Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| 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 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and 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 | copy fasta | chr14 | 31095117 | 31212793 |
| a0002 | 0/0 | 2610 | 19 | 0 | 6 | 7 | 2 | 4 | 7 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0003 | 0/0 | 2610 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0004 | 0/0 | 2610 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0005 | 0/0 | 2610 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0006 | 0/0 | 2610 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0007 | 0/0 | 2610 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0008 | 0/0 | 2610 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0009 | 0/0 | 2610 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0010 | 0/0 | 2610 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 7833 | 114 | 25 | 23 | 45 | 6 | 14 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| c0002 | 0/0 | 7833 | 52 | 30 | 3 | 19 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| c0003 | 0/0 | 7833 | 37 | 3 | 5 | 17 | 1 | 11 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| c0004 | 0/0 | 7833 | 28 | 14 | 9 | 0 | 0 | 5 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| c0005 | 0/0 | 7833 | 18 | 0 | 6 | 7 | 1 | 4 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| c0006 | 0/0 | 7833 | 14 | 0 | 4 | 10 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| c0007 | 0/1 | 7833 | 14 | 0 | 6 | 0 | 4 | 3 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| c0008 | 0/0 | 7833 | 12 | 0 | 0 | 12 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| c0009 | 0/0 | 7833 | 8 | 0 | 0 | 8 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| c0010 | 0/0 | 7833 | 5 | 0 | 0 | 4 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| c0011 | 0/0 | 7833 | 4 | 4 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| c0012 | 0/0 | 7833 | 4 | 0 | 0 | 4 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| c0013 | 0/0 | 7833 | 3 | 0 | 1 | 2 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| c0014 | 0/0 | 7833 | 3 | 3 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| c0015 | 0/0 | 7833 | 2 | 0 | 0 | 0 | 0 | 2 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| c0016 | 0/0 | 7833 | 2 | 0 | 0 | 2 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| c0017 | 0/0 | 7833 | 2 | 2 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| c0018 | 0/0 | 7833 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| c0019 | 0/0 | 7833 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| c0020 | 0/0 | 7833 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| c0021 | 0/0 | 7833 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| c0022 | 0/0 | 7833 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| c0023 | 0/0 | 7833 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| c0024 | 0/0 | 7833 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| c0025 | 0/0 | 7833 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| c0026 | 0/0 | 7833 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| c0027 | 0/0 | 7833 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| c0028 | 0/0 | 7833 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| c0029 | 0/0 | 7833 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| c0030 | 0/0 | 7833 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| c0031 | 0/0 | 7833 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| c0032 | 0/0 | 7833 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| c0033 | 0/0 | 7833 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| c0034 | 0/0 | 7833 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| c0035 | 0/0 | 7833 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| c0036 | 0/0 | 7833 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| c0037 | 0/0 | 7833 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1613 | 295 | 76 | 52 | 116 | 12 | 37 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| t0002 | 0/0 | 1613 | 12 | 0 | 4 | 8 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| t0003 | 0/0 | 1613 | 8 | 0 | 0 | 8 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| t0004 | 0/0 | 1613 | 6 | 0 | 0 | 5 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| t0005 | 0/0 | 1613 | 5 | 4 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| t0006 | 0/0 | 1613 | 3 | 2 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| t0007 | 0/0 | 1613 | 3 | 0 | 1 | 0 | 2 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| t0008 | 0/0 | 1613 | 2 | 0 | 0 | 0 | 0 | 2 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| t0009 | 0/0 | 1613 | 2 | 2 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| t0010 | 0/0 | 1613 | 2 | 1 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| t0011 | 0/0 | 1613 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| t0012 | 0/0 | 1613 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| t0013 | 0/0 | 1613 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| t0014 | 0/0 | 1613 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0028 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0217 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 7833 | 114 | 25 | 23 | 45 | 6 | 14 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0002 | 0/0 | 7833 | 52 | 30 | 3 | 19 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0003 | 0/0 | 7833 | 37 | 3 | 5 | 17 | 1 | 11 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0004 | 0/0 | 7833 | 28 | 14 | 9 | 0 | 0 | 5 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0006 | 0/0 | 7833 | 14 | 0 | 4 | 10 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0007 | 0/1 | 7833 | 14 | 0 | 6 | 0 | 4 | 3 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0008 | 0/0 | 7833 | 12 | 0 | 0 | 12 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0009 | 0/0 | 7833 | 8 | 0 | 0 | 8 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0010 | 0/0 | 7833 | 5 | 0 | 0 | 4 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0011 | 0/0 | 7833 | 4 | 4 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0012 | 0/0 | 7833 | 4 | 0 | 0 | 4 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0013 | 0/0 | 7833 | 3 | 0 | 1 | 2 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0017 | 0/0 | 7833 | 2 | 2 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0018 | 0/0 | 7833 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0021 | 0/0 | 7833 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0022 | 0/0 | 7833 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0023 | 0/0 | 7833 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0025 | 0/0 | 7833 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0026 | 0/0 | 7833 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0029 | 0/0 | 7833 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0030 | 0/0 | 7833 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0031 | 0/0 | 7833 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0033 | 0/0 | 7833 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0034 | 0/0 | 7833 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0035 | 0/0 | 7833 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0036 | 0/0 | 7833 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0037 | 0/0 | 7833 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0002c0005 | 0/0 | 7833 | 18 | 0 | 6 | 7 | 1 | 4 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0002c0020 | 0/0 | 7833 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0003c0014 | 0/0 | 7833 | 3 | 3 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0004c0015 | 0/0 | 7833 | 2 | 0 | 0 | 0 | 0 | 2 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0005c0016 | 0/0 | 7833 | 2 | 0 | 0 | 2 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0006c0027 | 0/0 | 7833 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0007c0028 | 0/0 | 7833 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0008c0024 | 0/0 | 7833 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0009c0019 | 0/0 | 7833 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0010c0032 | 0/0 | 7833 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | 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 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0001t0002 | 0/0 | 9445 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0001t0012 | 0/0 | 9445 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0002t0001 | 0/0 | 9445 | 45 | 26 | 0 | 19 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0002t0006 | 0/0 | 9445 | 3 | 2 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0002t0010 | 0/0 | 9445 | 2 | 1 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0002t0013 | 0/0 | 9445 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0002t0014 | 0/0 | 9445 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0003t0001 | 0/0 | 9445 | 36 | 3 | 5 | 16 | 1 | 11 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0003t0011 | 0/0 | 9445 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0004t0001 | 0/0 | 9445 | 21 | 10 | 8 | 0 | 0 | 3 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0004t0005 | 0/0 | 9445 | 5 | 4 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0004t0008 | 0/0 | 9445 | 2 | 0 | 0 | 0 | 0 | 2 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0006t0001 | 0/0 | 9445 | 3 | 0 | 0 | 3 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0006t0002 | 0/0 | 9445 | 11 | 0 | 4 | 7 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0007t0001 | 0/1 | 9445 | 11 | 0 | 5 | 0 | 2 | 3 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0007t0007 | 0/0 | 9445 | 3 | 0 | 1 | 0 | 2 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0008t0001 | 0/0 | 9445 | 12 | 0 | 0 | 12 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0009t0003 | 0/0 | 9445 | 8 | 0 | 0 | 8 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0010t0004 | 0/0 | 9445 | 5 | 0 | 0 | 4 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0011t0001 | 0/0 | 9445 | 4 | 4 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0012t0001 | 0/0 | 9445 | 4 | 0 | 0 | 4 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0013t0001 | 0/0 | 9445 | 3 | 0 | 1 | 2 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0017t0009 | 0/0 | 9445 | 2 | 2 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0018t0004 | 0/0 | 9445 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0021t0001 | 0/0 | 9445 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0022t0001 | 0/0 | 9445 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0023t0001 | 0/0 | 9445 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0025t0001 | 0/0 | 9445 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0026t0001 | 0/0 | 9445 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0029t0001 | 0/0 | 9445 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0030t0001 | 0/0 | 9445 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0031t0001 | 0/0 | 9445 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0033t0001 | 0/0 | 9445 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0034t0001 | 0/0 | 9445 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0035t0001 | 0/0 | 9445 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0036t0001 | 0/0 | 9445 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0001c0037t0001 | 0/0 | 9445 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0002c0005t0001 | 0/0 | 9445 | 18 | 0 | 6 | 7 | 1 | 4 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0002c0020t0001 | 0/0 | 9445 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0003c0014t0001 | 0/0 | 9445 | 3 | 3 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0004c0015t0001 | 0/0 | 9445 | 2 | 0 | 0 | 0 | 0 | 2 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0005c0016t0001 | 0/0 | 9445 | 2 | 0 | 0 | 2 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0006c0027t0001 | 0/0 | 9445 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0007c0028t0001 | 0/0 | 9445 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0008c0024t0001 | 0/0 | 9445 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0009c0019t0001 | 0/0 | 9445 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| a0010c0032t0001 | 0/0 | 9445 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | copy fasta | chr14 | 31095117 | 31212793 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0217 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 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 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0001t0012g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0002t0001g0056 | 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 |
| a0001c0002t0001g0060 | 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 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0070 | 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 |
| a0001c0002t0001g0075 | 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 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0006g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0006g0021 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0002t0010g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0010g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0013g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0002t0014g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0003t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0003t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0003t0011g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0001g0033 | 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 |
| a0001c0004t0001g0035 | 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 |
| a0001c0004t0001g0064 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0004t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0005g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0005g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0005g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0005g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0005g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0008g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0004t0008g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0006t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0006t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0006t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0006t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0006t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0006t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0006t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0006t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0006t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0006t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0006t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0006t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0006t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0006t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0007t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0007t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0007t0001g0028 | 0/1 | 1 | 0 | 0 | 0 | 0 | 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 |
| a0001c0007t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 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 |
| a0001c0007t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0007t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0007t0007g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0007t0007g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0007t0007g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0008t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0008t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0008t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0008t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0008t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0008t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0008t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0008t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0008t0001g0278 | 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 |
| a0001c0008t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0008t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0009t0003g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0009t0003g0002 | 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 |
| a0001c0010t0004g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0010t0004g0013 | 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 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0011t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 |
| a0001c0012t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0012t0001g0054 | 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 |
| a0001c0012t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0013t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0013t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0013t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0017t0009g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0017t0009g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0018t0004g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0021t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0022t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0023t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0025t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0026t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0029t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0030t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0031t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0033t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0034t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0001c0035t0001g0063 | 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 |
| a0001c0037t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0002c0005t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0002c0005t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0002c0005t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0002c0005t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0002c0005t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0002c0005t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0002c0005t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0002c0005t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0002c0005t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0002c0005t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0002c0005t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0002c0005t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0002c0005t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0002c0005t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0002c0005t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0002c0005t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0002c0005t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0002c0005t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0002c0020t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0003c0014t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 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 |
| a0004c0015t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0005c0016t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0005c0016t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0006c0027t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0007c0028t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0008c0024t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0009c0019t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| a0010c0032t0001g0086 | 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 | g0045 | EUR | GBR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0126 | EUR | GBR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00140 | hp1 | a0001 | c0003 | t0001 | g0250 | EUR | GBR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00140 | hp2 | a0002 | c0005 | t0001 | g0331 | EUR | GBR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0133 | EUR | FIN | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00280 | hp2 | a0002 | c0020 | t0001 | g0234 | EUR | FIN | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00323 | hp1 | a0001 | c0007 | t0007 | g0026 | EUR | FIN | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0224 | EUR | FIN | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00423 | hp2 | a0001 | c0003 | t0001 | g0247 | EAS | CHS | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00544 | hp2 | a0001 | c0008 | t0001 | g0266 | EAS | CHS | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00558 | hp1 | a0001 | c0009 | t0003 | g0004 | EAS | CHS | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00609 | hp2 | a0001 | c0009 | t0003 | g0003 | EAS | CHS | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00621 | hp2 | a0001 | c0035 | t0001 | g0063 | EAS | CHS | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00639 | hp2 | a0001 | c0002 | t0006 | g0021 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00673 | hp1 | a0001 | c0034 | t0001 | g0269 | EAS | CHS | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00733 | hp1 | a0002 | c0005 | t0001 | g0335 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0202 | 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 | g0209 | 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 | g0032 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01069 | hp2 | a0001 | c0004 | t0001 | g0066 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01071 | hp2 | a0001 | c0004 | t0001 | g0067 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01074 | hp1 | a0001 | c0007 | t0001 | g0029 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01074 | hp2 | a0001 | c0006 | t0002 | g0193 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01081 | hp2 | a0001 | c0003 | t0001 | g0236 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01099 | hp1 | a0001 | c0013 | t0001 | g0111 | 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 | g0300 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01109 | hp1 | a0001 | c0029 | t0001 | g0285 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01109 | hp2 | a0001 | c0002 | t0013 | g0341 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01168 | hp2 | a0002 | c0005 | t0001 | g0332 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01175 | hp2 | a0001 | c0003 | t0001 | g0286 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01192 | hp2 | a0001 | c0003 | t0001 | g0257 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01243 | hp1 | a0001 | c0003 | t0001 | g0276 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01243 | hp2 | a0002 | c0005 | t0001 | g0336 | AMR | PUR | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01255 | hp1 | a0001 | c0001 | t0012 | g0160 | AMR | CLM | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01255 | hp2 | a0001 | c0007 | t0001 | g0023 | AMR | CLM | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01256 | hp1 | a0001 | c0007 | t0007 | g0031 | AMR | CLM | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01261 | hp2 | a0001 | c0004 | t0001 | g0064 | AMR | CLM | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01346 | hp2 | a0001 | c0003 | t0001 | g0271 | AMR | CLM | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01358 | hp1 | a0002 | c0005 | t0001 | g0326 | AMR | CLM | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0181 | 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 | g0226 | AMR | CLM | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01496 | hp2 | a0001 | c0037 | t0001 | g0322 | AMR | CLM | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0218 | EUR | IBS | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01516 | hp2 | a0001 | c0007 | t0007 | g0030 | EUR | IBS | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0094 | AFR | ACB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0310 | AFR | ACB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01891 | hp2 | a0001 | c0004 | t0001 | g0025 | AFR | ACB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01928 | hp1 | a0002 | c0005 | t0001 | g0323 | AMR | PEL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01928 | hp2 | a0001 | c0004 | t0001 | g0077 | AMR | PEL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01943 | hp1 | a0008 | c0024 | t0001 | g0073 | AMR | PEL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01952 | hp1 | a0001 | c0030 | t0001 | g0238 | AMR | PEL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01952 | hp2 | a0001 | c0006 | t0002 | g0287 | AMR | PEL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01975 | hp1 | a0001 | c0004 | t0001 | g0079 | AMR | PEL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01993 | hp2 | a0001 | c0002 | t0010 | g0096 | AMR | PEL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02015 | hp1 | a0001 | c0003 | t0001 | g0248 | EAS | KHV | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0320 | AFR | ACB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | ACB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02056 | hp2 | a0001 | c0003 | t0001 | g0291 | EAS | KHV | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02071 | hp1 | a0001 | c0023 | t0001 | g0161 | EAS | KHV | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02071 | hp2 | a0001 | c0009 | t0003 | g0006 | EAS | KHV | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02074 | hp1 | a0001 | c0010 | t0004 | g0012 | EAS | KHV | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0078 | EAS | KHV | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02080 | hp1 | a0001 | c0003 | t0001 | g0270 | EAS | KHV | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0062 | EAS | KHV | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | KHV | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02083 | hp2 | a0001 | c0006 | t0001 | g0130 | EAS | KHV | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02129 | hp1 | a0001 | c0003 | t0001 | g0274 | EAS | KHV | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | KHV | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02145 | hp1 | a0003 | c0014 | t0001 | g0080 | AFR | ACB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02155 | hp1 | a0001 | c0033 | t0001 | g0277 | EAS | CDX | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02155 | hp2 | a0001 | c0009 | t0003 | g0001 | EAS | CDX | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0317 | AFR | ACB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02257 | hp2 | a0001 | c0025 | t0001 | g0299 | AFR | ACB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02258 | hp1 | a0001 | c0002 | t0006 | g0022 | AFR | ACB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02273 | hp1 | a0001 | c0006 | t0002 | g0207 | AMR | PEL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0318 | AFR | ACB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02280 | hp2 | a0001 | c0017 | t0009 | g0018 | AFR | ACB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02300 | hp1 | a0001 | c0006 | t0002 | g0192 | AMR | PEL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02300 | hp2 | a0001 | c0004 | t0001 | g0065 | AMR | PEL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02451 | hp2 | a0007 | c0028 | t0001 | g0069 | AFR | ACB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02572 | hp1 | a0001 | c0021 | t0001 | g0212 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02572 | hp2 | a0001 | c0004 | t0005 | g0302 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02602 | hp1 | a0001 | c0003 | t0001 | g0263 | SAS | PJL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02602 | hp2 | a0002 | c0005 | t0001 | g0324 | SAS | PJL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0313 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0093 | 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 | g0314 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02683 | hp1 | a0001 | c0004 | t0001 | g0087 | SAS | PJL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02698 | hp1 | a0001 | c0003 | t0001 | g0240 | SAS | PJL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02698 | hp2 | a0001 | c0007 | t0001 | g0044 | SAS | PJL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0085 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02809 | hp1 | a0001 | c0011 | t0001 | g0047 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0084 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02818 | hp1 | a0001 | c0002 | t0014 | g0342 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0308 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0092 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0091 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02922 | hp1 | a0001 | c0011 | t0001 | g0046 | AFR | ESN | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ESN | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0315 | AFR | ESN | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02965 | hp2 | a0001 | c0004 | t0001 | g0027 | AFR | ESN | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02970 | hp1 | a0001 | c0017 | t0009 | g0019 | AFR | ESN | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02970 | hp2 | a0001 | c0004 | t0001 | g0034 | AFR | ESN | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03017 | hp2 | a0001 | c0003 | t0001 | g0262 | SAS | PJL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03041 | hp1 | a0001 | c0002 | t0010 | g0095 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03041 | hp2 | a0001 | c0011 | t0001 | g0048 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | MSL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0090 | AFR | MSL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0316 | AFR | ESN | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03130 | hp2 | a0001 | c0026 | t0001 | g0298 | AFR | ESN | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0312 | AFR | ESN | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ESN | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0319 | AFR | ESN | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0293 | AFR | ESN | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0235 | AFR | MSL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03209 | hp2 | a0001 | c0004 | t0005 | g0301 | AFR | MSL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03225 | hp2 | a0001 | c0004 | t0001 | g0296 | AFR | MSL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03239 | hp1 | a0001 | c0003 | t0001 | g0259 | SAS | PJL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | MSL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0233 | AFR | MSL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | MSL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03490 | hp2 | a0004 | c0015 | t0001 | g0144 | SAS | PJL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03492 | hp2 | a0004 | c0015 | t0001 | g0125 | SAS | PJL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03516 | hp1 | a0003 | c0014 | t0001 | g0081 | AFR | ESN | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | ESN | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03540 | hp1 | a0001 | c0002 | t0006 | g0020 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03540 | hp2 | a0006 | c0027 | t0001 | g0307 | AFR | GWD | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | MSL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03579 | hp2 | a0001 | c0004 | t0005 | g0303 | AFR | MSL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03654 | hp1 | a0001 | c0003 | t0001 | g0280 | SAS | PJL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0145 | 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 | g0137 | SAS | PJL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03704 | hp1 | a0001 | c0004 | t0008 | g0010 | SAS | PJL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03704 | hp2 | a0002 | c0005 | t0001 | g0337 | SAS | PJL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03710 | hp2 | a0001 | c0003 | t0001 | g0273 | SAS | PJL | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03831 | hp1 | a0002 | c0005 | t0001 | g0334 | SAS | BEB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0205 | 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 | g0260 | SAS | BEB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | BEB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03927 | hp2 | a0001 | c0004 | t0001 | g0305 | SAS | BEB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | BEB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG03942 | hp2 | a0001 | c0010 | t0004 | g0016 | SAS | BEB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | STU | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG04115 | hp2 | a0001 | c0003 | t0001 | g0282 | SAS | STU | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG04184 | hp1 | a0001 | c0003 | t0001 | g0258 | SAS | BEB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG04184 | hp2 | a0001 | c0004 | t0008 | g0011 | SAS | BEB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | STU | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG04199 | hp2 | a0001 | c0003 | t0001 | g0252 | SAS | STU | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG04204 | hp1 | a0001 | c0004 | t0001 | g0304 | SAS | STU | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG04204 | hp2 | a0002 | c0005 | t0001 | g0325 | SAS | STU | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CHB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0071 | 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 | g0183 | AFR | YRI | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18939 | hp1 | a0001 | c0003 | t0001 | g0253 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18943 | hp1 | a0001 | c0012 | t0001 | g0059 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18943 | hp2 | a0001 | c0006 | t0002 | g0170 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18946 | hp1 | a0001 | c0008 | t0001 | g0245 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18947 | hp1 | a0001 | c0003 | t0001 | g0279 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18947 | hp2 | a0001 | c0006 | t0002 | g0215 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18948 | hp1 | a0001 | c0003 | t0001 | g0246 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18953 | hp2 | a0001 | c0003 | t0001 | g0261 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18954 | hp2 | a0001 | c0003 | t0001 | g0267 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18956 | hp2 | a0001 | c0008 | t0001 | g0284 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18957 | hp1 | a0001 | c0012 | t0001 | g0054 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18957 | hp2 | a0001 | c0006 | t0001 | g0244 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18961 | hp2 | a0001 | c0022 | t0001 | g0242 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18966 | hp1 | a0001 | c0012 | t0001 | g0055 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18968 | hp1 | a0001 | c0003 | t0001 | g0292 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18968 | hp2 | a0001 | c0012 | t0001 | g0051 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18969 | hp1 | a0001 | c0013 | t0001 | g0164 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18969 | hp2 | a0001 | c0008 | t0001 | g0268 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18970 | hp2 | a0002 | c0005 | t0001 | g0328 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18971 | hp1 | a0001 | c0010 | t0004 | g0013 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18975 | hp1 | a0001 | c0003 | t0011 | g0009 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18977 | hp2 | a0001 | c0008 | t0001 | g0278 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18982 | hp1 | a0001 | c0009 | t0003 | g0008 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18987 | hp1 | a0001 | c0003 | t0001 | g0272 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18987 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18992 | hp1 | a0001 | c0018 | t0004 | g0017 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18994 | hp1 | a0001 | c0003 | t0001 | g0288 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18994 | hp2 | a0001 | c0006 | t0002 | g0214 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18995 | hp1 | a0001 | c0008 | t0001 | g0283 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18999 | hp1 | a0002 | c0005 | t0001 | g0327 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA18999 | hp2 | a0001 | c0006 | t0001 | g0281 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19000 | hp2 | a0001 | c0008 | t0001 | g0239 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19001 | hp1 | a0002 | c0005 | t0001 | g0338 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19002 | hp2 | a0001 | c0008 | t0001 | g0289 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19005 | hp2 | a0002 | c0005 | t0001 | g0330 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19006 | hp1 | a0002 | c0005 | t0001 | g0295 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19009 | hp1 | a0001 | c0006 | t0002 | g0175 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19011 | hp2 | a0001 | c0008 | t0001 | g0264 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19012 | hp1 | a0001 | c0013 | t0001 | g0148 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19012 | hp2 | a0001 | c0003 | t0001 | g0254 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19043 | hp1 | a0001 | c0003 | t0001 | g0275 | AFR | LWK | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19043 | hp2 | a0001 | c0004 | t0005 | g0297 | AFR | LWK | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19055 | hp1 | a0001 | c0008 | t0001 | g0241 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19055 | hp2 | a0001 | c0009 | t0003 | g0007 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19057 | hp1 | a0001 | c0010 | t0004 | g0015 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19062 | hp1 | a0001 | c0003 | t0001 | g0290 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19065 | hp1 | a0001 | c0008 | t0001 | g0265 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19065 | hp2 | a0001 | c0006 | t0002 | g0146 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19067 | hp1 | a0009 | c0019 | t0001 | g0194 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19067 | hp2 | a0001 | c0006 | t0002 | g0190 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19068 | hp1 | a0001 | c0008 | t0001 | g0237 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19074 | hp2 | a0001 | c0009 | t0003 | g0005 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19075 | hp2 | a0001 | c0010 | t0004 | g0014 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19076 | hp1 | a0010 | c0032 | t0001 | g0086 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19076 | hp2 | a0001 | c0006 | t0002 | g0106 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19077 | hp2 | a0001 | c0009 | t0003 | g0002 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19078 | hp1 | a0005 | c0016 | t0001 | g0118 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19078 | hp2 | a0002 | c0005 | t0001 | g0333 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19082 | hp1 | a0001 | c0003 | t0001 | g0243 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19082 | hp2 | a0005 | c0016 | t0001 | g0115 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19087 | hp1 | a0002 | c0005 | t0001 | g0321 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | YRI | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0311 | AFR | YRI | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA20129 | hp1 | a0001 | c0003 | t0001 | g0249 | AFR | ASW | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA20129 | hp2 | a0001 | c0003 | t0001 | g0256 | AFR | ASW | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA20752 | hp1 | a0001 | c0007 | t0001 | g0024 | EUR | TSI | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0219 | EUR | TSI | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0155 | EUR | TSI | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA20805 | hp2 | a0001 | c0031 | t0001 | g0251 | EUR | TSI | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | GIH | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA20905 | hp2 | a0001 | c0003 | t0001 | g0255 | SAS | GIH | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01123 | hp1 | a0001 | c0004 | t0001 | g0074 | AMR | CLM | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG01123 | hp2 | a0002 | c0005 | t0001 | g0329 | AMR | CLM | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0294 | AFR | ACB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0309 | 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 | g0082 | AFR | ACB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02559 | hp1 | a0001 | c0004 | t0001 | g0035 | AFR | ACB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0306 | AFR | ACB | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG06807 | hp1 | a0001 | c0004 | t0001 | g0033 | AFR | USA | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0050 | AFR | USA | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA20300 | hp1 | a0001 | c0004 | t0001 | g0072 | AFR | USA | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0340 | AFR | USA | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA21309 | hp1 | a0001 | c0004 | t0001 | g0339 | AFR | LWK | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | LWK | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0007 | t0001 | g0028 | REF | REF | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0217 | REF | REF | HECTD1_chr14_31095117_31212793 | HECTD1 | chr14 | 31095117 | 31212793 |
| 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 | a0008 | 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 | a0006 | 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 |
| 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 | a0001c0002a0001c0003a0001c0008others(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 | a0001c0002a0001c0003a0001c0004others(25): Show | 203 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(200): 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 | a0001c0008a0001c0030a0001c0033others(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 | a0001c0003a0001c0008a0001c0029others(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 | a0001c0011a0001c0026 | 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 | a0001c0002a0001c0003a0001c0008others(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 | a0001c0010a0001c0018 | 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 | a0001c0012a0001c0035 | 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 | a0001c0002a0001c0003a0001c0004others(25): Show | 216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): 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 | a0001c0010a0001c0018 | 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 | a0001c0007a0001c0036 | 15 | HG00099.hp1 HG00323.hp1 HG00738.hp2 others(12): 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 | a0001c0037a0002c0005 | 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 |
| 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 | a0001c0001t0002a0001c0006t0002 | 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 | a0001c0010t0004a0001c0018t0004 | 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 | a0001c0010t0004a0001c0018t0004 | 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 | a0001c0002t0013a0001c0002t0014 | 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 |
| 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 | a0001c0001t0001g0127 | 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 | a0001c0010t0004g0016 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0006g0022 | 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 | a0001c0001t0001g0105 | 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 | a0001c0002t0010g0095a0001c0002t0010g0096 | 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 | a0004c0015t0001g0125a0004c0015t0001g0144 | 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 | a0010c0032t0001g0086 | 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 | a0001c0009t0003g0001a0001c0009t0003g0002a0001c0009t0003g0003others(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 | a0001c0006t0002g0106a0001c0006t0002g0146a0001c0006t0002g0175 | 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 | a0001c0002t0001g0294 | 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 | a0001c0002t0006g0020a0001c0002t0006g0021a0001c0002t0006g0022 | 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 | a0001c0008t0001g0245 | 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 | a0001c0002t0013g0341a0001c0002t0014g0342 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | 100 | a0001c0001t0001g0088a0001c0001t0001g0128a0001c0001t0001g0152others(97): 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 | a0001c0002t0001g0075a0001c0002t0001g0090a0001c0003t0001g0254others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0001t0001g0151a0001c0001t0001g0196 | 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 | a0001c0001t0001g0188a0001c0002t0001g0050a0001c0002t0001g0052others(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 | 62 | a0001c0004t0001g0025a0001c0004t0001g0027a0001c0004t0001g0033others(59): Show | 62 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(59): 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0029t0001g0285 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0003c0014t0001g0080a0003c0014t0001g0081a0003c0014t0001g0082 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0009t0003g0001a0001c0009t0003g0002a0001c0009t0003g0003others(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 | a0001c0004t0001g0339 | 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 | a0001c0004t0001g0339 | 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 | a0001c0004t0001g0339 | 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 | a0001c0001t0001g0203 | 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 | a0003c0014t0001g0080a0003c0014t0001g0081a0003c0014t0001g0082 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0013g0341a0001c0002t0014g0342 | 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 | a0001c0002t0001g0294 | 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 | a0001c0002t0001g0235 | 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 | a0001c0002t0010g0095a0001c0002t0010g0096 | 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 | a0001c0002t0001g0050a0001c0003t0001g0252a0001c0003t0001g0260others(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 | a0001c0004t0008g0010a0001c0004t0008g0011 | 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 | a0001c0008t0001g0239a0001c0008t0001g0241a0001c0008t0001g0245others(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 | a0001c0010t0004g0016 | 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 | a0001c0002t0001g0235a0001c0002t0001g0293a0001c0002t0001g0294 | 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 | 202 | a0001c0002t0001g0050a0001c0002t0001g0052a0001c0002t0001g0053others(199): Show | 202 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(199): 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 | a0001c0001t0001g0112a0001c0001t0001g0119a0001c0001t0001g0157others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0001g0306a0001c0002t0001g0308a0001c0002t0001g0309others(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 | a0001c0008t0001g0241 | 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 | a0001c0017t0009g0018a0001c0017t0009g0019 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0007t0001g0029 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0004t0001g0339 | 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 | a0001c0001t0001g0181 | 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 | a0001c0004t0001g0339 | 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 | a0001c0002t0010g0095a0001c0002t0010g0096 | 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 | a0001c0002t0001g0306a0001c0002t0001g0309a0001c0002t0001g0310 | 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 | a0001c0002t0006g0022 | 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 | a0007c0028t0001g0069 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0003t0001g0254 | 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 | a0001c0017t0009g0018 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0006t0002g0215 | 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 | a0001c0004t0008g0010a0001c0004t0008g0011 | 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 | 204 | a0001c0002t0001g0050a0001c0002t0001g0052a0001c0002t0001g0053others(201): Show | 204 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(201): 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0001g0308 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | 24 | a0001c0004t0001g0064a0001c0004t0001g0065a0001c0004t0001g0066others(21): Show | 24 | HG00099.hp1 HG00323.hp1 HG00738.hp2 others(21): 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0001t0001g0152a0001c0001t0001g0180a0001c0001t0001g0181others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0003t0001g0243a0001c0004t0005g0302a0001c0009t0003g0001others(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 | 204 | a0001c0002t0001g0050a0001c0002t0001g0052a0001c0002t0001g0053others(201): Show | 204 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(201): 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 | a0001c0004t0001g0305 | 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 | a0001c0002t0001g0233a0001c0002t0001g0312a0001c0002t0001g0313others(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 | a0001c0001t0001g0104a0001c0001t0001g0121a0001c0001t0001g0220 | 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 | a0001c0002t0001g0306 | 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 | a0008c0024t0001g0073 | 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 | a0001c0002t0006g0020 | 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 | a0001c0009t0003g0003a0001c0009t0003g0004a0001c0009t0003g0005others(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 | a0001c0001t0001g0201 | 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 | 32 | a0001c0004t0001g0025a0001c0004t0001g0027a0001c0004t0001g0033others(29): Show | 32 | HG00099.hp1 HG00323.hp1 HG00738.hp2 others(29): 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 | a0001c0003t0001g0240 | 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 | a0001c0003t0001g0271 | 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 | a0001c0002t0001g0091a0001c0002t0001g0092 | 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 | a0001c0002t0001g0052a0001c0002t0001g0053a0001c0002t0001g0056others(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 | a0001c0009t0003g0001a0001c0009t0003g0002a0001c0009t0003g0003others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0001t0002g0173 | 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 | a0001c0001t0001g0128a0001c0001t0001g0223a0001c0002t0001g0235others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0004t0001g0339 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0001g0235a0001c0002t0001g0293a0001c0002t0001g0294 | 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 | a0001c0002t0006g0020 | 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 | a0001c0002t0013g0341a0001c0002t0014g0342 | 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 | a0001c0002t0001g0057a0001c0002t0001g0058 | 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 | a0003c0014t0001g0080a0003c0014t0001g0081a0003c0014t0001g0082 | 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 | a0001c0003t0001g0243 | 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 | a0001c0003t0001g0280 | 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 | a0001c0002t0001g0293 | 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 | a0001c0017t0009g0019 | 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 | a0001c0007t0001g0032a0001c0007t0001g0039 | 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 | a0002c0005t0001g0323 | 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 | a0007c0028t0001g0069 | 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 | a0001c0004t0001g0087a0001c0004t0001g0296a0001c0004t0001g0304others(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 | a0001c0002t0001g0052a0001c0002t0001g0053a0001c0002t0001g0056others(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 | a0001c0002t0001g0091a0001c0002t0001g0092a0001c0002t0001g0093others(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 | a0001c0001t0001g0174a0001c0001t0001g0227a0001c0002t0001g0050others(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 | a0001c0001t0001g0116 | 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 | a0001c0001t0001g0105 | 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 | a0003c0014t0001g0080a0003c0014t0001g0081a0003c0014t0001g0082 | 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 | a0010c0032t0001g0086 | 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 | a0001c0004t0008g0011 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0002c0005t0001g0324a0002c0005t0001g0325a0002c0020t0001g0234 | 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 | a0010c0032t0001g0086 | 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 | a0010c0032t0001g0086 | 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 | a0010c0032t0001g0086 | 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 | a0001c0002t0001g0294 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0001g0233a0001c0002t0001g0312a0001c0002t0001g0313others(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 | a0010c0032t0001g0086 | 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 | a0001c0002t0001g0233a0001c0002t0001g0312a0001c0002t0001g0313others(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 | a0001c0002t0006g0020a0001c0002t0006g0021a0001c0002t0006g0022 | 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 | a0001c0003t0001g0248 | 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 | a0003c0014t0001g0080a0003c0014t0001g0081a0003c0014t0001g0082 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | 205 | a0001c0001t0001g0097a0001c0002t0001g0050a0001c0002t0001g0052others(202): Show | 205 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(202): 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 | a0001c0002t0001g0050a0001c0002t0001g0052a0001c0002t0001g0053others(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 | a0001c0002t0001g0090 | 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 | a0001c0001t0001g0177a0009c0019t0001g0194 | 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 | a0001c0002t0010g0095a0001c0002t0010g0096a0001c0017t0009g0018others(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 | a0001c0001t0001g0119 | 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 | a0001c0002t0013g0341a0001c0002t0014g0342 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0010g0095a0001c0002t0010g0096a0001c0017t0009g0018others(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 | a0001c0003t0001g0263 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0001g0233a0001c0002t0001g0312a0001c0002t0001g0313others(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 | 65 | a0001c0004t0001g0025a0001c0004t0001g0027a0001c0004t0001g0033others(62): Show | 65 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(62): 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 | a0001c0004t0001g0087a0001c0004t0001g0296a0001c0004t0001g0304others(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 | a0001c0001t0001g0126 | 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 | a0001c0002t0001g0052a0001c0002t0001g0053a0001c0002t0001g0056others(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 | a0001c0006t0002g0207 | 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 | a0001c0025t0001g0299 | 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 | a0001c0001t0001g0089 | 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 | a0001c0011t0001g0046a0001c0011t0001g0047a0001c0011t0001g0048others(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 | a0001c0004t0005g0297a0001c0004t0005g0300a0001c0004t0005g0301others(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 | a0001c0003t0001g0240 | 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 | a0001c0001t0001g0134 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0004t0001g0087 | 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 | a0001c0001t0001g0139 | 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 | a0001c0004t0001g0025 | 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 | a0001c0004t0001g0025 | 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 | a0001c0002t0001g0091a0001c0002t0001g0092a0001c0002t0001g0093others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0001g0091a0001c0002t0001g0092a0001c0002t0001g0093others(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 | a0001c0017t0009g0018 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0001g0068a0001c0002t0001g0075a0001c0002t0001g0076others(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 | a0001c0002t0010g0095a0001c0002t0010g0096a0001c0017t0009g0018others(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 | a0001c0009t0003g0003a0001c0009t0003g0004a0001c0009t0003g0005others(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 | a0001c0001t0001g0209 | 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 | 50 | a0001c0004t0001g0025a0001c0004t0001g0027a0001c0004t0001g0033others(47): Show | 50 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(47): 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 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0119others(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 | a0001c0001t0001g0132a0001c0004t0001g0033a0001c0004t0001g0072others(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 | 54 | a0001c0004t0001g0025a0001c0004t0001g0027a0001c0004t0001g0034others(51): Show | 54 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(51): 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 | a0001c0002t0001g0075a0001c0002t0001g0078a0001c0002t0001g0090others(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 | a0001c0002t0001g0050a0001c0002t0001g0052a0001c0002t0001g0053others(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 | a0001c0002t0006g0020a0001c0003t0001g0236a0001c0003t0001g0240others(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 | a0001c0001t0001g0159 | 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 | a0001c0002t0001g0091a0001c0002t0001g0092a0001c0002t0001g0093others(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 | a0001c0004t0001g0033a0001c0004t0001g0072a0001c0007t0001g0036others(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 | 39 | a0001c0004t0001g0025a0001c0004t0001g0027a0001c0004t0001g0034others(36): Show | 39 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(36): 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 | a0001c0002t0013g0341a0001c0007t0007g0031 | 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 | a0001c0002t0014g0342 | 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 | a0001c0002t0001g0050a0001c0002t0001g0052a0001c0002t0001g0053others(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 | a0002c0005t0001g0336 | 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 | a0001c0003t0001g0288 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0010g0095a0001c0002t0010g0096a0001c0017t0009g0018others(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 | a0001c0002t0006g0022 | 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 | a0001c0002t0001g0068a0001c0002t0001g0075a0001c0002t0001g0076others(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 | a0001c0002t0006g0020 | 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 | a0001c0002t0001g0235a0001c0002t0001g0293a0001c0002t0001g0294 | 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 | a0001c0003t0001g0282 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0009t0003g0001a0001c0009t0003g0002a0001c0009t0003g0003others(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 | 52 | a0001c0004t0001g0025a0001c0004t0001g0027a0001c0004t0001g0033others(49): Show | 52 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(49): 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 | a0001c0002t0010g0095a0001c0002t0010g0096a0001c0017t0009g0018others(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 | a0003c0014t0001g0080a0003c0014t0001g0081a0003c0014t0001g0082 | 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 | a0001c0001t0001g0157 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.5239-447C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 28/42 | chr14 | 31120313 | ||||||
| chr14:31120427
|
C | A | 1 | a0001c0007t0001g0028 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.5239-561G>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 28/42 | chr14 | 31120427 | ||||||
| chr14:31120541
|
A | C | 6 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0025t0001g0299 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0001t0001g0122a0001c0001t0001g0153a0001c0001t0001g0191 | 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 | a0001c0002t0010g0095a0001c0002t0010g0096a0001c0017t0009g0018others(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 | a0001c0002t0001g0090 | 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 | a0001c0002t0001g0233a0001c0002t0001g0312a0001c0002t0001g0313others(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 | a0001c0002t0013g0341a0001c0002t0014g0342 | 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 | a0001c0002t0001g0061 | 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 | a0001c0002t0001g0293 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0001g0235a0001c0002t0001g0293a0001c0002t0001g0294 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0012t0001g0055a0001c0012t0001g0059 | 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 | a0001c0001t0001g0120 | 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 | a0001c0009t0003g0001a0001c0009t0003g0002a0001c0009t0003g0003others(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 | a0001c0001t0001g0132a0001c0010t0004g0012a0001c0010t0004g0013others(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 | a0001c0002t0001g0050a0001c0002t0001g0052a0001c0002t0001g0053others(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 | a0001c0002t0001g0050a0001c0002t0001g0052a0001c0002t0001g0053others(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 | a0001c0017t0009g0018a0001c0017t0009g0019 | 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 | a0001c0002t0001g0233a0001c0002t0001g0235a0001c0002t0001g0293others(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 | a0001c0001t0001g0168a0001c0002t0001g0052a0001c0002t0001g0058others(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 | a0001c0002t0001g0308a0001c0003t0001g0270a0002c0005t0001g0336 | 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 | 33 | a0001c0003t0001g0249a0001c0004t0001g0025a0001c0004t0001g0027others(30): 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 |
20 | a0001c0004t0001g0077a0001c0007t0001g0028a0001c0010t0004g0016others(17): Show | 20 | HG00140.hp2 HG00280.hp2 HG01168.hp2 others(17): 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0001g0233a0001c0002t0001g0235a0001c0002t0001g0293others(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 | a0001c0002t0006g0020a0001c0002t0006g0021a0001c0002t0006g0022 | 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 | a0001c0002t0001g0053a0001c0002t0001g0056a0001c0002t0001g0057others(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 | a0001c0002t0001g0235a0001c0002t0001g0293a0001c0002t0001g0294 | 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 | a0001c0002t0001g0294 | 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 | a0001c0004t0005g0297a0001c0004t0005g0301a0001c0004t0005g0302 | 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 | 153 | a0001c0001t0001g0088a0001c0002t0001g0052a0001c0002t0001g0053others(150): Show | 153 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(150): 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 | a0001c0002t0006g0020a0001c0007t0001g0044a0001c0007t0001g0045others(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 | a0001c0002t0001g0235a0001c0002t0001g0293a0001c0002t0001g0294 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0003c0014t0001g0080a0003c0014t0001g0081a0003c0014t0001g0082 | 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 | 202 | a0001c0002t0001g0050a0001c0002t0001g0052a0001c0002t0001g0053others(199): Show | 202 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(199): 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 | a0001c0002t0001g0235a0001c0002t0001g0293a0001c0002t0001g0294 | 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 | ||||||
| chr14:31122638
|
AG | A | 341 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0097others(338): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.5115+275delC | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 27/42 | chr14 | 31122638 | ||||||
| chr14:31122709
|
A | T | 6 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0001g0091a0001c0002t0001g0092a0001c0002t0001g0093others(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 | a0001c0002t0001g0091a0001c0002t0001g0092a0001c0002t0001g0093 | 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 | a0001c0007t0001g0044a0001c0007t0001g0045 | 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 | a0001c0001t0001g0171 | 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 | a0001c0002t0001g0235a0001c0002t0001g0293a0001c0002t0001g0294 | 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 | a0001c0003t0001g0247 | 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 | a0001c0009t0003g0002a0001c0009t0003g0008 | 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 | a0001c0003t0001g0254 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0003c0014t0001g0080a0003c0014t0001g0081a0003c0014t0001g0082 | 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 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0222others(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 | a0001c0003t0001g0243a0001c0003t0001g0246a0001c0003t0001g0253others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0001t0001g0179 | 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 | a0001c0006t0002g0190a0001c0006t0002g0214a0001c0006t0002g0215 | 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 | a0001c0025t0001g0299 | 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 | a0001c0002t0001g0235a0001c0002t0001g0293a0001c0002t0001g0294 | 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 | a0001c0003t0001g0256a0001c0003t0001g0263a0001c0003t0001g0271 | 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 | a0001c0002t0010g0095a0001c0002t0010g0096 | 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 | a0001c0002t0001g0306a0001c0002t0001g0309a0001c0002t0001g0310 | 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 | 181 | a0001c0001t0001g0140a0001c0002t0001g0050a0001c0002t0001g0052others(178): Show | 181 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.4982-1763delA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31124809 | ||||||
| chr14:31124809
|
ATT | A | 9 | a0001c0002t0001g0235a0001c0002t0001g0293a0001c0002t0001g0294others(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 | a0001c0009t0003g0001a0001c0009t0003g0002a0001c0009t0003g0003others(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 | a0001c0002t0010g0095a0001c0002t0010g0096 | 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 | a0001c0001t0001g0205 | 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 | 51 | a0001c0004t0001g0025a0001c0004t0001g0027a0001c0004t0001g0033others(48): Show | 51 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(48): 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 | a0001c0001t0001g0119a0001c0001t0001g0162a0001c0001t0001g0199others(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 | a0001c0001t0001g0138a0001c0001t0001g0218a0001c0001t0001g0224others(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 | a0001c0023t0001g0161 | 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 | a0001c0002t0001g0050a0001c0002t0001g0052a0001c0002t0001g0053others(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 | a0001c0004t0001g0087a0001c0004t0001g0296a0001c0004t0001g0304others(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 | a0001c0004t0001g0087 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0001t0001g0178 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4981+2225C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31125560 | ||||||
| chr14:31125693
|
C | T | 341 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0097others(338): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.4981+2092G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 26/42 | chr14 | 31125693 | ||||||
| chr14:31125789
|
A | G | 8 | a0001c0009t0003g0001a0001c0009t0003g0002a0001c0009t0003g0003others(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 | a0001c0002t0001g0050 | 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 | a0001c0002t0001g0091a0001c0002t0001g0235a0001c0002t0001g0294others(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 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0116 | 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 | a0001c0002t0001g0050a0001c0002t0001g0052a0001c0002t0001g0053others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0006t0001g0281 | 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 | a0001c0025t0001g0299 | 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 | a0001c0017t0009g0018a0001c0017t0009g0019 | 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 | a0001c0002t0010g0095a0001c0002t0010g0096 | 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 | a0001c0002t0006g0022 | 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 | a0001c0002t0001g0068a0001c0002t0001g0075a0001c0002t0001g0076others(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 | a0001c0001t0001g0114a0001c0001t0001g0116 | 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 | a0001c0003t0001g0250a0001c0003t0001g0257a0001c0003t0001g0259others(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 | a0001c0023t0001g0161 | 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 | a0001c0002t0001g0091a0001c0002t0001g0092a0001c0002t0001g0093others(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 | a0001c0001t0001g0340 | 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 | a0001c0001t0001g0134 | 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 | a0001c0001t0001g0205a0001c0002t0001g0052a0001c0002t0001g0053others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0013g0341a0001c0002t0014g0342 | 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 | a0009c0019t0001g0194 | 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 | a0001c0002t0013g0341a0001c0002t0014g0342 | 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 | a0001c0004t0001g0087a0001c0004t0001g0296a0001c0004t0001g0304others(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 | a0001c0009t0003g0006a0001c0009t0003g0007 | 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 | a0001c0001t0001g0122a0001c0001t0001g0153a0001c0001t0001g0191 | 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 | a0001c0030t0001g0238 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.4759+186G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 25/42 | chr14 | 31128426 | ||||||
| chr14:31128479
|
C | G | 341 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0097others(338): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.4759+133G>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 25/42 | chr14 | 31128479 | ||||||
| chr14:31129646
|
T | C | 1 | a0001c0002t0001g0101 | 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 | a0001c0001t0001g0226 | 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 | a0001c0017t0009g0018a0001c0017t0009g0019 | 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 | a0001c0001t0001g0143 | 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 | a0001c0002t0001g0050a0001c0002t0001g0052a0001c0002t0001g0053others(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 | a0001c0017t0009g0018a0001c0017t0009g0019 | 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 | a0001c0002t0001g0091a0001c0002t0001g0092a0001c0002t0001g0093others(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 | a0001c0001t0001g0137a0001c0002t0001g0050a0001c0011t0001g0046others(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 | a0001c0002t0001g0235a0001c0002t0001g0294a0001c0010t0004g0012others(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 | a0001c0001t0001g0129a0001c0001t0001g0143a0001c0001t0001g0167others(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 | a0001c0001t0001g0157 | 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 | a0001c0002t0001g0235a0001c0002t0001g0293a0001c0002t0001g0294 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0001g0293 | 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 | a0001c0001t0001g0109 | 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 | a0001c0002t0001g0057 | 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 | 168 | a0001c0001t0001g0089a0001c0001t0001g0199a0001c0001t0001g0201others(165): Show | 168 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.3923-1581dupT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31131028 | ||||||
| chr14:31131044
|
T | C | 1 | a0001c0008t0001g0241 | 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 | a0001c0008t0001g0266 | 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 | a0001c0013t0001g0164 | 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 | a0001c0002t0001g0050 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0001t0001g0103 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0004t0001g0339 | 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 | a0001c0017t0009g0018a0001c0017t0009g0019 | 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 | a0001c0001t0001g0097 | 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 | a0001c0001t0001g0108 | 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 | a0001c0002t0006g0021a0001c0002t0006g0022 | 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 | a0001c0001t0001g0104a0001c0001t0001g0110a0001c0001t0001g0114others(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 | 180 | a0001c0002t0001g0052a0001c0002t0001g0056a0001c0002t0001g0057others(177): Show | 180 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.3922+800delT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 24/42 | chr14 | 31132437 | ||||||
| chr14:31132437
|
CAA | C | 6 | a0001c0002t0001g0050a0001c0011t0001g0046a0001c0011t0001g0047others(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 | a0001c0001t0001g0132 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0001t0001g0107a0004c0015t0001g0125 | 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 | 201 | a0001c0002t0001g0050a0001c0002t0001g0052a0001c0002t0001g0053others(198): Show | 201 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(198): 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 | a0001c0002t0010g0095a0001c0002t0010g0096a0001c0017t0009g0018others(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 | a0001c0002t0010g0096 | 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 | a0001c0002t0001g0310 | 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 | a0001c0009t0003g0002a0001c0009t0003g0008 | 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 | a0003c0014t0001g0080a0003c0014t0001g0081a0003c0014t0001g0082 | 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 | a0001c0034t0001g0269 | 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 | a0001c0002t0001g0235a0001c0002t0001g0293a0001c0002t0001g0294 | 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 | a0001c0001t0001g0097 | 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 | a0001c0002t0006g0020 | 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 | a0001c0007t0001g0023a0001c0007t0001g0024a0001c0007t0001g0029others(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 | a0001c0002t0010g0095a0001c0002t0010g0096a0001c0017t0009g0019 | 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 | a0001c0001t0001g0195 | 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 | a0001c0004t0001g0079a0001c0007t0007g0026a0001c0009t0003g0001others(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 |
51 | a0001c0004t0001g0025a0001c0004t0001g0027a0001c0004t0001g0033others(48): Show | 51 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(48): 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 | a0002c0005t0001g0336 | 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 | a0001c0004t0001g0339 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0015others(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 | a0001c0004t0001g0296a0001c0004t0008g0010a0001c0010t0004g0014others(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 | a0001c0002t0013g0341a0001c0003t0001g0267a0001c0003t0001g0273others(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 | a0001c0002t0001g0091a0001c0002t0001g0092a0001c0002t0001g0093others(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 | a0001c0002t0001g0308a0001c0002t0001g0309a0001c0002t0001g0310others(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 | a0001c0002t0001g0053a0001c0002t0001g0056a0001c0002t0001g0060others(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 | a0001c0002t0001g0052a0001c0002t0001g0057a0001c0002t0001g0058others(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 | a0001c0011t0001g0046a0001c0011t0001g0047a0001c0011t0001g0048others(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 | a0001c0002t0001g0050a0001c0002t0001g0083a0001c0002t0001g0094 | 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 | a0001c0002t0001g0233a0001c0002t0001g0312a0001c0002t0001g0316others(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 | a0001c0002t0001g0313a0001c0002t0001g0314a0001c0002t0001g0315others(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 | a0001c0002t0001g0235 | 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 | a0001c0002t0001g0294 | 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 | a0001c0002t0001g0293 | 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 | a0001c0004t0005g0300 | 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 | a0001c0004t0005g0303 | 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 | a0001c0002t0001g0235a0001c0002t0001g0293a0001c0002t0001g0294 | 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 | a0001c0026t0001g0298 | 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 | a0001c0001t0001g0204 | 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 | a0001c0010t0004g0016 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0010g0095a0001c0002t0010g0096 | 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 | a0001c0001t0001g0112a0001c0001t0001g0127a0001c0001t0001g0182others(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 | a0001c0001t0001g0114a0001c0001t0001g0116a0001c0001t0001g0135others(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 | a0001c0001t0001g0210a0001c0006t0002g0192a0001c0009t0003g0004others(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 | a0001c0001t0001g0183a0001c0001t0001g0186a0001c0004t0001g0339others(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 | a0001c0002t0006g0020a0001c0002t0006g0022a0001c0009t0003g0002others(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 | a0001c0009t0003g0005a0002c0005t0001g0330 | 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 | a0002c0005t0001g0333a0002c0005t0001g0338 | 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 | a0002c0005t0001g0295a0002c0005t0001g0321a0002c0005t0001g0327 | 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 | a0001c0001t0001g0187a0001c0002t0006g0021a0001c0017t0009g0018others(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 | a0001c0001t0001g0105a0001c0010t0004g0012a0001c0010t0004g0013others(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 | a0001c0002t0001g0090a0001c0002t0001g0094a0001c0004t0001g0042others(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 | a0001c0002t0001g0053a0001c0002t0001g0091a0001c0002t0001g0092others(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 | a0001c0002t0001g0057a0001c0003t0001g0262 | 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 | a0001c0002t0001g0052a0001c0002t0001g0058a0001c0002t0001g0060others(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 | a0001c0002t0001g0056a0001c0002t0001g0068a0001c0002t0001g0070others(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 | a0001c0003t0001g0288a0001c0008t0001g0264a0001c0008t0001g0284others(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 | a0001c0002t0001g0050a0001c0011t0001g0046a0001c0011t0001g0048others(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 | a0001c0001t0001g0172a0001c0001t0001g0202 | 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 | a0001c0002t0001g0294 | 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 | 3 | a0001c0001t0001g0097a0001c0001t0001g0141a0001c0001t0001g0142 | 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 | a0001c0002t0001g0293 | 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 | a0006c0027t0001g0307 | 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 | a0001c0002t0001g0235 | 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 | a0001c0001t0001g0109a0001c0001t0001g0119a0001c0001t0001g0120others(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 | a0001c0025t0001g0299 | 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 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0137others(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 | a0001c0004t0005g0302 | 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 | a0001c0002t0010g0095a0001c0002t0010g0096a0001c0010t0004g0016others(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 | a0001c0001t0001g0088a0001c0001t0001g0104a0001c0001t0001g0113others(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 | a0001c0002t0001g0094a0001c0002t0010g0095a0001c0002t0010g0096others(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 | a0001c0001t0001g0102a0001c0001t0001g0110a0001c0001t0001g0122others(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 | a0001c0002t0001g0052a0001c0002t0001g0053a0001c0002t0001g0056others(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 | a0001c0002t0013g0341a0001c0002t0014g0342a0002c0005t0001g0335 | 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 | 24 | a0001c0001t0001g0089a0001c0001t0001g0136a0001c0001t0001g0152others(21): Show | 24 | HG00280.hp2 HG00673.hp2 HG00738.hp2 others(21): 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 | a0001c0004t0001g0065a0001c0004t0001g0079a0001c0004t0001g0305others(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 | a0001c0002t0010g0095a0001c0002t0010g0096a0001c0017t0009g0018others(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 | a0001c0001t0001g0103a0001c0001t0001g0112a0001c0001t0001g0114others(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 | a0001c0002t0006g0020a0001c0004t0001g0064a0001c0004t0001g0066others(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 | a0001c0002t0010g0095a0001c0002t0010g0096a0001c0017t0009g0018others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0001g0091a0001c0002t0001g0092a0001c0002t0001g0093others(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 | a0002c0005t0001g0295a0002c0005t0001g0327a0002c0005t0001g0330others(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 | a0001c0001t0001g0205 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0006t0001g0244a0001c0006t0001g0281 | 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 | a0001c0004t0001g0296 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0001t0001g0109a0001c0002t0001g0052a0001c0002t0001g0053others(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 | a0001c0002t0001g0235a0001c0002t0001g0293a0001c0002t0001g0294 | 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 | a0001c0001t0001g0138a0001c0001t0001g0150a0001c0001t0001g0199others(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 | a0001c0004t0001g0037a0001c0004t0001g0042 | 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 | a0001c0002t0001g0050a0001c0002t0010g0095a0001c0002t0010g0096others(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 | a0001c0002t0001g0094a0001c0002t0001g0233a0001c0002t0001g0312others(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 | 174 | a0001c0001t0001g0109a0001c0002t0001g0050a0001c0002t0001g0052others(171): Show | 174 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(171): 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 | a0001c0002t0001g0091a0001c0002t0001g0092a0001c0002t0001g0093others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0006g0021a0001c0002t0006g0022 | 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 | a0001c0004t0001g0079 | 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 | a0001c0013t0001g0111a0001c0013t0001g0148a0001c0013t0001g0164 | 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 | a0001c0004t0001g0296a0001c0025t0001g0299 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0010t0004g0016 | 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 | a0001c0002t0001g0091a0001c0002t0001g0092a0001c0002t0001g0093 | 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 | a0001c0003t0001g0256a0001c0003t0001g0263a0001c0003t0001g0271 | 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 | 70 | a0001c0001t0001g0097a0001c0001t0001g0102a0001c0001t0001g0109others(67): Show | 70 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.2980-457dupA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 19/42 | chr14 | 31137121 | ||||||
| chr14:31137121
|
C | CTT | 10 | a0001c0001t0001g0134a0001c0002t0001g0075a0001c0002t0001g0091others(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 | a0001c0003t0001g0270 | 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 | a0001c0009t0003g0001a0001c0009t0003g0002a0001c0009t0003g0003others(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 | a0001c0029t0001g0285 | 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 | a0001c0003t0001g0271 | 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 | a0001c0002t0001g0091a0001c0002t0001g0092a0001c0002t0001g0093others(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 | a0001c0034t0001g0269 | 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 | a0001c0002t0001g0306a0001c0002t0001g0308a0001c0002t0001g0309others(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 | a0003c0014t0001g0080a0003c0014t0001g0081a0003c0014t0001g0082 | 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 | a0001c0002t0001g0091a0001c0002t0001g0092a0001c0002t0001g0093others(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 | a0001c0004t0001g0087a0001c0004t0001g0296a0001c0004t0001g0304others(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 | a0001c0009t0003g0006a0001c0009t0003g0007 | 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 | a0001c0010t0004g0016 | 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 | a0001c0017t0009g0018a0001c0017t0009g0019 | 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 | a0003c0014t0001g0080a0003c0014t0001g0081a0003c0014t0001g0082 | 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 | a0001c0004t0001g0087a0001c0004t0001g0296a0001c0004t0001g0304others(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 | a0001c0004t0001g0296 | 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 | a0001c0001t0001g0204 | 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 | a0001c0013t0001g0148 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0001g0233a0001c0002t0001g0312a0001c0002t0001g0313others(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 | a0007c0028t0001g0069 | 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 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0108others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0003t0001g0236a0001c0003t0001g0240a0001c0003t0001g0243others(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 | 80 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0102others(77): 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 | a0001c0002t0001g0094 | 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 | a0001c0001t0001g0104 | 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 | a0001c0004t0001g0025 | 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 | a0001c0001t0001g0097 | 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 | a0001c0002t0001g0052a0001c0002t0001g0053a0001c0002t0001g0056others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0001g0091a0001c0002t0001g0092a0001c0002t0001g0093others(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 | a0001c0004t0005g0297a0001c0004t0005g0300a0001c0004t0005g0301others(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 | a0001c0002t0001g0233a0001c0002t0001g0312a0001c0002t0001g0313others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0003t0001g0255 | 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 | a0001c0001t0001g0182a0001c0001t0001g0211 | 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 | a0001c0004t0001g0339 | 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 | a0001c0002t0010g0095a0001c0002t0010g0096a0001c0017t0009g0018others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0001t0001g0097 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0004t0008g0010 | 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 | 68 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0102others(65): 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 | a0001c0002t0001g0094a0001c0002t0001g0233a0001c0002t0001g0312others(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 | 52 | a0001c0004t0001g0025a0001c0004t0001g0027a0001c0004t0001g0033others(49): Show | 52 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(49): 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 | a0001c0003t0001g0236a0001c0003t0001g0240a0001c0003t0001g0243others(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 | 233 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0097others(230): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.2873+925delA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 18/42 | chr14 | 31140932 | ||||||
| chr14:31141010
|
T | C | 131 | a0001c0002t0001g0050a0001c0002t0001g0052a0001c0002t0001g0053others(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 | a0001c0004t0001g0305 | 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 | a0001c0004t0001g0025 | 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 | a0001c0001t0001g0108a0001c0001t0001g0132a0001c0001t0001g0137others(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 | a0001c0001t0001g0151a0001c0001t0001g0196 | 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 | a0001c0002t0001g0050a0001c0011t0001g0046a0001c0011t0001g0047others(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 | a0002c0005t0001g0323 | 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 | a0001c0002t0001g0050a0001c0002t0001g0052a0001c0002t0001g0053others(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 | a0001c0003t0001g0274 | 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 | a0001c0001t0001g0105 | 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 | a0001c0002t0001g0293 | 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 | a0001c0003t0001g0292a0001c0010t0004g0012a0001c0010t0004g0013others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0001t0001g0340 | 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 | 52 | a0001c0004t0001g0025a0001c0004t0001g0027a0001c0004t0001g0033others(49): Show | 52 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(49): 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 | a0001c0002t0001g0052a0001c0002t0001g0053a0001c0002t0001g0056others(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 | a0001c0002t0001g0235a0001c0002t0001g0293a0001c0002t0001g0294others(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 | a0001c0002t0001g0094a0001c0002t0001g0233a0001c0002t0001g0312others(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 | a0001c0001t0001g0228 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0001g0293 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0013g0341a0001c0002t0014g0342 | 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 | a0001c0002t0001g0306a0001c0002t0001g0308a0001c0002t0001g0309others(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 | a0001c0002t0001g0294 | 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 | 21 | a0001c0001t0001g0158a0001c0002t0001g0308a0001c0002t0001g0311others(18): Show | 21 | HG01074.hp2 HG01952.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.2779-482dupA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 17/42 | chr14 | 31142433 | ||||||
| chr14:31142433
|
AT | A | 15 | a0001c0001t0001g0151a0001c0002t0001g0233a0001c0002t0001g0312others(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 | a0001c0001t0001g0228 | 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 | a0001c0001t0001g0188 | 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 | a0003c0014t0001g0080a0003c0014t0001g0081a0003c0014t0001g0082 | 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 | a0001c0002t0001g0293a0001c0002t0010g0095a0001c0002t0010g0096others(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 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0222others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0006g0020a0001c0002t0006g0021a0001c0002t0006g0022 | 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 | a0001c0002t0001g0235 | 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 | a0001c0008t0001g0241 | 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 | a0001c0001t0001g0123 | 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 | a0001c0004t0001g0296 | 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 | 3 | a0001c0004t0001g0033a0001c0004t0001g0034a0001c0004t0001g0035 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0001t0001g0107a0001c0001t0001g0126a0004c0015t0001g0125 | 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 | a0001c0009t0003g0001a0001c0009t0003g0002a0001c0009t0003g0003others(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 | a0001c0001t0001g0213 | 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 | a0003c0014t0001g0080a0003c0014t0001g0081a0003c0014t0001g0082 | 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 | a0001c0002t0001g0068a0001c0007t0001g0041 | 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 | a0001c0002t0001g0294 | 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 | 31 | a0001c0004t0001g0027a0001c0004t0001g0033a0001c0004t0001g0034others(28): Show | 31 | HG00099.hp1 HG00323.hp1 HG00738.hp2 others(28): 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | 31 | a0001c0004t0001g0027a0001c0004t0001g0033a0001c0004t0001g0034others(28): Show | 31 | HG00099.hp1 HG00323.hp1 HG00738.hp2 others(28): 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 | a0001c0030t0001g0238 | 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 | a0001c0001t0001g0174 | 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 | a0001c0001t0001g0176 | 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 | a0001c0009t0003g0005 | 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 | a0002c0005t0001g0332 | 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 | a0001c0002t0006g0020 | 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 | a0001c0002t0001g0294 | 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 | a0001c0002t0001g0306a0001c0002t0001g0308a0001c0002t0001g0309others(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 | 51 | a0001c0004t0001g0025a0001c0004t0001g0027a0001c0004t0001g0033others(48): Show | 51 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(48): 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 | a0002c0005t0001g0295a0002c0005t0001g0327 | 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 | a0001c0001t0001g0104a0001c0001t0001g0121a0001c0001t0001g0220 | 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 | a0001c0001t0001g0103a0001c0002t0001g0052a0001c0002t0001g0053others(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 | a0003c0014t0001g0081 | 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 | a0001c0001t0001g0089 | 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 | a0001c0006t0001g0244 | 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 | a0001c0002t0001g0235a0001c0002t0001g0293a0001c0002t0001g0294 | 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 | a0001c0006t0002g0175 | 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 | a0001c0002t0001g0306a0001c0002t0001g0308a0001c0002t0001g0309others(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 | a0001c0002t0001g0306a0001c0002t0001g0308a0001c0002t0001g0309others(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 | a0001c0002t0001g0078 | 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 | a0001c0009t0003g0001a0001c0009t0003g0002a0001c0009t0003g0003others(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 | a0001c0002t0001g0052a0001c0002t0001g0057a0001c0002t0001g0058 | 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 | a0006c0027t0001g0307 | 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 | a0001c0004t0001g0025 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0001g0050a0001c0011t0001g0046a0001c0011t0001g0047others(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 | a0002c0005t0001g0295a0002c0005t0001g0327a0002c0005t0001g0330others(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 | a0003c0014t0001g0080a0003c0014t0001g0081a0003c0014t0001g0082 | 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 | a0001c0002t0001g0052a0001c0002t0001g0053a0001c0002t0001g0056others(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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0208others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0004t0001g0296 | 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 | a0001c0002t0001g0294 | 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 | a0001c0002t0006g0021a0001c0002t0006g0022 | 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 | a0001c0001t0001g0159 | 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 | a0002c0005t0001g0295 | 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 | a0002c0005t0001g0326a0002c0005t0001g0331a0002c0005t0001g0332 | 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 | a0001c0009t0003g0001a0001c0009t0003g0002a0001c0009t0003g0003others(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 | a0001c0002t0001g0235a0001c0002t0001g0294 | 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 | a0001c0002t0001g0050a0001c0002t0001g0052a0001c0002t0001g0053others(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 | a0001c0009t0003g0001a0001c0009t0003g0002a0001c0009t0003g0003others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0009t0003g0001a0001c0009t0003g0002a0001c0009t0003g0003others(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 | a0001c0002t0001g0091a0001c0002t0001g0092a0001c0002t0001g0093others(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 | a0001c0001t0001g0204a0001c0001t0001g0229a0001c0002t0001g0075others(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 | a0001c0001t0001g0113a0001c0002t0001g0050a0001c0002t0001g0315others(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 | a0001c0010t0004g0016 | 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 | a0001c0004t0001g0025 | 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 | a0001c0001t0001g0134 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0003t0001g0291 | 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 | a0001c0002t0001g0052a0001c0002t0001g0053a0001c0002t0001g0056others(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 | a0001c0001t0001g0340 | 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 | a0001c0001t0001g0113 | 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 | a0001c0001t0001g0105 | 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 | a0001c0002t0001g0313 | 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 | a0001c0002t0006g0020a0001c0002t0006g0021a0001c0002t0006g0022 | 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 | a0001c0002t0001g0091a0001c0002t0001g0092a0001c0002t0001g0093others(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 | a0001c0001t0001g0097 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0001t0001g0097a0001c0001t0001g0123a0001c0001t0001g0159others(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 | a0001c0002t0001g0235a0001c0002t0001g0293a0001c0002t0001g0294others(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 | a0001c0002t0006g0020a0001c0010t0004g0012a0001c0010t0004g0013others(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 | a0001c0002t0013g0341a0001c0002t0014g0342a0001c0009t0003g0003others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0013g0341a0001c0002t0014g0342 | 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 | a0001c0001t0001g0089a0001c0010t0004g0012a0001c0010t0004g0013others(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 | a0001c0007t0007g0031 | 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 | a0001c0002t0001g0050a0001c0002t0001g0052a0001c0002t0001g0053others(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 | 136 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0102others(133): 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 | a0001c0002t0001g0094 | 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 | 80 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0102others(77): 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | 24 | a0001c0004t0001g0064a0001c0004t0001g0065a0001c0004t0001g0066others(21): Show | 24 | HG00099.hp1 HG00323.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.1933-2469C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31152690 | ||||||
| chr14:31152737
|
A | T | 341 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0097others(338): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.1933-2516T>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31152737 | ||||||
| chr14:31152942
|
C | T | 1 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0156a0001c0001t0001g0158a0001c0001t0001g0220others(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 | a0001c0002t0001g0308 | 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 | a0001c0002t0001g0308 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0004t0001g0087 | 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 | a0001c0001t0001g0171 | 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 | 204 | a0001c0002t0001g0050a0001c0002t0001g0052a0001c0002t0001g0053others(201): Show | 204 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.1933-3093A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31153314 | ||||||
| chr14:31153369
|
C | CA | 7 | a0001c0007t0001g0028a0001c0010t0004g0012a0001c0010t0004g0013others(4): Show | 7 | HG02074.hp1 HG03942.hp2 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.1933-3149dupT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31153369 | ||||||
| chr14:31153463
|
C | A | 1 | a0001c0002t0001g0056 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0001t0001g0105a0001c0002t0001g0050a0001c0002t0001g0052others(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 | a0001c0002t0013g0341a0001c0002t0014g0342 | 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 | a0001c0002t0001g0050a0001c0002t0001g0052a0001c0002t0001g0053others(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 | a0001c0002t0001g0313 | 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 | 51 | a0001c0004t0001g0025a0001c0004t0001g0027a0001c0004t0001g0033others(48): Show | 51 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(48): 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 | a0001c0002t0001g0293 | 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 | a0001c0007t0001g0032a0001c0007t0001g0039 | 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 | 9 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0141others(6): 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 | a0001c0002t0006g0021a0001c0002t0006g0022 | 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 | 201 | a0001c0002t0001g0050a0001c0002t0001g0052a0001c0002t0001g0053others(198): Show | 201 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(198): 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 | a0001c0013t0001g0111a0001c0013t0001g0148a0001c0013t0001g0164 | 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 | 202 | a0001c0002t0001g0050a0001c0002t0001g0052a0001c0002t0001g0053others(199): Show | 202 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.1932+2029delA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31154810 | ||||||
| chr14:31154917
|
C | G | 6 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | 201 | a0001c0001t0001g0103a0001c0001t0001g0129a0001c0002t0001g0050others(198): Show | 201 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.1932+1495delT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31155344 | ||||||
| chr14:31155568
|
C | A | 1 | a0001c0004t0005g0301 | 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 | a0001c0002t0001g0050a0001c0011t0001g0046a0001c0011t0001g0047others(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 | a0001c0002t0013g0341a0001c0002t0014g0342 | 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 | a0001c0001t0001g0128 | 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 | a0001c0010t0004g0016 | 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 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0222others(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 | a0001c0003t0001g0256 | 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 | a0001c0001t0001g0136 | 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 | a0001c0001t0001g0102a0001c0001t0001g0131 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0001g0050a0001c0002t0001g0052a0001c0002t0001g0053others(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 | a0001c0003t0001g0270 | 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 | a0001c0001t0001g0110a0001c0001t0001g0135a0001c0001t0001g0140others(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 | a0001c0001t0001g0171 | 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 | a0001c0002t0001g0094a0003c0014t0001g0080a0003c0014t0001g0081others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0003t0001g0236a0001c0003t0001g0240a0001c0003t0001g0246others(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 | 125 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0102others(122): 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 | a0001c0002t0001g0294 | 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 | a0001c0001t0001g0104a0001c0001t0001g0121a0001c0001t0001g0199others(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 | 19 | a0001c0001t0001g0220a0001c0002t0001g0083a0001c0002t0001g0090others(16): Show | 19 | HG00423.hp2 HG00544.hp2 HG00621.hp2 others(16): 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 | a0001c0002t0001g0094a0001c0002t0006g0021a0001c0002t0006g0022others(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 |
29 | a0001c0002t0001g0050a0001c0002t0001g0306a0001c0002t0001g0309others(26): 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 | a0001c0002t0001g0233a0001c0002t0001g0312a0001c0002t0001g0315others(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 | a0001c0002t0001g0308a0001c0002t0006g0020a0001c0004t0001g0339others(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 | a0001c0010t0004g0016 | 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 | a0001c0002t0001g0060a0001c0002t0001g0061a0001c0002t0001g0062others(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 | a0001c0001t0001g0097a0001c0001t0001g0151a0001c0001t0001g0167others(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 | a0001c0037t0001g0322 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(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 | a0001c0002t0001g0235a0001c0002t0001g0293a0001c0002t0001g0294others(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 | a0003c0014t0001g0080 | 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 | a0001c0001t0001g0141a0001c0003t0001g0240a0001c0004t0001g0072others(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 | a0001c0002t0013g0341a0001c0002t0014g0342 | 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 | a0001c0001t0001g0122a0001c0001t0001g0127a0001c0001t0001g0128others(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 | a0001c0001t0001g0104a0001c0001t0001g0121a0001c0001t0001g0220others(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 | 63 | a0001c0004t0001g0025a0001c0004t0001g0027a0001c0004t0001g0033others(60): Show | 63 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.1932+51delT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 12/42 | chr14 | 31156788 | ||||||
| chr14:31156821
|
T | C | 1 | a0001c0001t0001g0135 | 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 | a0001c0009t0003g0001a0001c0009t0003g0002a0001c0009t0003g0003others(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 | a0001c0013t0001g0148 | 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 | a0001c0003t0001g0261a0001c0003t0001g0272a0001c0003t0001g0288 | 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 | a0001c0004t0001g0025 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0009t0003g0001a0001c0009t0003g0002a0001c0009t0003g0003others(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 | a0001c0003t0001g0262a0001c0017t0009g0018a0001c0017t0009g0019 | 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 | a0001c0002t0001g0070a0001c0002t0001g0071 | 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 | a0001c0002t0001g0235a0001c0002t0001g0293a0001c0002t0001g0294 | 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 | a0001c0002t0001g0094a0003c0014t0001g0080a0003c0014t0001g0081others(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 | a0001c0001t0001g0114a0001c0001t0001g0172a0001c0001t0001g0174others(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 | a0001c0002t0001g0050a0001c0002t0001g0308a0001c0002t0001g0316others(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 | a0001c0004t0001g0064 | 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 | a0001c0002t0001g0306a0001c0002t0001g0308a0001c0002t0001g0309others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0004t0001g0339 | 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 | a0001c0002t0001g0094 | 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 | a0001c0013t0001g0148 | 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 | a0001c0008t0001g0245 | 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 | a0001c0009t0003g0001a0001c0009t0003g0002a0001c0009t0003g0003others(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 | a0001c0002t0001g0050a0001c0011t0001g0046a0001c0011t0001g0047others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0001t0001g0137 | 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 | a0001c0002t0001g0235a0001c0002t0001g0293a0001c0002t0001g0294 | 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 | a0001c0001t0001g0156a0001c0001t0001g0222a0001c0004t0008g0011others(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 | a0001c0002t0001g0306a0001c0002t0001g0308a0001c0002t0001g0309others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0004t0005g0300a0001c0004t0005g0303a0002c0005t0001g0330others(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 | a0001c0002t0001g0306a0001c0002t0001g0308a0001c0002t0001g0309others(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 | a0001c0002t0001g0052a0001c0002t0001g0053a0001c0002t0001g0056others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0001g0050a0001c0011t0001g0046a0001c0011t0001g0047others(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 | a0001c0002t0001g0094 | 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 | 200 | a0001c0002t0001g0050a0001c0002t0001g0052a0001c0002t0001g0053others(197): Show | 200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): 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 | a0001c0002t0001g0052a0001c0002t0001g0053a0001c0002t0001g0056others(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 | a0001c0009t0003g0001a0001c0009t0003g0002a0001c0009t0003g0003others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0006g0020a0001c0002t0006g0021a0001c0002t0006g0022 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0001t0001g0107a0001c0001t0001g0126a0004c0015t0001g0125 | 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 | a0001c0001t0001g0097 | 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 | a0001c0002t0010g0095a0001c0002t0010g0096a0001c0017t0009g0018others(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 | a0001c0002t0001g0052a0001c0002t0001g0053a0001c0002t0001g0056others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0001g0084a0001c0002t0001g0085 | 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 | a0001c0002t0001g0052a0001c0002t0001g0053a0001c0002t0001g0056others(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 | a0001c0002t0001g0052a0001c0002t0001g0053a0001c0002t0001g0056others(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 | a0001c0004t0001g0087a0001c0004t0001g0296a0001c0004t0001g0305others(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 | a0001c0001t0001g0110a0001c0001t0001g0135a0001c0001t0001g0140others(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 | a0001c0009t0003g0001a0001c0009t0003g0002a0001c0009t0003g0003others(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 | a0001c0002t0006g0021a0001c0002t0006g0022 | 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 | a0001c0002t0001g0050 | 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 | a0001c0009t0003g0001a0001c0009t0003g0002a0001c0009t0003g0003others(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 | a0001c0002t0001g0052a0001c0002t0001g0053a0001c0002t0001g0056others(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 | a0001c0002t0001g0091a0001c0002t0001g0092a0001c0002t0001g0093others(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 | a0001c0001t0001g0135a0001c0001t0001g0147 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | 190 | a0001c0002t0001g0052a0001c0002t0001g0053a0001c0002t0001g0056others(187): Show | 190 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.1623-4568delT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31161870 | ||||||
| chr14:31161994
|
C | G | 1 | a0001c0001t0001g0159 | 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 | a0001c0001t0001g0113 | 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 | a0001c0002t0001g0293a0001c0004t0001g0087a0001c0004t0001g0296others(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 | a0001c0001t0001g0123a0001c0002t0001g0084a0001c0002t0001g0085others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0004t0001g0339 | 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 | 70 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0145others(67): 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 | a0001c0009t0003g0002a0001c0009t0003g0008a0001c0010t0004g0012others(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 |
331 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0097others(328): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0009t0003g0002a0001c0009t0003g0008 | 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 | a0002c0005t0001g0328 | 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 | a0002c0005t0001g0328 | 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 | a0001c0008t0001g0265 | 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 | a0001c0009t0003g0001a0001c0009t0003g0002a0001c0009t0003g0003others(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 | a0001c0002t0013g0341a0001c0002t0014g0342 | 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 | 165 | a0001c0002t0001g0050a0001c0002t0001g0052a0001c0002t0001g0053others(162): 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 | a0001c0009t0003g0001a0001c0009t0003g0002a0001c0009t0003g0003others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0007t0001g0029a0001c0007t0001g0036a0001c0036t0001g0043 | 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 | ||||||
| chr14:31163493
|
G | C | 341 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0097others(338): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.1622+4805C>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 10/42 | chr14 | 31163493 | ||||||
| chr14:31163527
|
C | T | 3 | a0001c0003t0001g0261a0001c0003t0001g0272a0001c0003t0001g0288 | 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 | a0002c0005t0001g0295a0002c0005t0001g0321a0002c0005t0001g0323others(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 | a0001c0022t0001g0242 | 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 | a0001c0002t0001g0050a0001c0002t0001g0052a0001c0002t0001g0053others(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 | a0001c0013t0001g0164 | 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 | a0001c0002t0001g0235a0001c0002t0001g0293a0001c0002t0001g0294 | 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 | a0001c0002t0001g0235a0001c0002t0001g0293a0001c0002t0001g0294others(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 | a0001c0001t0001g0088 | 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 | a0001c0002t0001g0306 | 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 | a0001c0002t0006g0022 | 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 | a0001c0004t0001g0087a0001c0004t0001g0296a0001c0004t0001g0304others(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 | a0001c0002t0001g0235a0001c0002t0001g0293a0001c0002t0001g0294others(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 | a0001c0011t0001g0047 | 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 | a0001c0002t0001g0235a0001c0002t0001g0293a0001c0002t0001g0294others(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 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0002t0001g0085others(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 | a0001c0006t0002g0190a0001c0006t0002g0214a0001c0006t0002g0215 | 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 | a0001c0013t0001g0111 | 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 | a0001c0002t0006g0020 | 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 | a0001c0002t0001g0235 | 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 | 9 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0141others(6): 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 | a0001c0003t0001g0236a0001c0003t0001g0240a0001c0003t0001g0243others(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 | a0001c0006t0002g0106 | 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 | a0003c0014t0001g0080a0003c0014t0001g0081a0003c0014t0001g0082 | 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 | a0001c0010t0004g0016 | 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 | a0001c0002t0001g0050a0001c0002t0001g0052a0001c0002t0001g0053others(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 | a0001c0002t0001g0094 | 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 | a0001c0001t0001g0182a0001c0001t0001g0211 | 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 | a0001c0017t0009g0018a0001c0017t0009g0019 | 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 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(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 | a0001c0002t0001g0091a0001c0002t0001g0092a0001c0002t0001g0093 | 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 | a0001c0002t0001g0235a0001c0002t0001g0293a0001c0002t0001g0294others(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 | a0001c0004t0001g0339 | 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 | a0001c0002t0001g0050 | 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 | a0001c0001t0001g0117 | 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 | a0001c0001t0001g0210 | 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 | 61 | a0001c0002t0001g0306a0001c0002t0001g0308a0001c0002t0001g0309others(58): Show | 61 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(58): 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0004t0001g0087a0001c0004t0001g0304a0001c0004t0001g0305others(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 | a0001c0009t0003g0001a0001c0009t0003g0002a0001c0009t0003g0003others(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 | a0005c0016t0001g0115 | 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 | a0001c0001t0001g0168a0001c0007t0007g0031 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0013g0341a0001c0002t0014g0342 | 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 | a0001c0001t0001g0155 | 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 | a0001c0001t0001g0139 | 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 | a0001c0003t0001g0236a0001c0003t0001g0240a0001c0003t0001g0243others(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 | a0001c0002t0006g0020 | 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 | a0003c0014t0001g0081 | 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 | a0001c0003t0001g0263 | 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 | 204 | a0001c0002t0001g0050a0001c0002t0001g0052a0001c0002t0001g0053others(201): Show | 204 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(201): 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 | a0001c0001t0001g0139 | 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 | a0001c0001t0001g0139 | 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 | 3 | a0001c0004t0001g0033a0001c0004t0001g0034a0001c0004t0001g0035 | 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 | a0001c0001t0001g0119a0001c0001t0001g0123a0001c0001t0001g0124others(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 | a0001c0002t0001g0308a0001c0002t0001g0309a0001c0002t0001g0310others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0001g0084 | 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 | a0001c0002t0001g0294 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0010g0095a0001c0002t0010g0096a0001c0017t0009g0018others(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 | a0001c0002t0006g0020a0001c0002t0006g0021a0001c0002t0006g0022 | 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 | a0001c0001t0001g0119a0001c0001t0001g0123a0001c0001t0001g0124others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0001t0001g0185 | 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 | a0001c0006t0002g0106a0001c0006t0002g0175 | 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 | a0002c0005t0001g0326 | 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 | a0001c0033t0001g0277 | 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 | a0001c0003t0001g0272 | 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 | a0001c0010t0004g0016 | 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 | a0001c0001t0001g0089 | 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 | a0001c0001t0001g0165a0001c0001t0001g0196a0001c0001t0001g0208others(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 | 144 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0102others(141): 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 | a0001c0002t0001g0068 | 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 | a0007c0028t0001g0069 | 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 | a0001c0001t0001g0129a0001c0001t0001g0171a0001c0001t0001g0179others(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 | a0003c0014t0001g0080a0003c0014t0001g0081a0003c0014t0001g0082 | 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 | a0002c0005t0001g0324a0002c0005t0001g0325 | 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 | 42 | a0001c0004t0001g0025a0001c0004t0001g0027a0001c0004t0001g0033others(39): Show | 42 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(39): 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 | a0001c0003t0001g0236a0001c0003t0001g0249a0001c0003t0001g0275others(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 | a0001c0001t0001g0097 | 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 | a0001c0002t0001g0050a0001c0011t0001g0046a0001c0011t0001g0047others(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 | a0001c0017t0009g0018a0001c0017t0009g0019 | 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 | a0001c0003t0001g0248 | 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 | a0001c0004t0001g0087a0001c0004t0001g0296a0001c0004t0001g0304others(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 | a0001c0002t0010g0095a0001c0002t0010g0096 | 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 | a0001c0003t0001g0256 | 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 | a0001c0001t0001g0152a0001c0001t0001g0180a0001c0001t0001g0181others(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 | a0001c0004t0001g0087a0001c0004t0001g0296a0001c0004t0001g0304others(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 | a0001c0002t0001g0050a0001c0002t0001g0052a0001c0002t0001g0053others(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 | a0001c0003t0001g0256a0001c0003t0001g0263a0001c0003t0001g0271 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0001g0233a0001c0002t0001g0312a0001c0002t0001g0315others(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 | a0001c0006t0002g0170 | 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 | a0001c0002t0001g0293 | 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 | a0007c0028t0001g0069 | 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 | a0001c0017t0009g0019 | 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 | 22 | a0001c0004t0001g0027a0001c0004t0001g0033a0001c0004t0001g0034others(19): Show | 22 | HG00099.hp1 HG00323.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.1157-331C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 6/42 | chr14 | 31172453 | ||||||
| chr14:31172583
|
G | A | 79 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0102others(76): 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 | a0001c0002t0001g0052a0001c0002t0001g0053a0001c0002t0001g0056others(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 | ||||||
| chr14:31172960
|
C | T | 341 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0097others(338): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.1156+196G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 6/42 | chr14 | 31172960 | ||||||
| chr14:31172965
|
C | T | 61 | a0001c0002t0001g0235a0001c0002t0001g0293a0001c0002t0001g0294others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0001g0094 | 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 | a0001c0006t0002g0192a0001c0006t0002g0193a0001c0006t0002g0207others(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 | a0001c0004t0001g0064 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0001t0001g0223 | 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 | a0001c0003t0001g0272 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0006t0001g0130a0001c0006t0002g0106a0001c0006t0002g0146others(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 | a0001c0017t0009g0018 | 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 | 333 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0097others(330): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): 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 | a0001c0017t0009g0019 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0017t0009g0018a0001c0017t0009g0019 | 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 | a0001c0001t0001g0143 | 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 | a0001c0004t0001g0339 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0001t0001g0105a0001c0001t0001g0229a0001c0001t0001g0230others(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 | a0001c0002t0001g0235a0001c0002t0001g0293a0001c0002t0001g0294others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | 134 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0102others(131): 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 | a0001c0002t0001g0235a0001c0002t0001g0293a0001c0002t0001g0294 | 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 | a0001c0001t0001g0199 | 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 | a0001c0001t0001g0102a0001c0001t0001g0128a0001c0001t0001g0134others(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 | a0001c0001t0001g0097a0001c0002t0013g0341a0001c0003t0001g0240others(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 | a0001c0003t0001g0236a0001c0003t0001g0243a0001c0003t0001g0246others(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 | a0001c0003t0001g0247a0001c0003t0001g0248a0001c0003t0001g0273others(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 | a0001c0001t0001g0088a0001c0001t0001g0138a0001c0001t0001g0147others(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 | a0001c0009t0003g0001a0001c0009t0003g0002a0001c0009t0003g0003others(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 | a0001c0004t0001g0339 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0001g0235a0001c0002t0001g0293a0001c0002t0001g0294others(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 | a0006c0027t0001g0307 | 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 | a0001c0001t0001g0089 | 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 | a0001c0002t0001g0306a0001c0002t0001g0309a0001c0002t0001g0310 | 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 | a0001c0002t0001g0235a0001c0002t0006g0022a0001c0003t0001g0273others(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 | a0001c0002t0006g0021a0001c0004t0001g0087a0001c0004t0001g0296others(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 | a0001c0013t0001g0111a0001c0013t0001g0148a0001c0013t0001g0164 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0001g0052a0001c0002t0001g0053a0001c0002t0001g0056others(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 | a0001c0001t0001g0226 | 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 | a0003c0014t0001g0080a0003c0014t0001g0081a0003c0014t0001g0082 | 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 | 83 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0102others(80): 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0225others(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 | a0001c0002t0001g0306a0001c0002t0001g0308a0001c0002t0001g0309others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0009t0003g0001a0001c0009t0003g0002a0001c0009t0003g0003others(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 | a0001c0002t0001g0306a0001c0002t0001g0308a0001c0002t0001g0309others(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 | a0001c0002t0013g0341a0001c0002t0014g0342a0001c0003t0001g0236others(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 | a0001c0001t0001g0117a0001c0001t0001g0147a0001c0001t0001g0186others(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 | a0001c0002t0013g0341a0001c0002t0014g0342 | 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 | a0001c0035t0001g0063 | 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 | a0002c0005t0001g0325 | 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 | a0001c0003t0001g0247 | 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 | a0001c0008t0001g0283 | 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 | a0001c0002t0001g0293a0001c0003t0001g0257a0001c0003t0001g0286others(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 | a0001c0008t0001g0239 | 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 | a0001c0002t0013g0341a0001c0002t0014g0342a0001c0003t0001g0236others(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 | a0001c0003t0001g0243a0001c0003t0001g0253a0001c0003t0001g0254others(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 | a0001c0003t0001g0246 | 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 | a0001c0004t0005g0300a0001c0004t0005g0303a0001c0010t0004g0012others(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 | a0001c0002t0001g0052a0001c0002t0001g0053a0001c0002t0001g0056others(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 | a0001c0002t0001g0050a0001c0011t0001g0046a0001c0011t0001g0047others(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 | a0001c0011t0001g0046a0001c0011t0001g0047a0001c0011t0001g0048others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | 42 | a0001c0004t0001g0025a0001c0004t0001g0027a0001c0004t0001g0033others(39): Show | 42 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.141-1768delT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31180021 | ||||||
| chr14:31180078
|
T | A | 6 | a0001c0001t0001g0129a0001c0001t0001g0143a0001c0001t0001g0167others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0001g0091a0001c0002t0001g0092a0001c0002t0001g0093others(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 | a0001c0006t0001g0130 | 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 | a0001c0001t0001g0203 | 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 | a0001c0002t0001g0309a0001c0002t0001g0310 | 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 | a0001c0003t0001g0267 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0001g0094a0001c0002t0001g0233a0001c0002t0001g0312others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0001g0052a0001c0002t0001g0053a0001c0002t0001g0056others(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 | a0001c0002t0001g0091a0001c0002t0001g0092a0001c0002t0001g0093others(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 | a0001c0001t0001g0122a0001c0001t0001g0127a0001c0001t0001g0128others(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 | a0001c0001t0001g0104 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0001g0091a0001c0002t0001g0092a0001c0002t0001g0093others(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 | a0002c0005t0001g0329 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | 43 | a0001c0004t0001g0025a0001c0004t0001g0027a0001c0004t0001g0033others(40): Show | 43 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(40): 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 | a0001c0002t0001g0306 | 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 | a0001c0002t0013g0341a0001c0002t0014g0342a0001c0003t0001g0236others(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 | a0001c0002t0001g0306a0001c0002t0001g0308a0001c0002t0001g0309others(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 | a0001c0002t0001g0050a0001c0002t0001g0052a0001c0002t0001g0053others(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 | a0001c0009t0003g0001a0001c0009t0003g0002a0001c0009t0003g0003others(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 | a0006c0027t0001g0307 | 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 | 4 | a0001c0004t0001g0027a0001c0004t0001g0033a0001c0004t0001g0034others(1): Show | 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 | a0001c0002t0001g0235a0001c0002t0001g0293a0001c0002t0001g0294 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0222others(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 | a0001c0001t0001g0155a0001c0002t0001g0235a0001c0002t0001g0293others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0001t0001g0162 | 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 | a0001c0002t0001g0294 | 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 | a0001c0002t0013g0341a0001c0002t0014g0342a0001c0003t0001g0236others(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 | a0001c0009t0003g0002a0001c0009t0003g0008 | 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 | a0002c0005t0001g0336 | 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 | a0001c0002t0013g0341a0001c0002t0014g0342 | 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 | a0001c0002t0001g0090 | 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 | a0002c0005t0001g0329 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | 144 | a0001c0002t0001g0057a0001c0002t0001g0233a0001c0002t0001g0235others(141): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.141-5457dupA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31183710 | ||||||
| chr14:31183710
|
C | CTT | 53 | a0001c0002t0001g0050a0001c0002t0001g0052a0001c0002t0001g0053others(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 | a0001c0003t0001g0255 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | ||||||
| chr14:31183881
|
T | G | 341 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0097others(338): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.141-5627A>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31183881 | ||||||
| chr14:31184240
|
G | C | 13 | a0001c0004t0001g0087a0001c0004t0001g0296a0001c0004t0001g0304others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0002c0005t0001g0295a0002c0005t0001g0327a0002c0005t0001g0330others(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 | a0001c0002t0010g0095a0001c0002t0010g0096a0001c0017t0009g0018others(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 | a0001c0002t0001g0050a0001c0011t0001g0046a0001c0011t0001g0047others(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 | a0001c0002t0001g0306a0001c0002t0001g0308a0001c0002t0001g0309others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0006g0020 | 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 | a0001c0003t0001g0292 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0003t0001g0256a0003c0014t0001g0082 | 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 | a0001c0002t0006g0021a0001c0002t0006g0022 | 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 | a0001c0001t0001g0224 | 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 | a0001c0002t0001g0233a0001c0002t0001g0312a0001c0002t0001g0313others(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 | a0001c0003t0001g0236a0001c0003t0001g0240a0001c0003t0001g0243others(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 | 205 | a0001c0002t0001g0050a0001c0002t0001g0052a0001c0002t0001g0053others(202): Show | 205 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(202): 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0001g0312a0001c0002t0001g0317 | 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 | a0001c0007t0001g0029a0001c0007t0001g0036a0001c0036t0001g0043 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0009t0003g0001a0001c0009t0003g0002a0001c0009t0003g0003others(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 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(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 | a0001c0003t0001g0236a0001c0003t0001g0249a0001c0003t0001g0275others(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 | a0001c0009t0003g0004 | 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 | a0001c0009t0003g0001 | 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 | a0007c0028t0001g0069 | 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 | a0001c0001t0001g0102a0001c0001t0001g0163a0001c0001t0001g0171others(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 | a0001c0001t0001g0110a0001c0001t0001g0127a0001c0001t0001g0128others(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 | a0001c0002t0001g0311 | 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 | a0001c0004t0001g0087a0001c0004t0001g0296a0001c0004t0001g0304others(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 | a0001c0002t0001g0235a0001c0002t0001g0293a0001c0002t0001g0294others(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 | a0001c0004t0001g0087a0001c0004t0001g0296a0001c0004t0001g0304others(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 | a0001c0004t0001g0296 | 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 | a0001c0001t0001g0134a0001c0001t0001g0136a0001c0001t0001g0205others(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 | a0001c0002t0001g0062a0001c0002t0001g0078a0001c0002t0001g0090others(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 | 134 | a0001c0001t0001g0089a0001c0001t0001g0097a0001c0001t0001g0104others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(131): 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 | a0001c0002t0001g0084a0001c0002t0001g0085 | 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 | a0001c0002t0006g0021a0001c0002t0006g0022 | 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 | a0001c0003t0001g0270 | 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 | a0003c0014t0001g0080a0003c0014t0001g0081a0003c0014t0001g0082 | 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 | a0001c0002t0010g0095a0001c0002t0010g0096 | 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 | 201 | a0001c0002t0001g0050a0001c0002t0001g0052a0001c0002t0001g0053others(198): Show | 201 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(198): 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 | a0001c0004t0001g0339 | 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 | a0001c0002t0001g0050a0001c0002t0001g0052a0001c0002t0001g0053others(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 | a0001c0002t0006g0021 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0001g0052a0001c0002t0001g0053a0001c0002t0001g0056others(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 | a0001c0002t0001g0068 | 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 | a0001c0002t0001g0050 | 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 | a0001c0002t0001g0233a0001c0002t0001g0312a0001c0002t0001g0313others(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 | 72 | a0001c0002t0001g0233a0001c0002t0001g0306a0001c0002t0001g0308others(69): Show | 72 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(69): 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 | a0003c0014t0001g0080a0003c0014t0001g0081a0003c0014t0001g0082 | 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 | a0003c0014t0001g0080a0003c0014t0001g0081a0003c0014t0001g0082 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0001g0293 | 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 | a0001c0002t0001g0306a0001c0002t0001g0308a0001c0002t0001g0309others(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 | a0001c0003t0001g0247 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0002c0005t0001g0324a0002c0005t0001g0325 | 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 | a0001c0002t0001g0306a0001c0002t0001g0308a0001c0002t0001g0309others(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 | a0001c0001t0001g0120a0001c0001t0001g0172a0001c0001t0001g0202others(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 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0110others(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 | 97 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0097others(94): 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 | a0001c0001t0001g0109a0001c0001t0001g0132a0001c0001t0001g0135others(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 | a0001c0003t0001g0236a0001c0003t0001g0240a0001c0003t0001g0248others(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 | a0001c0003t0001g0247 | 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 | a0001c0001t0001g0134 | 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 | a0001c0004t0001g0065 | 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 | a0001c0017t0009g0018 | 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 | a0001c0002t0001g0235a0001c0002t0006g0021a0001c0002t0006g0022others(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 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0116others(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 | a0001c0002t0001g0056a0001c0011t0001g0049a0005c0016t0001g0115others(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 | a0001c0017t0009g0019 | 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 | a0001c0018t0004g0017 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0002c0005t0001g0321 | 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 | a0001c0002t0001g0235a0001c0002t0001g0294 | 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 | 262 | a0001c0001t0001g0089a0001c0001t0001g0102a0001c0001t0001g0103others(259): 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 | a0001c0001t0001g0088a0001c0001t0001g0104a0001c0001t0001g0121others(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 | 39 | a0001c0004t0001g0025a0001c0004t0001g0037a0001c0004t0001g0038others(36): Show | 39 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(36): 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0001g0235a0001c0002t0001g0293a0001c0002t0001g0294others(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 | a0001c0002t0014g0342 | 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 | a0001c0012t0001g0051 | 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 | a0001c0003t0001g0274 | 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 | a0001c0002t0001g0306a0001c0002t0001g0308a0001c0002t0001g0309others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0017t0009g0018a0001c0017t0009g0019 | 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 | 202 | a0001c0002t0001g0050a0001c0002t0001g0052a0001c0002t0001g0053others(199): Show | 202 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(199): 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 | a0001c0037t0001g0322 | 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 | a0001c0010t0004g0016 | 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 | a0003c0014t0001g0080a0003c0014t0001g0081a0003c0014t0001g0082 | 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 | a0001c0017t0009g0018a0001c0017t0009g0019 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0007t0007g0026 | 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 | a0001c0002t0001g0052a0001c0002t0001g0053a0001c0002t0001g0056others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | 202 | a0001c0002t0001g0050a0001c0002t0001g0052a0001c0002t0001g0053others(199): Show | 202 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.141-11380A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31189634 | ||||||
| chr14:31189640
|
T | C | 4 | a0001c0004t0001g0027a0001c0004t0001g0033a0001c0004t0001g0034others(1): Show | 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 | a0001c0002t0001g0075a0001c0002t0001g0076a0010c0032t0001g0086 | 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 | a0001c0002t0006g0021a0001c0002t0006g0022 | 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 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(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 | a0001c0002t0013g0341a0001c0002t0014g0342a0001c0003t0001g0236others(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 | a0001c0001t0001g0189 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0006t0002g0207 | 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 | a0001c0002t0001g0050a0001c0002t0001g0052a0001c0002t0001g0053others(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 | a0001c0002t0001g0094 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0007t0007g0030a0001c0007t0007g0031 | 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 | a0001c0003t0001g0236 | 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 | a0001c0002t0001g0083 | 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 | a0001c0004t0001g0296 | 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 | a0001c0002t0001g0313 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0004t0001g0087a0001c0004t0001g0304a0001c0004t0001g0305others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0001t0001g0203 | 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 | 162 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0097others(159): Show | 162 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.141-13292dupT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31191545 | ||||||
| chr14:31191545
|
CA | C | 12 | a0001c0002t0001g0083a0001c0002t0001g0233a0001c0002t0001g0312others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0006g0020 | 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 | 42 | a0001c0004t0001g0025a0001c0004t0001g0027a0001c0004t0001g0033others(39): Show | 42 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.141-13471C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31191725 | ||||||
| chr14:31191845
|
C | CA | 69 | a0001c0001t0001g0181a0001c0002t0001g0233a0001c0002t0001g0312others(66): Show | 69 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.141-13592dupT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31191845 | ||||||
| chr14:31191880
|
A | G | 2 | a0001c0002t0010g0095a0001c0002t0010g0096 | 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 | a0001c0004t0005g0300a0001c0004t0005g0303 | 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 | a0001c0004t0005g0297a0001c0010t0004g0012a0001c0010t0004g0013others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0001t0001g0116a0001c0010t0004g0016 | 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 | a0001c0002t0006g0021a0001c0002t0006g0022 | 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 | a0001c0002t0013g0341a0001c0002t0014g0342a0001c0003t0001g0236others(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 | 151 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0097others(148): 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 | a0001c0002t0001g0083a0001c0003t0001g0288a0001c0004t0001g0087others(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 | a0001c0033t0001g0277 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0013g0341a0001c0002t0014g0342 | 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 | a0001c0004t0001g0296a0001c0025t0001g0299 | 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 | a0001c0002t0001g0235a0001c0002t0001g0294 | 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 | a0001c0004t0001g0339 | 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 | a0001c0004t0001g0296 | 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 | a0001c0004t0005g0297a0001c0004t0005g0301a0001c0004t0005g0302others(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 | a0001c0006t0001g0244 | 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 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0222others(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 | a0001c0001t0001g0176 | 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 | a0001c0001t0001g0176 | 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 | a0001c0002t0001g0060a0001c0002t0001g0061a0001c0002t0001g0062 | 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 | a0001c0002t0001g0293 | 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 | a0001c0002t0001g0235a0001c0002t0001g0294 | 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 | a0001c0001t0001g0188 | 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 | a0001c0002t0001g0050a0001c0002t0001g0052a0001c0002t0001g0053others(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 | a0001c0033t0001g0277 | 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 | a0001c0004t0001g0339 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.140+11886G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31193911 | ||||||
| chr14:31193971
|
A | G | 1 | a0001c0007t0001g0028 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.140+11826T>C | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31193971 | ||||||
| chr14:31194175
|
T | C | 17 | a0001c0002t0001g0052a0001c0002t0001g0053a0001c0002t0001g0056others(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 | a0001c0006t0001g0130 | 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 | a0001c0009t0003g0001a0001c0009t0003g0002a0001c0009t0003g0003others(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 | a0001c0004t0001g0027 | 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 | a0001c0003t0001g0243 | 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 | a0001c0002t0010g0095a0001c0002t0010g0096 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0004t0001g0296 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0001t0001g0129a0001c0002t0001g0235a0001c0002t0001g0293others(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 | a0001c0001t0001g0177 | 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 | a0001c0001t0001g0205 | 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 | 200 | a0001c0002t0001g0050a0001c0002t0001g0052a0001c0002t0001g0053others(197): Show | 200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): 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 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0222others(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 | ||||||
| chr14:31195222
|
T | C | 341 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0097others(338): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.140+10575A>G | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31195222 | ||||||
| chr14:31195442
|
C | T | 1 | a0001c0017t0009g0018 | 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 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(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 | a0001c0004t0001g0339 | 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 | a0002c0005t0001g0336a0002c0005t0001g0337 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0004t0005g0297a0001c0004t0005g0300a0001c0004t0005g0301others(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 | a0001c0004t0001g0087a0001c0004t0001g0296a0001c0004t0001g0304others(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 | a0001c0002t0001g0050 | 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 | 43 | a0001c0004t0001g0025a0001c0004t0001g0027a0001c0004t0001g0033others(40): Show | 43 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(40): 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 | a0001c0001t0001g0117 | 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 | a0001c0002t0001g0090 | 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 | a0001c0017t0009g0018a0001c0017t0009g0019 | 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 | a0001c0002t0001g0233a0001c0002t0001g0235a0001c0002t0001g0312others(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 | a0001c0003t0001g0291 | 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 | a0001c0002t0010g0095a0001c0002t0010g0096 | 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 | a0003c0014t0001g0080a0003c0014t0001g0081a0003c0014t0001g0082 | 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 | a0001c0001t0001g0107a0001c0001t0001g0126a0004c0015t0001g0125 | 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 | a0002c0005t0001g0336a0002c0005t0001g0337 | 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 | a0001c0002t0013g0341a0001c0002t0014g0342 | 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 | a0001c0003t0011g0009 | 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 | a0001c0002t0001g0050a0001c0011t0001g0046a0001c0011t0001g0047others(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 | a0001c0008t0001g0241 | 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 | a0001c0001t0001g0103 | 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 | a0002c0005t0001g0326 | 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 | 119 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0102others(116): 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 | a0001c0002t0001g0233a0001c0002t0001g0312a0001c0002t0001g0313others(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 | a0001c0004t0001g0087a0001c0004t0001g0296a0001c0004t0001g0304others(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 | a0001c0003t0001g0291 | 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 | a0001c0001t0001g0178 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0004t0001g0087a0001c0004t0001g0296a0001c0004t0001g0304others(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 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0179others(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 | a0001c0001t0001g0108a0001c0004t0001g0087a0001c0004t0001g0296others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0001t0001g0103 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0013g0341a0001c0002t0014g0342a0001c0003t0001g0236others(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 | a0001c0017t0009g0018a0001c0017t0009g0019 | 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 | a0001c0010t0004g0016 | 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 | a0001c0010t0004g0014 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0015others(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 | a0001c0017t0009g0018a0001c0017t0009g0019 | 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 | a0001c0001t0001g0206a0001c0001t0001g0232a0001c0002t0001g0056others(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 | a0001c0001t0001g0340 | 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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0208others(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 | a0001c0001t0001g0102a0001c0001t0001g0182a0001c0001t0001g0183others(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 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0213others(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 | a0001c0001t0001g0107a0001c0001t0001g0121a0001c0001t0001g0122others(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 | a0001c0002t0001g0050a0001c0002t0001g0057a0001c0002t0001g0058others(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 | 66 | a0001c0002t0001g0052a0001c0002t0001g0053a0001c0002t0001g0056others(63): Show | 66 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(63): 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 | a0001c0002t0001g0235a0001c0002t0001g0293a0001c0002t0001g0294others(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 | a0001c0001t0001g0120 | 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 | a0001c0004t0001g0339 | 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 | a0001c0037t0001g0322a0002c0005t0001g0295a0002c0005t0001g0321others(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 | a0001c0002t0001g0233a0001c0002t0001g0312a0001c0002t0001g0313others(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 | a0001c0002t0001g0311 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0003c0014t0001g0080a0003c0014t0001g0081a0003c0014t0001g0082 | 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 | a0001c0001t0001g0119 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | 65 | a0001c0002t0001g0233a0001c0002t0001g0312a0001c0002t0001g0313others(62): Show | 65 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.140+5380C>T | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31200417 | ||||||
| chr14:31200489
|
TA | T | 194 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0097others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.140+5307delT | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 2/42 | chr14 | 31200489 | ||||||
| chr14:31200489
|
TAA | T | 87 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(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 | a0001c0002t0001g0052a0001c0002t0001g0053a0001c0002t0001g0056others(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 | a0001c0003t0001g0288 | 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 | a0001c0008t0001g0289 | 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 | a0001c0009t0003g0001a0001c0009t0003g0002a0001c0009t0003g0003others(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 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0001t0001g0221 | 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 | a0002c0005t0001g0321 | 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 | a0001c0009t0003g0001 | 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 | a0001c0017t0009g0018a0001c0017t0009g0019 | 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 | a0001c0001t0001g0088a0001c0001t0001g0102a0001c0002t0001g0052others(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 | a0001c0002t0001g0235 | 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 | a0001c0017t0009g0018a0001c0017t0009g0019 | 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 | a0001c0001t0001g0222 | 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 | a0001c0030t0001g0238 | 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 | a0001c0002t0010g0095a0001c0002t0010g0096 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0001g0050a0001c0011t0001g0046a0001c0011t0001g0047others(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 | a0001c0003t0001g0290a0001c0003t0001g0292a0001c0003t0011g0009 | 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 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0001t0001g0097a0001c0002t0001g0233a0001c0002t0001g0306others(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 | a0001c0004t0001g0339 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0010t0004g0015 | 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 | a0001c0017t0009g0018a0001c0017t0009g0019 | 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 | a0001c0004t0001g0339 | 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 | a0001c0001t0001g0228 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | 72 | a0001c0002t0001g0233a0001c0002t0001g0306a0001c0002t0001g0308others(69): Show | 72 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(69): 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(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 | a0001c0002t0001g0235a0001c0002t0001g0293a0001c0002t0001g0294others(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 | a0001c0002t0001g0235a0001c0002t0001g0293a0001c0002t0001g0294 | 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 | a0001c0017t0009g0018a0001c0017t0009g0019 | 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 | a0001c0002t0001g0050a0001c0002t0001g0052a0001c0002t0001g0053others(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 | a0001c0002t0001g0084a0001c0002t0001g0085 | 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 | a0001c0001t0001g0089 | 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 | a0001c0002t0006g0020 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0017t0009g0018a0001c0017t0009g0019 | 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 | 66 | a0001c0002t0001g0233a0001c0002t0001g0312a0001c0002t0001g0313others(63): Show | 66 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(63): 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 | a0001c0001t0001g0088 | 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 | a0001c0001t0001g0088 | 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 | a0001c0002t0001g0235a0001c0002t0001g0293a0001c0002t0001g0294others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0010t0004g0016 | 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 | a0001c0017t0009g0018a0001c0017t0009g0019 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0001g0235a0001c0002t0001g0293a0001c0002t0001g0294others(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 | a0001c0002t0001g0235a0001c0002t0001g0293a0001c0002t0001g0294others(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 | a0001c0003t0001g0236 | 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 | a0010c0032t0001g0086 | 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 | a0001c0002t0001g0052a0001c0002t0001g0053a0001c0002t0001g0056others(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 | a0001c0002t0001g0293a0001c0002t0001g0294a0001c0002t0013g0341others(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 | a0001c0004t0001g0087a0001c0004t0001g0296a0001c0004t0001g0304others(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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0002t0001g0052a0001c0002t0001g0053a0001c0002t0001g0056others(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 | a0001c0002t0001g0050a0001c0011t0001g0046a0001c0011t0001g0047others(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 | a0001c0018t0004g0017 | 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 | a0002c0005t0001g0295 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | 64 | a0001c0002t0001g0306a0001c0002t0001g0308a0001c0002t0001g0309others(61): Show | 64 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.-22+388delA | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 1/42 | chr14 | 31206627 | ||||||
| chr14:31206628
|
T | A | 3 | a0001c0004t0001g0339a0001c0007t0001g0044a0001c0007t0001g0045 | 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 | a0001c0010t0004g0012a0001c0010t0004g0013a0001c0010t0004g0014others(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 | a0001c0001t0001g0340 | 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 | 23 | a0001c0004t0001g0025a0001c0004t0001g0027a0001c0004t0001g0033others(20): Show | 23 | HG00099.hp1 HG00323.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.-22+25G>A | HECTD1 | ENSG00000092148.14 | transcript | ENST00000399332.6 | protein_coding | 1/42 | chr14 | 31206991 |