A>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31145403 | |||||||
| chr14:31145443 | A | C | 29 | a0001c0004t0001g0001 a0001c0004t0001g0026 a0001c0004t0001g0034 others(26): Show |
30 | HG00099.hp1 HG00323.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.2497-502T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31145443 | |||||||
| chr14:31145453 | A | C | 1 | a0001c0030t0001g0280 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2497-512T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31145453 | |||||||
| chr14:31145558 | C | A | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2497-617G>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31145558 | |||||||
| chr14:31145621 | A | T | 1 | a0001c0001t0001g0193 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2497-680T>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31145621 | |||||||
| chr14:31145727 | C | G | 1 | a0001c0009t0003g0008 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2497-786G>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31145727 | |||||||
| chr14:31145785 | T | C | 1 | a0002c0005t0001g0271 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2497-844A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31145785 | |||||||
| chr14:31145849 | C | T | 1 | a0001c0007t0001g0040 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2497-908G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31145849 | |||||||
| chr14:31145979 | C | T | 1 | a0001c0002t0006g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2497-1038G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31145979 | |||||||
| chr14:31145983 | A | G | 1 | a0001c0002t0001g0336 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2497-1042T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31145983 | |||||||
| chr14:31145986 | A | AT | 6 | a0001c0002t0001g0109 a0001c0002t0001g0111 a0001c0002t0001g0112 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2497-1046dupA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31145986 | |||||||
| chr14:31146069 | C | T | 49 | a0001c0004t0001g0001 a0001c0004t0001g0026 a0001c0004t0001g0034 others(46): Show |
50 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.2497-1128G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31146069 | |||||||
| chr14:31146204 | A | G | 2 | a0002c0005t0001g0046 a0002c0005t0001g0266 |
2 | NA18999.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.2497-1263T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31146204 | |||||||
| chr14:31146447 | G | A | 3 | a0001c0001t0001g0123 a0001c0001t0001g0140 a0001c0001t0001g0237 |
3 | NA18939.hp2 NA18982.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.2497-1506C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31146447 | |||||||
| chr14:31146496 | GA | G | 37 | a0001c0001t0001g0122 a0001c0002t0001g0053 a0001c0002t0001g0054 others(34): Show |
37 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.2497-1556delT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31146496 | |||||||
| chr14:31146624 | C | G | 1 | a0003c0014t0001g0082 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2497-1683G>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31146624 | |||||||
| chr14:31146625 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2497-1684C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31146625 | |||||||
| chr14:31146673 | T | C | 1 | a0001c0006t0001g0286 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2497-1732A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31146673 | |||||||
| chr14:31146701 | A | C | 3 | a0001c0002t0001g0335 a0001c0002t0001g0336 a0001c0002t0001g0337 |
3 | HG02109.hp1 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2497-1760T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31146701 | |||||||
| chr14:31146746 | G | T | 1 | a0001c0006t0002g0192 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2497-1805C>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31146746 | |||||||
| chr14:31146888 | CT | C | 6 | a0001c0002t0001g0109 a0001c0002t0001g0111 a0001c0002t0001g0112 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2496+1832delA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31146888 | |||||||
| chr14:31146891 | T | A | 6 | a0001c0002t0001g0109 a0001c0002t0001g0111 a0001c0002t0001g0112 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2496+1830A>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31146891 | |||||||
| chr14:31147068 | T | C | 1 | a0001c0002t0001g0079 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2496+1653A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31147068 | |||||||
| chr14:31147183 | C | T | 8 | a0001c0009t0003g0003 a0001c0009t0003g0004 a0001c0009t0003g0005 others(5): Show |
8 | HG00558.hp1 HG00609.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.2496+1538G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31147183 | |||||||
| chr14:31147205 | C | T | 3 | a0001c0002t0001g0053 a0001c0002t0001g0058 a0001c0002t0001g0059 |
3 | NA19057.hp2 NA19080.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.2496+1516G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31147205 | |||||||
| chr14:31147238 | G | A | 1 | a0008c0027t0001g0110 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2496+1483C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31147238 | |||||||
| chr14:31147284 | A | T | 1 | a0001c0004t0001g0044 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2496+1437T>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31147284 | |||||||
| chr14:31147586 | G | A | 5 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(2): Show |
5 | HG02074.hp1 NA18971.hp1 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.2496+1135C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31147586 | |||||||
| chr14:31147700 | G | A | 6 | a0001c0002t0001g0051 a0001c0011t0001g0047 a0001c0011t0001g0048 others(3): Show |
6 | HG02630.hp2 HG02809.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2496+1021C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31147700 | |||||||
| chr14:31147739 | G | C | 5 | a0002c0005t0001g0046 a0002c0005t0001g0266 a0002c0005t0001g0269 others(2): Show |
5 | NA18999.hp1 NA19001.hp1 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.2496+982C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31147739 | |||||||
| chr14:31147756 | A | AG | 3 | a0003c0014t0001g0081 a0003c0014t0001g0082 a0003c0014t0001g0083 |
3 | HG02145.hp1 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2496+964_2496+965i others(3): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31147756 | |||||||
| chr14:31147809 | C | A | 29 | a0001c0002t0001g0053 a0001c0002t0001g0054 a0001c0002t0001g0057 others(26): Show |
29 | HG00621.hp2 HG02074.hp2 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.2496+912G>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31147809 | |||||||
| chr14:31147831 | G | A | 4 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0225 others(1): Show |
4 | HG00741.hp1 HG01433.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.2496+890C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31147831 | |||||||
| chr14:31147838 | C | G | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.2496+883G>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31147838 | |||||||
| chr14:31147920 | C | T | 1 | a0001c0004t0001g0089 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2496+801G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31147920 | |||||||
| chr14:31147934 | T | C | 1 | a0001c0002t0001g0336 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2496+787A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31147934 | |||||||
| chr14:31147978 | C | T | 2 | a0001c0002t0006g0023 a0001c0002t0006g0024 |
2 | HG00639.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.2496+743G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31147978 | |||||||
| chr14:31148090 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2496+631G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31148090 | |||||||
| chr14:31148428 | A | T | 1 | a0002c0005t0001g0046 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2496+293T>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31148428 | |||||||
| chr14:31148516 | T | C | 3 | a0002c0005t0001g0265 a0002c0005t0001g0270 a0002c0005t0001g0271 |
3 | HG00140.hp2 HG01168.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.2496+205A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31148516 | |||||||
| chr14:31148554 | T | C | 8 | a0001c0009t0003g0003 a0001c0009t0003g0004 a0001c0009t0003g0005 others(5): Show |
8 | HG00558.hp1 HG00609.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.2496+167A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31148554 | |||||||
| chr14:31148562 | A | C | 2 | a0001c0002t0001g0336 a0001c0002t0001g0337 |
2 | HG02109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2496+159T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31148562 | |||||||
| chr14:31148674 | A | C | 131 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0054 others(128): Show |
131 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.2496+47T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31148674 | |||||||
| chr14:31148713 | A | G | 8 | a0001c0009t0003g0003 a0001c0009t0003g0004 a0001c0009t0003g0005 others(5): Show |
8 | HG00558.hp1 HG00609.hp2 HG02071.hp2 others(5): Show |
splice_region_variant&intron_variant | LOW | c.2496+8T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 15/42 | chr14 | 31148713 | |||||||
| chr14:31148842 | A | G | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.2420-45T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 14/42 | chr14 | 31148842 | |||||||
| chr14:31148844 | T | C | 1 | a0001c0011t0001g0049 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2420-47A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 14/42 | chr14 | 31148844 | |||||||
| chr14:31148866 | AC | A | 8 | a0001c0009t0003g0003 a0001c0009t0003g0004 a0001c0009t0003g0005 others(5): Show |
8 | HG00558.hp1 HG00609.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.2419+30delG | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 14/42 | chr14 | 31148866 | |||||||
| chr14:31149308 | C | A | 9 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(6): Show |
9 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.2156-148G>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 13/42 | chr14 | 31149308 | |||||||
| chr14:31149443 | C | CA | 19 | a0001c0001t0001g0221 a0001c0001t0001g0246 a0001c0002t0001g0076 others(16): Show |
19 | HG00140.hp2 HG01168.hp2 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.2156-284dupT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 13/42 | chr14 | 31149443 | |||||||
| chr14:31149443 | CA | C | 6 | a0001c0001t0001g0131 a0001c0002t0001g0051 a0001c0002t0001g0254 others(3): Show |
6 | HG02015.hp2 HG02145.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2156-284delT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 13/42 | chr14 | 31149443 | |||||||
| chr14:31149443 | CAAAAAAA others(3): Show |
C | 1 | a0001c0010t0004g0018 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2156-293_2156-284d others(12): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 13/42 | chr14 | 31149443 | |||||||
| chr14:31149448 | A | G | 1 | a0001c0004t0001g0044 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2156-288T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 13/42 | chr14 | 31149448 | |||||||
| chr14:31149596 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2155+403A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 13/42 | chr14 | 31149596 | |||||||
| chr14:31149622 | T | TTAAAAAT others(7): Show |
6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.2155+376_2155+377i others(16): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 13/42 | chr14 | 31149622 | |||||||
| chr14:31149623 | G | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.2155+376C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 13/42 | chr14 | 31149623 | |||||||
| chr14:31149624 | T | A | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.2155+375A>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 13/42 | chr14 | 31149624 | |||||||
| chr14:31149625 | T | A | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.2155+374A>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 13/42 | chr14 | 31149625 | |||||||
| chr14:31149626 | T | G | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.2155+373A>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 13/42 | chr14 | 31149626 | |||||||
| chr14:31149629 | A | AGGCG | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.2155+369_2155+370i others(6): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 13/42 | chr14 | 31149629 | |||||||
| chr14:31149683 | A | T | 1 | a0001c0003t0001g0333 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2155+316T>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 13/42 | chr14 | 31149683 | |||||||
| chr14:31149776 | G | A | 29 | a0001c0002t0001g0053 a0001c0002t0001g0054 a0001c0002t0001g0057 others(26): Show |
29 | HG00621.hp2 HG02074.hp2 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.2155+223C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 13/42 | chr14 | 31149776 | |||||||
| chr14:31149898 | G | A | 1 | a0001c0001t0001g0338 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2155+101C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 13/42 | chr14 | 31149898 | |||||||
| chr14:31149939 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2155+60T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 13/42 | chr14 | 31149939 | |||||||
| chr14:31149961 | G | C | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2155+38C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 13/42 | chr14 | 31149961 | |||||||
| chr14:31149982 | T | C | 1 | a0001c0002t0001g0251 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2155+17A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 13/42 | chr14 | 31149982 | |||||||
| chr14:31150224 | AAATGTGT others(2): Show |
A | 3 | a0001c0002t0006g0022 a0001c0002t0006g0023 a0001c0002t0006g0024 |
3 | HG00639.hp2 HG02258.hp1 HG03540.hp1 |
splice_region_variant&intron_variant | LOW | c.1933-12_1933-4delC others(8): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31150224 | |||||||
| chr14:31150254 | A | G | 9 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(6): Show |
9 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1933-33T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31150254 | |||||||
| chr14:31150376 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1933-155A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31150376 | |||||||
| chr14:31151302 | A | AATTC | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1933-1085_1933-108 others(8): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31151302 | |||||||
| chr14:31151390 | C | CT | 27 | a0001c0001t0001g0116 a0001c0001t0001g0142 a0001c0001t0001g0177 others(24): Show |
27 | HG00639.hp2 HG01175.hp1 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.1933-1170dupA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31151390 | |||||||
| chr14:31151390 | C | CTT | 7 | a0001c0002t0001g0251 a0001c0002t0001g0256 a0001c0002t0001g0335 others(4): Show |
7 | HG01109.hp2 HG02109.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1933-1171_1933-117 others(6): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31151390 | |||||||
| chr14:31151696 | G | GT | 7 | a0001c0002t0006g0022 a0001c0010t0004g0014 a0001c0010t0004g0015 others(4): Show |
7 | HG02074.hp1 HG03540.hp1 HG03942.hp2 others(4): Show |
intron_variant | MODIFIER | c.1933-1476dupA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31151696 | |||||||
| chr14:31151707 | T | A | 6 | a0001c0002t0013g0339 a0001c0002t0014g0340 a0001c0009t0003g0005 others(3): Show |
6 | HG00609.hp2 HG01109.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1933-1486A>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31151707 | |||||||
| chr14:31151708 | A | T | 7 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(4): Show |
7 | HG01109.hp1 HG02074.hp1 HG03942.hp2 others(4): Show |
intron_variant | MODIFIER | c.1933-1487T>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31151708 | |||||||
| chr14:31151767 | C | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1933-1546G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31151767 | |||||||
| chr14:31151844 | T | C | 2 | a0001c0002t0013g0339 a0001c0002t0014g0340 |
2 | HG01109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1933-1623A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31151844 | |||||||
| chr14:31151857 | C | T | 7 | a0001c0001t0001g0101 a0001c0010t0004g0014 a0001c0010t0004g0015 others(4): Show |
7 | HG02074.hp1 HG03710.hp1 HG03942.hp2 others(4): Show |
intron_variant | MODIFIER | c.1933-1636G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31151857 | |||||||
| chr14:31152159 | T | C | 1 | a0001c0007t0007g0032 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1933-1938A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31152159 | |||||||
| chr14:31152168 | T | C | 111 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0054 others(108): Show |
111 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.1933-1947A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31152168 | |||||||
| chr14:31152410 | G | A | 135 | a0001c0001t0001g0002 a0001c0001t0001g0100 a0001c0001t0001g0101 others(132): Show |
136 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.1933-2189C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31152410 | |||||||
| chr14:31152415 | C | T | 1 | a0001c0002t0001g0106 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1933-2194G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31152415 | |||||||
| chr14:31152427 | C | T | 79 | a0001c0001t0001g0002 a0001c0001t0001g0100 a0001c0001t0001g0101 others(76): Show |
80 | HG00280.hp1 HG00323.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.1933-2206G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31152427 | |||||||
| chr14:31152465 | C | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1933-2244G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31152465 | |||||||
| chr14:31152690 | G | A | 23 | a0001c0004t0001g0065 a0001c0004t0001g0066 a0001c0004t0001g0067 others(20): Show |
23 | HG00099.hp1 HG00323.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.1933-2469C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31152690 | |||||||
| chr14:31152942 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1933-2721G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31152942 | |||||||
| chr14:31153073 | C | CT | 18 | a0001c0001t0001g0174 a0001c0001t0001g0176 a0001c0001t0001g0237 others(15): Show |
18 | HG00639.hp2 HG01192.hp2 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.1933-2853dupA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31153073 | |||||||
| chr14:31153158 | C | T | 1 | a0001c0002t0001g0111 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1933-2937G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31153158 | |||||||
| chr14:31153159 | A | G | 1 | a0001c0002t0001g0111 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1933-2938T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31153159 | |||||||
| chr14:31153164 | G | A | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1933-2943C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31153164 | |||||||
| chr14:31153234 | T | C | 1 | a0001c0004t0001g0088 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1933-3013A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31153234 | |||||||
| chr14:31153249 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1933-3028C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31153249 | |||||||
| chr14:31153314 | T | C | 202 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0054 others(199): Show |
203 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.1933-3093A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31153314 | |||||||
| chr14:31153369 | C | CA | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1933-3149dupT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31153369 | |||||||
| chr14:31153463 | C | A | 1 | a0001c0002t0001g0057 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1933-3242G>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31153463 | |||||||
| chr14:31153475 | C | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1933-3254G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31153475 | |||||||
| chr14:31153500 | T | C | 112 | a0001c0001t0001g0124 a0001c0002t0001g0051 a0001c0002t0001g0053 others(109): Show |
112 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.1933-3279A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31153500 | |||||||
| chr14:31153526 | T | C | 2 | a0001c0002t0013g0339 a0001c0002t0014g0340 |
2 | HG01109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1933-3305A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31153526 | |||||||
| chr14:31153535 | G | A | 131 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0054 others(128): Show |
131 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.1932+3305C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31153535 | |||||||
| chr14:31153867 | T | G | 1 | a0001c0002t0001g0251 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1932+2973A>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31153867 | |||||||
| chr14:31153917 | A | T | 1 | a0001c0007t0001g0036 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1932+2923T>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31153917 | |||||||
| chr14:31154012 | C | T | 49 | a0001c0004t0001g0001 a0001c0004t0001g0026 a0001c0004t0001g0034 others(46): Show |
50 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.1932+2828G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31154012 | |||||||
| chr14:31154324 | G | A | 1 | a0001c0002t0001g0335 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1932+2516C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31154324 | |||||||
| chr14:31154336 | C | T | 2 | a0001c0007t0001g0033 a0001c0007t0001g0039 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.1932+2504G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31154336 | |||||||
| chr14:31154337 | G | A | 8 | a0001c0001t0001g0002 a0001c0001t0001g0152 a0001c0001t0001g0153 others(5): Show |
9 | HG00280.hp1 HG00323.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1932+2503C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31154337 | |||||||
| chr14:31154587 | T | G | 2 | a0001c0002t0006g0023 a0001c0002t0006g0024 |
2 | HG00639.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1932+2253A>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31154587 | |||||||
| chr14:31154612 | C | T | 199 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0054 others(196): Show |
200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.1932+2228G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31154612 | |||||||
| chr14:31154745 | C | T | 3 | a0001c0013t0001g0130 a0001c0013t0001g0165 a0001c0013t0001g0182 |
3 | HG01099.hp1 NA18969.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1932+2095G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31154745 | |||||||
| chr14:31154810 | AT | A | 200 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0054 others(197): Show |
201 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.1932+2029delA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31154810 | |||||||
| chr14:31154917 | C | G | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1932+1923G>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31154917 | |||||||
| chr14:31155344 | CA | C | 199 | a0001c0001t0001g0122 a0001c0001t0001g0148 a0001c0002t0001g0051 others(196): Show |
200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.1932+1495delT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31155344 | |||||||
| chr14:31155568 | C | A | 1 | a0001c0004t0005g0094 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1932+1272G>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31155568 | |||||||
| chr14:31155681 | C | T | 6 | a0001c0002t0001g0051 a0001c0011t0001g0047 a0001c0011t0001g0048 others(3): Show |
6 | HG02630.hp2 HG02809.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1932+1159G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31155681 | |||||||
| chr14:31155702 | A | T | 2 | a0001c0002t0013g0339 a0001c0002t0014g0340 |
2 | HG01109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1932+1138T>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31155702 | |||||||
| chr14:31155870 | A | C | 1 | a0001c0001t0001g0147 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1932+970T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31155870 | |||||||
| chr14:31155935 | T | C | 1 | a0001c0010t0004g0018 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1932+905A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31155935 | |||||||
| chr14:31155968 | C | T | 4 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0239 others(1): Show |
4 | HG02055.hp2 HG02647.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1932+872G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31155968 | |||||||
| chr14:31155970 | G | A | 1 | a0001c0003t0001g0298 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1932+870C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31155970 | |||||||
| chr14:31155985 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1932+855G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31155985 | |||||||
| chr14:31156019 | G | A | 2 | a0001c0001t0001g0121 a0001c0001t0001g0150 |
2 | NA18981.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.1932+821C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31156019 | |||||||
| chr14:31156026 | T | A | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1932+814A>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31156026 | |||||||
| chr14:31156121 | T | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1932+719A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31156121 | |||||||
| chr14:31156135 | T | C | 107 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0054 others(104): Show |
107 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.1932+705A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31156135 | |||||||
| chr14:31156140 | G | C | 1 | a0001c0003t0001g0312 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1932+700C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31156140 | |||||||
| chr14:31156164 | G | A | 11 | a0001c0001t0001g0129 a0001c0001t0001g0154 a0001c0001t0001g0159 others(8): Show |
11 | HG00738.hp1 HG01081.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.1932+676C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31156164 | |||||||
| chr14:31156174 | G | C | 1 | a0001c0001t0001g0190 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1932+666C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31156174 | |||||||
| chr14:31156196 | G | A | 4 | a0001c0002t0001g0106 a0003c0014t0001g0081 a0003c0014t0001g0082 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1932+644C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31156196 | |||||||
| chr14:31156202 | G | A | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1932+638C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31156202 | |||||||
| chr14:31156246 | C | CA | 61 | a0001c0003t0001g0099 a0001c0003t0001g0282 a0001c0003t0001g0288 others(58): Show |
61 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.1932+593dupT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31156246 | |||||||
| chr14:31156308 | G | A | 124 | a0001c0001t0001g0002 a0001c0001t0001g0100 a0001c0001t0001g0101 others(121): Show |
125 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.1932+532C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31156308 | |||||||
| chr14:31156492 | C | T | 1 | a0001c0002t0001g0336 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1932+348G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31156492 | |||||||
| chr14:31156516 | T | TAC | 77 | a0001c0001t0001g0123 a0001c0001t0001g0140 a0001c0001t0001g0216 others(74): Show |
77 | HG00140.hp1 HG00673.hp1 HG00741.hp2 others(74): Show |
intron_variant | MODIFIER | c.1932+322_1932+323d others(4): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31156516 | |||||||
| chr14:31156516 | T | TACAC | 18 | a0001c0001t0001g0237 a0001c0002t0001g0084 a0001c0002t0001g0102 others(15): Show |
18 | HG00423.hp2 HG00544.hp2 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.1932+320_1932+323d others(6): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31156516 | |||||||
| chr14:31156516 | T | TACACAC | 42 | a0001c0002t0001g0106 a0001c0002t0006g0023 a0001c0002t0006g0024 others(39): Show |
42 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.1932+318_1932+323d others(8): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31156516 | |||||||
| chr14:31156516 | T | TACACACA others(1): Show |
28 | a0001c0002t0001g0051 a0001c0002t0001g0109 a0001c0002t0001g0112 others(25): Show |
29 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.1932+316_1932+323d others(10): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31156516 | |||||||
| chr14:31156516 | T | TACACACA others(3): Show |
17 | a0001c0002t0001g0250 a0001c0002t0001g0253 a0001c0002t0001g0254 others(14): Show |
17 | HG00609.hp2 HG01928.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1932+314_1932+323d others(12): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31156516 | |||||||
| chr14:31156516 | T | TACACACA others(5): Show |
6 | a0001c0002t0001g0111 a0001c0002t0006g0022 a0001c0004t0001g0115 others(3): Show |
6 | HG02155.hp2 HG02257.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1932+312_1932+323d others(14): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31156516 | |||||||
| chr14:31156516 | T | TACACACA others(3): Show |
1 | a0001c0010t0004g0018 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1932+323_1932+324i others(12): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31156516 | |||||||
| chr14:31156516 | TAC | T | 4 | a0001c0002t0001g0061 a0001c0002t0001g0062 a0001c0002t0001g0063 others(1): Show |
4 | HG02080.hp2 HG02083.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1932+322_1932+323d others(4): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31156516 | |||||||
| chr14:31156516 | TACAC | T | 4 | a0001c0001t0001g0116 a0001c0001t0001g0168 a0001c0001t0001g0185 others(1): Show |
4 | HG00323.hp2 HG00639.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.1932+320_1932+323d others(6): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31156516 | |||||||
| chr14:31156516 | TACACACA others(5): Show |
T | 1 | a0001c0037t0001g0261 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1932+312_1932+323d others(14): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31156516 | |||||||
| chr14:31156520 | C | CACAT | 5 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(2): Show |
5 | HG02074.hp1 NA18971.hp1 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.1932+319_1932+320i others(6): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31156520 | |||||||
| chr14:31156546 | CACAA | C | 13 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(10): Show |
13 | HG01884.hp2 HG02572.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1932+290_1932+293d others(6): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31156546 | |||||||
| chr14:31156548 | CAA | C | 7 | a0001c0002t0001g0335 a0001c0002t0001g0336 a0001c0002t0001g0337 others(4): Show |
7 | HG01109.hp1 HG01346.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1932+290_1932+291d others(4): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31156548 | |||||||
| chr14:31156549 | A | ACACACAC others(4): Show |
1 | a0003c0014t0001g0081 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1932+290_1932+291i others(13): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31156549 | |||||||
| chr14:31156550 | A | C | 11 | a0001c0001t0001g0002 a0001c0003t0001g0282 a0001c0004t0001g0073 others(8): Show |
11 | HG00558.hp1 HG00609.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1932+290T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31156550 | |||||||
| chr14:31156595 | A | G | 2 | a0001c0002t0013g0339 a0001c0002t0014g0340 |
2 | HG01109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1932+245T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31156595 | |||||||
| chr14:31156724 | CAG | C | 8 | a0001c0001t0001g0141 a0001c0001t0001g0146 a0001c0001t0001g0147 others(5): Show |
8 | HG00733.hp2 HG02055.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1932+114_1932+115d others(4): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31156724 | |||||||
| chr14:31156788 | C | CA | 19 | a0001c0001t0001g0123 a0001c0001t0001g0140 a0001c0001t0001g0237 others(16): Show |
19 | HG00423.hp2 HG00558.hp1 HG00609.hp2 others(16): Show |
intron_variant | MODIFIER | c.1932+51dupT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31156788 | |||||||
| chr14:31156788 | CA | C | 61 | a0001c0004t0001g0001 a0001c0004t0001g0026 a0001c0004t0001g0034 others(58): Show |
62 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.1932+51delT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31156788 | |||||||
| chr14:31156821 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1932+19A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31156821 | |||||||
| chr14:31157379 | T | C | 8 | a0001c0009t0003g0003 a0001c0009t0003g0004 a0001c0009t0003g0005 others(5): Show |
8 | HG00558.hp1 HG00609.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.1623-76A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31157379 | |||||||
| chr14:31157447 | T | A | 1 | a0001c0013t0001g0165 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1623-144A>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31157447 | |||||||
| chr14:31157572 | C | G | 3 | a0001c0003t0001g0303 a0001c0003t0001g0315 a0001c0003t0001g0330 |
3 | NA18953.hp2 NA18987.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1623-269G>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31157572 | |||||||
| chr14:31157607 | T | A | 1 | a0001c0004t0001g0044 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1623-304A>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31157607 | |||||||
| chr14:31157617 | C | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1623-314G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31157617 | |||||||
| chr14:31157788 | C | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1623-485G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31157788 | |||||||
| chr14:31157842 | C | A | 8 | a0001c0009t0003g0003 a0001c0009t0003g0004 a0001c0009t0003g0005 others(5): Show |
8 | HG00558.hp1 HG00609.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.1623-539G>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31157842 | |||||||
| chr14:31157843 | G | A | 3 | a0001c0003t0001g0304 a0001c0017t0009g0020 a0001c0017t0009g0021 |
3 | HG02280.hp2 HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1623-540C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31157843 | |||||||
| chr14:31157898 | G | A | 2 | a0001c0002t0001g0071 a0001c0002t0001g0072 |
2 | HG02129.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.1623-595C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31157898 | |||||||
| chr14:31157989 | C | T | 3 | a0001c0002t0001g0335 a0001c0002t0001g0336 a0001c0002t0001g0337 |
3 | HG02109.hp1 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1623-686G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31157989 | |||||||
| chr14:31158098 | A | G | 4 | a0001c0002t0001g0106 a0003c0014t0001g0081 a0003c0014t0001g0082 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1623-795T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31158098 | |||||||
| chr14:31158248 | A | AT | 101 | a0001c0001t0001g0132 a0001c0001t0001g0187 a0001c0001t0001g0191 others(98): Show |
101 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.1623-946dupA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31158248 | |||||||
| chr14:31158248 | A | ATT | 21 | a0001c0002t0001g0051 a0001c0002t0001g0111 a0001c0002t0001g0255 others(18): Show |
21 | HG01175.hp2 HG01192.hp2 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.1623-947_1623-946d others(4): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31158248 | |||||||
| chr14:31158284 | C | G | 1 | a0001c0004t0001g0065 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1623-981G>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31158284 | |||||||
| chr14:31158299 | C | T | 6 | a0001c0002t0001g0109 a0001c0002t0001g0111 a0001c0002t0001g0112 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1623-996G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31158299 | |||||||
| chr14:31158349 | G | A | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1623-1046C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31158349 | |||||||
| chr14:31158540 | G | A | 1 | a0001c0004t0001g0115 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1623-1237C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31158540 | |||||||
| chr14:31158624 | C | T | 1 | a0001c0002t0001g0106 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1623-1321G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31158624 | |||||||
| chr14:31158675 | G | A | 1 | a0001c0013t0001g0165 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1623-1372C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31158675 | |||||||
| chr14:31158970 | G | T | 1 | a0001c0008t0001g0287 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1623-1667C>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31158970 | |||||||
| chr14:31159075 | G | GTGA | 8 | a0001c0009t0003g0003 a0001c0009t0003g0004 a0001c0009t0003g0005 others(5): Show |
8 | HG00558.hp1 HG00609.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.1623-1775_1623-177 others(7): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31159075 | |||||||
| chr14:31159403 | G | T | 6 | a0001c0002t0001g0051 a0001c0011t0001g0047 a0001c0011t0001g0048 others(3): Show |
6 | HG02630.hp2 HG02809.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1623-2100C>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31159403 | |||||||
| chr14:31159529 | G | A | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1623-2226C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31159529 | |||||||
| chr14:31159603 | C | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1623-2300G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31159603 | |||||||
| chr14:31159604 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1623-2301C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31159604 | |||||||
| chr14:31159628 | C | T | 3 | a0001c0002t0001g0335 a0001c0002t0001g0336 a0001c0002t0001g0337 |
3 | HG02109.hp1 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1623-2325G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31159628 | |||||||
| chr14:31159642 | A | AT | 10 | a0001c0001t0001g0174 a0001c0001t0001g0239 a0001c0004t0008g0013 others(7): Show |
10 | HG02055.hp2 HG02074.hp1 HG03942.hp2 others(7): Show |
intron_variant | MODIFIER | c.1623-2340dupA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31159642 | |||||||
| chr14:31159642 | AT | A | 7 | a0001c0002t0001g0109 a0001c0002t0001g0111 a0001c0002t0001g0112 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1623-2340delA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31159642 | |||||||
| chr14:31159767 | A | G | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1623-2464T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31159767 | |||||||
| chr14:31159774 | G | A | 4 | a0001c0004t0005g0093 a0001c0004t0005g0096 a0002c0005t0001g0269 others(1): Show |
4 | HG01106.hp1 HG03579.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.1623-2471C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31159774 | |||||||
| chr14:31159794 | C | T | 6 | a0001c0002t0001g0109 a0001c0002t0001g0111 a0001c0002t0001g0112 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1623-2491G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31159794 | |||||||
| chr14:31159892 | G | A | 30 | a0001c0002t0001g0053 a0001c0002t0001g0054 a0001c0002t0001g0057 others(27): Show |
30 | HG00099.hp1 HG00621.hp2 HG02074.hp2 others(27): Show |
intron_variant | MODIFIER | c.1623-2589C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31159892 | |||||||
| chr14:31159900 | G | A | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1623-2597C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31159900 | |||||||
| chr14:31160066 | T | C | 6 | a0001c0002t0001g0051 a0001c0011t0001g0047 a0001c0011t0001g0048 others(3): Show |
6 | HG02630.hp2 HG02809.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1623-2763A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31160066 | |||||||
| chr14:31160067 | A | C | 1 | a0001c0002t0001g0106 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1623-2764T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31160067 | |||||||
| chr14:31160078 | G | A | 198 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0054 others(195): Show |
199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.1623-2775C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31160078 | |||||||
| chr14:31160185 | C | A | 28 | a0001c0002t0001g0053 a0001c0002t0001g0054 a0001c0002t0001g0057 others(25): Show |
28 | HG00621.hp2 HG02074.hp2 HG02080.hp2 others(25): Show |
intron_variant | MODIFIER | c.1623-2882G>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31160185 | |||||||
| chr14:31160249 | A | C | 8 | a0001c0009t0003g0003 a0001c0009t0003g0004 a0001c0009t0003g0005 others(5): Show |
8 | HG00558.hp1 HG00609.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.1623-2946T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31160249 | |||||||
| chr14:31160337 | T | G | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1623-3034A>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31160337 | |||||||
| chr14:31160513 | GGTT | G | 3 | a0001c0002t0006g0022 a0001c0002t0006g0023 a0001c0002t0006g0024 |
3 | HG00639.hp2 HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1623-3213_1623-321 others(7): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31160513 | |||||||
| chr14:31160579 | A | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1623-3276T>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31160579 | |||||||
| chr14:31160677 | C | CTTT | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1623-3377_1623-337 others(7): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31160677 | |||||||
| chr14:31160752 | C | T | 3 | a0001c0001t0001g0126 a0001c0001t0001g0145 a0004c0015t0001g0144 |
3 | HG00099.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1623-3449G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31160752 | |||||||
| chr14:31160801 | G | C | 1 | a0001c0001t0001g0116 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1623-3498C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31160801 | |||||||
| chr14:31161158 | T | A | 4 | a0001c0002t0010g0107 a0001c0002t0010g0108 a0001c0017t0009g0020 others(1): Show |
4 | HG01993.hp2 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1623-3855A>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31161158 | |||||||
| chr14:31161265 | C | G | 17 | a0001c0002t0001g0053 a0001c0002t0001g0054 a0001c0002t0001g0057 others(14): Show |
17 | HG00621.hp2 HG02080.hp2 NA18943.hp1 others(14): Show |
intron_variant | MODIFIER | c.1623-3962G>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31161265 | |||||||
| chr14:31161385 | CT | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1623-4083delA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31161385 | |||||||
| chr14:31161391 | C | T | 2 | a0001c0002t0001g0085 a0001c0002t0001g0086 |
2 | HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1623-4088G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31161391 | |||||||
| chr14:31161565 | C | T | 84 | a0001c0002t0001g0053 a0001c0002t0001g0054 a0001c0002t0001g0057 others(81): Show |
84 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.1623-4262G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31161565 | |||||||
| chr14:31161570 | CAAAAAAA others(5): Show |
C | 105 | a0001c0002t0001g0053 a0001c0002t0001g0054 a0001c0002t0001g0057 others(102): Show |
105 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.1623-4279_1623-426 others(16): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31161570 | |||||||
| chr14:31161579 | AG | A | 11 | a0001c0004t0001g0088 a0001c0004t0001g0089 a0001c0004t0001g0098 others(8): Show |
11 | HG01106.hp1 HG02257.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1623-4277delC | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31161579 | |||||||
| chr14:31161580 | G | GA | 11 | a0001c0001t0001g0129 a0001c0001t0001g0154 a0001c0001t0001g0159 others(8): Show |
11 | HG00738.hp1 HG01081.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.1623-4278dupT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31161580 | |||||||
| chr14:31161597 | AAAAG | A | 8 | a0001c0009t0003g0003 a0001c0009t0003g0004 a0001c0009t0003g0005 others(5): Show |
8 | HG00558.hp1 HG00609.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.1623-4298_1623-429 others(8): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31161597 | |||||||
| chr14:31161602 | A | G | 2 | a0001c0002t0006g0023 a0001c0002t0006g0024 |
2 | HG00639.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1623-4299T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31161602 | |||||||
| chr14:31161649 | G | A | 1 | a0001c0002t0001g0051 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1623-4346C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31161649 | |||||||
| chr14:31161702 | G | A | 8 | a0001c0009t0003g0003 a0001c0009t0003g0004 a0001c0009t0003g0005 others(5): Show |
8 | HG00558.hp1 HG00609.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.1623-4399C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31161702 | |||||||
| chr14:31161712 | G | A | 102 | a0001c0002t0001g0053 a0001c0002t0001g0054 a0001c0002t0001g0057 others(99): Show |
102 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.1623-4409C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31161712 | |||||||
| chr14:31161718 | G | T | 9 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(6): Show |
9 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1623-4415C>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31161718 | |||||||
| chr14:31161836 | A | G | 2 | a0001c0001t0001g0154 a0001c0001t0001g0164 |
2 | HG01261.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1623-4533T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31161836 | |||||||
| chr14:31161854 | G | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1623-4551C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31161854 | |||||||
| chr14:31161870 | CA | C | 188 | a0001c0002t0001g0053 a0001c0002t0001g0054 a0001c0002t0001g0057 others(185): Show |
189 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1623-4568delT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31161870 | |||||||
| chr14:31161994 | C | G | 1 | a0001c0001t0001g0177 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1623-4691G>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31161994 | |||||||
| chr14:31162229 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1623-4926A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31162229 | |||||||
| chr14:31162305 | T | G | 14 | a0001c0002t0001g0335 a0001c0004t0001g0088 a0001c0004t0001g0089 others(11): Show |
14 | HG01106.hp1 HG02257.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1623-5002A>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31162305 | |||||||
| chr14:31162411 | A | AC | 5 | a0001c0001t0001g0142 a0001c0002t0001g0085 a0001c0002t0001g0086 others(2): Show |
5 | HG02723.hp2 HG02809.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.1623-5109dupG | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31162411 | |||||||
| chr14:31162531 | CAT | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1623-5230_1623-522 others(6): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31162531 | |||||||
| chr14:31162565 | A | G | 1 | a0001c0004t0001g0115 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1623-5262T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31162565 | |||||||
| chr14:31163060 | G | GAC | 69 | a0001c0001t0001g0002 a0001c0001t0001g0162 a0001c0001t0001g0220 others(66): Show |
70 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1622+5236_1622+523 others(6): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31163060 | |||||||
| chr14:31163079 | G | A | 8 | a0001c0009t0003g0004 a0001c0009t0003g0010 a0001c0010t0004g0014 others(5): Show |
8 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(5): Show |
intron_variant | MODIFIER | c.1622+5219C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31163079 | |||||||
| chr14:31163087 | A | ACACACAC others(1): Show |
328 | a0001c0001t0001g0002 a0001c0001t0001g0100 a0001c0001t0001g0101 others(325): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.1622+5203_1622+521 others(12): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31163087 | |||||||
| chr14:31163087 | A | ACG | 5 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(2): Show |
5 | HG02074.hp1 NA18971.hp1 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.1622+5210_1622+521 others(6): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31163087 | |||||||
| chr14:31163087 | A | G | 2 | a0001c0009t0003g0004 a0001c0009t0003g0010 |
2 | NA18982.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1622+5211T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31163087 | |||||||
| chr14:31163101 | A | ACGCACAC others(3): Show |
1 | a0002c0005t0001g0267 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1622+5196_1622+519 others(14): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31163101 | |||||||
| chr14:31163102 | T | C | 1 | a0002c0005t0001g0267 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1622+5196A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31163102 | |||||||
| chr14:31163119 | G | A | 1 | a0001c0008t0001g0307 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1622+5179C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31163119 | |||||||
| chr14:31163143 | C | T | 1 | a0001c0007t0001g0041 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1622+5155G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31163143 | |||||||
| chr14:31163161 | G | A | 8 | a0001c0009t0003g0003 a0001c0009t0003g0004 a0001c0009t0003g0005 others(5): Show |
8 | HG00558.hp1 HG00609.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.1622+5137C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31163161 | |||||||
| chr14:31163195 | G | A | 2 | a0001c0002t0013g0339 a0001c0002t0014g0340 |
2 | HG01109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1622+5103C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31163195 | |||||||
| chr14:31163259 | CA | C | 164 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0054 others(161): Show |
165 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.1622+5038delT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31163259 | |||||||
| chr14:31163259 | CAA | C | 14 | a0001c0009t0003g0003 a0001c0009t0003g0004 a0001c0009t0003g0005 others(11): Show |
14 | HG00558.hp1 HG00609.hp2 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1622+5037_1622+503 others(6): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31163259 | |||||||
| chr14:31163442 | T | TC | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1622+4855dupG | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31163442 | |||||||
| chr14:31163481 | T | G | 3 | a0001c0007t0001g0030 a0001c0007t0001g0036 a0001c0036t0001g0043 |
3 | HG00741.hp2 HG01074.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1622+4817A>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31163481 | |||||||
| chr14:31163527 | C | T | 3 | a0001c0003t0001g0303 a0001c0003t0001g0315 a0001c0003t0001g0330 |
3 | NA18953.hp2 NA18987.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1622+4771G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31163527 | |||||||
| chr14:31163823 | T | C | 17 | a0002c0005t0001g0046 a0002c0005t0001g0260 a0002c0005t0001g0262 others(14): Show |
17 | HG00140.hp2 HG00280.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.1622+4475A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31163823 | |||||||
| chr14:31163880 | T | C | 1 | a0001c0022t0001g0284 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1622+4418A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31163880 | |||||||
| chr14:31163912 | CA | C | 57 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0054 others(54): Show |
57 | HG00621.hp2 HG01069.hp2 HG01071.hp2 others(54): Show |
intron_variant | MODIFIER | c.1622+4385delT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31163912 | |||||||
| chr14:31163920 | A | C | 1 | a0001c0013t0001g0182 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1622+4378T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31163920 | |||||||
| chr14:31164069 | A | T | 3 | a0001c0002t0001g0335 a0001c0002t0001g0336 a0001c0002t0001g0337 |
3 | HG02109.hp1 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1622+4229T>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31164069 | |||||||
| chr14:31164107 | G | A | 61 | a0001c0002t0001g0335 a0001c0002t0001g0336 a0001c0002t0001g0337 others(58): Show |
61 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.1622+4191C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31164107 | |||||||
| chr14:31164299 | A | G | 1 | a0001c0001t0001g0100 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1622+3999T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31164299 | |||||||
| chr14:31164399 | T | C | 1 | a0001c0002t0001g0109 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1622+3899A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31164399 | |||||||
| chr14:31164591 | G | A | 1 | a0001c0002t0006g0024 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1622+3707C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31164591 | |||||||
| chr14:31164602 | A | G | 7 | a0001c0004t0001g0088 a0001c0004t0001g0089 a0001c0004t0001g0097 others(4): Show |
7 | HG02257.hp2 HG02683.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.1622+3696T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31164602 | |||||||
| chr14:31164830 | G | A | 61 | a0001c0002t0001g0335 a0001c0002t0001g0336 a0001c0002t0001g0337 others(58): Show |
61 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.1622+3468C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31164830 | |||||||
| chr14:31164850 | A | G | 1 | a0001c0011t0001g0048 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1622+3448T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31164850 | |||||||
| chr14:31164883 | A | C | 72 | a0001c0002t0001g0335 a0001c0002t0001g0336 a0001c0002t0001g0337 others(69): Show |
72 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.1622+3415T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31164883 | |||||||
| chr14:31164999 | TA | T | 69 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0002t0001g0086 others(66): Show |
69 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.1622+3298delT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31164999 | |||||||
| chr14:31165167 | T | C | 3 | a0001c0006t0002g0207 a0001c0006t0002g0231 a0001c0006t0002g0232 |
3 | NA18947.hp2 NA18994.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.1622+3131A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31165167 | |||||||
| chr14:31165264 | A | C | 1 | a0001c0013t0001g0130 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1622+3034T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31165264 | |||||||
| chr14:31165310 | A | T | 1 | a0001c0002t0006g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1622+2988T>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31165310 | |||||||
| chr14:31165335 | C | T | 1 | a0001c0002t0001g0337 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1622+2963G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31165335 | |||||||
| chr14:31165395 | T | A | 8 | a0001c0001t0001g0002 a0001c0001t0001g0152 a0001c0001t0001g0153 others(5): Show |
9 | HG00280.hp1 HG00323.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1622+2903A>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31165395 | |||||||
| chr14:31165519 | G | A | 56 | a0001c0003t0001g0099 a0001c0003t0001g0282 a0001c0003t0001g0285 others(53): Show |
56 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.1622+2779C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31165519 | |||||||
| chr14:31165723 | A | C | 1 | a0001c0006t0002g0125 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1622+2575T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31165723 | |||||||
| chr14:31165745 | T | C | 3 | a0003c0014t0001g0081 a0003c0014t0001g0082 a0003c0014t0001g0083 |
3 | HG02145.hp1 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1622+2553A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31165745 | |||||||
| chr14:31165832 | C | T | 1 | a0001c0010t0004g0018 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1622+2466G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31165832 | |||||||
| chr14:31165853 | C | CT | 60 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0054 others(57): Show |
60 | HG00621.hp2 HG01069.hp2 HG01071.hp2 others(57): Show |
intron_variant | MODIFIER | c.1622+2444dupA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31165853 | |||||||
| chr14:31165890 | G | A | 1 | a0001c0002t0001g0106 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1622+2408C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31165890 | |||||||
| chr14:31165903 | T | C | 2 | a0001c0001t0001g0199 a0001c0001t0001g0228 |
2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1622+2395A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31165903 | |||||||
| chr14:31165906 | C | T | 2 | a0001c0017t0009g0020 a0001c0017t0009g0021 |
2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1622+2392G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31165906 | |||||||
| chr14:31165975 | A | G | 7 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0134 others(4): Show |
7 | HG02015.hp2 HG03927.hp1 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.1622+2323T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31165975 | |||||||
| chr14:31166004 | C | T | 3 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 |
3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1622+2294G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31166004 | |||||||
| chr14:31166011 | A | G | 69 | a0001c0002t0001g0335 a0001c0002t0001g0336 a0001c0002t0001g0337 others(66): Show |
69 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.1622+2287T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31166011 | |||||||
| chr14:31166021 | T | C | 1 | a0001c0004t0001g0115 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1622+2277A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31166021 | |||||||
| chr14:31166032 | G | A | 1 | a0001c0002t0001g0051 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1622+2266C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31166032 | |||||||
| chr14:31166043 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1622+2255C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31166043 | |||||||
| chr14:31166048 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1622+2250C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31166048 | |||||||
| chr14:31166136 | G | T | 59 | a0001c0002t0001g0109 a0001c0002t0001g0111 a0001c0002t0001g0112 others(56): Show |
60 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.1622+2162C>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31166136 | |||||||
| chr14:31166528 | C | A | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1622+1770G>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31166528 | |||||||
| chr14:31166540 | A | G | 5 | a0001c0004t0001g0088 a0001c0004t0001g0097 a0001c0004t0001g0098 others(2): Show |
5 | HG02683.hp1 HG03704.hp1 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.1622+1758T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31166540 | |||||||
| chr14:31166593 | G | A | 8 | a0001c0009t0003g0003 a0001c0009t0003g0004 a0001c0009t0003g0005 others(5): Show |
8 | HG00558.hp1 HG00609.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.1622+1705C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31166593 | |||||||
| chr14:31166633 | T | A | 1 | a0005c0016t0001g0133 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1622+1665A>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31166633 | |||||||
| chr14:31166865 | A | T | 2 | a0001c0001t0001g0186 a0001c0007t0007g0032 |
2 | HG00621.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.1622+1433T>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31166865 | |||||||
| chr14:31166896 | C | CA | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1622+1401dupT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31166896 | |||||||
| chr14:31166964 | A | G | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1622+1334T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31166964 | |||||||
| chr14:31167045 | C | T | 2 | a0001c0002t0013g0339 a0001c0002t0014g0340 |
2 | HG01109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1622+1253G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31167045 | |||||||
| chr14:31167149 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1622+1149C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31167149 | |||||||
| chr14:31167151 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1622+1147C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31167151 | |||||||
| chr14:31167282 | G | A | 56 | a0001c0003t0001g0099 a0001c0003t0001g0282 a0001c0003t0001g0285 others(53): Show |
56 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.1622+1016C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31167282 | |||||||
| chr14:31167334 | T | C | 1 | a0001c0002t0006g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1622+964A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31167334 | |||||||
| chr14:31167349 | G | A | 1 | a0003c0014t0001g0082 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1622+949C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31167349 | |||||||
| chr14:31167538 | G | C | 1 | a0001c0003t0001g0305 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1622+760C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31167538 | |||||||
| chr14:31167557 | C | T | 202 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0054 others(199): Show |
203 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.1622+741G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31167557 | |||||||
| chr14:31167611 | A | T | 1 | a0001c0001t0001g0158 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1622+687T>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31167611 | |||||||
| chr14:31167665 | C | G | 1 | a0001c0001t0001g0158 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1622+633G>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31167665 | |||||||
| chr14:31167793 | C | A | 2 | a0001c0004t0001g0001 a0001c0004t0001g0034 |
3 | HG02559.hp1 HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1622+505G>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31167793 | |||||||
| chr14:31167801 | T | C | 7 | a0001c0001t0001g0138 a0001c0001t0001g0142 a0001c0001t0001g0143 others(4): Show |
7 | HG00609.hp1 NA18966.hp2 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.1622+497A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31167801 | |||||||
| chr14:31167896 | C | CT | 5 | a0001c0002t0001g0111 a0001c0002t0001g0112 a0001c0002t0001g0113 others(2): Show |
5 | HG01891.hp1 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1622+401dupA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31167896 | |||||||
| chr14:31167929 | G | A | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1622+369C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31167929 | |||||||
| chr14:31167955 | A | T | 1 | a0001c0002t0001g0085 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1622+343T>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31167955 | |||||||
| chr14:31168029 | A | G | 1 | a0001c0002t0001g0336 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1622+269T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31168029 | |||||||
| chr14:31168174 | A | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1622+124T>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31168174 | |||||||
| chr14:31168206 | A | C | 4 | a0001c0002t0010g0107 a0001c0002t0010g0108 a0001c0017t0009g0020 others(1): Show |
4 | HG01993.hp2 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1622+92T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31168206 | |||||||
| chr14:31168285 | T | C | 3 | a0001c0002t0006g0022 a0001c0002t0006g0023 a0001c0002t0006g0024 |
3 | HG00639.hp2 HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1622+13A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31168285 | |||||||
| chr14:31168609 | A | G | 64 | a0001c0001t0001g0138 a0001c0001t0001g0142 a0001c0001t0001g0143 others(61): Show |
64 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.1448-137T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 9/42 | chr14 | 31168609 | |||||||
| chr14:31168652 | T | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1448-180A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 9/42 | chr14 | 31168652 | |||||||
| chr14:31168696 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1448-224C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 9/42 | chr14 | 31168696 | |||||||
| chr14:31168754 | T | C | 2 | a0001c0006t0002g0125 a0001c0006t0002g0192 |
2 | NA19009.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.1448-282A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 9/42 | chr14 | 31168754 | |||||||
| chr14:31168795 | C | A | 1 | a0002c0005t0001g0265 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1448-323G>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 9/42 | chr14 | 31168795 | |||||||
| chr14:31168808 | C | T | 1 | a0001c0033t0001g0319 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1448-336G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 9/42 | chr14 | 31168808 | |||||||
| chr14:31168812 | A | G | 1 | a0001c0003t0001g0315 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1448-340T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 9/42 | chr14 | 31168812 | |||||||
| chr14:31168834 | A | C | 1 | a0001c0010t0004g0018 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1448-362T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 9/42 | chr14 | 31168834 | |||||||
| chr14:31168966 | C | A | 1 | a0001c0004t0001g0038 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1447+388G>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 9/42 | chr14 | 31168966 | |||||||
| chr14:31168969 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1447+385C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 9/42 | chr14 | 31168969 | |||||||
| chr14:31169043 | CA | C | 6 | a0001c0001t0001g0183 a0001c0001t0001g0213 a0001c0001t0001g0225 others(3): Show |
6 | HG01081.hp1 HG02273.hp2 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.1447+310delT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 9/42 | chr14 | 31169043 | |||||||
| chr14:31169058 | A | T | 143 | a0001c0001t0001g0002 a0001c0001t0001g0100 a0001c0001t0001g0101 others(140): Show |
144 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.1447+296T>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 9/42 | chr14 | 31169058 | |||||||
| chr14:31169200 | A | T | 1 | a0001c0002t0001g0069 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1447+154T>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 9/42 | chr14 | 31169200 | |||||||
| chr14:31169578 | C | T | 1 | a0007c0028t0001g0070 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1333-110G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 8/42 | chr14 | 31169578 | |||||||
| chr14:31169835 | G | A | 4 | a0001c0001t0001g0148 a0001c0001t0001g0190 a0001c0001t0001g0196 others(1): Show |
4 | HG01106.hp2 HG01256.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1333-367C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 8/42 | chr14 | 31169835 | |||||||
| chr14:31169896 | C | T | 3 | a0003c0014t0001g0081 a0003c0014t0001g0082 a0003c0014t0001g0083 |
3 | HG02145.hp1 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1333-428G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 8/42 | chr14 | 31169896 | |||||||
| chr14:31169904 | C | T | 2 | a0002c0005t0001g0263 a0002c0005t0001g0264 |
2 | HG02602.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1333-436G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 8/42 | chr14 | 31169904 | |||||||
| chr14:31169905 | C | T | 40 | a0001c0004t0001g0001 a0001c0004t0001g0026 a0001c0004t0001g0034 others(37): Show |
41 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.1333-437G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 8/42 | chr14 | 31169905 | |||||||
| chr14:31169909 | C | G | 4 | a0001c0003t0001g0099 a0001c0003t0001g0291 a0001c0003t0001g0317 others(1): Show |
4 | HG01081.hp2 HG01243.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1333-441G>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 8/42 | chr14 | 31169909 | |||||||
| chr14:31169940 | C | G | 1 | a0001c0001t0001g0116 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1333-472G>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 8/42 | chr14 | 31169940 | |||||||
| chr14:31169999 | C | T | 5 | a0001c0002t0001g0051 a0001c0011t0001g0047 a0001c0011t0001g0048 others(2): Show |
5 | HG02630.hp2 HG02809.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1333-531G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 8/42 | chr14 | 31169999 | |||||||
| chr14:31170012 | C | T | 2 | a0001c0017t0009g0020 a0001c0017t0009g0021 |
2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1333-544G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 8/42 | chr14 | 31170012 | |||||||
| chr14:31170133 | C | G | 1 | a0001c0003t0001g0290 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1333-665G>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 8/42 | chr14 | 31170133 | |||||||
| chr14:31170183 | G | A | 13 | a0001c0004t0001g0088 a0001c0004t0001g0089 a0001c0004t0001g0097 others(10): Show |
13 | HG01106.hp1 HG02257.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1333-715C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 8/42 | chr14 | 31170183 | |||||||
| chr14:31170312 | T | C | 2 | a0001c0002t0010g0107 a0001c0002t0010g0108 |
2 | HG01993.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1333-844A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 8/42 | chr14 | 31170312 | |||||||
| chr14:31170408 | G | A | 1 | a0001c0003t0001g0298 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1333-940C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 8/42 | chr14 | 31170408 | |||||||
| chr14:31170627 | T | C | 7 | a0001c0001t0001g0170 a0001c0001t0001g0197 a0001c0001t0001g0198 others(4): Show |
7 | HG00280.hp2 HG00741.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.1333-1159A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 8/42 | chr14 | 31170627 | |||||||
| chr14:31170667 | G | C | 13 | a0001c0004t0001g0088 a0001c0004t0001g0089 a0001c0004t0001g0097 others(10): Show |
13 | HG01106.hp1 HG02257.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1332+1194C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 8/42 | chr14 | 31170667 | |||||||
| chr14:31170704 | C | T | 62 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0054 others(59): Show |
62 | HG00621.hp2 HG00639.hp2 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.1332+1157G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 8/42 | chr14 | 31170704 | |||||||
| chr14:31170705 | G | A | 3 | a0001c0003t0001g0298 a0001c0003t0001g0305 a0001c0003t0001g0314 |
3 | HG01346.hp2 HG02602.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1332+1156C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 8/42 | chr14 | 31170705 | |||||||
| chr14:31171657 | A | G | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1332+204T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 8/42 | chr14 | 31171657 | |||||||
| chr14:31171736 | CACTT | C | 12 | a0001c0002t0001g0250 a0001c0002t0001g0253 a0001c0002t0001g0254 others(9): Show |
12 | HG01993.hp2 HG02055.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1332+121_1332+124d others(6): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 8/42 | chr14 | 31171736 | |||||||
| chr14:31172269 | A | G | 1 | a0001c0006t0002g0189 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1157-147T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 6/42 | chr14 | 31172269 | |||||||
| chr14:31172346 | G | A | 1 | a0001c0002t0001g0335 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1157-224C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 6/42 | chr14 | 31172346 | |||||||
| chr14:31172381 | A | T | 1 | a0007c0028t0001g0070 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1157-259T>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 6/42 | chr14 | 31172381 | |||||||
| chr14:31172400 | A | C | 1 | a0001c0017t0009g0021 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1157-278T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 6/42 | chr14 | 31172400 | |||||||
| chr14:31172453 | G | A | 20 | a0001c0004t0001g0001 a0001c0004t0001g0026 a0001c0004t0001g0034 others(17): Show |
21 | HG00099.hp1 HG00323.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.1157-331C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 6/42 | chr14 | 31172453 | |||||||
| chr14:31172583 | G | A | 78 | a0001c0001t0001g0002 a0001c0001t0001g0100 a0001c0001t0001g0101 others(75): Show |
79 | HG00280.hp1 HG00323.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.1157-461C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 6/42 | chr14 | 31172583 | |||||||
| chr14:31172675 | T | C | 37 | a0001c0002t0001g0053 a0001c0002t0001g0054 a0001c0002t0001g0057 others(34): Show |
37 | HG00621.hp2 HG01069.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.1156+481A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 6/42 | chr14 | 31172675 | |||||||
| chr14:31172965 | C | T | 61 | a0001c0002t0001g0335 a0001c0002t0001g0336 a0001c0002t0001g0337 others(58): Show |
61 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.1156+191G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 6/42 | chr14 | 31172965 | |||||||
| chr14:31173809 | A | G | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.604-3T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 4/42 | chr14 | 31173809 | |||||||
| chr14:31174147 | T | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.604-341A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 4/42 | chr14 | 31174147 | |||||||
| chr14:31174176 | C | T | 1 | a0001c0002t0001g0106 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.604-370G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 4/42 | chr14 | 31174176 | |||||||
| chr14:31174563 | A | G | 4 | a0001c0006t0002g0209 a0001c0006t0002g0210 a0001c0006t0002g0224 others(1): Show |
4 | HG01074.hp2 HG01952.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.603+348T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 4/42 | chr14 | 31174563 | |||||||
| chr14:31174795 | T | C | 1 | a0001c0004t0001g0065 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.603+116A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 4/42 | chr14 | 31174795 | |||||||
| chr14:31174873 | T | G | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.603+38A>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 4/42 | chr14 | 31174873 | |||||||
| chr14:31175465 | T | C | 1 | a0001c0001t0001g0240 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.376-327A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/42 | chr14 | 31175465 | |||||||
| chr14:31175501 | G | C | 1 | a0001c0003t0001g0315 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.376-363C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/42 | chr14 | 31175501 | |||||||
| chr14:31175552 | T | G | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.376-414A>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/42 | chr14 | 31175552 | |||||||
| chr14:31175662 | A | G | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.376-524T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/42 | chr14 | 31175662 | |||||||
| chr14:31175677 | A | G | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.376-539T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/42 | chr14 | 31175677 | |||||||
| chr14:31175720 | C | T | 12 | a0001c0006t0001g0149 a0001c0006t0002g0125 a0001c0006t0002g0163 others(9): Show |
12 | HG01074.hp2 HG01952.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.376-582G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/42 | chr14 | 31175720 | |||||||
| chr14:31175812 | C | T | 1 | a0001c0017t0009g0020 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.376-674G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/42 | chr14 | 31175812 | |||||||
| chr14:31175874 | A | T | 330 | a0001c0001t0001g0002 a0001c0001t0001g0100 a0001c0001t0001g0101 others(327): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.376-736T>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/42 | chr14 | 31175874 | |||||||
| chr14:31175896 | T | A | 1 | a0001c0017t0009g0021 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.376-758A>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/42 | chr14 | 31175896 | |||||||
| chr14:31176120 | G | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.376-982C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/42 | chr14 | 31176120 | |||||||
| chr14:31176274 | G | T | 2 | a0001c0017t0009g0020 a0001c0017t0009g0021 |
2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.376-1136C>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/42 | chr14 | 31176274 | |||||||
| chr14:31176445 | C | T | 1 | a0001c0001t0001g0160 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.376-1307G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/42 | chr14 | 31176445 | |||||||
| chr14:31176486 | A | G | 1 | a0001c0004t0001g0038 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.376-1348T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/42 | chr14 | 31176486 | |||||||
| chr14:31176510 | T | A | 1 | a0001c0004t0001g0115 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.376-1372A>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/42 | chr14 | 31176510 | |||||||
| chr14:31176586 | T | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.375+1434A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/42 | chr14 | 31176586 | |||||||
| chr14:31176612 | T | TA | 25 | a0001c0001t0001g0124 a0001c0001t0001g0246 a0001c0001t0001g0247 others(22): Show |
25 | HG01074.hp1 HG01106.hp1 HG02074.hp1 others(22): Show |
intron_variant | MODIFIER | c.375+1407dupT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/42 | chr14 | 31176612 | |||||||
| chr14:31176612 | TA | T | 63 | a0001c0002t0001g0335 a0001c0002t0001g0336 a0001c0002t0001g0337 others(60): Show |
63 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.375+1407delT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/42 | chr14 | 31176612 | |||||||
| chr14:31176807 | C | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.375+1213G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/42 | chr14 | 31176807 | |||||||
| chr14:31176834 | G | A | 133 | a0001c0001t0001g0002 a0001c0001t0001g0100 a0001c0001t0001g0101 others(130): Show |
134 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.375+1186C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/42 | chr14 | 31176834 | |||||||
| chr14:31176874 | T | C | 3 | a0001c0002t0001g0335 a0001c0002t0001g0336 a0001c0002t0001g0337 |
3 | HG02109.hp1 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.375+1146A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/42 | chr14 | 31176874 | |||||||
| chr14:31176930 | A | C | 1 | a0001c0001t0001g0216 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.375+1090T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/42 | chr14 | 31176930 | |||||||
| chr14:31176936 | C | CA | 55 | a0001c0001t0001g0121 a0001c0001t0001g0147 a0001c0001t0001g0153 others(52): Show |
55 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.375+1083dupT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/42 | chr14 | 31176936 | |||||||
| chr14:31176936 | C | CAA | 7 | a0001c0001t0001g0116 a0001c0002t0013g0339 a0001c0003t0001g0282 others(4): Show |
7 | HG01109.hp2 HG02698.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.375+1082_375+1083d others(4): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/42 | chr14 | 31176936 | |||||||
| chr14:31176936 | C | CAAA | 32 | a0001c0003t0001g0099 a0001c0003t0001g0285 a0001c0003t0001g0288 others(29): Show |
32 | HG00140.hp1 HG01081.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.375+1081_375+1083d others(5): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/42 | chr14 | 31176936 | |||||||
| chr14:31176936 | C | CAAAA | 19 | a0001c0003t0001g0289 a0001c0003t0001g0290 a0001c0003t0001g0313 others(16): Show |
19 | HG00423.hp2 HG00544.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.375+1080_375+1083d others(6): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/42 | chr14 | 31176936 | |||||||
| chr14:31176936 | CA | C | 8 | a0001c0001t0001g0100 a0001c0001t0001g0157 a0001c0001t0001g0164 others(5): Show |
8 | HG02280.hp2 HG02451.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.375+1083delT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/42 | chr14 | 31176936 | |||||||
| chr14:31176958 | AT | A | 8 | a0001c0009t0003g0003 a0001c0009t0003g0004 a0001c0009t0003g0005 others(5): Show |
8 | HG00558.hp1 HG00609.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.375+1061delA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/42 | chr14 | 31176958 | |||||||
| chr14:31177029 | G | A | 1 | a0001c0004t0001g0115 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.375+991C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/42 | chr14 | 31177029 | |||||||
| chr14:31177258 | C | A | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.375+762G>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/42 | chr14 | 31177258 | |||||||
| chr14:31177258 | C | G | 64 | a0001c0002t0001g0335 a0001c0002t0001g0336 a0001c0002t0001g0337 others(61): Show |
64 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.375+762G>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/42 | chr14 | 31177258 | |||||||
| chr14:31177316 | G | A | 1 | a0008c0027t0001g0110 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.375+704C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/42 | chr14 | 31177316 | |||||||
| chr14:31177366 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.375+654G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/42 | chr14 | 31177366 | |||||||
| chr14:31177461 | A | G | 3 | a0001c0002t0001g0109 a0001c0002t0001g0112 a0001c0002t0001g0113 |
3 | HG01891.hp1 HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.375+559T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/42 | chr14 | 31177461 | |||||||
| chr14:31177510 | C | CAAT | 4 | a0001c0002t0001g0337 a0001c0002t0006g0024 a0001c0003t0001g0313 others(1): Show |
4 | HG00673.hp1 HG02258.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.375+507_375+509dup others(3): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/42 | chr14 | 31177510 | |||||||
| chr14:31177510 | C | CAATAAT | 8 | a0001c0002t0006g0023 a0001c0004t0001g0088 a0001c0004t0001g0089 others(5): Show |
8 | HG00639.hp2 HG02257.hp2 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.375+504_375+509dup others(6): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/42 | chr14 | 31177510 | |||||||
| chr14:31177611 | A | G | 3 | a0001c0013t0001g0130 a0001c0013t0001g0165 a0001c0013t0001g0182 |
3 | HG01099.hp1 NA18969.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.375+409T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/42 | chr14 | 31177611 | |||||||
| chr14:31177625 | T | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.375+395A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/42 | chr14 | 31177625 | |||||||
| chr14:31177721 | G | A | 41 | a0001c0002t0001g0053 a0001c0002t0001g0054 a0001c0002t0001g0057 others(38): Show |
41 | HG00621.hp2 HG01069.hp2 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.375+299C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/42 | chr14 | 31177721 | |||||||
| chr14:31177763 | T | C | 1 | a0001c0001t0001g0243 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.375+257A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/42 | chr14 | 31177763 | |||||||
| chr14:31177882 | A | G | 3 | a0003c0014t0001g0081 a0003c0014t0001g0082 a0003c0014t0001g0083 |
3 | HG02145.hp1 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.375+138T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/42 | chr14 | 31177882 | |||||||
| chr14:31177889 | AT | A | 82 | a0001c0001t0001g0002 a0001c0001t0001g0100 a0001c0001t0001g0101 others(79): Show |
83 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.375+130delA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 3/42 | chr14 | 31177889 | |||||||
| chr14:31178296 | T | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.141-42A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31178296 | |||||||
| chr14:31178504 | T | TA | 7 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0242 others(4): Show |
7 | HG01175.hp2 HG02056.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.141-251dupT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31178504 | |||||||
| chr14:31178617 | C | T | 7 | a0001c0002t0001g0109 a0001c0002t0001g0111 a0001c0002t0001g0112 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.141-363G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31178617 | |||||||
| chr14:31178629 | T | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.141-375A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31178629 | |||||||
| chr14:31178681 | T | C | 8 | a0001c0009t0003g0003 a0001c0009t0003g0004 a0001c0009t0003g0005 others(5): Show |
8 | HG00558.hp1 HG00609.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.141-427A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31178681 | |||||||
| chr14:31178724 | G | A | 7 | a0001c0002t0001g0109 a0001c0002t0001g0111 a0001c0002t0001g0112 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.141-470C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31178724 | |||||||
| chr14:31178755 | C | T | 58 | a0001c0002t0013g0339 a0001c0002t0014g0340 a0001c0003t0001g0099 others(55): Show |
58 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.141-501G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31178755 | |||||||
| chr14:31178807 | GA | G | 68 | a0001c0001t0001g0136 a0001c0001t0001g0164 a0001c0001t0001g0203 others(65): Show |
68 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.141-554delT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31178807 | |||||||
| chr14:31178972 | A | G | 2 | a0001c0002t0013g0339 a0001c0002t0014g0340 |
2 | HG01109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.141-718T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31178972 | |||||||
| chr14:31179097 | CTTATAAA others(29): Show |
C | 1 | a0001c0035t0001g0064 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.141-879_141-844del others(36): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31179097 | |||||||
| chr14:31179185 | G | A | 1 | a0002c0005t0001g0264 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.141-931C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31179185 | |||||||
| chr14:31179298 | A | G | 1 | a0001c0003t0001g0289 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.141-1044T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31179298 | |||||||
| chr14:31179405 | C | T | 1 | a0001c0008t0001g0325 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.141-1151G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31179405 | |||||||
| chr14:31179429 | C | CATAAA | 5 | a0001c0002t0001g0335 a0001c0003t0001g0299 a0001c0003t0001g0328 others(2): Show |
5 | HG01175.hp2 HG01192.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.141-1180_141-1176d others(7): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31179429 | |||||||
| chr14:31179429 | C | CATAAAAT others(3): Show |
1 | a0001c0008t0001g0281 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.141-1185_141-1176d others(12): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31179429 | |||||||
| chr14:31179429 | C | CATAAAAT others(8): Show |
46 | a0001c0002t0013g0339 a0001c0002t0014g0340 a0001c0003t0001g0099 others(43): Show |
46 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.141-1190_141-1176d others(17): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31179429 | |||||||
| chr14:31179429 | C | CATAAAAT others(13): Show |
6 | a0001c0003t0001g0285 a0001c0003t0001g0295 a0001c0003t0001g0296 others(3): Show |
6 | NA18939.hp1 NA18947.hp1 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.141-1195_141-1176d others(22): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31179429 | |||||||
| chr14:31179429 | C | CATAAAAT others(18): Show |
1 | a0001c0003t0001g0288 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.141-1200_141-1176d others(27): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31179429 | |||||||
| chr14:31179429 | CATAAA | C | 8 | a0001c0004t0005g0093 a0001c0004t0005g0096 a0001c0010t0004g0014 others(5): Show |
8 | HG01106.hp1 HG02074.hp1 HG03579.hp2 others(5): Show |
intron_variant | MODIFIER | c.141-1180_141-1176d others(7): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31179429 | |||||||
| chr14:31179467 | AAAT | A | 33 | a0001c0002t0001g0053 a0001c0002t0001g0054 a0001c0002t0001g0057 others(30): Show |
33 | HG00621.hp2 HG01069.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.141-1216_141-1214d others(5): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31179467 | |||||||
| chr14:31179532 | G | A | 5 | a0001c0002t0001g0051 a0001c0011t0001g0047 a0001c0011t0001g0048 others(2): Show |
5 | HG02630.hp2 HG02809.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.141-1278C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31179532 | |||||||
| chr14:31179735 | C | T | 4 | a0001c0011t0001g0047 a0001c0011t0001g0048 a0001c0011t0001g0049 others(1): Show |
4 | HG02630.hp2 HG02809.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.141-1481G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31179735 | |||||||
| chr14:31179949 | G | A | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.141-1695C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31179949 | |||||||
| chr14:31180021 | CA | C | 40 | a0001c0004t0001g0001 a0001c0004t0001g0026 a0001c0004t0001g0034 others(37): Show |
41 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.141-1768delT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31180021 | |||||||
| chr14:31180078 | T | A | 6 | a0001c0001t0001g0148 a0001c0001t0001g0160 a0001c0001t0001g0185 others(3): Show |
6 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.141-1824A>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31180078 | |||||||
| chr14:31180124 | G | GC | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.141-1871dupG | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31180124 | |||||||
| chr14:31180170 | T | TA | 10 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(7): Show |
10 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.141-1917dupT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31180170 | |||||||
| chr14:31180309 | T | C | 1 | a0001c0006t0001g0149 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.141-2055A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31180309 | |||||||
| chr14:31180730 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.141-2476G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31180730 | |||||||
| chr14:31181039 | T | C | 2 | a0001c0002t0001g0112 a0001c0002t0001g0113 |
2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.141-2785A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31181039 | |||||||
| chr14:31181086 | T | C | 1 | a0001c0003t0001g0309 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.141-2832A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31181086 | |||||||
| chr14:31181172 | CA | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.141-2919delT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31181172 | |||||||
| chr14:31181178 | A | AT | 11 | a0001c0002t0001g0106 a0001c0002t0001g0250 a0001c0002t0001g0251 others(8): Show |
11 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.141-2925_141-2924i others(3): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31181178 | |||||||
| chr14:31181409 | C | G | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.141-3155G>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31181409 | |||||||
| chr14:31181632 | A | C | 36 | a0001c0002t0001g0053 a0001c0002t0001g0054 a0001c0002t0001g0057 others(33): Show |
36 | HG00621.hp2 HG01069.hp2 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.141-3378T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31181632 | |||||||
| chr14:31181850 | T | C | 9 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(6): Show |
9 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.141-3596A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31181850 | |||||||
| chr14:31181854 | CT | C | 8 | a0001c0001t0001g0141 a0001c0001t0001g0146 a0001c0001t0001g0147 others(5): Show |
8 | HG00733.hp2 HG02055.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.141-3601delA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31181854 | |||||||
| chr14:31181862 | T | A | 1 | a0001c0001t0001g0123 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.141-3608A>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31181862 | |||||||
| chr14:31181901 | C | CT | 7 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(4): Show |
7 | HG01109.hp1 HG02074.hp1 HG03942.hp2 others(4): Show |
intron_variant | MODIFIER | c.141-3648dupA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31181901 | |||||||
| chr14:31182094 | A | G | 9 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(6): Show |
9 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.141-3840T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31182094 | |||||||
| chr14:31182108 | G | C | 1 | a0002c0005t0001g0268 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.141-3854C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31182108 | |||||||
| chr14:31182208 | C | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.141-3954G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31182208 | |||||||
| chr14:31182294 | T | C | 41 | a0001c0004t0001g0001 a0001c0004t0001g0026 a0001c0004t0001g0034 others(38): Show |
42 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(39): Show |
intron_variant | MODIFIER | c.141-4040A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31182294 | |||||||
| chr14:31182350 | G | A | 1 | a0001c0002t0001g0109 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.141-4096C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31182350 | |||||||
| chr14:31182413 | G | A | 58 | a0001c0002t0013g0339 a0001c0002t0014g0340 a0001c0003t0001g0099 others(55): Show |
58 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.141-4159C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31182413 | |||||||
| chr14:31182439 | C | T | 7 | a0001c0002t0001g0109 a0001c0002t0001g0111 a0001c0002t0001g0112 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.141-4185G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31182439 | |||||||
| chr14:31182442 | C | T | 49 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0054 others(46): Show |
49 | HG00621.hp2 HG00639.hp2 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.141-4188G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31182442 | |||||||
| chr14:31182571 | G | T | 7 | a0001c0009t0003g0003 a0001c0009t0003g0004 a0001c0009t0003g0005 others(4): Show |
7 | HG00558.hp1 HG00609.hp2 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.141-4317C>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31182571 | |||||||
| chr14:31182590 | G | A | 1 | a0008c0027t0001g0110 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.141-4336C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31182590 | |||||||
| chr14:31182618 | G | A | 3 | a0001c0004t0001g0001 a0001c0004t0001g0026 a0001c0004t0001g0034 |
4 | HG02559.hp1 HG02965.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.141-4364C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31182618 | |||||||
| chr14:31182646 | G | C | 3 | a0001c0002t0001g0335 a0001c0002t0001g0336 a0001c0002t0001g0337 |
3 | HG02109.hp1 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.141-4392C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31182646 | |||||||
| chr14:31182672 | T | G | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.141-4418A>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31182672 | |||||||
| chr14:31182743 | T | TG | 4 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0239 others(1): Show |
4 | HG02055.hp2 HG02647.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.141-4490dupC | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31182743 | |||||||
| chr14:31182832 | T | C | 73 | a0001c0001t0001g0173 a0001c0002t0001g0335 a0001c0002t0001g0336 others(70): Show |
73 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.141-4578A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31182832 | |||||||
| chr14:31182913 | A | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.141-4659T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31182913 | |||||||
| chr14:31182999 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.141-4745C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31182999 | |||||||
| chr14:31183039 | C | G | 1 | a0001c0002t0001g0336 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.141-4785G>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31183039 | |||||||
| chr14:31183078 | T | TA | 60 | a0001c0002t0013g0339 a0001c0002t0014g0340 a0001c0003t0001g0099 others(57): Show |
60 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.141-4825dupT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31183078 | |||||||
| chr14:31183083 | A | C | 2 | a0001c0009t0003g0004 a0001c0009t0003g0010 |
2 | NA18982.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.141-4829T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31183083 | |||||||
| chr14:31183138 | C | T | 1 | a0002c0005t0001g0275 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.141-4884G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31183138 | |||||||
| chr14:31183164 | T | C | 2 | a0001c0002t0013g0339 a0001c0002t0014g0340 |
2 | HG01109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.141-4910A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31183164 | |||||||
| chr14:31183171 | T | C | 1 | a0001c0002t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.141-4917A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31183171 | |||||||
| chr14:31183363 | T | C | 1 | a0002c0005t0001g0268 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.141-5109A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31183363 | |||||||
| chr14:31183574 | A | AAATTCAG others(2): Show |
6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.141-5321_141-5320i others(11): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31183574 | |||||||
| chr14:31183710 | C | CT | 142 | a0001c0002t0001g0058 a0001c0002t0001g0109 a0001c0002t0001g0111 others(139): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.141-5457dupA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31183710 | |||||||
| chr14:31183710 | C | CTT | 53 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0054 others(50): Show |
53 | HG00621.hp2 HG00639.hp2 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.141-5458_141-5457d others(4): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31183710 | |||||||
| chr14:31183768 | C | A | 1 | a0001c0003t0001g0297 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.141-5514G>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31183768 | |||||||
| chr14:31183768 | C | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.141-5514G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31183768 | |||||||
| chr14:31184240 | G | C | 13 | a0001c0004t0001g0088 a0001c0004t0001g0089 a0001c0004t0001g0097 others(10): Show |
13 | HG01106.hp1 HG02257.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.141-5986C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31184240 | |||||||
| chr14:31184276 | C | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.141-6022G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31184276 | |||||||
| chr14:31184456 | C | T | 5 | a0002c0005t0001g0046 a0002c0005t0001g0266 a0002c0005t0001g0269 others(2): Show |
5 | NA18999.hp1 NA19001.hp1 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.141-6202G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31184456 | |||||||
| chr14:31184457 | G | A | 4 | a0001c0002t0010g0107 a0001c0002t0010g0108 a0001c0017t0009g0020 others(1): Show |
4 | HG01993.hp2 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.141-6203C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31184457 | |||||||
| chr14:31184545 | G | A | 5 | a0001c0002t0001g0051 a0001c0011t0001g0047 a0001c0011t0001g0048 others(2): Show |
5 | HG02630.hp2 HG02809.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.141-6291C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31184545 | |||||||
| chr14:31184583 | C | CA | 7 | a0001c0002t0001g0109 a0001c0002t0001g0111 a0001c0002t0001g0112 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.141-6330dupT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31184583 | |||||||
| chr14:31184661 | A | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.141-6407T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31184661 | |||||||
| chr14:31184697 | C | T | 1 | a0001c0002t0006g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.141-6443G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31184697 | |||||||
| chr14:31184698 | G | A | 1 | a0001c0003t0001g0334 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.141-6444C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31184698 | |||||||
| chr14:31184796 | T | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.141-6542A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31184796 | |||||||
| chr14:31184879 | G | A | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.141-6625C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31184879 | |||||||
| chr14:31185081 | G | A | 2 | a0001c0003t0001g0298 a0003c0014t0001g0083 |
2 | HG02486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.141-6827C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31185081 | |||||||
| chr14:31185132 | G | C | 2 | a0001c0002t0006g0023 a0001c0002t0006g0024 |
2 | HG00639.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.141-6878C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31185132 | |||||||
| chr14:31185215 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.141-6961C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31185215 | |||||||
| chr14:31185287 | C | T | 10 | a0001c0002t0001g0250 a0001c0002t0001g0251 a0001c0002t0001g0252 others(7): Show |
10 | HG02055.hp1 HG02257.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.141-7033G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31185287 | |||||||
| chr14:31185310 | G | C | 56 | a0001c0003t0001g0099 a0001c0003t0001g0282 a0001c0003t0001g0285 others(53): Show |
56 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.141-7056C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31185310 | |||||||
| chr14:31185326 | A | C | 1 | a0001c0004t0001g0038 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.141-7072T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31185326 | |||||||
| chr14:31185337 | A | G | 203 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0054 others(200): Show |
204 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.141-7083T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31185337 | |||||||
| chr14:31185368 | AC | A | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.141-7115delG | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31185368 | |||||||
| chr14:31185816 | G | A | 2 | a0001c0002t0001g0250 a0001c0002t0001g0256 |
2 | HG02257.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.141-7562C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31185816 | |||||||
| chr14:31185838 | C | T | 3 | a0001c0007t0001g0030 a0001c0007t0001g0036 a0001c0036t0001g0043 |
3 | HG00741.hp2 HG01074.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.141-7584G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31185838 | |||||||
| chr14:31185923 | T | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.141-7669A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31185923 | |||||||
| chr14:31185960 | A | G | 8 | a0001c0009t0003g0003 a0001c0009t0003g0004 a0001c0009t0003g0005 others(5): Show |
8 | HG00558.hp1 HG00609.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.141-7706T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31185960 | |||||||
| chr14:31186005 | T | A | 6 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 others(3): Show |
6 | HG02572.hp1 HG02615.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.141-7751A>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31186005 | |||||||
| chr14:31186321 | A | AC | 4 | a0001c0003t0001g0099 a0001c0003t0001g0291 a0001c0003t0001g0317 others(1): Show |
4 | HG01081.hp2 HG01243.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.141-8068dupG | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31186321 | |||||||
| chr14:31186454 | G | A | 1 | a0001c0009t0003g0006 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.141-8200C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31186454 | |||||||
| chr14:31186459 | G | A | 1 | a0001c0009t0003g0003 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.141-8205C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31186459 | |||||||
| chr14:31186558 | C | T | 1 | a0007c0028t0001g0070 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.141-8304G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31186558 | |||||||
| chr14:31186688 | C | CA | 52 | a0001c0001t0001g0121 a0001c0001t0001g0181 a0001c0001t0001g0190 others(49): Show |
52 | HG00609.hp1 HG00621.hp2 HG01069.hp2 others(49): Show |
intron_variant | MODIFIER | c.141-8435dupT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31186688 | |||||||
| chr14:31186688 | CA | C | 60 | a0001c0001t0001g0129 a0001c0001t0001g0146 a0001c0001t0001g0147 others(57): Show |
60 | HG00140.hp1 HG00544.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.141-8435delT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31186688 | |||||||
| chr14:31186775 | C | T | 1 | a0001c0002t0001g0114 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.141-8521G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31186775 | |||||||
| chr14:31186880 | G | A | 13 | a0001c0004t0001g0088 a0001c0004t0001g0089 a0001c0004t0001g0097 others(10): Show |
13 | HG01106.hp1 HG02257.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.141-8626C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31186880 | |||||||
| chr14:31186970 | C | A | 62 | a0001c0002t0001g0335 a0001c0002t0001g0336 a0001c0002t0001g0337 others(59): Show |
62 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.141-8716G>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31186970 | |||||||
| chr14:31186972 | G | A | 7 | a0001c0004t0001g0088 a0001c0004t0001g0089 a0001c0004t0001g0097 others(4): Show |
7 | HG02257.hp2 HG02683.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.141-8718C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31186972 | |||||||
| chr14:31187018 | C | T | 1 | a0001c0004t0001g0089 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.141-8764G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31187018 | |||||||
| chr14:31187027 | C | CA | 54 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0222 others(51): Show |
54 | HG00423.hp2 HG00673.hp1 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.141-8774dupT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31187027 | |||||||
| chr14:31187027 | C | CAA | 13 | a0001c0002t0001g0063 a0001c0002t0001g0079 a0001c0002t0001g0102 others(10): Show |
13 | HG00621.hp2 HG01123.hp1 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.141-8775_141-8774d others(4): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31187027 | |||||||
| chr14:31187027 | CA | C | 132 | a0001c0001t0001g0002 a0001c0001t0001g0101 a0001c0001t0001g0116 others(129): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.141-8774delT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31187027 | |||||||
| chr14:31187027 | CAAAAAAA others(6): Show |
C | 2 | a0001c0002t0001g0085 a0001c0002t0001g0086 |
2 | HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.141-8786_141-8774d others(15): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31187027 | |||||||
| chr14:31187027 | CAAAAAAA others(7): Show |
C | 2 | a0001c0002t0006g0023 a0001c0002t0006g0024 |
2 | HG00639.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.141-8787_141-8774d others(16): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31187027 | |||||||
| chr14:31187045 | A | C | 1 | a0001c0003t0001g0312 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.141-8791T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31187045 | |||||||
| chr14:31187052 | A | AC | 3 | a0003c0014t0001g0081 a0003c0014t0001g0082 a0003c0014t0001g0083 |
3 | HG02145.hp1 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.141-8799dupG | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31187052 | |||||||
| chr14:31187074 | G | A | 2 | a0001c0002t0010g0107 a0001c0002t0010g0108 |
2 | HG01993.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.141-8820C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31187074 | |||||||
| chr14:31187085 | C | T | 199 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0054 others(196): Show |
200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.141-8831G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31187085 | |||||||
| chr14:31187111 | G | T | 1 | a0001c0004t0001g0115 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.141-8857C>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31187111 | |||||||
| chr14:31187156 | T | C | 55 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0054 others(52): Show |
55 | HG00621.hp2 HG00639.hp2 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.141-8902A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31187156 | |||||||
| chr14:31187192 | C | T | 1 | a0001c0002t0006g0023 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.141-8938G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31187192 | |||||||
| chr14:31187245 | CCTG | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.141-8994_141-8992d others(5): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31187245 | |||||||
| chr14:31187305 | C | T | 41 | a0001c0002t0001g0053 a0001c0002t0001g0054 a0001c0002t0001g0057 others(38): Show |
41 | HG00621.hp2 HG01069.hp2 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.141-9051G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31187305 | |||||||
| chr14:31187314 | C | T | 1 | a0001c0002t0001g0069 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.141-9060G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31187314 | |||||||
| chr14:31187357 | A | T | 1 | a0001c0002t0001g0051 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.141-9103T>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31187357 | |||||||
| chr14:31187410 | C | CA | 10 | a0001c0002t0001g0250 a0001c0002t0001g0251 a0001c0002t0001g0252 others(7): Show |
10 | HG02055.hp1 HG02257.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.141-9157dupT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31187410 | |||||||
| chr14:31187684 | A | G | 70 | a0001c0002t0001g0109 a0001c0002t0001g0111 a0001c0002t0001g0112 others(67): Show |
71 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.141-9430T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31187684 | |||||||
| chr14:31187696 | A | G | 3 | a0003c0014t0001g0081 a0003c0014t0001g0082 a0003c0014t0001g0083 |
3 | HG02145.hp1 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.141-9442T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31187696 | |||||||
| chr14:31187710 | G | A | 3 | a0003c0014t0001g0081 a0003c0014t0001g0082 a0003c0014t0001g0083 |
3 | HG02145.hp1 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.141-9456C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31187710 | |||||||
| chr14:31187749 | GGTT | G | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.141-9498_141-9496d others(5): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31187749 | |||||||
| chr14:31187807 | G | A | 1 | a0001c0002t0001g0335 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.141-9553C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31187807 | |||||||
| chr14:31187824 | T | C | 7 | a0001c0002t0001g0109 a0001c0002t0001g0111 a0001c0002t0001g0112 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.141-9570A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31187824 | |||||||
| chr14:31187825 | C | A | 1 | a0001c0003t0001g0289 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.141-9571G>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31187825 | |||||||
| chr14:31187862 | G | A | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.141-9608C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31187862 | |||||||
| chr14:31187964 | T | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.141-9710A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31187964 | |||||||
| chr14:31187972 | T | C | 2 | a0002c0005t0001g0263 a0002c0005t0001g0264 |
2 | HG02602.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.141-9718A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31187972 | |||||||
| chr14:31188036 | G | A | 6 | a0001c0002t0001g0109 a0001c0002t0001g0111 a0001c0002t0001g0112 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.141-9782C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31188036 | |||||||
| chr14:31188089 | G | GTAGA | 10 | a0001c0001t0001g0139 a0001c0001t0001g0191 a0001c0001t0001g0219 others(7): Show |
10 | HG00738.hp1 HG01175.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.141-9839_141-9836d others(6): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31188089 | |||||||
| chr14:31188089 | GTAGA | G | 113 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0129 others(110): Show |
113 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.141-9839_141-9836d others(6): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31188089 | |||||||
| chr14:31188089 | GTAGATAG others(1): Show |
G | 95 | a0001c0001t0001g0002 a0001c0001t0001g0100 a0001c0001t0001g0101 others(92): Show |
97 | HG00323.hp1 HG00544.hp2 HG00621.hp2 others(94): Show |
intron_variant | MODIFIER | c.141-9843_141-9836d others(10): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31188089 | |||||||
| chr14:31188089 | GTAGATAG others(5): Show |
G | 51 | a0001c0001t0001g0128 a0001c0001t0001g0151 a0001c0001t0001g0154 others(48): Show |
51 | HG00099.hp1 HG00140.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.141-9847_141-9836d others(14): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31188089 | |||||||
| chr14:31188089 | GTAGATAG others(9): Show |
G | 6 | a0001c0003t0001g0099 a0001c0003t0001g0282 a0001c0003t0001g0290 others(3): Show |
6 | HG01081.hp2 HG01952.hp1 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.141-9851_141-9836d others(18): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31188089 | |||||||
| chr14:31188089 | GTAGATAG others(13): Show |
G | 1 | a0001c0003t0001g0289 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.141-9855_141-9836d others(22): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31188089 | |||||||
| chr14:31188117 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.141-9863T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31188117 | |||||||
| chr14:31188134 | TAGATAGA others(5): Show |
T | 1 | a0001c0004t0001g0066 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.141-9892_141-9881d others(14): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31188134 | |||||||
| chr14:31188138 | T | C | 1 | a0001c0017t0009g0020 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.141-9884A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31188138 | |||||||
| chr14:31188138 | TAGATAGA others(1): Show |
T | 6 | a0001c0002t0001g0337 a0001c0002t0006g0023 a0001c0002t0006g0024 others(3): Show |
6 | HG00639.hp2 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.141-9892_141-9885d others(10): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31188138 | |||||||
| chr14:31188142 | T | C | 20 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0135 others(17): Show |
20 | HG01993.hp2 HG02015.hp2 HG02071.hp2 others(17): Show |
intron_variant | MODIFIER | c.141-9888A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31188142 | |||||||
| chr14:31188142 | T | TAGAC | 4 | a0001c0002t0001g0057 a0001c0011t0001g0049 a0005c0016t0001g0133 others(1): Show |
4 | HG02630.hp2 NA19003.hp1 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.141-9892_141-9889d others(6): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31188142 | |||||||
| chr14:31188142 | T | TAGATAGA others(5): Show |
1 | a0001c0017t0009g0021 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.141-9889_141-9888i others(14): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31188142 | |||||||
| chr14:31188142 | T | TAGATAGA others(17): Show |
1 | a0001c0018t0004g0019 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.141-9889_141-9888i others(26): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31188142 | |||||||
| chr14:31188142 | T | TAGATGGA others(13): Show |
5 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(2): Show |
5 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.141-9889_141-9888i others(22): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31188142 | |||||||
| chr14:31188154 | T | A | 1 | a0002c0005t0001g0260 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.141-9900A>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31188154 | |||||||
| chr14:31188181 | C | T | 2 | a0001c0002t0001g0336 a0001c0002t0001g0337 |
2 | HG02109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.141-9927G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31188181 | |||||||
| chr14:31188237 | C | CT | 261 | a0001c0001t0001g0002 a0001c0001t0001g0101 a0001c0001t0001g0121 others(258): Show |
262 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.141-9984dupA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31188237 | |||||||
| chr14:31188237 | C | CTT | 18 | a0001c0001t0001g0100 a0001c0001t0001g0123 a0001c0001t0001g0140 others(15): Show |
18 | HG00280.hp1 HG01261.hp2 HG02129.hp1 others(15): Show |
intron_variant | MODIFIER | c.141-9985_141-9984d others(4): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31188237 | |||||||
| chr14:31188242 | T | TC | 38 | a0001c0004t0001g0037 a0001c0004t0001g0038 a0001c0004t0001g0042 others(35): Show |
38 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(35): Show |
intron_variant | MODIFIER | c.141-9989_141-9988i others(3): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31188242 | |||||||
| chr14:31188299 | A | G | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.141-10045T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31188299 | |||||||
| chr14:31188378 | G | C | 5 | a0001c0002t0001g0335 a0001c0002t0001g0336 a0001c0002t0001g0337 others(2): Show |
5 | HG01109.hp2 HG02109.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.141-10124C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31188378 | |||||||
| chr14:31188380 | C | T | 1 | a0001c0002t0014g0340 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.141-10126G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31188380 | |||||||
| chr14:31188546 | C | G | 1 | a0001c0012t0001g0052 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.141-10292G>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31188546 | |||||||
| chr14:31188658 | G | A | 1 | a0001c0003t0001g0316 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.141-10404C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31188658 | |||||||
| chr14:31188714 | CAG | C | 6 | a0001c0002t0001g0109 a0001c0002t0001g0111 a0001c0002t0001g0112 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.141-10462_141-1046 others(6): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31188714 | |||||||
| chr14:31188789 | C | G | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.141-10535G>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31188789 | |||||||
| chr14:31188835 | A | G | 2 | a0001c0017t0009g0020 a0001c0017t0009g0021 |
2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.141-10581T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31188835 | |||||||
| chr14:31188872 | T | C | 200 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0054 others(197): Show |
201 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.141-10618A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31188872 | |||||||
| chr14:31188877 | A | G | 1 | a0001c0037t0001g0261 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.141-10623T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31188877 | |||||||
| chr14:31188925 | C | T | 1 | a0001c0010t0004g0018 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.141-10671G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31188925 | |||||||
| chr14:31188965 | C | G | 3 | a0003c0014t0001g0081 a0003c0014t0001g0082 a0003c0014t0001g0083 |
3 | HG02145.hp1 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.141-10711G>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31188965 | |||||||
| chr14:31189129 | A | G | 2 | a0001c0017t0009g0020 a0001c0017t0009g0021 |
2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.141-10875T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31189129 | |||||||
| chr14:31189161 | G | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.141-10907C>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31189161 | |||||||
| chr14:31189422 | A | G | 1 | a0001c0007t0007g0025 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.141-11168T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31189422 | |||||||
| chr14:31189460 | G | A | 39 | a0001c0002t0001g0053 a0001c0002t0001g0054 a0001c0002t0001g0057 others(36): Show |
39 | HG00621.hp2 HG01069.hp2 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.141-11206C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31189460 | |||||||
| chr14:31189529 | C | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.141-11275G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31189529 | |||||||
| chr14:31189634 | T | C | 200 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0054 others(197): Show |
201 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.141-11380A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31189634 | |||||||
| chr14:31189640 | T | C | 3 | a0001c0004t0001g0001 a0001c0004t0001g0026 a0001c0004t0001g0034 |
4 | HG02559.hp1 HG02965.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.141-11386A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31189640 | |||||||
| chr14:31189715 | T | C | 3 | a0001c0002t0001g0076 a0001c0002t0001g0077 a0010c0032t0001g0087 |
3 | NA18977.hp1 NA18987.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.141-11461A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31189715 | |||||||
| chr14:31189963 | C | T | 2 | a0001c0002t0006g0023 a0001c0002t0006g0024 |
2 | HG00639.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.141-11709G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31189963 | |||||||
| chr14:31190019 | G | A | 13 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(10): Show |
13 | HG01884.hp2 HG02572.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.141-11765C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31190019 | |||||||
| chr14:31190127 | G | A | 58 | a0001c0002t0013g0339 a0001c0002t0014g0340 a0001c0003t0001g0099 others(55): Show |
58 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.141-11873C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31190127 | |||||||
| chr14:31190230 | C | G | 1 | a0001c0001t0001g0206 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.141-11976G>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31190230 | |||||||
| chr14:31190267 | C | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.141-12013G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31190267 | |||||||
| chr14:31190297 | C | A | 1 | a0001c0006t0002g0224 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.141-12043G>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31190297 | |||||||
| chr14:31190400 | G | A | 48 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0054 others(45): Show |
48 | HG00621.hp2 HG01069.hp2 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.141-12146C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31190400 | |||||||
| chr14:31190423 | A | C | 1 | a0001c0002t0001g0106 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.141-12169T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31190423 | |||||||
| chr14:31190425 | C | T | 5 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(2): Show |
5 | HG02074.hp1 NA18971.hp1 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.141-12171G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31190425 | |||||||
| chr14:31190468 | T | C | 2 | a0001c0007t0007g0031 a0001c0007t0007g0032 |
2 | HG01256.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.141-12214A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31190468 | |||||||
| chr14:31190706 | A | G | 1 | a0001c0003t0001g0099 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.141-12452T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31190706 | |||||||
| chr14:31190786 | G | A | 1 | a0001c0002t0001g0084 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.141-12532C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31190786 | |||||||
| chr14:31190807 | C | A | 1 | a0001c0004t0001g0089 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.141-12553G>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31190807 | |||||||
| chr14:31190921 | C | T | 1 | a0001c0002t0001g0251 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.141-12667G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31190921 | |||||||
| chr14:31190922 | G | A | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.141-12668C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31190922 | |||||||
| chr14:31191144 | T | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.141-12890A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31191144 | |||||||
| chr14:31191166 | T | G | 5 | a0001c0004t0001g0088 a0001c0004t0001g0097 a0001c0004t0001g0098 others(2): Show |
5 | HG02683.hp1 HG03704.hp1 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.141-12912A>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31191166 | |||||||
| chr14:31191489 | C | T | 5 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(2): Show |
5 | HG02074.hp1 NA18971.hp1 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.141-13235G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31191489 | |||||||
| chr14:31191525 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.141-13271C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31191525 | |||||||
| chr14:31191545 | C | CA | 159 | a0001c0001t0001g0002 a0001c0001t0001g0100 a0001c0001t0001g0101 others(156): Show |
161 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.141-13292dupT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31191545 | |||||||
| chr14:31191545 | CA | C | 12 | a0001c0002t0001g0084 a0001c0002t0001g0250 a0001c0002t0001g0251 others(9): Show |
12 | HG02055.hp1 HG02257.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.141-13292delT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31191545 | |||||||
| chr14:31191545 | CAA | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.141-13293_141-1329 others(6): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31191545 | |||||||
| chr14:31191610 | A | G | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.141-13356T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31191610 | |||||||
| chr14:31191626 | A | T | 1 | a0001c0002t0006g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.141-13372T>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31191626 | |||||||
| chr14:31191725 | G | A | 40 | a0001c0004t0001g0001 a0001c0004t0001g0026 a0001c0004t0001g0034 others(37): Show |
41 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.141-13471C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31191725 | |||||||
| chr14:31191845 | C | CA | 67 | a0001c0001t0001g0198 a0001c0002t0001g0250 a0001c0002t0001g0251 others(64): Show |
68 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.141-13592dupT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31191845 | |||||||
| chr14:31191880 | A | G | 2 | a0001c0002t0010g0107 a0001c0002t0010g0108 |
2 | HG01993.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.141-13626T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31191880 | |||||||
| chr14:31191917 | G | A | 2 | a0001c0004t0005g0093 a0001c0004t0005g0096 |
2 | HG01106.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.141-13663C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31191917 | |||||||
| chr14:31192014 | A | G | 7 | a0001c0004t0005g0090 a0001c0010t0004g0014 a0001c0010t0004g0015 others(4): Show |
7 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.141-13760T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31192014 | |||||||
| chr14:31192067 | T | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.140+13730A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31192067 | |||||||
| chr14:31192068 | G | A | 2 | a0001c0001t0001g0135 a0001c0010t0004g0018 |
2 | HG03942.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.140+13729C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31192068 | |||||||
| chr14:31192207 | G | A | 2 | a0001c0002t0006g0023 a0001c0002t0006g0024 |
2 | HG00639.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.140+13590C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31192207 | |||||||
| chr14:31192323 | G | T | 58 | a0001c0002t0013g0339 a0001c0002t0014g0340 a0001c0003t0001g0099 others(55): Show |
58 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.140+13474C>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31192323 | |||||||
| chr14:31192335 | C | CA | 149 | a0001c0001t0001g0002 a0001c0001t0001g0100 a0001c0001t0001g0101 others(146): Show |
151 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.140+13461dupT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31192335 | |||||||
| chr14:31192335 | CA | C | 6 | a0001c0002t0001g0084 a0001c0003t0001g0330 a0001c0004t0001g0088 others(3): Show |
6 | HG02683.hp1 NA18946.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.140+13461delT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31192335 | |||||||
| chr14:31192466 | T | A | 1 | a0001c0033t0001g0319 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.140+13331A>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31192466 | |||||||
| chr14:31192479 | T | G | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.140+13318A>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31192479 | |||||||
| chr14:31192620 | A | C | 2 | a0001c0002t0013g0339 a0001c0002t0014g0340 |
2 | HG01109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.140+13177T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31192620 | |||||||
| chr14:31192633 | C | T | 2 | a0001c0004t0001g0089 a0001c0025t0001g0092 |
2 | HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.140+13164G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31192633 | |||||||
| chr14:31192698 | G | A | 2 | a0001c0002t0001g0336 a0001c0002t0001g0337 |
2 | HG02109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.140+13099C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31192698 | |||||||
| chr14:31192716 | C | T | 1 | a0001c0004t0001g0115 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.140+13081G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31192716 | |||||||
| chr14:31192718 | A | G | 1 | a0001c0004t0001g0089 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.140+13079T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31192718 | |||||||
| chr14:31192805 | G | A | 4 | a0001c0004t0005g0090 a0001c0004t0005g0094 a0001c0004t0005g0095 others(1): Show |
4 | HG02572.hp2 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.140+12992C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31192805 | |||||||
| chr14:31192819 | C | T | 1 | a0001c0006t0001g0286 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.140+12978G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31192819 | |||||||
| chr14:31192832 | C | T | 4 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0239 others(1): Show |
4 | HG02055.hp2 HG02647.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.140+12965G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31192832 | |||||||
| chr14:31192907 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.140+12890C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31192907 | |||||||
| chr14:31192908 | C | A | 1 | a0001c0001t0001g0193 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.140+12889G>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31192908 | |||||||
| chr14:31192963 | G | A | 3 | a0001c0002t0001g0061 a0001c0002t0001g0062 a0001c0002t0001g0063 |
3 | HG02080.hp2 NA18950.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.140+12834C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31192963 | |||||||
| chr14:31193034 | G | A | 1 | a0001c0002t0001g0335 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.140+12763C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31193034 | |||||||
| chr14:31193115 | C | T | 2 | a0001c0002t0001g0336 a0001c0002t0001g0337 |
2 | HG02109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.140+12682G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31193115 | |||||||
| chr14:31193185 | T | G | 1 | a0001c0001t0001g0205 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.140+12612A>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31193185 | |||||||
| chr14:31193249 | A | C | 52 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0054 others(49): Show |
52 | HG00621.hp2 HG01069.hp2 HG01071.hp2 others(49): Show |
intron_variant | MODIFIER | c.140+12548T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31193249 | |||||||
| chr14:31193302 | G | A | 1 | a0001c0033t0001g0319 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.140+12495C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31193302 | |||||||
| chr14:31193911 | C | T | 1 | a0001c0004t0001g0115 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.140+11886G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31193911 | |||||||
| chr14:31194175 | T | C | 17 | a0001c0002t0001g0053 a0001c0002t0001g0054 a0001c0002t0001g0057 others(14): Show |
17 | HG00621.hp2 HG02080.hp2 NA18943.hp1 others(14): Show |
intron_variant | MODIFIER | c.140+11622A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31194175 | |||||||
| chr14:31194201 | A | T | 1 | a0001c0006t0001g0149 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.140+11596T>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31194201 | |||||||
| chr14:31194233 | A | G | 8 | a0001c0009t0003g0003 a0001c0009t0003g0004 a0001c0009t0003g0005 others(5): Show |
8 | HG00558.hp1 HG00609.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.140+11564T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31194233 | |||||||
| chr14:31194244 | G | T | 1 | a0001c0004t0001g0026 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.140+11553C>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31194244 | |||||||
| chr14:31194313 | A | G | 1 | a0001c0003t0001g0285 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.140+11484T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31194313 | |||||||
| chr14:31194522 | C | A | 2 | a0001c0002t0010g0107 a0001c0002t0010g0108 |
2 | HG01993.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.140+11275G>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31194522 | |||||||
| chr14:31194534 | C | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.140+11263G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31194534 | |||||||
| chr14:31194782 | G | C | 1 | a0001c0004t0001g0089 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.140+11015C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31194782 | |||||||
| chr14:31194838 | T | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.140+10959A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31194838 | |||||||
| chr14:31194924 | A | T | 4 | a0001c0001t0001g0148 a0001c0002t0001g0335 a0001c0002t0001g0336 others(1): Show |
4 | HG01256.hp2 HG02109.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.140+10873T>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31194924 | |||||||
| chr14:31194948 | T | C | 1 | a0001c0001t0001g0194 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.140+10849A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31194948 | |||||||
| chr14:31194969 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.140+10828A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31194969 | |||||||
| chr14:31195061 | G | A | 198 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0054 others(195): Show |
199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.140+10736C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31195061 | |||||||
| chr14:31195090 | A | C | 4 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0239 others(1): Show |
4 | HG02055.hp2 HG02647.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.140+10707T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31195090 | |||||||
| chr14:31195442 | C | T | 1 | a0001c0017t0009g0020 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.140+10355G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31195442 | |||||||
| chr14:31195606 | C | T | 4 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
4 | NA18954.hp1 NA18970.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.140+10191G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31195606 | |||||||
| chr14:31195749 | C | T | 1 | a0001c0004t0001g0115 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.140+10048G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31195749 | |||||||
| chr14:31195768 | C | T | 2 | a0002c0005t0001g0275 a0002c0005t0001g0276 |
2 | HG01243.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.140+10029G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31195768 | |||||||
| chr14:31195812 | A | G | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.140+9985T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31195812 | |||||||
| chr14:31196051 | T | C | 6 | a0001c0004t0005g0090 a0001c0004t0005g0093 a0001c0004t0005g0094 others(3): Show |
6 | HG01106.hp1 HG02572.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.140+9746A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31196051 | |||||||
| chr14:31196087 | C | T | 13 | a0001c0004t0001g0088 a0001c0004t0001g0089 a0001c0004t0001g0097 others(10): Show |
13 | HG01106.hp1 HG02257.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.140+9710G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31196087 | |||||||
| chr14:31196235 | T | G | 1 | a0001c0002t0001g0051 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.140+9562A>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31196235 | |||||||
| chr14:31196570 | T | C | 41 | a0001c0004t0001g0001 a0001c0004t0001g0026 a0001c0004t0001g0034 others(38): Show |
42 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(39): Show |
intron_variant | MODIFIER | c.140+9227A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31196570 | |||||||
| chr14:31196712 | C | A | 1 | a0001c0001t0001g0136 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.140+9085G>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31196712 | |||||||
| chr14:31196748 | C | T | 1 | a0001c0002t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.140+9049G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31196748 | |||||||
| chr14:31196749 | G | A | 1 | a0001c0007t0001g0040 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.140+9048C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31196749 | |||||||
| chr14:31196821 | T | C | 2 | a0001c0017t0009g0020 a0001c0017t0009g0021 |
2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.140+8976A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31196821 | |||||||
| chr14:31196837 | T | TA | 14 | a0001c0002t0001g0250 a0001c0002t0001g0251 a0001c0002t0001g0252 others(11): Show |
14 | HG02055.hp1 HG02257.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.140+8959dupT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31196837 | |||||||
| chr14:31196961 | C | T | 1 | a0001c0003t0001g0333 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.140+8836G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31196961 | |||||||
| chr14:31197046 | G | A | 2 | a0001c0002t0010g0107 a0001c0002t0010g0108 |
2 | HG01993.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.140+8751C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31197046 | |||||||
| chr14:31197057 | C | T | 3 | a0003c0014t0001g0081 a0003c0014t0001g0082 a0003c0014t0001g0083 |
3 | HG02145.hp1 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.140+8740G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31197057 | |||||||
| chr14:31197245 | C | T | 3 | a0001c0001t0001g0126 a0001c0001t0001g0145 a0004c0015t0001g0144 |
3 | HG00099.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.140+8552G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31197245 | |||||||
| chr14:31197399 | C | T | 2 | a0002c0005t0001g0275 a0002c0005t0001g0276 |
2 | HG01243.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.140+8398G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31197399 | |||||||
| chr14:31197412 | C | T | 2 | a0001c0002t0013g0339 a0001c0002t0014g0340 |
2 | HG01109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.140+8385G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31197412 | |||||||
| chr14:31197641 | A | C | 1 | a0001c0003t0011g0011 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.140+8156T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31197641 | |||||||
| chr14:31197697 | T | C | 5 | a0001c0002t0001g0051 a0001c0011t0001g0047 a0001c0011t0001g0048 others(2): Show |
5 | HG02630.hp2 HG02809.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.140+8100A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31197697 | |||||||
| chr14:31197787 | A | G | 1 | a0001c0008t0001g0283 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.140+8010T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31197787 | |||||||
| chr14:31197915 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.140+7882G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31197915 | |||||||
| chr14:31197978 | C | T | 1 | a0002c0005t0001g0265 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.140+7819G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31197978 | |||||||
| chr14:31198204 | ATG | A | 118 | a0001c0001t0001g0002 a0001c0001t0001g0100 a0001c0001t0001g0101 others(115): Show |
119 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.140+7591_140+7592d others(4): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31198204 | |||||||
| chr14:31198240 | T | A | 10 | a0001c0002t0001g0250 a0001c0002t0001g0251 a0001c0002t0001g0252 others(7): Show |
10 | HG02055.hp1 HG02257.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.140+7557A>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31198240 | |||||||
| chr14:31198633 | T | C | 7 | a0001c0004t0001g0088 a0001c0004t0001g0089 a0001c0004t0001g0097 others(4): Show |
7 | HG02257.hp2 HG02683.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.140+7164A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31198633 | |||||||
| chr14:31198736 | G | A | 1 | a0001c0003t0001g0333 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.140+7061C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31198736 | |||||||
| chr14:31198809 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.140+6988C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31198809 | |||||||
| chr14:31198878 | TA | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.140+6918delT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31198878 | |||||||
| chr14:31198940 | G | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.140+6857C>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31198940 | |||||||
| chr14:31199017 | G | A | 13 | a0001c0004t0001g0088 a0001c0004t0001g0089 a0001c0004t0001g0097 others(10): Show |
13 | HG01106.hp1 HG02257.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.140+6780C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31199017 | |||||||
| chr14:31199033 | G | GA | 17 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0196 others(14): Show |
17 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.140+6763dupT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31199033 | |||||||
| chr14:31199033 | GA | G | 11 | a0001c0001t0001g0127 a0001c0004t0001g0088 a0001c0004t0001g0089 others(8): Show |
11 | HG00558.hp2 HG01496.hp2 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.140+6763delT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31199033 | |||||||
| chr14:31199033 | GAA | G | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.140+6762_140+6763d others(4): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31199033 | |||||||
| chr14:31199034 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.140+6763T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31199034 | |||||||
| chr14:31199043 | A | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.140+6754T>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31199043 | |||||||
| chr14:31199048 | A | C | 58 | a0001c0002t0013g0339 a0001c0002t0014g0340 a0001c0003t0001g0099 others(55): Show |
58 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.140+6749T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31199048 | |||||||
| chr14:31199059 | C | T | 2 | a0001c0017t0009g0020 a0001c0017t0009g0021 |
2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.140+6738G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31199059 | |||||||
| chr14:31199322 | C | CCCAAAAT others(326): Show |
1 | a0001c0010t0004g0018 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.140+6474_140+6475i others(335): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31199322 | |||||||
| chr14:31199322 | C | CCCAAAAT others(327): Show |
1 | a0001c0010t0004g0016 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.140+6474_140+6475i others(336): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31199322 | |||||||
| chr14:31199322 | C | CCCAAAAT others(326): Show |
4 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0017 others(1): Show |
4 | HG02074.hp1 NA18971.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.140+6474_140+6475i others(335): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31199322 | |||||||
| chr14:31199386 | T | C | 2 | a0001c0017t0009g0020 a0001c0017t0009g0021 |
2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.140+6411A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31199386 | |||||||
| chr14:31199394 | AT | A | 8 | a0001c0001t0001g0223 a0001c0001t0001g0249 a0001c0002t0001g0057 others(5): Show |
8 | HG01109.hp2 HG02273.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.140+6402delA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31199394 | |||||||
| chr14:31199456 | C | T | 1 | a0001c0001t0001g0338 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.140+6341G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31199456 | |||||||
| chr14:31199584 | G | A | 5 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0225 others(2): Show |
5 | HG00741.hp1 HG01433.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.140+6213C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31199584 | |||||||
| chr14:31199714 | C | CA | 35 | a0001c0001t0001g0121 a0001c0001t0001g0199 a0001c0001t0001g0200 others(32): Show |
35 | HG00423.hp1 HG00544.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.140+6082dupT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31199714 | |||||||
| chr14:31199714 | C | CAA | 7 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0230 others(4): Show |
7 | HG01978.hp2 HG02572.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.140+6081_140+6082d others(4): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31199714 | |||||||
| chr14:31199714 | CA | C | 20 | a0001c0001t0001g0126 a0001c0001t0001g0140 a0001c0001t0001g0141 others(17): Show |
20 | HG00733.hp1 HG01106.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.140+6082delT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31199714 | |||||||
| chr14:31199714 | CAA | C | 63 | a0001c0002t0001g0051 a0001c0002t0001g0058 a0001c0002t0001g0059 others(60): Show |
63 | HG00140.hp2 HG00639.hp2 HG00738.hp2 others(60): Show |
intron_variant | MODIFIER | c.140+6081_140+6082d others(4): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31199714 | |||||||
| chr14:31199714 | CAAA | C | 64 | a0001c0002t0001g0053 a0001c0002t0001g0054 a0001c0002t0001g0057 others(61): Show |
65 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.140+6080_140+6082d others(5): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31199714 | |||||||
| chr14:31199714 | CAAAA | C | 52 | a0001c0002t0001g0335 a0001c0002t0001g0336 a0001c0002t0001g0337 others(49): Show |
52 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.140+6079_140+6082d others(6): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31199714 | |||||||
| chr14:31199727 | A | C | 1 | a0001c0001t0001g0139 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.140+6070T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31199727 | |||||||
| chr14:31199755 | A | T | 1 | a0001c0004t0001g0115 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.140+6042T>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31199755 | |||||||
| chr14:31199853 | T | C | 19 | a0001c0037t0001g0261 a0002c0005t0001g0046 a0002c0005t0001g0260 others(16): Show |
19 | HG00140.hp2 HG00733.hp1 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.140+5944A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31199853 | |||||||
| chr14:31200149 | CCT | C | 10 | a0001c0002t0001g0250 a0001c0002t0001g0251 a0001c0002t0001g0252 others(7): Show |
10 | HG02055.hp1 HG02257.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.140+5646_140+5647d others(4): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31200149 | |||||||
| chr14:31200314 | T | C | 1 | a0001c0007t0001g0040 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.140+5483A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31200314 | |||||||
| chr14:31200333 | T | C | 1 | a0001c0002t0001g0114 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.140+5464A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31200333 | |||||||
| chr14:31200373 | C | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.140+5424G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31200373 | |||||||
| chr14:31200374 | G | A | 3 | a0003c0014t0001g0081 a0003c0014t0001g0082 a0003c0014t0001g0083 |
3 | HG02145.hp1 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.140+5423C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31200374 | |||||||
| chr14:31200400 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.140+5397G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31200400 | |||||||
| chr14:31200402 | C | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.140+5395G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31200402 | |||||||
| chr14:31200417 | G | A | 63 | a0001c0002t0001g0250 a0001c0002t0001g0251 a0001c0002t0001g0252 others(60): Show |
64 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.140+5380C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31200417 | |||||||
| chr14:31200489 | TA | T | 191 | a0001c0001t0001g0002 a0001c0001t0001g0100 a0001c0001t0001g0101 others(188): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.140+5307delT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31200489 | |||||||
| chr14:31200489 | TAA | T | 87 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(84): Show |
87 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.140+5306_140+5307d others(4): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31200489 | |||||||
| chr14:31200489 | TAAA | T | 37 | a0001c0002t0001g0053 a0001c0002t0001g0054 a0001c0002t0001g0057 others(34): Show |
37 | HG00621.hp2 HG01069.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.140+5305_140+5307d others(5): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31200489 | |||||||
| chr14:31200575 | T | C | 1 | a0001c0003t0001g0330 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.140+5222A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31200575 | |||||||
| chr14:31200597 | T | C | 1 | a0001c0008t0001g0331 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.140+5200A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31200597 | |||||||
| chr14:31200678 | G | A | 8 | a0001c0009t0003g0003 a0001c0009t0003g0004 a0001c0009t0003g0005 others(5): Show |
8 | HG00558.hp1 HG00609.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.140+5119C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31200678 | |||||||
| chr14:31200782 | GA | G | 24 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(21): Show |
24 | HG00140.hp2 HG00733.hp1 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.140+5014delT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31200782 | |||||||
| chr14:31201077 | G | GA | 5 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(2): Show |
5 | HG02074.hp1 NA18971.hp1 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.140+4719_140+4720i others(3): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31201077 | |||||||
| chr14:31201119 | T | A | 1 | a0001c0001t0001g0238 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.140+4678A>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31201119 | |||||||
| chr14:31201248 | C | T | 1 | a0002c0005t0001g0260 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.140+4549G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31201248 | |||||||
| chr14:31201334 | A | G | 1 | a0001c0009t0003g0003 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.140+4463T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31201334 | |||||||
| chr14:31201370 | T | C | 2 | a0001c0017t0009g0020 a0001c0017t0009g0021 |
2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.140+4427A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31201370 | |||||||
| chr14:31201510 | C | CT | 55 | a0001c0001t0001g0100 a0001c0001t0001g0121 a0001c0002t0001g0053 others(52): Show |
55 | HG00621.hp2 HG01069.hp2 HG01071.hp2 others(52): Show |
intron_variant | MODIFIER | c.140+4286dupA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31201510 | |||||||
| chr14:31201535 | G | A | 1 | a0001c0002t0001g0337 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.140+4262C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31201535 | |||||||
| chr14:31201567 | T | C | 2 | a0001c0017t0009g0020 a0001c0017t0009g0021 |
2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.140+4230A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31201567 | |||||||
| chr14:31201711 | T | C | 1 | a0001c0001t0001g0239 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.140+4086A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31201711 | |||||||
| chr14:31201730 | G | T | 1 | a0001c0030t0001g0280 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.140+4067C>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31201730 | |||||||
| chr14:31201806 | G | A | 2 | a0001c0002t0010g0107 a0001c0002t0010g0108 |
2 | HG01993.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.140+3991C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31201806 | |||||||
| chr14:31201955 | G | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.140+3842C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31201955 | |||||||
| chr14:31202008 | C | T | 5 | a0001c0002t0001g0051 a0001c0011t0001g0047 a0001c0011t0001g0048 others(2): Show |
5 | HG02630.hp2 HG02809.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.140+3789G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31202008 | |||||||
| chr14:31202051 | C | A | 3 | a0001c0003t0001g0332 a0001c0003t0001g0334 a0001c0003t0011g0011 |
3 | NA18968.hp1 NA18975.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.140+3746G>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31202051 | |||||||
| chr14:31202199 | C | CA | 19 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 others(16): Show |
19 | HG00323.hp2 HG00558.hp1 HG00609.hp2 others(16): Show |
intron_variant | MODIFIER | c.140+3597dupT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31202199 | |||||||
| chr14:31202199 | C | CAA | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.140+3596_140+3597d others(4): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31202199 | |||||||
| chr14:31202199 | CA | C | 23 | a0001c0001t0001g0116 a0001c0002t0001g0109 a0001c0002t0001g0250 others(20): Show |
23 | HG01106.hp1 HG02055.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.140+3597delT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31202199 | |||||||
| chr14:31202235 | C | T | 1 | a0001c0004t0001g0115 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.140+3562G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31202235 | |||||||
| chr14:31202243 | A | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.140+3554T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31202243 | |||||||
| chr14:31202326 | G | C | 1 | a0001c0010t0004g0017 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.140+3471C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31202326 | |||||||
| chr14:31202338 | C | T | 2 | a0001c0017t0009g0020 a0001c0017t0009g0021 |
2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.140+3459G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31202338 | |||||||
| chr14:31202530 | T | A | 1 | a0001c0004t0001g0115 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.140+3267A>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31202530 | |||||||
| chr14:31202593 | T | G | 1 | a0001c0001t0001g0245 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.140+3204A>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31202593 | |||||||
| chr14:31202719 | C | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.140+3078G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31202719 | |||||||
| chr14:31202768 | C | T | 70 | a0001c0002t0001g0109 a0001c0002t0001g0111 a0001c0002t0001g0112 others(67): Show |
71 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.140+3029G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31202768 | |||||||
| chr14:31203533 | C | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.140+2264G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31203533 | |||||||
| chr14:31203604 | T | TAAAAAAA others(2): Show |
6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.140+2192_140+2193i others(11): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31203604 | |||||||
| chr14:31203677 | G | GA | 4 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
4 | NA18954.hp1 NA18970.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.140+2119dupT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31203677 | |||||||
| chr14:31203750 | CT | C | 63 | a0001c0002t0001g0335 a0001c0002t0001g0336 a0001c0002t0001g0337 others(60): Show |
63 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.140+2046delA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31203750 | |||||||
| chr14:31203754 | T | G | 3 | a0001c0002t0001g0335 a0001c0002t0001g0336 a0001c0002t0001g0337 |
3 | HG02109.hp1 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.140+2043A>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31203754 | |||||||
| chr14:31203756 | T | A | 2 | a0001c0017t0009g0020 a0001c0017t0009g0021 |
2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.140+2041A>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31203756 | |||||||
| chr14:31203768 | C | T | 51 | a0001c0002t0001g0051 a0001c0002t0001g0053 a0001c0002t0001g0054 others(48): Show |
51 | HG00621.hp2 HG00639.hp2 HG01069.hp2 others(48): Show |
intron_variant | MODIFIER | c.140+2029G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31203768 | |||||||
| chr14:31203809 | T | G | 2 | a0001c0002t0001g0085 a0001c0002t0001g0086 |
2 | HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.140+1988A>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31203809 | |||||||
| chr14:31203897 | C | G | 1 | a0001c0001t0001g0101 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.140+1900G>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31203897 | |||||||
| chr14:31203898 | C | G | 1 | a0001c0002t0006g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.140+1899G>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31203898 | |||||||
| chr14:31203905 | T | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.140+1892A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31203905 | |||||||
| chr14:31204122 | C | T | 2 | a0001c0017t0009g0020 a0001c0017t0009g0021 |
2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.140+1675G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31204122 | |||||||
| chr14:31204175 | T | C | 64 | a0001c0002t0001g0250 a0001c0002t0001g0251 a0001c0002t0001g0252 others(61): Show |
65 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.140+1622A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31204175 | |||||||
| chr14:31204332 | C | A | 1 | a0001c0001t0001g0100 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.140+1465G>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31204332 | |||||||
| chr14:31204333 | A | C | 1 | a0001c0001t0001g0100 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.140+1464T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31204333 | |||||||
| chr14:31204460 | A | G | 63 | a0001c0002t0001g0335 a0001c0002t0001g0336 a0001c0002t0001g0337 others(60): Show |
63 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.140+1337T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31204460 | |||||||
| chr14:31204461 | TAAC | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.140+1333_140+1335d others(5): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31204461 | |||||||
| chr14:31204617 | G | C | 1 | a0001c0010t0004g0018 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.140+1180C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31204617 | |||||||
| chr14:31204661 | A | G | 2 | a0001c0017t0009g0020 a0001c0017t0009g0021 |
2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.140+1136T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31204661 | |||||||
| chr14:31204722 | T | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.140+1075A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31204722 | |||||||
| chr14:31204729 | A | G | 63 | a0001c0002t0001g0335 a0001c0002t0001g0336 a0001c0002t0001g0337 others(60): Show |
63 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.140+1068T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31204729 | |||||||
| chr14:31204788 | T | C | 63 | a0001c0002t0001g0335 a0001c0002t0001g0336 a0001c0002t0001g0337 others(60): Show |
63 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.140+1009A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31204788 | |||||||
| chr14:31204902 | A | C | 1 | a0001c0003t0001g0099 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.140+895T>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31204902 | |||||||
| chr14:31204916 | C | A | 1 | a0010c0032t0001g0087 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.140+881G>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31204916 | |||||||
| chr14:31205181 | TTC | T | 13 | a0001c0002t0001g0053 a0001c0002t0001g0054 a0001c0002t0001g0057 others(10): Show |
13 | HG00621.hp2 HG02080.hp2 NA18943.hp1 others(10): Show |
intron_variant | MODIFIER | c.140+614_140+615del others(2): Show |
HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31205181 | |||||||
| chr14:31205183 | C | A | 70 | a0001c0002t0001g0335 a0001c0002t0001g0336 a0001c0002t0013g0339 others(67): Show |
70 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.140+614G>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31205183 | |||||||
| chr14:31205256 | A | G | 13 | a0001c0004t0001g0088 a0001c0004t0001g0089 a0001c0004t0001g0097 others(10): Show |
13 | HG01106.hp1 HG02257.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.140+541T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31205256 | |||||||
| chr14:31205295 | C | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.140+502G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31205295 | |||||||
| chr14:31205383 | A | G | 36 | a0001c0002t0001g0053 a0001c0002t0001g0054 a0001c0002t0001g0057 others(33): Show |
36 | HG00621.hp2 HG01069.hp2 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.140+414T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31205383 | |||||||
| chr14:31205618 | C | T | 5 | a0001c0002t0001g0051 a0001c0011t0001g0047 a0001c0011t0001g0048 others(2): Show |
5 | HG02630.hp2 HG02809.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.140+179G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31205618 | |||||||
| chr14:31205703 | T | C | 1 | a0001c0018t0004g0019 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.140+94A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31205703 | |||||||
| chr14:31206310 | A | G | 1 | a0002c0005t0001g0046 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-21-353T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 1/42 | chr14 | 31206310 | |||||||
| chr14:31206414 | T | C | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.-21-457A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 1/42 | chr14 | 31206414 | |||||||
| chr14:31206627 | AT | A | 62 | a0001c0002t0001g0109 a0001c0002t0001g0111 a0001c0002t0001g0112 others(59): Show |
63 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.-22+388delA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 1/42 | chr14 | 31206627 | |||||||
| chr14:31206628 | T | A | 3 | a0001c0004t0001g0115 a0001c0007t0001g0027 a0001c0007t0001g0028 |
3 | HG00099.hp1 HG02698.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-22+388A>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 1/42 | chr14 | 31206628 | |||||||
| chr14:31206651 | C | T | 6 | a0001c0010t0004g0014 a0001c0010t0004g0015 a0001c0010t0004g0016 others(3): Show |
6 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.-22+365G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 1/42 | chr14 | 31206651 | |||||||
| chr14:31206884 | G | A | 1 | a0001c0001t0001g0338 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-22+132C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 1/42 | chr14 | 31206884 | |||||||
| chr14:31206991 | C | T | 21 | a0001c0004t0001g0001 a0001c0004t0001g0026 a0001c0004t0001g0034 others(18): Show |
22 | HG00099.hp1 HG00323.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.-22+25G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 1/42 | chr14 | 31206991 |