| geneid | 84236 |
|---|---|
| ensemblid | ENSG00000144468.17 |
| hgncid | 23081 |
| symbol | RHBDD1 |
| name | rhomboid domain containing 1 |
| refseq_nuc | NM_001167608.3 |
| refseq_prot | NP_001161080.1 |
| ensembl_nuc | ENST00000392062.7 |
| ensembl_prot | ENSP00000375914.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 226836054 |
| end | 226999210 |
| strand | + |
| ver | v1.2 |
| region | chr2:226836054-226999210 |
| region5000 | chr2:226831054-227004210 |
| regionname0 | RHBDD1_chr2_226836054_226999210 |
| regionname5000 | RHBDD1_chr2_226831054_227004210 |
| 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 | 315 | 247 | 58 | 38 | 117 | 8 | 24 | 87 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| a0002 | 0/0 | 315 | 12 | 10 | 0 | 0 | 0 | 2 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| a0003 | 0/0 | 315 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| a0004 | 0/0 | 315 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| 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 | 948 | 240 | 52 | 38 | 116 | 8 | 24 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| c0002 | 0/0 | 948 | 10 | 10 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| c0003 | 0/0 | 948 | 4 | 4 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| c0004 | 0/0 | 948 | 3 | 3 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| c0005 | 0/0 | 948 | 2 | 2 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| c0006 | 0/0 | 948 | 2 | 0 | 0 | 0 | 0 | 2 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| c0007 | 0/0 | 948 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| c0008 | 0/0 | 948 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| c0009 | 0/0 | 948 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| 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 | 4114 | 165 | 21 | 19 | 97 | 5 | 21 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| t0002 | 0/0 | 4114 | 51 | 26 | 8 | 15 | 1 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| t0003 | 0/0 | 4114 | 16 | 2 | 7 | 2 | 2 | 3 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| t0004 | 0/0 | 4114 | 10 | 10 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| t0005 | 0/0 | 4112 | 3 | 3 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| t0006 | 0/0 | 4114 | 3 | 3 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| t0007 | 0/0 | 4114 | 2 | 0 | 0 | 2 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| t0008 | 0/0 | 4114 | 2 | 0 | 2 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| t0009 | 0/0 | 4114 | 2 | 2 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| t0010 | 0/0 | 4112 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| t0011 | 0/0 | 4114 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| t0012 | 0/0 | 4114 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| t0013 | 0/0 | 4114 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| t0014 | 0/0 | 4114 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| t0015 | 0/0 | 4114 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| t0016 | 0/0 | 4114 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| t0017 | 0/0 | 4075 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| t0018 | 0/0 | 4114 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| t0019 | 0/0 | 4114 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| 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 | 0 | 0 | 0 | 2 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0096 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0138 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| 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 | 948 | 240 | 52 | 38 | 116 | 8 | 24 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| a0001c0004 | 0/0 | 948 | 3 | 3 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| a0001c0005 | 0/0 | 948 | 2 | 2 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| a0001c0007 | 0/0 | 948 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| a0001c0008 | 0/0 | 948 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| a0002c0002 | 0/0 | 948 | 10 | 10 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| a0002c0006 | 0/0 | 948 | 2 | 0 | 0 | 0 | 0 | 2 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| a0003c0003 | 0/0 | 948 | 4 | 4 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| a0004c0009 | 0/0 | 948 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 5061 | 159 | 19 | 19 | 95 | 5 | 19 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| a0001c0001t0002 | 0/0 | 5061 | 48 | 23 | 8 | 15 | 1 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| a0001c0001t0003 | 0/0 | 5061 | 16 | 2 | 7 | 2 | 2 | 3 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| a0001c0001t0005 | 0/0 | 5059 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| a0001c0001t0006 | 0/0 | 5061 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| a0001c0001t0007 | 0/0 | 5061 | 2 | 0 | 0 | 2 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| a0001c0001t0008 | 0/0 | 5061 | 2 | 0 | 2 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| a0001c0001t0009 | 0/0 | 5061 | 2 | 2 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| a0001c0001t0011 | 0/0 | 5061 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| a0001c0001t0012 | 0/0 | 5061 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| a0001c0001t0013 | 0/0 | 5061 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| a0001c0001t0014 | 0/0 | 5061 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| a0001c0001t0015 | 0/0 | 5061 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| a0001c0001t0016 | 0/0 | 5061 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| a0001c0001t0017 | 0/0 | 5022 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| a0001c0001t0018 | 0/0 | 5061 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| a0001c0001t0019 | 0/0 | 5061 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| a0001c0004t0002 | 0/0 | 5061 | 3 | 3 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| a0001c0005t0005 | 0/0 | 5059 | 2 | 2 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| a0001c0007t0010 | 0/0 | 5059 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| a0001c0008t0001 | 0/0 | 5061 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| a0002c0002t0001 | 0/0 | 5061 | 2 | 2 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| a0002c0002t0004 | 0/0 | 5061 | 6 | 6 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| a0002c0002t0006 | 0/0 | 5061 | 2 | 2 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| a0002c0006t0001 | 0/0 | 5061 | 2 | 0 | 0 | 0 | 0 | 2 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| a0003c0003t0004 | 0/0 | 5061 | 4 | 4 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| a0004c0009t0001 | 0/0 | 5061 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | copy fasta | chr2 | 226831054 | 227004210 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0096 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0138 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0005g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0006g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0007g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0007g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0008g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0008g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0009g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0009g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0011g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0012g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0013g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0014g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0015g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0016g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0017g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0018g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0019g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0004t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0004t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0004t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0005t0005g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0005t0005g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0007t0010g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0008t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0002c0002t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0002c0002t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0002c0002t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0002c0002t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0002c0002t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0002c0002t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0002c0002t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0002c0002t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0002c0002t0006g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0002c0002t0006g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0002c0006t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0002c0006t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0003c0003t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0003c0003t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0003c0003t0004g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0003c0003t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0004c0009t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | GBR | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0254 | EUR | GBR | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0135 | EUR | GBR | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0249 | EUR | GBR | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | CHS | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0255 | AMR | PUR | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0243 | AMR | PUR | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0045 | AMR | PUR | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG01071 | hp2 | a0001 | c0001 | t0008 | g0246 | AMR | PUR | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0258 | AMR | PUR | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0213 | AMR | PUR | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0061 | AMR | PUR | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0181 | AMR | PUR | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0252 | AMR | PUR | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0182 | AMR | PUR | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG01192 | hp1 | a0001 | c0001 | t0008 | g0247 | AMR | PUR | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0179 | AMR | PUR | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0223 | AMR | CLM | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG01358 | hp1 | a0001 | c0001 | t0011 | g0183 | AMR | CLM | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG01358 | hp2 | a0001 | c0001 | t0018 | g0128 | AMR | CLM | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0253 | AMR | CLM | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0241 | EUR | IBS | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0180 | EUR | IBS | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG01884 | hp1 | a0001 | c0004 | t0002 | g0202 | AFR | ACB | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG01884 | hp2 | a0001 | c0001 | t0009 | g0140 | AFR | ACB | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0185 | AMR | PEL | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02074 | hp1 | a0001 | c0001 | t0007 | g0069 | EAS | KHV | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | KHV | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02083 | hp2 | a0001 | c0001 | t0017 | g0107 | EAS | KHV | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02145 | hp1 | a0002 | c0002 | t0004 | g0015 | AFR | ACB | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02145 | hp2 | a0002 | c0002 | t0004 | g0237 | AFR | ACB | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0187 | AMR | PEL | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CDX | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CDX | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02258 | hp1 | a0002 | c0002 | t0004 | g0012 | AFR | ACB | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0184 | AFR | ACB | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0212 | AFR | ACB | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02451 | hp1 | a0001 | c0001 | t0019 | g0017 | AFR | ACB | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02572 | hp1 | a0001 | c0001 | t0016 | g0066 | AFR | GWD | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0214 | AFR | GWD | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0208 | AFR | GWD | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0178 | AFR | GWD | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0232 | AFR | GWD | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02818 | hp1 | a0001 | c0001 | t0013 | g0198 | AFR | GWD | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02818 | hp2 | a0003 | c0003 | t0004 | g0174 | AFR | GWD | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0217 | AFR | GWD | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0196 | AFR | GWD | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02896 | hp2 | a0003 | c0003 | t0004 | g0173 | AFR | GWD | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0210 | AFR | GWD | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02897 | hp2 | a0003 | c0003 | t0004 | g0172 | AFR | GWD | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0192 | AFR | ESN | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02922 | hp2 | a0001 | c0005 | t0005 | g0220 | AFR | ESN | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | ESN | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02965 | hp2 | a0003 | c0003 | t0004 | g0175 | AFR | ESN | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0234 | AFR | ESN | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG03041 | hp1 | a0002 | c0002 | t0004 | g0016 | AFR | GWD | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0218 | AFR | GWD | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0221 | AFR | MSL | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | MSL | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG03130 | hp1 | a0001 | c0005 | t0005 | g0219 | AFR | ESN | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | ESN | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG03139 | hp1 | a0001 | c0007 | t0010 | g0222 | AFR | ESN | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG03139 | hp2 | a0002 | c0002 | t0006 | g0230 | AFR | ESN | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0235 | AFR | ESN | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG03209 | hp1 | a0002 | c0002 | t0004 | g0238 | AFR | MSL | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | MSL | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG03225 | hp2 | a0001 | c0004 | t0002 | g0203 | AFR | MSL | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | MSL | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0194 | AFR | MSL | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0014 | AFR | MSL | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0257 | SAS | PJL | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0197 | AFR | ESN | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG03540 | hp1 | a0001 | c0001 | t0012 | g0231 | AFR | GWD | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0013 | AFR | GWD | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG03654 | hp1 | a0002 | c0006 | t0001 | g0177 | SAS | PJL | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | STU | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | STU | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG03710 | hp1 | a0001 | c0001 | t0015 | g0072 | SAS | PJL | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0245 | SAS | BEB | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0204 | SAS | BEB | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0043 | SAS | STU | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | STU | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | STU | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG04228 | hp2 | a0002 | c0006 | t0001 | g0176 | SAS | STU | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0244 | AFR | YRI | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | YRI | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18988 | hp1 | a0001 | c0001 | t0007 | g0057 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0256 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA19000 | hp1 | a0001 | c0008 | t0001 | g0076 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA19011 | hp1 | a0001 | c0001 | t0014 | g0211 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0233 | AFR | LWK | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | LWK | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA19056 | hp1 | a0004 | c0009 | t0001 | g0242 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0193 | AFR | ASW | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0251 | AFR | ASW | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0240 | EUR | TSI | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | TSI | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | GIH | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | GIH | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0188 | AMR | CLM | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0215 | AFR | ACB | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02559 | hp2 | a0001 | c0004 | t0002 | g0201 | AFR | ACB | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | MSL | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG03471 | hp2 | a0001 | c0001 | t0009 | g0149 | AFR | MSL | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | USA | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | USA | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA20300 | hp1 | a0002 | c0002 | t0004 | g0011 | AFR | USA | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0216 | AFR | USA | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0209 | AFR | LWK | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA21309 | hp2 | a0002 | c0002 | t0006 | g0229 | AFR | LWK | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0138 | REF | REF | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0096 | REF | REF | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:226864779
|
C | G | 1 | a0004 | 1 | NA19056.hp1 | missense_variant | MODERATE | c.86C>G | p.Pro29Arg | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 4/9 | 511/5061 | 86/948 | 29/315 | chr2 | 226864779 | ||
| chr2:226865021
|
G | A | 2 | a0002a0003 | 16 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(13): Show |
missense_variant | MODERATE | c.328G>A | p.Ala110Thr | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 4/9 | 753/5061 | 328/948 | 110/315 | chr2 | 226865021 | ||
| chr2:226865075
|
G | A | 1 | a0003 | 4 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
missense_variant | MODERATE | c.382G>A | p.Glu128Lys | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 4/9 | 807/5061 | 382/948 | 128/315 | chr2 | 226865075 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:226864997
|
A | C | 2 | a0002c0006a0003c0003 | 6 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
synonymous_variant | LOW | c.304A>C | p.Arg102Arg | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 4/9 | 729/5061 | 304/948 | 102/315 | chr2 | 226864997 | ||
| chr2:226914212
|
C | T | 1 | a0001c0008 | 1 | NA19000.hp1 | synonymous_variant | LOW | c.717C>T | p.Ser239Ser | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/9 | 1142/5061 | 717/948 | 239/315 | chr2 | 226914212 | ||
| chr2:226914350
|
A | G | 1 | a0001c0007 | 1 | HG03139.hp1 | splice_region_variant&synonymous_variant | LOW | c.855A>G | p.Arg285Arg | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/9 | 1280/5061 | 855/948 | 285/315 | chr2 | 226914350 | ||
| chr2:226995471
|
C | T | 1 | a0001c0004 | 3 | HG01884.hp1 HG02559.hp2 HG03225.hp2 |
synonymous_variant | LOW | c.897C>T | p.Leu299Leu | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 9/9 | 1322/5061 | 897/948 | 299/315 | chr2 | 226995471 | ||
| chr2:226995516
|
C | T | 2 | a0001c0005a0001c0007 | 3 | HG02922.hp2 HG03130.hp1 HG03139.hp1 |
synonymous_variant | LOW | c.942C>T | p.Ser314Ser | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 9/9 | 1367/5061 | 942/948 | 314/315 | chr2 | 226995516 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:226838077
|
C | T | 1 | a0001c0001t0009 | 2 | HG01884.hp2 HG03471.hp2 |
5_prime_UTR_variant | MODIFIER | c.-387C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 2/9 | 26617 | chr2 | 226838077 | |||||
| chr2:226838120
|
G | C | 1 | a0001c0001t0007 | 2 | HG02074.hp1 NA18988.hp1 |
5_prime_UTR_variant | MODIFIER | c.-344G>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 2/9 | 26574 | chr2 | 226838120 | |||||
| chr2:226839430
|
T | A | 9 | a0001c0001t0002a0001c0001t0005a0001c0001t0011others(6): Show | 59 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(56): Show |
5_prime_UTR_variant | MODIFIER | c.-288T>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/9 | 25264 | chr2 | 226839430 | |||||
| chr2:226839562
|
CTG | C | 3 | a0001c0001t0005a0001c0005t0005a0001c0007t0010 | 4 | HG02922.hp2 HG03098.hp1 HG03130.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-153_-152delTG | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/9 | 25128 | INFO_REALIGN_3_PRIME | chr2 | 226839562 | ||||
| chr2:226864644
|
C | T | 1 | a0001c0001t0019 | 1 | HG02451.hp1 | 5_prime_UTR_variant | MODIFIER | c.-50C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 4/9 | 50 | chr2 | 226864644 | |||||
| chr2:226995955
|
G | A | 2 | a0001c0001t0003a0001c0001t0011 | 17 | HG00140.hp2 HG00735.hp2 HG00738.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*433G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 9/9 | 433 | chr2 | 226995955 | |||||
| chr2:226996002
|
G | A | 6 | a0001c0001t0005a0001c0001t0012a0001c0005t0005others(3): Show | 15 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*480G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 9/9 | 480 | chr2 | 226996002 | |||||
| chr2:226996019
|
C | T | 6 | a0001c0001t0005a0001c0001t0012a0001c0005t0005others(3): Show | 15 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*497C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 9/9 | 497 | chr2 | 226996019 | |||||
| chr2:226996030
|
G | A | 1 | a0001c0001t0008 | 2 | HG01071.hp2 HG01192.hp1 |
3_prime_UTR_variant | MODIFIER | c.*508G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 9/9 | 508 | chr2 | 226996030 | |||||
| chr2:226996155
|
G | T | 1 | a0001c0001t0019 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*633G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 9/9 | 633 | chr2 | 226996155 | |||||
| chr2:226996687
|
C | G | 3 | a0001c0001t0006a0001c0001t0019a0002c0002t0006 | 4 | HG02451.hp1 HG03139.hp2 NA18906.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1165C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 9/9 | 1165 | chr2 | 226996687 | |||||
| chr2:226996862
|
C | G | 1 | a0001c0001t0018 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1340C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 9/9 | 1340 | chr2 | 226996862 | |||||
| chr2:226997032
|
ACCATGGA others(32): Show |
A | 1 | a0001c0001t0017 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1511_*1549delCCAT others(35): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 9/9 | 1511 | chr2 | 226997032 | |||||
| chr2:226997641
|
A | G | 1 | a0001c0007t0010 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2119A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 9/9 | 2119 | chr2 | 226997641 | |||||
| chr2:226998522
|
A | G | 1 | a0001c0001t0016 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3000A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 9/9 | 3000 | chr2 | 226998522 | |||||
| chr2:226998625
|
C | T | 1 | a0001c0001t0014 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3103C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 9/9 | 3103 | chr2 | 226998625 | |||||
| chr2:226998710
|
C | T | 1 | a0001c0001t0013 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3188C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 9/9 | 3188 | chr2 | 226998710 | |||||
| chr2:226998957
|
C | T | 1 | a0001c0001t0015 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3435C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 9/9 | 3435 | chr2 | 226998957 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:226836102
|
C | T | 19 | a0001c0001t0001g0240a0001c0001t0001g0248a0001c0001t0001g0254others(16): Show | 19 | HG00099.hp2 HG00140.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.-392+15C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 1/8 | chr2 | 226836102 | ||||||
| chr2:226836122
|
C | T | 1 | a0001c0001t0002g0239 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-392+35C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 1/8 | chr2 | 226836122 | ||||||
| chr2:226836143
|
C | G | 1 | a0002c0002t0004g0238 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-392+56C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 1/8 | chr2 | 226836143 | ||||||
| chr2:226836346
|
G | A | 2 | a0001c0001t0001g0008a0001c0001t0003g0007 | 2 | HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-392+259G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 1/8 | chr2 | 226836346 | ||||||
| chr2:226836369
|
C | A | 8 | a0001c0001t0001g0009a0001c0001t0001g0010a0002c0002t0001g0013others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-392+282C>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 1/8 | chr2 | 226836369 | ||||||
| chr2:226836409
|
G | A | 1 | a0001c0001t0019g0017 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-392+322G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 1/8 | chr2 | 226836409 | ||||||
| chr2:226836454
|
A | G | 1 | a0002c0002t0004g0237 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-392+367A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 1/8 | chr2 | 226836454 | ||||||
| chr2:226836567
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-392+480C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 1/8 | chr2 | 226836567 | ||||||
| chr2:226836612
|
G | T | 4 | a0001c0001t0002g0232a0001c0001t0002g0233a0001c0001t0002g0234others(1): Show | 4 | HG02809.hp2 HG02976.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-392+525G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 1/8 | chr2 | 226836612 | ||||||
| chr2:226836716
|
A | G | 1 | a0001c0001t0012g0231 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-392+629A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 1/8 | chr2 | 226836716 | ||||||
| chr2:226837051
|
A | G | 10 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0004g0011others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-392+964A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 1/8 | chr2 | 226837051 | ||||||
| chr2:226837251
|
G | A | 9 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0004g0011others(6): Show | 9 | HG02145.hp1 HG02258.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.-391-822G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 1/8 | chr2 | 226837251 | ||||||
| chr2:226837266
|
A | G | 1 | a0001c0001t0003g0258 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-391-807A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 1/8 | chr2 | 226837266 | ||||||
| chr2:226837532
|
C | T | 1 | a0002c0002t0004g0238 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-391-541C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 1/8 | chr2 | 226837532 | ||||||
| chr2:226837548
|
C | CTTTG | 74 | a0001c0001t0002g0006a0001c0001t0002g0178a0001c0001t0002g0179others(71): Show | 75 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(72): Show |
intron_variant | MODIFIER | c.-391-520_-391-517d others(6): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 226837548 | |||||
| chr2:226837638
|
A | G | 58 | a0001c0001t0002g0006a0001c0001t0002g0178a0001c0001t0002g0179others(55): Show | 59 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(56): Show |
intron_variant | MODIFIER | c.-391-435A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 1/8 | chr2 | 226837638 | ||||||
| chr2:226837702
|
A | G | 6 | a0001c0001t0002g0224a0001c0001t0002g0225a0001c0001t0002g0226others(3): Show | 6 | HG00673.hp2 HG03041.hp1 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.-391-371A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 1/8 | chr2 | 226837702 | ||||||
| chr2:226837901
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-391-172G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 1/8 | chr2 | 226837901 | ||||||
| chr2:226837941
|
C | T | 40 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0134others(37): Show | 42 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.-391-132C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 1/8 | chr2 | 226837941 | ||||||
| chr2:226838251
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-310+97A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 2/8 | chr2 | 226838251 | ||||||
| chr2:226838253
|
A | G | 58 | a0001c0001t0002g0006a0001c0001t0002g0178a0001c0001t0002g0179others(55): Show | 59 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(56): Show |
intron_variant | MODIFIER | c.-310+99A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 2/8 | chr2 | 226838253 | ||||||
| chr2:226838378
|
C | T | 58 | a0001c0001t0002g0006a0001c0001t0002g0178a0001c0001t0002g0179others(55): Show | 59 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(56): Show |
intron_variant | MODIFIER | c.-310+224C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 2/8 | chr2 | 226838378 | ||||||
| chr2:226838401
|
T | C | 68 | a0001c0001t0002g0006a0001c0001t0002g0178a0001c0001t0002g0179others(65): Show | 69 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(66): Show |
intron_variant | MODIFIER | c.-310+247T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 2/8 | chr2 | 226838401 | ||||||
| chr2:226838409
|
T | C | 58 | a0001c0001t0002g0006a0001c0001t0002g0178a0001c0001t0002g0179others(55): Show | 59 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(56): Show |
intron_variant | MODIFIER | c.-310+255T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 2/8 | chr2 | 226838409 | ||||||
| chr2:226838515
|
T | C | 2 | a0001c0001t0002g0006a0001c0001t0002g0178 | 3 | HG02647.hp1 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-310+361T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 2/8 | chr2 | 226838515 | ||||||
| chr2:226838555
|
C | T | 1 | a0001c0001t0002g0223 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-310+401C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 2/8 | chr2 | 226838555 | ||||||
| chr2:226838978
|
A | T | 1 | a0001c0007t0010g0222 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-309-431A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 2/8 | chr2 | 226838978 | ||||||
| chr2:226839228
|
G | C | 1 | a0001c0001t0001g0240 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-309-181G>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 2/8 | chr2 | 226839228 | ||||||
| chr2:226839392
|
A | G | 2 | a0002c0006t0001g0176a0002c0006t0001g0177 | 2 | HG03654.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-309-17A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 2/8 | chr2 | 226839392 | ||||||
| chr2:226839402
|
T | C | 1 | a0001c0001t0019g0017 | 1 | HG02451.hp1 | splice_region_variant&intron_variant | LOW | c.-309-7T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 2/8 | chr2 | 226839402 | ||||||
| chr2:226839729
|
G | GA | 54 | a0001c0001t0002g0006a0001c0001t0002g0178a0001c0001t0002g0179others(51): Show | 55 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(52): Show |
intron_variant | MODIFIER | c.-91+113dupA | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 226839729 | |||||
| chr2:226839731
|
A | G | 40 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0134others(37): Show | 42 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.-91+104A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226839731 | ||||||
| chr2:226839835
|
G | A | 58 | a0001c0001t0002g0006a0001c0001t0002g0178a0001c0001t0002g0179others(55): Show | 59 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(56): Show |
intron_variant | MODIFIER | c.-91+208G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226839835 | ||||||
| chr2:226840088
|
G | A | 2 | a0002c0006t0001g0176a0002c0006t0001g0177 | 2 | HG03654.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-91+461G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226840088 | ||||||
| chr2:226840300
|
A | C | 68 | a0001c0001t0002g0006a0001c0001t0002g0178a0001c0001t0002g0179others(65): Show | 69 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(66): Show |
intron_variant | MODIFIER | c.-91+673A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226840300 | ||||||
| chr2:226840314
|
C | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-91+687C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226840314 | ||||||
| chr2:226840360
|
G | T | 4 | a0001c0001t0005g0221a0001c0005t0005g0219a0001c0005t0005g0220others(1): Show | 4 | HG02922.hp2 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-91+733G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226840360 | ||||||
| chr2:226840364
|
T | C | 6 | a0002c0006t0001g0176a0002c0006t0001g0177a0003c0003t0004g0172others(3): Show | 6 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-91+737T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226840364 | ||||||
| chr2:226840445
|
T | G | 74 | a0001c0001t0002g0006a0001c0001t0002g0178a0001c0001t0002g0179others(71): Show | 75 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(72): Show |
intron_variant | MODIFIER | c.-91+818T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226840445 | ||||||
| chr2:226840495
|
C | T | 1 | a0001c0001t0003g0257 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-91+868C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226840495 | ||||||
| chr2:226840594
|
A | G | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-91+967A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226840594 | ||||||
| chr2:226840745
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-91+1118C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226840745 | ||||||
| chr2:226840881
|
T | A | 5 | a0001c0001t0002g0179a0001c0001t0002g0180a0001c0001t0002g0181others(2): Show | 5 | HG01168.hp1 HG01169.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.-91+1254T>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226840881 | ||||||
| chr2:226840883
|
G | C | 10 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0004g0011others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-91+1256G>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226840883 | ||||||
| chr2:226841066
|
G | A | 58 | a0001c0001t0002g0006a0001c0001t0002g0178a0001c0001t0002g0179others(55): Show | 59 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(56): Show |
intron_variant | MODIFIER | c.-91+1439G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226841066 | ||||||
| chr2:226841509
|
G | A | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-91+1882G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226841509 | ||||||
| chr2:226841902
|
T | C | 76 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0002g0006others(73): Show | 77 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(74): Show |
intron_variant | MODIFIER | c.-91+2275T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226841902 | ||||||
| chr2:226841948
|
G | A | 1 | a0001c0001t0001g0019 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-91+2321G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226841948 | ||||||
| chr2:226842177
|
CTG | C | 54 | a0001c0001t0002g0006a0001c0001t0002g0178a0001c0001t0002g0179others(51): Show | 55 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(52): Show |
intron_variant | MODIFIER | c.-91+2553_-91+2554d others(4): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 226842177 | |||||
| chr2:226842352
|
G | A | 7 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(4): Show | 7 | HG00408.hp1 HG00597.hp2 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.-91+2725G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226842352 | ||||||
| chr2:226842368
|
C | A | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-91+2741C>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226842368 | ||||||
| chr2:226842450
|
G | T | 1 | a0001c0001t0001g0129 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-91+2823G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226842450 | ||||||
| chr2:226842679
|
G | A | 64 | a0001c0001t0002g0006a0001c0001t0002g0178a0001c0001t0002g0179others(61): Show | 65 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(62): Show |
intron_variant | MODIFIER | c.-91+3052G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226842679 | ||||||
| chr2:226842815
|
T | C | 10 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0004g0011others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-91+3188T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226842815 | ||||||
| chr2:226843001
|
G | T | 16 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0004g0011others(13): Show | 16 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-91+3374G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226843001 | ||||||
| chr2:226843074
|
G | C | 16 | a0001c0001t0002g0179a0001c0001t0002g0180a0001c0001t0002g0181others(13): Show | 16 | HG01123.hp1 HG01168.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.-91+3447G>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226843074 | ||||||
| chr2:226843094
|
A | G | 2 | a0001c0001t0001g0018a0001c0001t0018g0128 | 2 | HG00735.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.-91+3467A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226843094 | ||||||
| chr2:226843170
|
G | T | 6 | a0002c0006t0001g0176a0002c0006t0001g0177a0003c0003t0004g0172others(3): Show | 6 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-91+3543G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226843170 | ||||||
| chr2:226843180
|
A | G | 54 | a0001c0001t0002g0006a0001c0001t0002g0178a0001c0001t0002g0179others(51): Show | 55 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(52): Show |
intron_variant | MODIFIER | c.-91+3553A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226843180 | ||||||
| chr2:226843498
|
G | A | 2 | a0002c0002t0006g0229a0002c0002t0006g0230 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-91+3871G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226843498 | ||||||
| chr2:226843588
|
G | T | 1 | a0001c0001t0005g0221 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-91+3961G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226843588 | ||||||
| chr2:226843605
|
C | T | 10 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0004g0011others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-91+3978C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226843605 | ||||||
| chr2:226843608
|
C | T | 6 | a0002c0006t0001g0176a0002c0006t0001g0177a0003c0003t0004g0172others(3): Show | 6 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-91+3981C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226843608 | ||||||
| chr2:226843629
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-91+4002G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226843629 | ||||||
| chr2:226843712
|
A | G | 2 | a0001c0001t0001g0126a0001c0001t0001g0127 | 2 | NA18995.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-91+4085A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226843712 | ||||||
| chr2:226843860
|
T | C | 1 | a0001c0001t0001g0028 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-91+4233T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226843860 | ||||||
| chr2:226844289
|
C | T | 1 | a0001c0001t0001g0171 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-91+4662C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226844289 | ||||||
| chr2:226844629
|
C | G | 1 | a0001c0001t0003g0256 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-91+5002C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226844629 | ||||||
| chr2:226844635
|
A | G | 1 | a0001c0007t0010g0222 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-91+5008A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226844635 | ||||||
| chr2:226845620
|
A | T | 1 | a0001c0001t0001g0125 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-91+5993A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226845620 | ||||||
| chr2:226845738
|
G | A | 1 | a0001c0001t0001g0001 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-91+6111G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226845738 | ||||||
| chr2:226845746
|
T | G | 1 | a0002c0002t0004g0238 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-91+6119T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226845746 | ||||||
| chr2:226845944
|
A | G | 6 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0215others(3): Show | 6 | HG01106.hp1 HG02109.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-91+6317A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226845944 | ||||||
| chr2:226846159
|
C | T | 1 | a0001c0001t0003g0255 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-91+6532C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226846159 | ||||||
| chr2:226846163
|
G | A | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(198): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.-91+6536G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226846163 | ||||||
| chr2:226846732
|
A | G | 1 | a0001c0001t0005g0221 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-91+7105A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226846732 | ||||||
| chr2:226846747
|
CA | C | 59 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0002g0006others(56): Show | 60 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(57): Show |
intron_variant | MODIFIER | c.-91+7138delA | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 226846747 | |||||
| chr2:226846767
|
G | T | 1 | a0001c0001t0001g0078 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-91+7140G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226846767 | ||||||
| chr2:226847024
|
A | G | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-91+7397A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226847024 | ||||||
| chr2:226847038
|
A | G | 1 | a0001c0001t0001g0254 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-91+7411A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226847038 | ||||||
| chr2:226847112
|
T | G | 1 | a0001c0001t0019g0017 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-91+7485T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226847112 | ||||||
| chr2:226847126
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-91+7499G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226847126 | ||||||
| chr2:226847242
|
G | A | 3 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG00099.hp1 HG01099.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.-91+7615G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226847242 | ||||||
| chr2:226847451
|
T | TTA | 74 | a0001c0001t0002g0006a0001c0001t0002g0178a0001c0001t0002g0179others(71): Show | 75 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(72): Show |
intron_variant | MODIFIER | c.-91+7826_-91+7827d others(4): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 226847451 | |||||
| chr2:226847477
|
A | G | 1 | a0001c0001t0003g0253 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-91+7850A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226847477 | ||||||
| chr2:226847673
|
G | A | 4 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(1): Show | 4 | HG00140.hp1 HG01255.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.-91+8046G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226847673 | ||||||
| chr2:226847821
|
G | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0075a0001c0001t0001g0077others(1): Show | 5 | HG00408.hp2 HG00423.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.-91+8194G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226847821 | ||||||
| chr2:226847860
|
A | T | 1 | a0001c0001t0002g0212 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-91+8233A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226847860 | ||||||
| chr2:226848108
|
A | G | 6 | a0002c0006t0001g0176a0002c0006t0001g0177a0003c0003t0004g0172others(3): Show | 6 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-91+8481A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226848108 | ||||||
| chr2:226848182
|
A | G | 1 | a0001c0001t0014g0211 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-91+8555A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226848182 | ||||||
| chr2:226848197
|
C | G | 1 | a0001c0001t0001g0001 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-91+8570C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226848197 | ||||||
| chr2:226848274
|
G | C | 10 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0004g0011others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-91+8647G>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226848274 | ||||||
| chr2:226848382
|
A | G | 2 | a0001c0001t0002g0006a0001c0001t0002g0178 | 3 | HG02647.hp1 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-91+8755A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226848382 | ||||||
| chr2:226848452
|
G | T | 57 | a0001c0001t0002g0006a0001c0001t0002g0178a0001c0001t0002g0179others(54): Show | 58 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(55): Show |
intron_variant | MODIFIER | c.-91+8825G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226848452 | ||||||
| chr2:226848799
|
C | G | 2 | a0001c0001t0001g0008a0001c0001t0003g0007 | 2 | HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-91+9172C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226848799 | ||||||
| chr2:226849339
|
C | T | 1 | a0001c0001t0002g0218 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-91+9712C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226849339 | ||||||
| chr2:226849500
|
G | A | 6 | a0002c0006t0001g0176a0002c0006t0001g0177a0003c0003t0004g0172others(3): Show | 6 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-91+9873G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226849500 | ||||||
| chr2:226849541
|
C | G | 4 | a0001c0001t0002g0208a0001c0001t0002g0209a0001c0001t0002g0210others(1): Show | 4 | HG02280.hp1 HG02622.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-91+9914C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226849541 | ||||||
| chr2:226849558
|
G | T | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG00558.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.-91+9931G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226849558 | ||||||
| chr2:226849740
|
ATATC | A | 3 | a0001c0005t0005g0219a0001c0005t0005g0220a0001c0007t0010g0222 | 3 | HG02922.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-91+10117_-91+1012 others(8): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 226849740 | |||||
| chr2:226849747
|
T | C | 2 | a0001c0001t0002g0224a0001c0001t0002g0225 | 2 | HG00673.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.-91+10120T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226849747 | ||||||
| chr2:226849789
|
A | G | 1 | a0001c0001t0001g0120 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-91+10162A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226849789 | ||||||
| chr2:226850116
|
T | C | 57 | a0001c0001t0002g0006a0001c0001t0002g0178a0001c0001t0002g0179others(54): Show | 58 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(55): Show |
intron_variant | MODIFIER | c.-91+10489T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226850116 | ||||||
| chr2:226850152
|
G | T | 2 | a0001c0001t0001g0018a0001c0001t0018g0128 | 2 | HG00735.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.-91+10525G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226850152 | ||||||
| chr2:226850242
|
A | G | 16 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0004g0011others(13): Show | 16 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-91+10615A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226850242 | ||||||
| chr2:226851049
|
C | G | 1 | a0001c0001t0001g0170 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-91+11422C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226851049 | ||||||
| chr2:226851174
|
C | T | 1 | a0001c0001t0002g0212 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-91+11547C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226851174 | ||||||
| chr2:226851301
|
C | G | 2 | a0002c0002t0006g0229a0002c0002t0006g0230 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-91+11674C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226851301 | ||||||
| chr2:226851387
|
T | G | 1 | a0001c0001t0005g0221 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-91+11760T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226851387 | ||||||
| chr2:226851883
|
C | T | 1 | a0002c0002t0006g0230 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-91+12256C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226851883 | ||||||
| chr2:226851890
|
G | A | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-91+12263G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226851890 | ||||||
| chr2:226852160
|
T | C | 1 | a0001c0001t0001g0139 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-90-12444T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226852160 | ||||||
| chr2:226852272
|
G | A | 1 | a0001c0001t0019g0017 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-90-12332G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226852272 | ||||||
| chr2:226852278
|
A | C | 2 | a0002c0002t0004g0237a0002c0002t0004g0238 | 2 | HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-90-12326A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226852278 | ||||||
| chr2:226852667
|
T | G | 1 | a0001c0001t0001g0032 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-90-11937T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226852667 | ||||||
| chr2:226852692
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-90-11912G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226852692 | ||||||
| chr2:226852747
|
G | C | 1 | a0001c0001t0001g0019 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-90-11857G>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226852747 | ||||||
| chr2:226852783
|
T | A | 6 | a0002c0006t0001g0176a0002c0006t0001g0177a0003c0003t0004g0172others(3): Show | 6 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-90-11821T>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226852783 | ||||||
| chr2:226852901
|
T | TTTA | 37 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0031others(34): Show | 38 | HG00140.hp2 HG00558.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.-90-11658_-90-1165 others(7): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 226852901 | |||||
| chr2:226852901
|
T | TTTATTA | 31 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0022others(28): Show | 31 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(28): Show |
intron_variant | MODIFIER | c.-90-11661_-90-1165 others(10): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 226852901 | |||||
| chr2:226852901
|
T | TTTATTAT others(2): Show |
6 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0034others(3): Show | 7 | HG01515.hp1 HG03490.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.-90-11664_-90-1165 others(13): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 226852901 | |||||
| chr2:226852901
|
T | TTTATTAT others(5): Show |
2 | a0001c0001t0001g0033a0001c0001t0001g0079 | 2 | HG00621.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.-90-11667_-90-1165 others(16): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 226852901 | |||||
| chr2:226852901
|
T | TTTATTAT others(2): Show |
13 | a0001c0001t0001g0074a0001c0001t0001g0118a0001c0001t0001g0142others(10): Show | 14 | HG00609.hp2 HG02004.hp1 HG03098.hp1 others(11): Show |
intron_variant | MODIFIER | c.-90-11695_-90-1169 others(13): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 226852901 | |||||
| chr2:226852901
|
T | TTTATTAT others(5): Show |
3 | a0001c0001t0001g0134a0001c0001t0001g0141a0001c0001t0002g0179 | 3 | HG00673.hp1 HG01192.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.-90-11695_-90-1169 others(16): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 226852901 | |||||
| chr2:226852901
|
TTTA | T | 9 | a0001c0001t0001g0032a0001c0001t0001g0070a0001c0001t0001g0071others(6): Show | 9 | HG00735.hp2 HG01168.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.-90-11658_-90-1165 others(7): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 226852901 | |||||
| chr2:226852901
|
TTTATTA | T | 3 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0002g0212 | 3 | HG02280.hp1 HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-90-11661_-90-1165 others(10): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 226852901 | |||||
| chr2:226852901
|
TTTATTAT others(5): Show |
T | 16 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0004g0011others(13): Show | 16 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-90-11667_-90-1165 others(16): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 226852901 | |||||
| chr2:226852904
|
A | ATTATTG | 31 | a0001c0001t0001g0119a0001c0001t0001g0135a0001c0001t0001g0136others(28): Show | 31 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.-90-11695_-90-1169 others(10): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 226852904 | |||||
| chr2:226852907
|
A | ATTG | 38 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0131others(35): Show | 40 | HG01123.hp1 HG01168.hp1 HG01169.hp2 others(37): Show |
intron_variant | MODIFIER | c.-90-11695_-90-1169 others(7): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 226852907 | |||||
| chr2:226852910
|
A | G | 17 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(14): Show | 17 | HG00673.hp2 HG01934.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.-90-11694A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226852910 | ||||||
| chr2:226852916
|
A | G | 1 | a0001c0001t0002g0212 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-90-11688A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226852916 | ||||||
| chr2:226852922
|
A | G | 16 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0004g0011others(13): Show | 16 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-90-11682A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226852922 | ||||||
| chr2:226852975
|
T | C | 73 | a0001c0001t0002g0006a0001c0001t0002g0178a0001c0001t0002g0179others(70): Show | 74 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(71): Show |
intron_variant | MODIFIER | c.-90-11629T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226852975 | ||||||
| chr2:226853154
|
G | T | 1 | a0001c0001t0001g0078 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-90-11450G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226853154 | ||||||
| chr2:226853523
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-90-11081G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226853523 | ||||||
| chr2:226853672
|
T | C | 1 | a0001c0001t0002g0188 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-90-10932T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226853672 | ||||||
| chr2:226853986
|
T | TGC | 74 | a0001c0001t0002g0006a0001c0001t0002g0178a0001c0001t0002g0179others(71): Show | 75 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(72): Show |
intron_variant | MODIFIER | c.-90-10618_-90-1061 others(6): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226853986 | ||||||
| chr2:226854097
|
T | C | 2 | a0001c0001t0009g0140a0001c0001t0009g0149 | 2 | HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-90-10507T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226854097 | ||||||
| chr2:226854392
|
A | C | 1 | a0001c0001t0005g0221 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-90-10212A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226854392 | ||||||
| chr2:226854465
|
G | A | 10 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0004g0011others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-90-10139G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226854465 | ||||||
| chr2:226854601
|
G | GA | 23 | a0001c0001t0001g0019a0001c0001t0001g0035a0001c0001t0001g0036others(20): Show | 23 | HG01934.hp1 HG01975.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.-90-9985dupA | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 226854601 | |||||
| chr2:226854601
|
G | GAA | 5 | a0001c0001t0002g0182a0001c0001t0002g0210a0001c0004t0002g0202others(2): Show | 5 | HG01169.hp2 HG01884.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-90-9986_-90-9985d others(4): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 226854601 | |||||
| chr2:226854601
|
G | GAAA | 48 | a0001c0001t0002g0006a0001c0001t0002g0180a0001c0001t0002g0181others(45): Show | 49 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(46): Show |
intron_variant | MODIFIER | c.-90-9987_-90-9985d others(5): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 226854601 | |||||
| chr2:226854622
|
C | T | 4 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0007g0057others(1): Show | 4 | HG00558.hp1 HG02074.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.-90-9982C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226854622 | ||||||
| chr2:226854812
|
T | C | 76 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0002g0006others(73): Show | 77 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(74): Show |
intron_variant | MODIFIER | c.-90-9792T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226854812 | ||||||
| chr2:226854843
|
A | G | 7 | a0001c0001t0001g0091a0002c0002t0001g0013a0002c0002t0001g0014others(4): Show | 7 | HG02145.hp1 HG02258.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.-90-9761A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226854843 | ||||||
| chr2:226855174
|
T | C | 1 | a0001c0001t0001g0133 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-90-9430T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226855174 | ||||||
| chr2:226855330
|
A | T | 1 | a0001c0001t0005g0221 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-90-9274A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226855330 | ||||||
| chr2:226855348
|
A | G | 1 | a0001c0001t0002g0223 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-90-9256A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226855348 | ||||||
| chr2:226855631
|
A | G | 1 | a0001c0001t0002g0207 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-90-8973A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226855631 | ||||||
| chr2:226855800
|
C | T | 10 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0004g0011others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-90-8804C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226855800 | ||||||
| chr2:226856313
|
A | G | 2 | a0001c0004t0002g0201a0001c0004t0002g0203 | 2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-90-8291A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226856313 | ||||||
| chr2:226856604
|
G | A | 10 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0004g0011others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-90-8000G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226856604 | ||||||
| chr2:226856743
|
C | T | 5 | a0001c0001t0002g0195a0001c0001t0002g0199a0001c0001t0002g0200others(2): Show | 5 | HG02083.hp1 NA18949.hp2 NA18956.hp1 others(2): Show |
intron_variant | MODIFIER | c.-90-7861C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226856743 | ||||||
| chr2:226856744
|
A | G | 55 | a0001c0001t0002g0006a0001c0001t0002g0178a0001c0001t0002g0179others(52): Show | 56 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(53): Show |
intron_variant | MODIFIER | c.-90-7860A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226856744 | ||||||
| chr2:226856998
|
A | G | 74 | a0001c0001t0002g0006a0001c0001t0002g0178a0001c0001t0002g0179others(71): Show | 75 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(72): Show |
intron_variant | MODIFIER | c.-90-7606A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226856998 | ||||||
| chr2:226857096
|
A | AGT | 5 | a0001c0001t0001g0003a0001c0001t0001g0091a0001c0001t0001g0092others(2): Show | 6 | HG02071.hp2 NA18945.hp2 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.-90-7489_-90-7488d others(4): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 226857096 | |||||
| chr2:226857096
|
AGT | A | 45 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0119others(42): Show | 47 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.-90-7489_-90-7488d others(4): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 226857096 | |||||
| chr2:226857096
|
AGTGT | A | 73 | a0001c0001t0002g0006a0001c0001t0002g0178a0001c0001t0002g0179others(70): Show | 74 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(71): Show |
intron_variant | MODIFIER | c.-90-7491_-90-7488d others(6): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 226857096 | |||||
| chr2:226857102
|
T | A | 1 | a0001c0004t0002g0201 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-90-7502T>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226857102 | ||||||
| chr2:226857385
|
A | G | 57 | a0001c0001t0002g0006a0001c0001t0002g0178a0001c0001t0002g0179others(54): Show | 58 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(55): Show |
intron_variant | MODIFIER | c.-90-7219A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226857385 | ||||||
| chr2:226857400
|
A | C | 9 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(6): Show | 9 | HG00423.hp1 HG00621.hp2 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.-90-7204A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226857400 | ||||||
| chr2:226857853
|
T | C | 3 | a0001c0001t0001g0083a0001c0001t0001g0094a0001c0001t0001g0117 | 3 | HG00558.hp2 HG00609.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.-90-6751T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226857853 | ||||||
| chr2:226858057
|
A | T | 54 | a0001c0001t0002g0006a0001c0001t0002g0178a0001c0001t0002g0179others(51): Show | 55 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(52): Show |
intron_variant | MODIFIER | c.-90-6547A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226858057 | ||||||
| chr2:226858467
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-90-6137G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226858467 | ||||||
| chr2:226858537
|
A | T | 1 | a0001c0001t0001g0028 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-90-6067A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226858537 | ||||||
| chr2:226858896
|
A | G | 4 | a0003c0003t0004g0172a0003c0003t0004g0173a0003c0003t0004g0174others(1): Show | 4 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-90-5708A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226858896 | ||||||
| chr2:226859250
|
G | C | 2 | a0002c0006t0001g0176a0002c0006t0001g0177 | 2 | HG03654.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-90-5354G>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226859250 | ||||||
| chr2:226859290
|
A | C | 54 | a0001c0001t0002g0006a0001c0001t0002g0178a0001c0001t0002g0179others(51): Show | 55 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(52): Show |
intron_variant | MODIFIER | c.-90-5314A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226859290 | ||||||
| chr2:226859330
|
A | G | 54 | a0001c0001t0002g0006a0001c0001t0002g0178a0001c0001t0002g0179others(51): Show | 55 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(52): Show |
intron_variant | MODIFIER | c.-90-5274A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226859330 | ||||||
| chr2:226859333
|
A | G | 44 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(41): Show | 46 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.-90-5271A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226859333 | ||||||
| chr2:226859528
|
G | T | 4 | a0003c0003t0004g0172a0003c0003t0004g0173a0003c0003t0004g0174others(1): Show | 4 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-90-5076G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226859528 | ||||||
| chr2:226859622
|
A | G | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-90-4982A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226859622 | ||||||
| chr2:226859766
|
C | T | 10 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0004g0011others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-90-4838C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226859766 | ||||||
| chr2:226859856
|
T | C | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | NA18972.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.-90-4748T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226859856 | ||||||
| chr2:226860009
|
TA | T | 66 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0002g0006others(63): Show | 67 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(64): Show |
intron_variant | MODIFIER | c.-90-4586delA | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 226860009 | |||||
| chr2:226860152
|
T | G | 58 | a0001c0001t0002g0006a0001c0001t0002g0178a0001c0001t0002g0179others(55): Show | 59 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(56): Show |
intron_variant | MODIFIER | c.-90-4452T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226860152 | ||||||
| chr2:226860315
|
A | G | 1 | a0001c0001t0001g0034 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-90-4289A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226860315 | ||||||
| chr2:226860390
|
A | G | 1 | a0001c0001t0003g0253 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-90-4214A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226860390 | ||||||
| chr2:226860551
|
C | T | 20 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(17): Show | 20 | HG01106.hp2 HG01255.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.-90-4053C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226860551 | ||||||
| chr2:226860788
|
C | T | 1 | a0001c0001t0003g0253 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-90-3816C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226860788 | ||||||
| chr2:226860871
|
C | T | 1 | a0001c0001t0003g0252 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-90-3733C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226860871 | ||||||
| chr2:226861025
|
A | G | 2 | a0001c0001t0002g0194a0001c0001t0013g0198 | 2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-90-3579A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226861025 | ||||||
| chr2:226861136
|
C | T | 6 | a0002c0006t0001g0176a0002c0006t0001g0177a0003c0003t0004g0172others(3): Show | 6 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-90-3468C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226861136 | ||||||
| chr2:226861366
|
C | T | 1 | a0001c0001t0019g0017 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-90-3238C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226861366 | ||||||
| chr2:226861427
|
A | G | 1 | a0001c0001t0017g0107 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-90-3177A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226861427 | ||||||
| chr2:226861722
|
G | C | 10 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0004g0011others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-90-2882G>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226861722 | ||||||
| chr2:226861741
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-90-2863C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226861741 | ||||||
| chr2:226861803
|
G | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0163 | 5 | NA18943.hp2 NA18993.hp1 NA19003.hp1 others(2): Show |
intron_variant | MODIFIER | c.-90-2801G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226861803 | ||||||
| chr2:226861810
|
G | A | 1 | a0001c0001t0003g0045 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-90-2794G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226861810 | ||||||
| chr2:226862032
|
A | G | 1 | a0001c0001t0001g0091 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-90-2572A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226862032 | ||||||
| chr2:226862039
|
T | C | 6 | a0002c0006t0001g0176a0002c0006t0001g0177a0003c0003t0004g0172others(3): Show | 6 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-90-2565T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226862039 | ||||||
| chr2:226862085
|
A | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-90-2519A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226862085 | ||||||
| chr2:226862310
|
G | C | 1 | a0002c0002t0004g0237 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-90-2294G>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226862310 | ||||||
| chr2:226862353
|
CT | C | 8 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(5): Show | 8 | HG00597.hp1 HG02559.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.-90-2233delT | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 226862353 | |||||
| chr2:226862668
|
G | A | 79 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(76): Show | 80 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(77): Show |
intron_variant | MODIFIER | c.-90-1936G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226862668 | ||||||
| chr2:226862688
|
T | C | 1 | a0001c0001t0003g0243 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-90-1916T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226862688 | ||||||
| chr2:226862694
|
G | A | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-90-1910G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226862694 | ||||||
| chr2:226862727
|
A | C | 2 | a0002c0006t0001g0176a0002c0006t0001g0177 | 2 | HG03654.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-90-1877A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226862727 | ||||||
| chr2:226862825
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-90-1779G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226862825 | ||||||
| chr2:226862861
|
C | G | 1 | a0001c0001t0005g0221 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-90-1743C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226862861 | ||||||
| chr2:226862948
|
T | A | 1 | a0001c0001t0001g0092 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-90-1656T>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226862948 | ||||||
| chr2:226863005
|
A | G | 58 | a0001c0001t0002g0006a0001c0001t0002g0178a0001c0001t0002g0179others(55): Show | 59 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(56): Show |
intron_variant | MODIFIER | c.-90-1599A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226863005 | ||||||
| chr2:226863196
|
A | G | 137 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(134): Show | 140 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.-90-1408A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226863196 | ||||||
| chr2:226863206
|
A | G | 74 | a0001c0001t0002g0006a0001c0001t0002g0178a0001c0001t0002g0179others(71): Show | 75 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(72): Show |
intron_variant | MODIFIER | c.-90-1398A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226863206 | ||||||
| chr2:226863412
|
C | T | 1 | a0001c0001t0003g0256 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-90-1192C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226863412 | ||||||
| chr2:226863415
|
G | A | 1 | a0001c0001t0002g0218 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-90-1189G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226863415 | ||||||
| chr2:226863476
|
G | C | 1 | a0001c0001t0001g0046 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-90-1128G>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226863476 | ||||||
| chr2:226863543
|
G | A | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-90-1061G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226863543 | ||||||
| chr2:226863582
|
T | G | 2 | a0002c0006t0001g0176a0002c0006t0001g0177 | 2 | HG03654.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-90-1022T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226863582 | ||||||
| chr2:226863620
|
T | G | 58 | a0001c0001t0002g0006a0001c0001t0002g0178a0001c0001t0002g0179others(55): Show | 59 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(56): Show |
intron_variant | MODIFIER | c.-90-984T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226863620 | ||||||
| chr2:226863677
|
T | G | 74 | a0001c0001t0002g0006a0001c0001t0002g0178a0001c0001t0002g0179others(71): Show | 75 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(72): Show |
intron_variant | MODIFIER | c.-90-927T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226863677 | ||||||
| chr2:226863828
|
G | T | 10 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0004g0011others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-90-776G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226863828 | ||||||
| chr2:226864076
|
G | C | 4 | a0001c0001t0001g0003a0001c0001t0001g0091a0001c0001t0001g0093others(1): Show | 5 | HG02071.hp2 NA18945.hp2 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.-90-528G>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226864076 | ||||||
| chr2:226864213
|
C | A | 1 | a0001c0001t0001g0046 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-90-391C>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226864213 | ||||||
| chr2:226864323
|
G | T | 74 | a0001c0001t0002g0006a0001c0001t0002g0178a0001c0001t0002g0179others(71): Show | 75 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(72): Show |
intron_variant | MODIFIER | c.-90-281G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226864323 | ||||||
| chr2:226865213
|
T | C | 1 | a0002c0002t0004g0238 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.433+87T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 4/8 | chr2 | 226865213 | ||||||
| chr2:226865520
|
CAG | C | 10 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0004g0011others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.433+397_433+398del others(2): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 226865520 | |||||
| chr2:226865609
|
G | A | 2 | a0001c0001t0001g0095a0001c0001t0001g0118 | 2 | NA18990.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.433+483G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 4/8 | chr2 | 226865609 | ||||||
| chr2:226865783
|
G | A | 2 | a0002c0006t0001g0176a0002c0006t0001g0177 | 2 | HG03654.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.433+657G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 4/8 | chr2 | 226865783 | ||||||
| chr2:226865855
|
C | T | 1 | a0001c0001t0001g0106 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.433+729C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 4/8 | chr2 | 226865855 | ||||||
| chr2:226866115
|
GC | G | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(254): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.433+991delC | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 226866115 | |||||
| chr2:226866156
|
C | T | 1 | a0001c0001t0003g0243 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.433+1030C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 4/8 | chr2 | 226866156 | ||||||
| chr2:226866191
|
C | T | 4 | a0001c0001t0005g0221a0001c0005t0005g0219a0001c0005t0005g0220others(1): Show | 4 | HG02922.hp2 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.434-995C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 4/8 | chr2 | 226866191 | ||||||
| chr2:226866279
|
C | A | 1 | a0001c0001t0014g0211 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.434-907C>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 4/8 | chr2 | 226866279 | ||||||
| chr2:226866450
|
G | T | 10 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0004g0011others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.434-736G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 4/8 | chr2 | 226866450 | ||||||
| chr2:226866584
|
A | G | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.434-602A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 4/8 | chr2 | 226866584 | ||||||
| chr2:226866603
|
T | C | 1 | a0002c0002t0004g0237 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.434-583T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 4/8 | chr2 | 226866603 | ||||||
| chr2:226866756
|
T | C | 1 | a0001c0001t0002g0218 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.434-430T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 4/8 | chr2 | 226866756 | ||||||
| chr2:226867119
|
T | C | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG02040.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.434-67T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 4/8 | chr2 | 226867119 | ||||||
| chr2:226867550
|
C | T | 16 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0004g0011others(13): Show | 16 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.566+232C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226867550 | ||||||
| chr2:226867581
|
T | A | 78 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(75): Show | 79 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(76): Show |
intron_variant | MODIFIER | c.566+263T>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226867581 | ||||||
| chr2:226867659
|
A | T | 2 | a0001c0001t0009g0140a0001c0001t0009g0149 | 2 | HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.566+341A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226867659 | ||||||
| chr2:226867725
|
T | C | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060 | 3 | HG02622.hp2 HG02886.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.566+407T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226867725 | ||||||
| chr2:226867929
|
G | A | 1 | a0001c0001t0002g0206 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.566+611G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226867929 | ||||||
| chr2:226868314
|
C | T | 2 | a0001c0001t0001g0089a0001c0001t0001g0090 | 2 | NA18977.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.566+996C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226868314 | ||||||
| chr2:226868414
|
T | C | 68 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0002g0006others(65): Show | 69 | HG00597.hp2 HG00673.hp2 HG01106.hp1 others(66): Show |
intron_variant | MODIFIER | c.566+1096T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226868414 | ||||||
| chr2:226868556
|
A | G | 51 | a0001c0001t0002g0006a0001c0001t0002g0178a0001c0001t0002g0179others(48): Show | 52 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(49): Show |
intron_variant | MODIFIER | c.566+1238A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226868556 | ||||||
| chr2:226868714
|
C | G | 3 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169 | 3 | HG01934.hp2 HG02451.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.566+1396C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226868714 | ||||||
| chr2:226868769
|
C | T | 76 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0002g0006others(73): Show | 77 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(74): Show |
intron_variant | MODIFIER | c.566+1451C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226868769 | ||||||
| chr2:226868785
|
G | A | 10 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0004g0011others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.566+1467G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226868785 | ||||||
| chr2:226868947
|
G | C | 2 | a0002c0002t0004g0011a0002c0002t0004g0012 | 2 | HG02258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.566+1629G>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226868947 | ||||||
| chr2:226869053
|
C | T | 58 | a0001c0001t0002g0006a0001c0001t0002g0178a0001c0001t0002g0179others(55): Show | 59 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(56): Show |
intron_variant | MODIFIER | c.566+1735C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226869053 | ||||||
| chr2:226869459
|
T | C | 76 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0002g0006others(73): Show | 77 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(74): Show |
intron_variant | MODIFIER | c.566+2141T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226869459 | ||||||
| chr2:226869516
|
G | A | 13 | a0001c0001t0002g0195a0001c0001t0002g0199a0001c0001t0002g0200others(10): Show | 13 | HG00673.hp2 HG02083.hp1 HG04184.hp2 others(10): Show |
intron_variant | MODIFIER | c.566+2198G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226869516 | ||||||
| chr2:226869717
|
C | T | 5 | a0001c0001t0001g0142a0001c0001t0001g0148a0001c0001t0001g0160others(2): Show | 5 | HG00609.hp2 HG02056.hp1 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.566+2399C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226869717 | ||||||
| chr2:226869936
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.566+2618C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226869936 | ||||||
| chr2:226869953
|
A | C | 1 | a0001c0001t0003g0243 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.566+2635A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226869953 | ||||||
| chr2:226870020
|
C | T | 1 | a0001c0001t0001g0147 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.566+2702C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226870020 | ||||||
| chr2:226870186
|
T | C | 58 | a0001c0001t0002g0006a0001c0001t0002g0178a0001c0001t0002g0179others(55): Show | 59 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(56): Show |
intron_variant | MODIFIER | c.566+2868T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226870186 | ||||||
| chr2:226870400
|
A | G | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG00558.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.566+3082A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226870400 | ||||||
| chr2:226870912
|
A | G | 1 | a0001c0001t0001g0027 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.566+3594A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226870912 | ||||||
| chr2:226871116
|
A | G | 6 | a0002c0006t0001g0176a0002c0006t0001g0177a0003c0003t0004g0172others(3): Show | 6 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.566+3798A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226871116 | ||||||
| chr2:226871205
|
A | T | 1 | a0001c0001t0003g0252 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.566+3887A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226871205 | ||||||
| chr2:226871250
|
ATTTATAA others(3829): Show |
A | 1 | a0001c0001t0001g0105 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.566+3936_566+7771d others(2): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 226871250 | |||||
| chr2:226871410
|
A | G | 10 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0004g0011others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.566+4092A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226871410 | ||||||
| chr2:226871430
|
T | C | 1 | a0001c0001t0001g0131 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.566+4112T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226871430 | ||||||
| chr2:226871457
|
C | T | 2 | a0001c0001t0002g0181a0001c0001t0002g0182 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.566+4139C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226871457 | ||||||
| chr2:226871539
|
T | C | 6 | a0002c0006t0001g0176a0002c0006t0001g0177a0003c0003t0004g0172others(3): Show | 6 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.566+4221T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226871539 | ||||||
| chr2:226871576
|
C | T | 58 | a0001c0001t0002g0006a0001c0001t0002g0178a0001c0001t0002g0179others(55): Show | 59 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(56): Show |
intron_variant | MODIFIER | c.566+4258C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226871576 | ||||||
| chr2:226871596
|
G | A | 74 | a0001c0001t0002g0006a0001c0001t0002g0178a0001c0001t0002g0179others(71): Show | 75 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(72): Show |
intron_variant | MODIFIER | c.566+4278G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226871596 | ||||||
| chr2:226871841
|
A | G | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | NA18972.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.566+4523A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226871841 | ||||||
| chr2:226871847
|
G | A | 58 | a0001c0001t0002g0006a0001c0001t0002g0178a0001c0001t0002g0179others(55): Show | 59 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(56): Show |
intron_variant | MODIFIER | c.566+4529G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226871847 | ||||||
| chr2:226871981
|
C | T | 6 | a0002c0006t0001g0176a0002c0006t0001g0177a0003c0003t0004g0172others(3): Show | 6 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.566+4663C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226871981 | ||||||
| chr2:226872220
|
G | C | 74 | a0001c0001t0002g0006a0001c0001t0002g0178a0001c0001t0002g0179others(71): Show | 75 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(72): Show |
intron_variant | MODIFIER | c.566+4902G>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226872220 | ||||||
| chr2:226872303
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.566+4985A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226872303 | ||||||
| chr2:226872374
|
A | G | 1 | a0001c0001t0001g0056 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.566+5056A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226872374 | ||||||
| chr2:226872414
|
A | G | 3 | a0001c0005t0005g0219a0001c0005t0005g0220a0001c0007t0010g0222 | 3 | HG02922.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.566+5096A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226872414 | ||||||
| chr2:226872633
|
A | G | 1 | a0001c0001t0001g0034 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.566+5315A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226872633 | ||||||
| chr2:226872694
|
A | C | 1 | a0002c0002t0004g0238 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.566+5376A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226872694 | ||||||
| chr2:226873124
|
G | A | 1 | a0002c0002t0006g0229 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.566+5806G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226873124 | ||||||
| chr2:226873144
|
T | C | 1 | a0001c0001t0001g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.566+5826T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226873144 | ||||||
| chr2:226873301
|
A | G | 10 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0004g0011others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.566+5983A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226873301 | ||||||
| chr2:226873782
|
A | C | 1 | a0002c0002t0004g0238 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.566+6464A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226873782 | ||||||
| chr2:226873794
|
G | A | 1 | a0001c0007t0010g0222 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.566+6476G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226873794 | ||||||
| chr2:226874157
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.566+6839A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226874157 | ||||||
| chr2:226874379
|
T | C | 6 | a0002c0006t0001g0176a0002c0006t0001g0177a0003c0003t0004g0172others(3): Show | 6 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.566+7061T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226874379 | ||||||
| chr2:226874584
|
T | C | 1 | a0001c0001t0019g0017 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.566+7266T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226874584 | ||||||
| chr2:226874682
|
A | G | 1 | a0001c0001t0001g0106 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.566+7364A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226874682 | ||||||
| chr2:226874749
|
C | A | 46 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(43): Show | 50 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.566+7431C>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226874749 | ||||||
| chr2:226875107
|
A | G | 100 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(97): Show | 105 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.566+7789A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226875107 | ||||||
| chr2:226875114
|
TCTTTAGG others(3814): Show |
T | 1 | a0001c0001t0001g0105 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.566+7799_566+11619 others(3): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 226875114 | |||||
| chr2:226875162
|
G | C | 1 | a0001c0001t0001g0078 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.566+7844G>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226875162 | ||||||
| chr2:226875296
|
C | T | 1 | a0001c0001t0001g0001 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.566+7978C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226875296 | ||||||
| chr2:226875406
|
G | A | 1 | a0001c0001t0002g0223 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.566+8088G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226875406 | ||||||
| chr2:226875495
|
A | G | 2 | a0001c0001t0002g0197a0001c0001t0012g0231 | 2 | HG03516.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.566+8177A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226875495 | ||||||
| chr2:226875538
|
C | G | 10 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0004g0011others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.566+8220C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226875538 | ||||||
| chr2:226875654
|
A | T | 16 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0004g0011others(13): Show | 16 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.566+8336A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226875654 | ||||||
| chr2:226875739
|
G | A | 1 | a0001c0001t0001g0240 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.566+8421G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226875739 | ||||||
| chr2:226875883
|
G | A | 5 | a0001c0001t0002g0179a0001c0001t0002g0180a0001c0001t0002g0181others(2): Show | 5 | HG01168.hp1 HG01169.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.566+8565G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226875883 | ||||||
| chr2:226875958
|
G | A | 2 | a0001c0001t0002g0181a0001c0001t0002g0182 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.566+8640G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226875958 | ||||||
| chr2:226876011
|
A | G | 2 | a0002c0002t0006g0229a0002c0002t0006g0230 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.566+8693A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226876011 | ||||||
| chr2:226876372
|
C | G | 1 | a0001c0001t0001g0088 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.566+9054C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226876372 | ||||||
| chr2:226876386
|
C | G | 1 | a0001c0001t0001g0022 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.566+9068C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226876386 | ||||||
| chr2:226876403
|
A | G | 1 | a0001c0001t0001g0022 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.566+9085A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226876403 | ||||||
| chr2:226876461
|
G | A | 17 | a0001c0001t0002g0223a0002c0002t0001g0013a0002c0002t0001g0014others(14): Show | 17 | HG01261.hp2 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.566+9143G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226876461 | ||||||
| chr2:226876703
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.566+9385G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226876703 | ||||||
| chr2:226876740
|
A | G | 6 | a0002c0006t0001g0176a0002c0006t0001g0177a0003c0003t0004g0172others(3): Show | 6 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.566+9422A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226876740 | ||||||
| chr2:226876812
|
CAT | C | 4 | a0003c0003t0004g0172a0003c0003t0004g0173a0003c0003t0004g0174others(1): Show | 4 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.566+9496_566+9497d others(4): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 226876812 | |||||
| chr2:226876881
|
A | G | 55 | a0001c0001t0001g0162a0001c0001t0002g0006a0001c0001t0002g0178others(52): Show | 56 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(53): Show |
intron_variant | MODIFIER | c.566+9563A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226876881 | ||||||
| chr2:226876970
|
C | G | 1 | a0001c0001t0001g0130 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.566+9652C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226876970 | ||||||
| chr2:226877042
|
T | C | 7 | a0001c0001t0002g0185a0001c0001t0002g0186a0001c0001t0002g0187others(4): Show | 7 | HG01123.hp1 HG02004.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.566+9724T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226877042 | ||||||
| chr2:226877183
|
C | G | 6 | a0002c0006t0001g0176a0002c0006t0001g0177a0003c0003t0004g0172others(3): Show | 6 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.566+9865C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226877183 | ||||||
| chr2:226877421
|
G | A | 1 | a0001c0001t0003g0061 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.566+10103G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226877421 | ||||||
| chr2:226877550
|
C | CT | 15 | a0001c0001t0001g0033a0001c0001t0001g0055a0001c0001t0001g0058others(12): Show | 16 | HG00621.hp1 HG00621.hp2 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.566+10252dupT | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 226877550 | |||||
| chr2:226877550
|
CT | C | 23 | a0001c0001t0001g0039a0001c0001t0001g0097a0001c0001t0002g0180others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG01515.hp2 others(20): Show |
intron_variant | MODIFIER | c.566+10252delT | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 226877550 | |||||
| chr2:226877750
|
C | T | 1 | a0001c0001t0002g0006 | 2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.566+10432C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226877750 | ||||||
| chr2:226877976
|
TA | T | 16 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0004g0011others(13): Show | 16 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.566+10666delA | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 226877976 | |||||
| chr2:226877977
|
A | T | 1 | a0001c0001t0001g0103 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.566+10659A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226877977 | ||||||
| chr2:226877992
|
T | A | 16 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0004g0011others(13): Show | 16 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.566+10674T>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226877992 | ||||||
| chr2:226878187
|
G | A | 2 | a0002c0002t0006g0229a0002c0002t0006g0230 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.566+10869G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226878187 | ||||||
| chr2:226878232
|
A | G | 75 | a0001c0001t0001g0162a0001c0001t0002g0006a0001c0001t0002g0178others(72): Show | 76 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(73): Show |
intron_variant | MODIFIER | c.566+10914A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226878232 | ||||||
| chr2:226878352
|
T | G | 1 | a0002c0002t0004g0016 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.566+11034T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226878352 | ||||||
| chr2:226878380
|
T | G | 10 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0004g0011others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.566+11062T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226878380 | ||||||
| chr2:226878392
|
A | G | 1 | a0001c0001t0001g0028 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.566+11074A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226878392 | ||||||
| chr2:226878402
|
G | A | 4 | a0001c0001t0005g0221a0001c0005t0005g0219a0001c0005t0005g0220others(1): Show | 4 | HG02922.hp2 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.566+11084G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226878402 | ||||||
| chr2:226878449
|
G | A | 1 | a0001c0001t0003g0249 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.566+11131G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226878449 | ||||||
| chr2:226878564
|
G | A | 4 | a0003c0003t0004g0172a0003c0003t0004g0173a0003c0003t0004g0174others(1): Show | 4 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.566+11246G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226878564 | ||||||
| chr2:226878881
|
C | T | 1 | a0001c0001t0007g0069 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.566+11563C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226878881 | ||||||
| chr2:226878973
|
C | T | 2 | a0002c0002t0004g0237a0002c0002t0004g0238 | 2 | HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.566+11655C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226878973 | ||||||
| chr2:226879038
|
G | A | 1 | a0001c0001t0001g0132 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.566+11720G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226879038 | ||||||
| chr2:226879072
|
C | CA | 67 | a0001c0001t0001g0032a0001c0001t0001g0089a0001c0001t0001g0109others(64): Show | 68 | HG00140.hp1 HG00544.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.566+11772dupA | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 226879072 | |||||
| chr2:226879072
|
CAA | C | 9 | a0001c0001t0001g0018a0002c0002t0001g0013a0002c0002t0001g0014others(6): Show | 9 | HG00735.hp1 HG02145.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.566+11771_566+1177 others(6): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 226879072 | |||||
| chr2:226879146
|
C | T | 1 | a0001c0001t0016g0066 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.566+11828C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226879146 | ||||||
| chr2:226879258
|
C | T | 8 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0004g0011others(5): Show | 8 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.566+11940C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226879258 | ||||||
| chr2:226879320
|
G | A | 1 | a0001c0001t0015g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.566+12002G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226879320 | ||||||
| chr2:226879420
|
C | A | 10 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0004g0011others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.566+12102C>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226879420 | ||||||
| chr2:226879906
|
G | T | 6 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0004g0011others(3): Show | 6 | HG02145.hp1 HG02258.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.566+12588G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226879906 | ||||||
| chr2:226880343
|
C | T | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.566+13025C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226880343 | ||||||
| chr2:226880511
|
G | A | 9 | a0001c0001t0003g0043a0001c0001t0003g0061a0001c0001t0003g0243others(6): Show | 9 | HG00140.hp2 HG00735.hp2 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.566+13193G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226880511 | ||||||
| chr2:226880581
|
C | G | 117 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(114): Show | 122 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.566+13263C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226880581 | ||||||
| chr2:226880887
|
C | T | 6 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0004g0011others(3): Show | 6 | HG02145.hp1 HG02258.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.566+13569C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226880887 | ||||||
| chr2:226880934
|
A | C | 3 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG00099.hp1 HG01099.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.566+13616A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226880934 | ||||||
| chr2:226881300
|
C | T | 58 | a0001c0001t0001g0162a0001c0001t0002g0006a0001c0001t0002g0178others(55): Show | 59 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(56): Show |
intron_variant | MODIFIER | c.566+13982C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226881300 | ||||||
| chr2:226881488
|
A | G | 1 | a0001c0001t0002g0207 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.566+14170A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226881488 | ||||||
| chr2:226881633
|
TC | T | 58 | a0001c0001t0001g0162a0001c0001t0002g0006a0001c0001t0002g0178others(55): Show | 59 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(56): Show |
intron_variant | MODIFIER | c.566+14316delC | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226881633 | ||||||
| chr2:226881811
|
C | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.566+14493C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226881811 | ||||||
| chr2:226882038
|
A | G | 3 | a0001c0001t0001g0146a0001c0001t0001g0157a0001c0001t0001g0165 | 3 | NA18994.hp2 NA18995.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.566+14720A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226882038 | ||||||
| chr2:226882227
|
C | T | 6 | a0002c0006t0001g0176a0002c0006t0001g0177a0003c0003t0004g0172others(3): Show | 6 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.566+14909C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226882227 | ||||||
| chr2:226882250
|
T | G | 1 | a0001c0001t0001g0164 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.566+14932T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226882250 | ||||||
| chr2:226882281
|
C | T | 58 | a0001c0001t0001g0162a0001c0001t0002g0006a0001c0001t0002g0178others(55): Show | 59 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(56): Show |
intron_variant | MODIFIER | c.566+14963C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226882281 | ||||||
| chr2:226882304
|
C | T | 18 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(15): Show | 18 | HG01255.hp1 HG02109.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.566+14986C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226882304 | ||||||
| chr2:226882430
|
C | CA | 13 | a0001c0001t0001g0023a0001c0001t0001g0098a0001c0001t0001g0109others(10): Show | 13 | HG00597.hp1 HG00609.hp2 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.566+15136dupA | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 226882430 | |||||
| chr2:226882430
|
C | CAA | 36 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(33): Show | 40 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(37): Show |
intron_variant | MODIFIER | c.566+15135_566+1513 others(6): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 226882430 | |||||
| chr2:226882430
|
CA | C | 11 | a0001c0001t0001g0042a0001c0001t0001g0058a0001c0001t0001g0059others(8): Show | 11 | HG01169.hp1 HG01975.hp1 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.566+15136delA | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 226882430 | |||||
| chr2:226882430
|
CAA | C | 5 | a0001c0001t0002g0184a0001c0001t0002g0186a0001c0001t0002g0190others(2): Show | 5 | HG02258.hp2 NA18946.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.566+15135_566+1513 others(6): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 226882430 | |||||
| chr2:226882430
|
CAAA | C | 49 | a0001c0001t0001g0162a0001c0001t0002g0006a0001c0001t0002g0178others(46): Show | 50 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(47): Show |
intron_variant | MODIFIER | c.566+15134_566+1513 others(7): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 226882430 | |||||
| chr2:226882452
|
AAAG | A | 9 | a0001c0001t0015g0072a0001c0001t0019g0017a0002c0002t0001g0013others(6): Show | 9 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.566+15152_566+1515 others(7): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 226882452 | |||||
| chr2:226882453
|
AAGAAG | A | 6 | a0002c0006t0001g0176a0002c0006t0001g0177a0003c0003t0004g0172others(3): Show | 6 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.566+15137_566+1514 others(9): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 226882453 | |||||
| chr2:226882495
|
T | G | 6 | a0002c0006t0001g0176a0002c0006t0001g0177a0003c0003t0004g0172others(3): Show | 6 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.566+15177T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226882495 | ||||||
| chr2:226882537
|
A | T | 1 | a0001c0001t0001g0165 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.566+15219A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226882537 | ||||||
| chr2:226882665
|
A | G | 3 | a0001c0005t0005g0219a0001c0005t0005g0220a0001c0007t0010g0222 | 3 | HG02922.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.566+15347A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226882665 | ||||||
| chr2:226882993
|
A | G | 6 | a0002c0006t0001g0176a0002c0006t0001g0177a0003c0003t0004g0172others(3): Show | 6 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.566+15675A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226882993 | ||||||
| chr2:226883237
|
A | G | 1 | a0001c0001t0003g0007 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.566+15919A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226883237 | ||||||
| chr2:226883473
|
G | A | 2 | a0001c0004t0002g0201a0001c0004t0002g0203 | 2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.566+16155G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226883473 | ||||||
| chr2:226883607
|
G | A | 6 | a0002c0006t0001g0176a0002c0006t0001g0177a0003c0003t0004g0172others(3): Show | 6 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.566+16289G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226883607 | ||||||
| chr2:226883627
|
A | T | 1 | a0001c0001t0001g0078 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.566+16309A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226883627 | ||||||
| chr2:226883713
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.566+16395A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226883713 | ||||||
| chr2:226883828
|
A | G | 1 | a0001c0001t0003g0257 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.566+16510A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226883828 | ||||||
| chr2:226883976
|
A | C | 1 | a0001c0001t0019g0017 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.566+16658A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226883976 | ||||||
| chr2:226884259
|
G | A | 1 | a0001c0001t0003g0045 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.566+16941G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226884259 | ||||||
| chr2:226884349
|
A | G | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.566+17031A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226884349 | ||||||
| chr2:226884442
|
T | A | 3 | a0001c0005t0005g0219a0001c0005t0005g0220a0001c0007t0010g0222 | 3 | HG02922.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.566+17124T>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226884442 | ||||||
| chr2:226884442
|
T | G | 6 | a0002c0006t0001g0176a0002c0006t0001g0177a0003c0003t0004g0172others(3): Show | 6 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.566+17124T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226884442 | ||||||
| chr2:226884492
|
C | T | 3 | a0001c0001t0001g0044a0001c0001t0001g0065a0001c0001t0001g0067 | 3 | HG02647.hp2 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.566+17174C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226884492 | ||||||
| chr2:226884746
|
C | A | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.566+17428C>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226884746 | ||||||
| chr2:226885247
|
A | G | 2 | a0001c0001t0001g0063a0001c0001t0001g0064 | 2 | HG01255.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.566+17929A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226885247 | ||||||
| chr2:226885387
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.566+18069A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226885387 | ||||||
| chr2:226885428
|
G | T | 1 | a0001c0001t0002g0193 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.566+18110G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226885428 | ||||||
| chr2:226886022
|
G | T | 55 | a0001c0001t0001g0162a0001c0001t0002g0006a0001c0001t0002g0178others(52): Show | 56 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(53): Show |
intron_variant | MODIFIER | c.566+18704G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226886022 | ||||||
| chr2:226886054
|
C | G | 55 | a0001c0001t0001g0162a0001c0001t0002g0006a0001c0001t0002g0178others(52): Show | 56 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(53): Show |
intron_variant | MODIFIER | c.566+18736C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226886054 | ||||||
| chr2:226886130
|
C | G | 55 | a0001c0001t0001g0162a0001c0001t0002g0006a0001c0001t0002g0178others(52): Show | 56 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(53): Show |
intron_variant | MODIFIER | c.566+18812C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226886130 | ||||||
| chr2:226886282
|
G | A | 1 | a0001c0001t0007g0057 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.566+18964G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226886282 | ||||||
| chr2:226886333
|
A | G | 75 | a0001c0001t0001g0162a0001c0001t0002g0006a0001c0001t0002g0178others(72): Show | 76 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(73): Show |
intron_variant | MODIFIER | c.566+19015A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226886333 | ||||||
| chr2:226886425
|
G | T | 58 | a0001c0001t0001g0162a0001c0001t0002g0006a0001c0001t0002g0178others(55): Show | 59 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(56): Show |
intron_variant | MODIFIER | c.566+19107G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226886425 | ||||||
| chr2:226886498
|
A | C | 55 | a0001c0001t0001g0162a0001c0001t0002g0006a0001c0001t0002g0178others(52): Show | 56 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(53): Show |
intron_variant | MODIFIER | c.566+19180A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226886498 | ||||||
| chr2:226886548
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.566+19230G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226886548 | ||||||
| chr2:226886852
|
A | T | 2 | a0001c0001t0001g0095a0001c0001t0001g0118 | 2 | NA18990.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.566+19534A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226886852 | ||||||
| chr2:226887039
|
GA | G | 3 | a0001c0001t0001g0087a0001c0001t0001g0119a0001c0001t0017g0107 | 3 | HG02083.hp2 NA18994.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.566+19727delA | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 226887039 | |||||
| chr2:226887086
|
C | T | 78 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0162others(75): Show | 79 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(76): Show |
intron_variant | MODIFIER | c.567-19707C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226887086 | ||||||
| chr2:226887146
|
G | A | 6 | a0002c0006t0001g0176a0002c0006t0001g0177a0003c0003t0004g0172others(3): Show | 6 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.567-19647G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226887146 | ||||||
| chr2:226887496
|
T | G | 1 | a0001c0001t0001g0048 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.567-19297T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226887496 | ||||||
| chr2:226887784
|
A | G | 58 | a0001c0001t0001g0162a0001c0001t0002g0006a0001c0001t0002g0178others(55): Show | 59 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(56): Show |
intron_variant | MODIFIER | c.567-19009A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226887784 | ||||||
| chr2:226888070
|
C | T | 1 | a0001c0001t0001g0001 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.567-18723C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226888070 | ||||||
| chr2:226888196
|
T | A | 13 | a0001c0001t0002g0195a0001c0001t0002g0199a0001c0001t0002g0200others(10): Show | 13 | HG00673.hp2 HG02083.hp1 HG04184.hp2 others(10): Show |
intron_variant | MODIFIER | c.567-18597T>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226888196 | ||||||
| chr2:226888285
|
A | G | 4 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(1): Show | 4 | HG00140.hp1 HG01255.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.567-18508A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226888285 | ||||||
| chr2:226888411
|
GT | G | 73 | a0001c0001t0001g0039a0001c0001t0001g0162a0001c0001t0002g0006others(70): Show | 74 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(71): Show |
intron_variant | MODIFIER | c.567-18371delT | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 226888411 | |||||
| chr2:226888441
|
A | T | 2 | a0001c0001t0002g0224a0001c0001t0002g0225 | 2 | HG00673.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.567-18352A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226888441 | ||||||
| chr2:226888477
|
T | C | 6 | a0002c0006t0001g0176a0002c0006t0001g0177a0003c0003t0004g0172others(3): Show | 6 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.567-18316T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226888477 | ||||||
| chr2:226888614
|
T | G | 1 | a0001c0001t0001g0049 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.567-18179T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226888614 | ||||||
| chr2:226888704
|
G | T | 1 | a0001c0001t0009g0140 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.567-18089G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226888704 | ||||||
| chr2:226888807
|
T | C | 3 | a0001c0005t0005g0219a0001c0005t0005g0220a0001c0007t0010g0222 | 3 | HG02922.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.567-17986T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226888807 | ||||||
| chr2:226889293
|
C | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.567-17500C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226889293 | ||||||
| chr2:226889472
|
A | C | 2 | a0002c0002t0006g0229a0002c0002t0006g0230 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.567-17321A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226889472 | ||||||
| chr2:226889595
|
T | C | 9 | a0001c0001t0005g0221a0002c0002t0001g0013a0002c0002t0001g0014others(6): Show | 9 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.567-17198T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226889595 | ||||||
| chr2:226889638
|
T | C | 55 | a0001c0001t0001g0162a0001c0001t0002g0006a0001c0001t0002g0178others(52): Show | 56 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(53): Show |
intron_variant | MODIFIER | c.567-17155T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226889638 | ||||||
| chr2:226889871
|
T | G | 1 | a0002c0002t0004g0237 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.567-16922T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226889871 | ||||||
| chr2:226890219
|
G | A | 2 | a0002c0002t0006g0229a0002c0002t0006g0230 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.567-16574G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226890219 | ||||||
| chr2:226890297
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.567-16496G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226890297 | ||||||
| chr2:226890393
|
C | T | 14 | a0001c0001t0002g0195a0001c0001t0002g0196a0001c0001t0002g0199others(11): Show | 14 | HG00673.hp2 HG02083.hp1 HG02896.hp1 others(11): Show |
intron_variant | MODIFIER | c.567-16400C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226890393 | ||||||
| chr2:226890618
|
G | T | 1 | a0001c0001t0003g0252 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.567-16175G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226890618 | ||||||
| chr2:226890832
|
T | A | 6 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0004g0011others(3): Show | 6 | HG02145.hp1 HG02258.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.567-15961T>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226890832 | ||||||
| chr2:226890944
|
T | G | 64 | a0001c0001t0001g0162a0001c0001t0002g0006a0001c0001t0002g0178others(61): Show | 65 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(62): Show |
intron_variant | MODIFIER | c.567-15849T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226890944 | ||||||
| chr2:226890989
|
C | T | 1 | a0001c0001t0002g0207 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.567-15804C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226890989 | ||||||
| chr2:226891199
|
A | T | 3 | a0001c0005t0005g0219a0001c0005t0005g0220a0001c0007t0010g0222 | 3 | HG02922.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.567-15594A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226891199 | ||||||
| chr2:226891487
|
T | C | 2 | a0002c0002t0006g0229a0002c0002t0006g0230 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.567-15306T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226891487 | ||||||
| chr2:226891559
|
G | A | 6 | a0002c0006t0001g0176a0002c0006t0001g0177a0003c0003t0004g0172others(3): Show | 6 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.567-15234G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226891559 | ||||||
| chr2:226891875
|
C | G | 1 | a0001c0001t0001g0025 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.567-14918C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226891875 | ||||||
| chr2:226891889
|
C | G | 1 | a0001c0001t0001g0046 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.567-14904C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226891889 | ||||||
| chr2:226891960
|
A | G | 67 | a0001c0001t0001g0162a0001c0001t0002g0006a0001c0001t0002g0178others(64): Show | 68 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(65): Show |
intron_variant | MODIFIER | c.567-14833A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226891960 | ||||||
| chr2:226892120
|
A | G | 6 | a0002c0006t0001g0176a0002c0006t0001g0177a0003c0003t0004g0172others(3): Show | 6 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.567-14673A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226892120 | ||||||
| chr2:226892427
|
AT | A | 58 | a0001c0001t0001g0162a0001c0001t0002g0006a0001c0001t0002g0178others(55): Show | 59 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(56): Show |
intron_variant | MODIFIER | c.567-14365delT | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226892427 | ||||||
| chr2:226892485
|
G | A | 2 | a0002c0006t0001g0176a0002c0006t0001g0177 | 2 | HG03654.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.567-14308G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226892485 | ||||||
| chr2:226892617
|
A | G | 58 | a0001c0001t0001g0162a0001c0001t0002g0006a0001c0001t0002g0178others(55): Show | 59 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(56): Show |
intron_variant | MODIFIER | c.567-14176A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226892617 | ||||||
| chr2:226892689
|
G | T | 6 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0004g0011others(3): Show | 6 | HG02145.hp1 HG02258.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.567-14104G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226892689 | ||||||
| chr2:226892692
|
T | C | 3 | a0001c0005t0005g0219a0001c0005t0005g0220a0001c0007t0010g0222 | 3 | HG02922.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.567-14101T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226892692 | ||||||
| chr2:226892776
|
C | A | 124 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(121): Show | 129 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.567-14017C>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226892776 | ||||||
| chr2:226892793
|
G | A | 1 | a0001c0001t0019g0017 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.567-14000G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226892793 | ||||||
| chr2:226892818
|
A | G | 1 | a0001c0001t0013g0198 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.567-13975A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226892818 | ||||||
| chr2:226892876
|
A | G | 6 | a0002c0006t0001g0176a0002c0006t0001g0177a0003c0003t0004g0172others(3): Show | 6 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.567-13917A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226892876 | ||||||
| chr2:226893166
|
C | T | 1 | a0001c0001t0003g0245 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.567-13627C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226893166 | ||||||
| chr2:226893421
|
T | C | 58 | a0001c0001t0001g0162a0001c0001t0002g0006a0001c0001t0002g0178others(55): Show | 59 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(56): Show |
intron_variant | MODIFIER | c.567-13372T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226893421 | ||||||
| chr2:226893678
|
C | T | 1 | a0001c0001t0002g0223 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.567-13115C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226893678 | ||||||
| chr2:226893871
|
C | T | 1 | a0001c0001t0002g0200 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.567-12922C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226893871 | ||||||
| chr2:226893958
|
T | G | 1 | a0001c0001t0001g0099 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.567-12835T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226893958 | ||||||
| chr2:226893963
|
G | T | 1 | a0001c0001t0001g0099 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.567-12830G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226893963 | ||||||
| chr2:226894296
|
G | A | 3 | a0001c0001t0005g0221a0002c0002t0004g0237a0002c0002t0004g0238 | 3 | HG02145.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.567-12497G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226894296 | ||||||
| chr2:226894313
|
G | A | 77 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0162others(74): Show | 78 | HG00673.hp2 HG01106.hp1 HG01123.hp1 others(75): Show |
intron_variant | MODIFIER | c.567-12480G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226894313 | ||||||
| chr2:226894372
|
T | C | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.567-12421T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226894372 | ||||||
| chr2:226894457
|
G | A | 6 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0004g0011others(3): Show | 6 | HG02145.hp1 HG02258.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.567-12336G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226894457 | ||||||
| chr2:226894481
|
G | A | 3 | a0001c0001t0005g0221a0002c0002t0004g0237a0002c0002t0004g0238 | 3 | HG02145.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.567-12312G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226894481 | ||||||
| chr2:226894739
|
A | C | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(96): Show | 104 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.567-12054A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226894739 | ||||||
| chr2:226894762
|
G | A | 3 | a0001c0005t0005g0219a0001c0005t0005g0220a0001c0007t0010g0222 | 3 | HG02922.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.567-12031G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226894762 | ||||||
| chr2:226895004
|
G | C | 91 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0027others(88): Show | 92 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(89): Show |
intron_variant | MODIFIER | c.567-11789G>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226895004 | ||||||
| chr2:226895174
|
C | T | 18 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(15): Show | 18 | HG01255.hp1 HG02109.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.567-11619C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226895174 | ||||||
| chr2:226895176
|
C | T | 103 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0027others(100): Show | 104 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(101): Show |
intron_variant | MODIFIER | c.567-11617C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226895176 | ||||||
| chr2:226895318
|
C | T | 90 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0027others(87): Show | 91 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(88): Show |
intron_variant | MODIFIER | c.567-11475C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226895318 | ||||||
| chr2:226895326
|
A | G | 1 | a0001c0001t0001g0248 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.567-11467A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226895326 | ||||||
| chr2:226895440
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.567-11353G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226895440 | ||||||
| chr2:226895441
|
A | G | 1 | a0001c0001t0001g0099 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.567-11352A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226895441 | ||||||
| chr2:226895805
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.567-10988C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226895805 | ||||||
| chr2:226896540
|
G | A | 115 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(112): Show | 116 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(113): Show |
intron_variant | MODIFIER | c.567-10253G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226896540 | ||||||
| chr2:226896553
|
T | C | 115 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(112): Show | 116 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(113): Show |
intron_variant | MODIFIER | c.567-10240T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226896553 | ||||||
| chr2:226896729
|
A | C | 95 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(92): Show | 96 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(93): Show |
intron_variant | MODIFIER | c.567-10064A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226896729 | ||||||
| chr2:226896761
|
G | A | 95 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(92): Show | 96 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(93): Show |
intron_variant | MODIFIER | c.567-10032G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226896761 | ||||||
| chr2:226896770
|
C | T | 1 | a0001c0001t0003g0241 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.567-10023C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226896770 | ||||||
| chr2:226896775
|
GC | G | 13 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0027others(10): Show | 13 | HG00099.hp1 HG00735.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.567-10015delC | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 226896775 | |||||
| chr2:226896840
|
T | C | 1 | a0001c0001t0002g0006 | 2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.567-9953T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226896840 | ||||||
| chr2:226896866
|
C | A | 113 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(110): Show | 114 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(111): Show |
intron_variant | MODIFIER | c.567-9927C>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226896866 | ||||||
| chr2:226896949
|
C | T | 10 | a0001c0001t0005g0221a0001c0001t0012g0231a0002c0002t0001g0013others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.567-9844C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226896949 | ||||||
| chr2:226896990
|
A | T | 1 | a0001c0001t0001g0090 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.567-9803A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226896990 | ||||||
| chr2:226897277
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.567-9516G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226897277 | ||||||
| chr2:226897308
|
G | GTGTC | 4 | a0001c0001t0001g0065a0001c0001t0001g0081a0001c0001t0001g0152others(1): Show | 4 | HG00597.hp1 HG02976.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.567-9456_567-9453d others(6): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 226897308 | |||||
| chr2:226897308
|
GTGTC | G | 97 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(94): Show | 98 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(95): Show |
intron_variant | MODIFIER | c.567-9456_567-9453d others(6): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 226897308 | |||||
| chr2:226897308
|
GTGTCTGT others(1): Show |
G | 13 | a0001c0001t0001g0047a0001c0001t0001g0110a0001c0001t0001g0236others(10): Show | 13 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.567-9460_567-9453d others(10): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 226897308 | |||||
| chr2:226897312
|
C | G | 1 | a0001c0001t0001g0161 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.567-9481C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226897312 | ||||||
| chr2:226897316
|
C | G | 5 | a0001c0001t0001g0019a0001c0001t0001g0035a0001c0001t0001g0036others(2): Show | 5 | HG01934.hp1 HG01975.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.567-9477C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226897316 | ||||||
| chr2:226897442
|
A | G | 1 | a0001c0001t0001g0020 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.567-9351A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226897442 | ||||||
| chr2:226897742
|
C | T | 3 | a0001c0001t0001g0044a0001c0001t0001g0065a0001c0001t0001g0067 | 3 | HG02647.hp2 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.567-9051C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226897742 | ||||||
| chr2:226897988
|
A | AAAC | 19 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(16): Show | 19 | HG01255.hp1 HG02109.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.567-8787_567-8785d others(5): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 226897988 | |||||
| chr2:226897993
|
AC | A | 6 | a0002c0006t0001g0176a0002c0006t0001g0177a0003c0003t0004g0172others(3): Show | 6 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.567-8799delC | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226897993 | ||||||
| chr2:226898099
|
G | C | 95 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(92): Show | 96 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(93): Show |
intron_variant | MODIFIER | c.567-8694G>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226898099 | ||||||
| chr2:226898226
|
C | A | 18 | a0001c0001t0005g0221a0001c0001t0012g0231a0002c0002t0001g0013others(15): Show | 18 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.567-8567C>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226898226 | ||||||
| chr2:226898350
|
C | G | 1 | a0001c0001t0001g0130 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.567-8443C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226898350 | ||||||
| chr2:226898408
|
C | T | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.567-8385C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226898408 | ||||||
| chr2:226898528
|
T | G | 92 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(89): Show | 93 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(90): Show |
intron_variant | MODIFIER | c.567-8265T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226898528 | ||||||
| chr2:226899049
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.567-7744C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226899049 | ||||||
| chr2:226899161
|
A | G | 1 | a0001c0001t0001g0109 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.567-7632A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226899161 | ||||||
| chr2:226899167
|
C | G | 2 | a0002c0002t0006g0229a0002c0002t0006g0230 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.567-7626C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226899167 | ||||||
| chr2:226899167
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.567-7626C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226899167 | ||||||
| chr2:226899277
|
C | A | 95 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(92): Show | 96 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(93): Show |
intron_variant | MODIFIER | c.567-7516C>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226899277 | ||||||
| chr2:226899341
|
A | G | 96 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(93): Show | 97 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(94): Show |
intron_variant | MODIFIER | c.567-7452A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226899341 | ||||||
| chr2:226899481
|
A | G | 6 | a0002c0006t0001g0176a0002c0006t0001g0177a0003c0003t0004g0172others(3): Show | 6 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.567-7312A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226899481 | ||||||
| chr2:226899512
|
G | T | 1 | a0001c0001t0001g0073 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.567-7281G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226899512 | ||||||
| chr2:226899983
|
A | G | 6 | a0002c0006t0001g0176a0002c0006t0001g0177a0003c0003t0004g0172others(3): Show | 6 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.567-6810A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226899983 | ||||||
| chr2:226900047
|
C | G | 1 | a0001c0005t0005g0220 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.567-6746C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226900047 | ||||||
| chr2:226900156
|
A | G | 93 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(90): Show | 94 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(91): Show |
intron_variant | MODIFIER | c.567-6637A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226900156 | ||||||
| chr2:226900233
|
G | T | 1 | a0001c0001t0003g0252 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.567-6560G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226900233 | ||||||
| chr2:226900238
|
T | G | 96 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(93): Show | 97 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(94): Show |
intron_variant | MODIFIER | c.567-6555T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226900238 | ||||||
| chr2:226900477
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.567-6316G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226900477 | ||||||
| chr2:226900493
|
G | A | 1 | a0001c0004t0002g0202 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.567-6300G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226900493 | ||||||
| chr2:226900534
|
C | A | 1 | a0001c0001t0019g0017 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.567-6259C>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226900534 | ||||||
| chr2:226900534
|
C | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.567-6259C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226900534 | ||||||
| chr2:226900772
|
G | A | 96 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(93): Show | 97 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(94): Show |
intron_variant | MODIFIER | c.567-6021G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226900772 | ||||||
| chr2:226900985
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.567-5808C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226900985 | ||||||
| chr2:226901175
|
C | T | 96 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(93): Show | 97 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(94): Show |
intron_variant | MODIFIER | c.567-5618C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226901175 | ||||||
| chr2:226901325
|
A | G | 6 | a0002c0006t0001g0176a0002c0006t0001g0177a0003c0003t0004g0172others(3): Show | 6 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.567-5468A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226901325 | ||||||
| chr2:226901391
|
A | T | 1 | a0001c0001t0001g0164 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.567-5402A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226901391 | ||||||
| chr2:226901396
|
T | C | 96 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(93): Show | 97 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(94): Show |
intron_variant | MODIFIER | c.567-5397T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226901396 | ||||||
| chr2:226901563
|
A | G | 1 | a0001c0001t0002g0216 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.567-5230A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226901563 | ||||||
| chr2:226901623
|
G | A | 95 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(92): Show | 96 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(93): Show |
intron_variant | MODIFIER | c.567-5170G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226901623 | ||||||
| chr2:226901733
|
T | C | 1 | a0001c0001t0001g0154 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.567-5060T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226901733 | ||||||
| chr2:226901742
|
T | C | 1 | a0002c0002t0004g0237 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.567-5051T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226901742 | ||||||
| chr2:226901789
|
A | G | 2 | a0001c0001t0001g0083a0001c0001t0001g0117 | 2 | HG00558.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.567-5004A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226901789 | ||||||
| chr2:226901930
|
C | T | 1 | a0001c0001t0003g0245 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.567-4863C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226901930 | ||||||
| chr2:226901947
|
C | T | 2 | a0002c0002t0006g0229a0002c0002t0006g0230 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.567-4846C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226901947 | ||||||
| chr2:226901997
|
A | G | 1 | a0001c0001t0001g0117 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.567-4796A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226901997 | ||||||
| chr2:226902106
|
C | G | 95 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(92): Show | 96 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(93): Show |
intron_variant | MODIFIER | c.567-4687C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226902106 | ||||||
| chr2:226902386
|
G | A | 5 | a0001c0001t0001g0019a0001c0001t0001g0035a0001c0001t0001g0036others(2): Show | 5 | HG01934.hp1 HG01975.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.567-4407G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226902386 | ||||||
| chr2:226902877
|
G | C | 95 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(92): Show | 96 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(93): Show |
intron_variant | MODIFIER | c.567-3916G>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226902877 | ||||||
| chr2:226903386
|
C | T | 1 | a0001c0007t0010g0222 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.567-3407C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226903386 | ||||||
| chr2:226903646
|
C | T | 94 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(91): Show | 95 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(92): Show |
intron_variant | MODIFIER | c.567-3147C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226903646 | ||||||
| chr2:226903771
|
A | G | 1 | a0001c0001t0001g0099 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.567-3022A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226903771 | ||||||
| chr2:226904042
|
A | G | 1 | a0001c0001t0013g0198 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.567-2751A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226904042 | ||||||
| chr2:226904152
|
G | A | 112 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(109): Show | 113 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(110): Show |
intron_variant | MODIFIER | c.567-2641G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226904152 | ||||||
| chr2:226904274
|
C | T | 2 | a0001c0001t0001g0095a0001c0001t0001g0118 | 2 | NA18990.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.567-2519C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226904274 | ||||||
| chr2:226904284
|
A | G | 102 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(99): Show | 103 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(100): Show |
intron_variant | MODIFIER | c.567-2509A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226904284 | ||||||
| chr2:226904369
|
G | A | 2 | a0002c0002t0006g0229a0002c0002t0006g0230 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.567-2424G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226904369 | ||||||
| chr2:226904393
|
C | A | 10 | a0001c0001t0005g0221a0001c0001t0012g0231a0002c0002t0001g0013others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.567-2400C>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226904393 | ||||||
| chr2:226904407
|
C | G | 109 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0018others(106): Show | 112 | HG00099.hp1 HG00609.hp2 HG00621.hp2 others(109): Show |
intron_variant | MODIFIER | c.567-2386C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226904407 | ||||||
| chr2:226904416
|
G | T | 3 | a0001c0001t0001g0083a0001c0001t0001g0094a0001c0001t0001g0117 | 3 | HG00558.hp2 HG00609.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.567-2377G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226904416 | ||||||
| chr2:226904418
|
G | GC | 4 | a0001c0001t0001g0050a0001c0001t0001g0084a0001c0001t0001g0104others(1): Show | 4 | HG00621.hp2 HG02135.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.567-2375_567-2374i others(3): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226904418 | ||||||
| chr2:226904423
|
A | G | 110 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0018others(107): Show | 113 | HG00099.hp1 HG00609.hp2 HG00621.hp2 others(110): Show |
intron_variant | MODIFIER | c.567-2370A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226904423 | ||||||
| chr2:226904427
|
G | C | 10 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0084others(7): Show | 10 | HG00621.hp2 HG01993.hp2 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.567-2366G>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226904427 | ||||||
| chr2:226904427
|
G | GC | 32 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0029others(29): Show | 33 | HG00099.hp1 HG00673.hp2 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.567-2366_567-2365i others(3): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226904427 | ||||||
| chr2:226904427
|
G | GGC | 55 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0021others(52): Show | 56 | HG00609.hp2 HG00673.hp1 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.567-2365_567-2364i others(4): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 226904427 | |||||
| chr2:226904427
|
G | GGGC | 9 | a0001c0001t0001g0049a0001c0001t0001g0056a0001c0001t0001g0074others(6): Show | 10 | HG01071.hp1 HG02897.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.567-2364_567-2363i others(5): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 226904427 | |||||
| chr2:226904512
|
G | A | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG02886.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.567-2281G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226904512 | ||||||
| chr2:226904535
|
C | A | 1 | a0001c0001t0002g0217 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.567-2258C>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226904535 | ||||||
| chr2:226904560
|
C | T | 3 | a0001c0001t0005g0221a0002c0002t0004g0237a0002c0002t0004g0238 | 3 | HG02145.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.567-2233C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226904560 | ||||||
| chr2:226904600
|
A | G | 1 | a0001c0001t0002g0223 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.567-2193A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226904600 | ||||||
| chr2:226904777
|
A | C | 112 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(109): Show | 113 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(110): Show |
intron_variant | MODIFIER | c.567-2016A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226904777 | ||||||
| chr2:226904783
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.567-2010C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226904783 | ||||||
| chr2:226904794
|
G | T | 1 | a0001c0001t0001g0153 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.567-1999G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226904794 | ||||||
| chr2:226904891
|
A | C | 94 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(91): Show | 95 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(92): Show |
intron_variant | MODIFIER | c.567-1902A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226904891 | ||||||
| chr2:226904924
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.567-1869C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226904924 | ||||||
| chr2:226904936
|
C | T | 41 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(38): Show | 45 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.567-1857C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226904936 | ||||||
| chr2:226904997
|
A | C | 1 | a0001c0001t0007g0069 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.567-1796A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226904997 | ||||||
| chr2:226905056
|
T | C | 2 | a0001c0001t0005g0221a0002c0002t0004g0238 | 2 | HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.567-1737T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226905056 | ||||||
| chr2:226905078
|
C | T | 53 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0027others(50): Show | 53 | HG00099.hp1 HG00621.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.567-1715C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226905078 | ||||||
| chr2:226905159
|
CT | C | 119 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(116): Show | 124 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.567-1620delT | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 226905159 | |||||
| chr2:226905266
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.567-1527C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226905266 | ||||||
| chr2:226905623
|
G | A | 12 | a0001c0001t0002g0178a0001c0001t0002g0213a0001c0001t0002g0214others(9): Show | 12 | HG01106.hp1 HG01261.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.567-1170G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226905623 | ||||||
| chr2:226905835
|
G | A | 10 | a0001c0001t0005g0221a0001c0001t0012g0231a0002c0002t0001g0013others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.567-958G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226905835 | ||||||
| chr2:226905876
|
T | C | 113 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(110): Show | 114 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(111): Show |
intron_variant | MODIFIER | c.567-917T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226905876 | ||||||
| chr2:226905971
|
AC | A | 93 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(90): Show | 94 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(91): Show |
intron_variant | MODIFIER | c.567-814delC | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 226905971 | |||||
| chr2:226905991
|
A | AT | 99 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(96): Show | 100 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(97): Show |
intron_variant | MODIFIER | c.567-802_567-801ins others(1): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226905991 | ||||||
| chr2:226906011
|
G | C | 93 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(90): Show | 94 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(91): Show |
intron_variant | MODIFIER | c.567-782G>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226906011 | ||||||
| chr2:226906120
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.567-673G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226906120 | ||||||
| chr2:226906128
|
T | C | 157 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(154): Show | 162 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.567-665T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226906128 | ||||||
| chr2:226906210
|
AGTTTGAA others(3): Show |
A | 1 | a0001c0001t0001g0110 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.567-582_567-573del others(10): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226906210 | ||||||
| chr2:226906384
|
A | G | 2 | a0002c0002t0006g0229a0002c0002t0006g0230 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.567-409A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226906384 | ||||||
| chr2:226906486
|
C | T | 1 | a0001c0001t0009g0149 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.567-307C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226906486 | ||||||
| chr2:226906571
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.567-222G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226906571 | ||||||
| chr2:226906624
|
G | A | 1 | a0003c0003t0004g0174 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.567-169G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226906624 | ||||||
| chr2:226906672
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.567-121C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226906672 | ||||||
| chr2:226906673
|
T | G | 111 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(108): Show | 112 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(109): Show |
intron_variant | MODIFIER | c.567-120T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226906673 | ||||||
| chr2:226906894
|
A | C | 1 | a0001c0001t0001g0110 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.655+13A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 6/8 | chr2 | 226906894 | ||||||
| chr2:226907034
|
G | A | 1 | a0001c0001t0001g0240 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.655+153G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 6/8 | chr2 | 226907034 | ||||||
| chr2:226907272
|
T | C | 93 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(90): Show | 94 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(91): Show |
intron_variant | MODIFIER | c.655+391T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 6/8 | chr2 | 226907272 | ||||||
| chr2:226907306
|
T | G | 1 | a0001c0001t0016g0066 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.655+425T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 6/8 | chr2 | 226907306 | ||||||
| chr2:226907322
|
G | A | 93 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(90): Show | 94 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(91): Show |
intron_variant | MODIFIER | c.655+441G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 6/8 | chr2 | 226907322 | ||||||
| chr2:226907439
|
A | T | 1 | a0001c0001t0001g0001 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.655+558A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 6/8 | chr2 | 226907439 | ||||||
| chr2:226907532
|
T | C | 93 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(90): Show | 94 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(91): Show |
intron_variant | MODIFIER | c.655+651T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 6/8 | chr2 | 226907532 | ||||||
| chr2:226907574
|
G | A | 1 | a0001c0001t0002g0185 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.655+693G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 6/8 | chr2 | 226907574 | ||||||
| chr2:226907764
|
T | C | 93 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(90): Show | 94 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(91): Show |
intron_variant | MODIFIER | c.655+883T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 6/8 | chr2 | 226907764 | ||||||
| chr2:226907786
|
A | G | 93 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(90): Show | 94 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(91): Show |
intron_variant | MODIFIER | c.655+905A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 6/8 | chr2 | 226907786 | ||||||
| chr2:226907953
|
T | G | 2 | a0002c0002t0006g0229a0002c0002t0006g0230 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.656-869T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 6/8 | chr2 | 226907953 | ||||||
| chr2:226908076
|
A | G | 1 | a0001c0001t0001g0084 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.656-746A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 6/8 | chr2 | 226908076 | ||||||
| chr2:226908096
|
T | A | 176 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(173): Show | 181 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.656-726T>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 6/8 | chr2 | 226908096 | ||||||
| chr2:226908252
|
C | T | 1 | a0001c0001t0002g0205 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.656-570C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 6/8 | chr2 | 226908252 | ||||||
| chr2:226908368
|
T | G | 6 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0215others(3): Show | 6 | HG01106.hp1 HG02109.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.656-454T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 6/8 | chr2 | 226908368 | ||||||
| chr2:226908441
|
C | A | 90 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(87): Show | 91 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(88): Show |
intron_variant | MODIFIER | c.656-381C>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 6/8 | chr2 | 226908441 | ||||||
| chr2:226908582
|
T | TAC | 25 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0027others(22): Show | 27 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.656-202_656-201dup others(2): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 226908582 | |||||
| chr2:226908582
|
T | TACAC | 7 | a0001c0001t0001g0092a0001c0001t0001g0095a0001c0001t0001g0100others(4): Show | 7 | HG01993.hp1 HG02280.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.656-204_656-201dup others(4): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 226908582 | |||||
| chr2:226908582
|
T | TACACAC | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0002c0002t0004g0237others(1): Show | 4 | HG01433.hp1 HG02145.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.656-206_656-201dup others(6): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 226908582 | |||||
| chr2:226908582
|
T | TACACACA others(15): Show |
1 | a0001c0001t0001g0132 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.656-222_656-201dup others(22): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 226908582 | |||||
| chr2:226908582
|
T | TACACACA others(17): Show |
1 | a0001c0001t0001g0131 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.656-224_656-201dup others(24): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 226908582 | |||||
| chr2:226908582
|
TAC | T | 33 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(30): Show | 33 | HG00408.hp1 HG01071.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.656-202_656-201del others(2): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 226908582 | |||||
| chr2:226908582
|
TACAC | T | 12 | a0001c0001t0001g0050a0001c0001t0001g0065a0001c0001t0001g0084others(9): Show | 12 | HG00621.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.656-204_656-201del others(4): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 226908582 | |||||
| chr2:226908582
|
TACACACA others(9): Show |
T | 6 | a0002c0006t0001g0176a0002c0006t0001g0177a0003c0003t0004g0172others(3): Show | 6 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.656-216_656-201del others(16): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 226908582 | |||||
| chr2:226908582
|
TACACACA others(13): Show |
T | 1 | a0001c0001t0019g0017 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.656-220_656-201del others(20): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 226908582 | |||||
| chr2:226908638
|
G | GAC | 93 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(90): Show | 94 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(91): Show |
intron_variant | MODIFIER | c.656-173_656-172dup others(2): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 226908638 | |||||
| chr2:226908750
|
T | C | 93 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(90): Show | 94 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(91): Show |
intron_variant | MODIFIER | c.656-72T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 6/8 | chr2 | 226908750 | ||||||
| chr2:226908921
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.712+43A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226908921 | ||||||
| chr2:226909040
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.712+162G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226909040 | ||||||
| chr2:226909196
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.712+318G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226909196 | ||||||
| chr2:226909208
|
A | G | 114 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(111): Show | 115 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(112): Show |
intron_variant | MODIFIER | c.712+330A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226909208 | ||||||
| chr2:226909323
|
T | C | 1 | a0001c0001t0002g0006 | 2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.712+445T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226909323 | ||||||
| chr2:226909424
|
T | A | 43 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(40): Show | 47 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.712+546T>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226909424 | ||||||
| chr2:226909506
|
A | G | 3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0163 | 5 | NA18943.hp2 NA18993.hp1 NA19003.hp1 others(2): Show |
intron_variant | MODIFIER | c.712+628A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226909506 | ||||||
| chr2:226909528
|
G | C | 93 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(90): Show | 94 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(91): Show |
intron_variant | MODIFIER | c.712+650G>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226909528 | ||||||
| chr2:226909601
|
A | T | 3 | a0001c0005t0005g0219a0001c0005t0005g0220a0001c0007t0010g0222 | 3 | HG02922.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.712+723A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226909601 | ||||||
| chr2:226909787
|
C | G | 113 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(110): Show | 114 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(111): Show |
intron_variant | MODIFIER | c.712+909C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226909787 | ||||||
| chr2:226909831
|
T | C | 11 | a0001c0001t0005g0221a0001c0001t0012g0231a0001c0001t0019g0017others(8): Show | 11 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.712+953T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226909831 | ||||||
| chr2:226909919
|
A | C | 95 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(92): Show | 97 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.712+1041A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226909919 | ||||||
| chr2:226910002
|
A | G | 2 | a0002c0002t0001g0014a0002c0002t0004g0015 | 2 | HG02145.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.712+1124A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226910002 | ||||||
| chr2:226910055
|
A | G | 3 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169 | 3 | HG01934.hp2 HG02451.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.712+1177A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226910055 | ||||||
| chr2:226910146
|
A | G | 25 | a0001c0001t0001g0021a0001c0001t0002g0194a0001c0001t0002g0195others(22): Show | 25 | HG00673.hp2 HG01884.hp1 HG02083.hp1 others(22): Show |
intron_variant | MODIFIER | c.712+1268A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226910146 | ||||||
| chr2:226910165
|
T | C | 15 | a0001c0001t0001g0021a0001c0001t0002g0195a0001c0001t0002g0196others(12): Show | 15 | HG00673.hp2 HG02083.hp1 HG02896.hp1 others(12): Show |
intron_variant | MODIFIER | c.712+1287T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226910165 | ||||||
| chr2:226910172
|
C | T | 98 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(95): Show | 100 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.712+1294C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226910172 | ||||||
| chr2:226910393
|
A | G | 1 | a0001c0001t0001g0248 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.712+1515A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226910393 | ||||||
| chr2:226910507
|
G | T | 157 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(154): Show | 162 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.712+1629G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226910507 | ||||||
| chr2:226910525
|
C | T | 1 | a0001c0001t0002g0235 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.712+1647C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226910525 | ||||||
| chr2:226910908
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.712+2030G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226910908 | ||||||
| chr2:226911000
|
A | G | 3 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169 | 3 | HG01934.hp2 HG02451.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.712+2122A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226911000 | ||||||
| chr2:226911313
|
G | T | 93 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(90): Show | 94 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(91): Show |
intron_variant | MODIFIER | c.712+2435G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226911313 | ||||||
| chr2:226911491
|
G | A | 2 | a0001c0001t0003g0250a0001c0001t0003g0256 | 2 | NA18975.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.712+2613G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226911491 | ||||||
| chr2:226911541
|
C | CT | 20 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0137others(17): Show | 21 | HG00099.hp2 HG01106.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.713-2645dupT | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 226911541 | |||||
| chr2:226911541
|
CT | C | 19 | a0001c0001t0001g0032a0001c0001t0001g0054a0001c0001t0001g0073others(16): Show | 19 | HG01169.hp1 HG01261.hp1 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.713-2645delT | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 226911541 | |||||
| chr2:226911541
|
CTT | C | 7 | a0001c0001t0001g0106a0002c0006t0001g0176a0002c0006t0001g0177others(4): Show | 7 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.713-2646_713-2645d others(4): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 226911541 | |||||
| chr2:226911611
|
T | C | 1 | a0001c0001t0001g0078 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.713-2597T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226911611 | ||||||
| chr2:226911712
|
A | G | 1 | a0001c0001t0006g0244 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.713-2496A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226911712 | ||||||
| chr2:226911805
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.713-2403A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226911805 | ||||||
| chr2:226911885
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.713-2323C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226911885 | ||||||
| chr2:226911931
|
C | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.713-2277C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226911931 | ||||||
| chr2:226912209
|
T | C | 1 | a0001c0001t0001g0001 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.713-1999T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226912209 | ||||||
| chr2:226912260
|
T | A | 98 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(95): Show | 100 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.713-1948T>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226912260 | ||||||
| chr2:226912379
|
A | G | 98 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(95): Show | 100 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.713-1829A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226912379 | ||||||
| chr2:226912488
|
G | A | 6 | a0002c0006t0001g0176a0002c0006t0001g0177a0003c0003t0004g0172others(3): Show | 6 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.713-1720G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226912488 | ||||||
| chr2:226912777
|
A | T | 98 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(95): Show | 100 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.713-1431A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226912777 | ||||||
| chr2:226912838
|
G | A | 98 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(95): Show | 100 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.713-1370G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226912838 | ||||||
| chr2:226912898
|
G | A | 1 | a0001c0001t0001g0028 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.713-1310G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226912898 | ||||||
| chr2:226912934
|
A | G | 104 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(101): Show | 106 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.713-1274A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226912934 | ||||||
| chr2:226913041
|
A | G | 98 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(95): Show | 100 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.713-1167A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226913041 | ||||||
| chr2:226913066
|
C | A | 1 | a0001c0001t0002g0196 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.713-1142C>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226913066 | ||||||
| chr2:226913170
|
T | G | 1 | a0001c0001t0001g0123 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.713-1038T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226913170 | ||||||
| chr2:226913252
|
T | C | 10 | a0001c0001t0005g0221a0001c0001t0012g0231a0002c0002t0001g0013others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.713-956T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226913252 | ||||||
| chr2:226913295
|
T | C | 6 | a0002c0006t0001g0176a0002c0006t0001g0177a0003c0003t0004g0172others(3): Show | 6 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.713-913T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226913295 | ||||||
| chr2:226913457
|
G | A | 97 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(94): Show | 99 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.713-751G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226913457 | ||||||
| chr2:226913672
|
T | G | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.713-536T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226913672 | ||||||
| chr2:226913681
|
G | A | 95 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(92): Show | 97 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.713-527G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226913681 | ||||||
| chr2:226913729
|
C | T | 94 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(91): Show | 96 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.713-479C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226913729 | ||||||
| chr2:226913860
|
G | C | 4 | a0001c0001t0001g0042a0001c0001t0001g0097a0001c0001t0001g0102others(1): Show | 4 | HG01169.hp1 HG01975.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.713-348G>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226913860 | ||||||
| chr2:226913906
|
A | C | 1 | a0001c0001t0001g0025 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.713-302A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226913906 | ||||||
| chr2:226913918
|
A | G | 1 | a0001c0001t0001g0161 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.713-290A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226913918 | ||||||
| chr2:226914126
|
G | A | 4 | a0001c0001t0002g0197a0001c0001t0006g0244a0002c0002t0006g0229others(1): Show | 4 | HG03139.hp2 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.713-82G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 7/8 | chr2 | 226914126 | ||||||
| chr2:226914406
|
G | T | 1 | a0001c0001t0001g0073 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.856+55G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226914406 | ||||||
| chr2:226914475
|
C | A | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(100): Show | 106 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.856+124C>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226914475 | ||||||
| chr2:226914496
|
A | T | 6 | a0001c0001t0012g0231a0002c0002t0001g0014a0002c0002t0004g0011others(3): Show | 6 | HG02145.hp1 HG02258.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.856+145A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226914496 | ||||||
| chr2:226914696
|
A | C | 1 | a0001c0001t0001g0010 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.856+345A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226914696 | ||||||
| chr2:226914724
|
A | G | 1 | a0001c0001t0002g0197 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.856+373A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226914724 | ||||||
| chr2:226914827
|
T | C | 1 | a0001c0001t0013g0198 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.856+476T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226914827 | ||||||
| chr2:226914960
|
G | A | 35 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0081others(32): Show | 37 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.856+609G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226914960 | ||||||
| chr2:226915031
|
A | G | 2 | a0002c0006t0001g0176a0002c0006t0001g0177 | 2 | HG03654.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.856+680A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226915031 | ||||||
| chr2:226915080
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.856+729C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226915080 | ||||||
| chr2:226915299
|
G | A | 1 | a0001c0001t0002g0190 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.856+948G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226915299 | ||||||
| chr2:226915402
|
G | T | 1 | a0001c0001t0002g0218 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.856+1051G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226915402 | ||||||
| chr2:226915550
|
G | C | 105 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0027others(102): Show | 105 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.856+1199G>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226915550 | ||||||
| chr2:226915561
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.856+1210A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226915561 | ||||||
| chr2:226915583
|
T | C | 3 | a0001c0005t0005g0219a0001c0005t0005g0220a0001c0007t0010g0222 | 3 | HG02922.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.856+1232T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226915583 | ||||||
| chr2:226915654
|
A | G | 1 | a0001c0001t0002g0209 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.856+1303A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226915654 | ||||||
| chr2:226915687
|
C | T | 1 | a0001c0001t0001g0023 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.856+1336C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226915687 | ||||||
| chr2:226915726
|
C | A | 3 | a0001c0001t0001g0008a0001c0001t0003g0007a0002c0002t0001g0013 | 3 | HG03516.hp1 HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.856+1375C>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226915726 | ||||||
| chr2:226915761
|
G | A | 1 | a0001c0001t0001g0039 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.856+1410G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226915761 | ||||||
| chr2:226915845
|
C | T | 6 | a0001c0001t0012g0231a0002c0002t0001g0014a0002c0002t0004g0011others(3): Show | 6 | HG02145.hp1 HG02258.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.856+1494C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226915845 | ||||||
| chr2:226915950
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.856+1599C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226915950 | ||||||
| chr2:226916119
|
T | C | 1 | a0001c0001t0001g0068 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.856+1768T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226916119 | ||||||
| chr2:226916229
|
C | A | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(157): Show | 165 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.856+1878C>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226916229 | ||||||
| chr2:226916229
|
C | G | 2 | a0002c0006t0001g0176a0002c0006t0001g0177 | 2 | HG03654.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.856+1878C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226916229 | ||||||
| chr2:226916231
|
C | G | 3 | a0001c0005t0005g0219a0001c0005t0005g0220a0001c0007t0010g0222 | 3 | HG02922.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.856+1880C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226916231 | ||||||
| chr2:226916428
|
A | T | 1 | a0001c0001t0001g0062 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.856+2077A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226916428 | ||||||
| chr2:226916434
|
A | G | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(162): Show | 170 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.856+2083A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226916434 | ||||||
| chr2:226916447
|
A | G | 3 | a0001c0005t0005g0219a0001c0005t0005g0220a0001c0007t0010g0222 | 3 | HG02922.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.856+2096A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226916447 | ||||||
| chr2:226916742
|
A | G | 1 | a0001c0005t0005g0220 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.856+2391A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226916742 | ||||||
| chr2:226916884
|
T | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(117): Show | 122 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.856+2533T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226916884 | ||||||
| chr2:226916885
|
G | A | 1 | a0001c0001t0002g0179 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.856+2534G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226916885 | ||||||
| chr2:226917026
|
G | A | 6 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0111others(3): Show | 6 | HG00423.hp1 HG02056.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.856+2675G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226917026 | ||||||
| chr2:226917147
|
G | A | 120 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(117): Show | 122 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.856+2796G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226917147 | ||||||
| chr2:226917556
|
CT | C | 5 | a0001c0001t0002g0178a0001c0001t0002g0232a0001c0001t0002g0233others(2): Show | 5 | HG02647.hp1 HG02809.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.856+3208delT | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226917556 | |||||
| chr2:226917639
|
A | T | 1 | a0001c0001t0001g0155 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.856+3288A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226917639 | ||||||
| chr2:226917776
|
G | T | 1 | a0001c0001t0003g0245 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.856+3425G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226917776 | ||||||
| chr2:226917783
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.856+3432T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226917783 | ||||||
| chr2:226917848
|
C | T | 3 | a0001c0005t0005g0219a0001c0005t0005g0220a0001c0007t0010g0222 | 3 | HG02922.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.856+3497C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226917848 | ||||||
| chr2:226917849
|
G | T | 1 | a0001c0001t0003g0245 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.856+3498G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226917849 | ||||||
| chr2:226918114
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.856+3763A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226918114 | ||||||
| chr2:226918243
|
A | C | 1 | a0001c0001t0001g0081 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.856+3892A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226918243 | ||||||
| chr2:226918327
|
A | C | 2 | a0002c0006t0001g0176a0002c0006t0001g0177 | 2 | HG03654.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.856+3976A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226918327 | ||||||
| chr2:226918611
|
A | G | 2 | a0002c0006t0001g0176a0002c0006t0001g0177 | 2 | HG03654.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.856+4260A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226918611 | ||||||
| chr2:226919613
|
T | G | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(250): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.856+5262T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226919613 | ||||||
| chr2:226919782
|
C | T | 1 | a0001c0001t0001g0147 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.856+5431C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226919782 | ||||||
| chr2:226919848
|
A | G | 1 | a0001c0001t0001g0037 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.856+5497A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226919848 | ||||||
| chr2:226920140
|
A | T | 3 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG00099.hp1 HG01099.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.856+5789A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226920140 | ||||||
| chr2:226920245
|
A | G | 120 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(117): Show | 122 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.856+5894A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226920245 | ||||||
| chr2:226920794
|
A | G | 2 | a0001c0001t0001g0056a0001c0001t0001g0139 | 2 | NA18985.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.856+6443A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226920794 | ||||||
| chr2:226920819
|
G | A | 120 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(117): Show | 122 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.856+6468G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226920819 | ||||||
| chr2:226921266
|
G | A | 1 | a0001c0001t0001g0040 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.856+6915G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226921266 | ||||||
| chr2:226921393
|
C | G | 3 | a0001c0001t0005g0221a0002c0002t0004g0237a0002c0002t0004g0238 | 3 | HG02145.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.856+7042C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226921393 | ||||||
| chr2:226921439
|
G | A | 2 | a0001c0001t0005g0221a0002c0002t0004g0238 | 2 | HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.856+7088G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226921439 | ||||||
| chr2:226921651
|
C | G | 1 | a0001c0001t0015g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.856+7300C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226921651 | ||||||
| chr2:226921714
|
G | C | 1 | a0001c0001t0001g0023 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.856+7363G>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226921714 | ||||||
| chr2:226921741
|
T | G | 1 | a0001c0001t0002g0224 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.856+7390T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226921741 | ||||||
| chr2:226921798
|
T | C | 112 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(109): Show | 114 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.856+7447T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226921798 | ||||||
| chr2:226922202
|
C | CT | 50 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0021others(47): Show | 52 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.856+7874dupT | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226922202 | |||||
| chr2:226922202
|
C | CTT | 13 | a0001c0001t0001g0002a0001c0001t0001g0054a0001c0001t0001g0081others(10): Show | 14 | HG00408.hp2 HG00423.hp2 HG02738.hp1 others(11): Show |
intron_variant | MODIFIER | c.856+7873_856+7874d others(4): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226922202 | |||||
| chr2:226922202
|
CT | C | 10 | a0001c0001t0001g0083a0001c0001t0003g0250a0001c0001t0003g0256others(7): Show | 10 | HG00558.hp2 HG02074.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.856+7874delT | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226922202 | |||||
| chr2:226922231
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.856+7880G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226922231 | ||||||
| chr2:226922278
|
G | T | 1 | a0001c0001t0001g0092 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.856+7927G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226922278 | ||||||
| chr2:226922454
|
A | G | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(182): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.856+8103A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226922454 | ||||||
| chr2:226922454
|
A | T | 1 | a0001c0001t0002g0235 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.856+8103A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226922454 | ||||||
| chr2:226922457
|
T | C | 1 | a0002c0002t0004g0237 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.856+8106T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226922457 | ||||||
| chr2:226922623
|
T | C | 3 | a0001c0001t0006g0244a0002c0002t0006g0229a0002c0002t0006g0230 | 3 | HG03139.hp2 NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.856+8272T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226922623 | ||||||
| chr2:226922705
|
T | G | 7 | a0001c0005t0005g0219a0001c0005t0005g0220a0001c0007t0010g0222others(4): Show | 7 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.856+8354T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226922705 | ||||||
| chr2:226922872
|
A | ACAAGCAA others(1): Show |
4 | a0001c0001t0001g0050a0001c0001t0001g0084a0001c0001t0001g0104others(1): Show | 4 | HG00621.hp2 HG02135.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.856+8533_856+8540d others(10): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226922872 | |||||
| chr2:226923097
|
T | G | 2 | a0002c0006t0001g0176a0002c0006t0001g0177 | 2 | HG03654.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.856+8746T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226923097 | ||||||
| chr2:226923110
|
C | G | 14 | a0001c0001t0001g0021a0001c0001t0002g0195a0001c0001t0002g0199others(11): Show | 14 | HG00673.hp2 HG02083.hp1 HG04184.hp2 others(11): Show |
intron_variant | MODIFIER | c.856+8759C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226923110 | ||||||
| chr2:226923148
|
A | G | 1 | a0001c0001t0003g0257 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.856+8797A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226923148 | ||||||
| chr2:226923324
|
A | T | 1 | a0002c0002t0004g0237 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.856+8973A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226923324 | ||||||
| chr2:226923356
|
C | T | 1 | a0002c0002t0004g0237 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.856+9005C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226923356 | ||||||
| chr2:226923482
|
A | G | 9 | a0001c0001t0003g0043a0001c0001t0003g0061a0001c0001t0003g0243others(6): Show | 9 | HG00140.hp2 HG00735.hp2 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.856+9131A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226923482 | ||||||
| chr2:226923643
|
C | A | 1 | a0001c0005t0005g0220 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.856+9292C>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226923643 | ||||||
| chr2:226923743
|
G | A | 4 | a0003c0003t0004g0172a0003c0003t0004g0173a0003c0003t0004g0174others(1): Show | 4 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.856+9392G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226923743 | ||||||
| chr2:226923748
|
C | T | 4 | a0003c0003t0004g0172a0003c0003t0004g0173a0003c0003t0004g0174others(1): Show | 4 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.856+9397C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226923748 | ||||||
| chr2:226923820
|
C | T | 3 | a0001c0005t0005g0219a0001c0005t0005g0220a0001c0007t0010g0222 | 3 | HG02922.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.856+9469C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226923820 | ||||||
| chr2:226923827
|
A | T | 4 | a0001c0001t0001g0042a0001c0001t0001g0097a0001c0001t0001g0102others(1): Show | 4 | HG01169.hp1 HG01975.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.856+9476A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226923827 | ||||||
| chr2:226923876
|
T | C | 121 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(118): Show | 123 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.856+9525T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226923876 | ||||||
| chr2:226923961
|
G | C | 1 | a0001c0001t0002g0184 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.856+9610G>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226923961 | ||||||
| chr2:226923996
|
C | T | 3 | a0001c0001t0002g0189a0001c0001t0002g0192a0001c0001t0002g0193 | 3 | HG02922.hp1 HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.856+9645C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226923996 | ||||||
| chr2:226924270
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.856+9919G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226924270 | ||||||
| chr2:226924552
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.856+10201C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226924552 | ||||||
| chr2:226924856
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.856+10505A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226924856 | ||||||
| chr2:226925093
|
C | A | 1 | a0001c0001t0001g0036 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.856+10742C>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226925093 | ||||||
| chr2:226925274
|
T | C | 2 | a0001c0005t0005g0219a0001c0005t0005g0220 | 2 | HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.856+10923T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226925274 | ||||||
| chr2:226925376
|
G | C | 1 | a0001c0001t0001g0022 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.856+11025G>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226925376 | ||||||
| chr2:226925401
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.856+11050T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226925401 | ||||||
| chr2:226925447
|
A | C | 1 | a0001c0001t0003g0241 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.856+11096A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226925447 | ||||||
| chr2:226925471
|
A | C | 99 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(96): Show | 101 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.856+11120A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226925471 | ||||||
| chr2:226925497
|
A | G | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | HG02622.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.856+11146A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226925497 | ||||||
| chr2:226925546
|
C | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(105): Show | 110 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.856+11195C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226925546 | ||||||
| chr2:226925812
|
T | C | 2 | a0001c0001t0001g0100a0001c0001t0001g0105 | 2 | NA18985.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.856+11461T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226925812 | ||||||
| chr2:226926027
|
C | T | 2 | a0002c0006t0001g0176a0002c0006t0001g0177 | 2 | HG03654.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.856+11676C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226926027 | ||||||
| chr2:226926223
|
TA | T | 107 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0018others(104): Show | 109 | HG00544.hp2 HG00558.hp1 HG00621.hp2 others(106): Show |
intron_variant | MODIFIER | c.856+11888delA | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226926223 | |||||
| chr2:226926502
|
T | C | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(160): Show | 168 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.856+12151T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226926502 | ||||||
| chr2:226926573
|
A | G | 5 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0075others(2): Show | 6 | HG00408.hp2 HG00423.hp2 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.856+12222A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226926573 | ||||||
| chr2:226926987
|
G | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(105): Show | 110 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.856+12636G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226926987 | ||||||
| chr2:226927129
|
A | G | 13 | a0001c0001t0001g0042a0001c0001t0001g0054a0001c0001t0001g0085others(10): Show | 13 | HG01169.hp1 HG01975.hp1 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.856+12778A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226927129 | ||||||
| chr2:226927144
|
T | C | 2 | a0001c0001t0005g0221a0002c0002t0004g0238 | 2 | HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.856+12793T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226927144 | ||||||
| chr2:226927146
|
C | T | 4 | a0003c0003t0004g0172a0003c0003t0004g0173a0003c0003t0004g0174others(1): Show | 4 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.856+12795C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226927146 | ||||||
| chr2:226927207
|
G | A | 1 | a0001c0001t0002g0196 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.856+12856G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226927207 | ||||||
| chr2:226927248
|
T | A | 1 | a0001c0001t0002g0194 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.856+12897T>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226927248 | ||||||
| chr2:226927249
|
G | C | 1 | a0001c0001t0002g0194 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.856+12898G>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226927249 | ||||||
| chr2:226927250
|
T | A | 1 | a0001c0001t0002g0194 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.856+12899T>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226927250 | ||||||
| chr2:226927251
|
T | A | 1 | a0001c0001t0002g0194 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.856+12900T>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226927251 | ||||||
| chr2:226927282
|
AT | A | 4 | a0001c0001t0001g0050a0001c0001t0001g0084a0001c0001t0001g0104others(1): Show | 4 | HG00621.hp2 HG02135.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.856+12939delT | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226927282 | |||||
| chr2:226927334
|
G | GT | 108 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(105): Show | 110 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.856+12992dupT | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226927334 | |||||
| chr2:226927364
|
T | C | 2 | a0001c0001t0005g0221a0002c0002t0004g0238 | 2 | HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.856+13013T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226927364 | ||||||
| chr2:226927443
|
G | A | 1 | a0001c0001t0002g0212 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.856+13092G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226927443 | ||||||
| chr2:226927448
|
G | A | 7 | a0001c0005t0005g0219a0001c0005t0005g0220a0001c0007t0010g0222others(4): Show | 7 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.856+13097G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226927448 | ||||||
| chr2:226927643
|
T | C | 1 | a0001c0001t0002g0194 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.856+13292T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226927643 | ||||||
| chr2:226927814
|
T | A | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(160): Show | 168 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.856+13463T>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226927814 | ||||||
| chr2:226927824
|
G | A | 58 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(55): Show | 59 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.856+13473G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226927824 | ||||||
| chr2:226927905
|
T | C | 1 | a0001c0001t0016g0066 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.856+13554T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226927905 | ||||||
| chr2:226928013
|
A | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(105): Show | 110 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.856+13662A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226928013 | ||||||
| chr2:226928115
|
A | G | 2 | a0001c0001t0002g0181a0001c0001t0002g0182 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.856+13764A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226928115 | ||||||
| chr2:226928689
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.856+14338C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226928689 | ||||||
| chr2:226928833
|
A | G | 1 | a0001c0001t0001g0171 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.856+14482A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226928833 | ||||||
| chr2:226928872
|
C | T | 2 | a0001c0001t0003g0045a0001c0001t0003g0252 | 2 | HG01071.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.856+14521C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226928872 | ||||||
| chr2:226929056
|
C | T | 7 | a0001c0005t0005g0219a0001c0005t0005g0220a0001c0007t0010g0222others(4): Show | 7 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.856+14705C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226929056 | ||||||
| chr2:226929126
|
G | A | 1 | a0001c0001t0002g0227 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.856+14775G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226929126 | ||||||
| chr2:226929205
|
A | G | 4 | a0001c0001t0006g0244a0001c0001t0019g0017a0002c0002t0006g0229others(1): Show | 4 | HG02451.hp1 HG03139.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.856+14854A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226929205 | ||||||
| chr2:226929232
|
G | A | 1 | a0001c0001t0002g0197 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.856+14881G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226929232 | ||||||
| chr2:226929290
|
C | G | 2 | a0001c0001t0001g0034a0001c0001t0001g0124 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.856+14939C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226929290 | ||||||
| chr2:226929352
|
A | T | 1 | a0001c0001t0001g0038 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.856+15001A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226929352 | ||||||
| chr2:226929594
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.856+15243A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226929594 | ||||||
| chr2:226929607
|
C | T | 4 | a0003c0003t0004g0172a0003c0003t0004g0173a0003c0003t0004g0174others(1): Show | 4 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.856+15256C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226929607 | ||||||
| chr2:226929704
|
T | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(105): Show | 110 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.856+15353T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226929704 | ||||||
| chr2:226929736
|
G | A | 112 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(109): Show | 114 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.856+15385G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226929736 | ||||||
| chr2:226929930
|
A | G | 1 | a0001c0001t0001g0091 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.856+15579A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226929930 | ||||||
| chr2:226930228
|
A | G | 117 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(114): Show | 119 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.856+15877A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226930228 | ||||||
| chr2:226930259
|
A | G | 2 | a0002c0006t0001g0176a0002c0006t0001g0177 | 2 | HG03654.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.856+15908A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226930259 | ||||||
| chr2:226930339
|
C | T | 1 | a0001c0001t0001g0087 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.856+15988C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226930339 | ||||||
| chr2:226930340
|
C | G | 4 | a0001c0001t0006g0244a0001c0001t0019g0017a0002c0002t0006g0229others(1): Show | 4 | HG02451.hp1 HG03139.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.856+15989C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226930340 | ||||||
| chr2:226930494
|
A | G | 1 | a0001c0001t0001g0001 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.856+16143A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226930494 | ||||||
| chr2:226930748
|
G | A | 108 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(105): Show | 110 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.856+16397G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226930748 | ||||||
| chr2:226930858
|
A | G | 1 | a0001c0001t0002g0205 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.856+16507A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226930858 | ||||||
| chr2:226931289
|
T | C | 1 | a0001c0001t0019g0017 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.856+16938T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226931289 | ||||||
| chr2:226931334
|
C | T | 1 | a0001c0001t0012g0231 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.856+16983C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226931334 | ||||||
| chr2:226931480
|
G | A | 1 | a0002c0002t0004g0237 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.856+17129G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226931480 | ||||||
| chr2:226931679
|
C | A | 1 | a0001c0001t0001g0059 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.856+17328C>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226931679 | ||||||
| chr2:226931872
|
GA | G | 112 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(109): Show | 114 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.856+17531delA | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226931872 | |||||
| chr2:226931967
|
A | G | 7 | a0001c0005t0005g0219a0001c0005t0005g0220a0001c0007t0010g0222others(4): Show | 7 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.856+17616A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226931967 | ||||||
| chr2:226931994
|
G | C | 4 | a0001c0001t0006g0244a0001c0001t0019g0017a0002c0002t0006g0229others(1): Show | 4 | HG02451.hp1 HG03139.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.856+17643G>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226931994 | ||||||
| chr2:226932195
|
T | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(105): Show | 110 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.856+17844T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226932195 | ||||||
| chr2:226932239
|
A | T | 3 | a0001c0001t0006g0244a0002c0002t0006g0229a0002c0002t0006g0230 | 3 | HG03139.hp2 NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.856+17888A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226932239 | ||||||
| chr2:226932385
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.856+18034C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226932385 | ||||||
| chr2:226932632
|
C | T | 7 | a0001c0005t0005g0219a0001c0005t0005g0220a0001c0007t0010g0222others(4): Show | 7 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.856+18281C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226932632 | ||||||
| chr2:226933025
|
G | A | 1 | a0001c0007t0010g0222 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.856+18674G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226933025 | ||||||
| chr2:226933037
|
G | C | 1 | a0001c0001t0001g0078 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.856+18686G>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226933037 | ||||||
| chr2:226933094
|
G | C | 3 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0002g0194 | 3 | HG03453.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.856+18743G>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226933094 | ||||||
| chr2:226933173
|
G | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0124 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.856+18822G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226933173 | ||||||
| chr2:226933683
|
A | G | 1 | a0001c0001t0001g0147 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.856+19332A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226933683 | ||||||
| chr2:226934093
|
T | G | 4 | a0001c0001t0006g0244a0001c0001t0019g0017a0002c0002t0006g0229others(1): Show | 4 | HG02451.hp1 HG03139.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.856+19742T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226934093 | ||||||
| chr2:226934265
|
G | A | 108 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(105): Show | 110 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.856+19914G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226934265 | ||||||
| chr2:226934287
|
C | A | 2 | a0001c0001t0008g0246a0001c0001t0008g0247 | 2 | HG01071.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.856+19936C>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226934287 | ||||||
| chr2:226934517
|
G | A | 2 | a0002c0006t0001g0176a0002c0006t0001g0177 | 2 | HG03654.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.856+20166G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226934517 | ||||||
| chr2:226934678
|
C | A | 2 | a0001c0001t0001g0032a0001c0001t0001g0048 | 2 | HG03704.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.856+20327C>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226934678 | ||||||
| chr2:226934752
|
T | C | 1 | a0001c0001t0001g0111 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.856+20401T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226934752 | ||||||
| chr2:226934798
|
T | G | 1 | a0001c0001t0001g0070 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.856+20447T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226934798 | ||||||
| chr2:226934863
|
CT | C | 107 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(104): Show | 109 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.856+20523delT | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226934863 | |||||
| chr2:226934936
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.856+20585A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226934936 | ||||||
| chr2:226935061
|
T | C | 1 | a0001c0001t0001g0032 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.856+20710T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226935061 | ||||||
| chr2:226935137
|
A | G | 99 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(96): Show | 101 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.856+20786A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226935137 | ||||||
| chr2:226935362
|
A | G | 2 | a0001c0001t0001g0145a0001c0001t0001g0166 | 2 | NA18988.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.856+21011A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226935362 | ||||||
| chr2:226935489
|
T | C | 99 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(96): Show | 101 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.856+21138T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226935489 | ||||||
| chr2:226935572
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.856+21221C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226935572 | ||||||
| chr2:226935634
|
AT | A | 108 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(105): Show | 110 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.856+21295delT | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226935634 | |||||
| chr2:226935637
|
T | A | 108 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(105): Show | 110 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.856+21286T>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226935637 | ||||||
| chr2:226935639
|
T | A | 1 | a0001c0001t0001g0138 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.856+21288T>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226935639 | ||||||
| chr2:226935909
|
A | G | 1 | a0001c0001t0002g0208 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.856+21558A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226935909 | ||||||
| chr2:226936012
|
T | C | 1 | a0001c0004t0002g0203 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.856+21661T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226936012 | ||||||
| chr2:226936041
|
T | G | 4 | a0001c0001t0006g0244a0001c0001t0019g0017a0002c0002t0006g0229others(1): Show | 4 | HG02451.hp1 HG03139.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.856+21690T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226936041 | ||||||
| chr2:226936045
|
A | T | 3 | a0001c0005t0005g0219a0001c0005t0005g0220a0001c0007t0010g0222 | 3 | HG02922.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.856+21694A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226936045 | ||||||
| chr2:226936060
|
A | G | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(160): Show | 168 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.856+21709A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226936060 | ||||||
| chr2:226936371
|
G | T | 28 | a0001c0001t0001g0021a0001c0001t0001g0131a0001c0001t0001g0132others(25): Show | 28 | HG00673.hp2 HG01261.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.856+22020G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226936371 | ||||||
| chr2:226936387
|
T | C | 1 | a0001c0001t0002g0225 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.856+22036T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226936387 | ||||||
| chr2:226936418
|
A | G | 2 | a0002c0002t0004g0011a0002c0002t0004g0012 | 2 | HG02258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.856+22067A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226936418 | ||||||
| chr2:226936572
|
C | A | 2 | a0001c0001t0001g0135a0001c0001t0001g0138 | 2 | HG00140.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.856+22221C>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226936572 | ||||||
| chr2:226936578
|
A | G | 1 | a0001c0001t0002g0200 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.856+22227A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226936578 | ||||||
| chr2:226936600
|
A | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(105): Show | 110 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.856+22249A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226936600 | ||||||
| chr2:226936628
|
T | C | 1 | a0001c0001t0001g0078 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.856+22277T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226936628 | ||||||
| chr2:226936641
|
G | A | 1 | a0001c0001t0001g0056 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.856+22290G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226936641 | ||||||
| chr2:226936991
|
T | A | 1 | a0001c0001t0001g0130 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.856+22640T>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226936991 | ||||||
| chr2:226937322
|
C | T | 5 | a0001c0001t0002g0178a0001c0001t0002g0232a0001c0001t0002g0233others(2): Show | 5 | HG02647.hp1 HG02809.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.856+22971C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226937322 | ||||||
| chr2:226937638
|
G | A | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(159): Show | 167 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.856+23287G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226937638 | ||||||
| chr2:226937783
|
T | C | 107 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(104): Show | 109 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.856+23432T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226937783 | ||||||
| chr2:226937802
|
A | T | 1 | a0001c0001t0001g0093 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.856+23451A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226937802 | ||||||
| chr2:226937812
|
C | T | 107 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(104): Show | 109 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.856+23461C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226937812 | ||||||
| chr2:226938097
|
G | A | 107 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(104): Show | 109 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.856+23746G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226938097 | ||||||
| chr2:226938151
|
G | A | 1 | a0001c0001t0002g0180 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.856+23800G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226938151 | ||||||
| chr2:226938258
|
T | A | 2 | a0001c0001t0001g0019a0001c0001t0001g0040 | 2 | NA20752.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.856+23907T>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226938258 | ||||||
| chr2:226938545
|
A | G | 4 | a0001c0001t0006g0244a0001c0001t0019g0017a0002c0002t0006g0229others(1): Show | 4 | HG02451.hp1 HG03139.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.856+24194A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226938545 | ||||||
| chr2:226938665
|
G | A | 1 | a0001c0001t0002g0208 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.856+24314G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226938665 | ||||||
| chr2:226938744
|
G | GA | 8 | a0001c0001t0002g0226a0001c0001t0006g0244a0001c0001t0019g0017others(5): Show | 8 | HG02451.hp1 HG02922.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.856+24403dupA | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226938744 | |||||
| chr2:226938846
|
A | C | 1 | a0001c0001t0013g0198 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.856+24495A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226938846 | ||||||
| chr2:226938862
|
T | C | 3 | a0001c0005t0005g0219a0001c0005t0005g0220a0001c0007t0010g0222 | 3 | HG02922.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.856+24511T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226938862 | ||||||
| chr2:226939623
|
A | C | 1 | a0001c0007t0010g0222 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.856+25272A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226939623 | ||||||
| chr2:226939772
|
A | C | 1 | a0002c0002t0004g0016 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.856+25421A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226939772 | ||||||
| chr2:226940006
|
CA | C | 99 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(96): Show | 101 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.856+25657delA | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226940006 | |||||
| chr2:226940101
|
T | TAAAAAAA others(555): Show |
1 | a0001c0001t0001g0062 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.856+25764_856+2576 others(566): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226940101 | |||||
| chr2:226940103
|
A | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(105): Show | 110 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.856+25752A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226940103 | ||||||
| chr2:226940127
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.856+25776A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226940127 | ||||||
| chr2:226940211
|
A | G | 1 | a0001c0001t0015g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.856+25860A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226940211 | ||||||
| chr2:226940294
|
G | A | 121 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(118): Show | 123 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.856+25943G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226940294 | ||||||
| chr2:226940710
|
C | A | 108 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(105): Show | 110 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.856+26359C>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226940710 | ||||||
| chr2:226940813
|
A | G | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(160): Show | 168 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.856+26462A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226940813 | ||||||
| chr2:226940954
|
T | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(95): Show | 100 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.856+26603T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226940954 | ||||||
| chr2:226940955
|
T | C | 1 | a0001c0001t0002g0197 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.856+26604T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226940955 | ||||||
| chr2:226941033
|
A | G | 121 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(118): Show | 123 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.856+26682A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226941033 | ||||||
| chr2:226941051
|
ATCC | A | 108 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(105): Show | 110 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.856+26705_856+2670 others(7): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226941051 | |||||
| chr2:226941114
|
G | A | 5 | a0001c0001t0001g0019a0001c0001t0001g0035a0001c0001t0001g0036others(2): Show | 5 | HG01934.hp1 HG01975.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.856+26763G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226941114 | ||||||
| chr2:226941224
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.856+26873C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226941224 | ||||||
| chr2:226941227
|
A | C | 1 | a0001c0001t0001g0038 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.856+26876A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226941227 | ||||||
| chr2:226941258
|
G | A | 1 | a0001c0001t0001g0100 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.856+26907G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226941258 | ||||||
| chr2:226941692
|
A | G | 1 | a0001c0001t0001g0068 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.856+27341A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226941692 | ||||||
| chr2:226941822
|
A | C | 1 | a0001c0001t0008g0247 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.856+27471A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226941822 | ||||||
| chr2:226941834
|
G | A | 108 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(105): Show | 110 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.856+27483G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226941834 | ||||||
| chr2:226942009
|
A | G | 1 | a0001c0001t0001g0078 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.856+27658A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226942009 | ||||||
| chr2:226942160
|
G | A | 35 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(32): Show | 38 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.856+27809G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226942160 | ||||||
| chr2:226942241
|
C | CT | 108 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(105): Show | 110 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.856+27905dupT | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226942241 | |||||
| chr2:226942308
|
G | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG00558.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.856+27957G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226942308 | ||||||
| chr2:226942331
|
C | T | 1 | a0001c0001t0016g0066 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.856+27980C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226942331 | ||||||
| chr2:226942395
|
A | G | 1 | a0001c0001t0001g0056 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.856+28044A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226942395 | ||||||
| chr2:226942486
|
G | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(96): Show | 101 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.856+28135G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226942486 | ||||||
| chr2:226942661
|
C | T | 4 | a0001c0001t0006g0244a0001c0001t0019g0017a0002c0002t0006g0229others(1): Show | 4 | HG02451.hp1 HG03139.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.856+28310C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226942661 | ||||||
| chr2:226942891
|
A | G | 2 | a0002c0006t0001g0176a0002c0006t0001g0177 | 2 | HG03654.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.856+28540A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226942891 | ||||||
| chr2:226942990
|
C | T | 3 | a0001c0001t0002g0195a0001c0001t0002g0199a0001c0001t0002g0200 | 3 | HG02083.hp1 NA18956.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.856+28639C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226942990 | ||||||
| chr2:226943023
|
G | C | 1 | a0002c0002t0004g0237 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.856+28672G>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226943023 | ||||||
| chr2:226943412
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.856+29061G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226943412 | ||||||
| chr2:226943510
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.856+29159G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226943510 | ||||||
| chr2:226943609
|
A | G | 7 | a0001c0005t0005g0219a0001c0005t0005g0220a0001c0007t0010g0222others(4): Show | 7 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.856+29258A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226943609 | ||||||
| chr2:226943648
|
A | C | 7 | a0001c0001t0001g0153a0001c0001t0002g0186a0001c0001t0002g0187others(4): Show | 7 | HG00544.hp2 HG01123.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.856+29297A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226943648 | ||||||
| chr2:226943660
|
T | TG | 121 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(118): Show | 123 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.856+29310dupG | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226943660 | |||||
| chr2:226943842
|
C | T | 1 | a0001c0001t0002g0234 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.856+29491C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226943842 | ||||||
| chr2:226944084
|
A | G | 1 | a0001c0001t0002g0197 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.856+29733A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226944084 | ||||||
| chr2:226944095
|
A | AGT | 7 | a0001c0005t0005g0219a0001c0005t0005g0220a0001c0007t0010g0222others(4): Show | 7 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.856+29746_856+2974 others(6): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226944095 | |||||
| chr2:226944271
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.856+29920G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226944271 | ||||||
| chr2:226944507
|
G | A | 1 | a0001c0001t0001g0039 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.856+30156G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226944507 | ||||||
| chr2:226944557
|
G | A | 2 | a0002c0006t0001g0176a0002c0006t0001g0177 | 2 | HG03654.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.856+30206G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226944557 | ||||||
| chr2:226944727
|
T | G | 1 | a0001c0001t0002g0218 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.856+30376T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226944727 | ||||||
| chr2:226945114
|
T | C | 1 | a0001c0001t0002g0006 | 2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.856+30763T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226945114 | ||||||
| chr2:226945139
|
A | T | 2 | a0002c0006t0001g0176a0002c0006t0001g0177 | 2 | HG03654.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.856+30788A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226945139 | ||||||
| chr2:226945145
|
G | GATT | 35 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0026others(32): Show | 37 | HG00408.hp1 HG00609.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.856+30824_856+3082 others(7): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226945145 | |||||
| chr2:226945145
|
G | GATTATT | 6 | a0001c0001t0001g0084a0001c0001t0002g0006a0001c0001t0002g0209others(3): Show | 7 | HG01884.hp2 HG02280.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.856+30821_856+3082 others(10): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226945145 | |||||
| chr2:226945145
|
G | GATTATTA others(2): Show |
70 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0021others(67): Show | 71 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.856+30818_856+3082 others(13): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226945145 | |||||
| chr2:226945145
|
G | GATTATTA others(5): Show |
14 | a0001c0001t0001g0019a0001c0001t0001g0035a0001c0001t0001g0036others(11): Show | 14 | HG01934.hp1 HG03130.hp2 HG03516.hp2 others(11): Show |
intron_variant | MODIFIER | c.856+30815_856+3082 others(16): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226945145 | |||||
| chr2:226945145
|
G | GATTATTA others(8): Show |
3 | a0001c0001t0001g0082a0001c0001t0002g0181a0001c0001t0002g0182 | 3 | HG01168.hp1 HG01169.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.856+30812_856+3082 others(19): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226945145 | |||||
| chr2:226945227
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.856+30876G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226945227 | ||||||
| chr2:226945246
|
C | G | 161 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(158): Show | 166 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.856+30895C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226945246 | ||||||
| chr2:226945487
|
A | G | 3 | a0001c0005t0005g0219a0001c0005t0005g0220a0001c0007t0010g0222 | 3 | HG02922.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.856+31136A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226945487 | ||||||
| chr2:226945621
|
C | G | 1 | a0001c0001t0002g0223 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.856+31270C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226945621 | ||||||
| chr2:226945636
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.856+31285A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226945636 | ||||||
| chr2:226945785
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.856+31434G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226945785 | ||||||
| chr2:226945926
|
A | G | 6 | a0001c0001t0012g0231a0002c0002t0001g0014a0002c0002t0004g0011others(3): Show | 6 | HG02145.hp1 HG02258.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.856+31575A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226945926 | ||||||
| chr2:226946050
|
C | A | 1 | a0001c0001t0001g0084 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.856+31699C>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226946050 | ||||||
| chr2:226946059
|
G | A | 14 | a0001c0001t0001g0021a0001c0001t0002g0195a0001c0001t0002g0199others(11): Show | 14 | HG00673.hp2 HG02083.hp1 HG04184.hp2 others(11): Show |
intron_variant | MODIFIER | c.856+31708G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226946059 | ||||||
| chr2:226946090
|
A | G | 14 | a0001c0001t0001g0021a0001c0001t0002g0195a0001c0001t0002g0199others(11): Show | 14 | HG00673.hp2 HG02083.hp1 HG04184.hp2 others(11): Show |
intron_variant | MODIFIER | c.856+31739A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226946090 | ||||||
| chr2:226946149
|
T | G | 1 | a0001c0001t0002g0196 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.856+31798T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226946149 | ||||||
| chr2:226946213
|
A | C | 1 | a0001c0004t0002g0202 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.856+31862A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226946213 | ||||||
| chr2:226946230
|
A | G | 4 | a0001c0001t0006g0244a0001c0001t0019g0017a0002c0002t0006g0229others(1): Show | 4 | HG02451.hp1 HG03139.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.856+31879A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226946230 | ||||||
| chr2:226946361
|
G | A | 1 | a0001c0007t0010g0222 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.856+32010G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226946361 | ||||||
| chr2:226946402
|
A | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(105): Show | 110 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.856+32051A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226946402 | ||||||
| chr2:226946457
|
G | A | 4 | a0003c0003t0004g0172a0003c0003t0004g0173a0003c0003t0004g0174others(1): Show | 4 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.856+32106G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226946457 | ||||||
| chr2:226946914
|
A | G | 2 | a0002c0006t0001g0176a0002c0006t0001g0177 | 2 | HG03654.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.856+32563A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226946914 | ||||||
| chr2:226947096
|
C | T | 1 | a0001c0001t0001g0087 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.856+32745C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226947096 | ||||||
| chr2:226947107
|
T | C | 1 | a0001c0008t0001g0076 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.856+32756T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226947107 | ||||||
| chr2:226947242
|
C | T | 4 | a0001c0001t0006g0244a0001c0001t0019g0017a0002c0002t0006g0229others(1): Show | 4 | HG02451.hp1 HG03139.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.856+32891C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226947242 | ||||||
| chr2:226947279
|
A | T | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG00558.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.856+32928A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226947279 | ||||||
| chr2:226947590
|
T | C | 4 | a0001c0001t0006g0244a0001c0001t0019g0017a0002c0002t0006g0229others(1): Show | 4 | HG02451.hp1 HG03139.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.856+33239T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226947590 | ||||||
| chr2:226947840
|
A | T | 4 | a0001c0001t0001g0049a0001c0001t0001g0053a0001c0001t0001g0056others(1): Show | 4 | NA18939.hp2 NA18989.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.856+33489A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226947840 | ||||||
| chr2:226948121
|
T | C | 1 | a0001c0001t0001g0133 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.856+33770T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226948121 | ||||||
| chr2:226948164
|
G | A | 108 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(105): Show | 110 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.856+33813G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226948164 | ||||||
| chr2:226948166
|
G | A | 1 | a0001c0001t0019g0017 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.856+33815G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226948166 | ||||||
| chr2:226948166
|
G | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(105): Show | 110 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.856+33815G>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226948166 | ||||||
| chr2:226948474
|
G | A | 1 | a0001c0001t0001g0075 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.856+34123G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226948474 | ||||||
| chr2:226948491
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.856+34140G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226948491 | ||||||
| chr2:226948532
|
C | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(105): Show | 110 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.856+34181C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226948532 | ||||||
| chr2:226948556
|
T | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(105): Show | 110 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.856+34205T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226948556 | ||||||
| chr2:226948563
|
A | T | 4 | a0001c0001t0006g0244a0001c0001t0019g0017a0002c0002t0006g0229others(1): Show | 4 | HG02451.hp1 HG03139.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.856+34212A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226948563 | ||||||
| chr2:226948564
|
T | TA | 39 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0023others(36): Show | 40 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.856+34234dupA | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226948564 | |||||
| chr2:226948564
|
T | TAA | 20 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0081others(17): Show | 22 | HG00140.hp1 HG00609.hp2 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.856+34233_856+3423 others(6): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226948564 | |||||
| chr2:226948564
|
T | TAAA | 6 | a0001c0001t0001g0008a0001c0001t0001g0119a0001c0001t0001g0141others(3): Show | 6 | HG03516.hp1 NA18949.hp1 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.856+34232_856+3423 others(7): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226948564 | |||||
| chr2:226948570
|
A | AAAAT | 108 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(105): Show | 110 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.856+34222_856+3422 others(8): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226948570 | |||||
| chr2:226948576
|
A | AT | 4 | a0001c0001t0006g0244a0001c0001t0019g0017a0002c0002t0006g0229others(1): Show | 4 | HG02451.hp1 HG03139.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.856+34225_856+3422 others(5): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226948576 | ||||||
| chr2:226948576
|
A | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(105): Show | 110 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.856+34225A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226948576 | ||||||
| chr2:226948581
|
A | T | 4 | a0001c0001t0006g0244a0001c0001t0019g0017a0002c0002t0006g0229others(1): Show | 4 | HG02451.hp1 HG03139.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.856+34230A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226948581 | ||||||
| chr2:226948587
|
G | A | 4 | a0001c0001t0006g0244a0001c0001t0019g0017a0002c0002t0006g0229others(1): Show | 4 | HG02451.hp1 HG03139.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.856+34236G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226948587 | ||||||
| chr2:226948601
|
T | TA | 120 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(117): Show | 122 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.856+34259dupA | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226948601 | |||||
| chr2:226948645
|
A | T | 5 | a0001c0001t0001g0054a0001c0001t0001g0085a0001c0001t0001g0100others(2): Show | 5 | NA18951.hp2 NA18972.hp2 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.856+34294A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226948645 | ||||||
| chr2:226948728
|
A | T | 42 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(39): Show | 45 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.856+34377A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226948728 | ||||||
| chr2:226948797
|
A | G | 3 | a0001c0001t0005g0221a0002c0002t0004g0237a0002c0002t0004g0238 | 3 | HG02145.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.856+34446A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226948797 | ||||||
| chr2:226948821
|
G | A | 4 | a0001c0001t0006g0244a0001c0001t0019g0017a0002c0002t0006g0229others(1): Show | 4 | HG02451.hp1 HG03139.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.856+34470G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226948821 | ||||||
| chr2:226948842
|
T | G | 1 | a0001c0001t0001g0129 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.856+34491T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226948842 | ||||||
| chr2:226948894
|
C | T | 1 | a0001c0001t0001g0165 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.856+34543C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226948894 | ||||||
| chr2:226948960
|
A | T | 2 | a0002c0006t0001g0176a0002c0006t0001g0177 | 2 | HG03654.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.856+34609A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226948960 | ||||||
| chr2:226949050
|
A | G | 1 | a0001c0001t0001g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.856+34699A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226949050 | ||||||
| chr2:226949283
|
A | G | 1 | a0001c0001t0007g0057 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.856+34932A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226949283 | ||||||
| chr2:226949363
|
G | C | 1 | a0001c0001t0001g0135 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.856+35012G>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226949363 | ||||||
| chr2:226949736
|
C | T | 2 | a0002c0006t0001g0176a0002c0006t0001g0177 | 2 | HG03654.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.856+35385C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226949736 | ||||||
| chr2:226949769
|
T | A | 1 | a0004c0009t0001g0242 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.856+35418T>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226949769 | ||||||
| chr2:226949793
|
CT | C | 3 | a0001c0001t0002g0195a0001c0001t0002g0199a0001c0001t0002g0200 | 3 | HG02083.hp1 NA18956.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.856+35445delT | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226949793 | |||||
| chr2:226950027
|
A | G | 4 | a0003c0003t0004g0172a0003c0003t0004g0173a0003c0003t0004g0174others(1): Show | 4 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.856+35676A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226950027 | ||||||
| chr2:226950041
|
T | C | 121 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(118): Show | 123 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.856+35690T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226950041 | ||||||
| chr2:226950311
|
CTTATT | C | 2 | a0002c0006t0001g0176a0002c0006t0001g0177 | 2 | HG03654.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.856+35967_856+3597 others(9): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226950311 | |||||
| chr2:226950349
|
C | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(116): Show | 121 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.856+35998C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226950349 | ||||||
| chr2:226950491
|
C | T | 3 | a0001c0001t0002g0189a0001c0001t0002g0192a0001c0001t0002g0193 | 3 | HG02922.hp1 HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.856+36140C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226950491 | ||||||
| chr2:226950495
|
A | G | 4 | a0001c0001t0006g0244a0001c0001t0019g0017a0002c0002t0006g0229others(1): Show | 4 | HG02451.hp1 HG03139.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.856+36144A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226950495 | ||||||
| chr2:226950570
|
A | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(105): Show | 110 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.856+36219A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226950570 | ||||||
| chr2:226950647
|
T | TC | 7 | a0001c0005t0005g0219a0001c0005t0005g0220a0001c0007t0010g0222others(4): Show | 7 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.856+36297dupC | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226950647 | |||||
| chr2:226951039
|
G | A | 1 | a0001c0001t0001g0047 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.856+36688G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226951039 | ||||||
| chr2:226951080
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.856+36729C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226951080 | ||||||
| chr2:226951342
|
T | C | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | NA18972.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.856+36991T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226951342 | ||||||
| chr2:226951484
|
T | A | 121 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(118): Show | 123 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.856+37133T>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226951484 | ||||||
| chr2:226951624
|
A | G | 6 | a0001c0001t0012g0231a0002c0002t0001g0014a0002c0002t0004g0011others(3): Show | 6 | HG02145.hp1 HG02258.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.856+37273A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226951624 | ||||||
| chr2:226952083
|
G | A | 1 | a0002c0002t0004g0237 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.856+37732G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226952083 | ||||||
| chr2:226952200
|
A | G | 1 | a0001c0001t0003g0061 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.856+37849A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226952200 | ||||||
| chr2:226952220
|
T | G | 1 | a0001c0001t0001g0117 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.856+37869T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226952220 | ||||||
| chr2:226952283
|
T | G | 1 | a0001c0001t0002g0196 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.856+37932T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226952283 | ||||||
| chr2:226952293
|
GT | G | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(191): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.856+37964delT | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226952293 | |||||
| chr2:226952293
|
GTT | G | 5 | a0001c0001t0001g0059a0001c0001t0001g0075a0001c0001t0001g0083others(2): Show | 5 | HG00558.hp2 HG01168.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.856+37963_856+3796 others(6): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226952293 | |||||
| chr2:226952438
|
C | T | 2 | a0002c0006t0001g0176a0002c0006t0001g0177 | 2 | HG03654.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.856+38087C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226952438 | ||||||
| chr2:226952733
|
C | A | 1 | a0001c0001t0001g0019 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.856+38382C>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226952733 | ||||||
| chr2:226952852
|
A | C | 1 | a0001c0001t0001g0119 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.856+38501A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226952852 | ||||||
| chr2:226953276
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.856+38925A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226953276 | ||||||
| chr2:226953376
|
C | A | 10 | a0001c0001t0001g0042a0001c0001t0001g0054a0001c0001t0001g0085others(7): Show | 10 | HG01169.hp1 HG01975.hp1 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.856+39025C>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226953376 | ||||||
| chr2:226953499
|
G | A | 2 | a0001c0001t0002g0206a0001c0001t0002g0207 | 2 | NA18949.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.856+39148G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226953499 | ||||||
| chr2:226953913
|
C | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(95): Show | 100 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.856+39562C>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226953913 | ||||||
| chr2:226953938
|
G | A | 4 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(1): Show | 4 | HG00140.hp1 HG01255.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.856+39587G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226953938 | ||||||
| chr2:226954024
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.856+39673C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226954024 | ||||||
| chr2:226954157
|
C | T | 1 | a0001c0001t0012g0231 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.856+39806C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226954157 | ||||||
| chr2:226954185
|
G | A | 4 | a0001c0001t0006g0244a0001c0001t0019g0017a0002c0002t0006g0229others(1): Show | 4 | HG02451.hp1 HG03139.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.856+39834G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226954185 | ||||||
| chr2:226954307
|
C | G | 39 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(36): Show | 42 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.856+39956C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226954307 | ||||||
| chr2:226954334
|
C | A | 108 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(105): Show | 110 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.856+39983C>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226954334 | ||||||
| chr2:226954379
|
G | A | 4 | a0001c0001t0006g0244a0001c0001t0019g0017a0002c0002t0006g0229others(1): Show | 4 | HG02451.hp1 HG03139.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.856+40028G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226954379 | ||||||
| chr2:226954416
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.856+40065G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226954416 | ||||||
| chr2:226955019
|
G | A | 1 | a0001c0001t0009g0140 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.857-40412G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226955019 | ||||||
| chr2:226955023
|
T | C | 1 | a0001c0001t0001g0099 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.857-40408T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226955023 | ||||||
| chr2:226955612
|
A | C | 1 | a0001c0001t0001g0086 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.857-39819A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226955612 | ||||||
| chr2:226955785
|
A | G | 1 | a0001c0007t0010g0222 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.857-39646A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226955785 | ||||||
| chr2:226955808
|
A | G | 7 | a0001c0005t0005g0219a0001c0005t0005g0220a0001c0007t0010g0222others(4): Show | 7 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.857-39623A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226955808 | ||||||
| chr2:226955913
|
G | C | 4 | a0001c0001t0006g0244a0001c0001t0019g0017a0002c0002t0006g0229others(1): Show | 4 | HG02451.hp1 HG03139.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.857-39518G>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226955913 | ||||||
| chr2:226956176
|
C | G | 1 | a0001c0001t0001g0073 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.857-39255C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226956176 | ||||||
| chr2:226956193
|
G | A | 2 | a0001c0001t0001g0126a0001c0001t0001g0127 | 2 | NA18995.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.857-39238G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226956193 | ||||||
| chr2:226956227
|
G | A | 107 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(104): Show | 109 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.857-39204G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226956227 | ||||||
| chr2:226956304
|
A | T | 42 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(39): Show | 45 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.857-39127A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226956304 | ||||||
| chr2:226956363
|
G | A | 4 | a0001c0001t0001g0042a0001c0001t0001g0097a0001c0001t0001g0102others(1): Show | 4 | HG01169.hp1 HG01975.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.857-39068G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226956363 | ||||||
| chr2:226956454
|
A | G | 2 | a0001c0001t0007g0057a0001c0001t0007g0069 | 2 | HG02074.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.857-38977A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226956454 | ||||||
| chr2:226956487
|
C | T | 1 | a0001c0001t0001g0171 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.857-38944C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226956487 | ||||||
| chr2:226956863
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.857-38568G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226956863 | ||||||
| chr2:226957118
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.857-38313G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226957118 | ||||||
| chr2:226957129
|
A | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(105): Show | 110 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.857-38302A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226957129 | ||||||
| chr2:226957174
|
C | T | 5 | a0001c0001t0002g0178a0001c0001t0002g0232a0001c0001t0002g0233others(2): Show | 5 | HG02647.hp1 HG02809.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.857-38257C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226957174 | ||||||
| chr2:226957570
|
CA | C | 118 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(115): Show | 120 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.857-37851delA | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226957570 | |||||
| chr2:226957724
|
T | C | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(184): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.857-37707T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226957724 | ||||||
| chr2:226957901
|
C | T | 2 | a0001c0001t0001g0110a0001c0001t0001g0114 | 2 | NA18956.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.857-37530C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226957901 | ||||||
| chr2:226957988
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0124 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.857-37443G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226957988 | ||||||
| chr2:226958053
|
G | A | 1 | a0001c0001t0003g0258 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.857-37378G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226958053 | ||||||
| chr2:226958287
|
C | A | 1 | a0001c0001t0001g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.857-37144C>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226958287 | ||||||
| chr2:226958318
|
T | G | 3 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169 | 3 | HG01934.hp2 HG02451.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.857-37113T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226958318 | ||||||
| chr2:226958342
|
G | C | 1 | a0001c0001t0002g0197 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.857-37089G>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226958342 | ||||||
| chr2:226958418
|
G | A | 42 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(39): Show | 45 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.857-37013G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226958418 | ||||||
| chr2:226958702
|
C | CTG | 72 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(69): Show | 74 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.857-36687_857-3668 others(6): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226958702 | |||||
| chr2:226958702
|
C | CTGTG | 40 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0031others(37): Show | 40 | HG00544.hp1 HG00544.hp2 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.857-36689_857-3668 others(8): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226958702 | |||||
| chr2:226958702
|
C | CTGTGTG | 13 | a0001c0001t0001g0021a0001c0001t0001g0036a0001c0001t0001g0051others(10): Show | 13 | HG00609.hp1 HG01123.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.857-36691_857-3668 others(10): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226958702 | |||||
| chr2:226958702
|
C | CTGTGTGT others(1): Show |
5 | a0001c0001t0001g0086a0001c0001t0002g0179a0001c0001t0002g0190others(2): Show | 5 | HG01192.hp2 HG02074.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.857-36693_857-3668 others(12): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226958702 | |||||
| chr2:226958702
|
C | CTGTGTGT others(5): Show |
1 | a0001c0001t0002g0208 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.857-36697_857-3668 others(16): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226958702 | |||||
| chr2:226958702
|
CTG | C | 29 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(26): Show | 31 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(28): Show |
intron_variant | MODIFIER | c.857-36687_857-3668 others(6): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226958702 | |||||
| chr2:226958702
|
CTGTG | C | 33 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0047others(30): Show | 35 | HG00140.hp1 HG00609.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.857-36689_857-3668 others(8): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226958702 | |||||
| chr2:226958702
|
CTGTGTGT others(5): Show |
C | 1 | a0001c0001t0002g0194 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.857-36697_857-3668 others(16): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226958702 | |||||
| chr2:226958702
|
CTGTGTGT others(7): Show |
C | 3 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0013g0198 | 3 | HG02818.hp1 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.857-36699_857-3668 others(18): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226958702 | |||||
| chr2:226958919
|
C | A | 1 | a0001c0007t0010g0222 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.857-36512C>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226958919 | ||||||
| chr2:226959132
|
G | A | 3 | a0001c0001t0001g0083a0001c0001t0001g0094a0001c0001t0001g0117 | 3 | HG00558.hp2 HG00609.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.857-36299G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226959132 | ||||||
| chr2:226959705
|
A | G | 4 | a0001c0001t0006g0244a0001c0001t0019g0017a0002c0002t0006g0229others(1): Show | 4 | HG02451.hp1 HG03139.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.857-35726A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226959705 | ||||||
| chr2:226959898
|
C | T | 98 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(95): Show | 100 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.857-35533C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226959898 | ||||||
| chr2:226960030
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.857-35401A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226960030 | ||||||
| chr2:226960061
|
A | G | 1 | a0001c0001t0002g0206 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.857-35370A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226960061 | ||||||
| chr2:226960119
|
G | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(95): Show | 99 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.857-35312G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226960119 | ||||||
| chr2:226960355
|
G | C | 7 | a0001c0005t0005g0219a0001c0005t0005g0220a0001c0007t0010g0222others(4): Show | 7 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.857-35076G>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226960355 | ||||||
| chr2:226960394
|
G | A | 8 | a0001c0001t0001g0033a0001c0001t0001g0108a0001c0001t0001g0110others(5): Show | 8 | HG00423.hp1 HG00621.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.857-35037G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226960394 | ||||||
| chr2:226960484
|
A | C | 1 | a0001c0001t0002g0209 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.857-34947A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226960484 | ||||||
| chr2:226960635
|
C | G | 6 | a0001c0001t0012g0231a0002c0002t0001g0014a0002c0002t0004g0011others(3): Show | 6 | HG02145.hp1 HG02258.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.857-34796C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226960635 | ||||||
| chr2:226960648
|
A | C | 1 | a0001c0001t0001g0088 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.857-34783A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226960648 | ||||||
| chr2:226960666
|
G | T | 9 | a0001c0001t0005g0221a0001c0001t0012g0231a0002c0002t0001g0014others(6): Show | 9 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.857-34765G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226960666 | ||||||
| chr2:226960900
|
A | G | 4 | a0001c0001t0006g0244a0001c0001t0019g0017a0002c0002t0006g0229others(1): Show | 4 | HG02451.hp1 HG03139.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.857-34531A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226960900 | ||||||
| chr2:226961051
|
G | T | 1 | a0001c0001t0001g0093 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.857-34380G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226961051 | ||||||
| chr2:226961060
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.857-34371G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226961060 | ||||||
| chr2:226961121
|
C | A | 1 | a0001c0001t0001g0078 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.857-34310C>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226961121 | ||||||
| chr2:226961535
|
T | G | 1 | a0001c0001t0001g0018 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.857-33896T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226961535 | ||||||
| chr2:226961542
|
A | AT | 98 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(95): Show | 100 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.857-33880dupT | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226961542 | |||||
| chr2:226961679
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.857-33752T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226961679 | ||||||
| chr2:226961954
|
T | C | 4 | a0001c0001t0006g0244a0001c0001t0019g0017a0002c0002t0006g0229others(1): Show | 4 | HG02451.hp1 HG03139.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.857-33477T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226961954 | ||||||
| chr2:226962263
|
A | G | 2 | a0001c0001t0001g0110a0001c0001t0001g0114 | 2 | NA18956.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.857-33168A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226962263 | ||||||
| chr2:226962371
|
T | C | 1 | a0001c0001t0001g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.857-33060T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226962371 | ||||||
| chr2:226962491
|
C | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.857-32940C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226962491 | ||||||
| chr2:226963024
|
G | T | 98 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(95): Show | 100 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.857-32407G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226963024 | ||||||
| chr2:226963184
|
TA | T | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(254): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.857-32239delA | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226963184 | |||||
| chr2:226963232
|
T | C | 9 | a0001c0001t0005g0221a0001c0001t0012g0231a0002c0002t0001g0014others(6): Show | 9 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.857-32199T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226963232 | ||||||
| chr2:226963561
|
A | G | 4 | a0003c0003t0004g0172a0003c0003t0004g0173a0003c0003t0004g0174others(1): Show | 4 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.857-31870A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226963561 | ||||||
| chr2:226963619
|
A | T | 121 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(118): Show | 123 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.857-31812A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226963619 | ||||||
| chr2:226963734
|
C | T | 1 | a0001c0007t0010g0222 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.857-31697C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226963734 | ||||||
| chr2:226963738
|
A | G | 7 | a0001c0001t0006g0244a0001c0001t0019g0017a0001c0005t0005g0219others(4): Show | 7 | HG02451.hp1 HG02922.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.857-31693A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226963738 | ||||||
| chr2:226963876
|
C | G | 2 | a0001c0001t0009g0140a0001c0001t0009g0149 | 2 | HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.857-31555C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226963876 | ||||||
| chr2:226963943
|
T | G | 1 | a0001c0001t0001g0144 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.857-31488T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226963943 | ||||||
| chr2:226963952
|
T | C | 7 | a0001c0005t0005g0219a0001c0005t0005g0220a0001c0007t0010g0222others(4): Show | 7 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.857-31479T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226963952 | ||||||
| chr2:226964007
|
C | T | 4 | a0003c0003t0004g0172a0003c0003t0004g0173a0003c0003t0004g0174others(1): Show | 4 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.857-31424C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226964007 | ||||||
| chr2:226964718
|
G | T | 2 | a0002c0006t0001g0176a0002c0006t0001g0177 | 2 | HG03654.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.857-30713G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226964718 | ||||||
| chr2:226964922
|
A | T | 9 | a0001c0001t0005g0221a0001c0001t0012g0231a0002c0002t0001g0014others(6): Show | 9 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.857-30509A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226964922 | ||||||
| chr2:226964990
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.857-30441G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226964990 | ||||||
| chr2:226965150
|
G | A | 1 | a0001c0001t0001g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.857-30281G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226965150 | ||||||
| chr2:226965364
|
A | G | 6 | a0001c0001t0012g0231a0002c0002t0001g0014a0002c0002t0004g0011others(3): Show | 6 | HG02145.hp1 HG02258.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.857-30067A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226965364 | ||||||
| chr2:226965465
|
G | T | 1 | a0001c0001t0002g0217 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.857-29966G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226965465 | ||||||
| chr2:226965639
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.857-29792A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226965639 | ||||||
| chr2:226965698
|
G | T | 98 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(95): Show | 100 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.857-29733G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226965698 | ||||||
| chr2:226965727
|
C | T | 2 | a0002c0006t0001g0176a0002c0006t0001g0177 | 2 | HG03654.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.857-29704C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226965727 | ||||||
| chr2:226965767
|
T | C | 4 | a0001c0005t0005g0219a0001c0005t0005g0220a0001c0007t0010g0222others(1): Show | 4 | HG02258.hp1 HG02922.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.857-29664T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226965767 | ||||||
| chr2:226966097
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.857-29334G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226966097 | ||||||
| chr2:226966264
|
A | C | 1 | a0001c0001t0001g0081 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.857-29167A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226966264 | ||||||
| chr2:226966295
|
C | A | 1 | a0001c0001t0001g0037 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.857-29136C>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226966295 | ||||||
| chr2:226966344
|
A | G | 1 | a0001c0001t0019g0017 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.857-29087A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226966344 | ||||||
| chr2:226966357
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.857-29074C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226966357 | ||||||
| chr2:226966373
|
T | C | 3 | a0001c0005t0005g0219a0001c0005t0005g0220a0001c0007t0010g0222 | 3 | HG02922.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.857-29058T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226966373 | ||||||
| chr2:226966419
|
C | T | 1 | a0001c0001t0002g0179 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.857-29012C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226966419 | ||||||
| chr2:226966420
|
G | A | 12 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0002g0194others(9): Show | 12 | HG01884.hp1 HG02280.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.857-29011G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226966420 | ||||||
| chr2:226966431
|
G | A | 1 | a0001c0001t0001g0154 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.857-29000G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226966431 | ||||||
| chr2:226966464
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.857-28967C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226966464 | ||||||
| chr2:226966837
|
A | AT | 20 | a0001c0001t0001g0133a0001c0001t0005g0221a0001c0001t0006g0244others(17): Show | 20 | HG02109.hp2 HG02145.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.857-28580dupT | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226966837 | |||||
| chr2:226966837
|
AT | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(96): Show | 101 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.857-28580delT | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226966837 | |||||
| chr2:226967122
|
A | T | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060 | 3 | HG02622.hp2 HG02886.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.857-28309A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226967122 | ||||||
| chr2:226967153
|
C | T | 4 | a0001c0001t0006g0244a0001c0001t0019g0017a0002c0002t0006g0229others(1): Show | 4 | HG02451.hp1 HG03139.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.857-28278C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226967153 | ||||||
| chr2:226967168
|
G | A | 1 | a0001c0001t0015g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.857-28263G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226967168 | ||||||
| chr2:226967208
|
G | A | 1 | a0001c0001t0002g0235 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.857-28223G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226967208 | ||||||
| chr2:226967515
|
C | T | 1 | a0001c0001t0001g0025 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.857-27916C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226967515 | ||||||
| chr2:226967677
|
T | A | 4 | a0003c0003t0004g0172a0003c0003t0004g0173a0003c0003t0004g0174others(1): Show | 4 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.857-27754T>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226967677 | ||||||
| chr2:226967706
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.857-27725G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226967706 | ||||||
| chr2:226967735
|
A | G | 4 | a0001c0001t0006g0244a0001c0001t0019g0017a0002c0002t0006g0229others(1): Show | 4 | HG02451.hp1 HG03139.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.857-27696A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226967735 | ||||||
| chr2:226967914
|
C | G | 3 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0082 | 3 | HG01934.hp1 HG01975.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.857-27517C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226967914 | ||||||
| chr2:226968399
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.857-27032C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226968399 | ||||||
| chr2:226968527
|
C | G | 1 | a0001c0001t0001g0041 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.857-26904C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226968527 | ||||||
| chr2:226968540
|
T | C | 3 | a0001c0001t0001g0146a0001c0001t0001g0157a0001c0001t0001g0165 | 3 | NA18994.hp2 NA18995.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.857-26891T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226968540 | ||||||
| chr2:226968840
|
C | G | 1 | a0001c0001t0019g0017 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.857-26591C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226968840 | ||||||
| chr2:226968942
|
GT | G | 104 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(101): Show | 106 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.857-26487delT | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226968942 | |||||
| chr2:226969153
|
G | A | 102 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(99): Show | 104 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.857-26278G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226969153 | ||||||
| chr2:226969229
|
T | A | 1 | a0001c0001t0001g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.857-26202T>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226969229 | ||||||
| chr2:226969271
|
T | G | 1 | a0001c0001t0019g0017 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.857-26160T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226969271 | ||||||
| chr2:226969341
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.857-26090C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226969341 | ||||||
| chr2:226969394
|
C | CT | 6 | a0001c0001t0001g0083a0001c0001t0006g0244a0002c0002t0006g0229others(3): Show | 6 | HG00558.hp2 HG03139.hp2 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.857-26017dupT | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226969394 | |||||
| chr2:226969394
|
C | CTTT | 5 | a0001c0001t0001g0123a0001c0001t0002g0181a0001c0001t0002g0210others(2): Show | 5 | HG01168.hp1 HG02897.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.857-26019_857-2601 others(7): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226969394 | |||||
| chr2:226969394
|
C | CTTTT | 89 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(86): Show | 91 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.857-26020_857-2601 others(8): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226969394 | |||||
| chr2:226969605
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.857-25826G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226969605 | ||||||
| chr2:226969633
|
T | G | 98 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(95): Show | 100 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.857-25798T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226969633 | ||||||
| chr2:226969989
|
T | TC | 84 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(81): Show | 86 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.857-25432dupC | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226969989 | |||||
| chr2:226969989
|
T | TCC | 22 | a0001c0001t0001g0021a0001c0001t0001g0035a0001c0001t0001g0036others(19): Show | 22 | HG00673.hp2 HG01192.hp2 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.857-25433_857-2543 others(6): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226969989 | |||||
| chr2:226970497
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.857-24934C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226970497 | ||||||
| chr2:226970746
|
T | C | 3 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169 | 3 | HG01934.hp2 HG02451.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.857-24685T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226970746 | ||||||
| chr2:226970864
|
C | T | 42 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(39): Show | 45 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.857-24567C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226970864 | ||||||
| chr2:226970965
|
C | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(96): Show | 101 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.857-24466C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226970965 | ||||||
| chr2:226971369
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.857-24062G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226971369 | ||||||
| chr2:226971523
|
C | G | 105 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(102): Show | 107 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.857-23908C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226971523 | ||||||
| chr2:226971546
|
A | G | 99 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(96): Show | 101 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.857-23885A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226971546 | ||||||
| chr2:226971571
|
G | T | 4 | a0001c0001t0006g0244a0001c0001t0019g0017a0002c0002t0006g0229others(1): Show | 4 | HG02451.hp1 HG03139.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.857-23860G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226971571 | ||||||
| chr2:226971621
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.857-23810G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226971621 | ||||||
| chr2:226971909
|
CT | C | 101 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(98): Show | 103 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.857-23508delT | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226971909 | |||||
| chr2:226971918
|
T | C | 1 | a0002c0002t0006g0229 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.857-23513T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226971918 | ||||||
| chr2:226971992
|
C | T | 1 | a0001c0001t0002g0233 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.857-23439C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226971992 | ||||||
| chr2:226972026
|
T | G | 121 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(118): Show | 123 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.857-23405T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226972026 | ||||||
| chr2:226972104
|
G | C | 1 | a0001c0001t0001g0038 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.857-23327G>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226972104 | ||||||
| chr2:226972268
|
G | T | 121 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(118): Show | 123 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.857-23163G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226972268 | ||||||
| chr2:226972448
|
G | A | 3 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169 | 3 | HG01934.hp2 HG02451.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.857-22983G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226972448 | ||||||
| chr2:226972522
|
A | G | 3 | a0001c0001t0005g0221a0002c0002t0004g0237a0002c0002t0004g0238 | 3 | HG02145.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.857-22909A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226972522 | ||||||
| chr2:226972690
|
A | G | 3 | a0001c0005t0005g0219a0001c0005t0005g0220a0001c0007t0010g0222 | 3 | HG02922.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.857-22741A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226972690 | ||||||
| chr2:226972929
|
C | CA | 61 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(58): Show | 64 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.857-22486dupA | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226972929 | |||||
| chr2:226972929
|
C | CAA | 8 | a0001c0001t0001g0047a0001c0001t0001g0075a0001c0001t0001g0137others(5): Show | 8 | HG01255.hp2 HG02922.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.857-22487_857-2248 others(6): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226972929 | |||||
| chr2:226972929
|
CA | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(91): Show | 96 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.857-22486delA | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226972929 | |||||
| chr2:226972946
|
C | A | 3 | a0001c0005t0005g0219a0001c0005t0005g0220a0001c0007t0010g0222 | 3 | HG02922.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.857-22485C>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226972946 | ||||||
| chr2:226973324
|
T | G | 121 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(118): Show | 123 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.857-22107T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226973324 | ||||||
| chr2:226973822
|
G | A | 18 | a0001c0001t0001g0139a0001c0001t0001g0153a0001c0001t0001g0170others(15): Show | 18 | HG00544.hp2 HG01123.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.857-21609G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226973822 | ||||||
| chr2:226973893
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.857-21538C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226973893 | ||||||
| chr2:226973930
|
A | T | 4 | a0003c0003t0004g0172a0003c0003t0004g0173a0003c0003t0004g0174others(1): Show | 4 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.857-21501A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226973930 | ||||||
| chr2:226974173
|
G | C | 4 | a0001c0001t0006g0244a0001c0001t0019g0017a0002c0002t0006g0229others(1): Show | 4 | HG02451.hp1 HG03139.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.857-21258G>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226974173 | ||||||
| chr2:226974225
|
T | TTTTTA | 7 | a0001c0005t0005g0219a0001c0005t0005g0220a0001c0007t0010g0222others(4): Show | 7 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.857-21181_857-2117 others(9): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226974225 | |||||
| chr2:226974225
|
T | TTTTTATT others(3): Show |
104 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(101): Show | 106 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.857-21186_857-2117 others(14): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226974225 | |||||
| chr2:226974225
|
T | TTTTTATT others(8): Show |
4 | a0001c0001t0002g0179a0001c0001t0002g0195a0001c0001t0002g0199others(1): Show | 4 | HG01192.hp2 HG02818.hp1 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.857-21191_857-2117 others(19): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226974225 | |||||
| chr2:226974276
|
C | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0248a0002c0002t0001g0013 | 3 | HG03516.hp1 HG03540.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.857-21155C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226974276 | ||||||
| chr2:226974459
|
G | C | 1 | a0001c0001t0014g0211 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.857-20972G>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226974459 | ||||||
| chr2:226974562
|
C | A | 121 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(118): Show | 123 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.857-20869C>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226974562 | ||||||
| chr2:226974692
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.857-20739A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226974692 | ||||||
| chr2:226974760
|
GGCTGAGA others(17): Show |
G | 1 | a0001c0008t0001g0076 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.857-20654_857-2063 others(28): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226974760 | |||||
| chr2:226974823
|
C | T | 23 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(20): Show | 23 | HG00099.hp2 HG01071.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.857-20608C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226974823 | ||||||
| chr2:226974824
|
G | A | 2 | a0001c0001t0001g0041a0001c0001t0001g0052 | 2 | HG00738.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.857-20607G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226974824 | ||||||
| chr2:226974864
|
C | T | 1 | a0001c0001t0001g0084 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.857-20567C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226974864 | ||||||
| chr2:226974995
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.857-20436G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226974995 | ||||||
| chr2:226975161
|
T | C | 6 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0215others(3): Show | 6 | HG01106.hp1 HG02109.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.857-20270T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226975161 | ||||||
| chr2:226975389
|
G | A | 2 | a0001c0001t0001g0060a0001c0001t0002g0006 | 3 | HG03209.hp2 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.857-20042G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226975389 | ||||||
| chr2:226975578
|
C | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(96): Show | 101 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.857-19853C>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226975578 | ||||||
| chr2:226975623
|
G | A | 2 | a0001c0001t0003g0043a0001c0001t0003g0061 | 2 | HG01106.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.857-19808G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226975623 | ||||||
| chr2:226975826
|
A | C | 16 | a0001c0001t0005g0221a0001c0001t0012g0231a0001c0005t0005g0219others(13): Show | 16 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.857-19605A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226975826 | ||||||
| chr2:226975948
|
G | T | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | HG01255.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.857-19483G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226975948 | ||||||
| chr2:226976049
|
G | T | 2 | a0001c0001t0009g0140a0001c0001t0009g0149 | 2 | HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.857-19382G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226976049 | ||||||
| chr2:226976207
|
G | T | 98 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(95): Show | 100 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.857-19224G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226976207 | ||||||
| chr2:226976225
|
A | G | 1 | a0001c0001t0002g0207 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.857-19206A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226976225 | ||||||
| chr2:226976703
|
C | A | 1 | a0001c0001t0019g0017 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.857-18728C>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226976703 | ||||||
| chr2:226976743
|
A | G | 4 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0001g0147others(1): Show | 4 | NA18939.hp1 NA18978.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.857-18688A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226976743 | ||||||
| chr2:226977076
|
A | C | 121 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(118): Show | 123 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.857-18355A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226977076 | ||||||
| chr2:226977194
|
G | A | 1 | a0001c0001t0003g0249 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.857-18237G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226977194 | ||||||
| chr2:226977312
|
A | G | 251 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(248): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.857-18119A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226977312 | ||||||
| chr2:226977357
|
C | T | 1 | a0001c0001t0002g0179 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.857-18074C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226977357 | ||||||
| chr2:226977385
|
T | G | 1 | a0001c0001t0002g0216 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.857-18046T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226977385 | ||||||
| chr2:226977425
|
G | T | 1 | a0001c0001t0013g0198 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.857-18006G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226977425 | ||||||
| chr2:226977509
|
A | G | 16 | a0001c0001t0005g0221a0001c0001t0012g0231a0001c0005t0005g0219others(13): Show | 16 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.857-17922A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226977509 | ||||||
| chr2:226978176
|
C | T | 2 | a0001c0001t0009g0140a0001c0001t0009g0149 | 2 | HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.857-17255C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226978176 | ||||||
| chr2:226978282
|
A | T | 1 | a0001c0004t0002g0202 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.857-17149A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226978282 | ||||||
| chr2:226978294
|
C | T | 98 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(95): Show | 100 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.857-17137C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226978294 | ||||||
| chr2:226978419
|
T | C | 1 | a0001c0001t0002g0217 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.857-17012T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226978419 | ||||||
| chr2:226978683
|
A | T | 1 | a0001c0001t0009g0140 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.857-16748A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226978683 | ||||||
| chr2:226978773
|
C | T | 120 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(117): Show | 122 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.857-16658C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226978773 | ||||||
| chr2:226978918
|
C | G | 98 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(95): Show | 100 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.857-16513C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226978918 | ||||||
| chr2:226978919
|
G | A | 4 | a0003c0003t0004g0172a0003c0003t0004g0173a0003c0003t0004g0174others(1): Show | 4 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.857-16512G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226978919 | ||||||
| chr2:226979286
|
A | G | 1 | a0001c0001t0002g0184 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.857-16145A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226979286 | ||||||
| chr2:226979320
|
G | A | 1 | a0001c0001t0003g0241 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.857-16111G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226979320 | ||||||
| chr2:226979474
|
C | G | 1 | a0001c0001t0003g0256 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.857-15957C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226979474 | ||||||
| chr2:226979549
|
T | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(95): Show | 100 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.857-15882T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226979549 | ||||||
| chr2:226979705
|
G | A | 1 | a0001c0001t0002g0194 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.857-15726G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226979705 | ||||||
| chr2:226979740
|
G | A | 5 | a0001c0005t0005g0219a0003c0003t0004g0172a0003c0003t0004g0173others(2): Show | 5 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.857-15691G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226979740 | ||||||
| chr2:226979803
|
C | A | 1 | a0001c0001t0001g0032 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.857-15628C>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226979803 | ||||||
| chr2:226979966
|
T | C | 6 | a0001c0001t0006g0244a0001c0001t0019g0017a0002c0002t0006g0229others(3): Show | 6 | HG02451.hp1 HG03139.hp2 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.857-15465T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226979966 | ||||||
| chr2:226980005
|
A | G | 4 | a0001c0001t0002g0179a0001c0001t0002g0180a0001c0001t0002g0181others(1): Show | 4 | HG01168.hp1 HG01169.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.857-15426A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226980005 | ||||||
| chr2:226980295
|
C | T | 8 | a0001c0001t0001g0033a0001c0001t0001g0108a0001c0001t0001g0110others(5): Show | 8 | HG00423.hp1 HG00621.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.857-15136C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226980295 | ||||||
| chr2:226980700
|
A | G | 22 | a0001c0001t0005g0221a0001c0001t0006g0244a0001c0001t0012g0231others(19): Show | 22 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.857-14731A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226980700 | ||||||
| chr2:226980723
|
G | A | 3 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0109 | 3 | HG02040.hp2 NA19000.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.857-14708G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226980723 | ||||||
| chr2:226980829
|
T | C | 2 | a0001c0001t0009g0140a0001c0001t0009g0149 | 2 | HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.857-14602T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226980829 | ||||||
| chr2:226980935
|
C | T | 1 | a0001c0001t0001g0240 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.857-14496C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226980935 | ||||||
| chr2:226980939
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.857-14492G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226980939 | ||||||
| chr2:226981110
|
C | T | 1 | a0003c0003t0004g0175 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.857-14321C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226981110 | ||||||
| chr2:226981435
|
CA | C | 6 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0068others(3): Show | 6 | HG01515.hp1 HG03516.hp1 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.857-13982delA | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226981435 | |||||
| chr2:226981569
|
T | TAC | 112 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(109): Show | 114 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.857-13845_857-1384 others(6): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226981569 | |||||
| chr2:226981569
|
T | TACAC | 17 | a0001c0001t0001g0131a0001c0001t0002g0178a0001c0001t0002g0213others(14): Show | 17 | HG01106.hp1 HG02109.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.857-13847_857-1384 others(8): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226981569 | |||||
| chr2:226981569
|
T | TACACACA others(1): Show |
12 | a0001c0001t0005g0221a0001c0001t0012g0231a0001c0005t0005g0219others(9): Show | 12 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.857-13851_857-1384 others(12): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226981569 | |||||
| chr2:226981569
|
T | TACACACA others(7): Show |
4 | a0003c0003t0004g0172a0003c0003t0004g0173a0003c0003t0004g0174others(1): Show | 4 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.857-13857_857-1384 others(18): Show |
RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 226981569 | |||||
| chr2:226981709
|
G | A | 15 | a0001c0001t0001g0037a0001c0001t0001g0044a0001c0001t0001g0058others(12): Show | 15 | HG00099.hp2 HG01071.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.857-13722G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226981709 | ||||||
| chr2:226981808
|
A | G | 99 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(96): Show | 101 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.857-13623A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226981808 | ||||||
| chr2:226981936
|
G | A | 3 | a0001c0001t0001g0021a0001c0001t0002g0224a0001c0001t0002g0225 | 3 | HG00673.hp2 NA18979.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.857-13495G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226981936 | ||||||
| chr2:226982161
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.857-13270C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226982161 | ||||||
| chr2:226982203
|
T | C | 1 | a0001c0001t0002g0213 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.857-13228T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226982203 | ||||||
| chr2:226982216
|
A | G | 99 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(96): Show | 101 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.857-13215A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226982216 | ||||||
| chr2:226982340
|
C | T | 4 | a0001c0001t0001g0049a0001c0001t0001g0053a0001c0001t0001g0056others(1): Show | 4 | NA18939.hp2 NA18989.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.857-13091C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226982340 | ||||||
| chr2:226982502
|
T | C | 1 | a0001c0001t0002g0224 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.857-12929T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226982502 | ||||||
| chr2:226982690
|
G | A | 2 | a0001c0001t0001g0008a0001c0001t0001g0248 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.857-12741G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226982690 | ||||||
| chr2:226982914
|
T | G | 99 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(96): Show | 101 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.857-12517T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226982914 | ||||||
| chr2:226983243
|
A | G | 1 | a0001c0007t0010g0222 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.857-12188A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226983243 | ||||||
| chr2:226983267
|
C | T | 3 | a0001c0001t0005g0221a0002c0002t0004g0237a0002c0002t0004g0238 | 3 | HG02145.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.857-12164C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226983267 | ||||||
| chr2:226983378
|
G | T | 3 | a0001c0001t0006g0244a0002c0002t0006g0229a0002c0002t0006g0230 | 3 | HG03139.hp2 NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.857-12053G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226983378 | ||||||
| chr2:226983403
|
C | A | 2 | a0002c0006t0001g0176a0002c0006t0001g0177 | 2 | HG03654.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.857-12028C>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226983403 | ||||||
| chr2:226983414
|
G | A | 2 | a0002c0006t0001g0176a0002c0006t0001g0177 | 2 | HG03654.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.857-12017G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226983414 | ||||||
| chr2:226983886
|
G | T | 4 | a0001c0001t0006g0244a0001c0001t0019g0017a0002c0002t0006g0229others(1): Show | 4 | HG02451.hp1 HG03139.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.857-11545G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226983886 | ||||||
| chr2:226983909
|
C | T | 1 | a0001c0001t0002g0187 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.857-11522C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226983909 | ||||||
| chr2:226983939
|
A | G | 1 | a0001c0001t0001g0165 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.857-11492A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226983939 | ||||||
| chr2:226983988
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.857-11443G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226983988 | ||||||
| chr2:226984148
|
G | A | 4 | a0003c0003t0004g0172a0003c0003t0004g0173a0003c0003t0004g0174others(1): Show | 4 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.857-11283G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226984148 | ||||||
| chr2:226984149
|
T | C | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(254): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.857-11282T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226984149 | ||||||
| chr2:226984152
|
G | C | 3 | a0001c0005t0005g0219a0001c0005t0005g0220a0001c0007t0010g0222 | 3 | HG02922.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.857-11279G>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226984152 | ||||||
| chr2:226984493
|
T | G | 1 | a0001c0001t0001g0123 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.857-10938T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226984493 | ||||||
| chr2:226984539
|
T | A | 121 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(118): Show | 123 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.857-10892T>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226984539 | ||||||
| chr2:226984596
|
G | A | 3 | a0001c0005t0005g0219a0001c0005t0005g0220a0001c0007t0010g0222 | 3 | HG02922.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.857-10835G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226984596 | ||||||
| chr2:226984640
|
T | A | 1 | a0001c0001t0001g0123 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.857-10791T>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226984640 | ||||||
| chr2:226984968
|
T | C | 6 | a0001c0001t0012g0231a0002c0002t0001g0014a0002c0002t0004g0011others(3): Show | 6 | HG02145.hp1 HG02258.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.857-10463T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226984968 | ||||||
| chr2:226985493
|
G | C | 41 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(38): Show | 44 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.857-9938G>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226985493 | ||||||
| chr2:226985559
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.857-9872G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226985559 | ||||||
| chr2:226985645
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.857-9786T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226985645 | ||||||
| chr2:226985749
|
C | G | 101 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(98): Show | 103 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.857-9682C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226985749 | ||||||
| chr2:226985884
|
T | A | 4 | a0001c0001t0006g0244a0001c0001t0019g0017a0002c0002t0006g0229others(1): Show | 4 | HG02451.hp1 HG03139.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.857-9547T>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226985884 | ||||||
| chr2:226985887
|
C | T | 1 | a0002c0002t0004g0237 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.857-9544C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226985887 | ||||||
| chr2:226986060
|
A | G | 105 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(102): Show | 107 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.857-9371A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226986060 | ||||||
| chr2:226986138
|
C | G | 1 | a0001c0001t0001g0100 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.857-9293C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226986138 | ||||||
| chr2:226986157
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.857-9274T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226986157 | ||||||
| chr2:226986273
|
C | T | 4 | a0003c0003t0004g0172a0003c0003t0004g0173a0003c0003t0004g0174others(1): Show | 4 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.857-9158C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226986273 | ||||||
| chr2:226986452
|
A | C | 3 | a0001c0001t0001g0044a0001c0001t0001g0065a0001c0001t0001g0067 | 3 | HG02647.hp2 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.857-8979A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226986452 | ||||||
| chr2:226986562
|
C | T | 1 | a0001c0001t0001g0162 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.857-8869C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226986562 | ||||||
| chr2:226986570
|
A | C | 24 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(21): Show | 24 | HG00099.hp2 HG01071.hp2 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.857-8861A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226986570 | ||||||
| chr2:226986658
|
G | A | 1 | a0001c0001t0011g0183 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.857-8773G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226986658 | ||||||
| chr2:226986877
|
C | T | 4 | a0001c0001t0006g0244a0001c0001t0019g0017a0002c0002t0006g0229others(1): Show | 4 | HG02451.hp1 HG03139.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.857-8554C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226986877 | ||||||
| chr2:226986878
|
G | C | 2 | a0001c0001t0001g0146a0001c0001t0001g0157 | 2 | NA18994.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.857-8553G>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226986878 | ||||||
| chr2:226986927
|
C | G | 2 | a0001c0001t0001g0034a0001c0001t0001g0124 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.857-8504C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226986927 | ||||||
| chr2:226987221
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.857-8210A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226987221 | ||||||
| chr2:226987271
|
A | T | 1 | a0001c0001t0001g0052 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.857-8160A>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226987271 | ||||||
| chr2:226987367
|
G | T | 4 | a0003c0003t0004g0172a0003c0003t0004g0173a0003c0003t0004g0174others(1): Show | 4 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.857-8064G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226987367 | ||||||
| chr2:226987414
|
T | C | 1 | a0001c0001t0002g0223 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.857-8017T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226987414 | ||||||
| chr2:226987886
|
T | A | 2 | a0001c0001t0003g0250a0001c0001t0003g0256 | 2 | NA18975.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.857-7545T>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226987886 | ||||||
| chr2:226988365
|
T | C | 4 | a0003c0003t0004g0172a0003c0003t0004g0173a0003c0003t0004g0174others(1): Show | 4 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.857-7066T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226988365 | ||||||
| chr2:226988455
|
T | C | 1 | a0001c0001t0003g0255 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.857-6976T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226988455 | ||||||
| chr2:226988502
|
C | T | 3 | a0001c0001t0005g0221a0002c0002t0004g0237a0002c0002t0004g0238 | 3 | HG02145.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.857-6929C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226988502 | ||||||
| chr2:226988628
|
T | G | 1 | a0001c0001t0001g0105 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.857-6803T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226988628 | ||||||
| chr2:226988723
|
T | C | 1 | a0001c0001t0001g0078 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.857-6708T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226988723 | ||||||
| chr2:226988731
|
T | G | 1 | a0001c0001t0001g0032 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.857-6700T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226988731 | ||||||
| chr2:226988998
|
G | A | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG01934.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.857-6433G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226988998 | ||||||
| chr2:226989904
|
G | C | 3 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169 | 3 | HG01934.hp2 HG02451.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.857-5527G>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226989904 | ||||||
| chr2:226990026
|
G | A | 1 | a0001c0001t0018g0128 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.857-5405G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226990026 | ||||||
| chr2:226990292
|
A | G | 1 | a0001c0001t0001g0157 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.857-5139A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226990292 | ||||||
| chr2:226990777
|
A | C | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(160): Show | 168 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.857-4654A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226990777 | ||||||
| chr2:226990807
|
C | T | 1 | a0001c0001t0002g0212 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.857-4624C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226990807 | ||||||
| chr2:226991025
|
G | A | 4 | a0001c0001t0006g0244a0001c0001t0019g0017a0002c0002t0006g0229others(1): Show | 4 | HG02451.hp1 HG03139.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.857-4406G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226991025 | ||||||
| chr2:226991616
|
C | G | 24 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(21): Show | 24 | HG00099.hp2 HG01071.hp2 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.857-3815C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226991616 | ||||||
| chr2:226991769
|
G | A | 2 | a0001c0001t0001g0063a0001c0001t0001g0064 | 2 | HG01255.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.857-3662G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226991769 | ||||||
| chr2:226991836
|
A | G | 100 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(97): Show | 102 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.857-3595A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226991836 | ||||||
| chr2:226992132
|
G | A | 1 | a0001c0001t0001g0068 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.857-3299G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226992132 | ||||||
| chr2:226992246
|
C | T | 1 | a0001c0001t0009g0140 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.857-3185C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226992246 | ||||||
| chr2:226992291
|
C | G | 4 | a0001c0001t0006g0244a0001c0001t0019g0017a0002c0002t0006g0229others(1): Show | 4 | HG02451.hp1 HG03139.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.857-3140C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226992291 | ||||||
| chr2:226992534
|
T | G | 16 | a0001c0001t0005g0221a0001c0001t0012g0231a0001c0005t0005g0219others(13): Show | 16 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.857-2897T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226992534 | ||||||
| chr2:226992781
|
G | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(113): Show | 118 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.857-2650G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226992781 | ||||||
| chr2:226992785
|
T | C | 3 | a0001c0001t0001g0021a0001c0001t0002g0224a0001c0001t0002g0225 | 3 | HG00673.hp2 NA18979.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.857-2646T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226992785 | ||||||
| chr2:226993047
|
T | C | 100 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(97): Show | 102 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.857-2384T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226993047 | ||||||
| chr2:226993283
|
T | C | 2 | a0001c0001t0001g0060a0001c0001t0002g0006 | 3 | HG03209.hp2 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.857-2148T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226993283 | ||||||
| chr2:226993339
|
C | G | 1 | a0001c0001t0003g0245 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.857-2092C>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226993339 | ||||||
| chr2:226993504
|
A | G | 1 | a0001c0001t0001g0032 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.857-1927A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226993504 | ||||||
| chr2:226993676
|
A | G | 3 | a0001c0001t0005g0221a0002c0002t0004g0237a0002c0002t0004g0238 | 3 | HG02145.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.857-1755A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226993676 | ||||||
| chr2:226993876
|
G | A | 4 | a0003c0003t0004g0172a0003c0003t0004g0173a0003c0003t0004g0174others(1): Show | 4 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.857-1555G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226993876 | ||||||
| chr2:226993893
|
T | C | 101 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(98): Show | 103 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.857-1538T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226993893 | ||||||
| chr2:226994009
|
T | C | 15 | a0001c0001t0005g0221a0001c0001t0012g0231a0001c0005t0005g0219others(12): Show | 15 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.857-1422T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226994009 | ||||||
| chr2:226994075
|
G | T | 2 | a0001c0001t0001g0099a0001c0001t0001g0130 | 2 | HG00544.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.857-1356G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226994075 | ||||||
| chr2:226994197
|
T | A | 4 | a0003c0003t0004g0172a0003c0003t0004g0173a0003c0003t0004g0174others(1): Show | 4 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.857-1234T>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226994197 | ||||||
| chr2:226994198
|
G | T | 4 | a0003c0003t0004g0172a0003c0003t0004g0173a0003c0003t0004g0174others(1): Show | 4 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.857-1233G>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226994198 | ||||||
| chr2:226994246
|
C | A | 2 | a0001c0001t0002g0197a0002c0002t0001g0014 | 2 | HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.857-1185C>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226994246 | ||||||
| chr2:226994392
|
C | T | 101 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(98): Show | 103 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.857-1039C>T | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226994392 | ||||||
| chr2:226994508
|
A | G | 101 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(98): Show | 103 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.857-923A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226994508 | ||||||
| chr2:226994610
|
G | A | 101 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(98): Show | 103 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.857-821G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226994610 | ||||||
| chr2:226994817
|
T | C | 15 | a0001c0001t0005g0221a0001c0001t0012g0231a0001c0005t0005g0219others(12): Show | 15 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.857-614T>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226994817 | ||||||
| chr2:226994942
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.857-489G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226994942 | ||||||
| chr2:226994977
|
T | G | 61 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(58): Show | 62 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.857-454T>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226994977 | ||||||
| chr2:226995126
|
G | A | 1 | a0001c0001t0003g0241 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.857-305G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226995126 | ||||||
| chr2:226995175
|
A | G | 1 | a0001c0001t0002g0185 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.857-256A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226995175 | ||||||
| chr2:226995249
|
A | C | 4 | a0001c0001t0006g0244a0001c0001t0019g0017a0002c0002t0006g0229others(1): Show | 4 | HG02451.hp1 HG03139.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.857-182A>C | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226995249 | ||||||
| chr2:226995391
|
G | A | 1 | a0001c0001t0002g0214 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.857-40G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 8/8 | chr2 | 226995391 |