Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 283450 |
|---|---|
| ensemblid | ENSG00000173064.14 |
| hgncid | 26611 |
| symbol | HECTD4 |
| name | HECT domain E3 ubiquitin protein ligase 4 |
| refseq_nuc | NM_001388303.1 |
| refseq_prot | NP_001375232.1 |
| ensembl_nuc | ENST00000682272.1 |
| ensembl_prot | ENSP00000507687.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 112160195 |
| end | 112382431 |
| strand | - |
| ver | v1.2 |
| region | chr12:112160195-112382431 |
| region5000 | chr12:112155195-112387431 |
| regionname0 | HECTD4_chr12_112160195_112382431 |
| regionname5000 | HECTD4_chr12_112155195_112387431 |
| 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 | 4418 | 234 | 67 | 39 | 108 | 4 | 14 | 88 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0002 | 0/0 | 3245 | 21 | 5 | 3 | 11 | 0 | 2 | 9 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0003 | 0/0 | 4418 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0004 | 0/0 | 4418 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0005 | 0/0 | 4418 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0006 | 0/0 | 4418 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0007 | 0/0 | 4418 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0008 | 0/0 | 3245 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0009 | 0/0 | 4418 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0010 | 0/0 | 4418 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0011 | 0/0 | 4418 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0012 | 0/0 | 4418 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0013 | 0/0 | 4418 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0014 | 0/0 | 4418 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0015 | 0/0 | 4418 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0016 | 0/0 | 4418 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| 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 | 0/0 | 13257 | 113 | 46 | 12 | 44 | 3 | 8 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| c0002 | 0/0 | 13257 | 65 | 7 | 11 | 45 | 0 | 2 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| c0003 | 1/1 | 13257 | 39 | 6 | 14 | 12 | 1 | 4 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| c0004 | 0/0 | 13258 | 9 | 4 | 1 | 3 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| c0005 | 0/0 | 13258 | 7 | 0 | 1 | 6 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| c0006 | 0/0 | 13258 | 4 | 0 | 1 | 2 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| c0007 | 0/0 | 13257 | 2 | 0 | 0 | 2 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| c0008 | 0/0 | 13257 | 2 | 0 | 0 | 2 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| c0009 | 0/0 | 13257 | 2 | 2 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| c0010 | 0/0 | 13257 | 2 | 2 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| c0011 | 0/0 | 13257 | 2 | 0 | 0 | 2 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| c0012 | 0/0 | 13257 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| c0013 | 0/0 | 13257 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| c0014 | 0/0 | 13257 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| c0015 | 0/0 | 13257 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| c0016 | 0/0 | 13257 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| c0017 | 0/0 | 13258 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| c0018 | 0/0 | 13257 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| c0019 | 0/0 | 13257 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| c0020 | 0/0 | 13257 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| c0021 | 0/0 | 13257 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| c0022 | 0/0 | 13257 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| c0023 | 0/0 | 13257 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| c0024 | 0/0 | 13257 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| c0025 | 0/0 | 13257 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| c0026 | 0/0 | 13258 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| c0027 | 0/0 | 13257 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| c0028 | 0/0 | 13257 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| c0029 | 0/0 | 13257 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| c0030 | 0/0 | 13257 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| c0031 | 0/0 | 13257 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| c0032 | 0/0 | 13257 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| c0033 | 0/0 | 13257 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| c0034 | 0/0 | 13257 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| 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 | 0/0 | 2504 | 117 | 23 | 20 | 65 | 2 | 7 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| t0002 | 1/1 | 2496 | 44 | 5 | 17 | 13 | 1 | 6 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| t0003 | 0/0 | 2499 | 36 | 0 | 2 | 28 | 1 | 5 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| t0004 | 0/0 | 2501 | 19 | 18 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| t0005 | 0/0 | 2499 | 14 | 11 | 3 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| t0006 | 0/0 | 2508 | 9 | 0 | 0 | 9 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| t0007 | 0/0 | 2501 | 6 | 5 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| t0008 | 0/0 | 2507 | 5 | 3 | 0 | 2 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| t0009 | 0/0 | 2493 | 3 | 1 | 1 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| t0010 | 0/0 | 2502 | 3 | 0 | 0 | 3 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| t0011 | 0/0 | 2510 | 3 | 3 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| t0012 | 0/0 | 2502 | 2 | 2 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| t0013 | 0/0 | 2496 | 2 | 0 | 0 | 2 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| t0014 | 0/0 | 2504 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| t0015 | 0/0 | 2504 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| t0016 | 0/0 | 2514 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| t0017 | 0/0 | 2517 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| t0018 | 0/0 | 2522 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| t0019 | 0/0 | 2538 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| t0020 | 0/0 | 2540 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| 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 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0082 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0138 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| 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 | 0/0 | 13257 | 113 | 46 | 12 | 44 | 3 | 8 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0002 | 0/0 | 13257 | 65 | 7 | 11 | 45 | 0 | 2 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0003 | 1/1 | 13257 | 39 | 6 | 14 | 12 | 1 | 4 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0007 | 0/0 | 13257 | 2 | 0 | 0 | 2 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0009 | 0/0 | 13257 | 2 | 2 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0010 | 0/0 | 13257 | 2 | 2 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0011 | 0/0 | 13257 | 2 | 0 | 0 | 2 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0012 | 0/0 | 13257 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0013 | 0/0 | 13257 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0016 | 0/0 | 13257 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0018 | 0/0 | 13257 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0029 | 0/0 | 13257 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0030 | 0/0 | 13257 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0031 | 0/0 | 13257 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0032 | 0/0 | 13257 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0033 | 0/0 | 13257 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0002c0004 | 0/0 | 13258 | 9 | 4 | 1 | 3 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0002c0005 | 0/0 | 13258 | 7 | 0 | 1 | 6 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0002c0006 | 0/0 | 13258 | 4 | 0 | 1 | 2 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0002c0026 | 0/0 | 13258 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0003c0008 | 0/0 | 13257 | 2 | 0 | 0 | 2 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0004c0034 | 0/0 | 13257 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0005c0022 | 0/0 | 13257 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0006c0023 | 0/0 | 13257 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0007c0015 | 0/0 | 13257 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0008c0017 | 0/0 | 13258 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0009c0024 | 0/0 | 13257 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0010c0014 | 0/0 | 13257 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0011c0028 | 0/0 | 13257 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0012c0027 | 0/0 | 13257 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0013c0025 | 0/0 | 13257 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0014c0021 | 0/0 | 13257 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0015c0020 | 0/0 | 13257 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0016c0019 | 0/0 | 13257 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 15760 | 32 | 12 | 6 | 8 | 2 | 4 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0001t0003 | 0/0 | 15755 | 31 | 0 | 2 | 24 | 1 | 4 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0001t0004 | 0/0 | 15757 | 16 | 15 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0001t0005 | 0/0 | 15755 | 12 | 9 | 3 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0001t0006 | 0/0 | 15764 | 8 | 0 | 0 | 8 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0001t0007 | 0/0 | 15757 | 4 | 3 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0001t0008 | 0/0 | 15763 | 2 | 2 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0001t0010 | 0/0 | 15758 | 2 | 0 | 0 | 2 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0001t0011 | 0/0 | 15766 | 2 | 2 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0001t0012 | 0/0 | 15758 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0001t0014 | 0/0 | 15760 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0001t0015 | 0/0 | 15760 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0001t0019 | 0/0 | 15794 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0002t0001 | 0/0 | 15760 | 62 | 7 | 11 | 42 | 0 | 2 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0002t0008 | 0/0 | 15763 | 2 | 0 | 0 | 2 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0002t0020 | 0/0 | 15796 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0003t0002 | 1/1 | 15752 | 34 | 4 | 14 | 9 | 1 | 4 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0003t0004 | 0/0 | 15757 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0003t0009 | 0/0 | 15749 | 2 | 1 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0003t0013 | 0/0 | 15752 | 2 | 0 | 0 | 2 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0007t0001 | 0/0 | 15760 | 2 | 0 | 0 | 2 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0009t0016 | 0/0 | 15770 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0009t0018 | 0/0 | 15778 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0010t0001 | 0/0 | 15760 | 2 | 2 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0011t0001 | 0/0 | 15760 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0011t0010 | 0/0 | 15758 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0012t0002 | 0/0 | 15752 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0013t0012 | 0/0 | 15758 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0016t0001 | 0/0 | 15760 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0018t0001 | 0/0 | 15760 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0029t0001 | 0/0 | 15760 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0030t0007 | 0/0 | 15757 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0031t0008 | 0/0 | 15763 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0032t0011 | 0/0 | 15766 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0001c0033t0002 | 0/0 | 15752 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0002c0004t0001 | 0/0 | 15761 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0002c0004t0003 | 0/0 | 15756 | 4 | 0 | 0 | 3 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0002c0004t0004 | 0/0 | 15758 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0002c0004t0005 | 0/0 | 15756 | 2 | 2 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0002c0004t0007 | 0/0 | 15758 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0002c0005t0001 | 0/0 | 15761 | 7 | 0 | 1 | 6 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0002c0006t0002 | 0/0 | 15753 | 4 | 0 | 1 | 2 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0002c0026t0001 | 0/0 | 15761 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0003c0008t0001 | 0/0 | 15760 | 2 | 0 | 0 | 2 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0004c0034t0001 | 0/0 | 15760 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0005c0022t0002 | 0/0 | 15752 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0006c0023t0009 | 0/0 | 15749 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0007c0015t0001 | 0/0 | 15760 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0008c0017t0001 | 0/0 | 15761 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0009c0024t0002 | 0/0 | 15752 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0010c0014t0001 | 0/0 | 15760 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0011c0028t0006 | 0/0 | 15764 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0012c0027t0004 | 0/0 | 15757 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0013c0025t0002 | 0/0 | 15752 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0014c0021t0017 | 0/0 | 15773 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0015c0020t0003 | 0/0 | 15755 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| a0016c0019t0002 | 0/0 | 15752 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | copy fasta | chr12 | 112155195 | 112387431 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0003g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0004g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0004g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0005g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0005g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0005g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0005g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0005g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0005g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0005g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0005g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0006g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0006g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0006g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0006g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0006g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0006g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0006g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0006g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0007g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0007g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0007g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0007g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0008g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0008g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0010g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0010g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0011g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0011g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0012g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0014g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0015g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0001t0019g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0008g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0008g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0002t0020g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0003t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0003t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0003t0002g0082 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0003t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0003t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0003t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0003t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0003t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0003t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0003t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0003t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0003t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0003t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0003t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0003t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0003t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0003t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0003t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0003t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0003t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0003t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0003t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0003t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0003t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0003t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0003t0002g0138 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0003t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0003t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0003t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0003t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0003t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0003t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0003t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0003t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0003t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0003t0009g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0003t0009g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0003t0013g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0003t0013g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0007t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0007t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0009t0016g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0009t0018g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0010t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0010t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0011t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0011t0010g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0012t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0013t0012g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0016t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0018t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0029t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0030t0007g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0031t0008g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0032t0011g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0001c0033t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0002c0004t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0002c0004t0003g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0002c0004t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0002c0004t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0002c0004t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0002c0004t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0002c0004t0005g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0002c0004t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0002c0004t0007g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0002c0005t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0002c0005t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0002c0005t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0002c0005t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0002c0005t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0002c0005t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0002c0005t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0002c0006t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0002c0006t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0002c0006t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0002c0006t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0002c0026t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0003c0008t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0003c0008t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0004c0034t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0005c0022t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0006c0023t0009g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0007c0015t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0008c0017t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0009c0024t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0010c0014t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0011c0028t0006g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0012c0027t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0013c0025t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0014c0021t0017g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0015c0020t0003g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| a0016c0019t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0131 | EUR | GBR | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG00140 | hp2 | a0001 | c0003 | t0002 | g0134 | EUR | GBR | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0227 | EAS | CHS | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG00544 | hp2 | a0013 | c0025 | t0002 | g0095 | EAS | CHS | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG00597 | hp1 | a0001 | c0016 | t0001 | g0168 | EAS | CHS | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG00597 | hp2 | a0001 | c0001 | t0006 | g0254 | EAS | CHS | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG00735 | hp1 | a0001 | c0003 | t0002 | g0143 | AMR | PUR | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0189 | AMR | PUR | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG00738 | hp2 | a0001 | c0003 | t0002 | g0080 | AMR | PUR | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0184 | AMR | PUR | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG01071 | hp2 | a0001 | c0012 | t0002 | g0093 | AMR | PUR | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG01081 | hp1 | a0001 | c0001 | t0005 | g0044 | AMR | PUR | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0176 | AMR | PUR | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG01099 | hp1 | a0001 | c0001 | t0005 | g0053 | AMR | PUR | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG01106 | hp2 | a0001 | c0003 | t0002 | g0136 | AMR | PUR | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG01109 | hp1 | a0006 | c0023 | t0009 | g0003 | AMR | PUR | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0043 | AMR | PUR | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG01167 | hp1 | a0001 | c0003 | t0002 | g0144 | AMR | PUR | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG01167 | hp2 | a0001 | c0001 | t0005 | g0049 | AMR | PUR | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG01175 | hp1 | a0002 | c0004 | t0001 | g0155 | AMR | PUR | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG01175 | hp2 | a0001 | c0003 | t0002 | g0101 | AMR | PUR | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0042 | AMR | PUR | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0179 | AMR | CLM | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG01256 | hp2 | a0001 | c0003 | t0002 | g0141 | AMR | CLM | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG01258 | hp1 | a0001 | c0003 | t0002 | g0104 | AMR | CLM | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0178 | AMR | CLM | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG01433 | hp1 | a0002 | c0005 | t0001 | g0199 | AMR | CLM | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG01433 | hp2 | a0001 | c0003 | t0002 | g0142 | AMR | CLM | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG01496 | hp1 | a0001 | c0003 | t0002 | g0123 | AMR | CLM | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0194 | AMR | CLM | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0078 | AFR | ACB | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | ACB | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0213 | AMR | PEL | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG01928 | hp2 | a0009 | c0024 | t0002 | g0108 | AMR | PEL | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG01934 | hp1 | a0002 | c0006 | t0002 | g0094 | AMR | PEL | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG01934 | hp2 | a0001 | c0018 | t0001 | g0162 | AMR | PEL | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG01943 | hp1 | a0001 | c0001 | t0007 | g0025 | AMR | PEL | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG01943 | hp2 | a0001 | c0003 | t0002 | g0140 | AMR | PEL | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0187 | AMR | PEL | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG01952 | hp2 | a0001 | c0003 | t0002 | g0106 | AMR | PEL | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG01978 | hp2 | a0001 | c0003 | t0002 | g0086 | AMR | PEL | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0186 | AMR | PEL | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | KHV | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0198 | EAS | KHV | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02055 | hp1 | a0002 | c0004 | t0005 | g0048 | AFR | ACB | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02055 | hp2 | a0002 | c0004 | t0004 | g0063 | AFR | ACB | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02056 | hp1 | a0002 | c0006 | t0002 | g0097 | EAS | KHV | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02056 | hp2 | a0001 | c0001 | t0006 | g0258 | EAS | KHV | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02071 | hp1 | a0002 | c0005 | t0001 | g0197 | EAS | KHV | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02071 | hp2 | a0011 | c0028 | t0006 | g0261 | EAS | KHV | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0191 | EAS | KHV | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0058 | EAS | KHV | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02080 | hp1 | a0001 | c0003 | t0013 | g0105 | EAS | KHV | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0188 | EAS | KHV | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02129 | hp1 | a0001 | c0001 | t0006 | g0262 | EAS | KHV | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0226 | EAS | KHV | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0225 | EAS | KHV | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02132 | hp2 | a0001 | c0001 | t0006 | g0259 | EAS | KHV | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0210 | EAS | KHV | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02135 | hp2 | a0001 | c0011 | t0001 | g0133 | EAS | KHV | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0185 | AMR | PEL | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02148 | hp2 | a0001 | c0003 | t0002 | g0102 | AMR | PEL | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02165 | hp1 | a0001 | c0003 | t0002 | g0088 | EAS | CDX | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0161 | EAS | CDX | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02257 | hp1 | a0001 | c0001 | t0007 | g0007 | AFR | ACB | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0204 | AFR | ACB | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02258 | hp1 | a0001 | c0003 | t0002 | g0137 | AFR | ACB | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0061 | AFR | ACB | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02273 | hp1 | a0001 | c0003 | t0002 | g0124 | AMR | PEL | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0167 | AMR | PEL | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02451 | hp1 | a0001 | c0003 | t0002 | g0139 | AFR | ACB | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0071 | AFR | ACB | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02523 | hp1 | a0001 | c0001 | t0006 | g0260 | EAS | KHV | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02523 | hp2 | a0001 | c0003 | t0002 | g0087 | EAS | KHV | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02572 | hp1 | a0001 | c0003 | t0002 | g0103 | AFR | GWD | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0064 | AFR | GWD | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0068 | AFR | GWD | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02622 | hp2 | a0001 | c0009 | t0016 | g0266 | AFR | GWD | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02630 | hp1 | a0001 | c0001 | t0011 | g0264 | AFR | GWD | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02630 | hp2 | a0001 | c0003 | t0002 | g0107 | AFR | GWD | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02647 | hp1 | a0004 | c0034 | t0001 | g0154 | AFR | GWD | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0060 | AFR | GWD | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02683 | hp1 | a0001 | c0003 | t0002 | g0247 | SAS | PJL | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0045 | SAS | PJL | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0202 | AFR | GWD | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02717 | hp2 | a0001 | c0030 | t0007 | g0035 | AFR | GWD | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02738 | hp1 | a0002 | c0004 | t0003 | g0008 | SAS | PJL | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02738 | hp2 | a0001 | c0003 | t0002 | g0109 | SAS | PJL | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0205 | AFR | GWD | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02809 | hp2 | a0002 | c0004 | t0007 | g0036 | AFR | GWD | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0055 | AFR | GWD | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0067 | AFR | GWD | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02896 | hp2 | a0016 | c0019 | t0002 | g0135 | AFR | GWD | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02897 | hp1 | a0001 | c0009 | t0018 | g0268 | AFR | GWD | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0070 | AFR | GWD | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02922 | hp1 | a0001 | c0001 | t0012 | g0151 | AFR | ESN | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0021 | AFR | ESN | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02965 | hp1 | a0001 | c0001 | t0007 | g0024 | AFR | ESN | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02965 | hp2 | a0001 | c0010 | t0001 | g0214 | AFR | ESN | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02976 | hp1 | a0001 | c0031 | t0008 | g0251 | AFR | ESN | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0219 | SAS | PJL | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0203 | AFR | GWD | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG03041 | hp2 | a0001 | c0003 | t0009 | g0002 | AFR | GWD | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG03098 | hp1 | a0001 | c0010 | t0001 | g0217 | AFR | MSL | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | MSL | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0023 | AFR | ESN | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG03130 | hp2 | a0001 | c0001 | t0008 | g0253 | AFR | ESN | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0072 | AFR | ESN | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG03195 | hp1 | a0001 | c0003 | t0004 | g0004 | AFR | ESN | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG03225 | hp1 | a0001 | c0001 | t0011 | g0265 | AFR | MSL | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG03225 | hp2 | a0014 | c0021 | t0017 | g0267 | AFR | MSL | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG03239 | hp1 | a0001 | c0003 | t0002 | g0081 | SAS | PJL | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG03239 | hp2 | a0007 | c0015 | t0001 | g0173 | SAS | PJL | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0065 | AFR | MSL | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0076 | AFR | MSL | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG03516 | hp1 | a0002 | c0004 | t0005 | g0057 | AFR | ESN | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0062 | AFR | MSL | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0046 | AFR | MSL | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG03654 | hp1 | a0002 | c0006 | t0002 | g0126 | SAS | PJL | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0033 | SAS | PJL | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG03704 | hp2 | a0005 | c0022 | t0002 | g0092 | SAS | PJL | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG03927 | hp1 | a0001 | c0003 | t0002 | g0150 | SAS | BEB | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0006 | SAS | BEB | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | STU | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0037 | SAS | STU | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0175 | SAS | STU | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | STU | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0054 | AFR | YRI | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18522 | hp2 | a0001 | c0001 | t0008 | g0252 | AFR | YRI | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18906 | hp1 | a0012 | c0027 | t0004 | g0066 | AFR | YRI | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0206 | AFR | YRI | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18942 | hp1 | a0001 | c0002 | t0008 | g0250 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18945 | hp1 | a0001 | c0002 | t0020 | g0270 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18947 | hp2 | a0002 | c0005 | t0001 | g0165 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0192 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18950 | hp2 | a0002 | c0004 | t0003 | g0015 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0177 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18964 | hp1 | a0003 | c0008 | t0001 | g0212 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18964 | hp2 | a0001 | c0001 | t0010 | g0147 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18965 | hp2 | a0001 | c0001 | t0019 | g0269 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18968 | hp2 | a0001 | c0011 | t0010 | g0146 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18969 | hp1 | a0001 | c0002 | t0008 | g0249 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18971 | hp2 | a0015 | c0020 | t0003 | g0009 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18980 | hp2 | a0002 | c0005 | t0001 | g0231 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18984 | hp2 | a0001 | c0003 | t0002 | g0085 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18986 | hp1 | a0001 | c0003 | t0009 | g0001 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18989 | hp1 | a0002 | c0005 | t0001 | g0170 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18994 | hp1 | a0002 | c0005 | t0001 | g0246 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19000 | hp1 | a0008 | c0017 | t0001 | g0190 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19000 | hp2 | a0001 | c0001 | t0006 | g0255 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0163 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19002 | hp2 | a0001 | c0003 | t0002 | g0091 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19004 | hp2 | a0001 | c0029 | t0001 | g0122 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19007 | hp1 | a0003 | c0008 | t0001 | g0207 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19007 | hp2 | a0001 | c0033 | t0002 | g0110 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19009 | hp2 | a0001 | c0001 | t0006 | g0256 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19030 | hp1 | a0002 | c0026 | t0001 | g0215 | AFR | LWK | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19030 | hp2 | a0001 | c0001 | t0007 | g0034 | AFR | LWK | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19043 | hp1 | a0001 | c0013 | t0012 | g0145 | AFR | LWK | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | LWK | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0240 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19056 | hp2 | a0001 | c0003 | t0002 | g0090 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19057 | hp2 | a0001 | c0007 | t0001 | g0172 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19067 | hp1 | a0002 | c0004 | t0003 | g0052 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19068 | hp2 | a0002 | c0004 | t0003 | g0039 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19070 | hp1 | a0010 | c0014 | t0001 | g0195 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19079 | hp1 | a0001 | c0003 | t0002 | g0100 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0243 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19080 | hp1 | a0002 | c0006 | t0002 | g0089 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0236 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0073 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19084 | hp2 | a0001 | c0001 | t0010 | g0149 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19085 | hp2 | a0001 | c0003 | t0002 | g0111 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19086 | hp1 | a0001 | c0003 | t0002 | g0084 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19086 | hp2 | a0001 | c0007 | t0001 | g0183 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19087 | hp2 | a0001 | c0003 | t0002 | g0098 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19088 | hp1 | a0001 | c0001 | t0006 | g0257 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19091 | hp2 | a0002 | c0005 | t0001 | g0239 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | YRI | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0069 | AFR | YRI | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0077 | AFR | ASW | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA20129 | hp2 | a0001 | c0001 | t0014 | g0148 | AFR | ASW | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0128 | EUR | TSI | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0022 | EUR | TSI | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0201 | AFR | ACB | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02486 | hp1 | a0001 | c0001 | t0015 | g0248 | AFR | ACB | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0047 | AFR | ACB | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0074 | AFR | ACB | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG02559 | hp2 | a0001 | c0032 | t0011 | g0263 | AFR | ACB | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0056 | AFR | MSL | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | MSL | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18955 | hp1 | a0001 | c0003 | t0013 | g0096 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0221 | AFR | USA | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0075 | AFR | USA | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0002 | g0138 | REF | REF | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0002 | g0082 | REF | REF | HECTD4_chr12_112155195_112387431 | HECTD4 | chr12 | 112155195 | 112387431 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:112178962
|
C | T | 1 | a0011 | 1 | HG02071.hp2 | missense_variant | MODERATE | c.11332G>A | p.Ala3778Thr | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 64/76 | 11635/15752 | 11332/13257 | 3778/4418 | chr12 | 112178962 | ||
| chr12:112179289
|
G | A | 1 | a0010 | 1 | NA19070.hp1 | missense_variant | MODERATE | c.11096C>T | p.Ser3699Phe | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 63/76 | 11399/15752 | 11096/13257 | 3699/4418 | chr12 | 112179289 | ||
| chr12:112184240
|
G | C | 1 | a0005 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.10726C>G | p.Leu3576Val | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 61/76 | 11029/15752 | 10726/13257 | 3576/4418 | chr12 | 112184240 | ||
| chr12:112185003
|
C | G | 1 | a0012 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.9963G>C | p.Lys3321Asn | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 61/76 | 10266/15752 | 9963/13257 | 3321/4418 | chr12 | 112185003 | ||
| chr12:112185233
|
C | A | 1 | a0009 | 1 | HG01928.hp2 | missense_variant | MODERATE | c.9733G>T | p.Gly3245Cys | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 61/76 | 10036/15752 | 9733/13257 | 3245/4418 | chr12 | 112185233 | ||
| chr12:112185241
|
G | A | 1 | a0013 | 1 | HG00544.hp2 | missense_variant | MODERATE | c.9725C>T | p.Ala3242Val | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 61/76 | 10028/15752 | 9725/13257 | 3242/4418 | chr12 | 112185241 | ||
| chr12:112185241
|
G | GC | 2 | a0002a0008 | 22 | HG01175.hp1 HG01433.hp1 HG01934.hp1 others(19): Show |
frameshift_variant | HIGH | c.9724dupG | p.Ala3242fs | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 61/76 | 10027/15752 | 9724/13257 | 3242/4418 | chr12 | 112185241 | ||
| chr12:112185266
|
C | T | 1 | a0014 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.9700G>A | p.Gly3234Ser | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 61/76 | 10003/15752 | 9700/13257 | 3234/4418 | chr12 | 112185266 | ||
| chr12:112192617
|
T | C | 1 | a0008 | 1 | NA19000.hp1 | missense_variant | MODERATE | c.9235A>G | p.Thr3079Ala | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 59/76 | 9538/15752 | 9235/13257 | 3079/4418 | chr12 | 112192617 | ||
| chr12:112192728
|
C | T | 1 | a0007 | 1 | HG03239.hp2 | missense_variant | MODERATE | c.9124G>A | p.Val3042Ile | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 59/76 | 9427/15752 | 9124/13257 | 3042/4418 | chr12 | 112192728 | ||
| chr12:112203754
|
C | T | 1 | a0006 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.8288G>A | p.Arg2763His | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 54/76 | 8591/15752 | 8288/13257 | 2763/4418 | chr12 | 112203754 | ||
| chr12:112216884
|
T | A | 1 | a0003 | 2 | NA18964.hp1 NA19007.hp1 |
missense_variant | MODERATE | c.7274A>T | p.Tyr2425Phe | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 47/76 | 7577/15752 | 7274/13257 | 2425/4418 | chr12 | 112216884 | ||
| chr12:112228714
|
C | T | 1 | a0005 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.6617G>A | p.Arg2206Lys | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 42/76 | 6920/15752 | 6617/13257 | 2206/4418 | chr12 | 112228714 | ||
| chr12:112251008
|
C | T | 1 | a0015 | 1 | NA18971.hp2 | missense_variant | MODERATE | c.3679G>A | p.Ala1227Thr | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 24/76 | 3982/15752 | 3679/13257 | 1227/4418 | chr12 | 112251008 | ||
| chr12:112251027
|
T | A | 1 | a0004 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.3660A>T | p.Glu1220Asp | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 24/76 | 3963/15752 | 3660/13257 | 1220/4418 | chr12 | 112251027 | ||
| chr12:112261323
|
A | G | 1 | a0016 | 1 | HG02896.hp2 | missense_variant | MODERATE | c.2855T>C | p.Ile952Thr | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 18/76 | 3158/15752 | 2855/13257 | 952/4418 | chr12 | 112261323 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:112163563
|
G | A | 1 | a0001c0029 | 1 | NA19004.hp2 | synonymous_variant | LOW | c.12876C>T | p.Tyr4292Tyr | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 74/76 | 13179/15752 | 12876/13257 | 4292/4418 | chr12 | 112163563 | ||
| chr12:112167443
|
G | A | 1 | a0001c0031 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.12408C>T | p.Asp4136Asp | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 72/76 | 12711/15752 | 12408/13257 | 4136/4418 | chr12 | 112167443 | ||
| chr12:112171142
|
G | A | 1 | a0001c0030 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.11907C>T | p.Ile3969Ile | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 68/76 | 12210/15752 | 11907/13257 | 3969/4418 | chr12 | 112171142 | ||
| chr12:112184508
|
G | A | 1 | a0001c0007 | 2 | NA19057.hp2 NA19086.hp2 |
synonymous_variant | LOW | c.10458C>T | p.Ser3486Ser | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 61/76 | 10761/15752 | 10458/13257 | 3486/4418 | chr12 | 112184508 | ||
| chr12:112185330
|
C | T | 1 | a0001c0016 | 1 | HG00597.hp1 | synonymous_variant | LOW | c.9636G>A | p.Leu3212Leu | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 61/76 | 9939/15752 | 9636/13257 | 3212/4418 | chr12 | 112185330 | ||
| chr12:112204583
|
G | A | 1 | a0001c0018 | 1 | HG01934.hp2 | synonymous_variant | LOW | c.8172C>T | p.Tyr2724Tyr | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 53/76 | 8475/15752 | 8172/13257 | 2724/4418 | chr12 | 112204583 | ||
| chr12:112212579
|
G | T | 1 | a0010c0014 | 1 | NA19070.hp1 | synonymous_variant | LOW | c.7537C>A | p.Arg2513Arg | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 49/76 | 7840/15752 | 7537/13257 | 2513/4418 | chr12 | 112212579 | ||
| chr12:112212598
|
C | T | 2 | a0001c0010a0002c0026 | 3 | HG02965.hp2 HG03098.hp1 NA19030.hp1 |
synonymous_variant | LOW | c.7518G>A | p.Pro2506Pro | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 49/76 | 7821/15752 | 7518/13257 | 2506/4418 | chr12 | 112212598 | ||
| chr12:112212646
|
G | A | 1 | a0001c0011 | 2 | HG02135.hp2 NA18968.hp2 |
synonymous_variant | LOW | c.7470C>T | p.Asp2490Asp | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 49/76 | 7773/15752 | 7470/13257 | 2490/4418 | chr12 | 112212646 | ||
| chr12:112216859
|
T | G | 1 | a0001c0031 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.7299A>C | p.Gly2433Gly | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 47/76 | 7602/15752 | 7299/13257 | 2433/4418 | chr12 | 112216859 | ||
| chr12:112229871
|
T | G | 25 | a0001c0001a0001c0002a0001c0007others(22): Show | 220 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(217): Show |
synonymous_variant | LOW | c.6346A>C | p.Arg2116Arg | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 41/76 | 6649/15752 | 6346/13257 | 2116/4418 | chr12 | 112229871 | ||
| chr12:112235120
|
G | T | 2 | a0001c0009a0014c0021 | 3 | HG02622.hp2 HG02897.hp1 HG03225.hp2 |
synonymous_variant | LOW | c.5872C>A | p.Arg1958Arg | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 37/76 | 6175/15752 | 5872/13257 | 1958/4418 | chr12 | 112235120 | ||
| chr12:112235670
|
G | A | 1 | a0001c0032 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.5559C>T | p.Cys1853Cys | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 36/76 | 5862/15752 | 5559/13257 | 1853/4418 | chr12 | 112235670 | ||
| chr12:112243752
|
G | A | 1 | a0001c0033 | 1 | NA19007.hp2 | synonymous_variant | LOW | c.4659C>T | p.His1553His | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 31/76 | 4962/15752 | 4659/13257 | 1553/4418 | chr12 | 112243752 | ||
| chr12:112256425
|
G | A | 1 | a0001c0013 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.3222C>T | p.Pro1074Pro | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 21/76 | 3525/15752 | 3222/13257 | 1074/4418 | chr12 | 112256425 | ||
| chr12:112265928
|
A | C | 9 | a0001c0002a0001c0007a0001c0016others(6): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
synonymous_variant | LOW | c.2448T>G | p.Ala816Ala | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 15/76 | 2751/15752 | 2448/13257 | 816/4418 | chr12 | 112265928 | ||
| chr12:112269790
|
C | T | 1 | a0001c0013 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.2235G>A | p.Arg745Arg | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 13/76 | 2538/15752 | 2235/13257 | 745/4418 | chr12 | 112269790 | ||
| chr12:112306103
|
C | T | 1 | a0001c0012 | 1 | HG01071.hp2 | synonymous_variant | LOW | c.1296G>A | p.Pro432Pro | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/76 | 1599/15752 | 1296/13257 | 432/4418 | chr12 | 112306103 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:112160517
|
G | A | 8 | a0001c0001t0003a0001c0001t0006a0001c0001t0010others(5): Show | 49 | HG00597.hp2 HG01109.hp2 HG01243.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*1870C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 76/76 | 1870 | chr12 | 112160517 | |||||
| chr12:112161257
|
T | TGCACTGG others(1): Show |
46 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(43): Show | 221 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(218): Show |
3_prime_UTR_variant | MODIFIER | c.*1129_*1130insCCCA others(4): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 76/76 | 1129 | chr12 | 112161257 | |||||
| chr12:112161461
|
C | T | 4 | a0001c0001t0007a0001c0001t0014a0001c0030t0007others(1): Show | 7 | HG01943.hp1 HG02257.hp1 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*926G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 76/76 | 926 | chr12 | 112161461 | |||||
| chr12:112161479
|
C | A | 4 | a0001c0001t0007a0001c0001t0014a0001c0030t0007others(1): Show | 7 | HG01943.hp1 HG02257.hp1 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*908G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 76/76 | 908 | chr12 | 112161479 | |||||
| chr12:112161862
|
C | T | 1 | a0001c0003t0013 | 2 | HG02080.hp1 NA18955.hp1 |
3_prime_UTR_variant | MODIFIER | c.*525G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 76/76 | 525 | chr12 | 112161862 | |||||
| chr12:112162131
|
GAC | G | 14 | a0001c0001t0003a0001c0001t0005a0001c0001t0006others(11): Show | 67 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*254_*255delGT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 76/76 | 254 | chr12 | 112162131 | |||||
| chr12:112382174
|
G | A | 1 | a0001c0009t0018 | 1 | HG02897.hp1 | 5_prime_UTR_variant | MODIFIER | c.-46C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/76 | 46 | chr12 | 112382174 | |||||
| chr12:112382277
|
G | A | 1 | a0001c0001t0015 | 1 | HG02486.hp1 | 5_prime_UTR_variant | MODIFIER | c.-149C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/76 | 149 | chr12 | 112382277 | |||||
| chr12:112382327
|
T | TGCC | 3 | a0001c0001t0008a0001c0002t0008a0001c0031t0008 | 5 | HG02976.hp1 HG03130.hp2 NA18522.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-202_-200dupGGC | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/76 | 200 | chr12 | 112382327 | |||||
| chr12:112382327
|
T | TGCCGCC | 4 | a0001c0001t0006a0001c0001t0011a0001c0032t0011others(1): Show | 12 | HG00597.hp2 HG02056.hp2 HG02071.hp2 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-205_-200dupGGCGGC | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/76 | 200 | chr12 | 112382327 | |||||
| chr12:112382327
|
T | TGCCGCCG others(5): Show |
1 | a0001c0009t0016 | 1 | HG02622.hp2 | 5_prime_UTR_variant | MODIFIER | c.-211_-200dupGGCGGC others(6): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/76 | 200 | chr12 | 112382327 | |||||
| chr12:112382327
|
T | TGCCGCCG others(8): Show |
1 | a0014c0021t0017 | 1 | HG03225.hp2 | 5_prime_UTR_variant | MODIFIER | c.-214_-200dupGGCGGC others(9): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/76 | 200 | chr12 | 112382327 | |||||
| chr12:112382327
|
T | TGCCGCCG others(11): Show |
1 | a0001c0009t0018 | 1 | HG02897.hp1 | 5_prime_UTR_variant | MODIFIER | c.-217_-200dupGGCGGC others(12): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/76 | 200 | chr12 | 112382327 | |||||
| chr12:112382327
|
T | TGCCGCCG others(29): Show |
2 | a0001c0001t0019a0001c0002t0020 | 2 | NA18945.hp1 NA18965.hp2 |
5_prime_UTR_variant | MODIFIER | c.-200_-199insGGCGGC others(30): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/76 | 200 | chr12 | 112382327 | |||||
| chr12:112382327
|
TGCC | T | 14 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(11): Show | 78 | HG01081.hp1 HG01099.hp1 HG01109.hp1 others(75): Show |
5_prime_UTR_variant | MODIFIER | c.-202_-200delGGC | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/76 | 200 | chr12 | 112382327 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:112162621
|
G | A | 8 | a0001c0001t0001g0099a0001c0001t0001g0125a0001c0001t0001g0128others(5): Show | 8 | HG00140.hp1 HG00738.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.13121-98C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 75/75 | chr12 | 112162621 | ||||||
| chr12:112162675
|
C | T | 2 | a0001c0001t0004g0067a0001c0009t0018g0268 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.13121-152G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 75/75 | chr12 | 112162675 | ||||||
| chr12:112162768
|
CT | C | 5 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0004g0074others(2): Show | 5 | HG01167.hp1 HG02559.hp1 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.13121-246delA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 75/75 | chr12 | 112162768 | ||||||
| chr12:112162989
|
C | T | 6 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(3): Show | 6 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.13120+53G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 75/75 | chr12 | 112162989 | ||||||
| chr12:112163298
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.12898-34C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 74/75 | chr12 | 112163298 | ||||||
| chr12:112163372
|
G | A | 1 | a0001c0002t0001g0174 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.12898-108C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 74/75 | chr12 | 112163372 | ||||||
| chr12:112163437
|
G | C | 2 | a0001c0001t0001g0156a0001c0001t0001g0220 | 2 | HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.12897+105C>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 74/75 | chr12 | 112163437 | ||||||
| chr12:112163446
|
G | A | 81 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(78): Show | 81 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(78): Show |
intron_variant | MODIFIER | c.12897+96C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 74/75 | chr12 | 112163446 | ||||||
| chr12:112163455
|
C | T | 1 | a0001c0001t0005g0060 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.12897+87G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 74/75 | chr12 | 112163455 | ||||||
| chr12:112163794
|
G | A | 1 | a0002c0006t0002g0126 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.12702-57C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 73/75 | chr12 | 112163794 | ||||||
| chr12:112163929
|
T | A | 2 | a0001c0001t0003g0022a0001c0001t0003g0037 | 2 | HG04115.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.12701+180A>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 73/75 | chr12 | 112163929 | ||||||
| chr12:112164004
|
T | G | 74 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(71): Show | 74 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(71): Show |
intron_variant | MODIFIER | c.12701+105A>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 73/75 | chr12 | 112164004 | ||||||
| chr12:112164382
|
C | T | 5 | a0001c0001t0004g0062a0001c0001t0004g0064a0001c0001t0004g0065others(2): Show | 5 | HG02055.hp2 HG02572.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.12535-107G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 72/75 | chr12 | 112164382 | ||||||
| chr12:112164642
|
C | T | 3 | a0001c0001t0005g0070a0001c0009t0016g0266a0014c0021t0017g0267 | 3 | HG02622.hp2 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.12535-367G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 72/75 | chr12 | 112164642 | ||||||
| chr12:112164822
|
A | G | 1 | a0001c0002t0001g0241 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.12535-547T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 72/75 | chr12 | 112164822 | ||||||
| chr12:112164917
|
C | T | 2 | a0001c0001t0004g0074a0001c0001t0004g0078 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.12535-642G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 72/75 | chr12 | 112164917 | ||||||
| chr12:112165222
|
CT | C | 8 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0019others(5): Show | 8 | HG01167.hp1 NA18946.hp2 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.12535-948delA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 72/75 | chr12 | 112165222 | ||||||
| chr12:112165349
|
A | AT | 13 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(10): Show | 13 | HG01934.hp1 HG02135.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.12535-1075dupA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 72/75 | chr12 | 112165349 | ||||||
| chr12:112165349
|
AT | A | 20 | a0001c0001t0001g0152a0001c0001t0004g0023a0001c0001t0004g0068others(17): Show | 20 | HG01099.hp2 HG01175.hp1 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.12535-1075delA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 72/75 | chr12 | 112165349 | ||||||
| chr12:112165349
|
ATT | A | 152 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(149): Show | 152 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(149): Show |
intron_variant | MODIFIER | c.12535-1076_12535-1 others(8): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 72/75 | chr12 | 112165349 | ||||||
| chr12:112165349
|
ATTT | A | 7 | a0001c0001t0003g0030a0001c0001t0004g0071a0001c0001t0004g0074others(4): Show | 7 | HG01256.hp1 HG01891.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.12535-1077_12535-1 others(9): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 72/75 | chr12 | 112165349 | ||||||
| chr12:112165404
|
T | C | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG02109.hp1 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.12535-1129A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 72/75 | chr12 | 112165404 | ||||||
| chr12:112165412
|
C | T | 2 | a0001c0002t0001g0203a0001c0002t0001g0204 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.12535-1137G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 72/75 | chr12 | 112165412 | ||||||
| chr12:112165542
|
G | A | 1 | a0001c0002t0001g0242 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.12535-1267C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 72/75 | chr12 | 112165542 | ||||||
| chr12:112165558
|
A | G | 3 | a0001c0001t0005g0070a0001c0009t0016g0266a0014c0021t0017g0267 | 3 | HG02622.hp2 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.12535-1283T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 72/75 | chr12 | 112165558 | ||||||
| chr12:112165568
|
G | A | 61 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(58): Show | 61 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(58): Show |
intron_variant | MODIFIER | c.12535-1293C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 72/75 | chr12 | 112165568 | ||||||
| chr12:112166800
|
G | A | 3 | a0001c0010t0001g0214a0001c0010t0001g0217a0002c0026t0001g0215 | 3 | HG02965.hp2 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.12534+517C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 72/75 | chr12 | 112166800 | ||||||
| chr12:112166871
|
G | A | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.12534+446C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 72/75 | chr12 | 112166871 | ||||||
| chr12:112166875
|
C | T | 1 | a0001c0001t0004g0068 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.12534+442G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 72/75 | chr12 | 112166875 | ||||||
| chr12:112166880
|
G | A | 1 | a0001c0001t0004g0023 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.12534+437C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 72/75 | chr12 | 112166880 | ||||||
| chr12:112166924
|
C | T | 1 | a0001c0001t0004g0061 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.12534+393G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 72/75 | chr12 | 112166924 | ||||||
| chr12:112167027
|
C | T | 1 | a0001c0001t0005g0070 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.12534+290G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 72/75 | chr12 | 112167027 | ||||||
| chr12:112167222
|
C | T | 1 | a0001c0001t0003g0016 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.12534+95G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 72/75 | chr12 | 112167222 | ||||||
| chr12:112167267
|
C | T | 2 | a0001c0003t0002g0101a0002c0006t0002g0126 | 2 | HG01175.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.12534+50G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 72/75 | chr12 | 112167267 | ||||||
| chr12:112167553
|
G | A | 1 | a0001c0002t0001g0187 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.12313-15C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 71/75 | chr12 | 112167553 | ||||||
| chr12:112167569
|
G | C | 1 | a0001c0002t0001g0182 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.12313-31C>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 71/75 | chr12 | 112167569 | ||||||
| chr12:112167765
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.12312+49C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 71/75 | chr12 | 112167765 | ||||||
| chr12:112167807
|
T | C | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
splice_region_variant&intron_variant | LOW | c.12312+7A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 71/75 | chr12 | 112167807 | ||||||
| chr12:112168008
|
A | C | 3 | a0001c0002t0001g0175a0001c0002t0001g0219a0007c0015t0001g0173 | 3 | HG03017.hp2 HG03239.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.12209-91T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 70/75 | chr12 | 112168008 | ||||||
| chr12:112168181
|
C | T | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.12209-264G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 70/75 | chr12 | 112168181 | ||||||
| chr12:112168217
|
G | C | 75 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(72): Show | 75 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.12209-300C>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 70/75 | chr12 | 112168217 | ||||||
| chr12:112168224
|
G | A | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG02109.hp1 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.12209-307C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 70/75 | chr12 | 112168224 | ||||||
| chr12:112168367
|
G | A | 8 | a0001c0001t0004g0061a0001c0001t0004g0067a0001c0001t0004g0068others(5): Show | 8 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.12209-450C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 70/75 | chr12 | 112168367 | ||||||
| chr12:112168672
|
C | T | 8 | a0001c0001t0004g0023a0001c0001t0007g0007a0001c0001t0007g0024others(5): Show | 8 | HG01943.hp1 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.12209-755G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 70/75 | chr12 | 112168672 | ||||||
| chr12:112168781
|
G | A | 3 | a0001c0001t0003g0031a0001c0001t0003g0032a0015c0020t0003g0009 | 3 | NA18971.hp2 NA18980.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.12208+722C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 70/75 | chr12 | 112168781 | ||||||
| chr12:112168860
|
T | C | 4 | a0001c0001t0003g0020a0001c0001t0003g0029a0001c0001t0003g0030others(1): Show | 4 | NA18942.hp2 NA18960.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.12208+643A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 70/75 | chr12 | 112168860 | ||||||
| chr12:112168941
|
C | A | 1 | a0001c0002t0001g0193 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.12208+562G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 70/75 | chr12 | 112168941 | ||||||
| chr12:112168991
|
G | A | 2 | a0001c0001t0001g0153a0004c0034t0001g0154 | 2 | HG02647.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.12208+512C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 70/75 | chr12 | 112168991 | ||||||
| chr12:112169191
|
GCACA | G | 6 | a0001c0002t0001g0201a0001c0002t0001g0202a0001c0002t0001g0203others(3): Show | 6 | HG02109.hp2 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.12208+308_12208+31 others(8): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 70/75 | chr12 | 112169191 | ||||||
| chr12:112169240
|
G | A | 1 | a0001c0029t0001g0122 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.12208+263C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 70/75 | chr12 | 112169240 | ||||||
| chr12:112169281
|
G | C | 8 | a0001c0001t0004g0023a0001c0001t0007g0007a0001c0001t0007g0024others(5): Show | 8 | HG01943.hp1 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.12208+222C>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 70/75 | chr12 | 112169281 | ||||||
| chr12:112169326
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.12208+177C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 70/75 | chr12 | 112169326 | ||||||
| chr12:112169477
|
G | A | 1 | a0001c0029t0001g0122 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.12208+26C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 70/75 | chr12 | 112169477 | ||||||
| chr12:112169778
|
C | T | 2 | a0001c0001t0004g0074a0001c0001t0004g0078 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.12053-120G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 69/75 | chr12 | 112169778 | ||||||
| chr12:112169939
|
C | A | 1 | a0001c0001t0003g0058 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.12053-281G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 69/75 | chr12 | 112169939 | ||||||
| chr12:112170118
|
G | C | 8 | a0001c0001t0004g0023a0001c0001t0007g0007a0001c0001t0007g0024others(5): Show | 8 | HG01943.hp1 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.12052+215C>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 69/75 | chr12 | 112170118 | ||||||
| chr12:112170508
|
TCCC | T | 72 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(69): Show | 72 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(69): Show |
intron_variant | MODIFIER | c.11933-59_11933-57d others(5): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 68/75 | chr12 | 112170508 | ||||||
| chr12:112170580
|
T | G | 1 | a0016c0019t0002g0135 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.11933-128A>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 68/75 | chr12 | 112170580 | ||||||
| chr12:112170613
|
A | G | 2 | a0001c0003t0002g0103a0001c0003t0002g0107 | 2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.11933-161T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 68/75 | chr12 | 112170613 | ||||||
| chr12:112170732
|
A | C | 11 | a0001c0001t0001g0083a0001c0001t0001g0112a0001c0001t0001g0113others(8): Show | 11 | HG01993.hp2 HG02135.hp2 HG04115.hp1 others(8): Show |
intron_variant | MODIFIER | c.11933-280T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 68/75 | chr12 | 112170732 | ||||||
| chr12:112171417
|
A | G | 4 | a0001c0001t0001g0079a0001c0001t0001g0156a0001c0001t0001g0160others(1): Show | 4 | HG01884.hp1 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.11786-154T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 67/75 | chr12 | 112171417 | ||||||
| chr12:112171556
|
C | A | 1 | a0001c0001t0004g0023 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.11786-293G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 67/75 | chr12 | 112171556 | ||||||
| chr12:112171996
|
C | T | 8 | a0001c0001t0004g0023a0001c0001t0007g0007a0001c0001t0007g0024others(5): Show | 8 | HG01943.hp1 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.11785+675G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 67/75 | chr12 | 112171996 | ||||||
| chr12:112172052
|
C | T | 8 | a0001c0001t0004g0023a0001c0001t0007g0007a0001c0001t0007g0024others(5): Show | 8 | HG01943.hp1 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.11785+619G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 67/75 | chr12 | 112172052 | ||||||
| chr12:112172194
|
C | T | 81 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(78): Show | 81 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(78): Show |
intron_variant | MODIFIER | c.11785+477G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 67/75 | chr12 | 112172194 | ||||||
| chr12:112172529
|
C | G | 1 | a0001c0001t0004g0061 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.11785+142G>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 67/75 | chr12 | 112172529 | ||||||
| chr12:112172588
|
A | T | 3 | a0001c0001t0005g0070a0001c0009t0016g0266a0014c0021t0017g0267 | 3 | HG02622.hp2 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.11785+83T>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 67/75 | chr12 | 112172588 | ||||||
| chr12:112172910
|
G | A | 10 | a0001c0003t0002g0136a0001c0003t0002g0137a0001c0003t0002g0138others(7): Show | 10 | HG00735.hp1 HG01106.hp2 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.11595-49C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 66/75 | chr12 | 112172910 | ||||||
| chr12:112173057
|
C | T | 4 | a0001c0002t0001g0169a0001c0002t0001g0198a0001c0002t0001g0200others(1): Show | 4 | HG02027.hp2 HG02135.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.11595-196G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 66/75 | chr12 | 112173057 | ||||||
| chr12:112173266
|
C | T | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.11595-405G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 66/75 | chr12 | 112173266 | ||||||
| chr12:112173585
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.11595-724C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 66/75 | chr12 | 112173585 | ||||||
| chr12:112173685
|
C | T | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.11595-824G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 66/75 | chr12 | 112173685 | ||||||
| chr12:112173702
|
A | AT | 6 | a0001c0001t0004g0023a0001c0001t0007g0024a0001c0001t0007g0025others(3): Show | 6 | HG01943.hp1 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.11595-842dupA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 66/75 | chr12 | 112173702 | ||||||
| chr12:112173964
|
C | T | 1 | a0001c0001t0001g0119 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.11595-1103G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 66/75 | chr12 | 112173964 | ||||||
| chr12:112173980
|
CT | C | 5 | a0001c0001t0003g0019a0001c0001t0010g0149a0001c0002t0001g0240others(2): Show | 5 | HG02559.hp2 HG02976.hp1 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.11595-1120delA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 66/75 | chr12 | 112173980 | ||||||
| chr12:112174009
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.11595-1148G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 66/75 | chr12 | 112174009 | ||||||
| chr12:112174038
|
C | T | 1 | a0001c0001t0004g0077 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.11595-1177G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 66/75 | chr12 | 112174038 | ||||||
| chr12:112174087
|
C | T | 4 | a0001c0002t0001g0176a0001c0002t0001g0189a0001c0002t0001g0194others(1): Show | 4 | HG00735.hp2 HG01081.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.11595-1226G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 66/75 | chr12 | 112174087 | ||||||
| chr12:112174123
|
G | A | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.11595-1262C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 66/75 | chr12 | 112174123 | ||||||
| chr12:112174267
|
C | CT | 80 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(77): Show | 80 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(77): Show |
intron_variant | MODIFIER | c.11595-1407dupA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 66/75 | chr12 | 112174267 | ||||||
| chr12:112174349
|
A | T | 170 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(167): Show | 170 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(167): Show |
intron_variant | MODIFIER | c.11594+1387T>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 66/75 | chr12 | 112174349 | ||||||
| chr12:112174656
|
C | A | 3 | a0001c0003t0002g0090a0001c0003t0002g0100a0002c0006t0002g0089 | 3 | NA19056.hp2 NA19079.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.11594+1080G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 66/75 | chr12 | 112174656 | ||||||
| chr12:112174682
|
A | G | 1 | a0001c0001t0003g0022 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.11594+1054T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 66/75 | chr12 | 112174682 | ||||||
| chr12:112174737
|
T | C | 1 | a0001c0003t0002g0080 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.11594+999A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 66/75 | chr12 | 112174737 | ||||||
| chr12:112174757
|
T | A | 1 | a0001c0001t0004g0071 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.11594+979A>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 66/75 | chr12 | 112174757 | ||||||
| chr12:112174776
|
C | T | 1 | a0005c0022t0002g0092 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.11594+960G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 66/75 | chr12 | 112174776 | ||||||
| chr12:112174838
|
C | T | 3 | a0001c0001t0011g0264a0001c0001t0011g0265a0001c0031t0008g0251 | 3 | HG02630.hp1 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.11594+898G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 66/75 | chr12 | 112174838 | ||||||
| chr12:112174908
|
C | T | 2 | a0001c0001t0004g0067a0001c0009t0018g0268 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.11594+828G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 66/75 | chr12 | 112174908 | ||||||
| chr12:112174990
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.11594+746T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 66/75 | chr12 | 112174990 | ||||||
| chr12:112175048
|
T | G | 8 | a0001c0001t0004g0023a0001c0001t0007g0007a0001c0001t0007g0024others(5): Show | 8 | HG01943.hp1 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.11594+688A>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 66/75 | chr12 | 112175048 | ||||||
| chr12:112175294
|
C | T | 1 | a0001c0002t0001g0161 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.11594+442G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 66/75 | chr12 | 112175294 | ||||||
| chr12:112175435
|
C | T | 8 | a0001c0001t0004g0023a0001c0001t0007g0007a0001c0001t0007g0024others(5): Show | 8 | HG01943.hp1 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.11594+301G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 66/75 | chr12 | 112175435 | ||||||
| chr12:112176025
|
C | A | 1 | a0005c0022t0002g0092 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.11471-166G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 65/75 | chr12 | 112176025 | ||||||
| chr12:112176032
|
G | C | 2 | a0001c0003t0002g0085a0001c0003t0009g0001 | 2 | NA18984.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.11471-173C>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 65/75 | chr12 | 112176032 | ||||||
| chr12:112176195
|
T | C | 5 | a0001c0001t0004g0062a0001c0001t0004g0064a0001c0001t0004g0065others(2): Show | 5 | HG02055.hp2 HG02572.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.11471-336A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 65/75 | chr12 | 112176195 | ||||||
| chr12:112176522
|
G | C | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159 | 3 | HG03098.hp2 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.11470+74C>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 65/75 | chr12 | 112176522 | ||||||
| chr12:112176542
|
T | C | 3 | a0001c0003t0004g0004a0001c0003t0009g0002a0006c0023t0009g0003 | 3 | HG01109.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.11470+54A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 65/75 | chr12 | 112176542 | ||||||
| chr12:112176743
|
C | T | 1 | a0001c0003t0002g0085 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.11364-41G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 64/75 | chr12 | 112176743 | ||||||
| chr12:112176836
|
G | A | 3 | a0001c0001t0005g0070a0001c0009t0016g0266a0014c0021t0017g0267 | 3 | HG02622.hp2 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.11364-134C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 64/75 | chr12 | 112176836 | ||||||
| chr12:112177301
|
G | A | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.11364-599C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 64/75 | chr12 | 112177301 | ||||||
| chr12:112177375
|
C | CT | 7 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(4): Show | 7 | HG02109.hp1 HG02486.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.11364-674dupA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 64/75 | chr12 | 112177375 | ||||||
| chr12:112177375
|
C | CTT | 3 | a0001c0001t0004g0062a0001c0001t0004g0065a0012c0027t0004g0066 | 3 | HG03453.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.11364-674_11364-67 others(6): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 64/75 | chr12 | 112177375 | ||||||
| chr12:112177377
|
A | AT | 19 | a0001c0001t0001g0117a0001c0001t0001g0129a0001c0001t0001g0220others(16): Show | 19 | HG01106.hp1 HG01943.hp1 HG02135.hp2 others(16): Show |
intron_variant | MODIFIER | c.11364-676dupA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 64/75 | chr12 | 112177377 | ||||||
| chr12:112177377
|
A | T | 17 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0216others(14): Show | 17 | HG01099.hp2 HG01175.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.11364-675T>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 64/75 | chr12 | 112177377 | ||||||
| chr12:112177377
|
AT | A | 78 | a0001c0001t0001g0156a0001c0001t0004g0074a0001c0001t0004g0078others(75): Show | 78 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.11364-676delA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 64/75 | chr12 | 112177377 | ||||||
| chr12:112177473
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.11364-771C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 64/75 | chr12 | 112177473 | ||||||
| chr12:112177540
|
C | T | 2 | a0001c0001t0008g0252a0001c0001t0008g0253 | 2 | HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.11364-838G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 64/75 | chr12 | 112177540 | ||||||
| chr12:112177570
|
C | T | 81 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(78): Show | 81 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(78): Show |
intron_variant | MODIFIER | c.11364-868G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 64/75 | chr12 | 112177570 | ||||||
| chr12:112177573
|
G | A | 72 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(69): Show | 72 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(69): Show |
intron_variant | MODIFIER | c.11364-871C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 64/75 | chr12 | 112177573 | ||||||
| chr12:112177621
|
C | T | 12 | a0001c0002t0001g0163a0001c0002t0001g0164a0001c0002t0001g0176others(9): Show | 12 | HG00735.hp2 HG01081.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.11364-919G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 64/75 | chr12 | 112177621 | ||||||
| chr12:112177632
|
G | A | 2 | a0001c0001t0005g0053a0001c0001t0012g0151 | 2 | HG01099.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.11364-930C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 64/75 | chr12 | 112177632 | ||||||
| chr12:112177734
|
A | G | 67 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(64): Show | 67 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(64): Show |
intron_variant | MODIFIER | c.11364-1032T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 64/75 | chr12 | 112177734 | ||||||
| chr12:112177978
|
T | A | 170 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(167): Show | 170 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(167): Show |
intron_variant | MODIFIER | c.11363+953A>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 64/75 | chr12 | 112177978 | ||||||
| chr12:112178046
|
C | T | 1 | a0002c0005t0001g0197 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.11363+885G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 64/75 | chr12 | 112178046 | ||||||
| chr12:112178104
|
G | A | 1 | a0001c0003t0002g0134 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.11363+827C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 64/75 | chr12 | 112178104 | ||||||
| chr12:112178115
|
A | C | 59 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(56): Show | 59 | HG00597.hp2 HG01109.hp2 HG01167.hp2 others(56): Show |
intron_variant | MODIFIER | c.11363+816T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 64/75 | chr12 | 112178115 | ||||||
| chr12:112178363
|
T | C | 80 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(77): Show | 80 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(77): Show |
intron_variant | MODIFIER | c.11363+568A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 64/75 | chr12 | 112178363 | ||||||
| chr12:112178627
|
G | C | 175 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(172): Show | 175 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(172): Show |
intron_variant | MODIFIER | c.11363+304C>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 64/75 | chr12 | 112178627 | ||||||
| chr12:112178869
|
C | A | 1 | a0001c0001t0003g0006 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.11363+62G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 64/75 | chr12 | 112178869 | ||||||
| chr12:112178871
|
C | T | 2 | a0001c0001t0001g0156a0001c0001t0001g0220 | 2 | HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.11363+60G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 64/75 | chr12 | 112178871 | ||||||
| chr12:112179143
|
C | T | 1 | a0001c0011t0001g0133 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.11211+31G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 63/75 | chr12 | 112179143 | ||||||
| chr12:112179679
|
C | T | 1 | a0001c0001t0006g0260 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.10988-282G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 62/75 | chr12 | 112179679 | ||||||
| chr12:112179706
|
T | G | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.10988-309A>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 62/75 | chr12 | 112179706 | ||||||
| chr12:112179940
|
T | C | 2 | a0001c0001t0004g0065a0002c0004t0004g0063 | 2 | HG02055.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.10988-543A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 62/75 | chr12 | 112179940 | ||||||
| chr12:112180114
|
G | A | 64 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(61): Show | 64 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(61): Show |
intron_variant | MODIFIER | c.10988-717C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 62/75 | chr12 | 112180114 | ||||||
| chr12:112180396
|
G | A | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.10988-999C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 62/75 | chr12 | 112180396 | ||||||
| chr12:112180532
|
A | T | 1 | a0001c0001t0001g0127 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.10988-1135T>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 62/75 | chr12 | 112180532 | ||||||
| chr12:112180542
|
A | C | 68 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(65): Show | 68 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(65): Show |
intron_variant | MODIFIER | c.10988-1145T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 62/75 | chr12 | 112180542 | ||||||
| chr12:112180557
|
A | C | 1 | a0001c0001t0003g0037 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.10988-1160T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 62/75 | chr12 | 112180557 | ||||||
| chr12:112180665
|
A | C | 170 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(167): Show | 170 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(167): Show |
intron_variant | MODIFIER | c.10988-1268T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 62/75 | chr12 | 112180665 | ||||||
| chr12:112180709
|
G | A | 3 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0077 | 3 | HG03453.hp2 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.10988-1312C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 62/75 | chr12 | 112180709 | ||||||
| chr12:112180753
|
C | A | 1 | a0001c0030t0007g0035 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.10988-1356G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 62/75 | chr12 | 112180753 | ||||||
| chr12:112180966
|
T | TA | 8 | a0001c0001t0004g0061a0001c0001t0004g0067a0001c0001t0004g0068others(5): Show | 8 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.10988-1570dupT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 62/75 | chr12 | 112180966 | ||||||
| chr12:112180966
|
TA | T | 6 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(3): Show | 6 | HG02976.hp1 HG03098.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.10988-1570delT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 62/75 | chr12 | 112180966 | ||||||
| chr12:112181167
|
C | CA | 78 | a0001c0002t0001g0161a0001c0002t0001g0164a0001c0002t0001g0166others(75): Show | 78 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.10988-1771dupT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 62/75 | chr12 | 112181167 | ||||||
| chr12:112181703
|
A | G | 3 | a0001c0001t0007g0024a0001c0001t0007g0025a0001c0030t0007g0035 | 3 | HG01943.hp1 HG02717.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.10987+1356T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 62/75 | chr12 | 112181703 | ||||||
| chr12:112181711
|
T | C | 170 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(167): Show | 170 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(167): Show |
intron_variant | MODIFIER | c.10987+1348A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 62/75 | chr12 | 112181711 | ||||||
| chr12:112181957
|
C | T | 80 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(77): Show | 80 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(77): Show |
intron_variant | MODIFIER | c.10987+1102G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 62/75 | chr12 | 112181957 | ||||||
| chr12:112181961
|
G | A | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.10987+1098C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 62/75 | chr12 | 112181961 | ||||||
| chr12:112182023
|
G | A | 1 | a0001c0001t0003g0042 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.10987+1036C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 62/75 | chr12 | 112182023 | ||||||
| chr12:112182092
|
T | TA | 86 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(83): Show | 86 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(83): Show |
intron_variant | MODIFIER | c.10987+966dupT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 62/75 | chr12 | 112182092 | ||||||
| chr12:112182175
|
A | T | 1 | a0001c0003t0002g0104 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.10987+884T>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 62/75 | chr12 | 112182175 | ||||||
| chr12:112182384
|
TA | T | 170 | a0001c0001t0001g0116a0001c0001t0003g0006a0001c0001t0003g0010others(167): Show | 170 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(167): Show |
intron_variant | MODIFIER | c.10987+674delT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 62/75 | chr12 | 112182384 | ||||||
| chr12:112182506
|
A | T | 1 | a0002c0005t0001g0170 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.10987+553T>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 62/75 | chr12 | 112182506 | ||||||
| chr12:112182629
|
G | A | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.10987+430C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 62/75 | chr12 | 112182629 | ||||||
| chr12:112182842
|
T | A | 3 | a0001c0001t0005g0070a0001c0009t0016g0266a0014c0021t0017g0267 | 3 | HG02622.hp2 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.10987+217A>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 62/75 | chr12 | 112182842 | ||||||
| chr12:112182846
|
A | C | 1 | a0001c0002t0001g0218 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.10987+213T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 62/75 | chr12 | 112182846 | ||||||
| chr12:112183946
|
C | A | 6 | a0001c0001t0004g0023a0001c0001t0007g0024a0001c0001t0007g0025others(3): Show | 6 | HG01943.hp1 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.10779+241G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 61/75 | chr12 | 112183946 | ||||||
| chr12:112184082
|
C | T | 67 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(64): Show | 67 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(64): Show |
intron_variant | MODIFIER | c.10779+105G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 61/75 | chr12 | 112184082 | ||||||
| chr12:112185551
|
C | T | 1 | a0002c0004t0001g0155 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.9473-58G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 60/75 | chr12 | 112185551 | ||||||
| chr12:112185786
|
T | C | 2 | a0001c0001t0001g0079a0001c0001t0001g0160 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.9473-293A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 60/75 | chr12 | 112185786 | ||||||
| chr12:112186118
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.9473-625C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 60/75 | chr12 | 112186118 | ||||||
| chr12:112186306
|
CT | C | 13 | a0001c0001t0004g0023a0001c0001t0004g0067a0001c0001t0007g0007others(10): Show | 13 | HG01167.hp1 HG01943.hp1 HG02165.hp2 others(10): Show |
intron_variant | MODIFIER | c.9473-814delA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 60/75 | chr12 | 112186306 | ||||||
| chr12:112186324
|
T | A | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.9473-831A>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 60/75 | chr12 | 112186324 | ||||||
| chr12:112186328
|
T | A | 1 | a0001c0001t0001g0119 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.9473-835A>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 60/75 | chr12 | 112186328 | ||||||
| chr12:112186341
|
A | AT | 5 | a0001c0001t0001g0113a0001c0001t0003g0011a0001c0001t0004g0067others(2): Show | 5 | HG02896.hp1 NA18968.hp2 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.9473-849dupA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 60/75 | chr12 | 112186341 | ||||||
| chr12:112186341
|
A | ATT | 76 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0012others(73): Show | 76 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(73): Show |
intron_variant | MODIFIER | c.9473-850_9473-849d others(4): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 60/75 | chr12 | 112186341 | ||||||
| chr12:112186341
|
AT | A | 10 | a0001c0001t0004g0023a0001c0001t0007g0007a0001c0001t0007g0024others(7): Show | 10 | HG01943.hp1 HG02257.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.9473-849delA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 60/75 | chr12 | 112186341 | ||||||
| chr12:112186635
|
G | A | 1 | a0001c0003t0002g0085 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.9473-1142C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 60/75 | chr12 | 112186635 | ||||||
| chr12:112186664
|
T | C | 1 | a0001c0003t0002g0142 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.9473-1171A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 60/75 | chr12 | 112186664 | ||||||
| chr12:112186813
|
A | G | 1 | a0001c0001t0003g0026 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.9473-1320T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 60/75 | chr12 | 112186813 | ||||||
| chr12:112187042
|
T | C | 170 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(167): Show | 170 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(167): Show |
intron_variant | MODIFIER | c.9473-1549A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 60/75 | chr12 | 112187042 | ||||||
| chr12:112187267
|
C | T | 2 | a0001c0001t0004g0074a0001c0001t0004g0078 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.9473-1774G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 60/75 | chr12 | 112187267 | ||||||
| chr12:112187276
|
G | A | 3 | a0001c0001t0005g0070a0001c0009t0016g0266a0014c0021t0017g0267 | 3 | HG02622.hp2 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.9473-1783C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 60/75 | chr12 | 112187276 | ||||||
| chr12:112187622
|
C | CT | 6 | a0001c0001t0004g0068a0001c0001t0006g0255a0001c0001t0006g0256others(3): Show | 6 | HG00735.hp1 HG02622.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.9473-2130dupA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 60/75 | chr12 | 112187622 | ||||||
| chr12:112187622
|
CT | C | 167 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0099others(164): Show | 167 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(164): Show |
intron_variant | MODIFIER | c.9473-2130delA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 60/75 | chr12 | 112187622 | ||||||
| chr12:112187775
|
C | T | 1 | a0001c0001t0004g0074 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.9473-2282G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 60/75 | chr12 | 112187775 | ||||||
| chr12:112187820
|
G | A | 8 | a0001c0001t0004g0023a0001c0001t0007g0007a0001c0001t0007g0024others(5): Show | 8 | HG01943.hp1 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.9473-2327C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 60/75 | chr12 | 112187820 | ||||||
| chr12:112187827
|
T | C | 3 | a0001c0010t0001g0214a0001c0010t0001g0217a0002c0026t0001g0215 | 3 | HG02965.hp2 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.9473-2334A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 60/75 | chr12 | 112187827 | ||||||
| chr12:112187906
|
A | G | 9 | a0001c0001t0004g0061a0001c0001t0004g0067a0001c0001t0004g0068others(6): Show | 9 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.9473-2413T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 60/75 | chr12 | 112187906 | ||||||
| chr12:112188364
|
G | A | 1 | a0001c0001t0003g0059 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.9472+2422C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 60/75 | chr12 | 112188364 | ||||||
| chr12:112188420
|
C | G | 64 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(61): Show | 64 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(61): Show |
intron_variant | MODIFIER | c.9472+2366G>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 60/75 | chr12 | 112188420 | ||||||
| chr12:112189041
|
T | C | 80 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(77): Show | 80 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(77): Show |
intron_variant | MODIFIER | c.9472+1745A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 60/75 | chr12 | 112189041 | ||||||
| chr12:112189166
|
G | A | 5 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0118others(2): Show | 5 | NA18952.hp2 NA18973.hp2 NA19054.hp2 others(2): Show |
intron_variant | MODIFIER | c.9472+1620C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 60/75 | chr12 | 112189166 | ||||||
| chr12:112189367
|
A | G | 1 | a0001c0001t0004g0075 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.9472+1419T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 60/75 | chr12 | 112189367 | ||||||
| chr12:112189486
|
A | AG | 269 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0099others(266): Show | 269 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(266): Show |
intron_variant | MODIFIER | c.9472+1299_9472+130 others(5): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 60/75 | chr12 | 112189486 | ||||||
| chr12:112189546
|
G | A | 21 | a0001c0002t0001g0225a0001c0002t0001g0227a0001c0002t0001g0228others(18): Show | 21 | HG00544.hp1 HG02132.hp1 NA18946.hp1 others(18): Show |
intron_variant | MODIFIER | c.9472+1240C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 60/75 | chr12 | 112189546 | ||||||
| chr12:112189550
|
C | CA | 85 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0118others(82): Show | 85 | HG00544.hp1 HG00597.hp1 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.9472+1235dupT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 60/75 | chr12 | 112189550 | ||||||
| chr12:112189550
|
C | CAA | 11 | a0001c0002t0001g0181a0001c0002t0001g0198a0001c0002t0001g0204others(8): Show | 11 | HG01928.hp1 HG02027.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.9472+1234_9472+123 others(6): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 60/75 | chr12 | 112189550 | ||||||
| chr12:112189550
|
C | CAAAAAA | 33 | a0001c0001t0003g0010a0001c0001t0003g0012a0001c0001t0003g0013others(30): Show | 33 | HG01167.hp2 HG01243.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.9472+1230_9472+123 others(10): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 60/75 | chr12 | 112189550 | ||||||
| chr12:112189550
|
C | CAAAAAAA | 31 | a0001c0001t0003g0006a0001c0001t0003g0011a0001c0001t0003g0014others(28): Show | 31 | HG00597.hp2 HG01099.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.9472+1229_9472+123 others(11): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 60/75 | chr12 | 112189550 | ||||||
| chr12:112189550
|
C | CAAAAAAA others(3): Show |
2 | a0001c0001t0004g0067a0001c0009t0018g0268 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.9472+1226_9472+123 others(14): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 60/75 | chr12 | 112189550 | ||||||
| chr12:112189550
|
C | CAAAAAAA others(4): Show |
3 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0078 | 3 | HG01891.hp1 HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.9472+1225_9472+123 others(15): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 60/75 | chr12 | 112189550 | ||||||
| chr12:112189550
|
C | CAAAAAAA others(5): Show |
5 | a0001c0001t0004g0061a0001c0001t0004g0073a0001c0001t0004g0077others(2): Show | 5 | HG02258.hp2 HG02897.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.9472+1224_9472+123 others(16): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 60/75 | chr12 | 112189550 | ||||||
| chr12:112189550
|
C | CAAAAAAA others(6): Show |
1 | a0001c0009t0016g0266 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.9472+1223_9472+123 others(17): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 60/75 | chr12 | 112189550 | ||||||
| chr12:112189550
|
C | CAAAAAAA others(10): Show |
1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.9472+1219_9472+123 others(21): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 60/75 | chr12 | 112189550 | ||||||
| chr12:112189962
|
A | G | 5 | a0001c0001t0004g0062a0001c0001t0004g0064a0001c0001t0004g0065others(2): Show | 5 | HG02055.hp2 HG02572.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.9472+824T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 60/75 | chr12 | 112189962 | ||||||
| chr12:112190055
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.9472+731C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 60/75 | chr12 | 112190055 | ||||||
| chr12:112190136
|
C | T | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.9472+650G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 60/75 | chr12 | 112190136 | ||||||
| chr12:112190172
|
G | A | 2 | a0001c0001t0005g0046a0001c0001t0005g0049 | 2 | HG01167.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.9472+614C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 60/75 | chr12 | 112190172 | ||||||
| chr12:112190504
|
T | C | 8 | a0001c0001t0004g0023a0001c0001t0007g0007a0001c0001t0007g0024others(5): Show | 8 | HG01943.hp1 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.9472+282A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 60/75 | chr12 | 112190504 | ||||||
| chr12:112190761
|
C | T | 2 | a0001c0001t0001g0156a0001c0001t0001g0220 | 2 | HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.9472+25G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 60/75 | chr12 | 112190761 | ||||||
| chr12:112191029
|
A | G | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.9293-64T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 59/75 | chr12 | 112191029 | ||||||
| chr12:112191239
|
G | C | 1 | a0001c0001t0003g0050 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.9293-274C>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 59/75 | chr12 | 112191239 | ||||||
| chr12:112191445
|
C | A | 2 | a0001c0001t0011g0264a0001c0001t0011g0265 | 2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.9293-480G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 59/75 | chr12 | 112191445 | ||||||
| chr12:112191909
|
G | A | 1 | a0001c0003t0002g0140 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.9292+651C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 59/75 | chr12 | 112191909 | ||||||
| chr12:112191911
|
G | A | 1 | a0001c0001t0003g0006 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.9292+649C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 59/75 | chr12 | 112191911 | ||||||
| chr12:112191994
|
G | A | 2 | a0001c0001t0011g0264a0001c0001t0011g0265 | 2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.9292+566C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 59/75 | chr12 | 112191994 | ||||||
| chr12:112192282
|
T | G | 2 | a0001c0001t0011g0264a0001c0001t0011g0265 | 2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.9292+278A>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 59/75 | chr12 | 112192282 | ||||||
| chr12:112192454
|
T | C | 1 | a0001c0003t0002g0080 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.9292+106A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 59/75 | chr12 | 112192454 | ||||||
| chr12:112193682
|
C | T | 1 | a0001c0029t0001g0122 | 1 | NA19004.hp2 | splice_region_variant&intron_variant | LOW | c.8750-8G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 56/75 | chr12 | 112193682 | ||||||
| chr12:112193803
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.8750-129G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 56/75 | chr12 | 112193803 | ||||||
| chr12:112193978
|
A | G | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.8750-304T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 56/75 | chr12 | 112193978 | ||||||
| chr12:112194296
|
C | T | 1 | a0001c0001t0007g0025 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.8749+589G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 56/75 | chr12 | 112194296 | ||||||
| chr12:112194345
|
C | G | 170 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(167): Show | 170 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(167): Show |
intron_variant | MODIFIER | c.8749+540G>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 56/75 | chr12 | 112194345 | ||||||
| chr12:112194388
|
C | A | 1 | a0001c0001t0014g0148 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.8749+497G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 56/75 | chr12 | 112194388 | ||||||
| chr12:112194417
|
A | T | 8 | a0001c0001t0004g0061a0001c0001t0004g0067a0001c0001t0004g0068others(5): Show | 8 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.8749+468T>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 56/75 | chr12 | 112194417 | ||||||
| chr12:112195151
|
A | C | 2 | a0001c0001t0006g0258a0001c0001t0006g0262 | 2 | HG02056.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.8568-85T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 55/75 | chr12 | 112195151 | ||||||
| chr12:112195262
|
C | T | 2 | a0001c0001t0001g0079a0001c0001t0001g0160 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.8568-196G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 55/75 | chr12 | 112195262 | ||||||
| chr12:112195307
|
G | A | 1 | a0001c0003t0002g0084 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.8568-241C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 55/75 | chr12 | 112195307 | ||||||
| chr12:112195348
|
C | T | 5 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(2): Show | 5 | HG00140.hp1 HG00738.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.8568-282G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 55/75 | chr12 | 112195348 | ||||||
| chr12:112195500
|
C | A | 67 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(64): Show | 67 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(64): Show |
intron_variant | MODIFIER | c.8568-434G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 55/75 | chr12 | 112195500 | ||||||
| chr12:112195558
|
C | A | 1 | a0001c0001t0001g0083 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.8568-492G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 55/75 | chr12 | 112195558 | ||||||
| chr12:112195655
|
A | C | 1 | a0001c0001t0003g0027 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.8568-589T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 55/75 | chr12 | 112195655 | ||||||
| chr12:112195811
|
T | A | 1 | a0001c0001t0001g0216 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.8568-745A>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 55/75 | chr12 | 112195811 | ||||||
| chr12:112195887
|
C | T | 2 | a0001c0001t0004g0074a0001c0001t0004g0078 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.8568-821G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 55/75 | chr12 | 112195887 | ||||||
| chr12:112196017
|
T | G | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.8568-951A>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 55/75 | chr12 | 112196017 | ||||||
| chr12:112196783
|
G | A | 1 | a0001c0001t0005g0060 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.8568-1717C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 55/75 | chr12 | 112196783 | ||||||
| chr12:112196865
|
G | A | 2 | a0001c0001t0011g0264a0001c0001t0011g0265 | 2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.8568-1799C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 55/75 | chr12 | 112196865 | ||||||
| chr12:112196881
|
C | A | 1 | a0003c0008t0001g0207 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.8568-1815G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 55/75 | chr12 | 112196881 | ||||||
| chr12:112196989
|
C | A | 1 | a0001c0003t0002g0150 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.8568-1923G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 55/75 | chr12 | 112196989 | ||||||
| chr12:112197213
|
T | G | 1 | a0012c0027t0004g0066 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.8568-2147A>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 55/75 | chr12 | 112197213 | ||||||
| chr12:112197311
|
C | T | 1 | a0001c0001t0003g0027 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.8568-2245G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 55/75 | chr12 | 112197311 | ||||||
| chr12:112197387
|
G | A | 59 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(56): Show | 59 | HG00597.hp2 HG01109.hp2 HG01167.hp2 others(56): Show |
intron_variant | MODIFIER | c.8568-2321C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 55/75 | chr12 | 112197387 | ||||||
| chr12:112197625
|
C | T | 1 | a0001c0001t0004g0075 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.8568-2559G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 55/75 | chr12 | 112197625 | ||||||
| chr12:112197788
|
A | G | 2 | a0001c0001t0004g0074a0001c0001t0004g0078 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.8568-2722T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 55/75 | chr12 | 112197788 | ||||||
| chr12:112197934
|
C | G | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.8567+2704G>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 55/75 | chr12 | 112197934 | ||||||
| chr12:112198124
|
C | T | 1 | a0001c0001t0005g0054 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.8567+2514G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 55/75 | chr12 | 112198124 | ||||||
| chr12:112198377
|
G | A | 1 | a0001c0002t0001g0191 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.8567+2261C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 55/75 | chr12 | 112198377 | ||||||
| chr12:112198670
|
G | A | 1 | a0001c0033t0002g0110 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.8567+1968C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 55/75 | chr12 | 112198670 | ||||||
| chr12:112200155
|
AT | A | 10 | a0001c0001t0004g0061a0001c0001t0004g0067a0001c0001t0004g0068others(7): Show | 10 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.8567+482delA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 55/75 | chr12 | 112200155 | ||||||
| chr12:112200155
|
ATT | A | 79 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(76): Show | 79 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.8567+481_8567+482d others(4): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 55/75 | chr12 | 112200155 | ||||||
| chr12:112200156
|
T | C | 12 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(9): Show | 12 | HG02055.hp2 HG02109.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.8567+482A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 55/75 | chr12 | 112200156 | ||||||
| chr12:112200344
|
C | T | 1 | a0001c0002t0001g0230 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.8567+294G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 55/75 | chr12 | 112200344 | ||||||
| chr12:112200362
|
C | T | 5 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0118others(2): Show | 5 | NA18952.hp2 NA18973.hp2 NA19054.hp2 others(2): Show |
intron_variant | MODIFIER | c.8567+276G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 55/75 | chr12 | 112200362 | ||||||
| chr12:112200466
|
G | A | 1 | a0001c0001t0004g0078 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.8567+172C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 55/75 | chr12 | 112200466 | ||||||
| chr12:112200632
|
T | C | 1 | a0001c0011t0010g0146 | 1 | NA18968.hp2 | splice_region_variant&intron_variant | LOW | c.8567+6A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 55/75 | chr12 | 112200632 | ||||||
| chr12:112200849
|
ATGTGTGC others(13): Show |
A | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.8407-71_8407-52del others(20): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 54/75 | chr12 | 112200849 | ||||||
| chr12:112200872
|
T | C | 3 | a0001c0010t0001g0214a0001c0010t0001g0217a0002c0026t0001g0215 | 3 | HG02965.hp2 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.8407-74A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 54/75 | chr12 | 112200872 | ||||||
| chr12:112200872
|
T | TGTGC | 7 | a0001c0002t0001g0163a0001c0002t0001g0164a0001c0002t0001g0177others(4): Show | 7 | NA18942.hp1 NA18959.hp2 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.8407-78_8407-75dup others(4): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 54/75 | chr12 | 112200872 | ||||||
| chr12:112200880
|
CGTGCGT | C | 3 | a0001c0010t0001g0214a0001c0010t0001g0217a0002c0026t0001g0215 | 3 | HG02965.hp2 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.8407-88_8407-83del others(6): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 54/75 | chr12 | 112200880 | ||||||
| chr12:112200884
|
C | CGTGTGT | 56 | a0001c0002t0001g0161a0001c0002t0001g0166a0001c0002t0001g0167others(53): Show | 56 | HG00544.hp1 HG00597.hp1 HG02027.hp2 others(53): Show |
intron_variant | MODIFIER | c.8407-92_8407-87dup others(6): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 54/75 | chr12 | 112200884 | ||||||
| chr12:112200884
|
C | CGTGTGTG others(1): Show |
12 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0184others(9): Show | 12 | HG01071.hp1 HG01256.hp1 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.8407-94_8407-87dup others(8): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 54/75 | chr12 | 112200884 | ||||||
| chr12:112200884
|
CGT | C | 76 | a0001c0001t0001g0083a0001c0001t0001g0099a0001c0001t0001g0112others(73): Show | 76 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.8407-88_8407-87del others(2): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 54/75 | chr12 | 112200884 | ||||||
| chr12:112200884
|
CGTGT | C | 6 | a0001c0001t0001g0117a0001c0001t0001g0222a0001c0001t0001g0223others(3): Show | 6 | HG02109.hp1 HG02886.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.8407-90_8407-87del others(4): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 54/75 | chr12 | 112200884 | ||||||
| chr12:112200888
|
T | C | 65 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(62): Show | 65 | HG00597.hp2 HG00735.hp2 HG01081.hp1 others(62): Show |
intron_variant | MODIFIER | c.8407-90A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 54/75 | chr12 | 112200888 | ||||||
| chr12:112200890
|
T | C | 3 | a0001c0001t0003g0038a0001c0001t0003g0051a0001c0001t0008g0253 | 3 | HG03130.hp2 NA18959.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.8407-92A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 54/75 | chr12 | 112200890 | ||||||
| chr12:112200892
|
T | C | 3 | a0001c0001t0003g0045a0001c0001t0005g0005a0001c0001t0008g0252 | 3 | HG01891.hp2 HG02683.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.8407-94A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 54/75 | chr12 | 112200892 | ||||||
| chr12:112200950
|
C | T | 1 | a0001c0001t0015g0248 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.8407-152G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 54/75 | chr12 | 112200950 | ||||||
| chr12:112200967
|
G | T | 3 | a0001c0002t0001g0203a0001c0002t0001g0204a0001c0002t0001g0206 | 3 | HG02257.hp2 HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.8407-169C>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 54/75 | chr12 | 112200967 | ||||||
| chr12:112201024
|
T | C | 1 | a0001c0003t0002g0084 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.8407-226A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 54/75 | chr12 | 112201024 | ||||||
| chr12:112201427
|
T | C | 2 | a0001c0007t0001g0172a0001c0007t0001g0183 | 2 | NA19057.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.8407-629A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 54/75 | chr12 | 112201427 | ||||||
| chr12:112201473
|
GA | G | 88 | a0001c0001t0004g0061a0001c0001t0004g0067a0001c0001t0004g0068others(85): Show | 88 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(85): Show |
intron_variant | MODIFIER | c.8407-676delT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 54/75 | chr12 | 112201473 | ||||||
| chr12:112201799
|
A | G | 2 | a0001c0002t0001g0202a0001c0002t0001g0205 | 2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.8407-1001T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 54/75 | chr12 | 112201799 | ||||||
| chr12:112202228
|
C | T | 3 | a0001c0010t0001g0214a0001c0010t0001g0217a0002c0026t0001g0215 | 3 | HG02965.hp2 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.8406+1408G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 54/75 | chr12 | 112202228 | ||||||
| chr12:112202322
|
C | T | 1 | a0001c0001t0003g0050 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.8406+1314G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 54/75 | chr12 | 112202322 | ||||||
| chr12:112202361
|
A | G | 89 | a0001c0001t0004g0061a0001c0001t0004g0067a0001c0001t0004g0068others(86): Show | 89 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(86): Show |
intron_variant | MODIFIER | c.8406+1275T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 54/75 | chr12 | 112202361 | ||||||
| chr12:112202488
|
G | T | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159 | 3 | HG03098.hp2 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.8406+1148C>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 54/75 | chr12 | 112202488 | ||||||
| chr12:112202750
|
G | A | 8 | a0001c0001t0001g0099a0001c0001t0001g0125a0001c0001t0001g0128others(5): Show | 8 | HG00140.hp1 HG00738.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.8406+886C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 54/75 | chr12 | 112202750 | ||||||
| chr12:112202987
|
G | A | 1 | a0001c0003t0002g0098 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.8406+649C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 54/75 | chr12 | 112202987 | ||||||
| chr12:112203011
|
C | T | 1 | a0001c0003t0002g0102 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.8406+625G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 54/75 | chr12 | 112203011 | ||||||
| chr12:112203165
|
C | T | 2 | a0001c0003t0002g0103a0001c0003t0002g0107 | 2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.8406+471G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 54/75 | chr12 | 112203165 | ||||||
| chr12:112203573
|
T | G | 89 | a0001c0001t0004g0061a0001c0001t0004g0067a0001c0001t0004g0068others(86): Show | 89 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(86): Show |
intron_variant | MODIFIER | c.8406+63A>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 54/75 | chr12 | 112203573 | ||||||
| chr12:112203886
|
A | C | 1 | a0001c0002t0001g0234 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.8270-114T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 53/75 | chr12 | 112203886 | ||||||
| chr12:112203903
|
G | A | 67 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(64): Show | 67 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(64): Show |
intron_variant | MODIFIER | c.8270-131C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 53/75 | chr12 | 112203903 | ||||||
| chr12:112203918
|
C | G | 1 | a0001c0001t0005g0005 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.8270-146G>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 53/75 | chr12 | 112203918 | ||||||
| chr12:112204102
|
G | A | 8 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0012others(5): Show | 8 | NA18946.hp2 NA18950.hp2 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.8270-330C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 53/75 | chr12 | 112204102 | ||||||
| chr12:112204246
|
A | G | 1 | a0001c0003t0002g0150 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.8269+240T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 53/75 | chr12 | 112204246 | ||||||
| chr12:112204657
|
A | G | 1 | a0001c0003t0002g0109 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.8132-34T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 52/75 | chr12 | 112204657 | ||||||
| chr12:112205132
|
C | CA | 151 | a0001c0001t0001g0118a0001c0001t0001g0127a0001c0001t0001g0220others(148): Show | 151 | HG00597.hp2 HG00735.hp2 HG01071.hp1 others(148): Show |
intron_variant | MODIFIER | c.8132-510dupT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 52/75 | chr12 | 112205132 | ||||||
| chr12:112205132
|
C | CAA | 24 | a0001c0001t0003g0016a0001c0001t0003g0037a0001c0001t0003g0058others(21): Show | 24 | HG00544.hp1 HG00597.hp1 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.8132-511_8132-510d others(4): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 52/75 | chr12 | 112205132 | ||||||
| chr12:112205156
|
C | G | 1 | a0001c0001t0001g0118 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.8132-533G>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 52/75 | chr12 | 112205156 | ||||||
| chr12:112205295
|
A | G | 1 | a0001c0003t0002g0090 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.8132-672T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 52/75 | chr12 | 112205295 | ||||||
| chr12:112205302
|
C | T | 3 | a0001c0001t0003g0027a0001c0001t0003g0038a0001c0001t0003g0051 | 3 | NA18959.hp1 NA18994.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.8132-679G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 52/75 | chr12 | 112205302 | ||||||
| chr12:112205808
|
G | T | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.8132-1185C>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 52/75 | chr12 | 112205808 | ||||||
| chr12:112206043
|
T | C | 5 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(2): Show | 5 | HG00140.hp1 HG00738.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.8132-1420A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 52/75 | chr12 | 112206043 | ||||||
| chr12:112206261
|
C | T | 1 | a0001c0001t0010g0147 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.8131+1613G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 52/75 | chr12 | 112206261 | ||||||
| chr12:112206354
|
G | T | 3 | a0001c0001t0003g0018a0001c0001t0003g0019a0002c0004t0003g0052 | 3 | HG02027.hp1 NA18969.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.8131+1520C>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 52/75 | chr12 | 112206354 | ||||||
| chr12:112206533
|
C | CT | 19 | a0001c0001t0001g0083a0001c0001t0001g0112a0001c0001t0001g0113others(16): Show | 19 | HG01099.hp2 HG01106.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.8131+1340dupA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 52/75 | chr12 | 112206533 | ||||||
| chr12:112206533
|
CT | C | 147 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(144): Show | 147 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(144): Show |
intron_variant | MODIFIER | c.8131+1340delA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 52/75 | chr12 | 112206533 | ||||||
| chr12:112206642
|
T | C | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.8131+1232A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 52/75 | chr12 | 112206642 | ||||||
| chr12:112206787
|
T | C | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.8131+1087A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 52/75 | chr12 | 112206787 | ||||||
| chr12:112206952
|
G | A | 5 | a0001c0001t0001g0083a0001c0001t0001g0112a0001c0001t0001g0113others(2): Show | 5 | HG01993.hp2 HG02135.hp2 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.8131+922C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 52/75 | chr12 | 112206952 | ||||||
| chr12:112207106
|
A | ATGTG | 70 | a0001c0001t0001g0079a0001c0001t0001g0160a0001c0002t0001g0161others(67): Show | 70 | HG00544.hp1 HG00597.hp1 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.8131+764_8131+767d others(6): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 52/75 | chr12 | 112207106 | ||||||
| chr12:112207108
|
GTGTGTGT others(13): Show |
G | 5 | a0001c0001t0004g0062a0001c0001t0004g0064a0001c0001t0004g0065others(2): Show | 5 | HG02055.hp2 HG02572.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.8131+746_8131+765d others(22): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 52/75 | chr12 | 112207108 | ||||||
| chr12:112207116
|
G | A | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0002c0004t0001g0155 | 3 | HG01099.hp2 HG01175.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.8131+758C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 52/75 | chr12 | 112207116 | ||||||
| chr12:112207116
|
G | GTGTA | 94 | a0001c0001t0001g0099a0001c0001t0001g0125a0001c0001t0001g0127others(91): Show | 94 | HG00140.hp1 HG00597.hp2 HG00738.hp1 others(91): Show |
intron_variant | MODIFIER | c.8131+754_8131+757d others(6): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 52/75 | chr12 | 112207116 | ||||||
| chr12:112207116
|
G | GTGTATGT others(1): Show |
5 | a0001c0001t0003g0027a0001c0001t0003g0038a0001c0001t0003g0051others(2): Show | 5 | HG02257.hp1 HG03579.hp2 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.8131+750_8131+757d others(10): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 52/75 | chr12 | 112207116 | ||||||
| chr12:112207116
|
G | GTGTATGT others(5): Show |
1 | a0001c0001t0005g0049 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.8131+746_8131+757d others(14): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 52/75 | chr12 | 112207116 | ||||||
| chr12:112207116
|
G | GTGTGTGT others(1): Show |
13 | a0001c0002t0001g0163a0001c0002t0001g0164a0001c0002t0001g0176others(10): Show | 13 | HG00735.hp2 HG01081.hp2 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.8131+757_8131+758i others(10): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 52/75 | chr12 | 112207116 | ||||||
| chr12:112207116
|
GTGTATGT others(5): Show |
G | 2 | a0001c0003t0002g0103a0001c0003t0002g0107 | 2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.8131+746_8131+757d others(14): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 52/75 | chr12 | 112207116 | ||||||
| chr12:112207427
|
G | GC | 269 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0099others(266): Show | 269 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(266): Show |
intron_variant | MODIFIER | c.8131+446dupG | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 52/75 | chr12 | 112207427 | ||||||
| chr12:112207564
|
T | A | 1 | a0001c0003t0002g0107 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.8131+310A>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 52/75 | chr12 | 112207564 | ||||||
| chr12:112207597
|
G | A | 16 | a0001c0002t0001g0225a0001c0002t0001g0228a0001c0002t0001g0230others(13): Show | 16 | HG02132.hp1 NA18951.hp1 NA18952.hp1 others(13): Show |
intron_variant | MODIFIER | c.8131+277C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 52/75 | chr12 | 112207597 | ||||||
| chr12:112207622
|
GA | G | 3 | a0001c0010t0001g0214a0001c0010t0001g0217a0002c0026t0001g0215 | 3 | HG02965.hp2 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.8131+251delT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 52/75 | chr12 | 112207622 | ||||||
| chr12:112207624
|
G | T | 3 | a0001c0010t0001g0214a0001c0010t0001g0217a0002c0026t0001g0215 | 3 | HG02965.hp2 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.8131+250C>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 52/75 | chr12 | 112207624 | ||||||
| chr12:112207625
|
T | A | 3 | a0001c0010t0001g0214a0001c0010t0001g0217a0002c0026t0001g0215 | 3 | HG02965.hp2 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.8131+249A>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 52/75 | chr12 | 112207625 | ||||||
| chr12:112207627
|
T | A | 3 | a0001c0010t0001g0214a0001c0010t0001g0217a0002c0026t0001g0215 | 3 | HG02965.hp2 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.8131+247A>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 52/75 | chr12 | 112207627 | ||||||
| chr12:112207628
|
C | A | 3 | a0001c0010t0001g0214a0001c0010t0001g0217a0002c0026t0001g0215 | 3 | HG02965.hp2 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.8131+246G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 52/75 | chr12 | 112207628 | ||||||
| chr12:112208197
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.8005-197C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 51/75 | chr12 | 112208197 | ||||||
| chr12:112208388
|
C | T | 1 | a0001c0002t0001g0180 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.8004+106G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 51/75 | chr12 | 112208388 | ||||||
| chr12:112208893
|
C | CT | 92 | a0001c0001t0001g0079a0001c0001t0001g0119a0001c0001t0001g0152others(89): Show | 92 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.7868-264dupA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 50/75 | chr12 | 112208893 | ||||||
| chr12:112208893
|
C | CTT | 72 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0012others(69): Show | 72 | HG00597.hp2 HG01099.hp1 HG01109.hp2 others(69): Show |
intron_variant | MODIFIER | c.7868-265_7868-264d others(4): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 50/75 | chr12 | 112208893 | ||||||
| chr12:112208893
|
C | CTTT | 11 | a0001c0001t0003g0006a0001c0001t0003g0020a0001c0001t0003g0042others(8): Show | 11 | HG01081.hp1 HG01243.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.7868-266_7868-264d others(5): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 50/75 | chr12 | 112208893 | ||||||
| chr12:112209177
|
G | A | 1 | a0001c0001t0001g0115 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.7868-547C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 50/75 | chr12 | 112209177 | ||||||
| chr12:112209218
|
C | G | 6 | a0001c0001t0004g0062a0001c0001t0004g0064a0001c0001t0004g0065others(3): Show | 6 | HG02055.hp2 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.7868-588G>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 50/75 | chr12 | 112209218 | ||||||
| chr12:112209327
|
G | GT | 8 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0003t0013g0096others(5): Show | 8 | HG00738.hp1 HG01106.hp1 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.7867+687dupA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 50/75 | chr12 | 112209327 | ||||||
| chr12:112209421
|
G | C | 1 | a0001c0001t0006g0254 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.7867+594C>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 50/75 | chr12 | 112209421 | ||||||
| chr12:112209485
|
C | G | 1 | a0001c0001t0003g0018 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.7867+530G>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 50/75 | chr12 | 112209485 | ||||||
| chr12:112209515
|
G | A | 78 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(75): Show | 78 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(75): Show |
intron_variant | MODIFIER | c.7867+500C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 50/75 | chr12 | 112209515 | ||||||
| chr12:112209705
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.7867+310T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 50/75 | chr12 | 112209705 | ||||||
| chr12:112209873
|
C | G | 1 | a0002c0004t0007g0036 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.7867+142G>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 50/75 | chr12 | 112209873 | ||||||
| chr12:112209940
|
A | C | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.7867+75T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 50/75 | chr12 | 112209940 | ||||||
| chr12:112209968
|
T | C | 7 | a0001c0003t0002g0080a0001c0003t0002g0081a0001c0003t0002g0086others(4): Show | 7 | HG00738.hp2 HG01928.hp2 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.7867+47A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 50/75 | chr12 | 112209968 | ||||||
| chr12:112210421
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.7630-169T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 49/75 | chr12 | 112210421 | ||||||
| chr12:112210652
|
C | T | 4 | a0001c0001t0003g0006a0001c0001t0003g0027a0001c0001t0003g0038others(1): Show | 4 | HG03927.hp2 NA18959.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.7630-400G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 49/75 | chr12 | 112210652 | ||||||
| chr12:112210794
|
A | C | 1 | a0001c0002t0001g0161 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.7630-542T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 49/75 | chr12 | 112210794 | ||||||
| chr12:112211118
|
G | A | 2 | a0001c0001t0005g0047a0002c0004t0005g0048 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.7630-866C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 49/75 | chr12 | 112211118 | ||||||
| chr12:112211144
|
G | A | 2 | a0001c0001t0001g0156a0001c0001t0001g0220 | 2 | HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.7630-892C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 49/75 | chr12 | 112211144 | ||||||
| chr12:112211148
|
A | G | 1 | a0001c0002t0001g0185 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.7630-896T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 49/75 | chr12 | 112211148 | ||||||
| chr12:112211177
|
T | C | 219 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0099others(216): Show | 219 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(216): Show |
intron_variant | MODIFIER | c.7630-925A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 49/75 | chr12 | 112211177 | ||||||
| chr12:112211294
|
C | T | 2 | a0001c0001t0004g0067a0001c0009t0018g0268 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.7630-1042G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 49/75 | chr12 | 112211294 | ||||||
| chr12:112211532
|
A | G | 1 | a0001c0002t0001g0176 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.7629+955T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 49/75 | chr12 | 112211532 | ||||||
| chr12:112211541
|
A | C | 2 | a0001c0001t0001g0156a0001c0001t0001g0220 | 2 | HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.7629+946T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 49/75 | chr12 | 112211541 | ||||||
| chr12:112211727
|
A | G | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.7629+760T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 49/75 | chr12 | 112211727 | ||||||
| chr12:112211943
|
T | C | 1 | a0005c0022t0002g0092 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.7629+544A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 49/75 | chr12 | 112211943 | ||||||
| chr12:112212245
|
T | C | 169 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(166): Show | 169 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(166): Show |
intron_variant | MODIFIER | c.7629+242A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 49/75 | chr12 | 112212245 | ||||||
| chr12:112212254
|
A | G | 170 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(167): Show | 170 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(167): Show |
intron_variant | MODIFIER | c.7629+233T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 49/75 | chr12 | 112212254 | ||||||
| chr12:112212323
|
A | G | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.7629+164T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 49/75 | chr12 | 112212323 | ||||||
| chr12:112212332
|
C | T | 2 | a0001c0001t0005g0046a0001c0001t0005g0049 | 2 | HG01167.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.7629+155G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 49/75 | chr12 | 112212332 | ||||||
| chr12:112212788
|
G | GTTAT | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.7466-142_7466-139d others(6): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 48/75 | chr12 | 112212788 | ||||||
| chr12:112212818
|
C | T | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0002c0004t0001g0155 | 3 | HG01099.hp2 HG01175.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.7466-168G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 48/75 | chr12 | 112212818 | ||||||
| chr12:112212903
|
T | C | 170 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(167): Show | 170 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(167): Show |
intron_variant | MODIFIER | c.7466-253A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 48/75 | chr12 | 112212903 | ||||||
| chr12:112213048
|
G | A | 1 | a0001c0002t0001g0174 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.7466-398C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 48/75 | chr12 | 112213048 | ||||||
| chr12:112213244
|
G | T | 4 | a0001c0001t0004g0068a0001c0001t0004g0069a0001c0001t0004g0071others(1): Show | 4 | HG02451.hp2 HG02622.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.7466-594C>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 48/75 | chr12 | 112213244 | ||||||
| chr12:112213602
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.7466-952G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 48/75 | chr12 | 112213602 | ||||||
| chr12:112213699
|
C | CAT | 15 | a0001c0001t0001g0079a0001c0001t0001g0099a0001c0001t0001g0121others(12): Show | 15 | HG00738.hp2 HG01099.hp2 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.7466-1051_7466-105 others(6): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 48/75 | chr12 | 112213699 | ||||||
| chr12:112213699
|
CAT | C | 160 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(157): Show | 160 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(157): Show |
intron_variant | MODIFIER | c.7466-1051_7466-105 others(6): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 48/75 | chr12 | 112213699 | ||||||
| chr12:112213722
|
T | A | 269 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0099others(266): Show | 269 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(266): Show |
intron_variant | MODIFIER | c.7466-1072A>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 48/75 | chr12 | 112213722 | ||||||
| chr12:112213889
|
G | C | 1 | a0002c0026t0001g0215 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.7466-1239C>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 48/75 | chr12 | 112213889 | ||||||
| chr12:112213904
|
C | A | 1 | a0001c0003t0002g0101 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.7466-1254G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 48/75 | chr12 | 112213904 | ||||||
| chr12:112213905
|
C | CACACTAG others(5): Show |
1 | a0001c0003t0002g0101 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.7466-1256_7466-125 others(16): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 48/75 | chr12 | 112213905 | ||||||
| chr12:112213932
|
G | T | 1 | a0001c0002t0001g0174 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.7466-1282C>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 48/75 | chr12 | 112213932 | ||||||
| chr12:112214202
|
T | G | 170 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(167): Show | 170 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(167): Show |
intron_variant | MODIFIER | c.7466-1552A>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 48/75 | chr12 | 112214202 | ||||||
| chr12:112214284
|
G | A | 1 | a0001c0001t0004g0073 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.7466-1634C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 48/75 | chr12 | 112214284 | ||||||
| chr12:112214712
|
C | T | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.7465+1580G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 48/75 | chr12 | 112214712 | ||||||
| chr12:112214712
|
CCT | C | 5 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(2): Show | 5 | HG00140.hp1 HG00738.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.7465+1578_7465+157 others(6): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 48/75 | chr12 | 112214712 | ||||||
| chr12:112214719
|
T | C | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.7465+1573A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 48/75 | chr12 | 112214719 | ||||||
| chr12:112214983
|
G | A | 1 | a0001c0002t0008g0249 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.7465+1309C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 48/75 | chr12 | 112214983 | ||||||
| chr12:112215087
|
A | G | 8 | a0001c0001t0004g0061a0001c0001t0004g0067a0001c0001t0004g0068others(5): Show | 8 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.7465+1205T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 48/75 | chr12 | 112215087 | ||||||
| chr12:112215181
|
C | CA | 6 | a0001c0001t0003g0040a0001c0002t0001g0175a0001c0002t0001g0181others(3): Show | 6 | HG02027.hp2 HG02559.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.7465+1110dupT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 48/75 | chr12 | 112215181 | ||||||
| chr12:112215380
|
T | C | 2 | a0001c0001t0005g0070a0001c0009t0016g0266 | 2 | HG02622.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.7465+912A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 48/75 | chr12 | 112215380 | ||||||
| chr12:112215589
|
G | T | 1 | a0001c0001t0015g0248 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.7465+703C>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 48/75 | chr12 | 112215589 | ||||||
| chr12:112215696
|
G | A | 1 | a0001c0009t0016g0266 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.7465+596C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 48/75 | chr12 | 112215696 | ||||||
| chr12:112215943
|
C | G | 6 | a0001c0001t0004g0062a0001c0001t0004g0064a0001c0001t0004g0065others(3): Show | 6 | HG02055.hp2 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.7465+349G>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 48/75 | chr12 | 112215943 | ||||||
| chr12:112216149
|
G | C | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG02109.hp1 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.7465+143C>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 48/75 | chr12 | 112216149 | ||||||
| chr12:112216403
|
A | C | 1 | a0001c0001t0004g0075 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.7386-32T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 47/75 | chr12 | 112216403 | ||||||
| chr12:112216536
|
T | C | 1 | a0001c0033t0002g0110 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.7386-165A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 47/75 | chr12 | 112216536 | ||||||
| chr12:112217297
|
G | GCATACAC others(11): Show |
2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.7075-120_7075-103d others(20): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 45/75 | chr12 | 112217297 | ||||||
| chr12:112217297
|
GCATACAC others(11): Show |
G | 1 | a0001c0001t0001g0083 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.7075-120_7075-103d others(20): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 45/75 | chr12 | 112217297 | ||||||
| chr12:112217302
|
CACACACA others(9): Show |
C | 5 | a0001c0001t0005g0053a0001c0001t0005g0054a0001c0001t0005g0055others(2): Show | 5 | HG01099.hp1 HG02886.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.7075-123_7075-108d others(18): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 45/75 | chr12 | 112217302 | ||||||
| chr12:112217304
|
CACACACA others(7): Show |
C | 1 | a0001c0001t0005g0044 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.7075-123_7075-110d others(16): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 45/75 | chr12 | 112217304 | ||||||
| chr12:112217318
|
T | C | 162 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(159): Show | 162 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(159): Show |
intron_variant | MODIFIER | c.7075-123A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 45/75 | chr12 | 112217318 | ||||||
| chr12:112217320
|
C | T | 162 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(159): Show | 162 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(159): Show |
intron_variant | MODIFIER | c.7075-125G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 45/75 | chr12 | 112217320 | ||||||
| chr12:112217336
|
T | C | 1 | a0001c0001t0014g0148 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.7075-141A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 45/75 | chr12 | 112217336 | ||||||
| chr12:112217336
|
TAC | T | 167 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(164): Show | 167 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(164): Show |
intron_variant | MODIFIER | c.7075-143_7075-142d others(4): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 45/75 | chr12 | 112217336 | ||||||
| chr12:112217338
|
C | T | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.7075-143G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 45/75 | chr12 | 112217338 | ||||||
| chr12:112217857
|
C | T | 1 | a0001c0003t0002g0103 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.7075-662G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 45/75 | chr12 | 112217857 | ||||||
| chr12:112218082
|
C | T | 5 | a0001c0003t0002g0090a0001c0003t0002g0091a0001c0003t0002g0100others(2): Show | 5 | NA19002.hp2 NA19056.hp2 NA19079.hp1 others(2): Show |
intron_variant | MODIFIER | c.7075-887G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 45/75 | chr12 | 112218082 | ||||||
| chr12:112218144
|
T | C | 220 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0099others(217): Show | 220 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(217): Show |
intron_variant | MODIFIER | c.7075-949A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 45/75 | chr12 | 112218144 | ||||||
| chr12:112218434
|
C | A | 42 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(39): Show | 42 | HG00597.hp2 HG01109.hp2 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.7074+952G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 45/75 | chr12 | 112218434 | ||||||
| chr12:112218576
|
T | C | 1 | a0001c0002t0001g0232 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.7074+810A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 45/75 | chr12 | 112218576 | ||||||
| chr12:112219242
|
G | A | 1 | a0001c0001t0003g0033 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.7074+144C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 45/75 | chr12 | 112219242 | ||||||
| chr12:112219328
|
CTTACTCA others(8): Show |
C | 6 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(3): Show | 6 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.7074+43_7074+57del others(15): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 45/75 | chr12 | 112219328 | ||||||
| chr12:112219495
|
G | A | 1 | a0001c0002t0001g0196 | 1 | NA18981.hp2 | splice_region_variant&intron_variant | LOW | c.6971-6C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112219495 | ||||||
| chr12:112219557
|
T | C | 2 | a0001c0001t0001g0152a0002c0004t0001g0155 | 2 | HG01099.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.6971-68A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112219557 | ||||||
| chr12:112219585
|
C | T | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.6971-96G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112219585 | ||||||
| chr12:112219602
|
A | AT | 5 | a0001c0001t0003g0020a0001c0001t0005g0070a0001c0009t0016g0266others(2): Show | 5 | HG02071.hp2 HG02622.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.6971-114dupA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112219602 | ||||||
| chr12:112219685
|
T | C | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.6971-196A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112219685 | ||||||
| chr12:112219750
|
C | A | 1 | a0001c0001t0001g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.6971-261G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112219750 | ||||||
| chr12:112219844
|
C | T | 1 | a0001c0001t0003g0033 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.6971-355G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112219844 | ||||||
| chr12:112219852
|
A | G | 173 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(170): Show | 173 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(170): Show |
intron_variant | MODIFIER | c.6971-363T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112219852 | ||||||
| chr12:112219864
|
T | G | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.6971-375A>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112219864 | ||||||
| chr12:112219934
|
A | T | 8 | a0001c0001t0004g0023a0001c0001t0007g0007a0001c0001t0007g0024others(5): Show | 8 | HG01943.hp1 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.6971-445T>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112219934 | ||||||
| chr12:112220248
|
G | A | 2 | a0001c0001t0008g0252a0001c0001t0008g0253 | 2 | HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.6971-759C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112220248 | ||||||
| chr12:112220464
|
C | T | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.6971-975G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112220464 | ||||||
| chr12:112220470
|
T | G | 1 | a0001c0011t0010g0146 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.6971-981A>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112220470 | ||||||
| chr12:112220702
|
C | T | 1 | a0001c0001t0005g0046 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6971-1213G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112220702 | ||||||
| chr12:112220705
|
G | A | 2 | a0001c0001t0006g0258a0001c0001t0006g0262 | 2 | HG02056.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.6971-1216C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112220705 | ||||||
| chr12:112220919
|
A | G | 1 | a0001c0001t0001g0118 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.6971-1430T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112220919 | ||||||
| chr12:112220943
|
C | T | 1 | a0001c0002t0001g0174 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.6971-1454G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112220943 | ||||||
| chr12:112221010
|
G | A | 1 | a0003c0008t0001g0207 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.6971-1521C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112221010 | ||||||
| chr12:112221029
|
G | A | 1 | a0003c0008t0001g0207 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.6971-1540C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112221029 | ||||||
| chr12:112221220
|
C | T | 2 | a0001c0001t0003g0058a0001c0001t0003g0059 | 2 | HG02074.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.6971-1731G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112221220 | ||||||
| chr12:112221306
|
T | A | 2 | a0001c0001t0008g0252a0001c0001t0008g0253 | 2 | HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.6971-1817A>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112221306 | ||||||
| chr12:112221337
|
T | G | 1 | a0001c0003t0002g0150 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.6971-1848A>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112221337 | ||||||
| chr12:112221382
|
G | A | 1 | a0002c0004t0003g0008 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.6971-1893C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112221382 | ||||||
| chr12:112221700
|
T | C | 2 | a0001c0003t0009g0002a0006c0023t0009g0003 | 2 | HG01109.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.6971-2211A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112221700 | ||||||
| chr12:112221758
|
C | CT | 10 | a0001c0001t0003g0012a0001c0001t0004g0023a0001c0001t0007g0007others(7): Show | 10 | HG01943.hp1 HG02257.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.6971-2270dupA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112221758 | ||||||
| chr12:112221927
|
C | CT | 12 | a0001c0001t0004g0023a0001c0001t0005g0070a0001c0001t0007g0007others(9): Show | 12 | HG01943.hp1 HG02257.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.6971-2439dupA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112221927 | ||||||
| chr12:112221927
|
C | CTT | 66 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(63): Show | 66 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(63): Show |
intron_variant | MODIFIER | c.6971-2440_6971-243 others(6): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112221927 | ||||||
| chr12:112222525
|
C | T | 2 | a0001c0003t0013g0096a0001c0003t0013g0105 | 2 | HG02080.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.6971-3036G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112222525 | ||||||
| chr12:112222604
|
T | C | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.6971-3115A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112222604 | ||||||
| chr12:112222625
|
C | T | 1 | a0001c0001t0004g0062 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.6971-3136G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112222625 | ||||||
| chr12:112222665
|
T | C | 1 | a0001c0001t0006g0262 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.6971-3176A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112222665 | ||||||
| chr12:112222710
|
T | C | 12 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(9): Show | 12 | HG02055.hp2 HG02109.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.6971-3221A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112222710 | ||||||
| chr12:112222788
|
C | A | 79 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(76): Show | 79 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.6971-3299G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112222788 | ||||||
| chr12:112222967
|
G | A | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.6971-3478C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112222967 | ||||||
| chr12:112223114
|
T | C | 2 | a0001c0001t0008g0252a0001c0001t0008g0253 | 2 | HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.6970+3529A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112223114 | ||||||
| chr12:112223183
|
C | T | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.6970+3460G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112223183 | ||||||
| chr12:112223300
|
G | A | 24 | a0001c0001t0001g0083a0001c0001t0001g0099a0001c0001t0001g0112others(21): Show | 24 | HG00140.hp1 HG00738.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.6970+3343C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112223300 | ||||||
| chr12:112223459
|
T | G | 194 | a0001c0001t0001g0079a0001c0001t0001g0152a0001c0001t0001g0153others(191): Show | 194 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(191): Show |
intron_variant | MODIFIER | c.6970+3184A>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112223459 | ||||||
| chr12:112223465
|
G | T | 67 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(64): Show | 67 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(64): Show |
intron_variant | MODIFIER | c.6970+3178C>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112223465 | ||||||
| chr12:112223569
|
C | G | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00140.hp1 HG00738.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.6970+3074G>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112223569 | ||||||
| chr12:112223678
|
C | T | 1 | a0001c0001t0004g0069 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.6970+2965G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112223678 | ||||||
| chr12:112223781
|
T | G | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.6970+2862A>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112223781 | ||||||
| chr12:112223808
|
C | T | 2 | a0001c0001t0001g0216a0001c0001t0004g0074 | 2 | HG01243.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.6970+2835G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112223808 | ||||||
| chr12:112224358
|
C | T | 2 | a0001c0001t0008g0252a0001c0001t0008g0253 | 2 | HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.6970+2285G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112224358 | ||||||
| chr12:112224493
|
C | T | 1 | a0001c0001t0006g0258 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.6970+2150G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112224493 | ||||||
| chr12:112224514
|
C | T | 1 | a0001c0001t0011g0265 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.6970+2129G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112224514 | ||||||
| chr12:112224695
|
A | G | 1 | a0001c0001t0015g0248 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.6970+1948T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112224695 | ||||||
| chr12:112224787
|
T | C | 4 | a0001c0001t0004g0068a0001c0001t0004g0069a0001c0001t0004g0071others(1): Show | 4 | HG02451.hp2 HG02622.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.6970+1856A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112224787 | ||||||
| chr12:112225023
|
A | T | 1 | a0001c0003t0002g0143 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.6970+1620T>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112225023 | ||||||
| chr12:112225327
|
C | CA | 8 | a0001c0001t0001g0118a0001c0001t0001g0159a0001c0001t0001g0216others(5): Show | 8 | HG01243.hp2 HG02258.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.6970+1315dupT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112225327 | ||||||
| chr12:112225327
|
CA | C | 11 | a0001c0001t0001g0152a0001c0001t0001g0156a0001c0001t0003g0016others(8): Show | 11 | HG01099.hp2 HG02055.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.6970+1315delT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112225327 | ||||||
| chr12:112225419
|
T | C | 1 | a0001c0001t0003g0022 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.6970+1224A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112225419 | ||||||
| chr12:112225564
|
A | G | 4 | a0001c0001t0001g0152a0001c0001t0001g0153a0002c0004t0001g0155others(1): Show | 4 | HG01099.hp2 HG01175.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.6970+1079T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112225564 | ||||||
| chr12:112225602
|
CACAA | C | 3 | a0001c0001t0003g0042a0001c0001t0003g0043a0001c0001t0003g0045 | 3 | HG01109.hp2 HG01243.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.6970+1037_6970+104 others(8): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112225602 | ||||||
| chr12:112225620
|
C | CA | 7 | a0001c0001t0003g0020a0001c0001t0004g0023a0001c0001t0005g0005others(4): Show | 7 | HG01891.hp2 HG03130.hp1 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.6970+1022dupT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112225620 | ||||||
| chr12:112225736
|
A | G | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.6970+907T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112225736 | ||||||
| chr12:112225803
|
A | G | 2 | a0001c0001t0004g0074a0001c0001t0004g0078 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.6970+840T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112225803 | ||||||
| chr12:112226112
|
A | T | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.6970+531T>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112226112 | ||||||
| chr12:112226192
|
T | TAC | 7 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(4): Show | 7 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.6970+449_6970+450d others(4): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112226192 | ||||||
| chr12:112226192
|
T | TACACAC | 59 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(56): Show | 59 | HG00597.hp1 HG00735.hp2 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.6970+445_6970+450d others(8): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112226192 | ||||||
| chr12:112226192
|
T | TACACACA others(1): Show |
21 | a0001c0002t0001g0225a0001c0002t0001g0227a0001c0002t0001g0228others(18): Show | 21 | HG00544.hp1 HG02132.hp1 NA18946.hp1 others(18): Show |
intron_variant | MODIFIER | c.6970+443_6970+450d others(10): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112226192 | ||||||
| chr12:112226197
|
ACACACAC others(5): Show |
A | 1 | a0001c0001t0001g0216 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.6970+434_6970+445d others(14): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112226197 | ||||||
| chr12:112226609
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.6970+34T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 44/75 | chr12 | 112226609 | ||||||
| chr12:112227209
|
C | T | 88 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(85): Show | 88 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(85): Show |
intron_variant | MODIFIER | c.6855-451G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 43/75 | chr12 | 112227209 | ||||||
| chr12:112227305
|
T | C | 1 | a0001c0002t0001g0196 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.6855-547A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 43/75 | chr12 | 112227305 | ||||||
| chr12:112227560
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.6854+529A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 43/75 | chr12 | 112227560 | ||||||
| chr12:112228029
|
C | T | 1 | a0001c0013t0012g0145 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.6854+60G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 43/75 | chr12 | 112228029 | ||||||
| chr12:112228363
|
A | T | 1 | a0001c0002t0001g0189 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.6685-105T>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 42/75 | chr12 | 112228363 | ||||||
| chr12:112228872
|
G | A | 1 | a0001c0001t0007g0034 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.6520-61C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 41/75 | chr12 | 112228872 | ||||||
| chr12:112229035
|
G | A | 2 | a0001c0001t0001g0079a0001c0001t0001g0160 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.6520-224C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 41/75 | chr12 | 112229035 | ||||||
| chr12:112229200
|
A | G | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.6520-389T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 41/75 | chr12 | 112229200 | ||||||
| chr12:112229327
|
A | AAAAC | 15 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(12): Show | 15 | HG02258.hp2 HG02451.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.6519+367_6519+370d others(6): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 41/75 | chr12 | 112229327 | ||||||
| chr12:112229327
|
AAAAC | A | 82 | a0001c0001t0005g0044a0001c0002t0001g0161a0001c0002t0001g0163others(79): Show | 82 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(79): Show |
intron_variant | MODIFIER | c.6519+367_6519+370d others(6): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 41/75 | chr12 | 112229327 | ||||||
| chr12:112230059
|
C | G | 1 | a0001c0001t0004g0061 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.6337-179G>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 40/75 | chr12 | 112230059 | ||||||
| chr12:112230328
|
T | A | 3 | a0001c0010t0001g0214a0001c0010t0001g0217a0002c0026t0001g0215 | 3 | HG02965.hp2 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.6336+359A>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 40/75 | chr12 | 112230328 | ||||||
| chr12:112230422
|
C | T | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.6336+265G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 40/75 | chr12 | 112230422 | ||||||
| chr12:112230471
|
C | G | 1 | a0002c0004t0003g0008 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.6336+216G>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 40/75 | chr12 | 112230471 | ||||||
| chr12:112230530
|
G | C | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.6336+157C>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 40/75 | chr12 | 112230530 | ||||||
| chr12:112230539
|
T | C | 171 | a0001c0001t0001g0158a0001c0001t0003g0006a0001c0001t0003g0010others(168): Show | 171 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(168): Show |
intron_variant | MODIFIER | c.6336+148A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 40/75 | chr12 | 112230539 | ||||||
| chr12:112230951
|
G | A | 50 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(47): Show | 50 | HG00597.hp2 HG01109.hp2 HG01243.hp1 others(47): Show |
intron_variant | MODIFIER | c.6201-129C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 39/75 | chr12 | 112230951 | ||||||
| chr12:112231313
|
A | C | 2 | a0001c0003t0002g0090a0001c0003t0002g0100 | 2 | NA19056.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.6200+200T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 39/75 | chr12 | 112231313 | ||||||
| chr12:112231384
|
A | G | 1 | a0001c0002t0001g0218 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.6200+129T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 39/75 | chr12 | 112231384 | ||||||
| chr12:112231718
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG03704.hp1 | splice_region_variant&intron_variant | LOW | c.5998-3C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 38/75 | chr12 | 112231718 | ||||||
| chr12:112231936
|
C | T | 4 | a0001c0001t0001g0152a0001c0001t0001g0153a0002c0004t0001g0155others(1): Show | 4 | HG01099.hp2 HG01175.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.5998-221G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 38/75 | chr12 | 112231936 | ||||||
| chr12:112231978
|
G | T | 1 | a0001c0001t0005g0046 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5998-263C>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 38/75 | chr12 | 112231978 | ||||||
| chr12:112232008
|
A | T | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.5998-293T>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 38/75 | chr12 | 112232008 | ||||||
| chr12:112232289
|
T | C | 170 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(167): Show | 170 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(167): Show |
intron_variant | MODIFIER | c.5998-574A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 38/75 | chr12 | 112232289 | ||||||
| chr12:112232755
|
T | C | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.5997+249A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 38/75 | chr12 | 112232755 | ||||||
| chr12:112232795
|
G | C | 1 | a0001c0029t0001g0122 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.5997+209C>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 38/75 | chr12 | 112232795 | ||||||
| chr12:112233135
|
A | G | 1 | a0001c0003t0002g0139 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.5916-50T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 37/75 | chr12 | 112233135 | ||||||
| chr12:112233214
|
C | CT | 35 | a0001c0001t0001g0099a0001c0001t0001g0113a0001c0001t0001g0125others(32): Show | 35 | HG00140.hp1 HG00738.hp1 HG01433.hp2 others(32): Show |
intron_variant | MODIFIER | c.5916-130dupA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 37/75 | chr12 | 112233214 | ||||||
| chr12:112233214
|
CT | C | 12 | a0001c0001t0003g0010a0001c0001t0003g0012a0001c0001t0003g0013others(9): Show | 12 | HG01256.hp1 HG01256.hp2 HG02897.hp2 others(9): Show |
intron_variant | MODIFIER | c.5916-130delA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 37/75 | chr12 | 112233214 | ||||||
| chr12:112233214
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0129 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.5916-139_5916-130d others(12): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 37/75 | chr12 | 112233214 | ||||||
| chr12:112233644
|
G | A | 2 | a0001c0003t0002g0098a0001c0003t0002g0150 | 2 | HG03927.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.5916-559C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 37/75 | chr12 | 112233644 | ||||||
| chr12:112233826
|
C | T | 3 | a0001c0010t0001g0214a0001c0010t0001g0217a0002c0026t0001g0215 | 3 | HG02965.hp2 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.5916-741G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 37/75 | chr12 | 112233826 | ||||||
| chr12:112233845
|
GT | G | 170 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(167): Show | 170 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(167): Show |
intron_variant | MODIFIER | c.5916-761delA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 37/75 | chr12 | 112233845 | ||||||
| chr12:112233858
|
A | G | 1 | a0001c0011t0001g0133 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.5916-773T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 37/75 | chr12 | 112233858 | ||||||
| chr12:112233873
|
A | T | 3 | a0001c0001t0003g0042a0001c0001t0003g0043a0001c0001t0003g0045 | 3 | HG01109.hp2 HG01243.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.5916-788T>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 37/75 | chr12 | 112233873 | ||||||
| chr12:112233881
|
T | C | 1 | a0001c0001t0001g0115 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.5916-796A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 37/75 | chr12 | 112233881 | ||||||
| chr12:112234104
|
T | G | 8 | a0001c0001t0004g0061a0001c0001t0004g0067a0001c0001t0004g0068others(5): Show | 8 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.5915+973A>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 37/75 | chr12 | 112234104 | ||||||
| chr12:112234249
|
G | C | 2 | a0001c0001t0005g0021a0001c0001t0012g0151 | 2 | HG02922.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.5915+828C>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 37/75 | chr12 | 112234249 | ||||||
| chr12:112234371
|
T | C | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159 | 3 | HG03098.hp2 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.5915+706A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 37/75 | chr12 | 112234371 | ||||||
| chr12:112234560
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.5915+517C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 37/75 | chr12 | 112234560 | ||||||
| chr12:112234631
|
C | A | 1 | a0001c0001t0004g0076 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5915+446G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 37/75 | chr12 | 112234631 | ||||||
| chr12:112235952
|
T | C | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5445-168A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 35/75 | chr12 | 112235952 | ||||||
| chr12:112235958
|
C | T | 75 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(72): Show | 75 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.5445-174G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 35/75 | chr12 | 112235958 | ||||||
| chr12:112236553
|
G | A | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.5444+392C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 35/75 | chr12 | 112236553 | ||||||
| chr12:112236613
|
C | T | 2 | a0001c0002t0001g0208a0001c0002t0001g0209 | 2 | NA18943.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.5444+332G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 35/75 | chr12 | 112236613 | ||||||
| chr12:112236672
|
T | C | 1 | a0001c0002t0001g0196 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.5444+273A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 35/75 | chr12 | 112236672 | ||||||
| chr12:112236711
|
C | G | 3 | a0001c0002t0001g0166a0001c0016t0001g0168a0002c0005t0001g0165 | 3 | HG00597.hp1 NA18947.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.5444+234G>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 35/75 | chr12 | 112236711 | ||||||
| chr12:112236872
|
C | T | 1 | a0001c0001t0003g0032 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.5444+73G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 35/75 | chr12 | 112236872 | ||||||
| chr12:112236914
|
C | T | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG00140.hp1 HG00738.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.5444+31G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 35/75 | chr12 | 112236914 | ||||||
| chr12:112237291
|
G | C | 1 | a0001c0001t0001g0128 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.5291-193C>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 34/75 | chr12 | 112237291 | ||||||
| chr12:112237329
|
T | C | 175 | a0001c0001t0001g0079a0001c0001t0001g0157a0001c0001t0001g0158others(172): Show | 175 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(172): Show |
intron_variant | MODIFIER | c.5291-231A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 34/75 | chr12 | 112237329 | ||||||
| chr12:112237371
|
T | C | 1 | a0001c0001t0005g0060 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.5291-273A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 34/75 | chr12 | 112237371 | ||||||
| chr12:112237562
|
C | T | 6 | a0001c0001t0005g0044a0001c0001t0005g0053a0001c0001t0005g0054others(3): Show | 6 | HG01081.hp1 HG01099.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.5291-464G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 34/75 | chr12 | 112237562 | ||||||
| chr12:112237839
|
C | T | 2 | a0001c0001t0001g0079a0001c0001t0001g0160 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.5291-741G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 34/75 | chr12 | 112237839 | ||||||
| chr12:112237875
|
C | T | 15 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(12): Show | 15 | HG02055.hp2 HG02109.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.5291-777G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 34/75 | chr12 | 112237875 | ||||||
| chr12:112237903
|
T | C | 1 | a0001c0001t0007g0007 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.5291-805A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 34/75 | chr12 | 112237903 | ||||||
| chr12:112238291
|
C | T | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5290+761G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 34/75 | chr12 | 112238291 | ||||||
| chr12:112238864
|
G | A | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.5290+188C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 34/75 | chr12 | 112238864 | ||||||
| chr12:112239003
|
C | T | 1 | a0010c0014t0001g0195 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.5290+49G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 34/75 | chr12 | 112239003 | ||||||
| chr12:112239475
|
A | G | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.5106-239T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 33/75 | chr12 | 112239475 | ||||||
| chr12:112239683
|
G | T | 1 | a0001c0001t0003g0022 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.5105+198C>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 33/75 | chr12 | 112239683 | ||||||
| chr12:112239700
|
T | A | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.5105+181A>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 33/75 | chr12 | 112239700 | ||||||
| chr12:112239844
|
G | A | 1 | a0003c0008t0001g0207 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.5105+37C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 33/75 | chr12 | 112239844 | ||||||
| chr12:112240223
|
C | T | 1 | a0001c0011t0010g0146 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.4959-196G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 32/75 | chr12 | 112240223 | ||||||
| chr12:112240318
|
G | A | 1 | a0014c0021t0017g0267 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4959-291C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 32/75 | chr12 | 112240318 | ||||||
| chr12:112240330
|
C | T | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.4959-303G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 32/75 | chr12 | 112240330 | ||||||
| chr12:112240434
|
T | TTTTTCTT others(3): Show |
1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4959-417_4959-408d others(12): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 32/75 | chr12 | 112240434 | ||||||
| chr12:112240577
|
G | A | 1 | a0001c0001t0010g0149 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.4959-550C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 32/75 | chr12 | 112240577 | ||||||
| chr12:112240664
|
T | C | 1 | a0001c0001t0001g0157 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4959-637A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 32/75 | chr12 | 112240664 | ||||||
| chr12:112240885
|
C | G | 1 | a0001c0003t0004g0004 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4959-858G>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 32/75 | chr12 | 112240885 | ||||||
| chr12:112240893
|
G | A | 50 | a0001c0002t0001g0161a0001c0002t0001g0166a0001c0002t0001g0167others(47): Show | 50 | HG00544.hp1 HG00597.hp1 HG02027.hp2 others(47): Show |
intron_variant | MODIFIER | c.4959-866C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 32/75 | chr12 | 112240893 | ||||||
| chr12:112240932
|
A | G | 2 | a0001c0001t0004g0069a0001c0001t0004g0072 | 2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4959-905T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 32/75 | chr12 | 112240932 | ||||||
| chr12:112241124
|
T | C | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.4959-1097A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 32/75 | chr12 | 112241124 | ||||||
| chr12:112241142
|
T | C | 1 | a0001c0001t0001g0157 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4959-1115A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 32/75 | chr12 | 112241142 | ||||||
| chr12:112241231
|
G | A | 1 | a0001c0001t0003g0013 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.4959-1204C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 32/75 | chr12 | 112241231 | ||||||
| chr12:112241269
|
G | A | 2 | a0001c0001t0001g0079a0001c0001t0001g0160 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.4959-1242C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 32/75 | chr12 | 112241269 | ||||||
| chr12:112241301
|
C | A | 1 | a0001c0003t0009g0002 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.4959-1274G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 32/75 | chr12 | 112241301 | ||||||
| chr12:112241372
|
C | T | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.4959-1345G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 32/75 | chr12 | 112241372 | ||||||
| chr12:112241487
|
T | G | 1 | a0001c0001t0005g0060 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4959-1460A>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 32/75 | chr12 | 112241487 | ||||||
| chr12:112241653
|
T | C | 2 | a0001c0001t0001g0153a0004c0034t0001g0154 | 2 | HG02647.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.4959-1626A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 32/75 | chr12 | 112241653 | ||||||
| chr12:112241967
|
A | T | 1 | a0001c0001t0005g0060 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4958+1386T>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 32/75 | chr12 | 112241967 | ||||||
| chr12:112242241
|
C | T | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.4958+1112G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 32/75 | chr12 | 112242241 | ||||||
| chr12:112242298
|
T | A | 1 | a0001c0001t0001g0222 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4958+1055A>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 32/75 | chr12 | 112242298 | ||||||
| chr12:112242408
|
T | C | 1 | a0001c0001t0001g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4958+945A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 32/75 | chr12 | 112242408 | ||||||
| chr12:112242486
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.4958+867C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 32/75 | chr12 | 112242486 | ||||||
| chr12:112242536
|
C | A | 1 | a0001c0001t0015g0248 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4958+817G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 32/75 | chr12 | 112242536 | ||||||
| chr12:112242550
|
G | T | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4958+803C>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 32/75 | chr12 | 112242550 | ||||||
| chr12:112242612
|
TA | T | 88 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(85): Show | 88 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(85): Show |
intron_variant | MODIFIER | c.4958+740delT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 32/75 | chr12 | 112242612 | ||||||
| chr12:112242637
|
C | T | 75 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(72): Show | 75 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(72): Show |
intron_variant | MODIFIER | c.4958+716G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 32/75 | chr12 | 112242637 | ||||||
| chr12:112242669
|
G | C | 1 | a0003c0008t0001g0212 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.4958+684C>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 32/75 | chr12 | 112242669 | ||||||
| chr12:112243182
|
C | T | 1 | a0001c0032t0011g0263 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4958+171G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 32/75 | chr12 | 112243182 | ||||||
| chr12:112243269
|
C | T | 1 | a0008c0017t0001g0190 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.4958+84G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 32/75 | chr12 | 112243269 | ||||||
| chr12:112243305
|
C | T | 3 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0077 | 3 | HG03453.hp2 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.4958+48G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 32/75 | chr12 | 112243305 | ||||||
| chr12:112243547
|
C | G | 1 | a0001c0001t0001g0129 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.4792-28G>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 31/75 | chr12 | 112243547 | ||||||
| chr12:112243603
|
C | T | 1 | a0003c0008t0001g0207 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.4791+17G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 31/75 | chr12 | 112243603 | ||||||
| chr12:112244034
|
C | T | 8 | a0001c0001t0004g0061a0001c0001t0004g0067a0001c0001t0004g0068others(5): Show | 8 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.4514-25G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 29/75 | chr12 | 112244034 | ||||||
| chr12:112244206
|
TA | T | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.4514-198delT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 29/75 | chr12 | 112244206 | ||||||
| chr12:112244399
|
C | T | 1 | a0001c0002t0001g0200 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.4514-390G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 29/75 | chr12 | 112244399 | ||||||
| chr12:112244472
|
A | G | 220 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0099others(217): Show | 220 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(217): Show |
intron_variant | MODIFIER | c.4514-463T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 29/75 | chr12 | 112244472 | ||||||
| chr12:112244761
|
T | C | 1 | a0001c0003t0002g0109 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.4514-752A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 29/75 | chr12 | 112244761 | ||||||
| chr12:112244802
|
G | A | 2 | a0001c0002t0001g0203a0001c0002t0001g0204 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.4514-793C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 29/75 | chr12 | 112244802 | ||||||
| chr12:112245112
|
C | T | 5 | a0001c0001t0001g0083a0001c0001t0001g0112a0001c0001t0001g0113others(2): Show | 5 | HG01993.hp2 HG02135.hp2 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.4514-1103G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 29/75 | chr12 | 112245112 | ||||||
| chr12:112245231
|
T | C | 2 | a0001c0002t0001g0178a0001c0002t0001g0179 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.4514-1222A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 29/75 | chr12 | 112245231 | ||||||
| chr12:112245409
|
C | G | 6 | a0001c0001t0004g0062a0001c0001t0004g0064a0001c0001t0004g0065others(3): Show | 6 | HG02055.hp2 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.4514-1400G>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 29/75 | chr12 | 112245409 | ||||||
| chr12:112245454
|
T | G | 1 | a0001c0002t0001g0174 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.4514-1445A>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 29/75 | chr12 | 112245454 | ||||||
| chr12:112245625
|
C | T | 3 | a0001c0009t0016g0266a0001c0009t0018g0268a0014c0021t0017g0267 | 3 | HG02622.hp2 HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.4513+1276G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 29/75 | chr12 | 112245625 | ||||||
| chr12:112245679
|
G | A | 3 | a0001c0010t0001g0214a0001c0010t0001g0217a0002c0026t0001g0215 | 3 | HG02965.hp2 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.4513+1222C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 29/75 | chr12 | 112245679 | ||||||
| chr12:112245711
|
T | A | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.4513+1190A>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 29/75 | chr12 | 112245711 | ||||||
| chr12:112245823
|
T | C | 4 | a0001c0003t0002g0086a0001c0003t0002g0102a0002c0006t0002g0094others(1): Show | 4 | HG01928.hp2 HG01934.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.4513+1078A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 29/75 | chr12 | 112245823 | ||||||
| chr12:112245867
|
C | T | 3 | a0001c0010t0001g0214a0001c0010t0001g0217a0002c0026t0001g0215 | 3 | HG02965.hp2 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.4513+1034G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 29/75 | chr12 | 112245867 | ||||||
| chr12:112245897
|
T | C | 1 | a0001c0032t0011g0263 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4513+1004A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 29/75 | chr12 | 112245897 | ||||||
| chr12:112246085
|
T | C | 1 | a0001c0002t0001g0218 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.4513+816A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 29/75 | chr12 | 112246085 | ||||||
| chr12:112246141
|
A | AAAAAT | 86 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(83): Show | 86 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(83): Show |
intron_variant | MODIFIER | c.4513+755_4513+759d others(7): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 29/75 | chr12 | 112246141 | ||||||
| chr12:112246141
|
A | AAAAATAA others(3): Show |
4 | a0001c0001t0003g0045a0001c0001t0006g0258a0001c0031t0008g0251others(1): Show | 4 | HG02056.hp2 HG02683.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.4513+750_4513+759d others(12): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 29/75 | chr12 | 112246141 | ||||||
| chr12:112246141
|
A | AAAAATAA others(8): Show |
2 | a0001c0002t0020g0270a0002c0005t0001g0197 | 2 | HG02071.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.4513+745_4513+759d others(17): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 29/75 | chr12 | 112246141 | ||||||
| chr12:112246141
|
A | AAAAATAA others(13): Show |
75 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(72): Show | 75 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.4513+740_4513+759d others(22): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 29/75 | chr12 | 112246141 | ||||||
| chr12:112246141
|
A | AAAAATAA others(18): Show |
2 | a0001c0002t0001g0171a0001c0002t0001g0187 | 2 | HG01952.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.4513+735_4513+759d others(27): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 29/75 | chr12 | 112246141 | ||||||
| chr12:112246141
|
A | AAAAATAA others(23): Show |
1 | a0001c0002t0008g0249 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.4513+730_4513+759d others(32): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 29/75 | chr12 | 112246141 | ||||||
| chr12:112246417
|
A | T | 259 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0099others(256): Show | 259 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(256): Show |
intron_variant | MODIFIER | c.4513+484T>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 29/75 | chr12 | 112246417 | ||||||
| chr12:112246489
|
A | G | 1 | a0001c0003t0009g0001 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.4513+412T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 29/75 | chr12 | 112246489 | ||||||
| chr12:112246528
|
A | G | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.4513+373T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 29/75 | chr12 | 112246528 | ||||||
| chr12:112246826
|
G | T | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4513+75C>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 29/75 | chr12 | 112246826 | ||||||
| chr12:112246875
|
G | A | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159 | 3 | HG03098.hp2 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.4513+26C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 29/75 | chr12 | 112246875 | ||||||
| chr12:112247149
|
A | G | 2 | a0001c0001t0004g0067a0001c0001t0005g0070 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.4338-73T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 28/75 | chr12 | 112247149 | ||||||
| chr12:112247977
|
T | TAC | 59 | a0001c0001t0003g0006a0001c0001t0003g0018a0001c0001t0003g0019others(56): Show | 59 | HG00597.hp2 HG01071.hp2 HG01081.hp1 others(56): Show |
intron_variant | MODIFIER | c.4248+88_4248+89dup others(2): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 27/75 | chr12 | 112247977 | ||||||
| chr12:112247977
|
T | TACAC | 22 | a0001c0001t0001g0156a0001c0001t0001g0220a0001c0001t0003g0010others(19): Show | 22 | HG02132.hp2 HG02523.hp1 HG02622.hp2 others(19): Show |
intron_variant | MODIFIER | c.4248+86_4248+89dup others(4): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 27/75 | chr12 | 112247977 | ||||||
| chr12:112247977
|
T | TACACACA others(1): Show |
4 | a0001c0002t0001g0164a0001c0002t0001g0177a0001c0002t0001g0208others(1): Show | 4 | NA18943.hp1 NA18959.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.4248+82_4248+89dup others(8): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 27/75 | chr12 | 112247977 | ||||||
| chr12:112247977
|
T | TACACACA others(3): Show |
2 | a0001c0002t0001g0180a0001c0002t0001g0196 | 2 | NA18981.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.4248+80_4248+89dup others(10): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 27/75 | chr12 | 112247977 | ||||||
| chr12:112247977
|
T | TACACACA others(5): Show |
70 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0166others(67): Show | 70 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.4248+78_4248+89dup others(12): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 27/75 | chr12 | 112247977 | ||||||
| chr12:112247977
|
T | TACACACA others(7): Show |
4 | a0001c0002t0001g0174a0001c0002t0001g0191a0001c0002t0001g0192others(1): Show | 4 | HG02074.hp1 NA18950.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.4248+76_4248+89dup others(14): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 27/75 | chr12 | 112247977 | ||||||
| chr12:112247977
|
T | TACACACA others(9): Show |
1 | a0001c0002t0001g0167 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.4248+74_4248+89dup others(16): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 27/75 | chr12 | 112247977 | ||||||
| chr12:112247977
|
TAC | T | 12 | a0001c0001t0001g0083a0001c0001t0001g0112a0001c0001t0001g0113others(9): Show | 12 | HG01993.hp2 HG02135.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.4248+88_4248+89del others(2): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 27/75 | chr12 | 112247977 | ||||||
| chr12:112248209
|
A | T | 1 | a0001c0001t0001g0129 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.4144-38T>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 26/75 | chr12 | 112248209 | ||||||
| chr12:112248516
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG03516.hp2 | splice_region_variant&intron_variant | LOW | c.3951-4A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 25/75 | chr12 | 112248516 | ||||||
| chr12:112249069
|
A | G | 1 | a0001c0012t0002g0093 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.3951-557T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 25/75 | chr12 | 112249069 | ||||||
| chr12:112249183
|
C | T | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.3951-671G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 25/75 | chr12 | 112249183 | ||||||
| chr12:112249311
|
A | G | 177 | a0001c0001t0001g0079a0001c0001t0001g0157a0001c0001t0001g0158others(174): Show | 177 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(174): Show |
intron_variant | MODIFIER | c.3951-799T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 25/75 | chr12 | 112249311 | ||||||
| chr12:112249353
|
C | CA | 11 | a0001c0001t0001g0083a0001c0001t0001g0222a0001c0001t0001g0223others(8): Show | 11 | HG01993.hp2 HG02109.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.3950+790dupT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 25/75 | chr12 | 112249353 | ||||||
| chr12:112249389
|
T | C | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159 | 3 | HG03098.hp2 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3950+755A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 25/75 | chr12 | 112249389 | ||||||
| chr12:112249429
|
G | A | 8 | a0001c0001t0004g0061a0001c0001t0004g0067a0001c0001t0004g0068others(5): Show | 8 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.3950+715C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 25/75 | chr12 | 112249429 | ||||||
| chr12:112249476
|
A | G | 2 | a0001c0001t0003g0026a0001c0001t0003g0050 | 2 | NA19056.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.3950+668T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 25/75 | chr12 | 112249476 | ||||||
| chr12:112249529
|
A | G | 1 | a0001c0002t0001g0204 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3950+615T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 25/75 | chr12 | 112249529 | ||||||
| chr12:112249939
|
G | A | 1 | a0004c0034t0001g0154 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3950+205C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 25/75 | chr12 | 112249939 | ||||||
| chr12:112249955
|
C | A | 2 | a0001c0001t0001g0079a0001c0001t0001g0160 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.3950+189G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 25/75 | chr12 | 112249955 | ||||||
| chr12:112250426
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3717-49A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 24/75 | chr12 | 112250426 | ||||||
| chr12:112250451
|
A | T | 2 | a0001c0001t0004g0067a0001c0001t0005g0070 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.3717-74T>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 24/75 | chr12 | 112250451 | ||||||
| chr12:112251305
|
C | T | 1 | a0004c0034t0001g0154 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3553-171G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 23/75 | chr12 | 112251305 | ||||||
| chr12:112251334
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3553-200T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 23/75 | chr12 | 112251334 | ||||||
| chr12:112251392
|
T | C | 4 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0077others(1): Show | 4 | HG01891.hp1 HG03453.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.3553-258A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 23/75 | chr12 | 112251392 | ||||||
| chr12:112251803
|
C | G | 2 | a0001c0001t0008g0252a0001c0001t0008g0253 | 2 | HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.3552+621G>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 23/75 | chr12 | 112251803 | ||||||
| chr12:112251886
|
C | G | 1 | a0011c0028t0006g0261 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3552+538G>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 23/75 | chr12 | 112251886 | ||||||
| chr12:112252546
|
G | C | 1 | a0001c0001t0001g0113 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.3448-18C>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 22/75 | chr12 | 112252546 | ||||||
| chr12:112252694
|
C | G | 1 | a0001c0001t0001g0220 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3448-166G>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 22/75 | chr12 | 112252694 | ||||||
| chr12:112252810
|
A | AT | 9 | a0001c0001t0001g0079a0001c0001t0001g0160a0001c0001t0003g0027others(6): Show | 9 | HG01884.hp1 HG02683.hp1 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.3448-283dupA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 22/75 | chr12 | 112252810 | ||||||
| chr12:112252810
|
AT | A | 95 | a0001c0001t0001g0156a0001c0001t0001g0222a0001c0001t0001g0223others(92): Show | 95 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.3448-283delA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 22/75 | chr12 | 112252810 | ||||||
| chr12:112253371
|
C | T | 1 | a0001c0003t0002g0150 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3447+672G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 22/75 | chr12 | 112253371 | ||||||
| chr12:112253469
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.3447+574C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 22/75 | chr12 | 112253469 | ||||||
| chr12:112253483
|
T | C | 1 | a0001c0001t0006g0260 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3447+560A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 22/75 | chr12 | 112253483 | ||||||
| chr12:112253500
|
G | A | 3 | a0001c0010t0001g0214a0001c0010t0001g0217a0002c0026t0001g0215 | 3 | HG02965.hp2 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3447+543C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 22/75 | chr12 | 112253500 | ||||||
| chr12:112253574
|
C | G | 80 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(77): Show | 80 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(77): Show |
intron_variant | MODIFIER | c.3447+469G>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 22/75 | chr12 | 112253574 | ||||||
| chr12:112253847
|
G | A | 8 | a0001c0001t0004g0061a0001c0001t0004g0067a0001c0001t0004g0068others(5): Show | 8 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.3447+196C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 22/75 | chr12 | 112253847 | ||||||
| chr12:112254503
|
C | T | 2 | a0001c0007t0001g0172a0001c0007t0001g0183 | 2 | NA19057.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.3328-341G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 21/75 | chr12 | 112254503 | ||||||
| chr12:112254638
|
A | C | 9 | a0001c0001t0001g0099a0001c0001t0001g0125a0001c0001t0001g0127others(6): Show | 9 | HG00140.hp1 HG00738.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.3328-476T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 21/75 | chr12 | 112254638 | ||||||
| chr12:112254871
|
T | C | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.3328-709A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 21/75 | chr12 | 112254871 | ||||||
| chr12:112255657
|
G | A | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159 | 3 | HG03098.hp2 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3327+663C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 21/75 | chr12 | 112255657 | ||||||
| chr12:112255717
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3327+603G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 21/75 | chr12 | 112255717 | ||||||
| chr12:112255728
|
A | G | 4 | a0001c0001t0001g0079a0001c0001t0001g0156a0001c0001t0001g0160others(1): Show | 4 | HG01884.hp1 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3327+592T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 21/75 | chr12 | 112255728 | ||||||
| chr12:112255751
|
A | C | 8 | a0001c0001t0004g0023a0001c0001t0007g0007a0001c0001t0007g0024others(5): Show | 8 | HG01943.hp1 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.3327+569T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 21/75 | chr12 | 112255751 | ||||||
| chr12:112255835
|
T | C | 1 | a0001c0003t0002g0104 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.3327+485A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 21/75 | chr12 | 112255835 | ||||||
| chr12:112255972
|
T | C | 5 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(2): Show | 5 | HG01891.hp1 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.3327+348A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 21/75 | chr12 | 112255972 | ||||||
| chr12:112256062
|
C | G | 1 | a0001c0002t0001g0164 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.3327+258G>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 21/75 | chr12 | 112256062 | ||||||
| chr12:112256111
|
A | G | 8 | a0001c0001t0004g0023a0001c0001t0007g0007a0001c0001t0007g0024others(5): Show | 8 | HG01943.hp1 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.3327+209T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 21/75 | chr12 | 112256111 | ||||||
| chr12:112256625
|
C | G | 1 | a0001c0003t0002g0247 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3129-107G>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 20/75 | chr12 | 112256625 | ||||||
| chr12:112256861
|
G | GA | 83 | a0001c0001t0005g0060a0001c0001t0014g0148a0001c0002t0001g0161others(80): Show | 83 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.3129-344dupT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 20/75 | chr12 | 112256861 | ||||||
| chr12:112257075
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.3129-557C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 20/75 | chr12 | 112257075 | ||||||
| chr12:112257129
|
C | T | 1 | a0001c0003t0013g0096 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.3129-611G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 20/75 | chr12 | 112257129 | ||||||
| chr12:112257448
|
T | C | 1 | a0001c0001t0005g0060 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3129-930A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 20/75 | chr12 | 112257448 | ||||||
| chr12:112257629
|
T | C | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.3128+867A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 20/75 | chr12 | 112257629 | ||||||
| chr12:112257646
|
CATT | C | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.3128+847_3128+849d others(5): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 20/75 | chr12 | 112257646 | ||||||
| chr12:112257698
|
T | C | 1 | a0004c0034t0001g0154 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3128+798A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 20/75 | chr12 | 112257698 | ||||||
| chr12:112257704
|
G | C | 8 | a0001c0001t0004g0061a0001c0001t0004g0067a0001c0001t0004g0068others(5): Show | 8 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.3128+792C>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 20/75 | chr12 | 112257704 | ||||||
| chr12:112257955
|
T | C | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.3128+541A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 20/75 | chr12 | 112257955 | ||||||
| chr12:112258146
|
G | A | 1 | a0001c0012t0002g0093 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.3128+350C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 20/75 | chr12 | 112258146 | ||||||
| chr12:112258190
|
GA | G | 169 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(166): Show | 169 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(166): Show |
intron_variant | MODIFIER | c.3128+305delT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 20/75 | chr12 | 112258190 | ||||||
| chr12:112258373
|
T | C | 4 | a0001c0002t0001g0164a0001c0002t0001g0177a0001c0002t0001g0181others(1): Show | 4 | NA18959.hp2 NA18967.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.3128+123A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 20/75 | chr12 | 112258373 | ||||||
| chr12:112258379
|
C | T | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3128+117G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 20/75 | chr12 | 112258379 | ||||||
| chr12:112258419
|
T | C | 2 | a0001c0001t0004g0067a0001c0001t0005g0070 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.3128+77A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 20/75 | chr12 | 112258419 | ||||||
| chr12:112258768
|
C | T | 8 | a0001c0001t0006g0254a0001c0001t0006g0255a0001c0001t0006g0256others(5): Show | 8 | HG00597.hp2 HG02056.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.3028-172G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 19/75 | chr12 | 112258768 | ||||||
| chr12:112259517
|
C | CT | 87 | a0001c0001t0001g0083a0001c0001t0001g0224a0001c0001t0003g0006others(84): Show | 87 | HG00597.hp2 HG00738.hp2 HG01081.hp1 others(84): Show |
intron_variant | MODIFIER | c.2874-253dupA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 18/75 | chr12 | 112259517 | ||||||
| chr12:112259517
|
C | CTT | 7 | a0001c0001t0003g0020a0001c0001t0003g0033a0001c0001t0004g0075others(4): Show | 7 | HG03579.hp2 HG03654.hp2 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.2874-254_2874-253d others(4): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 18/75 | chr12 | 112259517 | ||||||
| chr12:112259517
|
CTT | C | 79 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(76): Show | 79 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.2874-254_2874-253d others(4): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 18/75 | chr12 | 112259517 | ||||||
| chr12:112259582
|
C | T | 9 | a0001c0001t0003g0030a0001c0001t0004g0061a0001c0001t0004g0067others(6): Show | 9 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2874-317G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 18/75 | chr12 | 112259582 | ||||||
| chr12:112259697
|
T | A | 1 | a0002c0026t0001g0215 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2874-432A>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 18/75 | chr12 | 112259697 | ||||||
| chr12:112259850
|
T | C | 1 | a0001c0003t0002g0123 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2874-585A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 18/75 | chr12 | 112259850 | ||||||
| chr12:112260073
|
T | C | 5 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(2): Show | 5 | HG01891.hp1 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.2874-808A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 18/75 | chr12 | 112260073 | ||||||
| chr12:112260579
|
A | AT | 7 | a0001c0001t0003g0022a0001c0001t0003g0029a0001c0001t0003g0030others(4): Show | 7 | HG03654.hp2 HG04115.hp2 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.2873+725dupA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 18/75 | chr12 | 112260579 | ||||||
| chr12:112260743
|
A | AT | 8 | a0001c0001t0001g0079a0001c0001t0001g0158a0001c0001t0001g0159others(5): Show | 8 | HG01258.hp1 HG01884.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.2873+561dupA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 18/75 | chr12 | 112260743 | ||||||
| chr12:112260743
|
AT | A | 87 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0019g0269others(84): Show | 87 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.2873+561delA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 18/75 | chr12 | 112260743 | ||||||
| chr12:112261024
|
T | C | 1 | a0001c0002t0001g0206 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2873+281A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 18/75 | chr12 | 112261024 | ||||||
| chr12:112261252
|
C | T | 1 | a0001c0001t0004g0064 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2873+53G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 18/75 | chr12 | 112261252 | ||||||
| chr12:112261480
|
G | A | 1 | a0001c0003t0002g0136 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2749-51C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112261480 | ||||||
| chr12:112261664
|
C | T | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2749-235G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112261664 | ||||||
| chr12:112261736
|
T | C | 220 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0099others(217): Show | 220 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(217): Show |
intron_variant | MODIFIER | c.2749-307A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112261736 | ||||||
| chr12:112262208
|
A | G | 4 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0077others(1): Show | 4 | HG01891.hp1 HG03453.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.2749-779T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112262208 | ||||||
| chr12:112262339
|
C | T | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2749-910G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112262339 | ||||||
| chr12:112262464
|
C | T | 3 | a0001c0001t0003g0027a0001c0001t0003g0038a0001c0001t0003g0051 | 3 | NA18959.hp1 NA18994.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.2749-1035G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112262464 | ||||||
| chr12:112262465
|
G | A | 1 | a0001c0003t0002g0137 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2749-1036C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112262465 | ||||||
| chr12:112262508
|
T | A | 1 | a0001c0002t0001g0186 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2749-1079A>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112262508 | ||||||
| chr12:112262515
|
C | CA | 45 | a0001c0001t0001g0099a0001c0001t0001g0115a0001c0001t0001g0116others(42): Show | 45 | HG00140.hp1 HG00140.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.2749-1087dupT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112262515 | ||||||
| chr12:112262515
|
C | CAA | 79 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0112others(76): Show | 79 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(76): Show |
intron_variant | MODIFIER | c.2749-1088_2749-108 others(6): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112262515 | ||||||
| chr12:112262515
|
C | CAAA | 22 | a0001c0001t0003g0018a0001c0001t0003g0020a0001c0001t0003g0029others(19): Show | 22 | HG01109.hp2 HG01891.hp2 HG02027.hp1 others(19): Show |
intron_variant | MODIFIER | c.2749-1089_2749-108 others(7): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112262515 | ||||||
| chr12:112262515
|
C | CAAAA | 60 | a0001c0002t0001g0161a0001c0002t0001g0164a0001c0002t0001g0166others(57): Show | 60 | HG00544.hp1 HG01071.hp1 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.2749-1090_2749-108 others(8): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112262515 | ||||||
| chr12:112262515
|
C | CAAAAA | 16 | a0001c0002t0001g0178a0001c0002t0001g0185a0001c0002t0001g0189others(13): Show | 16 | HG00597.hp1 HG00735.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.2749-1091_2749-108 others(9): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112262515 | ||||||
| chr12:112262515
|
C | CAAAAAAA others(3): Show |
2 | a0001c0001t0004g0067a0001c0001t0005g0070 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2749-1096_2749-108 others(14): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112262515 | ||||||
| chr12:112262515
|
C | CAAAAAAA others(4): Show |
3 | a0001c0001t0004g0061a0001c0001t0004g0069a0001c0001t0004g0072 | 3 | HG02258.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2749-1097_2749-108 others(15): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112262515 | ||||||
| chr12:112262515
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0004g0071 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2749-1098_2749-108 others(16): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112262515 | ||||||
| chr12:112262515
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0004g0068 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2749-1099_2749-108 others(17): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112262515 | ||||||
| chr12:112262558
|
A | G | 1 | a0001c0033t0002g0110 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2749-1129T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112262558 | ||||||
| chr12:112262625
|
A | ATTATTT | 199 | a0001c0001t0001g0079a0001c0001t0001g0152a0001c0001t0001g0153others(196): Show | 199 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(196): Show |
intron_variant | MODIFIER | c.2749-1197_2749-119 others(10): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112262625 | ||||||
| chr12:112262625
|
A | T | 1 | a0001c0001t0001g0121 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2749-1196T>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112262625 | ||||||
| chr12:112262657
|
C | T | 3 | a0001c0009t0016g0266a0001c0009t0018g0268a0014c0021t0017g0267 | 3 | HG02622.hp2 HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2749-1228G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112262657 | ||||||
| chr12:112262709
|
G | A | 1 | a0002c0006t0002g0097 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2749-1280C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112262709 | ||||||
| chr12:112263014
|
T | G | 89 | a0001c0001t0004g0061a0001c0001t0004g0067a0001c0001t0004g0068others(86): Show | 89 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(86): Show |
intron_variant | MODIFIER | c.2748+1070A>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112263014 | ||||||
| chr12:112263079
|
T | TA | 89 | a0001c0001t0004g0061a0001c0001t0004g0067a0001c0001t0004g0068others(86): Show | 89 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(86): Show |
intron_variant | MODIFIER | c.2748+1004_2748+100 others(5): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112263079 | ||||||
| chr12:112263080
|
T | A | 89 | a0001c0001t0004g0061a0001c0001t0004g0067a0001c0001t0004g0068others(86): Show | 89 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(86): Show |
intron_variant | MODIFIER | c.2748+1004A>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112263080 | ||||||
| chr12:112263387
|
A | T | 170 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(167): Show | 170 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(167): Show |
intron_variant | MODIFIER | c.2748+697T>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112263387 | ||||||
| chr12:112263564
|
G | A | 1 | a0001c0002t0001g0225 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2748+520C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112263564 | ||||||
| chr12:112263703
|
ATT | A | 5 | a0001c0001t0004g0068a0001c0001t0004g0069a0001c0001t0004g0071others(2): Show | 5 | HG02451.hp2 HG02622.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.2748+379_2748+380d others(4): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112263703 | ||||||
| chr12:112263705
|
T | TTATATA | 18 | a0001c0002t0001g0163a0001c0002t0001g0176a0001c0002t0001g0178others(15): Show | 18 | HG00735.hp2 HG01081.hp2 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.2748+378_2748+379i others(8): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112263705 | ||||||
| chr12:112263705
|
T | TTATATAT others(1): Show |
40 | a0001c0002t0001g0161a0001c0002t0001g0164a0001c0002t0001g0166others(37): Show | 40 | HG00544.hp1 HG00597.hp1 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.2748+378_2748+379i others(10): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112263705 | ||||||
| chr12:112263705
|
T | TTATATAT others(3): Show |
14 | a0001c0002t0001g0169a0001c0002t0001g0174a0001c0002t0001g0181others(11): Show | 14 | HG02027.hp2 HG02071.hp1 HG02129.hp2 others(11): Show |
intron_variant | MODIFIER | c.2748+378_2748+379i others(12): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112263705 | ||||||
| chr12:112263705
|
T | TTATATAT others(5): Show |
6 | a0001c0002t0001g0202a0001c0002t0001g0203a0001c0002t0001g0205others(3): Show | 6 | HG02717.hp1 HG02809.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2748+378_2748+379i others(14): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112263705 | ||||||
| chr12:112263705
|
T | TTATATAT others(7): Show |
1 | a0001c0002t0001g0234 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2748+378_2748+379i others(16): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112263705 | ||||||
| chr12:112263705
|
T | TTATATAT others(9): Show |
1 | a0001c0002t0001g0206 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2748+378_2748+379i others(18): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112263705 | ||||||
| chr12:112263707
|
T | A | 84 | a0001c0001t0004g0061a0001c0001t0004g0067a0001c0001t0005g0070others(81): Show | 84 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.2748+377A>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112263707 | ||||||
| chr12:112263707
|
T | TTA | 10 | a0001c0001t0001g0152a0001c0001t0004g0062a0001c0001t0004g0064others(7): Show | 10 | HG01099.hp2 HG01175.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.2748+375_2748+376d others(4): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112263707 | ||||||
| chr12:112263707
|
T | TTATA | 4 | a0001c0001t0007g0007a0001c0009t0016g0266a0001c0009t0018g0268others(1): Show | 4 | HG02257.hp1 HG02622.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2748+373_2748+376d others(6): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112263707 | ||||||
| chr12:112263707
|
TTA | T | 3 | a0001c0001t0003g0037a0001c0001t0005g0047a0002c0004t0005g0048 | 3 | HG02055.hp1 HG02486.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.2748+375_2748+376d others(4): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112263707 | ||||||
| chr12:112263722
|
TATACAC | T | 9 | a0001c0001t0001g0099a0001c0001t0001g0125a0001c0001t0001g0127others(6): Show | 9 | HG00140.hp1 HG00738.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.2748+356_2748+361d others(8): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112263722 | ||||||
| chr12:112263724
|
T | TAC | 12 | a0001c0001t0001g0153a0001c0001t0001g0157a0001c0001t0001g0158others(9): Show | 12 | HG01109.hp2 HG01243.hp1 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.2748+358_2748+359d others(4): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112263724 | ||||||
| chr12:112263724
|
TACAC | T | 11 | a0001c0001t0001g0083a0001c0001t0001g0112a0001c0001t0001g0113others(8): Show | 11 | HG01993.hp2 HG02135.hp2 HG04115.hp1 others(8): Show |
intron_variant | MODIFIER | c.2748+356_2748+359d others(6): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112263724 | ||||||
| chr12:112263726
|
C | T | 91 | a0001c0001t0004g0061a0001c0001t0004g0067a0001c0001t0004g0068others(88): Show | 91 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(88): Show |
intron_variant | MODIFIER | c.2748+358G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112263726 | ||||||
| chr12:112263728
|
C | T | 89 | a0001c0001t0004g0061a0001c0001t0004g0067a0001c0001t0004g0068others(86): Show | 89 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(86): Show |
intron_variant | MODIFIER | c.2748+356G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112263728 | ||||||
| chr12:112263730
|
C | T | 89 | a0001c0001t0004g0061a0001c0001t0004g0067a0001c0001t0004g0068others(86): Show | 89 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(86): Show |
intron_variant | MODIFIER | c.2748+354G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112263730 | ||||||
| chr12:112263732
|
C | T | 89 | a0001c0001t0004g0061a0001c0001t0004g0067a0001c0001t0004g0068others(86): Show | 89 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(86): Show |
intron_variant | MODIFIER | c.2748+352G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112263732 | ||||||
| chr12:112263734
|
C | T | 7 | a0001c0001t0004g0067a0001c0001t0004g0068a0001c0001t0004g0069others(4): Show | 7 | HG02451.hp2 HG02622.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.2748+350G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112263734 | ||||||
| chr12:112263752
|
T | C | 1 | a0001c0002t0001g0202 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2748+332A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112263752 | ||||||
| chr12:112263922
|
T | C | 89 | a0001c0001t0004g0061a0001c0001t0004g0067a0001c0001t0004g0068others(86): Show | 89 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(86): Show |
intron_variant | MODIFIER | c.2748+162A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 17/75 | chr12 | 112263922 | ||||||
| chr12:112264408
|
C | T | 1 | a0001c0001t0001g0118 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2620-196G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 16/75 | chr12 | 112264408 | ||||||
| chr12:112264682
|
G | A | 1 | a0001c0001t0003g0045 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2620-470C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 16/75 | chr12 | 112264682 | ||||||
| chr12:112264739
|
A | C | 1 | a0001c0001t0006g0255 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2619+436T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 16/75 | chr12 | 112264739 | ||||||
| chr12:112265057
|
G | A | 8 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0012others(5): Show | 8 | NA18946.hp2 NA18950.hp2 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.2619+118C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 16/75 | chr12 | 112265057 | ||||||
| chr12:112265154
|
A | G | 8 | a0001c0001t0004g0061a0001c0001t0004g0067a0001c0001t0004g0068others(5): Show | 8 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2619+21T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 16/75 | chr12 | 112265154 | ||||||
| chr12:112265775
|
C | T | 1 | a0001c0001t0003g0006 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2498+103G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 15/75 | chr12 | 112265775 | ||||||
| chr12:112266101
|
G | A | 1 | a0001c0001t0004g0073 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2393-118C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 14/75 | chr12 | 112266101 | ||||||
| chr12:112266209
|
T | C | 4 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0216others(1): Show | 4 | HG01099.hp2 HG01175.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.2393-226A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 14/75 | chr12 | 112266209 | ||||||
| chr12:112266361
|
C | T | 1 | a0001c0002t0008g0250 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2393-378G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 14/75 | chr12 | 112266361 | ||||||
| chr12:112267157
|
A | G | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.2322-175T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 13/75 | chr12 | 112267157 | ||||||
| chr12:112267209
|
C | T | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.2322-227G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 13/75 | chr12 | 112267209 | ||||||
| chr12:112267251
|
G | A | 1 | a0001c0001t0004g0071 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2322-269C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 13/75 | chr12 | 112267251 | ||||||
| chr12:112267425
|
A | G | 2 | a0001c0002t0001g0236a0001c0002t0001g0244 | 2 | NA18955.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.2322-443T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 13/75 | chr12 | 112267425 | ||||||
| chr12:112267755
|
T | C | 1 | a0001c0012t0002g0093 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2322-773A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 13/75 | chr12 | 112267755 | ||||||
| chr12:112268058
|
G | A | 8 | a0001c0001t0004g0061a0001c0001t0004g0067a0001c0001t0004g0068others(5): Show | 8 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2322-1076C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 13/75 | chr12 | 112268058 | ||||||
| chr12:112268198
|
C | T | 75 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(72): Show | 75 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.2322-1216G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 13/75 | chr12 | 112268198 | ||||||
| chr12:112268325
|
C | G | 2 | a0001c0003t0002g0087a0001c0003t0002g0088 | 2 | HG02165.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.2322-1343G>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 13/75 | chr12 | 112268325 | ||||||
| chr12:112268571
|
C | A | 1 | a0001c0001t0001g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2321+1133G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 13/75 | chr12 | 112268571 | ||||||
| chr12:112268751
|
C | T | 2 | a0001c0001t0003g0017a0002c0004t0003g0015 | 2 | NA18950.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.2321+953G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 13/75 | chr12 | 112268751 | ||||||
| chr12:112268796
|
AC | A | 82 | a0001c0001t0005g0046a0001c0001t0005g0049a0001c0002t0001g0161others(79): Show | 82 | HG00544.hp1 HG00597.hp1 HG01071.hp1 others(79): Show |
intron_variant | MODIFIER | c.2321+907delG | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 13/75 | chr12 | 112268796 | ||||||
| chr12:112268797
|
C | A | 1 | a0001c0002t0001g0189 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2321+907G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 13/75 | chr12 | 112268797 | ||||||
| chr12:112268802
|
CA | C | 80 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(77): Show | 80 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(77): Show |
intron_variant | MODIFIER | c.2321+901delT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 13/75 | chr12 | 112268802 | ||||||
| chr12:112268868
|
G | GT | 82 | a0001c0001t0001g0079a0001c0001t0001g0127a0001c0001t0001g0129others(79): Show | 82 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.2321+835dupA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 13/75 | chr12 | 112268868 | ||||||
| chr12:112268868
|
G | GTT | 44 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0003g0006others(41): Show | 44 | HG01099.hp1 HG01109.hp2 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.2321+834_2321+835d others(4): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 13/75 | chr12 | 112268868 | ||||||
| chr12:112268868
|
GT | G | 50 | a0001c0001t0001g0083a0001c0001t0001g0112a0001c0001t0001g0113others(47): Show | 50 | HG00544.hp1 HG01099.hp2 HG01928.hp1 others(47): Show |
intron_variant | MODIFIER | c.2321+835delA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 13/75 | chr12 | 112268868 | ||||||
| chr12:112268868
|
GTT | G | 40 | a0001c0002t0001g0161a0001c0002t0001g0166a0001c0002t0001g0167others(37): Show | 40 | HG00597.hp1 HG00735.hp2 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.2321+834_2321+835d others(4): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 13/75 | chr12 | 112268868 | ||||||
| chr12:112268868
|
GTTTTTTT others(4): Show |
G | 1 | a0001c0009t0018g0268 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.2321+825_2321+835d others(13): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 13/75 | chr12 | 112268868 | ||||||
| chr12:112268897
|
C | T | 4 | a0001c0003t0002g0104a0001c0003t0002g0106a0001c0003t0002g0123others(1): Show | 4 | HG01258.hp1 HG01496.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.2321+807G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 13/75 | chr12 | 112268897 | ||||||
| chr12:112268999
|
C | T | 1 | a0001c0032t0011g0263 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2321+705G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 13/75 | chr12 | 112268999 | ||||||
| chr12:112269019
|
A | C | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.2321+685T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 13/75 | chr12 | 112269019 | ||||||
| chr12:112269457
|
TTTTG | T | 3 | a0001c0009t0016g0266a0001c0009t0018g0268a0014c0021t0017g0267 | 3 | HG02622.hp2 HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2321+243_2321+246d others(6): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 13/75 | chr12 | 112269457 | ||||||
| chr12:112269531
|
C | T | 2 | a0001c0002t0001g0171a0001c0002t0001g0193 | 2 | NA18965.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.2321+173G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 13/75 | chr12 | 112269531 | ||||||
| chr12:112269594
|
T | C | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.2321+110A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 13/75 | chr12 | 112269594 | ||||||
| chr12:112270527
|
T | C | 170 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(167): Show | 170 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(167): Show |
intron_variant | MODIFIER | c.1943-68A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 11/75 | chr12 | 112270527 | ||||||
| chr12:112270622
|
T | C | 88 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(85): Show | 88 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(85): Show |
intron_variant | MODIFIER | c.1943-163A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 11/75 | chr12 | 112270622 | ||||||
| chr12:112270649
|
T | C | 1 | a0001c0001t0005g0044 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1943-190A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 11/75 | chr12 | 112270649 | ||||||
| chr12:112270709
|
T | C | 1 | a0007c0015t0001g0173 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1943-250A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 11/75 | chr12 | 112270709 | ||||||
| chr12:112271317
|
G | A | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.1943-858C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 11/75 | chr12 | 112271317 | ||||||
| chr12:112271415
|
A | G | 1 | a0004c0034t0001g0154 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1943-956T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 11/75 | chr12 | 112271415 | ||||||
| chr12:112271419
|
A | G | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.1943-960T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 11/75 | chr12 | 112271419 | ||||||
| chr12:112271490
|
A | T | 1 | a0001c0002t0001g0196 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1943-1031T>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 11/75 | chr12 | 112271490 | ||||||
| chr12:112271762
|
T | G | 176 | a0001c0001t0001g0116a0001c0001t0001g0157a0001c0001t0001g0158others(173): Show | 176 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(173): Show |
intron_variant | MODIFIER | c.1943-1303A>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 11/75 | chr12 | 112271762 | ||||||
| chr12:112271901
|
C | T | 3 | a0001c0001t0003g0031a0001c0001t0003g0032a0015c0020t0003g0009 | 3 | NA18971.hp2 NA18980.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1943-1442G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 11/75 | chr12 | 112271901 | ||||||
| chr12:112272402
|
T | G | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.1942+1253A>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 11/75 | chr12 | 112272402 | ||||||
| chr12:112272478
|
C | T | 6 | a0001c0001t0004g0062a0001c0001t0004g0064a0001c0001t0004g0065others(3): Show | 6 | HG02055.hp2 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1942+1177G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 11/75 | chr12 | 112272478 | ||||||
| chr12:112272526
|
G | A | 2 | a0001c0002t0001g0171a0001c0002t0001g0193 | 2 | NA18965.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1942+1129C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 11/75 | chr12 | 112272526 | ||||||
| chr12:112272669
|
A | G | 1 | a0001c0011t0010g0146 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1942+986T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 11/75 | chr12 | 112272669 | ||||||
| chr12:112272775
|
CTGTT | C | 15 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(12): Show | 15 | HG02055.hp2 HG02109.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.1942+876_1942+879d others(6): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 11/75 | chr12 | 112272775 | ||||||
| chr12:112273119
|
G | A | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.1942+536C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 11/75 | chr12 | 112273119 | ||||||
| chr12:112273150
|
G | A | 21 | a0001c0001t0001g0083a0001c0001t0001g0099a0001c0001t0001g0112others(18): Show | 21 | HG00140.hp1 HG00738.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.1942+505C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 11/75 | chr12 | 112273150 | ||||||
| chr12:112273279
|
G | A | 1 | a0008c0017t0001g0190 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1942+376C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 11/75 | chr12 | 112273279 | ||||||
| chr12:112273981
|
T | A | 1 | a0001c0001t0004g0073 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1802-186A>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 10/75 | chr12 | 112273981 | ||||||
| chr12:112274033
|
C | T | 2 | a0001c0001t0005g0046a0001c0001t0005g0049 | 2 | HG01167.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1802-238G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 10/75 | chr12 | 112274033 | ||||||
| chr12:112274401
|
T | C | 1 | a0001c0001t0004g0078 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1801+446A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 10/75 | chr12 | 112274401 | ||||||
| chr12:112274705
|
CAAACA | C | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.1801+137_1801+141d others(7): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 10/75 | chr12 | 112274705 | ||||||
| chr12:112274724
|
C | A | 1 | a0001c0001t0006g0258 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1801+123G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 10/75 | chr12 | 112274724 | ||||||
| chr12:112275216
|
C | T | 8 | a0001c0001t0004g0023a0001c0001t0007g0007a0001c0001t0007g0024others(5): Show | 8 | HG01943.hp1 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1688-256G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 9/75 | chr12 | 112275216 | ||||||
| chr12:112275405
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1688-445C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 9/75 | chr12 | 112275405 | ||||||
| chr12:112275490
|
T | G | 1 | a0001c0029t0001g0122 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1688-530A>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 9/75 | chr12 | 112275490 | ||||||
| chr12:112275619
|
C | CAT | 10 | a0001c0001t0001g0114a0001c0001t0004g0067a0001c0001t0004g0068others(7): Show | 10 | HG01175.hp2 HG02129.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1688-661_1688-660d others(4): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 9/75 | chr12 | 112275619 | ||||||
| chr12:112275619
|
CAT | C | 4 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0077others(1): Show | 4 | HG01891.hp1 HG03453.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1688-661_1688-660d others(4): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 9/75 | chr12 | 112275619 | ||||||
| chr12:112276091
|
G | A | 72 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(69): Show | 72 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(69): Show |
intron_variant | MODIFIER | c.1688-1131C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 9/75 | chr12 | 112276091 | ||||||
| chr12:112276464
|
T | A | 1 | a0001c0001t0001g0127 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1688-1504A>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 9/75 | chr12 | 112276464 | ||||||
| chr12:112276492
|
G | C | 1 | a0002c0005t0001g0197 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1688-1532C>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 9/75 | chr12 | 112276492 | ||||||
| chr12:112276708
|
T | C | 2 | a0001c0001t0001g0079a0001c0001t0001g0160 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1688-1748A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 9/75 | chr12 | 112276708 | ||||||
| chr12:112276760
|
AAATGGAT others(15): Show |
A | 1 | a0001c0003t0002g0088 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1688-1822_1688-180 others(26): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 9/75 | chr12 | 112276760 | ||||||
| chr12:112276769
|
A | C | 8 | a0001c0001t0004g0061a0001c0001t0004g0067a0001c0001t0004g0068others(5): Show | 8 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1688-1809T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 9/75 | chr12 | 112276769 | ||||||
| chr12:112276787
|
G | T | 1 | a0001c0003t0002g0088 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1688-1827C>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 9/75 | chr12 | 112276787 | ||||||
| chr12:112276788
|
A | C | 1 | a0001c0003t0002g0088 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1688-1828T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 9/75 | chr12 | 112276788 | ||||||
| chr12:112277030
|
C | G | 75 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(72): Show | 75 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.1688-2070G>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 9/75 | chr12 | 112277030 | ||||||
| chr12:112277230
|
T | A | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.1687+1998A>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 9/75 | chr12 | 112277230 | ||||||
| chr12:112277520
|
G | A | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.1687+1708C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 9/75 | chr12 | 112277520 | ||||||
| chr12:112277858
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1687+1370C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 9/75 | chr12 | 112277858 | ||||||
| chr12:112278111
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1687+1117C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 9/75 | chr12 | 112278111 | ||||||
| chr12:112278233
|
G | A | 88 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(85): Show | 88 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(85): Show |
intron_variant | MODIFIER | c.1687+995C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 9/75 | chr12 | 112278233 | ||||||
| chr12:112278335
|
C | T | 6 | a0001c0001t0004g0062a0001c0001t0004g0064a0001c0001t0004g0065others(3): Show | 6 | HG02055.hp2 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1687+893G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 9/75 | chr12 | 112278335 | ||||||
| chr12:112278367
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1687+861C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 9/75 | chr12 | 112278367 | ||||||
| chr12:112278580
|
A | G | 8 | a0001c0001t0004g0023a0001c0001t0007g0007a0001c0001t0007g0024others(5): Show | 8 | HG01943.hp1 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1687+648T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 9/75 | chr12 | 112278580 | ||||||
| chr12:112278590
|
T | C | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1687+638A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 9/75 | chr12 | 112278590 | ||||||
| chr12:112278718
|
C | T | 1 | a0001c0001t0005g0060 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1687+510G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 9/75 | chr12 | 112278718 | ||||||
| chr12:112279196
|
C | T | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.1687+32G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 9/75 | chr12 | 112279196 | ||||||
| chr12:112279760
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1529-374C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 8/75 | chr12 | 112279760 | ||||||
| chr12:112280042
|
A | G | 1 | a0001c0003t0009g0001 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1529-656T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 8/75 | chr12 | 112280042 | ||||||
| chr12:112280063
|
T | C | 1 | a0001c0016t0001g0168 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1529-677A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 8/75 | chr12 | 112280063 | ||||||
| chr12:112280116
|
T | C | 220 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0099others(217): Show | 220 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(217): Show |
intron_variant | MODIFIER | c.1529-730A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 8/75 | chr12 | 112280116 | ||||||
| chr12:112280394
|
G | A | 88 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(85): Show | 88 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(85): Show |
intron_variant | MODIFIER | c.1529-1008C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 8/75 | chr12 | 112280394 | ||||||
| chr12:112280408
|
A | G | 1 | a0001c0002t0001g0169 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1529-1022T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 8/75 | chr12 | 112280408 | ||||||
| chr12:112280476
|
A | G | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG02109.hp1 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1529-1090T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 8/75 | chr12 | 112280476 | ||||||
| chr12:112280706
|
C | A | 220 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0099others(217): Show | 220 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(217): Show |
intron_variant | MODIFIER | c.1529-1320G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 8/75 | chr12 | 112280706 | ||||||
| chr12:112280784
|
C | CT | 9 | a0001c0001t0001g0121a0001c0001t0004g0062a0001c0001t0004g0064others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.1529-1399dupA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 8/75 | chr12 | 112280784 | ||||||
| chr12:112280784
|
CT | C | 86 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0012others(83): Show | 86 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(83): Show |
intron_variant | MODIFIER | c.1529-1399delA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 8/75 | chr12 | 112280784 | ||||||
| chr12:112280784
|
CTT | C | 81 | a0001c0001t0005g0049a0001c0002t0001g0161a0001c0002t0001g0163others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.1529-1400_1529-139 others(6): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 8/75 | chr12 | 112280784 | ||||||
| chr12:112280849
|
A | C | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.1529-1463T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 8/75 | chr12 | 112280849 | ||||||
| chr12:112280952
|
G | A | 1 | a0001c0001t0005g0005 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1529-1566C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 8/75 | chr12 | 112280952 | ||||||
| chr12:112281206
|
C | A | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.1529-1820G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 8/75 | chr12 | 112281206 | ||||||
| chr12:112281250
|
A | G | 3 | a0001c0009t0016g0266a0001c0009t0018g0268a0014c0021t0017g0267 | 3 | HG02622.hp2 HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1528+1860T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 8/75 | chr12 | 112281250 | ||||||
| chr12:112281265
|
G | GTT | 80 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(77): Show | 80 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(77): Show |
intron_variant | MODIFIER | c.1528+1843_1528+184 others(6): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 8/75 | chr12 | 112281265 | ||||||
| chr12:112281273
|
T | A | 1 | a0001c0001t0001g0116 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1528+1837A>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 8/75 | chr12 | 112281273 | ||||||
| chr12:112281274
|
A | T | 6 | a0001c0001t0003g0033a0001c0002t0001g0163a0001c0002t0008g0250others(3): Show | 6 | HG02965.hp2 HG03098.hp1 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.1528+1836T>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 8/75 | chr12 | 112281274 | ||||||
| chr12:112281362
|
C | T | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.1528+1748G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 8/75 | chr12 | 112281362 | ||||||
| chr12:112281540
|
A | G | 1 | a0001c0001t0008g0253 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1528+1570T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 8/75 | chr12 | 112281540 | ||||||
| chr12:112281644
|
C | G | 1 | a0001c0011t0010g0146 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1528+1466G>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 8/75 | chr12 | 112281644 | ||||||
| chr12:112281884
|
A | G | 1 | a0001c0001t0001g0113 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1528+1226T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 8/75 | chr12 | 112281884 | ||||||
| chr12:112282107
|
G | C | 2 | a0001c0001t0006g0254a0001c0001t0006g0256 | 2 | HG00597.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1528+1003C>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 8/75 | chr12 | 112282107 | ||||||
| chr12:112282199
|
C | T | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1528+911G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 8/75 | chr12 | 112282199 | ||||||
| chr12:112282243
|
C | T | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1528+867G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 8/75 | chr12 | 112282243 | ||||||
| chr12:112282334
|
G | C | 1 | a0001c0001t0001g0121 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1528+776C>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 8/75 | chr12 | 112282334 | ||||||
| chr12:112282394
|
A | C | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1528+716T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 8/75 | chr12 | 112282394 | ||||||
| chr12:112282823
|
C | T | 1 | a0001c0011t0010g0146 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1528+287G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 8/75 | chr12 | 112282823 | ||||||
| chr12:112283495
|
T | C | 2 | a0001c0001t0001g0153a0004c0034t0001g0154 | 2 | HG02647.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1336-193A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112283495 | ||||||
| chr12:112283724
|
C | T | 4 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0216others(1): Show | 4 | HG01099.hp2 HG01175.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.1336-422G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112283724 | ||||||
| chr12:112283878
|
T | C | 1 | a0002c0006t0002g0126 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1336-576A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112283878 | ||||||
| chr12:112283955
|
C | CT | 6 | a0001c0001t0001g0216a0001c0001t0004g0068a0001c0001t0004g0069others(3): Show | 6 | HG01243.hp2 HG02486.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1336-654dupA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112283955 | ||||||
| chr12:112283955
|
CT | C | 8 | a0001c0001t0001g0079a0001c0001t0001g0156a0001c0001t0001g0160others(5): Show | 8 | HG01167.hp1 HG01884.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1336-654delA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112283955 | ||||||
| chr12:112283958
|
T | C | 5 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(2): Show | 5 | HG02071.hp2 HG02109.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1336-656A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112283958 | ||||||
| chr12:112284453
|
G | A | 1 | a0001c0001t0004g0074 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1336-1151C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112284453 | ||||||
| chr12:112284754
|
G | A | 4 | a0001c0001t0004g0068a0001c0001t0004g0069a0001c0001t0004g0071others(1): Show | 4 | HG02451.hp2 HG02622.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1336-1452C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112284754 | ||||||
| chr12:112284880
|
C | G | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.1336-1578G>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112284880 | ||||||
| chr12:112285197
|
G | A | 5 | a0001c0001t0004g0062a0001c0001t0004g0064a0001c0001t0004g0065others(2): Show | 5 | HG02055.hp2 HG02572.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1336-1895C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112285197 | ||||||
| chr12:112285478
|
T | A | 1 | a0001c0001t0019g0269 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1336-2176A>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112285478 | ||||||
| chr12:112285595
|
G | A | 4 | a0001c0001t0001g0079a0001c0001t0001g0156a0001c0001t0001g0160others(1): Show | 4 | HG01884.hp1 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1336-2293C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112285595 | ||||||
| chr12:112285607
|
A | G | 2 | a0001c0001t0001g0079a0001c0001t0001g0160 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1336-2305T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112285607 | ||||||
| chr12:112285897
|
T | C | 1 | a0001c0001t0003g0059 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1336-2595A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112285897 | ||||||
| chr12:112286586
|
G | T | 2 | a0001c0003t0002g0098a0001c0003t0002g0150 | 2 | HG03927.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1336-3284C>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112286586 | ||||||
| chr12:112286709
|
A | C | 1 | a0001c0001t0011g0264 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1336-3407T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112286709 | ||||||
| chr12:112286889
|
C | T | 5 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(2): Show | 5 | HG01891.hp1 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1336-3587G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112286889 | ||||||
| chr12:112286964
|
G | A | 77 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(74): Show | 77 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(74): Show |
intron_variant | MODIFIER | c.1336-3662C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112286964 | ||||||
| chr12:112286998
|
C | T | 4 | a0001c0002t0001g0164a0001c0002t0001g0177a0001c0002t0001g0181others(1): Show | 4 | NA18959.hp2 NA18967.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.1336-3696G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112286998 | ||||||
| chr12:112287344
|
A | G | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.1336-4042T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112287344 | ||||||
| chr12:112287495
|
A | G | 1 | a0001c0002t0001g0185 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1336-4193T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112287495 | ||||||
| chr12:112287500
|
AAAATAGC others(18): Show |
A | 1 | a0001c0003t0002g0090 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1336-4223_1336-419 others(29): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112287500 | ||||||
| chr12:112287745
|
C | A | 5 | a0001c0001t0004g0062a0001c0001t0004g0064a0001c0001t0004g0065others(2): Show | 5 | HG02055.hp2 HG02572.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1336-4443G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112287745 | ||||||
| chr12:112288010
|
C | CT | 12 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(9): Show | 12 | HG02109.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1336-4709dupA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112288010 | ||||||
| chr12:112288057
|
G | A | 5 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(2): Show | 5 | HG01891.hp1 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1336-4755C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112288057 | ||||||
| chr12:112288318
|
C | CA | 122 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(119): Show | 122 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.1336-5017dupT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112288318 | ||||||
| chr12:112288318
|
C | CAA | 7 | a0001c0002t0001g0163a0001c0002t0001g0164a0001c0002t0001g0169others(4): Show | 7 | NA18942.hp1 NA18959.hp2 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.1336-5018_1336-501 others(6): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112288318 | ||||||
| chr12:112288345
|
A | G | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.1336-5043T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112288345 | ||||||
| chr12:112288449
|
C | CA | 3 | a0001c0010t0001g0214a0001c0010t0001g0217a0002c0026t0001g0215 | 3 | HG02965.hp2 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1336-5148dupT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112288449 | ||||||
| chr12:112288496
|
C | A | 80 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(77): Show | 80 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(77): Show |
intron_variant | MODIFIER | c.1336-5194G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112288496 | ||||||
| chr12:112289083
|
T | C | 1 | a0002c0004t0003g0008 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1336-5781A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112289083 | ||||||
| chr12:112289924
|
G | A | 2 | a0001c0001t0003g0043a0001c0001t0003g0045 | 2 | HG01109.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1336-6622C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112289924 | ||||||
| chr12:112289974
|
G | A | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.1336-6672C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112289974 | ||||||
| chr12:112290269
|
G | A | 2 | a0001c0007t0001g0172a0001c0007t0001g0183 | 2 | NA19057.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1336-6967C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112290269 | ||||||
| chr12:112290327
|
AT | A | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0166others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.1336-7026delA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112290327 | ||||||
| chr12:112290398
|
G | C | 5 | a0001c0001t0004g0062a0001c0001t0004g0064a0001c0001t0004g0065others(2): Show | 5 | HG02055.hp2 HG02572.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1336-7096C>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112290398 | ||||||
| chr12:112290637
|
C | T | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.1336-7335G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112290637 | ||||||
| chr12:112290848
|
C | CA | 52 | a0001c0001t0003g0010a0001c0001t0003g0013a0001c0001t0003g0014others(49): Show | 52 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(49): Show |
intron_variant | MODIFIER | c.1336-7547dupT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112290848 | ||||||
| chr12:112290848
|
C | CAA | 27 | a0001c0001t0003g0006a0001c0001t0003g0011a0001c0001t0003g0012others(24): Show | 27 | HG02027.hp1 HG02055.hp1 HG02071.hp2 others(24): Show |
intron_variant | MODIFIER | c.1336-7548_1336-754 others(6): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112290848 | ||||||
| chr12:112290848
|
C | CAAAAAAA others(4): Show |
4 | a0001c0002t0001g0174a0001c0002t0001g0176a0001c0002t0001g0179others(1): Show | 4 | HG01071.hp1 HG01081.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.1336-7547_1336-754 others(15): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112290848 | ||||||
| chr12:112290848
|
C | CAAAAAAA others(5): Show |
36 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(33): Show | 36 | HG00735.hp2 HG01258.hp2 HG01433.hp1 others(33): Show |
intron_variant | MODIFIER | c.1336-7547_1336-754 others(16): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112290848 | ||||||
| chr12:112290848
|
C | CAAAAAAA others(6): Show |
23 | a0001c0002t0001g0171a0001c0002t0001g0175a0001c0002t0001g0177others(20): Show | 23 | HG02129.hp2 HG02132.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.1336-7547_1336-754 others(17): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112290848 | ||||||
| chr12:112290848
|
C | CAAAAAAA others(7): Show |
15 | a0001c0002t0001g0166a0001c0002t0001g0169a0001c0002t0001g0188others(12): Show | 15 | HG00544.hp1 HG00597.hp1 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.1336-7547_1336-754 others(18): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112290848 | ||||||
| chr12:112290848
|
C | CAAAAAAA others(8): Show |
2 | a0002c0005t0001g0165a0003c0008t0001g0207 | 2 | NA18947.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1336-7547_1336-754 others(19): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112290848 | ||||||
| chr12:112290850
|
AAAAAAAA others(6): Show |
A | 5 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(2): Show | 5 | HG01891.hp1 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1336-7561_1336-754 others(17): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112290850 | ||||||
| chr12:112290854
|
A | C | 15 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(12): Show | 15 | HG02055.hp2 HG02109.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.1336-7552T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112290854 | ||||||
| chr12:112290858
|
C | A | 164 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(161): Show | 164 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(161): Show |
intron_variant | MODIFIER | c.1336-7556G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112290858 | ||||||
| chr12:112290862
|
A | C | 10 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(7): Show | 10 | HG02559.hp2 HG02630.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.1336-7560T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112290862 | ||||||
| chr12:112290863
|
C | A | 185 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(182): Show | 185 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(182): Show |
intron_variant | MODIFIER | c.1336-7561G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112290863 | ||||||
| chr12:112290866
|
A | C | 5 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(2): Show | 5 | HG03098.hp2 HG03130.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1336-7564T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112290866 | ||||||
| chr12:112290868
|
A | C | 14 | a0001c0001t0001g0083a0001c0001t0001g0112a0001c0001t0001g0113others(11): Show | 14 | HG01884.hp2 HG01952.hp2 HG01993.hp2 others(11): Show |
intron_variant | MODIFIER | c.1336-7566T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112290868 | ||||||
| chr12:112291383
|
T | A | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.1336-8081A>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112291383 | ||||||
| chr12:112291384
|
A | G | 1 | a0001c0002t0001g0180 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1336-8082T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112291384 | ||||||
| chr12:112291562
|
C | T | 1 | a0001c0003t0002g0138 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1336-8260G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112291562 | ||||||
| chr12:112291833
|
C | T | 4 | a0001c0001t0004g0068a0001c0001t0004g0069a0001c0001t0004g0071others(1): Show | 4 | HG02451.hp2 HG02622.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1336-8531G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112291833 | ||||||
| chr12:112292056
|
A | G | 1 | a0001c0001t0006g0259 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1336-8754T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112292056 | ||||||
| chr12:112292133
|
C | T | 1 | a0001c0003t0013g0105 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1336-8831G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112292133 | ||||||
| chr12:112292223
|
A | C | 8 | a0001c0001t0004g0061a0001c0001t0004g0067a0001c0001t0004g0068others(5): Show | 8 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1336-8921T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112292223 | ||||||
| chr12:112292593
|
T | G | 1 | a0001c0011t0010g0146 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1336-9291A>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112292593 | ||||||
| chr12:112292789
|
G | A | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.1336-9487C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112292789 | ||||||
| chr12:112293103
|
C | T | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.1336-9801G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112293103 | ||||||
| chr12:112293364
|
C | CA | 22 | a0001c0001t0003g0006a0001c0001t0003g0012a0001c0001t0003g0020others(19): Show | 22 | HG00597.hp2 HG01928.hp2 HG01978.hp2 others(19): Show |
intron_variant | MODIFIER | c.1336-10063dupT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112293364 | ||||||
| chr12:112293364
|
CA | C | 80 | a0001c0001t0001g0158a0001c0001t0005g0070a0001c0002t0001g0161others(77): Show | 80 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(77): Show |
intron_variant | MODIFIER | c.1336-10063delT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112293364 | ||||||
| chr12:112293490
|
C | T | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1336-10188G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112293490 | ||||||
| chr12:112293543
|
A | AAATCAAT others(1): Show |
142 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0099others(139): Show | 142 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(139): Show |
intron_variant | MODIFIER | c.1336-10249_1336-10 others(14): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112293543 | ||||||
| chr12:112293543
|
A | AAATCAAT others(5): Show |
78 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(75): Show | 78 | HG01081.hp1 HG01099.hp1 HG01109.hp2 others(75): Show |
intron_variant | MODIFIER | c.1336-10253_1336-10 others(18): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112293543 | ||||||
| chr12:112293634
|
C | A | 1 | a0001c0002t0001g0174 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1336-10332G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112293634 | ||||||
| chr12:112293648
|
A | T | 2 | a0001c0001t0005g0056a0002c0004t0005g0057 | 2 | HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1336-10346T>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112293648 | ||||||
| chr12:112293699
|
G | C | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.1336-10397C>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112293699 | ||||||
| chr12:112293703
|
G | A | 21 | a0001c0001t0001g0083a0001c0001t0001g0099a0001c0001t0001g0112others(18): Show | 21 | HG00140.hp1 HG00738.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.1336-10401C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112293703 | ||||||
| chr12:112293914
|
C | T | 5 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(2): Show | 5 | HG01891.hp1 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1336-10612G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112293914 | ||||||
| chr12:112294045
|
A | G | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.1336-10743T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112294045 | ||||||
| chr12:112294113
|
A | G | 1 | a0001c0001t0012g0151 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1336-10811T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112294113 | ||||||
| chr12:112294204
|
T | A | 1 | a0001c0001t0005g0046 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1336-10902A>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112294204 | ||||||
| chr12:112294221
|
T | C | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.1336-10919A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112294221 | ||||||
| chr12:112294547
|
C | T | 2 | a0001c0001t0006g0258a0001c0001t0006g0262 | 2 | HG02056.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.1336-11245G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112294547 | ||||||
| chr12:112294560
|
C | T | 1 | a0001c0001t0003g0006 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1336-11258G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112294560 | ||||||
| chr12:112294613
|
T | C | 1 | a0001c0032t0011g0263 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1336-11311A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112294613 | ||||||
| chr12:112294703
|
C | T | 4 | a0001c0001t0001g0152a0001c0001t0001g0153a0002c0004t0001g0155others(1): Show | 4 | HG01099.hp2 HG01175.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1335+11361G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112294703 | ||||||
| chr12:112294804
|
T | A | 88 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(85): Show | 88 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(85): Show |
intron_variant | MODIFIER | c.1335+11260A>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112294804 | ||||||
| chr12:112294945
|
T | TTTAA | 9 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(6): Show | 9 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1335+11115_1335+11 others(10): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112294945 | ||||||
| chr12:112294960
|
A | C | 88 | a0001c0001t0001g0079a0001c0001t0001g0160a0001c0001t0007g0007others(85): Show | 88 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(85): Show |
intron_variant | MODIFIER | c.1335+11104T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112294960 | ||||||
| chr12:112295126
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1335+10938C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112295126 | ||||||
| chr12:112295148
|
A | AAGAG | 218 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0099others(215): Show | 218 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(215): Show |
intron_variant | MODIFIER | c.1335+10912_1335+10 others(10): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112295148 | ||||||
| chr12:112295148
|
A | G | 2 | a0001c0002t0001g0188a0001c0002t0001g0211 | 2 | HG02080.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.1335+10916T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112295148 | ||||||
| chr12:112295326
|
A | C | 1 | a0002c0004t0003g0052 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1335+10738T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112295326 | ||||||
| chr12:112295367
|
A | AT | 28 | a0001c0001t0004g0023a0001c0001t0004g0061a0001c0001t0004g0067others(25): Show | 28 | HG00735.hp2 HG01081.hp2 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.1335+10696dupA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112295367 | ||||||
| chr12:112295367
|
A | ATT | 63 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(60): Show | 63 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(60): Show |
intron_variant | MODIFIER | c.1335+10695_1335+10 others(8): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112295367 | ||||||
| chr12:112295414
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1335+10650C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112295414 | ||||||
| chr12:112295457
|
C | A | 2 | a0001c0002t0001g0203a0001c0002t0001g0204 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1335+10607G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112295457 | ||||||
| chr12:112295677
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1335+10387G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112295677 | ||||||
| chr12:112295757
|
T | A | 1 | a0001c0001t0004g0064 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1335+10307A>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112295757 | ||||||
| chr12:112295770
|
T | C | 1 | a0002c0005t0001g0231 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1335+10294A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112295770 | ||||||
| chr12:112295795
|
T | C | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159 | 3 | HG03098.hp2 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1335+10269A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112295795 | ||||||
| chr12:112295802
|
A | T | 1 | a0002c0004t0003g0008 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1335+10262T>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112295802 | ||||||
| chr12:112295808
|
A | T | 6 | a0001c0001t0001g0156a0001c0001t0004g0023a0001c0001t0007g0024others(3): Show | 6 | HG01943.hp1 HG02717.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1335+10256T>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112295808 | ||||||
| chr12:112295810
|
A | T | 129 | a0001c0001t0001g0099a0001c0001t0001g0112a0001c0001t0001g0121others(126): Show | 129 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.1335+10254T>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112295810 | ||||||
| chr12:112295822
|
T | TAC | 63 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(60): Show | 63 | HG00597.hp2 HG01109.hp2 HG01167.hp2 others(60): Show |
intron_variant | MODIFIER | c.1335+10241_1335+10 others(8): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112295822 | ||||||
| chr12:112295822
|
T | TACAC | 7 | a0001c0001t0005g0021a0001c0001t0005g0044a0001c0001t0005g0053others(4): Show | 7 | HG01081.hp1 HG01099.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1335+10241_1335+10 others(10): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112295822 | ||||||
| chr12:112295824
|
T | C | 74 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(71): Show | 74 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(71): Show |
intron_variant | MODIFIER | c.1335+10240A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112295824 | ||||||
| chr12:112295824
|
T | TAC | 15 | a0001c0001t0004g0061a0001c0001t0004g0068a0001c0001t0004g0069others(12): Show | 15 | HG01891.hp1 HG02258.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1335+10238_1335+10 others(8): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112295824 | ||||||
| chr12:112295836
|
C | A | 1 | a0001c0002t0001g0193 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1335+10228G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112295836 | ||||||
| chr12:112296104
|
T | C | 1 | a0001c0001t0015g0248 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1335+9960A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112296104 | ||||||
| chr12:112296200
|
TGTAGGTG others(9): Show |
T | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.1335+9848_1335+986 others(20): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112296200 | ||||||
| chr12:112296471
|
G | A | 1 | a0001c0002t0001g0232 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1335+9593C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112296471 | ||||||
| chr12:112296577
|
ATGTAGGT others(8): Show |
A | 1 | a0001c0003t0002g0111 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1335+9472_1335+948 others(19): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112296577 | ||||||
| chr12:112296758
|
ATGTAGGT others(8): Show |
A | 4 | a0001c0001t0004g0078a0001c0001t0014g0148a0001c0002t0001g0237others(1): Show | 4 | HG01891.hp1 NA19081.hp1 NA19087.hp2 others(1): Show |
intron_variant | MODIFIER | c.1335+9291_1335+930 others(19): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112296758 | ||||||
| chr12:112296771
|
T | G | 1 | a0001c0001t0005g0060 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1335+9293A>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112296771 | ||||||
| chr12:112297116
|
G | GATGTAGA others(68): Show |
1 | a0001c0001t0003g0016 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1335+8947_1335+894 others(79): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112297116 | ||||||
| chr12:112297116
|
G | GATGTAGG others(68): Show |
1 | a0001c0002t0001g0189 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1335+8947_1335+894 others(79): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112297116 | ||||||
| chr12:112297116
|
G | GATGTAGG others(68): Show |
218 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0099others(215): Show | 218 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(215): Show |
intron_variant | MODIFIER | c.1335+8873_1335+894 others(79): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112297116 | ||||||
| chr12:112297233
|
G | A | 1 | a0013c0025t0002g0095 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1335+8831C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112297233 | ||||||
| chr12:112297236
|
G | A | 1 | a0001c0003t0002g0103 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1335+8828C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112297236 | ||||||
| chr12:112297536
|
G | A | 1 | a0001c0002t0001g0232 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1335+8528C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112297536 | ||||||
| chr12:112297688
|
A | G | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.1335+8376T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112297688 | ||||||
| chr12:112297693
|
T | C | 8 | a0001c0001t0001g0099a0001c0001t0001g0125a0001c0001t0001g0128others(5): Show | 8 | HG00140.hp1 HG00738.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1335+8371A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112297693 | ||||||
| chr12:112297741
|
G | A | 1 | a0013c0025t0002g0095 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1335+8323C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112297741 | ||||||
| chr12:112298279
|
G | C | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.1335+7785C>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112298279 | ||||||
| chr12:112298314
|
A | G | 20 | a0001c0002t0001g0225a0001c0002t0001g0227a0001c0002t0001g0228others(17): Show | 20 | HG00544.hp1 HG02132.hp1 NA18946.hp1 others(17): Show |
intron_variant | MODIFIER | c.1335+7750T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112298314 | ||||||
| chr12:112298317
|
C | A | 1 | a0001c0001t0004g0078 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1335+7747G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112298317 | ||||||
| chr12:112298448
|
C | T | 1 | a0001c0001t0003g0028 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1335+7616G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112298448 | ||||||
| chr12:112298480
|
A | AT | 163 | a0001c0001t0001g0117a0001c0001t0003g0006a0001c0001t0003g0010others(160): Show | 163 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.1335+7583dupA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112298480 | ||||||
| chr12:112298480
|
A | ATT | 9 | a0001c0001t0003g0020a0001c0001t0003g0040a0001c0001t0003g0059others(6): Show | 9 | HG01934.hp2 HG02738.hp1 NA18947.hp1 others(6): Show |
intron_variant | MODIFIER | c.1335+7582_1335+758 others(6): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112298480 | ||||||
| chr12:112298480
|
A | T | 1 | a0001c0001t0003g0027 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1335+7584T>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112298480 | ||||||
| chr12:112298700
|
C | T | 88 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(85): Show | 88 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(85): Show |
intron_variant | MODIFIER | c.1335+7364G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112298700 | ||||||
| chr12:112298881
|
C | CA | 11 | a0001c0001t0001g0114a0001c0001t0001g0130a0001c0001t0001g0157others(8): Show | 11 | HG00738.hp1 HG02027.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.1335+7182dupT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112298881 | ||||||
| chr12:112298881
|
CAA | C | 77 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(74): Show | 77 | HG00544.hp1 HG00735.hp2 HG01071.hp1 others(74): Show |
intron_variant | MODIFIER | c.1335+7181_1335+718 others(6): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112298881 | ||||||
| chr12:112298926
|
C | T | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.1335+7138G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112298926 | ||||||
| chr12:112299005
|
G | A | 1 | a0001c0002t0001g0193 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1335+7059C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112299005 | ||||||
| chr12:112299562
|
G | T | 1 | a0001c0001t0003g0043 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1335+6502C>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112299562 | ||||||
| chr12:112299623
|
A | AAAAC | 25 | a0001c0001t0001g0099a0001c0001t0001g0125a0001c0001t0001g0128others(22): Show | 25 | HG00140.hp1 HG00544.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.1335+6437_1335+644 others(8): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112299623 | ||||||
| chr12:112299623
|
AAAAC | A | 22 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0216others(19): Show | 22 | HG00738.hp2 HG01099.hp2 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.1335+6437_1335+644 others(8): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112299623 | ||||||
| chr12:112299623
|
AAAACAAA others(5): Show |
A | 64 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(61): Show | 64 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(61): Show |
intron_variant | MODIFIER | c.1335+6429_1335+644 others(16): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112299623 | ||||||
| chr12:112299714
|
C | T | 1 | a0001c0001t0004g0078 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1335+6350G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112299714 | ||||||
| chr12:112299846
|
C | T | 1 | a0002c0005t0001g0197 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1335+6218G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112299846 | ||||||
| chr12:112300056
|
C | T | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.1335+6008G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112300056 | ||||||
| chr12:112300151
|
C | A | 4 | a0001c0001t0001g0152a0001c0001t0001g0153a0002c0004t0001g0155others(1): Show | 4 | HG01099.hp2 HG01175.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1335+5913G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112300151 | ||||||
| chr12:112300307
|
C | CA | 79 | a0001c0001t0003g0018a0001c0001t0004g0069a0001c0002t0001g0161others(76): Show | 79 | HG00544.hp1 HG01071.hp1 HG01256.hp1 others(76): Show |
intron_variant | MODIFIER | c.1335+5756dupT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112300307 | ||||||
| chr12:112300307
|
C | CAA | 6 | a0001c0002t0001g0176a0001c0002t0001g0189a0001c0002t0001g0194others(3): Show | 6 | HG00597.hp1 HG00735.hp2 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.1335+5755_1335+575 others(6): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112300307 | ||||||
| chr12:112300308
|
A | C | 1 | a0001c0011t0010g0146 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1335+5756T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112300308 | ||||||
| chr12:112300342
|
G | C | 1 | a0001c0032t0011g0263 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1335+5722C>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112300342 | ||||||
| chr12:112300641
|
A | G | 5 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0118others(2): Show | 5 | NA18952.hp2 NA18973.hp2 NA19054.hp2 others(2): Show |
intron_variant | MODIFIER | c.1335+5423T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112300641 | ||||||
| chr12:112300815
|
G | A | 6 | a0001c0002t0001g0201a0001c0002t0001g0202a0001c0002t0001g0203others(3): Show | 6 | HG02109.hp2 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1335+5249C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112300815 | ||||||
| chr12:112300886
|
C | CT | 9 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0184others(6): Show | 9 | HG01071.hp1 HG01256.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1335+5177dupA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112300886 | ||||||
| chr12:112300892
|
C | T | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.1335+5172G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112300892 | ||||||
| chr12:112301009
|
C | T | 2 | a0001c0001t0001g0156a0001c0001t0001g0220 | 2 | HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1335+5055G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112301009 | ||||||
| chr12:112301029
|
T | C | 170 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(167): Show | 170 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(167): Show |
intron_variant | MODIFIER | c.1335+5035A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112301029 | ||||||
| chr12:112301041
|
T | C | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.1335+5023A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112301041 | ||||||
| chr12:112301043
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1335+5021G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112301043 | ||||||
| chr12:112301051
|
AT | A | 8 | a0001c0001t0004g0061a0001c0001t0004g0067a0001c0001t0004g0068others(5): Show | 8 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1335+5012delA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112301051 | ||||||
| chr12:112301138
|
G | A | 72 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(69): Show | 72 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(69): Show |
intron_variant | MODIFIER | c.1335+4926C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112301138 | ||||||
| chr12:112301181
|
C | T | 88 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(85): Show | 88 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(85): Show |
intron_variant | MODIFIER | c.1335+4883G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112301181 | ||||||
| chr12:112301245
|
C | T | 8 | a0001c0001t0001g0099a0001c0001t0001g0125a0001c0001t0001g0128others(5): Show | 8 | HG00140.hp1 HG00738.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1335+4819G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112301245 | ||||||
| chr12:112301258
|
G | A | 4 | a0001c0001t0001g0152a0001c0001t0001g0153a0002c0004t0001g0155others(1): Show | 4 | HG01099.hp2 HG01175.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1335+4806C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112301258 | ||||||
| chr12:112301331
|
C | A | 1 | a0001c0003t0002g0150 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1335+4733G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112301331 | ||||||
| chr12:112301638
|
T | G | 3 | a0001c0009t0016g0266a0001c0009t0018g0268a0014c0021t0017g0267 | 3 | HG02622.hp2 HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1335+4426A>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112301638 | ||||||
| chr12:112301800
|
GT | G | 211 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0099others(208): Show | 211 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(208): Show |
intron_variant | MODIFIER | c.1335+4263delA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112301800 | ||||||
| chr12:112301896
|
T | C | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.1335+4168A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112301896 | ||||||
| chr12:112301980
|
C | T | 4 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0077others(1): Show | 4 | HG01891.hp1 HG03453.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1335+4084G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112301980 | ||||||
| chr12:112302496
|
G | A | 1 | a0003c0008t0001g0212 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1335+3568C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112302496 | ||||||
| chr12:112302511
|
G | A | 88 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(85): Show | 88 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(85): Show |
intron_variant | MODIFIER | c.1335+3553C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112302511 | ||||||
| chr12:112302614
|
A | G | 75 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(72): Show | 75 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.1335+3450T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112302614 | ||||||
| chr12:112302668
|
G | A | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.1335+3396C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112302668 | ||||||
| chr12:112302905
|
T | C | 75 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(72): Show | 75 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(72): Show |
intron_variant | MODIFIER | c.1335+3159A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112302905 | ||||||
| chr12:112302978
|
C | CT | 12 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0118others(9): Show | 12 | HG01928.hp2 HG01934.hp1 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.1335+3085dupA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112302978 | ||||||
| chr12:112302978
|
CT | C | 159 | a0001c0001t0001g0152a0001c0001t0001g0156a0001c0001t0003g0006others(156): Show | 159 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(156): Show |
intron_variant | MODIFIER | c.1335+3085delA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112302978 | ||||||
| chr12:112302978
|
CTT | C | 19 | a0001c0001t0001g0153a0001c0001t0003g0019a0001c0001t0004g0061others(16): Show | 19 | HG01256.hp1 HG01943.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.1335+3084_1335+308 others(6): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112302978 | ||||||
| chr12:112303408
|
C | T | 1 | a0001c0001t0005g0046 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1335+2656G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112303408 | ||||||
| chr12:112303862
|
TA | T | 31 | a0001c0001t0001g0079a0001c0001t0001g0121a0001c0001t0001g0152others(28): Show | 31 | HG01099.hp2 HG01175.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.1335+2201delT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112303862 | ||||||
| chr12:112303862
|
TAA | T | 168 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(165): Show | 168 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(165): Show |
intron_variant | MODIFIER | c.1335+2200_1335+220 others(6): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112303862 | ||||||
| chr12:112303876
|
A | G | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1335+2188T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112303876 | ||||||
| chr12:112303901
|
A | G | 4 | a0001c0001t0003g0020a0001c0001t0003g0029a0001c0001t0003g0030others(1): Show | 4 | NA18942.hp2 NA18960.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.1335+2163T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112303901 | ||||||
| chr12:112303908
|
G | T | 1 | a0001c0001t0007g0007 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1335+2156C>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112303908 | ||||||
| chr12:112304007
|
G | A | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.1335+2057C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112304007 | ||||||
| chr12:112304132
|
A | G | 1 | a0001c0001t0004g0073 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1335+1932T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112304132 | ||||||
| chr12:112304238
|
A | AT | 75 | a0001c0001t0001g0112a0001c0001t0001g0119a0001c0001t0003g0006others(72): Show | 75 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(72): Show |
intron_variant | MODIFIER | c.1335+1825dupA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112304238 | ||||||
| chr12:112304238
|
A | ATT | 9 | a0001c0001t0001g0127a0001c0001t0003g0018a0001c0001t0003g0020others(6): Show | 9 | HG01978.hp1 HG02027.hp1 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.1335+1824_1335+182 others(6): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112304238 | ||||||
| chr12:112304238
|
A | ATTTTT | 53 | a0001c0002t0001g0163a0001c0002t0001g0164a0001c0002t0001g0167others(50): Show | 53 | HG00544.hp1 HG00597.hp1 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.1335+1821_1335+182 others(9): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112304238 | ||||||
| chr12:112304238
|
A | ATTTTTT | 24 | a0001c0002t0001g0166a0001c0002t0001g0169a0001c0002t0001g0178others(21): Show | 24 | HG00735.hp2 HG01256.hp1 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.1335+1820_1335+182 others(10): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112304238 | ||||||
| chr12:112304238
|
AT | A | 9 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0004g0068others(6): Show | 9 | HG01106.hp2 HG01256.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1335+1825delA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112304238 | ||||||
| chr12:112304316
|
C | T | 8 | a0001c0001t0004g0061a0001c0001t0004g0067a0001c0001t0004g0068others(5): Show | 8 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1335+1748G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112304316 | ||||||
| chr12:112304678
|
TAA | T | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.1335+1384_1335+138 others(6): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112304678 | ||||||
| chr12:112305239
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1335+825C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112305239 | ||||||
| chr12:112305398
|
G | A | 1 | a0001c0001t0005g0005 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1335+666C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112305398 | ||||||
| chr12:112305486
|
C | T | 2 | a0001c0002t0001g0163a0001c0002t0008g0250 | 2 | NA18942.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1335+578G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112305486 | ||||||
| chr12:112305523
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1335+541C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112305523 | ||||||
| chr12:112305681
|
T | C | 1 | a0009c0024t0002g0108 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1335+383A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112305681 | ||||||
| chr12:112305855
|
A | G | 1 | a0001c0002t0001g0203 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1335+209T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112305855 | ||||||
| chr12:112305969
|
C | T | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.1335+95G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112305969 | ||||||
| chr12:112306039
|
T | C | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.1335+25A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 7/75 | chr12 | 112306039 | ||||||
| chr12:112306604
|
T | G | 1 | a0005c0022t0002g0092 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1165-370A>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 6/75 | chr12 | 112306604 | ||||||
| chr12:112306737
|
C | T | 1 | a0001c0001t0003g0043 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1165-503G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 6/75 | chr12 | 112306737 | ||||||
| chr12:112306830
|
T | C | 170 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(167): Show | 170 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(167): Show |
intron_variant | MODIFIER | c.1165-596A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 6/75 | chr12 | 112306830 | ||||||
| chr12:112306972
|
A | T | 1 | a0001c0003t0002g0134 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1165-738T>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 6/75 | chr12 | 112306972 | ||||||
| chr12:112307588
|
T | A | 1 | a0001c0001t0004g0073 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1164+1165A>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 6/75 | chr12 | 112307588 | ||||||
| chr12:112307952
|
A | G | 1 | a0001c0002t0001g0189 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1164+801T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 6/75 | chr12 | 112307952 | ||||||
| chr12:112308034
|
G | A | 8 | a0001c0001t0004g0061a0001c0001t0004g0067a0001c0001t0004g0068others(5): Show | 8 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1164+719C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 6/75 | chr12 | 112308034 | ||||||
| chr12:112308435
|
C | CA | 8 | a0001c0001t0001g0156a0001c0001t0001g0220a0001c0001t0003g0040others(5): Show | 8 | HG01106.hp2 HG02965.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.1164+317dupT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 6/75 | chr12 | 112308435 | ||||||
| chr12:112308446
|
AC | A | 72 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0166others(69): Show | 72 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(69): Show |
intron_variant | MODIFIER | c.1164+306delG | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 6/75 | chr12 | 112308446 | ||||||
| chr12:112308447
|
C | A | 8 | a0001c0002t0001g0164a0001c0002t0001g0181a0001c0002t0001g0191others(5): Show | 8 | HG02071.hp1 HG02074.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.1164+306G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 6/75 | chr12 | 112308447 | ||||||
| chr12:112308453
|
C | A | 1 | a0001c0002t0001g0193 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1164+300G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 6/75 | chr12 | 112308453 | ||||||
| chr12:112308457
|
AC | A | 78 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(75): Show | 78 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.1164+295delG | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 6/75 | chr12 | 112308457 | ||||||
| chr12:112308458
|
C | A | 3 | a0001c0002t0001g0181a0001c0002t0001g0193a0001c0002t0001g0210 | 3 | HG02135.hp1 NA18965.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1164+295G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 6/75 | chr12 | 112308458 | ||||||
| chr12:112308463
|
A | C | 4 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG02109.hp1 HG02559.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1164+290T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 6/75 | chr12 | 112308463 | ||||||
| chr12:112308465
|
A | C | 80 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(77): Show | 80 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(77): Show |
intron_variant | MODIFIER | c.1164+288T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 6/75 | chr12 | 112308465 | ||||||
| chr12:112308479
|
T | C | 5 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(2): Show | 5 | HG01891.hp1 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1164+274A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 6/75 | chr12 | 112308479 | ||||||
| chr12:112309112
|
G | C | 3 | a0001c0001t0003g0031a0001c0001t0003g0032a0015c0020t0003g0009 | 3 | NA18971.hp2 NA18980.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1026-221C>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 5/75 | chr12 | 112309112 | ||||||
| chr12:112309301
|
T | C | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.1025+260A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 5/75 | chr12 | 112309301 | ||||||
| chr12:112309678
|
G | A | 2 | a0001c0002t0001g0175a0001c0002t0001g0219 | 2 | HG03017.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.917-9C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 4/75 | chr12 | 112309678 | ||||||
| chr12:112309728
|
C | T | 8 | a0001c0001t0004g0061a0001c0001t0004g0067a0001c0001t0004g0068others(5): Show | 8 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.917-59G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 4/75 | chr12 | 112309728 | ||||||
| chr12:112309858
|
G | A | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.917-189C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 4/75 | chr12 | 112309858 | ||||||
| chr12:112310032
|
C | T | 1 | a0001c0001t0010g0149 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.917-363G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 4/75 | chr12 | 112310032 | ||||||
| chr12:112310089
|
A | T | 8 | a0001c0001t0004g0061a0001c0001t0004g0067a0001c0001t0004g0068others(5): Show | 8 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.917-420T>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 4/75 | chr12 | 112310089 | ||||||
| chr12:112310113
|
G | A | 2 | a0001c0001t0006g0258a0001c0001t0006g0262 | 2 | HG02056.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.917-444C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 4/75 | chr12 | 112310113 | ||||||
| chr12:112310351
|
A | G | 3 | a0001c0001t0003g0031a0001c0001t0003g0032a0015c0020t0003g0009 | 3 | NA18971.hp2 NA18980.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.917-682T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 4/75 | chr12 | 112310351 | ||||||
| chr12:112310765
|
C | T | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.917-1096G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 4/75 | chr12 | 112310765 | ||||||
| chr12:112310802
|
G | T | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.917-1133C>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 4/75 | chr12 | 112310802 | ||||||
| chr12:112310832
|
G | A | 5 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(2): Show | 5 | HG01891.hp1 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.917-1163C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 4/75 | chr12 | 112310832 | ||||||
| chr12:112310993
|
G | A | 1 | a0001c0003t0002g0086 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.917-1324C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 4/75 | chr12 | 112310993 | ||||||
| chr12:112311257
|
T | C | 175 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(172): Show | 175 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(172): Show |
intron_variant | MODIFIER | c.917-1588A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 4/75 | chr12 | 112311257 | ||||||
| chr12:112311258
|
G | A | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.917-1589C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 4/75 | chr12 | 112311258 | ||||||
| chr12:112311323
|
G | A | 5 | a0001c0001t0005g0046a0001c0001t0005g0047a0001c0001t0005g0049others(2): Show | 5 | HG01167.hp2 HG02055.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.917-1654C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 4/75 | chr12 | 112311323 | ||||||
| chr12:112311342
|
A | G | 5 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0216others(2): Show | 5 | HG01099.hp2 HG01175.hp1 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.917-1673T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 4/75 | chr12 | 112311342 | ||||||
| chr12:112311437
|
CATAA | C | 260 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0099others(257): Show | 260 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(257): Show |
intron_variant | MODIFIER | c.916+1576_916+1579d others(6): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 4/75 | chr12 | 112311437 | ||||||
| chr12:112311481
|
A | C | 4 | a0001c0001t0001g0079a0001c0001t0001g0156a0001c0001t0001g0160others(1): Show | 4 | HG01884.hp1 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.916+1536T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 4/75 | chr12 | 112311481 | ||||||
| chr12:112311607
|
G | A | 2 | a0001c0001t0003g0040a0001c0001t0003g0041 | 2 | NA18945.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.916+1410C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 4/75 | chr12 | 112311607 | ||||||
| chr12:112311619
|
C | CA | 10 | a0001c0001t0003g0006a0001c0001t0004g0023a0001c0001t0007g0024others(7): Show | 10 | HG01943.hp1 HG02717.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.916+1397dupT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 4/75 | chr12 | 112311619 | ||||||
| chr12:112311876
|
T | C | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.916+1141A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 4/75 | chr12 | 112311876 | ||||||
| chr12:112312032
|
A | C | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.916+985T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 4/75 | chr12 | 112312032 | ||||||
| chr12:112312127
|
ACT | A | 7 | a0001c0001t0005g0021a0001c0001t0005g0044a0001c0001t0005g0053others(4): Show | 7 | HG01081.hp1 HG01099.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.916+888_916+889del others(2): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 4/75 | chr12 | 112312127 | ||||||
| chr12:112312311
|
G | T | 1 | a0001c0001t0003g0028 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.916+706C>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 4/75 | chr12 | 112312311 | ||||||
| chr12:112312361
|
G | A | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.916+656C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 4/75 | chr12 | 112312361 | ||||||
| chr12:112312396
|
C | T | 1 | a0001c0003t0002g0098 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.916+621G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 4/75 | chr12 | 112312396 | ||||||
| chr12:112312597
|
T | G | 2 | a0001c0001t0008g0252a0001c0001t0008g0253 | 2 | HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.916+420A>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 4/75 | chr12 | 112312597 | ||||||
| chr12:112312616
|
A | G | 5 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(2): Show | 5 | HG00140.hp1 HG00738.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.916+401T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 4/75 | chr12 | 112312616 | ||||||
| chr12:112312620
|
G | A | 2 | a0001c0003t0002g0087a0001c0003t0002g0088 | 2 | HG02165.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.916+397C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 4/75 | chr12 | 112312620 | ||||||
| chr12:112312673
|
G | A | 1 | a0001c0002t0020g0270 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.916+344C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 4/75 | chr12 | 112312673 | ||||||
| chr12:112313009
|
T | C | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
splice_region_variant&intron_variant | LOW | c.916+8A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 4/75 | chr12 | 112313009 | ||||||
| chr12:112313174
|
A | G | 1 | a0001c0001t0005g0060 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.786-27T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 3/75 | chr12 | 112313174 | ||||||
| chr12:112313175
|
A | T | 1 | a0001c0001t0005g0060 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.786-28T>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 3/75 | chr12 | 112313175 | ||||||
| chr12:112313481
|
A | AT | 148 | a0001c0001t0001g0079a0001c0001t0001g0117a0001c0001t0001g0127others(145): Show | 148 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(145): Show |
intron_variant | MODIFIER | c.786-335dupA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 3/75 | chr12 | 112313481 | ||||||
| chr12:112313481
|
A | ATT | 27 | a0001c0001t0003g0018a0001c0001t0003g0051a0001c0001t0003g0058others(24): Show | 27 | HG01081.hp1 HG01099.hp1 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.786-336_786-335dup others(2): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 3/75 | chr12 | 112313481 | ||||||
| chr12:112313526
|
C | T | 1 | a0001c0002t0001g0221 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.786-379G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 3/75 | chr12 | 112313526 | ||||||
| chr12:112313641
|
T | TC | 5 | a0001c0002t0001g0166a0001c0002t0001g0171a0001c0002t0001g0193others(2): Show | 5 | HG00597.hp1 NA18947.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.786-495dupG | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 3/75 | chr12 | 112313641 | ||||||
| chr12:112314003
|
T | A | 1 | a0001c0001t0012g0151 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.785+454A>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 3/75 | chr12 | 112314003 | ||||||
| chr12:112314192
|
C | A | 1 | a0002c0004t0003g0008 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.785+265G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 3/75 | chr12 | 112314192 | ||||||
| chr12:112314319
|
A | G | 3 | a0001c0003t0004g0004a0001c0003t0009g0002a0006c0023t0009g0003 | 3 | HG01109.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.785+138T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 3/75 | chr12 | 112314319 | ||||||
| chr12:112314851
|
G | A | 75 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(72): Show | 75 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.696-305C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 2/75 | chr12 | 112314851 | ||||||
| chr12:112315517
|
G | A | 173 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(170): Show | 173 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(170): Show |
intron_variant | MODIFIER | c.696-971C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 2/75 | chr12 | 112315517 | ||||||
| chr12:112315646
|
C | A | 2 | a0001c0009t0016g0266a0001c0009t0018g0268 | 2 | HG02622.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.696-1100G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 2/75 | chr12 | 112315646 | ||||||
| chr12:112315732
|
T | A | 1 | a0001c0001t0004g0068 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.696-1186A>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 2/75 | chr12 | 112315732 | ||||||
| chr12:112315895
|
T | TA | 13 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0003g0051others(10): Show | 13 | HG01928.hp2 HG02056.hp1 HG02148.hp1 others(10): Show |
intron_variant | MODIFIER | c.696-1350dupT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 2/75 | chr12 | 112315895 | ||||||
| chr12:112315895
|
TA | T | 6 | a0001c0001t0001g0216a0001c0001t0005g0070a0001c0002t0001g0218others(3): Show | 6 | HG01243.hp2 HG01256.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.696-1350delT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 2/75 | chr12 | 112315895 | ||||||
| chr12:112316645
|
G | A | 88 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(85): Show | 88 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(85): Show |
intron_variant | MODIFIER | c.696-2099C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 2/75 | chr12 | 112316645 | ||||||
| chr12:112317045
|
A | G | 1 | a0001c0001t0011g0264 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.695+2180T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 2/75 | chr12 | 112317045 | ||||||
| chr12:112317315
|
A | C | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.695+1910T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 2/75 | chr12 | 112317315 | ||||||
| chr12:112317472
|
C | T | 1 | a0001c0030t0007g0035 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.695+1753G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 2/75 | chr12 | 112317472 | ||||||
| chr12:112317940
|
G | C | 8 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0012others(5): Show | 8 | NA18946.hp2 NA18950.hp2 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.695+1285C>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 2/75 | chr12 | 112317940 | ||||||
| chr12:112317956
|
C | CA | 79 | a0001c0001t0001g0117a0001c0001t0001g0157a0001c0001t0001g0216others(76): Show | 79 | HG00544.hp1 HG00597.hp1 HG01081.hp2 others(76): Show |
intron_variant | MODIFIER | c.695+1268dupT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 2/75 | chr12 | 112317956 | ||||||
| chr12:112317956
|
C | CAA | 17 | a0001c0002t0001g0169a0001c0002t0001g0180a0001c0002t0001g0184others(14): Show | 17 | HG00735.hp2 HG01071.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.695+1267_695+1268d others(4): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 2/75 | chr12 | 112317956 | ||||||
| chr12:112317956
|
CA | C | 75 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(72): Show | 75 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(72): Show |
intron_variant | MODIFIER | c.695+1268delT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 2/75 | chr12 | 112317956 | ||||||
| chr12:112318031
|
C | T | 89 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(86): Show | 89 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(86): Show |
intron_variant | MODIFIER | c.695+1194G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 2/75 | chr12 | 112318031 | ||||||
| chr12:112318205
|
T | C | 89 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(86): Show | 89 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(86): Show |
intron_variant | MODIFIER | c.695+1020A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 2/75 | chr12 | 112318205 | ||||||
| chr12:112318285
|
G | A | 1 | a0010c0014t0001g0195 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.695+940C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 2/75 | chr12 | 112318285 | ||||||
| chr12:112318334
|
A | G | 1 | a0001c0003t0002g0111 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.695+891T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 2/75 | chr12 | 112318334 | ||||||
| chr12:112318710
|
A | C | 22 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0216others(19): Show | 22 | HG01099.hp2 HG01175.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.695+515T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 2/75 | chr12 | 112318710 | ||||||
| chr12:112319215
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.695+10A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 2/75 | chr12 | 112319215 | ||||||
| chr12:112319754
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.178-12C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112319754 | ||||||
| chr12:112320022
|
C | T | 2 | a0001c0001t0003g0026a0001c0001t0003g0050 | 2 | NA19056.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.178-280G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112320022 | ||||||
| chr12:112320301
|
T | A | 88 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(85): Show | 88 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(85): Show |
intron_variant | MODIFIER | c.178-559A>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112320301 | ||||||
| chr12:112320470
|
C | T | 2 | a0001c0001t0008g0252a0001c0001t0008g0253 | 2 | HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.178-728G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112320470 | ||||||
| chr12:112320599
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.178-857G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112320599 | ||||||
| chr12:112320700
|
T | TA | 8 | a0001c0001t0001g0099a0001c0001t0001g0125a0001c0001t0001g0128others(5): Show | 8 | HG00140.hp1 HG00738.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.178-959dupT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112320700 | ||||||
| chr12:112321004
|
C | T | 4 | a0001c0001t0001g0152a0001c0001t0001g0153a0002c0004t0001g0155others(1): Show | 4 | HG01099.hp2 HG01175.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-1262G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112321004 | ||||||
| chr12:112321161
|
T | C | 5 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0216others(2): Show | 5 | HG01099.hp2 HG01175.hp1 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.178-1419A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112321161 | ||||||
| chr12:112321795
|
C | T | 1 | a0001c0001t0015g0248 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.178-2053G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112321795 | ||||||
| chr12:112322068
|
T | C | 2 | a0001c0001t0001g0079a0001c0001t0001g0160 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.178-2326A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112322068 | ||||||
| chr12:112322107
|
TA | T | 109 | a0001c0001t0001g0079a0001c0001t0001g0152a0001c0001t0001g0153others(106): Show | 109 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(106): Show |
intron_variant | MODIFIER | c.178-2366delT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112322107 | ||||||
| chr12:112322329
|
C | T | 1 | a0001c0003t0002g0101 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.178-2587G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112322329 | ||||||
| chr12:112322367
|
T | A | 1 | a0001c0001t0004g0074 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.178-2625A>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112322367 | ||||||
| chr12:112322415
|
A | G | 2 | a0001c0001t0007g0034a0002c0004t0007g0036 | 2 | HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.178-2673T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112322415 | ||||||
| chr12:112322668
|
G | A | 1 | a0001c0003t0002g0142 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.178-2926C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112322668 | ||||||
| chr12:112322670
|
T | G | 170 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(167): Show | 170 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(167): Show |
intron_variant | MODIFIER | c.178-2928A>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112322670 | ||||||
| chr12:112322935
|
T | C | 2 | a0001c0001t0003g0058a0001c0001t0003g0059 | 2 | HG02074.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.178-3193A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112322935 | ||||||
| chr12:112322973
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.178-3231C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112322973 | ||||||
| chr12:112322991
|
G | A | 8 | a0001c0001t0004g0023a0001c0001t0007g0007a0001c0001t0007g0024others(5): Show | 8 | HG01943.hp1 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.178-3249C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112322991 | ||||||
| chr12:112323107
|
G | C | 2 | a0001c0009t0016g0266a0001c0009t0018g0268 | 2 | HG02622.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.178-3365C>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323107 | ||||||
| chr12:112323238
|
A | T | 1 | a0001c0001t0003g0006 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.178-3496T>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323238 | ||||||
| chr12:112323494
|
T | C | 1 | a0001c0001t0003g0045 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.178-3752A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323494 | ||||||
| chr12:112323590
|
T | C | 5 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.178-3848A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323590 | ||||||
| chr12:112323596
|
G | GA | 6 | a0001c0001t0001g0079a0001c0003t0002g0086a0001c0003t0002g0109others(3): Show | 6 | HG01884.hp1 HG01978.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.178-3855dupT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323596 | ||||||
| chr12:112323850
|
C | G | 1 | a0001c0002t0001g0161 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.178-4108G>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323850 | ||||||
| chr12:112323947
|
C | CTTCTTCC others(9): Show |
2 | a0001c0001t0001g0129a0001c0001t0001g0131 | 2 | HG00140.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.178-4206_178-4205i others(18): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323947 | ||||||
| chr12:112323947
|
C | CTTCTTCC others(13): Show |
1 | a0001c0001t0001g0128 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.178-4206_178-4205i others(22): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323947 | ||||||
| chr12:112323947
|
C | CTTCTTCC others(21): Show |
1 | a0001c0001t0001g0132 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.178-4206_178-4205i others(30): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323947 | ||||||
| chr12:112323947
|
C | CTTCTTTC others(21): Show |
1 | a0001c0001t0001g0125 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.178-4206_178-4205i others(30): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323947 | ||||||
| chr12:112323947
|
C | CTTCTTTC others(25): Show |
1 | a0001c0003t0002g0085 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.178-4206_178-4205i others(34): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323947 | ||||||
| chr12:112323947
|
C | CTTCTTTC others(29): Show |
1 | a0001c0003t0002g0086 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.178-4206_178-4205i others(38): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323947 | ||||||
| chr12:112323947
|
C | CTTCTTTC others(17): Show |
1 | a0001c0003t0009g0001 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.178-4206_178-4205i others(26): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323947 | ||||||
| chr12:112323947
|
C | CTTCTTTC others(25): Show |
1 | a0001c0001t0001g0079 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.178-4206_178-4205i others(34): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323947 | ||||||
| chr12:112323947
|
C | CTTCTTTC others(40): Show |
1 | a0002c0006t0002g0097 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.178-4206_178-4205i others(49): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323947 | ||||||
| chr12:112323947
|
C | CTTCTTTC others(37): Show |
1 | a0002c0006t0002g0094 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.178-4206_178-4205i others(46): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323947 | ||||||
| chr12:112323947
|
C | CTTCTTTC others(20): Show |
1 | a0001c0003t0002g0247 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.178-4206_178-4205i others(29): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323947 | ||||||
| chr12:112323947
|
C | CTTCTTTC others(13): Show |
1 | a0001c0012t0002g0093 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.178-4225_178-4206d others(22): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323947 | ||||||
| chr12:112323947
|
C | CTTCTTTC others(25): Show |
1 | a0001c0001t0001g0118 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.178-4206_178-4205i others(34): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323947 | ||||||
| chr12:112323947
|
C | CTTCTTTC others(29): Show |
1 | a0006c0023t0009g0003 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.178-4206_178-4205i others(38): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323947 | ||||||
| chr12:112323947
|
CTTCT | C | 4 | a0001c0001t0011g0264a0001c0003t0002g0081a0001c0003t0002g0150others(1): Show | 4 | HG02630.hp1 HG03239.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-4209_178-4206d others(6): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323947 | ||||||
| chr12:112323947
|
CTTCTTTC others(5): Show |
C | 2 | a0001c0003t0002g0101a0005c0022t0002g0092 | 2 | HG01175.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.178-4217_178-4206d others(14): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323947 | ||||||
| chr12:112323948
|
T | G | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159 | 3 | HG03098.hp2 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.178-4206A>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323948 | ||||||
| chr12:112323949
|
T | TCTTTCTT others(9): Show |
1 | a0001c0003t0002g0107 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.178-4208_178-4207i others(18): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323949 | ||||||
| chr12:112323949
|
T | TCTTTCTT others(9): Show |
2 | a0001c0003t0002g0134a0013c0025t0002g0095 | 2 | HG00140.hp2 HG00544.hp2 |
intron_variant | MODIFIER | c.178-4208_178-4207i others(18): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323949 | ||||||
| chr12:112323949
|
TCTTTCTT others(29): Show |
T | 1 | a0001c0001t0001g0130 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.178-4243_178-4208d others(38): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323949 | ||||||
| chr12:112323953
|
T | TCTTTCTT others(9): Show |
1 | a0001c0001t0011g0265 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.178-4212_178-4211i others(18): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323953 | ||||||
| chr12:112323953
|
TCTTTCTT others(9): Show |
T | 1 | a0001c0003t0002g0140 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.178-4227_178-4212d others(18): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323953 | ||||||
| chr12:112323953
|
TCTTTCTT others(85): Show |
T | 1 | a0001c0011t0010g0146 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.178-4303_178-4212d others(94): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323953 | ||||||
| chr12:112323957
|
T | C | 1 | a0001c0029t0001g0122 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.178-4215A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323957 | ||||||
| chr12:112323957
|
TCTTTCTT others(9): Show |
T | 2 | a0001c0001t0008g0252a0001c0001t0008g0253 | 2 | HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.178-4231_178-4216d others(18): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323957 | ||||||
| chr12:112323957
|
TCTTTCTT others(13): Show |
T | 2 | a0001c0003t0002g0080a0002c0006t0002g0126 | 2 | HG00738.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.178-4235_178-4216d others(22): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323957 | ||||||
| chr12:112323957
|
TCTTTCTT others(81): Show |
T | 3 | a0001c0001t0004g0072a0001c0001t0005g0046a0001c0009t0018g0268 | 3 | HG02897.hp1 HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.178-4303_178-4216d others(90): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323957 | ||||||
| chr12:112323961
|
T | C | 3 | a0001c0003t0002g0104a0001c0003t0002g0150a0001c0029t0001g0122 | 3 | HG01258.hp1 HG03927.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.178-4219A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323961 | ||||||
| chr12:112323961
|
TCTTTCTT others(1): Show |
T | 3 | a0001c0001t0001g0160a0001c0003t0002g0136a0001c0032t0011g0263 | 3 | HG01106.hp2 HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.178-4227_178-4220d others(10): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323961 | ||||||
| chr12:112323961
|
TCTTTCTT others(5): Show |
T | 1 | a0016c0019t0002g0135 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.178-4231_178-4220d others(14): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323961 | ||||||
| chr12:112323961
|
TCTTTCTT others(41): Show |
T | 1 | a0001c0001t0001g0127 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.178-4267_178-4220d others(50): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323961 | ||||||
| chr12:112323961
|
TCTTTCTT others(57): Show |
T | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.178-4283_178-4220d others(66): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323961 | ||||||
| chr12:112323961
|
TCTTTCTT others(77): Show |
T | 7 | a0001c0001t0001g0121a0001c0001t0004g0067a0001c0001t0004g0069others(4): Show | 7 | HG00597.hp2 HG01884.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.178-4303_178-4220d others(86): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323961 | ||||||
| chr12:112323965
|
T | C | 12 | a0001c0001t0001g0099a0001c0001t0001g0222a0001c0001t0001g0223others(9): Show | 12 | HG01167.hp1 HG01258.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.178-4223A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323965 | ||||||
| chr12:112323965
|
TCTTCCTT others(25): Show |
T | 1 | a0001c0003t0009g0002 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.178-4255_178-4224d others(34): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323965 | ||||||
| chr12:112323965
|
TCTTCCTT others(37): Show |
T | 1 | a0010c0014t0001g0195 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.178-4267_178-4224d others(46): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323965 | ||||||
| chr12:112323965
|
TCTTCCTT others(41): Show |
T | 7 | a0001c0002t0001g0167a0001c0002t0001g0178a0001c0002t0001g0179others(4): Show | 7 | HG01256.hp1 HG01258.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.178-4271_178-4224d others(50): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323965 | ||||||
| chr12:112323965
|
TCTTCCTT others(45): Show |
T | 16 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0171others(13): Show | 16 | HG00597.hp1 HG01928.hp1 HG01993.hp1 others(13): Show |
intron_variant | MODIFIER | c.178-4275_178-4224d others(54): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323965 | ||||||
| chr12:112323965
|
TCTTCCTT others(49): Show |
T | 16 | a0001c0001t0001g0158a0001c0002t0001g0176a0001c0002t0001g0180others(13): Show | 16 | HG00735.hp2 HG01081.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.178-4279_178-4224d others(58): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323965 | ||||||
| chr12:112323965
|
TCTTCCTT others(53): Show |
T | 35 | a0001c0001t0001g0083a0001c0001t0001g0157a0001c0001t0001g0159others(32): Show | 35 | HG00544.hp1 HG01071.hp1 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.178-4283_178-4224d others(62): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323965 | ||||||
| chr12:112323965
|
TCTTCCTT others(57): Show |
T | 10 | a0001c0001t0001g0220a0001c0002t0001g0181a0001c0002t0001g0226others(7): Show | 10 | HG01934.hp2 HG02129.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.178-4287_178-4224d others(66): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323965 | ||||||
| chr12:112323965
|
TCTTCCTT others(61): Show |
T | 4 | a0001c0001t0003g0020a0001c0001t0003g0042a0001c0001t0006g0257others(1): Show | 4 | HG01243.hp1 HG02109.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.178-4291_178-4224d others(70): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323965 | ||||||
| chr12:112323965
|
TCTTCCTT others(65): Show |
T | 14 | a0001c0001t0001g0156a0001c0001t0003g0030a0001c0001t0003g0058others(11): Show | 14 | HG01081.hp1 HG02056.hp2 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.178-4295_178-4224d others(74): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323965 | ||||||
| chr12:112323965
|
TCTTCCTT others(69): Show |
T | 19 | a0001c0001t0003g0006a0001c0001t0003g0011a0001c0001t0003g0013others(16): Show | 19 | HG01099.hp1 HG01109.hp2 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.178-4299_178-4224d others(78): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323965 | ||||||
| chr12:112323965
|
TCTTCCTT others(73): Show |
T | 43 | a0001c0001t0003g0010a0001c0001t0003g0012a0001c0001t0003g0016others(40): Show | 43 | HG01891.hp1 HG01891.hp2 HG01943.hp1 others(40): Show |
intron_variant | MODIFIER | c.178-4303_178-4224d others(82): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323965 | ||||||
| chr12:112323969
|
C | CCTTTCTT others(9): Show |
2 | a0001c0010t0001g0217a0002c0004t0004g0063 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.178-4228_178-4227i others(18): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323969 | ||||||
| chr12:112323969
|
C | CCTTTCTT others(17): Show |
1 | a0001c0010t0001g0214 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.178-4228_178-4227i others(26): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323969 | ||||||
| chr12:112323969
|
C | CCTTTCTT others(21): Show |
1 | a0001c0003t0002g0109 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.178-4228_178-4227i others(30): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323969 | ||||||
| chr12:112323969
|
C | CCTTTCTT others(25): Show |
1 | a0001c0003t0002g0088 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.178-4228_178-4227i others(34): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323969 | ||||||
| chr12:112323969
|
C | CCTTTCTT others(29): Show |
1 | a0001c0001t0001g0115 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.178-4228_178-4227i others(38): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323969 | ||||||
| chr12:112323969
|
C | CCTTTCTT others(33): Show |
1 | a0001c0003t0002g0102 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.178-4228_178-4227i others(42): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323969 | ||||||
| chr12:112323969
|
C | CTTTCTTT others(12): Show |
1 | a0001c0001t0004g0065 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.178-4228_178-4227i others(21): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323969 | ||||||
| chr12:112323969
|
C | CTTTCTTT others(16): Show |
1 | a0002c0026t0001g0215 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.178-4228_178-4227i others(25): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323969 | ||||||
| chr12:112323969
|
C | CTTTCTTT others(32): Show |
1 | a0001c0003t0002g0084 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.178-4228_178-4227i others(41): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323969 | ||||||
| chr12:112323969
|
C | T | 31 | a0001c0001t0001g0079a0001c0001t0001g0099a0001c0001t0001g0112others(28): Show | 31 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.178-4227G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323969 | ||||||
| chr12:112323969
|
CCTTCCTT others(77): Show |
C | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0216 | 3 | HG01099.hp2 HG01243.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.178-4311_178-4228d others(86): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323969 | ||||||
| chr12:112323969
|
CCTTCCTT others(81): Show |
C | 1 | a0004c0034t0001g0154 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.178-4315_178-4228d others(90): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323969 | ||||||
| chr12:112323972
|
T | C | 1 | a0001c0001t0011g0264 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.178-4230A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323972 | ||||||
| chr12:112323973
|
C | CCTTTCTT others(37): Show |
1 | a0001c0001t0001g0112 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.178-4232_178-4231i others(46): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323973 | ||||||
| chr12:112323973
|
C | T | 37 | a0001c0001t0001g0079a0001c0001t0001g0099a0001c0001t0001g0115others(34): Show | 37 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.178-4231G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323973 | ||||||
| chr12:112323975
|
TTCCTTCC others(40): Show |
T | 1 | a0001c0002t0001g0203 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.178-4280_178-4234d others(49): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323975 | ||||||
| chr12:112323975
|
TTCCTTCC others(44): Show |
T | 1 | a0001c0002t0001g0204 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.178-4284_178-4234d others(53): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323975 | ||||||
| chr12:112323977
|
C | CCTTTCTT others(5): Show |
1 | a0009c0024t0002g0108 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.178-4236_178-4235i others(14): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323977 | ||||||
| chr12:112323977
|
C | T | 45 | a0001c0001t0001g0079a0001c0001t0001g0099a0001c0001t0001g0112others(42): Show | 45 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.178-4235G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323977 | ||||||
| chr12:112323981
|
C | CCTTTCTT others(5): Show |
1 | a0001c0001t0015g0248 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.178-4240_178-4239i others(14): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323981 | ||||||
| chr12:112323981
|
C | CCTTTCTT others(33): Show |
1 | a0001c0001t0004g0062 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.178-4240_178-4239i others(42): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323981 | ||||||
| chr12:112323981
|
C | T | 45 | a0001c0001t0001g0079a0001c0001t0001g0099a0001c0001t0001g0112others(42): Show | 45 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.178-4239G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323981 | ||||||
| chr12:112323981
|
CCTTCCTT others(61): Show |
C | 1 | a0001c0001t0001g0117 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.178-4307_178-4240d others(70): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323981 | ||||||
| chr12:112323982
|
C | T | 1 | a0001c0001t0001g0120 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.178-4240G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323982 | ||||||
| chr12:112323985
|
C | CCTTTCTT others(33): Show |
1 | a0001c0033t0002g0110 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.178-4244_178-4243i others(42): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323985 | ||||||
| chr12:112323985
|
C | T | 48 | a0001c0001t0001g0079a0001c0001t0001g0099a0001c0001t0001g0112others(45): Show | 48 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.178-4243G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323985 | ||||||
| chr12:112323986
|
C | T | 1 | a0001c0001t0001g0120 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.178-4244G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323986 | ||||||
| chr12:112323989
|
C | T | 49 | a0001c0001t0001g0079a0001c0001t0001g0099a0001c0001t0001g0112others(46): Show | 49 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.178-4247G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323989 | ||||||
| chr12:112323990
|
C | T | 1 | a0001c0001t0001g0120 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.178-4248G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323990 | ||||||
| chr12:112323993
|
C | CCTTTCCT others(38): Show |
1 | a0001c0001t0001g0222 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.178-4252_178-4251i others(47): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323993 | ||||||
| chr12:112323993
|
C | CCTTTCCT others(42): Show |
1 | a0001c0001t0001g0224 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.178-4252_178-4251i others(51): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323993 | ||||||
| chr12:112323993
|
C | CCTTTCCT others(15): Show |
1 | a0001c0001t0001g0223 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.178-4252_178-4251i others(24): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323993 | ||||||
| chr12:112323993
|
C | CCTTTCTT others(25): Show |
1 | a0001c0011t0001g0133 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.178-4252_178-4251i others(34): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323993 | ||||||
| chr12:112323993
|
C | T | 50 | a0001c0001t0001g0079a0001c0001t0001g0099a0001c0001t0001g0112others(47): Show | 50 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.178-4251G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323993 | ||||||
| chr12:112323994
|
C | T | 1 | a0001c0001t0001g0120 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.178-4252G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323994 | ||||||
| chr12:112323997
|
C | T | 53 | a0001c0001t0001g0079a0001c0001t0001g0099a0001c0001t0001g0112others(50): Show | 53 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.178-4255G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323997 | ||||||
| chr12:112323998
|
C | T | 1 | a0001c0001t0001g0120 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.178-4256G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112323998 | ||||||
| chr12:112324001
|
C | T | 55 | a0001c0001t0001g0079a0001c0001t0001g0099a0001c0001t0001g0112others(52): Show | 55 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.178-4259G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324001 | ||||||
| chr12:112324002
|
C | T | 1 | a0001c0001t0001g0120 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.178-4260G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324002 | ||||||
| chr12:112324005
|
C | CCTTTCTT others(5): Show |
1 | a0001c0003t0002g0124 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.178-4264_178-4263i others(14): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324005 | ||||||
| chr12:112324005
|
C | T | 56 | a0001c0001t0001g0079a0001c0001t0001g0099a0001c0001t0001g0112others(53): Show | 56 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.178-4263G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324005 | ||||||
| chr12:112324006
|
C | T | 1 | a0001c0001t0001g0120 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.178-4264G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324006 | ||||||
| chr12:112324009
|
C | T | 57 | a0001c0001t0001g0079a0001c0001t0001g0099a0001c0001t0001g0112others(54): Show | 57 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.178-4267G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324009 | ||||||
| chr12:112324010
|
C | T | 1 | a0001c0001t0001g0120 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.178-4268G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324010 | ||||||
| chr12:112324013
|
C | T | 58 | a0001c0001t0001g0079a0001c0001t0001g0099a0001c0001t0001g0112others(55): Show | 58 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.178-4271G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324013 | ||||||
| chr12:112324014
|
C | T | 1 | a0001c0001t0001g0120 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.178-4272G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324014 | ||||||
| chr12:112324017
|
C | CTCTTTCT others(15): Show |
1 | a0001c0001t0001g0114 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.178-4276_178-4275i others(24): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324017 | ||||||
| chr12:112324017
|
C | T | 64 | a0001c0001t0001g0079a0001c0001t0001g0099a0001c0001t0001g0112others(61): Show | 64 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.178-4275G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324017 | ||||||
| chr12:112324018
|
C | T | 1 | a0001c0001t0001g0120 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.178-4276G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324018 | ||||||
| chr12:112324021
|
C | CCTTTCTT others(25): Show |
1 | a0001c0003t0002g0106 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.178-4280_178-4279i others(34): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324021 | ||||||
| chr12:112324021
|
C | T | 74 | a0001c0001t0001g0079a0001c0001t0001g0099a0001c0001t0001g0112others(71): Show | 74 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.178-4279G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324021 | ||||||
| chr12:112324022
|
C | T | 1 | a0001c0001t0001g0120 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.178-4280G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324022 | ||||||
| chr12:112324023
|
T | C | 1 | a0001c0001t0001g0119 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.178-4281A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324023 | ||||||
| chr12:112324025
|
C | CCTTTCTT others(9): Show |
1 | a0001c0003t0002g0143 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.178-4284_178-4283i others(18): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324025 | ||||||
| chr12:112324025
|
C | T | 83 | a0001c0001t0001g0079a0001c0001t0001g0099a0001c0001t0001g0112others(80): Show | 83 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.178-4283G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324025 | ||||||
| chr12:112324026
|
C | T | 2 | a0001c0001t0001g0120a0001c0002t0001g0203 | 2 | HG03041.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.178-4284G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324026 | ||||||
| chr12:112324029
|
C | T | 120 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0099others(117): Show | 120 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.178-4287G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324029 | ||||||
| chr12:112324030
|
C | T | 1 | a0001c0002t0001g0204 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.178-4288G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324030 | ||||||
| chr12:112324033
|
C | CCTTTCTT others(25): Show |
1 | a0001c0003t0002g0123 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.178-4292_178-4291i others(34): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324033 | ||||||
| chr12:112324033
|
C | T | 118 | a0001c0001t0001g0079a0001c0001t0001g0099a0001c0001t0001g0112others(115): Show | 118 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.178-4291G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324033 | ||||||
| chr12:112324037
|
C | CCTTTCTT others(5): Show |
1 | a0001c0003t0002g0091 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.178-4296_178-4295i others(14): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324037 | ||||||
| chr12:112324037
|
C | T | 157 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0099others(154): Show | 157 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.178-4295G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324037 | ||||||
| chr12:112324041
|
C | T | 181 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0099others(178): Show | 181 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(178): Show |
intron_variant | MODIFIER | c.178-4299G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324041 | ||||||
| chr12:112324042
|
C | T | 1 | a0001c0003t0002g0098 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.178-4300G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324042 | ||||||
| chr12:112324045
|
C | CCTTCCTT others(9): Show |
1 | a0001c0003t0002g0137 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.178-4304_178-4303i others(18): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324045 | ||||||
| chr12:112324045
|
C | CCTTTCTT others(5): Show |
2 | a0001c0003t0002g0100a0001c0003t0002g0139 | 2 | HG02451.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.178-4315_178-4304d others(14): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324045 | ||||||
| chr12:112324045
|
C | T | 202 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0099others(199): Show | 202 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(199): Show |
intron_variant | MODIFIER | c.178-4303G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324045 | ||||||
| chr12:112324057
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.178-4315A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324057 | ||||||
| chr12:112324078
|
CTTT | C | 17 | a0001c0001t0004g0061a0001c0001t0004g0067a0001c0001t0004g0068others(14): Show | 17 | HG00597.hp2 HG02258.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.178-4339_178-4337d others(5): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324078 | ||||||
| chr12:112324082
|
CTTT | C | 16 | a0001c0001t0003g0016a0001c0001t0003g0022a0001c0001t0003g0037others(13): Show | 16 | HG02132.hp2 HG02257.hp1 HG02717.hp2 others(13): Show |
intron_variant | MODIFIER | c.178-4343_178-4341d others(5): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324082 | ||||||
| chr12:112324084
|
T | C | 17 | a0001c0001t0004g0061a0001c0001t0004g0067a0001c0001t0004g0068others(14): Show | 17 | HG00597.hp2 HG02258.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.178-4342A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324084 | ||||||
| chr12:112324085
|
T | C | 1 | a0001c0001t0005g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.178-4343A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324085 | ||||||
| chr12:112324085
|
T | TC | 138 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(135): Show | 138 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(135): Show |
intron_variant | MODIFIER | c.178-4344dupG | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324085 | ||||||
| chr12:112324088
|
T | C | 173 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(170): Show | 173 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(170): Show |
intron_variant | MODIFIER | c.178-4346A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324088 | ||||||
| chr12:112324092
|
T | C | 156 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(153): Show | 156 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(153): Show |
intron_variant | MODIFIER | c.178-4350A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324092 | ||||||
| chr12:112324100
|
TTCC | T | 156 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(153): Show | 156 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(153): Show |
intron_variant | MODIFIER | c.178-4361_178-4359d others(5): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324100 | ||||||
| chr12:112324100
|
TTCCTCTC | T | 17 | a0001c0001t0004g0061a0001c0001t0004g0067a0001c0001t0004g0068others(14): Show | 17 | HG00597.hp2 HG02258.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.178-4365_178-4359d others(9): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324100 | ||||||
| chr12:112324102
|
C | CTTTCTTT others(4): Show |
1 | a0001c0029t0001g0122 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.178-4361_178-4360i others(13): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324102 | ||||||
| chr12:112324103
|
C | T | 2 | a0001c0003t0013g0096a0001c0003t0013g0105 | 2 | HG02080.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.178-4361G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324103 | ||||||
| chr12:112324104
|
T | TTCTTTCT others(35): Show |
2 | a0001c0003t0013g0096a0001c0003t0013g0105 | 2 | HG02080.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.178-4363_178-4362i others(44): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324104 | ||||||
| chr12:112324105
|
C | T | 1 | a0001c0029t0001g0122 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.178-4363G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324105 | ||||||
| chr12:112324107
|
C | T | 156 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(153): Show | 156 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(153): Show |
intron_variant | MODIFIER | c.178-4365G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324107 | ||||||
| chr12:112324113
|
T | C | 1 | a0001c0029t0001g0122 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.178-4371A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324113 | ||||||
| chr12:112324384
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.178-4642A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324384 | ||||||
| chr12:112324536
|
C | T | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.178-4794G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324536 | ||||||
| chr12:112324710
|
G | A | 8 | a0001c0001t0004g0023a0001c0001t0007g0007a0001c0001t0007g0024others(5): Show | 8 | HG01943.hp1 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.178-4968C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324710 | ||||||
| chr12:112324945
|
T | C | 1 | a0001c0001t0006g0259 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.178-5203A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112324945 | ||||||
| chr12:112325008
|
T | C | 1 | a0001c0003t0002g0142 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.178-5266A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112325008 | ||||||
| chr12:112325276
|
T | C | 1 | a0009c0024t0002g0108 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.178-5534A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112325276 | ||||||
| chr12:112325499
|
C | T | 1 | a0001c0003t0002g0111 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.178-5757G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112325499 | ||||||
| chr12:112325724
|
G | A | 72 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(69): Show | 72 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(69): Show |
intron_variant | MODIFIER | c.178-5982C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112325724 | ||||||
| chr12:112325790
|
C | T | 1 | a0001c0001t0004g0061 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.178-6048G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112325790 | ||||||
| chr12:112325813
|
G | GT | 19 | a0001c0001t0001g0112a0001c0001t0003g0051a0001c0001t0015g0248others(16): Show | 19 | HG01109.hp1 HG01496.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.178-6072dupA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112325813 | ||||||
| chr12:112325813
|
GT | G | 8 | a0001c0001t0004g0061a0001c0001t0004g0067a0001c0001t0004g0068others(5): Show | 8 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.178-6072delA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112325813 | ||||||
| chr12:112325905
|
T | C | 3 | a0001c0001t0003g0020a0001c0001t0003g0029a0001c0001t0003g0030 | 3 | NA18942.hp2 NA18960.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.178-6163A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112325905 | ||||||
| chr12:112326079
|
G | A | 2 | a0001c0007t0001g0172a0001c0007t0001g0183 | 2 | NA19057.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.178-6337C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112326079 | ||||||
| chr12:112326454
|
C | T | 1 | a0001c0001t0006g0254 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.178-6712G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112326454 | ||||||
| chr12:112326530
|
T | A | 1 | a0001c0003t0002g0111 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.178-6788A>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112326530 | ||||||
| chr12:112326596
|
T | C | 2 | a0001c0002t0001g0184a0002c0005t0001g0199 | 2 | HG01071.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.178-6854A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112326596 | ||||||
| chr12:112326739
|
C | T | 88 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(85): Show | 88 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(85): Show |
intron_variant | MODIFIER | c.178-6997G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112326739 | ||||||
| chr12:112326772
|
C | T | 8 | a0001c0001t0004g0061a0001c0001t0004g0067a0001c0001t0004g0068others(5): Show | 8 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.178-7030G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112326772 | ||||||
| chr12:112326826
|
G | T | 1 | a0001c0003t0002g0085 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.178-7084C>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112326826 | ||||||
| chr12:112326920
|
T | G | 1 | a0001c0003t0002g0101 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.178-7178A>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112326920 | ||||||
| chr12:112327054
|
G | A | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.178-7312C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112327054 | ||||||
| chr12:112327173
|
C | T | 2 | a0001c0001t0001g0152a0002c0004t0001g0155 | 2 | HG01099.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.178-7431G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112327173 | ||||||
| chr12:112327242
|
G | A | 2 | a0003c0008t0001g0207a0003c0008t0001g0212 | 2 | NA18964.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.178-7500C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112327242 | ||||||
| chr12:112327526
|
T | C | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.178-7784A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112327526 | ||||||
| chr12:112328110
|
C | CTATT | 26 | a0001c0001t0001g0157a0001c0001t0001g0160a0001c0001t0004g0062others(23): Show | 26 | HG01109.hp1 HG02055.hp2 HG02080.hp2 others(23): Show |
intron_variant | MODIFIER | c.178-8372_178-8369d others(6): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112328110 | ||||||
| chr12:112328110
|
C | CTATTTAT others(1): Show |
70 | a0001c0001t0001g0216a0001c0001t0011g0265a0001c0002t0001g0164others(67): Show | 70 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.178-8376_178-8369d others(10): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112328110 | ||||||
| chr12:112328110
|
C | CTATTTAT others(5): Show |
6 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0167others(3): Show | 6 | HG02165.hp2 HG02273.hp2 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.178-8380_178-8369d others(14): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112328110 | ||||||
| chr12:112328110
|
CTATT | C | 65 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(62): Show | 65 | HG01081.hp1 HG01099.hp1 HG01109.hp2 others(62): Show |
intron_variant | MODIFIER | c.178-8372_178-8369d others(6): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112328110 | ||||||
| chr12:112328110
|
CTATTTAT others(1): Show |
C | 21 | a0001c0001t0001g0083a0001c0001t0001g0099a0001c0001t0001g0112others(18): Show | 21 | HG00140.hp1 HG00738.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.178-8376_178-8369d others(10): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112328110 | ||||||
| chr12:112328110
|
CTATTTAT others(9): Show |
C | 8 | a0001c0001t0004g0023a0001c0001t0007g0007a0001c0001t0007g0024others(5): Show | 8 | HG01943.hp1 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.178-8384_178-8369d others(18): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112328110 | ||||||
| chr12:112328120
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.178-8378T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112328120 | ||||||
| chr12:112328140
|
A | G | 1 | a0001c0001t0004g0074 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.178-8398T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112328140 | ||||||
| chr12:112328312
|
C | A | 88 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(85): Show | 88 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(85): Show |
intron_variant | MODIFIER | c.178-8570G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112328312 | ||||||
| chr12:112328442
|
C | T | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.178-8700G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112328442 | ||||||
| chr12:112328650
|
C | T | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.178-8908G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112328650 | ||||||
| chr12:112328937
|
G | A | 2 | a0001c0001t0008g0252a0001c0001t0008g0253 | 2 | HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.178-9195C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112328937 | ||||||
| chr12:112329341
|
A | C | 1 | a0001c0001t0001g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.178-9599T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112329341 | ||||||
| chr12:112329368
|
TTG | T | 6 | a0001c0001t0004g0067a0001c0001t0004g0068a0001c0001t0004g0069others(3): Show | 6 | HG02622.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.178-9628_178-9627d others(4): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112329368 | ||||||
| chr12:112329370
|
G | T | 2 | a0001c0003t0002g0101a0006c0023t0009g0003 | 2 | HG01109.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.178-9628C>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112329370 | ||||||
| chr12:112329370
|
GT | G | 195 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0099others(192): Show | 195 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(192): Show |
intron_variant | MODIFIER | c.178-9629delA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112329370 | ||||||
| chr12:112329390
|
C | A | 1 | a0001c0001t0004g0071 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.178-9648G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112329390 | ||||||
| chr12:112329426
|
G | C | 4 | a0001c0003t0002g0086a0001c0003t0002g0102a0002c0006t0002g0094others(1): Show | 4 | HG01928.hp2 HG01934.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.178-9684C>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112329426 | ||||||
| chr12:112329478
|
G | A | 8 | a0001c0001t0001g0099a0001c0001t0001g0125a0001c0001t0001g0128others(5): Show | 8 | HG00140.hp1 HG00738.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.178-9736C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112329478 | ||||||
| chr12:112329620
|
G | A | 3 | a0001c0001t0003g0027a0001c0001t0003g0038a0001c0001t0003g0051 | 3 | NA18959.hp1 NA18994.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.178-9878C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112329620 | ||||||
| chr12:112330014
|
C | G | 8 | a0001c0001t0004g0061a0001c0001t0004g0067a0001c0001t0004g0068others(5): Show | 8 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.178-10272G>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112330014 | ||||||
| chr12:112330047
|
T | C | 89 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(86): Show | 89 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(86): Show |
intron_variant | MODIFIER | c.178-10305A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112330047 | ||||||
| chr12:112330110
|
C | T | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.178-10368G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112330110 | ||||||
| chr12:112330276
|
CA | C | 83 | a0001c0001t0001g0114a0001c0001t0003g0013a0001c0002t0001g0161others(80): Show | 83 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.178-10535delT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112330276 | ||||||
| chr12:112330412
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.178-10670G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112330412 | ||||||
| chr12:112330748
|
T | C | 1 | a0001c0002t0001g0174 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.178-11006A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112330748 | ||||||
| chr12:112330932
|
GC | G | 4 | a0001c0001t0003g0006a0001c0001t0003g0027a0001c0001t0003g0038others(1): Show | 4 | HG03927.hp2 NA18959.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.178-11191delG | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112330932 | ||||||
| chr12:112331021
|
A | C | 1 | a0001c0001t0001g0099 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.178-11279T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112331021 | ||||||
| chr12:112331048
|
G | GT | 5 | a0001c0001t0015g0248a0001c0002t0001g0208a0001c0003t0002g0086others(2): Show | 5 | HG01978.hp2 HG02056.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.178-11307dupA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112331048 | ||||||
| chr12:112331125
|
G | T | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG02109.hp1 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.178-11383C>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112331125 | ||||||
| chr12:112331140
|
C | G | 1 | a0011c0028t0006g0261 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.178-11398G>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112331140 | ||||||
| chr12:112331156
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.178-11414G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112331156 | ||||||
| chr12:112331380
|
T | C | 1 | a0001c0033t0002g0110 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.178-11638A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112331380 | ||||||
| chr12:112331434
|
T | G | 1 | a0001c0002t0001g0182 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.178-11692A>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112331434 | ||||||
| chr12:112331795
|
A | T | 1 | a0001c0012t0002g0093 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.178-12053T>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112331795 | ||||||
| chr12:112332141
|
T | TACAAGAA others(24): Show |
1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.178-12400_178-1239 others(35): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112332141 | ||||||
| chr12:112332143
|
G | A | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.178-12401C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112332143 | ||||||
| chr12:112332322
|
C | T | 1 | a0001c0033t0002g0110 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.178-12580G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112332322 | ||||||
| chr12:112332327
|
G | A | 2 | a0001c0001t0006g0258a0001c0001t0006g0262 | 2 | HG02056.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.178-12585C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112332327 | ||||||
| chr12:112332479
|
T | G | 1 | a0001c0003t0002g0247 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.178-12737A>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112332479 | ||||||
| chr12:112332540
|
C | CA | 94 | a0001c0001t0001g0216a0001c0001t0001g0220a0001c0001t0001g0222others(91): Show | 94 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(91): Show |
intron_variant | MODIFIER | c.178-12799dupT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112332540 | ||||||
| chr12:112332540
|
C | CAA | 7 | a0001c0001t0003g0031a0001c0001t0003g0042a0001c0001t0003g0059others(4): Show | 7 | HG01243.hp1 HG02055.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.178-12800_178-1279 others(6): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112332540 | ||||||
| chr12:112332540
|
C | CAAA | 72 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(69): Show | 72 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(69): Show |
intron_variant | MODIFIER | c.178-12801_178-1279 others(7): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112332540 | ||||||
| chr12:112332577
|
T | C | 6 | a0001c0002t0001g0201a0001c0002t0001g0202a0001c0002t0001g0203others(3): Show | 6 | HG02109.hp2 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.178-12835A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112332577 | ||||||
| chr12:112332811
|
C | CA | 76 | a0001c0001t0001g0156a0001c0002t0001g0161a0001c0002t0001g0163others(73): Show | 76 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(73): Show |
intron_variant | MODIFIER | c.178-13070dupT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112332811 | ||||||
| chr12:112332811
|
CA | C | 87 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(84): Show | 87 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(84): Show |
intron_variant | MODIFIER | c.178-13070delT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112332811 | ||||||
| chr12:112333259
|
T | G | 220 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0099others(217): Show | 220 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(217): Show |
intron_variant | MODIFIER | c.178-13517A>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112333259 | ||||||
| chr12:112333522
|
A | G | 1 | a0001c0001t0015g0248 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.178-13780T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112333522 | ||||||
| chr12:112333803
|
T | C | 1 | a0001c0001t0015g0248 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.178-14061A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112333803 | ||||||
| chr12:112333863
|
A | G | 8 | a0001c0001t0006g0254a0001c0001t0006g0255a0001c0001t0006g0256others(5): Show | 8 | HG00597.hp2 HG02056.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.178-14121T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112333863 | ||||||
| chr12:112333937
|
G | A | 1 | a0006c0023t0009g0003 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.178-14195C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112333937 | ||||||
| chr12:112333990
|
C | T | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.178-14248G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112333990 | ||||||
| chr12:112334081
|
G | A | 1 | a0001c0003t0004g0004 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.178-14339C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112334081 | ||||||
| chr12:112334180
|
G | A | 2 | a0001c0001t0004g0067a0001c0001t0005g0070 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.178-14438C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112334180 | ||||||
| chr12:112334207
|
T | TTAAA | 10 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0002t0001g0182others(7): Show | 10 | HG00140.hp2 HG01928.hp2 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.178-14469_178-1446 others(8): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112334207 | ||||||
| chr12:112334207
|
TTAAA | T | 91 | a0001c0001t0001g0083a0001c0001t0001g0112a0001c0001t0001g0113others(88): Show | 91 | HG00597.hp2 HG01071.hp1 HG01071.hp2 others(88): Show |
intron_variant | MODIFIER | c.178-14469_178-1446 others(8): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112334207 | ||||||
| chr12:112334207
|
TTAAATAA others(1): Show |
T | 3 | a0001c0001t0001g0159a0001c0003t0002g0098a0001c0003t0002g0136 | 3 | HG01106.hp2 HG03516.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.178-14473_178-1446 others(12): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112334207 | ||||||
| chr12:112334207
|
TTAAATAA others(13): Show |
T | 1 | a0001c0001t0001g0158 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.178-14485_178-1446 others(24): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112334207 | ||||||
| chr12:112334329
|
G | C | 2 | a0001c0003t0013g0096a0001c0003t0013g0105 | 2 | HG02080.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.178-14587C>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112334329 | ||||||
| chr12:112334547
|
C | T | 1 | a0001c0001t0004g0071 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.178-14805G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112334547 | ||||||
| chr12:112334591
|
G | A | 1 | a0001c0001t0003g0050 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.178-14849C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112334591 | ||||||
| chr12:112334637
|
C | CA | 13 | a0001c0001t0001g0159a0001c0002t0001g0181a0001c0002t0001g0196others(10): Show | 13 | HG01952.hp2 HG02055.hp2 HG02165.hp1 others(10): Show |
intron_variant | MODIFIER | c.178-14896dupT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112334637 | ||||||
| chr12:112334637
|
CA | C | 11 | a0001c0001t0003g0011a0001c0001t0003g0028a0001c0001t0005g0021others(8): Show | 11 | HG01081.hp1 HG01099.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.178-14896delT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112334637 | ||||||
| chr12:112334718
|
G | A | 1 | a0001c0001t0004g0073 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.178-14976C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112334718 | ||||||
| chr12:112334810
|
CA | C | 83 | a0001c0001t0001g0079a0001c0001t0001g0160a0001c0002t0001g0161others(80): Show | 83 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.178-15069delT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112334810 | ||||||
| chr12:112334843
|
T | C | 2 | a0001c0001t0003g0026a0001c0001t0003g0050 | 2 | NA19056.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.178-15101A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112334843 | ||||||
| chr12:112335088
|
A | G | 2 | a0001c0009t0016g0266a0001c0009t0018g0268 | 2 | HG02622.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.178-15346T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112335088 | ||||||
| chr12:112335143
|
T | TACAC | 3 | a0001c0001t0005g0047a0001c0002t0001g0176a0002c0004t0005g0048 | 3 | HG01081.hp2 HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.178-15405_178-1540 others(8): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112335143 | ||||||
| chr12:112335143
|
T | TACACAC | 3 | a0001c0001t0003g0006a0001c0001t0003g0059a0001c0001t0007g0007 | 3 | HG02257.hp1 HG03927.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.178-15407_178-1540 others(10): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112335143 | ||||||
| chr12:112335143
|
T | TACACACA others(1): Show |
24 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0012others(21): Show | 24 | HG01109.hp2 HG01243.hp1 HG01943.hp1 others(21): Show |
intron_variant | MODIFIER | c.178-15409_178-1540 others(12): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112335143 | ||||||
| chr12:112335143
|
T | TACACACA others(3): Show |
29 | a0001c0001t0003g0013a0001c0001t0003g0018a0001c0001t0003g0022others(26): Show | 29 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.178-15411_178-1540 others(14): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112335143 | ||||||
| chr12:112335143
|
T | TACACACA others(5): Show |
11 | a0001c0001t0003g0016a0001c0001t0003g0031a0001c0001t0003g0032others(8): Show | 11 | HG02523.hp1 HG02559.hp1 HG02976.hp1 others(8): Show |
intron_variant | MODIFIER | c.178-15413_178-1540 others(16): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112335143 | ||||||
| chr12:112335143
|
T | TACACACA others(7): Show |
6 | a0001c0001t0003g0019a0001c0001t0004g0077a0001c0001t0005g0005others(3): Show | 6 | HG01496.hp2 HG01891.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.178-15415_178-1540 others(18): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112335143 | ||||||
| chr12:112335143
|
T | TACACACA others(9): Show |
11 | a0001c0001t0004g0061a0001c0001t0004g0073a0001c0001t0004g0078others(8): Show | 11 | HG01891.hp1 HG02080.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.178-15417_178-1540 others(20): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112335143 | ||||||
| chr12:112335143
|
T | TACACACA others(11): Show |
37 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0005g0060others(34): Show | 37 | HG00597.hp1 HG00735.hp2 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.178-15419_178-1540 others(22): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112335143 | ||||||
| chr12:112335143
|
T | TACACACA others(13): Show |
18 | a0001c0001t0001g0157a0001c0002t0001g0161a0001c0002t0001g0167others(15): Show | 18 | HG01256.hp1 HG01258.hp2 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.178-15421_178-1540 others(24): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112335143 | ||||||
| chr12:112335143
|
T | TACACACA others(15): Show |
21 | a0001c0001t0004g0068a0001c0002t0001g0196a0001c0002t0001g0225others(18): Show | 21 | HG00544.hp1 HG02132.hp1 HG02622.hp1 others(18): Show |
intron_variant | MODIFIER | c.178-15423_178-1540 others(26): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112335143 | ||||||
| chr12:112335143
|
T | TACACACA others(17): Show |
5 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0004g0069others(2): Show | 5 | HG02451.hp2 HG03516.hp2 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.178-15402_178-1540 others(28): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112335143 | ||||||
| chr12:112335143
|
T | TACACACA others(19): Show |
4 | a0001c0001t0004g0067a0001c0001t0004g0072a0001c0001t0005g0070others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.178-15402_178-1540 others(30): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112335143 | ||||||
| chr12:112335143
|
T | TACACACA others(21): Show |
1 | a0014c0021t0017g0267 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.178-15402_178-1540 others(32): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112335143 | ||||||
| chr12:112335167
|
G | C | 73 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(70): Show | 73 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(70): Show |
intron_variant | MODIFIER | c.178-15425C>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112335167 | ||||||
| chr12:112335389
|
G | T | 1 | a0001c0001t0004g0023 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.178-15647C>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112335389 | ||||||
| chr12:112335600
|
A | C | 3 | a0001c0009t0016g0266a0001c0009t0018g0268a0014c0021t0017g0267 | 3 | HG02622.hp2 HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.178-15858T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112335600 | ||||||
| chr12:112335896
|
C | T | 1 | a0001c0001t0004g0061 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.178-16154G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112335896 | ||||||
| chr12:112336249
|
C | T | 1 | a0001c0001t0001g0114 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.178-16507G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112336249 | ||||||
| chr12:112336259
|
C | G | 8 | a0001c0001t0001g0099a0001c0001t0001g0125a0001c0001t0001g0128others(5): Show | 8 | HG00140.hp1 HG00738.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.178-16517G>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112336259 | ||||||
| chr12:112336355
|
C | G | 3 | a0001c0009t0016g0266a0001c0009t0018g0268a0014c0021t0017g0267 | 3 | HG02622.hp2 HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.178-16613G>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112336355 | ||||||
| chr12:112336522
|
C | CA | 8 | a0001c0001t0004g0061a0001c0001t0004g0067a0001c0001t0004g0068others(5): Show | 8 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.178-16781dupT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112336522 | ||||||
| chr12:112336792
|
T | C | 1 | a0001c0001t0003g0014 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.178-17050A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112336792 | ||||||
| chr12:112337006
|
G | T | 1 | a0009c0024t0002g0108 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.178-17264C>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112337006 | ||||||
| chr12:112337084
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.178-17342T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112337084 | ||||||
| chr12:112337097
|
G | A | 9 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0184others(6): Show | 9 | HG01071.hp1 HG01256.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.178-17355C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112337097 | ||||||
| chr12:112337546
|
C | T | 5 | a0001c0002t0001g0166a0001c0002t0001g0171a0001c0002t0001g0193others(2): Show | 5 | HG00597.hp1 NA18947.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.178-17804G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112337546 | ||||||
| chr12:112337670
|
C | T | 89 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(86): Show | 89 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(86): Show |
intron_variant | MODIFIER | c.178-17928G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112337670 | ||||||
| chr12:112337675
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.178-17933T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112337675 | ||||||
| chr12:112337777
|
G | A | 1 | a0001c0011t0010g0146 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.178-18035C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112337777 | ||||||
| chr12:112337883
|
C | T | 5 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.178-18141G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112337883 | ||||||
| chr12:112338238
|
T | C | 199 | a0001c0001t0001g0079a0001c0001t0001g0152a0001c0001t0001g0153others(196): Show | 199 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(196): Show |
intron_variant | MODIFIER | c.178-18496A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112338238 | ||||||
| chr12:112338488
|
G | C | 4 | a0001c0002t0001g0174a0001c0002t0001g0188a0001c0002t0001g0211others(1): Show | 4 | HG02080.hp2 NA18961.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-18746C>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112338488 | ||||||
| chr12:112338534
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.178-18792G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112338534 | ||||||
| chr12:112338899
|
G | A | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.178-19157C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112338899 | ||||||
| chr12:112339059
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.178-19317G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112339059 | ||||||
| chr12:112339065
|
A | G | 1 | a0001c0002t0001g0191 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.178-19323T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112339065 | ||||||
| chr12:112339293
|
G | A | 170 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(167): Show | 170 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(167): Show |
intron_variant | MODIFIER | c.178-19551C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112339293 | ||||||
| chr12:112339310
|
C | CAAGAAAA others(341): Show |
1 | a0001c0001t0003g0042 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.178-19569_178-1956 others(352): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112339310 | ||||||
| chr12:112339310
|
C | CAAGAAAA others(370): Show |
1 | a0001c0001t0003g0043 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.178-19569_178-1956 others(381): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112339310 | ||||||
| chr12:112339310
|
C | CAAGAAAA others(367): Show |
1 | a0001c0001t0003g0041 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.178-19569_178-1956 others(378): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112339310 | ||||||
| chr12:112339310
|
C | CAAGAAAA others(366): Show |
1 | a0001c0009t0018g0268 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.178-19569_178-1956 others(377): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112339310 | ||||||
| chr12:112339310
|
C | CAAGAAAA others(363): Show |
1 | a0001c0001t0003g0040 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.178-19569_178-1956 others(374): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112339310 | ||||||
| chr12:112339310
|
C | CAAGAAAA others(362): Show |
1 | a0001c0001t0003g0037 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.178-19569_178-1956 others(373): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112339310 | ||||||
| chr12:112339310
|
C | CAAGAAAA others(359): Show |
1 | a0001c0001t0003g0033 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.178-19569_178-1956 others(370): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112339310 | ||||||
| chr12:112339310
|
C | CAAGAAAA others(360): Show |
1 | a0001c0009t0016g0266 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.178-19569_178-1956 others(371): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112339310 | ||||||
| chr12:112339310
|
C | CAAGAAAA others(350): Show |
1 | a0001c0013t0012g0145 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.178-19569_178-1956 others(361): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112339310 | ||||||
| chr12:112339310
|
C | CAAGAAAA others(359): Show |
2 | a0001c0001t0003g0019a0001c0001t0007g0034 | 2 | NA18969.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.178-19569_178-1956 others(370): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112339310 | ||||||
| chr12:112339310
|
C | CAAGAAAA others(358): Show |
3 | a0001c0001t0003g0026a0001c0001t0004g0023a0002c0004t0007g0036 | 3 | HG02809.hp2 HG03130.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.178-19569_178-1956 others(369): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112339310 | ||||||
| chr12:112339310
|
C | CAAGAAAA others(357): Show |
3 | a0001c0001t0005g0005a0001c0001t0019g0269a0014c0021t0017g0267 | 3 | HG01891.hp2 HG03225.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.178-19569_178-1956 others(368): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112339310 | ||||||
| chr12:112339310
|
C | CAAGAAAA others(356): Show |
3 | a0001c0001t0003g0018a0001c0001t0003g0020a0001c0001t0010g0147 | 3 | HG02027.hp1 NA18964.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.178-19569_178-1956 others(367): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112339310 | ||||||
| chr12:112339310
|
C | CAAGAAAA others(341): Show |
1 | a0002c0004t0003g0008 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.178-19569_178-1956 others(352): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112339310 | ||||||
| chr12:112339310
|
C | CAAGAAAA others(355): Show |
11 | a0001c0001t0003g0010a0001c0001t0003g0014a0001c0001t0003g0017others(8): Show | 11 | HG00597.hp2 HG02132.hp2 HG03579.hp2 others(8): Show |
intron_variant | MODIFIER | c.178-19569_178-1956 others(366): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112339310 | ||||||
| chr12:112339310
|
C | CAAGAAAA others(354): Show |
19 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(16): Show | 19 | HG01943.hp1 HG02055.hp1 HG02071.hp2 others(16): Show |
intron_variant | MODIFIER | c.178-19569_178-1956 others(365): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112339310 | ||||||
| chr12:112339310
|
C | CAAGAAAA others(353): Show |
5 | a0001c0001t0003g0030a0001c0001t0005g0049a0001c0001t0007g0024others(2): Show | 5 | HG01167.hp2 HG02717.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.178-19569_178-1956 others(364): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112339310 | ||||||
| chr12:112339310
|
C | CAAGAAAA others(352): Show |
1 | a0001c0001t0014g0148 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.178-19569_178-1956 others(363): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112339310 | ||||||
| chr12:112339310
|
C | CAAGAAAA others(350): Show |
1 | a0001c0001t0003g0058 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.178-19569_178-1956 others(361): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112339310 | ||||||
| chr12:112339310
|
C | CAAGAAAA others(349): Show |
1 | a0001c0001t0003g0027 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.178-19569_178-1956 others(360): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112339310 | ||||||
| chr12:112339310
|
C | CAAGAAAA others(348): Show |
1 | a0001c0001t0003g0051 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.178-19569_178-1956 others(359): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112339310 | ||||||
| chr12:112339310
|
C | CAAGAAAA others(347): Show |
1 | a0001c0001t0003g0038 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.178-19569_178-1956 others(358): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112339310 | ||||||
| chr12:112339310
|
C | CAAGAAAA others(354): Show |
1 | a0001c0001t0006g0258 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.178-19569_178-1956 others(365): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112339310 | ||||||
| chr12:112339310
|
C | CAAGAAAA others(342): Show |
2 | a0001c0001t0003g0006a0001c0001t0006g0255 | 2 | HG03927.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.178-19569_178-1956 others(353): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112339310 | ||||||
| chr12:112339310
|
C | CAAGAAAA others(336): Show |
1 | a0001c0001t0003g0022 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.178-19569_178-1956 others(347): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112339310 | ||||||
| chr12:112339310
|
C | CAAGAAAA others(334): Show |
1 | a0001c0001t0003g0045 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.178-19569_178-1956 others(345): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112339310 | ||||||
| chr12:112339310
|
C | CAAGAAAA others(333): Show |
7 | a0001c0001t0005g0021a0001c0001t0005g0044a0001c0001t0005g0053others(4): Show | 7 | HG01081.hp1 HG01099.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.178-19569_178-1956 others(344): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112339310 | ||||||
| chr12:112339310
|
C | CAAGAAAA others(332): Show |
8 | a0001c0001t0004g0061a0001c0001t0004g0067a0001c0001t0004g0068others(5): Show | 8 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.178-19569_178-1956 others(343): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112339310 | ||||||
| chr12:112339310
|
C | CAAGAAAA others(331): Show |
1 | a0001c0001t0003g0059 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.178-19569_178-1956 others(342): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112339310 | ||||||
| chr12:112339310
|
C | CAAGAAAA others(330): Show |
1 | a0001c0001t0004g0077 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.178-19569_178-1956 others(341): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112339310 | ||||||
| chr12:112339310
|
C | CAAGAAAA others(329): Show |
5 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(2): Show | 5 | HG01891.hp1 HG02559.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.178-19569_178-1956 others(340): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112339310 | ||||||
| chr12:112339629
|
T | C | 174 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(171): Show | 174 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(171): Show |
intron_variant | MODIFIER | c.178-19887A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112339629 | ||||||
| chr12:112340042
|
C | CA | 8 | a0001c0001t0006g0254a0001c0001t0006g0255a0001c0001t0006g0256others(5): Show | 8 | HG00597.hp2 HG02056.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.178-20301dupT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112340042 | ||||||
| chr12:112340214
|
A | G | 1 | a0001c0001t0005g0005 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.178-20472T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112340214 | ||||||
| chr12:112340402
|
G | A | 3 | a0001c0001t0003g0018a0001c0001t0003g0019a0002c0004t0003g0052 | 3 | HG02027.hp1 NA18969.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.178-20660C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112340402 | ||||||
| chr12:112340421
|
G | GGA | 90 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(87): Show | 90 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(87): Show |
intron_variant | MODIFIER | c.178-20680_178-2067 others(6): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112340421 | ||||||
| chr12:112340484
|
G | A | 1 | a0001c0001t0001g0113 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.178-20742C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112340484 | ||||||
| chr12:112340639
|
T | C | 2 | a0001c0003t0002g0101a0002c0006t0002g0126 | 2 | HG01175.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.178-20897A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112340639 | ||||||
| chr12:112340801
|
C | T | 1 | a0001c0003t0002g0100 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.178-21059G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112340801 | ||||||
| chr12:112342138
|
C | A | 2 | a0001c0002t0001g0175a0001c0002t0001g0219 | 2 | HG03017.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.178-22396G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112342138 | ||||||
| chr12:112342216
|
G | C | 4 | a0001c0003t0002g0090a0001c0003t0002g0091a0001c0003t0002g0100others(1): Show | 4 | NA19002.hp2 NA19056.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-22474C>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112342216 | ||||||
| chr12:112342243
|
C | G | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.178-22501G>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112342243 | ||||||
| chr12:112343029
|
CTTCTT | C | 4 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0077others(1): Show | 4 | HG01891.hp1 HG03453.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-23292_178-2328 others(9): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112343029 | ||||||
| chr12:112343070
|
AT | A | 21 | a0001c0001t0001g0083a0001c0001t0001g0099a0001c0001t0001g0112others(18): Show | 21 | HG00140.hp1 HG00738.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.178-23329delA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112343070 | ||||||
| chr12:112343230
|
G | T | 1 | a0010c0014t0001g0195 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.178-23488C>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112343230 | ||||||
| chr12:112343313
|
C | A | 87 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(84): Show | 87 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(84): Show |
intron_variant | MODIFIER | c.178-23571G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112343313 | ||||||
| chr12:112343488
|
G | C | 5 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(2): Show | 5 | HG00140.hp1 HG00738.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.178-23746C>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112343488 | ||||||
| chr12:112344040
|
C | T | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.178-24298G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112344040 | ||||||
| chr12:112344048
|
C | T | 87 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(84): Show | 87 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(84): Show |
intron_variant | MODIFIER | c.178-24306G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112344048 | ||||||
| chr12:112344114
|
C | G | 1 | a0001c0001t0007g0024 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.178-24372G>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112344114 | ||||||
| chr12:112344390
|
T | C | 1 | a0001c0002t0001g0182 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.178-24648A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112344390 | ||||||
| chr12:112344746
|
C | T | 8 | a0001c0001t0005g0021a0001c0001t0005g0044a0001c0001t0005g0053others(5): Show | 8 | HG01081.hp1 HG01099.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.178-25004G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112344746 | ||||||
| chr12:112344913
|
C | T | 8 | a0001c0001t0006g0254a0001c0001t0006g0255a0001c0001t0006g0256others(5): Show | 8 | HG00597.hp2 HG02056.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.178-25171G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112344913 | ||||||
| chr12:112345000
|
TC | T | 7 | a0001c0001t0005g0021a0001c0001t0005g0044a0001c0001t0005g0053others(4): Show | 7 | HG01081.hp1 HG01099.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.178-25259delG | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112345000 | ||||||
| chr12:112345054
|
G | C | 7 | a0001c0001t0004g0067a0001c0001t0004g0068a0001c0001t0004g0069others(4): Show | 7 | HG02451.hp2 HG02622.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.178-25312C>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112345054 | ||||||
| chr12:112345098
|
C | A | 1 | a0001c0033t0002g0110 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.178-25356G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112345098 | ||||||
| chr12:112345250
|
A | C | 5 | a0001c0002t0001g0161a0001c0002t0001g0180a0001c0002t0001g0182others(2): Show | 5 | HG02071.hp1 HG02165.hp2 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.178-25508T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112345250 | ||||||
| chr12:112345258
|
C | A | 1 | a0002c0004t0005g0057 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.178-25516G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112345258 | ||||||
| chr12:112345739
|
C | G | 7 | a0001c0001t0005g0021a0001c0001t0005g0044a0001c0001t0005g0053others(4): Show | 7 | HG01081.hp1 HG01099.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.178-25997G>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112345739 | ||||||
| chr12:112345787
|
C | T | 3 | a0001c0003t0004g0004a0001c0003t0009g0002a0006c0023t0009g0003 | 3 | HG01109.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.178-26045G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112345787 | ||||||
| chr12:112345819
|
C | T | 1 | a0001c0001t0005g0054 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-26077G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112345819 | ||||||
| chr12:112345822
|
G | A | 11 | a0001c0002t0001g0163a0001c0002t0001g0164a0001c0002t0001g0176others(8): Show | 11 | HG00735.hp2 HG01081.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.178-26080C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112345822 | ||||||
| chr12:112345979
|
G | A | 1 | a0001c0001t0003g0033 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.178-26237C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112345979 | ||||||
| chr12:112346046
|
C | A | 1 | a0006c0023t0009g0003 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.178-26304G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112346046 | ||||||
| chr12:112346051
|
T | C | 1 | a0001c0001t0006g0260 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.178-26309A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112346051 | ||||||
| chr12:112346128
|
G | A | 1 | a0001c0001t0001g0158 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.178-26386C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112346128 | ||||||
| chr12:112346200
|
T | C | 1 | a0001c0002t0001g0213 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.178-26458A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112346200 | ||||||
| chr12:112346402
|
A | T | 2 | a0001c0001t0005g0047a0002c0004t0005g0048 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.178-26660T>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112346402 | ||||||
| chr12:112346572
|
C | T | 3 | a0001c0010t0001g0214a0001c0010t0001g0217a0002c0026t0001g0215 | 3 | HG02965.hp2 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.178-26830G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112346572 | ||||||
| chr12:112347423
|
C | T | 1 | a0001c0003t0002g0109 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.178-27681G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112347423 | ||||||
| chr12:112347500
|
A | C | 5 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(2): Show | 5 | HG00140.hp1 HG00738.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.178-27758T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112347500 | ||||||
| chr12:112347547
|
C | A | 1 | a0001c0003t0002g0111 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.178-27805G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112347547 | ||||||
| chr12:112347677
|
A | G | 4 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0077others(1): Show | 4 | HG01891.hp1 HG03453.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-27935T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112347677 | ||||||
| chr12:112347702
|
C | T | 8 | a0001c0001t0004g0023a0001c0001t0007g0007a0001c0001t0007g0024others(5): Show | 8 | HG01943.hp1 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.178-27960G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112347702 | ||||||
| chr12:112347735
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.178-27993G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112347735 | ||||||
| chr12:112347767
|
T | C | 173 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(170): Show | 173 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(170): Show |
intron_variant | MODIFIER | c.178-28025A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112347767 | ||||||
| chr12:112347778
|
T | C | 90 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(87): Show | 90 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(87): Show |
intron_variant | MODIFIER | c.178-28036A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112347778 | ||||||
| chr12:112347851
|
C | T | 2 | a0001c0003t0002g0103a0001c0003t0002g0107 | 2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.178-28109G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112347851 | ||||||
| chr12:112347953
|
C | T | 1 | a0002c0004t0007g0036 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.178-28211G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112347953 | ||||||
| chr12:112347956
|
A | C | 1 | a0001c0001t0006g0255 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.178-28214T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112347956 | ||||||
| chr12:112348523
|
C | T | 1 | a0001c0001t0006g0254 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.178-28781G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112348523 | ||||||
| chr12:112348763
|
A | G | 2 | a0001c0003t0002g0101a0002c0006t0002g0126 | 2 | HG01175.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.178-29021T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112348763 | ||||||
| chr12:112349003
|
G | T | 1 | a0002c0006t0002g0094 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.178-29261C>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112349003 | ||||||
| chr12:112349190
|
C | T | 1 | a0010c0014t0001g0195 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.178-29448G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112349190 | ||||||
| chr12:112349219
|
C | A | 1 | a0001c0002t0008g0249 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.178-29477G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112349219 | ||||||
| chr12:112349342
|
C | G | 1 | a0001c0001t0001g0099 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.178-29600G>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112349342 | ||||||
| chr12:112349388
|
C | CA | 92 | a0001c0001t0001g0099a0001c0001t0001g0117a0001c0001t0001g0222others(89): Show | 92 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.178-29647dupT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112349388 | ||||||
| chr12:112349388
|
C | CAA | 67 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0012others(64): Show | 67 | HG00597.hp2 HG01099.hp1 HG01109.hp2 others(64): Show |
intron_variant | MODIFIER | c.178-29648_178-2964 others(6): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112349388 | ||||||
| chr12:112349388
|
C | CAAA | 16 | a0001c0001t0003g0006a0001c0001t0003g0027a0001c0001t0003g0042others(13): Show | 16 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.178-29649_178-2964 others(7): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112349388 | ||||||
| chr12:112349388
|
CAAAAAAA others(3): Show |
C | 8 | a0001c0001t0004g0023a0001c0001t0007g0007a0001c0001t0007g0024others(5): Show | 8 | HG01943.hp1 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.178-29656_178-2964 others(14): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112349388 | ||||||
| chr12:112349388
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0012t0002g0093 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.178-29657_178-2964 others(15): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112349388 | ||||||
| chr12:112349433
|
T | G | 8 | a0001c0001t0004g0061a0001c0001t0004g0067a0001c0001t0004g0068others(5): Show | 8 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.178-29691A>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112349433 | ||||||
| chr12:112350234
|
C | T | 1 | a0001c0001t0004g0074 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.178-30492G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112350234 | ||||||
| chr12:112350445
|
T | G | 1 | a0001c0001t0001g0125 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.178-30703A>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112350445 | ||||||
| chr12:112350712
|
C | T | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.178-30970G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112350712 | ||||||
| chr12:112351030
|
G | A | 1 | a0001c0001t0003g0006 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.177+30922C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112351030 | ||||||
| chr12:112351229
|
G | A | 6 | a0001c0002t0001g0201a0001c0002t0001g0202a0001c0002t0001g0203others(3): Show | 6 | HG02109.hp2 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.177+30723C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112351229 | ||||||
| chr12:112351303
|
C | T | 6 | a0001c0001t0004g0067a0001c0001t0004g0068a0001c0001t0004g0069others(3): Show | 6 | HG02451.hp2 HG02622.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.177+30649G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112351303 | ||||||
| chr12:112351340
|
C | T | 1 | a0005c0022t0002g0092 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.177+30612G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112351340 | ||||||
| chr12:112351734
|
T | C | 1 | a0001c0013t0012g0145 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.177+30218A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112351734 | ||||||
| chr12:112351750
|
T | C | 2 | a0001c0001t0001g0079a0001c0001t0001g0160 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.177+30202A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112351750 | ||||||
| chr12:112351796
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.177+30156A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112351796 | ||||||
| chr12:112352273
|
C | T | 1 | a0001c0032t0011g0263 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.177+29679G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112352273 | ||||||
| chr12:112352335
|
C | CT | 80 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(77): Show | 80 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(77): Show |
intron_variant | MODIFIER | c.177+29616dupA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112352335 | ||||||
| chr12:112352618
|
CT | C | 3 | a0001c0003t0002g0084a0001c0003t0002g0085a0001c0003t0009g0001 | 3 | NA18984.hp2 NA18986.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.177+29333delA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112352618 | ||||||
| chr12:112352757
|
C | A | 1 | a0001c0003t0002g0111 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.177+29195G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112352757 | ||||||
| chr12:112352780
|
G | T | 2 | a0001c0001t0001g0112a0001c0002t0001g0167 | 2 | HG02273.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.177+29172C>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112352780 | ||||||
| chr12:112352782
|
T | C | 3 | a0001c0001t0003g0018a0001c0001t0003g0019a0002c0004t0003g0052 | 3 | HG02027.hp1 NA18969.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.177+29170A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112352782 | ||||||
| chr12:112352803
|
C | T | 2 | a0001c0001t0004g0067a0001c0001t0005g0070 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.177+29149G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112352803 | ||||||
| chr12:112352827
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.177+29125C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112352827 | ||||||
| chr12:112352844
|
T | C | 221 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0099others(218): Show | 221 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(218): Show |
intron_variant | MODIFIER | c.177+29108A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112352844 | ||||||
| chr12:112353274
|
T | TGAGGGAT others(325): Show |
1 | a0001c0001t0003g0030 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.177+28677_177+2867 others(336): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112353274 | ||||||
| chr12:112353274
|
T | TGAGGGAT others(350): Show |
1 | a0001c0001t0003g0029 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.177+28677_177+2867 others(361): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112353274 | ||||||
| chr12:112353274
|
T | TGAGGGAT others(351): Show |
1 | a0001c0001t0003g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.177+28677_177+2867 others(362): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112353274 | ||||||
| chr12:112353293
|
A | G | 1 | a0001c0001t0005g0060 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.177+28659T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112353293 | ||||||
| chr12:112353319
|
T | C | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.177+28633A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112353319 | ||||||
| chr12:112353435
|
T | C | 1 | a0001c0001t0003g0059 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.177+28517A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112353435 | ||||||
| chr12:112353493
|
T | C | 2 | a0001c0001t0007g0024a0001c0001t0007g0025 | 2 | HG01943.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.177+28459A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112353493 | ||||||
| chr12:112353569
|
G | T | 88 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(85): Show | 88 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(85): Show |
intron_variant | MODIFIER | c.177+28383C>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112353569 | ||||||
| chr12:112353656
|
C | T | 1 | a0001c0030t0007g0035 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.177+28296G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112353656 | ||||||
| chr12:112353675
|
A | G | 1 | a0016c0019t0002g0135 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.177+28277T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112353675 | ||||||
| chr12:112353740
|
T | C | 1 | a0001c0001t0003g0018 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.177+28212A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112353740 | ||||||
| chr12:112354362
|
C | CT | 76 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(73): Show | 76 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(73): Show |
intron_variant | MODIFIER | c.177+27589dupA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112354362 | ||||||
| chr12:112354515
|
C | T | 1 | a0001c0030t0007g0035 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.177+27437G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112354515 | ||||||
| chr12:112354780
|
A | C | 170 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(167): Show | 170 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(167): Show |
intron_variant | MODIFIER | c.177+27172T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112354780 | ||||||
| chr12:112354990
|
T | C | 1 | a0001c0001t0011g0265 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.177+26962A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112354990 | ||||||
| chr12:112355067
|
G | A | 2 | a0001c0002t0001g0203a0001c0002t0001g0204 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.177+26885C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112355067 | ||||||
| chr12:112355265
|
G | T | 4 | a0001c0001t0001g0152a0001c0001t0001g0153a0002c0004t0001g0155others(1): Show | 4 | HG01099.hp2 HG01175.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.177+26687C>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112355265 | ||||||
| chr12:112355274
|
G | A | 5 | a0001c0001t0004g0062a0001c0001t0004g0064a0001c0001t0004g0065others(2): Show | 5 | HG02055.hp2 HG02572.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.177+26678C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112355274 | ||||||
| chr12:112355287
|
C | A | 1 | a0001c0001t0001g0127 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.177+26665G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112355287 | ||||||
| chr12:112355287
|
C | CA | 229 | a0001c0001t0001g0079a0001c0001t0001g0099a0001c0001t0001g0121others(226): Show | 229 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(226): Show |
intron_variant | MODIFIER | c.177+26664dupT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112355287 | ||||||
| chr12:112355287
|
C | CAA | 25 | a0001c0001t0001g0083a0001c0001t0001g0112a0001c0001t0001g0113others(22): Show | 25 | HG01175.hp2 HG01243.hp2 HG01993.hp2 others(22): Show |
intron_variant | MODIFIER | c.177+26663_177+2666 others(6): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112355287 | ||||||
| chr12:112355386
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.177+26566C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112355386 | ||||||
| chr12:112355620
|
C | T | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.177+26332G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112355620 | ||||||
| chr12:112355756
|
T | C | 89 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(86): Show | 89 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(86): Show |
intron_variant | MODIFIER | c.177+26196A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112355756 | ||||||
| chr12:112356252
|
G | A | 4 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0077others(1): Show | 4 | HG01891.hp1 HG03453.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.177+25700C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112356252 | ||||||
| chr12:112356264
|
G | A | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.177+25688C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112356264 | ||||||
| chr12:112356368
|
C | A | 2 | a0001c0002t0001g0178a0001c0002t0001g0179 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.177+25584G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112356368 | ||||||
| chr12:112356813
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.177+25139G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112356813 | ||||||
| chr12:112356875
|
C | A | 1 | a0001c0001t0005g0005 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.177+25077G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112356875 | ||||||
| chr12:112356910
|
T | G | 200 | a0001c0001t0001g0079a0001c0001t0001g0152a0001c0001t0001g0153others(197): Show | 200 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(197): Show |
intron_variant | MODIFIER | c.177+25042A>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112356910 | ||||||
| chr12:112356947
|
T | C | 1 | a0001c0003t0002g0098 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.177+25005A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112356947 | ||||||
| chr12:112357013
|
C | T | 1 | a0001c0029t0001g0122 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.177+24939G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112357013 | ||||||
| chr12:112357015
|
G | C | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.177+24937C>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112357015 | ||||||
| chr12:112357482
|
T | C | 1 | a0002c0006t0002g0097 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.177+24470A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112357482 | ||||||
| chr12:112357494
|
T | A | 170 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(167): Show | 170 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(167): Show |
intron_variant | MODIFIER | c.177+24458A>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112357494 | ||||||
| chr12:112357587
|
A | C | 16 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0012others(13): Show | 16 | HG02132.hp2 HG02523.hp1 NA18942.hp2 others(13): Show |
intron_variant | MODIFIER | c.177+24365T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112357587 | ||||||
| chr12:112357838
|
G | T | 3 | a0001c0010t0001g0214a0001c0010t0001g0217a0002c0026t0001g0215 | 3 | HG02965.hp2 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.177+24114C>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112357838 | ||||||
| chr12:112357940
|
T | C | 221 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0099others(218): Show | 221 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(218): Show |
intron_variant | MODIFIER | c.177+24012A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112357940 | ||||||
| chr12:112358064
|
A | G | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.177+23888T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112358064 | ||||||
| chr12:112358433
|
T | C | 1 | a0001c0001t0014g0148 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.177+23519A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112358433 | ||||||
| chr12:112358701
|
C | T | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.177+23251G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112358701 | ||||||
| chr12:112358844
|
G | A | 2 | a0001c0001t0011g0264a0001c0001t0011g0265 | 2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.177+23108C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112358844 | ||||||
| chr12:112358889
|
C | T | 1 | a0001c0011t0001g0133 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.177+23063G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112358889 | ||||||
| chr12:112359293
|
C | CT | 9 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0077others(6): Show | 9 | HG02622.hp2 HG02897.hp1 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.177+22658dupA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112359293 | ||||||
| chr12:112359443
|
G | A | 75 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(72): Show | 75 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.177+22509C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112359443 | ||||||
| chr12:112359507
|
C | T | 1 | a0001c0002t0001g0238 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.177+22445G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112359507 | ||||||
| chr12:112359667
|
C | G | 1 | a0001c0032t0011g0263 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.177+22285G>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112359667 | ||||||
| chr12:112359732
|
T | C | 1 | a0001c0002t0008g0249 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.177+22220A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112359732 | ||||||
| chr12:112359747
|
C | G | 3 | a0001c0009t0016g0266a0001c0009t0018g0268a0014c0021t0017g0267 | 3 | HG02622.hp2 HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.177+22205G>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112359747 | ||||||
| chr12:112359946
|
C | A | 2 | a0001c0001t0001g0156a0001c0001t0001g0220 | 2 | HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.177+22006G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112359946 | ||||||
| chr12:112360706
|
G | A | 1 | a0001c0001t0008g0252 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.177+21246C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112360706 | ||||||
| chr12:112360715
|
G | T | 3 | a0001c0009t0016g0266a0001c0009t0018g0268a0014c0021t0017g0267 | 3 | HG02622.hp2 HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.177+21237C>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112360715 | ||||||
| chr12:112360732
|
C | A | 1 | a0014c0021t0017g0267 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.177+21220G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112360732 | ||||||
| chr12:112360735
|
G | A | 1 | a0002c0006t0002g0126 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.177+21217C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112360735 | ||||||
| chr12:112360817
|
C | T | 3 | a0001c0001t0003g0027a0001c0001t0003g0038a0001c0001t0003g0051 | 3 | NA18959.hp1 NA18994.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.177+21135G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112360817 | ||||||
| chr12:112361123
|
T | C | 1 | a0001c0002t0020g0270 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.177+20829A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112361123 | ||||||
| chr12:112361199
|
C | T | 3 | a0001c0009t0016g0266a0001c0009t0018g0268a0014c0021t0017g0267 | 3 | HG02622.hp2 HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.177+20753G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112361199 | ||||||
| chr12:112361224
|
T | G | 1 | a0001c0001t0004g0074 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.177+20728A>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112361224 | ||||||
| chr12:112361656
|
G | A | 2 | a0001c0001t0005g0047a0002c0004t0005g0048 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.177+20296C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112361656 | ||||||
| chr12:112361960
|
T | C | 1 | a0001c0001t0001g0216 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.177+19992A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112361960 | ||||||
| chr12:112361973
|
T | C | 1 | a0001c0002t0001g0221 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.177+19979A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112361973 | ||||||
| chr12:112362004
|
G | A | 1 | a0001c0001t0007g0007 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.177+19948C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112362004 | ||||||
| chr12:112362093
|
C | T | 3 | a0001c0001t0007g0024a0001c0001t0007g0025a0001c0030t0007g0035 | 3 | HG01943.hp1 HG02717.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.177+19859G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112362093 | ||||||
| chr12:112362166
|
A | G | 1 | a0001c0002t0001g0198 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.177+19786T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112362166 | ||||||
| chr12:112362530
|
G | C | 3 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0077 | 3 | HG03453.hp2 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.177+19422C>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112362530 | ||||||
| chr12:112362706
|
A | T | 1 | a0001c0001t0001g0099 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.177+19246T>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112362706 | ||||||
| chr12:112362706
|
AT | A | 5 | a0001c0001t0001g0119a0001c0002t0001g0191a0001c0002t0001g0203others(2): Show | 5 | HG02074.hp1 HG03017.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.177+19245delA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112362706 | ||||||
| chr12:112362739
|
T | C | 2 | a0001c0002t0001g0163a0001c0002t0008g0250 | 2 | NA18942.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.177+19213A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112362739 | ||||||
| chr12:112362804
|
C | G | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159 | 3 | HG03098.hp2 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.177+19148G>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112362804 | ||||||
| chr12:112362982
|
A | G | 170 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(167): Show | 170 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(167): Show |
intron_variant | MODIFIER | c.177+18970T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112362982 | ||||||
| chr12:112363203
|
C | A | 82 | a0001c0001t0006g0258a0001c0002t0001g0161a0001c0002t0001g0163others(79): Show | 82 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(79): Show |
intron_variant | MODIFIER | c.177+18749G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112363203 | ||||||
| chr12:112363688
|
A | T | 1 | a0001c0001t0001g0157 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.177+18264T>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112363688 | ||||||
| chr12:112363804
|
A | G | 221 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0099others(218): Show | 221 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(218): Show |
intron_variant | MODIFIER | c.177+18148T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112363804 | ||||||
| chr12:112363844
|
C | T | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.177+18108G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112363844 | ||||||
| chr12:112363990
|
T | G | 1 | a0001c0003t0009g0001 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.177+17962A>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112363990 | ||||||
| chr12:112363992
|
C | CA | 82 | a0001c0001t0001g0114a0001c0001t0001g0120a0001c0001t0003g0006others(79): Show | 82 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(79): Show |
intron_variant | MODIFIER | c.177+17959dupT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112363992 | ||||||
| chr12:112363992
|
C | CAA | 19 | a0001c0001t0001g0099a0001c0001t0003g0019a0001c0001t0003g0045others(16): Show | 19 | HG01891.hp1 HG01891.hp2 HG02074.hp2 others(16): Show |
intron_variant | MODIFIER | c.177+17958_177+1795 others(6): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112363992 | ||||||
| chr12:112364355
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.177+17597G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112364355 | ||||||
| chr12:112364416
|
A | AT | 87 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(84): Show | 87 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(84): Show |
intron_variant | MODIFIER | c.177+17535_177+1753 others(5): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112364416 | ||||||
| chr12:112364420
|
A | T | 111 | a0001c0001t0001g0079a0001c0001t0001g0099a0001c0001t0001g0160others(108): Show | 111 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(108): Show |
intron_variant | MODIFIER | c.177+17532T>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112364420 | ||||||
| chr12:112364421
|
A | T | 2 | a0001c0001t0001g0153a0004c0034t0001g0154 | 2 | HG02647.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.177+17531T>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112364421 | ||||||
| chr12:112364450
|
C | A | 1 | a0001c0003t0009g0001 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.177+17502G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112364450 | ||||||
| chr12:112364487
|
T | C | 1 | a0001c0001t0001g0216 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.177+17465A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112364487 | ||||||
| chr12:112364622
|
T | C | 4 | a0001c0001t0001g0152a0001c0001t0001g0153a0002c0004t0001g0155others(1): Show | 4 | HG01099.hp2 HG01175.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.177+17330A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112364622 | ||||||
| chr12:112365065
|
T | C | 1 | a0001c0013t0012g0145 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.177+16887A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112365065 | ||||||
| chr12:112365439
|
T | A | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.177+16513A>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112365439 | ||||||
| chr12:112365725
|
C | G | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.177+16227G>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112365725 | ||||||
| chr12:112365772
|
G | T | 6 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.177+16180C>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112365772 | ||||||
| chr12:112365772
|
GT | G | 226 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0099others(223): Show | 226 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(223): Show |
intron_variant | MODIFIER | c.177+16179delA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112365772 | ||||||
| chr12:112365773
|
T | G | 6 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.177+16179A>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112365773 | ||||||
| chr12:112365776
|
T | G | 1 | a0001c0001t0003g0037 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.177+16176A>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112365776 | ||||||
| chr12:112365778
|
T | G | 1 | a0001c0001t0001g0216 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.177+16174A>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112365778 | ||||||
| chr12:112365780
|
T | G | 1 | a0001c0002t0008g0249 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.177+16172A>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112365780 | ||||||
| chr12:112365802
|
C | T | 1 | a0001c0001t0014g0148 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.177+16150G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112365802 | ||||||
| chr12:112365901
|
G | A | 1 | a0001c0002t0001g0237 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.177+16051C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112365901 | ||||||
| chr12:112366345
|
C | T | 1 | a0001c0009t0018g0268 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.177+15607G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112366345 | ||||||
| chr12:112366419
|
C | T | 2 | a0001c0001t0001g0222a0001c0001t0001g0224 | 2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.177+15533G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112366419 | ||||||
| chr12:112366683
|
C | T | 1 | a0001c0001t0003g0037 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.177+15269G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112366683 | ||||||
| chr12:112366932
|
A | AT | 8 | a0001c0001t0004g0067a0001c0001t0004g0068a0001c0001t0004g0069others(5): Show | 8 | HG02129.hp2 HG02451.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.177+15019dupA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112366932 | ||||||
| chr12:112367222
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.177+14730G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112367222 | ||||||
| chr12:112367306
|
A | AAAAG | 6 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0003t0002g0081others(3): Show | 6 | HG02559.hp2 HG02683.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.177+14642_177+1464 others(8): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112367306 | ||||||
| chr12:112367306
|
A | AAAAGAAA others(13): Show |
1 | a0001c0001t0001g0157 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.177+14626_177+1464 others(24): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112367306 | ||||||
| chr12:112367306
|
AAAAG | A | 119 | a0001c0001t0001g0099a0001c0001t0001g0125a0001c0001t0001g0127others(116): Show | 119 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.177+14642_177+1464 others(8): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112367306 | ||||||
| chr12:112367306
|
AAAAGAAA others(1): Show |
A | 45 | a0001c0001t0001g0079a0001c0001t0001g0152a0001c0001t0001g0153others(42): Show | 45 | HG01081.hp1 HG01099.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.177+14638_177+1464 others(12): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112367306 | ||||||
| chr12:112367306
|
AAAAGAAA others(5): Show |
A | 58 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0216others(55): Show | 58 | HG00597.hp2 HG01109.hp2 HG01167.hp2 others(55): Show |
intron_variant | MODIFIER | c.177+14634_177+1464 others(16): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112367306 | ||||||
| chr12:112367306
|
AAAAGAAA others(9): Show |
A | 7 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(4): Show | 7 | HG01891.hp1 HG02559.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.177+14630_177+1464 others(20): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112367306 | ||||||
| chr12:112367357
|
A | G | 21 | a0001c0001t0001g0083a0001c0001t0001g0099a0001c0001t0001g0112others(18): Show | 21 | HG00140.hp1 HG00738.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.177+14595T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112367357 | ||||||
| chr12:112367361
|
G | T | 169 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(166): Show | 169 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(166): Show |
intron_variant | MODIFIER | c.177+14591C>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112367361 | ||||||
| chr12:112367473
|
T | C | 1 | a0001c0001t0001g0157 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.177+14479A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112367473 | ||||||
| chr12:112367807
|
G | T | 1 | a0010c0014t0001g0195 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.177+14145C>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112367807 | ||||||
| chr12:112367820
|
C | CA | 48 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0099others(45): Show | 48 | HG00140.hp1 HG00735.hp1 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.177+14131dupT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112367820 | ||||||
| chr12:112367820
|
C | CAA | 12 | a0001c0001t0001g0152a0001c0001t0001g0224a0001c0001t0004g0064others(9): Show | 12 | HG01099.hp2 HG01175.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.177+14130_177+1413 others(6): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112367820 | ||||||
| chr12:112367820
|
C | CAAA | 39 | a0001c0001t0015g0248a0001c0002t0001g0161a0001c0002t0001g0169others(36): Show | 39 | HG00544.hp1 HG01081.hp2 HG01256.hp1 others(36): Show |
intron_variant | MODIFIER | c.177+14129_177+1413 others(7): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112367820 | ||||||
| chr12:112367820
|
C | CAAAA | 38 | a0001c0002t0001g0163a0001c0002t0001g0180a0001c0002t0001g0181others(35): Show | 38 | HG00735.hp2 HG01071.hp1 HG01433.hp1 others(35): Show |
intron_variant | MODIFIER | c.177+14128_177+1413 others(8): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112367820 | ||||||
| chr12:112367820
|
CA | C | 34 | a0001c0001t0001g0158a0001c0001t0003g0011a0001c0001t0003g0012others(31): Show | 34 | HG01081.hp1 HG01099.hp1 HG01943.hp1 others(31): Show |
intron_variant | MODIFIER | c.177+14131delT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112367820 | ||||||
| chr12:112367820
|
CAAAAAAA others(3): Show |
C | 2 | a0001c0002t0001g0166a0002c0005t0001g0165 | 2 | NA18947.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.177+14122_177+1413 others(14): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112367820 | ||||||
| chr12:112367820
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0002t0001g0164 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.177+14118_177+1413 others(18): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112367820 | ||||||
| chr12:112367832
|
A | C | 1 | a0001c0009t0016g0266 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.177+14120T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112367832 | ||||||
| chr12:112367833
|
A | C | 2 | a0001c0009t0018g0268a0014c0021t0017g0267 | 2 | HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.177+14119T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112367833 | ||||||
| chr12:112367836
|
A | C | 1 | a0001c0001t0005g0060 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.177+14116T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112367836 | ||||||
| chr12:112367837
|
A | C | 2 | a0001c0009t0016g0266a0001c0009t0018g0268 | 2 | HG02622.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.177+14115T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112367837 | ||||||
| chr12:112367838
|
A | C | 2 | a0001c0003t0002g0087a0001c0003t0002g0088 | 2 | HG02165.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.177+14114T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112367838 | ||||||
| chr12:112367849
|
C | T | 1 | a0001c0003t0009g0002 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.177+14103G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112367849 | ||||||
| chr12:112368105
|
C | T | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.177+13847G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112368105 | ||||||
| chr12:112368265
|
T | C | 1 | a0001c0002t0001g0192 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.177+13687A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112368265 | ||||||
| chr12:112368275
|
T | C | 3 | a0001c0001t0005g0047a0001c0001t0012g0151a0002c0004t0005g0048 | 3 | HG02055.hp1 HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.177+13677A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112368275 | ||||||
| chr12:112368667
|
T | C | 1 | a0001c0001t0003g0043 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.177+13285A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112368667 | ||||||
| chr12:112368709
|
C | T | 1 | a0001c0001t0003g0022 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.177+13243G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112368709 | ||||||
| chr12:112368913
|
A | G | 2 | a0001c0001t0001g0079a0001c0001t0001g0160 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.177+13039T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112368913 | ||||||
| chr12:112369020
|
C | T | 7 | a0001c0001t0005g0021a0001c0001t0005g0044a0001c0001t0005g0053others(4): Show | 7 | HG01081.hp1 HG01099.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.177+12932G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112369020 | ||||||
| chr12:112369143
|
A | G | 2 | a0001c0001t0001g0112a0001c0001t0001g0113 | 2 | NA18943.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.177+12809T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112369143 | ||||||
| chr12:112369163
|
T | C | 1 | a0001c0002t0001g0193 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.177+12789A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112369163 | ||||||
| chr12:112369285
|
T | C | 1 | a0001c0001t0001g0224 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.177+12667A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112369285 | ||||||
| chr12:112369340
|
C | CT | 12 | a0001c0001t0001g0121a0001c0001t0005g0021a0001c0001t0005g0053others(9): Show | 12 | HG01099.hp1 HG01884.hp2 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.177+12611dupA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112369340 | ||||||
| chr12:112369340
|
CT | C | 8 | a0001c0001t0001g0153a0001c0001t0003g0045a0001c0001t0003g0050others(5): Show | 8 | HG01081.hp1 HG01167.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.177+12611delA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112369340 | ||||||
| chr12:112369749
|
G | A | 81 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.177+12203C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112369749 | ||||||
| chr12:112369925
|
A | G | 1 | a0001c0003t0009g0001 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.177+12027T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112369925 | ||||||
| chr12:112370650
|
G | A | 1 | a0001c0001t0015g0248 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.177+11302C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112370650 | ||||||
| chr12:112370734
|
A | G | 16 | a0001c0001t0001g0083a0001c0001t0001g0112a0001c0001t0001g0113others(13): Show | 16 | HG01884.hp2 HG01934.hp2 HG01993.hp2 others(13): Show |
intron_variant | MODIFIER | c.177+11218T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112370734 | ||||||
| chr12:112370924
|
G | T | 1 | a0001c0001t0001g0127 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.177+11028C>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112370924 | ||||||
| chr12:112370939
|
A | T | 1 | a0001c0002t0001g0161 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.177+11013T>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112370939 | ||||||
| chr12:112371002
|
G | A | 5 | a0001c0001t0005g0046a0001c0001t0005g0047a0001c0001t0005g0049others(2): Show | 5 | HG01167.hp2 HG02055.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.177+10950C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112371002 | ||||||
| chr12:112371504
|
G | A | 1 | a0010c0014t0001g0195 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.177+10448C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112371504 | ||||||
| chr12:112371622
|
T | C | 173 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(170): Show | 173 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(170): Show |
intron_variant | MODIFIER | c.177+10330A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112371622 | ||||||
| chr12:112371886
|
C | CA | 87 | a0001c0001t0001g0127a0001c0001t0001g0131a0001c0001t0003g0006others(84): Show | 87 | HG00140.hp1 HG01081.hp1 HG01099.hp1 others(84): Show |
intron_variant | MODIFIER | c.177+10065dupT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112371886 | ||||||
| chr12:112371902
|
A | AG | 3 | a0001c0001t0003g0018a0001c0001t0003g0019a0002c0004t0003g0052 | 3 | HG02027.hp1 NA18969.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.177+10049_177+1005 others(5): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112371902 | ||||||
| chr12:112371938
|
CCAAA | C | 7 | a0001c0001t0004g0067a0001c0001t0004g0068a0001c0001t0004g0069others(4): Show | 7 | HG02451.hp2 HG02622.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.177+10010_177+1001 others(8): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112371938 | ||||||
| chr12:112372047
|
C | T | 173 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(170): Show | 173 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(170): Show |
intron_variant | MODIFIER | c.177+9905G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112372047 | ||||||
| chr12:112372061
|
G | A | 5 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(2): Show | 5 | HG01891.hp1 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.177+9891C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112372061 | ||||||
| chr12:112372073
|
G | C | 1 | a0001c0001t0004g0073 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.177+9879C>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112372073 | ||||||
| chr12:112372104
|
C | CT | 97 | a0001c0001t0001g0083a0001c0001t0001g0112a0001c0001t0001g0113others(94): Show | 97 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(94): Show |
intron_variant | MODIFIER | c.177+9847dupA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112372104 | ||||||
| chr12:112372251
|
C | G | 4 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(1): Show | 4 | HG02135.hp2 NA18943.hp2 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.177+9701G>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112372251 | ||||||
| chr12:112372471
|
G | A | 7 | a0001c0001t0004g0067a0001c0001t0004g0068a0001c0001t0004g0069others(4): Show | 7 | HG02451.hp2 HG02622.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.177+9481C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112372471 | ||||||
| chr12:112372517
|
CGT | C | 269 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0099others(266): Show | 269 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(266): Show |
intron_variant | MODIFIER | c.177+9433_177+9434d others(4): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112372517 | ||||||
| chr12:112372690
|
A | G | 1 | a0001c0001t0015g0248 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.177+9262T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112372690 | ||||||
| chr12:112372953
|
TTGCCA | T | 75 | a0001c0002t0001g0161a0001c0002t0001g0163a0001c0002t0001g0164others(72): Show | 75 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.177+8994_177+8998d others(7): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112372953 | ||||||
| chr12:112373010
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.177+8942C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112373010 | ||||||
| chr12:112373117
|
A | T | 8 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0012others(5): Show | 8 | NA18946.hp2 NA18950.hp2 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.177+8835T>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112373117 | ||||||
| chr12:112373278
|
C | T | 1 | a0001c0001t0003g0051 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.177+8674G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112373278 | ||||||
| chr12:112373385
|
T | G | 1 | a0003c0008t0001g0207 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.177+8567A>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112373385 | ||||||
| chr12:112373387
|
G | C | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.177+8565C>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112373387 | ||||||
| chr12:112373453
|
C | T | 73 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(70): Show | 73 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(70): Show |
intron_variant | MODIFIER | c.177+8499G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112373453 | ||||||
| chr12:112373644
|
A | G | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.177+8308T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112373644 | ||||||
| chr12:112373979
|
A | G | 89 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(86): Show | 89 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(86): Show |
intron_variant | MODIFIER | c.177+7973T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112373979 | ||||||
| chr12:112374003
|
C | CA | 20 | a0001c0001t0001g0079a0001c0001t0001g0156a0001c0001t0001g0160others(17): Show | 20 | HG01099.hp1 HG01884.hp1 HG02135.hp1 others(17): Show |
intron_variant | MODIFIER | c.177+7948dupT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112374003 | ||||||
| chr12:112374310
|
T | A | 1 | a0001c0033t0002g0110 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.177+7642A>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112374310 | ||||||
| chr12:112374478
|
C | T | 7 | a0001c0001t0004g0067a0001c0001t0004g0068a0001c0001t0004g0069others(4): Show | 7 | HG02451.hp2 HG02622.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.177+7474G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112374478 | ||||||
| chr12:112374490
|
C | T | 1 | a0015c0020t0003g0009 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.177+7462G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112374490 | ||||||
| chr12:112374983
|
T | C | 5 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(2): Show | 5 | HG00140.hp1 HG00738.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.177+6969A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112374983 | ||||||
| chr12:112375100
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.177+6852G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112375100 | ||||||
| chr12:112375611
|
T | C | 200 | a0001c0001t0001g0079a0001c0001t0001g0152a0001c0001t0001g0153others(197): Show | 200 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(197): Show |
intron_variant | MODIFIER | c.177+6341A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112375611 | ||||||
| chr12:112375666
|
G | T | 1 | a0001c0002t0001g0226 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.177+6286C>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112375666 | ||||||
| chr12:112375889
|
C | T | 7 | a0001c0001t0004g0067a0001c0001t0004g0068a0001c0001t0004g0069others(4): Show | 7 | HG02451.hp2 HG02622.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.177+6063G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112375889 | ||||||
| chr12:112375914
|
C | CA | 7 | a0001c0001t0003g0058a0001c0001t0003g0059a0001c0001t0015g0248others(4): Show | 7 | HG01928.hp1 HG02074.hp2 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.177+6037dupT | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112375914 | ||||||
| chr12:112375928
|
A | C | 1 | a0002c0004t0003g0008 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.177+6024T>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112375928 | ||||||
| chr12:112376085
|
T | A | 5 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(2): Show | 5 | HG01891.hp1 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.177+5867A>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112376085 | ||||||
| chr12:112376332
|
C | T | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.177+5620G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112376332 | ||||||
| chr12:112376725
|
A | G | 1 | a0001c0013t0012g0145 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.177+5227T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112376725 | ||||||
| chr12:112376777
|
C | T | 7 | a0001c0001t0004g0067a0001c0001t0004g0068a0001c0001t0004g0069others(4): Show | 7 | HG02451.hp2 HG02622.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.177+5175G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112376777 | ||||||
| chr12:112376870
|
T | C | 1 | a0001c0003t0002g0144 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.177+5082A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112376870 | ||||||
| chr12:112376941
|
A | G | 89 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(86): Show | 89 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(86): Show |
intron_variant | MODIFIER | c.177+5011T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112376941 | ||||||
| chr12:112377279
|
A | T | 4 | a0001c0001t0006g0254a0001c0001t0006g0255a0001c0001t0006g0256others(1): Show | 4 | HG00597.hp2 NA18965.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.177+4673T>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112377279 | ||||||
| chr12:112377281
|
A | T | 2 | a0001c0001t0001g0156a0001c0001t0001g0220 | 2 | HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.177+4671T>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112377281 | ||||||
| chr12:112377285
|
T | A | 1 | a0001c0001t0004g0061 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.177+4667A>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112377285 | ||||||
| chr12:112377542
|
T | C | 1 | a0001c0031t0008g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.177+4410A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112377542 | ||||||
| chr12:112377570
|
T | C | 1 | a0001c0001t0005g0060 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.177+4382A>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112377570 | ||||||
| chr12:112377818
|
C | T | 2 | a0001c0003t0002g0080a0001c0003t0002g0081 | 2 | HG00738.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.177+4134G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112377818 | ||||||
| chr12:112377841
|
G | C | 1 | a0002c0004t0001g0155 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.177+4111C>G | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112377841 | ||||||
| chr12:112377856
|
A | G | 1 | a0001c0003t0002g0080 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.177+4096T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112377856 | ||||||
| chr12:112377864
|
C | T | 1 | a0001c0001t0004g0074 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.177+4088G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112377864 | ||||||
| chr12:112377894
|
A | G | 4 | a0001c0001t0001g0152a0001c0001t0001g0153a0002c0004t0001g0155others(1): Show | 4 | HG01099.hp2 HG01175.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.177+4058T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112377894 | ||||||
| chr12:112378064
|
A | G | 1 | a0001c0003t0002g0134 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.177+3888T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112378064 | ||||||
| chr12:112378394
|
AT | A | 170 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(167): Show | 170 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(167): Show |
intron_variant | MODIFIER | c.177+3557delA | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112378394 | ||||||
| chr12:112378414
|
C | T | 1 | a0001c0001t0005g0005 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.177+3538G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112378414 | ||||||
| chr12:112378594
|
C | T | 1 | a0001c0032t0011g0263 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.177+3358G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112378594 | ||||||
| chr12:112378746
|
A | T | 81 | a0001c0001t0003g0006a0001c0001t0003g0010a0001c0001t0003g0011others(78): Show | 81 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(78): Show |
intron_variant | MODIFIER | c.177+3206T>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112378746 | ||||||
| chr12:112378809
|
C | T | 7 | a0001c0001t0004g0067a0001c0001t0004g0068a0001c0001t0004g0069others(4): Show | 7 | HG02451.hp2 HG02622.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.177+3143G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112378809 | ||||||
| chr12:112379001
|
C | G | 1 | a0001c0001t0007g0007 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.177+2951G>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112379001 | ||||||
| chr12:112379053
|
C | A | 1 | a0001c0001t0004g0061 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.177+2899G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112379053 | ||||||
| chr12:112379127
|
C | T | 1 | a0001c0001t0003g0006 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.177+2825G>A | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112379127 | ||||||
| chr12:112379336
|
C | G | 1 | a0001c0002t0001g0225 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.177+2616G>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112379336 | ||||||
| chr12:112379552
|
G | A | 1 | a0001c0003t0002g0111 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.177+2400C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112379552 | ||||||
| chr12:112379708
|
A | G | 1 | a0001c0001t0005g0005 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.177+2244T>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112379708 | ||||||
| chr12:112379715
|
T | TTA | 5 | a0001c0001t0004g0062a0001c0001t0004g0064a0001c0001t0004g0065others(2): Show | 5 | HG02055.hp2 HG02572.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.177+2236_177+2237i others(4): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112379715 | ||||||
| chr12:112379717
|
T | A | 18 | a0001c0001t0001g0220a0001c0001t0004g0062a0001c0001t0004g0064others(15): Show | 18 | HG00140.hp2 HG00735.hp1 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.177+2235A>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112379717 | ||||||
| chr12:112379717
|
T | TTA | 34 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(31): Show | 34 | HG00140.hp1 HG00738.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.177+2233_177+2234d others(4): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112379717 | ||||||
| chr12:112379717
|
T | TTATATA | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | HG02109.hp1 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.177+2229_177+2234d others(8): Show |
HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112379717 | ||||||
| chr12:112379979
|
T | A | 22 | a0001c0002t0001g0225a0001c0002t0001g0226a0001c0002t0001g0227others(19): Show | 22 | HG00544.hp1 HG02129.hp2 HG02132.hp1 others(19): Show |
intron_variant | MODIFIER | c.177+1973A>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112379979 | ||||||
| chr12:112380043
|
T | G | 200 | a0001c0001t0001g0079a0001c0001t0001g0152a0001c0001t0001g0153others(197): Show | 200 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(197): Show |
intron_variant | MODIFIER | c.177+1909A>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112380043 | ||||||
| chr12:112380855
|
C | A | 7 | a0001c0001t0004g0067a0001c0001t0004g0068a0001c0001t0004g0069others(4): Show | 7 | HG02451.hp2 HG02622.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.177+1097G>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112380855 | ||||||
| chr12:112381076
|
G | A | 1 | a0001c0003t0002g0247 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.177+876C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112381076 | ||||||
| chr12:112381618
|
G | A | 5 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(2): Show | 5 | HG01891.hp1 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.177+334C>T | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112381618 | ||||||
| chr12:112381841
|
C | G | 1 | a0001c0001t0001g0079 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.177+111G>C | HECTD4 | ENSG00000173064.14 | transcript | ENST00000682272.1 | protein_coding | 1/75 | chr12 | 112381841 |