Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MQRRS others(310): Show |
chr2 | 226831054 | 227004210 |
| a0002 | 0/0 | 315 | 12 | 10 | 0 | 0 | 0 | 2 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | MQRRS others(310): Show |
chr2 | 226831054 | 227004210 |
| a0003 | 0/0 | 315 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | MQRRS others(310): Show |
chr2 | 226831054 | 227004210 |
| a0004 | 0/0 | 315 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | MQRRS others(310): Show |
chr2 | 226831054 | 227004210 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 945 | 240 | 52 | 38 | 116 | 8 | 24 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | ATGCA others(940): Show |
chr2 | 226831054 | 227004210 | ||
| a0001c0004 | 0/0 | 945 | 3 | 3 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | ATGCA others(940): Show |
chr2 | 226831054 | 227004210 | ||
| a0001c0005 | 0/0 | 945 | 2 | 2 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | ATGCA others(940): Show |
chr2 | 226831054 | 227004210 | ||
| a0001c0007 | 0/0 | 945 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | ATGCA others(940): Show |
chr2 | 226831054 | 227004210 | ||
| a0001c0008 | 0/0 | 945 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | ATGCA others(940): Show |
chr2 | 226831054 | 227004210 | ||
| a0002c0002 | 0/0 | 945 | 10 | 10 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | ATGCA others(940): Show |
chr2 | 226831054 | 227004210 | ||
| a0002c0006 | 0/0 | 945 | 2 | 0 | 0 | 0 | 0 | 2 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | ATGCA others(940): Show |
chr2 | 226831054 | 227004210 | ||
| a0003c0003 | 0/0 | 945 | 4 | 4 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | ATGCA others(940): Show |
chr2 | 226831054 | 227004210 | ||
| a0004c0009 | 0/0 | 945 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | ATGCA others(940): Show |
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 | GAAGA others(5056): Show |
chr2 | 226831054 | 227004210 |
| a0001c0001t0002 | 0/0 | 5061 | 48 | 23 | 8 | 15 | 1 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | GAAGA others(5056): Show |
chr2 | 226831054 | 227004210 |
| a0001c0001t0003 | 0/0 | 5061 | 16 | 2 | 7 | 2 | 2 | 3 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | GAAGA others(5056): Show |
chr2 | 226831054 | 227004210 |
| a0001c0001t0005 | 0/0 | 5059 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | GAAGA others(5054): Show |
chr2 | 226831054 | 227004210 |
| a0001c0001t0006 | 0/0 | 5061 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | GAAGA others(5056): Show |
chr2 | 226831054 | 227004210 |
| a0001c0001t0007 | 0/0 | 5061 | 2 | 0 | 0 | 2 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | GAAGA others(5056): Show |
chr2 | 226831054 | 227004210 |
| a0001c0001t0008 | 0/0 | 5061 | 2 | 0 | 2 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | GAAGA others(5056): Show |
chr2 | 226831054 | 227004210 |
| a0001c0001t0009 | 0/0 | 5061 | 2 | 2 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | GAAGA others(5056): Show |
chr2 | 226831054 | 227004210 |
| a0001c0001t0011 | 0/0 | 5061 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | GAAGA others(5056): Show |
chr2 | 226831054 | 227004210 |
| a0001c0001t0012 | 0/0 | 5061 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | GAAGA others(5056): Show |
chr2 | 226831054 | 227004210 |
| a0001c0001t0013 | 0/0 | 5061 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | GAAGA others(5056): Show |
chr2 | 226831054 | 227004210 |
| a0001c0001t0014 | 0/0 | 5061 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | GAAGA others(5056): Show |
chr2 | 226831054 | 227004210 |
| a0001c0001t0015 | 0/0 | 5061 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | GAAGA others(5056): Show |
chr2 | 226831054 | 227004210 |
| a0001c0001t0016 | 0/0 | 5061 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | GAAGA others(5056): Show |
chr2 | 226831054 | 227004210 |
| a0001c0001t0017 | 0/0 | 5022 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | GAAGA others(5017): Show |
chr2 | 226831054 | 227004210 |
| a0001c0001t0018 | 0/0 | 5061 | 1 | 0 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | GAAGA others(5056): Show |
chr2 | 226831054 | 227004210 |
| a0001c0001t0019 | 0/0 | 5061 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | GAAGA others(5056): Show |
chr2 | 226831054 | 227004210 |
| a0001c0004t0002 | 0/0 | 5061 | 3 | 3 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | GAAGA others(5056): Show |
chr2 | 226831054 | 227004210 |
| a0001c0005t0005 | 0/0 | 5059 | 2 | 2 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | GAAGA others(5054): Show |
chr2 | 226831054 | 227004210 |
| a0001c0007t0010 | 0/0 | 5059 | 1 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | GAAGA others(5054): Show |
chr2 | 226831054 | 227004210 |
| a0001c0008t0001 | 0/0 | 5061 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | GAAGA others(5056): Show |
chr2 | 226831054 | 227004210 |
| a0002c0002t0001 | 0/0 | 5061 | 2 | 2 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | GAAGA others(5056): Show |
chr2 | 226831054 | 227004210 |
| a0002c0002t0004 | 0/0 | 5061 | 6 | 6 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | GAAGA others(5056): Show |
chr2 | 226831054 | 227004210 |
| a0002c0002t0006 | 0/0 | 5061 | 2 | 2 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | GAAGA others(5056): Show |
chr2 | 226831054 | 227004210 |
| a0002c0006t0001 | 0/0 | 5061 | 2 | 0 | 0 | 0 | 0 | 2 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | GAAGA others(5056): Show |
chr2 | 226831054 | 227004210 |
| a0003c0003t0004 | 0/0 | 5061 | 4 | 4 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | GAAGA others(5056): Show |
chr2 | 226831054 | 227004210 |
| a0004c0009t0001 | 0/0 | 5061 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | GAAGA others(5056): Show |
chr2 | 226831054 | 227004210 |
| actghapid | grch38/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 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0066 | 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 | 1 | 0 | 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 | 0 | 1 | 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 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1/0 | 1 | 0 | 0 | 0 | 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 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0003g0242 | 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 |
| a0001c0001t0016g0067 | 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 |
| a0004c0009t0001g0241 | 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 | g0113 | 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 | g0111 | 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 | g0103 | 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 | g0242 | 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 | g0168 | 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 | g0102 | AMR | PEL | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0050 | 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 | g0161 | 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 | g0100 | 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 | g0114 | EAS | KHV | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0049 | 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 | g0104 | 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 | g0167 | AFR | ACB | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| HG02572 | hp1 | a0001 | c0001 | t0016 | g0067 | 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 | g0197 | 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 | g0066 | 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 | g0051 | 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 | g0065 | 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 | g0196 | 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 | g0047 | 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 | g0131 | 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 | g0115 | 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 | g0088 | EAS | JPT | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0160 | 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 | g0098 | 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 | g0116 | 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 | g0099 | 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 | g0097 | 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 | g0112 | 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 | g0132 | AFR | LWK | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| NA19056 | hp1 | a0004 | c0009 | t0001 | g0241 | 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 | g0052 | 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 | g0056 | 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 | g0162 | 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 | g0048 | 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 | g0096 | 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 | g0086 | 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 | a0001 | c0001 | t0001 | g0138 | REF | REF | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0101 | REF | REF | RHBDD1_chr2_226831054_227004210 | RHBDD1 | chr2 | 226831054 | 227004210 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0002 a0003 |
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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:226864997 | A | C | 2 | a0002c0006 a0003c0003 |
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 | a0001c0005 a0001c0007 |
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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0011 others(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 | a0001c0001t0005 a0001c0005t0005 a0001c0007t0010 |
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 | a0001c0001t0003 a0001c0001t0011 |
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 | a0001c0001t0005 a0001c0001t0012 a0001c0005t0005 others(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 | a0001c0001t0005 a0001c0001t0012 a0001c0005t0005 others(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 | a0001c0001t0006 a0001c0001t0019 a0002c0002t0006 |
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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:226836102 | C | T | 19 | a0001c0001t0001g0240 a0001c0001t0001g0248 a0001c0001t0001g0254 others(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 | a0001c0001t0001g0008 a0001c0001t0003g0007 |
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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0002c0002t0001g0013 others(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 | a0001c0001t0002g0232 a0001c0001t0002g0233 a0001c0001t0002g0234 others(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 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0004g0011 others(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 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0004g0011 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | a0001c0001t0002g0224 a0001c0001t0002g0225 a0001c0001t0002g0226 others(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 | 39 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0134 others(36): Show |
41 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(38): 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 | a0001c0001t0002g0006 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0178 |
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 | a0002c0006t0001g0176 a0002c0006t0001g0177 |
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 | a0001c0001t0002g0006 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | 39 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0134 others(36): Show |
41 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(38): 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 | a0001c0001t0002g0006 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | a0002c0006t0001g0176 a0002c0006t0001g0177 |
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 | a0001c0001t0002g0006 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
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 | a0001c0001t0005g0221 a0001c0005t0005g0219 a0001c0005t0005g0220 others(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 | a0002c0006t0001g0176 a0002c0006t0001g0177 a0003c0003t0004g0172 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
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 | a0001c0001t0002g0179 a0001c0001t0002g0180 a0001c0001t0002g0181 others(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 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0004g0011 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
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 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0002g0006 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0010 |
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 | a0001c0001t0002g0006 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0004g0011 others(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 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0004g0011 others(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 | a0001c0001t0002g0179 a0001c0001t0002g0180 a0001c0001t0002g0181 others(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 | a0001c0001t0001g0018 a0001c0001t0018g0128 |
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 | a0002c0006t0001g0176 a0002c0006t0001g0177 a0003c0003t0004g0172 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | a0002c0002t0006g0229 a0002c0002t0006g0230 |
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 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0004g0011 others(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 | a0002c0006t0001g0176 a0002c0006t0001g0177 a0003c0003t0004g0172 others(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 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
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 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 others(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 | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(197): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): 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 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0002g0006 others(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 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
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 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 |
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 | a0001c0001t0002g0006 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 |
3 | HG00140.hp1 HG01255.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-91+8046G>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 3/8 | chr2 | 226847673 | |||||||
| chr2:226847821 | G | T | 4 | a0001c0001t0001g0002 a0001c0001t0001g0075 a0001c0001t0001g0077 others(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 | a0002c0006t0001g0176 a0002c0006t0001g0177 a0003c0003t0004g0172 others(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 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0004g0011 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0178 |
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 | a0001c0001t0002g0006 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | a0001c0001t0001g0008 a0001c0001t0003g0007 |
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 | a0002c0006t0001g0176 a0002c0006t0001g0177 a0003c0003t0004g0172 others(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 | a0001c0001t0002g0208 a0001c0001t0002g0209 a0001c0001t0002g0210 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
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 | a0001c0005t0005g0219 a0001c0005t0005g0220 a0001c0007t0010g0222 |
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 | a0001c0001t0002g0224 a0001c0001t0002g0225 |
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 | a0001c0001t0002g0006 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | a0001c0001t0001g0018 a0001c0001t0018g0128 |
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 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0004g0011 others(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 | a0002c0002t0006g0229 a0002c0002t0006g0230 |
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 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
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 | a0002c0002t0004g0237 a0002c0002t0004g0238 |
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 | a0002c0006t0001g0176 a0002c0006t0001g0177 a0003c0003t0004g0172 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0034 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0079 |
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 | a0001c0001t0001g0074 a0001c0001t0001g0118 a0001c0001t0001g0142 others(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 | a0001c0001t0001g0134 a0001c0001t0001g0141 a0001c0001t0002g0179 |
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 | a0001c0001t0001g0032 a0001c0001t0001g0070 a0001c0001t0001g0071 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0002g0212 |
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 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0004g0011 others(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 | 30 | a0001c0001t0001g0119 a0001c0001t0001g0135 a0001c0001t0001g0136 others(27): Show |
30 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(27): 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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0131 others(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 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 others(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 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0004g0011 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | a0001c0001t0009g0140 a0001c0001t0009g0149 |
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 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0004g0011 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0035 a0001c0001t0001g0036 others(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 | a0001c0001t0002g0182 a0001c0001t0002g0210 a0001c0004t0002g0202 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0180 a0001c0001t0002g0181 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0007g0057 others(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 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0002g0006 others(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 | a0001c0001t0001g0091 a0002c0002t0001g0013 a0002c0002t0001g0014 others(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 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0004g0011 others(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 | a0001c0004t0002g0201 a0001c0004t0002g0203 |
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 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0004g0011 others(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 | a0001c0001t0002g0195 a0001c0001t0002g0199 a0001c0001t0002g0200 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0092 others(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 | 44 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0119 others(41): Show |
46 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(43): 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 | a0001c0001t0002g0006 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(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 | a0001c0001t0001g0083 a0001c0001t0001g0094 a0001c0001t0001g0117 |
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 | a0001c0001t0002g0006 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | a0003c0003t0004g0172 a0003c0003t0004g0173 a0003c0003t0004g0174 others(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 | a0002c0006t0001g0176 a0002c0006t0001g0177 |
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 | a0001c0001t0002g0006 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(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 | a0003c0003t0004g0172 a0003c0003t0004g0173 a0003c0003t0004g0174 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0010 |
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 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0004g0011 others(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 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
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 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0002g0006 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0002g0194 a0001c0001t0013g0198 |
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 | a0002c0006t0001g0176 a0002c0006t0001g0177 a0003c0003t0004g0172 others(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 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0004g0011 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0163 |
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 | a0002c0006t0001g0176 a0002c0006t0001g0177 a0003c0003t0004g0172 others(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 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
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 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(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 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(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 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
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 | a0002c0006t0001g0176 a0002c0006t0001g0177 |
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 | a0001c0001t0002g0006 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | 136 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(133): Show |
139 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(136): 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 | a0001c0001t0002g0006 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0010 |
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 | a0002c0006t0001g0176 a0002c0006t0001g0177 |
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 | a0001c0001t0002g0006 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0004g0011 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0093 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0004g0011 others(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 | a0001c0001t0001g0095 a0001c0001t0001g0118 |
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 | a0002c0006t0001g0176 a0002c0006t0001g0177 |
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 | |||||||
| chr2:226866156 | 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 | a0001c0001t0005g0221 a0001c0005t0005g0219 a0001c0005t0005g0220 others(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 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0004g0011 others(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 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
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 | a0001c0001t0001g0079 a0001c0001t0001g0080 |
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 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0004g0011 others(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 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(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 | a0001c0001t0009g0140 a0001c0001t0009g0149 |
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 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 |
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 | a0001c0001t0001g0089 a0001c0001t0001g0090 |
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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0002g0006 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 |
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 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0002g0006 others(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 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0004g0011 others(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 | a0002c0002t0004g0011 a0002c0002t0004g0012 |
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 | a0001c0001t0002g0006 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0002g0006 others(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 | a0001c0001t0002g0195 a0001c0001t0002g0199 a0001c0001t0002g0200 others(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 | a0001c0001t0001g0142 a0001c0001t0001g0148 a0001c0001t0001g0160 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
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 | a0002c0006t0001g0176 a0002c0006t0001g0177 a0003c0003t0004g0172 others(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 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0004g0011 others(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 | a0001c0001t0001g0132 | 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 | a0001c0001t0002g0181 a0001c0001t0002g0182 |
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 | a0002c0006t0001g0176 a0002c0006t0001g0177 a0003c0003t0004g0172 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
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 | a0001c0001t0002g0006 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | a0002c0006t0001g0176 a0002c0006t0001g0177 a0003c0003t0004g0172 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | a0001c0001t0001g0167 | 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 | a0001c0001t0001g0052 | 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 | a0001c0005t0005g0219 a0001c0005t0005g0220 a0001c0007t0010g0222 |
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 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0004g0011 others(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 | a0001c0001t0001g0065 | 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 | a0002c0006t0001g0176 a0002c0006t0001g0177 a0003c0003t0004g0172 others(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 | 45 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(42): Show |
49 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.566+7431C>A | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226874749 | |||||||
| chr2:226875107 | A | G | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
104 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(101): 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 | a0001c0001t0002g0196 a0001c0001t0012g0231 |
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 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0004g0011 others(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 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0004g0011 others(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 | a0001c0001t0002g0179 a0001c0001t0002g0180 a0001c0001t0002g0181 others(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 | a0001c0001t0002g0181 a0001c0001t0002g0182 |
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 | a0002c0002t0006g0229 a0002c0002t0006g0230 |
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 | a0001c0001t0001g0086 | 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 | a0001c0001t0002g0223 a0002c0002t0001g0013 a0002c0002t0001g0014 others(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 | a0002c0006t0001g0176 a0002c0006t0001g0177 a0003c0003t0004g0172 others(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 | a0003c0003t0004g0172 a0003c0003t0004g0173 a0003c0003t0004g0174 others(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 | a0001c0001t0001g0160 a0001c0001t0002g0006 a0001c0001t0002g0178 others(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 | a0001c0001t0002g0185 a0001c0001t0002g0186 a0001c0001t0002g0187 others(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 | a0002c0006t0001g0176 a0002c0006t0001g0177 a0003c0003t0004g0172 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0055 a0001c0001t0001g0058 others(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 | a0001c0001t0001g0039 a0001c0001t0001g0103 a0001c0001t0002g0180 others(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 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0004g0011 others(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 | a0001c0001t0001g0102 | 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 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0004g0011 others(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 | a0002c0002t0006g0229 a0002c0002t0006g0230 |
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 | a0001c0001t0001g0160 a0001c0001t0002g0006 a0001c0001t0002g0178 others(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 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0004g0011 others(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 | a0001c0001t0005g0221 a0001c0005t0005g0219 a0001c0005t0005g0220 others(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 | a0003c0003t0004g0172 a0003c0003t0004g0173 a0003c0003t0004g0174 others(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 | a0002c0002t0004g0237 a0002c0002t0004g0238 |
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 | a0001c0001t0001g0131 | 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 | 66 | a0001c0001t0001g0032 a0001c0001t0001g0089 a0001c0001t0001g0109 others(63): Show |
67 | HG00140.hp1 HG00544.hp2 HG00673.hp2 others(64): 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 | a0001c0001t0001g0018 a0002c0002t0001g0013 a0002c0002t0001g0014 others(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 | a0001c0001t0016g0067 | 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 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0004g0011 others(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 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0004g0011 others(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 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0004g0011 others(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 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
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 | a0001c0001t0003g0043 a0001c0001t0003g0061 a0001c0001t0003g0243 others(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 | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(113): Show |
121 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(118): 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 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0004g0011 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 |
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 | a0001c0001t0001g0160 a0001c0001t0002g0006 a0001c0001t0002g0178 others(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 | a0001c0001t0001g0160 a0001c0001t0002g0006 a0001c0001t0002g0178 others(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 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
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 | a0001c0001t0001g0146 a0001c0001t0001g0157 a0001c0001t0001g0165 |
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 | a0002c0006t0001g0176 a0002c0006t0001g0177 a0003c0003t0004g0172 others(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 | a0001c0001t0001g0160 a0001c0001t0002g0006 a0001c0001t0002g0178 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0096 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0042 a0001c0001t0001g0058 a0001c0001t0001g0059 others(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 | a0001c0001t0002g0184 a0001c0001t0002g0186 a0001c0001t0002g0190 others(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 | a0001c0001t0001g0160 a0001c0001t0002g0006 a0001c0001t0002g0178 others(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 | a0001c0001t0015g0072 a0001c0001t0019g0017 a0002c0002t0001g0013 others(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 | a0002c0006t0001g0176 a0002c0006t0001g0177 a0003c0003t0004g0172 others(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 | a0002c0006t0001g0176 a0002c0006t0001g0177 a0003c0003t0004g0172 others(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 | a0001c0005t0005g0219 a0001c0005t0005g0220 a0001c0007t0010g0222 |
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 | a0002c0006t0001g0176 a0002c0006t0001g0177 a0003c0003t0004g0172 others(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 | a0001c0004t0002g0201 a0001c0004t0002g0203 |
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 | a0002c0006t0001g0176 a0002c0006t0001g0177 a0003c0003t0004g0172 others(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 | a0001c0001t0001g0066 | 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 | a0001c0005t0005g0219 a0001c0005t0005g0220 a0001c0007t0010g0222 |
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 | a0002c0006t0001g0176 a0002c0006t0001g0177 a0003c0003t0004g0172 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0065 a0001c0001t0001g0066 |
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 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
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 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
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 | a0001c0001t0001g0160 a0001c0001t0002g0006 a0001c0001t0002g0178 others(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 | a0001c0001t0001g0160 a0001c0001t0002g0006 a0001c0001t0002g0178 others(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 | a0001c0001t0001g0160 a0001c0001t0002g0006 a0001c0001t0002g0178 others(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 | a0001c0001t0001g0160 a0001c0001t0002g0006 a0001c0001t0002g0178 others(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 | a0001c0001t0001g0160 a0001c0001t0002g0006 a0001c0001t0002g0178 others(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 | a0001c0001t0001g0160 a0001c0001t0002g0006 a0001c0001t0002g0178 others(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 | a0001c0001t0001g0095 a0001c0001t0001g0118 |
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 | a0001c0001t0001g0087 a0001c0001t0001g0119 a0001c0001t0017g0107 |
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 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0160 others(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 | a0002c0006t0001g0176 a0002c0006t0001g0177 a0003c0003t0004g0172 others(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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0160 a0001c0001t0002g0006 a0001c0001t0002g0178 others(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 | a0001c0001t0002g0195 a0001c0001t0002g0199 a0001c0001t0002g0200 others(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 | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 |
3 | HG00140.hp1 HG01255.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.567-18508A>G | RHBDD1 | ENSG00000144468.17 | transcript | ENST00000392062.7 | protein_coding | 5/8 | chr2 | 226888285 | |||||||
| chr2:226888411 | GT | G | 73 | a0001c0001t0001g0039 a0001c0001t0001g0160 a0001c0001t0002g0006 others(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 | a0001c0001t0002g0224 a0001c0001t0002g0225 |
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 | a0002c0006t0001g0176 a0002c0006t0001g0177 a0003c0003t0004g0172 others(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 | a0001c0001t0001g0048 | 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 | a0001c0005t0005g0219 a0001c0005t0005g0220 a0001c0007t0010g0222 |
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 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
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 | a0002c0002t0006g0229 a0002c0002t0006g0230 |
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 | a0001c0001t0005g0221 a0002c0002t0001g0013 a0002c0002t0001g0014 others(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 | a0001c0001t0001g0160 a0001c0001t0002g0006 a0001c0001t0002g0178 others(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 | a0002c0002t0006g0229 a0002c0002t0006g0230 |
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 | a0001c0001t0002g0195 a0001c0001t0002g0197 a0001c0001t0002g0199 others(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 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0004g0011 others(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 | a0001c0001t0001g0160 a0001c0001t0002g0006 a0001c0001t0002g0178 others(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 | a0001c0005t0005g0219 a0001c0005t0005g0220 a0001c0007t0010g0222 |
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 | a0002c0002t0006g0229 a0002c0002t0006g0230 |
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 | a0002c0006t0001g0176 a0002c0006t0001g0177 a0003c0003t0004g0172 others(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 | a0001c0001t0001g0160 a0001c0001t0002g0006 a0001c0001t0002g0178 others(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 | a0002c0006t0001g0176 a0002c0006t0001g0177 a0003c0003t0004g0172 others(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 | a0001c0001t0001g0160 a0001c0001t0002g0006 a0001c0001t0002g0178 others(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 | a0002c0006t0001g0176 a0002c0006t0001g0177 |
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 | a0001c0001t0001g0160 a0001c0001t0002g0006 a0001c0001t0002g0178 others(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 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0004g0011 others(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 | a0001c0005t0005g0219 a0001c0005t0005g0220 a0001c0007t0010g0222 |
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 | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(120): Show |
128 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(125): 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 | a0002c0006t0001g0176 a0002c0006t0001g0177 a0003c0003t0004g0172 others(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 | a0001c0001t0001g0160 a0001c0001t0002g0006 a0001c0001t0002g0178 others(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 | a0001c0001t0001g0097 | 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 | a0001c0001t0001g0097 | 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 | a0001c0001t0005g0221 a0002c0002t0004g0237 a0002c0002t0004g0238 |
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 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
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 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0004g0011 others(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 | a0001c0001t0005g0221 a0002c0002t0004g0237 a0002c0002t0004g0238 |
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 | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(95): Show |
103 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(100): 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 | a0001c0005t0005g0219 a0001c0005t0005g0220 a0001c0007t0010g0222 |
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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0097 | 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 | a0001c0001t0001g0097 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(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 | a0001c0001t0003g0242 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(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 | a0001c0001t0005g0221 a0001c0001t0012g0231 a0002c0002t0001g0013 others(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 | a0001c0001t0001g0066 a0001c0001t0001g0081 a0001c0001t0001g0152 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0056 a0001c0001t0001g0110 a0001c0001t0001g0236 others(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 | a0001c0001t0001g0162 | 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 | a0001c0001t0001g0019 a0001c0001t0001g0035 a0001c0001t0001g0036 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0065 a0001c0001t0001g0066 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0002c0006t0001g0176 a0002c0006t0001g0177 a0003c0003t0004g0172 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(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 | a0001c0001t0005g0221 a0001c0001t0012g0231 a0002c0002t0001g0013 others(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 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(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 | a0002c0002t0006g0229 a0002c0002t0006g0230 |
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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(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 | a0002c0006t0001g0176 a0002c0006t0001g0177 a0003c0003t0004g0172 others(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 | a0002c0006t0001g0176 a0002c0006t0001g0177 a0003c0003t0004g0172 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(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 | a0002c0006t0001g0176 a0002c0006t0001g0177 a0003c0003t0004g0172 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0083 a0001c0001t0001g0117 |
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 | a0002c0002t0006g0229 a0002c0002t0006g0230 |
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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0035 a0001c0001t0001g0036 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0097 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0095 a0001c0001t0001g0118 |
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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(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 | a0002c0002t0006g0229 a0002c0002t0006g0230 |
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 | a0001c0001t0005g0221 a0001c0001t0012g0231 a0002c0002t0001g0013 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0018 others(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 | a0001c0001t0001g0083 a0001c0001t0001g0094 a0001c0001t0001g0117 |
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 | a0001c0001t0001g0049 a0001c0001t0001g0084 a0001c0001t0001g0098 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0018 others(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 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0084 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0048 a0001c0001t0001g0052 a0001c0001t0001g0074 others(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 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
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 | a0001c0001t0005g0221 a0002c0002t0004g0237 a0002c0002t0004g0238 |
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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(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 | 40 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(37): Show |
44 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(41): 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 | a0001c0001t0005g0221 a0002c0002t0004g0238 |
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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0027 others(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 | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(115): Show |
123 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(120): 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 | a0001c0001t0002g0178 a0001c0001t0002g0213 a0001c0001t0002g0214 others(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 | a0001c0001t0005g0221 a0001c0001t0012g0231 a0002c0002t0001g0013 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(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 | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(153): Show |
161 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(158): 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 | a0002c0002t0006g0229 a0002c0002t0006g0230 |
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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(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 | a0001c0001t0016g0067 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(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 | a0002c0002t0006g0229 a0002c0002t0006g0230 |
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 | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(172): Show |
180 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(177): 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 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0092 a0001c0001t0001g0095 a0001c0001t0001g0099 others(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 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0002c0002t0004g0237 others(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 | a0001c0001t0001g0131 | 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 | a0001c0001t0001g0132 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0049 a0001c0001t0001g0066 a0001c0001t0001g0084 others(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 | a0002c0006t0001g0176 a0002c0006t0001g0177 a0003c0003t0004g0172 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(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 | 42 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(39): Show |
46 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(43): 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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0163 |
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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(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 | a0001c0005t0005g0219 a0001c0005t0005g0220 a0001c0007t0010g0222 |
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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(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 | a0001c0001t0005g0221 a0001c0001t0012g0231 a0001c0001t0019g0017 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0002c0002t0001g0014 a0002c0002t0004g0015 |
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 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 |
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 | a0001c0001t0001g0021 a0001c0001t0002g0194 a0001c0001t0002g0195 others(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 | a0001c0001t0001g0021 a0001c0001t0002g0195 a0001c0001t0002g0197 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(153): Show |
161 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(158): 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 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 |
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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(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 | a0001c0001t0003g0250 a0001c0001t0003g0256 |
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 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0137 others(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 | 18 | a0001c0001t0001g0032 a0001c0001t0001g0054 a0001c0001t0001g0073 others(15): Show |
18 | HG01169.hp1 HG01261.hp1 HG01515.hp2 others(15): 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 | a0001c0001t0001g0106 a0002c0006t0001g0176 a0002c0006t0001g0177 others(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 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0002c0006t0001g0176 a0002c0006t0001g0177 a0003c0003t0004g0172 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0002g0197 | 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 | a0001c0001t0005g0221 a0001c0001t0012g0231 a0002c0002t0001g0013 others(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 | a0002c0006t0001g0176 a0002c0006t0001g0177 a0003c0003t0004g0172 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0042 a0001c0001t0001g0102 a0001c0001t0001g0103 others(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 | a0001c0001t0001g0162 | 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 | a0001c0001t0002g0196 a0001c0001t0006g0244 a0002c0002t0006g0229 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(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 | a0001c0001t0012g0231 a0002c0002t0001g0014 a0002c0002t0004g0011 others(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 | a0001c0001t0002g0196 | 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 | 34 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0081 others(31): Show |
36 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(33): 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 | a0002c0006t0001g0176 a0002c0006t0001g0177 |
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 | 104 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0027 others(101): Show |
104 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(101): 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 | a0001c0005t0005g0219 a0001c0005t0005g0220 a0001c0007t0010g0222 |
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 | a0001c0001t0001g0008 a0001c0001t0003g0007 a0002c0002t0001g0013 |
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 | a0001c0001t0012g0231 a0002c0002t0001g0014 a0002c0002t0004g0011 others(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 | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(156): Show |
164 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(161): 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 | a0002c0006t0001g0176 a0002c0006t0001g0177 |
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 | a0001c0005t0005g0219 a0001c0005t0005g0220 a0001c0007t0010g0222 |
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 | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(161): Show |
169 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(166): 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 | a0001c0005t0005g0219 a0001c0005t0005g0220 a0001c0007t0010g0222 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0108 a0001c0001t0001g0110 a0001c0001t0001g0112 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0002g0178 a0001c0001t0002g0232 a0001c0001t0002g0233 others(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 | a0001c0005t0005g0219 a0001c0005t0005g0220 a0001c0007t0010g0222 |
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 | a0002c0006t0001g0176 a0002c0006t0001g0177 |
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 | a0002c0006t0001g0176 a0002c0006t0001g0177 |
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 | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): 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 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0052 a0001c0001t0001g0139 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0005g0221 a0002c0002t0004g0237 a0002c0002t0004g0238 |
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 | a0001c0001t0005g0221 a0002c0002t0004g0238 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | 49 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0021 others(46): Show |
51 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(48): 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 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0081 others(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 | a0001c0001t0001g0083 a0001c0001t0003g0250 a0001c0001t0003g0256 others(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 | a0001c0001t0001g0167 | 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 | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(181): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): 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 | a0001c0001t0006g0244 a0002c0002t0006g0229 a0002c0002t0006g0230 |
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 | a0001c0005t0005g0219 a0001c0005t0005g0220 a0001c0007t0010g0222 others(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 | a0001c0001t0001g0049 a0001c0001t0001g0084 a0001c0001t0001g0098 others(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 | a0002c0006t0001g0176 a0002c0006t0001g0177 |
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 | a0001c0001t0001g0021 a0001c0001t0002g0195 a0001c0001t0002g0199 others(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 | a0001c0001t0003g0043 a0001c0001t0003g0061 a0001c0001t0003g0243 others(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 | a0003c0003t0004g0172 a0003c0003t0004g0173 a0003c0003t0004g0174 others(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 | a0003c0003t0004g0172 a0003c0003t0004g0173 a0003c0003t0004g0174 others(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 | a0001c0005t0005g0219 a0001c0005t0005g0220 a0001c0007t0010g0222 |
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 | a0001c0001t0001g0042 a0001c0001t0001g0102 a0001c0001t0001g0103 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0002g0189 a0001c0001t0002g0192 a0001c0001t0002g0193 |
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 | a0001c0001t0001g0050 | 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 | a0001c0005t0005g0219 a0001c0005t0005g0220 |
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 | a0001c0001t0003g0242 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0099 a0001c0001t0001g0105 |
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 | a0002c0006t0001g0176 a0002c0006t0001g0177 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0018 others(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 | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(159): Show |
167 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(164): 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 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0075 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0042 a0001c0001t0001g0054 a0001c0001t0001g0085 others(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 | a0001c0001t0005g0221 a0002c0002t0004g0238 |
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 | a0003c0003t0004g0172 a0003c0003t0004g0173 a0003c0003t0004g0174 others(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 | a0001c0001t0002g0197 | 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 | a0001c0001t0001g0049 a0001c0001t0001g0084 a0001c0001t0001g0098 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0005g0221 a0002c0002t0004g0238 |
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 | a0001c0005t0005g0219 a0001c0005t0005g0220 a0001c0007t0010g0222 others(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 | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(159): Show |
167 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(164): 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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0016g0067 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0002g0181 a0001c0001t0002g0182 |
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 | a0001c0001t0003g0045 a0001c0001t0003g0252 |
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 | a0001c0005t0005g0219 a0001c0005t0005g0220 a0001c0007t0010g0222 others(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 | a0001c0001t0006g0244 a0001c0001t0019g0017 a0002c0002t0006g0229 others(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 | a0001c0001t0002g0196 | 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 | a0001c0001t0001g0034 a0001c0001t0001g0124 |
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 | a0003c0003t0004g0172 a0003c0003t0004g0173 a0003c0003t0004g0174 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0002c0006t0001g0176 a0002c0006t0001g0177 |
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 | a0001c0001t0006g0244 a0001c0001t0019g0017 a0002c0002t0006g0229 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0005t0005g0219 a0001c0005t0005g0220 a0001c0007t0010g0222 others(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 | a0001c0001t0006g0244 a0001c0001t0019g0017 a0002c0002t0006g0229 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0006g0244 a0002c0002t0006g0229 a0002c0002t0006g0230 |
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 | a0001c0001t0001g0066 | 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 | a0001c0005t0005g0219 a0001c0005t0005g0220 a0001c0007t0010g0222 others(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 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0002g0194 |
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 | a0001c0001t0001g0034 a0001c0001t0001g0124 |
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 | a0001c0001t0006g0244 a0001c0001t0019g0017 a0002c0002t0006g0229 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0008g0246 a0001c0001t0008g0247 |
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 | a0002c0006t0001g0176 a0002c0006t0001g0177 |
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 | a0001c0001t0001g0032 a0001c0001t0001g0047 |
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 | a0001c0001t0001g0112 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0145 a0001c0001t0001g0166 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | |||||||
| chr2:226935909 | 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 | a0001c0001t0006g0244 a0001c0001t0019g0017 a0002c0002t0006g0229 others(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 | a0001c0005t0005g0219 a0001c0005t0005g0220 a0001c0007t0010g0222 |
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 | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(159): Show |
167 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(164): 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 | a0001c0001t0001g0021 a0001c0001t0001g0131 a0001c0001t0001g0132 others(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 | a0002c0002t0004g0011 a0002c0002t0004g0012 |
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 | 1 | a0001c0001t0001g0135 | 1 | HG00140.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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0052 | 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 | a0001c0001t0002g0178 a0001c0001t0002g0232 a0001c0001t0002g0233 others(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 | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(158): Show |
166 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(163): 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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0040 |
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 | a0001c0001t0006g0244 a0001c0001t0019g0017 a0002c0002t0006g0229 others(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 | a0001c0001t0002g0226 a0001c0001t0006g0244 a0001c0001t0019g0017 others(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 | a0001c0005t0005g0219 a0001c0005t0005g0220 a0001c0007t0010g0222 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(159): Show |
167 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(164): 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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0002g0196 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0035 a0001c0001t0001g0036 others(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 | a0001c0001t0001g0099 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | 34 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(31): Show |
37 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(34): 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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
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 | a0001c0001t0016g0067 | 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 | a0001c0001t0001g0052 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0006g0244 a0001c0001t0019g0017 a0002c0002t0006g0229 others(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 | a0002c0006t0001g0176 a0002c0006t0001g0177 |
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 | a0001c0001t0002g0195 a0001c0001t0002g0199 a0001c0001t0002g0200 |
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 | a0001c0001t0001g0066 | 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 | a0001c0005t0005g0219 a0001c0005t0005g0220 a0001c0007t0010g0222 others(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 | a0001c0001t0001g0153 a0001c0001t0002g0186 a0001c0001t0002g0187 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0002g0196 | 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 | a0001c0005t0005g0219 a0001c0005t0005g0220 a0001c0007t0010g0222 others(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 | a0002c0006t0001g0176 a0002c0006t0001g0177 |
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 | a0002c0006t0001g0176 a0002c0006t0001g0177 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0084 a0001c0001t0002g0006 a0001c0001t0002g0209 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0035 a0001c0001t0001g0036 others(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 | a0001c0001t0001g0082 a0001c0001t0002g0181 a0001c0001t0002g0182 |
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 | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(157): Show |
165 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(162): 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 | a0001c0005t0005g0219 a0001c0005t0005g0220 a0001c0007t0010g0222 |
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 | a0001c0001t0001g0161 | 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 | a0001c0001t0012g0231 a0002c0002t0001g0014 a0002c0002t0004g0011 others(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 | a0001c0001t0001g0021 a0001c0001t0002g0195 a0001c0001t0002g0199 others(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 | a0001c0001t0001g0021 a0001c0001t0002g0195 a0001c0001t0002g0199 others(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 | a0001c0001t0002g0197 | 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 | a0001c0001t0006g0244 a0001c0001t0019g0017 a0002c0002t0006g0229 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0003c0003t0004g0172 a0003c0003t0004g0173 a0003c0003t0004g0174 others(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 | a0002c0006t0001g0176 a0002c0006t0001g0177 |
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 | a0001c0001t0006g0244 a0001c0001t0019g0017 a0002c0002t0006g0229 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
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 | a0001c0001t0006g0244 a0001c0001t0019g0017 a0002c0002t0006g0229 others(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 | a0001c0001t0001g0048 a0001c0001t0001g0052 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0006g0244 a0001c0001t0019g0017 a0002c0002t0006g0229 others(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 | 38 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0023 others(35): Show |
39 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(36): 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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0081 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0119 a0001c0001t0001g0141 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0006g0244 a0001c0001t0019g0017 a0002c0002t0006g0229 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0006g0244 a0001c0001t0019g0017 a0002c0002t0006g0229 others(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 | a0001c0001t0006g0244 a0001c0001t0019g0017 a0002c0002t0006g0229 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0054 a0001c0001t0001g0085 a0001c0001t0001g0099 others(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 | 41 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(38): Show |
44 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(41): 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 | a0001c0001t0005g0221 a0002c0002t0004g0237 a0002c0002t0004g0238 |
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 | a0001c0001t0006g0244 a0001c0001t0019g0017 a0002c0002t0006g0229 others(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 | a0002c0006t0001g0176 a0002c0006t0001g0177 |
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 | a0002c0006t0001g0176 a0002c0006t0001g0177 |
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 | a0004c0009t0001g0241 | 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 | a0001c0001t0002g0195 a0001c0001t0002g0199 a0001c0001t0002g0200 |
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 | a0003c0003t0004g0172 a0003c0003t0004g0173 a0003c0003t0004g0174 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0002c0006t0001g0176 a0002c0006t0001g0177 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0002g0189 a0001c0001t0002g0192 a0001c0001t0002g0193 |
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 | a0001c0001t0006g0244 a0001c0001t0019g0017 a0002c0002t0006g0229 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0005t0005g0219 a0001c0005t0005g0220 a0001c0007t0010g0222 others(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 | a0001c0001t0001g0056 | 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 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0012g0231 a0002c0002t0001g0014 a0002c0002t0004g0011 others(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 | a0001c0001t0002g0197 | 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 | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(190): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(194): 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 | a0001c0001t0001g0059 a0001c0001t0001g0075 a0001c0001t0001g0083 others(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 | a0002c0006t0001g0176 a0002c0006t0001g0177 |
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 | a0001c0001t0001g0042 a0001c0001t0001g0054 a0001c0001t0001g0085 others(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 | a0001c0001t0002g0206 a0001c0001t0002g0207 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 |
3 | HG00140.hp1 HG01255.hp2 HG01258.hp1 |
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 | a0001c0001t0006g0244 a0001c0001t0019g0017 a0002c0002t0006g0229 others(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 | 38 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(35): Show |
41 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(38): 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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0006g0244 a0001c0001t0019g0017 a0002c0002t0006g0229 others(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 | a0001c0001t0001g0097 | 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 | a0001c0001t0001g0088 | 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 | a0001c0005t0005g0219 a0001c0005t0005g0220 a0001c0007t0010g0222 others(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 | a0001c0001t0006g0244 a0001c0001t0019g0017 a0002c0002t0006g0229 others(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 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | 41 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(38): Show |
44 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(41): 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 | a0001c0001t0001g0042 a0001c0001t0001g0102 a0001c0001t0001g0103 others(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 | a0001c0001t0007g0057 a0001c0001t0007g0069 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0002g0178 a0001c0001t0002g0232 a0001c0001t0002g0233 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(183): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): 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 | a0001c0001t0001g0110 a0001c0001t0001g0115 |
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 | a0001c0001t0001g0034 a0001c0001t0001g0124 |
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 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 |
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 | a0001c0001t0002g0196 | 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 | 41 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(38): Show |
44 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(41): 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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0036 a0001c0001t0001g0050 others(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 | a0001c0001t0001g0088 a0001c0001t0002g0179 a0001c0001t0002g0190 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0022 others(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 | 32 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0056 others(29): Show |
34 | HG00140.hp1 HG00609.hp2 HG00673.hp1 others(31): 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 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0013g0198 |
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 | a0001c0001t0001g0083 a0001c0001t0001g0094 a0001c0001t0001g0117 |
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 | a0001c0001t0006g0244 a0001c0001t0019g0017 a0002c0002t0006g0229 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0005t0005g0219 a0001c0005t0005g0220 a0001c0007t0010g0222 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0108 a0001c0001t0001g0110 others(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 | a0001c0001t0012g0231 a0002c0002t0001g0014 a0002c0002t0004g0011 others(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 | a0001c0001t0001g0086 | 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 | a0001c0001t0005g0221 a0001c0001t0012g0231 a0002c0002t0001g0014 others(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 | a0001c0001t0006g0244 a0001c0001t0019g0017 a0002c0002t0006g0229 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0006g0244 a0001c0001t0019g0017 a0002c0002t0006g0229 others(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 | a0001c0001t0001g0110 a0001c0001t0001g0115 |
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 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | |||||||
| chr2:226963232 | T | C | 9 | a0001c0001t0005g0221 a0001c0001t0012g0231 a0002c0002t0001g0014 others(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 | a0003c0003t0004g0172 a0003c0003t0004g0173 a0003c0003t0004g0174 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0006g0244 a0001c0001t0019g0017 a0001c0005t0005g0219 others(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 | a0001c0001t0009g0140 a0001c0001t0009g0149 |
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 | a0001c0005t0005g0219 a0001c0005t0005g0220 a0001c0007t0010g0222 others(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 | a0003c0003t0004g0172 a0003c0003t0004g0173 a0003c0003t0004g0174 others(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 | a0002c0006t0001g0176 a0002c0006t0001g0177 |
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 | a0001c0001t0005g0221 a0001c0001t0012g0231 a0002c0002t0001g0014 others(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 | a0001c0001t0012g0231 a0002c0002t0001g0014 a0002c0002t0004g0011 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0002c0006t0001g0176 a0002c0006t0001g0177 |
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 | a0001c0005t0005g0219 a0001c0005t0005g0220 a0001c0007t0010g0222 others(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 | a0001c0001t0001g0160 | 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 | a0001c0005t0005g0219 a0001c0005t0005g0220 a0001c0007t0010g0222 |
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 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0002g0194 others(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 | a0001c0001t0001g0133 a0001c0001t0005g0221 a0001c0001t0006g0244 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 |
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 | a0001c0001t0006g0244 a0001c0001t0019g0017 a0002c0002t0006g0229 others(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 | a0003c0003t0004g0172 a0003c0003t0004g0173 a0003c0003t0004g0174 others(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 | a0001c0001t0006g0244 a0001c0001t0019g0017 a0002c0002t0006g0229 others(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 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0082 |
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 | a0001c0001t0001g0146 a0001c0001t0001g0157 a0001c0001t0001g0165 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0083 a0001c0001t0006g0244 a0002c0002t0006g0229 others(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 | a0001c0001t0001g0123 a0001c0001t0002g0181 a0001c0001t0002g0210 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0066 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0035 a0001c0001t0001g0036 others(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 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 |
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 | 41 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(38): Show |
44 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(41): 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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0006g0244 a0001c0001t0019g0017 a0002c0002t0006g0229 others(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 | a0001c0001t0001g0161 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 |
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 | a0001c0001t0005g0221 a0002c0002t0004g0237 a0002c0002t0004g0238 |
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 | a0001c0005t0005g0219 a0001c0005t0005g0220 a0001c0007t0010g0222 |
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 | 60 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(57): Show |
63 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(60): 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 | a0001c0001t0001g0056 a0001c0001t0001g0075 a0001c0001t0001g0137 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0005t0005g0219 a0001c0005t0005g0220 a0001c0007t0010g0222 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0139 a0001c0001t0001g0153 a0001c0001t0001g0170 others(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 | a0003c0003t0004g0172 a0003c0003t0004g0173 a0003c0003t0004g0174 others(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 | a0001c0001t0006g0244 a0001c0001t0019g0017 a0002c0002t0006g0229 others(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 | a0001c0005t0005g0219 a0001c0005t0005g0220 a0001c0007t0010g0222 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0002g0179 a0001c0001t0002g0195 a0001c0001t0002g0199 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0248 a0002c0002t0001g0013 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0104 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0051 |
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 | a0001c0001t0001g0097 | 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 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 others(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 | a0001c0001t0001g0060 a0001c0001t0002g0006 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0003g0043 a0001c0001t0003g0061 |
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 | a0001c0001t0005g0221 a0001c0001t0012g0231 a0001c0005t0005g0219 others(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 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
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 | a0001c0001t0009g0140 a0001c0001t0009g0149 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0141 a0001c0001t0001g0143 a0001c0001t0001g0147 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): 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 | a0001c0001t0005g0221 a0001c0001t0012g0231 a0001c0005t0005g0219 others(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 | a0001c0001t0009g0140 a0001c0001t0009g0149 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0003c0003t0004g0172 a0003c0003t0004g0173 a0003c0003t0004g0174 others(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 | a0001c0001t0003g0242 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0005t0005g0219 a0003c0003t0004g0172 a0003c0003t0004g0173 others(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 | a0001c0001t0006g0244 a0001c0001t0019g0017 a0002c0002t0006g0229 others(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 | a0001c0001t0002g0179 a0001c0001t0002g0180 a0001c0001t0002g0181 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0108 a0001c0001t0001g0110 others(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 | a0001c0001t0005g0221 a0001c0001t0006g0244 a0001c0001t0012g0231 others(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 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0109 |
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 | a0001c0001t0009g0140 a0001c0001t0009g0149 |
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 | a0001c0001t0001g0050 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0048 a0001c0001t0001g0068 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0132 a0001c0001t0002g0178 a0001c0001t0002g0213 others(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 | a0001c0001t0005g0221 a0001c0001t0012g0231 a0001c0005t0005g0219 others(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 | a0003c0003t0004g0172 a0003c0003t0004g0173 a0003c0003t0004g0174 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0044 a0001c0001t0001g0058 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0021 a0001c0001t0002g0224 a0001c0001t0002g0225 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0048 a0001c0001t0001g0052 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0248 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0005g0221 a0002c0002t0004g0237 a0002c0002t0004g0238 |
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 | a0001c0001t0006g0244 a0002c0002t0006g0229 a0002c0002t0006g0230 |
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 | a0002c0006t0001g0176 a0002c0006t0001g0177 |
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 | a0002c0006t0001g0176 a0002c0006t0001g0177 |
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 | a0001c0001t0006g0244 a0001c0001t0019g0017 a0002c0002t0006g0229 others(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 | a0003c0003t0004g0172 a0003c0003t0004g0173 a0003c0003t0004g0174 others(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 | |||||||
| chr2:226984152 | G | C | 3 | a0001c0005t0005g0219 a0001c0005t0005g0220 a0001c0007t0010g0222 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0005t0005g0219 a0001c0005t0005g0220 a0001c0007t0010g0222 |
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 | a0001c0001t0012g0231 a0002c0002t0001g0014 a0002c0002t0004g0011 others(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 | 40 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(37): Show |
43 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(40): 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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0006g0244 a0001c0001t0019g0017 a0002c0002t0006g0229 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0099 | 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 | a0003c0003t0004g0172 a0003c0003t0004g0173 a0003c0003t0004g0174 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0065 a0001c0001t0001g0066 |
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 | a0001c0001t0001g0160 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0006g0244 a0001c0001t0019g0017 a0002c0002t0006g0229 others(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 | a0001c0001t0001g0146 a0001c0001t0001g0157 |
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 | a0001c0001t0001g0034 a0001c0001t0001g0124 |
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 | a0001c0001t0001g0051 | 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 | a0003c0003t0004g0172 a0003c0003t0004g0173 a0003c0003t0004g0174 others(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 | a0001c0001t0003g0250 a0001c0001t0003g0256 |
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 | a0003c0003t0004g0172 a0003c0003t0004g0173 a0003c0003t0004g0174 others(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 | a0001c0001t0005g0221 a0002c0002t0004g0237 a0002c0002t0004g0238 |
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 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
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 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 |
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 | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(159): Show |
167 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(164): 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 | a0001c0001t0006g0244 a0001c0001t0019g0017 a0002c0002t0006g0229 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0006g0244 a0001c0001t0019g0017 a0002c0002t0006g0229 others(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 | a0001c0001t0005g0221 a0001c0001t0012g0231 a0001c0005t0005g0219 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0021 a0001c0001t0002g0224 a0001c0001t0002g0225 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0060 a0001c0001t0002g0006 |
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 | a0001c0001t0005g0221 a0002c0002t0004g0237 a0002c0002t0004g0238 |
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 | a0003c0003t0004g0172 a0003c0003t0004g0173 a0003c0003t0004g0174 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0005g0221 a0001c0001t0012g0231 a0001c0005t0005g0219 others(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 | a0001c0001t0001g0097 a0001c0001t0001g0130 |
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 | a0003c0003t0004g0172 a0003c0003t0004g0173 a0003c0003t0004g0174 others(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 | a0003c0003t0004g0172 a0003c0003t0004g0173 a0003c0003t0004g0174 others(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 | a0001c0001t0002g0196 a0002c0002t0001g0014 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0005g0221 a0001c0001t0012g0231 a0001c0005t0005g0219 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0003g0242 | 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 | a0001c0001t0006g0244 a0001c0001t0019g0017 a0002c0002t0006g0229 others(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 |