Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 285605 |
|---|---|
| ensemblid | ENSG00000169570.10 |
| hgncid | 19334 |
| symbol | DTWD2 |
| name | DTW domain containing 2 |
| refseq_nuc | NM_173666.4 |
| refseq_prot | NP_775937.1 |
| ensembl_nuc | ENST00000510708.6 |
| ensembl_prot | ENSP00000425048.1 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 118836074 |
| end | 118988547 |
| strand | - |
| ver | v1.2 |
| region | chr5:118836074-118988547 |
| region5000 | chr5:118831074-118993547 |
| regionname0 | DTWD2_chr5_118836074_118988547 |
| regionname5000 | DTWD2_chr5_118831074_118993547 |
| 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 | 298 | 237 | 85 | 62 | 47 | 12 | 29 | 33 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0002 | 0/0 | 298 | 4 | 0 | 0 | 3 | 0 | 1 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0003 | 0/0 | 7 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 897 | 231 | 80 | 62 | 46 | 12 | 29 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| c0002 | 0/0 | 897 | 5 | 5 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| c0003 | 0/0 | 897 | 4 | 0 | 0 | 3 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| c0004 | 0/0 | 897 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| c0005 | 0/0 | 897 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 4880 | 106 | 20 | 31 | 33 | 8 | 12 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| t0002 | 0/0 | 4882 | 20 | 1 | 11 | 2 | 3 | 3 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| t0003 | 0/0 | 4884 | 11 | 8 | 3 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| t0004 | 0/0 | 4878 | 10 | 9 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| t0005 | 0/0 | 4881 | 9 | 2 | 2 | 0 | 1 | 4 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| t0006 | 0/0 | 4880 | 9 | 0 | 5 | 0 | 0 | 4 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| t0007 | 0/0 | 4879 | 8 | 8 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| t0008 | 0/0 | 4875 | 6 | 6 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| t0009 | 0/0 | 4880 | 5 | 0 | 1 | 4 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| t0010 | 0/0 | 4879 | 5 | 0 | 0 | 4 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| t0011 | 0/0 | 4880 | 5 | 0 | 0 | 5 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| t0012 | 0/0 | 4880 | 5 | 5 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| t0013 | 0/0 | 4878 | 4 | 4 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| t0014 | 0/0 | 4880 | 4 | 4 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| t0015 | 0/0 | 4878 | 3 | 3 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| t0016 | 0/0 | 4878 | 2 | 2 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| t0017 | 0/0 | 4880 | 2 | 0 | 0 | 0 | 0 | 2 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| t0018 | 0/0 | 4879 | 2 | 0 | 2 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| t0019 | 0/0 | 4880 | 2 | 0 | 1 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| t0020 | 0/0 | 4879 | 2 | 1 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| t0021 | 0/0 | 4878 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| t0022 | 0/0 | 4881 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| t0023 | 0/0 | 4881 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| t0024 | 0/0 | 4878 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| t0025 | 0/0 | 4882 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| t0026 | 0/0 | 4879 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| t0027 | 0/0 | 4881 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| t0028 | 0/0 | 4878 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| t0029 | 0/0 | 4879 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| t0030 | 0/0 | 4879 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| t0031 | 0/0 | 4880 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| t0032 | 0/0 | 4879 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| t0033 | 0/0 | 4880 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| t0034 | 0/0 | 4880 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| t0035 | 0/0 | 4880 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| t0036 | 0/0 | 4880 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| t0037 | 0/0 | 4880 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| t0038 | 0/0 | 4880 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| t0039 | 0/0 | 4880 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| t0040 | 0/0 | 4880 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| t0041 | 0/0 | 4880 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| t0042 | 0/0 | 4880 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| 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 | 2 | 0 | 2 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0071 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0169 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 897 | 231 | 80 | 62 | 46 | 12 | 29 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0001c0002 | 0/0 | 897 | 5 | 5 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0001c0004 | 0/0 | 897 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0002c0003 | 0/0 | 897 | 4 | 0 | 0 | 3 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0003c0005 | 0/0 | 897 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 5776 | 101 | 16 | 31 | 32 | 8 | 12 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0001c0001t0002 | 0/0 | 5778 | 19 | 1 | 11 | 2 | 3 | 2 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0001c0001t0003 | 0/0 | 5780 | 11 | 8 | 3 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0001c0001t0004 | 0/0 | 5774 | 10 | 9 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0001c0001t0005 | 0/0 | 5777 | 9 | 2 | 2 | 0 | 1 | 4 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0001c0001t0006 | 0/0 | 5776 | 9 | 0 | 5 | 0 | 0 | 4 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0001c0001t0007 | 0/0 | 5775 | 8 | 8 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0001c0001t0008 | 0/0 | 5771 | 6 | 6 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0001c0001t0009 | 0/0 | 5776 | 5 | 0 | 1 | 4 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0001c0001t0010 | 0/0 | 5775 | 2 | 0 | 0 | 1 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0001c0001t0011 | 0/0 | 5776 | 5 | 0 | 0 | 5 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0001c0001t0012 | 0/0 | 5776 | 5 | 5 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0001c0001t0013 | 0/0 | 5774 | 4 | 4 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0001c0001t0014 | 0/0 | 5776 | 4 | 4 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0001c0001t0015 | 0/0 | 5774 | 3 | 3 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0001c0001t0016 | 0/0 | 5774 | 2 | 2 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0001c0001t0017 | 0/0 | 5776 | 2 | 0 | 0 | 0 | 0 | 2 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0001c0001t0018 | 0/0 | 5775 | 2 | 0 | 2 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0001c0001t0019 | 0/0 | 5776 | 2 | 0 | 1 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0001c0001t0020 | 0/0 | 5775 | 2 | 1 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0001c0001t0021 | 0/0 | 5774 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0001c0001t0022 | 0/0 | 5777 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0001c0001t0023 | 0/0 | 5777 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0001c0001t0024 | 0/0 | 5774 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0001c0001t0025 | 0/0 | 5778 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0001c0001t0026 | 0/0 | 5775 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0001c0001t0027 | 0/0 | 5777 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0001c0001t0028 | 0/0 | 5774 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0001c0001t0029 | 0/0 | 5775 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0001c0001t0030 | 0/0 | 5775 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0001c0001t0031 | 0/0 | 5776 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0001c0001t0032 | 0/0 | 5775 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0001c0001t0033 | 0/0 | 5776 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0001c0001t0034 | 0/0 | 5776 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0001c0001t0035 | 0/0 | 5776 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0001c0001t0036 | 0/0 | 5776 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0001c0001t0038 | 0/0 | 5776 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0001c0001t0039 | 0/0 | 5776 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0001c0001t0040 | 0/0 | 5776 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0001c0001t0041 | 0/0 | 5776 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0001c0002t0001 | 0/0 | 5776 | 4 | 4 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0001c0002t0037 | 0/0 | 5776 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0001c0004t0001 | 0/0 | 5776 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0002c0003t0002 | 0/0 | 5778 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0002c0003t0010 | 0/0 | 5775 | 3 | 0 | 0 | 3 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| a0003c0005t0042 | 0/0 | 5776 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | copy fasta | chr5 | 118831074 | 118993547 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0071 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0169 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0004g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0005g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0005g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0005g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0005g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0005g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0005g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0005g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0005g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0005g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0006g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0006g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0006g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0006g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0006g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0006g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0006g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0006g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0006g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0007g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0007g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0007g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0007g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0007g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0007g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0007g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0007g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0008g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0008g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0008g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0008g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0008g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0008g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0009g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0009g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0009g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0009g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0009g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0010g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0010g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0011g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0011g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0011g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0011g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0011g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0012g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0012g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0012g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0012g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0012g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0013g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0013g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0013g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0013g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0014g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0014g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0014g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0014g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0015g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0015g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0015g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0016g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0016g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0017g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0017g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0018g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0019g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0019g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0020g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0020g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0021g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0022g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0023g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0024g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0025g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0026g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0027g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0028g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0029g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0030g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0031g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0032g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0033g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0034g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0035g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0036g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0038g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0039g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0040g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0001t0041g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0002t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0002t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0002t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0002t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0002t0037g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0001c0004t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0002c0003t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0002c0003t0010g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0002c0003t0010g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0002c0003t0010g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| a0003c0005t0042g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0196 | EUR | GBR | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0143 | EUR | GBR | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0202 | EUR | GBR | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0101 | EUR | GBR | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0179 | EUR | FIN | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | FIN | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0153 | EUR | FIN | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0085 | EUR | FIN | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG00423 | hp1 | a0002 | c0003 | t0010 | g0237 | EAS | CHS | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG00544 | hp1 | a0002 | c0003 | t0010 | g0238 | EAS | CHS | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG00639 | hp1 | a0001 | c0001 | t0006 | g0047 | AMR | PUR | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG00642 | hp1 | a0001 | c0001 | t0018 | g0001 | AMR | PUR | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0174 | AMR | PUR | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG00733 | hp1 | a0001 | c0001 | t0036 | g0178 | AMR | PUR | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG00733 | hp2 | a0001 | c0001 | t0005 | g0155 | AMR | PUR | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG00741 | hp1 | a0001 | c0001 | t0024 | g0206 | AMR | PUR | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | PUR | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01074 | hp1 | a0001 | c0001 | t0018 | g0001 | AMR | PUR | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0160 | AMR | PUR | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01106 | hp1 | a0001 | c0001 | t0020 | g0121 | AMR | PUR | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0151 | AMR | PUR | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01168 | hp2 | a0001 | c0001 | t0006 | g0092 | AMR | PUR | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01169 | hp2 | a0001 | c0001 | t0006 | g0093 | AMR | PUR | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01243 | hp1 | a0001 | c0001 | t0039 | g0119 | AMR | PUR | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0018 | AMR | CLM | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0129 | AMR | CLM | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0130 | AMR | CLM | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01261 | hp1 | a0001 | c0001 | t0019 | g0023 | AMR | CLM | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01261 | hp2 | a0001 | c0001 | t0025 | g0045 | AMR | CLM | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0078 | AMR | CLM | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01358 | hp2 | a0001 | c0001 | t0006 | g0059 | AMR | CLM | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0137 | AMR | CLM | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01496 | hp2 | a0001 | c0001 | t0009 | g0159 | AMR | CLM | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01884 | hp1 | a0001 | c0001 | t0015 | g0133 | AFR | ACB | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0118 | AFR | ACB | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01891 | hp1 | a0001 | c0001 | t0013 | g0142 | AFR | ACB | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01891 | hp2 | a0001 | c0001 | t0008 | g0223 | AFR | ACB | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0060 | AMR | PEL | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PEL | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | PEL | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | ACB | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02056 | hp1 | a0001 | c0001 | t0010 | g0027 | EAS | KHV | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02056 | hp2 | a0001 | c0001 | t0022 | g0082 | EAS | KHV | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | KHV | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02257 | hp1 | a0001 | c0001 | t0029 | g0132 | AFR | ACB | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02257 | hp2 | a0001 | c0001 | t0041 | g0110 | AFR | ACB | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02258 | hp1 | a0001 | c0001 | t0012 | g0198 | AFR | ACB | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | ACB | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | ACB | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0136 | AFR | GWD | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02572 | hp2 | a0001 | c0001 | t0026 | g0212 | AFR | GWD | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02602 | hp1 | a0001 | c0001 | t0040 | g0084 | SAS | PJL | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02602 | hp2 | a0001 | c0001 | t0006 | g0083 | SAS | PJL | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02615 | hp1 | a0001 | c0002 | t0037 | g0002 | AFR | GWD | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02622 | hp1 | a0001 | c0001 | t0008 | g0231 | AFR | GWD | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0123 | AFR | GWD | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02630 | hp1 | a0001 | c0001 | t0007 | g0141 | AFR | GWD | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02630 | hp2 | a0001 | c0001 | t0032 | g0236 | AFR | GWD | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02647 | hp1 | a0001 | c0001 | t0012 | g0201 | AFR | GWD | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | GWD | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02683 | hp1 | a0002 | c0003 | t0002 | g0239 | SAS | PJL | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02683 | hp2 | a0001 | c0001 | t0005 | g0156 | SAS | PJL | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02717 | hp1 | a0001 | c0001 | t0012 | g0167 | AFR | GWD | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0124 | AFR | GWD | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02723 | hp1 | a0001 | c0001 | t0021 | g0010 | AFR | GWD | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02723 | hp2 | a0001 | c0001 | t0008 | g0222 | AFR | GWD | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02735 | hp1 | a0001 | c0001 | t0031 | g0170 | SAS | PJL | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02735 | hp2 | a0001 | c0001 | t0035 | g0207 | SAS | PJL | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0126 | SAS | PJL | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02738 | hp2 | a0001 | c0001 | t0006 | g0029 | SAS | PJL | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0068 | AFR | GWD | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02886 | hp1 | a0001 | c0001 | t0008 | g0204 | AFR | GWD | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02895 | hp2 | a0001 | c0001 | t0007 | g0213 | AFR | GWD | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | GWD | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0180 | AFR | GWD | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02897 | hp1 | a0003 | c0005 | t0042 | g0241 | AFR | GWD | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02922 | hp1 | a0001 | c0001 | t0007 | g0210 | AFR | ESN | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0120 | AFR | ESN | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02970 | hp1 | a0001 | c0001 | t0014 | g0230 | AFR | ESN | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02970 | hp2 | a0001 | c0001 | t0012 | g0199 | AFR | ESN | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0006 | AFR | ESN | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02976 | hp2 | a0001 | c0001 | t0016 | g0232 | AFR | ESN | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG03041 | hp1 | a0001 | c0001 | t0033 | g0205 | AFR | GWD | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG03041 | hp2 | a0001 | c0001 | t0013 | g0219 | AFR | GWD | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG03098 | hp1 | a0001 | c0001 | t0020 | g0122 | AFR | MSL | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG03098 | hp2 | a0001 | c0001 | t0008 | g0221 | AFR | MSL | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | ESN | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0116 | AFR | ESN | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ESN | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG03139 | hp2 | a0001 | c0001 | t0028 | g0138 | AFR | ESN | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG03195 | hp1 | a0001 | c0001 | t0007 | g0208 | AFR | ESN | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG03195 | hp2 | a0001 | c0001 | t0027 | g0009 | AFR | ESN | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG03209 | hp1 | a0001 | c0001 | t0014 | g0229 | AFR | MSL | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG03225 | hp1 | a0001 | c0001 | t0015 | g0135 | AFR | MSL | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG03225 | hp2 | a0001 | c0001 | t0007 | g0215 | AFR | MSL | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG03239 | hp1 | a0001 | c0001 | t0005 | g0162 | SAS | PJL | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG03239 | hp2 | a0001 | c0001 | t0006 | g0072 | SAS | PJL | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG03486 | hp1 | a0001 | c0001 | t0034 | g0228 | AFR | MSL | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0139 | AFR | MSL | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG03492 | hp2 | a0001 | c0001 | t0005 | g0161 | SAS | PJL | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG03516 | hp1 | a0001 | c0001 | t0007 | g0214 | AFR | ESN | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | ESN | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG03540 | hp1 | a0001 | c0001 | t0030 | g0225 | AFR | GWD | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | MSL | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0158 | AFR | MSL | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG03688 | hp1 | a0001 | c0001 | t0005 | g0154 | SAS | STU | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG03688 | hp2 | a0001 | c0001 | t0017 | g0140 | SAS | STU | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | BEB | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | BEB | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0070 | SAS | BEB | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | BEB | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG04115 | hp1 | a0001 | c0001 | t0010 | g0063 | SAS | STU | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | STU | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | STU | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG04199 | hp2 | a0001 | c0001 | t0017 | g0146 | SAS | STU | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | STU | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG04204 | hp2 | a0001 | c0001 | t0019 | g0025 | SAS | STU | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG04228 | hp1 | a0001 | c0001 | t0006 | g0091 | SAS | STU | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | STU | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA18522 | hp1 | a0001 | c0001 | t0013 | g0218 | AFR | YRI | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA18522 | hp2 | a0001 | c0001 | t0014 | g0227 | AFR | YRI | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CHB | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CHB | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHB | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | CHB | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA18906 | hp1 | a0001 | c0001 | t0015 | g0134 | AFR | YRI | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0209 | AFR | YRI | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA18951 | hp2 | a0001 | c0001 | t0011 | g0111 | EAS | JPT | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA18959 | hp2 | a0001 | c0001 | t0009 | g0148 | EAS | JPT | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA18964 | hp2 | a0001 | c0001 | t0011 | g0040 | EAS | JPT | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA18970 | hp1 | a0001 | c0001 | t0011 | g0112 | EAS | JPT | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA18974 | hp1 | a0002 | c0003 | t0010 | g0240 | EAS | JPT | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA18999 | hp1 | a0001 | c0001 | t0009 | g0149 | EAS | JPT | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA18999 | hp2 | a0001 | c0004 | t0001 | g0032 | EAS | JPT | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA19030 | hp1 | a0001 | c0001 | t0023 | g0226 | AFR | LWK | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA19030 | hp2 | a0001 | c0001 | t0013 | g0011 | AFR | LWK | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA19043 | hp1 | a0001 | c0001 | t0014 | g0115 | AFR | LWK | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | LWK | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA19058 | hp1 | a0001 | c0001 | t0011 | g0080 | EAS | JPT | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA19058 | hp2 | a0001 | c0001 | t0009 | g0144 | EAS | JPT | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA19063 | hp2 | a0001 | c0001 | t0011 | g0073 | EAS | JPT | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA19084 | hp2 | a0001 | c0001 | t0038 | g0054 | EAS | JPT | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA19090 | hp2 | a0001 | c0001 | t0009 | g0147 | EAS | JPT | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA19240 | hp1 | a0001 | c0001 | t0016 | g0233 | AFR | YRI | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0168 | AFR | YRI | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | ASW | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0157 | AFR | ASW | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0097 | EUR | TSI | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA20752 | hp2 | a0001 | c0001 | t0005 | g0184 | EUR | TSI | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0086 | EUR | TSI | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0131 | EUR | TSI | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG01123 | hp2 | a0001 | c0001 | t0006 | g0075 | AMR | CLM | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | ACB | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02486 | hp1 | a0001 | c0001 | t0007 | g0211 | AFR | ACB | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0117 | AFR | ACB | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG03471 | hp1 | a0001 | c0001 | t0008 | g0220 | AFR | MSL | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | MSL | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA20300 | hp1 | a0001 | c0001 | t0012 | g0200 | AFR | USA | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | USA | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0071 | REF | REF | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0169 | REF | REF | DTWD2_chr5_118831074_118993547 | DTWD2 | chr5 | 118831074 | 118993547 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:118988418
|
G | C | 1 | a0002 | 4 | HG00423.hp1 HG00544.hp1 HG02683.hp1 others(1): Show |
missense_variant | MODERATE | c.94C>G | p.Arg32Gly | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/6 | 130/5776 | 94/897 | 32/298 | chr5 | 118988418 | ||
| chr5:118988453
|
G | C | 1 | a0003 | 1 | HG02897.hp1 | missense_variant | MODERATE | c.59C>G | p.Ala20Gly | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/6 | 95/5776 | 59/897 | 20/298 | chr5 | 118988453 | ||
| chr5:118988454
|
C | T | 1 | a0003 | 1 | HG02897.hp1 | missense_variant | MODERATE | c.58G>A | p.Ala20Thr | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/6 | 94/5776 | 58/897 | 20/298 | chr5 | 118988454 | ||
| chr5:118988456
|
C | T | 1 | a0003 | 1 | HG02897.hp1 | missense_variant | MODERATE | c.56G>A | p.Gly19Glu | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/6 | 92/5776 | 56/897 | 19/298 | chr5 | 118988456 | ||
| chr5:118988462
|
G | C | 1 | a0003 | 1 | HG02897.hp1 | missense_variant | MODERATE | c.50C>G | p.Pro17Arg | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/6 | 86/5776 | 50/897 | 17/298 | chr5 | 118988462 | ||
| chr5:118988472
|
C | G | 1 | a0003 | 1 | HG02897.hp1 | missense_variant | MODERATE | c.40G>C | p.Val14Leu | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/6 | 76/5776 | 40/897 | 14/298 | chr5 | 118988472 | ||
| chr5:118988474
|
G | A | 1 | a0003 | 1 | HG02897.hp1 | missense_variant | MODERATE | c.38C>T | p.Pro13Leu | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/6 | 74/5776 | 38/897 | 13/298 | chr5 | 118988474 | ||
| chr5:118988477
|
T | G | 1 | a0003 | 1 | HG02897.hp1 | missense_variant | MODERATE | c.35A>C | p.Glu12Ala | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/6 | 71/5776 | 35/897 | 12/298 | chr5 | 118988477 | ||
| chr5:118988480
|
T | G | 1 | a0003 | 1 | HG02897.hp1 | missense_variant | MODERATE | c.32A>C | p.Gln11Pro | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/6 | 68/5776 | 32/897 | 11/298 | chr5 | 118988480 | ||
| chr5:118988492
|
G | C | 1 | a0003 | 1 | HG02897.hp1 | missense_variant | MODERATE | c.20C>G | p.Ala7Gly | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/6 | 56/5776 | 20/897 | 7/298 | chr5 | 118988492 | ||
| chr5:118988493
|
C | G | 1 | a0003 | 1 | HG02897.hp1 | missense_variant | MODERATE | c.19G>C | p.Ala7Pro | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/6 | 55/5776 | 19/897 | 7/298 | chr5 | 118988493 | ||
| chr5:118988495
|
T | A | 1 | a0003 | 1 | HG02897.hp1 | missense_variant | MODERATE | c.17A>T | p.Glu6Val | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/6 | 53/5776 | 17/897 | 6/298 | chr5 | 118988495 | ||
| chr5:118988497
|
T | G | 1 | a0003 | 1 | HG02897.hp1 | missense_variant | MODERATE | c.15A>C | p.Lys5Asn | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/6 | 51/5776 | 15/897 | 5/298 | chr5 | 118988497 | ||
| chr5:118988499
|
T | G | 1 | a0003 | 1 | HG02897.hp1 | missense_variant | MODERATE | c.13A>C | p.Lys5Gln | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/6 | 49/5776 | 13/897 | 5/298 | chr5 | 118988499 | ||
| chr5:118988505
|
A | G | 1 | a0003 | 1 | HG02897.hp1 | missense_variant | MODERATE | c.7T>C | p.Ser3Pro | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/6 | 43/5776 | 7/897 | 3/298 | chr5 | 118988505 | ||
| chr5:118988510
|
A | C | 1 | a0003 | 1 | HG02897.hp1 | start_lost | HIGH | c.2T>G | p.Met1? | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/6 | 38/5776 | 2/897 | 1/298 | chr5 | 118988510 | ||
| chr5:118988511
|
T | C | 1 | a0003 | 1 | HG02897.hp1 | start_lost | HIGH | c.1A>G | p.Met1? | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/6 | 37/5776 | 1/897 | 1/298 | chr5 | 118988511 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:118848216
|
C | T | 1 | a0001c0004 | 1 | NA18999.hp2 | splice_region_variant&synonymous_variant | LOW | c.600G>A | p.Val200Val | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/6 | 636/5776 | 600/897 | 200/298 | chr5 | 118848216 | ||
| chr5:118988419
|
C | G | 2 | a0001c0002a0003c0005 | 6 | HG02055.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
synonymous_variant | LOW | c.93G>C | p.Arg31Arg | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/6 | 129/5776 | 93/897 | 31/298 | chr5 | 118988419 | ||
| chr5:118988485
|
T | G | 1 | a0003c0005 | 1 | HG02897.hp1 | synonymous_variant | LOW | c.27A>C | p.Thr9Thr | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/6 | 63/5776 | 27/897 | 9/298 | chr5 | 118988485 | ||
| chr5:118988491
|
T | G | 1 | a0003c0005 | 1 | HG02897.hp1 | synonymous_variant | LOW | c.21A>C | p.Ala7Ala | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/6 | 57/5776 | 21/897 | 7/298 | chr5 | 118988491 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:118836081
|
A | T | 7 | a0001c0001t0010a0001c0001t0014a0001c0001t0020others(4): Show | 14 | HG00423.hp1 HG00544.hp1 HG01106.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4836T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 4836 | chr5 | 118836081 | |||||
| chr5:118836158
|
A | C | 1 | a0001c0001t0034 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4759T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 4759 | chr5 | 118836158 | |||||
| chr5:118836160
|
T | C | 2 | a0001c0001t0013a0001c0001t0021 | 5 | HG01891.hp1 HG02723.hp1 HG03041.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4757A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 4757 | chr5 | 118836160 | |||||
| chr5:118836173
|
C | A | 2 | a0001c0001t0020a0001c0001t0032 | 3 | HG01106.hp1 HG02630.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4744G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 4744 | chr5 | 118836173 | |||||
| chr5:118836226
|
G | A | 1 | a0001c0001t0006 | 9 | HG00639.hp1 HG01123.hp2 HG01168.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4691C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 4691 | chr5 | 118836226 | |||||
| chr5:118836280
|
G | A | 23 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(20): Show | 92 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*4637C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 4637 | chr5 | 118836280 | |||||
| chr5:118836295
|
C | G | 1 | a0001c0001t0033 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4622G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 4622 | chr5 | 118836295 | |||||
| chr5:118836475
|
G | C | 2 | a0001c0001t0010a0002c0003t0010 | 5 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4442C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 4442 | chr5 | 118836475 | |||||
| chr5:118836650
|
G | T | 30 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(27): Show | 106 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*4267C>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 4267 | chr5 | 118836650 | |||||
| chr5:118836738
|
G | A | 1 | a0001c0001t0025 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4179C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 4179 | chr5 | 118836738 | |||||
| chr5:118836774
|
C | A | 1 | a0001c0002t0037 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4143G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 4143 | chr5 | 118836774 | |||||
| chr5:118836775
|
C | G | 1 | a0001c0002t0037 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4142G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 4142 | chr5 | 118836775 | |||||
| chr5:118836955
|
G | A | 1 | a0001c0001t0019 | 2 | HG01261.hp1 HG04204.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3962C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 3962 | chr5 | 118836955 | |||||
| chr5:118837157
|
G | A | 7 | a0001c0001t0010a0001c0001t0014a0001c0001t0020others(4): Show | 14 | HG00423.hp1 HG00544.hp1 HG01106.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3760C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 3760 | chr5 | 118837157 | |||||
| chr5:118837159
|
G | A | 2 | a0001c0001t0010a0002c0003t0010 | 5 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3758C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 3758 | chr5 | 118837159 | |||||
| chr5:118837165
|
C | T | 3 | a0001c0001t0018a0001c0001t0029a0001c0001t0030 | 4 | HG00642.hp1 HG01074.hp1 HG02257.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3752G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 3752 | chr5 | 118837165 | |||||
| chr5:118837426
|
A | G | 1 | a0001c0001t0021 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3491T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 3491 | chr5 | 118837426 | |||||
| chr5:118837451
|
G | C | 1 | a0001c0001t0012 | 5 | HG02258.hp1 HG02647.hp1 HG02717.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3466C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 3466 | chr5 | 118837451 | |||||
| chr5:118837492
|
C | A | 1 | a0001c0001t0038 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3425G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 3425 | chr5 | 118837492 | |||||
| chr5:118837688
|
G | A | 1 | a0001c0001t0022 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3229C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 3229 | chr5 | 118837688 | |||||
| chr5:118837745
|
TA | T | 2 | a0001c0001t0009a0001c0001t0017 | 7 | HG01496.hp2 HG03688.hp2 HG04199.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3171delT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 3171 | chr5 | 118837745 | |||||
| chr5:118837957
|
A | G | 23 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(20): Show | 92 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*2960T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 2960 | chr5 | 118837957 | |||||
| chr5:118838142
|
T | C | 1 | a0001c0001t0039 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2775A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 2775 | chr5 | 118838142 | |||||
| chr5:118838286
|
C | T | 23 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(20): Show | 92 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*2631G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 2631 | chr5 | 118838286 | |||||
| chr5:118838308
|
G | C | 30 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(27): Show | 106 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*2609C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 2609 | chr5 | 118838308 | |||||
| chr5:118838375
|
A | G | 1 | a0001c0001t0011 | 5 | NA18951.hp2 NA18964.hp2 NA18970.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2542T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 2542 | chr5 | 118838375 | |||||
| chr5:118838392
|
GA | G | 27 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(24): Show | 100 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*2524delT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 2524 | chr5 | 118838392 | |||||
| chr5:118838429
|
G | C | 1 | a0001c0001t0035 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2488C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 2488 | chr5 | 118838429 | |||||
| chr5:118838480
|
A | G | 23 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(20): Show | 92 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*2437T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 2437 | chr5 | 118838480 | |||||
| chr5:118838544
|
AACTT | A | 1 | a0001c0001t0008 | 6 | HG01891.hp2 HG02622.hp1 HG02723.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2369_*2372delAAGT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 2369 | chr5 | 118838544 | |||||
| chr5:118838574
|
G | A | 1 | a0001c0001t0020 | 2 | HG01106.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2343C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 2343 | chr5 | 118838574 | |||||
| chr5:118838726
|
T | C | 1 | a0001c0001t0026 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2191A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 2191 | chr5 | 118838726 | |||||
| chr5:118838762
|
CA | C | 23 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(20): Show | 92 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*2154delT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 2154 | chr5 | 118838762 | |||||
| chr5:118838826
|
A | C | 1 | a0001c0001t0036 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2091T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 2091 | chr5 | 118838826 | |||||
| chr5:118838917
|
C | T | 1 | a0001c0001t0035 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2000G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 2000 | chr5 | 118838917 | |||||
| chr5:118839115
|
T | C | 1 | a0001c0001t0030 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1802A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 1802 | chr5 | 118839115 | |||||
| chr5:118839141
|
G | A | 1 | a0001c0001t0040 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1776C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 1776 | chr5 | 118839141 | |||||
| chr5:118839162
|
A | AAAT | 1 | a0001c0001t0003 | 11 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1752_*1754dupATT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 1754 | chr5 | 118839162 | |||||
| chr5:118839162
|
AAAT | A | 13 | a0001c0001t0004a0001c0001t0007a0001c0001t0008others(10): Show | 41 | HG00642.hp1 HG00741.hp1 HG01074.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1752_*1754delATT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 1752 | chr5 | 118839162 | |||||
| chr5:118839217
|
A | C | 1 | a0001c0001t0017 | 2 | HG03688.hp2 HG04199.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1700T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 1700 | chr5 | 118839217 | |||||
| chr5:118839325
|
A | G | 27 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(24): Show | 100 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*1592T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 1592 | chr5 | 118839325 | |||||
| chr5:118839384
|
T | G | 1 | a0001c0001t0023 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1533A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 1533 | chr5 | 118839384 | |||||
| chr5:118839386
|
A | T | 1 | a0001c0001t0021 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1531T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 1531 | chr5 | 118839386 | |||||
| chr5:118839461
|
C | A | 1 | a0001c0001t0041 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1456G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 1456 | chr5 | 118839461 | |||||
| chr5:118839524
|
A | AT | 9 | a0001c0001t0002a0001c0001t0007a0001c0001t0008others(6): Show | 40 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1392dupA | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 1392 | chr5 | 118839524 | |||||
| chr5:118839651
|
T | C | 1 | a0001c0001t0024 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1266A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 1266 | chr5 | 118839651 | |||||
| chr5:118839945
|
C | G | 23 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(20): Show | 92 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*972G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 972 | chr5 | 118839945 | |||||
| chr5:118839979
|
C | T | 21 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(18): Show | 66 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*938G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 938 | chr5 | 118839979 | |||||
| chr5:118840027
|
A | C | 1 | a0001c0001t0031 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*890T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 890 | chr5 | 118840027 | |||||
| chr5:118840229
|
A | G | 1 | a0001c0001t0016 | 2 | HG02976.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*688T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 688 | chr5 | 118840229 | |||||
| chr5:118840503
|
A | T | 2 | a0001c0001t0004a0001c0001t0028 | 11 | HG01496.hp1 HG01884.hp2 HG02486.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*414T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 414 | chr5 | 118840503 | |||||
| chr5:118840667
|
G | C | 1 | a0001c0001t0020 | 2 | HG01106.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*250C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 250 | chr5 | 118840667 | |||||
| chr5:118840712
|
T | C | 2 | a0001c0001t0003a0001c0001t0027 | 12 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*205A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 205 | chr5 | 118840712 | |||||
| chr5:118840723
|
G | A | 1 | a0001c0001t0028 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*194C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 194 | chr5 | 118840723 | |||||
| chr5:118840757
|
G | A | 2 | a0001c0001t0029a0001c0001t0030 | 2 | HG02257.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*160C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 160 | chr5 | 118840757 | |||||
| chr5:118840814
|
C | CATT | 23 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(20): Show | 92 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*102_*103insAAT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 6/6 | 102 | chr5 | 118840814 | |||||
| chr5:118988512
|
G | T | 1 | a0003c0005t0042 | 1 | HG02897.hp1 | 5_prime_UTR_variant | MODIFIER | c.-1C>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/6 | 1 | chr5 | 118988512 | |||||
| chr5:118988519
|
A | G | 1 | a0003c0005t0042 | 1 | HG02897.hp1 | 5_prime_UTR_variant | MODIFIER | c.-8T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/6 | 8 | chr5 | 118988519 | |||||
| chr5:118988521
|
T | A | 1 | a0003c0005t0042 | 1 | HG02897.hp1 | 5_prime_UTR_variant | MODIFIER | c.-10A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/6 | 10 | chr5 | 118988521 | |||||
| chr5:118988522
|
C | G | 1 | a0003c0005t0042 | 1 | HG02897.hp1 | 5_prime_UTR_variant | MODIFIER | c.-11G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/6 | 11 | chr5 | 118988522 | |||||
| chr5:118988523
|
C | A | 1 | a0003c0005t0042 | 1 | HG02897.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-12G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/6 | chr5 | 118988523 | ||||||
| chr5:118988528
|
A | G | 1 | a0003c0005t0042 | 1 | HG02897.hp1 | 5_prime_UTR_variant | MODIFIER | c.-17T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/6 | 17 | chr5 | 118988528 | |||||
| chr5:118988531
|
C | A | 1 | a0003c0005t0042 | 1 | HG02897.hp1 | 5_prime_UTR_variant | MODIFIER | c.-20G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/6 | 20 | chr5 | 118988531 | |||||
| chr5:118988534
|
T | A | 1 | a0003c0005t0042 | 1 | HG02897.hp1 | 5_prime_UTR_variant | MODIFIER | c.-23A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/6 | 23 | chr5 | 118988534 | |||||
| chr5:118988539
|
T | G | 1 | a0003c0005t0042 | 1 | HG02897.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-28A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/6 | chr5 | 118988539 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:118841132
|
A | G | 2 | a0001c0001t0016g0232a0001c0001t0016g0233 | 2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.727-45T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118841132 | ||||||
| chr5:118841147
|
T | C | 91 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(88): Show | 92 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.727-60A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118841147 | ||||||
| chr5:118841378
|
A | G | 91 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(88): Show | 92 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.727-291T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118841378 | ||||||
| chr5:118841541
|
G | A | 12 | a0001c0001t0004g0068a0001c0001t0004g0116a0001c0001t0004g0117others(9): Show | 12 | HG01496.hp1 HG01884.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.727-454C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118841541 | ||||||
| chr5:118841862
|
A | G | 91 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(88): Show | 92 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.727-775T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118841862 | ||||||
| chr5:118841930
|
A | G | 1 | a0001c0001t0002g0174 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.727-843T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118841930 | ||||||
| chr5:118842057
|
C | A | 91 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(88): Show | 92 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.727-970G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118842057 | ||||||
| chr5:118842242
|
T | A | 1 | a0001c0001t0032g0236 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.727-1155A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118842242 | ||||||
| chr5:118842451
|
C | T | 91 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(88): Show | 92 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.727-1364G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118842451 | ||||||
| chr5:118842483
|
T | C | 29 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(26): Show | 29 | HG00423.hp2 HG01192.hp2 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.727-1396A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118842483 | ||||||
| chr5:118842518
|
T | A | 1 | a0001c0001t0001g0187 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.727-1431A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118842518 | ||||||
| chr5:118842662
|
C | T | 2 | a0001c0001t0014g0227a0001c0001t0034g0228 | 2 | HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.727-1575G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118842662 | ||||||
| chr5:118842741
|
C | T | 91 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(88): Show | 92 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.727-1654G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118842741 | ||||||
| chr5:118842770
|
TAA | T | 91 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(88): Show | 92 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.727-1685_727-1684d others(4): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118842770 | ||||||
| chr5:118842861
|
C | T | 1 | a0001c0001t0022g0082 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.727-1774G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118842861 | ||||||
| chr5:118842950
|
CCT | C | 5 | a0001c0001t0010g0027a0001c0001t0010g0063a0002c0003t0010g0237others(2): Show | 5 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.727-1865_727-1864d others(4): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118842950 | ||||||
| chr5:118842953
|
CT | C | 68 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0203others(65): Show | 69 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.727-1867delA | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118842953 | ||||||
| chr5:118842953
|
CTT | C | 15 | a0001c0001t0002g0035a0001c0001t0002g0174a0001c0001t0005g0151others(12): Show | 15 | HG00642.hp2 HG00741.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.727-1868_727-1867d others(4): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118842953 | ||||||
| chr5:118843116
|
C | T | 1 | a0001c0001t0009g0149 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.727-2029G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118843116 | ||||||
| chr5:118843143
|
G | C | 1 | a0001c0001t0001g0061 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.727-2056C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118843143 | ||||||
| chr5:118843163
|
G | A | 1 | a0001c0001t0001g0079 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.727-2076C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118843163 | ||||||
| chr5:118843168
|
G | C | 5 | a0001c0001t0010g0027a0001c0001t0010g0063a0002c0003t0010g0237others(2): Show | 5 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.727-2081C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118843168 | ||||||
| chr5:118843207
|
G | A | 11 | a0001c0001t0004g0068a0001c0001t0004g0116a0001c0001t0004g0117others(8): Show | 11 | HG01496.hp1 HG01884.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.727-2120C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118843207 | ||||||
| chr5:118843351
|
GAGGGAGG others(9): Show |
G | 41 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(38): Show | 41 | HG00639.hp2 HG00733.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.727-2280_727-2265d others(18): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118843351 | ||||||
| chr5:118843371
|
G | GAGGAAGG others(13): Show |
1 | a0001c0001t0018g0001 | 2 | HG00642.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.727-2285_727-2284i others(22): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118843371 | ||||||
| chr5:118843371
|
G | GAGGAAGG others(17): Show |
30 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(27): Show | 30 | HG00099.hp1 HG00642.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.727-2285_727-2284i others(26): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118843371 | ||||||
| chr5:118843371
|
G | GAGGAAGG others(25): Show |
8 | a0001c0001t0004g0116a0001c0001t0004g0117a0001c0001t0004g0118others(5): Show | 8 | HG01884.hp2 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.727-2285_727-2284i others(34): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118843371 | ||||||
| chr5:118843371
|
G | GAGGAAGG others(29): Show |
2 | a0001c0001t0004g0136a0001c0001t0004g0137 | 2 | HG01496.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.727-2285_727-2284i others(38): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118843371 | ||||||
| chr5:118843371
|
G | GAGGAAGG others(21): Show |
9 | a0001c0001t0007g0141a0001c0001t0007g0208a0001c0001t0007g0209others(6): Show | 9 | HG02486.hp1 HG02572.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.727-2285_727-2284i others(30): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118843371 | ||||||
| chr5:118843409
|
T | C | 46 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(43): Show | 46 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.727-2322A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118843409 | ||||||
| chr5:118843436
|
A | G | 2 | a0001c0001t0020g0121a0001c0001t0020g0122 | 2 | HG01106.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.727-2349T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118843436 | ||||||
| chr5:118843465
|
G | A | 105 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(102): Show | 106 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.727-2378C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118843465 | ||||||
| chr5:118843560
|
C | T | 2 | a0001c0001t0020g0121a0001c0001t0020g0122 | 2 | HG01106.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.727-2473G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118843560 | ||||||
| chr5:118843680
|
T | C | 1 | a0001c0001t0003g0016 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.727-2593A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118843680 | ||||||
| chr5:118843717
|
A | G | 11 | a0001c0001t0001g0235a0001c0001t0012g0167a0001c0001t0012g0198others(8): Show | 11 | HG02055.hp2 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.727-2630T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118843717 | ||||||
| chr5:118843828
|
T | C | 3 | a0001c0001t0004g0117a0001c0001t0004g0136a0001c0001t0004g0137 | 3 | HG01496.hp1 HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.727-2741A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118843828 | ||||||
| chr5:118843871
|
T | C | 5 | a0001c0001t0010g0027a0001c0001t0010g0063a0002c0003t0010g0237others(2): Show | 5 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.727-2784A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118843871 | ||||||
| chr5:118844029
|
A | G | 2 | a0001c0001t0015g0133a0001c0001t0015g0134 | 2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.727-2942T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118844029 | ||||||
| chr5:118844043
|
T | A | 50 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(47): Show | 51 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.727-2956A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118844043 | ||||||
| chr5:118844160
|
T | C | 2 | a0001c0001t0020g0121a0001c0001t0020g0122 | 2 | HG01106.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.727-3073A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118844160 | ||||||
| chr5:118844174
|
C | T | 5 | a0001c0001t0010g0027a0001c0001t0010g0063a0002c0003t0010g0237others(2): Show | 5 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.727-3087G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118844174 | ||||||
| chr5:118844556
|
G | A | 9 | a0001c0001t0014g0115a0001c0001t0014g0227a0001c0001t0014g0229others(6): Show | 9 | HG01106.hp1 HG02630.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.727-3469C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118844556 | ||||||
| chr5:118844578
|
A | G | 5 | a0001c0001t0010g0027a0001c0001t0010g0063a0002c0003t0010g0237others(2): Show | 5 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.727-3491T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118844578 | ||||||
| chr5:118844636
|
T | G | 1 | a0001c0001t0003g0012 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.726+3454A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118844636 | ||||||
| chr5:118844653
|
A | G | 1 | a0001c0001t0030g0225 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.726+3437T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118844653 | ||||||
| chr5:118844965
|
C | T | 12 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(9): Show | 12 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.726+3125G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118844965 | ||||||
| chr5:118844977
|
T | A | 1 | a0001c0001t0001g0109 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.726+3113A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118844977 | ||||||
| chr5:118845240
|
T | C | 27 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(24): Show | 27 | HG00099.hp1 HG00642.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.726+2850A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118845240 | ||||||
| chr5:118845243
|
T | C | 3 | a0001c0001t0018g0001a0001c0001t0029g0132a0001c0001t0030g0225 | 4 | HG00642.hp1 HG01074.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.726+2847A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118845243 | ||||||
| chr5:118845340
|
G | A | 11 | a0001c0001t0001g0235a0001c0001t0012g0167a0001c0001t0012g0198others(8): Show | 11 | HG02055.hp2 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.726+2750C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118845340 | ||||||
| chr5:118845368
|
T | C | 5 | a0001c0001t0010g0027a0001c0001t0010g0063a0002c0003t0010g0237others(2): Show | 5 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.726+2722A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118845368 | ||||||
| chr5:118845382
|
C | G | 54 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(51): Show | 54 | HG00099.hp1 HG00642.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.726+2708G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118845382 | ||||||
| chr5:118845384
|
C | T | 105 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(102): Show | 106 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.726+2706G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118845384 | ||||||
| chr5:118845387
|
C | T | 27 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(24): Show | 27 | HG00099.hp1 HG00642.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.726+2703G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118845387 | ||||||
| chr5:118845511
|
C | T | 4 | a0001c0001t0015g0133a0001c0001t0015g0134a0001c0001t0015g0135others(1): Show | 4 | HG00741.hp1 HG01884.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.726+2579G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118845511 | ||||||
| chr5:118845850
|
T | G | 6 | a0001c0001t0001g0064a0001c0001t0013g0011a0001c0001t0013g0142others(3): Show | 6 | HG01255.hp1 HG01891.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.726+2240A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118845850 | ||||||
| chr5:118845874
|
T | A | 3 | a0001c0001t0018g0001a0001c0001t0029g0132a0001c0001t0030g0225 | 4 | HG00642.hp1 HG01074.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.726+2216A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118845874 | ||||||
| chr5:118846026
|
A | C | 1 | a0001c0001t0001g0099 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.726+2064T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118846026 | ||||||
| chr5:118846497
|
C | T | 1 | a0001c0001t0009g0147 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.726+1593G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118846497 | ||||||
| chr5:118846504
|
C | A | 12 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(9): Show | 12 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.726+1586G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118846504 | ||||||
| chr5:118846729
|
G | A | 1 | a0001c0001t0028g0138 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.726+1361C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118846729 | ||||||
| chr5:118846763
|
A | G | 2 | a0001c0001t0001g0177a0001c0001t0001g0179 | 2 | HG00280.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.726+1327T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118846763 | ||||||
| chr5:118846920
|
G | GCA | 12 | a0001c0001t0001g0051a0001c0001t0001g0061a0001c0001t0001g0062others(9): Show | 12 | HG00280.hp2 HG00323.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.726+1168_726+1169d others(4): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118846920 | ||||||
| chr5:118846920
|
G | GCACA | 29 | a0001c0001t0001g0031a0001c0001t0001g0036a0001c0001t0001g0037others(26): Show | 29 | HG00140.hp2 HG00544.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.726+1166_726+1169d others(6): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118846920 | ||||||
| chr5:118846920
|
G | GCACACA | 5 | a0001c0001t0001g0049a0001c0001t0001g0064a0001c0001t0001g0071others(2): Show | 5 | HG01255.hp1 HG01256.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.726+1164_726+1169d others(8): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118846920 | ||||||
| chr5:118846920
|
GCA | G | 33 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0069others(30): Show | 33 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.726+1168_726+1169d others(4): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118846920 | ||||||
| chr5:118846920
|
GCACA | G | 8 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0183others(5): Show | 8 | HG01257.hp2 HG01258.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.726+1166_726+1169d others(6): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118846920 | ||||||
| chr5:118846920
|
GCACACA | G | 10 | a0001c0001t0002g0160a0001c0001t0007g0141a0001c0001t0007g0208others(7): Show | 10 | HG01081.hp1 HG02486.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.726+1164_726+1169d others(8): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118846920 | ||||||
| chr5:118846920
|
GCACACAC others(1): Show |
G | 27 | a0001c0001t0002g0126a0001c0001t0002g0129a0001c0001t0002g0130others(24): Show | 27 | HG00733.hp2 HG01109.hp1 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.726+1162_726+1169d others(10): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118846920 | ||||||
| chr5:118846920
|
GCACACAC others(3): Show |
G | 27 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(24): Show | 27 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.726+1160_726+1169d others(12): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118846920 | ||||||
| chr5:118846920
|
GCACACAC others(5): Show |
G | 14 | a0001c0001t0004g0117a0001c0001t0004g0118a0001c0001t0004g0120others(11): Show | 14 | HG01496.hp1 HG01884.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.726+1158_726+1169d others(14): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118846920 | ||||||
| chr5:118846920
|
GCACACAC others(7): Show |
G | 3 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0004g0116 | 3 | HG00423.hp2 HG03130.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.726+1156_726+1169d others(16): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118846920 | ||||||
| chr5:118846920
|
GCACACAC others(23): Show |
G | 23 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(20): Show | 24 | HG00639.hp2 HG00642.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.726+1140_726+1169d others(32): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118846920 | ||||||
| chr5:118846959
|
C | T | 5 | a0001c0001t0010g0027a0001c0001t0010g0063a0002c0003t0010g0237others(2): Show | 5 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.726+1131G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118846959 | ||||||
| chr5:118847231
|
G | A | 3 | a0001c0001t0015g0133a0001c0001t0015g0134a0001c0001t0015g0135 | 3 | HG01884.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.726+859C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118847231 | ||||||
| chr5:118847266
|
G | A | 2 | a0001c0001t0019g0023a0001c0001t0019g0025 | 2 | HG01261.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.726+824C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118847266 | ||||||
| chr5:118847302
|
G | T | 1 | a0001c0001t0003g0017 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.726+788C>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118847302 | ||||||
| chr5:118847333
|
T | C | 3 | a0001c0001t0018g0001a0001c0001t0029g0132a0001c0001t0030g0225 | 4 | HG00642.hp1 HG01074.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.726+757A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118847333 | ||||||
| chr5:118847473
|
A | C | 1 | a0001c0001t0001g0101 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.726+617T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118847473 | ||||||
| chr5:118847565
|
A | G | 1 | a0001c0001t0005g0154 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.726+525T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118847565 | ||||||
| chr5:118847609
|
A | AT | 82 | a0001c0001t0001g0037a0001c0001t0001g0095a0001c0001t0002g0033others(79): Show | 83 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.726+480dupA | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118847609 | ||||||
| chr5:118847613
|
T | G | 1 | a0001c0001t0001g0182 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.726+477A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118847613 | ||||||
| chr5:118847753
|
C | A | 5 | a0001c0001t0010g0027a0001c0001t0010g0063a0002c0003t0010g0237others(2): Show | 5 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.726+337G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118847753 | ||||||
| chr5:118847914
|
AAC | A | 103 | a0001c0001t0001g0037a0001c0001t0001g0095a0001c0001t0002g0033others(100): Show | 104 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.726+174_726+175del others(2): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118847914 | ||||||
| chr5:118847926
|
G | A | 12 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(9): Show | 12 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.726+164C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 5/5 | chr5 | 118847926 | ||||||
| chr5:118848390
|
A | C | 11 | a0001c0001t0004g0068a0001c0001t0004g0116a0001c0001t0004g0117others(8): Show | 11 | HG01496.hp1 HG01884.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.598-172T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118848390 | ||||||
| chr5:118848418
|
C | T | 6 | a0001c0001t0013g0011a0001c0001t0013g0142a0001c0001t0013g0218others(3): Show | 6 | HG00741.hp1 HG01891.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.598-200G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118848418 | ||||||
| chr5:118848429
|
C | A | 9 | a0001c0001t0006g0029a0001c0001t0006g0047a0001c0001t0006g0059others(6): Show | 9 | HG00639.hp1 HG01123.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.598-211G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118848429 | ||||||
| chr5:118848537
|
G | C | 3 | a0001c0001t0020g0121a0001c0001t0020g0122a0001c0001t0032g0236 | 3 | HG01106.hp1 HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.598-319C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118848537 | ||||||
| chr5:118848598
|
T | C | 1 | a0001c0001t0001g0036 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.598-380A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118848598 | ||||||
| chr5:118848608
|
T | C | 1 | a0001c0001t0032g0236 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.598-390A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118848608 | ||||||
| chr5:118848653
|
G | C | 4 | a0001c0001t0014g0115a0001c0001t0014g0229a0001c0001t0014g0230others(1): Show | 4 | HG02970.hp1 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.598-435C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118848653 | ||||||
| chr5:118848759
|
C | A | 1 | a0001c0002t0037g0002 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.598-541G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118848759 | ||||||
| chr5:118848857
|
C | A | 10 | a0001c0001t0004g0116a0001c0001t0004g0117a0001c0001t0004g0118others(7): Show | 10 | HG01496.hp1 HG01884.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.598-639G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118848857 | ||||||
| chr5:118848945
|
C | T | 2 | a0001c0001t0020g0121a0001c0001t0020g0122 | 2 | HG01106.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.598-727G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118848945 | ||||||
| chr5:118849121
|
G | A | 105 | a0001c0001t0001g0037a0001c0001t0001g0095a0001c0001t0002g0033others(102): Show | 106 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.598-903C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118849121 | ||||||
| chr5:118849177
|
G | C | 7 | a0001c0001t0001g0098a0001c0001t0001g0103a0001c0001t0001g0104others(4): Show | 7 | HG00738.hp1 HG00741.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.598-959C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118849177 | ||||||
| chr5:118849243
|
T | A | 1 | a0001c0001t0008g0231 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.598-1025A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118849243 | ||||||
| chr5:118849333
|
C | T | 3 | a0001c0001t0009g0159a0001c0001t0017g0140a0001c0001t0017g0146 | 3 | HG01496.hp2 HG03688.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.598-1115G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118849333 | ||||||
| chr5:118849479
|
C | T | 6 | a0001c0001t0014g0115a0001c0001t0014g0227a0001c0001t0014g0229others(3): Show | 6 | HG02970.hp1 HG03041.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.598-1261G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118849479 | ||||||
| chr5:118849558
|
T | C | 5 | a0001c0001t0010g0027a0001c0001t0010g0063a0002c0003t0010g0237others(2): Show | 5 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.598-1340A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118849558 | ||||||
| chr5:118849766
|
T | A | 1 | a0001c0001t0001g0109 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.598-1548A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118849766 | ||||||
| chr5:118849767
|
A | C | 1 | a0001c0001t0001g0109 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.598-1549T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118849767 | ||||||
| chr5:118849951
|
C | T | 25 | a0001c0001t0001g0037a0001c0001t0001g0074a0001c0001t0001g0095others(22): Show | 25 | HG00099.hp1 HG00642.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.598-1733G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118849951 | ||||||
| chr5:118850072
|
G | C | 56 | a0001c0001t0001g0037a0001c0001t0001g0095a0001c0001t0002g0033others(53): Show | 56 | HG00099.hp1 HG00642.hp2 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.598-1854C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118850072 | ||||||
| chr5:118850151
|
A | G | 5 | a0001c0001t0010g0027a0001c0001t0010g0063a0002c0003t0010g0237others(2): Show | 5 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.598-1933T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118850151 | ||||||
| chr5:118850192
|
A | G | 34 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(31): Show | 35 | HG00639.hp2 HG00642.hp1 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.598-1974T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118850192 | ||||||
| chr5:118850309
|
C | CA | 47 | a0001c0001t0001g0030a0001c0001t0001g0064a0001c0001t0001g0076others(44): Show | 47 | HG00423.hp1 HG00544.hp1 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.598-2092dupT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118850309 | ||||||
| chr5:118850309
|
CA | C | 19 | a0001c0001t0004g0068a0001c0001t0004g0116a0001c0001t0004g0117others(16): Show | 20 | HG00642.hp1 HG00741.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.598-2092delT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118850309 | ||||||
| chr5:118850477
|
C | CA | 59 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(56): Show | 59 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.598-2260dupT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118850477 | ||||||
| chr5:118850477
|
C | CAA | 23 | a0001c0001t0001g0019a0001c0001t0001g0024a0001c0001t0001g0038others(20): Show | 23 | HG00140.hp2 HG00544.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.598-2261_598-2260d others(4): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118850477 | ||||||
| chr5:118850477
|
C | CAAA | 5 | a0001c0001t0001g0030a0001c0001t0001g0039a0001c0001t0001g0051others(2): Show | 5 | HG00733.hp1 HG02615.hp2 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.598-2262_598-2260d others(5): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118850477 | ||||||
| chr5:118850477
|
C | CAAAAAAA others(26): Show |
1 | a0001c0001t0014g0227 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.598-2292_598-2260d others(35): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118850477 | ||||||
| chr5:118850477
|
CA | C | 22 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0193others(19): Show | 22 | HG01070.hp1 HG01099.hp1 HG01168.hp2 others(19): Show |
intron_variant | MODIFIER | c.598-2260delT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118850477 | ||||||
| chr5:118850477
|
CAA | C | 21 | a0001c0001t0001g0037a0001c0001t0001g0095a0001c0001t0002g0033others(18): Show | 21 | HG00099.hp1 HG00642.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.598-2261_598-2260d others(4): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118850477 | ||||||
| chr5:118850477
|
CAAA | C | 15 | a0001c0001t0005g0162a0001c0001t0007g0209a0001c0001t0007g0214others(12): Show | 15 | HG01106.hp1 HG01496.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.598-2262_598-2260d others(5): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118850477 | ||||||
| chr5:118850477
|
CAAAA | C | 19 | a0001c0001t0005g0151a0001c0001t0005g0154a0001c0001t0005g0155others(16): Show | 19 | HG00733.hp2 HG01109.hp1 HG02056.hp2 others(16): Show |
intron_variant | MODIFIER | c.598-2263_598-2260d others(6): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118850477 | ||||||
| chr5:118850477
|
CAAAAAAA others(3): Show |
C | 14 | a0001c0001t0004g0116a0001c0001t0004g0117a0001c0001t0004g0118others(11): Show | 15 | HG00642.hp1 HG01074.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.598-2269_598-2260d others(12): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118850477 | ||||||
| chr5:118850477
|
CAAAAAAA others(6): Show |
C | 5 | a0001c0001t0010g0027a0001c0001t0010g0063a0002c0003t0010g0237others(2): Show | 5 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.598-2272_598-2260d others(15): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118850477 | ||||||
| chr5:118850512
|
T | G | 2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | HG01099.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.598-2294A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118850512 | ||||||
| chr5:118850568
|
A | AAGAAAAC others(1): Show |
5 | a0001c0001t0006g0029a0001c0001t0006g0083a0001c0001t0006g0091others(2): Show | 5 | HG01168.hp2 HG01169.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.598-2358_598-2351d others(10): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118850568 | ||||||
| chr5:118850956
|
C | T | 1 | a0001c0001t0021g0010 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.598-2738G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118850956 | ||||||
| chr5:118851006
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.598-2788C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118851006 | ||||||
| chr5:118851047
|
G | C | 1 | a0001c0001t0001g0030 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.598-2829C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118851047 | ||||||
| chr5:118851136
|
T | C | 12 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(9): Show | 12 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.598-2918A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118851136 | ||||||
| chr5:118851163
|
G | A | 5 | a0001c0001t0010g0027a0001c0001t0010g0063a0002c0003t0010g0237others(2): Show | 5 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.598-2945C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118851163 | ||||||
| chr5:118851218
|
C | CA | 49 | a0001c0001t0001g0026a0001c0001t0001g0031a0001c0001t0001g0041others(46): Show | 49 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.598-3001dupT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118851218 | ||||||
| chr5:118851218
|
C | CAA | 10 | a0001c0001t0004g0116a0001c0001t0004g0117a0001c0001t0004g0118others(7): Show | 10 | HG01496.hp1 HG01884.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.598-3002_598-3001d others(4): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118851218 | ||||||
| chr5:118851218
|
CA | C | 13 | a0001c0001t0001g0021a0001c0001t0001g0048a0001c0001t0001g0095others(10): Show | 13 | HG00099.hp2 HG00733.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.598-3001delT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118851218 | ||||||
| chr5:118851234
|
A | G | 2 | a0001c0001t0001g0081a0001c0001t0007g0213 | 2 | HG02895.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.598-3016T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118851234 | ||||||
| chr5:118851386
|
T | TATCG | 18 | a0001c0001t0005g0151a0001c0001t0005g0154a0001c0001t0005g0155others(15): Show | 18 | HG00733.hp2 HG01109.hp1 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.598-3172_598-3169d others(6): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118851386 | ||||||
| chr5:118851417
|
A | G | 5 | a0001c0001t0010g0027a0001c0001t0010g0063a0002c0003t0010g0237others(2): Show | 5 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.598-3199T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118851417 | ||||||
| chr5:118851586
|
GC | G | 5 | a0001c0001t0012g0167a0001c0001t0012g0198a0001c0001t0012g0199others(2): Show | 5 | HG02258.hp1 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.598-3369delG | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118851586 | ||||||
| chr5:118851643
|
A | T | 3 | a0001c0001t0009g0159a0001c0001t0017g0140a0001c0001t0017g0146 | 3 | HG01496.hp2 HG03688.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.598-3425T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118851643 | ||||||
| chr5:118851775
|
C | T | 1 | a0001c0001t0036g0178 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.598-3557G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118851775 | ||||||
| chr5:118851808
|
G | A | 2 | a0001c0001t0006g0092a0001c0001t0006g0093 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.598-3590C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118851808 | ||||||
| chr5:118851839
|
T | TA | 7 | a0001c0001t0001g0049a0001c0001t0001g0172a0001c0001t0012g0167others(4): Show | 7 | HG01981.hp2 HG02258.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.598-3622dupT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118851839 | ||||||
| chr5:118851839
|
TA | T | 48 | a0001c0001t0001g0173a0001c0001t0005g0151a0001c0001t0005g0154others(45): Show | 49 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.598-3622delT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118851839 | ||||||
| chr5:118851839
|
TAA | T | 18 | a0001c0001t0004g0116a0001c0001t0004g0117a0001c0001t0004g0118others(15): Show | 18 | HG01106.hp1 HG01496.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.598-3623_598-3622d others(4): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118851839 | ||||||
| chr5:118852014
|
G | A | 20 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(17): Show | 20 | HG00639.hp2 HG00741.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.598-3796C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118852014 | ||||||
| chr5:118852283
|
A | G | 12 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(9): Show | 12 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.598-4065T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118852283 | ||||||
| chr5:118852359
|
G | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0028 | 2 | HG00423.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.598-4141C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118852359 | ||||||
| chr5:118852365
|
AAAGT | A | 6 | a0001c0001t0008g0204a0001c0001t0008g0220a0001c0001t0008g0221others(3): Show | 6 | HG01891.hp2 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.598-4151_598-4148d others(6): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118852365 | ||||||
| chr5:118852485
|
C | T | 12 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(9): Show | 12 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.598-4267G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118852485 | ||||||
| chr5:118852555
|
G | C | 1 | a0001c0001t0039g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.598-4337C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118852555 | ||||||
| chr5:118852568
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.598-4350T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118852568 | ||||||
| chr5:118852647
|
G | A | 2 | a0001c0001t0029g0132a0001c0001t0030g0225 | 2 | HG02257.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.598-4429C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118852647 | ||||||
| chr5:118852666
|
C | G | 2 | a0001c0001t0014g0227a0001c0001t0034g0228 | 2 | HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.598-4448G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118852666 | ||||||
| chr5:118852717
|
GAT | G | 174 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(171): Show | 175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.598-4501_598-4500d others(4): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118852717 | ||||||
| chr5:118852802
|
A | C | 1 | a0001c0001t0002g0043 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.598-4584T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118852802 | ||||||
| chr5:118852843
|
G | C | 10 | a0001c0001t0004g0116a0001c0001t0004g0117a0001c0001t0004g0118others(7): Show | 10 | HG01496.hp1 HG01884.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.598-4625C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118852843 | ||||||
| chr5:118852996
|
G | C | 1 | a0001c0001t0020g0122 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.598-4778C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118852996 | ||||||
| chr5:118853196
|
T | C | 2 | a0001c0001t0016g0232a0001c0001t0016g0233 | 2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.598-4978A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118853196 | ||||||
| chr5:118853198
|
C | T | 20 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(17): Show | 20 | HG00639.hp2 HG00741.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.598-4980G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118853198 | ||||||
| chr5:118853388
|
C | T | 1 | a0001c0001t0009g0148 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.598-5170G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118853388 | ||||||
| chr5:118853473
|
T | C | 1 | a0001c0001t0001g0172 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.598-5255A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118853473 | ||||||
| chr5:118853519
|
T | C | 6 | a0001c0001t0013g0011a0001c0001t0013g0142a0001c0001t0013g0218others(3): Show | 6 | HG00741.hp1 HG01891.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.598-5301A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118853519 | ||||||
| chr5:118853525
|
A | T | 27 | a0001c0001t0005g0151a0001c0001t0005g0154a0001c0001t0005g0155others(24): Show | 27 | HG00733.hp2 HG01109.hp1 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.598-5307T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118853525 | ||||||
| chr5:118853771
|
G | C | 3 | a0001c0001t0015g0133a0001c0001t0015g0134a0001c0001t0015g0135 | 3 | HG01884.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.598-5553C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118853771 | ||||||
| chr5:118853840
|
G | A | 1 | a0001c0001t0026g0212 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.598-5622C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118853840 | ||||||
| chr5:118853856
|
A | C | 6 | a0001c0001t0014g0115a0001c0001t0014g0227a0001c0001t0014g0229others(3): Show | 6 | HG02970.hp1 HG03041.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.598-5638T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118853856 | ||||||
| chr5:118854266
|
T | C | 27 | a0001c0001t0005g0151a0001c0001t0005g0154a0001c0001t0005g0155others(24): Show | 27 | HG00733.hp2 HG01109.hp1 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.598-6048A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118854266 | ||||||
| chr5:118854454
|
A | G | 18 | a0001c0001t0005g0151a0001c0001t0005g0154a0001c0001t0005g0155others(15): Show | 18 | HG00733.hp2 HG01109.hp1 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.598-6236T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118854454 | ||||||
| chr5:118854514
|
GA | G | 11 | a0001c0001t0004g0068a0001c0001t0004g0116a0001c0001t0004g0117others(8): Show | 11 | HG01496.hp1 HG01884.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.598-6297delT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118854514 | ||||||
| chr5:118854628
|
TACACACA others(9): Show |
T | 5 | a0001c0001t0010g0027a0001c0001t0010g0063a0002c0003t0010g0237others(2): Show | 5 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.598-6426_598-6411d others(18): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118854628 | ||||||
| chr5:118854715
|
G | A | 20 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(17): Show | 20 | HG00639.hp2 HG00741.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.598-6497C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118854715 | ||||||
| chr5:118854886
|
G | T | 183 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(180): Show | 184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.598-6668C>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118854886 | ||||||
| chr5:118854990
|
C | G | 5 | a0001c0001t0010g0027a0001c0001t0010g0063a0002c0003t0010g0237others(2): Show | 5 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.598-6772G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118854990 | ||||||
| chr5:118855101
|
A | G | 1 | a0001c0001t0001g0039 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.598-6883T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118855101 | ||||||
| chr5:118855176
|
A | T | 2 | a0001c0001t0016g0232a0001c0001t0016g0233 | 2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.598-6958T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118855176 | ||||||
| chr5:118855178
|
AT | A | 3 | a0001c0001t0005g0161a0001c0001t0005g0162a0001c0001t0005g0184 | 3 | HG03239.hp1 HG03492.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.598-6961delA | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118855178 | ||||||
| chr5:118855192
|
T | C | 5 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(2): Show | 5 | HG01071.hp2 HG01261.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.598-6974A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118855192 | ||||||
| chr5:118855195
|
C | T | 138 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(135): Show | 138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.598-6977G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118855195 | ||||||
| chr5:118855199
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.598-6981G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118855199 | ||||||
| chr5:118855239
|
GTAAAACT others(3): Show |
G | 1 | a0001c0001t0030g0225 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.598-7031_598-7022d others(12): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118855239 | ||||||
| chr5:118855245
|
C | A | 13 | a0001c0001t0004g0068a0001c0001t0004g0116a0001c0001t0004g0117others(10): Show | 14 | HG00642.hp1 HG01074.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.598-7027G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118855245 | ||||||
| chr5:118855246
|
T | G | 13 | a0001c0001t0004g0068a0001c0001t0004g0116a0001c0001t0004g0117others(10): Show | 14 | HG00642.hp1 HG01074.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.598-7028A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118855246 | ||||||
| chr5:118855300
|
A | C | 1 | a0001c0004t0001g0032 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.598-7082T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118855300 | ||||||
| chr5:118855415
|
A | T | 3 | a0001c0001t0015g0133a0001c0001t0015g0134a0001c0001t0015g0135 | 3 | HG01884.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.598-7197T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118855415 | ||||||
| chr5:118855435
|
TA | T | 20 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(17): Show | 20 | HG00639.hp2 HG00741.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.598-7218delT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118855435 | ||||||
| chr5:118855485
|
A | T | 20 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(17): Show | 20 | HG00639.hp2 HG00741.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.598-7267T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118855485 | ||||||
| chr5:118855768
|
C | T | 1 | a0001c0001t0008g0221 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.598-7550G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118855768 | ||||||
| chr5:118855909
|
T | A | 1 | a0001c0001t0021g0010 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.598-7691A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118855909 | ||||||
| chr5:118856103
|
G | A | 32 | a0001c0001t0001g0031a0001c0001t0001g0037a0001c0001t0001g0041others(29): Show | 32 | HG00280.hp2 HG00323.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.598-7885C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118856103 | ||||||
| chr5:118856204
|
C | A | 6 | a0001c0001t0001g0235a0001c0002t0001g0003a0001c0002t0001g0004others(3): Show | 6 | HG02055.hp2 HG02145.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.598-7986G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118856204 | ||||||
| chr5:118856273
|
T | C | 20 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(17): Show | 20 | HG00639.hp2 HG00741.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.598-8055A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118856273 | ||||||
| chr5:118856310
|
C | T | 14 | a0001c0001t0004g0068a0001c0001t0004g0116a0001c0001t0004g0117others(11): Show | 15 | HG00642.hp1 HG01074.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.598-8092G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118856310 | ||||||
| chr5:118856595
|
T | C | 1 | a0001c0001t0001g0024 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.598-8377A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118856595 | ||||||
| chr5:118856615
|
A | G | 3 | a0001c0001t0015g0133a0001c0001t0015g0134a0001c0001t0015g0135 | 3 | HG01884.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.598-8397T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118856615 | ||||||
| chr5:118856623
|
C | T | 1 | a0001c0001t0001g0164 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.598-8405G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118856623 | ||||||
| chr5:118856764
|
C | CT | 115 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0024others(112): Show | 116 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.598-8547dupA | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118856764 | ||||||
| chr5:118856764
|
C | CTT | 9 | a0001c0001t0001g0049a0001c0001t0001g0090a0001c0001t0001g0235others(6): Show | 9 | HG01256.hp1 HG01891.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.598-8548_598-8547d others(4): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118856764 | ||||||
| chr5:118856764
|
C | CTTT | 48 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(45): Show | 48 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.598-8549_598-8547d others(5): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118856764 | ||||||
| chr5:118856764
|
CT | C | 21 | a0001c0001t0001g0164a0001c0001t0003g0007a0001c0001t0003g0012others(18): Show | 21 | HG01243.hp2 HG01255.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.598-8547delA | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118856764 | ||||||
| chr5:118856775
|
T | C | 3 | a0001c0001t0013g0011a0001c0001t0013g0218a0001c0001t0013g0219 | 3 | HG03041.hp2 NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.598-8557A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118856775 | ||||||
| chr5:118856846
|
C | A | 2 | a0001c0001t0014g0229a0001c0001t0014g0230 | 2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.598-8628G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118856846 | ||||||
| chr5:118856869
|
C | T | 99 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(96): Show | 100 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.598-8651G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118856869 | ||||||
| chr5:118856876
|
G | C | 6 | a0001c0001t0008g0204a0001c0001t0008g0220a0001c0001t0008g0221others(3): Show | 6 | HG01891.hp2 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.598-8658C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118856876 | ||||||
| chr5:118856917
|
T | C | 96 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(93): Show | 97 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.598-8699A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118856917 | ||||||
| chr5:118856936
|
T | G | 1 | a0001c0001t0001g0128 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.598-8718A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118856936 | ||||||
| chr5:118857075
|
C | A | 2 | a0001c0001t0001g0186a0001c0001t0001g0188 | 2 | HG01123.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.598-8857G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118857075 | ||||||
| chr5:118857114
|
T | C | 1 | a0001c0001t0002g0035 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.598-8896A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118857114 | ||||||
| chr5:118857148
|
G | T | 1 | a0001c0001t0001g0098 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.598-8930C>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118857148 | ||||||
| chr5:118857165
|
G | A | 5 | a0001c0001t0010g0027a0001c0001t0010g0063a0002c0003t0010g0237others(2): Show | 5 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.598-8947C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118857165 | ||||||
| chr5:118857289
|
T | C | 1 | a0002c0003t0010g0240 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.598-9071A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118857289 | ||||||
| chr5:118857300
|
G | A | 1 | a0001c0001t0001g0164 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.598-9082C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118857300 | ||||||
| chr5:118857378
|
T | A | 3 | a0001c0001t0015g0133a0001c0001t0015g0134a0001c0001t0015g0135 | 3 | HG01884.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.598-9160A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118857378 | ||||||
| chr5:118857570
|
T | C | 6 | a0001c0001t0013g0011a0001c0001t0013g0142a0001c0001t0013g0218others(3): Show | 6 | HG00741.hp1 HG01891.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.598-9352A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118857570 | ||||||
| chr5:118857733
|
G | A | 13 | a0001c0001t0004g0068a0001c0001t0004g0116a0001c0001t0004g0117others(10): Show | 13 | HG01496.hp1 HG01884.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.598-9515C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118857733 | ||||||
| chr5:118858094
|
T | C | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG01192.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.598-9876A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118858094 | ||||||
| chr5:118858172
|
C | CA | 6 | a0001c0001t0008g0204a0001c0001t0008g0220a0001c0001t0008g0221others(3): Show | 6 | HG01891.hp2 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.598-9955dupT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118858172 | ||||||
| chr5:118858209
|
A | T | 30 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(27): Show | 30 | HG00639.hp2 HG00733.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.598-9991T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118858209 | ||||||
| chr5:118858317
|
T | C | 1 | a0001c0001t0018g0001 | 2 | HG00642.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.598-10099A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118858317 | ||||||
| chr5:118858371
|
T | C | 3 | a0001c0001t0015g0133a0001c0001t0015g0134a0001c0001t0015g0135 | 3 | HG01884.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.598-10153A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118858371 | ||||||
| chr5:118858441
|
G | A | 6 | a0001c0001t0013g0011a0001c0001t0013g0142a0001c0001t0013g0218others(3): Show | 6 | HG00741.hp1 HG01891.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.598-10223C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118858441 | ||||||
| chr5:118858487
|
G | C | 1 | a0001c0001t0004g0068 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.598-10269C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118858487 | ||||||
| chr5:118858702
|
A | G | 2 | a0001c0001t0029g0132a0001c0001t0030g0225 | 2 | HG02257.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.598-10484T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118858702 | ||||||
| chr5:118859089
|
T | C | 6 | a0001c0001t0013g0011a0001c0001t0013g0142a0001c0001t0013g0218others(3): Show | 6 | HG00741.hp1 HG01891.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.598-10871A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118859089 | ||||||
| chr5:118859145
|
T | C | 6 | a0001c0001t0014g0115a0001c0001t0014g0227a0001c0001t0014g0229others(3): Show | 6 | HG02970.hp1 HG03041.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.598-10927A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118859145 | ||||||
| chr5:118859173
|
G | A | 1 | a0001c0001t0005g0184 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.598-10955C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118859173 | ||||||
| chr5:118859186
|
T | C | 1 | a0001c0001t0003g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.598-10968A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118859186 | ||||||
| chr5:118859206
|
GA | G | 6 | a0001c0001t0001g0030a0001c0001t0001g0175a0001c0001t0001g0194others(3): Show | 6 | HG01106.hp1 HG02280.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.598-10989delT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118859206 | ||||||
| chr5:118859216
|
A | C | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG01934.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.598-10998T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118859216 | ||||||
| chr5:118859243
|
C | T | 1 | a0001c0001t0024g0206 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.598-11025G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118859243 | ||||||
| chr5:118859273
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.598-11055T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118859273 | ||||||
| chr5:118859414
|
A | C | 96 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(93): Show | 97 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.598-11196T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118859414 | ||||||
| chr5:118859481
|
T | C | 1 | a0001c0001t0001g0024 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.598-11263A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118859481 | ||||||
| chr5:118859773
|
T | C | 2 | a0001c0001t0020g0121a0001c0001t0020g0122 | 2 | HG01106.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.598-11555A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118859773 | ||||||
| chr5:118859984
|
A | G | 30 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(27): Show | 30 | HG00639.hp2 HG00733.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.598-11766T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118859984 | ||||||
| chr5:118860067
|
A | G | 2 | a0001c0001t0016g0232a0001c0001t0016g0233 | 2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.598-11849T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118860067 | ||||||
| chr5:118860356
|
T | C | 2 | a0001c0001t0014g0229a0001c0001t0014g0230 | 2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.598-12138A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118860356 | ||||||
| chr5:118860435
|
C | A | 1 | a0001c0001t0004g0120 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.598-12217G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118860435 | ||||||
| chr5:118860470
|
T | C | 2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | HG01099.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.598-12252A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118860470 | ||||||
| chr5:118860753
|
T | C | 6 | a0001c0001t0014g0115a0001c0001t0014g0227a0001c0001t0014g0229others(3): Show | 6 | HG02970.hp1 HG03041.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.598-12535A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118860753 | ||||||
| chr5:118860819
|
C | G | 28 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(25): Show | 29 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.598-12601G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118860819 | ||||||
| chr5:118860829
|
C | A | 1 | a0001c0001t0001g0066 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.598-12611G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118860829 | ||||||
| chr5:118860991
|
T | C | 8 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(5): Show | 8 | HG01243.hp2 HG01255.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.598-12773A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118860991 | ||||||
| chr5:118861042
|
A | G | 1 | a0001c0001t0033g0205 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.598-12824T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118861042 | ||||||
| chr5:118861108
|
T | C | 1 | a0001c0001t0032g0236 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.598-12890A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118861108 | ||||||
| chr5:118861221
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.598-13003C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118861221 | ||||||
| chr5:118861252
|
G | C | 1 | a0001c0001t0032g0236 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.598-13034C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118861252 | ||||||
| chr5:118861359
|
T | A | 2 | a0001c0001t0002g0129a0001c0001t0002g0130 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.598-13141A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118861359 | ||||||
| chr5:118861559
|
G | A | 6 | a0001c0001t0014g0115a0001c0001t0014g0227a0001c0001t0014g0229others(3): Show | 6 | HG02970.hp1 HG03041.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.598-13341C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118861559 | ||||||
| chr5:118861574
|
A | AT | 15 | a0001c0001t0005g0151a0001c0001t0005g0154a0001c0001t0005g0155others(12): Show | 15 | HG00733.hp2 HG01109.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.598-13357dupA | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118861574 | ||||||
| chr5:118861583
|
T | TA | 3 | a0001c0001t0005g0161a0001c0001t0005g0162a0001c0001t0005g0184 | 3 | HG03239.hp1 HG03492.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.598-13366dupT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118861583 | ||||||
| chr5:118861583
|
T | TTA | 12 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(9): Show | 12 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.598-13366_598-1336 others(6): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118861583 | ||||||
| chr5:118861584
|
A | T | 1 | a0001c0001t0001g0143 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.598-13366T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118861584 | ||||||
| chr5:118861613
|
C | G | 1 | a0001c0001t0007g0209 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.598-13395G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118861613 | ||||||
| chr5:118861633
|
A | G | 3 | a0001c0001t0007g0141a0001c0001t0007g0208a0001c0001t0007g0209 | 3 | HG02630.hp1 HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.598-13415T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118861633 | ||||||
| chr5:118861770
|
T | C | 14 | a0001c0001t0004g0068a0001c0001t0004g0116a0001c0001t0004g0117others(11): Show | 15 | HG00642.hp1 HG01074.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.598-13552A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118861770 | ||||||
| chr5:118861852
|
G | A | 2 | a0001c0001t0015g0133a0001c0001t0015g0134 | 2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.598-13634C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118861852 | ||||||
| chr5:118862067
|
T | G | 8 | a0001c0001t0013g0011a0001c0001t0013g0142a0001c0001t0013g0218others(5): Show | 8 | HG00741.hp1 HG01891.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.598-13849A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118862067 | ||||||
| chr5:118862224
|
T | C | 11 | a0001c0001t0004g0068a0001c0001t0004g0116a0001c0001t0004g0117others(8): Show | 11 | HG01496.hp1 HG01884.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.598-14006A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118862224 | ||||||
| chr5:118862225
|
C | T | 14 | a0001c0001t0004g0068a0001c0001t0004g0116a0001c0001t0004g0117others(11): Show | 15 | HG00642.hp1 HG01074.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.598-14007G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118862225 | ||||||
| chr5:118862331
|
A | G | 3 | a0001c0001t0015g0133a0001c0001t0015g0134a0001c0001t0015g0135 | 3 | HG01884.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.598-14113T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118862331 | ||||||
| chr5:118862496
|
T | C | 1 | a0001c0001t0003g0013 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.598-14278A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118862496 | ||||||
| chr5:118862591
|
T | C | 1 | a0001c0001t0005g0158 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.598-14373A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118862591 | ||||||
| chr5:118862615
|
A | G | 1 | a0001c0001t0008g0221 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.598-14397T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118862615 | ||||||
| chr5:118862675
|
T | G | 2 | a0001c0001t0002g0129a0001c0001t0002g0130 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.598-14457A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118862675 | ||||||
| chr5:118862839
|
T | C | 1 | a0001c0001t0001g0071 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.598-14621A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118862839 | ||||||
| chr5:118863026
|
A | G | 11 | a0001c0001t0004g0068a0001c0001t0004g0116a0001c0001t0004g0117others(8): Show | 11 | HG01496.hp1 HG01884.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.598-14808T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118863026 | ||||||
| chr5:118863055
|
T | TA | 51 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(48): Show | 51 | HG00423.hp2 HG00544.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.598-14838dupT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118863055 | ||||||
| chr5:118863085
|
G | A | 1 | a0001c0001t0014g0115 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.598-14867C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118863085 | ||||||
| chr5:118863555
|
G | A | 2 | a0001c0001t0020g0122a0001c0001t0032g0236 | 2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.598-15337C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118863555 | ||||||
| chr5:118863701
|
T | C | 1 | a0001c0001t0008g0221 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.598-15483A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118863701 | ||||||
| chr5:118864023
|
G | T | 3 | a0001c0001t0015g0133a0001c0001t0015g0134a0001c0001t0015g0135 | 3 | HG01884.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.598-15805C>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118864023 | ||||||
| chr5:118864064
|
T | TG | 97 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(94): Show | 98 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.598-15847_598-1584 others(5): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118864064 | ||||||
| chr5:118864065
|
T | C | 97 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(94): Show | 98 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.598-15847A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118864065 | ||||||
| chr5:118864069
|
C | T | 97 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(94): Show | 98 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.598-15851G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118864069 | ||||||
| chr5:118864070
|
A | AGTTTCCT others(2445): Show |
1 | a0001c0001t0002g0058 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.598-15853_598-1585 others(2456): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118864070 | ||||||
| chr5:118864070
|
A | AGTTTCTT others(2445): Show |
1 | a0001c0001t0023g0226 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.598-15853_598-1585 others(2456): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118864070 | ||||||
| chr5:118864070
|
A | AGTTTCTT others(2445): Show |
1 | a0001c0001t0008g0221 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.598-15853_598-1585 others(2456): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118864070 | ||||||
| chr5:118864070
|
A | AGTTTCTT others(2445): Show |
2 | a0001c0001t0004g0139a0001c0001t0028g0138 | 2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.598-15853_598-1585 others(2456): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118864070 | ||||||
| chr5:118864070
|
A | AGTTTCTT others(2445): Show |
5 | a0001c0001t0010g0027a0001c0001t0010g0063a0002c0003t0010g0237others(2): Show | 5 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.598-15853_598-1585 others(2456): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118864070 | ||||||
| chr5:118864070
|
A | AGTTTCTT others(2445): Show |
1 | a0001c0001t0004g0117 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.598-15853_598-1585 others(2456): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118864070 | ||||||
| chr5:118864070
|
A | AGTTTCTT others(2445): Show |
1 | a0001c0001t0024g0206 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.598-15853_598-1585 others(2456): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118864070 | ||||||
| chr5:118864070
|
A | AGTTTCTT others(2445): Show |
50 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(47): Show | 51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.598-15853_598-1585 others(2456): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118864070 | ||||||
| chr5:118864070
|
A | AGTTTCTT others(2445): Show |
1 | a0001c0001t0005g0156 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.598-15853_598-1585 others(2456): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118864070 | ||||||
| chr5:118864070
|
A | AGTTTCTT others(2445): Show |
32 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(29): Show | 32 | HG00099.hp1 HG00642.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.598-15853_598-1585 others(2456): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118864070 | ||||||
| chr5:118864070
|
A | AGTTTCTT others(2445): Show |
1 | a0001c0001t0029g0132 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.598-15853_598-1585 others(2456): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118864070 | ||||||
| chr5:118864070
|
A | AGTTTCTT others(2445): Show |
1 | a0001c0001t0030g0225 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.598-15853_598-1585 others(2456): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118864070 | ||||||
| chr5:118864072
|
A | C | 97 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(94): Show | 98 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.598-15854T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118864072 | ||||||
| chr5:118864075
|
C | G | 97 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(94): Show | 98 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.598-15857G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118864075 | ||||||
| chr5:118864080
|
T | C | 97 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(94): Show | 98 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.598-15862A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118864080 | ||||||
| chr5:118864094
|
G | A | 96 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(93): Show | 97 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.598-15876C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118864094 | ||||||
| chr5:118864096
|
C | T | 2 | a0001c0001t0001g0076a0001c0001t0001g0077 | 2 | HG00735.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.598-15878G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118864096 | ||||||
| chr5:118864106
|
A | G | 3 | a0001c0001t0001g0175a0001c0001t0001g0194a0001c0002t0037g0002 | 3 | HG02280.hp1 HG02615.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.598-15888T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118864106 | ||||||
| chr5:118864272
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.598-16054A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118864272 | ||||||
| chr5:118864298
|
C | A | 5 | a0001c0001t0012g0167a0001c0001t0012g0198a0001c0001t0012g0199others(2): Show | 5 | HG02258.hp1 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.598-16080G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118864298 | ||||||
| chr5:118864524
|
A | G | 9 | a0001c0001t0007g0141a0001c0001t0007g0208a0001c0001t0007g0209others(6): Show | 9 | HG02486.hp1 HG02572.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.598-16306T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118864524 | ||||||
| chr5:118864529
|
TA | T | 7 | a0001c0001t0001g0109a0001c0001t0001g0177a0001c0001t0007g0210others(4): Show | 7 | HG01081.hp2 HG02486.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.598-16312delT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118864529 | ||||||
| chr5:118864641
|
AT | A | 25 | a0001c0001t0001g0066a0001c0001t0004g0068a0001c0001t0007g0141others(22): Show | 26 | HG00642.hp1 HG01074.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.598-16424delA | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118864641 | ||||||
| chr5:118864757
|
A | G | 68 | a0001c0001t0001g0164a0001c0001t0003g0007a0001c0001t0003g0008others(65): Show | 69 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.598-16539T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118864757 | ||||||
| chr5:118864828
|
C | T | 2 | a0001c0001t0014g0229a0001c0001t0014g0230 | 2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.598-16610G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118864828 | ||||||
| chr5:118865008
|
G | C | 1 | a0001c0001t0001g0224 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.598-16790C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118865008 | ||||||
| chr5:118865129
|
T | C | 1 | a0001c0001t0001g0234 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.598-16911A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118865129 | ||||||
| chr5:118865244
|
G | A | 2 | a0001c0001t0004g0139a0001c0001t0028g0138 | 2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.598-17026C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118865244 | ||||||
| chr5:118865377
|
T | C | 2 | a0001c0001t0029g0132a0001c0001t0030g0225 | 2 | HG02257.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.598-17159A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118865377 | ||||||
| chr5:118865402
|
C | T | 2 | a0001c0001t0016g0232a0001c0001t0016g0233 | 2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.598-17184G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118865402 | ||||||
| chr5:118865448
|
A | T | 1 | a0001c0001t0019g0023 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.598-17230T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118865448 | ||||||
| chr5:118865626
|
A | G | 1 | a0001c0001t0005g0154 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.598-17408T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118865626 | ||||||
| chr5:118865762
|
C | T | 1 | a0001c0001t0001g0095 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.598-17544G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118865762 | ||||||
| chr5:118865821
|
T | C | 6 | a0001c0001t0014g0115a0001c0001t0014g0227a0001c0001t0014g0229others(3): Show | 6 | HG02970.hp1 HG03041.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.598-17603A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118865821 | ||||||
| chr5:118865883
|
G | A | 5 | a0001c0001t0014g0227a0001c0001t0014g0229a0001c0001t0014g0230others(2): Show | 5 | HG02970.hp1 HG03041.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.598-17665C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118865883 | ||||||
| chr5:118865885
|
C | T | 12 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(9): Show | 12 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.598-17667G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118865885 | ||||||
| chr5:118865995
|
C | CGT | 3 | a0001c0001t0001g0094a0001c0001t0006g0072a0001c0002t0001g0004 | 3 | HG02055.hp2 HG03239.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.598-17779_598-1777 others(6): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118865995 | ||||||
| chr5:118865995
|
CGTGT | C | 17 | a0001c0001t0010g0027a0001c0001t0010g0063a0001c0001t0014g0115others(14): Show | 17 | HG00423.hp1 HG00544.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.598-17781_598-1777 others(8): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118865995 | ||||||
| chr5:118866004
|
GTGTGTGT others(9): Show |
G | 2 | a0001c0001t0014g0227a0001c0001t0034g0228 | 2 | HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.598-17802_598-1778 others(20): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118866004 | ||||||
| chr5:118866140
|
T | C | 1 | a0001c0001t0002g0174 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.598-17922A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118866140 | ||||||
| chr5:118866182
|
A | C | 1 | a0001c0001t0039g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.598-17964T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118866182 | ||||||
| chr5:118866201
|
C | T | 1 | a0001c0001t0004g0139 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.598-17983G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118866201 | ||||||
| chr5:118866515
|
C | T | 1 | a0001c0001t0001g0044 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.598-18297G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118866515 | ||||||
| chr5:118866570
|
A | G | 11 | a0001c0001t0004g0068a0001c0001t0004g0116a0001c0001t0004g0117others(8): Show | 11 | HG01496.hp1 HG01884.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.598-18352T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118866570 | ||||||
| chr5:118866621
|
T | C | 27 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(24): Show | 27 | HG00099.hp1 HG00642.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.598-18403A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118866621 | ||||||
| chr5:118866648
|
G | T | 1 | a0001c0001t0012g0167 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.598-18430C>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118866648 | ||||||
| chr5:118866812
|
G | A | 1 | a0001c0001t0018g0001 | 2 | HG00642.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.598-18594C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118866812 | ||||||
| chr5:118867136
|
T | C | 1 | a0001c0001t0002g0196 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.598-18918A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118867136 | ||||||
| chr5:118867421
|
T | C | 60 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0085others(57): Show | 60 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.598-19203A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118867421 | ||||||
| chr5:118867574
|
A | G | 1 | a0002c0003t0010g0240 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.598-19356T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118867574 | ||||||
| chr5:118867768
|
C | T | 1 | a0001c0001t0008g0231 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.598-19550G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118867768 | ||||||
| chr5:118867826
|
G | A | 5 | a0001c0001t0014g0227a0001c0001t0015g0133a0001c0001t0015g0134others(2): Show | 5 | HG01884.hp1 HG03225.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.598-19608C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118867826 | ||||||
| chr5:118867958
|
A | G | 1 | a0001c0001t0009g0159 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.598-19740T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118867958 | ||||||
| chr5:118868094
|
C | T | 1 | a0001c0001t0008g0221 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.598-19876G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118868094 | ||||||
| chr5:118868210
|
A | C | 5 | a0001c0001t0010g0027a0001c0001t0010g0063a0002c0003t0010g0237others(2): Show | 5 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.598-19992T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118868210 | ||||||
| chr5:118868292
|
T | A | 3 | a0001c0001t0001g0094a0001c0001t0001g0099a0001c0001t0001g0166 | 3 | NA18948.hp2 NA18981.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.598-20074A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118868292 | ||||||
| chr5:118868296
|
A | G | 24 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0085others(21): Show | 24 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.598-20078T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118868296 | ||||||
| chr5:118868315
|
A | G | 1 | a0001c0001t0007g0211 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.598-20097T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118868315 | ||||||
| chr5:118868339
|
C | G | 1 | a0001c0001t0001g0114 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.598-20121G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118868339 | ||||||
| chr5:118868346
|
G | A | 1 | a0001c0001t0005g0161 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.598-20128C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118868346 | ||||||
| chr5:118868381
|
C | T | 4 | a0001c0001t0014g0115a0001c0001t0014g0229a0001c0001t0014g0230others(1): Show | 4 | HG02970.hp1 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.598-20163G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118868381 | ||||||
| chr5:118868386
|
C | T | 14 | a0001c0001t0004g0068a0001c0001t0004g0116a0001c0001t0004g0117others(11): Show | 15 | HG00642.hp1 HG01074.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.598-20168G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118868386 | ||||||
| chr5:118868401
|
A | C | 1 | a0001c0001t0001g0022 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.598-20183T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118868401 | ||||||
| chr5:118868448
|
A | C | 4 | a0001c0001t0007g0210a0001c0001t0007g0211a0001c0001t0007g0213others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.598-20230T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118868448 | ||||||
| chr5:118868456
|
C | A | 33 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(30): Show | 34 | HG00639.hp2 HG00642.hp1 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.598-20238G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118868456 | ||||||
| chr5:118868794
|
G | A | 1 | a0001c0001t0009g0159 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.598-20576C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118868794 | ||||||
| chr5:118868838
|
T | TA | 30 | a0001c0001t0001g0164a0001c0001t0001g0181a0001c0001t0001g0217others(27): Show | 30 | HG00733.hp2 HG01109.hp1 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.598-20621dupT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118868838 | ||||||
| chr5:118868838
|
T | TAA | 5 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0085others(2): Show | 5 | HG00280.hp2 HG00323.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.598-20622_598-2062 others(6): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118868838 | ||||||
| chr5:118868838
|
TA | T | 32 | a0001c0001t0001g0038a0001c0001t0001g0067a0001c0001t0001g0079others(29): Show | 32 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.598-20621delT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118868838 | ||||||
| chr5:118868924
|
C | T | 3 | a0001c0001t0013g0011a0001c0001t0013g0218a0001c0001t0013g0219 | 3 | HG03041.hp2 NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.598-20706G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118868924 | ||||||
| chr5:118869118
|
ATGG | A | 7 | a0001c0001t0001g0175a0001c0001t0001g0194a0001c0001t0013g0011others(4): Show | 7 | HG01891.hp1 HG02280.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.598-20903_598-2090 others(7): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118869118 | ||||||
| chr5:118869202
|
G | A | 1 | a0001c0001t0001g0066 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.598-20984C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118869202 | ||||||
| chr5:118869226
|
C | G | 27 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(24): Show | 27 | HG00099.hp1 HG00642.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.598-21008G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118869226 | ||||||
| chr5:118869362
|
A | G | 3 | a0001c0001t0001g0094a0001c0001t0001g0099a0001c0001t0001g0166 | 3 | NA18948.hp2 NA18981.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.598-21144T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118869362 | ||||||
| chr5:118869445
|
T | C | 2 | a0001c0001t0014g0227a0001c0001t0034g0228 | 2 | HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.598-21227A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118869445 | ||||||
| chr5:118869742
|
C | A | 9 | a0001c0001t0007g0141a0001c0001t0007g0208a0001c0001t0007g0209others(6): Show | 9 | HG02486.hp1 HG02572.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.598-21524G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118869742 | ||||||
| chr5:118869867
|
G | C | 8 | a0001c0001t0004g0117a0001c0001t0004g0118a0001c0001t0004g0120others(5): Show | 8 | HG01496.hp1 HG01884.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.598-21649C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118869867 | ||||||
| chr5:118869960
|
C | T | 7 | a0001c0001t0001g0098a0001c0001t0001g0103a0001c0001t0001g0104others(4): Show | 7 | HG00738.hp1 HG00741.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.598-21742G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118869960 | ||||||
| chr5:118870261
|
T | C | 5 | a0001c0001t0010g0027a0001c0001t0010g0063a0002c0003t0010g0237others(2): Show | 5 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.598-22043A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118870261 | ||||||
| chr5:118870315
|
C | T | 1 | a0001c0001t0011g0040 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.598-22097G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118870315 | ||||||
| chr5:118870378
|
G | A | 14 | a0001c0001t0004g0068a0001c0001t0004g0116a0001c0001t0004g0117others(11): Show | 15 | HG00642.hp1 HG01074.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.598-22160C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118870378 | ||||||
| chr5:118870774
|
C | A | 1 | a0001c0001t0002g0042 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.598-22556G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118870774 | ||||||
| chr5:118870777
|
C | T | 5 | a0001c0001t0001g0189a0001c0001t0001g0191a0001c0001t0001g0192others(2): Show | 5 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.598-22559G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118870777 | ||||||
| chr5:118870932
|
CTT | C | 5 | a0001c0001t0010g0027a0001c0001t0010g0063a0002c0003t0010g0237others(2): Show | 5 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.598-22716_598-2271 others(6): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118870932 | ||||||
| chr5:118870952
|
C | T | 163 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(160): Show | 164 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.598-22734G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118870952 | ||||||
| chr5:118871063
|
A | T | 14 | a0001c0001t0004g0068a0001c0001t0004g0116a0001c0001t0004g0117others(11): Show | 15 | HG00642.hp1 HG01074.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.598-22845T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118871063 | ||||||
| chr5:118871275
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.598-23057A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118871275 | ||||||
| chr5:118871293
|
A | G | 27 | a0001c0001t0005g0151a0001c0001t0005g0154a0001c0001t0005g0155others(24): Show | 27 | HG00733.hp2 HG01109.hp1 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.598-23075T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118871293 | ||||||
| chr5:118871333
|
C | T | 32 | a0001c0001t0005g0151a0001c0001t0005g0154a0001c0001t0005g0155others(29): Show | 32 | HG00733.hp2 HG01109.hp1 HG01496.hp2 others(29): Show |
intron_variant | MODIFIER | c.598-23115G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118871333 | ||||||
| chr5:118871862
|
G | T | 9 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(6): Show | 9 | HG00639.hp2 HG01255.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.598-23644C>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118871862 | ||||||
| chr5:118871889
|
T | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0028 | 2 | HG00423.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.598-23671A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118871889 | ||||||
| chr5:118871900
|
G | C | 2 | a0001c0001t0015g0133a0001c0001t0015g0134 | 2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.598-23682C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118871900 | ||||||
| chr5:118871937
|
G | C | 1 | a0001c0001t0040g0084 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.598-23719C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118871937 | ||||||
| chr5:118871939
|
G | A | 9 | a0001c0001t0006g0029a0001c0001t0006g0047a0001c0001t0006g0059others(6): Show | 9 | HG00639.hp1 HG01123.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.598-23721C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118871939 | ||||||
| chr5:118872023
|
C | T | 8 | a0001c0001t0013g0011a0001c0001t0013g0142a0001c0001t0013g0218others(5): Show | 8 | HG00741.hp1 HG01891.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.598-23805G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118872023 | ||||||
| chr5:118872110
|
T | A | 5 | a0001c0001t0012g0167a0001c0001t0012g0198a0001c0001t0012g0199others(2): Show | 5 | HG02258.hp1 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.598-23892A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118872110 | ||||||
| chr5:118872142
|
G | A | 11 | a0001c0001t0004g0068a0001c0001t0004g0116a0001c0001t0004g0117others(8): Show | 11 | HG01496.hp1 HG01884.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.598-23924C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118872142 | ||||||
| chr5:118872159
|
G | A | 5 | a0001c0001t0012g0167a0001c0001t0012g0198a0001c0001t0012g0199others(2): Show | 5 | HG02258.hp1 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.598-23941C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118872159 | ||||||
| chr5:118872362
|
A | G | 1 | a0001c0004t0001g0032 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.598-24144T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118872362 | ||||||
| chr5:118872448
|
A | G | 12 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(9): Show | 12 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.598-24230T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118872448 | ||||||
| chr5:118872456
|
G | A | 35 | a0001c0001t0005g0151a0001c0001t0005g0154a0001c0001t0005g0155others(32): Show | 36 | HG00642.hp1 HG00733.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.598-24238C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118872456 | ||||||
| chr5:118872501
|
G | C | 1 | a0001c0001t0001g0046 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.598-24283C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118872501 | ||||||
| chr5:118872602
|
T | C | 1 | a0001c0001t0006g0083 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.598-24384A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118872602 | ||||||
| chr5:118872608
|
A | G | 1 | a0001c0002t0001g0005 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.598-24390T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118872608 | ||||||
| chr5:118872660
|
C | G | 1 | a0001c0001t0001g0202 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.598-24442G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118872660 | ||||||
| chr5:118872793
|
G | A | 5 | a0001c0001t0013g0011a0001c0001t0013g0142a0001c0001t0013g0218others(2): Show | 5 | HG01891.hp1 HG02723.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.598-24575C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118872793 | ||||||
| chr5:118872805
|
C | T | 6 | a0001c0001t0001g0235a0001c0002t0001g0003a0001c0002t0001g0004others(3): Show | 6 | HG02055.hp2 HG02145.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.598-24587G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118872805 | ||||||
| chr5:118872932
|
C | T | 78 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(75): Show | 79 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.598-24714G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118872932 | ||||||
| chr5:118872991
|
C | T | 12 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(9): Show | 12 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.598-24773G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118872991 | ||||||
| chr5:118873222
|
C | T | 3 | a0001c0001t0020g0121a0001c0001t0020g0122a0001c0001t0032g0236 | 3 | HG01106.hp1 HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.598-25004G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118873222 | ||||||
| chr5:118873393
|
C | T | 1 | a0001c0001t0006g0047 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.598-25175G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118873393 | ||||||
| chr5:118873824
|
A | T | 2 | a0001c0001t0014g0227a0001c0001t0034g0228 | 2 | HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.598-25606T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118873824 | ||||||
| chr5:118873826
|
T | G | 1 | a0001c0001t0007g0213 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.598-25608A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118873826 | ||||||
| chr5:118874062
|
G | A | 3 | a0001c0001t0015g0133a0001c0001t0015g0134a0001c0001t0015g0135 | 3 | HG01884.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.598-25844C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118874062 | ||||||
| chr5:118874079
|
T | C | 4 | a0001c0001t0001g0044a0001c0001t0001g0094a0001c0001t0001g0099others(1): Show | 4 | NA18948.hp2 NA18981.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.598-25861A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118874079 | ||||||
| chr5:118874368
|
A | T | 1 | a0001c0001t0032g0236 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.598-26150T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118874368 | ||||||
| chr5:118874420
|
C | T | 32 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0085others(29): Show | 32 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.598-26202G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118874420 | ||||||
| chr5:118874473
|
G | A | 21 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(18): Show | 21 | HG00099.hp1 HG00642.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.598-26255C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118874473 | ||||||
| chr5:118874508
|
A | C | 5 | a0001c0001t0013g0011a0001c0001t0013g0142a0001c0001t0013g0218others(2): Show | 5 | HG01891.hp1 HG02723.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.598-26290T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118874508 | ||||||
| chr5:118874681
|
T | G | 2 | a0001c0001t0014g0229a0001c0001t0014g0230 | 2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.598-26463A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118874681 | ||||||
| chr5:118874721
|
A | G | 1 | a0002c0003t0002g0239 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.598-26503T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118874721 | ||||||
| chr5:118874737
|
T | A | 1 | a0001c0001t0001g0031 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.598-26519A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118874737 | ||||||
| chr5:118874744
|
A | G | 3 | a0001c0001t0001g0235a0001c0002t0001g0003a0003c0005t0042g0241 | 3 | HG02145.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.598-26526T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118874744 | ||||||
| chr5:118874776
|
T | A | 3 | a0001c0001t0001g0235a0001c0002t0001g0003a0003c0005t0042g0241 | 3 | HG02145.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.598-26558A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118874776 | ||||||
| chr5:118874782
|
AC | A | 4 | a0001c0001t0014g0115a0001c0001t0014g0229a0001c0001t0014g0230others(1): Show | 4 | HG02970.hp1 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.598-26565delG | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118874782 | ||||||
| chr5:118875037
|
A | G | 1 | a0001c0001t0004g0068 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.598-26819T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118875037 | ||||||
| chr5:118875042
|
T | C | 1 | a0001c0001t0011g0080 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.598-26824A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118875042 | ||||||
| chr5:118875120
|
C | T | 1 | a0001c0001t0003g0012 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.598-26902G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118875120 | ||||||
| chr5:118875140
|
T | C | 39 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0085others(36): Show | 39 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.598-26922A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118875140 | ||||||
| chr5:118875154
|
A | G | 5 | a0001c0001t0001g0189a0001c0001t0001g0191a0001c0001t0001g0192others(2): Show | 5 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.598-26936T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118875154 | ||||||
| chr5:118875191
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.598-26973C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118875191 | ||||||
| chr5:118875210
|
A | C | 1 | a0001c0001t0001g0145 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.598-26992T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118875210 | ||||||
| chr5:118875540
|
T | C | 3 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0057 | 3 | HG00738.hp2 HG01070.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.598-27322A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118875540 | ||||||
| chr5:118875563
|
G | GA | 12 | a0001c0001t0001g0038a0001c0001t0001g0079a0001c0001t0001g0081others(9): Show | 12 | HG00544.hp2 HG01175.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.598-27346dupT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118875563 | ||||||
| chr5:118875563
|
GA | G | 51 | a0001c0001t0001g0031a0001c0001t0001g0036a0001c0001t0001g0037others(48): Show | 52 | HG00639.hp2 HG00642.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.598-27346delT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118875563 | ||||||
| chr5:118875563
|
GAA | G | 28 | a0001c0001t0001g0065a0001c0001t0001g0235a0001c0001t0004g0116others(25): Show | 28 | HG00423.hp1 HG00544.hp1 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.598-27347_598-2734 others(6): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118875563 | ||||||
| chr5:118875571
|
A | G | 1 | a0001c0001t0020g0122 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.598-27353T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118875571 | ||||||
| chr5:118875701
|
C | T | 1 | a0001c0001t0017g0140 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.598-27483G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118875701 | ||||||
| chr5:118875726
|
A | G | 11 | a0001c0001t0001g0235a0001c0001t0013g0011a0001c0001t0013g0142others(8): Show | 11 | HG00741.hp1 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.598-27508T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118875726 | ||||||
| chr5:118875764
|
T | C | 3 | a0001c0001t0015g0133a0001c0001t0015g0134a0001c0001t0015g0135 | 3 | HG01884.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.598-27546A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118875764 | ||||||
| chr5:118875945
|
T | G | 5 | a0001c0001t0013g0011a0001c0001t0013g0142a0001c0001t0013g0218others(2): Show | 5 | HG01891.hp1 HG02723.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.598-27727A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118875945 | ||||||
| chr5:118875967
|
C | T | 14 | a0001c0001t0004g0068a0001c0001t0004g0116a0001c0001t0004g0117others(11): Show | 15 | HG00642.hp1 HG01074.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.598-27749G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118875967 | ||||||
| chr5:118876407
|
A | C | 2 | a0001c0001t0020g0121a0001c0001t0020g0122 | 2 | HG01106.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.598-28189T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118876407 | ||||||
| chr5:118876480
|
C | T | 5 | a0001c0001t0013g0011a0001c0001t0013g0142a0001c0001t0013g0218others(2): Show | 5 | HG01891.hp1 HG02723.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.598-28262G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118876480 | ||||||
| chr5:118876546
|
G | C | 1 | a0001c0001t0005g0154 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.598-28328C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118876546 | ||||||
| chr5:118876590
|
G | C | 1 | a0001c0001t0001g0096 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.598-28372C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118876590 | ||||||
| chr5:118876946
|
A | G | 5 | a0001c0001t0001g0235a0001c0001t0016g0232a0001c0001t0016g0233others(2): Show | 5 | HG02145.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.598-28728T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118876946 | ||||||
| chr5:118877194
|
C | T | 24 | a0001c0001t0001g0125a0001c0001t0001g0143a0001c0001t0001g0150others(21): Show | 24 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(21): Show |
intron_variant | MODIFIER | c.598-28976G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118877194 | ||||||
| chr5:118877195
|
G | A | 16 | a0001c0001t0007g0141a0001c0001t0007g0208a0001c0001t0007g0209others(13): Show | 17 | HG00642.hp1 HG01074.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.598-28977C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118877195 | ||||||
| chr5:118877297
|
C | T | 1 | a0001c0001t0001g0046 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.598-29079G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118877297 | ||||||
| chr5:118877364
|
T | C | 11 | a0001c0001t0004g0068a0001c0001t0004g0116a0001c0001t0004g0117others(8): Show | 11 | HG01496.hp1 HG01884.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.598-29146A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118877364 | ||||||
| chr5:118877420
|
G | A | 1 | a0001c0001t0011g0073 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.598-29202C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118877420 | ||||||
| chr5:118877444
|
C | A | 1 | a0001c0001t0001g0100 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.598-29226G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118877444 | ||||||
| chr5:118877467
|
G | A | 13 | a0001c0001t0002g0107a0001c0001t0003g0007a0001c0001t0003g0008others(10): Show | 13 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.598-29249C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118877467 | ||||||
| chr5:118877530
|
A | T | 1 | a0001c0001t0024g0206 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.598-29312T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118877530 | ||||||
| chr5:118877557
|
TA | T | 3 | a0001c0001t0015g0133a0001c0001t0015g0134a0001c0001t0015g0135 | 3 | HG01884.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.598-29340delT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118877557 | ||||||
| chr5:118877578
|
A | T | 21 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(18): Show | 21 | HG00099.hp1 HG00642.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.598-29360T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118877578 | ||||||
| chr5:118877819
|
T | G | 1 | a0001c0001t0001g0164 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.598-29601A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118877819 | ||||||
| chr5:118877983
|
C | T | 3 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021 | 3 | HG01192.hp2 HG03491.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.598-29765G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118877983 | ||||||
| chr5:118878188
|
G | C | 1 | a0001c0001t0007g0210 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.598-29970C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118878188 | ||||||
| chr5:118878292
|
T | C | 1 | a0001c0001t0004g0136 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.598-30074A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118878292 | ||||||
| chr5:118878469
|
T | C | 1 | a0001c0001t0004g0117 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.598-30251A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118878469 | ||||||
| chr5:118878595
|
G | A | 32 | a0001c0001t0001g0031a0001c0001t0001g0037a0001c0001t0001g0041others(29): Show | 32 | HG00280.hp2 HG00323.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.598-30377C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118878595 | ||||||
| chr5:118878666
|
A | T | 1 | a0001c0001t0001g0114 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.598-30448T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118878666 | ||||||
| chr5:118878759
|
A | G | 36 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(33): Show | 36 | HG00099.hp1 HG00642.hp2 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.598-30541T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118878759 | ||||||
| chr5:118878778
|
G | A | 86 | a0001c0001t0001g0235a0001c0001t0003g0007a0001c0001t0003g0008others(83): Show | 87 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.598-30560C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118878778 | ||||||
| chr5:118878839
|
G | A | 11 | a0001c0001t0004g0068a0001c0001t0004g0116a0001c0001t0004g0117others(8): Show | 11 | HG01496.hp1 HG01884.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.598-30621C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118878839 | ||||||
| chr5:118878894
|
A | G | 4 | a0001c0001t0013g0011a0001c0001t0013g0142a0001c0001t0013g0218others(1): Show | 4 | HG01891.hp1 HG03041.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.598-30676T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118878894 | ||||||
| chr5:118878941
|
C | T | 4 | a0001c0001t0014g0115a0001c0001t0014g0229a0001c0001t0014g0230others(1): Show | 4 | HG02970.hp1 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.598-30723G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118878941 | ||||||
| chr5:118879035
|
T | TG | 42 | a0001c0001t0001g0164a0001c0001t0001g0235a0001c0001t0003g0007others(39): Show | 42 | HG00639.hp2 HG00733.hp2 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.598-30818dupC | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118879035 | ||||||
| chr5:118879132
|
A | G | 9 | a0001c0001t0007g0141a0001c0001t0007g0208a0001c0001t0007g0209others(6): Show | 9 | HG02486.hp1 HG02572.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.598-30914T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118879132 | ||||||
| chr5:118879183
|
C | T | 1 | a0001c0001t0012g0167 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.598-30965G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118879183 | ||||||
| chr5:118879186
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.598-30968C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118879186 | ||||||
| chr5:118879236
|
C | A | 1 | a0001c0001t0003g0008 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.598-31018G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118879236 | ||||||
| chr5:118879334
|
C | T | 1 | a0001c0001t0032g0236 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.598-31116G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118879334 | ||||||
| chr5:118879422
|
C | A | 3 | a0001c0001t0001g0235a0001c0002t0001g0003a0003c0005t0042g0241 | 3 | HG02145.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.598-31204G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118879422 | ||||||
| chr5:118879609
|
C | CA | 6 | a0001c0001t0001g0024a0001c0001t0002g0107a0001c0001t0004g0068others(3): Show | 6 | HG02055.hp2 HG02074.hp2 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.598-31392dupT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118879609 | ||||||
| chr5:118879609
|
CA | C | 15 | a0001c0001t0001g0049a0001c0001t0001g0176a0001c0001t0005g0157others(12): Show | 15 | HG00423.hp1 HG00544.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.598-31392delT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118879609 | ||||||
| chr5:118879697
|
G | T | 1 | a0001c0001t0001g0089 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.598-31479C>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118879697 | ||||||
| chr5:118879770
|
T | A | 11 | a0001c0001t0004g0068a0001c0001t0004g0116a0001c0001t0004g0117others(8): Show | 11 | HG01496.hp1 HG01884.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.598-31552A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118879770 | ||||||
| chr5:118880114
|
A | G | 1 | a0001c0001t0001g0086 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.598-31896T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118880114 | ||||||
| chr5:118880157
|
G | T | 237 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(234): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.598-31939C>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118880157 | ||||||
| chr5:118880161
|
G | C | 22 | a0001c0001t0001g0235a0001c0001t0003g0007a0001c0001t0003g0008others(19): Show | 22 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.598-31943C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118880161 | ||||||
| chr5:118880189
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.598-31971T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118880189 | ||||||
| chr5:118880362
|
T | C | 41 | a0001c0001t0001g0164a0001c0001t0001g0235a0001c0001t0003g0007others(38): Show | 41 | HG00639.hp2 HG00733.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.598-32144A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118880362 | ||||||
| chr5:118880428
|
G | C | 4 | a0001c0001t0004g0118a0001c0001t0004g0120a0001c0001t0004g0139others(1): Show | 4 | HG01884.hp2 HG02922.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.598-32210C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118880428 | ||||||
| chr5:118880531
|
G | A | 1 | a0001c0001t0006g0047 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.598-32313C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118880531 | ||||||
| chr5:118880577
|
A | G | 47 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(44): Show | 48 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.598-32359T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118880577 | ||||||
| chr5:118880623
|
C | T | 100 | a0001c0001t0001g0235a0001c0001t0002g0033a0001c0001t0002g0034others(97): Show | 101 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.598-32405G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118880623 | ||||||
| chr5:118880864
|
C | T | 3 | a0001c0001t0001g0235a0001c0002t0001g0003a0003c0005t0042g0241 | 3 | HG02145.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.598-32646G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118880864 | ||||||
| chr5:118880888
|
A | G | 1 | a0002c0003t0010g0238 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.598-32670T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118880888 | ||||||
| chr5:118881032
|
T | C | 17 | a0001c0001t0010g0027a0001c0001t0010g0063a0001c0001t0014g0115others(14): Show | 17 | HG00423.hp1 HG00544.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.598-32814A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118881032 | ||||||
| chr5:118881043
|
G | A | 61 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0085others(58): Show | 61 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.598-32825C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118881043 | ||||||
| chr5:118881100
|
T | C | 1 | a0001c0001t0032g0236 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.598-32882A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118881100 | ||||||
| chr5:118881101
|
T | A | 60 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0085others(57): Show | 60 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.598-32883A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118881101 | ||||||
| chr5:118881200
|
G | C | 1 | a0001c0001t0004g0068 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.598-32982C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118881200 | ||||||
| chr5:118881363
|
T | A | 1 | a0001c0001t0001g0197 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.598-33145A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118881363 | ||||||
| chr5:118881602
|
A | G | 61 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0085others(58): Show | 61 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.598-33384T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118881602 | ||||||
| chr5:118881623
|
A | G | 1 | a0001c0001t0015g0135 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.598-33405T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118881623 | ||||||
| chr5:118881638
|
TG | T | 17 | a0001c0001t0010g0027a0001c0001t0010g0063a0001c0001t0014g0115others(14): Show | 17 | HG00423.hp1 HG00544.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.598-33421delC | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118881638 | ||||||
| chr5:118881779
|
C | T | 88 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0085others(85): Show | 89 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.598-33561G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118881779 | ||||||
| chr5:118881802
|
A | T | 1 | a0001c0001t0001g0096 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.598-33584T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118881802 | ||||||
| chr5:118881901
|
A | G | 6 | a0001c0001t0014g0115a0001c0001t0014g0227a0001c0001t0014g0229others(3): Show | 6 | HG02970.hp1 HG03041.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.598-33683T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118881901 | ||||||
| chr5:118882141
|
A | G | 2 | a0001c0001t0002g0129a0001c0001t0002g0130 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.598-33923T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118882141 | ||||||
| chr5:118882307
|
C | T | 89 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0085others(86): Show | 90 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.598-34089G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118882307 | ||||||
| chr5:118882337
|
C | T | 5 | a0001c0001t0008g0204a0001c0001t0008g0220a0001c0001t0008g0221others(2): Show | 5 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.598-34119G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118882337 | ||||||
| chr5:118882565
|
C | T | 2 | a0001c0001t0016g0232a0001c0001t0016g0233 | 2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.598-34347G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118882565 | ||||||
| chr5:118882812
|
C | T | 9 | a0001c0001t0007g0141a0001c0001t0007g0208a0001c0001t0007g0209others(6): Show | 9 | HG02486.hp1 HG02572.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.598-34594G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118882812 | ||||||
| chr5:118883313
|
A | G | 1 | a0001c0001t0013g0011 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.598-35095T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118883313 | ||||||
| chr5:118883527
|
T | C | 5 | a0001c0001t0013g0011a0001c0001t0013g0142a0001c0001t0013g0218others(2): Show | 5 | HG01891.hp1 HG02723.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.598-35309A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118883527 | ||||||
| chr5:118883566
|
G | A | 1 | a0001c0001t0004g0068 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.598-35348C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118883566 | ||||||
| chr5:118883655
|
C | T | 1 | a0001c0001t0007g0211 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.598-35437G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118883655 | ||||||
| chr5:118883941
|
T | C | 1 | a0001c0001t0003g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.598-35723A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118883941 | ||||||
| chr5:118884164
|
A | G | 5 | a0001c0001t0013g0011a0001c0001t0013g0142a0001c0001t0013g0218others(2): Show | 5 | HG01891.hp1 HG02723.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.598-35946T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118884164 | ||||||
| chr5:118884167
|
G | C | 19 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(16): Show | 19 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.598-35949C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118884167 | ||||||
| chr5:118884380
|
C | A | 3 | a0001c0001t0014g0229a0001c0001t0014g0230a0001c0001t0033g0205 | 3 | HG02970.hp1 HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.598-36162G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118884380 | ||||||
| chr5:118884589
|
T | G | 2 | a0001c0001t0016g0232a0001c0001t0016g0233 | 2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.598-36371A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118884589 | ||||||
| chr5:118884759
|
C | A | 1 | a0001c0001t0001g0024 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.598-36541G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118884759 | ||||||
| chr5:118884821
|
A | G | 1 | a0001c0001t0001g0164 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.598-36603T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118884821 | ||||||
| chr5:118884832
|
C | T | 1 | a0001c0001t0032g0236 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.598-36614G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118884832 | ||||||
| chr5:118884836
|
C | A | 1 | a0001c0001t0014g0115 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.598-36618G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118884836 | ||||||
| chr5:118884928
|
G | A | 53 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(50): Show | 54 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.598-36710C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118884928 | ||||||
| chr5:118884962
|
C | T | 3 | a0001c0001t0015g0133a0001c0001t0015g0134a0001c0001t0015g0135 | 3 | HG01884.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.598-36744G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118884962 | ||||||
| chr5:118884992
|
T | C | 2 | a0001c0001t0018g0001a0001c0001t0029g0132 | 3 | HG00642.hp1 HG01074.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.598-36774A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118884992 | ||||||
| chr5:118884996
|
C | CA | 58 | a0001c0001t0001g0024a0001c0001t0001g0076a0001c0001t0001g0077others(55): Show | 58 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.598-36779dupT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118884996 | ||||||
| chr5:118884996
|
C | CAA | 10 | a0001c0001t0002g0042a0001c0001t0002g0126a0001c0001t0005g0154others(7): Show | 10 | HG00423.hp1 HG02056.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.598-36780_598-3677 others(6): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118884996 | ||||||
| chr5:118884996
|
C | CAAA | 7 | a0001c0001t0004g0068a0001c0001t0004g0118a0001c0001t0004g0120others(4): Show | 7 | HG01884.hp2 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.598-36781_598-3677 others(7): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118884996 | ||||||
| chr5:118884996
|
C | CAAAAAAA others(2): Show |
5 | a0001c0001t0003g0014a0001c0001t0003g0016a0001c0001t0003g0018others(2): Show | 5 | HG01255.hp2 HG02280.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.598-36787_598-3677 others(13): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118884996 | ||||||
| chr5:118884996
|
C | CAAAAAAA others(3): Show |
6 | a0001c0001t0003g0008a0001c0001t0003g0012a0001c0001t0003g0013others(3): Show | 6 | HG00639.hp2 HG01243.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.598-36788_598-3677 others(14): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118884996 | ||||||
| chr5:118884996
|
CAA | C | 5 | a0001c0001t0013g0142a0001c0001t0013g0218a0001c0001t0013g0219others(2): Show | 6 | HG00642.hp1 HG01074.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.598-36780_598-3677 others(6): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118884996 | ||||||
| chr5:118884996
|
CAAA | C | 6 | a0001c0001t0001g0235a0001c0001t0016g0232a0001c0001t0016g0233others(3): Show | 6 | HG02145.hp2 HG02257.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.598-36781_598-3677 others(7): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118884996 | ||||||
| chr5:118885066
|
T | C | 22 | a0001c0001t0001g0235a0001c0001t0003g0007a0001c0001t0003g0008others(19): Show | 22 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.598-36848A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118885066 | ||||||
| chr5:118885073
|
C | A | 5 | a0001c0001t0001g0235a0001c0001t0016g0232a0001c0001t0016g0233others(2): Show | 5 | HG02145.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.598-36855G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118885073 | ||||||
| chr5:118885078
|
G | A | 1 | a0001c0001t0019g0025 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.598-36860C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118885078 | ||||||
| chr5:118885082
|
G | A | 3 | a0001c0001t0015g0133a0001c0001t0015g0134a0001c0001t0015g0135 | 3 | HG01884.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.598-36864C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118885082 | ||||||
| chr5:118885154
|
A | G | 5 | a0001c0001t0001g0235a0001c0001t0016g0232a0001c0001t0016g0233others(2): Show | 5 | HG02145.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.598-36936T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118885154 | ||||||
| chr5:118885154
|
A | T | 50 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(47): Show | 50 | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.598-36936T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118885154 | ||||||
| chr5:118885155
|
A | T | 2 | a0001c0001t0002g0057a0001c0001t0002g0196 | 2 | HG00099.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.598-36937T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118885155 | ||||||
| chr5:118885176
|
G | A | 3 | a0001c0001t0015g0133a0001c0001t0015g0134a0001c0001t0015g0135 | 3 | HG01884.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.598-36958C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118885176 | ||||||
| chr5:118885377
|
G | A | 25 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(22): Show | 25 | HG00099.hp1 HG00642.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.598-37159C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118885377 | ||||||
| chr5:118885379
|
G | T | 5 | a0001c0001t0013g0011a0001c0001t0013g0142a0001c0001t0013g0218others(2): Show | 5 | HG01891.hp1 HG02723.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.598-37161C>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118885379 | ||||||
| chr5:118885381
|
G | A | 1 | a0002c0003t0010g0240 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.598-37163C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118885381 | ||||||
| chr5:118885431
|
T | G | 1 | a0001c0001t0001g0172 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.598-37213A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118885431 | ||||||
| chr5:118885439
|
A | G | 1 | a0001c0001t0002g0107 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.598-37221T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118885439 | ||||||
| chr5:118885456
|
C | CA | 71 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0039others(68): Show | 71 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(68): Show |
intron_variant | MODIFIER | c.598-37239dupT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118885456 | ||||||
| chr5:118885456
|
C | CAA | 20 | a0001c0001t0001g0024a0001c0001t0001g0044a0001c0001t0001g0048others(17): Show | 20 | HG01243.hp2 HG01255.hp1 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.598-37240_598-3723 others(6): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118885456 | ||||||
| chr5:118885456
|
CA | C | 25 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0187others(22): Show | 25 | HG00423.hp1 HG00544.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.598-37239delT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118885456 | ||||||
| chr5:118885494
|
AGTGGCTC others(6): Show |
A | 1 | a0001c0002t0001g0004 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.598-37289_598-3727 others(17): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118885494 | ||||||
| chr5:118885520
|
C | T | 1 | a0001c0001t0011g0111 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.598-37302G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118885520 | ||||||
| chr5:118885658
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.598-37440C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118885658 | ||||||
| chr5:118885690
|
C | A | 4 | a0001c0001t0010g0027a0002c0003t0010g0237a0002c0003t0010g0238others(1): Show | 4 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.598-37472G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118885690 | ||||||
| chr5:118885707
|
A | T | 2 | a0001c0001t0017g0140a0001c0001t0017g0146 | 2 | HG03688.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.598-37489T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118885707 | ||||||
| chr5:118885775
|
A | T | 2 | a0001c0001t0016g0232a0001c0001t0016g0233 | 2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.598-37557T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118885775 | ||||||
| chr5:118885788
|
T | C | 3 | a0001c0001t0020g0121a0001c0001t0020g0122a0001c0001t0032g0236 | 3 | HG01106.hp1 HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.598-37570A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118885788 | ||||||
| chr5:118885894
|
G | A | 9 | a0001c0001t0001g0173a0001c0001t0001g0175a0001c0001t0001g0176others(6): Show | 9 | HG01099.hp1 HG01169.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.598-37676C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118885894 | ||||||
| chr5:118885985
|
A | G | 5 | a0001c0001t0001g0235a0001c0001t0016g0232a0001c0001t0016g0233others(2): Show | 5 | HG02145.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.598-37767T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118885985 | ||||||
| chr5:118885990
|
C | A | 2 | a0001c0001t0001g0102a0001c0001t0031g0170 | 2 | HG02735.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.598-37772G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118885990 | ||||||
| chr5:118886223
|
C | T | 2 | a0001c0001t0001g0173a0001c0001t0001g0176 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.598-38005G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118886223 | ||||||
| chr5:118886293
|
G | A | 2 | a0001c0001t0005g0155a0001c0001t0005g0157 | 2 | HG00733.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.598-38075C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118886293 | ||||||
| chr5:118886418
|
T | C | 2 | a0001c0001t0018g0001a0001c0001t0029g0132 | 3 | HG00642.hp1 HG01074.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.598-38200A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118886418 | ||||||
| chr5:118886492
|
G | A | 1 | a0001c0001t0001g0053 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.598-38274C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118886492 | ||||||
| chr5:118886524
|
A | C | 1 | a0001c0001t0005g0156 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.598-38306T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118886524 | ||||||
| chr5:118886567
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.598-38349C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118886567 | ||||||
| chr5:118887013
|
T | C | 1 | a0001c0001t0032g0236 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.598-38795A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118887013 | ||||||
| chr5:118887067
|
T | C | 1 | a0001c0001t0007g0210 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.598-38849A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118887067 | ||||||
| chr5:118887084
|
T | A | 5 | a0001c0001t0013g0011a0001c0001t0013g0142a0001c0001t0013g0218others(2): Show | 5 | HG01891.hp1 HG02723.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.598-38866A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118887084 | ||||||
| chr5:118887221
|
A | G | 1 | a0001c0002t0001g0004 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.598-39003T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118887221 | ||||||
| chr5:118887293
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.598-39075G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118887293 | ||||||
| chr5:118887422
|
T | C | 1 | a0001c0001t0024g0206 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.598-39204A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118887422 | ||||||
| chr5:118887434
|
C | G | 2 | a0001c0001t0020g0121a0001c0001t0020g0122 | 2 | HG01106.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.598-39216G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118887434 | ||||||
| chr5:118887695
|
C | T | 6 | a0001c0001t0008g0204a0001c0001t0008g0220a0001c0001t0008g0221others(3): Show | 6 | HG01891.hp2 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.598-39477G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118887695 | ||||||
| chr5:118887712
|
G | A | 5 | a0001c0001t0013g0011a0001c0001t0013g0142a0001c0001t0013g0218others(2): Show | 5 | HG01891.hp1 HG02723.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.598-39494C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118887712 | ||||||
| chr5:118887731
|
G | A | 3 | a0001c0001t0001g0079a0001c0001t0001g0088a0001c0001t0001g0089 | 3 | HG02015.hp2 NA18951.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.598-39513C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118887731 | ||||||
| chr5:118887780
|
G | A | 1 | a0001c0001t0015g0135 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.598-39562C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118887780 | ||||||
| chr5:118887785
|
A | G | 1 | a0001c0001t0001g0048 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.598-39567T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118887785 | ||||||
| chr5:118887880
|
A | C | 1 | a0001c0001t0004g0123 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.598-39662T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118887880 | ||||||
| chr5:118888027
|
G | A | 12 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(9): Show | 12 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.598-39809C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118888027 | ||||||
| chr5:118888074
|
T | TTA | 227 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(224): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.598-39858_598-3985 others(6): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118888074 | ||||||
| chr5:118888091
|
T | C | 4 | a0001c0001t0010g0027a0002c0003t0010g0237a0002c0003t0010g0238others(1): Show | 4 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.598-39873A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118888091 | ||||||
| chr5:118888242
|
G | A | 1 | a0001c0001t0004g0117 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.598-40024C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118888242 | ||||||
| chr5:118888357
|
G | A | 1 | a0001c0001t0032g0236 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.598-40139C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118888357 | ||||||
| chr5:118888554
|
T | C | 3 | a0001c0001t0015g0133a0001c0001t0015g0134a0001c0001t0015g0135 | 3 | HG01884.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.597+39983A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118888554 | ||||||
| chr5:118888669
|
A | G | 2 | a0001c0001t0020g0121a0001c0001t0020g0122 | 2 | HG01106.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.597+39868T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118888669 | ||||||
| chr5:118888686
|
G | A | 1 | a0001c0001t0001g0044 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+39851C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118888686 | ||||||
| chr5:118888828
|
T | A | 3 | a0001c0001t0015g0133a0001c0001t0015g0134a0001c0001t0015g0135 | 3 | HG01884.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.597+39709A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118888828 | ||||||
| chr5:118888854
|
T | C | 12 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(9): Show | 12 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.597+39683A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118888854 | ||||||
| chr5:118888957
|
A | T | 20 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(17): Show | 20 | HG00639.hp2 HG00741.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.597+39580T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118888957 | ||||||
| chr5:118889152
|
A | T | 10 | a0001c0001t0004g0116a0001c0001t0004g0117a0001c0001t0004g0118others(7): Show | 10 | HG01496.hp1 HG01884.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.597+39385T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118889152 | ||||||
| chr5:118889427
|
A | G | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG03834.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.597+39110T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118889427 | ||||||
| chr5:118889474
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.597+39063T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118889474 | ||||||
| chr5:118889544
|
AT | A | 5 | a0001c0001t0010g0027a0001c0001t0010g0063a0002c0003t0010g0237others(2): Show | 5 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.597+38992delA | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118889544 | ||||||
| chr5:118889622
|
G | A | 2 | a0001c0001t0018g0001a0001c0001t0029g0132 | 3 | HG00642.hp1 HG01074.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.597+38915C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118889622 | ||||||
| chr5:118889701
|
A | G | 12 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(9): Show | 12 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.597+38836T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118889701 | ||||||
| chr5:118889870
|
A | G | 102 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(99): Show | 103 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.597+38667T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118889870 | ||||||
| chr5:118889921
|
C | T | 70 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(67): Show | 70 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.597+38616G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118889921 | ||||||
| chr5:118889936
|
T | C | 9 | a0001c0001t0001g0173a0001c0001t0001g0175a0001c0001t0001g0176others(6): Show | 9 | HG01099.hp1 HG01169.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.597+38601A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118889936 | ||||||
| chr5:118890019
|
T | A | 18 | a0001c0001t0005g0151a0001c0001t0005g0154a0001c0001t0005g0155others(15): Show | 18 | HG00733.hp2 HG01109.hp1 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.597+38518A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118890019 | ||||||
| chr5:118890129
|
T | C | 1 | a0001c0001t0001g0024 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.597+38408A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118890129 | ||||||
| chr5:118890337
|
C | G | 4 | a0001c0001t0001g0143a0001c0001t0001g0150a0001c0001t0001g0152others(1): Show | 4 | HG00099.hp2 HG00323.hp1 HG00735.hp1 others(1): Show |
intron_variant | MODIFIER | c.597+38200G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118890337 | ||||||
| chr5:118890385
|
T | C | 3 | a0001c0001t0020g0121a0001c0001t0020g0122a0001c0001t0032g0236 | 3 | HG01106.hp1 HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.597+38152A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118890385 | ||||||
| chr5:118890429
|
AT | A | 3 | a0001c0001t0020g0121a0001c0001t0020g0122a0001c0001t0032g0236 | 3 | HG01106.hp1 HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.597+38107delA | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118890429 | ||||||
| chr5:118890562
|
C | CT | 77 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0031others(74): Show | 77 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.597+37974dupA | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118890562 | ||||||
| chr5:118890562
|
C | CTT | 8 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0077others(5): Show | 8 | HG00423.hp2 HG00735.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.597+37973_597+3797 others(6): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118890562 | ||||||
| chr5:118890562
|
CT | C | 56 | a0001c0001t0001g0173a0001c0001t0001g0175a0001c0001t0001g0176others(53): Show | 57 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.597+37974delA | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118890562 | ||||||
| chr5:118890562
|
CTT | C | 10 | a0001c0001t0007g0210a0001c0001t0007g0211a0001c0001t0007g0213others(7): Show | 10 | HG01106.hp1 HG02257.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.597+37973_597+3797 others(6): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118890562 | ||||||
| chr5:118890659
|
C | T | 4 | a0001c0001t0001g0143a0001c0001t0001g0150a0001c0001t0001g0152others(1): Show | 4 | HG00099.hp2 HG00323.hp1 HG00735.hp1 others(1): Show |
intron_variant | MODIFIER | c.597+37878G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118890659 | ||||||
| chr5:118890776
|
G | C | 8 | a0001c0001t0013g0011a0001c0001t0013g0142a0001c0001t0013g0218others(5): Show | 8 | HG00741.hp1 HG01891.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.597+37761C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118890776 | ||||||
| chr5:118890787
|
T | G | 1 | a0001c0001t0001g0052 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.597+37750A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118890787 | ||||||
| chr5:118890873
|
T | A | 69 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(66): Show | 69 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.597+37664A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118890873 | ||||||
| chr5:118890892
|
C | G | 82 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(79): Show | 83 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.597+37645G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118890892 | ||||||
| chr5:118890948
|
C | T | 6 | a0001c0001t0014g0115a0001c0001t0014g0227a0001c0001t0014g0229others(3): Show | 6 | HG02970.hp1 HG03041.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.597+37589G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118890948 | ||||||
| chr5:118890968
|
T | C | 1 | a0001c0001t0032g0236 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.597+37569A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118890968 | ||||||
| chr5:118891024
|
A | AAATACGT others(44): Show |
1 | a0001c0001t0001g0127 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.597+37462_597+3751 others(55): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118891024 | ||||||
| chr5:118891046
|
C | T | 5 | a0001c0001t0012g0167a0001c0001t0012g0198a0001c0001t0012g0199others(2): Show | 5 | HG02258.hp1 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.597+37491G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118891046 | ||||||
| chr5:118891202
|
G | GA | 7 | a0001c0001t0001g0101a0001c0001t0001g0172a0001c0001t0001g0190others(4): Show | 7 | HG00140.hp1 HG00140.hp2 HG00733.hp1 others(4): Show |
intron_variant | MODIFIER | c.597+37334dupT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118891202 | ||||||
| chr5:118891252
|
T | G | 3 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021 | 3 | HG01192.hp2 HG03491.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.597+37285A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118891252 | ||||||
| chr5:118891333
|
T | C | 2 | a0001c0001t0005g0151a0001c0001t0005g0156 | 2 | HG01109.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.597+37204A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118891333 | ||||||
| chr5:118891408
|
A | T | 32 | a0001c0001t0005g0151a0001c0001t0005g0154a0001c0001t0005g0155others(29): Show | 32 | HG00733.hp2 HG01109.hp1 HG01496.hp2 others(29): Show |
intron_variant | MODIFIER | c.597+37129T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118891408 | ||||||
| chr5:118891417
|
G | C | 4 | a0001c0001t0010g0027a0002c0003t0010g0237a0002c0003t0010g0238others(1): Show | 4 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.597+37120C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118891417 | ||||||
| chr5:118891545
|
C | T | 65 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(62): Show | 66 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.597+36992G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118891545 | ||||||
| chr5:118891737
|
A | G | 1 | a0001c0001t0005g0151 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.597+36800T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118891737 | ||||||
| chr5:118891767
|
T | C | 1 | a0001c0001t0001g0046 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.597+36770A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118891767 | ||||||
| chr5:118892401
|
G | A | 1 | a0001c0001t0002g0107 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.597+36136C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118892401 | ||||||
| chr5:118892530
|
A | G | 5 | a0001c0001t0001g0235a0001c0001t0016g0232a0001c0001t0016g0233others(2): Show | 5 | HG02145.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.597+36007T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118892530 | ||||||
| chr5:118892649
|
T | A | 5 | a0001c0001t0001g0235a0001c0001t0016g0232a0001c0001t0016g0233others(2): Show | 5 | HG02145.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.597+35888A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118892649 | ||||||
| chr5:118892689
|
T | C | 1 | a0001c0001t0002g0097 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.597+35848A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118892689 | ||||||
| chr5:118892798
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.597+35739G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118892798 | ||||||
| chr5:118893012
|
G | T | 1 | a0001c0001t0001g0074 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.597+35525C>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118893012 | ||||||
| chr5:118893019
|
TA | T | 17 | a0001c0001t0001g0076a0001c0001t0001g0101a0001c0001t0001g0171others(14): Show | 17 | HG00140.hp1 HG00140.hp2 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.597+35517delT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118893019 | ||||||
| chr5:118893071
|
T | C | 1 | a0001c0001t0006g0059 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.597+35466A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118893071 | ||||||
| chr5:118893074
|
A | T | 1 | a0001c0001t0001g0194 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.597+35463T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118893074 | ||||||
| chr5:118893168
|
A | G | 28 | a0001c0001t0001g0164a0001c0001t0005g0151a0001c0001t0005g0154others(25): Show | 28 | HG00733.hp2 HG01109.hp1 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.597+35369T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118893168 | ||||||
| chr5:118893256
|
G | C | 4 | a0001c0001t0005g0154a0001c0001t0005g0155a0001c0001t0005g0157others(1): Show | 4 | HG00733.hp2 HG03579.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.597+35281C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118893256 | ||||||
| chr5:118893268
|
C | T | 6 | a0001c0001t0014g0115a0001c0001t0014g0227a0001c0001t0014g0229others(3): Show | 6 | HG02970.hp1 HG03041.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.597+35269G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118893268 | ||||||
| chr5:118893360
|
C | CA | 14 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(11): Show | 14 | HG00639.hp2 HG01243.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.597+35176dupT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118893360 | ||||||
| chr5:118893360
|
CA | C | 23 | a0001c0001t0001g0021a0001c0001t0001g0028a0001c0001t0001g0062others(20): Show | 23 | HG00099.hp1 HG01070.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.597+35176delT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118893360 | ||||||
| chr5:118893489
|
T | C | 3 | a0001c0001t0007g0141a0001c0001t0007g0208a0001c0001t0007g0209 | 3 | HG02630.hp1 HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.597+35048A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118893489 | ||||||
| chr5:118893557
|
T | C | 1 | a0001c0001t0001g0164 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.597+34980A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118893557 | ||||||
| chr5:118893638
|
A | G | 1 | a0001c0001t0002g0058 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.597+34899T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118893638 | ||||||
| chr5:118893763
|
AT | A | 6 | a0001c0001t0014g0115a0001c0001t0014g0227a0001c0001t0014g0229others(3): Show | 6 | HG02970.hp1 HG03041.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.597+34773delA | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118893763 | ||||||
| chr5:118893797
|
C | G | 1 | a0001c0001t0001g0217 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.597+34740G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118893797 | ||||||
| chr5:118893940
|
C | A | 85 | a0001c0001t0001g0235a0001c0001t0003g0007a0001c0001t0003g0008others(82): Show | 86 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.597+34597G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118893940 | ||||||
| chr5:118893986
|
T | C | 9 | a0001c0001t0014g0115a0001c0001t0014g0227a0001c0001t0014g0229others(6): Show | 9 | HG01106.hp1 HG02630.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.597+34551A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118893986 | ||||||
| chr5:118893991
|
T | A | 10 | a0001c0001t0004g0116a0001c0001t0004g0117a0001c0001t0004g0118others(7): Show | 10 | HG01496.hp1 HG01884.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.597+34546A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118893991 | ||||||
| chr5:118894040
|
C | CA | 18 | a0001c0001t0001g0187a0001c0001t0010g0027a0001c0001t0013g0011others(15): Show | 18 | HG00423.hp1 HG00544.hp1 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.597+34496dupT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118894040 | ||||||
| chr5:118894134
|
C | A | 4 | a0001c0001t0001g0143a0001c0001t0001g0150a0001c0001t0001g0152others(1): Show | 4 | HG00099.hp2 HG00323.hp1 HG00735.hp1 others(1): Show |
intron_variant | MODIFIER | c.597+34403G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118894134 | ||||||
| chr5:118894183
|
C | G | 1 | a0001c0001t0005g0158 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.597+34354G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118894183 | ||||||
| chr5:118894287
|
A | G | 1 | a0001c0001t0001g0049 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.597+34250T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118894287 | ||||||
| chr5:118894844
|
C | T | 69 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(66): Show | 69 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.597+33693G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118894844 | ||||||
| chr5:118894868
|
T | C | 5 | a0001c0001t0013g0011a0001c0001t0013g0142a0001c0001t0013g0218others(2): Show | 5 | HG01891.hp1 HG02723.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.597+33669A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118894868 | ||||||
| chr5:118894945
|
G | A | 9 | a0001c0001t0001g0173a0001c0001t0001g0175a0001c0001t0001g0176others(6): Show | 9 | HG01099.hp1 HG01169.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.597+33592C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118894945 | ||||||
| chr5:118894976
|
C | T | 82 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(79): Show | 83 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.597+33561G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118894976 | ||||||
| chr5:118894991
|
T | G | 3 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0057 | 3 | HG00738.hp2 HG01070.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.597+33546A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118894991 | ||||||
| chr5:118895009
|
G | C | 2 | a0001c0001t0016g0232a0001c0001t0016g0233 | 2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.597+33528C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118895009 | ||||||
| chr5:118895078
|
T | G | 2 | a0001c0001t0003g0008a0001c0001t0027g0009 | 2 | HG00639.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.597+33459A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118895078 | ||||||
| chr5:118895168
|
G | C | 2 | a0001c0001t0018g0001a0001c0001t0029g0132 | 3 | HG00642.hp1 HG01074.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.597+33369C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118895168 | ||||||
| chr5:118895284
|
G | A | 13 | a0001c0001t0004g0068a0001c0001t0004g0116a0001c0001t0004g0117others(10): Show | 14 | HG00642.hp1 HG01074.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.597+33253C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118895284 | ||||||
| chr5:118895290
|
T | C | 3 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021 | 3 | HG01192.hp2 HG03491.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.597+33247A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118895290 | ||||||
| chr5:118895389
|
G | A | 1 | a0001c0001t0008g0221 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.597+33148C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118895389 | ||||||
| chr5:118895665
|
T | C | 3 | a0001c0001t0001g0022a0001c0001t0001g0100a0001c0001t0002g0196 | 3 | HG00099.hp1 HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.597+32872A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118895665 | ||||||
| chr5:118895794
|
G | C | 3 | a0001c0001t0015g0133a0001c0001t0015g0134a0001c0001t0015g0135 | 3 | HG01884.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.597+32743C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118895794 | ||||||
| chr5:118895885
|
G | C | 6 | a0001c0001t0013g0011a0001c0001t0013g0142a0001c0001t0013g0218others(3): Show | 6 | HG00741.hp1 HG01891.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.597+32652C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118895885 | ||||||
| chr5:118896125
|
A | T | 6 | a0001c0001t0014g0115a0001c0001t0014g0227a0001c0001t0014g0229others(3): Show | 6 | HG02970.hp1 HG03041.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.597+32412T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118896125 | ||||||
| chr5:118896358
|
G | T | 1 | a0001c0001t0029g0132 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.597+32179C>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118896358 | ||||||
| chr5:118896412
|
T | A | 5 | a0001c0001t0010g0027a0001c0001t0010g0063a0002c0003t0010g0237others(2): Show | 5 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.597+32125A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118896412 | ||||||
| chr5:118896446
|
T | C | 1 | a0001c0001t0029g0132 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.597+32091A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118896446 | ||||||
| chr5:118896461
|
G | C | 1 | a0001c0001t0002g0097 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.597+32076C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118896461 | ||||||
| chr5:118896466
|
GA | G | 11 | a0001c0001t0004g0068a0001c0001t0004g0116a0001c0001t0004g0117others(8): Show | 11 | HG01496.hp1 HG01884.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.597+32070delT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118896466 | ||||||
| chr5:118896466
|
GAA | G | 73 | a0001c0001t0001g0235a0001c0001t0003g0007a0001c0001t0003g0008others(70): Show | 74 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.597+32069_597+3207 others(6): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118896466 | ||||||
| chr5:118896825
|
T | G | 1 | a0001c0001t0004g0068 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.597+31712A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118896825 | ||||||
| chr5:118896834
|
T | C | 1 | a0001c0001t0009g0149 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.597+31703A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118896834 | ||||||
| chr5:118896882
|
G | A | 1 | a0001c0001t0004g0116 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.597+31655C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118896882 | ||||||
| chr5:118897012
|
T | C | 1 | a0001c0001t0032g0236 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.597+31525A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118897012 | ||||||
| chr5:118897191
|
T | A | 81 | a0001c0001t0001g0235a0001c0001t0003g0007a0001c0001t0003g0008others(78): Show | 82 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.597+31346A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118897191 | ||||||
| chr5:118897285
|
G | C | 10 | a0001c0001t0004g0116a0001c0001t0004g0117a0001c0001t0004g0118others(7): Show | 10 | HG01496.hp1 HG01884.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.597+31252C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118897285 | ||||||
| chr5:118897332
|
T | C | 22 | a0001c0001t0001g0235a0001c0001t0003g0007a0001c0001t0003g0008others(19): Show | 22 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.597+31205A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118897332 | ||||||
| chr5:118897432
|
T | A | 4 | a0001c0001t0010g0027a0002c0003t0010g0237a0002c0003t0010g0238others(1): Show | 4 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.597+31105A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118897432 | ||||||
| chr5:118897546
|
T | C | 3 | a0001c0001t0006g0029a0001c0001t0006g0092a0001c0001t0006g0093 | 3 | HG01168.hp2 HG01169.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.597+30991A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118897546 | ||||||
| chr5:118897658
|
C | T | 1 | a0001c0001t0001g0056 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.597+30879G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118897658 | ||||||
| chr5:118897728
|
T | G | 35 | a0001c0001t0001g0235a0001c0001t0003g0007a0001c0001t0003g0008others(32): Show | 36 | HG00639.hp2 HG00642.hp1 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.597+30809A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118897728 | ||||||
| chr5:118897742
|
T | C | 3 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0057 | 3 | HG00738.hp2 HG01070.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.597+30795A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118897742 | ||||||
| chr5:118898033
|
T | G | 2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | HG01099.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.597+30504A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118898033 | ||||||
| chr5:118898227
|
T | C | 1 | a0001c0001t0010g0027 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.597+30310A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118898227 | ||||||
| chr5:118898331
|
T | A | 4 | a0001c0001t0001g0044a0001c0001t0001g0094a0001c0001t0001g0099others(1): Show | 4 | NA18948.hp2 NA18981.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.597+30206A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118898331 | ||||||
| chr5:118898382
|
G | C | 12 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(9): Show | 12 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.597+30155C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118898382 | ||||||
| chr5:118898414
|
T | C | 1 | a0001c0001t0032g0236 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.597+30123A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118898414 | ||||||
| chr5:118898489
|
C | T | 2 | a0001c0001t0020g0121a0001c0001t0020g0122 | 2 | HG01106.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.597+30048G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118898489 | ||||||
| chr5:118898496
|
GA | G | 7 | a0001c0001t0014g0115a0001c0001t0014g0227a0001c0001t0014g0229others(4): Show | 7 | HG02257.hp1 HG02970.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.597+30040delT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118898496 | ||||||
| chr5:118898528
|
G | A | 1 | a0001c0001t0022g0082 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.597+30009C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118898528 | ||||||
| chr5:118898530
|
G | A | 3 | a0001c0001t0001g0235a0001c0002t0001g0003a0003c0005t0042g0241 | 3 | HG02145.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.597+30007C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118898530 | ||||||
| chr5:118898590
|
C | T | 2 | a0001c0001t0018g0001a0001c0001t0029g0132 | 3 | HG00642.hp1 HG01074.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.597+29947G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118898590 | ||||||
| chr5:118898601
|
G | C | 4 | a0001c0001t0010g0027a0002c0003t0010g0237a0002c0003t0010g0238others(1): Show | 4 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.597+29936C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118898601 | ||||||
| chr5:118898658
|
C | CA | 68 | a0001c0001t0001g0103a0001c0001t0001g0164a0001c0001t0001g0172others(65): Show | 68 | HG00099.hp1 HG00639.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.597+29878dupT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118898658 | ||||||
| chr5:118898722
|
A | C | 1 | a0001c0001t0024g0206 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.597+29815T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118898722 | ||||||
| chr5:118898805
|
A | T | 5 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(2): Show | 5 | HG01071.hp2 HG01261.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.597+29732T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118898805 | ||||||
| chr5:118899404
|
T | C | 1 | a0001c0001t0018g0001 | 2 | HG00642.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.597+29133A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118899404 | ||||||
| chr5:118899447
|
G | C | 1 | a0001c0001t0029g0132 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.597+29090C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118899447 | ||||||
| chr5:118899688
|
G | A | 5 | a0001c0001t0013g0011a0001c0001t0013g0142a0001c0001t0013g0218others(2): Show | 5 | HG01891.hp1 HG02723.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.597+28849C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118899688 | ||||||
| chr5:118899757
|
G | A | 1 | a0001c0001t0014g0115 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.597+28780C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118899757 | ||||||
| chr5:118899799
|
CT | C | 47 | a0001c0001t0001g0173a0001c0001t0001g0193a0001c0001t0002g0057others(44): Show | 48 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.597+28737delA | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118899799 | ||||||
| chr5:118899804
|
T | C | 11 | a0001c0001t0003g0008a0001c0001t0003g0012a0001c0001t0003g0013others(8): Show | 11 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.597+28733A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118899804 | ||||||
| chr5:118899895
|
G | A | 2 | a0001c0001t0020g0121a0001c0001t0020g0122 | 2 | HG01106.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.597+28642C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118899895 | ||||||
| chr5:118900001
|
C | T | 3 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0224 | 3 | HG01099.hp1 HG01169.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.597+28536G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118900001 | ||||||
| chr5:118900072
|
G | C | 3 | a0001c0001t0003g0014a0001c0001t0003g0017a0001c0001t0003g0168 | 3 | HG02647.hp2 HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.597+28465C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118900072 | ||||||
| chr5:118900271
|
T | C | 2 | a0001c0001t0016g0232a0001c0001t0016g0233 | 2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.597+28266A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118900271 | ||||||
| chr5:118900295
|
C | G | 33 | a0001c0001t0001g0164a0001c0001t0005g0151a0001c0001t0005g0154others(30): Show | 33 | HG00733.hp2 HG01109.hp1 HG01496.hp2 others(30): Show |
intron_variant | MODIFIER | c.597+28242G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118900295 | ||||||
| chr5:118900378
|
A | G | 10 | a0001c0001t0004g0116a0001c0001t0004g0117a0001c0001t0004g0118others(7): Show | 10 | HG01496.hp1 HG01884.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.597+28159T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118900378 | ||||||
| chr5:118900667
|
C | A | 1 | a0001c0001t0028g0138 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.597+27870G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118900667 | ||||||
| chr5:118900693
|
A | G | 104 | a0001c0001t0001g0171a0001c0001t0002g0033a0001c0001t0002g0034others(101): Show | 105 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.597+27844T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118900693 | ||||||
| chr5:118900709
|
A | G | 12 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(9): Show | 12 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.597+27828T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118900709 | ||||||
| chr5:118900830
|
C | T | 15 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(12): Show | 15 | HG00639.hp2 HG00741.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.597+27707G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118900830 | ||||||
| chr5:118901207
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.597+27330T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118901207 | ||||||
| chr5:118901478
|
T | C | 1 | a0001c0001t0001g0055 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.597+27059A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118901478 | ||||||
| chr5:118901805
|
A | T | 5 | a0001c0001t0008g0204a0001c0001t0008g0220a0001c0001t0008g0221others(2): Show | 5 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.597+26732T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118901805 | ||||||
| chr5:118901821
|
T | A | 13 | a0001c0001t0004g0068a0001c0001t0004g0116a0001c0001t0004g0117others(10): Show | 14 | HG00642.hp1 HG01074.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.597+26716A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118901821 | ||||||
| chr5:118901893
|
C | A | 2 | a0001c0001t0003g0007a0001c0001t0003g0180 | 2 | HG02896.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.597+26644G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118901893 | ||||||
| chr5:118902116
|
T | C | 1 | a0001c0001t0001g0191 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.597+26421A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118902116 | ||||||
| chr5:118902321
|
T | C | 1 | a0001c0001t0023g0226 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.597+26216A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118902321 | ||||||
| chr5:118902364
|
C | T | 1 | a0001c0001t0020g0121 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.597+26173G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118902364 | ||||||
| chr5:118902403
|
T | C | 1 | a0001c0001t0001g0074 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.597+26134A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118902403 | ||||||
| chr5:118902465
|
A | G | 1 | a0001c0001t0001g0046 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.597+26072T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118902465 | ||||||
| chr5:118902862
|
T | G | 1 | a0001c0001t0003g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.597+25675A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118902862 | ||||||
| chr5:118903113
|
ATTTG | A | 7 | a0001c0001t0013g0011a0001c0001t0013g0142a0001c0001t0013g0218others(4): Show | 7 | HG01891.hp1 HG02723.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.597+25420_597+2542 others(8): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118903113 | ||||||
| chr5:118903146
|
T | TA | 8 | a0001c0001t0001g0065a0001c0001t0001g0202a0001c0001t0001g0216others(5): Show | 8 | HG00140.hp1 HG01891.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.597+25390dupT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118903146 | ||||||
| chr5:118903146
|
TA | T | 69 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(66): Show | 69 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.597+25390delT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118903146 | ||||||
| chr5:118903159
|
A | C | 1 | a0001c0001t0001g0224 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.597+25378T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118903159 | ||||||
| chr5:118903189
|
G | T | 1 | a0001c0001t0017g0146 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.597+25348C>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118903189 | ||||||
| chr5:118903212
|
T | C | 10 | a0001c0001t0004g0116a0001c0001t0004g0117a0001c0001t0004g0118others(7): Show | 10 | HG01496.hp1 HG01884.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.597+25325A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118903212 | ||||||
| chr5:118903456
|
T | A | 7 | a0001c0001t0013g0011a0001c0001t0013g0142a0001c0001t0013g0218others(4): Show | 7 | HG01891.hp1 HG02723.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.597+25081A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118903456 | ||||||
| chr5:118903493
|
C | G | 1 | a0001c0001t0009g0149 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.597+25044G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118903493 | ||||||
| chr5:118903503
|
A | G | 6 | a0001c0001t0013g0011a0001c0001t0013g0142a0001c0001t0013g0218others(3): Show | 6 | HG00741.hp1 HG01891.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.597+25034T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118903503 | ||||||
| chr5:118903603
|
G | A | 2 | a0001c0001t0002g0126a0001c0001t0002g0131 | 2 | HG02738.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.597+24934C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118903603 | ||||||
| chr5:118903780
|
G | A | 1 | a0001c0001t0005g0151 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.597+24757C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118903780 | ||||||
| chr5:118903876
|
TAA | T | 13 | a0001c0001t0004g0068a0001c0001t0004g0116a0001c0001t0004g0117others(10): Show | 14 | HG00642.hp1 HG01074.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.597+24659_597+2466 others(6): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118903876 | ||||||
| chr5:118903953
|
A | G | 10 | a0001c0001t0001g0173a0001c0001t0001g0175a0001c0001t0001g0176others(7): Show | 10 | HG01099.hp1 HG01169.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.597+24584T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118903953 | ||||||
| chr5:118904061
|
A | G | 27 | a0001c0001t0005g0151a0001c0001t0005g0154a0001c0001t0005g0155others(24): Show | 27 | HG00733.hp2 HG01109.hp1 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.597+24476T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118904061 | ||||||
| chr5:118904174
|
G | A | 7 | a0001c0001t0013g0011a0001c0001t0013g0142a0001c0001t0013g0218others(4): Show | 7 | HG01891.hp1 HG02723.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.597+24363C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118904174 | ||||||
| chr5:118904310
|
A | G | 6 | a0001c0001t0001g0172a0001c0001t0001g0190a0001c0001t0001g0195others(3): Show | 6 | HG00140.hp1 HG00733.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.597+24227T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118904310 | ||||||
| chr5:118904328
|
G | A | 1 | a0001c0001t0014g0227 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.597+24209C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118904328 | ||||||
| chr5:118904356
|
T | C | 9 | a0001c0001t0007g0141a0001c0001t0007g0208a0001c0001t0007g0209others(6): Show | 9 | HG02486.hp1 HG02572.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.597+24181A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118904356 | ||||||
| chr5:118904472
|
C | A | 1 | a0001c0001t0001g0128 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.597+24065G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118904472 | ||||||
| chr5:118904539
|
G | A | 1 | a0001c0001t0001g0050 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.597+23998C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118904539 | ||||||
| chr5:118904571
|
A | G | 2 | a0001c0001t0011g0111a0001c0001t0011g0112 | 2 | NA18951.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.597+23966T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118904571 | ||||||
| chr5:118904628
|
A | C | 12 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(9): Show | 12 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.597+23909T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118904628 | ||||||
| chr5:118904755
|
G | A | 2 | a0001c0001t0020g0121a0001c0001t0020g0122 | 2 | HG01106.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.597+23782C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118904755 | ||||||
| chr5:118904812
|
A | T | 89 | a0001c0001t0002g0058a0001c0001t0002g0078a0001c0001t0002g0107others(86): Show | 90 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.597+23725T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118904812 | ||||||
| chr5:118904899
|
T | C | 1 | a0001c0001t0004g0068 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.597+23638A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118904899 | ||||||
| chr5:118904924
|
A | T | 1 | a0001c0001t0013g0142 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.597+23613T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118904924 | ||||||
| chr5:118904953
|
G | C | 1 | a0001c0001t0001g0051 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.597+23584C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118904953 | ||||||
| chr5:118904978
|
G | T | 1 | a0001c0001t0004g0068 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.597+23559C>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118904978 | ||||||
| chr5:118905288
|
G | A | 12 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(9): Show | 12 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.597+23249C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118905288 | ||||||
| chr5:118905558
|
C | T | 12 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(9): Show | 12 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.597+22979G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118905558 | ||||||
| chr5:118905659
|
G | T | 5 | a0001c0001t0010g0027a0001c0001t0010g0063a0002c0003t0010g0237others(2): Show | 5 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.597+22878C>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118905659 | ||||||
| chr5:118905723
|
A | T | 101 | a0001c0001t0001g0164a0001c0001t0002g0033a0001c0001t0002g0034others(98): Show | 102 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.597+22814T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118905723 | ||||||
| chr5:118905788
|
T | G | 12 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(9): Show | 12 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.597+22749A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118905788 | ||||||
| chr5:118905839
|
C | T | 24 | a0001c0001t0001g0125a0001c0001t0001g0143a0001c0001t0001g0150others(21): Show | 24 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(21): Show |
intron_variant | MODIFIER | c.597+22698G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118905839 | ||||||
| chr5:118906007
|
G | A | 2 | a0001c0001t0003g0008a0001c0001t0027g0009 | 2 | HG00639.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.597+22530C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118906007 | ||||||
| chr5:118906159
|
A | G | 51 | a0001c0001t0001g0194a0001c0001t0002g0034a0001c0001t0002g0042others(48): Show | 52 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.597+22378T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118906159 | ||||||
| chr5:118906286
|
G | T | 4 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0086others(1): Show | 4 | HG00735.hp2 HG01175.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.597+22251C>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118906286 | ||||||
| chr5:118906391
|
C | T | 78 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(75): Show | 79 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.597+22146G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118906391 | ||||||
| chr5:118906395
|
T | C | 9 | a0001c0001t0007g0141a0001c0001t0007g0208a0001c0001t0007g0209others(6): Show | 9 | HG02486.hp1 HG02572.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.597+22142A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118906395 | ||||||
| chr5:118906456
|
T | A | 3 | a0001c0001t0015g0133a0001c0001t0015g0134a0001c0001t0015g0135 | 3 | HG01884.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.597+22081A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118906456 | ||||||
| chr5:118906913
|
C | T | 2 | a0001c0001t0007g0214a0001c0001t0007g0215 | 2 | HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.597+21624G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118906913 | ||||||
| chr5:118906919
|
T | C | 5 | a0001c0001t0007g0141a0001c0001t0013g0011a0001c0001t0013g0142others(2): Show | 5 | HG01891.hp1 HG02630.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.597+21618A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118906919 | ||||||
| chr5:118906937
|
G | T | 2 | a0001c0001t0001g0192a0001c0001t0001g0193 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.597+21600C>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118906937 | ||||||
| chr5:118907127
|
C | T | 2 | a0001c0001t0016g0232a0001c0001t0016g0233 | 2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.597+21410G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118907127 | ||||||
| chr5:118907168
|
T | C | 2 | a0001c0001t0016g0232a0001c0001t0016g0233 | 2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.597+21369A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118907168 | ||||||
| chr5:118907181
|
T | A | 4 | a0001c0001t0010g0027a0002c0003t0010g0237a0002c0003t0010g0238others(1): Show | 4 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.597+21356A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118907181 | ||||||
| chr5:118907281
|
A | C | 1 | a0001c0001t0002g0107 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.597+21256T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118907281 | ||||||
| chr5:118907312
|
G | T | 1 | a0001c0001t0035g0207 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.597+21225C>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118907312 | ||||||
| chr5:118907318
|
C | T | 3 | a0001c0001t0015g0133a0001c0001t0015g0134a0001c0001t0015g0135 | 3 | HG01884.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.597+21219G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118907318 | ||||||
| chr5:118907348
|
G | T | 74 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(71): Show | 74 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.597+21189C>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118907348 | ||||||
| chr5:118907350
|
G | T | 5 | a0001c0001t0008g0221a0001c0001t0014g0115a0001c0001t0014g0229others(2): Show | 5 | HG02257.hp1 HG02970.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.597+21187C>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118907350 | ||||||
| chr5:118907529
|
G | A | 2 | a0001c0001t0012g0199a0001c0001t0033g0205 | 2 | HG02970.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.597+21008C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118907529 | ||||||
| chr5:118907727
|
CA | C | 21 | a0001c0001t0005g0151a0001c0001t0005g0154a0001c0001t0005g0155others(18): Show | 21 | HG00544.hp1 HG00733.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.597+20809delT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118907727 | ||||||
| chr5:118907931
|
G | C | 162 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(159): Show | 163 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.597+20606C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118907931 | ||||||
| chr5:118907973
|
T | C | 4 | a0001c0001t0003g0012a0001c0001t0003g0014a0001c0001t0003g0017others(1): Show | 4 | HG02647.hp2 HG03130.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.597+20564A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118907973 | ||||||
| chr5:118908019
|
C | T | 1 | a0001c0001t0012g0167 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.597+20518G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118908019 | ||||||
| chr5:118908101
|
T | C | 6 | a0001c0001t0008g0204a0001c0001t0008g0220a0001c0001t0008g0221others(3): Show | 6 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.597+20436A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118908101 | ||||||
| chr5:118908181
|
G | T | 1 | a0001c0002t0001g0004 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.597+20356C>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118908181 | ||||||
| chr5:118908282
|
G | A | 1 | a0001c0001t0029g0132 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.597+20255C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118908282 | ||||||
| chr5:118908374
|
T | C | 1 | a0001c0001t0033g0205 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.597+20163A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118908374 | ||||||
| chr5:118908435
|
T | C | 4 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0086others(1): Show | 4 | HG00735.hp2 HG01175.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.597+20102A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118908435 | ||||||
| chr5:118908656
|
C | CA | 9 | a0001c0001t0007g0141a0001c0001t0013g0011a0001c0001t0013g0142others(6): Show | 9 | HG00741.hp1 HG01884.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.597+19880dupT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118908656 | ||||||
| chr5:118908670
|
G | A | 31 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(28): Show | 31 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.597+19867C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118908670 | ||||||
| chr5:118908885
|
T | C | 1 | a0001c0001t0008g0221 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.597+19652A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118908885 | ||||||
| chr5:118909323
|
C | T | 1 | a0001c0001t0004g0118 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.597+19214G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118909323 | ||||||
| chr5:118909328
|
G | T | 4 | a0001c0001t0010g0027a0002c0003t0010g0237a0002c0003t0010g0238others(1): Show | 4 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.597+19209C>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118909328 | ||||||
| chr5:118909498
|
T | C | 47 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0031others(44): Show | 47 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.597+19039A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118909498 | ||||||
| chr5:118909526
|
C | G | 1 | a0001c0001t0001g0100 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.597+19011G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118909526 | ||||||
| chr5:118909647
|
T | C | 3 | a0001c0001t0020g0121a0001c0001t0020g0122a0001c0001t0021g0010 | 3 | HG01106.hp1 HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.597+18890A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118909647 | ||||||
| chr5:118909690
|
C | T | 2 | a0001c0001t0030g0225a0001c0001t0033g0205 | 2 | HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.597+18847G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118909690 | ||||||
| chr5:118909782
|
T | A | 1 | a0001c0001t0001g0145 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.597+18755A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118909782 | ||||||
| chr5:118909818
|
A | G | 1 | a0001c0001t0009g0159 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.597+18719T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118909818 | ||||||
| chr5:118909841
|
G | A | 11 | a0001c0001t0010g0027a0001c0001t0010g0063a0001c0001t0014g0115others(8): Show | 11 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.597+18696C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118909841 | ||||||
| chr5:118910171
|
C | A | 1 | a0001c0001t0004g0068 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.597+18366G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118910171 | ||||||
| chr5:118910364
|
T | A | 2 | a0001c0001t0030g0225a0001c0001t0033g0205 | 2 | HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.597+18173A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118910364 | ||||||
| chr5:118910380
|
A | T | 1 | a0001c0002t0037g0002 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.597+18157T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118910380 | ||||||
| chr5:118910661
|
T | C | 5 | a0001c0001t0014g0115a0001c0001t0014g0227a0001c0001t0014g0229others(2): Show | 5 | HG02970.hp1 HG03209.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.597+17876A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118910661 | ||||||
| chr5:118910664
|
T | A | 2 | a0001c0001t0030g0225a0001c0001t0033g0205 | 2 | HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.597+17873A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118910664 | ||||||
| chr5:118910667
|
T | C | 1 | a0001c0001t0005g0158 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.597+17870A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118910667 | ||||||
| chr5:118910738
|
A | C | 1 | a0001c0001t0001g0024 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.597+17799T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118910738 | ||||||
| chr5:118910863
|
C | A | 14 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(11): Show | 14 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.597+17674G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118910863 | ||||||
| chr5:118910900
|
T | G | 5 | a0001c0001t0014g0115a0001c0001t0014g0227a0001c0001t0014g0229others(2): Show | 5 | HG02970.hp1 HG03209.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.597+17637A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118910900 | ||||||
| chr5:118910962
|
G | T | 1 | a0002c0003t0010g0238 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.597+17575C>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118910962 | ||||||
| chr5:118911104
|
C | CT | 11 | a0001c0001t0004g0068a0001c0001t0004g0116a0001c0001t0004g0117others(8): Show | 11 | HG01496.hp1 HG01884.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.597+17432dupA | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118911104 | ||||||
| chr5:118911110
|
T | C | 2 | a0001c0001t0016g0232a0001c0001t0016g0233 | 2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.597+17427A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118911110 | ||||||
| chr5:118911514
|
A | G | 1 | a0001c0001t0018g0001 | 2 | HG00642.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.597+17023T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118911514 | ||||||
| chr5:118911615
|
C | T | 11 | a0001c0001t0010g0027a0001c0001t0010g0063a0001c0001t0014g0115others(8): Show | 11 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.597+16922G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118911615 | ||||||
| chr5:118911976
|
A | G | 10 | a0001c0001t0004g0116a0001c0001t0004g0117a0001c0001t0004g0118others(7): Show | 10 | HG01496.hp1 HG01884.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.597+16561T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118911976 | ||||||
| chr5:118912076
|
A | G | 11 | a0001c0001t0004g0068a0001c0001t0004g0116a0001c0001t0004g0117others(8): Show | 11 | HG01496.hp1 HG01884.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.597+16461T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118912076 | ||||||
| chr5:118912115
|
G | C | 1 | a0001c0001t0002g0160 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.597+16422C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118912115 | ||||||
| chr5:118912115
|
G | T | 1 | a0001c0001t0004g0068 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.597+16422C>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118912115 | ||||||
| chr5:118912178
|
T | A | 1 | a0001c0001t0004g0068 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.597+16359A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118912178 | ||||||
| chr5:118912281
|
G | A | 1 | a0001c0001t0032g0236 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.597+16256C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118912281 | ||||||
| chr5:118912473
|
C | A | 21 | a0001c0001t0007g0208a0001c0001t0007g0209a0001c0001t0007g0210others(18): Show | 21 | HG01496.hp2 HG01891.hp2 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.597+16064G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118912473 | ||||||
| chr5:118912513
|
T | G | 22 | a0001c0001t0007g0208a0001c0001t0007g0209a0001c0001t0007g0210others(19): Show | 22 | HG01496.hp2 HG01891.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.597+16024A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118912513 | ||||||
| chr5:118912527
|
G | A | 3 | a0001c0001t0015g0133a0001c0001t0015g0134a0001c0001t0015g0135 | 3 | HG01884.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.597+16010C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118912527 | ||||||
| chr5:118912644
|
C | T | 21 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(18): Show | 21 | HG01192.hp2 HG02015.hp2 HG02074.hp2 others(18): Show |
intron_variant | MODIFIER | c.597+15893G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118912644 | ||||||
| chr5:118912657
|
GC | G | 76 | a0001c0001t0001g0235a0001c0001t0003g0007a0001c0001t0003g0008others(73): Show | 77 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.597+15879delG | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118912657 | ||||||
| chr5:118912734
|
A | G | 3 | a0001c0001t0009g0144a0001c0001t0009g0147a0001c0001t0009g0148 | 3 | NA18959.hp2 NA19058.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.597+15803T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118912734 | ||||||
| chr5:118912749
|
G | A | 1 | a0001c0001t0001g0048 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.597+15788C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118912749 | ||||||
| chr5:118912889
|
T | C | 2 | a0001c0001t0001g0026a0001c0001t0001g0028 | 2 | HG00423.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.597+15648A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118912889 | ||||||
| chr5:118912942
|
A | C | 7 | a0001c0001t0007g0141a0001c0001t0013g0011a0001c0001t0013g0142others(4): Show | 7 | HG01891.hp1 HG02630.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.597+15595T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118912942 | ||||||
| chr5:118913083
|
T | C | 2 | a0001c0001t0030g0225a0001c0001t0033g0205 | 2 | HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.597+15454A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118913083 | ||||||
| chr5:118913244
|
A | C | 1 | a0001c0001t0002g0107 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.597+15293T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118913244 | ||||||
| chr5:118913335
|
A | G | 1 | a0001c0001t0001g0049 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.597+15202T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118913335 | ||||||
| chr5:118913372
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.597+15165G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118913372 | ||||||
| chr5:118913390
|
TATATATA others(3): Show |
T | 7 | a0001c0001t0001g0096a0001c0001t0008g0223a0001c0001t0010g0027others(4): Show | 7 | HG00423.hp1 HG00544.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.597+15137_597+1514 others(14): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118913390 | ||||||
| chr5:118913407
|
A | G | 1 | a0001c0001t0001g0166 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.597+15130T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118913407 | ||||||
| chr5:118913410
|
GATATATA others(5): Show |
G | 3 | a0001c0001t0020g0121a0001c0001t0020g0122a0001c0001t0021g0010 | 3 | HG01106.hp1 HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.597+15115_597+1512 others(16): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118913410 | ||||||
| chr5:118913420
|
GAT | G | 5 | a0001c0001t0007g0141a0001c0001t0013g0011a0001c0001t0013g0142others(2): Show | 5 | HG01891.hp1 HG02630.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.597+15115_597+1511 others(6): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118913420 | ||||||
| chr5:118913432
|
T | C | 7 | a0001c0001t0001g0164a0001c0001t0001g0235a0001c0001t0004g0068others(4): Show | 7 | HG02145.hp2 HG02809.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.597+15105A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118913432 | ||||||
| chr5:118913432
|
T | TAC | 65 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(62): Show | 65 | HG00280.hp1 HG00639.hp1 HG00741.hp1 others(62): Show |
intron_variant | MODIFIER | c.597+15103_597+1510 others(6): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118913432 | ||||||
| chr5:118913434
|
C | T | 3 | a0001c0001t0020g0121a0001c0001t0020g0122a0001c0001t0021g0010 | 3 | HG01106.hp1 HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.597+15103G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118913434 | ||||||
| chr5:118913581
|
G | C | 1 | a0001c0001t0014g0115 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.597+14956C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118913581 | ||||||
| chr5:118913738
|
T | G | 12 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(9): Show | 12 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.597+14799A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118913738 | ||||||
| chr5:118913752
|
A | G | 1 | a0001c0001t0008g0204 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.597+14785T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118913752 | ||||||
| chr5:118913875
|
C | T | 1 | a0001c0001t0030g0225 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.597+14662G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118913875 | ||||||
| chr5:118913968
|
C | CAATAAA | 76 | a0001c0001t0001g0235a0001c0001t0003g0007a0001c0001t0003g0008others(73): Show | 77 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.597+14563_597+1456 others(10): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118913968 | ||||||
| chr5:118913996
|
T | C | 5 | a0001c0001t0010g0027a0001c0001t0010g0063a0002c0003t0010g0237others(2): Show | 5 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.597+14541A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118913996 | ||||||
| chr5:118914004
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.597+14533A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118914004 | ||||||
| chr5:118914181
|
C | T | 5 | a0001c0001t0014g0115a0001c0001t0014g0227a0001c0001t0014g0229others(2): Show | 5 | HG02970.hp1 HG03209.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.597+14356G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118914181 | ||||||
| chr5:118914279
|
C | G | 76 | a0001c0001t0001g0235a0001c0001t0003g0007a0001c0001t0003g0008others(73): Show | 77 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.597+14258G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118914279 | ||||||
| chr5:118914338
|
A | C | 1 | a0001c0001t0001g0030 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.597+14199T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118914338 | ||||||
| chr5:118914463
|
C | T | 3 | a0001c0001t0015g0133a0001c0001t0015g0134a0001c0001t0015g0135 | 3 | HG01884.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.597+14074G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118914463 | ||||||
| chr5:118914465
|
C | T | 14 | a0001c0001t0004g0068a0001c0001t0004g0116a0001c0001t0004g0117others(11): Show | 14 | HG01496.hp1 HG01884.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.597+14072G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118914465 | ||||||
| chr5:118914474
|
C | G | 3 | a0001c0001t0020g0121a0001c0001t0020g0122a0001c0001t0021g0010 | 3 | HG01106.hp1 HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.597+14063G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118914474 | ||||||
| chr5:118914545
|
TATA | T | 5 | a0001c0001t0007g0141a0001c0001t0013g0011a0001c0001t0013g0142others(2): Show | 5 | HG01891.hp1 HG02630.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.597+13989_597+1399 others(7): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118914545 | ||||||
| chr5:118914644
|
C | T | 5 | a0001c0001t0007g0141a0001c0001t0013g0011a0001c0001t0013g0142others(2): Show | 5 | HG01891.hp1 HG02630.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.597+13893G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118914644 | ||||||
| chr5:118914665
|
C | T | 5 | a0001c0001t0014g0115a0001c0001t0014g0227a0001c0001t0014g0229others(2): Show | 5 | HG02970.hp1 HG03209.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.597+13872G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118914665 | ||||||
| chr5:118914767
|
T | C | 12 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(9): Show | 12 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.597+13770A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118914767 | ||||||
| chr5:118914890
|
T | C | 90 | a0001c0001t0001g0143a0001c0001t0001g0150a0001c0001t0001g0152others(87): Show | 91 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.597+13647A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118914890 | ||||||
| chr5:118914897
|
A | T | 3 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006 | 3 | HG02055.hp2 HG02976.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.597+13640T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118914897 | ||||||
| chr5:118914952
|
T | C | 5 | a0001c0001t0007g0141a0001c0001t0013g0011a0001c0001t0013g0142others(2): Show | 5 | HG01891.hp1 HG02630.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.597+13585A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118914952 | ||||||
| chr5:118914969
|
A | G | 1 | a0001c0001t0001g0066 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.597+13568T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118914969 | ||||||
| chr5:118914998
|
G | A | 1 | a0001c0001t0001g0074 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.597+13539C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118914998 | ||||||
| chr5:118915244
|
GAAAAAAA others(3228): Show |
G | 1 | a0001c0004t0001g0032 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.597+10058_597+1329 others(4): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118915244 | ||||||
| chr5:118915374
|
A | AT | 16 | a0001c0001t0001g0066a0001c0001t0001g0114a0001c0001t0001g0143others(13): Show | 16 | HG00099.hp2 HG00323.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.597+13162dupA | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118915374 | ||||||
| chr5:118915374
|
AT | A | 34 | a0001c0001t0001g0235a0001c0001t0004g0068a0001c0001t0004g0116others(31): Show | 34 | HG00423.hp1 HG00544.hp1 HG01496.hp1 others(31): Show |
intron_variant | MODIFIER | c.597+13162delA | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118915374 | ||||||
| chr5:118915424
|
G | C | 1 | a0001c0001t0004g0068 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.597+13113C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118915424 | ||||||
| chr5:118915443
|
C | T | 50 | a0001c0001t0001g0235a0001c0001t0003g0007a0001c0001t0003g0008others(47): Show | 50 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.597+13094G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118915443 | ||||||
| chr5:118915444
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.597+13093C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118915444 | ||||||
| chr5:118915461
|
A | G | 1 | a0001c0001t0012g0198 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.597+13076T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118915461 | ||||||
| chr5:118915520
|
G | A | 1 | a0001c0001t0007g0141 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.597+13017C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118915520 | ||||||
| chr5:118915626
|
G | A | 1 | a0001c0001t0030g0225 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.597+12911C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118915626 | ||||||
| chr5:118915669
|
C | A | 1 | a0001c0001t0030g0225 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.597+12868G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118915669 | ||||||
| chr5:118915673
|
C | T | 1 | a0001c0001t0004g0118 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.597+12864G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118915673 | ||||||
| chr5:118915740
|
T | C | 4 | a0001c0001t0010g0027a0002c0003t0010g0237a0002c0003t0010g0238others(1): Show | 4 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.597+12797A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118915740 | ||||||
| chr5:118915839
|
T | C | 1 | a0001c0001t0003g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.597+12698A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118915839 | ||||||
| chr5:118916170
|
T | C | 1 | a0001c0001t0018g0001 | 2 | HG00642.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.597+12367A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118916170 | ||||||
| chr5:118916311
|
T | C | 5 | a0001c0001t0007g0141a0001c0001t0013g0011a0001c0001t0013g0142others(2): Show | 5 | HG01891.hp1 HG02630.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.597+12226A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118916311 | ||||||
| chr5:118916360
|
C | A | 5 | a0001c0001t0010g0027a0001c0001t0010g0063a0002c0003t0010g0237others(2): Show | 5 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.597+12177G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118916360 | ||||||
| chr5:118916455
|
C | T | 1 | a0001c0001t0032g0236 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.597+12082G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118916455 | ||||||
| chr5:118916464
|
G | A | 1 | a0001c0001t0003g0017 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.597+12073C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118916464 | ||||||
| chr5:118916570
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.597+11967G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118916570 | ||||||
| chr5:118916665
|
C | CA | 38 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0095others(35): Show | 38 | HG00099.hp1 HG00280.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.597+11871dupT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118916665 | ||||||
| chr5:118916767
|
C | T | 73 | a0001c0001t0001g0235a0001c0001t0003g0007a0001c0001t0003g0008others(70): Show | 74 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.597+11770G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118916767 | ||||||
| chr5:118916923
|
G | A | 1 | a0001c0001t0006g0059 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.597+11614C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118916923 | ||||||
| chr5:118917069
|
C | T | 2 | a0001c0001t0030g0225a0001c0001t0033g0205 | 2 | HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.597+11468G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118917069 | ||||||
| chr5:118917099
|
T | C | 1 | a0001c0001t0009g0159 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.597+11438A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118917099 | ||||||
| chr5:118917168
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.597+11369C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118917168 | ||||||
| chr5:118917358
|
C | T | 6 | a0001c0001t0008g0204a0001c0001t0008g0220a0001c0001t0008g0221others(3): Show | 6 | HG01891.hp2 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.597+11179G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118917358 | ||||||
| chr5:118917408
|
G | T | 74 | a0001c0001t0001g0235a0001c0001t0003g0007a0001c0001t0003g0008others(71): Show | 75 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.597+11129C>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118917408 | ||||||
| chr5:118917635
|
G | C | 1 | a0001c0001t0032g0236 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.597+10902C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118917635 | ||||||
| chr5:118917900
|
C | T | 2 | a0001c0001t0016g0232a0001c0001t0016g0233 | 2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.597+10637G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118917900 | ||||||
| chr5:118917901
|
G | A | 3 | a0001c0001t0001g0177a0001c0001t0001g0179a0001c0001t0001g0185 | 3 | HG00280.hp1 HG01081.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.597+10636C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118917901 | ||||||
| chr5:118917908
|
T | A | 1 | a0001c0001t0023g0226 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.597+10629A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118917908 | ||||||
| chr5:118917960
|
C | CA | 12 | a0001c0001t0002g0033a0001c0001t0007g0141a0001c0001t0009g0148others(9): Show | 12 | HG00423.hp1 HG00544.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.597+10576dupT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118917960 | ||||||
| chr5:118917979
|
A | AATTTCAT others(1): Show |
5 | a0001c0001t0010g0027a0001c0001t0010g0063a0002c0003t0010g0237others(2): Show | 5 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.597+10550_597+1055 others(12): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118917979 | ||||||
| chr5:118918160
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.597+10377A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118918160 | ||||||
| chr5:118918322
|
AG | A | 5 | a0001c0001t0001g0235a0001c0001t0016g0232a0001c0001t0016g0233others(2): Show | 5 | HG02145.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.597+10214delC | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118918322 | ||||||
| chr5:118918334
|
A | T | 9 | a0001c0001t0006g0029a0001c0001t0006g0047a0001c0001t0006g0072others(6): Show | 9 | HG00639.hp1 HG01123.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.597+10203T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118918334 | ||||||
| chr5:118918420
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.597+10117C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118918420 | ||||||
| chr5:118918472
|
A | AG | 52 | a0001c0001t0001g0143a0001c0001t0001g0150a0001c0001t0001g0153others(49): Show | 53 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.597+10064dupC | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118918472 | ||||||
| chr5:118918555
|
TCCCAGAA others(104): Show |
T | 1 | a0001c0004t0001g0032 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.597+9871_597+9981d others(2): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118918555 | ||||||
| chr5:118918580
|
C | T | 1 | a0001c0001t0039g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.597+9957G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118918580 | ||||||
| chr5:118918682
|
C | T | 14 | a0001c0001t0010g0027a0001c0001t0010g0063a0001c0001t0014g0115others(11): Show | 14 | HG00423.hp1 HG00544.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.597+9855G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118918682 | ||||||
| chr5:118918700
|
G | A | 3 | a0001c0001t0001g0235a0001c0002t0001g0003a0003c0005t0042g0241 | 3 | HG02145.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.597+9837C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118918700 | ||||||
| chr5:118918803
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.597+9734G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118918803 | ||||||
| chr5:118918826
|
A | AG | 5 | a0001c0001t0014g0115a0001c0001t0014g0227a0001c0001t0014g0229others(2): Show | 5 | HG02970.hp1 HG03209.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.597+9710dupC | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118918826 | ||||||
| chr5:118918858
|
C | T | 2 | a0001c0001t0009g0144a0001c0001t0009g0148 | 2 | NA18959.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.597+9679G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118918858 | ||||||
| chr5:118918859
|
C | A | 4 | a0001c0001t0001g0044a0001c0001t0001g0094a0001c0001t0001g0099others(1): Show | 4 | NA18948.hp2 NA18981.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.597+9678G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118918859 | ||||||
| chr5:118918936
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.597+9601G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118918936 | ||||||
| chr5:118918962
|
G | C | 1 | a0001c0001t0016g0232 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.597+9575C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118918962 | ||||||
| chr5:118918991
|
C | A | 1 | a0001c0001t0004g0124 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.597+9546G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118918991 | ||||||
| chr5:118918991
|
C | T | 1 | a0001c0001t0032g0236 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.597+9546G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118918991 | ||||||
| chr5:118919050
|
G | A | 5 | a0001c0001t0001g0235a0001c0001t0016g0232a0001c0001t0016g0233others(2): Show | 5 | HG02145.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.597+9487C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118919050 | ||||||
| chr5:118919165
|
C | G | 1 | a0001c0004t0001g0032 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.597+9372G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118919165 | ||||||
| chr5:118919348
|
C | T | 1 | a0001c0001t0023g0226 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.597+9189G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118919348 | ||||||
| chr5:118919443
|
C | A | 1 | a0001c0001t0009g0147 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.597+9094G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118919443 | ||||||
| chr5:118919531
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.597+9006C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118919531 | ||||||
| chr5:118919648
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.597+8889T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118919648 | ||||||
| chr5:118919655
|
A | C | 24 | a0001c0001t0001g0235a0001c0001t0003g0007a0001c0001t0003g0008others(21): Show | 24 | HG00639.hp2 HG00741.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.597+8882T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118919655 | ||||||
| chr5:118919879
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.597+8658A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118919879 | ||||||
| chr5:118919894
|
T | C | 37 | a0001c0001t0001g0143a0001c0001t0001g0150a0001c0001t0001g0152others(34): Show | 37 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.597+8643A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118919894 | ||||||
| chr5:118920006
|
TA | T | 8 | a0001c0001t0003g0180a0001c0001t0014g0115a0001c0001t0014g0227others(5): Show | 8 | HG02630.hp2 HG02896.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.597+8530delT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118920006 | ||||||
| chr5:118920007
|
A | T | 9 | a0001c0001t0009g0144a0001c0001t0009g0147a0001c0001t0009g0148others(6): Show | 9 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.597+8530T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118920007 | ||||||
| chr5:118920008
|
A | T | 2 | a0001c0001t0014g0229a0001c0001t0014g0230 | 2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.597+8529T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118920008 | ||||||
| chr5:118920019
|
T | G | 1 | a0001c0001t0001g0235 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.597+8518A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118920019 | ||||||
| chr5:118920244
|
C | T | 1 | a0001c0001t0018g0001 | 2 | HG00642.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.597+8293G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118920244 | ||||||
| chr5:118920303
|
T | A | 24 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(21): Show | 24 | HG01192.hp2 HG01255.hp1 HG02015.hp2 others(21): Show |
intron_variant | MODIFIER | c.597+8234A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118920303 | ||||||
| chr5:118920316
|
A | C | 1 | a0001c0001t0001g0100 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.597+8221T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118920316 | ||||||
| chr5:118920380
|
C | A | 1 | a0001c0001t0001g0125 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.597+8157G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118920380 | ||||||
| chr5:118920464
|
T | C | 1 | a0001c0001t0006g0047 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.597+8073A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118920464 | ||||||
| chr5:118920508
|
T | C | 1 | a0001c0001t0001g0046 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.597+8029A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118920508 | ||||||
| chr5:118920569
|
G | C | 8 | a0001c0001t0004g0117a0001c0001t0004g0118a0001c0001t0004g0120others(5): Show | 8 | HG01496.hp1 HG01884.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.597+7968C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118920569 | ||||||
| chr5:118920608
|
A | ATTC | 88 | a0001c0001t0001g0143a0001c0001t0001g0150a0001c0001t0001g0152others(85): Show | 89 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.597+7926_597+7928d others(5): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118920608 | ||||||
| chr5:118920711
|
G | A | 6 | a0001c0001t0008g0204a0001c0001t0008g0220a0001c0001t0008g0221others(3): Show | 6 | HG01891.hp2 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.597+7826C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118920711 | ||||||
| chr5:118920751
|
A | G | 3 | a0001c0001t0001g0235a0001c0002t0001g0003a0003c0005t0042g0241 | 3 | HG02145.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.597+7786T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118920751 | ||||||
| chr5:118920889
|
C | G | 3 | a0001c0001t0008g0220a0001c0001t0008g0222a0001c0001t0008g0223 | 3 | HG01891.hp2 HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.597+7648G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118920889 | ||||||
| chr5:118921163
|
AG | A | 12 | a0001c0001t0004g0068a0001c0001t0004g0116a0001c0001t0004g0117others(9): Show | 12 | HG01496.hp1 HG01884.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.597+7373delC | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118921163 | ||||||
| chr5:118921197
|
A | G | 22 | a0001c0001t0004g0068a0001c0001t0004g0116a0001c0001t0004g0117others(19): Show | 23 | HG00642.hp1 HG01074.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.597+7340T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118921197 | ||||||
| chr5:118921320
|
T | G | 31 | a0001c0001t0001g0143a0001c0001t0001g0150a0001c0001t0001g0152others(28): Show | 31 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.597+7217A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118921320 | ||||||
| chr5:118921377
|
T | C | 1 | a0001c0001t0004g0136 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.597+7160A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118921377 | ||||||
| chr5:118921442
|
C | T | 22 | a0001c0001t0004g0068a0001c0001t0004g0116a0001c0001t0004g0117others(19): Show | 23 | HG00642.hp1 HG01074.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.597+7095G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118921442 | ||||||
| chr5:118921449
|
G | A | 12 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(9): Show | 12 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.597+7088C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118921449 | ||||||
| chr5:118921470
|
T | C | 6 | a0001c0001t0007g0141a0001c0001t0013g0011a0001c0001t0013g0142others(3): Show | 6 | HG01891.hp1 HG02630.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.597+7067A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118921470 | ||||||
| chr5:118921481
|
G | A | 7 | a0001c0001t0008g0204a0001c0001t0008g0220a0001c0001t0008g0221others(4): Show | 8 | HG00642.hp1 HG01074.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.597+7056C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118921481 | ||||||
| chr5:118921497
|
G | T | 5 | a0001c0001t0010g0027a0001c0001t0010g0063a0002c0003t0010g0237others(2): Show | 5 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.597+7040C>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118921497 | ||||||
| chr5:118921498
|
C | A | 5 | a0001c0001t0010g0027a0001c0001t0010g0063a0002c0003t0010g0237others(2): Show | 5 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.597+7039G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118921498 | ||||||
| chr5:118921499
|
A | C | 5 | a0001c0001t0010g0027a0001c0001t0010g0063a0002c0003t0010g0237others(2): Show | 5 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.597+7038T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118921499 | ||||||
| chr5:118921521
|
T | TA | 12 | a0001c0001t0001g0173a0001c0001t0001g0175a0001c0001t0001g0176others(9): Show | 12 | HG01099.hp1 HG01106.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.597+7015dupT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118921521 | ||||||
| chr5:118921523
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.597+7014T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118921523 | ||||||
| chr5:118921615
|
G | C | 1 | a0001c0001t0029g0132 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.597+6922C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118921615 | ||||||
| chr5:118921674
|
G | T | 10 | a0001c0001t0004g0116a0001c0001t0004g0117a0001c0001t0004g0118others(7): Show | 10 | HG01496.hp1 HG01884.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.597+6863C>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118921674 | ||||||
| chr5:118921739
|
G | A | 29 | a0001c0001t0001g0113a0001c0001t0001g0125a0001c0001t0001g0171others(26): Show | 29 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.597+6798C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118921739 | ||||||
| chr5:118921982
|
C | T | 1 | a0001c0001t0020g0122 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.597+6555G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118921982 | ||||||
| chr5:118922249
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.597+6288T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118922249 | ||||||
| chr5:118922652
|
G | C | 2 | a0001c0001t0014g0229a0001c0001t0014g0230 | 2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.597+5885C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118922652 | ||||||
| chr5:118922719
|
T | C | 17 | a0001c0001t0001g0235a0001c0001t0003g0007a0001c0001t0003g0008others(14): Show | 17 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.597+5818A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118922719 | ||||||
| chr5:118922788
|
G | A | 31 | a0001c0001t0001g0235a0001c0001t0003g0007a0001c0001t0003g0008others(28): Show | 31 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.597+5749C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118922788 | ||||||
| chr5:118922833
|
G | C | 90 | a0001c0001t0001g0143a0001c0001t0001g0150a0001c0001t0001g0152others(87): Show | 91 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.597+5704C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118922833 | ||||||
| chr5:118923215
|
CT | C | 6 | a0001c0001t0014g0115a0001c0001t0014g0227a0001c0001t0014g0229others(3): Show | 6 | HG02630.hp2 HG02970.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.597+5321delA | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118923215 | ||||||
| chr5:118923323
|
G | A | 3 | a0001c0001t0015g0133a0001c0001t0015g0134a0001c0001t0015g0135 | 3 | HG01884.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.597+5214C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118923323 | ||||||
| chr5:118923388
|
T | G | 24 | a0001c0001t0001g0235a0001c0001t0003g0007a0001c0001t0003g0008others(21): Show | 24 | HG00639.hp2 HG00741.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.597+5149A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118923388 | ||||||
| chr5:118923697
|
C | G | 1 | a0001c0001t0008g0204 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.597+4840G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118923697 | ||||||
| chr5:118923759
|
G | A | 1 | a0001c0001t0023g0226 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.597+4778C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118923759 | ||||||
| chr5:118924071
|
A | G | 1 | a0001c0002t0001g0004 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.597+4466T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118924071 | ||||||
| chr5:118924103
|
A | G | 1 | a0001c0001t0032g0236 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.597+4434T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118924103 | ||||||
| chr5:118924108
|
G | A | 1 | a0001c0001t0001g0037 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.597+4429C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118924108 | ||||||
| chr5:118924183
|
G | C | 1 | a0001c0001t0001g0038 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.597+4354C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118924183 | ||||||
| chr5:118924199
|
T | C | 32 | a0001c0001t0001g0143a0001c0001t0001g0150a0001c0001t0001g0152others(29): Show | 32 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.597+4338A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118924199 | ||||||
| chr5:118924199
|
T | G | 1 | a0001c0001t0018g0001 | 2 | HG00642.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.597+4338A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118924199 | ||||||
| chr5:118924208
|
C | A | 91 | a0001c0001t0001g0143a0001c0001t0001g0150a0001c0001t0001g0152others(88): Show | 92 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.597+4329G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118924208 | ||||||
| chr5:118924217
|
GTATCTCC others(15): Show |
G | 1 | a0001c0001t0002g0174 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.597+4298_597+4319d others(24): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118924217 | ||||||
| chr5:118924474
|
T | A | 5 | a0001c0001t0010g0027a0001c0001t0010g0063a0002c0003t0010g0237others(2): Show | 5 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.597+4063A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118924474 | ||||||
| chr5:118924879
|
T | C | 1 | a0001c0001t0018g0001 | 2 | HG00642.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.597+3658A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118924879 | ||||||
| chr5:118925093
|
A | C | 52 | a0001c0001t0001g0143a0001c0001t0001g0150a0001c0001t0001g0152others(49): Show | 52 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.597+3444T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118925093 | ||||||
| chr5:118925162
|
A | T | 1 | a0001c0001t0005g0157 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.597+3375T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118925162 | ||||||
| chr5:118925195
|
G | T | 1 | a0001c0001t0001g0189 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.597+3342C>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118925195 | ||||||
| chr5:118925307
|
A | G | 1 | a0001c0001t0001g0066 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.597+3230T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118925307 | ||||||
| chr5:118925434
|
C | T | 84 | a0001c0001t0001g0143a0001c0001t0001g0150a0001c0001t0001g0152others(81): Show | 85 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.597+3103G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118925434 | ||||||
| chr5:118925642
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.597+2895C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118925642 | ||||||
| chr5:118925702
|
G | A | 5 | a0001c0001t0007g0141a0001c0001t0013g0011a0001c0001t0013g0142others(2): Show | 5 | HG01891.hp1 HG02630.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.597+2835C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118925702 | ||||||
| chr5:118925705
|
C | T | 5 | a0001c0001t0007g0141a0001c0001t0013g0011a0001c0001t0013g0142others(2): Show | 5 | HG01891.hp1 HG02630.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.597+2832G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118925705 | ||||||
| chr5:118925707
|
C | T | 5 | a0001c0001t0007g0141a0001c0001t0013g0011a0001c0001t0013g0142others(2): Show | 5 | HG01891.hp1 HG02630.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.597+2830G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118925707 | ||||||
| chr5:118925708
|
A | G | 5 | a0001c0001t0007g0141a0001c0001t0013g0011a0001c0001t0013g0142others(2): Show | 5 | HG01891.hp1 HG02630.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.597+2829T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118925708 | ||||||
| chr5:118925714
|
G | A | 5 | a0001c0001t0007g0141a0001c0001t0013g0011a0001c0001t0013g0142others(2): Show | 5 | HG01891.hp1 HG02630.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.597+2823C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118925714 | ||||||
| chr5:118925717
|
T | C | 5 | a0001c0001t0007g0141a0001c0001t0013g0011a0001c0001t0013g0142others(2): Show | 5 | HG01891.hp1 HG02630.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.597+2820A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118925717 | ||||||
| chr5:118925718
|
A | C | 5 | a0001c0001t0007g0141a0001c0001t0013g0011a0001c0001t0013g0142others(2): Show | 5 | HG01891.hp1 HG02630.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.597+2819T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118925718 | ||||||
| chr5:118925725
|
G | C | 5 | a0001c0001t0007g0141a0001c0001t0013g0011a0001c0001t0013g0142others(2): Show | 5 | HG01891.hp1 HG02630.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.597+2812C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118925725 | ||||||
| chr5:118925738
|
A | G | 5 | a0001c0001t0007g0141a0001c0001t0013g0011a0001c0001t0013g0142others(2): Show | 5 | HG01891.hp1 HG02630.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.597+2799T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118925738 | ||||||
| chr5:118925782
|
T | C | 5 | a0001c0001t0014g0115a0001c0001t0014g0227a0001c0001t0014g0229others(2): Show | 5 | HG02970.hp1 HG03209.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.597+2755A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118925782 | ||||||
| chr5:118926129
|
C | T | 8 | a0001c0001t0007g0208a0001c0001t0007g0209a0001c0001t0007g0210others(5): Show | 8 | HG02486.hp1 HG02572.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.597+2408G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118926129 | ||||||
| chr5:118926316
|
G | A | 5 | a0001c0001t0014g0115a0001c0001t0014g0227a0001c0001t0014g0229others(2): Show | 5 | HG02970.hp1 HG03209.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.597+2221C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118926316 | ||||||
| chr5:118926430
|
C | T | 5 | a0001c0001t0012g0167a0001c0001t0012g0198a0001c0001t0012g0199others(2): Show | 5 | HG02258.hp1 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.597+2107G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118926430 | ||||||
| chr5:118926685
|
C | G | 5 | a0001c0001t0018g0001a0001c0001t0020g0121a0001c0001t0020g0122others(2): Show | 6 | HG00642.hp1 HG01074.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.597+1852G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118926685 | ||||||
| chr5:118927460
|
T | C | 17 | a0001c0001t0001g0235a0001c0001t0003g0007a0001c0001t0003g0008others(14): Show | 17 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.597+1077A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118927460 | ||||||
| chr5:118927617
|
C | A | 11 | a0001c0001t0004g0068a0001c0001t0004g0116a0001c0001t0004g0117others(8): Show | 11 | HG01496.hp1 HG01884.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.597+920G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118927617 | ||||||
| chr5:118927792
|
C | G | 1 | a0001c0001t0024g0206 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.597+745G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118927792 | ||||||
| chr5:118928243
|
T | G | 63 | a0001c0001t0001g0164a0001c0001t0002g0174a0001c0001t0003g0007others(60): Show | 64 | HG00639.hp2 HG00642.hp1 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.597+294A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 4/5 | chr5 | 118928243 | ||||||
| chr5:118928744
|
T | A | 3 | a0001c0001t0001g0030a0001c0001t0001g0165a0001c0001t0030g0225 | 3 | HG02615.hp2 HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.405-15A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118928744 | ||||||
| chr5:118929112
|
C | A | 1 | a0001c0001t0001g0055 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.405-383G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118929112 | ||||||
| chr5:118929119
|
A | T | 1 | a0001c0001t0005g0157 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.405-390T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118929119 | ||||||
| chr5:118929171
|
C | A | 81 | a0001c0001t0001g0164a0001c0001t0001g0235a0001c0001t0002g0174others(78): Show | 82 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.405-442G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118929171 | ||||||
| chr5:118929207
|
T | C | 1 | a0001c0001t0011g0073 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.405-478A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118929207 | ||||||
| chr5:118929489
|
C | CT | 56 | a0001c0001t0001g0087a0001c0001t0001g0096a0001c0001t0001g0098others(53): Show | 57 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.405-761dupA | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118929489 | ||||||
| chr5:118929526
|
G | A | 1 | a0001c0001t0019g0025 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.405-797C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118929526 | ||||||
| chr5:118929842
|
A | C | 59 | a0001c0001t0001g0074a0001c0001t0001g0127a0001c0001t0001g0128others(56): Show | 60 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.405-1113T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118929842 | ||||||
| chr5:118929849
|
G | A | 3 | a0001c0001t0001g0235a0001c0002t0001g0003a0003c0005t0042g0241 | 3 | HG02145.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.405-1120C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118929849 | ||||||
| chr5:118930107
|
G | A | 1 | a0001c0001t0005g0158 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.405-1378C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118930107 | ||||||
| chr5:118930120
|
T | G | 19 | a0001c0001t0001g0235a0001c0001t0003g0007a0001c0001t0003g0008others(16): Show | 19 | HG00639.hp2 HG00741.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.405-1391A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118930120 | ||||||
| chr5:118930643
|
A | G | 1 | a0001c0001t0032g0236 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.405-1914T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118930643 | ||||||
| chr5:118930739
|
C | G | 8 | a0001c0001t0007g0208a0001c0001t0007g0209a0001c0001t0007g0210others(5): Show | 8 | HG02486.hp1 HG02572.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.405-2010G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118930739 | ||||||
| chr5:118930817
|
AAC | A | 6 | a0001c0001t0008g0204a0001c0001t0014g0115a0001c0001t0014g0227others(3): Show | 6 | HG02886.hp1 HG02970.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.405-2090_405-2089d others(4): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118930817 | ||||||
| chr5:118930856
|
C | T | 12 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(9): Show | 12 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.405-2127G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118930856 | ||||||
| chr5:118930948
|
TTGAC | T | 3 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006 | 3 | HG02055.hp2 HG02976.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.405-2223_405-2220d others(6): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118930948 | ||||||
| chr5:118931120
|
C | T | 15 | a0001c0001t0001g0022a0001c0001t0001g0096a0001c0001t0001g0098others(12): Show | 15 | HG00738.hp1 HG00741.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.405-2391G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118931120 | ||||||
| chr5:118931150
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.405-2421A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118931150 | ||||||
| chr5:118931292
|
A | G | 3 | a0001c0001t0015g0133a0001c0001t0015g0134a0001c0001t0015g0135 | 3 | HG01884.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.405-2563T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118931292 | ||||||
| chr5:118931322
|
G | A | 1 | a0001c0001t0033g0205 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.405-2593C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118931322 | ||||||
| chr5:118931335
|
C | T | 5 | a0001c0001t0010g0027a0001c0001t0010g0063a0002c0003t0010g0237others(2): Show | 5 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.405-2606G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118931335 | ||||||
| chr5:118931398
|
T | TA | 16 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(13): Show | 16 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.405-2670dupT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118931398 | ||||||
| chr5:118931398
|
T | TAA | 7 | a0001c0001t0003g0013a0001c0001t0003g0015a0001c0001t0003g0016others(4): Show | 7 | HG01243.hp2 HG02258.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.405-2671_405-2670d others(4): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118931398 | ||||||
| chr5:118931398
|
T | TAAA | 6 | a0001c0001t0001g0235a0001c0001t0007g0141a0001c0001t0013g0011others(3): Show | 6 | HG01891.hp1 HG02145.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.405-2672_405-2670d others(5): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118931398 | ||||||
| chr5:118931398
|
TA | T | 25 | a0001c0001t0001g0041a0001c0001t0001g0048a0001c0001t0001g0053others(22): Show | 26 | HG00099.hp1 HG00642.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.405-2670delT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118931398 | ||||||
| chr5:118931479
|
T | A | 3 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021 | 3 | HG01192.hp2 HG03491.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.405-2750A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118931479 | ||||||
| chr5:118931727
|
AT | A | 34 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0031others(31): Show | 34 | HG00323.hp2 HG00423.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.405-2999delA | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118931727 | ||||||
| chr5:118931866
|
A | G | 7 | a0001c0001t0008g0204a0001c0001t0014g0115a0001c0001t0014g0227others(4): Show | 7 | HG02630.hp2 HG02886.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.405-3137T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118931866 | ||||||
| chr5:118931938
|
C | T | 32 | a0001c0001t0002g0174a0001c0001t0005g0151a0001c0001t0005g0154others(29): Show | 32 | HG00642.hp2 HG00733.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.405-3209G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118931938 | ||||||
| chr5:118931980
|
G | A | 1 | a0001c0001t0001g0095 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.405-3251C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118931980 | ||||||
| chr5:118931989
|
G | A | 1 | a0001c0001t0029g0132 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.405-3260C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118931989 | ||||||
| chr5:118932096
|
A | G | 5 | a0001c0001t0010g0027a0001c0001t0010g0063a0002c0003t0010g0237others(2): Show | 5 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.405-3367T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118932096 | ||||||
| chr5:118932279
|
C | A | 3 | a0001c0001t0001g0235a0001c0002t0001g0003a0003c0005t0042g0241 | 3 | HG02145.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.405-3550G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118932279 | ||||||
| chr5:118932323
|
TA | T | 5 | a0001c0001t0001g0048a0001c0001t0006g0092a0001c0001t0007g0213others(2): Show | 5 | HG01168.hp2 HG02258.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.405-3595delT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118932323 | ||||||
| chr5:118932521
|
C | T | 2 | a0001c0001t0002g0129a0001c0001t0002g0130 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.405-3792G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118932521 | ||||||
| chr5:118932588
|
T | C | 1 | a0001c0001t0001g0079 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.405-3859A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118932588 | ||||||
| chr5:118932757
|
C | G | 1 | a0001c0001t0030g0225 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.405-4028G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118932757 | ||||||
| chr5:118932800
|
T | G | 3 | a0001c0001t0020g0121a0001c0001t0020g0122a0001c0001t0021g0010 | 3 | HG01106.hp1 HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.405-4071A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118932800 | ||||||
| chr5:118933199
|
G | C | 3 | a0001c0001t0015g0133a0001c0001t0015g0134a0001c0001t0015g0135 | 3 | HG01884.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.405-4470C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118933199 | ||||||
| chr5:118933548
|
C | T | 1 | a0001c0001t0001g0095 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.405-4819G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118933548 | ||||||
| chr5:118933711
|
T | C | 22 | a0001c0001t0004g0068a0001c0001t0004g0116a0001c0001t0004g0117others(19): Show | 23 | HG00642.hp1 HG01074.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.405-4982A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118933711 | ||||||
| chr5:118933760
|
C | G | 1 | a0001c0001t0001g0094 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.405-5031G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118933760 | ||||||
| chr5:118933859
|
A | C | 28 | a0001c0001t0001g0164a0001c0001t0002g0174a0001c0001t0005g0151others(25): Show | 28 | HG00642.hp2 HG00733.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.405-5130T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118933859 | ||||||
| chr5:118933878
|
C | CTAAA | 9 | a0001c0001t0001g0101a0001c0001t0001g0127a0001c0001t0001g0128others(6): Show | 9 | HG00140.hp2 HG01081.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.405-5153_405-5150d others(6): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118933878 | ||||||
| chr5:118933878
|
CTAAA | C | 41 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(38): Show | 41 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.405-5153_405-5150d others(6): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118933878 | ||||||
| chr5:118933878
|
CTAAATAA others(1): Show |
C | 9 | a0001c0001t0001g0175a0001c0001t0001g0177a0001c0001t0001g0179others(6): Show | 9 | HG00280.hp1 HG01081.hp2 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.405-5157_405-5150d others(10): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118933878 | ||||||
| chr5:118933878
|
CTAAATAA others(5): Show |
C | 13 | a0001c0001t0007g0141a0001c0001t0008g0204a0001c0001t0008g0220others(10): Show | 13 | HG00741.hp1 HG01891.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.405-5161_405-5150d others(14): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118933878 | ||||||
| chr5:118934055
|
A | G | 1 | a0001c0001t0024g0206 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.404+5141T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118934055 | ||||||
| chr5:118934059
|
C | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0071 | 2 | HG01255.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.404+5137G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118934059 | ||||||
| chr5:118934272
|
T | TA | 113 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(110): Show | 113 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.404+4923dupT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118934272 | ||||||
| chr5:118934272
|
T | TAA | 29 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0052others(26): Show | 29 | HG00544.hp2 HG00642.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.404+4922_404+4923d others(4): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118934272 | ||||||
| chr5:118934272
|
T | TAAA | 8 | a0001c0001t0001g0039a0001c0001t0001g0069a0001c0001t0001g0089others(5): Show | 8 | HG01106.hp2 HG02015.hp2 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.404+4921_404+4923d others(5): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118934272 | ||||||
| chr5:118934272
|
TA | T | 19 | a0001c0001t0004g0068a0001c0001t0004g0116a0001c0001t0007g0208others(16): Show | 19 | HG01106.hp1 HG02486.hp1 HG02572.hp2 others(16): Show |
intron_variant | MODIFIER | c.404+4923delT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118934272 | ||||||
| chr5:118934272
|
TAA | T | 5 | a0001c0001t0009g0144a0001c0001t0009g0148a0001c0001t0009g0149others(2): Show | 5 | HG01496.hp2 HG04199.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.404+4922_404+4923d others(4): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118934272 | ||||||
| chr5:118934272
|
TAAAAAAA others(3): Show |
T | 20 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0002g0033others(17): Show | 20 | HG00099.hp1 HG01071.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.404+4914_404+4923d others(12): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118934272 | ||||||
| chr5:118934429
|
C | CA | 12 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(9): Show | 12 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.404+4766dupT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118934429 | ||||||
| chr5:118934442
|
G | A | 11 | a0001c0001t0002g0174a0001c0001t0005g0151a0001c0001t0005g0154others(8): Show | 11 | HG00642.hp2 HG00733.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.404+4754C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118934442 | ||||||
| chr5:118934756
|
ATAAACTC others(6): Show |
A | 1 | a0001c0001t0002g0107 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.404+4427_404+4439d others(15): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118934756 | ||||||
| chr5:118934784
|
T | C | 12 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(9): Show | 12 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.404+4412A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118934784 | ||||||
| chr5:118934839
|
C | T | 10 | a0001c0001t0004g0116a0001c0001t0004g0117a0001c0001t0004g0118others(7): Show | 10 | HG01496.hp1 HG01884.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.404+4357G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118934839 | ||||||
| chr5:118934860
|
G | A | 1 | a0001c0001t0013g0219 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.404+4336C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118934860 | ||||||
| chr5:118934941
|
C | T | 8 | a0001c0001t0007g0208a0001c0001t0007g0209a0001c0001t0007g0210others(5): Show | 8 | HG02486.hp1 HG02572.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.404+4255G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118934941 | ||||||
| chr5:118935107
|
G | A | 5 | a0001c0001t0007g0141a0001c0001t0013g0011a0001c0001t0013g0142others(2): Show | 5 | HG01891.hp1 HG02630.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.404+4089C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118935107 | ||||||
| chr5:118935229
|
C | T | 1 | a0001c0001t0031g0170 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.404+3967G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118935229 | ||||||
| chr5:118935230
|
G | A | 3 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021 | 3 | HG01192.hp2 HG03491.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.404+3966C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118935230 | ||||||
| chr5:118935243
|
A | G | 23 | a0001c0001t0001g0235a0001c0001t0003g0007a0001c0001t0003g0008others(20): Show | 23 | HG00639.hp2 HG00741.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.404+3953T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118935243 | ||||||
| chr5:118935330
|
A | C | 3 | a0001c0001t0001g0087a0001c0001t0001g0102a0001c0001t0001g0109 | 3 | HG00544.hp2 NA19003.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.404+3866T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118935330 | ||||||
| chr5:118935721
|
G | A | 36 | a0001c0001t0001g0235a0001c0001t0003g0007a0001c0001t0003g0008others(33): Show | 37 | HG00639.hp2 HG00642.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.404+3475C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118935721 | ||||||
| chr5:118935783
|
C | T | 12 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(9): Show | 12 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.404+3413G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118935783 | ||||||
| chr5:118935822
|
T | C | 1 | a0001c0001t0018g0001 | 2 | HG00642.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.404+3374A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118935822 | ||||||
| chr5:118935836
|
T | C | 1 | a0001c0001t0033g0205 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.404+3360A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118935836 | ||||||
| chr5:118936109
|
G | C | 3 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021 | 3 | HG01192.hp2 HG03491.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.404+3087C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118936109 | ||||||
| chr5:118936368
|
G | A | 1 | a0001c0001t0022g0082 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.404+2828C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118936368 | ||||||
| chr5:118936531
|
A | G | 3 | a0001c0001t0001g0235a0001c0002t0001g0003a0003c0005t0042g0241 | 3 | HG02145.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.404+2665T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118936531 | ||||||
| chr5:118936542
|
C | T | 1 | a0001c0001t0002g0070 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.404+2654G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118936542 | ||||||
| chr5:118936587
|
T | C | 1 | a0001c0001t0029g0132 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.404+2609A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118936587 | ||||||
| chr5:118936655
|
A | T | 11 | a0001c0001t0001g0235a0001c0001t0007g0141a0001c0001t0013g0011others(8): Show | 11 | HG00741.hp1 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.404+2541T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118936655 | ||||||
| chr5:118936707
|
T | C | 1 | a0001c0001t0010g0063 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.404+2489A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118936707 | ||||||
| chr5:118936910
|
G | C | 1 | a0001c0001t0033g0205 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.404+2286C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118936910 | ||||||
| chr5:118936990
|
G | A | 11 | a0001c0001t0004g0068a0001c0001t0004g0116a0001c0001t0004g0117others(8): Show | 11 | HG01496.hp1 HG01884.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.404+2206C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118936990 | ||||||
| chr5:118937131
|
T | C | 1 | a0001c0001t0001g0056 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.404+2065A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118937131 | ||||||
| chr5:118937142
|
T | C | 8 | a0001c0001t0007g0208a0001c0001t0007g0209a0001c0001t0007g0210others(5): Show | 8 | HG02486.hp1 HG02572.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.404+2054A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118937142 | ||||||
| chr5:118937285
|
T | C | 1 | a0001c0001t0032g0236 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.404+1911A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118937285 | ||||||
| chr5:118937363
|
G | A | 1 | a0001c0001t0012g0201 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.404+1833C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118937363 | ||||||
| chr5:118937383
|
CA | C | 214 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(211): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.404+1812delT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118937383 | ||||||
| chr5:118937391
|
A | G | 4 | a0001c0001t0001g0177a0001c0001t0001g0179a0001c0001t0001g0185others(1): Show | 4 | HG00280.hp1 HG01081.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.404+1805T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118937391 | ||||||
| chr5:118937603
|
A | G | 1 | a0001c0001t0004g0137 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.404+1593T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118937603 | ||||||
| chr5:118937715
|
C | T | 1 | a0001c0001t0033g0205 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.404+1481G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118937715 | ||||||
| chr5:118937776
|
C | G | 3 | a0001c0001t0001g0175a0001c0001t0001g0194a0001c0002t0037g0002 | 3 | HG02280.hp1 HG02615.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.404+1420G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118937776 | ||||||
| chr5:118937963
|
G | A | 53 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0028others(50): Show | 53 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.404+1233C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118937963 | ||||||
| chr5:118937972
|
T | TTTG | 234 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(231): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.404+1223_404+1224i others(5): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118937972 | ||||||
| chr5:118938016
|
C | T | 6 | a0001c0001t0014g0115a0001c0001t0014g0227a0001c0001t0014g0229others(3): Show | 6 | HG02630.hp2 HG02970.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.404+1180G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118938016 | ||||||
| chr5:118938087
|
G | A | 1 | a0001c0001t0002g0196 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.404+1109C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118938087 | ||||||
| chr5:118938789
|
T | A | 1 | a0001c0001t0002g0196 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.404+407A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118938789 | ||||||
| chr5:118938808
|
CA | C | 13 | a0001c0001t0001g0095a0001c0001t0004g0116a0001c0001t0004g0117others(10): Show | 13 | HG01496.hp1 HG01884.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.404+387delT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118938808 | ||||||
| chr5:118938834
|
A | G | 1 | a0001c0001t0033g0205 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.404+362T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118938834 | ||||||
| chr5:118938845
|
G | GA | 25 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(22): Show | 25 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.404+350dupT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118938845 | ||||||
| chr5:118938923
|
T | A | 1 | a0001c0001t0001g0114 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.404+273A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118938923 | ||||||
| chr5:118938958
|
T | C | 3 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021 | 3 | HG01192.hp2 HG03491.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.404+238A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 3/5 | chr5 | 118938958 | ||||||
| chr5:118939384
|
C | T | 87 | a0001c0001t0001g0143a0001c0001t0001g0150a0001c0001t0001g0152others(84): Show | 88 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.310-94G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118939384 | ||||||
| chr5:118939585
|
A | G | 1 | a0001c0001t0033g0205 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.310-295T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118939585 | ||||||
| chr5:118939660
|
T | A | 1 | a0001c0001t0032g0236 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.310-370A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118939660 | ||||||
| chr5:118939662
|
C | T | 2 | a0001c0001t0003g0008a0001c0001t0027g0009 | 2 | HG00639.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.310-372G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118939662 | ||||||
| chr5:118939715
|
G | A | 11 | a0001c0001t0001g0235a0001c0001t0004g0068a0001c0001t0007g0141others(8): Show | 11 | HG01891.hp1 HG02145.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.310-425C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118939715 | ||||||
| chr5:118939835
|
T | C | 1 | a0001c0001t0033g0205 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.310-545A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118939835 | ||||||
| chr5:118939836
|
T | G | 1 | a0001c0001t0004g0068 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.310-546A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118939836 | ||||||
| chr5:118940174
|
T | G | 32 | a0001c0001t0001g0143a0001c0001t0001g0150a0001c0001t0001g0152others(29): Show | 32 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.310-884A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118940174 | ||||||
| chr5:118940310
|
G | A | 6 | a0001c0001t0008g0204a0001c0001t0008g0220a0001c0001t0008g0221others(3): Show | 6 | HG01891.hp2 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.310-1020C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118940310 | ||||||
| chr5:118940356
|
T | C | 1 | a0001c0001t0013g0142 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.310-1066A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118940356 | ||||||
| chr5:118940491
|
T | C | 6 | a0001c0001t0007g0141a0001c0001t0013g0011a0001c0001t0013g0142others(3): Show | 6 | HG01891.hp1 HG02630.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.310-1201A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118940491 | ||||||
| chr5:118940557
|
A | T | 1 | a0001c0001t0001g0127 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.310-1267T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118940557 | ||||||
| chr5:118940836
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.310-1546G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118940836 | ||||||
| chr5:118940854
|
CTAA | C | 6 | a0001c0001t0001g0235a0001c0001t0004g0068a0001c0001t0016g0232others(3): Show | 6 | HG02145.hp2 HG02809.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.310-1567_310-1565d others(5): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118940854 | ||||||
| chr5:118940898
|
G | A | 1 | a0001c0001t0036g0178 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.310-1608C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118940898 | ||||||
| chr5:118940982
|
C | T | 2 | a0001c0001t0018g0001a0001c0001t0029g0132 | 3 | HG00642.hp1 HG01074.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.310-1692G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118940982 | ||||||
| chr5:118941033
|
T | G | 32 | a0001c0001t0001g0143a0001c0001t0001g0150a0001c0001t0001g0152others(29): Show | 32 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.310-1743A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118941033 | ||||||
| chr5:118941098
|
C | G | 3 | a0001c0001t0015g0133a0001c0001t0015g0134a0001c0001t0015g0135 | 3 | HG01884.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.310-1808G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118941098 | ||||||
| chr5:118941127
|
C | G | 1 | a0001c0001t0018g0001 | 2 | HG00642.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.310-1837G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118941127 | ||||||
| chr5:118941144
|
C | T | 3 | a0001c0001t0018g0001a0001c0001t0021g0010a0001c0001t0029g0132 | 4 | HG00642.hp1 HG01074.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.310-1854G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118941144 | ||||||
| chr5:118941390
|
T | C | 12 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(9): Show | 12 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.310-2100A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118941390 | ||||||
| chr5:118941447
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.310-2157C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118941447 | ||||||
| chr5:118941451
|
T | C | 6 | a0001c0001t0007g0141a0001c0001t0013g0011a0001c0001t0013g0142others(3): Show | 6 | HG01891.hp1 HG02630.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.310-2161A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118941451 | ||||||
| chr5:118941494
|
C | A | 1 | a0001c0001t0001g0039 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.310-2204G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118941494 | ||||||
| chr5:118941499
|
G | C | 1 | a0001c0001t0004g0123 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.310-2209C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118941499 | ||||||
| chr5:118941534
|
T | C | 32 | a0001c0001t0001g0143a0001c0001t0001g0150a0001c0001t0001g0152others(29): Show | 32 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.310-2244A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118941534 | ||||||
| chr5:118941568
|
C | A | 2 | a0001c0001t0002g0126a0001c0001t0002g0131 | 2 | HG02738.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.310-2278G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118941568 | ||||||
| chr5:118941590
|
T | A | 14 | a0001c0001t0010g0027a0001c0001t0010g0063a0001c0001t0014g0115others(11): Show | 14 | HG00423.hp1 HG00544.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.310-2300A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118941590 | ||||||
| chr5:118941647
|
A | G | 1 | a0001c0001t0009g0147 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.310-2357T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118941647 | ||||||
| chr5:118941748
|
C | T | 3 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0088 | 3 | HG03834.hp1 NA18951.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.310-2458G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118941748 | ||||||
| chr5:118941864
|
C | T | 1 | a0001c0001t0032g0236 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.310-2574G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118941864 | ||||||
| chr5:118941887
|
G | C | 48 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(45): Show | 48 | HG00639.hp1 HG00741.hp1 HG01106.hp1 others(45): Show |
intron_variant | MODIFIER | c.310-2597C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118941887 | ||||||
| chr5:118941954
|
T | C | 2 | a0001c0001t0016g0232a0001c0001t0016g0233 | 2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.309+2605A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118941954 | ||||||
| chr5:118942007
|
T | C | 107 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0143others(104): Show | 108 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.309+2552A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118942007 | ||||||
| chr5:118942023
|
GTTCT | G | 2 | a0001c0001t0019g0023a0001c0001t0019g0025 | 2 | HG01261.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.309+2532_309+2535d others(6): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118942023 | ||||||
| chr5:118942248
|
G | A | 5 | a0001c0001t0008g0204a0001c0001t0008g0220a0001c0001t0008g0221others(2): Show | 5 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.309+2311C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118942248 | ||||||
| chr5:118942438
|
A | C | 10 | a0001c0001t0004g0116a0001c0001t0004g0117a0001c0001t0004g0118others(7): Show | 10 | HG01496.hp1 HG01884.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.309+2121T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118942438 | ||||||
| chr5:118942447
|
T | A | 6 | a0001c0001t0001g0235a0001c0001t0004g0068a0001c0001t0016g0232others(3): Show | 6 | HG02145.hp2 HG02809.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.309+2112A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118942447 | ||||||
| chr5:118942518
|
A | T | 1 | a0001c0001t0033g0205 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.309+2041T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118942518 | ||||||
| chr5:118942547
|
C | T | 2 | a0001c0001t0001g0128a0001c0001t0023g0226 | 2 | NA18952.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.309+2012G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118942547 | ||||||
| chr5:118942548
|
G | A | 1 | a0001c0001t0005g0162 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.309+2011C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118942548 | ||||||
| chr5:118942552
|
G | A | 2 | a0001c0001t0002g0129a0001c0001t0002g0130 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.309+2007C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118942552 | ||||||
| chr5:118942729
|
C | A | 6 | a0001c0001t0008g0204a0001c0001t0008g0220a0001c0001t0008g0221others(3): Show | 6 | HG01891.hp2 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.309+1830G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118942729 | ||||||
| chr5:118942828
|
G | T | 2 | a0001c0001t0014g0227a0001c0001t0034g0228 | 2 | HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.309+1731C>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118942828 | ||||||
| chr5:118942954
|
C | A | 1 | a0001c0001t0001g0127 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.309+1605G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118942954 | ||||||
| chr5:118942966
|
C | A | 3 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006 | 3 | HG02055.hp2 HG02976.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.309+1593G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118942966 | ||||||
| chr5:118942992
|
T | C | 5 | a0001c0001t0007g0141a0001c0001t0013g0011a0001c0001t0013g0142others(2): Show | 5 | HG01891.hp1 HG02630.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.309+1567A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118942992 | ||||||
| chr5:118943001
|
G | A | 1 | a0001c0001t0033g0205 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.309+1558C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118943001 | ||||||
| chr5:118943040
|
G | A | 8 | a0001c0001t0006g0029a0001c0001t0006g0059a0001c0001t0006g0072others(5): Show | 8 | HG01123.hp2 HG01168.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.309+1519C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118943040 | ||||||
| chr5:118943087
|
A | G | 1 | a0001c0001t0001g0202 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.309+1472T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118943087 | ||||||
| chr5:118943379
|
G | A | 12 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(9): Show | 12 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.309+1180C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118943379 | ||||||
| chr5:118943410
|
G | T | 1 | a0001c0001t0019g0023 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.309+1149C>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118943410 | ||||||
| chr5:118943550
|
C | CA | 16 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(13): Show | 16 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.309+1008dupT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118943550 | ||||||
| chr5:118943557
|
A | G | 3 | a0001c0001t0001g0175a0001c0001t0001g0194a0001c0002t0037g0002 | 3 | HG02280.hp1 HG02615.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.309+1002T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118943557 | ||||||
| chr5:118943799
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.309+760G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118943799 | ||||||
| chr5:118943871
|
A | C | 23 | a0001c0001t0001g0164a0001c0001t0007g0208a0001c0001t0007g0209others(20): Show | 23 | HG01496.hp2 HG01891.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.309+688T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118943871 | ||||||
| chr5:118944015
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.309+544G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118944015 | ||||||
| chr5:118944038
|
A | T | 11 | a0001c0001t0001g0235a0001c0001t0004g0068a0001c0001t0007g0141others(8): Show | 11 | HG01891.hp1 HG02145.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.309+521T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118944038 | ||||||
| chr5:118944059
|
G | C | 1 | a0001c0001t0021g0010 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.309+500C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118944059 | ||||||
| chr5:118944060
|
A | G | 1 | a0001c0001t0001g0031 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.309+499T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118944060 | ||||||
| chr5:118944322
|
A | T | 17 | a0001c0001t0001g0164a0001c0001t0007g0208a0001c0001t0007g0209others(14): Show | 17 | HG01496.hp2 HG02486.hp1 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.309+237T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118944322 | ||||||
| chr5:118944455
|
T | C | 1 | a0001c0001t0002g0033 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.309+104A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118944455 | ||||||
| chr5:118944491
|
G | A | 11 | a0001c0001t0001g0235a0001c0001t0004g0068a0001c0001t0007g0141others(8): Show | 11 | HG01891.hp1 HG02145.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.309+68C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118944491 | ||||||
| chr5:118944535
|
A | C | 12 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(9): Show | 12 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.309+24T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 2/5 | chr5 | 118944535 | ||||||
| chr5:118944807
|
G | C | 10 | a0001c0001t0004g0116a0001c0001t0004g0117a0001c0001t0004g0118others(7): Show | 10 | HG01496.hp1 HG01884.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.219-158C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118944807 | ||||||
| chr5:118944877
|
A | G | 1 | a0001c0001t0004g0068 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.219-228T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118944877 | ||||||
| chr5:118945254
|
A | G | 2 | a0001c0001t0001g0076a0001c0001t0001g0077 | 2 | HG00735.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.219-605T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118945254 | ||||||
| chr5:118945323
|
A | C | 1 | a0001c0002t0001g0006 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.219-674T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118945323 | ||||||
| chr5:118945342
|
TCCAG | T | 10 | a0001c0001t0004g0116a0001c0001t0004g0117a0001c0001t0004g0118others(7): Show | 10 | HG01496.hp1 HG01884.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.219-697_219-694del others(4): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118945342 | ||||||
| chr5:118945493
|
G | A | 5 | a0001c0001t0014g0115a0001c0001t0014g0227a0001c0001t0014g0229others(2): Show | 5 | HG02970.hp1 HG03209.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.219-844C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118945493 | ||||||
| chr5:118945683
|
T | A | 5 | a0001c0001t0007g0141a0001c0001t0013g0011a0001c0001t0013g0142others(2): Show | 5 | HG01891.hp1 HG02630.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-1034A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118945683 | ||||||
| chr5:118945751
|
C | T | 1 | a0001c0001t0014g0115 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.219-1102G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118945751 | ||||||
| chr5:118945761
|
A | T | 73 | a0001c0001t0001g0235a0001c0001t0003g0007a0001c0001t0003g0008others(70): Show | 74 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.219-1112T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118945761 | ||||||
| chr5:118945774
|
A | AAAAGAAA others(5): Show |
2 | a0001c0001t0003g0180a0001c0001t0004g0068 | 2 | HG02809.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.219-1137_219-1126d others(14): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118945774 | ||||||
| chr5:118945774
|
A | AAAAGAAA others(9): Show |
1 | a0001c0001t0001g0235 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.219-1141_219-1126d others(18): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118945774 | ||||||
| chr5:118945774
|
A | AAAAGAAA others(13): Show |
6 | a0001c0001t0003g0008a0001c0001t0003g0012a0001c0001t0003g0017others(3): Show | 6 | HG00639.hp2 HG02647.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.219-1145_219-1126d others(22): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118945774 | ||||||
| chr5:118945774
|
A | AAAAGAAA others(17): Show |
4 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0168others(1): Show | 4 | HG01243.hp2 HG03130.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.219-1149_219-1126d others(26): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118945774 | ||||||
| chr5:118945774
|
A | AAAAGAAA others(21): Show |
2 | a0001c0001t0003g0018a0001c0001t0016g0232 | 2 | HG01255.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.219-1153_219-1126d others(30): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118945774 | ||||||
| chr5:118945774
|
A | AAAAGAAA others(25): Show |
3 | a0001c0001t0003g0016a0001c0001t0013g0218a0001c0001t0013g0219 | 3 | HG02280.hp2 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.219-1157_219-1126d others(34): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118945774 | ||||||
| chr5:118945774
|
A | AAAAGAAA others(29): Show |
1 | a0001c0001t0013g0011 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.219-1161_219-1126d others(38): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118945774 | ||||||
| chr5:118945774
|
A | AAAAGAAA others(33): Show |
1 | a0001c0001t0007g0141 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.219-1126_219-1125i others(42): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118945774 | ||||||
| chr5:118945774
|
A | AAAAGAAA others(73): Show |
1 | a0001c0001t0013g0142 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.219-1126_219-1125i others(82): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118945774 | ||||||
| chr5:118945774
|
A | AAGAAAGA others(23): Show |
2 | a0001c0001t0003g0007a0001c0001t0003g0015 | 2 | HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.219-1126_219-1125i others(32): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118945774 | ||||||
| chr5:118945774
|
AAAAG | A | 116 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.219-1129_219-1126d others(6): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118945774 | ||||||
| chr5:118945774
|
AAAAGAAA others(1): Show |
A | 45 | a0001c0001t0004g0116a0001c0001t0004g0117a0001c0001t0004g0118others(42): Show | 45 | HG00423.hp1 HG00544.hp1 HG01496.hp1 others(42): Show |
intron_variant | MODIFIER | c.219-1133_219-1126d others(10): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118945774 | ||||||
| chr5:118945774
|
AAAAGAAA others(5): Show |
A | 3 | a0001c0001t0001g0096a0001c0001t0015g0133a0001c0001t0018g0001 | 4 | HG00642.hp1 HG01074.hp1 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.219-1137_219-1126d others(14): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118945774 | ||||||
| chr5:118945774
|
AAAAGAAA others(9): Show |
A | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG03834.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.219-1141_219-1126d others(18): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118945774 | ||||||
| chr5:118945846
|
T | C | 23 | a0001c0001t0001g0235a0001c0001t0003g0007a0001c0001t0003g0008others(20): Show | 23 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.219-1197A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118945846 | ||||||
| chr5:118945982
|
T | C | 1 | a0001c0001t0003g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.219-1333A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118945982 | ||||||
| chr5:118946137
|
G | A | 14 | a0001c0001t0010g0027a0001c0001t0010g0063a0001c0001t0014g0115others(11): Show | 14 | HG00423.hp1 HG00544.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.219-1488C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118946137 | ||||||
| chr5:118946182
|
C | T | 1 | a0002c0003t0010g0238 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.219-1533G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118946182 | ||||||
| chr5:118946254
|
T | C | 6 | a0001c0001t0008g0204a0001c0001t0008g0220a0001c0001t0008g0221others(3): Show | 6 | HG01891.hp2 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.219-1605A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118946254 | ||||||
| chr5:118946315
|
G | C | 1 | a0001c0001t0003g0180 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.219-1666C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118946315 | ||||||
| chr5:118946751
|
A | T | 3 | a0001c0001t0015g0133a0001c0001t0015g0134a0001c0001t0015g0135 | 3 | HG01884.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.219-2102T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118946751 | ||||||
| chr5:118946753
|
C | A | 1 | a0001c0001t0030g0225 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.219-2104G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118946753 | ||||||
| chr5:118946879
|
T | C | 6 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(3): Show | 6 | HG01071.hp2 HG01261.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.219-2230A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118946879 | ||||||
| chr5:118947107
|
G | A | 2 | a0001c0001t0005g0151a0001c0001t0005g0156 | 2 | HG01109.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.219-2458C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118947107 | ||||||
| chr5:118947109
|
G | A | 5 | a0001c0001t0007g0141a0001c0001t0013g0011a0001c0001t0013g0142others(2): Show | 5 | HG01891.hp1 HG02630.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-2460C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118947109 | ||||||
| chr5:118947115
|
G | T | 4 | a0001c0001t0001g0235a0001c0001t0004g0068a0001c0002t0001g0003others(1): Show | 4 | HG02145.hp2 HG02809.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.219-2466C>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118947115 | ||||||
| chr5:118947119
|
G | C | 1 | a0002c0003t0010g0237 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.219-2470C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118947119 | ||||||
| chr5:118947199
|
A | C | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG01934.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.219-2550T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118947199 | ||||||
| chr5:118947236
|
T | C | 1 | a0001c0001t0007g0211 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.219-2587A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118947236 | ||||||
| chr5:118947243
|
C | G | 5 | a0001c0001t0014g0115a0001c0001t0014g0227a0001c0001t0014g0229others(2): Show | 5 | HG02970.hp1 HG03209.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.219-2594G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118947243 | ||||||
| chr5:118947279
|
A | C | 1 | a0001c0001t0009g0159 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.219-2630T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118947279 | ||||||
| chr5:118947280
|
C | A | 3 | a0001c0001t0001g0056a0001c0001t0001g0095a0001c0001t0009g0159 | 3 | HG01496.hp2 NA18953.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.219-2631G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118947280 | ||||||
| chr5:118947467
|
A | C | 1 | a0001c0001t0014g0115 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.219-2818T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118947467 | ||||||
| chr5:118947692
|
C | T | 1 | a0001c0001t0006g0083 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.219-3043G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118947692 | ||||||
| chr5:118947765
|
T | C | 1 | a0001c0002t0001g0006 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.219-3116A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118947765 | ||||||
| chr5:118947855
|
A | T | 4 | a0001c0001t0001g0079a0001c0001t0001g0087a0001c0001t0001g0088others(1): Show | 4 | HG00544.hp2 HG02015.hp2 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.219-3206T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118947855 | ||||||
| chr5:118948014
|
T | C | 8 | a0001c0001t0007g0208a0001c0001t0007g0209a0001c0001t0007g0210others(5): Show | 8 | HG02486.hp1 HG02572.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.219-3365A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118948014 | ||||||
| chr5:118948038
|
G | C | 1 | a0001c0001t0001g0096 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.219-3389C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118948038 | ||||||
| chr5:118948203
|
C | T | 6 | a0001c0001t0008g0204a0001c0001t0008g0220a0001c0001t0008g0221others(3): Show | 6 | HG01891.hp2 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.219-3554G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118948203 | ||||||
| chr5:118948213
|
C | T | 1 | a0001c0001t0002g0126 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.219-3564G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118948213 | ||||||
| chr5:118948311
|
T | C | 5 | a0001c0001t0010g0027a0001c0001t0010g0063a0002c0003t0010g0237others(2): Show | 5 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.219-3662A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118948311 | ||||||
| chr5:118948541
|
G | A | 1 | a0001c0001t0032g0236 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.219-3892C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118948541 | ||||||
| chr5:118948577
|
C | T | 1 | a0001c0001t0001g0039 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.219-3928G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118948577 | ||||||
| chr5:118948720
|
G | A | 1 | a0001c0001t0001g0038 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.219-4071C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118948720 | ||||||
| chr5:118948870
|
C | G | 3 | a0001c0001t0015g0133a0001c0001t0015g0134a0001c0001t0015g0135 | 3 | HG01884.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.219-4221G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118948870 | ||||||
| chr5:118948990
|
T | C | 12 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(9): Show | 12 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.219-4341A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118948990 | ||||||
| chr5:118949027
|
T | C | 5 | a0001c0001t0014g0115a0001c0001t0014g0227a0001c0001t0014g0229others(2): Show | 5 | HG02970.hp1 HG03209.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.219-4378A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118949027 | ||||||
| chr5:118949106
|
GA | G | 12 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0012others(9): Show | 12 | HG00639.hp2 HG01243.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.219-4458delT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118949106 | ||||||
| chr5:118949357
|
G | A | 1 | a0001c0001t0003g0016 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.219-4708C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118949357 | ||||||
| chr5:118949439
|
T | G | 2 | a0001c0001t0006g0092a0001c0001t0006g0093 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.219-4790A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118949439 | ||||||
| chr5:118949701
|
G | A | 133 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(130): Show | 133 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.219-5052C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118949701 | ||||||
| chr5:118949795
|
C | T | 9 | a0001c0001t0009g0144a0001c0001t0009g0147a0001c0001t0009g0148others(6): Show | 9 | HG01496.hp2 HG02572.hp2 HG03688.hp2 others(6): Show |
intron_variant | MODIFIER | c.219-5146G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118949795 | ||||||
| chr5:118949887
|
G | A | 1 | a0001c0001t0029g0132 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.219-5238C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118949887 | ||||||
| chr5:118949911
|
A | G | 1 | a0001c0001t0033g0205 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.219-5262T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118949911 | ||||||
| chr5:118949914
|
G | T | 1 | a0001c0001t0002g0196 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.219-5265C>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118949914 | ||||||
| chr5:118949915
|
A | C | 3 | a0001c0001t0015g0133a0001c0001t0015g0134a0001c0001t0015g0135 | 3 | HG01884.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.219-5266T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118949915 | ||||||
| chr5:118949919
|
T | C | 1 | a0001c0001t0001g0052 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.219-5270A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118949919 | ||||||
| chr5:118949996
|
G | C | 6 | a0001c0001t0008g0204a0001c0001t0008g0220a0001c0001t0008g0221others(3): Show | 6 | HG01891.hp2 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.219-5347C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118949996 | ||||||
| chr5:118950149
|
GTAT | G | 66 | a0001c0001t0001g0235a0001c0001t0003g0007a0001c0001t0003g0008others(63): Show | 67 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.219-5503_219-5501d others(5): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118950149 | ||||||
| chr5:118950213
|
C | CA | 36 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0028others(33): Show | 36 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.219-5565dupT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118950213 | ||||||
| chr5:118950213
|
CA | C | 22 | a0001c0001t0004g0068a0001c0001t0004g0116a0001c0001t0004g0117others(19): Show | 23 | HG00642.hp1 HG01074.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.219-5565delT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118950213 | ||||||
| chr5:118950317
|
T | C | 8 | a0001c0001t0001g0235a0001c0001t0004g0068a0001c0001t0007g0214others(5): Show | 8 | HG02145.hp2 HG02809.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.219-5668A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118950317 | ||||||
| chr5:118950547
|
T | A | 1 | a0001c0001t0001g0086 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.219-5898A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118950547 | ||||||
| chr5:118950612
|
G | T | 1 | a0001c0001t0002g0196 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.219-5963C>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118950612 | ||||||
| chr5:118950662
|
G | A | 4 | a0001c0001t0014g0115a0001c0002t0001g0004a0001c0002t0001g0005others(1): Show | 4 | HG02055.hp2 HG02976.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.219-6013C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118950662 | ||||||
| chr5:118950666
|
T | C | 5 | a0001c0001t0010g0027a0001c0001t0010g0063a0002c0003t0010g0237others(2): Show | 5 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.219-6017A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118950666 | ||||||
| chr5:118950769
|
T | C | 1 | a0001c0001t0039g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.219-6120A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118950769 | ||||||
| chr5:118950929
|
T | C | 4 | a0001c0001t0001g0235a0001c0001t0004g0068a0001c0002t0001g0003others(1): Show | 4 | HG02145.hp2 HG02809.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.219-6280A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118950929 | ||||||
| chr5:118950956
|
A | T | 7 | a0001c0001t0014g0227a0001c0001t0014g0229a0001c0001t0014g0230others(4): Show | 7 | HG02630.hp2 HG02970.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.219-6307T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118950956 | ||||||
| chr5:118950962
|
G | A | 1 | a0001c0001t0033g0205 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.219-6313C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118950962 | ||||||
| chr5:118951052
|
GA | G | 6 | a0001c0001t0007g0141a0001c0001t0013g0011a0001c0001t0013g0142others(3): Show | 6 | HG00741.hp1 HG01891.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.219-6404delT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118951052 | ||||||
| chr5:118951146
|
T | C | 1 | a0001c0001t0001g0100 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.219-6497A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118951146 | ||||||
| chr5:118951177
|
G | A | 8 | a0001c0001t0009g0144a0001c0001t0009g0147a0001c0001t0009g0148others(5): Show | 8 | HG01496.hp2 HG03688.hp2 HG04199.hp2 others(5): Show |
intron_variant | MODIFIER | c.219-6528C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118951177 | ||||||
| chr5:118951190
|
G | A | 1 | a0001c0001t0014g0230 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.219-6541C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118951190 | ||||||
| chr5:118951204
|
G | A | 3 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0057 | 3 | HG00738.hp2 HG01070.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.219-6555C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118951204 | ||||||
| chr5:118951207
|
C | A | 5 | a0001c0001t0010g0027a0001c0001t0010g0063a0002c0003t0010g0237others(2): Show | 5 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.219-6558G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118951207 | ||||||
| chr5:118951249
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.219-6600T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118951249 | ||||||
| chr5:118951285
|
G | A | 10 | a0001c0001t0004g0116a0001c0001t0004g0117a0001c0001t0004g0118others(7): Show | 10 | HG01496.hp1 HG01884.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.219-6636C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118951285 | ||||||
| chr5:118951307
|
G | C | 6 | a0001c0001t0007g0141a0001c0001t0013g0011a0001c0001t0013g0142others(3): Show | 6 | HG00741.hp1 HG01891.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.219-6658C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118951307 | ||||||
| chr5:118951357
|
C | T | 1 | a0001c0001t0001g0056 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.219-6708G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118951357 | ||||||
| chr5:118951490
|
C | A | 1 | a0001c0001t0004g0120 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.219-6841G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118951490 | ||||||
| chr5:118951506
|
C | T | 5 | a0001c0001t0010g0027a0001c0001t0010g0063a0002c0003t0010g0237others(2): Show | 5 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.219-6857G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118951506 | ||||||
| chr5:118951582
|
G | A | 1 | a0001c0001t0001g0056 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.219-6933C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118951582 | ||||||
| chr5:118951600
|
C | T | 4 | a0001c0001t0015g0133a0001c0001t0015g0134a0001c0001t0015g0135others(1): Show | 4 | HG01884.hp1 HG02723.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.219-6951G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118951600 | ||||||
| chr5:118951902
|
G | A | 1 | a0001c0001t0001g0079 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.219-7253C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118951902 | ||||||
| chr5:118951909
|
T | C | 1 | a0001c0001t0015g0135 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.219-7260A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118951909 | ||||||
| chr5:118952196
|
C | G | 1 | a0001c0001t0001g0127 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.219-7547G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118952196 | ||||||
| chr5:118952197
|
G | A | 7 | a0001c0001t0001g0125a0001c0001t0008g0204a0001c0001t0008g0220others(4): Show | 7 | HG01106.hp2 HG01891.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.219-7548C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118952197 | ||||||
| chr5:118952394
|
C | T | 1 | a0002c0003t0002g0239 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.219-7745G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118952394 | ||||||
| chr5:118952544
|
TCAGTTAG others(13): Show |
T | 1 | a0001c0001t0032g0236 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.219-7915_219-7896d others(22): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118952544 | ||||||
| chr5:118952689
|
T | C | 10 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0002g0107others(7): Show | 10 | HG00099.hp1 HG01081.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.219-8040A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118952689 | ||||||
| chr5:118952692
|
A | T | 1 | a0001c0001t0001g0053 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.219-8043T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118952692 | ||||||
| chr5:118952764
|
T | A | 1 | a0001c0001t0001g0224 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.219-8115A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118952764 | ||||||
| chr5:118952893
|
G | A | 5 | a0001c0001t0007g0141a0001c0001t0013g0011a0001c0001t0013g0142others(2): Show | 5 | HG01891.hp1 HG02630.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-8244C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118952893 | ||||||
| chr5:118952920
|
A | C | 7 | a0001c0001t0001g0098a0001c0001t0001g0103a0001c0001t0001g0104others(4): Show | 7 | HG00738.hp1 HG00741.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.219-8271T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118952920 | ||||||
| chr5:118952978
|
C | T | 1 | a0001c0001t0011g0111 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.219-8329G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118952978 | ||||||
| chr5:118953000
|
C | G | 2 | a0001c0001t0020g0121a0001c0001t0020g0122 | 2 | HG01106.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.219-8351G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118953000 | ||||||
| chr5:118953116
|
C | T | 3 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0057 | 3 | HG00738.hp2 HG01070.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.219-8467G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118953116 | ||||||
| chr5:118953170
|
T | C | 5 | a0001c0001t0010g0027a0001c0001t0010g0063a0002c0003t0010g0237others(2): Show | 5 | HG00423.hp1 HG00544.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.219-8521A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118953170 | ||||||
| chr5:118953263
|
C | T | 1 | a0001c0001t0001g0049 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.219-8614G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118953263 | ||||||
| chr5:118953315
|
C | A | 1 | a0001c0002t0037g0002 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.219-8666G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118953315 | ||||||
| chr5:118953775
|
G | C | 1 | a0001c0001t0002g0107 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.219-9126C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118953775 | ||||||
| chr5:118953889
|
A | C | 3 | a0001c0001t0001g0235a0001c0002t0001g0003a0003c0005t0042g0241 | 3 | HG02145.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.219-9240T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118953889 | ||||||
| chr5:118953890
|
C | T | 3 | a0001c0001t0001g0235a0001c0002t0001g0003a0003c0005t0042g0241 | 3 | HG02145.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.219-9241G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118953890 | ||||||
| chr5:118954133
|
C | T | 5 | a0001c0001t0004g0116a0001c0001t0004g0123a0001c0001t0004g0139others(2): Show | 5 | HG01243.hp1 HG02622.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-9484G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118954133 | ||||||
| chr5:118954409
|
T | A | 1 | a0001c0001t0001g0052 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.219-9760A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118954409 | ||||||
| chr5:118954447
|
C | A | 2 | a0001c0001t0001g0105a0001c0001t0001g0106 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.219-9798G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118954447 | ||||||
| chr5:118954525
|
C | CT | 12 | a0001c0001t0004g0116a0001c0001t0004g0117a0001c0001t0004g0118others(9): Show | 12 | HG01106.hp1 HG01243.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.219-9877dupA | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118954525 | ||||||
| chr5:118954537
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.219-9888G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118954537 | ||||||
| chr5:118954570
|
G | C | 32 | a0001c0001t0001g0145a0001c0001t0001g0163a0001c0001t0001g0164others(29): Show | 33 | HG00642.hp1 HG01074.hp1 HG01256.hp2 others(30): Show |
intron_variant | MODIFIER | c.219-9921C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118954570 | ||||||
| chr5:118955030
|
A | T | 2 | a0001c0001t0014g0227a0001c0001t0034g0228 | 2 | HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.219-10381T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118955030 | ||||||
| chr5:118955040
|
G | A | 8 | a0001c0001t0008g0204a0001c0001t0008g0220a0001c0001t0008g0221others(5): Show | 8 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.219-10391C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118955040 | ||||||
| chr5:118955075
|
A | G | 1 | a0002c0003t0010g0240 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.219-10426T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118955075 | ||||||
| chr5:118955204
|
T | C | 1 | a0001c0001t0001g0095 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.219-10555A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118955204 | ||||||
| chr5:118955480
|
A | G | 1 | a0001c0001t0009g0159 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.219-10831T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118955480 | ||||||
| chr5:118955586
|
A | G | 2 | a0001c0001t0006g0092a0001c0001t0006g0093 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.219-10937T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118955586 | ||||||
| chr5:118955762
|
C | T | 13 | a0001c0001t0004g0116a0001c0001t0004g0117a0001c0001t0004g0118others(10): Show | 13 | HG01106.hp1 HG01243.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.219-11113G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118955762 | ||||||
| chr5:118955798
|
TA | T | 5 | a0001c0001t0008g0231a0001c0001t0009g0148a0001c0001t0015g0133others(2): Show | 5 | HG01884.hp1 HG02622.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.219-11150delT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118955798 | ||||||
| chr5:118955841
|
T | C | 1 | a0001c0001t0009g0148 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.219-11192A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118955841 | ||||||
| chr5:118955874
|
C | G | 4 | a0001c0001t0008g0231a0001c0001t0015g0133a0001c0001t0015g0134others(1): Show | 4 | HG01884.hp1 HG02622.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.219-11225G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118955874 | ||||||
| chr5:118955906
|
AT | A | 5 | a0001c0001t0001g0079a0001c0001t0006g0092a0001c0001t0006g0093others(2): Show | 5 | HG01168.hp2 HG01169.hp2 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-11258delA | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118955906 | ||||||
| chr5:118955932
|
G | A | 1 | a0001c0001t0002g0058 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.219-11283C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118955932 | ||||||
| chr5:118956075
|
T | C | 2 | a0001c0001t0013g0011a0001c0001t0021g0010 | 2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.219-11426A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118956075 | ||||||
| chr5:118956141
|
G | A | 2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | HG01099.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.219-11492C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118956141 | ||||||
| chr5:118956418
|
C | T | 1 | a0001c0001t0032g0236 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.219-11769G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118956418 | ||||||
| chr5:118956433
|
A | C | 1 | a0001c0001t0004g0124 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.219-11784T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118956433 | ||||||
| chr5:118956584
|
A | C | 37 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0150others(34): Show | 37 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.219-11935T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118956584 | ||||||
| chr5:118956911
|
A | G | 1 | a0001c0001t0002g0097 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.219-12262T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118956911 | ||||||
| chr5:118956932
|
T | TCTGCTGT others(335): Show |
1 | a0001c0001t0007g0215 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.219-12284_219-1228 others(346): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118956932 | ||||||
| chr5:118956932
|
T | TCTGCTGT others(320): Show |
2 | a0001c0001t0007g0208a0001c0001t0007g0209 | 2 | HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.219-12284_219-1228 others(331): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118956932 | ||||||
| chr5:118956932
|
T | TCTGCTGT others(335): Show |
2 | a0001c0001t0007g0211a0001c0001t0026g0212 | 2 | HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.219-12284_219-1228 others(346): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118956932 | ||||||
| chr5:118956932
|
T | TCTGCTGT others(336): Show |
2 | a0001c0001t0007g0210a0001c0001t0007g0214 | 2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.219-12284_219-1228 others(347): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118956932 | ||||||
| chr5:118956932
|
T | TCTGCTGT others(337): Show |
1 | a0001c0001t0007g0213 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.219-12284_219-1228 others(348): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118956932 | ||||||
| chr5:118957103
|
T | G | 8 | a0001c0001t0001g0234a0001c0001t0003g0007a0001c0001t0003g0008others(5): Show | 8 | HG00639.hp2 HG01884.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.219-12454A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118957103 | ||||||
| chr5:118957129
|
T | C | 1 | a0001c0001t0009g0149 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.219-12480A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118957129 | ||||||
| chr5:118957192
|
G | A | 19 | a0001c0001t0001g0125a0001c0001t0001g0127a0001c0001t0002g0126others(16): Show | 19 | HG01106.hp1 HG01106.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.219-12543C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118957192 | ||||||
| chr5:118957589
|
C | T | 115 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(112): Show | 115 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.219-12940G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118957589 | ||||||
| chr5:118957776
|
T | C | 9 | a0001c0001t0008g0231a0001c0001t0015g0133a0001c0001t0015g0134others(6): Show | 9 | HG00423.hp1 HG00544.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.219-13127A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118957776 | ||||||
| chr5:118957805
|
C | T | 1 | a0001c0001t0033g0205 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.219-13156G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118957805 | ||||||
| chr5:118957806
|
G | T | 185 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(182): Show | 185 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.219-13157C>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118957806 | ||||||
| chr5:118957930
|
T | C | 3 | a0001c0001t0001g0235a0001c0001t0016g0232a0001c0001t0016g0233 | 3 | HG02145.hp2 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.219-13281A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118957930 | ||||||
| chr5:118958015
|
T | C | 5 | a0001c0001t0014g0227a0001c0001t0014g0229a0001c0001t0014g0230others(2): Show | 5 | HG02970.hp1 HG03041.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.219-13366A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118958015 | ||||||
| chr5:118958066
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.219-13417A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118958066 | ||||||
| chr5:118958382
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.219-13733G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118958382 | ||||||
| chr5:118958460
|
AAAC | A | 6 | a0001c0001t0001g0046a0001c0001t0001g0081a0001c0001t0011g0073others(3): Show | 6 | NA18951.hp2 NA18964.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.219-13814_219-1381 others(7): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118958460 | ||||||
| chr5:118958576
|
C | T | 2 | a0001c0001t0013g0011a0001c0001t0021g0010 | 2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.219-13927G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118958576 | ||||||
| chr5:118958584
|
CA | C | 121 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(118): Show | 122 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.219-13936delT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118958584 | ||||||
| chr5:118958584
|
CAA | C | 5 | a0001c0001t0032g0236a0002c0003t0002g0239a0002c0003t0010g0237others(2): Show | 5 | HG00423.hp1 HG00544.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-13937_219-1393 others(6): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118958584 | ||||||
| chr5:118958684
|
A | T | 1 | a0001c0001t0001g0127 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.219-14035T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118958684 | ||||||
| chr5:118958723
|
A | G | 1 | a0001c0001t0018g0001 | 2 | HG00642.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.219-14074T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118958723 | ||||||
| chr5:118958926
|
C | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0028 | 2 | HG00423.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.219-14277G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118958926 | ||||||
| chr5:118958977
|
C | A | 116 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(113): Show | 116 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.219-14328G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118958977 | ||||||
| chr5:118959001
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.219-14352C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118959001 | ||||||
| chr5:118959106
|
C | A | 151 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(148): Show | 151 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.219-14457G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118959106 | ||||||
| chr5:118959178
|
A | G | 1 | a0001c0001t0001g0224 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.219-14529T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118959178 | ||||||
| chr5:118959318
|
C | T | 2 | a0001c0001t0014g0227a0001c0001t0034g0228 | 2 | HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.219-14669G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118959318 | ||||||
| chr5:118959319
|
G | A | 4 | a0002c0003t0002g0239a0002c0003t0010g0237a0002c0003t0010g0238others(1): Show | 4 | HG00423.hp1 HG00544.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.219-14670C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118959319 | ||||||
| chr5:118959602
|
T | C | 125 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(122): Show | 125 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.219-14953A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118959602 | ||||||
| chr5:118959680
|
A | G | 3 | a0001c0001t0001g0235a0001c0001t0016g0232a0001c0001t0016g0233 | 3 | HG02145.hp2 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.219-15031T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118959680 | ||||||
| chr5:118959956
|
A | T | 1 | a0001c0001t0001g0096 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.219-15307T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118959956 | ||||||
| chr5:118960031
|
T | C | 126 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(123): Show | 126 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.219-15382A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118960031 | ||||||
| chr5:118960070
|
A | T | 1 | a0001c0001t0001g0165 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.219-15421T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118960070 | ||||||
| chr5:118960252
|
A | G | 1 | a0001c0001t0001g0049 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.219-15603T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118960252 | ||||||
| chr5:118960330
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.219-15681G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118960330 | ||||||
| chr5:118960748
|
T | TA | 6 | a0001c0001t0001g0234a0001c0001t0003g0007a0001c0001t0003g0008others(3): Show | 6 | HG00639.hp2 HG03041.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.219-16100dupT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118960748 | ||||||
| chr5:118960748
|
T | TAA | 6 | a0001c0001t0001g0125a0001c0001t0001g0127a0001c0001t0002g0126others(3): Show | 6 | HG01106.hp2 HG01256.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.219-16101_219-1610 others(6): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118960748 | ||||||
| chr5:118960748
|
T | TAAA | 12 | a0001c0001t0004g0116a0001c0001t0004g0117a0001c0001t0004g0118others(9): Show | 12 | HG01106.hp1 HG01243.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.219-16102_219-1610 others(7): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118960748 | ||||||
| chr5:118960766
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.219-16117A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118960766 | ||||||
| chr5:118961078
|
T | TA | 205 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(202): Show | 206 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.219-16430dupT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118961078 | ||||||
| chr5:118961092
|
T | G | 3 | a0001c0001t0001g0173a0001c0001t0001g0176a0001c0001t0003g0180 | 3 | HG02895.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.219-16443A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118961092 | ||||||
| chr5:118961488
|
T | TCCCA | 8 | a0001c0001t0007g0208a0001c0001t0007g0209a0001c0001t0007g0210others(5): Show | 8 | HG02486.hp1 HG02572.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.219-16843_219-1684 others(8): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118961488 | ||||||
| chr5:118961709
|
C | T | 2 | a0001c0001t0013g0011a0001c0001t0021g0010 | 2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.219-17060G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118961709 | ||||||
| chr5:118961900
|
A | G | 3 | a0001c0001t0001g0173a0001c0001t0001g0176a0001c0001t0003g0180 | 3 | HG02895.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.219-17251T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118961900 | ||||||
| chr5:118961962
|
C | T | 8 | a0001c0001t0008g0204a0001c0001t0008g0220a0001c0001t0008g0221others(5): Show | 8 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.219-17313G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118961962 | ||||||
| chr5:118962013
|
G | A | 8 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(5): Show | 8 | HG00280.hp2 HG00323.hp2 HG00735.hp2 others(5): Show |
intron_variant | MODIFIER | c.219-17364C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118962013 | ||||||
| chr5:118962151
|
T | C | 1 | a0002c0003t0002g0239 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.219-17502A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118962151 | ||||||
| chr5:118962365
|
TA | T | 4 | a0002c0003t0002g0239a0002c0003t0010g0237a0002c0003t0010g0238others(1): Show | 4 | HG00423.hp1 HG00544.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.219-17717delT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118962365 | ||||||
| chr5:118962379
|
T | A | 1 | a0001c0001t0003g0017 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.219-17730A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118962379 | ||||||
| chr5:118962799
|
T | C | 8 | a0001c0001t0007g0208a0001c0001t0007g0209a0001c0001t0007g0210others(5): Show | 8 | HG02486.hp1 HG02572.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.219-18150A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118962799 | ||||||
| chr5:118962935
|
T | C | 8 | a0001c0001t0008g0204a0001c0001t0008g0220a0001c0001t0008g0221others(5): Show | 8 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.219-18286A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118962935 | ||||||
| chr5:118962942
|
T | C | 1 | a0001c0001t0001g0071 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.219-18293A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118962942 | ||||||
| chr5:118963144
|
G | A | 1 | a0001c0001t0002g0174 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.219-18495C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118963144 | ||||||
| chr5:118963291
|
G | C | 8 | a0001c0001t0001g0235a0001c0001t0014g0227a0001c0001t0014g0229others(5): Show | 8 | HG02145.hp2 HG02970.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.219-18642C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118963291 | ||||||
| chr5:118963477
|
C | G | 2 | a0001c0001t0013g0011a0001c0001t0021g0010 | 2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.219-18828G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118963477 | ||||||
| chr5:118963492
|
T | C | 7 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(4): Show | 7 | HG01074.hp2 HG01123.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.219-18843A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118963492 | ||||||
| chr5:118963505
|
A | G | 1 | a0001c0001t0024g0206 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.219-18856T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118963505 | ||||||
| chr5:118963521
|
C | T | 158 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(155): Show | 158 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.219-18872G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118963521 | ||||||
| chr5:118963847
|
A | T | 204 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(201): Show | 205 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.219-19198T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118963847 | ||||||
| chr5:118963940
|
T | C | 51 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0031others(48): Show | 51 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.219-19291A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118963940 | ||||||
| chr5:118963975
|
C | A | 2 | a0001c0001t0013g0011a0001c0001t0021g0010 | 2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.219-19326G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118963975 | ||||||
| chr5:118964152
|
T | C | 1 | a0001c0001t0006g0075 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.219-19503A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118964152 | ||||||
| chr5:118964217
|
C | CA | 9 | a0001c0001t0001g0038a0001c0001t0001g0074a0001c0001t0001g0095others(6): Show | 9 | HG00280.hp1 HG01978.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.219-19569dupT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118964217 | ||||||
| chr5:118964217
|
CA | C | 29 | a0001c0001t0001g0055a0001c0001t0001g0062a0001c0001t0001g0172others(26): Show | 29 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.219-19569delT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118964217 | ||||||
| chr5:118964416
|
C | T | 117 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(114): Show | 117 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.219-19767G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118964416 | ||||||
| chr5:118964555
|
T | G | 3 | a0001c0001t0001g0024a0001c0001t0001g0064a0001c0001t0001g0071 | 3 | HG01255.hp1 HG02074.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.219-19906A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118964555 | ||||||
| chr5:118964556
|
C | A | 3 | a0001c0001t0001g0024a0001c0001t0001g0064a0001c0001t0001g0071 | 3 | HG01255.hp1 HG02074.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.219-19907G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118964556 | ||||||
| chr5:118964557
|
A | AT | 3 | a0001c0001t0001g0024a0001c0001t0001g0064a0001c0001t0001g0071 | 3 | HG01255.hp1 HG02074.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.219-19909_219-1990 others(5): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118964557 | ||||||
| chr5:118964612
|
G | A | 34 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0150others(31): Show | 34 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.219-19963C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118964612 | ||||||
| chr5:118964616
|
T | A | 34 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0150others(31): Show | 34 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.219-19967A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118964616 | ||||||
| chr5:118964656
|
G | A | 1 | a0001c0001t0001g0166 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.219-20007C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118964656 | ||||||
| chr5:118964675
|
C | T | 1 | a0001c0001t0020g0121 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.219-20026G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118964675 | ||||||
| chr5:118964773
|
G | A | 34 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0150others(31): Show | 34 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.219-20124C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118964773 | ||||||
| chr5:118964931
|
C | T | 1 | a0001c0001t0001g0044 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.219-20282G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118964931 | ||||||
| chr5:118965038
|
A | G | 124 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(121): Show | 124 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.219-20389T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118965038 | ||||||
| chr5:118965078
|
ACTGCCCG others(309): Show |
A | 1 | a0001c0001t0027g0009 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.219-20745_219-2043 others(4): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118965078 | ||||||
| chr5:118965079
|
C | T | 5 | a0001c0001t0032g0236a0002c0003t0002g0239a0002c0003t0010g0237others(2): Show | 5 | HG00423.hp1 HG00544.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-20430G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118965079 | ||||||
| chr5:118965115
|
G | A | 1 | a0001c0001t0015g0134 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.219-20466C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118965115 | ||||||
| chr5:118965151
|
C | A | 8 | a0001c0001t0001g0235a0001c0001t0014g0227a0001c0001t0014g0229others(5): Show | 8 | HG02145.hp2 HG02970.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.219-20502G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118965151 | ||||||
| chr5:118965173
|
T | C | 196 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(193): Show | 197 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.219-20524A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118965173 | ||||||
| chr5:118965188
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.219-20539C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118965188 | ||||||
| chr5:118965202
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.219-20553T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118965202 | ||||||
| chr5:118965209
|
G | A | 3 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021 | 3 | HG01192.hp2 HG03491.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.219-20560C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118965209 | ||||||
| chr5:118965331
|
A | AC | 54 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0024others(51): Show | 54 | HG00642.hp2 HG00735.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.219-20683dupG | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118965331 | ||||||
| chr5:118965378
|
G | T | 1 | a0001c0001t0029g0132 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.219-20729C>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118965378 | ||||||
| chr5:118965408
|
A | AC | 18 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0026others(15): Show | 18 | HG00423.hp2 HG01081.hp2 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.219-20760dupG | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118965408 | ||||||
| chr5:118965437
|
C | G | 130 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(127): Show | 130 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.219-20788G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118965437 | ||||||
| chr5:118965462
|
T | TG | 240 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(237): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.219-20814dupC | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118965462 | ||||||
| chr5:118965609
|
G | C | 1 | a0001c0001t0027g0009 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.219-20960C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118965609 | ||||||
| chr5:118965735
|
G | A | 128 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(125): Show | 128 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.219-21086C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118965735 | ||||||
| chr5:118965836
|
A | G | 31 | a0001c0001t0001g0125a0001c0001t0001g0127a0001c0001t0001g0234others(28): Show | 31 | HG00639.hp2 HG01106.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.219-21187T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118965836 | ||||||
| chr5:118965902
|
C | T | 5 | a0001c0001t0014g0227a0001c0001t0014g0229a0001c0001t0014g0230others(2): Show | 5 | HG02970.hp1 HG03041.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.219-21253G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118965902 | ||||||
| chr5:118965964
|
T | G | 70 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0028others(67): Show | 70 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.219-21315A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118965964 | ||||||
| chr5:118965994
|
C | G | 1 | a0001c0001t0011g0080 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.219-21345G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118965994 | ||||||
| chr5:118966085
|
T | A | 19 | a0001c0001t0001g0125a0001c0001t0001g0127a0001c0001t0002g0126others(16): Show | 19 | HG01106.hp1 HG01106.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.219-21436A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118966085 | ||||||
| chr5:118966094
|
G | C | 1 | a0001c0001t0001g0175 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.219-21445C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118966094 | ||||||
| chr5:118966104
|
A | G | 1 | a0001c0001t0001g0235 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.219-21455T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118966104 | ||||||
| chr5:118966109
|
T | G | 2 | a0001c0001t0001g0192a0001c0001t0001g0193 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.219-21460A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118966109 | ||||||
| chr5:118966220
|
G | A | 6 | a0001c0001t0001g0125a0001c0001t0001g0127a0001c0001t0002g0126others(3): Show | 6 | HG01106.hp2 HG01256.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.219-21571C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118966220 | ||||||
| chr5:118966263
|
A | G | 4 | a0001c0001t0008g0231a0001c0001t0015g0133a0001c0001t0015g0134others(1): Show | 4 | HG01884.hp1 HG02622.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.219-21614T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118966263 | ||||||
| chr5:118966272
|
T | C | 2 | a0001c0001t0006g0092a0001c0001t0006g0093 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.219-21623A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118966272 | ||||||
| chr5:118966303
|
T | C | 1 | a0001c0001t0038g0054 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.219-21654A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118966303 | ||||||
| chr5:118966447
|
T | C | 37 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(34): Show | 37 | HG00544.hp2 HG01071.hp2 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.219-21798A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118966447 | ||||||
| chr5:118966544
|
G | C | 2 | a0001c0001t0001g0036a0001c0001t0001g0039 | 2 | NA18953.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.218+21750C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118966544 | ||||||
| chr5:118966605
|
A | G | 5 | a0001c0001t0014g0227a0001c0001t0014g0229a0001c0001t0014g0230others(2): Show | 5 | HG02970.hp1 HG03041.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.218+21689T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118966605 | ||||||
| chr5:118966616
|
T | C | 1 | a0001c0001t0004g0118 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.218+21678A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118966616 | ||||||
| chr5:118966660
|
G | A | 6 | a0001c0001t0004g0118a0001c0001t0004g0120a0001c0001t0004g0139others(3): Show | 6 | HG01106.hp1 HG01884.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.218+21634C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118966660 | ||||||
| chr5:118966828
|
G | A | 1 | a0002c0003t0010g0238 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.218+21466C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118966828 | ||||||
| chr5:118966829
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.218+21465T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118966829 | ||||||
| chr5:118966859
|
G | A | 1 | a0001c0001t0018g0001 | 2 | HG00642.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.218+21435C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118966859 | ||||||
| chr5:118966866
|
T | C | 4 | a0001c0001t0001g0234a0001c0001t0003g0007a0001c0001t0003g0008others(1): Show | 4 | HG00639.hp2 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+21428A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118966866 | ||||||
| chr5:118966890
|
C | A | 8 | a0001c0001t0008g0204a0001c0001t0008g0220a0001c0001t0008g0221others(5): Show | 8 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.218+21404G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118966890 | ||||||
| chr5:118966893
|
G | C | 1 | a0001c0001t0032g0236 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.218+21401C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118966893 | ||||||
| chr5:118966982
|
G | C | 8 | a0001c0001t0008g0204a0001c0001t0008g0220a0001c0001t0008g0221others(5): Show | 8 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.218+21312C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118966982 | ||||||
| chr5:118966983
|
A | G | 2 | a0001c0001t0007g0214a0001c0001t0007g0215 | 2 | HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.218+21311T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118966983 | ||||||
| chr5:118967001
|
A | T | 3 | a0001c0001t0003g0168a0001c0001t0007g0141a0001c0001t0013g0142 | 3 | HG01891.hp1 HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.218+21293T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118967001 | ||||||
| chr5:118967029
|
C | CA | 8 | a0001c0001t0007g0208a0001c0001t0007g0209a0001c0001t0007g0210others(5): Show | 8 | HG02486.hp1 HG02572.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.218+21264dupT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118967029 | ||||||
| chr5:118967323
|
G | C | 2 | a0001c0001t0013g0011a0001c0001t0021g0010 | 2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.218+20971C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118967323 | ||||||
| chr5:118967762
|
T | C | 1 | a0001c0001t0004g0068 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.218+20532A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118967762 | ||||||
| chr5:118967786
|
G | A | 201 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(198): Show | 202 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.218+20508C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118967786 | ||||||
| chr5:118967828
|
G | C | 1 | a0001c0001t0029g0132 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.218+20466C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118967828 | ||||||
| chr5:118967931
|
C | A | 3 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183 | 3 | HG01099.hp1 HG01168.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.218+20363G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118967931 | ||||||
| chr5:118967936
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.218+20358C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118967936 | ||||||
| chr5:118968094
|
A | T | 8 | a0001c0001t0008g0204a0001c0001t0008g0220a0001c0001t0008g0221others(5): Show | 8 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.218+20200T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118968094 | ||||||
| chr5:118968102
|
C | A | 4 | a0001c0001t0001g0234a0001c0001t0003g0007a0001c0001t0003g0008others(1): Show | 4 | HG00639.hp2 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+20192G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118968102 | ||||||
| chr5:118968279
|
T | C | 180 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(177): Show | 180 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.218+20015A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118968279 | ||||||
| chr5:118968434
|
G | A | 2 | a0001c0001t0001g0036a0001c0001t0001g0039 | 2 | NA18953.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.218+19860C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118968434 | ||||||
| chr5:118968638
|
C | A | 13 | a0001c0001t0004g0116a0001c0001t0004g0117a0001c0001t0004g0118others(10): Show | 13 | HG01106.hp1 HG01243.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.218+19656G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118968638 | ||||||
| chr5:118968695
|
A | G | 197 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(194): Show | 198 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.218+19599T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118968695 | ||||||
| chr5:118968898
|
G | T | 1 | a0001c0001t0032g0236 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.218+19396C>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118968898 | ||||||
| chr5:118969107
|
T | C | 205 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(202): Show | 206 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.218+19187A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118969107 | ||||||
| chr5:118969198
|
G | A | 1 | a0001c0001t0001g0046 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.218+19096C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118969198 | ||||||
| chr5:118969340
|
T | C | 8 | a0001c0001t0007g0208a0001c0001t0007g0209a0001c0001t0007g0210others(5): Show | 8 | HG02486.hp1 HG02572.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.218+18954A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118969340 | ||||||
| chr5:118969520
|
C | T | 1 | a0001c0001t0024g0206 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.218+18774G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118969520 | ||||||
| chr5:118969805
|
T | G | 31 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(28): Show | 31 | HG00544.hp2 HG01071.hp2 HG01192.hp2 others(28): Show |
intron_variant | MODIFIER | c.218+18489A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118969805 | ||||||
| chr5:118969847
|
G | T | 4 | a0002c0003t0002g0239a0002c0003t0010g0237a0002c0003t0010g0238others(1): Show | 4 | HG00423.hp1 HG00544.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+18447C>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118969847 | ||||||
| chr5:118969860
|
G | C | 1 | a0001c0001t0001g0203 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.218+18434C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118969860 | ||||||
| chr5:118969944
|
T | C | 8 | a0001c0001t0001g0098a0001c0001t0001g0103a0001c0001t0001g0104others(5): Show | 8 | HG00738.hp1 HG00741.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.218+18350A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118969944 | ||||||
| chr5:118969965
|
C | T | 175 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(172): Show | 175 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.218+18329G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118969965 | ||||||
| chr5:118970017
|
A | G | 1 | a0001c0001t0018g0001 | 2 | HG00642.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.218+18277T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118970017 | ||||||
| chr5:118970047
|
C | T | 2 | a0001c0001t0013g0011a0001c0001t0021g0010 | 2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.218+18247G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118970047 | ||||||
| chr5:118970058
|
T | C | 2 | a0001c0001t0016g0232a0001c0001t0016g0233 | 2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.218+18236A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118970058 | ||||||
| chr5:118970230
|
C | G | 1 | a0001c0001t0014g0227 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.218+18064G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118970230 | ||||||
| chr5:118970388
|
C | T | 13 | a0001c0001t0004g0116a0001c0001t0004g0117a0001c0001t0004g0118others(10): Show | 13 | HG01106.hp1 HG01243.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.218+17906G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118970388 | ||||||
| chr5:118970393
|
C | T | 1 | a0001c0001t0029g0132 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.218+17901G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118970393 | ||||||
| chr5:118970399
|
C | A | 2 | a0001c0001t0013g0011a0001c0001t0021g0010 | 2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.218+17895G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118970399 | ||||||
| chr5:118970478
|
T | C | 1 | a0001c0001t0015g0134 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.218+17816A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118970478 | ||||||
| chr5:118970489
|
G | A | 4 | a0001c0001t0008g0231a0001c0001t0015g0133a0001c0001t0015g0134others(1): Show | 4 | HG01884.hp1 HG02622.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+17805C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118970489 | ||||||
| chr5:118970681
|
G | A | 4 | a0001c0001t0008g0231a0001c0001t0015g0133a0001c0001t0015g0134others(1): Show | 4 | HG01884.hp1 HG02622.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+17613C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118970681 | ||||||
| chr5:118970688
|
A | T | 174 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(171): Show | 174 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.218+17606T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118970688 | ||||||
| chr5:118970751
|
T | G | 2 | a0001c0001t0001g0036a0001c0001t0001g0039 | 2 | NA18953.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.218+17543A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118970751 | ||||||
| chr5:118970884
|
A | C | 238 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(235): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.218+17410T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118970884 | ||||||
| chr5:118970939
|
G | GA | 4 | a0002c0003t0002g0239a0002c0003t0010g0237a0002c0003t0010g0238others(1): Show | 4 | HG00423.hp1 HG00544.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+17354_218+1735 others(5): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118970939 | ||||||
| chr5:118971062
|
A | G | 174 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(171): Show | 174 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.218+17232T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118971062 | ||||||
| chr5:118971098
|
C | G | 4 | a0001c0001t0001g0234a0001c0001t0003g0007a0001c0001t0003g0008others(1): Show | 4 | HG00639.hp2 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+17196G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118971098 | ||||||
| chr5:118971157
|
G | A | 10 | a0001c0001t0008g0231a0001c0001t0015g0133a0001c0001t0015g0134others(7): Show | 10 | HG00423.hp1 HG00544.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.218+17137C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118971157 | ||||||
| chr5:118971392
|
C | T | 1 | a0001c0001t0024g0206 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.218+16902G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118971392 | ||||||
| chr5:118971393
|
G | A | 28 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(25): Show | 28 | HG01071.hp2 HG01192.hp2 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.218+16901C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118971393 | ||||||
| chr5:118971452
|
C | T | 3 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0027g0009 | 3 | HG00639.hp2 HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.218+16842G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118971452 | ||||||
| chr5:118971795
|
A | C | 7 | a0001c0001t0001g0125a0001c0001t0001g0127a0001c0001t0001g0128others(4): Show | 7 | HG01106.hp2 HG01256.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.218+16499T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118971795 | ||||||
| chr5:118971871
|
T | C | 4 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0195others(1): Show | 4 | HG01993.hp2 HG02109.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+16423A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118971871 | ||||||
| chr5:118971996
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.218+16298G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118971996 | ||||||
| chr5:118972062
|
C | T | 1 | a0001c0002t0001g0005 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.218+16232G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118972062 | ||||||
| chr5:118972222
|
T | G | 13 | a0001c0001t0004g0116a0001c0001t0004g0117a0001c0001t0004g0118others(10): Show | 13 | HG01106.hp1 HG01243.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.218+16072A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118972222 | ||||||
| chr5:118972263
|
G | A | 1 | a0001c0001t0005g0157 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.218+16031C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118972263 | ||||||
| chr5:118972447
|
A | G | 1 | a0001c0001t0018g0001 | 2 | HG00642.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.218+15847T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118972447 | ||||||
| chr5:118972554
|
G | A | 1 | a0001c0001t0004g0123 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.218+15740C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118972554 | ||||||
| chr5:118972794
|
T | C | 2 | a0001c0001t0014g0227a0001c0001t0034g0228 | 2 | HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.218+15500A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118972794 | ||||||
| chr5:118972848
|
G | A | 4 | a0001c0001t0008g0231a0001c0001t0015g0133a0001c0001t0015g0134others(1): Show | 4 | HG01884.hp1 HG02622.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+15446C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118972848 | ||||||
| chr5:118972946
|
G | A | 1 | a0001c0002t0001g0006 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.218+15348C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118972946 | ||||||
| chr5:118972986
|
C | A | 1 | a0001c0001t0022g0082 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.218+15308G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118972986 | ||||||
| chr5:118973074
|
A | AC | 6 | a0001c0001t0001g0036a0001c0001t0001g0048a0001c0001t0001g0095others(3): Show | 6 | HG01243.hp2 HG02738.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.218+15219dupG | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118973074 | ||||||
| chr5:118973079
|
CT | C | 29 | a0001c0001t0001g0089a0001c0001t0001g0100a0001c0001t0001g0176others(26): Show | 30 | HG00639.hp2 HG00642.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.218+15214delA | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118973079 | ||||||
| chr5:118973080
|
T | C | 108 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(105): Show | 108 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.218+15214A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118973080 | ||||||
| chr5:118973081
|
T | C | 17 | a0001c0001t0001g0089a0001c0001t0001g0100a0001c0001t0004g0068others(14): Show | 17 | HG00639.hp1 HG00741.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.218+15213A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118973081 | ||||||
| chr5:118973089
|
T | C | 34 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0150others(31): Show | 34 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.218+15205A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118973089 | ||||||
| chr5:118973219
|
C | G | 1 | a0001c0001t0005g0184 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.218+15075G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118973219 | ||||||
| chr5:118973323
|
T | A | 1 | a0001c0001t0024g0206 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.218+14971A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118973323 | ||||||
| chr5:118973406
|
C | A | 4 | a0001c0001t0008g0231a0001c0001t0015g0133a0001c0001t0015g0134others(1): Show | 4 | HG01884.hp1 HG02622.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+14888G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118973406 | ||||||
| chr5:118973427
|
G | A | 7 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0003g0007others(4): Show | 7 | HG00639.hp2 HG02145.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.218+14867C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118973427 | ||||||
| chr5:118973439
|
A | G | 8 | a0001c0001t0008g0204a0001c0001t0008g0220a0001c0001t0008g0221others(5): Show | 8 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.218+14855T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118973439 | ||||||
| chr5:118973505
|
C | T | 4 | a0001c0002t0001g0003a0001c0002t0001g0005a0001c0002t0037g0002others(1): Show | 4 | HG02615.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+14789G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118973505 | ||||||
| chr5:118973511
|
T | C | 4 | a0001c0001t0008g0231a0001c0001t0015g0133a0001c0001t0015g0134others(1): Show | 4 | HG01884.hp1 HG02622.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+14783A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118973511 | ||||||
| chr5:118973566
|
C | T | 4 | a0001c0001t0008g0231a0001c0001t0015g0133a0001c0001t0015g0134others(1): Show | 4 | HG01884.hp1 HG02622.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+14728G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118973566 | ||||||
| chr5:118973606
|
C | CGCCTCCT others(11): Show |
22 | a0001c0001t0001g0234a0001c0001t0003g0007a0001c0001t0003g0008others(19): Show | 23 | HG00639.hp2 HG00642.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.218+14670_218+1468 others(22): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118973606 | ||||||
| chr5:118973606
|
C | CGCCTCCT others(29): Show |
2 | a0001c0001t0013g0011a0001c0001t0021g0010 | 2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.218+14652_218+1468 others(40): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118973606 | ||||||
| chr5:118973606
|
C | CGCCTCCT others(11): Show |
2 | a0001c0001t0015g0133a0001c0001t0015g0134 | 2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.218+14687_218+1468 others(22): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118973606 | ||||||
| chr5:118973606
|
CGCCTCCT others(11): Show |
C | 157 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(154): Show | 157 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.218+14670_218+1468 others(22): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118973606 | ||||||
| chr5:118973606
|
CGCCTCCT others(29): Show |
C | 5 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(2): Show | 5 | HG01071.hp2 HG01261.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.218+14652_218+1468 others(40): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118973606 | ||||||
| chr5:118973657
|
G | C | 1 | a0001c0001t0011g0040 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.218+14637C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118973657 | ||||||
| chr5:118973657
|
G | GGCAGCCT others(11): Show |
1 | a0001c0001t0004g0118 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.218+14636_218+1463 others(22): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118973657 | ||||||
| chr5:118973657
|
G | GGCAGCCT others(11): Show |
4 | a0002c0003t0002g0239a0002c0003t0010g0237a0002c0003t0010g0238others(1): Show | 4 | HG00423.hp1 HG00544.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+14619_218+1463 others(22): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118973657 | ||||||
| chr5:118973678
|
A | G | 2 | a0001c0001t0016g0232a0001c0001t0016g0233 | 2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.218+14616T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118973678 | ||||||
| chr5:118973682
|
G | A | 8 | a0001c0001t0001g0173a0001c0001t0001g0175a0001c0001t0001g0176others(5): Show | 8 | HG01099.hp1 HG01168.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.218+14612C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118973682 | ||||||
| chr5:118973693
|
G | A | 1 | a0001c0001t0018g0001 | 2 | HG00642.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.218+14601C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118973693 | ||||||
| chr5:118973707
|
G | A | 1 | a0001c0001t0029g0132 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.218+14587C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118973707 | ||||||
| chr5:118973779
|
C | A | 10 | a0001c0001t0008g0231a0001c0001t0011g0040a0001c0001t0015g0133others(7): Show | 10 | HG00423.hp1 HG00544.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.218+14515G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118973779 | ||||||
| chr5:118973782
|
C | T | 3 | a0001c0001t0001g0235a0001c0001t0016g0232a0001c0001t0016g0233 | 3 | HG02145.hp2 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.218+14512G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118973782 | ||||||
| chr5:118973811
|
G | A | 1 | a0001c0001t0001g0235 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.218+14483C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118973811 | ||||||
| chr5:118973866
|
T | C | 13 | a0001c0001t0004g0116a0001c0001t0004g0117a0001c0001t0004g0118others(10): Show | 13 | HG01106.hp1 HG01243.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.218+14428A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118973866 | ||||||
| chr5:118973884
|
G | A | 1 | a0001c0001t0003g0018 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.218+14410C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118973884 | ||||||
| chr5:118973938
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.218+14356G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118973938 | ||||||
| chr5:118974039
|
G | A | 1 | a0001c0001t0007g0211 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.218+14255C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118974039 | ||||||
| chr5:118974041
|
G | C | 3 | a0001c0001t0015g0133a0001c0001t0015g0134a0001c0001t0015g0135 | 3 | HG01884.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.218+14253C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118974041 | ||||||
| chr5:118974237
|
C | T | 10 | a0001c0001t0001g0234a0001c0001t0003g0007a0001c0001t0003g0008others(7): Show | 10 | HG00639.hp2 HG01891.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.218+14057G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118974237 | ||||||
| chr5:118974274
|
G | A | 1 | a0001c0001t0003g0008 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.218+14020C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118974274 | ||||||
| chr5:118974383
|
T | G | 4 | a0002c0003t0002g0239a0002c0003t0010g0237a0002c0003t0010g0238others(1): Show | 4 | HG00423.hp1 HG00544.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+13911A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118974383 | ||||||
| chr5:118974474
|
G | A | 3 | a0001c0001t0001g0235a0001c0001t0016g0232a0001c0001t0016g0233 | 3 | HG02145.hp2 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.218+13820C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118974474 | ||||||
| chr5:118974555
|
T | TA | 12 | a0001c0001t0004g0117a0001c0001t0004g0118a0001c0001t0004g0120others(9): Show | 12 | HG01106.hp1 HG01243.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.218+13738dupT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118974555 | ||||||
| chr5:118974742
|
T | C | 1 | a0001c0001t0006g0072 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.218+13552A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118974742 | ||||||
| chr5:118974821
|
T | A | 1 | a0001c0001t0002g0107 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.218+13473A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118974821 | ||||||
| chr5:118974910
|
C | T | 5 | a0001c0001t0014g0227a0001c0001t0014g0229a0001c0001t0014g0230others(2): Show | 5 | HG02970.hp1 HG03041.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.218+13384G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118974910 | ||||||
| chr5:118975019
|
A | G | 8 | a0001c0001t0001g0224a0001c0001t0006g0029a0001c0001t0006g0047others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.218+13275T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118975019 | ||||||
| chr5:118975219
|
G | A | 1 | a0001c0001t0015g0135 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.218+13075C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118975219 | ||||||
| chr5:118975227
|
T | G | 6 | a0001c0001t0008g0231a0001c0001t0015g0133a0001c0001t0015g0134others(3): Show | 6 | HG01884.hp1 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.218+13067A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118975227 | ||||||
| chr5:118975276
|
A | G | 1 | a0001c0001t0001g0128 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.218+13018T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118975276 | ||||||
| chr5:118975312
|
G | A | 4 | a0001c0001t0001g0234a0001c0001t0003g0007a0001c0001t0003g0008others(1): Show | 4 | HG00639.hp2 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+12982C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118975312 | ||||||
| chr5:118975402
|
G | A | 4 | a0001c0001t0014g0227a0001c0001t0014g0229a0001c0001t0014g0230others(1): Show | 4 | HG02970.hp1 HG03209.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+12892C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118975402 | ||||||
| chr5:118975485
|
C | T | 1 | a0001c0001t0024g0206 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.218+12809G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118975485 | ||||||
| chr5:118975525
|
T | A | 6 | a0001c0001t0008g0204a0001c0001t0008g0220a0001c0001t0008g0221others(3): Show | 6 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.218+12769A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118975525 | ||||||
| chr5:118975633
|
T | G | 4 | a0001c0001t0008g0231a0001c0001t0015g0133a0001c0001t0015g0134others(1): Show | 4 | HG01884.hp1 HG02622.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+12661A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118975633 | ||||||
| chr5:118975641
|
G | T | 4 | a0001c0001t0008g0231a0001c0001t0015g0133a0001c0001t0015g0134others(1): Show | 4 | HG01884.hp1 HG02622.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+12653C>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118975641 | ||||||
| chr5:118975799
|
A | T | 1 | a0001c0002t0001g0004 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.218+12495T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118975799 | ||||||
| chr5:118975871
|
C | A | 1 | a0001c0001t0018g0001 | 2 | HG00642.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.218+12423G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118975871 | ||||||
| chr5:118975887
|
A | G | 1 | a0001c0001t0003g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.218+12407T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118975887 | ||||||
| chr5:118975931
|
C | T | 4 | a0001c0001t0001g0234a0001c0001t0003g0007a0001c0001t0003g0008others(1): Show | 4 | HG00639.hp2 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+12363G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118975931 | ||||||
| chr5:118976187
|
C | T | 1 | a0001c0001t0001g0095 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.218+12107G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118976187 | ||||||
| chr5:118976193
|
G | A | 34 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0150others(31): Show | 34 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.218+12101C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118976193 | ||||||
| chr5:118976260
|
C | G | 1 | a0001c0001t0017g0140 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.218+12034G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118976260 | ||||||
| chr5:118976365
|
CA | C | 3 | a0001c0001t0001g0235a0001c0001t0016g0232a0001c0001t0016g0233 | 3 | HG02145.hp2 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.218+11928delT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118976365 | ||||||
| chr5:118976455
|
A | C | 4 | a0002c0003t0002g0239a0002c0003t0010g0237a0002c0003t0010g0238others(1): Show | 4 | HG00423.hp1 HG00544.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+11839T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118976455 | ||||||
| chr5:118976459
|
GA | G | 4 | a0001c0001t0014g0227a0001c0001t0014g0229a0001c0001t0014g0230others(1): Show | 4 | HG02970.hp1 HG03209.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+11834delT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118976459 | ||||||
| chr5:118976588
|
A | C | 10 | a0001c0001t0008g0231a0001c0001t0015g0133a0001c0001t0015g0134others(7): Show | 10 | HG00423.hp1 HG00544.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.218+11706T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118976588 | ||||||
| chr5:118976664
|
C | G | 1 | a0001c0001t0004g0117 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.218+11630G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118976664 | ||||||
| chr5:118976716
|
A | G | 34 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0150others(31): Show | 34 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.218+11578T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118976716 | ||||||
| chr5:118976792
|
T | C | 1 | a0001c0001t0006g0072 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.218+11502A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118976792 | ||||||
| chr5:118976802
|
T | G | 1 | a0001c0001t0001g0041 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.218+11492A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118976802 | ||||||
| chr5:118977135
|
C | T | 2 | a0001c0001t0001g0046a0001c0004t0001g0032 | 2 | NA18970.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.218+11159G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118977135 | ||||||
| chr5:118977320
|
T | C | 1 | a0001c0001t0018g0001 | 2 | HG00642.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.218+10974A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118977320 | ||||||
| chr5:118977427
|
T | C | 3 | a0001c0001t0015g0133a0001c0001t0015g0134a0001c0001t0015g0135 | 3 | HG01884.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.218+10867A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118977427 | ||||||
| chr5:118977614
|
G | C | 3 | a0001c0001t0001g0235a0001c0001t0016g0232a0001c0001t0016g0233 | 3 | HG02145.hp2 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.218+10680C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118977614 | ||||||
| chr5:118977632
|
G | A | 1 | a0001c0001t0004g0124 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.218+10662C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118977632 | ||||||
| chr5:118977726
|
C | G | 1 | a0001c0001t0024g0206 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.218+10568G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118977726 | ||||||
| chr5:118977895
|
G | C | 45 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0150others(42): Show | 45 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.218+10399C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118977895 | ||||||
| chr5:118977963
|
C | T | 4 | a0001c0001t0018g0001a0001c0001t0023g0226a0001c0001t0029g0132others(1): Show | 5 | HG00642.hp1 HG01074.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.218+10331G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118977963 | ||||||
| chr5:118977970
|
A | G | 34 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0150others(31): Show | 34 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.218+10324T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118977970 | ||||||
| chr5:118978110
|
C | T | 2 | a0001c0001t0023g0226a0001c0001t0030g0225 | 2 | HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.218+10184G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118978110 | ||||||
| chr5:118978115
|
CT | C | 173 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(170): Show | 173 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.218+10178delA | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118978115 | ||||||
| chr5:118978169
|
A | C | 34 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0150others(31): Show | 34 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.218+10125T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118978169 | ||||||
| chr5:118978174
|
G | A | 2 | a0001c0001t0013g0218a0001c0001t0013g0219 | 2 | HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.218+10120C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118978174 | ||||||
| chr5:118978241
|
C | T | 1 | a0001c0001t0008g0231 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.218+10053G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118978241 | ||||||
| chr5:118978495
|
T | C | 1 | a0001c0001t0001g0052 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.218+9799A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118978495 | ||||||
| chr5:118978560
|
G | A | 4 | a0001c0001t0001g0234a0001c0001t0003g0007a0001c0001t0003g0008others(1): Show | 4 | HG00639.hp2 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+9734C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118978560 | ||||||
| chr5:118978690
|
A | T | 13 | a0001c0001t0004g0116a0001c0001t0004g0117a0001c0001t0004g0118others(10): Show | 13 | HG01106.hp1 HG01243.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.218+9604T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118978690 | ||||||
| chr5:118978917
|
G | A | 2 | a0001c0001t0013g0011a0001c0001t0021g0010 | 2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.218+9377C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118978917 | ||||||
| chr5:118979029
|
G | C | 1 | a0001c0001t0003g0012 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.218+9265C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118979029 | ||||||
| chr5:118979031
|
G | A | 1 | a0001c0001t0001g0164 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.218+9263C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118979031 | ||||||
| chr5:118979032
|
C | T | 1 | a0001c0001t0025g0045 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.218+9262G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118979032 | ||||||
| chr5:118979061
|
T | G | 1 | a0001c0001t0032g0236 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.218+9233A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118979061 | ||||||
| chr5:118979260
|
T | C | 175 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(172): Show | 175 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.218+9034A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118979260 | ||||||
| chr5:118979288
|
A | G | 13 | a0001c0001t0001g0235a0001c0001t0008g0231a0001c0001t0013g0011others(10): Show | 13 | HG00423.hp1 HG00544.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.218+9006T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118979288 | ||||||
| chr5:118979312
|
T | A | 4 | a0001c0001t0018g0001a0001c0001t0023g0226a0001c0001t0029g0132others(1): Show | 5 | HG00642.hp1 HG01074.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.218+8982A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118979312 | ||||||
| chr5:118979381
|
AAAAAG | A | 5 | a0001c0001t0012g0167a0001c0001t0012g0198a0001c0001t0012g0199others(2): Show | 5 | HG02258.hp1 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.218+8908_218+8912d others(7): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118979381 | ||||||
| chr5:118979523
|
T | C | 2 | a0001c0001t0016g0232a0001c0001t0016g0233 | 2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.218+8771A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118979523 | ||||||
| chr5:118979634
|
T | C | 1 | a0001c0001t0026g0212 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.218+8660A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118979634 | ||||||
| chr5:118979700
|
G | A | 13 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0031others(10): Show | 13 | HG00423.hp2 HG02056.hp1 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.218+8594C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118979700 | ||||||
| chr5:118979780
|
T | C | 5 | a0001c0001t0012g0167a0001c0001t0012g0198a0001c0001t0012g0199others(2): Show | 5 | HG02258.hp1 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.218+8514A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118979780 | ||||||
| chr5:118979835
|
T | C | 4 | a0001c0001t0007g0210a0001c0001t0007g0211a0001c0001t0007g0213others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+8459A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118979835 | ||||||
| chr5:118979869
|
C | T | 2 | a0001c0001t0014g0229a0001c0001t0014g0230 | 2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.218+8425G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118979869 | ||||||
| chr5:118980049
|
C | G | 138 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(135): Show | 138 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.218+8245G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118980049 | ||||||
| chr5:118980247
|
C | T | 2 | a0001c0001t0001g0102a0001c0001t0001g0109 | 2 | NA19003.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.218+8047G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118980247 | ||||||
| chr5:118980387
|
T | C | 1 | a0001c0001t0008g0231 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.218+7907A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118980387 | ||||||
| chr5:118980540
|
G | C | 1 | a0001c0001t0029g0132 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.218+7754C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118980540 | ||||||
| chr5:118980604
|
A | G | 2 | a0001c0001t0011g0111a0001c0001t0011g0112 | 2 | NA18951.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.218+7690T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118980604 | ||||||
| chr5:118980760
|
G | T | 4 | a0001c0001t0008g0231a0001c0001t0015g0133a0001c0001t0015g0134others(1): Show | 4 | HG01884.hp1 HG02622.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+7534C>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118980760 | ||||||
| chr5:118981080
|
C | T | 4 | a0001c0001t0008g0231a0001c0001t0015g0133a0001c0001t0015g0134others(1): Show | 4 | HG01884.hp1 HG02622.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+7214G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118981080 | ||||||
| chr5:118981304
|
T | C | 1 | a0001c0001t0038g0054 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.218+6990A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118981304 | ||||||
| chr5:118981392
|
G | C | 1 | a0001c0001t0001g0235 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.218+6902C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118981392 | ||||||
| chr5:118981503
|
T | C | 2 | a0001c0001t0013g0011a0001c0001t0021g0010 | 2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.218+6791A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118981503 | ||||||
| chr5:118981546
|
G | GA | 122 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(119): Show | 122 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.218+6747dupT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118981546 | ||||||
| chr5:118981708
|
A | G | 1 | a0001c0001t0002g0058 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.218+6586T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118981708 | ||||||
| chr5:118981833
|
C | T | 13 | a0001c0001t0004g0116a0001c0001t0004g0117a0001c0001t0004g0118others(10): Show | 13 | HG01106.hp1 HG01243.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.218+6461G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118981833 | ||||||
| chr5:118981969
|
T | C | 2 | a0001c0001t0001g0235a0001c0001t0033g0205 | 2 | HG02145.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.218+6325A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118981969 | ||||||
| chr5:118982117
|
G | A | 2 | a0001c0001t0001g0235a0001c0001t0033g0205 | 2 | HG02145.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.218+6177C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118982117 | ||||||
| chr5:118982123
|
A | T | 176 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(173): Show | 176 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.218+6171T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118982123 | ||||||
| chr5:118982199
|
A | C | 2 | a0001c0001t0007g0208a0001c0001t0007g0209 | 2 | HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.218+6095T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118982199 | ||||||
| chr5:118982278
|
T | C | 13 | a0001c0001t0001g0235a0001c0001t0008g0231a0001c0001t0013g0011others(10): Show | 13 | HG00423.hp1 HG00544.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.218+6016A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118982278 | ||||||
| chr5:118982386
|
C | T | 4 | a0001c0001t0014g0227a0001c0001t0014g0229a0001c0001t0014g0230others(1): Show | 4 | HG02970.hp1 HG03209.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+5908G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118982386 | ||||||
| chr5:118982423
|
T | C | 1 | a0001c0001t0024g0206 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.218+5871A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118982423 | ||||||
| chr5:118982655
|
T | A | 2 | a0001c0001t0013g0011a0001c0001t0021g0010 | 2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.218+5639A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118982655 | ||||||
| chr5:118982686
|
C | CT | 43 | a0001c0001t0001g0044a0001c0001t0001g0109a0001c0001t0001g0143others(40): Show | 43 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.218+5607dupA | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118982686 | ||||||
| chr5:118982686
|
CT | C | 16 | a0001c0001t0001g0101a0001c0001t0001g0176a0001c0001t0001g0195others(13): Show | 16 | HG00099.hp1 HG00140.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.218+5607delA | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118982686 | ||||||
| chr5:118982720
|
G | A | 2 | a0001c0001t0016g0232a0001c0001t0016g0233 | 2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.218+5574C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118982720 | ||||||
| chr5:118982728
|
G | A | 4 | a0001c0001t0014g0227a0001c0001t0014g0229a0001c0001t0014g0230others(1): Show | 4 | HG02970.hp1 HG03209.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+5566C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118982728 | ||||||
| chr5:118982775
|
G | A | 1 | a0001c0001t0033g0205 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.218+5519C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118982775 | ||||||
| chr5:118982892
|
C | T | 171 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(168): Show | 171 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.218+5402G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118982892 | ||||||
| chr5:118982909
|
G | A | 2 | a0001c0001t0002g0126a0001c0001t0002g0131 | 2 | HG02738.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.218+5385C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118982909 | ||||||
| chr5:118982927
|
G | A | 3 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0010g0027 | 3 | HG00423.hp2 HG02056.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.218+5367C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118982927 | ||||||
| chr5:118982957
|
G | A | 1 | a0001c0001t0018g0001 | 2 | HG00642.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.218+5337C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118982957 | ||||||
| chr5:118983041
|
C | G | 2 | a0001c0001t0014g0229a0001c0001t0014g0230 | 2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.218+5253G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118983041 | ||||||
| chr5:118983130
|
A | G | 4 | a0001c0001t0018g0001a0001c0001t0023g0226a0001c0001t0029g0132others(1): Show | 5 | HG00642.hp1 HG01074.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.218+5164T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118983130 | ||||||
| chr5:118983140
|
G | T | 7 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(4): Show | 7 | HG01243.hp2 HG01255.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.218+5154C>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118983140 | ||||||
| chr5:118983214
|
T | A | 4 | a0002c0003t0002g0239a0002c0003t0010g0237a0002c0003t0010g0238others(1): Show | 4 | HG00423.hp1 HG00544.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+5080A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118983214 | ||||||
| chr5:118983511
|
T | TTC | 5 | a0001c0001t0001g0127a0001c0001t0013g0011a0001c0001t0021g0010others(2): Show | 5 | HG01346.hp1 HG02257.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.218+4781_218+4782d others(4): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118983511 | ||||||
| chr5:118983529
|
CTT | C | 13 | a0001c0001t0004g0116a0001c0001t0004g0117a0001c0001t0004g0118others(10): Show | 13 | HG01106.hp1 HG01243.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.218+4763_218+4764d others(4): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118983529 | ||||||
| chr5:118983711
|
C | G | 3 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0057 | 3 | HG00738.hp2 HG01070.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.218+4583G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118983711 | ||||||
| chr5:118983849
|
T | G | 3 | a0001c0001t0015g0133a0001c0001t0015g0134a0001c0001t0015g0135 | 3 | HG01884.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.218+4445A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118983849 | ||||||
| chr5:118983861
|
A | G | 1 | a0001c0001t0012g0167 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.218+4433T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118983861 | ||||||
| chr5:118983876
|
G | A | 1 | a0001c0001t0018g0001 | 2 | HG00642.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.218+4418C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118983876 | ||||||
| chr5:118984096
|
G | A | 2 | a0001c0001t0014g0227a0001c0001t0034g0228 | 2 | HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.218+4198C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118984096 | ||||||
| chr5:118984132
|
C | T | 1 | a0001c0001t0032g0236 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.218+4162G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118984132 | ||||||
| chr5:118984322
|
G | A | 1 | a0001c0001t0001g0056 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.218+3972C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118984322 | ||||||
| chr5:118984353
|
C | G | 4 | a0002c0003t0002g0239a0002c0003t0010g0237a0002c0003t0010g0238others(1): Show | 4 | HG00423.hp1 HG00544.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+3941G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118984353 | ||||||
| chr5:118984424
|
G | A | 1 | a0001c0001t0001g0164 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.218+3870C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118984424 | ||||||
| chr5:118984460
|
CA | C | 9 | a0001c0001t0001g0173a0001c0001t0001g0234a0001c0001t0003g0007others(6): Show | 9 | HG00639.hp2 HG01884.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.218+3833delT | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118984460 | ||||||
| chr5:118984623
|
G | A | 63 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0150others(60): Show | 64 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.218+3671C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118984623 | ||||||
| chr5:118985006
|
T | C | 2 | a0001c0001t0013g0011a0001c0001t0021g0010 | 2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.218+3288A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118985006 | ||||||
| chr5:118985036
|
G | A | 4 | a0001c0001t0008g0231a0001c0001t0015g0133a0001c0001t0015g0134others(1): Show | 4 | HG01884.hp1 HG02622.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+3258C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118985036 | ||||||
| chr5:118985091
|
G | A | 4 | a0001c0001t0001g0234a0001c0001t0003g0007a0001c0001t0003g0008others(1): Show | 4 | HG00639.hp2 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+3203C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118985091 | ||||||
| chr5:118985092
|
G | A | 4 | a0001c0001t0001g0234a0001c0001t0003g0007a0001c0001t0003g0008others(1): Show | 4 | HG00639.hp2 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+3202C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118985092 | ||||||
| chr5:118985174
|
T | C | 8 | a0001c0001t0007g0208a0001c0001t0007g0209a0001c0001t0007g0210others(5): Show | 8 | HG02486.hp1 HG02572.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.218+3120A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118985174 | ||||||
| chr5:118985486
|
ATT | A | 10 | a0001c0001t0001g0235a0001c0001t0004g0116a0001c0001t0008g0220others(7): Show | 11 | HG00642.hp1 HG01074.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.218+2806_218+2807d others(4): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118985486 | ||||||
| chr5:118985488
|
TTTTA | T | 7 | a0001c0001t0005g0161a0001c0001t0005g0162a0001c0001t0008g0204others(4): Show | 7 | HG02622.hp1 HG02886.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.218+2802_218+2805d others(6): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118985488 | ||||||
| chr5:118985488
|
TTTTATA | T | 3 | a0001c0001t0015g0133a0001c0001t0015g0134a0001c0001t0015g0135 | 3 | HG01884.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.218+2800_218+2805d others(8): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118985488 | ||||||
| chr5:118985490
|
T | A | 17 | a0001c0001t0004g0117a0001c0001t0004g0118a0001c0001t0004g0120others(14): Show | 17 | HG01106.hp1 HG01243.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.218+2804A>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118985490 | ||||||
| chr5:118985490
|
T | TATATATA others(6): Show |
1 | a0001c0001t0001g0074 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.218+2803_218+2804i others(15): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118985490 | ||||||
| chr5:118985490
|
T | TTATA | 6 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0164others(3): Show | 6 | HG00423.hp2 HG02056.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.218+2800_218+2803d others(6): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118985490 | ||||||
| chr5:118985490
|
T | TTATATA | 4 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0172others(1): Show | 4 | HG01981.hp2 HG02129.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+2798_218+2803d others(8): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118985490 | ||||||
| chr5:118985490
|
T | TTATATAT others(1): Show |
14 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(11): Show | 14 | HG00642.hp2 HG01071.hp2 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.218+2796_218+2803d others(10): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118985490 | ||||||
| chr5:118985490
|
T | TTATATAT others(3): Show |
22 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0048others(19): Show | 22 | HG00280.hp1 HG00639.hp1 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.218+2794_218+2803d others(12): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118985490 | ||||||
| chr5:118985490
|
T | TTATATAT others(5): Show |
21 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(18): Show | 21 | HG01070.hp2 HG01074.hp2 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.218+2792_218+2803d others(14): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118985490 | ||||||
| chr5:118985490
|
T | TTATATAT others(7): Show |
17 | a0001c0001t0001g0071a0001c0001t0001g0165a0001c0001t0001g0189others(14): Show | 17 | HG00099.hp1 HG01070.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.218+2790_218+2803d others(16): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118985490 | ||||||
| chr5:118985490
|
T | TTATATAT others(9): Show |
9 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(6): Show | 9 | HG00735.hp2 HG01123.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.218+2788_218+2803d others(18): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118985490 | ||||||
| chr5:118985490
|
T | TTATATAT others(11): Show |
14 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(11): Show | 14 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(11): Show |
intron_variant | MODIFIER | c.218+2786_218+2803d others(20): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118985490 | ||||||
| chr5:118985490
|
T | TTATATAT others(13): Show |
2 | a0001c0001t0001g0090a0001c0001t0001g0114 | 2 | HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.218+2784_218+2803d others(22): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118985490 | ||||||
| chr5:118985490
|
T | TTATATAT others(15): Show |
1 | a0001c0001t0012g0201 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.218+2782_218+2803d others(24): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118985490 | ||||||
| chr5:118985490
|
T | TTATATAT others(17): Show |
1 | a0001c0001t0006g0091 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.218+2780_218+2803d others(26): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118985490 | ||||||
| chr5:118985490
|
T | TTATATAT others(19): Show |
1 | a0001c0001t0012g0167 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.218+2778_218+2803d others(28): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118985490 | ||||||
| chr5:118985490
|
T | TTTTATAT others(9): Show |
1 | a0001c0001t0001g0069 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.218+2803_218+2804i others(18): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118985490 | ||||||
| chr5:118985490
|
TTA | T | 3 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021 | 3 | HG01192.hp2 HG03491.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.218+2802_218+2803d others(4): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118985490 | ||||||
| chr5:118985490
|
TTATATAT others(5): Show |
T | 7 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(4): Show | 7 | HG01243.hp2 HG01255.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.218+2792_218+2803d others(14): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118985490 | ||||||
| chr5:118985513
|
TATATAC | T | 8 | a0001c0001t0004g0139a0001c0001t0007g0208a0001c0001t0007g0209others(5): Show | 8 | HG02486.hp1 HG02572.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.218+2775_218+2780d others(8): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118985513 | ||||||
| chr5:118985515
|
T | C | 2 | a0001c0001t0023g0226a0001c0001t0030g0225 | 2 | HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.218+2779A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118985515 | ||||||
| chr5:118985515
|
TATAC | T | 22 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0150others(19): Show | 22 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.218+2775_218+2778d others(6): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118985515 | ||||||
| chr5:118985517
|
T | C | 16 | a0001c0001t0004g0116a0001c0001t0004g0117a0001c0001t0004g0118others(13): Show | 17 | HG00642.hp1 HG01074.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.218+2777A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118985517 | ||||||
| chr5:118985517
|
T | TAC | 9 | a0001c0001t0004g0120a0001c0001t0004g0123a0001c0001t0004g0124others(6): Show | 9 | HG01106.hp1 HG01496.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.218+2775_218+2776d others(4): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118985517 | ||||||
| chr5:118985517
|
T | TATAC | 3 | a0001c0001t0014g0229a0001c0001t0014g0230a0001c0001t0033g0205 | 3 | HG02970.hp1 HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.218+2776_218+2777i others(6): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118985517 | ||||||
| chr5:118985517
|
T | TATATATA others(3): Show |
4 | a0001c0001t0001g0094a0001c0001t0001g0224a0001c0001t0006g0092others(1): Show | 4 | HG01168.hp2 HG01169.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+2776_218+2777i others(12): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118985517 | ||||||
| chr5:118985517
|
T | TATATATA others(5): Show |
8 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0098others(5): Show | 8 | HG00140.hp2 HG01106.hp2 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.218+2776_218+2777i others(14): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118985517 | ||||||
| chr5:118985517
|
T | TATATATA others(7): Show |
8 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(5): Show | 8 | HG00738.hp1 HG01109.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.218+2776_218+2777i others(16): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118985517 | ||||||
| chr5:118985517
|
T | TATATATA others(9): Show |
5 | a0001c0001t0001g0108a0001c0001t0001g0128a0001c0001t0002g0129others(2): Show | 5 | HG00741.hp2 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.218+2776_218+2777i others(18): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118985517 | ||||||
| chr5:118985517
|
T | TATATATA others(11): Show |
3 | a0001c0001t0001g0109a0001c0001t0011g0111a0001c0001t0041g0110 | 3 | HG02257.hp2 NA18951.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.218+2776_218+2777i others(20): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118985517 | ||||||
| chr5:118985517
|
T | TATATATA others(13): Show |
1 | a0001c0001t0011g0112 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.218+2776_218+2777i others(22): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118985517 | ||||||
| chr5:118985517
|
T | TATATATA others(15): Show |
1 | a0001c0001t0001g0202 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.218+2776_218+2777i others(24): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118985517 | ||||||
| chr5:118985517
|
TAC | T | 4 | a0001c0001t0002g0160a0001c0001t0009g0159a0001c0001t0013g0011others(1): Show | 4 | HG01081.hp1 HG01496.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+2775_218+2776d others(4): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118985517 | ||||||
| chr5:118985519
|
C | T | 12 | a0001c0001t0001g0164a0001c0001t0001g0234a0001c0001t0001g0235others(9): Show | 12 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.218+2775G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118985519 | ||||||
| chr5:118985555
|
A | G | 1 | a0001c0001t0012g0167 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.218+2739T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118985555 | ||||||
| chr5:118985614
|
G | A | 2 | a0001c0001t0001g0203a0001c0001t0033g0205 | 2 | HG01192.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.218+2680C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118985614 | ||||||
| chr5:118985622
|
A | G | 3 | a0001c0001t0015g0133a0001c0001t0015g0134a0001c0001t0015g0135 | 3 | HG01884.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.218+2672T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118985622 | ||||||
| chr5:118986209
|
T | C | 1 | a0002c0003t0010g0240 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.218+2085A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118986209 | ||||||
| chr5:118986295
|
G | A | 1 | a0001c0001t0032g0236 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.218+1999C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118986295 | ||||||
| chr5:118986299
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.218+1995C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118986299 | ||||||
| chr5:118986347
|
G | T | 111 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(108): Show | 111 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.218+1947C>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118986347 | ||||||
| chr5:118986364
|
T | C | 3 | a0001c0001t0023g0226a0001c0001t0029g0132a0001c0001t0030g0225 | 3 | HG02257.hp1 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.218+1930A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118986364 | ||||||
| chr5:118986417
|
A | T | 1 | a0001c0001t0001g0164 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.218+1877T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118986417 | ||||||
| chr5:118986419
|
G | C | 1 | a0001c0001t0001g0164 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.218+1875C>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118986419 | ||||||
| chr5:118986517
|
A | C | 4 | a0001c0001t0001g0234a0001c0001t0003g0007a0001c0001t0003g0008others(1): Show | 4 | HG00639.hp2 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+1777T>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118986517 | ||||||
| chr5:118986579
|
C | A | 5 | a0001c0001t0014g0227a0001c0001t0014g0229a0001c0001t0014g0230others(2): Show | 5 | HG02970.hp1 HG03041.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.218+1715G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118986579 | ||||||
| chr5:118986611
|
C | A | 4 | a0001c0001t0008g0231a0001c0001t0015g0133a0001c0001t0015g0134others(1): Show | 4 | HG01884.hp1 HG02622.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+1683G>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118986611 | ||||||
| chr5:118986634
|
A | T | 2 | a0001c0001t0013g0011a0001c0001t0021g0010 | 2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.218+1660T>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118986634 | ||||||
| chr5:118986731
|
GTTAAAGC others(91): Show |
G | 1 | a0001c0001t0008g0204 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.218+1465_218+1562d others(100): Show |
DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118986731 | ||||||
| chr5:118986755
|
A | G | 3 | a0001c0001t0001g0235a0001c0001t0032g0236a0001c0001t0033g0205 | 3 | HG02145.hp2 HG02630.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.218+1539T>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118986755 | ||||||
| chr5:118987293
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.218+1001A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118987293 | ||||||
| chr5:118987426
|
T | C | 204 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(201): Show | 205 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.218+868A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118987426 | ||||||
| chr5:118987489
|
T | C | 3 | a0001c0001t0015g0133a0001c0001t0015g0134a0001c0001t0015g0135 | 3 | HG01884.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.218+805A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118987489 | ||||||
| chr5:118987494
|
T | C | 2 | a0001c0001t0004g0136a0001c0001t0004g0137 | 2 | HG01496.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.218+800A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118987494 | ||||||
| chr5:118987515
|
T | G | 30 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0150others(27): Show | 30 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.218+779A>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118987515 | ||||||
| chr5:118987527
|
T | C | 1 | a0001c0001t0001g0166 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.218+767A>G | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118987527 | ||||||
| chr5:118987552
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.218+742G>A | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118987552 | ||||||
| chr5:118987849
|
C | G | 174 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(171): Show | 175 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.218+445G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118987849 | ||||||
| chr5:118988006
|
C | G | 3 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0027g0009 | 3 | HG00639.hp2 HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.218+288G>C | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118988006 | ||||||
| chr5:118988145
|
G | A | 3 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0032g0236 | 3 | HG02145.hp2 HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.218+149C>T | DTWD2 | ENSG00000169570.10 | transcript | ENST00000510708.6 | protein_coding | 1/5 | chr5 | 118988145 |