Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6006 |
| ensemblid | ENSG00000188672.19 |
| hgncid | 10008 |
| symbol | RHCE |
| name | Rh blood group CcEe antigens |
| refseq_nuc | NM_020485.8 |
| refseq_prot | NP_065231.4 |
| ensembl_nuc | ENST00000294413.13 |
| ensembl_prot | ENSP00000294413.6 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 25362249 |
| end | 25420825 |
| strand | - |
| ver | v1.2 |
| region | chr1:25362249-25420825 |
| region5000 | chr1:25357249-25425825 |
| regionname0 | RHCE_chr1_25362249_25420825 |
| regionname5000 | RHCE_chr1_25357249_25425825 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 417 | 130 | 3 | 31 | 73 | 5 | 17 | 56 | RHCE_chr1_25357249_25425825 | RHCE | MSSKY others(412): Show |
chr1 | 25357249 | 25425825 |
| a0002 | 0/0 | 417 | 71 | 5 | 8 | 50 | 3 | 5 | 37 | RHCE_chr1_25357249_25425825 | RHCE | MSSKY others(412): Show |
chr1 | 25357249 | 25425825 |
| a0003 | 0/0 | 417 | 43 | 13 | 13 | 3 | 6 | 8 | 2 | RHCE_chr1_25357249_25425825 | RHCE | MSSKY others(412): Show |
chr1 | 25357249 | 25425825 |
| a0004 | 1/0 | 417 | 26 | 18 | 2 | 5 | 0 | 0 | 4 | RHCE_chr1_25357249_25425825 | RHCE | MSSKY others(412): Show |
chr1 | 25357249 | 25425825 |
| a0005 | 0/0 | 417 | 18 | 15 | 3 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | MSSKY others(412): Show |
chr1 | 25357249 | 25425825 |
| a0006 | 0/0 | 417 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | MSSKY others(412): Show |
chr1 | 25357249 | 25425825 |
| a0007 | 0/0 | 417 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | MSSKY others(412): Show |
chr1 | 25357249 | 25425825 |
| a0008 | 0/0 | 417 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | MSSKY others(412): Show |
chr1 | 25357249 | 25425825 |
| a0009 | 0/0 | 417 | 4 | 3 | 0 | 0 | 0 | 1 | 0 | RHCE_chr1_25357249_25425825 | RHCE | MSSKY others(412): Show |
chr1 | 25357249 | 25425825 |
| a0010 | 0/0 | 417 | 3 | 0 | 0 | 3 | 0 | 0 | 1 | RHCE_chr1_25357249_25425825 | RHCE | MSSKY others(412): Show |
chr1 | 25357249 | 25425825 |
| a0011 | 0/0 | 417 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | MSSKY others(412): Show |
chr1 | 25357249 | 25425825 |
| a0012 | 0/0 | 417 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | MSSKY others(412): Show |
chr1 | 25357249 | 25425825 |
| a0013 | 0/0 | 417 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | MSSKY others(412): Show |
chr1 | 25357249 | 25425825 |
| a0014 | 0/0 | 417 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | MSSKY others(412): Show |
chr1 | 25357249 | 25425825 |
| a0015 | 0/0 | 417 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | MSSKY others(412): Show |
chr1 | 25357249 | 25425825 |
| a0016 | 0/0 | 417 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | RHCE_chr1_25357249_25425825 | RHCE | MSSKY others(412): Show |
chr1 | 25357249 | 25425825 |
| a0017 | 0/0 | 417 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | RHCE_chr1_25357249_25425825 | RHCE | MSSKY others(412): Show |
chr1 | 25357249 | 25425825 |
| a0018 | 0/0 | 417 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | MSSKY others(412): Show |
chr1 | 25357249 | 25425825 |
| a0019 | 0/0 | 417 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | MSSKY others(412): Show |
chr1 | 25357249 | 25425825 |
| a0020 | 0/0 | 417 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | MSSKY others(412): Show |
chr1 | 25357249 | 25425825 |
| a0021 | 0/0 | 417 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | MSSKY others(412): Show |
chr1 | 25357249 | 25425825 |
| a0022 | 0/0 | 417 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | MSSKY others(412): Show |
chr1 | 25357249 | 25425825 |
| a0023 | 0/0 | 417 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RHCE_chr1_25357249_25425825 | RHCE | MSSKY others(412): Show |
chr1 | 25357249 | 25425825 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1251 | 129 | 3 | 31 | 72 | 5 | 17 | RHCE_chr1_25357249_25425825 | RHCE | ATGAG others(1246): Show |
chr1 | 25357249 | 25425825 | ||
| a0001c0025 | 0/0 | 1251 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | ATGAG others(1246): Show |
chr1 | 25357249 | 25425825 | ||
| a0002c0002 | 0/0 | 1251 | 71 | 5 | 8 | 50 | 3 | 5 | RHCE_chr1_25357249_25425825 | RHCE | ATGAG others(1246): Show |
chr1 | 25357249 | 25425825 | ||
| a0003c0003 | 0/0 | 1251 | 43 | 13 | 13 | 3 | 6 | 8 | RHCE_chr1_25357249_25425825 | RHCE | ATGAG others(1246): Show |
chr1 | 25357249 | 25425825 | ||
| a0004c0004 | 1/0 | 1251 | 25 | 18 | 1 | 5 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | ATGAG others(1246): Show |
chr1 | 25357249 | 25425825 | ||
| a0004c0024 | 0/0 | 1251 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | ATGAG others(1246): Show |
chr1 | 25357249 | 25425825 | ||
| a0005c0005 | 0/0 | 1251 | 18 | 15 | 3 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | ATGAG others(1246): Show |
chr1 | 25357249 | 25425825 | ||
| a0006c0006 | 0/0 | 1251 | 8 | 8 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | ATGAG others(1246): Show |
chr1 | 25357249 | 25425825 | ||
| a0007c0007 | 0/0 | 1251 | 6 | 6 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | ATGAG others(1246): Show |
chr1 | 25357249 | 25425825 | ||
| a0008c0008 | 0/0 | 1251 | 5 | 4 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | ATGAG others(1246): Show |
chr1 | 25357249 | 25425825 | ||
| a0009c0009 | 0/0 | 1251 | 4 | 3 | 0 | 0 | 0 | 1 | RHCE_chr1_25357249_25425825 | RHCE | ATGAG others(1246): Show |
chr1 | 25357249 | 25425825 | ||
| a0010c0015 | 0/0 | 1251 | 2 | 0 | 0 | 2 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | ATGAG others(1246): Show |
chr1 | 25357249 | 25425825 | ||
| a0010c0022 | 0/0 | 1251 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | ATGAG others(1246): Show |
chr1 | 25357249 | 25425825 | ||
| a0011c0014 | 0/0 | 1251 | 2 | 1 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | ATGAG others(1246): Show |
chr1 | 25357249 | 25425825 | ||
| a0012c0010 | 0/0 | 1251 | 2 | 1 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | ATGAG others(1246): Show |
chr1 | 25357249 | 25425825 | ||
| a0013c0012 | 0/0 | 1251 | 2 | 1 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | ATGAG others(1246): Show |
chr1 | 25357249 | 25425825 | ||
| a0014c0013 | 0/0 | 1251 | 2 | 2 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | ATGAG others(1246): Show |
chr1 | 25357249 | 25425825 | ||
| a0015c0011 | 0/0 | 1251 | 2 | 2 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | ATGAG others(1246): Show |
chr1 | 25357249 | 25425825 | ||
| a0016c0017 | 0/0 | 1251 | 2 | 0 | 0 | 2 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | ATGAG others(1246): Show |
chr1 | 25357249 | 25425825 | ||
| a0017c0016 | 0/0 | 1251 | 2 | 0 | 0 | 2 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | ATGAG others(1246): Show |
chr1 | 25357249 | 25425825 | ||
| a0018c0021 | 0/0 | 1251 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | ATGAG others(1246): Show |
chr1 | 25357249 | 25425825 | ||
| a0019c0019 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | ATGAG others(1246): Show |
chr1 | 25357249 | 25425825 | ||
| a0020c0026 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | ATGAG others(1246): Show |
chr1 | 25357249 | 25425825 | ||
| a0021c0020 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | ATGAG others(1246): Show |
chr1 | 25357249 | 25425825 | ||
| a0022c0018 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | ATGAG others(1246): Show |
chr1 | 25357249 | 25425825 | ||
| a0023c0023 | 0/0 | 1251 | 1 | 0 | 0 | 0 | 0 | 1 | RHCE_chr1_25357249_25425825 | RHCE | ATGAG others(1246): Show |
chr1 | 25357249 | 25425825 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1571 | 129 | 3 | 31 | 72 | 5 | 17 | RHCE_chr1_25357249_25425825 | RHCE | CTGGT others(1566): Show |
chr1 | 25357249 | 25425825 |
| a0001c0025t0001 | 0/0 | 1571 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | CTGGT others(1566): Show |
chr1 | 25357249 | 25425825 |
| a0002c0002t0001 | 0/0 | 1571 | 71 | 5 | 8 | 50 | 3 | 5 | RHCE_chr1_25357249_25425825 | RHCE | CTGGT others(1566): Show |
chr1 | 25357249 | 25425825 |
| a0003c0003t0001 | 0/0 | 1571 | 43 | 13 | 13 | 3 | 6 | 8 | RHCE_chr1_25357249_25425825 | RHCE | CTGGT others(1566): Show |
chr1 | 25357249 | 25425825 |
| a0004c0004t0001 | 1/0 | 1571 | 25 | 18 | 1 | 5 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | CTGGT others(1566): Show |
chr1 | 25357249 | 25425825 |
| a0004c0024t0001 | 0/0 | 1571 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | CTGGT others(1566): Show |
chr1 | 25357249 | 25425825 |
| a0005c0005t0001 | 0/0 | 1571 | 18 | 15 | 3 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | CTGGT others(1566): Show |
chr1 | 25357249 | 25425825 |
| a0006c0006t0001 | 0/0 | 1571 | 8 | 8 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | CTGGT others(1566): Show |
chr1 | 25357249 | 25425825 |
| a0007c0007t0001 | 0/0 | 1571 | 5 | 5 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | CTGGT others(1566): Show |
chr1 | 25357249 | 25425825 |
| a0007c0007t0002 | 0/0 | 1571 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | CTGGT others(1566): Show |
chr1 | 25357249 | 25425825 |
| a0008c0008t0001 | 0/0 | 1571 | 5 | 4 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | CTGGT others(1566): Show |
chr1 | 25357249 | 25425825 |
| a0009c0009t0001 | 0/0 | 1571 | 4 | 3 | 0 | 0 | 0 | 1 | RHCE_chr1_25357249_25425825 | RHCE | CTGGT others(1566): Show |
chr1 | 25357249 | 25425825 |
| a0010c0015t0001 | 0/0 | 1571 | 2 | 0 | 0 | 2 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | CTGGT others(1566): Show |
chr1 | 25357249 | 25425825 |
| a0010c0022t0001 | 0/0 | 1571 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | CTGGT others(1566): Show |
chr1 | 25357249 | 25425825 |
| a0011c0014t0001 | 0/0 | 1571 | 2 | 1 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | CTGGT others(1566): Show |
chr1 | 25357249 | 25425825 |
| a0012c0010t0001 | 0/0 | 1571 | 2 | 1 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | CTGGT others(1566): Show |
chr1 | 25357249 | 25425825 |
| a0013c0012t0001 | 0/0 | 1571 | 2 | 1 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | CTGGT others(1566): Show |
chr1 | 25357249 | 25425825 |
| a0014c0013t0001 | 0/0 | 1571 | 2 | 2 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | CTGGT others(1566): Show |
chr1 | 25357249 | 25425825 |
| a0015c0011t0001 | 0/0 | 1571 | 2 | 2 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | CTGGT others(1566): Show |
chr1 | 25357249 | 25425825 |
| a0016c0017t0001 | 0/0 | 1571 | 2 | 0 | 0 | 2 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | CTGGT others(1566): Show |
chr1 | 25357249 | 25425825 |
| a0017c0016t0001 | 0/0 | 1571 | 2 | 0 | 0 | 2 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | CTGGT others(1566): Show |
chr1 | 25357249 | 25425825 |
| a0018c0021t0001 | 0/0 | 1571 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | CTGGT others(1566): Show |
chr1 | 25357249 | 25425825 |
| a0019c0019t0001 | 0/0 | 1571 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | CTGGT others(1566): Show |
chr1 | 25357249 | 25425825 |
| a0020c0026t0001 | 0/0 | 1571 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | CTGGT others(1566): Show |
chr1 | 25357249 | 25425825 |
| a0021c0020t0001 | 0/0 | 1571 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | CTGGT others(1566): Show |
chr1 | 25357249 | 25425825 |
| a0022c0018t0001 | 0/0 | 1571 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | CTGGT others(1566): Show |
chr1 | 25357249 | 25425825 |
| a0023c0023t0001 | 0/0 | 1571 | 1 | 0 | 0 | 0 | 0 | 1 | RHCE_chr1_25357249_25425825 | RHCE | CTGGT others(1566): Show |
chr1 | 25357249 | 25425825 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0039 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0001c0025t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0003c0003t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0003c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0003c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0003c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0003c0003t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0003c0003t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0003c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0003c0003t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0003c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0003c0003t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0003c0003t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0003c0003t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0003c0003t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0003c0003t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0003c0003t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0003c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0003c0003t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0003c0003t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0003c0003t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0003c0003t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0003c0003t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0003c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0003c0003t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0003c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0003c0003t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0003c0003t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0003c0003t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0003c0003t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0003c0003t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0003c0003t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0003c0003t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0003c0003t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0003c0003t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0003c0003t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0003c0003t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0003c0003t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0003c0003t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0003c0003t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0003c0003t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0003c0003t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0003c0003t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0003c0003t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0004c0004t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0004c0004t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0004c0004t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0004c0004t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0004c0004t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0004c0004t0001g0103 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0004c0004t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0004c0004t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0004c0004t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0004c0004t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0004c0004t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0004c0004t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0004c0004t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0004c0004t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0004c0004t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0004c0004t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0004c0004t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0004c0004t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0004c0004t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0004c0004t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0004c0004t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0004c0004t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0004c0024t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0005c0005t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0005c0005t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0005c0005t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0005c0005t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0005c0005t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0005c0005t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0005c0005t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0005c0005t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0005c0005t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0005c0005t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0005c0005t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0005c0005t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0005c0005t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0005c0005t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0005c0005t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0005c0005t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0005c0005t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0006c0006t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0006c0006t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0006c0006t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0006c0006t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0006c0006t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0006c0006t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0006c0006t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0006c0006t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0007c0007t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0007c0007t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0007c0007t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0007c0007t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0007c0007t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0008c0008t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0008c0008t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0008c0008t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0008c0008t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0008c0008t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0009c0009t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0009c0009t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0009c0009t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0009c0009t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0010c0015t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0010c0015t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0010c0022t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0011c0014t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0011c0014t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0012c0010t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0012c0010t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0013c0012t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0013c0012t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0014c0013t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0014c0013t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0015c0011t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0015c0011t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0016c0017t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0016c0017t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0017c0016t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0017c0016t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0018c0021t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0019c0019t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0020c0026t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0021c0020t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0022c0018t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| a0023c0023t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0003 | t0001 | g0190 | EUR | GBR | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0080 | EUR | GBR | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0053 | EUR | GBR | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG00140 | hp2 | a0003 | c0003 | t0001 | g0257 | EUR | GBR | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0248 | EUR | FIN | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG00280 | hp2 | a0003 | c0003 | t0001 | g0192 | EUR | FIN | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0198 | EAS | CHS | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0213 | EAS | CHS | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0241 | EAS | CHS | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0238 | EAS | CHS | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0274 | EAS | CHS | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG00639 | hp1 | a0003 | c0003 | t0001 | g0227 | AMR | PUR | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0186 | AMR | PUR | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0267 | EAS | CHS | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG00733 | hp2 | a0003 | c0003 | t0001 | g0279 | AMR | PUR | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG00738 | hp1 | a0003 | c0003 | t0001 | g0255 | AMR | PUR | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG00741 | hp1 | a0003 | c0003 | t0001 | g0276 | AMR | PUR | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01069 | hp1 | a0005 | c0005 | t0001 | g0311 | AMR | PUR | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01069 | hp2 | a0003 | c0003 | t0001 | g0283 | AMR | PUR | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01070 | hp1 | a0005 | c0005 | t0001 | g0015 | AMR | PUR | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0252 | AMR | PUR | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01071 | hp1 | a0003 | c0003 | t0001 | g0284 | AMR | PUR | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01071 | hp2 | a0005 | c0005 | t0001 | g0015 | AMR | PUR | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0185 | AMR | PUR | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01099 | hp2 | a0011 | c0014 | t0001 | g0157 | AMR | PUR | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01106 | hp1 | a0012 | c0010 | t0001 | g0020 | AMR | PUR | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01106 | hp2 | a0004 | c0004 | t0001 | g0176 | AMR | PUR | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01109 | hp1 | a0008 | c0008 | t0001 | g0147 | AMR | PUR | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01109 | hp2 | a0003 | c0003 | t0001 | g0251 | AMR | PUR | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01167 | hp2 | a0013 | c0012 | t0001 | g0170 | AMR | PUR | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01168 | hp2 | a0003 | c0003 | t0001 | g0253 | AMR | PUR | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01169 | hp1 | a0003 | c0003 | t0001 | g0265 | AMR | PUR | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01175 | hp1 | a0003 | c0003 | t0001 | g0193 | AMR | PUR | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01243 | hp1 | a0004 | c0024 | t0001 | g0182 | AMR | PUR | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01258 | hp2 | a0003 | c0003 | t0001 | g0261 | AMR | CLM | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01261 | hp1 | a0003 | c0003 | t0001 | g0205 | AMR | CLM | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0212 | EUR | IBS | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0117 | EUR | IBS | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01516 | hp1 | a0003 | c0003 | t0001 | g0014 | EUR | IBS | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0123 | EUR | IBS | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01517 | hp1 | a0003 | c0003 | t0001 | g0014 | EUR | IBS | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0116 | EUR | IBS | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01891 | hp1 | a0004 | c0004 | t0001 | g0016 | AFR | ACB | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01891 | hp2 | a0004 | c0004 | t0001 | g0005 | AFR | ACB | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01934 | hp2 | a0018 | c0021 | t0001 | g0050 | AMR | PEL | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0188 | AMR | PEL | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0187 | AMR | PEL | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0197 | EAS | KHV | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02027 | hp2 | a0010 | c0015 | t0001 | g0109 | EAS | KHV | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0236 | EAS | KHV | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02055 | hp1 | a0003 | c0003 | t0001 | g0280 | AFR | ACB | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02055 | hp2 | a0008 | c0008 | t0001 | g0178 | AFR | ACB | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02056 | hp2 | a0004 | c0004 | t0001 | g0037 | EAS | KHV | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0242 | EAS | KHV | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02071 | hp2 | a0003 | c0003 | t0001 | g0249 | EAS | KHV | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0196 | EAS | KHV | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02080 | hp2 | a0010 | c0022 | t0001 | g0135 | EAS | KHV | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0281 | EAS | KHV | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02145 | hp1 | a0014 | c0013 | t0001 | g0026 | AFR | ACB | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02145 | hp2 | a0003 | c0003 | t0001 | g0287 | AFR | ACB | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0224 | AMR | PEL | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0237 | EAS | CDX | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | CDX | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02257 | hp1 | a0003 | c0003 | t0001 | g0215 | AFR | ACB | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02257 | hp2 | a0006 | c0006 | t0001 | g0296 | AFR | ACB | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02258 | hp1 | a0019 | c0019 | t0001 | g0021 | AFR | ACB | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02258 | hp2 | a0007 | c0007 | t0002 | g0172 | AFR | ACB | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0199 | AMR | PEL | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02572 | hp1 | a0007 | c0007 | t0001 | g0173 | AFR | GWD | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02572 | hp2 | a0008 | c0008 | t0001 | g0177 | AFR | GWD | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0204 | SAS | PJL | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02615 | hp1 | a0005 | c0005 | t0001 | g0312 | AFR | GWD | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02615 | hp2 | a0009 | c0009 | t0001 | g0073 | AFR | GWD | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0245 | AFR | GWD | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02630 | hp1 | a0005 | c0005 | t0001 | g0309 | AFR | GWD | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02630 | hp2 | a0020 | c0026 | t0001 | g0222 | AFR | GWD | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02647 | hp1 | a0004 | c0004 | t0001 | g0041 | AFR | GWD | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02647 | hp2 | a0011 | c0014 | t0001 | g0175 | AFR | GWD | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0217 | SAS | PJL | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0256 | SAS | PJL | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02717 | hp1 | a0004 | c0004 | t0001 | g0144 | AFR | GWD | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0194 | AFR | GWD | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0271 | AFR | GWD | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02723 | hp2 | a0005 | c0005 | t0001 | g0299 | AFR | GWD | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0189 | SAS | PJL | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02738 | hp2 | a0003 | c0003 | t0001 | g0202 | SAS | PJL | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02809 | hp1 | a0007 | c0007 | t0001 | g0010 | AFR | GWD | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02809 | hp2 | a0004 | c0004 | t0001 | g0009 | AFR | GWD | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02818 | hp1 | a0004 | c0004 | t0001 | g0166 | AFR | GWD | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02818 | hp2 | a0005 | c0005 | t0001 | g0302 | AFR | GWD | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02886 | hp1 | a0007 | c0007 | t0001 | g0010 | AFR | GWD | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02886 | hp2 | a0021 | c0020 | t0001 | g0167 | AFR | GWD | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02895 | hp1 | a0009 | c0009 | t0001 | g0075 | AFR | GWD | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02895 | hp2 | a0015 | c0011 | t0001 | g0160 | AFR | GWD | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02896 | hp1 | a0004 | c0004 | t0001 | g0163 | AFR | GWD | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02896 | hp2 | a0004 | c0004 | t0001 | g0169 | AFR | GWD | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02897 | hp1 | a0009 | c0009 | t0001 | g0074 | AFR | GWD | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02897 | hp2 | a0004 | c0004 | t0001 | g0164 | AFR | GWD | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02922 | hp1 | a0006 | c0006 | t0001 | g0294 | AFR | ESN | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02922 | hp2 | a0004 | c0004 | t0001 | g0168 | AFR | ESN | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02965 | hp1 | a0004 | c0004 | t0001 | g0165 | AFR | ESN | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02965 | hp2 | a0003 | c0003 | t0001 | g0201 | AFR | ESN | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02970 | hp2 | a0004 | c0004 | t0001 | g0005 | AFR | ESN | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02976 | hp1 | a0006 | c0006 | t0001 | g0292 | AFR | ESN | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02976 | hp2 | a0008 | c0008 | t0001 | g0146 | AFR | ESN | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG03017 | hp2 | a0003 | c0003 | t0001 | g0263 | SAS | PJL | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG03041 | hp1 | a0006 | c0006 | t0001 | g0293 | AFR | GWD | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG03041 | hp2 | a0005 | c0005 | t0001 | g0310 | AFR | GWD | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG03130 | hp1 | a0005 | c0005 | t0001 | g0297 | AFR | ESN | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG03130 | hp2 | a0003 | c0003 | t0001 | g0313 | AFR | ESN | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG03139 | hp1 | a0004 | c0004 | t0001 | g0005 | AFR | ESN | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG03139 | hp2 | a0005 | c0005 | t0001 | g0307 | AFR | ESN | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG03195 | hp1 | a0004 | c0004 | t0001 | g0009 | AFR | ESN | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG03195 | hp2 | a0003 | c0003 | t0001 | g0288 | AFR | ESN | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG03209 | hp1 | a0005 | c0005 | t0001 | g0304 | AFR | MSL | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG03209 | hp2 | a0003 | c0003 | t0001 | g0277 | AFR | MSL | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG03225 | hp1 | a0008 | c0008 | t0001 | g0148 | AFR | MSL | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG03225 | hp2 | a0003 | c0003 | t0001 | g0289 | AFR | MSL | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG03239 | hp2 | a0003 | c0003 | t0001 | g0258 | SAS | PJL | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG03453 | hp1 | a0004 | c0004 | t0001 | g0162 | AFR | MSL | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG03453 | hp2 | a0003 | c0003 | t0001 | g0273 | AFR | MSL | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0278 | AFR | MSL | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG03486 | hp2 | a0015 | c0011 | t0001 | g0161 | AFR | MSL | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG03540 | hp1 | a0006 | c0006 | t0001 | g0290 | AFR | GWD | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG03540 | hp2 | a0022 | c0018 | t0001 | g0155 | AFR | GWD | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG03579 | hp1 | a0004 | c0004 | t0001 | g0159 | AFR | MSL | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG03579 | hp2 | a0006 | c0006 | t0001 | g0285 | AFR | MSL | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0225 | SAS | PJL | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG03710 | hp1 | a0003 | c0003 | t0001 | g0184 | SAS | PJL | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | BEB | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG03831 | hp2 | a0009 | c0009 | t0001 | g0064 | SAS | BEB | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG03942 | hp1 | a0023 | c0023 | t0001 | g0054 | SAS | BEB | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG04115 | hp1 | a0003 | c0003 | t0001 | g0272 | SAS | STU | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | STU | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG04199 | hp2 | a0003 | c0003 | t0001 | g0260 | SAS | STU | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG04204 | hp1 | a0003 | c0003 | t0001 | g0203 | SAS | STU | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | STU | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | STU | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | STU | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18522 | hp1 | a0004 | c0004 | t0001 | g0158 | AFR | YRI | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18522 | hp2 | a0005 | c0005 | t0001 | g0298 | AFR | YRI | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHB | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0219 | EAS | CHB | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHB | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0223 | AFR | YRI | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18906 | hp2 | a0005 | c0005 | t0001 | g0306 | AFR | YRI | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0208 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18940 | hp1 | a0002 | c0002 | t0001 | g0247 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0234 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0270 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18946 | hp1 | a0004 | c0004 | t0001 | g0114 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0221 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18951 | hp2 | a0016 | c0017 | t0001 | g0055 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0218 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18960 | hp1 | a0003 | c0003 | t0001 | g0250 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18960 | hp2 | a0017 | c0016 | t0001 | g0086 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0210 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0240 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18974 | hp2 | a0001 | c0025 | t0001 | g0181 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0207 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18978 | hp1 | a0002 | c0002 | t0001 | g0231 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0209 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0183 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18986 | hp2 | a0017 | c0016 | t0001 | g0087 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0229 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0244 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18994 | hp2 | a0004 | c0004 | t0001 | g0134 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0264 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0243 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19012 | hp1 | a0016 | c0017 | t0001 | g0082 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19030 | hp1 | a0014 | c0013 | t0001 | g0025 | AFR | LWK | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19030 | hp2 | a0004 | c0004 | t0001 | g0156 | AFR | LWK | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19043 | hp1 | a0005 | c0005 | t0001 | g0305 | AFR | LWK | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | LWK | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19057 | hp2 | a0002 | c0002 | t0001 | g0226 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0195 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0239 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0220 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19066 | hp1 | a0004 | c0004 | t0001 | g0133 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0269 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19072 | hp1 | a0002 | c0002 | t0001 | g0275 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19076 | hp1 | a0004 | c0004 | t0001 | g0132 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19076 | hp2 | a0010 | c0015 | t0001 | g0106 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0246 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0206 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0228 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0268 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0259 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA20129 | hp1 | a0005 | c0005 | t0001 | g0303 | AFR | ASW | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA20129 | hp2 | a0003 | c0003 | t0001 | g0233 | AFR | ASW | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0211 | EUR | TSI | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA20752 | hp2 | a0003 | c0003 | t0001 | g0191 | EUR | TSI | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | GIH | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA20905 | hp2 | a0003 | c0003 | t0001 | g0262 | SAS | GIH | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0214 | AMR | CLM | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG01123 | hp2 | a0003 | c0003 | t0001 | g0254 | AMR | CLM | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02109 | hp1 | a0007 | c0007 | t0001 | g0174 | AFR | ACB | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02109 | hp2 | a0003 | c0003 | t0001 | g0282 | AFR | ACB | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02486 | hp1 | a0007 | c0007 | t0001 | g0145 | AFR | ACB | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02486 | hp2 | a0006 | c0006 | t0001 | g0295 | AFR | ACB | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02559 | hp1 | a0012 | c0010 | t0001 | g0019 | AFR | ACB | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG02559 | hp2 | a0006 | c0006 | t0001 | g0291 | AFR | ACB | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG03471 | hp1 | a0013 | c0012 | t0001 | g0171 | AFR | MSL | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| HG03471 | hp2 | a0005 | c0005 | t0001 | g0308 | AFR | MSL | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0216 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA18955 | hp2 | a0003 | c0003 | t0001 | g0200 | EAS | JPT | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA20300 | hp1 | a0005 | c0005 | t0001 | g0300 | AFR | USA | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA20300 | hp2 | a0003 | c0003 | t0001 | g0232 | AFR | USA | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA21309 | hp1 | a0005 | c0005 | t0001 | g0301 | AFR | LWK | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| NA21309 | hp2 | a0003 | c0003 | t0001 | g0286 | AFR | LWK | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0039 | REF | REF | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| homoSapiens | grch38p0 | a0004 | c0004 | t0001 | g0103 | REF | REF | RHCE_chr1_25357249_25425825 | RHCE | chr1 | 25357249 | 25425825 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:25370501 | A | T | 2 | a0010 a0012 |
5 | HG01106.hp1 HG02027.hp2 HG02080.hp2 others(2): Show |
missense_variant | MODERATE | c.1193T>A | p.Val398Glu | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/10 | 1232/1571 | 1193/1254 | 398/417 | chr1 | 25370501 | |||
| chr1:25375366 | G | A | 1 | a0015 | 2 | HG02895.hp2 HG03486.hp2 |
missense_variant | MODERATE | c.1136C>T | p.Thr379Met | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/10 | 1175/1571 | 1136/1254 | 379/417 | chr1 | 25375366 | |||
| chr1:25375379 | C | T | 1 | a0020 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.1123G>A | p.Val375Met | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/10 | 1162/1571 | 1123/1254 | 375/417 | chr1 | 25375379 | |||
| chr1:25385759 | G | A | 1 | a0008 | 5 | HG01109.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
missense_variant | MODERATE | c.1025C>T | p.Thr342Ile | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/10 | 1064/1571 | 1025/1254 | 342/417 | chr1 | 25385759 | |||
| chr1:25385778 | C | A | 1 | a0014 | 2 | HG02145.hp1 NA19030.hp1 |
missense_variant | MODERATE | c.1006G>T | p.Gly336Cys | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/10 | 1045/1571 | 1006/1254 | 336/417 | chr1 | 25385778 | |||
| chr1:25385843 | A | G | 1 | a0013 | 2 | HG01167.hp2 HG03471.hp1 |
missense_variant&splice_region_variant | MODERATE | c.941T>C | p.Val314Ala | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/10 | 980/1571 | 941/1254 | 314/417 | chr1 | 25385843 | |||
| chr1:25388999 | T | C | 1 | a0019 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.916A>G | p.Ile306Val | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/10 | 955/1571 | 916/1254 | 306/417 | chr1 | 25388999 | |||
| chr1:25390750 | A | T | 1 | a0019 | 1 | HG02258.hp1 | missense_variant&splice_region_variant | MODERATE | c.800T>A | p.Met267Lys | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 5/10 | 839/1571 | 800/1254 | 267/417 | chr1 | 25390750 | |||
| chr1:25390763 | T | C | 1 | a0019 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.787A>G | p.Arg263Gly | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 5/10 | 826/1571 | 787/1254 | 263/417 | chr1 | 25390763 | |||
| chr1:25390817 | G | C | 5 | a0005 a0007 a0013 others(2): Show |
29 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(26): Show |
missense_variant | MODERATE | c.733C>G | p.Leu245Val | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 5/10 | 772/1571 | 733/1254 | 245/417 | chr1 | 25390817 | |||
| chr1:25390838 | T | C | 1 | a0019 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.712A>G | p.Met238Val | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 5/10 | 751/1571 | 712/1254 | 238/417 | chr1 | 25390838 | |||
| chr1:25390854 | G | C | 1 | a0021 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.696C>G | p.Ile232Met | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 5/10 | 735/1571 | 696/1254 | 232/417 | chr1 | 25390854 | |||
| chr1:25390874 | C | G | 4 | a0002 a0018 a0020 others(1): Show |
74 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(71): Show |
missense_variant | MODERATE | c.676G>C | p.Ala226Pro | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 5/10 | 715/1571 | 676/1254 | 226/417 | chr1 | 25390874 | |||
| chr1:25390883 | C | A | 1 | a0011 | 2 | HG01099.hp2 HG02647.hp2 |
missense_variant | MODERATE | c.667G>T | p.Val223Phe | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 5/10 | 706/1571 | 667/1254 | 223/417 | chr1 | 25390883 | |||
| chr1:25392026 | C | G | 1 | a0009 | 4 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
missense_variant | MODERATE | c.602G>C | p.Arg201Thr | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 4/10 | 641/1571 | 602/1254 | 201/417 | chr1 | 25392026 | |||
| chr1:25392034 | A | T | 1 | a0009 | 4 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
missense_variant | MODERATE | c.594T>A | p.Asn198Lys | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 4/10 | 633/1571 | 594/1254 | 198/417 | chr1 | 25392034 | |||
| chr1:25392051 | T | C | 1 | a0009 | 4 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
missense_variant | MODERATE | c.577A>G | p.Lys193Glu | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 4/10 | 616/1571 | 577/1254 | 193/417 | chr1 | 25392051 | |||
| chr1:25392084 | T | A | 1 | a0009 | 4 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
missense_variant | MODERATE | c.544A>T | p.Thr182Ser | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 4/10 | 583/1571 | 544/1254 | 182/417 | chr1 | 25392084 | |||
| chr1:25392114 | A | T | 1 | a0009 | 4 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
missense_variant | MODERATE | c.514T>A | p.Phe172Ile | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 4/10 | 553/1571 | 514/1254 | 172/417 | chr1 | 25392114 | |||
| chr1:25392119 | C | A | 1 | a0009 | 4 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
missense_variant | MODERATE | c.509G>T | p.Arg170Met | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 4/10 | 548/1571 | 509/1254 | 170/417 | chr1 | 25392119 | |||
| chr1:25392123 | G | T | 1 | a0009 | 4 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
missense_variant | MODERATE | c.505C>A | p.Leu169Met | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 4/10 | 544/1571 | 505/1254 | 169/417 | chr1 | 25392123 | |||
| chr1:25402627 | G | T | 1 | a0023 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.455C>A | p.Thr152Asn | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/10 | 494/1571 | 455/1254 | 152/417 | chr1 | 25402627 | |||
| chr1:25402678 | T | C | 1 | a0017 | 2 | NA18960.hp2 NA18986.hp2 |
missense_variant | MODERATE | c.404A>G | p.Asn135Ser | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/10 | 443/1571 | 404/1254 | 135/417 | chr1 | 25402678 | |||
| chr1:25402699 | C | T | 1 | a0023 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.383G>A | p.Gly128Asp | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/10 | 422/1571 | 383/1254 | 128/417 | chr1 | 25402699 | |||
| chr1:25402702 | G | A | 1 | a0023 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.380C>T | p.Ala127Val | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/10 | 419/1571 | 380/1254 | 127/417 | chr1 | 25402702 | |||
| chr1:25402721 | T | A | 2 | a0016 a0023 |
3 | HG03942.hp1 NA18951.hp2 NA19012.hp1 |
missense_variant | MODERATE | c.361A>T | p.Met121Leu | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/10 | 400/1571 | 361/1254 | 121/417 | chr1 | 25402721 | |||
| chr1:25408711 | G | A | 7 | a0001 a0009 a0010 others(4): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
missense_variant | MODERATE | c.307C>T | p.Pro103Ser | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/10 | 346/1571 | 307/1254 | 103/417 | chr1 | 25408711 | |||
| chr1:25408764 | G | C | 1 | a0006 | 8 | HG02257.hp2 HG02486.hp2 HG02559.hp2 others(5): Show |
missense_variant | MODERATE | c.254C>G | p.Ala85Gly | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/10 | 293/1571 | 254/1254 | 85/417 | chr1 | 25408764 | |||
| chr1:25408815 | T | C | 7 | a0001 a0009 a0010 others(4): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
missense_variant | MODERATE | c.203A>G | p.Asn68Ser | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/10 | 242/1571 | 203/1254 | 68/417 | chr1 | 25408815 | |||
| chr1:25408840 | G | T | 7 | a0001 a0009 a0010 others(4): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
missense_variant | MODERATE | c.178C>A | p.Leu60Ile | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/10 | 217/1571 | 178/1254 | 60/417 | chr1 | 25408840 | |||
| chr1:25420739 | G | C | 5 | a0002 a0003 a0005 others(2): Show |
141 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(138): Show |
missense_variant | MODERATE | c.48C>G | p.Cys16Trp | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/10 | 87/1571 | 48/1254 | 16/417 | chr1 | 25420739 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:25370524 | G | A | 2 | a0010c0015 a0012c0010 |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
synonymous_variant | LOW | c.1170C>T | p.Leu390Leu | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/10 | 1209/1571 | 1170/1254 | 390/417 | chr1 | 25370524 | |||
| chr1:25408817 | T | C | 9 | a0001c0001 a0001c0025 a0009c0009 others(6): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
synonymous_variant | LOW | c.201A>G | p.Ser67Ser | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/10 | 240/1571 | 201/1254 | 67/417 | chr1 | 25408817 | |||
| chr1:25408868 | G | A | 9 | a0001c0001 a0001c0025 a0009c0009 others(6): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
splice_region_variant&synonymous_variant | LOW | c.150C>T | p.Val50Val | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/10 | 189/1571 | 150/1254 | 50/417 | chr1 | 25408868 | |||
| chr1:25420682 | G | A | 2 | a0001c0025 a0004c0024 |
2 | HG01243.hp1 NA18974.hp2 |
synonymous_variant | LOW | c.105C>T | p.Asp35Asp | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/10 | 144/1571 | 105/1254 | 35/417 | chr1 | 25420682 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:25362392 | T | A | 1 | a0007c0007t0002 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*135A>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 10/10 | 135 | chr1 | 25362392 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:25362681 | A | G | 1 | a0005c0005t0001g0299 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1228-128T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25362681 | |||||||
| chr1:25362780 | G | A | 5 | a0008c0008t0001g0146 a0008c0008t0001g0147 a0008c0008t0001g0148 others(2): Show |
5 | HG01109.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1228-227C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25362780 | |||||||
| chr1:25362915 | A | G | 31 | a0002c0002t0001g0189 a0003c0003t0001g0014 a0003c0003t0001g0184 others(28): Show |
32 | HG00099.hp1 HG00140.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.1228-362T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25362915 | |||||||
| chr1:25362951 | T | G | 35 | a0003c0003t0001g0313 a0005c0005t0001g0015 a0005c0005t0001g0297 others(32): Show |
37 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.1228-398A>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25362951 | |||||||
| chr1:25363037 | G | A | 59 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(56): Show |
62 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.1228-484C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25363037 | |||||||
| chr1:25363081 | C | T | 1 | a0003c0003t0001g0201 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1228-528G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25363081 | |||||||
| chr1:25363193 | C | T | 3 | a0001c0001t0001g0046 a0001c0001t0001g0080 a0001c0001t0001g0081 |
3 | HG00099.hp2 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1228-640G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25363193 | |||||||
| chr1:25363217 | C | T | 6 | a0007c0007t0001g0010 a0007c0007t0001g0145 a0007c0007t0001g0173 others(3): Show |
7 | HG01167.hp2 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1228-664G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25363217 | |||||||
| chr1:25363222 | G | A | 3 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0180 |
3 | HG00639.hp2 HG01243.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1228-669C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25363222 | |||||||
| chr1:25363250 | G | A | 1 | a0019c0019t0001g0021 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1228-697C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25363250 | |||||||
| chr1:25363273 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1228-720G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25363273 | |||||||
| chr1:25363476 | A | C | 14 | a0006c0006t0001g0285 a0006c0006t0001g0290 a0006c0006t0001g0291 others(11): Show |
15 | HG01167.hp2 HG02109.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1228-923T>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25363476 | |||||||
| chr1:25363724 | G | A | 1 | a0004c0004t0001g0132 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1228-1171C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25363724 | |||||||
| chr1:25363758 | T | C | 1 | a0015c0011t0001g0161 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1228-1205A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25363758 | |||||||
| chr1:25363781 | T | C | 2 | a0010c0015t0001g0106 a0010c0015t0001g0109 |
2 | HG02027.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.1228-1228A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25363781 | |||||||
| chr1:25363783 | T | C | 113 | a0001c0001t0001g0034 a0001c0001t0001g0063 a0001c0001t0001g0097 others(110): Show |
117 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.1228-1230A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25363783 | |||||||
| chr1:25363883 | C | A | 2 | a0003c0003t0001g0253 a0003c0003t0001g0265 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1228-1330G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25363883 | |||||||
| chr1:25363919 | A | C | 1 | a0003c0003t0001g0233 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1228-1366T>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25363919 | |||||||
| chr1:25364095 | C | T | 34 | a0003c0003t0001g0313 a0005c0005t0001g0015 a0005c0005t0001g0297 others(31): Show |
36 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.1228-1542G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25364095 | |||||||
| chr1:25364146 | T | C | 1 | a0019c0019t0001g0021 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1228-1593A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25364146 | |||||||
| chr1:25364271 | C | T | 1 | a0008c0008t0001g0148 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1228-1718G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25364271 | |||||||
| chr1:25364323 | G | A | 37 | a0003c0003t0001g0313 a0005c0005t0001g0015 a0005c0005t0001g0297 others(34): Show |
39 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.1228-1770C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25364323 | |||||||
| chr1:25364413 | TTC | T | 6 | a0003c0003t0001g0215 a0003c0003t0001g0227 a0003c0003t0001g0232 others(3): Show |
6 | HG00639.hp1 HG02055.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1228-1862_1228-186 others(6): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25364413 | |||||||
| chr1:25364415 | C | T | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(282): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.1228-1862G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25364415 | |||||||
| chr1:25364785 | T | G | 2 | a0005c0005t0001g0307 a0005c0005t0001g0312 |
2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1228-2232A>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25364785 | |||||||
| chr1:25365068 | G | A | 3 | a0001c0001t0001g0085 a0017c0016t0001g0086 a0017c0016t0001g0087 |
3 | NA18960.hp2 NA18986.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1228-2515C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25365068 | |||||||
| chr1:25365124 | C | T | 1 | a0002c0002t0001g0230 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1228-2571G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25365124 | |||||||
| chr1:25365673 | T | A | 1 | a0001c0001t0001g0140 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1228-3120A>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25365673 | |||||||
| chr1:25365738 | T | C | 1 | a0004c0004t0001g0176 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1228-3185A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25365738 | |||||||
| chr1:25365902 | G | A | 1 | a0003c0003t0001g0254 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1228-3349C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25365902 | |||||||
| chr1:25365984 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1228-3431A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25365984 | |||||||
| chr1:25366033 | T | C | 113 | a0001c0001t0001g0034 a0001c0001t0001g0063 a0001c0001t0001g0097 others(110): Show |
117 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.1228-3480A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25366033 | |||||||
| chr1:25366050 | C | CA | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.1228-3498dupT | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25366050 | |||||||
| chr1:25366050 | C | CAA | 10 | a0001c0001t0001g0040 a0001c0001t0001g0042 a0001c0001t0001g0045 others(7): Show |
10 | HG01106.hp1 HG02080.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1228-3499_1228-349 others(6): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25366050 | |||||||
| chr1:25366052 | A | G | 1 | a0004c0004t0001g0169 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1228-3499T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25366052 | |||||||
| chr1:25366134 | G | A | 1 | a0003c0003t0001g0257 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1228-3581C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25366134 | |||||||
| chr1:25366170 | C | T | 2 | a0001c0001t0001g0047 a0001c0001t0001g0149 |
2 | HG01433.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.1228-3617G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25366170 | |||||||
| chr1:25366395 | T | C | 1 | a0002c0002t0001g0199 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1228-3842A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25366395 | |||||||
| chr1:25366396 | T | TC | 18 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(15): Show |
19 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.1228-3844dupG | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25366396 | |||||||
| chr1:25366493 | C | T | 1 | a0004c0004t0001g0176 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1228-3940G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25366493 | |||||||
| chr1:25366593 | T | G | 1 | a0002c0002t0001g0271 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1227+3874A>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25366593 | |||||||
| chr1:25366712 | A | G | 122 | a0001c0001t0001g0034 a0001c0001t0001g0063 a0001c0001t0001g0097 others(119): Show |
128 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.1227+3755T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25366712 | |||||||
| chr1:25366815 | T | C | 4 | a0003c0003t0001g0286 a0003c0003t0001g0287 a0003c0003t0001g0288 others(1): Show |
4 | HG02145.hp2 HG03195.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1227+3652A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25366815 | |||||||
| chr1:25366912 | G | A | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(290): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.1227+3555C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25366912 | |||||||
| chr1:25367052 | C | T | 2 | a0012c0010t0001g0019 a0012c0010t0001g0020 |
2 | HG01106.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1227+3415G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25367052 | |||||||
| chr1:25367080 | G | A | 2 | a0012c0010t0001g0019 a0012c0010t0001g0020 |
2 | HG01106.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1227+3387C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25367080 | |||||||
| chr1:25367164 | G | A | 3 | a0005c0005t0001g0304 a0005c0005t0001g0310 a0005c0005t0001g0312 |
3 | HG02615.hp1 HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1227+3303C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25367164 | |||||||
| chr1:25367206 | T | G | 1 | a0003c0003t0001g0184 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1227+3261A>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25367206 | |||||||
| chr1:25367256 | G | A | 3 | a0003c0003t0001g0313 a0014c0013t0001g0025 a0014c0013t0001g0026 |
3 | HG02145.hp1 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1227+3211C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25367256 | |||||||
| chr1:25367310 | C | G | 90 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(87): Show |
99 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.1227+3157G>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25367310 | |||||||
| chr1:25367316 | A | G | 2 | a0003c0003t0001g0253 a0003c0003t0001g0265 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1227+3151T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25367316 | |||||||
| chr1:25367351 | G | A | 2 | a0012c0010t0001g0019 a0012c0010t0001g0020 |
2 | HG01106.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1227+3116C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25367351 | |||||||
| chr1:25367541 | G | A | 2 | a0012c0010t0001g0019 a0012c0010t0001g0020 |
2 | HG01106.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1227+2926C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25367541 | |||||||
| chr1:25367636 | G | A | 60 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(57): Show |
69 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.1227+2831C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25367636 | |||||||
| chr1:25367656 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1227+2811C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25367656 | |||||||
| chr1:25367738 | C | G | 2 | a0003c0003t0001g0277 a0020c0026t0001g0222 |
2 | HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1227+2729G>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25367738 | |||||||
| chr1:25367764 | T | G | 27 | a0003c0003t0001g0313 a0005c0005t0001g0015 a0005c0005t0001g0297 others(24): Show |
29 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1227+2703A>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25367764 | |||||||
| chr1:25367826 | T | G | 1 | a0001c0001t0001g0071 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1227+2641A>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25367826 | |||||||
| chr1:25367833 | C | G | 31 | a0002c0002t0001g0245 a0003c0003t0001g0313 a0005c0005t0001g0015 others(28): Show |
33 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.1227+2634G>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25367833 | |||||||
| chr1:25367878 | G | C | 2 | a0012c0010t0001g0019 a0012c0010t0001g0020 |
2 | HG01106.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1227+2589C>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25367878 | |||||||
| chr1:25367922 | T | C | 17 | a0001c0001t0001g0153 a0002c0002t0001g0194 a0002c0002t0001g0216 others(14): Show |
19 | HG00597.hp1 HG01069.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.1227+2545A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25367922 | |||||||
| chr1:25367970 | G | A | 3 | a0006c0006t0001g0291 a0006c0006t0001g0292 a0006c0006t0001g0294 |
3 | HG02559.hp2 HG02922.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1227+2497C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25367970 | |||||||
| chr1:25367996 | C | T | 11 | a0001c0001t0001g0153 a0003c0003t0001g0277 a0003c0003t0001g0283 others(8): Show |
13 | HG01069.hp2 HG01071.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.1227+2471G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25367996 | |||||||
| chr1:25368042 | G | A | 1 | a0012c0010t0001g0020 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1227+2425C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25368042 | |||||||
| chr1:25368058 | A | G | 11 | a0001c0001t0001g0102 a0001c0001t0001g0153 a0003c0003t0001g0283 others(8): Show |
13 | HG01069.hp2 HG01071.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.1227+2409T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25368058 | |||||||
| chr1:25368134 | G | C | 5 | a0008c0008t0001g0146 a0008c0008t0001g0147 a0008c0008t0001g0148 others(2): Show |
5 | HG01109.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1227+2333C>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25368134 | |||||||
| chr1:25368154 | C | T | 2 | a0004c0004t0001g0037 a0004c0004t0001g0132 |
2 | HG02056.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.1227+2313G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25368154 | |||||||
| chr1:25368306 | C | T | 1 | a0001c0001t0001g0022 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1227+2161G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25368306 | |||||||
| chr1:25368314 | G | A | 1 | a0004c0004t0001g0159 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1227+2153C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25368314 | |||||||
| chr1:25368389 | C | T | 26 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(23): Show |
28 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.1227+2078G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25368389 | |||||||
| chr1:25368465 | C | T | 6 | a0004c0004t0001g0144 a0004c0004t0001g0159 a0004c0004t0001g0162 others(3): Show |
6 | HG02717.hp1 HG02895.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1227+2002G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25368465 | |||||||
| chr1:25368506 | C | T | 5 | a0008c0008t0001g0146 a0008c0008t0001g0147 a0008c0008t0001g0148 others(2): Show |
5 | HG01109.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1227+1961G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25368506 | |||||||
| chr1:25368587 | C | G | 6 | a0002c0002t0001g0218 a0003c0003t0001g0277 a0010c0015t0001g0106 others(3): Show |
6 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1227+1880G>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25368587 | |||||||
| chr1:25368609 | A | T | 1 | a0003c0003t0001g0289 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1227+1858T>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25368609 | |||||||
| chr1:25368856 | GTTCAAGT others(971): Show |
G | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227+633_1227+1610 others(3): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25368856 | |||||||
| chr1:25368863 | T | C | 3 | a0009c0009t0001g0073 a0009c0009t0001g0074 a0009c0009t0001g0075 |
3 | HG02615.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1227+1604A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25368863 | |||||||
| chr1:25368950 | G | A | 24 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(21): Show |
26 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.1227+1517C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25368950 | |||||||
| chr1:25369156 | G | A | 1 | a0001c0001t0001g0090 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1227+1311C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25369156 | |||||||
| chr1:25369217 | T | C | 1 | a0001c0001t0001g0090 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1227+1250A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25369217 | |||||||
| chr1:25369344 | G | A | 72 | a0001c0001t0001g0034 a0001c0001t0001g0097 a0001c0001t0001g0128 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.1227+1123C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25369344 | |||||||
| chr1:25369459 | T | C | 4 | a0008c0008t0001g0147 a0008c0008t0001g0148 a0008c0008t0001g0177 others(1): Show |
4 | HG01109.hp1 HG02055.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1227+1008A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25369459 | |||||||
| chr1:25369545 | C | A | 1 | a0001c0001t0001g0089 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1227+922G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25369545 | |||||||
| chr1:25369730 | A | AT | 41 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0058 others(38): Show |
43 | HG00642.hp1 HG01069.hp1 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.1227+736dupA | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25369730 | |||||||
| chr1:25369730 | A | ATT | 64 | a0001c0001t0001g0034 a0001c0001t0001g0097 a0001c0001t0001g0129 others(61): Show |
66 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.1227+735_1227+736d others(4): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25369730 | |||||||
| chr1:25369730 | A | ATTT | 40 | a0001c0001t0001g0128 a0002c0002t0001g0189 a0002c0002t0001g0214 others(37): Show |
41 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.1227+734_1227+736d others(5): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25369730 | |||||||
| chr1:25369730 | A | ATTTT | 8 | a0003c0003t0001g0201 a0003c0003t0001g0215 a0003c0003t0001g0232 others(5): Show |
8 | HG00733.hp2 HG00741.hp1 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.1227+733_1227+736d others(6): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25369730 | |||||||
| chr1:25369730 | AT | A | 25 | a0001c0001t0001g0038 a0001c0001t0001g0048 a0001c0001t0001g0085 others(22): Show |
26 | HG00639.hp2 HG01099.hp2 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.1227+736delA | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25369730 | |||||||
| chr1:25369778 | A | G | 27 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(24): Show |
29 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1227+689T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25369778 | |||||||
| chr1:25369799 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1227+668G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25369799 | |||||||
| chr1:25369807 | C | T | 1 | a0001c0001t0001g0038 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1227+660G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25369807 | |||||||
| chr1:25369841 | C | T | 4 | a0001c0001t0001g0044 a0001c0001t0001g0107 a0001c0001t0001g0108 others(1): Show |
4 | NA18969.hp2 NA18977.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1227+626G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25369841 | |||||||
| chr1:25369849 | T | C | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227+618A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25369849 | |||||||
| chr1:25369890 | T | C | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227+577A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25369890 | |||||||
| chr1:25369896 | G | A | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227+571C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25369896 | |||||||
| chr1:25369935 | T | C | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227+532A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25369935 | |||||||
| chr1:25370012 | T | C | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227+455A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25370012 | |||||||
| chr1:25370021 | C | G | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227+446G>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25370021 | |||||||
| chr1:25370035 | A | G | 27 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(24): Show |
29 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1227+432T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25370035 | |||||||
| chr1:25370136 | C | T | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227+331G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25370136 | |||||||
| chr1:25370137 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1227+330C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25370137 | |||||||
| chr1:25370160 | A | G | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227+307T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25370160 | |||||||
| chr1:25370192 | C | G | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227+275G>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25370192 | |||||||
| chr1:25370193 | G | A | 1 | a0004c0004t0001g0156 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1227+274C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25370193 | |||||||
| chr1:25370229 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1227+238G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25370229 | |||||||
| chr1:25370263 | T | C | 27 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(24): Show |
29 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1227+204A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25370263 | |||||||
| chr1:25370405 | C | T | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227+62G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 9/9 | chr1 | 25370405 | |||||||
| chr1:25370607 | A | G | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-67T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25370607 | |||||||
| chr1:25370613 | TTG | T | 31 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(28): Show |
33 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.1154-75_1154-74del others(2): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25370613 | |||||||
| chr1:25370635 | G | A | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-95C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25370635 | |||||||
| chr1:25370685 | C | A | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-145G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25370685 | |||||||
| chr1:25370720 | A | C | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-180T>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25370720 | |||||||
| chr1:25370721 | C | CTATTT | 106 | a0001c0001t0001g0034 a0001c0001t0001g0052 a0001c0001t0001g0056 others(103): Show |
110 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.1154-186_1154-182d others(7): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25370721 | |||||||
| chr1:25370721 | C | CTATTTTA others(3): Show |
14 | a0001c0001t0001g0129 a0002c0002t0001g0185 a0002c0002t0001g0186 others(11): Show |
14 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.1154-191_1154-182d others(12): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25370721 | |||||||
| chr1:25370721 | C | CTATTTTA others(8): Show |
3 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 |
3 | HG02027.hp2 HG02559.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.1154-196_1154-182d others(17): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25370721 | |||||||
| chr1:25370721 | CTATTT | C | 29 | a0001c0001t0001g0076 a0001c0001t0001g0154 a0002c0002t0001g0238 others(26): Show |
31 | HG00280.hp2 HG00621.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.1154-186_1154-182d others(7): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25370721 | |||||||
| chr1:25370721 | CTATTTTA others(3): Show |
C | 2 | a0002c0002t0001g0259 a0002c0002t0001g0264 |
2 | NA19011.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1154-191_1154-182d others(12): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25370721 | |||||||
| chr1:25370775 | G | A | 2 | a0012c0010t0001g0019 a0012c0010t0001g0020 |
2 | HG01106.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1154-235C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25370775 | |||||||
| chr1:25370788 | A | G | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-248T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25370788 | |||||||
| chr1:25370804 | C | A | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-264G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25370804 | |||||||
| chr1:25370805 | G | A | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-265C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25370805 | |||||||
| chr1:25370810 | A | G | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-270T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25370810 | |||||||
| chr1:25370818 | G | A | 1 | a0003c0003t0001g0202 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1154-278C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25370818 | |||||||
| chr1:25370856 | C | A | 6 | a0002c0002t0001g0209 a0002c0002t0001g0248 a0010c0015t0001g0106 others(3): Show |
6 | HG00280.hp1 HG01106.hp1 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.1154-316G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25370856 | |||||||
| chr1:25370882 | A | G | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-342T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25370882 | |||||||
| chr1:25370893 | C | T | 2 | a0012c0010t0001g0019 a0012c0010t0001g0020 |
2 | HG01106.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1154-353G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25370893 | |||||||
| chr1:25370915 | A | AT | 13 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(10): Show |
13 | HG00621.hp1 HG01106.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.1154-376dupA | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25370915 | |||||||
| chr1:25370915 | AT | A | 15 | a0001c0001t0001g0023 a0001c0001t0001g0081 a0001c0001t0001g0090 others(12): Show |
15 | HG01109.hp1 HG01169.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.1154-376delA | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25370915 | |||||||
| chr1:25370941 | G | GA | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-402_1154-401i others(3): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25370941 | |||||||
| chr1:25370947 | G | A | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-407C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25370947 | |||||||
| chr1:25370983 | T | C | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-443A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25370983 | |||||||
| chr1:25371019 | T | G | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-479A>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25371019 | |||||||
| chr1:25371031 | T | C | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-491A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25371031 | |||||||
| chr1:25371038 | A | G | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-498T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25371038 | |||||||
| chr1:25371051 | C | T | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-511G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25371051 | |||||||
| chr1:25371065 | A | G | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-525T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25371065 | |||||||
| chr1:25371068 | A | ATT | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-529_1154-528i others(4): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25371068 | |||||||
| chr1:25371069 | A | AT | 28 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(25): Show |
30 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.1154-530dupA | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25371069 | |||||||
| chr1:25371069 | A | T | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-529T>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25371069 | |||||||
| chr1:25371155 | C | T | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-615G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25371155 | |||||||
| chr1:25371162 | G | A | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-622C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25371162 | |||||||
| chr1:25371167 | G | T | 2 | a0012c0010t0001g0019 a0012c0010t0001g0020 |
2 | HG01106.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1154-627C>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25371167 | |||||||
| chr1:25371179 | C | G | 2 | a0012c0010t0001g0019 a0012c0010t0001g0020 |
2 | HG01106.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1154-639G>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25371179 | |||||||
| chr1:25371215 | C | T | 6 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(3): Show |
6 | HG01106.hp1 HG02027.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1154-675G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25371215 | |||||||
| chr1:25371216 | G | A | 1 | a0002c0002t0001g0199 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1154-676C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25371216 | |||||||
| chr1:25371223 | G | A | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-683C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25371223 | |||||||
| chr1:25371391 | A | G | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-851T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25371391 | |||||||
| chr1:25371396 | G | A | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-856C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25371396 | |||||||
| chr1:25371464 | A | G | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-924T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25371464 | |||||||
| chr1:25371467 | C | G | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-927G>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25371467 | |||||||
| chr1:25371468 | A | T | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-928T>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25371468 | |||||||
| chr1:25371477 | C | T | 1 | a0002c0002t0001g0183 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1154-937G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25371477 | |||||||
| chr1:25371479 | C | T | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-939G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25371479 | |||||||
| chr1:25371481 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1154-941G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25371481 | |||||||
| chr1:25371494 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1154-954G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25371494 | |||||||
| chr1:25371513 | A | G | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-973T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25371513 | |||||||
| chr1:25371529 | C | T | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-989G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25371529 | |||||||
| chr1:25371538 | T | G | 3 | a0010c0015t0001g0109 a0012c0010t0001g0019 a0012c0010t0001g0020 |
3 | HG01106.hp1 HG02027.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1154-998A>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25371538 | |||||||
| chr1:25371539 | T | G | 1 | a0010c0015t0001g0106 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1154-999A>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25371539 | |||||||
| chr1:25371544 | T | G | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-1004A>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25371544 | |||||||
| chr1:25371562 | G | A | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-1022C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25371562 | |||||||
| chr1:25371565 | G | A | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-1025C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25371565 | |||||||
| chr1:25371566 | T | C | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-1026A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25371566 | |||||||
| chr1:25371636 | G | T | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-1096C>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25371636 | |||||||
| chr1:25371643 | A | G | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-1103T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25371643 | |||||||
| chr1:25371700 | G | A | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-1160C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25371700 | |||||||
| chr1:25371732 | C | T | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-1192G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25371732 | |||||||
| chr1:25371737 | C | T | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-1197G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25371737 | |||||||
| chr1:25371741 | C | A | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-1201G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25371741 | |||||||
| chr1:25371770 | A | G | 5 | a0001c0001t0001g0112 a0010c0015t0001g0106 a0010c0015t0001g0109 others(2): Show |
5 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1154-1230T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25371770 | |||||||
| chr1:25371863 | T | C | 185 | a0001c0001t0001g0034 a0001c0001t0001g0097 a0001c0001t0001g0099 others(182): Show |
194 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.1154-1323A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25371863 | |||||||
| chr1:25371912 | A | T | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-1372T>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25371912 | |||||||
| chr1:25371948 | GTTA | G | 31 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(28): Show |
33 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.1154-1411_1154-140 others(7): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25371948 | |||||||
| chr1:25371973 | T | C | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-1433A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25371973 | |||||||
| chr1:25372090 | A | T | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-1550T>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25372090 | |||||||
| chr1:25372091 | A | T | 3 | a0010c0015t0001g0106 a0012c0010t0001g0019 a0012c0010t0001g0020 |
3 | HG01106.hp1 HG02559.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.1154-1551T>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25372091 | |||||||
| chr1:25372156 | T | G | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-1616A>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25372156 | |||||||
| chr1:25372163 | C | T | 2 | a0010c0015t0001g0106 a0010c0015t0001g0109 |
2 | HG02027.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.1154-1623G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25372163 | |||||||
| chr1:25372164 | G | A | 27 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(24): Show |
29 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1154-1624C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25372164 | |||||||
| chr1:25372178 | G | T | 2 | a0012c0010t0001g0019 a0012c0010t0001g0020 |
2 | HG01106.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1154-1638C>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25372178 | |||||||
| chr1:25372233 | T | C | 2 | a0003c0003t0001g0283 a0003c0003t0001g0284 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1154-1693A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25372233 | |||||||
| chr1:25372237 | T | C | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-1697A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25372237 | |||||||
| chr1:25372242 | G | A | 1 | a0004c0004t0001g0158 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1154-1702C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25372242 | |||||||
| chr1:25372244 | G | T | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-1704C>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25372244 | |||||||
| chr1:25372246 | A | G | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-1706T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25372246 | |||||||
| chr1:25372258 | G | C | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-1718C>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25372258 | |||||||
| chr1:25372292 | G | T | 2 | a0012c0010t0001g0019 a0012c0010t0001g0020 |
2 | HG01106.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1154-1752C>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25372292 | |||||||
| chr1:25372379 | C | T | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-1839G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25372379 | |||||||
| chr1:25372412 | A | G | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-1872T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25372412 | |||||||
| chr1:25372425 | A | G | 27 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(24): Show |
29 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1154-1885T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25372425 | |||||||
| chr1:25372451 | G | T | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-1911C>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25372451 | |||||||
| chr1:25372459 | C | T | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-1919G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25372459 | |||||||
| chr1:25372460 | G | A | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-1920C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25372460 | |||||||
| chr1:25372461 | T | G | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-1921A>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25372461 | |||||||
| chr1:25372513 | C | G | 5 | a0001c0001t0001g0040 a0010c0015t0001g0106 a0010c0015t0001g0109 others(2): Show |
5 | HG01106.hp1 HG02027.hp2 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.1154-1973G>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25372513 | |||||||
| chr1:25372537 | T | G | 2 | a0002c0002t0001g0220 a0002c0002t0001g0243 |
2 | NA19011.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1154-1997A>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25372537 | |||||||
| chr1:25372575 | C | T | 6 | a0007c0007t0001g0010 a0007c0007t0001g0145 a0007c0007t0001g0173 others(3): Show |
7 | HG01167.hp2 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1154-2035G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25372575 | |||||||
| chr1:25372611 | C | T | 4 | a0007c0007t0001g0010 a0007c0007t0001g0145 a0007c0007t0001g0173 others(1): Show |
5 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1154-2071G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25372611 | |||||||
| chr1:25372680 | C | T | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-2140G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25372680 | |||||||
| chr1:25372690 | G | A | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-2150C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25372690 | |||||||
| chr1:25372693 | T | C | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-2153A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25372693 | |||||||
| chr1:25372705 | C | T | 6 | a0007c0007t0001g0010 a0007c0007t0001g0173 a0010c0015t0001g0106 others(3): Show |
7 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1154-2165G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25372705 | |||||||
| chr1:25372724 | G | A | 5 | a0005c0005t0001g0300 a0010c0015t0001g0106 a0010c0015t0001g0109 others(2): Show |
5 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1154-2184C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25372724 | |||||||
| chr1:25372736 | G | T | 5 | a0005c0005t0001g0300 a0010c0015t0001g0106 a0010c0015t0001g0109 others(2): Show |
5 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1154-2196C>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25372736 | |||||||
| chr1:25372769 | T | G | 5 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(2): Show |
5 | HG01106.hp1 HG01167.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.1154-2229A>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25372769 | |||||||
| chr1:25372783 | C | T | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-2243G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25372783 | |||||||
| chr1:25372867 | C | T | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-2327G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25372867 | |||||||
| chr1:25372929 | G | A | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-2389C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25372929 | |||||||
| chr1:25372960 | A | G | 5 | a0004c0004t0001g0165 a0010c0015t0001g0106 a0010c0015t0001g0109 others(2): Show |
5 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1153+2389T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25372960 | |||||||
| chr1:25373004 | TAGG | T | 31 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(28): Show |
33 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.1153+2342_1153+234 others(7): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25373004 | |||||||
| chr1:25373008 | A | G | 31 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(28): Show |
33 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.1153+2341T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25373008 | |||||||
| chr1:25373045 | C | A | 5 | a0008c0008t0001g0146 a0008c0008t0001g0147 a0008c0008t0001g0148 others(2): Show |
5 | HG01109.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1153+2304G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25373045 | |||||||
| chr1:25373058 | T | C | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+2291A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25373058 | |||||||
| chr1:25373063 | A | G | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+2286T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25373063 | |||||||
| chr1:25373116 | C | T | 1 | a0002c0002t0001g0217 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1153+2233G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25373116 | |||||||
| chr1:25373142 | A | G | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+2207T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25373142 | |||||||
| chr1:25373147 | G | A | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+2202C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25373147 | |||||||
| chr1:25373215 | G | A | 1 | a0002c0002t0001g0214 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1153+2134C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25373215 | |||||||
| chr1:25373221 | C | A | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+2128G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25373221 | |||||||
| chr1:25373235 | C | T | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+2114G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25373235 | |||||||
| chr1:25373238 | G | T | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+2111C>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25373238 | |||||||
| chr1:25373276 | C | T | 5 | a0001c0001t0001g0111 a0010c0015t0001g0106 a0010c0015t0001g0109 others(2): Show |
5 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1153+2073G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25373276 | |||||||
| chr1:25373280 | T | C | 32 | a0001c0001t0001g0111 a0005c0005t0001g0015 a0005c0005t0001g0297 others(29): Show |
34 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.1153+2069A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25373280 | |||||||
| chr1:25373299 | A | G | 27 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(24): Show |
29 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1153+2050T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25373299 | |||||||
| chr1:25373304 | T | G | 1 | a0012c0010t0001g0020 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1153+2045A>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25373304 | |||||||
| chr1:25373354 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1153+1995A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25373354 | |||||||
| chr1:25373356 | G | T | 5 | a0001c0001t0001g0111 a0010c0015t0001g0106 a0010c0015t0001g0109 others(2): Show |
5 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1153+1993C>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25373356 | |||||||
| chr1:25373358 | G | A | 5 | a0001c0001t0001g0111 a0010c0015t0001g0106 a0010c0015t0001g0109 others(2): Show |
5 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1153+1991C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25373358 | |||||||
| chr1:25373451 | G | A | 3 | a0002c0002t0001g0011 a0002c0002t0001g0224 a0002c0002t0001g0240 |
4 | HG02148.hp1 NA18951.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+1898C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25373451 | |||||||
| chr1:25373457 | A | G | 1 | a0012c0010t0001g0020 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1153+1892T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25373457 | |||||||
| chr1:25373460 | T | G | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+1889A>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25373460 | |||||||
| chr1:25373485 | C | A | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+1864G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25373485 | |||||||
| chr1:25373495 | C | A | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+1854G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25373495 | |||||||
| chr1:25373513 | AT | A | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+1835delA | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25373513 | |||||||
| chr1:25373514 | T | A | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1153+1835A>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25373514 | |||||||
| chr1:25373563 | A | G | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+1786T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25373563 | |||||||
| chr1:25373576 | T | A | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+1773A>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25373576 | |||||||
| chr1:25373583 | C | G | 3 | a0003c0003t0001g0287 a0003c0003t0001g0288 a0003c0003t0001g0289 |
3 | HG02145.hp2 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1153+1766G>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25373583 | |||||||
| chr1:25373673 | G | A | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+1676C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25373673 | |||||||
| chr1:25373689 | T | C | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+1660A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25373689 | |||||||
| chr1:25373691 | TCAC | T | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+1655_1153+165 others(7): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25373691 | |||||||
| chr1:25373740 | C | T | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+1609G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25373740 | |||||||
| chr1:25373804 | A | AAAGGTG | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+1544_1153+154 others(10): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25373804 | |||||||
| chr1:25373806 | C | A | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+1543G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25373806 | |||||||
| chr1:25373807 | A | C | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+1542T>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25373807 | |||||||
| chr1:25373836 | C | CT | 74 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0097 others(71): Show |
77 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.1153+1512dupA | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25373836 | |||||||
| chr1:25373836 | CT | C | 6 | a0001c0001t0001g0085 a0004c0004t0001g0163 a0004c0004t0001g0169 others(3): Show |
6 | HG01069.hp1 HG02896.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1153+1512delA | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25373836 | |||||||
| chr1:25373877 | C | CTGGAGGG others(3): Show |
4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+1471_1153+147 others(14): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25373877 | |||||||
| chr1:25373889 | T | C | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+1460A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25373889 | |||||||
| chr1:25373891 | G | A | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+1458C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25373891 | |||||||
| chr1:25373940 | C | T | 2 | a0003c0003t0001g0232 a0003c0003t0001g0233 |
2 | NA20129.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1153+1409G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25373940 | |||||||
| chr1:25373946 | G | C | 5 | a0002c0002t0001g0236 a0010c0015t0001g0106 a0010c0015t0001g0109 others(2): Show |
5 | HG01106.hp1 HG02027.hp2 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.1153+1403C>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25373946 | |||||||
| chr1:25373970 | A | G | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+1379T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25373970 | |||||||
| chr1:25374003 | C | T | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+1346G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25374003 | |||||||
| chr1:25374018 | C | G | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+1331G>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25374018 | |||||||
| chr1:25374056 | G | A | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+1293C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25374056 | |||||||
| chr1:25374069 | C | T | 4 | a0010c0015t0001g0106 a0010c0015t0001g0109 a0012c0010t0001g0019 others(1): Show |
4 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+1280G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25374069 | |||||||
| chr1:25374112 | T | C | 6 | a0001c0001t0001g0032 a0001c0001t0001g0038 a0010c0015t0001g0106 others(3): Show |
6 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1153+1237A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25374112 | |||||||
| chr1:25374113 | G | A | 6 | a0001c0001t0001g0032 a0001c0001t0001g0038 a0010c0015t0001g0106 others(3): Show |
6 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1153+1236C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25374113 | |||||||
| chr1:25374136 | T | TTTTTTTC | 6 | a0001c0001t0001g0032 a0001c0001t0001g0038 a0010c0015t0001g0106 others(3): Show |
6 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1153+1212_1153+121 others(11): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25374136 | |||||||
| chr1:25374161 | C | T | 6 | a0001c0001t0001g0032 a0001c0001t0001g0038 a0010c0015t0001g0106 others(3): Show |
6 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1153+1188G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25374161 | |||||||
| chr1:25374187 | T | C | 6 | a0001c0001t0001g0032 a0001c0001t0001g0038 a0010c0015t0001g0106 others(3): Show |
6 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1153+1162A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25374187 | |||||||
| chr1:25374198 | C | A | 6 | a0001c0001t0001g0032 a0001c0001t0001g0038 a0010c0015t0001g0106 others(3): Show |
6 | HG01106.hp1 HG02027.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1153+1151G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25374198 | |||||||
| chr1:25374226 | TTACAGGT others(2): Show |
T | 4 | a0001c0001t0001g0032 a0001c0001t0001g0038 a0010c0015t0001g0106 others(1): Show |
4 | HG02027.hp2 NA18985.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+1114_1153+112 others(13): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25374226 | |||||||
| chr1:25374239 | C | A | 4 | a0001c0001t0001g0032 a0001c0001t0001g0038 a0010c0015t0001g0106 others(1): Show |
4 | HG02027.hp2 NA18985.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+1110G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25374239 | |||||||
| chr1:25374246 | G | A | 1 | a0001c0001t0001g0034 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1153+1103C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25374246 | |||||||
| chr1:25374254 | A | T | 4 | a0001c0001t0001g0032 a0001c0001t0001g0038 a0010c0015t0001g0106 others(1): Show |
4 | HG02027.hp2 NA18985.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+1095T>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25374254 | |||||||
| chr1:25374265 | T | C | 2 | a0001c0001t0001g0032 a0001c0001t0001g0038 |
2 | NA18985.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1153+1084A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25374265 | |||||||
| chr1:25374277 | C | T | 4 | a0001c0001t0001g0032 a0001c0001t0001g0038 a0010c0015t0001g0106 others(1): Show |
4 | HG02027.hp2 NA18985.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+1072G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25374277 | |||||||
| chr1:25374278 | A | G | 4 | a0001c0001t0001g0032 a0001c0001t0001g0038 a0010c0015t0001g0106 others(1): Show |
4 | HG02027.hp2 NA18985.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+1071T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25374278 | |||||||
| chr1:25374299 | G | T | 4 | a0001c0001t0001g0032 a0001c0001t0001g0038 a0010c0015t0001g0106 others(1): Show |
4 | HG02027.hp2 NA18985.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+1050C>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25374299 | |||||||
| chr1:25374318 | C | T | 4 | a0001c0001t0001g0032 a0001c0001t0001g0038 a0010c0015t0001g0106 others(1): Show |
4 | HG02027.hp2 NA18985.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+1031G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25374318 | |||||||
| chr1:25374357 | C | G | 54 | a0004c0004t0001g0005 a0004c0004t0001g0009 a0004c0004t0001g0016 others(51): Show |
59 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(56): Show |
intron_variant | MODIFIER | c.1153+992G>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25374357 | |||||||
| chr1:25374358 | A | G | 55 | a0003c0003t0001g0277 a0004c0004t0001g0005 a0004c0004t0001g0009 others(52): Show |
60 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(57): Show |
intron_variant | MODIFIER | c.1153+991T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25374358 | |||||||
| chr1:25374451 | T | G | 5 | a0001c0001t0001g0032 a0001c0001t0001g0038 a0010c0015t0001g0106 others(2): Show |
5 | HG02027.hp2 HG02630.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.1153+898A>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25374451 | |||||||
| chr1:25374459 | G | T | 4 | a0001c0001t0001g0032 a0001c0001t0001g0038 a0010c0015t0001g0106 others(1): Show |
4 | HG02027.hp2 NA18985.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+890C>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25374459 | |||||||
| chr1:25374535 | G | T | 26 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(23): Show |
28 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.1153+814C>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25374535 | |||||||
| chr1:25374565 | T | C | 29 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(26): Show |
31 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.1153+784A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25374565 | |||||||
| chr1:25374568 | T | C | 29 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(26): Show |
31 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.1153+781A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25374568 | |||||||
| chr1:25374589 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0097 |
2 | NA18985.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1153+760G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25374589 | |||||||
| chr1:25374618 | C | A | 29 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(26): Show |
31 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.1153+731G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25374618 | |||||||
| chr1:25374813 | A | G | 3 | a0001c0001t0001g0118 a0012c0010t0001g0019 a0012c0010t0001g0020 |
3 | HG01106.hp1 HG02559.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1153+536T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25374813 | |||||||
| chr1:25374860 | G | A | 2 | a0012c0010t0001g0019 a0012c0010t0001g0020 |
2 | HG01106.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1153+489C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25374860 | |||||||
| chr1:25374887 | A | G | 28 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(25): Show |
30 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.1153+462T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25374887 | |||||||
| chr1:25374923 | A | G | 4 | a0007c0007t0001g0010 a0007c0007t0001g0145 a0007c0007t0001g0173 others(1): Show |
5 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1153+426T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25374923 | |||||||
| chr1:25374926 | G | A | 27 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(24): Show |
29 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1153+423C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25374926 | |||||||
| chr1:25374963 | A | T | 27 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(24): Show |
29 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1153+386T>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25374963 | |||||||
| chr1:25375124 | G | A | 3 | a0002c0002t0001g0013 a0002c0002t0001g0244 a0002c0002t0001g0247 |
4 | NA18940.hp1 NA18941.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+225C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25375124 | |||||||
| chr1:25375176 | C | G | 1 | a0001c0001t0001g0098 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1153+173G>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25375176 | |||||||
| chr1:25375224 | C | G | 1 | a0003c0003t0001g0250 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1153+125G>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25375224 | |||||||
| chr1:25375263 | T | C | 1 | a0001c0001t0001g0105 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1153+86A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 8/9 | chr1 | 25375263 | |||||||
| chr1:25375475 | AG | A | 5 | a0008c0008t0001g0146 a0008c0008t0001g0147 a0008c0008t0001g0148 others(2): Show |
5 | HG01109.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1074-48delC | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25375475 | |||||||
| chr1:25375755 | T | C | 30 | a0001c0001t0001g0091 a0001c0001t0001g0141 a0005c0005t0001g0015 others(27): Show |
32 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.1074-327A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25375755 | |||||||
| chr1:25375757 | T | C | 30 | a0001c0001t0001g0091 a0001c0001t0001g0141 a0005c0005t0001g0015 others(27): Show |
32 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.1074-329A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25375757 | |||||||
| chr1:25375791 | CT | C | 30 | a0001c0001t0001g0084 a0001c0001t0001g0092 a0002c0002t0001g0212 others(27): Show |
34 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.1074-364delA | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25375791 | |||||||
| chr1:25375791 | CTT | C | 17 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(14): Show |
18 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.1074-365_1074-364d others(4): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25375791 | |||||||
| chr1:25375793 | T | C | 2 | a0001c0001t0001g0029 a0001c0001t0001g0115 |
2 | HG01175.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1074-365A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25375793 | |||||||
| chr1:25375794 | T | C | 3 | a0004c0004t0001g0005 a0004c0004t0001g0156 a0004c0004t0001g0176 |
5 | HG01106.hp2 HG01891.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1074-366A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25375794 | |||||||
| chr1:25375804 | T | C | 2 | a0012c0010t0001g0019 a0012c0010t0001g0020 |
2 | HG01106.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1074-376A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25375804 | |||||||
| chr1:25375806 | T | G | 2 | a0012c0010t0001g0019 a0012c0010t0001g0020 |
2 | HG01106.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1074-378A>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25375806 | |||||||
| chr1:25375815 | T | A | 2 | a0012c0010t0001g0019 a0012c0010t0001g0020 |
2 | HG01106.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1074-387A>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25375815 | |||||||
| chr1:25375874 | C | T | 27 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(24): Show |
29 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1074-446G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25375874 | |||||||
| chr1:25375886 | T | C | 27 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(24): Show |
29 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1074-458A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25375886 | |||||||
| chr1:25375896 | T | C | 2 | a0012c0010t0001g0019 a0012c0010t0001g0020 |
2 | HG01106.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1074-468A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25375896 | |||||||
| chr1:25375923 | T | C | 2 | a0012c0010t0001g0019 a0012c0010t0001g0020 |
2 | HG01106.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1074-495A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25375923 | |||||||
| chr1:25375993 | G | A | 1 | a0002c0002t0001g0281 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1074-565C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25375993 | |||||||
| chr1:25375998 | C | T | 5 | a0008c0008t0001g0146 a0008c0008t0001g0147 a0008c0008t0001g0148 others(2): Show |
5 | HG01109.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1074-570G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25375998 | |||||||
| chr1:25376054 | T | G | 27 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(24): Show |
29 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1074-626A>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25376054 | |||||||
| chr1:25376217 | C | A | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG02056.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1074-789G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25376217 | |||||||
| chr1:25376317 | A | C | 1 | a0003c0003t0001g0289 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1074-889T>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25376317 | |||||||
| chr1:25376554 | C | G | 1 | a0002c0002t0001g0236 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1074-1126G>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25376554 | |||||||
| chr1:25376665 | C | T | 63 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(60): Show |
66 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.1074-1237G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25376665 | |||||||
| chr1:25376680 | C | G | 2 | a0014c0013t0001g0025 a0014c0013t0001g0026 |
2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1074-1252G>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25376680 | |||||||
| chr1:25376785 | G | A | 8 | a0006c0006t0001g0285 a0006c0006t0001g0290 a0006c0006t0001g0291 others(5): Show |
8 | HG02257.hp2 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1074-1357C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25376785 | |||||||
| chr1:25376842 | A | C | 1 | a0002c0002t0001g0199 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1074-1414T>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25376842 | |||||||
| chr1:25377082 | A | C | 29 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(26): Show |
31 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.1074-1654T>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25377082 | |||||||
| chr1:25377153 | G | C | 27 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(24): Show |
29 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1074-1725C>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25377153 | |||||||
| chr1:25377285 | A | G | 170 | a0001c0001t0001g0034 a0001c0001t0001g0097 a0001c0001t0001g0128 others(167): Show |
179 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.1074-1857T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25377285 | |||||||
| chr1:25377316 | C | T | 29 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(26): Show |
31 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.1074-1888G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25377316 | |||||||
| chr1:25377354 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1074-1926C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25377354 | |||||||
| chr1:25377421 | C | T | 2 | a0014c0013t0001g0025 a0014c0013t0001g0026 |
2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1074-1993G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25377421 | |||||||
| chr1:25377652 | T | G | 1 | a0002c0002t0001g0206 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1074-2224A>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25377652 | |||||||
| chr1:25377703 | G | T | 1 | a0002c0002t0001g0242 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1074-2275C>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25377703 | |||||||
| chr1:25377756 | T | C | 2 | a0014c0013t0001g0025 a0014c0013t0001g0026 |
2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1074-2328A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25377756 | |||||||
| chr1:25377879 | T | A | 3 | a0005c0005t0001g0299 a0005c0005t0001g0302 a0005c0005t0001g0303 |
3 | HG02723.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1074-2451A>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25377879 | |||||||
| chr1:25378120 | A | C | 2 | a0016c0017t0001g0055 a0016c0017t0001g0082 |
2 | NA18951.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1074-2692T>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25378120 | |||||||
| chr1:25378211 | T | A | 1 | a0019c0019t0001g0021 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1074-2783A>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25378211 | |||||||
| chr1:25378226 | C | T | 2 | a0013c0012t0001g0170 a0013c0012t0001g0171 |
2 | HG01167.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1074-2798G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25378226 | |||||||
| chr1:25378277 | T | G | 3 | a0001c0001t0001g0044 a0001c0001t0001g0107 a0001c0001t0001g0108 |
3 | NA18969.hp2 NA18977.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1074-2849A>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25378277 | |||||||
| chr1:25378291 | C | T | 1 | a0003c0003t0001g0201 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1074-2863G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25378291 | |||||||
| chr1:25378297 | A | T | 5 | a0008c0008t0001g0146 a0008c0008t0001g0147 a0008c0008t0001g0148 others(2): Show |
5 | HG01109.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1074-2869T>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25378297 | |||||||
| chr1:25378310 | G | A | 4 | a0002c0002t0001g0013 a0002c0002t0001g0210 a0002c0002t0001g0244 others(1): Show |
5 | NA18940.hp1 NA18941.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.1074-2882C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25378310 | |||||||
| chr1:25378381 | C | T | 2 | a0012c0010t0001g0019 a0012c0010t0001g0020 |
2 | HG01106.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1074-2953G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25378381 | |||||||
| chr1:25378484 | T | G | 2 | a0003c0003t0001g0283 a0003c0003t0001g0284 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1074-3056A>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25378484 | |||||||
| chr1:25378489 | T | A | 1 | a0001c0001t0001g0060 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1074-3061A>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25378489 | |||||||
| chr1:25378515 | C | T | 29 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(26): Show |
31 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.1074-3087G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25378515 | |||||||
| chr1:25378565 | G | A | 1 | a0005c0005t0001g0015 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1074-3137C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25378565 | |||||||
| chr1:25378632 | C | T | 1 | a0003c0003t0001g0313 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1074-3204G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25378632 | |||||||
| chr1:25378716 | G | T | 2 | a0012c0010t0001g0019 a0012c0010t0001g0020 |
2 | HG01106.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1074-3288C>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25378716 | |||||||
| chr1:25378780 | A | T | 1 | a0007c0007t0002g0172 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1074-3352T>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25378780 | |||||||
| chr1:25378933 | C | T | 1 | a0003c0003t0001g0263 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1074-3505G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25378933 | |||||||
| chr1:25379071 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0125 |
2 | HG02735.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1074-3643A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379071 | |||||||
| chr1:25379161 | G | A | 2 | a0014c0013t0001g0025 a0014c0013t0001g0026 |
2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1074-3733C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379161 | |||||||
| chr1:25379199 | A | T | 1 | a0008c0008t0001g0177 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1074-3771T>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379199 | |||||||
| chr1:25379217 | G | T | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1074-3789C>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379217 | |||||||
| chr1:25379391 | G | T | 1 | a0002c0002t0001g0240 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1074-3963C>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379391 | |||||||
| chr1:25379419 | G | A | 27 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(24): Show |
29 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1074-3991C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379419 | |||||||
| chr1:25379451 | G | GTATATAT others(7): Show |
1 | a0001c0001t0001g0142 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1074-4037_1074-402 others(18): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379451 | |||||||
| chr1:25379451 | G | GTGTGTAT others(15): Show |
1 | a0006c0006t0001g0285 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1074-4024_1074-402 others(26): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379451 | |||||||
| chr1:25379451 | GTATATAT others(3): Show |
G | 4 | a0001c0001t0001g0078 a0001c0001t0001g0096 a0001c0001t0001g0113 others(1): Show |
4 | HG00733.hp1 HG02056.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.1074-4033_1074-402 others(14): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379451 | |||||||
| chr1:25379451 | GTATATAT others(5): Show |
G | 14 | a0001c0001t0001g0017 a0001c0001t0001g0024 a0001c0001t0001g0040 others(11): Show |
14 | HG00280.hp2 HG00673.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.1074-4035_1074-402 others(16): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379451 | |||||||
| chr1:25379451 | GTATATAT others(7): Show |
G | 5 | a0001c0001t0001g0062 a0001c0001t0001g0080 a0001c0001t0001g0118 others(2): Show |
5 | HG00099.hp2 HG02300.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1074-4037_1074-402 others(18): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379451 | |||||||
| chr1:25379451 | GTATATAT others(13): Show |
G | 1 | a0004c0004t0001g0041 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1074-4043_1074-402 others(24): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379451 | |||||||
| chr1:25379453 | A | G | 9 | a0006c0006t0001g0290 a0006c0006t0001g0291 a0006c0006t0001g0292 others(6): Show |
9 | HG01106.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1074-4025T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379453 | |||||||
| chr1:25379455 | A | G | 7 | a0006c0006t0001g0290 a0006c0006t0001g0291 a0006c0006t0001g0292 others(4): Show |
7 | HG02257.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1074-4027T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379455 | |||||||
| chr1:25379459 | A | G | 1 | a0006c0006t0001g0285 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1074-4031T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379459 | |||||||
| chr1:25379465 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1074-4037T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379465 | |||||||
| chr1:25379465 | ATATATAT others(33): Show |
A | 1 | a0003c0003t0001g0288 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1074-4077_1074-403 others(44): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379465 | |||||||
| chr1:25379471 | ATATATAT others(28): Show |
A | 2 | a0013c0012t0001g0170 a0013c0012t0001g0171 |
2 | HG01167.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1074-4078_1074-404 others(39): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379471 | |||||||
| chr1:25379473 | ATATATAT others(26): Show |
A | 3 | a0007c0007t0001g0145 a0007c0007t0001g0174 a0019c0019t0001g0021 |
3 | HG02109.hp1 HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1074-4078_1074-404 others(37): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379473 | |||||||
| chr1:25379473 | ATATATAT others(28): Show |
A | 5 | a0005c0005t0001g0297 a0005c0005t0001g0298 a0005c0005t0001g0299 others(2): Show |
5 | HG02723.hp2 HG02818.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1074-4080_1074-404 others(39): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379473 | |||||||
| chr1:25379475 | ATATATAT others(23): Show |
A | 2 | a0002c0002t0001g0216 a0002c0002t0001g0241 |
2 | HG00597.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.1074-4077_1074-404 others(34): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379475 | |||||||
| chr1:25379475 | ATATATAT others(26): Show |
A | 3 | a0005c0005t0001g0015 a0007c0007t0001g0010 a0007c0007t0001g0173 |
5 | HG01070.hp1 HG01071.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1074-4080_1074-404 others(37): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379475 | |||||||
| chr1:25379475 | ATATATAT others(27): Show |
A | 3 | a0005c0005t0001g0309 a0005c0005t0001g0310 a0005c0005t0001g0311 |
3 | HG01069.hp1 HG02630.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1074-4081_1074-404 others(38): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379475 | |||||||
| chr1:25379475 | ATATATAT others(28): Show |
A | 1 | a0007c0007t0002g0172 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1074-4082_1074-404 others(39): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379475 | |||||||
| chr1:25379475 | ATATATAT others(29): Show |
A | 2 | a0003c0003t0001g0283 a0003c0003t0001g0284 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1074-4083_1074-404 others(40): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379475 | |||||||
| chr1:25379477 | ATATATAT others(19): Show |
A | 2 | a0002c0002t0001g0271 a0002c0002t0001g0281 |
2 | HG02135.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1074-4075_1074-405 others(30): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379477 | |||||||
| chr1:25379477 | ATATATAT others(20): Show |
A | 1 | a0002c0002t0001g0218 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1074-4076_1074-405 others(31): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379477 | |||||||
| chr1:25379477 | ATATATAT others(25): Show |
A | 4 | a0005c0005t0001g0300 a0005c0005t0001g0301 a0005c0005t0001g0307 others(1): Show |
4 | HG03139.hp2 HG03471.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.1074-4081_1074-405 others(36): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379477 | |||||||
| chr1:25379477 | ATATATAT others(26): Show |
A | 2 | a0005c0005t0001g0304 a0005c0005t0001g0306 |
2 | HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1074-4082_1074-405 others(37): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379477 | |||||||
| chr1:25379478 | TATATATA others(6): Show |
T | 1 | a0001c0001t0001g0028 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1074-4063_1074-405 others(17): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379478 | |||||||
| chr1:25379479 | ATATATAT others(17): Show |
A | 1 | a0002c0002t0001g0229 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1074-4075_1074-405 others(28): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379479 | |||||||
| chr1:25379479 | ATATATAT others(18): Show |
A | 3 | a0002c0002t0001g0183 a0002c0002t0001g0185 a0002c0002t0001g0186 |
3 | HG00642.hp2 HG01099.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.1074-4076_1074-405 others(29): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379479 | |||||||
| chr1:25379479 | ATATATAT others(19): Show |
A | 19 | a0002c0002t0001g0013 a0002c0002t0001g0194 a0002c0002t0001g0204 others(16): Show |
19 | HG00621.hp1 HG00621.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.1074-4077_1074-405 others(30): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379479 | |||||||
| chr1:25379479 | ATATATAT others(20): Show |
A | 5 | a0002c0002t0001g0013 a0002c0002t0001g0217 a0002c0002t0001g0239 others(2): Show |
5 | HG02145.hp1 HG02683.hp1 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.1074-4078_1074-405 others(31): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379479 | |||||||
| chr1:25379479 | ATATATAT others(27): Show |
A | 2 | a0005c0005t0001g0305 a0005c0005t0001g0312 |
2 | HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1074-4085_1074-405 others(38): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379479 | |||||||
| chr1:25379480 | TATATATA others(6): Show |
T | 1 | a0001c0001t0001g0051 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1074-4065_1074-405 others(17): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379480 | |||||||
| chr1:25379481 | ATATATAT others(8): Show |
A | 1 | a0001c0001t0001g0112 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1074-4068_1074-405 others(19): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379481 | |||||||
| chr1:25379481 | ATATATAT others(15): Show |
A | 2 | a0002c0002t0001g0012 a0022c0018t0001g0155 |
2 | HG03540.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1074-4075_1074-405 others(26): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379481 | |||||||
| chr1:25379481 | ATATATAT others(16): Show |
A | 2 | a0002c0002t0001g0196 a0004c0024t0001g0182 |
2 | HG01243.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.1074-4076_1074-405 others(27): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379481 | |||||||
| chr1:25379481 | ATATATAT others(17): Show |
A | 5 | a0002c0002t0001g0207 a0002c0002t0001g0209 a0002c0002t0001g0223 others(2): Show |
5 | HG00280.hp1 HG02630.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.1074-4077_1074-405 others(28): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379481 | |||||||
| chr1:25379481 | ATATATAT others(18): Show |
A | 4 | a0002c0002t0001g0187 a0002c0002t0001g0188 a0002c0002t0001g0267 others(1): Show |
4 | HG00673.hp1 HG01952.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1074-4078_1074-405 others(29): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379481 | |||||||
| chr1:25379481 | ATATATAT others(19): Show |
A | 6 | a0001c0001t0001g0097 a0001c0001t0001g0128 a0001c0001t0001g0129 others(3): Show |
6 | HG01123.hp1 HG02622.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1074-4079_1074-405 others(30): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379481 | |||||||
| chr1:25379482 | TATATATA others(4): Show |
T | 3 | a0001c0001t0001g0056 a0001c0001t0001g0065 a0001c0001t0001g0180 |
3 | HG00639.hp2 HG02622.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1074-4065_1074-405 others(15): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379482 | |||||||
| chr1:25379482 | TATATATA others(6): Show |
T | 4 | a0001c0001t0001g0046 a0001c0001t0001g0081 a0001c0001t0001g0095 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1074-4067_1074-405 others(17): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379482 | |||||||
| chr1:25379483 | ATATATAT others(6): Show |
A | 12 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0035 others(9): Show |
12 | HG00408.hp2 HG00423.hp2 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.1074-4068_1074-405 others(17): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379483 | |||||||
| chr1:25379483 | ATATATAT others(7): Show |
A | 3 | a0001c0001t0001g0002 a0001c0001t0001g0085 a0017c0016t0001g0087 |
3 | HG02004.hp1 NA18986.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1074-4069_1074-405 others(18): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379483 | |||||||
| chr1:25379483 | ATATATAT others(8): Show |
A | 1 | a0017c0016t0001g0086 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1074-4070_1074-405 others(19): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379483 | |||||||
| chr1:25379483 | ATATATAT others(10): Show |
A | 1 | a0003c0003t0001g0313 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1074-4072_1074-405 others(21): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379483 | |||||||
| chr1:25379483 | ATATATAT others(13): Show |
A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0071 others(1): Show |
4 | NA18939.hp2 NA18947.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.1074-4075_1074-405 others(24): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379483 | |||||||
| chr1:25379483 | ATATATAT others(14): Show |
A | 1 | a0002c0002t0001g0011 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1074-4076_1074-405 others(25): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379483 | |||||||
| chr1:25379483 | ATATATAT others(15): Show |
A | 12 | a0002c0002t0001g0012 a0002c0002t0001g0198 a0002c0002t0001g0206 others(9): Show |
12 | HG00408.hp1 HG02040.hp1 HG02148.hp1 others(9): Show |
intron_variant | MODIFIER | c.1074-4077_1074-405 others(26): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379483 | |||||||
| chr1:25379483 | ATATATAT others(18): Show |
A | 1 | a0002c0002t0001g0269 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1074-4080_1074-405 others(29): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379483 | |||||||
| chr1:25379484 | TATATATA others(4): Show |
T | 7 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0018 others(4): Show |
7 | HG00642.hp1 HG01243.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.1074-4067_1074-405 others(15): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379484 | |||||||
| chr1:25379485 | ATATATAT others(4): Show |
A | 3 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0115 |
3 | HG01175.hp2 NA18971.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1074-4068_1074-405 others(15): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379485 | |||||||
| chr1:25379485 | ATATATAT others(5): Show |
A | 4 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0053 others(1): Show |
4 | HG00140.hp1 HG01517.hp2 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.1074-4069_1074-405 others(16): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379485 | |||||||
| chr1:25379485 | ATATATAT others(6): Show |
A | 5 | a0001c0001t0001g0031 a0001c0001t0001g0047 a0001c0001t0001g0048 others(2): Show |
5 | HG01496.hp2 HG01515.hp2 HG02080.hp2 others(2): Show |
intron_variant | MODIFIER | c.1074-4070_1074-405 others(17): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379485 | |||||||
| chr1:25379485 | ATATATAT others(11): Show |
A | 2 | a0001c0001t0001g0105 a0004c0004t0001g0009 |
2 | HG02809.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.1074-4075_1074-405 others(22): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379485 | |||||||
| chr1:25379485 | ATATATAT others(12): Show |
A | 3 | a0001c0001t0001g0003 a0003c0003t0001g0227 a0003c0003t0001g0257 |
3 | HG00140.hp2 HG00639.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.1074-4076_1074-405 others(23): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379485 | |||||||
| chr1:25379485 | ATATATAT others(13): Show |
A | 9 | a0002c0002t0001g0199 a0002c0002t0001g0213 a0002c0002t0001g0235 others(6): Show |
9 | HG00423.hp1 HG02071.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1074-4077_1074-405 others(24): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379485 | |||||||
| chr1:25379485 | ATATATAT others(14): Show |
A | 3 | a0001c0001t0001g0093 a0002c0002t0001g0011 a0002c0002t0001g0197 |
3 | HG02027.hp1 NA18951.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1074-4078_1074-405 others(25): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379485 | |||||||
| chr1:25379485 | ATATATAT others(18): Show |
A | 2 | a0002c0002t0001g0268 a0002c0002t0001g0270 |
2 | NA18944.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1074-4082_1074-405 others(29): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379485 | |||||||
| chr1:25379487 | ATATATAT others(2): Show |
A | 12 | a0001c0001t0001g0008 a0001c0001t0001g0030 a0001c0001t0001g0038 others(9): Show |
13 | HG00597.hp2 HG01952.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.1074-4068_1074-406 others(13): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379487 | |||||||
| chr1:25379487 | ATATATAT others(3): Show |
A | 6 | a0001c0001t0001g0001 a0001c0001t0001g0110 a0001c0001t0001g0120 others(3): Show |
6 | HG01433.hp1 HG01433.hp2 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.1074-4069_1074-406 others(14): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379487 | |||||||
| chr1:25379487 | ATATATAT others(4): Show |
A | 7 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0049 others(4): Show |
7 | HG01168.hp1 HG01358.hp2 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.1074-4070_1074-406 others(15): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379487 | |||||||
| chr1:25379487 | ATATATAT others(5): Show |
A | 3 | a0001c0001t0001g0068 a0001c0001t0001g0098 a0001c0001t0001g0126 |
3 | HG01934.hp1 HG01978.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1074-4071_1074-406 others(16): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379487 | |||||||
| chr1:25379487 | ATATATAT others(6): Show |
A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0122 |
2 | NA18972.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1074-4072_1074-406 others(17): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379487 | |||||||
| chr1:25379487 | ATATATAT others(9): Show |
A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0138 others(1): Show |
4 | HG03195.hp1 NA18974.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.1074-4075_1074-406 others(20): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379487 | |||||||
| chr1:25379487 | ATATATAT others(10): Show |
A | 6 | a0003c0003t0001g0203 a0003c0003t0001g0254 a0003c0003t0001g0255 others(3): Show |
6 | HG00738.hp1 HG00741.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.1074-4076_1074-406 others(21): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379487 | |||||||
| chr1:25379487 | ATATATAT others(11): Show |
A | 6 | a0001c0001t0001g0036 a0001c0001t0001g0152 a0002c0002t0001g0208 others(3): Show |
6 | HG01106.hp2 HG02135.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1074-4077_1074-406 others(22): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379487 | |||||||
| chr1:25379487 | ATATATAT others(12): Show |
A | 7 | a0003c0003t0001g0014 a0003c0003t0001g0205 a0003c0003t0001g0232 others(4): Show |
8 | HG00733.hp2 HG01258.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1074-4078_1074-406 others(23): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379487 | |||||||
| chr1:25379487 | ATATATAT others(13): Show |
A | 1 | a0003c0003t0001g0263 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1074-4079_1074-406 others(24): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379487 | |||||||
| chr1:25379487 | ATATATAT others(16): Show |
A | 1 | a0002c0002t0001g0266 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1074-4082_1074-406 others(27): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379487 | |||||||
| chr1:25379489 | ATATATAT others(4): Show |
A | 1 | a0001c0001t0001g0007 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1074-4072_1074-406 others(15): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379489 | |||||||
| chr1:25379489 | ATATATAT others(7): Show |
A | 1 | a0001c0001t0001g0004 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1074-4075_1074-406 others(18): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379489 | |||||||
| chr1:25379489 | ATATATAT others(8): Show |
A | 2 | a0003c0003t0001g0215 a0003c0003t0001g0280 |
2 | HG02055.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1074-4076_1074-406 others(19): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379489 | |||||||
| chr1:25379489 | ATATATAT others(9): Show |
A | 3 | a0004c0004t0001g0162 a0004c0004t0001g0168 a0021c0020t0001g0167 |
3 | HG02886.hp2 HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1074-4077_1074-406 others(20): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379489 | |||||||
| chr1:25379489 | ATATATAT others(10): Show |
A | 3 | a0002c0002t0001g0195 a0004c0004t0001g0114 a0004c0004t0001g0144 |
3 | HG02717.hp1 NA18946.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1074-4078_1074-406 others(21): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379489 | |||||||
| chr1:25379489 | ATATATAT others(11): Show |
A | 2 | a0002c0002t0001g0240 a0004c0004t0001g0134 |
2 | NA18971.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1074-4079_1074-406 others(22): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379489 | |||||||
| chr1:25379491 | ATATATTT others(3): Show |
A | 1 | a0004c0004t0001g0165 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1074-4073_1074-406 others(14): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379491 | |||||||
| chr1:25379491 | ATATATTT others(4): Show |
A | 1 | a0001c0001t0001g0119 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1074-4074_1074-406 others(15): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379491 | |||||||
| chr1:25379491 | ATATATTT others(5): Show |
A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0104 |
2 | NA18942.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.1074-4075_1074-406 others(16): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379491 | |||||||
| chr1:25379491 | ATATATTT others(6): Show |
A | 1 | a0004c0004t0001g0005 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1074-4076_1074-406 others(17): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379491 | |||||||
| chr1:25379491 | ATATATTT others(7): Show |
A | 6 | a0002c0002t0001g0275 a0003c0003t0001g0286 a0004c0004t0001g0163 others(3): Show |
6 | HG02895.hp2 HG02896.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1074-4077_1074-406 others(18): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379491 | |||||||
| chr1:25379491 | ATATATTT others(8): Show |
A | 3 | a0003c0003t0001g0251 a0003c0003t0001g0260 a0004c0004t0001g0016 |
3 | HG01109.hp2 HG01891.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1074-4078_1074-406 others(19): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379491 | |||||||
| chr1:25379491 | ATATATTT others(9): Show |
A | 2 | a0003c0003t0001g0184 a0011c0014t0001g0175 |
2 | HG02647.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1074-4079_1074-406 others(20): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379491 | |||||||
| chr1:25379493 | A | T | 5 | a0001c0001t0001g0028 a0001c0001t0001g0118 a0001c0001t0001g0127 others(2): Show |
5 | HG01192.hp2 HG02615.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1074-4065T>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379493 | |||||||
| chr1:25379493 | ATATTTTT others(5): Show |
A | 2 | a0004c0004t0001g0005 a0011c0014t0001g0157 |
2 | HG01099.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1074-4077_1074-406 others(16): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379493 | |||||||
| chr1:25379493 | ATATTTTT others(6): Show |
A | 6 | a0002c0002t0001g0189 a0003c0003t0001g0190 a0003c0003t0001g0191 others(3): Show |
6 | HG00099.hp1 HG02735.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1074-4078_1074-406 others(17): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379493 | |||||||
| chr1:25379493 | ATATTTTT others(7): Show |
A | 1 | a0003c0003t0001g0272 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1074-4079_1074-406 others(18): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379493 | |||||||
| chr1:25379493 | ATATTTTT others(8): Show |
A | 1 | a0003c0003t0001g0262 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1074-4080_1074-406 others(19): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379493 | |||||||
| chr1:25379495 | A | T | 16 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0040 others(13): Show |
16 | HG00639.hp2 HG00673.hp2 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.1074-4067T>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379495 | |||||||
| chr1:25379495 | ATTTTTTT others(3): Show |
A | 2 | a0004c0004t0001g0005 a0008c0008t0001g0148 |
2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1074-4077_1074-406 others(14): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379495 | |||||||
| chr1:25379497 | T | A | 5 | a0001c0001t0001g0142 a0003c0003t0001g0200 a0008c0008t0001g0177 others(2): Show |
5 | HG02055.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1074-4069A>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379497 | |||||||
| chr1:25379498 | T | A | 4 | a0006c0006t0001g0285 a0006c0006t0001g0290 a0006c0006t0001g0293 others(1): Show |
4 | HG02486.hp2 HG03041.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1074-4070A>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379498 | |||||||
| chr1:25379499 | T | A | 4 | a0003c0003t0001g0200 a0008c0008t0001g0177 a0008c0008t0001g0178 others(1): Show |
4 | HG02055.hp2 HG02559.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1074-4071A>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379499 | |||||||
| chr1:25379500 | T | A | 7 | a0006c0006t0001g0285 a0006c0006t0001g0290 a0006c0006t0001g0291 others(4): Show |
7 | HG02486.hp2 HG02559.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1074-4072A>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379500 | |||||||
| chr1:25379501 | T | A | 6 | a0003c0003t0001g0200 a0003c0003t0001g0265 a0006c0006t0001g0296 others(3): Show |
6 | HG01169.hp1 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1074-4073A>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379501 | |||||||
| chr1:25379502 | T | A | 1 | a0003c0003t0001g0253 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1074-4074A>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379502 | |||||||
| chr1:25379503 | T | A | 14 | a0003c0003t0001g0200 a0003c0003t0001g0265 a0004c0004t0001g0159 others(11): Show |
14 | HG01169.hp1 HG02055.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.1074-4075A>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379503 | |||||||
| chr1:25379504 | T | A | 2 | a0003c0003t0001g0253 a0006c0006t0001g0296 |
2 | HG01168.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1074-4076A>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379504 | |||||||
| chr1:25379505 | T | A | 8 | a0003c0003t0001g0200 a0003c0003t0001g0265 a0004c0004t0001g0159 others(5): Show |
8 | HG01106.hp1 HG01169.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1074-4077A>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379505 | |||||||
| chr1:25379506 | T | A | 3 | a0003c0003t0001g0193 a0003c0003t0001g0253 a0003c0003t0001g0258 |
3 | HG01168.hp2 HG01175.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1074-4078A>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379506 | |||||||
| chr1:25379507 | T | A | 6 | a0003c0003t0001g0200 a0008c0008t0001g0146 a0008c0008t0001g0177 others(3): Show |
6 | HG01106.hp1 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1074-4079A>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379507 | |||||||
| chr1:25379508 | T | A | 1 | a0003c0003t0001g0258 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1074-4080A>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379508 | |||||||
| chr1:25379509 | T | A | 1 | a0008c0008t0001g0146 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1074-4081A>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379509 | |||||||
| chr1:25379649 | C | T | 1 | a0004c0004t0001g0041 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1074-4221G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379649 | |||||||
| chr1:25379716 | C | T | 27 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(24): Show |
29 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1074-4288G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379716 | |||||||
| chr1:25379738 | G | A | 1 | a0003c0003t0001g0279 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1074-4310C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379738 | |||||||
| chr1:25379763 | C | T | 2 | a0012c0010t0001g0019 a0012c0010t0001g0020 |
2 | HG01106.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1074-4335G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379763 | |||||||
| chr1:25379804 | A | G | 2 | a0012c0010t0001g0019 a0012c0010t0001g0020 |
2 | HG01106.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1074-4376T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379804 | |||||||
| chr1:25379833 | C | A | 1 | a0001c0001t0001g0038 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1074-4405G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379833 | |||||||
| chr1:25379878 | A | G | 1 | a0001c0001t0001g0061 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1074-4450T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25379878 | |||||||
| chr1:25380328 | GA | G | 29 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(26): Show |
31 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.1074-4901delT | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25380328 | |||||||
| chr1:25380404 | T | C | 2 | a0008c0008t0001g0147 a0008c0008t0001g0178 |
2 | HG01109.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1074-4976A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25380404 | |||||||
| chr1:25380526 | C | T | 2 | a0002c0002t0001g0198 a0002c0002t0001g0208 |
2 | HG00408.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.1074-5098G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25380526 | |||||||
| chr1:25380624 | A | G | 20 | a0004c0004t0001g0005 a0004c0004t0001g0009 a0004c0004t0001g0016 others(17): Show |
23 | HG01099.hp2 HG01106.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.1073+5087T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25380624 | |||||||
| chr1:25380648 | C | T | 18 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(15): Show |
19 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.1073+5063G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25380648 | |||||||
| chr1:25380655 | C | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0042 a0001c0001t0001g0110 others(4): Show |
8 | HG00597.hp2 HG02074.hp1 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.1073+5056G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25380655 | |||||||
| chr1:25380717 | C | A | 27 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(24): Show |
29 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1073+4994G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25380717 | |||||||
| chr1:25380718 | A | C | 28 | a0001c0001t0001g0084 a0005c0005t0001g0015 a0005c0005t0001g0297 others(25): Show |
30 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.1073+4993T>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25380718 | |||||||
| chr1:25380860 | C | A | 2 | a0003c0003t0001g0283 a0003c0003t0001g0284 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1073+4851G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25380860 | |||||||
| chr1:25380899 | C | CT | 30 | a0001c0001t0001g0042 a0001c0001t0001g0060 a0001c0001t0001g0127 others(27): Show |
33 | HG01099.hp2 HG01106.hp2 HG01192.hp1 others(30): Show |
intron_variant | MODIFIER | c.1073+4811dupA | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25380899 | |||||||
| chr1:25380899 | CT | C | 17 | a0001c0001t0001g0048 a0001c0001t0001g0088 a0001c0001t0001g0104 others(14): Show |
17 | HG01099.hp1 HG01168.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.1073+4811delA | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25380899 | |||||||
| chr1:25380964 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1073+4747G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25380964 | |||||||
| chr1:25380970 | C | T | 2 | a0001c0001t0001g0059 a0003c0003t0001g0286 |
2 | HG02040.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1073+4741G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25380970 | |||||||
| chr1:25380971 | G | A | 18 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(15): Show |
19 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.1073+4740C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25380971 | |||||||
| chr1:25381051 | A | G | 29 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(26): Show |
31 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.1073+4660T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25381051 | |||||||
| chr1:25381201 | C | A | 3 | a0003c0003t0001g0203 a0003c0003t0001g0255 a0003c0003t0001g0276 |
3 | HG00738.hp1 HG00741.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1073+4510G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25381201 | |||||||
| chr1:25381457 | C | CT | 37 | a0001c0001t0001g0044 a0001c0001t0001g0108 a0001c0001t0001g0110 others(34): Show |
39 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.1073+4253dupA | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25381457 | |||||||
| chr1:25381457 | C | CTT | 12 | a0001c0001t0001g0008 a0001c0001t0001g0042 a0001c0001t0001g0111 others(9): Show |
13 | HG00597.hp2 HG02027.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1073+4252_1073+425 others(6): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25381457 | |||||||
| chr1:25381457 | CT | C | 10 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0002c0002t0001g0211 others(7): Show |
10 | HG01169.hp2 HG01515.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.1073+4253delA | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25381457 | |||||||
| chr1:25381591 | G | A | 1 | a0001c0001t0001g0018 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1073+4120C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25381591 | |||||||
| chr1:25381610 | G | C | 1 | a0001c0001t0001g0065 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1073+4101C>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25381610 | |||||||
| chr1:25381611 | A | C | 1 | a0001c0001t0001g0065 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1073+4100T>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25381611 | |||||||
| chr1:25381612 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1073+4099C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25381612 | |||||||
| chr1:25381613 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1073+4098A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25381613 | |||||||
| chr1:25381737 | T | C | 27 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(24): Show |
29 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1073+3974A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25381737 | |||||||
| chr1:25381743 | C | A | 27 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(24): Show |
29 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1073+3968G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25381743 | |||||||
| chr1:25381756 | C | G | 5 | a0003c0003t0001g0286 a0003c0003t0001g0287 a0003c0003t0001g0288 others(2): Show |
5 | HG02145.hp2 HG03130.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1073+3955G>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25381756 | |||||||
| chr1:25381757 | C | A | 27 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(24): Show |
29 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1073+3954G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25381757 | |||||||
| chr1:25381857 | T | C | 2 | a0003c0003t0001g0184 a0003c0003t0001g0260 |
2 | HG03710.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1073+3854A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25381857 | |||||||
| chr1:25381894 | T | C | 1 | a0001c0001t0001g0102 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1073+3817A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25381894 | |||||||
| chr1:25381918 | T | C | 20 | a0004c0004t0001g0005 a0004c0004t0001g0009 a0004c0004t0001g0016 others(17): Show |
23 | HG01099.hp2 HG01106.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.1073+3793A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25381918 | |||||||
| chr1:25382070 | G | A | 2 | a0003c0003t0001g0215 a0003c0003t0001g0280 |
2 | HG02055.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1073+3641C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25382070 | |||||||
| chr1:25382193 | A | C | 25 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(22): Show |
27 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.1073+3518T>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25382193 | |||||||
| chr1:25382195 | T | A | 29 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(26): Show |
31 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.1073+3516A>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25382195 | |||||||
| chr1:25382197 | G | C | 29 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(26): Show |
31 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.1073+3514C>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25382197 | |||||||
| chr1:25382229 | T | C | 29 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(26): Show |
31 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.1073+3482A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25382229 | |||||||
| chr1:25382298 | C | G | 1 | a0001c0001t0001g0139 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1073+3413G>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25382298 | |||||||
| chr1:25382369 | G | A | 29 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(26): Show |
31 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.1073+3342C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25382369 | |||||||
| chr1:25382455 | T | TTTGGGG | 29 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(26): Show |
31 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.1073+3255_1073+325 others(10): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25382455 | |||||||
| chr1:25382611 | G | A | 27 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(24): Show |
29 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1073+3100C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25382611 | |||||||
| chr1:25382613 | C | G | 109 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(106): Show |
113 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.1073+3098G>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25382613 | |||||||
| chr1:25382683 | A | G | 20 | a0004c0004t0001g0005 a0004c0004t0001g0009 a0004c0004t0001g0016 others(17): Show |
23 | HG01099.hp2 HG01106.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.1073+3028T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25382683 | |||||||
| chr1:25382686 | A | G | 29 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(26): Show |
31 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.1073+3025T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25382686 | |||||||
| chr1:25382739 | A | C | 1 | a0002c0002t0001g0252 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1073+2972T>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25382739 | |||||||
| chr1:25382742 | A | G | 1 | a0002c0002t0001g0252 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1073+2969T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25382742 | |||||||
| chr1:25382767 | A | C | 170 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(167): Show |
179 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.1073+2944T>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25382767 | |||||||
| chr1:25382849 | A | C | 27 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(24): Show |
29 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1073+2862T>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25382849 | |||||||
| chr1:25382870 | A | T | 2 | a0002c0002t0001g0209 a0003c0003t0001g0272 |
2 | HG04115.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.1073+2841T>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25382870 | |||||||
| chr1:25383035 | T | C | 2 | a0012c0010t0001g0019 a0012c0010t0001g0020 |
2 | HG01106.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1073+2676A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25383035 | |||||||
| chr1:25383142 | T | C | 2 | a0012c0010t0001g0019 a0012c0010t0001g0020 |
2 | HG01106.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1073+2569A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25383142 | |||||||
| chr1:25383380 | G | A | 2 | a0003c0003t0001g0283 a0003c0003t0001g0284 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1073+2331C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25383380 | |||||||
| chr1:25383420 | T | C | 1 | a0002c0002t0001g0248 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1073+2291A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25383420 | |||||||
| chr1:25383659 | T | C | 2 | a0013c0012t0001g0170 a0013c0012t0001g0171 |
2 | HG01167.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1073+2052A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25383659 | |||||||
| chr1:25383718 | G | A | 1 | a0022c0018t0001g0155 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1073+1993C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25383718 | |||||||
| chr1:25383762 | G | A | 1 | a0015c0011t0001g0161 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1073+1949C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25383762 | |||||||
| chr1:25383826 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1073+1885C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25383826 | |||||||
| chr1:25383827 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1073+1884G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25383827 | |||||||
| chr1:25383833 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1073+1878G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25383833 | |||||||
| chr1:25383844 | T | C | 1 | a0001c0001t0001g0040 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1073+1867A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25383844 | |||||||
| chr1:25383863 | T | C | 1 | a0001c0001t0001g0040 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1073+1848A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25383863 | |||||||
| chr1:25383901 | A | G | 5 | a0008c0008t0001g0146 a0008c0008t0001g0147 a0008c0008t0001g0148 others(2): Show |
5 | HG01109.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1073+1810T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25383901 | |||||||
| chr1:25383947 | C | T | 2 | a0001c0001t0001g0040 a0004c0004t0001g0158 |
2 | HG02080.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1073+1764G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25383947 | |||||||
| chr1:25383954 | C | A | 1 | a0001c0001t0001g0040 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1073+1757G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25383954 | |||||||
| chr1:25384271 | A | G | 2 | a0012c0010t0001g0019 a0012c0010t0001g0020 |
2 | HG01106.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1073+1440T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25384271 | |||||||
| chr1:25384356 | G | A | 1 | a0001c0001t0001g0045 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1073+1355C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25384356 | |||||||
| chr1:25384477 | G | A | 29 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(26): Show |
31 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.1073+1234C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25384477 | |||||||
| chr1:25384521 | C | T | 11 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0036 others(8): Show |
15 | HG00558.hp2 HG02135.hp1 NA18612.hp1 others(12): Show |
intron_variant | MODIFIER | c.1073+1190G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25384521 | |||||||
| chr1:25384577 | G | A | 6 | a0007c0007t0001g0010 a0007c0007t0001g0145 a0007c0007t0001g0173 others(3): Show |
7 | HG01167.hp2 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1073+1134C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25384577 | |||||||
| chr1:25384703 | G | A | 18 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(15): Show |
19 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.1073+1008C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25384703 | |||||||
| chr1:25384968 | G | C | 1 | a0001c0001t0001g0030 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1073+743C>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25384968 | |||||||
| chr1:25385008 | C | A | 1 | a0001c0001t0001g0136 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1073+703G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25385008 | |||||||
| chr1:25385258 | G | A | 1 | a0002c0002t0001g0208 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1073+453C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25385258 | |||||||
| chr1:25385311 | AG | A | 4 | a0004c0004t0001g0005 a0004c0004t0001g0016 a0004c0004t0001g0156 others(1): Show |
6 | HG01106.hp2 HG01891.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.1073+399delC | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25385311 | |||||||
| chr1:25385400 | C | G | 2 | a0001c0001t0001g0136 a0019c0019t0001g0021 |
2 | HG02258.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1073+311G>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25385400 | |||||||
| chr1:25385412 | C | A | 18 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(15): Show |
19 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.1073+299G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25385412 | |||||||
| chr1:25385559 | T | G | 8 | a0001c0001t0001g0008 a0001c0001t0001g0042 a0001c0001t0001g0110 others(5): Show |
9 | HG00597.hp2 HG02074.hp1 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.1073+152A>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 7/9 | chr1 | 25385559 | |||||||
| chr1:25385953 | A | G | 1 | a0004c0004t0001g0041 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.940-109T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25385953 | |||||||
| chr1:25386060 | G | C | 2 | a0002c0002t0001g0195 a0005c0005t0001g0308 |
2 | HG03471.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.940-216C>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25386060 | |||||||
| chr1:25386065 | T | G | 1 | a0003c0003t0001g0263 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.940-221A>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25386065 | |||||||
| chr1:25386100 | C | G | 2 | a0013c0012t0001g0170 a0013c0012t0001g0171 |
2 | HG01167.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.940-256G>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25386100 | |||||||
| chr1:25386101 | A | G | 29 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(26): Show |
31 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.940-257T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25386101 | |||||||
| chr1:25386142 | C | T | 2 | a0013c0012t0001g0170 a0013c0012t0001g0171 |
2 | HG01167.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.940-298G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25386142 | |||||||
| chr1:25386189 | T | C | 25 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0195 others(22): Show |
27 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.940-345A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25386189 | |||||||
| chr1:25386453 | G | A | 1 | a0003c0003t0001g0261 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.940-609C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25386453 | |||||||
| chr1:25386561 | C | T | 1 | a0003c0003t0001g0262 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.940-717G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25386561 | |||||||
| chr1:25386611 | A | G | 2 | a0002c0002t0001g0271 a0022c0018t0001g0155 |
2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.940-767T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25386611 | |||||||
| chr1:25386612 | A | G | 2 | a0002c0002t0001g0271 a0022c0018t0001g0155 |
2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.940-768T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25386612 | |||||||
| chr1:25386734 | A | G | 2 | a0005c0005t0001g0297 a0005c0005t0001g0298 |
2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.940-890T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25386734 | |||||||
| chr1:25386743 | A | T | 108 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(105): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.940-899T>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25386743 | |||||||
| chr1:25386770 | C | G | 2 | a0002c0002t0001g0271 a0022c0018t0001g0155 |
2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.940-926G>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25386770 | |||||||
| chr1:25386839 | C | CAACAA | 3 | a0012c0010t0001g0019 a0014c0013t0001g0025 a0014c0013t0001g0026 |
3 | HG02145.hp1 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.940-996_940-995ins others(5): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25386839 | |||||||
| chr1:25386841 | A | AC | 6 | a0005c0005t0001g0015 a0005c0005t0001g0309 a0007c0007t0001g0010 others(3): Show |
8 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.940-998_940-997ins others(1): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25386841 | |||||||
| chr1:25386842 | A | AAC | 34 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0023 others(31): Show |
36 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.940-1000_940-999du others(3): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25386842 | |||||||
| chr1:25386842 | A | AACAC | 6 | a0001c0001t0001g0093 a0001c0001t0001g0095 a0008c0008t0001g0147 others(3): Show |
6 | HG01109.hp1 HG02055.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.940-1002_940-999du others(5): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25386842 | |||||||
| chr1:25386842 | A | C | 22 | a0005c0005t0001g0297 a0005c0005t0001g0298 a0005c0005t0001g0299 others(19): Show |
22 | HG01069.hp1 HG01106.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.940-998T>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25386842 | |||||||
| chr1:25386842 | AAC | A | 4 | a0002c0002t0001g0223 a0002c0002t0001g0256 a0002c0002t0001g0278 others(1): Show |
4 | HG01099.hp2 HG02698.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.940-1000_940-999de others(3): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25386842 | |||||||
| chr1:25386842 | AACACAC | A | 29 | a0002c0002t0001g0189 a0003c0003t0001g0014 a0003c0003t0001g0184 others(26): Show |
30 | HG00099.hp1 HG00140.hp2 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.940-1004_940-999de others(7): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25386842 | |||||||
| chr1:25386842 | AACACACA others(9): Show |
A | 1 | a0003c0003t0001g0262 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.940-1014_940-999de others(17): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25386842 | |||||||
| chr1:25386843 | AC | A | 15 | a0005c0005t0001g0297 a0005c0005t0001g0298 a0005c0005t0001g0299 others(12): Show |
15 | HG01069.hp1 HG02258.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.940-1000delG | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25386843 | |||||||
| chr1:25386843 | ACAC | A | 3 | a0013c0012t0001g0170 a0013c0012t0001g0171 a0019c0019t0001g0021 |
3 | HG01167.hp2 HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.940-1002_940-1000d others(5): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25386843 | |||||||
| chr1:25386844 | C | A | 6 | a0005c0005t0001g0015 a0005c0005t0001g0309 a0007c0007t0001g0010 others(3): Show |
8 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.940-1000G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25386844 | |||||||
| chr1:25386846 | C | A | 15 | a0005c0005t0001g0297 a0005c0005t0001g0298 a0005c0005t0001g0299 others(12): Show |
15 | HG01069.hp1 HG02258.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.940-1002G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25386846 | |||||||
| chr1:25386848 | C | A | 3 | a0013c0012t0001g0170 a0013c0012t0001g0171 a0019c0019t0001g0021 |
3 | HG01167.hp2 HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.940-1004G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25386848 | |||||||
| chr1:25387017 | C | T | 2 | a0003c0003t0001g0283 a0003c0003t0001g0284 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.940-1173G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25387017 | |||||||
| chr1:25387247 | C | T | 7 | a0006c0006t0001g0290 a0006c0006t0001g0291 a0006c0006t0001g0292 others(4): Show |
7 | HG02257.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.940-1403G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25387247 | |||||||
| chr1:25387294 | G | A | 1 | a0013c0012t0001g0170 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.940-1450C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25387294 | |||||||
| chr1:25387425 | G | A | 1 | a0003c0003t0001g0313 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.939+1551C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25387425 | |||||||
| chr1:25387585 | T | C | 1 | a0015c0011t0001g0161 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.939+1391A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25387585 | |||||||
| chr1:25387651 | T | C | 1 | a0003c0003t0001g0263 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.939+1325A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25387651 | |||||||
| chr1:25387699 | T | C | 2 | a0012c0010t0001g0019 a0012c0010t0001g0020 |
2 | HG01106.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.939+1277A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25387699 | |||||||
| chr1:25387717 | T | C | 5 | a0008c0008t0001g0146 a0008c0008t0001g0147 a0008c0008t0001g0148 others(2): Show |
5 | HG01109.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.939+1259A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25387717 | |||||||
| chr1:25387740 | G | T | 2 | a0012c0010t0001g0019 a0012c0010t0001g0020 |
2 | HG01106.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.939+1236C>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25387740 | |||||||
| chr1:25387743 | C | T | 2 | a0012c0010t0001g0019 a0012c0010t0001g0020 |
2 | HG01106.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.939+1233G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25387743 | |||||||
| chr1:25387759 | G | T | 1 | a0003c0003t0001g0273 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.939+1217C>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25387759 | |||||||
| chr1:25387860 | G | A | 2 | a0013c0012t0001g0170 a0013c0012t0001g0171 |
2 | HG01167.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.939+1116C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25387860 | |||||||
| chr1:25388074 | C | T | 1 | a0002c0002t0001g0244 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.939+902G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25388074 | |||||||
| chr1:25388075 | T | C | 1 | a0002c0002t0001g0244 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.939+901A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25388075 | |||||||
| chr1:25388174 | A | G | 2 | a0013c0012t0001g0170 a0013c0012t0001g0171 |
2 | HG01167.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.939+802T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25388174 | |||||||
| chr1:25388225 | T | G | 1 | a0002c0002t0001g0244 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.939+751A>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25388225 | |||||||
| chr1:25388313 | G | A | 8 | a0006c0006t0001g0285 a0006c0006t0001g0290 a0006c0006t0001g0291 others(5): Show |
8 | HG02257.hp2 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.939+663C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25388313 | |||||||
| chr1:25388529 | T | C | 1 | a0001c0001t0001g0027 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.939+447A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25388529 | |||||||
| chr1:25388553 | C | G | 1 | a0002c0002t0001g0267 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.939+423G>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25388553 | |||||||
| chr1:25388615 | G | T | 1 | a0007c0007t0002g0172 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.939+361C>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25388615 | |||||||
| chr1:25388653 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.939+323C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25388653 | |||||||
| chr1:25388681 | T | G | 1 | a0007c0007t0002g0172 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.939+295A>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25388681 | |||||||
| chr1:25388692 | C | G | 1 | a0001c0001t0001g0031 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.939+284G>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25388692 | |||||||
| chr1:25388924 | G | A | 6 | a0008c0008t0001g0146 a0008c0008t0001g0147 a0008c0008t0001g0148 others(3): Show |
6 | HG01109.hp1 HG02055.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.939+52C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 6/9 | chr1 | 25388924 | |||||||
| chr1:25389286 | C | T | 18 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(15): Show |
19 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.802-173G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 5/9 | chr1 | 25389286 | |||||||
| chr1:25389288 | G | A | 18 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(15): Show |
19 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.802-175C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 5/9 | chr1 | 25389288 | |||||||
| chr1:25389394 | C | A | 108 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(105): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.802-281G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 5/9 | chr1 | 25389394 | |||||||
| chr1:25389739 | G | C | 3 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0180 |
3 | HG00639.hp2 HG01243.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.802-626C>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 5/9 | chr1 | 25389739 | |||||||
| chr1:25389800 | T | C | 20 | a0004c0004t0001g0005 a0004c0004t0001g0009 a0004c0004t0001g0016 others(17): Show |
23 | HG01099.hp2 HG01106.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.802-687A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 5/9 | chr1 | 25389800 | |||||||
| chr1:25389824 | A | G | 29 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(26): Show |
31 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.802-711T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 5/9 | chr1 | 25389824 | |||||||
| chr1:25389834 | C | T | 26 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(23): Show |
28 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.802-721G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 5/9 | chr1 | 25389834 | |||||||
| chr1:25389904 | C | T | 1 | a0005c0005t0001g0303 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.802-791G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 5/9 | chr1 | 25389904 | |||||||
| chr1:25390185 | T | C | 1 | a0002c0002t0001g0199 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.801+564A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 5/9 | chr1 | 25390185 | |||||||
| chr1:25390199 | A | G | 5 | a0008c0008t0001g0146 a0008c0008t0001g0147 a0008c0008t0001g0148 others(2): Show |
5 | HG01109.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.801+550T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 5/9 | chr1 | 25390199 | |||||||
| chr1:25390201 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.801+548A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 5/9 | chr1 | 25390201 | |||||||
| chr1:25390382 | A | C | 7 | a0003c0003t0001g0215 a0003c0003t0001g0227 a0003c0003t0001g0232 others(4): Show |
7 | HG00639.hp1 HG02055.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.801+367T>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 5/9 | chr1 | 25390382 | |||||||
| chr1:25390391 | G | C | 5 | a0008c0008t0001g0146 a0008c0008t0001g0147 a0008c0008t0001g0148 others(2): Show |
5 | HG01109.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.801+358C>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 5/9 | chr1 | 25390391 | |||||||
| chr1:25390491 | C | G | 5 | a0003c0003t0001g0286 a0003c0003t0001g0287 a0003c0003t0001g0288 others(2): Show |
5 | HG02145.hp2 HG03130.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.801+258G>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 5/9 | chr1 | 25390491 | |||||||
| chr1:25390579 | C | A | 1 | a0003c0003t0001g0277 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.801+170G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 5/9 | chr1 | 25390579 | |||||||
| chr1:25390648 | C | T | 149 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(146): Show |
156 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.801+101G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 5/9 | chr1 | 25390648 | |||||||
| chr1:25391048 | C | T | 2 | a0002c0002t0001g0216 a0002c0002t0001g0241 |
2 | HG00597.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.635-133G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 4/9 | chr1 | 25391048 | |||||||
| chr1:25391161 | TGATGGTC others(645): Show |
T | 1 | a0009c0009t0001g0064 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.634+181_635-247del | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 4/9 | chr1 | 25391161 | |||||||
| chr1:25391247 | C | T | 7 | a0003c0003t0001g0283 a0003c0003t0001g0284 a0003c0003t0001g0286 others(4): Show |
7 | HG01069.hp2 HG01071.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.635-332G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 4/9 | chr1 | 25391247 | |||||||
| chr1:25391275 | C | T | 4 | a0012c0010t0001g0019 a0012c0010t0001g0020 a0014c0013t0001g0025 others(1): Show |
4 | HG01106.hp1 HG02145.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.635-360G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 4/9 | chr1 | 25391275 | |||||||
| chr1:25391335 | C | T | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.635-420G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 4/9 | chr1 | 25391335 | |||||||
| chr1:25391350 | G | A | 174 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(171): Show |
183 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.635-435C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 4/9 | chr1 | 25391350 | |||||||
| chr1:25391485 | C | A | 18 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(15): Show |
19 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.634+509G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 4/9 | chr1 | 25391485 | |||||||
| chr1:25391491 | C | T | 9 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0048 others(6): Show |
9 | HG00738.hp2 HG01168.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.634+503G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 4/9 | chr1 | 25391491 | |||||||
| chr1:25391499 | T | TA | 21 | a0003c0003t0001g0201 a0004c0004t0001g0005 a0004c0004t0001g0009 others(18): Show |
24 | HG01099.hp2 HG01106.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.634+494_634+495ins others(1): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 4/9 | chr1 | 25391499 | |||||||
| chr1:25391547 | T | C | 18 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(15): Show |
19 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.634+447A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 4/9 | chr1 | 25391547 | |||||||
| chr1:25391578 | C | T | 1 | a0002c0002t0001g0198 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.634+416G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 4/9 | chr1 | 25391578 | |||||||
| chr1:25391598 | C | T | 1 | a0002c0002t0001g0204 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.634+396G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 4/9 | chr1 | 25391598 | |||||||
| chr1:25391815 | A | T | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG02083.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.634+179T>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 4/9 | chr1 | 25391815 | |||||||
| chr1:25391862 | G | A | 1 | a0009c0009t0001g0064 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.634+132C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 4/9 | chr1 | 25391862 | |||||||
| chr1:25391900 | G | C | 8 | a0007c0007t0001g0010 a0007c0007t0001g0145 a0007c0007t0001g0173 others(5): Show |
9 | HG01167.hp2 HG02109.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.634+94C>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 4/9 | chr1 | 25391900 | |||||||
| chr1:25391965 | T | G | 23 | a0001c0001t0001g0043 a0002c0002t0001g0207 a0002c0002t0001g0209 others(20): Show |
24 | HG00280.hp1 HG00738.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.634+29A>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 4/9 | chr1 | 25391965 | |||||||
| chr1:25392188 | CA | C | 4 | a0009c0009t0001g0064 a0009c0009t0001g0073 a0009c0009t0001g0074 others(1): Show |
4 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.487-48delT | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25392188 | |||||||
| chr1:25392194 | A | C | 4 | a0009c0009t0001g0064 a0009c0009t0001g0073 a0009c0009t0001g0074 others(1): Show |
4 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.487-53T>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25392194 | |||||||
| chr1:25392205 | G | A | 4 | a0009c0009t0001g0064 a0009c0009t0001g0073 a0009c0009t0001g0074 others(1): Show |
4 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.487-64C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25392205 | |||||||
| chr1:25392256 | C | T | 7 | a0002c0002t0001g0266 a0002c0002t0001g0268 a0002c0002t0001g0270 others(4): Show |
7 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.487-115G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25392256 | |||||||
| chr1:25392299 | T | C | 9 | a0003c0003t0001g0286 a0003c0003t0001g0287 a0003c0003t0001g0288 others(6): Show |
9 | HG02145.hp2 HG02615.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.487-158A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25392299 | |||||||
| chr1:25392370 | T | C | 2 | a0003c0003t0001g0283 a0003c0003t0001g0284 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.487-229A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25392370 | |||||||
| chr1:25392460 | C | T | 5 | a0003c0003t0001g0286 a0003c0003t0001g0287 a0003c0003t0001g0288 others(2): Show |
5 | HG02145.hp2 HG03130.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.487-319G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25392460 | |||||||
| chr1:25392562 | C | CT | 94 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(91): Show |
98 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.487-422dupA | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25392562 | |||||||
| chr1:25392562 | C | CTT | 13 | a0002c0002t0001g0195 a0002c0002t0001g0196 a0002c0002t0001g0199 others(10): Show |
13 | HG00597.hp1 HG01175.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.487-423_487-422dup others(2): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25392562 | |||||||
| chr1:25392562 | CT | C | 16 | a0001c0001t0001g0017 a0001c0001t0001g0028 a0001c0001t0001g0032 others(13): Show |
16 | HG01106.hp1 HG02056.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.487-422delA | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25392562 | |||||||
| chr1:25392562 | CTT | C | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(124): Show |
140 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.487-423_487-422del others(2): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25392562 | |||||||
| chr1:25392562 | CTTT | C | 6 | a0001c0001t0001g0088 a0001c0001t0001g0141 a0003c0003t0001g0282 others(3): Show |
6 | HG02109.hp2 NA18941.hp1 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.487-424_487-422del others(3): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25392562 | |||||||
| chr1:25392744 | A | C | 169 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(166): Show |
177 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.487-603T>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25392744 | |||||||
| chr1:25392924 | G | T | 7 | a0007c0007t0001g0010 a0007c0007t0001g0145 a0007c0007t0001g0173 others(4): Show |
8 | HG01167.hp2 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.487-783C>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25392924 | |||||||
| chr1:25393020 | T | C | 131 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(128): Show |
136 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.487-879A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25393020 | |||||||
| chr1:25393103 | A | G | 8 | a0006c0006t0001g0285 a0006c0006t0001g0290 a0006c0006t0001g0291 others(5): Show |
8 | HG02257.hp2 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.487-962T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25393103 | |||||||
| chr1:25393108 | T | A | 169 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(166): Show |
177 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.487-967A>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25393108 | |||||||
| chr1:25393289 | G | A | 22 | a0003c0003t0001g0286 a0003c0003t0001g0287 a0003c0003t0001g0288 others(19): Show |
23 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.487-1148C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25393289 | |||||||
| chr1:25393428 | C | A | 1 | a0003c0003t0001g0265 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.487-1287G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25393428 | |||||||
| chr1:25393554 | G | C | 131 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(128): Show |
136 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.487-1413C>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25393554 | |||||||
| chr1:25393559 | T | C | 4 | a0008c0008t0001g0147 a0008c0008t0001g0148 a0008c0008t0001g0177 others(1): Show |
4 | HG01109.hp1 HG02055.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.487-1418A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25393559 | |||||||
| chr1:25393587 | C | T | 5 | a0008c0008t0001g0146 a0008c0008t0001g0147 a0008c0008t0001g0148 others(2): Show |
5 | HG01109.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.487-1446G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25393587 | |||||||
| chr1:25393597 | G | A | 196 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(193): Show |
206 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.487-1456C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25393597 | |||||||
| chr1:25393606 | G | C | 1 | a0003c0003t0001g0280 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.487-1465C>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25393606 | |||||||
| chr1:25393608 | G | GACACT | 4 | a0012c0010t0001g0019 a0012c0010t0001g0020 a0014c0013t0001g0025 others(1): Show |
4 | HG01106.hp1 HG02145.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.487-1468_487-1467i others(7): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25393608 | |||||||
| chr1:25393610 | G | C | 196 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(193): Show |
206 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.487-1469C>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25393610 | |||||||
| chr1:25393641 | G | A | 2 | a0003c0003t0001g0283 a0003c0003t0001g0284 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.487-1500C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25393641 | |||||||
| chr1:25393713 | G | T | 165 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(162): Show |
173 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.487-1572C>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25393713 | |||||||
| chr1:25393757 | C | G | 107 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(104): Show |
111 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.487-1616G>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25393757 | |||||||
| chr1:25393777 | A | C | 2 | a0003c0003t0001g0283 a0003c0003t0001g0284 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.487-1636T>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25393777 | |||||||
| chr1:25393810 | C | T | 131 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(128): Show |
136 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.487-1669G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25393810 | |||||||
| chr1:25393879 | A | G | 169 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(166): Show |
177 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.487-1738T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25393879 | |||||||
| chr1:25394021 | G | A | 20 | a0004c0004t0001g0005 a0004c0004t0001g0009 a0004c0004t0001g0016 others(17): Show |
23 | HG01099.hp2 HG01106.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.487-1880C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25394021 | |||||||
| chr1:25394070 | A | C | 3 | a0004c0004t0001g0005 a0004c0004t0001g0156 a0004c0004t0001g0176 |
5 | HG01106.hp2 HG01891.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.487-1929T>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25394070 | |||||||
| chr1:25394073 | T | C | 3 | a0004c0004t0001g0005 a0004c0004t0001g0156 a0004c0004t0001g0176 |
5 | HG01106.hp2 HG01891.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.487-1932A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25394073 | |||||||
| chr1:25394079 | A | G | 3 | a0004c0004t0001g0005 a0004c0004t0001g0156 a0004c0004t0001g0176 |
5 | HG01106.hp2 HG01891.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.487-1938T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25394079 | |||||||
| chr1:25394080 | C | T | 3 | a0004c0004t0001g0005 a0004c0004t0001g0156 a0004c0004t0001g0176 |
5 | HG01106.hp2 HG01891.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.487-1939G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25394080 | |||||||
| chr1:25394143 | T | C | 33 | a0004c0004t0001g0005 a0004c0004t0001g0009 a0004c0004t0001g0016 others(30): Show |
37 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.487-2002A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25394143 | |||||||
| chr1:25394191 | G | T | 7 | a0007c0007t0001g0010 a0007c0007t0001g0145 a0007c0007t0001g0173 others(4): Show |
8 | HG01167.hp2 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.487-2050C>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25394191 | |||||||
| chr1:25394196 | C | T | 1 | a0004c0004t0001g0005 | 3 | HG01891.hp2 HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.487-2055G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25394196 | |||||||
| chr1:25394302 | A | G | 1 | a0019c0019t0001g0021 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.487-2161T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25394302 | |||||||
| chr1:25394358 | C | G | 8 | a0006c0006t0001g0285 a0006c0006t0001g0290 a0006c0006t0001g0291 others(5): Show |
8 | HG02257.hp2 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.487-2217G>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25394358 | |||||||
| chr1:25394394 | G | A | 8 | a0006c0006t0001g0285 a0006c0006t0001g0290 a0006c0006t0001g0291 others(5): Show |
8 | HG02257.hp2 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.487-2253C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25394394 | |||||||
| chr1:25394404 | C | T | 6 | a0004c0004t0001g0144 a0004c0004t0001g0159 a0004c0004t0001g0162 others(3): Show |
6 | HG02717.hp1 HG02895.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.487-2263G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25394404 | |||||||
| chr1:25394456 | G | A | 3 | a0001c0001t0001g0044 a0001c0001t0001g0107 a0001c0001t0001g0108 |
3 | NA18969.hp2 NA18977.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.487-2315C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25394456 | |||||||
| chr1:25394476 | C | T | 2 | a0003c0003t0001g0283 a0003c0003t0001g0284 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.487-2335G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25394476 | |||||||
| chr1:25394493 | C | A | 1 | a0019c0019t0001g0021 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.487-2352G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25394493 | |||||||
| chr1:25394627 | A | T | 1 | a0020c0026t0001g0222 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.487-2486T>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25394627 | |||||||
| chr1:25394656 | G | C | 7 | a0003c0003t0001g0283 a0003c0003t0001g0284 a0003c0003t0001g0286 others(4): Show |
7 | HG01069.hp2 HG01071.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.487-2515C>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25394656 | |||||||
| chr1:25394663 | A | G | 106 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(103): Show |
110 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.487-2522T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25394663 | |||||||
| chr1:25394831 | T | A | 7 | a0007c0007t0001g0010 a0007c0007t0001g0145 a0007c0007t0001g0173 others(4): Show |
8 | HG01167.hp2 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.487-2690A>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25394831 | |||||||
| chr1:25394908 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.487-2767G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25394908 | |||||||
| chr1:25394910 | A | G | 1 | a0002c0002t0001g0228 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.487-2769T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25394910 | |||||||
| chr1:25394966 | G | C | 175 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(172): Show |
184 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.487-2825C>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25394966 | |||||||
| chr1:25395101 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.487-2960C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25395101 | |||||||
| chr1:25395402 | A | G | 1 | a0019c0019t0001g0021 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.487-3261T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25395402 | |||||||
| chr1:25395499 | T | C | 7 | a0007c0007t0001g0010 a0007c0007t0001g0145 a0007c0007t0001g0173 others(4): Show |
8 | HG01167.hp2 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.487-3358A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25395499 | |||||||
| chr1:25395521 | T | G | 7 | a0007c0007t0001g0010 a0007c0007t0001g0145 a0007c0007t0001g0173 others(4): Show |
8 | HG01167.hp2 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.487-3380A>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25395521 | |||||||
| chr1:25395599 | A | G | 172 | a0001c0001t0001g0066 a0002c0002t0001g0011 a0002c0002t0001g0012 others(169): Show |
181 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.487-3458T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25395599 | |||||||
| chr1:25395687 | T | C | 5 | a0008c0008t0001g0146 a0008c0008t0001g0147 a0008c0008t0001g0148 others(2): Show |
5 | HG01109.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.487-3546A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25395687 | |||||||
| chr1:25395715 | T | C | 171 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(168): Show |
180 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.487-3574A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25395715 | |||||||
| chr1:25395731 | C | T | 4 | a0001c0001t0001g0004 a0001c0001t0001g0036 a0001c0001t0001g0104 others(1): Show |
6 | HG00558.hp2 HG02135.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.487-3590G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25395731 | |||||||
| chr1:25395734 | A | G | 4 | a0001c0001t0001g0004 a0001c0001t0001g0036 a0001c0001t0001g0104 others(1): Show |
6 | HG00558.hp2 HG02135.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.487-3593T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25395734 | |||||||
| chr1:25395736 | A | G | 26 | a0004c0004t0001g0005 a0004c0004t0001g0009 a0004c0004t0001g0016 others(23): Show |
29 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.487-3595T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25395736 | |||||||
| chr1:25395782 | G | A | 1 | a0002c0002t0001g0238 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.487-3641C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25395782 | |||||||
| chr1:25395790 | C | A | 1 | a0003c0003t0001g0313 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.487-3649G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25395790 | |||||||
| chr1:25395900 | T | C | 1 | a0003c0003t0001g0286 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.487-3759A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25395900 | |||||||
| chr1:25395999 | C | T | 8 | a0006c0006t0001g0285 a0006c0006t0001g0290 a0006c0006t0001g0291 others(5): Show |
8 | HG02257.hp2 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.487-3858G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25395999 | |||||||
| chr1:25396117 | A | T | 17 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(14): Show |
18 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.487-3976T>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25396117 | |||||||
| chr1:25396208 | T | C | 1 | a0001c0001t0001g0111 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.487-4067A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25396208 | |||||||
| chr1:25396341 | T | G | 1 | a0001c0001t0001g0065 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.487-4200A>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25396341 | |||||||
| chr1:25396395 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.487-4254A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25396395 | |||||||
| chr1:25396432 | T | A | 7 | a0007c0007t0001g0010 a0007c0007t0001g0145 a0007c0007t0001g0173 others(4): Show |
8 | HG01167.hp2 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.487-4291A>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25396432 | |||||||
| chr1:25396494 | G | A | 3 | a0007c0007t0002g0172 a0013c0012t0001g0170 a0013c0012t0001g0171 |
3 | HG01167.hp2 HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.487-4353C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25396494 | |||||||
| chr1:25396515 | C | A | 1 | a0002c0002t0001g0210 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.487-4374G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25396515 | |||||||
| chr1:25396612 | G | T | 33 | a0003c0003t0001g0215 a0003c0003t0001g0227 a0003c0003t0001g0232 others(30): Show |
36 | HG00639.hp1 HG01099.hp2 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.487-4471C>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25396612 | |||||||
| chr1:25396630 | G | C | 1 | a0004c0024t0001g0182 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.487-4489C>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25396630 | |||||||
| chr1:25396743 | A | G | 6 | a0003c0003t0001g0313 a0008c0008t0001g0146 a0008c0008t0001g0147 others(3): Show |
6 | HG01109.hp1 HG02055.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.487-4602T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25396743 | |||||||
| chr1:25396749 | C | A | 5 | a0008c0008t0001g0146 a0008c0008t0001g0147 a0008c0008t0001g0148 others(2): Show |
5 | HG01109.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.487-4608G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25396749 | |||||||
| chr1:25396852 | G | A | 4 | a0008c0008t0001g0146 a0008c0008t0001g0147 a0008c0008t0001g0148 others(1): Show |
4 | HG01109.hp1 HG02055.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.487-4711C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25396852 | |||||||
| chr1:25396992 | ATC | A | 26 | a0004c0004t0001g0005 a0004c0004t0001g0009 a0004c0004t0001g0016 others(23): Show |
29 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.487-4853_487-4852d others(4): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25396992 | |||||||
| chr1:25397057 | A | G | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.487-4916T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25397057 | |||||||
| chr1:25397089 | G | GTGAT | 17 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(14): Show |
18 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.487-4952_487-4949d others(6): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25397089 | |||||||
| chr1:25397111 | C | CA | 132 | a0001c0001t0001g0036 a0001c0001t0001g0053 a0001c0001t0001g0089 others(129): Show |
137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.487-4971dupT | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25397111 | |||||||
| chr1:25397111 | C | CAA | 8 | a0002c0002t0001g0186 a0002c0002t0001g0195 a0002c0002t0001g0199 others(5): Show |
8 | HG00642.hp2 HG01109.hp1 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.487-4972_487-4971d others(4): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25397111 | |||||||
| chr1:25397111 | CAAAAAA | C | 17 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(14): Show |
18 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.487-4976_487-4971d others(8): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25397111 | |||||||
| chr1:25397121 | A | G | 17 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(14): Show |
18 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.487-4980T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25397121 | |||||||
| chr1:25397357 | C | T | 1 | a0003c0003t0001g0262 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.487-5216G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25397357 | |||||||
| chr1:25397432 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.486+5164C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25397432 | |||||||
| chr1:25397446 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.486+5150C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25397446 | |||||||
| chr1:25397484 | C | G | 1 | a0002c0002t0001g0214 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.486+5112G>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25397484 | |||||||
| chr1:25397514 | C | T | 170 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(167): Show |
179 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.486+5082G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25397514 | |||||||
| chr1:25397625 | T | C | 4 | a0007c0007t0001g0010 a0007c0007t0001g0145 a0007c0007t0001g0173 others(1): Show |
5 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.486+4971A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25397625 | |||||||
| chr1:25397629 | C | T | 2 | a0001c0001t0001g0139 a0002c0002t0001g0274 |
2 | HG00621.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.486+4967G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25397629 | |||||||
| chr1:25397655 | T | C | 175 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(172): Show |
184 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.486+4941A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25397655 | |||||||
| chr1:25397815 | C | A | 20 | a0004c0004t0001g0005 a0004c0004t0001g0009 a0004c0004t0001g0016 others(17): Show |
23 | HG01099.hp2 HG01106.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.486+4781G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25397815 | |||||||
| chr1:25397875 | G | A | 106 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(103): Show |
110 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.486+4721C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25397875 | |||||||
| chr1:25398010 | A | G | 47 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0017 others(44): Show |
51 | HG00099.hp2 HG00140.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.486+4586T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25398010 | |||||||
| chr1:25398033 | G | T | 24 | a0004c0004t0001g0005 a0004c0004t0001g0009 a0004c0004t0001g0016 others(21): Show |
28 | HG01099.hp2 HG01106.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.486+4563C>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25398033 | |||||||
| chr1:25398047 | C | T | 4 | a0007c0007t0001g0010 a0007c0007t0001g0145 a0007c0007t0001g0173 others(1): Show |
5 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.486+4549G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25398047 | |||||||
| chr1:25398129 | G | A | 4 | a0007c0007t0001g0010 a0007c0007t0001g0145 a0007c0007t0001g0173 others(1): Show |
5 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.486+4467C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25398129 | |||||||
| chr1:25398292 | T | C | 141 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(138): Show |
146 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.486+4304A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25398292 | |||||||
| chr1:25398470 | A | G | 7 | a0003c0003t0001g0283 a0003c0003t0001g0284 a0003c0003t0001g0286 others(4): Show |
7 | HG01069.hp2 HG01071.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.486+4126T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25398470 | |||||||
| chr1:25398485 | C | T | 5 | a0008c0008t0001g0146 a0008c0008t0001g0147 a0008c0008t0001g0148 others(2): Show |
5 | HG01109.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.486+4111G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25398485 | |||||||
| chr1:25398662 | C | T | 1 | a0002c0002t0001g0213 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.486+3934G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25398662 | |||||||
| chr1:25398665 | A | C | 1 | a0013c0012t0001g0171 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.486+3931T>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25398665 | |||||||
| chr1:25398731 | T | C | 5 | a0003c0003t0001g0286 a0003c0003t0001g0287 a0003c0003t0001g0288 others(2): Show |
5 | HG02145.hp2 HG03130.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.486+3865A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25398731 | |||||||
| chr1:25398758 | C | T | 1 | a0003c0003t0001g0288 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.486+3838G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25398758 | |||||||
| chr1:25398907 | T | C | 2 | a0009c0009t0001g0074 a0009c0009t0001g0075 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.486+3689A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25398907 | |||||||
| chr1:25399235 | T | C | 1 | a0012c0010t0001g0020 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.486+3361A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25399235 | |||||||
| chr1:25399263 | A | G | 1 | a0003c0003t0001g0202 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.486+3333T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25399263 | |||||||
| chr1:25399412 | G | A | 1 | a0002c0002t0001g0278 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.486+3184C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25399412 | |||||||
| chr1:25399722 | A | C | 1 | a0003c0003t0001g0232 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.486+2874T>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25399722 | |||||||
| chr1:25399814 | T | C | 1 | a0001c0001t0001g0085 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.486+2782A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25399814 | |||||||
| chr1:25399835 | C | CATTGTAA others(132): Show |
1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.486+2622_486+2760d others(141): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25399835 | |||||||
| chr1:25400345 | C | T | 137 | a0001c0001t0001g0141 a0002c0002t0001g0011 a0002c0002t0001g0012 others(134): Show |
142 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.486+2251G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25400345 | |||||||
| chr1:25400698 | C | T | 1 | a0013c0012t0001g0171 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.486+1898G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25400698 | |||||||
| chr1:25400707 | A | ACACCC | 3 | a0012c0010t0001g0019 a0012c0010t0001g0020 a0019c0019t0001g0021 |
3 | HG01106.hp1 HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.486+1888_486+1889i others(7): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25400707 | |||||||
| chr1:25400710 | C | T | 3 | a0012c0010t0001g0019 a0012c0010t0001g0020 a0019c0019t0001g0021 |
3 | HG01106.hp1 HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.486+1886G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25400710 | |||||||
| chr1:25400711 | G | C | 3 | a0012c0010t0001g0019 a0012c0010t0001g0020 a0019c0019t0001g0021 |
3 | HG01106.hp1 HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.486+1885C>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25400711 | |||||||
| chr1:25400731 | G | A | 3 | a0007c0007t0002g0172 a0013c0012t0001g0170 a0013c0012t0001g0171 |
3 | HG01167.hp2 HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.486+1865C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25400731 | |||||||
| chr1:25400788 | T | C | 4 | a0002c0002t0001g0221 a0012c0010t0001g0019 a0012c0010t0001g0020 others(1): Show |
4 | HG01106.hp1 HG02258.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.486+1808A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25400788 | |||||||
| chr1:25400820 | T | C | 3 | a0012c0010t0001g0019 a0012c0010t0001g0020 a0019c0019t0001g0021 |
3 | HG01106.hp1 HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.486+1776A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25400820 | |||||||
| chr1:25400895 | C | T | 171 | a0001c0001t0001g0141 a0002c0002t0001g0011 a0002c0002t0001g0012 others(168): Show |
180 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.486+1701G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25400895 | |||||||
| chr1:25400947 | C | T | 174 | a0001c0001t0001g0141 a0002c0002t0001g0011 a0002c0002t0001g0012 others(171): Show |
183 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.486+1649G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25400947 | |||||||
| chr1:25400986 | C | A | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.486+1610G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25400986 | |||||||
| chr1:25400995 | T | C | 177 | a0001c0001t0001g0141 a0002c0002t0001g0011 a0002c0002t0001g0012 others(174): Show |
186 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.486+1601A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25400995 | |||||||
| chr1:25401056 | G | A | 1 | a0002c0002t0001g0224 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.486+1540C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25401056 | |||||||
| chr1:25401084 | A | G | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.486+1512T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25401084 | |||||||
| chr1:25401139 | A | C | 3 | a0007c0007t0002g0172 a0013c0012t0001g0170 a0013c0012t0001g0171 |
3 | HG01167.hp2 HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.486+1457T>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25401139 | |||||||
| chr1:25401153 | T | C | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.486+1443A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25401153 | |||||||
| chr1:25401196 | G | A | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.486+1400C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25401196 | |||||||
| chr1:25401205 | T | C | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.486+1391A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25401205 | |||||||
| chr1:25401273 | C | T | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.486+1323G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25401273 | |||||||
| chr1:25401279 | A | G | 6 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(3): Show |
7 | HG01070.hp1 HG01071.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.486+1317T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25401279 | |||||||
| chr1:25401345 | C | A | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.486+1251G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25401345 | |||||||
| chr1:25401382 | T | C | 1 | a0015c0011t0001g0161 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.486+1214A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25401382 | |||||||
| chr1:25401477 | C | T | 172 | a0001c0001t0001g0141 a0002c0002t0001g0011 a0002c0002t0001g0012 others(169): Show |
181 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.486+1119G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25401477 | |||||||
| chr1:25401542 | G | T | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.486+1054C>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25401542 | |||||||
| chr1:25401590 | C | T | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.486+1006G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25401590 | |||||||
| chr1:25401627 | G | A | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.486+969C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25401627 | |||||||
| chr1:25401642 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.486+954G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25401642 | |||||||
| chr1:25401725 | C | T | 2 | a0003c0003t0001g0313 a0023c0023t0001g0054 |
2 | HG03130.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.486+871G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25401725 | |||||||
| chr1:25401737 | C | T | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.486+859G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25401737 | |||||||
| chr1:25401745 | A | G | 1 | a0003c0003t0001g0286 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.486+851T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25401745 | |||||||
| chr1:25401787 | C | T | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.486+809G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25401787 | |||||||
| chr1:25401823 | C | T | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.486+773G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25401823 | |||||||
| chr1:25401832 | C | A | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.486+764G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25401832 | |||||||
| chr1:25401842 | G | A | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.486+754C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25401842 | |||||||
| chr1:25401842 | GTATC | G | 5 | a0008c0008t0001g0146 a0008c0008t0001g0147 a0008c0008t0001g0148 others(2): Show |
5 | HG01109.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.486+750_486+753del others(4): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25401842 | |||||||
| chr1:25401883 | T | A | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.486+713A>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25401883 | |||||||
| chr1:25401885 | T | C | 2 | a0005c0005t0001g0297 a0005c0005t0001g0298 |
2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.486+711A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25401885 | |||||||
| chr1:25401888 | T | A | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.486+708A>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25401888 | |||||||
| chr1:25401889 | T | A | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.486+707A>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25401889 | |||||||
| chr1:25401893 | G | T | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.486+703C>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25401893 | |||||||
| chr1:25401939 | C | T | 1 | a0003c0003t0001g0255 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.486+657G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25401939 | |||||||
| chr1:25401946 | A | G | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.486+650T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25401946 | |||||||
| chr1:25401947 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.486+649C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25401947 | |||||||
| chr1:25401966 | C | T | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.486+630G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25401966 | |||||||
| chr1:25401967 | T | C | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.486+629A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25401967 | |||||||
| chr1:25401968 | C | T | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.486+628G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25401968 | |||||||
| chr1:25402022 | A | G | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.486+574T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25402022 | |||||||
| chr1:25402036 | G | C | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.486+560C>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25402036 | |||||||
| chr1:25402100 | C | T | 4 | a0007c0007t0001g0010 a0007c0007t0001g0145 a0007c0007t0001g0173 others(1): Show |
5 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.486+496G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25402100 | |||||||
| chr1:25402175 | C | CCTGT | 5 | a0003c0003t0001g0014 a0003c0003t0001g0193 a0003c0003t0001g0273 others(2): Show |
6 | HG00733.hp2 HG01175.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.486+417_486+420dup others(4): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25402175 | |||||||
| chr1:25402175 | CCTGT | C | 28 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0031 others(25): Show |
30 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.486+417_486+420del others(4): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25402175 | |||||||
| chr1:25402175 | CCTGTCTG others(1): Show |
C | 5 | a0005c0005t0001g0299 a0007c0007t0001g0010 a0007c0007t0001g0145 others(2): Show |
6 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.486+413_486+420del others(8): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25402175 | |||||||
| chr1:25402198 | G | A | 2 | a0007c0007t0002g0172 a0013c0012t0001g0171 |
2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.486+398C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25402198 | |||||||
| chr1:25402198 | G | GTCTA | 6 | a0004c0004t0001g0009 a0005c0005t0001g0308 a0005c0005t0001g0309 others(3): Show |
7 | HG01069.hp1 HG02630.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.486+397_486+398ins others(4): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25402198 | |||||||
| chr1:25402198 | GTCTGTCT others(17): Show |
G | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.486+374_486+397del others(24): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25402198 | |||||||
| chr1:25402202 | G | A | 32 | a0004c0004t0001g0005 a0004c0004t0001g0009 a0004c0004t0001g0016 others(29): Show |
35 | HG01069.hp1 HG01099.hp2 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.486+394C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25402202 | |||||||
| chr1:25402202 | G | GTCTA | 20 | a0002c0002t0001g0012 a0002c0002t0001g0223 a0002c0002t0001g0224 others(17): Show |
21 | HG02109.hp2 HG02148.hp1 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.486+393_486+394ins others(4): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25402202 | |||||||
| chr1:25402206 | G | A | 75 | a0001c0001t0001g0018 a0001c0001t0001g0029 a0001c0001t0001g0089 others(72): Show |
80 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(77): Show |
intron_variant | MODIFIER | c.486+390C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25402206 | |||||||
| chr1:25402206 | G | GTCTA | 20 | a0001c0001t0001g0033 a0001c0001t0001g0038 a0001c0001t0001g0040 others(17): Show |
20 | HG00099.hp2 HG00558.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.486+386_486+389dup others(4): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25402206 | |||||||
| chr1:25402206 | G | GTCTATCT others(1): Show |
49 | a0001c0001t0001g0141 a0002c0002t0001g0011 a0002c0002t0001g0013 others(46): Show |
51 | HG00280.hp1 HG00423.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.486+382_486+389dup others(8): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25402206 | |||||||
| chr1:25402206 | G | GTCTATCT others(5): Show |
7 | a0002c0002t0001g0196 a0002c0002t0001g0198 a0002c0002t0001g0206 others(4): Show |
7 | HG00408.hp1 HG02074.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.486+378_486+389dup others(12): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25402206 | |||||||
| chr1:25402206 | G | GTCTATCT others(9): Show |
1 | a0002c0002t0001g0210 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.486+374_486+389dup others(16): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25402206 | |||||||
| chr1:25402206 | G | GTCTGTCT others(1): Show |
20 | a0002c0002t0001g0195 a0002c0002t0001g0259 a0002c0002t0001g0264 others(17): Show |
20 | HG00099.hp1 HG00738.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.486+389_486+390ins others(8): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25402206 | |||||||
| chr1:25402206 | G | GTCTGTCT others(5): Show |
5 | a0002c0002t0001g0189 a0002c0002t0001g0271 a0003c0003t0001g0192 others(2): Show |
5 | HG00280.hp2 HG00741.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.486+389_486+390ins others(12): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25402206 | |||||||
| chr1:25402206 | G | GTCTGTCT others(5): Show |
3 | a0002c0002t0001g0204 a0002c0002t0001g0252 a0002c0002t0001g0256 |
3 | HG01070.hp2 HG02602.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.486+389_486+390ins others(12): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25402206 | |||||||
| chr1:25402206 | G | GTCTGTCT others(9): Show |
1 | a0003c0003t0001g0262 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.486+389_486+390ins others(16): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25402206 | |||||||
| chr1:25402206 | GTCTA | G | 3 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0004c0004t0001g0041 |
3 | HG02647.hp1 NA18963.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.486+386_486+389del others(4): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25402206 | |||||||
| chr1:25402210 | A | G | 3 | a0001c0001t0001g0042 a0001c0001t0001g0094 a0003c0003t0001g0257 |
3 | HG00140.hp2 HG00408.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.486+386T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25402210 | |||||||
| chr1:25402238 | A | G | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.486+358T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25402238 | |||||||
| chr1:25402281 | A | G | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.486+315T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25402281 | |||||||
| chr1:25402290 | G | C | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.486+306C>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25402290 | |||||||
| chr1:25402292 | T | C | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.486+304A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25402292 | |||||||
| chr1:25402293 | C | G | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.486+303G>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25402293 | |||||||
| chr1:25402294 | A | G | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.486+302T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25402294 | |||||||
| chr1:25402297 | T | C | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.486+299A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25402297 | |||||||
| chr1:25402315 | G | A | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.486+281C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25402315 | |||||||
| chr1:25402356 | C | G | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.486+240G>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25402356 | |||||||
| chr1:25402439 | G | T | 177 | a0001c0001t0001g0141 a0002c0002t0001g0011 a0002c0002t0001g0012 others(174): Show |
186 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.486+157C>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25402439 | |||||||
| chr1:25402472 | C | T | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.486+124G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25402472 | |||||||
| chr1:25402479 | A | G | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.486+117T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25402479 | |||||||
| chr1:25402527 | C | T | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.486+69G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25402527 | |||||||
| chr1:25402532 | G | A | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.486+64C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 3/9 | chr1 | 25402532 | |||||||
| chr1:25402754 | T | A | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | splice_region_variant&intron_variant | LOW | c.336-8A>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25402754 | |||||||
| chr1:25402759 | A | G | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.336-13T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25402759 | |||||||
| chr1:25402772 | T | C | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.336-26A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25402772 | |||||||
| chr1:25402778 | A | G | 5 | a0008c0008t0001g0146 a0008c0008t0001g0147 a0008c0008t0001g0148 others(2): Show |
5 | HG01109.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.336-32T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25402778 | |||||||
| chr1:25402798 | CTCAT | C | 21 | a0004c0004t0001g0005 a0004c0004t0001g0009 a0004c0004t0001g0016 others(18): Show |
24 | HG01099.hp2 HG01106.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.336-56_336-53delAT others(2): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25402798 | |||||||
| chr1:25402821 | A | ATTCATTC others(5): Show |
1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.336-76_336-75insAG others(10): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25402821 | |||||||
| chr1:25402837 | T | C | 5 | a0008c0008t0001g0146 a0008c0008t0001g0147 a0008c0008t0001g0148 others(2): Show |
5 | HG01109.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.336-91A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25402837 | |||||||
| chr1:25402858 | A | G | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.336-112T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25402858 | |||||||
| chr1:25402964 | G | A | 33 | a0004c0004t0001g0005 a0004c0004t0001g0009 a0004c0004t0001g0016 others(30): Show |
37 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.336-218C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25402964 | |||||||
| chr1:25403117 | C | T | 1 | a0003c0003t0001g0201 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.336-371G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25403117 | |||||||
| chr1:25403178 | T | C | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.336-432A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25403178 | |||||||
| chr1:25403206 | C | G | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.336-460G>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25403206 | |||||||
| chr1:25403253 | C | T | 2 | a0014c0013t0001g0025 a0014c0013t0001g0026 |
2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.336-507G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25403253 | |||||||
| chr1:25403429 | C | T | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.336-683G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25403429 | |||||||
| chr1:25403440 | A | G | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.336-694T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25403440 | |||||||
| chr1:25403455 | A | G | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.336-709T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25403455 | |||||||
| chr1:25403462 | C | T | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.336-716G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25403462 | |||||||
| chr1:25403477 | C | T | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.336-731G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25403477 | |||||||
| chr1:25403502 | G | T | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.336-756C>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25403502 | |||||||
| chr1:25403526 | G | A | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.336-780C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25403526 | |||||||
| chr1:25403528 | T | A | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.336-782A>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25403528 | |||||||
| chr1:25403540 | A | G | 1 | a0003c0003t0001g0279 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.336-794T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25403540 | |||||||
| chr1:25403664 | A | G | 1 | a0004c0024t0001g0182 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.336-918T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25403664 | |||||||
| chr1:25403775 | A | G | 7 | a0007c0007t0001g0010 a0007c0007t0001g0145 a0007c0007t0001g0173 others(4): Show |
8 | HG01167.hp2 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.336-1029T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25403775 | |||||||
| chr1:25403893 | C | T | 18 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(15): Show |
19 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.336-1147G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25403893 | |||||||
| chr1:25404107 | G | T | 2 | a0001c0001t0001g0123 a0023c0023t0001g0054 |
2 | HG01516.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.336-1361C>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25404107 | |||||||
| chr1:25404108 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.336-1362G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25404108 | |||||||
| chr1:25404112 | C | G | 2 | a0001c0001t0001g0123 a0023c0023t0001g0054 |
2 | HG01516.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.336-1366G>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25404112 | |||||||
| chr1:25404113 | A | G | 2 | a0001c0001t0001g0123 a0023c0023t0001g0054 |
2 | HG01516.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.336-1367T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25404113 | |||||||
| chr1:25404121 | T | C | 2 | a0001c0001t0001g0123 a0023c0023t0001g0054 |
2 | HG01516.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.336-1375A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25404121 | |||||||
| chr1:25404134 | C | T | 21 | a0004c0004t0001g0005 a0004c0004t0001g0009 a0004c0004t0001g0016 others(18): Show |
24 | HG01099.hp2 HG01106.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.336-1388G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25404134 | |||||||
| chr1:25404147 | G | A | 2 | a0001c0001t0001g0123 a0023c0023t0001g0054 |
2 | HG01516.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.336-1401C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25404147 | |||||||
| chr1:25404164 | T | C | 2 | a0001c0001t0001g0123 a0023c0023t0001g0054 |
2 | HG01516.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.336-1418A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25404164 | |||||||
| chr1:25404169 | C | CA | 28 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0022 others(25): Show |
31 | HG00423.hp2 HG01175.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.336-1424dupT | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25404169 | |||||||
| chr1:25404169 | C | CAA | 7 | a0001c0001t0001g0007 a0001c0001t0001g0051 a0001c0001t0001g0088 others(4): Show |
8 | HG03130.hp2 NA18942.hp2 NA18972.hp1 others(5): Show |
intron_variant | MODIFIER | c.336-1425_336-1424d others(4): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25404169 | |||||||
| chr1:25404169 | C | CAAA | 104 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(101): Show |
109 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.336-1426_336-1424d others(5): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25404169 | |||||||
| chr1:25404169 | C | CAAAA | 29 | a0002c0002t0001g0186 a0002c0002t0001g0195 a0002c0002t0001g0199 others(26): Show |
29 | HG00639.hp1 HG00642.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.336-1427_336-1424d others(6): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25404169 | |||||||
| chr1:25404169 | CA | C | 11 | a0004c0004t0001g0114 a0007c0007t0001g0010 a0007c0007t0001g0145 others(8): Show |
12 | HG01167.hp2 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.336-1424delT | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25404169 | |||||||
| chr1:25404176 | A | C | 2 | a0001c0001t0001g0123 a0023c0023t0001g0054 |
2 | HG01516.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.336-1430T>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25404176 | |||||||
| chr1:25404178 | A | C | 2 | a0001c0001t0001g0123 a0023c0023t0001g0054 |
2 | HG01516.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.336-1432T>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25404178 | |||||||
| chr1:25404180 | A | C | 2 | a0001c0001t0001g0123 a0023c0023t0001g0054 |
2 | HG01516.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.336-1434T>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25404180 | |||||||
| chr1:25404182 | A | C | 2 | a0001c0001t0001g0123 a0023c0023t0001g0054 |
2 | HG01516.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.336-1436T>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25404182 | |||||||
| chr1:25404222 | G | A | 175 | a0001c0001t0001g0123 a0002c0002t0001g0011 a0002c0002t0001g0012 others(172): Show |
184 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.336-1476C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25404222 | |||||||
| chr1:25404252 | G | A | 3 | a0007c0007t0002g0172 a0013c0012t0001g0170 a0013c0012t0001g0171 |
3 | HG01167.hp2 HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.336-1506C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25404252 | |||||||
| chr1:25404426 | T | G | 171 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(168): Show |
180 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.336-1680A>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25404426 | |||||||
| chr1:25404488 | T | C | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.336-1742A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25404488 | |||||||
| chr1:25404726 | C | T | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.336-1980G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25404726 | |||||||
| chr1:25404817 | C | T | 1 | a0001c0001t0001g0030 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.336-2071G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25404817 | |||||||
| chr1:25404892 | A | G | 5 | a0008c0008t0001g0146 a0008c0008t0001g0147 a0008c0008t0001g0148 others(2): Show |
5 | HG01109.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.336-2146T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25404892 | |||||||
| chr1:25404941 | A | C | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.336-2195T>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25404941 | |||||||
| chr1:25405034 | C | CA | 44 | a0001c0001t0001g0030 a0001c0001t0001g0089 a0001c0001t0001g0090 others(41): Show |
45 | HG00597.hp2 HG01071.hp1 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.336-2289dupT | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25405034 | |||||||
| chr1:25405038 | A | AG | 5 | a0003c0003t0001g0286 a0003c0003t0001g0287 a0003c0003t0001g0288 others(2): Show |
5 | HG02145.hp2 HG03130.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.336-2293_336-2292i others(3): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25405038 | |||||||
| chr1:25405059 | C | T | 171 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(168): Show |
180 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.336-2313G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25405059 | |||||||
| chr1:25405117 | C | T | 1 | a0001c0001t0001g0031 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.336-2371G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25405117 | |||||||
| chr1:25405118 | G | A | 11 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0002c0002t0001g0235 others(8): Show |
12 | HG01167.hp2 HG01515.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.336-2372C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25405118 | |||||||
| chr1:25405199 | G | A | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.336-2453C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25405199 | |||||||
| chr1:25405201 | C | T | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.336-2455G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25405201 | |||||||
| chr1:25405236 | T | C | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.336-2490A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25405236 | |||||||
| chr1:25405251 | A | G | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.336-2505T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25405251 | |||||||
| chr1:25405290 | C | T | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.336-2544G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25405290 | |||||||
| chr1:25405308 | T | C | 4 | a0004c0004t0001g0005 a0004c0004t0001g0156 a0004c0004t0001g0176 others(1): Show |
6 | HG01106.hp2 HG01891.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.336-2562A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25405308 | |||||||
| chr1:25405361 | C | A | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.336-2615G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25405361 | |||||||
| chr1:25405374 | C | T | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.336-2628G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25405374 | |||||||
| chr1:25405377 | G | A | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.336-2631C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25405377 | |||||||
| chr1:25405424 | G | A | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.336-2678C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25405424 | |||||||
| chr1:25405443 | A | G | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.336-2697T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25405443 | |||||||
| chr1:25405451 | G | A | 3 | a0003c0003t0001g0232 a0003c0003t0001g0233 a0003c0003t0001g0282 |
3 | HG02109.hp2 NA20129.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.336-2705C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25405451 | |||||||
| chr1:25405451 | G | C | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.336-2705C>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25405451 | |||||||
| chr1:25405482 | G | T | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.336-2736C>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25405482 | |||||||
| chr1:25405484 | C | G | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.336-2738G>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25405484 | |||||||
| chr1:25405496 | C | T | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.336-2750G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25405496 | |||||||
| chr1:25405509 | C | A | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.336-2763G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25405509 | |||||||
| chr1:25405527 | T | C | 8 | a0001c0001t0001g0008 a0001c0001t0001g0042 a0001c0001t0001g0110 others(5): Show |
9 | HG00597.hp2 HG02074.hp1 HG03942.hp1 others(6): Show |
intron_variant | MODIFIER | c.336-2781A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25405527 | |||||||
| chr1:25405530 | G | A | 34 | a0004c0004t0001g0005 a0004c0004t0001g0009 a0004c0004t0001g0016 others(31): Show |
38 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.336-2784C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25405530 | |||||||
| chr1:25405587 | G | C | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.336-2841C>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25405587 | |||||||
| chr1:25405592 | T | TGCAATGA others(102): Show |
1 | a0001c0001t0001g0136 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.336-2847_336-2846i others(111): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25405592 | |||||||
| chr1:25405592 | T | TGCAATGA others(102): Show |
127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(124): Show |
139 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.336-2847_336-2846i others(111): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25405592 | |||||||
| chr1:25405592 | T | TGCAATGA others(102): Show |
1 | a0001c0001t0001g0142 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.336-2847_336-2846i others(111): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25405592 | |||||||
| chr1:25405596 | G | A | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(129): Show |
144 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.336-2850C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25405596 | |||||||
| chr1:25405627 | C | A | 4 | a0002c0002t0001g0185 a0002c0002t0001g0186 a0002c0002t0001g0187 others(1): Show |
4 | HG00642.hp2 HG01099.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.336-2881G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25405627 | |||||||
| chr1:25405649 | G | A | 1 | a0023c0023t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.336-2903C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25405649 | |||||||
| chr1:25405659 | AAAT | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.336-2916_336-2914d others(5): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25405659 | |||||||
| chr1:25405674 | A | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.336-2928T>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25405674 | |||||||
| chr1:25405695 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.336-2949C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25405695 | |||||||
| chr1:25405701 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.336-2955T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25405701 | |||||||
| chr1:25405718 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+2965A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25405718 | |||||||
| chr1:25405763 | C | G | 173 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(170): Show |
182 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.335+2920G>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25405763 | |||||||
| chr1:25405769 | C | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0180 |
3 | HG00639.hp2 HG01243.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.335+2914G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25405769 | |||||||
| chr1:25405918 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.335+2765C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25405918 | |||||||
| chr1:25405930 | G | A | 1 | a0001c0001t0001g0093 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.335+2753C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25405930 | |||||||
| chr1:25405988 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+2695T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25405988 | |||||||
| chr1:25405992 | A | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
180 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.335+2691T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25405992 | |||||||
| chr1:25405995 | G | A | 136 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(133): Show |
141 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.335+2688C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25405995 | |||||||
| chr1:25406033 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+2650T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406033 | |||||||
| chr1:25406038 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+2645G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406038 | |||||||
| chr1:25406041 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+2642C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406041 | |||||||
| chr1:25406041 | G | C | 3 | a0002c0002t0001g0012 a0002c0002t0001g0234 a0002c0002t0001g0235 |
4 | NA18942.hp1 NA18970.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.335+2642C>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406041 | |||||||
| chr1:25406056 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+2627A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406056 | |||||||
| chr1:25406056 | TG | T | 7 | a0007c0007t0001g0010 a0007c0007t0001g0145 a0007c0007t0001g0173 others(4): Show |
8 | HG01167.hp2 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.335+2626delC | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406056 | |||||||
| chr1:25406057 | G | A | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(290): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.335+2626C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406057 | |||||||
| chr1:25406081 | T | C | 1 | a0003c0003t0001g0280 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.335+2602A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406081 | |||||||
| chr1:25406084 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+2599T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406084 | |||||||
| chr1:25406178 | T | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+2505A>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406178 | |||||||
| chr1:25406179 | TC | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+2503delG | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406179 | |||||||
| chr1:25406205 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+2478A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406205 | |||||||
| chr1:25406215 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+2468A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406215 | |||||||
| chr1:25406216 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+2467C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406216 | |||||||
| chr1:25406230 | CGGGCGTG others(19): Show |
C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+2427_335+2452d others(28): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406230 | |||||||
| chr1:25406232 | G | GGCGT | 22 | a0002c0002t0001g0189 a0002c0002t0001g0195 a0002c0002t0001g0204 others(19): Show |
22 | HG00099.hp1 HG00140.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.335+2447_335+2450d others(6): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406232 | |||||||
| chr1:25406246 | CGTGCGTG others(3): Show |
C | 1 | a0003c0003t0001g0313 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.335+2427_335+2436d others(12): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406246 | |||||||
| chr1:25406250 | CGT | C | 24 | a0002c0002t0001g0236 a0002c0002t0001g0237 a0003c0003t0001g0283 others(21): Show |
25 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.335+2431_335+2432d others(4): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406250 | |||||||
| chr1:25406250 | CGTGT | C | 22 | a0002c0002t0001g0012 a0002c0002t0001g0185 a0002c0002t0001g0186 others(19): Show |
23 | HG00642.hp2 HG01099.hp1 HG01952.hp2 others(20): Show |
intron_variant | MODIFIER | c.335+2429_335+2432d others(6): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406250 | |||||||
| chr1:25406250 | CGTGTGT | C | 3 | a0004c0004t0001g0037 a0004c0004t0001g0144 a0008c0008t0001g0146 |
3 | HG02056.hp2 HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.335+2427_335+2432d others(8): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406250 | |||||||
| chr1:25406250 | CGTGTGTG others(1): Show |
C | 11 | a0004c0004t0001g0159 a0004c0004t0001g0162 a0004c0004t0001g0163 others(8): Show |
11 | HG01109.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.335+2425_335+2432d others(10): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406250 | |||||||
| chr1:25406250 | CGTGTGTG others(3): Show |
C | 15 | a0004c0004t0001g0005 a0004c0004t0001g0009 a0004c0004t0001g0016 others(12): Show |
18 | HG01099.hp2 HG01106.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.335+2423_335+2432d others(12): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406250 | |||||||
| chr1:25406252 | T | TGC | 18 | a0002c0002t0001g0194 a0002c0002t0001g0259 a0003c0003t0001g0193 others(15): Show |
19 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.335+2430_335+2431i others(4): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406252 | |||||||
| chr1:25406254 | T | C | 86 | a0002c0002t0001g0011 a0002c0002t0001g0013 a0002c0002t0001g0183 others(83): Show |
89 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.335+2429A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406254 | |||||||
| chr1:25406256 | T | C | 40 | a0002c0002t0001g0194 a0002c0002t0001g0236 a0002c0002t0001g0237 others(37): Show |
42 | HG00280.hp2 HG00733.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.335+2427A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406256 | |||||||
| chr1:25406258 | T | C | 81 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(78): Show |
85 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.335+2425A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406258 | |||||||
| chr1:25406260 | T | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(148): Show |
164 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.335+2423A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406260 | |||||||
| chr1:25406261 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+2422C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406261 | |||||||
| chr1:25406262 | T | C | 4 | a0002c0002t0001g0187 a0002c0002t0001g0238 a0002c0002t0001g0239 others(1): Show |
4 | HG00621.hp1 HG01978.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.335+2421A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406262 | |||||||
| chr1:25406264 | T | C | 1 | a0005c0005t0001g0308 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.335+2419A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406264 | |||||||
| chr1:25406268 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+2415A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406268 | |||||||
| chr1:25406284 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+2399G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406284 | |||||||
| chr1:25406286 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+2397G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406286 | |||||||
| chr1:25406302 | T | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+2381A>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406302 | |||||||
| chr1:25406303 | A | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+2380T>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406303 | |||||||
| chr1:25406307 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+2376A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406307 | |||||||
| chr1:25406308 | G | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+2375C>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406308 | |||||||
| chr1:25406336 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+2347C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406336 | |||||||
| chr1:25406373 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+2310G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406373 | |||||||
| chr1:25406401 | C | G | 1 | a0003c0003t0001g0286 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.335+2282G>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406401 | |||||||
| chr1:25406465 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+2218T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406465 | |||||||
| chr1:25406467 | A | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+2216T>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406467 | |||||||
| chr1:25406469 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+2214A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406469 | |||||||
| chr1:25406470 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+2213C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406470 | |||||||
| chr1:25406475 | G | A | 1 | a0004c0024t0001g0182 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.335+2208C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406475 | |||||||
| chr1:25406526 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+2157G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406526 | |||||||
| chr1:25406534 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+2149T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406534 | |||||||
| chr1:25406557 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+2126A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406557 | |||||||
| chr1:25406560 | GT | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+2122delA | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406560 | |||||||
| chr1:25406618 | CTGT | C | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(124): Show |
139 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.335+2062_335+2064d others(5): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406618 | |||||||
| chr1:25406620 | GTTGT | G | 3 | a0001c0001t0001g0030 a0001c0001t0001g0042 a0023c0023t0001g0054 |
3 | HG03942.hp1 NA19072.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.335+2059_335+2062d others(6): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406620 | |||||||
| chr1:25406629 | G | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0042 a0023c0023t0001g0054 |
3 | HG03942.hp1 NA19072.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.335+2054C>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406629 | |||||||
| chr1:25406629 | GGT | G | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(124): Show |
139 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.335+2052_335+2053d others(4): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406629 | |||||||
| chr1:25406630 | G | GT | 19 | a0002c0002t0001g0195 a0002c0002t0001g0198 a0002c0002t0001g0212 others(16): Show |
19 | HG00408.hp1 HG00597.hp1 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.335+2052dupA | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406630 | |||||||
| chr1:25406630 | GT | G | 30 | a0004c0004t0001g0005 a0004c0004t0001g0009 a0004c0004t0001g0016 others(27): Show |
34 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.335+2052delA | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406630 | |||||||
| chr1:25406649 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+2034T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406649 | |||||||
| chr1:25406665 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+2018C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406665 | |||||||
| chr1:25406674 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+2009T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406674 | |||||||
| chr1:25406689 | G | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+1994C>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406689 | |||||||
| chr1:25406697 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+1986G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406697 | |||||||
| chr1:25406718 | A | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(148): Show |
166 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.335+1965T>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406718 | |||||||
| chr1:25406719 | A | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(148): Show |
166 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.335+1964T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406719 | |||||||
| chr1:25406775 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+1908C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406775 | |||||||
| chr1:25406787 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+1896T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406787 | |||||||
| chr1:25406803 | G | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+1880C>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406803 | |||||||
| chr1:25406810 | C | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+1873G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406810 | |||||||
| chr1:25406847 | C | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+1836G>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406847 | |||||||
| chr1:25406867 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+1816A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406867 | |||||||
| chr1:25406868 | G | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+1815C>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406868 | |||||||
| chr1:25406872 | A | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
180 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.335+1811T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406872 | |||||||
| chr1:25406875 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+1808G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406875 | |||||||
| chr1:25406876 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+1807G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406876 | |||||||
| chr1:25406877 | C | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+1806G>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406877 | |||||||
| chr1:25406878 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+1805T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406878 | |||||||
| chr1:25406909 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+1774C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406909 | |||||||
| chr1:25406910 | C | T | 17 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(14): Show |
18 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.335+1773G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406910 | |||||||
| chr1:25406914 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+1769G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406914 | |||||||
| chr1:25406968 | G | A | 8 | a0006c0006t0001g0285 a0006c0006t0001g0290 a0006c0006t0001g0291 others(5): Show |
8 | HG02257.hp2 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.335+1715C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406968 | |||||||
| chr1:25406976 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+1707T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25406976 | |||||||
| chr1:25407008 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+1675C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25407008 | |||||||
| chr1:25407079 | C | T | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | HG00140.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.335+1604G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25407079 | |||||||
| chr1:25407115 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+1568C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25407115 | |||||||
| chr1:25407124 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+1559G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25407124 | |||||||
| chr1:25407128 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+1555C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25407128 | |||||||
| chr1:25407129 | C | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+1554G>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25407129 | |||||||
| chr1:25407142 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+1541G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25407142 | |||||||
| chr1:25407148 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+1535G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25407148 | |||||||
| chr1:25407175 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+1508T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25407175 | |||||||
| chr1:25407177 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+1506G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25407177 | |||||||
| chr1:25407202 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+1481G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25407202 | |||||||
| chr1:25407249 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+1434G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25407249 | |||||||
| chr1:25407253 | C | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+1430G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25407253 | |||||||
| chr1:25407262 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+1421A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25407262 | |||||||
| chr1:25407267 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+1416A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25407267 | |||||||
| chr1:25407275 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+1408C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25407275 | |||||||
| chr1:25407278 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+1405T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25407278 | |||||||
| chr1:25407310 | C | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+1373G>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25407310 | |||||||
| chr1:25407340 | A | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+1343T>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25407340 | |||||||
| chr1:25407349 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+1334T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25407349 | |||||||
| chr1:25407421 | C | G | 34 | a0004c0004t0001g0005 a0004c0004t0001g0009 a0004c0004t0001g0016 others(31): Show |
38 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.335+1262G>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25407421 | |||||||
| chr1:25407447 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+1236A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25407447 | |||||||
| chr1:25407564 | TGGCCTTG others(3): Show |
T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+1109_335+1118d others(12): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25407564 | |||||||
| chr1:25407626 | G | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+1057C>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25407626 | |||||||
| chr1:25407630 | T | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+1053A>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25407630 | |||||||
| chr1:25407631 | G | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+1052C>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25407631 | |||||||
| chr1:25407634 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+1049T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25407634 | |||||||
| chr1:25407688 | G | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+995C>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25407688 | |||||||
| chr1:25407694 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+989A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25407694 | |||||||
| chr1:25407722 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+961A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25407722 | |||||||
| chr1:25407761 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+922G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25407761 | |||||||
| chr1:25407786 | G | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+897C>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25407786 | |||||||
| chr1:25407787 | G | A | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | NA18963.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.335+896C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25407787 | |||||||
| chr1:25407789 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+894G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25407789 | |||||||
| chr1:25407813 | A | G | 1 | a0003c0003t0001g0282 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.335+870T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25407813 | |||||||
| chr1:25407837 | C | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+846G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25407837 | |||||||
| chr1:25407897 | G | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+786C>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25407897 | |||||||
| chr1:25407902 | C | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+781G>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25407902 | |||||||
| chr1:25407949 | C | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+734G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25407949 | |||||||
| chr1:25407958 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+725A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25407958 | |||||||
| chr1:25407962 | T | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+721A>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25407962 | |||||||
| chr1:25408027 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+656G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25408027 | |||||||
| chr1:25408039 | G | C | 1 | a0002c0002t0001g0240 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.335+644C>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25408039 | |||||||
| chr1:25408059 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+624T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25408059 | |||||||
| chr1:25408063 | C | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+620G>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25408063 | |||||||
| chr1:25408065 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+618C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25408065 | |||||||
| chr1:25408106 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+577T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25408106 | |||||||
| chr1:25408147 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+536A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25408147 | |||||||
| chr1:25408149 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+534A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25408149 | |||||||
| chr1:25408164 | A | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
180 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.335+519T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25408164 | |||||||
| chr1:25408183 | A | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+500T>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25408183 | |||||||
| chr1:25408274 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+409G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25408274 | |||||||
| chr1:25408287 | C | CA | 9 | a0004c0004t0001g0163 a0004c0004t0001g0164 a0007c0007t0001g0010 others(6): Show |
10 | HG01167.hp2 HG02109.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.335+395dupT | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25408287 | |||||||
| chr1:25408292 | AAG | A | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
136 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.335+389_335+390del others(2): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25408292 | |||||||
| chr1:25408293 | AG | A | 4 | a0001c0001t0001g0042 a0001c0001t0001g0091 a0001c0001t0001g0118 others(1): Show |
4 | NA18964.hp1 NA18975.hp2 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.335+389delC | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25408293 | |||||||
| chr1:25408294 | G | A | 34 | a0004c0004t0001g0005 a0004c0004t0001g0009 a0004c0004t0001g0016 others(31): Show |
38 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.335+389C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25408294 | |||||||
| chr1:25408322 | GGT | G | 8 | a0006c0006t0001g0285 a0006c0006t0001g0290 a0006c0006t0001g0291 others(5): Show |
8 | HG02257.hp2 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.335+359_335+360del others(2): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25408322 | |||||||
| chr1:25408327 | G | T | 1 | a0006c0006t0001g0290 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.335+356C>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25408327 | |||||||
| chr1:25408385 | A | G | 1 | a0011c0014t0001g0157 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.335+298T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25408385 | |||||||
| chr1:25408386 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+297G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25408386 | |||||||
| chr1:25408476 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+207T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25408476 | |||||||
| chr1:25408513 | TA | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+169delT | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25408513 | |||||||
| chr1:25408548 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.335+135G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 2/9 | chr1 | 25408548 | |||||||
| chr1:25408889 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.149-20A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25408889 | |||||||
| chr1:25408898 | G | C | 1 | a0001c0001t0001g0129 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.149-29C>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25408898 | |||||||
| chr1:25408972 | A | G | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.149-103T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25408972 | |||||||
| chr1:25409073 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.149-204C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25409073 | |||||||
| chr1:25409145 | T | C | 5 | a0008c0008t0001g0146 a0008c0008t0001g0147 a0008c0008t0001g0148 others(2): Show |
5 | HG01109.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.149-276A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25409145 | |||||||
| chr1:25409157 | T | A | 2 | a0012c0010t0001g0019 a0012c0010t0001g0020 |
2 | HG01106.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.149-288A>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25409157 | |||||||
| chr1:25409194 | T | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(128): Show |
143 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.149-325A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25409194 | |||||||
| chr1:25409207 | T | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(128): Show |
143 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.149-338A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25409207 | |||||||
| chr1:25409245 | T | C | 1 | a0004c0024t0001g0182 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.149-376A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25409245 | |||||||
| chr1:25409275 | C | T | 1 | a0001c0001t0001g0140 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.149-406G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25409275 | |||||||
| chr1:25409288 | A | G | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(128): Show |
143 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.149-419T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25409288 | |||||||
| chr1:25409345 | T | A | 1 | a0002c0002t0001g0197 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.149-476A>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25409345 | |||||||
| chr1:25409354 | T | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(136): Show |
152 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.149-485A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25409354 | |||||||
| chr1:25409482 | A | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(132): Show |
148 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.149-613T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25409482 | |||||||
| chr1:25409530 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.149-661A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25409530 | |||||||
| chr1:25409552 | C | T | 1 | a0001c0001t0001g0051 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.149-683G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25409552 | |||||||
| chr1:25409627 | G | A | 7 | a0007c0007t0001g0010 a0007c0007t0001g0145 a0007c0007t0001g0173 others(4): Show |
8 | HG01167.hp2 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-758C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25409627 | |||||||
| chr1:25409635 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.149-766A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25409635 | |||||||
| chr1:25409650 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.149-781T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25409650 | |||||||
| chr1:25409655 | G | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.149-786C>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25409655 | |||||||
| chr1:25409675 | G | A | 25 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 others(22): Show |
25 | HG00408.hp2 HG00673.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.149-806C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25409675 | |||||||
| chr1:25409676 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.149-807C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25409676 | |||||||
| chr1:25409808 | A | G | 1 | a0004c0024t0001g0182 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.149-939T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25409808 | |||||||
| chr1:25409808 | A | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.149-939T>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25409808 | |||||||
| chr1:25409852 | G | T | 3 | a0003c0003t0001g0287 a0003c0003t0001g0288 a0003c0003t0001g0289 |
3 | HG02145.hp2 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.149-983C>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25409852 | |||||||
| chr1:25409866 | T | C | 2 | a0001c0001t0001g0029 a0001c0001t0001g0115 |
2 | HG01175.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.149-997A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25409866 | |||||||
| chr1:25409878 | C | T | 33 | a0002c0002t0001g0189 a0002c0002t0001g0204 a0002c0002t0001g0252 others(30): Show |
34 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(31): Show |
intron_variant | MODIFIER | c.149-1009G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25409878 | |||||||
| chr1:25409913 | T | C | 5 | a0001c0001t0001g0004 a0001c0001t0001g0036 a0001c0001t0001g0104 others(2): Show |
7 | HG00558.hp2 HG02135.hp1 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.149-1044A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25409913 | |||||||
| chr1:25410011 | A | C | 2 | a0012c0010t0001g0019 a0012c0010t0001g0020 |
2 | HG01106.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.149-1142T>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25410011 | |||||||
| chr1:25410046 | A | G | 4 | a0001c0001t0001g0029 a0001c0001t0001g0115 a0002c0002t0001g0211 others(1): Show |
4 | HG01175.hp2 HG01515.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.149-1177T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25410046 | |||||||
| chr1:25410052 | G | A | 5 | a0008c0008t0001g0146 a0008c0008t0001g0147 a0008c0008t0001g0148 others(2): Show |
5 | HG01109.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.149-1183C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25410052 | |||||||
| chr1:25410080 | A | G | 5 | a0008c0008t0001g0146 a0008c0008t0001g0147 a0008c0008t0001g0148 others(2): Show |
5 | HG01109.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.149-1211T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25410080 | |||||||
| chr1:25410149 | G | C | 13 | a0001c0001t0001g0008 a0001c0001t0001g0042 a0001c0001t0001g0044 others(10): Show |
14 | HG00597.hp2 HG02027.hp2 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.149-1280C>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25410149 | |||||||
| chr1:25410241 | T | C | 1 | a0001c0001t0001g0112 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.149-1372A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25410241 | |||||||
| chr1:25410298 | G | A | 34 | a0004c0004t0001g0005 a0004c0004t0001g0009 a0004c0004t0001g0016 others(31): Show |
38 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.149-1429C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25410298 | |||||||
| chr1:25410311 | T | C | 17 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(14): Show |
18 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.149-1442A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25410311 | |||||||
| chr1:25410390 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.149-1521A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25410390 | |||||||
| chr1:25410522 | C | T | 7 | a0007c0007t0001g0010 a0007c0007t0001g0145 a0007c0007t0001g0173 others(4): Show |
8 | HG01167.hp2 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-1653G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25410522 | |||||||
| chr1:25410625 | C | T | 4 | a0003c0003t0001g0203 a0003c0003t0001g0254 a0003c0003t0001g0255 others(1): Show |
4 | HG00738.hp1 HG00741.hp1 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.149-1756G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25410625 | |||||||
| chr1:25410919 | G | A | 5 | a0008c0008t0001g0146 a0008c0008t0001g0147 a0008c0008t0001g0148 others(2): Show |
5 | HG01109.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.149-2050C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25410919 | |||||||
| chr1:25411006 | C | T | 1 | a0002c0002t0001g0267 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.149-2137G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25411006 | |||||||
| chr1:25411017 | A | G | 1 | a0004c0004t0001g0144 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.149-2148T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25411017 | |||||||
| chr1:25411028 | G | T | 1 | a0005c0005t0001g0299 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.149-2159C>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25411028 | |||||||
| chr1:25411092 | A | AAAAT | 30 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0004c0004t0001g0009 others(27): Show |
32 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.149-2227_149-2224d others(6): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25411092 | |||||||
| chr1:25411231 | A | C | 5 | a0008c0008t0001g0146 a0008c0008t0001g0147 a0008c0008t0001g0148 others(2): Show |
5 | HG01109.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.149-2362T>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25411231 | |||||||
| chr1:25411237 | G | A | 34 | a0004c0004t0001g0005 a0004c0004t0001g0009 a0004c0004t0001g0016 others(31): Show |
38 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.149-2368C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25411237 | |||||||
| chr1:25411301 | A | C | 1 | a0001c0001t0001g0042 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.149-2432T>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25411301 | |||||||
| chr1:25411329 | T | C | 3 | a0007c0007t0002g0172 a0013c0012t0001g0170 a0013c0012t0001g0171 |
3 | HG01167.hp2 HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.149-2460A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25411329 | |||||||
| chr1:25411519 | C | A | 1 | a0019c0019t0001g0021 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.149-2650G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25411519 | |||||||
| chr1:25411563 | C | T | 7 | a0007c0007t0001g0010 a0007c0007t0001g0145 a0007c0007t0001g0173 others(4): Show |
8 | HG01167.hp2 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-2694G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25411563 | |||||||
| chr1:25411638 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.149-2769C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25411638 | |||||||
| chr1:25411834 | C | T | 2 | a0014c0013t0001g0025 a0014c0013t0001g0026 |
2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.149-2965G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25411834 | |||||||
| chr1:25411917 | A | G | 7 | a0003c0003t0001g0283 a0003c0003t0001g0284 a0003c0003t0001g0286 others(4): Show |
7 | HG01069.hp2 HG01071.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.149-3048T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25411917 | |||||||
| chr1:25412246 | G | A | 1 | a0004c0024t0001g0182 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.149-3377C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25412246 | |||||||
| chr1:25412385 | T | C | 1 | a0019c0019t0001g0021 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.149-3516A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25412385 | |||||||
| chr1:25412388 | C | T | 34 | a0004c0004t0001g0005 a0004c0004t0001g0009 a0004c0004t0001g0016 others(31): Show |
38 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.149-3519G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25412388 | |||||||
| chr1:25412392 | G | C | 1 | a0002c0002t0001g0264 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.149-3523C>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25412392 | |||||||
| chr1:25412526 | A | C | 1 | a0001c0001t0001g0049 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.149-3657T>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25412526 | |||||||
| chr1:25412573 | G | A | 104 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(101): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.149-3704C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25412573 | |||||||
| chr1:25412581 | A | G | 7 | a0007c0007t0001g0010 a0007c0007t0001g0145 a0007c0007t0001g0173 others(4): Show |
8 | HG01167.hp2 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3712T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25412581 | |||||||
| chr1:25412694 | G | A | 21 | a0004c0004t0001g0005 a0004c0004t0001g0009 a0004c0004t0001g0016 others(18): Show |
24 | HG01099.hp2 HG01106.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.149-3825C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25412694 | |||||||
| chr1:25412708 | CT | C | 26 | a0002c0002t0001g0189 a0002c0002t0001g0208 a0002c0002t0001g0209 others(23): Show |
27 | HG01069.hp1 HG01069.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.149-3840delA | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25412708 | |||||||
| chr1:25412714 | T | TA | 21 | a0002c0002t0001g0013 a0002c0002t0001g0188 a0002c0002t0001g0197 others(18): Show |
22 | HG00597.hp1 HG01071.hp1 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.149-3846_149-3845i others(3): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25412714 | |||||||
| chr1:25412715 | T | A | 148 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(145): Show |
156 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.149-3846A>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25412715 | |||||||
| chr1:25412715 | T | TA | 21 | a0001c0001t0001g0028 a0001c0001t0001g0036 a0001c0001t0001g0115 others(18): Show |
21 | HG01175.hp2 HG01192.hp2 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.149-3847dupT | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25412715 | |||||||
| chr1:25412715 | TA | T | 6 | a0001c0001t0001g0006 a0001c0001t0001g0045 a0001c0001t0001g0046 others(3): Show |
7 | HG01167.hp1 HG01496.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.149-3847delT | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25412715 | |||||||
| chr1:25412718 | A | AAT | 28 | a0004c0004t0001g0005 a0004c0004t0001g0009 a0004c0004t0001g0016 others(25): Show |
32 | HG01099.hp2 HG01106.hp2 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.149-3850_149-3849i others(4): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25412718 | |||||||
| chr1:25412719 | A | T | 2 | a0014c0013t0001g0025 a0014c0013t0001g0026 |
2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.149-3850T>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25412719 | |||||||
| chr1:25412725 | A | T | 22 | a0004c0004t0001g0005 a0004c0004t0001g0009 a0004c0004t0001g0016 others(19): Show |
25 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.149-3856T>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25412725 | |||||||
| chr1:25412726 | A | T | 4 | a0007c0007t0001g0010 a0007c0007t0001g0145 a0007c0007t0001g0173 others(1): Show |
5 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.149-3857T>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25412726 | |||||||
| chr1:25412728 | A | T | 3 | a0007c0007t0002g0172 a0013c0012t0001g0170 a0013c0012t0001g0171 |
3 | HG01167.hp2 HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.149-3859T>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25412728 | |||||||
| chr1:25412730 | A | T | 4 | a0007c0007t0001g0010 a0007c0007t0001g0145 a0007c0007t0001g0173 others(1): Show |
5 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.149-3861T>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25412730 | |||||||
| chr1:25412733 | A | T | 3 | a0007c0007t0002g0172 a0013c0012t0001g0170 a0013c0012t0001g0171 |
3 | HG01167.hp2 HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.149-3864T>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25412733 | |||||||
| chr1:25412734 | A | T | 6 | a0004c0004t0001g0166 a0007c0007t0001g0010 a0007c0007t0001g0145 others(3): Show |
7 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.149-3865T>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25412734 | |||||||
| chr1:25412738 | A | T | 34 | a0004c0004t0001g0005 a0004c0004t0001g0009 a0004c0004t0001g0016 others(31): Show |
38 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.149-3869T>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25412738 | |||||||
| chr1:25412747 | G | A | 18 | a0002c0002t0001g0183 a0005c0005t0001g0015 a0005c0005t0001g0297 others(15): Show |
19 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.149-3878C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25412747 | |||||||
| chr1:25413074 | C | T | 1 | a0012c0010t0001g0019 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.149-4205G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25413074 | |||||||
| chr1:25413075 | G | A | 8 | a0006c0006t0001g0285 a0006c0006t0001g0290 a0006c0006t0001g0291 others(5): Show |
8 | HG02257.hp2 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-4206C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25413075 | |||||||
| chr1:25413312 | T | C | 175 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(172): Show |
184 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.149-4443A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25413312 | |||||||
| chr1:25413337 | G | A | 1 | a0004c0004t0001g0165 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.149-4468C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25413337 | |||||||
| chr1:25413351 | C | T | 1 | a0003c0003t0001g0202 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.149-4482G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25413351 | |||||||
| chr1:25413504 | G | A | 7 | a0003c0003t0001g0283 a0003c0003t0001g0284 a0003c0003t0001g0286 others(4): Show |
7 | HG01069.hp2 HG01071.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.149-4635C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25413504 | |||||||
| chr1:25413546 | G | A | 1 | a0010c0022t0001g0135 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.149-4677C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25413546 | |||||||
| chr1:25413618 | C | T | 15 | a0003c0003t0001g0283 a0003c0003t0001g0284 a0003c0003t0001g0286 others(12): Show |
15 | HG01069.hp2 HG01071.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.149-4749G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25413618 | |||||||
| chr1:25413629 | G | A | 1 | a0003c0003t0001g0282 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.149-4760C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25413629 | |||||||
| chr1:25413699 | C | T | 119 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(116): Show |
123 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.149-4830G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25413699 | |||||||
| chr1:25413702 | G | T | 1 | a0002c0002t0001g0197 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.149-4833C>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25413702 | |||||||
| chr1:25413728 | C | T | 1 | a0001c0001t0001g0038 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.149-4859G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25413728 | |||||||
| chr1:25414027 | G | A | 2 | a0003c0003t0001g0283 a0003c0003t0001g0284 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.149-5158C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25414027 | |||||||
| chr1:25414049 | C | T | 1 | a0002c0002t0001g0207 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.149-5180G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25414049 | |||||||
| chr1:25414050 | G | A | 7 | a0003c0003t0001g0283 a0003c0003t0001g0284 a0003c0003t0001g0286 others(4): Show |
7 | HG01069.hp2 HG01071.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.149-5181C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25414050 | |||||||
| chr1:25414110 | A | AC | 5 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(2): Show |
5 | HG00738.hp2 HG01109.hp2 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.149-5242dupG | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25414110 | |||||||
| chr1:25414181 | G | C | 4 | a0004c0004t0001g0166 a0004c0004t0001g0168 a0004c0004t0001g0169 others(1): Show |
4 | HG02818.hp1 HG02886.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.149-5312C>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25414181 | |||||||
| chr1:25414258 | G | A | 34 | a0004c0004t0001g0005 a0004c0004t0001g0009 a0004c0004t0001g0016 others(31): Show |
38 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.149-5389C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25414258 | |||||||
| chr1:25414288 | A | G | 34 | a0004c0004t0001g0005 a0004c0004t0001g0009 a0004c0004t0001g0016 others(31): Show |
38 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.149-5419T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25414288 | |||||||
| chr1:25414340 | G | C | 1 | a0002c0002t0001g0199 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.149-5471C>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25414340 | |||||||
| chr1:25414351 | G | T | 1 | a0002c0002t0001g0199 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.149-5482C>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25414351 | |||||||
| chr1:25414354 | G | C | 1 | a0002c0002t0001g0199 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.149-5485C>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25414354 | |||||||
| chr1:25414356 | A | C | 172 | a0001c0001t0001g0040 a0002c0002t0001g0011 a0002c0002t0001g0012 others(169): Show |
181 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.149-5487T>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25414356 | |||||||
| chr1:25414369 | C | T | 1 | a0003c0003t0001g0201 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.149-5500G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25414369 | |||||||
| chr1:25414391 | C | G | 3 | a0003c0003t0001g0200 a0003c0003t0001g0249 a0003c0003t0001g0250 |
3 | HG02071.hp2 NA18955.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.149-5522G>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25414391 | |||||||
| chr1:25414576 | T | C | 1 | a0002c0002t0001g0248 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.149-5707A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25414576 | |||||||
| chr1:25414703 | T | A | 1 | a0001c0001t0001g0136 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.149-5834A>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25414703 | |||||||
| chr1:25414972 | T | C | 1 | a0003c0003t0001g0286 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.148+5667A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25414972 | |||||||
| chr1:25414979 | C | T | 8 | a0006c0006t0001g0285 a0006c0006t0001g0290 a0006c0006t0001g0291 others(5): Show |
8 | HG02257.hp2 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.148+5660G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25414979 | |||||||
| chr1:25415138 | C | A | 173 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(170): Show |
182 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.148+5501G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25415138 | |||||||
| chr1:25415383 | T | C | 7 | a0003c0003t0001g0283 a0003c0003t0001g0284 a0003c0003t0001g0286 others(4): Show |
7 | HG01069.hp2 HG01071.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.148+5256A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25415383 | |||||||
| chr1:25415418 | C | T | 7 | a0006c0006t0001g0290 a0006c0006t0001g0291 a0006c0006t0001g0292 others(4): Show |
7 | HG02257.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.148+5221G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25415418 | |||||||
| chr1:25415508 | C | T | 7 | a0003c0003t0001g0283 a0003c0003t0001g0284 a0003c0003t0001g0286 others(4): Show |
7 | HG01069.hp2 HG01071.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.148+5131G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25415508 | |||||||
| chr1:25415592 | C | T | 4 | a0004c0004t0001g0005 a0004c0004t0001g0156 a0004c0004t0001g0176 others(1): Show |
6 | HG01106.hp2 HG01891.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.148+5047G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25415592 | |||||||
| chr1:25415759 | A | T | 1 | a0004c0024t0001g0182 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.148+4880T>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25415759 | |||||||
| chr1:25415899 | T | C | 17 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(14): Show |
18 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.148+4740A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25415899 | |||||||
| chr1:25415905 | G | A | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | NA18963.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.148+4734C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25415905 | |||||||
| chr1:25416003 | G | A | 2 | a0014c0013t0001g0025 a0014c0013t0001g0026 |
2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.148+4636C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25416003 | |||||||
| chr1:25416094 | A | T | 128 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(125): Show |
133 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.148+4545T>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25416094 | |||||||
| chr1:25416115 | C | T | 175 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(172): Show |
184 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.148+4524G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25416115 | |||||||
| chr1:25416125 | G | A | 175 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(172): Show |
184 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.148+4514C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25416125 | |||||||
| chr1:25416203 | C | T | 70 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(67): Show |
73 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.148+4436G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25416203 | |||||||
| chr1:25416204 | G | A | 7 | a0007c0007t0001g0010 a0007c0007t0001g0145 a0007c0007t0001g0173 others(4): Show |
8 | HG01167.hp2 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.148+4435C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25416204 | |||||||
| chr1:25416254 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.148+4385A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25416254 | |||||||
| chr1:25416324 | T | C | 5 | a0008c0008t0001g0146 a0008c0008t0001g0147 a0008c0008t0001g0148 others(2): Show |
5 | HG01109.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.148+4315A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25416324 | |||||||
| chr1:25416364 | C | T | 1 | a0003c0003t0001g0279 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.148+4275G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25416364 | |||||||
| chr1:25416392 | T | A | 1 | a0002c0002t0001g0275 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.148+4247A>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25416392 | |||||||
| chr1:25416465 | A | G | 34 | a0004c0004t0001g0005 a0004c0004t0001g0009 a0004c0004t0001g0016 others(31): Show |
38 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.148+4174T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25416465 | |||||||
| chr1:25416556 | C | G | 1 | a0001c0001t0001g0029 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.148+4083G>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25416556 | |||||||
| chr1:25416624 | C | T | 170 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(167): Show |
179 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.148+4015G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25416624 | |||||||
| chr1:25416686 | G | A | 2 | a0001c0001t0001g0140 a0001c0001t0001g0143 |
2 | NA18957.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.148+3953C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25416686 | |||||||
| chr1:25416767 | C | A | 1 | a0001c0001t0001g0038 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.148+3872G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25416767 | |||||||
| chr1:25416790 | C | A | 8 | a0002c0002t0001g0194 a0003c0003t0001g0283 a0003c0003t0001g0284 others(5): Show |
8 | HG01069.hp2 HG01071.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.148+3849G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25416790 | |||||||
| chr1:25416792 | G | GT | 11 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(8): Show |
11 | HG00558.hp1 HG02004.hp2 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.148+3846dupA | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25416792 | |||||||
| chr1:25416792 | GT | G | 43 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0003c0003t0001g0265 others(40): Show |
48 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.148+3846delA | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25416792 | |||||||
| chr1:25416792 | GTT | G | 8 | a0004c0024t0001g0182 a0005c0005t0001g0310 a0005c0005t0001g0311 others(5): Show |
8 | HG01069.hp1 HG01109.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.148+3845_148+3846d others(4): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25416792 | |||||||
| chr1:25416792 | GTTT | G | 10 | a0002c0002t0001g0183 a0002c0002t0001g0185 a0002c0002t0001g0186 others(7): Show |
10 | HG00642.hp2 HG00673.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.148+3844_148+3846d others(5): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25416792 | |||||||
| chr1:25416819 | C | CG | 104 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0154 others(101): Show |
109 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.148+3819dupC | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25416819 | |||||||
| chr1:25416819 | C | CGG | 35 | a0002c0002t0001g0197 a0002c0002t0001g0198 a0002c0002t0001g0199 others(32): Show |
36 | HG00408.hp1 HG00733.hp2 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.148+3818_148+3819d others(4): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25416819 | |||||||
| chr1:25416819 | C | CGGG | 25 | a0002c0002t0001g0195 a0002c0002t0001g0196 a0003c0003t0001g0286 others(22): Show |
28 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.148+3817_148+3819d others(5): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25416819 | |||||||
| chr1:25416874 | A | G | 1 | a0002c0002t0001g0194 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.148+3765T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25416874 | |||||||
| chr1:25416914 | GT | G | 47 | a0001c0001t0001g0143 a0002c0002t0001g0275 a0003c0003t0001g0283 others(44): Show |
49 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(46): Show |
intron_variant | MODIFIER | c.148+3724delA | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25416914 | |||||||
| chr1:25416914 | GTT | G | 4 | a0004c0004t0001g0005 a0004c0004t0001g0156 a0004c0004t0001g0176 others(1): Show |
6 | HG01106.hp2 HG01891.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.148+3723_148+3724d others(4): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25416914 | |||||||
| chr1:25416917 | T | G | 1 | a0002c0002t0001g0274 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.148+3722A>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25416917 | |||||||
| chr1:25416937 | A | G | 5 | a0002c0002t0001g0189 a0003c0003t0001g0190 a0003c0003t0001g0191 others(2): Show |
5 | HG00099.hp1 HG00280.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.148+3702T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25416937 | |||||||
| chr1:25416971 | G | T | 4 | a0002c0002t0001g0185 a0002c0002t0001g0186 a0002c0002t0001g0187 others(1): Show |
4 | HG00642.hp2 HG01099.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.148+3668C>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25416971 | |||||||
| chr1:25417068 | T | A | 1 | a0002c0002t0001g0275 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.148+3571A>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25417068 | |||||||
| chr1:25417148 | CA | C | 140 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(137): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.148+3490delT | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25417148 | |||||||
| chr1:25417149 | A | AAAAAC | 34 | a0004c0004t0001g0005 a0004c0004t0001g0009 a0004c0004t0001g0016 others(31): Show |
38 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.148+3489_148+3490i others(7): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25417149 | |||||||
| chr1:25417440 | T | A | 5 | a0008c0008t0001g0146 a0008c0008t0001g0147 a0008c0008t0001g0148 others(2): Show |
5 | HG01109.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.148+3199A>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25417440 | |||||||
| chr1:25417514 | C | T | 5 | a0008c0008t0001g0146 a0008c0008t0001g0147 a0008c0008t0001g0148 others(2): Show |
5 | HG01109.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.148+3125G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25417514 | |||||||
| chr1:25417674 | C | T | 170 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(167): Show |
179 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.148+2965G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25417674 | |||||||
| chr1:25417817 | G | A | 7 | a0003c0003t0001g0283 a0003c0003t0001g0284 a0003c0003t0001g0286 others(4): Show |
7 | HG01069.hp2 HG01071.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.148+2822C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25417817 | |||||||
| chr1:25417908 | C | T | 4 | a0004c0004t0001g0005 a0004c0004t0001g0156 a0004c0004t0001g0176 others(1): Show |
6 | HG01106.hp2 HG01891.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.148+2731G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25417908 | |||||||
| chr1:25417934 | G | A | 1 | a0003c0003t0001g0276 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.148+2705C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25417934 | |||||||
| chr1:25417977 | C | T | 136 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(133): Show |
141 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.148+2662G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25417977 | |||||||
| chr1:25418113 | A | T | 1 | a0001c0001t0001g0024 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.148+2526T>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25418113 | |||||||
| chr1:25418274 | G | A | 5 | a0008c0008t0001g0146 a0008c0008t0001g0147 a0008c0008t0001g0148 others(2): Show |
5 | HG01109.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.148+2365C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25418274 | |||||||
| chr1:25418464 | G | A | 1 | a0003c0003t0001g0277 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.148+2175C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25418464 | |||||||
| chr1:25418478 | A | C | 1 | a0003c0003t0001g0184 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.148+2161T>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25418478 | |||||||
| chr1:25418570 | T | C | 170 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(167): Show |
179 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.148+2069A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25418570 | |||||||
| chr1:25418571 | G | T | 1 | a0001c0001t0001g0023 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.148+2068C>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25418571 | |||||||
| chr1:25418634 | G | A | 1 | a0002c0002t0001g0278 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.148+2005C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25418634 | |||||||
| chr1:25418637 | A | G | 7 | a0003c0003t0001g0283 a0003c0003t0001g0284 a0003c0003t0001g0286 others(4): Show |
7 | HG01069.hp2 HG01071.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.148+2002T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25418637 | |||||||
| chr1:25418713 | G | T | 171 | a0001c0001t0001g0022 a0002c0002t0001g0011 a0002c0002t0001g0012 others(168): Show |
180 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.148+1926C>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25418713 | |||||||
| chr1:25418814 | G | A | 34 | a0004c0004t0001g0005 a0004c0004t0001g0009 a0004c0004t0001g0016 others(31): Show |
38 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.148+1825C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25418814 | |||||||
| chr1:25418982 | C | T | 3 | a0012c0010t0001g0019 a0012c0010t0001g0020 a0019c0019t0001g0021 |
3 | HG01106.hp1 HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.148+1657G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25418982 | |||||||
| chr1:25419096 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.148+1543A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25419096 | |||||||
| chr1:25419154 | C | T | 104 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(101): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.148+1485G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25419154 | |||||||
| chr1:25419321 | A | C | 2 | a0003c0003t0001g0283 a0003c0003t0001g0284 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.148+1318T>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25419321 | |||||||
| chr1:25419337 | A | G | 1 | a0002c0002t0001g0183 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.148+1302T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25419337 | |||||||
| chr1:25419452 | C | A | 1 | a0001c0001t0001g0150 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.148+1187G>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25419452 | |||||||
| chr1:25419823 | G | A | 128 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(125): Show |
133 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.148+816C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25419823 | |||||||
| chr1:25419837 | T | TG | 11 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(8): Show |
11 | HG00733.hp2 HG01106.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.148+801dupC | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25419837 | |||||||
| chr1:25419838 | G | C | 7 | a0006c0006t0001g0290 a0006c0006t0001g0291 a0006c0006t0001g0292 others(4): Show |
7 | HG02257.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.148+801C>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25419838 | |||||||
| chr1:25419865 | A | G | 2 | a0003c0003t0001g0283 a0003c0003t0001g0284 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.148+774T>C | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25419865 | |||||||
| chr1:25419877 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.148+762C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25419877 | |||||||
| chr1:25420016 | C | CAAAAAAA | 27 | a0004c0004t0001g0005 a0004c0004t0001g0009 a0004c0004t0001g0016 others(24): Show |
31 | HG01099.hp2 HG01106.hp2 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.148+616_148+622dup others(7): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25420016 | |||||||
| chr1:25420016 | C | CAAAAAAA others(3): Show |
2 | a0008c0008t0001g0177 a0008c0008t0001g0178 |
2 | HG02055.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.148+613_148+622dup others(10): Show |
RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25420016 | |||||||
| chr1:25420032 | T | A | 1 | a0001c0001t0001g0179 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.148+607A>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25420032 | |||||||
| chr1:25420072 | C | T | 121 | a0002c0002t0001g0011 a0002c0002t0001g0012 a0002c0002t0001g0013 others(118): Show |
126 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.148+567G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25420072 | |||||||
| chr1:25420085 | G | A | 17 | a0005c0005t0001g0015 a0005c0005t0001g0297 a0005c0005t0001g0298 others(14): Show |
18 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.148+554C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25420085 | |||||||
| chr1:25420125 | T | C | 1 | a0004c0024t0001g0182 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.148+514A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25420125 | |||||||
| chr1:25420230 | C | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0180 |
3 | HG00639.hp2 HG01243.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.148+409G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25420230 | |||||||
| chr1:25420231 | G | A | 1 | a0003c0003t0001g0313 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.148+408C>T | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25420231 | |||||||
| chr1:25420533 | C | T | 1 | a0004c0004t0001g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.148+106G>A | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25420533 | |||||||
| chr1:25420575 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.148+64A>G | RHCE | ENSG00000188672.19 | transcript | ENST00000294413.13 | protein_coding | 1/9 | chr1 | 25420575 |