Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10391 |
| ensemblid | ENSG00000103647.13 |
| hgncid | 2256 |
| symbol | CORO2B |
| name | coronin 2B |
| refseq_nuc | NM_006091.5 |
| refseq_prot | NP_006082.3 |
| ensembl_nuc | ENST00000261861.10 |
| ensembl_prot | ENSP00000261861.6 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 68578993 |
| end | 68727806 |
| strand | + |
| ver | v1.2 |
| region | chr15:68578993-68727806 |
| region5000 | chr15:68573993-68732806 |
| regionname0 | CORO2B_chr15_68578993_68727806 |
| regionname5000 | CORO2B_chr15_68573993_68732806 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 480 | 253 | 84 | 50 | 71 | 10 | 36 | 42 | CORO2B_chr15_68573993_68732806 | CORO2B | MTVTK others(475): Show |
chr15 | 68573993 | 68732806 |
| a0002 | 0/0 | 480 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | MTVTK others(475): Show |
chr15 | 68573993 | 68732806 |
| a0003 | 0/0 | 480 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | MTVTK others(475): Show |
chr15 | 68573993 | 68732806 |
| a0004 | 0/0 | 480 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | MTVTK others(475): Show |
chr15 | 68573993 | 68732806 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1440 | 214 | 68 | 39 | 66 | 8 | 32 | CORO2B_chr15_68573993_68732806 | CORO2B | ATGAC others(1435): Show |
chr15 | 68573993 | 68732806 | ||
| a0001c0002 | 0/1 | 1440 | 24 | 4 | 10 | 5 | 0 | 4 | CORO2B_chr15_68573993_68732806 | CORO2B | ATGAC others(1435): Show |
chr15 | 68573993 | 68732806 | ||
| a0001c0003 | 0/0 | 1440 | 7 | 7 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | ATGAC others(1435): Show |
chr15 | 68573993 | 68732806 | ||
| a0001c0004 | 0/0 | 1440 | 5 | 5 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | ATGAC others(1435): Show |
chr15 | 68573993 | 68732806 | ||
| a0001c0005 | 0/0 | 1440 | 3 | 0 | 1 | 0 | 2 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | ATGAC others(1435): Show |
chr15 | 68573993 | 68732806 | ||
| a0002c0008 | 0/0 | 1440 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | ATGAC others(1435): Show |
chr15 | 68573993 | 68732806 | ||
| a0003c0007 | 0/0 | 1440 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | ATGAC others(1435): Show |
chr15 | 68573993 | 68732806 | ||
| a0004c0006 | 0/0 | 1440 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | ATGAC others(1435): Show |
chr15 | 68573993 | 68732806 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3545 | 69 | 9 | 24 | 18 | 2 | 16 | CORO2B_chr15_68573993_68732806 | CORO2B | CTTCC others(3540): Show |
chr15 | 68573993 | 68732806 |
| a0001c0001t0002 | 0/0 | 3545 | 28 | 10 | 4 | 7 | 2 | 5 | CORO2B_chr15_68573993_68732806 | CORO2B | CTTCC others(3540): Show |
chr15 | 68573993 | 68732806 |
| a0001c0001t0003 | 0/0 | 3545 | 33 | 1 | 8 | 19 | 2 | 3 | CORO2B_chr15_68573993_68732806 | CORO2B | CTTCC others(3540): Show |
chr15 | 68573993 | 68732806 |
| a0001c0001t0004 | 1/0 | 3545 | 28 | 10 | 0 | 15 | 0 | 2 | CORO2B_chr15_68573993_68732806 | CORO2B | CTTCC others(3540): Show |
chr15 | 68573993 | 68732806 |
| a0001c0001t0005 | 0/0 | 3545 | 17 | 12 | 1 | 1 | 1 | 2 | CORO2B_chr15_68573993_68732806 | CORO2B | CTTCC others(3540): Show |
chr15 | 68573993 | 68732806 |
| a0001c0001t0006 | 0/0 | 3545 | 12 | 9 | 2 | 0 | 0 | 1 | CORO2B_chr15_68573993_68732806 | CORO2B | CTTCC others(3540): Show |
chr15 | 68573993 | 68732806 |
| a0001c0001t0007 | 0/0 | 3545 | 4 | 0 | 0 | 2 | 1 | 1 | CORO2B_chr15_68573993_68732806 | CORO2B | CTTCC others(3540): Show |
chr15 | 68573993 | 68732806 |
| a0001c0001t0008 | 0/0 | 3545 | 2 | 2 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | CTTCC others(3540): Show |
chr15 | 68573993 | 68732806 |
| a0001c0001t0009 | 0/0 | 3545 | 3 | 3 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | CTTCC others(3540): Show |
chr15 | 68573993 | 68732806 |
| a0001c0001t0010 | 0/0 | 3549 | 2 | 2 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | CTTCC others(3544): Show |
chr15 | 68573993 | 68732806 |
| a0001c0001t0011 | 0/0 | 3545 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | CTTCC others(3540): Show |
chr15 | 68573993 | 68732806 |
| a0001c0001t0013 | 0/0 | 3549 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | CTTCC others(3544): Show |
chr15 | 68573993 | 68732806 |
| a0001c0001t0014 | 0/0 | 3549 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | CTTCC others(3544): Show |
chr15 | 68573993 | 68732806 |
| a0001c0001t0015 | 0/0 | 3545 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | CTTCC others(3540): Show |
chr15 | 68573993 | 68732806 |
| a0001c0001t0016 | 0/0 | 3549 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | CTTCC others(3544): Show |
chr15 | 68573993 | 68732806 |
| a0001c0001t0017 | 0/0 | 3549 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | CTTCC others(3544): Show |
chr15 | 68573993 | 68732806 |
| a0001c0001t0018 | 0/0 | 3549 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | CTTCC others(3544): Show |
chr15 | 68573993 | 68732806 |
| a0001c0001t0019 | 0/0 | 3526 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | CTTCC others(3521): Show |
chr15 | 68573993 | 68732806 |
| a0001c0001t0020 | 0/0 | 3526 | 1 | 0 | 0 | 0 | 0 | 1 | CORO2B_chr15_68573993_68732806 | CORO2B | CTTCC others(3521): Show |
chr15 | 68573993 | 68732806 |
| a0001c0001t0021 | 0/0 | 3545 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | CTTCC others(3540): Show |
chr15 | 68573993 | 68732806 |
| a0001c0001t0022 | 0/0 | 3545 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | CTTCC others(3540): Show |
chr15 | 68573993 | 68732806 |
| a0001c0001t0023 | 0/0 | 3545 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | CTTCC others(3540): Show |
chr15 | 68573993 | 68732806 |
| a0001c0001t0024 | 0/0 | 3545 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | CTTCC others(3540): Show |
chr15 | 68573993 | 68732806 |
| a0001c0001t0025 | 0/0 | 3545 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | CTTCC others(3540): Show |
chr15 | 68573993 | 68732806 |
| a0001c0001t0026 | 0/0 | 3545 | 1 | 0 | 0 | 0 | 0 | 1 | CORO2B_chr15_68573993_68732806 | CORO2B | CTTCC others(3540): Show |
chr15 | 68573993 | 68732806 |
| a0001c0001t0027 | 0/0 | 3545 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | CTTCC others(3540): Show |
chr15 | 68573993 | 68732806 |
| a0001c0002t0001 | 0/0 | 3545 | 6 | 0 | 4 | 0 | 0 | 2 | CORO2B_chr15_68573993_68732806 | CORO2B | CTTCC others(3540): Show |
chr15 | 68573993 | 68732806 |
| a0001c0002t0002 | 0/0 | 3545 | 10 | 1 | 4 | 4 | 0 | 1 | CORO2B_chr15_68573993_68732806 | CORO2B | CTTCC others(3540): Show |
chr15 | 68573993 | 68732806 |
| a0001c0002t0003 | 0/1 | 3545 | 4 | 0 | 1 | 1 | 0 | 1 | CORO2B_chr15_68573993_68732806 | CORO2B | CTTCC others(3540): Show |
chr15 | 68573993 | 68732806 |
| a0001c0002t0005 | 0/0 | 3545 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | CTTCC others(3540): Show |
chr15 | 68573993 | 68732806 |
| a0001c0002t0006 | 0/0 | 3545 | 3 | 2 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | CTTCC others(3540): Show |
chr15 | 68573993 | 68732806 |
| a0001c0003t0001 | 0/0 | 3545 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | CTTCC others(3540): Show |
chr15 | 68573993 | 68732806 |
| a0001c0003t0006 | 0/0 | 3545 | 2 | 2 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | CTTCC others(3540): Show |
chr15 | 68573993 | 68732806 |
| a0001c0003t0008 | 0/0 | 3545 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | CTTCC others(3540): Show |
chr15 | 68573993 | 68732806 |
| a0001c0003t0011 | 0/0 | 3545 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | CTTCC others(3540): Show |
chr15 | 68573993 | 68732806 |
| a0001c0003t0012 | 0/0 | 3545 | 2 | 2 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | CTTCC others(3540): Show |
chr15 | 68573993 | 68732806 |
| a0001c0004t0005 | 0/0 | 3545 | 2 | 2 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | CTTCC others(3540): Show |
chr15 | 68573993 | 68732806 |
| a0001c0004t0006 | 0/0 | 3545 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | CTTCC others(3540): Show |
chr15 | 68573993 | 68732806 |
| a0001c0004t0007 | 0/0 | 3545 | 2 | 2 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | CTTCC others(3540): Show |
chr15 | 68573993 | 68732806 |
| a0001c0005t0002 | 0/0 | 3545 | 1 | 0 | 0 | 0 | 1 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | CTTCC others(3540): Show |
chr15 | 68573993 | 68732806 |
| a0001c0005t0003 | 0/0 | 3545 | 2 | 0 | 1 | 0 | 1 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | CTTCC others(3540): Show |
chr15 | 68573993 | 68732806 |
| a0002c0008t0002 | 0/0 | 3545 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | CTTCC others(3540): Show |
chr15 | 68573993 | 68732806 |
| a0003c0007t0006 | 0/0 | 3545 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | CTTCC others(3540): Show |
chr15 | 68573993 | 68732806 |
| a0004c0006t0002 | 0/0 | 3545 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | CTTCC others(3540): Show |
chr15 | 68573993 | 68732806 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0002g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0004g0050 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0004g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0005g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0005g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0005g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0005g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0005g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0005g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0005g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0005g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0005g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0005g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0005g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0005g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0005g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0006g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0006g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0006g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0006g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0006g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0006g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0006g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0006g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0006g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0006g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0006g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0006g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0007g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0007g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0007g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0007g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0008g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0008g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0009g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0009g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0009g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0010g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0010g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0011g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0013g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0014g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0015g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0016g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0017g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0018g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0019g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0020g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0021g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0022g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0023g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0024g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0025g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0026g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0001t0027g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0002t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0002t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0002t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0002t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0002t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0002t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0002t0003g0005 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0002t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0002t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0002t0003g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0002t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0002t0006g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0002t0006g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0002t0006g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0003t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0003t0006g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0003t0006g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0003t0008g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0003t0011g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0003t0012g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0003t0012g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0004t0005g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0004t0005g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0004t0006g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0004t0007g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0004t0007g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0005t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0005t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0001c0005t0003g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0002c0008t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0003c0007t0006g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| a0004c0006t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0171 | EUR | GBR | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0187 | EUR | GBR | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG00280 | hp1 | a0001 | c0001 | t0007 | g0162 | EUR | FIN | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG00280 | hp2 | a0001 | c0001 | t0005 | g0007 | EUR | FIN | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG00408 | hp1 | a0001 | c0001 | t0004 | g0109 | EAS | CHS | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG00408 | hp2 | a0002 | c0008 | t0002 | g0093 | EAS | CHS | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | CHS | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG00621 | hp1 | a0001 | c0001 | t0007 | g0151 | EAS | CHS | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0188 | AMR | PUR | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG00673 | hp1 | a0001 | c0001 | t0023 | g0209 | EAS | CHS | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | CHS | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0217 | AMR | PUR | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0069 | AMR | PUR | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG00741 | hp1 | a0001 | c0005 | t0003 | g0130 | AMR | PUR | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG00741 | hp2 | a0001 | c0002 | t0002 | g0099 | AMR | PUR | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0226 | AMR | PUR | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0045 | AMR | PUR | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0177 | AMR | PUR | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0225 | AMR | PUR | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01099 | hp1 | a0001 | c0001 | t0005 | g0072 | AMR | PUR | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01099 | hp2 | a0001 | c0002 | t0003 | g0198 | AMR | PUR | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | PUR | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01109 | hp2 | a0001 | c0001 | t0006 | g0237 | AMR | PUR | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01175 | hp2 | a0001 | c0001 | t0006 | g0218 | AMR | PUR | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0227 | AMR | PUR | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0070 | AMR | PUR | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0213 | AMR | CLM | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0242 | AMR | CLM | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0245 | AMR | CLM | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0246 | AMR | CLM | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01496 | hp1 | a0001 | c0002 | t0006 | g0137 | AMR | CLM | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0244 | AMR | CLM | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0220 | EUR | IBS | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01516 | hp2 | a0001 | c0005 | t0002 | g0043 | EUR | IBS | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0219 | EUR | IBS | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01517 | hp2 | a0001 | c0005 | t0003 | g0210 | EUR | IBS | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01884 | hp1 | a0001 | c0001 | t0019 | g0201 | AFR | ACB | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01884 | hp2 | a0001 | c0004 | t0007 | g0172 | AFR | ACB | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01891 | hp1 | a0001 | c0002 | t0002 | g0038 | AFR | ACB | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0018 | AFR | ACB | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01978 | hp2 | a0001 | c0002 | t0002 | g0170 | AMR | PEL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0241 | AMR | PEL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PEL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02015 | hp1 | a0001 | c0001 | t0005 | g0208 | EAS | KHV | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0127 | EAS | KHV | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | KHV | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | KHV | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02040 | hp1 | a0001 | c0001 | t0004 | g0205 | EAS | KHV | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02056 | hp1 | a0001 | c0001 | t0024 | g0120 | EAS | KHV | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | KHV | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0155 | EAS | KHV | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02080 | hp1 | a0001 | c0001 | t0025 | g0149 | EAS | KHV | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0059 | EAS | KHV | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | KHV | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0106 | EAS | KHV | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02132 | hp2 | a0001 | c0001 | t0015 | g0222 | EAS | KHV | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0239 | EAS | KHV | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02145 | hp1 | a0001 | c0003 | t0006 | g0145 | AFR | ACB | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | ACB | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | CDX | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CDX | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0078 | AFR | ACB | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0131 | AFR | ACB | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | ACB | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0029 | AFR | ACB | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0077 | AFR | ACB | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02280 | hp2 | a0001 | c0001 | t0011 | g0075 | AFR | ACB | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02451 | hp1 | a0001 | c0003 | t0008 | g0178 | AFR | ACB | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02451 | hp2 | a0001 | c0001 | t0008 | g0025 | AFR | ACB | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02523 | hp1 | a0001 | c0001 | t0004 | g0119 | EAS | KHV | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | KHV | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02572 | hp2 | a0001 | c0002 | t0006 | g0223 | AFR | GWD | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0140 | SAS | PJL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02615 | hp1 | a0001 | c0001 | t0006 | g0191 | AFR | GWD | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | GWD | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02622 | hp2 | a0001 | c0004 | t0006 | g0032 | AFR | GWD | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02630 | hp1 | a0001 | c0001 | t0017 | g0251 | AFR | GWD | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02647 | hp2 | a0001 | c0003 | t0006 | g0051 | AFR | GWD | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02698 | hp1 | a0001 | c0001 | t0004 | g0240 | SAS | PJL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02698 | hp2 | a0001 | c0002 | t0003 | g0256 | SAS | PJL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | GWD | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02717 | hp2 | a0001 | c0002 | t0005 | g0016 | AFR | GWD | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02735 | hp1 | a0001 | c0001 | t0026 | g0055 | SAS | PJL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02738 | hp2 | a0001 | c0001 | t0020 | g0203 | SAS | PJL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0195 | AFR | GWD | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0046 | AFR | GWD | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02818 | hp2 | a0001 | c0001 | t0010 | g0252 | AFR | GWD | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02886 | hp1 | a0001 | c0001 | t0006 | g0040 | AFR | GWD | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0164 | AFR | GWD | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02896 | hp1 | a0003 | c0007 | t0006 | g0186 | AFR | GWD | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02896 | hp2 | a0001 | c0001 | t0006 | g0021 | AFR | GWD | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0194 | AFR | ESN | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02922 | hp2 | a0001 | c0001 | t0021 | g0033 | AFR | ESN | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0141 | AFR | ESN | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02970 | hp1 | a0001 | c0001 | t0006 | g0004 | AFR | ESN | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02970 | hp2 | a0001 | c0001 | t0006 | g0236 | AFR | ESN | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | ESN | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0079 | AFR | ESN | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0214 | SAS | PJL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0146 | SAS | PJL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03041 | hp1 | a0001 | c0001 | t0018 | g0255 | AFR | GWD | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03041 | hp2 | a0001 | c0003 | t0012 | g0076 | AFR | GWD | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03098 | hp1 | a0001 | c0004 | t0005 | g0003 | AFR | MSL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0041 | AFR | MSL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0134 | AFR | ESN | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0012 | AFR | ESN | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03139 | hp1 | a0001 | c0003 | t0011 | g0247 | AFR | ESN | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03139 | hp2 | a0001 | c0001 | t0016 | g0250 | AFR | ESN | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0229 | AFR | ESN | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03195 | hp2 | a0001 | c0001 | t0009 | g0014 | AFR | ESN | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03209 | hp1 | a0001 | c0001 | t0006 | g0053 | AFR | MSL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03209 | hp2 | a0001 | c0001 | t0027 | g0034 | AFR | MSL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0216 | AFR | MSL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03225 | hp2 | a0001 | c0001 | t0013 | g0253 | AFR | MSL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03239 | hp2 | a0001 | c0001 | t0005 | g0113 | SAS | PJL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0019 | AFR | MSL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0024 | AFR | MSL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0135 | AFR | MSL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0008 | SAS | PJL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0196 | AFR | ESN | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03516 | hp2 | a0001 | c0001 | t0009 | g0030 | AFR | ESN | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03540 | hp1 | a0001 | c0001 | t0022 | g0049 | AFR | GWD | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0180 | AFR | GWD | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0020 | AFR | MSL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0035 | AFR | MSL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03669 | hp1 | a0001 | c0001 | t0006 | g0011 | SAS | PJL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03669 | hp2 | a0001 | c0001 | t0005 | g0073 | SAS | PJL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0117 | SAS | PJL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0054 | SAS | PJL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03834 | hp1 | a0001 | c0001 | t0007 | g0232 | SAS | BEB | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | BEB | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0167 | SAS | BEB | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0206 | SAS | BEB | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0152 | SAS | BEB | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0182 | SAS | BEB | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | STU | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | STU | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0160 | SAS | STU | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0221 | SAS | STU | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA18522 | hp1 | a0001 | c0001 | t0006 | g0031 | AFR | YRI | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0013 | AFR | YRI | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA18906 | hp1 | a0001 | c0001 | t0009 | g0238 | AFR | YRI | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA18906 | hp2 | a0001 | c0004 | t0005 | g0233 | AFR | YRI | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0071 | EAS | JPT | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA18949 | hp1 | a0001 | c0001 | t0004 | g0185 | EAS | JPT | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA18949 | hp2 | a0001 | c0002 | t0002 | g0142 | EAS | JPT | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0129 | EAS | JPT | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA18966 | hp2 | a0001 | c0001 | t0004 | g0103 | EAS | JPT | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA18971 | hp2 | a0001 | c0002 | t0002 | g0224 | EAS | JPT | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA18975 | hp1 | a0001 | c0001 | t0004 | g0058 | EAS | JPT | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA18977 | hp2 | a0001 | c0001 | t0004 | g0110 | EAS | JPT | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0112 | EAS | JPT | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA19001 | hp1 | a0001 | c0001 | t0004 | g0063 | EAS | JPT | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA19002 | hp2 | a0001 | c0001 | t0007 | g0193 | EAS | JPT | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA19012 | hp1 | a0001 | c0001 | t0004 | g0184 | EAS | JPT | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA19012 | hp2 | a0001 | c0002 | t0003 | g0107 | EAS | JPT | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0163 | AFR | LWK | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | LWK | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA19057 | hp1 | a0001 | c0001 | t0004 | g0207 | EAS | JPT | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA19084 | hp2 | a0001 | c0001 | t0004 | g0104 | EAS | JPT | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA19085 | hp1 | a0001 | c0001 | t0004 | g0092 | EAS | JPT | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA19088 | hp1 | a0001 | c0002 | t0002 | g0230 | EAS | JPT | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA19240 | hp1 | a0001 | c0001 | t0010 | g0249 | AFR | YRI | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA19240 | hp2 | a0001 | c0003 | t0012 | g0047 | AFR | YRI | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ASW | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0015 | AFR | ASW | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0116 | EUR | TSI | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0144 | EUR | TSI | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0181 | AFR | ACB | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02109 | hp2 | a0001 | c0003 | t0001 | g0057 | AFR | ACB | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ACB | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02486 | hp2 | a0001 | c0001 | t0014 | g0254 | AFR | ACB | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0166 | AFR | ACB | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG02559 | hp2 | a0001 | c0001 | t0008 | g0001 | AFR | ACB | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03471 | hp1 | a0004 | c0006 | t0002 | g0136 | AFR | MSL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0026 | AFR | MSL | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA20300 | hp1 | a0001 | c0002 | t0006 | g0248 | AFR | USA | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| NA20300 | hp2 | a0001 | c0004 | t0007 | g0023 | AFR | USA | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0003 | g0005 | REF | REF | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0050 | REF | REF | CORO2B_chr15_68573993_68732806 | CORO2B | chr15 | 68573993 | 68732806 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:68645356 | A | G | 1 | a0002 | 1 | HG00408.hp2 | missense_variant | MODERATE | c.212A>G | p.Glu71Gly | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/12 | 482/3545 | 212/1443 | 71/480 | chr15 | 68645356 | |||
| chr15:68711639 | T | A | 1 | a0004 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.581T>A | p.Leu194Gln | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 5/12 | 851/3545 | 581/1443 | 194/480 | chr15 | 68711639 | |||
| chr15:68725970 | G | A | 1 | a0003 | 1 | HG02896.hp1 | missense_variant | MODERATE | c.1439G>A | p.Cys480Tyr | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 12/12 | 1709/3545 | 1439/1443 | 480/480 | chr15 | 68725970 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:68711574 | G | A | 1 | a0001c0005 | 3 | HG00741.hp1 HG01516.hp2 HG01517.hp2 |
synonymous_variant | LOW | c.516G>A | p.Pro172Pro | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 5/12 | 786/3545 | 516/1443 | 172/480 | chr15 | 68711574 | |||
| chr15:68714570 | C | T | 2 | a0001c0003 a0001c0004 |
12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
synonymous_variant | LOW | c.777C>T | p.Ser259Ser | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 7/12 | 1047/3545 | 777/1443 | 259/480 | chr15 | 68714570 | |||
| chr15:68718780 | C | T | 3 | a0001c0002 a0001c0004 a0001c0005 |
31 | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(28): Show |
synonymous_variant | LOW | c.1050C>T | p.Ile350Ile | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 9/12 | 1320/3545 | 1050/1443 | 350/480 | chr15 | 68718780 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:68579093 | G | A | 2 | a0001c0001t0013 a0001c0001t0014 |
2 | HG02486.hp2 HG03225.hp2 |
5_prime_UTR_variant | MODIFIER | c.-170G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/12 | 170 | chr15 | 68579093 | ||||||
| chr15:68579112 | C | A | 1 | a0001c0001t0015 | 1 | HG02132.hp2 | 5_prime_UTR_variant | MODIFIER | c.-151C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/12 | 151 | chr15 | 68579112 | ||||||
| chr15:68579155 | C | T | 1 | a0001c0001t0027 | 1 | HG03209.hp2 | 5_prime_UTR_variant | MODIFIER | c.-108C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/12 | 108 | chr15 | 68579155 | ||||||
| chr15:68579187 | T | TC | 6 | a0001c0001t0010 a0001c0001t0013 a0001c0001t0014 others(3): Show |
7 | HG02486.hp2 HG02630.hp1 HG02818.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-74dupC | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/12 | 73 | INFO_REALIGN_3_PRIME | chr15 | 68579187 | |||||
| chr15:68579187 | TCCGCCGC others(12): Show |
T | 2 | a0001c0001t0019 a0001c0001t0020 |
2 | HG01884.hp1 HG02738.hp2 |
5_prime_UTR_variant | MODIFIER | c.-62_-44delGGGCCGCC others(11): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/12 | 44 | INFO_REALIGN_3_PRIME | chr15 | 68579187 | |||||
| chr15:68579201 | G | C | 1 | a0001c0001t0021 | 1 | HG02922.hp2 | 5_prime_UTR_variant | MODIFIER | c.-62G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/12 | 62 | chr15 | 68579201 | ||||||
| chr15:68579202 | G | GGCC | 6 | a0001c0001t0010 a0001c0001t0013 a0001c0001t0014 others(3): Show |
7 | HG02486.hp2 HG02630.hp1 HG02818.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-48_-46dupGCC | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/12 | 45 | INFO_REALIGN_3_PRIME | chr15 | 68579202 | |||||
| chr15:68726036 | C | A | 6 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0016 others(3): Show |
11 | HG00280.hp1 HG00621.hp1 HG01884.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*62C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 12/12 | 62 | chr15 | 68726036 | ||||||
| chr15:68726214 | G | T | 1 | a0001c0003t0012 | 2 | HG03041.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*240G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 12/12 | 240 | chr15 | 68726214 | ||||||
| chr15:68726340 | C | T | 8 | a0001c0001t0006 a0001c0001t0018 a0001c0001t0022 others(5): Show |
22 | HG01109.hp2 HG01175.hp2 HG01496.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*366C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 12/12 | 366 | chr15 | 68726340 | ||||||
| chr15:68726446 | C | T | 10 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0011 others(7): Show |
47 | HG00140.hp1 HG00597.hp1 HG00673.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*472C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 12/12 | 472 | chr15 | 68726446 | ||||||
| chr15:68726480 | G | A | 1 | a0001c0001t0023 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*506G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 12/12 | 506 | chr15 | 68726480 | ||||||
| chr15:68726509 | G | A | 1 | a0001c0001t0024 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*535G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 12/12 | 535 | chr15 | 68726509 | ||||||
| chr15:68726544 | A | G | 9 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0010 others(6): Show |
87 | HG00140.hp2 HG00280.hp1 HG00597.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*570A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 12/12 | 570 | chr15 | 68726544 | ||||||
| chr15:68726578 | C | T | 6 | a0001c0001t0002 a0001c0001t0021 a0001c0002t0002 others(3): Show |
42 | HG00408.hp2 HG00735.hp2 HG00741.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*604C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 12/12 | 604 | chr15 | 68726578 | ||||||
| chr15:68726620 | A | T | 9 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0010 others(6): Show |
87 | HG00140.hp2 HG00280.hp1 HG00597.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*646A>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 12/12 | 646 | chr15 | 68726620 | ||||||
| chr15:68726911 | T | C | 1 | a0001c0001t0025 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*937T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 12/12 | 937 | chr15 | 68726911 | ||||||
| chr15:68727138 | G | A | 2 | a0001c0001t0011 a0001c0003t0011 |
2 | HG02280.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1164G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 12/12 | 1164 | chr15 | 68727138 | ||||||
| chr15:68727192 | T | C | 1 | a0001c0001t0009 | 3 | HG03195.hp2 HG03516.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1218T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 12/12 | 1218 | chr15 | 68727192 | ||||||
| chr15:68727243 | G | C | 18 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(15): Show |
107 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*1269G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 12/12 | 1269 | chr15 | 68727243 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:68579346 | G | T | 1 | a0001c0002t0003g0256 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.15+69G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68579346 | |||||||
| chr15:68579366 | G | A | 4 | a0001c0001t0002g0002 a0001c0001t0006g0004 a0001c0001t0008g0001 others(1): Show |
4 | HG02559.hp2 HG02572.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+89G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68579366 | |||||||
| chr15:68579437 | G | T | 7 | a0001c0001t0010g0249 a0001c0001t0010g0252 a0001c0001t0013g0253 others(4): Show |
7 | HG02486.hp2 HG02630.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.15+160G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68579437 | |||||||
| chr15:68579485 | C | T | 2 | a0001c0002t0006g0248 a0001c0003t0011g0247 |
2 | HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.15+208C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68579485 | |||||||
| chr15:68579619 | C | T | 6 | a0001c0001t0001g0243 a0001c0001t0002g0241 a0001c0001t0002g0242 others(3): Show |
6 | HG01258.hp1 HG01261.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.15+342C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68579619 | |||||||
| chr15:68579774 | T | A | 1 | a0001c0002t0001g0006 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.15+497T>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68579774 | |||||||
| chr15:68580100 | G | T | 1 | a0001c0001t0004g0240 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.15+823G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68580100 | |||||||
| chr15:68580263 | G | A | 3 | a0001c0001t0001g0009 a0001c0001t0005g0007 a0001c0002t0001g0008 |
3 | HG00280.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.15+986G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68580263 | |||||||
| chr15:68580372 | TCAGATGG others(19): Show |
T | 168 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0087 others(165): Show |
168 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.15+1108_15+1133del others(26): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68580372 | ||||||
| chr15:68580643 | C | T | 1 | a0001c0001t0003g0239 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.15+1366C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68580643 | |||||||
| chr15:68580704 | A | G | 9 | a0001c0001t0002g0002 a0001c0001t0002g0078 a0001c0001t0002g0079 others(6): Show |
9 | HG02257.hp1 HG02280.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.15+1427A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68580704 | |||||||
| chr15:68580766 | G | A | 2 | a0001c0001t0001g0010 a0001c0001t0006g0011 |
2 | HG02602.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.15+1489G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68580766 | |||||||
| chr15:68580853 | C | T | 1 | a0001c0001t0018g0255 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.15+1576C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68580853 | |||||||
| chr15:68580868 | C | T | 2 | a0001c0001t0006g0237 a0001c0001t0009g0238 |
2 | HG01109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.15+1591C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68580868 | |||||||
| chr15:68581042 | G | T | 7 | a0001c0001t0010g0249 a0001c0001t0010g0252 a0001c0001t0013g0253 others(4): Show |
7 | HG02486.hp2 HG02630.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.15+1765G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68581042 | |||||||
| chr15:68581081 | G | A | 1 | a0001c0001t0010g0249 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.15+1804G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68581081 | |||||||
| chr15:68581443 | A | C | 1 | a0001c0001t0006g0236 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.15+2166A>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68581443 | |||||||
| chr15:68581687 | CTT | C | 17 | a0001c0001t0002g0022 a0001c0001t0002g0080 a0001c0001t0002g0081 others(14): Show |
17 | HG01891.hp2 HG02145.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.15+2412_15+2413del others(2): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68581687 | ||||||
| chr15:68581763 | C | T | 17 | a0001c0001t0002g0022 a0001c0001t0002g0080 a0001c0001t0002g0081 others(14): Show |
17 | HG01891.hp2 HG02145.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.15+2486C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68581763 | |||||||
| chr15:68581785 | G | T | 2 | a0001c0001t0002g0234 a0001c0001t0003g0235 |
2 | NA18944.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.15+2508G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68581785 | |||||||
| chr15:68581924 | C | A | 2 | a0001c0001t0002g0080 a0001c0001t0002g0081 |
2 | HG02145.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.15+2647C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68581924 | |||||||
| chr15:68582018 | A | G | 1 | a0001c0004t0005g0233 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.15+2741A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68582018 | |||||||
| chr15:68582231 | T | C | 209 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0028 others(206): Show |
209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.15+2954T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68582231 | |||||||
| chr15:68582435 | G | A | 1 | a0001c0001t0001g0027 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.15+3158G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68582435 | |||||||
| chr15:68582657 | A | G | 1 | a0001c0002t0002g0230 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.15+3380A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68582657 | |||||||
| chr15:68582696 | A | G | 16 | a0001c0001t0002g0002 a0001c0001t0002g0078 a0001c0001t0002g0079 others(13): Show |
16 | HG02257.hp1 HG02280.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.15+3419A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68582696 | |||||||
| chr15:68582827 | C | T | 1 | a0001c0002t0003g0256 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.15+3550C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68582827 | |||||||
| chr15:68582915 | C | T | 12 | a0001c0001t0002g0002 a0001c0001t0002g0078 a0001c0001t0002g0079 others(9): Show |
12 | HG02257.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.15+3638C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68582915 | |||||||
| chr15:68582941 | A | G | 1 | a0001c0001t0004g0229 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.15+3664A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68582941 | |||||||
| chr15:68583057 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.15+3780C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68583057 | |||||||
| chr15:68583103 | C | G | 2 | a0001c0001t0002g0080 a0001c0001t0002g0081 |
2 | HG02145.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.15+3826C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68583103 | |||||||
| chr15:68583644 | G | C | 2 | a0001c0001t0013g0253 a0001c0001t0014g0254 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.15+4367G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68583644 | |||||||
| chr15:68583736 | A | G | 15 | a0001c0001t0001g0243 a0001c0001t0002g0080 a0001c0001t0002g0081 others(12): Show |
15 | HG01070.hp1 HG01081.hp2 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.15+4459A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68583736 | |||||||
| chr15:68583883 | C | A | 1 | a0001c0001t0010g0249 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.15+4606C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68583883 | |||||||
| chr15:68583883 | C | T | 1 | a0001c0002t0002g0224 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.15+4606C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68583883 | |||||||
| chr15:68583943 | C | T | 2 | a0001c0001t0015g0222 a0001c0002t0006g0223 |
2 | HG02132.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.15+4666C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68583943 | |||||||
| chr15:68583961 | C | T | 2 | a0001c0001t0013g0253 a0001c0001t0014g0254 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.15+4684C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68583961 | |||||||
| chr15:68584107 | A | G | 28 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0202 others(25): Show |
28 | HG00673.hp1 HG00738.hp1 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.15+4830A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68584107 | |||||||
| chr15:68584152 | C | T | 1 | a0001c0001t0021g0033 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.15+4875C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68584152 | |||||||
| chr15:68584153 | G | A | 2 | a0001c0001t0013g0253 a0001c0001t0014g0254 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.15+4876G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68584153 | |||||||
| chr15:68584388 | G | C | 8 | a0001c0001t0004g0017 a0001c0001t0005g0012 a0001c0001t0005g0013 others(5): Show |
8 | HG02717.hp2 HG02976.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.15+5111G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68584388 | |||||||
| chr15:68584440 | G | A | 2 | a0001c0001t0013g0253 a0001c0001t0014g0254 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.15+5163G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68584440 | |||||||
| chr15:68584787 | A | G | 8 | a0001c0001t0004g0017 a0001c0001t0005g0012 a0001c0001t0005g0013 others(5): Show |
8 | HG02717.hp2 HG02976.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.15+5510A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68584787 | |||||||
| chr15:68584813 | G | C | 169 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0028 others(166): Show |
169 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.15+5536G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68584813 | |||||||
| chr15:68584855 | A | T | 1 | a0001c0001t0007g0193 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.15+5578A>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68584855 | |||||||
| chr15:68584934 | G | A | 1 | a0001c0001t0005g0194 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.15+5657G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68584934 | |||||||
| chr15:68584977 | G | A | 187 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0028 others(184): Show |
187 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.15+5700G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68584977 | |||||||
| chr15:68585096 | A | G | 188 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0028 others(185): Show |
188 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.15+5819A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68585096 | |||||||
| chr15:68585212 | G | A | 1 | a0001c0001t0016g0250 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.15+5935G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68585212 | |||||||
| chr15:68585473 | G | T | 1 | a0001c0001t0001g0192 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.15+6196G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68585473 | |||||||
| chr15:68585819 | T | C | 2 | a0001c0001t0013g0253 a0001c0001t0014g0254 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.15+6542T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68585819 | |||||||
| chr15:68585825 | G | A | 1 | a0001c0001t0010g0249 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.15+6548G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68585825 | |||||||
| chr15:68585893 | G | T | 4 | a0001c0001t0004g0024 a0001c0001t0004g0026 a0001c0001t0006g0004 others(1): Show |
4 | HG02451.hp2 HG02970.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+6616G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68585893 | |||||||
| chr15:68585908 | T | G | 168 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0028 others(165): Show |
168 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.15+6631T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68585908 | |||||||
| chr15:68585923 | C | T | 18 | a0001c0001t0001g0228 a0001c0001t0001g0243 a0001c0001t0002g0080 others(15): Show |
18 | HG01070.hp1 HG01081.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.15+6646C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68585923 | |||||||
| chr15:68586238 | A | G | 182 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0028 others(179): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.15+6961A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68586238 | |||||||
| chr15:68586470 | C | T | 1 | a0001c0001t0002g0079 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.15+7193C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68586470 | |||||||
| chr15:68586648 | G | C | 1 | a0001c0001t0001g0027 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.15+7371G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68586648 | |||||||
| chr15:68586686 | G | A | 2 | a0001c0001t0003g0082 a0001c0001t0003g0083 |
2 | HG00597.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.15+7409G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68586686 | |||||||
| chr15:68586717 | G | C | 210 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0028 others(207): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.15+7440G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68586717 | |||||||
| chr15:68586838 | C | T | 1 | a0001c0001t0005g0194 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.15+7561C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68586838 | |||||||
| chr15:68586912 | G | C | 2 | a0001c0001t0013g0253 a0001c0001t0014g0254 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.15+7635G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68586912 | |||||||
| chr15:68586946 | A | T | 7 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0001g0190 others(4): Show |
7 | HG00140.hp2 HG00642.hp1 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.15+7669A>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68586946 | |||||||
| chr15:68587001 | T | G | 1 | a0001c0001t0005g0029 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.15+7724T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68587001 | |||||||
| chr15:68587047 | TATAC | T | 7 | a0001c0001t0001g0028 a0001c0001t0001g0157 a0001c0001t0002g0148 others(4): Show |
7 | HG01496.hp1 HG01981.hp2 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.15+7772_15+7775del others(4): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68587047 | ||||||
| chr15:68587047 | TATACACA others(1): Show |
T | 48 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0037 others(45): Show |
48 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.15+7772_15+7779del others(8): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68587047 | ||||||
| chr15:68587047 | TATACACA others(3): Show |
T | 65 | a0001c0001t0001g0095 a0001c0001t0001g0101 a0001c0001t0001g0105 others(62): Show |
65 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.15+7772_15+7781del others(10): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68587047 | ||||||
| chr15:68587047 | TATACACA others(5): Show |
T | 7 | a0001c0001t0004g0106 a0001c0001t0006g0191 a0001c0001t0006g0218 others(4): Show |
7 | HG01175.hp2 HG02083.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.15+7772_15+7783del others(12): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68587047 | ||||||
| chr15:68587047 | TATACACA others(7): Show |
T | 47 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(44): Show |
47 | HG00673.hp1 HG00738.hp1 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.15+7772_15+7785del others(14): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68587047 | ||||||
| chr15:68587047 | TATACACA others(9): Show |
T | 4 | a0001c0001t0001g0199 a0001c0001t0002g0080 a0001c0001t0005g0018 others(1): Show |
4 | HG01891.hp2 HG02145.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+7772_15+7787del others(16): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68587047 | ||||||
| chr15:68587047 | TATACACA others(11): Show |
T | 2 | a0001c0001t0013g0253 a0001c0001t0014g0254 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.15+7772_15+7789del others(18): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68587047 | ||||||
| chr15:68587047 | TATACACA others(15): Show |
T | 1 | a0001c0001t0003g0155 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.15+7772_15+7793del others(22): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68587047 | ||||||
| chr15:68587049 | T | C | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0006g0040 |
3 | HG00621.hp2 HG02886.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.15+7772T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68587049 | |||||||
| chr15:68587049 | T | TAC | 9 | a0001c0001t0001g0056 a0001c0001t0002g0054 a0001c0001t0002g0231 others(6): Show |
9 | HG00280.hp2 HG00597.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.15+7818_15+7819dup others(2): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68587049 | ||||||
| chr15:68587049 | T | TACAC | 11 | a0001c0001t0001g0009 a0001c0001t0001g0060 a0001c0001t0001g0061 others(8): Show |
11 | HG01099.hp2 HG01106.hp2 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.15+7816_15+7819dup others(4): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68587049 | ||||||
| chr15:68587049 | T | TACACAC | 6 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0002g0221 others(3): Show |
6 | HG00738.hp2 HG01243.hp1 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+7814_15+7819dup others(6): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68587049 | ||||||
| chr15:68587049 | T | TACACACA others(1): Show |
3 | a0001c0001t0001g0039 a0001c0001t0005g0072 a0001c0002t0002g0071 |
3 | HG01099.hp1 HG01346.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.15+7812_15+7819dup others(8): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68587049 | ||||||
| chr15:68587049 | T | TACACACA others(3): Show |
1 | a0001c0001t0005g0073 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.15+7810_15+7819dup others(10): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68587049 | ||||||
| chr15:68587049 | TACACAC | T | 7 | a0001c0001t0001g0074 a0001c0001t0004g0077 a0001c0001t0021g0033 others(4): Show |
7 | HG02280.hp1 HG02922.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.15+7814_15+7819del others(6): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68587049 | ||||||
| chr15:68587049 | TACACACA others(1): Show |
T | 6 | a0001c0001t0002g0002 a0001c0001t0004g0024 a0001c0001t0004g0026 others(3): Show |
6 | HG02258.hp2 HG02451.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.15+7812_15+7819del others(8): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68587049 | ||||||
| chr15:68587049 | TACACACA others(3): Show |
T | 1 | a0001c0001t0006g0041 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.15+7810_15+7819del others(10): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68587049 | ||||||
| chr15:68587049 | TACACACA others(5): Show |
T | 6 | a0001c0001t0004g0017 a0001c0001t0005g0012 a0001c0001t0005g0013 others(3): Show |
6 | HG02717.hp2 HG02976.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+7808_15+7819del others(12): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68587049 | ||||||
| chr15:68587177 | C | T | 2 | a0001c0001t0010g0249 a0001c0001t0016g0250 |
2 | HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.15+7900C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68587177 | |||||||
| chr15:68587213 | A | C | 2 | a0001c0001t0004g0184 a0001c0001t0004g0185 |
2 | NA18949.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.15+7936A>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68587213 | |||||||
| chr15:68587218 | C | A | 1 | a0001c0002t0006g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.15+7941C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68587218 | |||||||
| chr15:68587372 | G | A | 1 | a0001c0001t0001g0199 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.15+8095G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68587372 | |||||||
| chr15:68587694 | A | T | 140 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0028 others(137): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.15+8417A>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68587694 | |||||||
| chr15:68587711 | A | T | 1 | a0001c0001t0006g0040 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.15+8434A>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68587711 | |||||||
| chr15:68587754 | T | C | 2 | a0001c0001t0004g0092 a0002c0008t0002g0093 |
2 | HG00408.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.15+8477T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68587754 | |||||||
| chr15:68587846 | C | A | 1 | a0001c0001t0001g0094 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.15+8569C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68587846 | |||||||
| chr15:68587981 | T | G | 1 | a0001c0001t0002g0002 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.15+8704T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68587981 | |||||||
| chr15:68588021 | A | G | 213 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0028 others(210): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.15+8744A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68588021 | |||||||
| chr15:68588362 | C | T | 2 | a0001c0001t0002g0219 a0001c0001t0002g0220 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.15+9085C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68588362 | |||||||
| chr15:68588553 | G | A | 1 | a0001c0004t0006g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.15+9276G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68588553 | |||||||
| chr15:68588564 | A | G | 1 | a0001c0001t0010g0249 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.15+9287A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68588564 | |||||||
| chr15:68588631 | C | G | 214 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0028 others(211): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.15+9354C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68588631 | |||||||
| chr15:68588822 | A | G | 44 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(41): Show |
44 | HG00673.hp1 HG00738.hp1 HG01175.hp2 others(41): Show |
intron_variant | MODIFIER | c.15+9545A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68588822 | |||||||
| chr15:68588856 | A | AG | 190 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0028 others(187): Show |
190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.15+9579_15+9580ins others(1): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68588856 | |||||||
| chr15:68588936 | C | T | 1 | a0001c0001t0003g0086 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.15+9659C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68588936 | |||||||
| chr15:68588988 | C | T | 2 | a0001c0001t0013g0253 a0001c0001t0014g0254 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.15+9711C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68588988 | |||||||
| chr15:68589059 | G | A | 3 | a0001c0001t0004g0024 a0001c0001t0004g0026 a0001c0001t0008g0025 |
3 | HG02451.hp2 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.15+9782G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68589059 | |||||||
| chr15:68589130 | C | T | 1 | a0001c0001t0006g0218 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.15+9853C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68589130 | |||||||
| chr15:68589185 | G | A | 139 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0028 others(136): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.15+9908G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68589185 | |||||||
| chr15:68589196 | T | C | 2 | a0001c0001t0002g0096 a0001c0001t0002g0097 |
2 | HG00735.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.15+9919T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68589196 | |||||||
| chr15:68589608 | G | A | 37 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(34): Show |
37 | HG00673.hp1 HG00738.hp1 HG01175.hp2 others(34): Show |
intron_variant | MODIFIER | c.15+10331G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68589608 | |||||||
| chr15:68589716 | G | A | 1 | a0001c0001t0004g0058 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.15+10439G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68589716 | |||||||
| chr15:68589910 | G | A | 7 | a0001c0001t0001g0009 a0001c0001t0002g0054 a0001c0001t0002g0197 others(4): Show |
7 | HG00280.hp2 HG02027.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.15+10633G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68589910 | |||||||
| chr15:68589927 | C | T | 1 | a0001c0001t0002g0002 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.15+10650C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68589927 | |||||||
| chr15:68589933 | G | T | 1 | a0001c0001t0010g0249 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.15+10656G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68589933 | |||||||
| chr15:68589965 | C | T | 1 | a0001c0001t0002g0091 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.15+10688C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68589965 | |||||||
| chr15:68590349 | G | C | 4 | a0001c0001t0001g0200 a0001c0001t0001g0202 a0001c0001t0019g0201 others(1): Show |
4 | HG01884.hp1 HG02735.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+11072G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68590349 | |||||||
| chr15:68590388 | T | G | 142 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0028 others(139): Show |
142 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.15+11111T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68590388 | |||||||
| chr15:68590391 | C | A | 1 | a0001c0001t0001g0098 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.15+11114C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68590391 | |||||||
| chr15:68590471 | A | G | 2 | a0001c0001t0002g0080 a0001c0001t0002g0081 |
2 | HG02145.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.15+11194A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68590471 | |||||||
| chr15:68590505 | G | A | 1 | a0001c0002t0006g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.15+11228G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68590505 | |||||||
| chr15:68590752 | G | C | 1 | a0001c0004t0005g0003 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.15+11475G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68590752 | |||||||
| chr15:68590879 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.15+11602C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68590879 | |||||||
| chr15:68590921 | C | T | 1 | a0001c0001t0003g0217 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.15+11644C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68590921 | |||||||
| chr15:68590997 | G | A | 201 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0028 others(198): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.15+11720G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68590997 | |||||||
| chr15:68591012 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.15+11735C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68591012 | |||||||
| chr15:68591074 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.15+11797G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68591074 | |||||||
| chr15:68591307 | G | A | 1 | a0001c0004t0006g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.15+12030G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68591307 | |||||||
| chr15:68591321 | C | T | 1 | a0001c0001t0002g0231 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.15+12044C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68591321 | |||||||
| chr15:68591400 | G | A | 5 | a0001c0001t0008g0001 a0001c0001t0010g0252 a0001c0001t0017g0251 others(2): Show |
5 | HG02109.hp2 HG02559.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+12123G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68591400 | |||||||
| chr15:68591500 | C | T | 1 | a0001c0001t0002g0182 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.15+12223C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68591500 | |||||||
| chr15:68591641 | G | A | 56 | a0001c0001t0001g0009 a0001c0001t0001g0087 a0001c0001t0001g0088 others(53): Show |
56 | HG00673.hp1 HG00738.hp1 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.15+12364G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68591641 | |||||||
| chr15:68591775 | G | A | 38 | a0001c0001t0001g0009 a0001c0001t0001g0087 a0001c0001t0001g0088 others(35): Show |
38 | HG00673.hp1 HG00738.hp1 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.15+12498G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68591775 | |||||||
| chr15:68591825 | G | A | 1 | a0001c0001t0018g0255 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.15+12548G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68591825 | |||||||
| chr15:68591865 | G | A | 143 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0028 others(140): Show |
143 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.15+12588G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68591865 | |||||||
| chr15:68592036 | A | T | 1 | a0001c0001t0006g0040 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.15+12759A>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68592036 | |||||||
| chr15:68592080 | G | C | 1 | a0001c0004t0005g0003 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.15+12803G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68592080 | |||||||
| chr15:68592146 | C | CCAGACTG | 3 | a0001c0001t0006g0191 a0001c0001t0013g0253 a0001c0001t0014g0254 |
3 | HG02486.hp2 HG02615.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.15+12871_15+12877d others(9): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68592146 | ||||||
| chr15:68592624 | A | G | 3 | a0001c0001t0001g0228 a0001c0001t0002g0195 a0001c0001t0005g0196 |
3 | HG02615.hp2 HG02809.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.15+13347A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68592624 | |||||||
| chr15:68592909 | T | A | 1 | a0001c0001t0001g0100 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.15+13632T>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68592909 | |||||||
| chr15:68592932 | C | T | 1 | a0001c0002t0003g0256 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.15+13655C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68592932 | |||||||
| chr15:68593007 | T | G | 205 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(202): Show |
205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.15+13730T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68593007 | |||||||
| chr15:68593035 | A | G | 205 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(202): Show |
205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.15+13758A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68593035 | |||||||
| chr15:68593113 | C | T | 2 | a0001c0001t0013g0253 a0001c0001t0014g0254 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.15+13836C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68593113 | |||||||
| chr15:68593244 | T | C | 228 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(225): Show |
228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.15+13967T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68593244 | |||||||
| chr15:68593343 | C | T | 1 | a0001c0002t0002g0177 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.15+14066C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68593343 | |||||||
| chr15:68593475 | G | A | 171 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(168): Show |
171 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.15+14198G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68593475 | |||||||
| chr15:68593518 | G | T | 4 | a0001c0001t0001g0215 a0001c0001t0003g0214 a0001c0001t0003g0217 others(1): Show |
4 | HG00738.hp1 HG01175.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+14241G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68593518 | |||||||
| chr15:68593538 | G | C | 1 | a0001c0001t0006g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.15+14261G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68593538 | |||||||
| chr15:68593600 | A | G | 1 | a0001c0001t0015g0222 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.15+14323A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68593600 | |||||||
| chr15:68594028 | G | A | 8 | a0001c0001t0001g0243 a0001c0001t0002g0242 a0001c0001t0003g0225 others(5): Show |
8 | HG01070.hp1 HG01081.hp2 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.15+14751G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68594028 | |||||||
| chr15:68594495 | A | T | 2 | a0001c0001t0002g0091 a0001c0001t0005g0035 |
2 | HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.15+15218A>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68594495 | |||||||
| chr15:68594558 | G | A | 14 | a0001c0001t0001g0028 a0001c0001t0001g0101 a0001c0001t0001g0105 others(11): Show |
14 | HG01981.hp1 HG02040.hp2 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.15+15281G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68594558 | |||||||
| chr15:68594559 | C | G | 1 | a0001c0001t0002g0182 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.15+15282C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68594559 | |||||||
| chr15:68594632 | G | A | 3 | a0001c0001t0002g0078 a0001c0001t0002g0079 a0001c0003t0012g0076 |
3 | HG02257.hp1 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.15+15355G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68594632 | |||||||
| chr15:68594743 | C | T | 1 | a0001c0003t0012g0076 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.15+15466C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68594743 | |||||||
| chr15:68594810 | C | T | 1 | a0001c0001t0006g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.15+15533C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68594810 | |||||||
| chr15:68595132 | G | A | 4 | a0001c0001t0001g0228 a0001c0001t0002g0195 a0001c0001t0004g0216 others(1): Show |
4 | HG02615.hp2 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+15855G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68595132 | |||||||
| chr15:68595255 | C | A | 21 | a0001c0001t0001g0048 a0001c0001t0001g0179 a0001c0001t0002g0002 others(18): Show |
21 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.15+15978C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68595255 | |||||||
| chr15:68595298 | G | A | 3 | a0001c0001t0001g0048 a0001c0001t0013g0253 a0001c0001t0014g0254 |
3 | HG02486.hp2 HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.15+16021G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68595298 | |||||||
| chr15:68595334 | G | A | 116 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0028 others(113): Show |
116 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.15+16057G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68595334 | |||||||
| chr15:68595509 | G | T | 17 | a0001c0001t0001g0179 a0001c0001t0002g0181 a0001c0001t0004g0017 others(14): Show |
17 | HG02109.hp1 HG02451.hp1 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.15+16232G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68595509 | |||||||
| chr15:68595701 | C | T | 1 | a0001c0001t0003g0064 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.15+16424C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68595701 | |||||||
| chr15:68595942 | G | A | 2 | a0001c0001t0001g0048 a0001c0001t0004g0024 |
2 | HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.15+16665G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68595942 | |||||||
| chr15:68595965 | C | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.15+16688C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68595965 | |||||||
| chr15:68596020 | G | A | 2 | a0001c0001t0013g0253 a0001c0001t0014g0254 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.15+16743G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68596020 | |||||||
| chr15:68596074 | G | C | 3 | a0001c0001t0003g0239 a0001c0001t0004g0109 a0001c0001t0004g0110 |
3 | HG00408.hp1 HG02135.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.15+16797G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68596074 | |||||||
| chr15:68596167 | C | A | 1 | a0001c0001t0003g0111 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.15+16890C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68596167 | |||||||
| chr15:68596405 | G | C | 14 | a0001c0001t0001g0179 a0001c0001t0002g0181 a0001c0001t0004g0017 others(11): Show |
14 | HG02109.hp1 HG02451.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.15+17128G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68596405 | |||||||
| chr15:68596437 | C | T | 99 | a0001c0001t0001g0010 a0001c0001t0001g0028 a0001c0001t0001g0042 others(96): Show |
99 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.15+17160C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68596437 | |||||||
| chr15:68596480 | C | G | 1 | a0001c0001t0002g0197 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.15+17203C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68596480 | |||||||
| chr15:68596570 | G | A | 1 | a0001c0001t0006g0021 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.15+17293G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68596570 | |||||||
| chr15:68596749 | G | A | 1 | a0001c0001t0002g0002 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.15+17472G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68596749 | |||||||
| chr15:68596814 | C | T | 2 | a0001c0001t0001g0098 a0001c0001t0002g0167 |
2 | HG01978.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.15+17537C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68596814 | |||||||
| chr15:68596817 | G | A | 1 | a0001c0001t0006g0040 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.15+17540G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68596817 | |||||||
| chr15:68597332 | T | G | 6 | a0001c0001t0002g0002 a0001c0001t0006g0237 a0001c0001t0009g0238 others(3): Show |
6 | HG01109.hp2 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.15+18055T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68597332 | |||||||
| chr15:68597453 | A | C | 3 | a0001c0001t0003g0225 a0001c0001t0003g0226 a0001c0001t0003g0227 |
3 | HG01070.hp1 HG01081.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.15+18176A>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68597453 | |||||||
| chr15:68597627 | C | CA | 13 | a0001c0001t0001g0065 a0001c0001t0001g0179 a0001c0001t0002g0181 others(10): Show |
13 | HG01106.hp2 HG01109.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.15+18363dupA | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68597627 | ||||||
| chr15:68597627 | CA | C | 25 | a0001c0001t0001g0100 a0001c0001t0001g0124 a0001c0001t0001g0128 others(22): Show |
25 | HG00408.hp1 HG01070.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.15+18363delA | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68597627 | ||||||
| chr15:68597627 | CAA | C | 13 | a0001c0001t0001g0228 a0001c0001t0002g0080 a0001c0001t0002g0081 others(10): Show |
13 | HG02145.hp2 HG02559.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.15+18362_15+18363d others(4): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68597627 | ||||||
| chr15:68597633 | A | T | 1 | a0001c0005t0003g0130 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.15+18356A>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68597633 | |||||||
| chr15:68597637 | A | AT | 6 | a0001c0001t0001g0048 a0001c0001t0004g0024 a0001c0001t0004g0026 others(3): Show |
6 | HG02280.hp2 HG02451.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.15+18360_15+18361i others(3): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68597637 | |||||||
| chr15:68597637 | A | T | 55 | a0001c0001t0001g0009 a0001c0001t0001g0037 a0001c0001t0001g0056 others(52): Show |
55 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.15+18360A>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68597637 | |||||||
| chr15:68597641 | T | A | 1 | a0001c0001t0005g0029 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.15+18364T>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68597641 | |||||||
| chr15:68597653 | A | T | 21 | a0001c0001t0001g0074 a0001c0001t0001g0228 a0001c0001t0001g0243 others(18): Show |
21 | HG01070.hp1 HG01081.hp2 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.15+18376A>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68597653 | |||||||
| chr15:68597670 | C | T | 2 | a0001c0001t0001g0122 a0001c0001t0002g0123 |
2 | NA18966.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.15+18393C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68597670 | |||||||
| chr15:68598044 | C | T | 1 | a0001c0001t0022g0049 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.15+18767C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68598044 | |||||||
| chr15:68598068 | A | C | 2 | a0001c0001t0006g0191 a0001c0001t0010g0249 |
2 | HG02615.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.15+18791A>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68598068 | |||||||
| chr15:68598213 | C | T | 2 | a0001c0001t0002g0078 a0001c0001t0002g0079 |
2 | HG02257.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.15+18936C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68598213 | |||||||
| chr15:68598218 | A | G | 15 | a0001c0001t0001g0179 a0001c0001t0002g0002 a0001c0001t0002g0181 others(12): Show |
15 | HG01109.hp2 HG02109.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.15+18941A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68598218 | |||||||
| chr15:68598333 | G | A | 1 | a0001c0001t0004g0205 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.15+19056G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68598333 | |||||||
| chr15:68598344 | C | T | 7 | a0001c0001t0002g0091 a0001c0001t0004g0019 a0001c0001t0005g0018 others(4): Show |
7 | HG01891.hp2 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.15+19067C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68598344 | |||||||
| chr15:68598486 | G | A | 2 | a0001c0001t0013g0253 a0001c0001t0014g0254 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.15+19209G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68598486 | |||||||
| chr15:68598749 | C | T | 2 | a0001c0001t0001g0048 a0001c0004t0005g0003 |
2 | HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.15+19472C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68598749 | |||||||
| chr15:68598786 | A | G | 2 | a0001c0001t0013g0253 a0001c0001t0014g0254 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.15+19509A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68598786 | |||||||
| chr15:68598812 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.15+19535G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68598812 | |||||||
| chr15:68598891 | A | G | 1 | a0001c0001t0001g0128 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.15+19614A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68598891 | |||||||
| chr15:68599051 | C | G | 2 | a0001c0001t0009g0238 a0001c0003t0011g0247 |
2 | HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.15+19774C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68599051 | |||||||
| chr15:68599208 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.15+19931C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68599208 | |||||||
| chr15:68599215 | G | A | 1 | a0001c0004t0006g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.15+19938G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68599215 | |||||||
| chr15:68599469 | G | A | 2 | a0001c0001t0006g0191 a0001c0001t0010g0249 |
2 | HG02615.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.15+20192G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68599469 | |||||||
| chr15:68599541 | T | G | 9 | a0001c0001t0001g0042 a0001c0001t0001g0074 a0001c0001t0006g0191 others(6): Show |
9 | HG02109.hp2 HG02559.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.15+20264T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68599541 | |||||||
| chr15:68599564 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.15+20287C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68599564 | |||||||
| chr15:68599565 | G | A | 18 | a0001c0001t0001g0179 a0001c0001t0002g0181 a0001c0001t0004g0017 others(15): Show |
18 | HG01109.hp2 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.15+20288G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68599565 | |||||||
| chr15:68599735 | C | T | 2 | a0001c0001t0001g0048 a0001c0004t0005g0003 |
2 | HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.15+20458C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68599735 | |||||||
| chr15:68599863 | T | C | 7 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0002g0135 others(4): Show |
7 | HG02809.hp1 HG02970.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.15+20586T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68599863 | |||||||
| chr15:68600339 | A | G | 1 | a0001c0001t0020g0203 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.15+21062A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68600339 | |||||||
| chr15:68600513 | G | A | 20 | a0001c0001t0001g0179 a0001c0001t0002g0002 a0001c0001t0002g0091 others(17): Show |
20 | HG01109.hp2 HG02109.hp1 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.15+21236G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68600513 | |||||||
| chr15:68600650 | C | T | 18 | a0001c0001t0001g0243 a0001c0001t0002g0078 a0001c0001t0002g0079 others(15): Show |
18 | HG01070.hp1 HG01081.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.15+21373C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68600650 | |||||||
| chr15:68601420 | A | T | 6 | a0001c0001t0001g0228 a0001c0001t0002g0195 a0001c0001t0004g0216 others(3): Show |
6 | HG02572.hp2 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+22143A>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68601420 | |||||||
| chr15:68601510 | G | T | 1 | a0001c0001t0002g0181 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.15+22233G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68601510 | |||||||
| chr15:68601516 | G | A | 2 | a0001c0001t0005g0046 a0001c0001t0005g0194 |
2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.15+22239G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68601516 | |||||||
| chr15:68601655 | A | G | 67 | a0001c0001t0001g0042 a0001c0001t0001g0048 a0001c0001t0001g0074 others(64): Show |
67 | HG00741.hp2 HG01070.hp1 HG01081.hp2 others(64): Show |
intron_variant | MODIFIER | c.15+22378A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68601655 | |||||||
| chr15:68601932 | T | G | 3 | a0001c0002t0002g0170 a0001c0005t0002g0043 a0001c0005t0003g0130 |
3 | HG00741.hp1 HG01516.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.15+22655T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68601932 | |||||||
| chr15:68601941 | G | T | 6 | a0001c0001t0004g0019 a0001c0001t0005g0012 a0001c0001t0005g0013 others(3): Show |
6 | HG01891.hp2 HG03130.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+22664G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68601941 | |||||||
| chr15:68601942 | G | C | 1 | a0001c0001t0001g0187 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.15+22665G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68601942 | |||||||
| chr15:68601993 | A | G | 1 | a0001c0001t0003g0213 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.15+22716A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68601993 | |||||||
| chr15:68602008 | CT | C | 34 | a0001c0001t0001g0173 a0001c0001t0001g0179 a0001c0001t0002g0002 others(31): Show |
34 | HG01070.hp2 HG01109.hp2 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.15+22749delT | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68602008 | ||||||
| chr15:68602220 | C | T | 67 | a0001c0001t0001g0042 a0001c0001t0001g0048 a0001c0001t0001g0074 others(64): Show |
67 | HG00741.hp2 HG01070.hp1 HG01081.hp2 others(64): Show |
intron_variant | MODIFIER | c.15+22943C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68602220 | |||||||
| chr15:68602384 | G | T | 31 | a0001c0001t0001g0042 a0001c0001t0001g0074 a0001c0001t0001g0179 others(28): Show |
31 | HG01109.hp2 HG01891.hp2 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.15+23107G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68602384 | |||||||
| chr15:68602407 | T | TCA | 51 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(48): Show |
51 | HG00408.hp1 HG00408.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.15+23172_15+23173d others(4): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68602407 | ||||||
| chr15:68602407 | T | TCACA | 14 | a0001c0001t0001g0101 a0001c0001t0001g0128 a0001c0001t0001g0243 others(11): Show |
14 | HG00673.hp2 HG00738.hp2 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.15+23170_15+23173d others(6): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68602407 | ||||||
| chr15:68602407 | T | TCACACA | 14 | a0001c0001t0001g0042 a0001c0001t0001g0074 a0001c0001t0001g0084 others(11): Show |
14 | HG00621.hp2 HG01070.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.15+23168_15+23173d others(8): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68602407 | ||||||
| chr15:68602407 | T | TCACACAC others(3): Show |
1 | a0001c0001t0003g0244 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.15+23164_15+23173d others(12): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68602407 | ||||||
| chr15:68602407 | TCA | T | 18 | a0001c0001t0001g0039 a0001c0001t0001g0048 a0001c0001t0001g0056 others(15): Show |
18 | HG00597.hp2 HG01071.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.15+23172_15+23173d others(4): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68602407 | ||||||
| chr15:68602407 | TCACA | T | 4 | a0001c0001t0004g0077 a0001c0001t0006g0031 a0001c0001t0027g0034 others(1): Show |
4 | HG02280.hp1 HG03209.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+23170_15+23173d others(6): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68602407 | ||||||
| chr15:68602407 | TCACACAC others(7): Show |
T | 6 | a0001c0001t0001g0228 a0001c0001t0002g0195 a0001c0001t0004g0216 others(3): Show |
6 | HG02572.hp2 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+23160_15+23173d others(16): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68602407 | ||||||
| chr15:68602407 | TCACACAC others(17): Show |
T | 1 | a0001c0001t0003g0163 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.15+23150_15+23173d others(26): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68602407 | ||||||
| chr15:68602562 | C | T | 5 | a0001c0001t0001g0228 a0001c0001t0002g0195 a0001c0001t0004g0216 others(2): Show |
5 | HG02572.hp2 HG02615.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.15+23285C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68602562 | |||||||
| chr15:68602584 | G | A | 14 | a0001c0001t0001g0179 a0001c0001t0002g0181 a0001c0001t0004g0019 others(11): Show |
14 | HG01109.hp2 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.15+23307G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68602584 | |||||||
| chr15:68602642 | C | T | 1 | a0001c0002t0006g0248 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.15+23365C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68602642 | |||||||
| chr15:68602701 | T | TG | 8 | a0001c0001t0001g0243 a0001c0001t0002g0242 a0001c0001t0003g0225 others(5): Show |
8 | HG01070.hp1 HG01081.hp2 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.15+23425dupG | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68602701 | ||||||
| chr15:68602744 | A | G | 1 | a0001c0002t0002g0099 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.15+23467A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68602744 | |||||||
| chr15:68602793 | A | C | 4 | a0001c0001t0001g0124 a0001c0001t0003g0125 a0001c0001t0003g0126 others(1): Show |
4 | HG02015.hp2 NA18968.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+23516A>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68602793 | |||||||
| chr15:68602938 | G | C | 3 | a0001c0001t0001g0100 a0001c0001t0001g0139 a0001c0001t0003g0140 |
3 | HG01109.hp1 HG02602.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.15+23661G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68602938 | |||||||
| chr15:68603183 | C | T | 1 | a0001c0001t0010g0249 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.15+23906C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68603183 | |||||||
| chr15:68603190 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.15+23913G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68603190 | |||||||
| chr15:68603206 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.15+23929C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68603206 | |||||||
| chr15:68603219 | C | T | 1 | a0001c0001t0005g0073 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.15+23942C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68603219 | |||||||
| chr15:68603292 | C | T | 31 | a0001c0001t0001g0179 a0001c0001t0001g0228 a0001c0001t0002g0002 others(28): Show |
31 | HG01109.hp2 HG01891.hp2 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.15+24015C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68603292 | |||||||
| chr15:68603609 | C | T | 1 | a0001c0002t0002g0099 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.15+24332C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68603609 | |||||||
| chr15:68603615 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.15+24338G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68603615 | |||||||
| chr15:68603680 | C | G | 60 | a0001c0001t0001g0042 a0001c0001t0001g0048 a0001c0001t0001g0074 others(57): Show |
60 | HG00741.hp2 HG01109.hp2 HG01258.hp1 others(57): Show |
intron_variant | MODIFIER | c.15+24403C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68603680 | |||||||
| chr15:68603681 | TC | T | 18 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0067 others(15): Show |
18 | HG00280.hp1 HG02040.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.15+24406delC | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68603681 | ||||||
| chr15:68603686 | A | G | 9 | a0001c0001t0002g0002 a0001c0001t0004g0077 a0001c0001t0005g0029 others(6): Show |
9 | HG02258.hp2 HG02280.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.15+24409A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68603686 | |||||||
| chr15:68603718 | G | A | 61 | a0001c0001t0001g0042 a0001c0001t0001g0048 a0001c0001t0001g0074 others(58): Show |
61 | HG01109.hp2 HG01258.hp1 HG01261.hp1 others(58): Show |
intron_variant | MODIFIER | c.15+24441G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68603718 | |||||||
| chr15:68603736 | G | C | 1 | a0001c0002t0001g0188 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.15+24459G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68603736 | |||||||
| chr15:68604063 | C | T | 21 | a0001c0001t0001g0228 a0001c0001t0002g0002 a0001c0001t0002g0091 others(18): Show |
21 | HG02258.hp2 HG02280.hp1 HG02486.hp2 others(18): Show |
intron_variant | MODIFIER | c.15+24786C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68604063 | |||||||
| chr15:68604090 | C | T | 24 | a0001c0001t0001g0042 a0001c0001t0001g0074 a0001c0001t0001g0228 others(21): Show |
24 | HG02258.hp2 HG02280.hp1 HG02486.hp2 others(21): Show |
intron_variant | MODIFIER | c.15+24813C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68604090 | |||||||
| chr15:68604282 | C | T | 2 | a0001c0001t0001g0175 a0001c0001t0001g0176 |
2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.15+25005C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68604282 | |||||||
| chr15:68604350 | A | G | 3 | a0001c0001t0001g0098 a0001c0001t0002g0167 a0001c0002t0002g0045 |
3 | HG01071.hp1 HG01978.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.15+25073A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68604350 | |||||||
| chr15:68604414 | C | G | 4 | a0001c0001t0002g0080 a0001c0001t0002g0081 a0001c0001t0006g0040 others(1): Show |
4 | HG02145.hp2 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+25137C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68604414 | |||||||
| chr15:68604419 | G | T | 1 | a0001c0001t0004g0112 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.15+25142G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68604419 | |||||||
| chr15:68604522 | C | T | 5 | a0001c0001t0001g0179 a0001c0001t0002g0181 a0001c0001t0004g0180 others(2): Show |
5 | HG02109.hp1 HG02451.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+25245C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68604522 | |||||||
| chr15:68604538 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.15+25261G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68604538 | |||||||
| chr15:68604619 | T | TA | 30 | a0001c0001t0001g0042 a0001c0001t0001g0074 a0001c0001t0001g0228 others(27): Show |
30 | HG02109.hp2 HG02258.hp2 HG02280.hp1 others(27): Show |
intron_variant | MODIFIER | c.15+25353dupA | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68604619 | ||||||
| chr15:68604664 | C | T | 1 | a0001c0001t0001g0048 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.15+25387C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68604664 | |||||||
| chr15:68604733 | G | T | 102 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0037 others(99): Show |
102 | HG00140.hp1 HG00621.hp2 HG00642.hp2 others(99): Show |
intron_variant | MODIFIER | c.15+25456G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68604733 | |||||||
| chr15:68604971 | A | G | 5 | a0001c0001t0004g0017 a0001c0001t0005g0015 a0001c0001t0016g0250 others(2): Show |
5 | HG02572.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+25694A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68604971 | |||||||
| chr15:68605109 | G | A | 2 | a0001c0001t0005g0046 a0001c0001t0005g0194 |
2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.15+25832G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68605109 | |||||||
| chr15:68605219 | C | T | 6 | a0001c0001t0002g0078 a0001c0001t0002g0079 a0001c0001t0011g0075 others(3): Show |
6 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+25942C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68605219 | |||||||
| chr15:68605326 | C | T | 1 | a0001c0001t0005g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.15+26049C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68605326 | |||||||
| chr15:68605346 | A | G | 49 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0037 others(46): Show |
49 | HG00140.hp1 HG00621.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.15+26069A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68605346 | |||||||
| chr15:68605378 | A | G | 16 | a0001c0001t0001g0048 a0001c0001t0001g0179 a0001c0001t0004g0077 others(13): Show |
16 | HG01109.hp2 HG02258.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.15+26101A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68605378 | |||||||
| chr15:68605380 | G | C | 1 | a0001c0003t0012g0047 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.15+26103G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68605380 | |||||||
| chr15:68605500 | C | T | 6 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0183 others(3): Show |
6 | HG00738.hp1 HG01070.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+26223C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68605500 | |||||||
| chr15:68605505 | G | A | 1 | a0001c0004t0006g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.15+26228G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68605505 | |||||||
| chr15:68605552 | C | T | 46 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0037 others(43): Show |
46 | HG00642.hp2 HG00738.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.15+26275C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68605552 | |||||||
| chr15:68605711 | G | GT | 88 | a0001c0001t0001g0010 a0001c0001t0001g0039 a0001c0001t0001g0044 others(85): Show |
88 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.15+26463dupT | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68605711 | ||||||
| chr15:68605711 | G | GTT | 29 | a0001c0001t0001g0027 a0001c0001t0001g0042 a0001c0001t0001g0052 others(26): Show |
29 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.15+26462_15+26463d others(4): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68605711 | ||||||
| chr15:68605711 | GT | G | 13 | a0001c0001t0001g0074 a0001c0001t0001g0087 a0001c0001t0001g0228 others(10): Show |
13 | HG01256.hp2 HG01891.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.15+26463delT | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68605711 | ||||||
| chr15:68605711 | GTTTTTTT others(3): Show |
G | 4 | a0001c0001t0001g0060 a0001c0001t0002g0219 a0001c0001t0002g0220 others(1): Show |
4 | HG01516.hp1 HG01517.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+26454_15+26463d others(12): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68605711 | ||||||
| chr15:68605721 | T | G | 5 | a0001c0001t0004g0216 a0001c0001t0005g0012 a0001c0001t0005g0013 others(2): Show |
5 | HG01891.hp2 HG03130.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.15+26444T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68605721 | |||||||
| chr15:68605731 | T | G | 5 | a0001c0001t0004g0216 a0001c0001t0005g0012 a0001c0001t0005g0013 others(2): Show |
5 | HG01891.hp2 HG03130.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.15+26454T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68605731 | |||||||
| chr15:68605753 | C | T | 1 | a0001c0002t0002g0099 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.15+26476C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68605753 | |||||||
| chr15:68605754 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.15+26477G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68605754 | |||||||
| chr15:68605806 | C | G | 57 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0037 others(54): Show |
57 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.15+26529C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68605806 | |||||||
| chr15:68605811 | A | G | 59 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0037 others(56): Show |
59 | HG00597.hp1 HG00621.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.15+26534A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68605811 | |||||||
| chr15:68605862 | T | C | 2 | a0001c0001t0004g0184 a0001c0001t0004g0185 |
2 | NA18949.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.15+26585T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68605862 | |||||||
| chr15:68605939 | A | T | 8 | a0001c0001t0001g0087 a0001c0001t0001g0089 a0001c0001t0001g0228 others(5): Show |
8 | HG00741.hp2 HG01256.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.15+26662A>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68605939 | |||||||
| chr15:68605956 | A | C | 58 | a0001c0001t0001g0039 a0001c0001t0001g0048 a0001c0001t0001g0065 others(55): Show |
58 | HG00642.hp2 HG00673.hp2 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.15+26679A>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68605956 | |||||||
| chr15:68605965 | T | C | 8 | a0001c0001t0001g0228 a0001c0001t0002g0002 a0001c0001t0002g0080 others(5): Show |
8 | HG02109.hp1 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.15+26688T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68605965 | |||||||
| chr15:68605966 | C | T | 8 | a0001c0001t0001g0228 a0001c0001t0002g0002 a0001c0001t0002g0080 others(5): Show |
8 | HG02109.hp1 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.15+26689C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68605966 | |||||||
| chr15:68605988 | T | C | 12 | a0001c0001t0001g0228 a0001c0001t0002g0002 a0001c0001t0002g0080 others(9): Show |
12 | HG02109.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.15+26711T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68605988 | |||||||
| chr15:68606060 | GA | G | 3 | a0001c0001t0005g0015 a0001c0001t0021g0033 a0003c0007t0006g0186 |
3 | HG02896.hp1 HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.15+26785delA | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68606060 | ||||||
| chr15:68606137 | A | G | 4 | a0001c0001t0004g0024 a0001c0001t0004g0026 a0001c0001t0005g0035 others(1): Show |
4 | HG02451.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+26860A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68606137 | |||||||
| chr15:68606200 | A | C | 11 | a0001c0001t0001g0048 a0001c0001t0002g0022 a0001c0001t0005g0029 others(8): Show |
11 | HG00741.hp2 HG01109.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.15+26923A>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68606200 | |||||||
| chr15:68606293 | G | A | 3 | a0001c0001t0005g0029 a0001c0001t0006g0031 a0001c0004t0007g0023 |
3 | HG02258.hp2 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.15+27016G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68606293 | |||||||
| chr15:68606339 | A | C | 13 | a0001c0001t0001g0042 a0001c0001t0001g0228 a0001c0001t0002g0002 others(10): Show |
13 | HG02109.hp1 HG02145.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.15+27062A>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68606339 | |||||||
| chr15:68606430 | C | G | 90 | a0001c0001t0001g0039 a0001c0001t0001g0042 a0001c0001t0001g0044 others(87): Show |
90 | HG00140.hp2 HG00597.hp1 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.15+27153C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68606430 | |||||||
| chr15:68606684 | C | A | 3 | a0001c0001t0001g0228 a0001c0001t0002g0080 a0001c0001t0002g0195 |
3 | HG02145.hp2 HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.15+27407C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68606684 | |||||||
| chr15:68606852 | C | A | 1 | a0001c0002t0002g0170 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.15+27575C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68606852 | |||||||
| chr15:68606852 | C | T | 1 | a0001c0001t0005g0208 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.15+27575C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68606852 | |||||||
| chr15:68606879 | C | A | 6 | a0001c0001t0001g0087 a0001c0001t0001g0089 a0001c0001t0001g0098 others(3): Show |
6 | HG00738.hp2 HG01192.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.15+27602C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68606879 | |||||||
| chr15:68607278 | T | C | 2 | a0001c0001t0005g0007 a0001c0002t0003g0198 |
2 | HG00280.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.15+28001T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68607278 | |||||||
| chr15:68607384 | G | A | 3 | a0001c0001t0003g0213 a0001c0002t0001g0188 a0001c0005t0003g0210 |
3 | HG00642.hp2 HG01256.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.15+28107G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68607384 | |||||||
| chr15:68607571 | A | G | 38 | a0001c0001t0001g0042 a0001c0001t0001g0048 a0001c0001t0001g0060 others(35): Show |
38 | HG00597.hp1 HG00642.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.15+28294A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68607571 | |||||||
| chr15:68607817 | C | CA | 11 | a0001c0001t0001g0228 a0001c0001t0002g0002 a0001c0001t0002g0022 others(8): Show |
11 | HG01175.hp2 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.15+28558dupA | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68607817 | ||||||
| chr15:68607817 | CA | C | 5 | a0001c0001t0001g0128 a0001c0001t0004g0129 a0001c0001t0006g0004 others(2): Show |
5 | HG02451.hp2 HG02615.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+28558delA | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68607817 | ||||||
| chr15:68607817 | CAA | C | 12 | a0001c0001t0002g0167 a0001c0001t0005g0015 a0001c0001t0005g0029 others(9): Show |
12 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.15+28557_15+28558d others(4): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68607817 | ||||||
| chr15:68607886 | A | G | 3 | a0001c0001t0004g0024 a0001c0001t0004g0026 a0001c0001t0008g0025 |
3 | HG02451.hp2 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.15+28609A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68607886 | |||||||
| chr15:68607938 | T | C | 1 | a0001c0004t0005g0233 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.15+28661T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68607938 | |||||||
| chr15:68607941 | T | G | 49 | a0001c0001t0001g0048 a0001c0001t0001g0060 a0001c0001t0001g0066 others(46): Show |
49 | HG00597.hp1 HG00642.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.15+28664T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68607941 | |||||||
| chr15:68608059 | C | T | 10 | a0001c0001t0001g0179 a0001c0001t0002g0022 a0001c0001t0004g0077 others(7): Show |
10 | HG01074.hp1 HG01175.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.15+28782C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68608059 | |||||||
| chr15:68608135 | G | A | 1 | a0001c0001t0015g0222 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.15+28858G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68608135 | |||||||
| chr15:68608349 | A | G | 1 | a0001c0001t0003g0111 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.15+29072A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68608349 | |||||||
| chr15:68608389 | G | T | 1 | a0001c0001t0006g0040 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.15+29112G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68608389 | |||||||
| chr15:68608477 | T | C | 13 | a0001c0001t0001g0048 a0001c0001t0002g0167 a0001c0001t0005g0015 others(10): Show |
13 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.15+29200T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68608477 | |||||||
| chr15:68608643 | G | A | 13 | a0001c0001t0001g0048 a0001c0001t0002g0167 a0001c0001t0005g0015 others(10): Show |
13 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.15+29366G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68608643 | |||||||
| chr15:68608655 | C | T | 5 | a0001c0001t0001g0179 a0001c0001t0004g0077 a0001c0001t0004g0180 others(2): Show |
5 | HG01074.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+29378C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68608655 | |||||||
| chr15:68608760 | A | G | 4 | a0001c0001t0004g0019 a0001c0001t0005g0194 a0001c0001t0006g0020 others(1): Show |
4 | HG02922.hp1 HG03041.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+29483A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68608760 | |||||||
| chr15:68608801 | A | G | 4 | a0001c0001t0004g0019 a0001c0001t0005g0194 a0001c0001t0006g0020 others(1): Show |
4 | HG02922.hp1 HG03041.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+29524A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68608801 | |||||||
| chr15:68608806 | G | C | 1 | a0001c0001t0002g0181 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.15+29529G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68608806 | |||||||
| chr15:68608936 | AAG | A | 36 | a0001c0001t0001g0060 a0001c0001t0001g0066 a0001c0001t0001g0095 others(33): Show |
36 | HG00597.hp1 HG00642.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.15+29672_15+29673d others(4): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68608936 | ||||||
| chr15:68609310 | G | A | 12 | a0001c0001t0001g0074 a0001c0001t0001g0087 a0001c0001t0001g0089 others(9): Show |
12 | HG00738.hp2 HG01192.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.15+30033G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68609310 | |||||||
| chr15:68609429 | G | A | 1 | a0001c0004t0005g0003 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.15+30152G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68609429 | |||||||
| chr15:68609538 | G | T | 1 | a0001c0001t0004g0110 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.15+30261G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68609538 | |||||||
| chr15:68609572 | T | C | 1 | a0001c0001t0003g0111 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.15+30295T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68609572 | |||||||
| chr15:68609578 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.15+30301G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68609578 | |||||||
| chr15:68609733 | A | G | 3 | a0001c0001t0002g0078 a0001c0001t0002g0079 a0001c0001t0005g0035 |
3 | HG02257.hp1 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.15+30456A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68609733 | |||||||
| chr15:68609746 | C | G | 4 | a0001c0001t0005g0029 a0001c0001t0006g0031 a0001c0004t0007g0023 others(1): Show |
4 | HG02258.hp2 HG02896.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+30469C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68609746 | |||||||
| chr15:68609850 | G | A | 2 | a0001c0001t0005g0046 a0001c0003t0012g0047 |
2 | HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.15+30573G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68609850 | |||||||
| chr15:68609880 | G | T | 1 | a0001c0001t0007g0162 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.15+30603G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68609880 | |||||||
| chr15:68609968 | T | C | 38 | a0001c0001t0001g0060 a0001c0001t0001g0066 a0001c0001t0001g0095 others(35): Show |
38 | HG00597.hp1 HG00642.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.15+30691T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68609968 | |||||||
| chr15:68610130 | T | C | 1 | a0001c0001t0007g0232 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.15+30853T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68610130 | |||||||
| chr15:68610248 | T | C | 2 | a0001c0001t0001g0128 a0001c0002t0003g0198 |
2 | HG01099.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.15+30971T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68610248 | |||||||
| chr15:68610260 | G | A | 15 | a0001c0001t0001g0039 a0001c0001t0001g0044 a0001c0001t0001g0052 others(12): Show |
15 | HG01346.hp2 HG02083.hp1 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.15+30983G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68610260 | |||||||
| chr15:68610341 | C | G | 1 | a0001c0001t0001g0028 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.15+31064C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68610341 | |||||||
| chr15:68610352 | C | G | 4 | a0001c0001t0001g0228 a0001c0001t0002g0080 a0001c0001t0002g0195 others(1): Show |
4 | HG02145.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+31075C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68610352 | |||||||
| chr15:68610478 | G | C | 2 | a0001c0001t0001g0108 a0001c0001t0003g0036 |
2 | HG02040.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.15+31201G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68610478 | |||||||
| chr15:68610540 | T | C | 2 | a0001c0001t0006g0236 a0001c0001t0027g0034 |
2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.15+31263T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68610540 | |||||||
| chr15:68610568 | C | T | 2 | a0001c0001t0013g0253 a0001c0001t0014g0254 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.15+31291C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68610568 | |||||||
| chr15:68610720 | A | AC | 43 | a0001c0001t0001g0060 a0001c0001t0001g0066 a0001c0001t0001g0095 others(40): Show |
43 | HG00597.hp1 HG00642.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.15+31444dupC | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68610720 | ||||||
| chr15:68610723 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.15+31446C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68610723 | |||||||
| chr15:68610928 | C | T | 9 | a0001c0001t0001g0179 a0001c0001t0002g0022 a0001c0001t0004g0077 others(6): Show |
9 | HG01074.hp1 HG01175.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.15+31651C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68610928 | |||||||
| chr15:68611070 | C | G | 43 | a0001c0001t0001g0060 a0001c0001t0001g0066 a0001c0001t0001g0095 others(40): Show |
43 | HG00597.hp1 HG00642.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.15+31793C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68611070 | |||||||
| chr15:68611070 | C | T | 1 | a0001c0001t0025g0149 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.15+31793C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68611070 | |||||||
| chr15:68611087 | C | CA | 4 | a0001c0001t0001g0228 a0001c0001t0002g0080 a0001c0001t0002g0195 others(1): Show |
4 | HG02145.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+31811dupA | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68611087 | ||||||
| chr15:68611139 | C | T | 1 | a0001c0001t0004g0024 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.15+31862C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68611139 | |||||||
| chr15:68611374 | G | C | 1 | a0001c0002t0006g0248 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.15+32097G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68611374 | |||||||
| chr15:68611465 | A | T | 1 | a0001c0001t0001g0211 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.15+32188A>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68611465 | |||||||
| chr15:68611483 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.15+32206T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68611483 | |||||||
| chr15:68611543 | T | C | 6 | a0001c0001t0001g0074 a0001c0001t0005g0012 a0001c0001t0005g0013 others(3): Show |
6 | HG01891.hp2 HG03130.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+32266T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68611543 | |||||||
| chr15:68611550 | A | G | 2 | a0001c0001t0013g0253 a0001c0001t0014g0254 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.15+32273A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68611550 | |||||||
| chr15:68611964 | T | C | 22 | a0001c0001t0001g0039 a0001c0001t0001g0042 a0001c0001t0001g0044 others(19): Show |
22 | HG01346.hp2 HG02083.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.15+32687T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68611964 | |||||||
| chr15:68612072 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.15+32795C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68612072 | |||||||
| chr15:68612104 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.15+32827G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68612104 | |||||||
| chr15:68612105 | A | T | 1 | a0001c0001t0002g0167 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.15+32828A>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68612105 | |||||||
| chr15:68612142 | G | T | 1 | a0001c0001t0003g0214 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.15+32865G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68612142 | |||||||
| chr15:68612380 | G | A | 1 | a0001c0001t0002g0167 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.16-32780G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68612380 | |||||||
| chr15:68612387 | A | C | 33 | a0001c0001t0001g0074 a0001c0001t0001g0087 a0001c0001t0001g0089 others(30): Show |
33 | HG00738.hp2 HG01070.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.16-32773A>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68612387 | |||||||
| chr15:68612423 | A | T | 2 | a0001c0001t0001g0094 a0001c0001t0004g0017 |
2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.16-32737A>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68612423 | |||||||
| chr15:68612500 | G | A | 2 | a0001c0001t0011g0075 a0001c0001t0017g0251 |
2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.16-32660G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68612500 | |||||||
| chr15:68612506 | G | C | 42 | a0001c0001t0001g0060 a0001c0001t0001g0066 a0001c0001t0001g0095 others(39): Show |
42 | HG00597.hp1 HG00642.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.16-32654G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68612506 | |||||||
| chr15:68612572 | G | C | 4 | a0001c0001t0002g0002 a0001c0001t0004g0024 a0001c0001t0004g0026 others(1): Show |
4 | HG02451.hp2 HG02572.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-32588G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68612572 | |||||||
| chr15:68612891 | T | C | 1 | a0001c0001t0002g0167 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.16-32269T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68612891 | |||||||
| chr15:68612896 | G | A | 1 | a0001c0001t0002g0091 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.16-32264G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68612896 | |||||||
| chr15:68613101 | A | G | 1 | a0001c0001t0002g0091 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.16-32059A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68613101 | |||||||
| chr15:68613157 | G | A | 1 | a0001c0002t0002g0224 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.16-32003G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68613157 | |||||||
| chr15:68613171 | C | G | 2 | a0001c0001t0013g0253 a0001c0001t0014g0254 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.16-31989C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68613171 | |||||||
| chr15:68613246 | T | C | 4 | a0001c0001t0001g0228 a0001c0001t0002g0080 a0001c0001t0002g0195 others(1): Show |
4 | HG02145.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-31914T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68613246 | |||||||
| chr15:68613404 | A | C | 1 | a0001c0001t0001g0139 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.16-31756A>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68613404 | |||||||
| chr15:68613461 | T | C | 1 | a0001c0001t0001g0204 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.16-31699T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68613461 | |||||||
| chr15:68613478 | G | T | 66 | a0001c0001t0001g0039 a0001c0001t0001g0042 a0001c0001t0001g0044 others(63): Show |
66 | HG00738.hp2 HG01074.hp1 HG01175.hp2 others(63): Show |
intron_variant | MODIFIER | c.16-31682G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68613478 | |||||||
| chr15:68613820 | T | C | 2 | a0001c0001t0005g0164 a0001c0001t0009g0238 |
2 | HG02886.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.16-31340T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68613820 | |||||||
| chr15:68614239 | G | A | 1 | a0001c0001t0005g0018 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.16-30921G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68614239 | |||||||
| chr15:68614276 | A | G | 3 | a0001c0001t0002g0078 a0001c0001t0002g0079 a0001c0001t0005g0035 |
3 | HG02257.hp1 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.16-30884A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68614276 | |||||||
| chr15:68614353 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.16-30807G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68614353 | |||||||
| chr15:68614457 | G | A | 1 | a0001c0001t0011g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.16-30703G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68614457 | |||||||
| chr15:68614549 | A | G | 30 | a0001c0001t0001g0074 a0001c0001t0001g0087 a0001c0001t0001g0089 others(27): Show |
30 | HG00738.hp2 HG01074.hp1 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.16-30611A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68614549 | |||||||
| chr15:68614802 | G | A | 1 | a0001c0001t0004g0184 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.16-30358G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68614802 | |||||||
| chr15:68614843 | G | A | 3 | a0001c0001t0005g0131 a0001c0001t0006g0021 a0001c0004t0006g0032 |
3 | HG02257.hp2 HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.16-30317G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68614843 | |||||||
| chr15:68615040 | A | G | 3 | a0001c0001t0002g0078 a0001c0001t0002g0079 a0001c0001t0005g0035 |
3 | HG02257.hp1 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.16-30120A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68615040 | |||||||
| chr15:68615160 | C | T | 1 | a0001c0001t0016g0250 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.16-30000C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68615160 | |||||||
| chr15:68615474 | G | A | 4 | a0001c0001t0001g0042 a0001c0001t0002g0081 a0001c0001t0008g0001 others(1): Show |
4 | HG02451.hp1 HG02559.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-29686G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68615474 | |||||||
| chr15:68615492 | A | G | 1 | a0001c0001t0003g0127 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.16-29668A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68615492 | |||||||
| chr15:68615595 | G | C | 5 | a0001c0001t0005g0164 a0001c0001t0006g0004 a0001c0001t0006g0237 others(2): Show |
5 | HG01109.hp2 HG02818.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-29565G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68615595 | |||||||
| chr15:68615768 | C | T | 1 | a0001c0001t0002g0167 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.16-29392C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68615768 | |||||||
| chr15:68615806 | C | A | 1 | a0001c0001t0001g0098 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.16-29354C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68615806 | |||||||
| chr15:68615833 | T | C | 1 | a0001c0001t0021g0033 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.16-29327T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68615833 | |||||||
| chr15:68615890 | A | G | 9 | a0001c0001t0002g0078 a0001c0001t0002g0079 a0001c0001t0002g0091 others(6): Show |
9 | HG01109.hp2 HG02257.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.16-29270A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68615890 | |||||||
| chr15:68615945 | T | C | 10 | a0001c0001t0002g0078 a0001c0001t0002g0079 a0001c0001t0002g0091 others(7): Show |
10 | HG01109.hp2 HG02257.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.16-29215T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68615945 | |||||||
| chr15:68615997 | C | G | 72 | a0001c0001t0001g0039 a0001c0001t0001g0042 a0001c0001t0001g0044 others(69): Show |
72 | HG00738.hp2 HG01070.hp2 HG01071.hp2 others(69): Show |
intron_variant | MODIFIER | c.16-29163C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68615997 | |||||||
| chr15:68616122 | C | G | 1 | a0001c0001t0021g0033 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.16-29038C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68616122 | |||||||
| chr15:68616157 | A | T | 1 | a0001c0001t0007g0232 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.16-29003A>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68616157 | |||||||
| chr15:68616193 | G | A | 6 | a0001c0001t0001g0100 a0001c0001t0001g0215 a0001c0001t0002g0096 others(3): Show |
6 | HG00140.hp1 HG00735.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.16-28967G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68616193 | |||||||
| chr15:68616199 | A | G | 2 | a0001c0001t0002g0078 a0001c0001t0002g0079 |
2 | HG02257.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.16-28961A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68616199 | |||||||
| chr15:68616203 | C | T | 4 | a0001c0001t0001g0228 a0001c0001t0002g0080 a0001c0001t0002g0195 others(1): Show |
4 | HG02145.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-28957C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68616203 | |||||||
| chr15:68616224 | G | T | 1 | a0001c0001t0004g0185 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.16-28936G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68616224 | |||||||
| chr15:68616498 | A | G | 3 | a0001c0001t0001g0192 a0001c0001t0003g0082 a0001c0001t0003g0239 |
3 | HG02135.hp1 HG02135.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.16-28662A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68616498 | |||||||
| chr15:68616563 | G | T | 9 | a0001c0001t0002g0078 a0001c0001t0002g0079 a0001c0001t0002g0091 others(6): Show |
9 | HG01109.hp2 HG02257.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.16-28597G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68616563 | |||||||
| chr15:68616596 | C | T | 9 | a0001c0001t0001g0048 a0001c0001t0004g0229 a0001c0001t0005g0015 others(6): Show |
9 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.16-28564C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68616596 | |||||||
| chr15:68616648 | C | T | 1 | a0002c0008t0002g0093 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.16-28512C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68616648 | |||||||
| chr15:68616706 | T | C | 9 | a0001c0001t0002g0078 a0001c0001t0002g0079 a0001c0001t0002g0167 others(6): Show |
9 | HG01109.hp2 HG02257.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.16-28454T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68616706 | |||||||
| chr15:68616781 | A | AG | 9 | a0001c0001t0002g0078 a0001c0001t0002g0079 a0001c0001t0002g0167 others(6): Show |
9 | HG01109.hp2 HG02257.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.16-28377dupG | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68616781 | ||||||
| chr15:68616908 | T | G | 2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.16-28252T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68616908 | |||||||
| chr15:68617068 | G | T | 5 | a0001c0001t0001g0044 a0001c0001t0001g0168 a0001c0001t0001g0169 others(2): Show |
5 | HG02735.hp1 HG03490.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.16-28092G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68617068 | |||||||
| chr15:68617109 | G | A | 1 | a0001c0001t0002g0091 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.16-28051G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68617109 | |||||||
| chr15:68617135 | C | G | 5 | a0001c0001t0005g0164 a0001c0001t0006g0004 a0001c0001t0006g0237 others(2): Show |
5 | HG01109.hp2 HG02818.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-28025C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68617135 | |||||||
| chr15:68617157 | T | G | 1 | a0001c0001t0001g0159 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.16-28003T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68617157 | |||||||
| chr15:68617161 | G | A | 1 | a0001c0001t0005g0012 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.16-27999G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68617161 | |||||||
| chr15:68617176 | T | C | 9 | a0001c0001t0002g0078 a0001c0001t0002g0079 a0001c0001t0002g0167 others(6): Show |
9 | HG01109.hp2 HG02257.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.16-27984T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68617176 | |||||||
| chr15:68617181 | T | C | 9 | a0001c0001t0002g0078 a0001c0001t0002g0079 a0001c0001t0002g0167 others(6): Show |
9 | HG01109.hp2 HG02257.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.16-27979T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68617181 | |||||||
| chr15:68617709 | G | A | 3 | a0001c0001t0002g0078 a0001c0001t0002g0079 a0001c0001t0005g0035 |
3 | HG02257.hp1 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.16-27451G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68617709 | |||||||
| chr15:68617983 | C | G | 1 | a0001c0001t0003g0062 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.16-27177C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68617983 | |||||||
| chr15:68618141 | C | T | 1 | a0001c0001t0004g0216 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.16-27019C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68618141 | |||||||
| chr15:68618184 | G | A | 3 | a0001c0001t0005g0131 a0001c0001t0006g0021 a0001c0004t0006g0032 |
3 | HG02257.hp2 HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.16-26976G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68618184 | |||||||
| chr15:68618320 | G | A | 3 | a0001c0001t0002g0078 a0001c0001t0002g0079 a0001c0001t0005g0035 |
3 | HG02257.hp1 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.16-26840G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68618320 | |||||||
| chr15:68618348 | A | G | 3 | a0001c0001t0002g0078 a0001c0001t0002g0079 a0001c0001t0005g0035 |
3 | HG02257.hp1 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.16-26812A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68618348 | |||||||
| chr15:68618532 | T | C | 1 | a0001c0001t0002g0167 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.16-26628T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68618532 | |||||||
| chr15:68618787 | A | G | 3 | a0001c0001t0002g0078 a0001c0001t0002g0079 a0001c0001t0005g0035 |
3 | HG02257.hp1 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.16-26373A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68618787 | |||||||
| chr15:68618999 | G | A | 1 | a0001c0004t0006g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.16-26161G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68618999 | |||||||
| chr15:68619213 | G | T | 1 | a0001c0002t0006g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.16-25947G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68619213 | |||||||
| chr15:68619472 | C | T | 4 | a0001c0001t0001g0228 a0001c0001t0002g0080 a0001c0001t0002g0195 others(1): Show |
4 | HG02145.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-25688C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68619472 | |||||||
| chr15:68619539 | A | G | 16 | a0001c0001t0001g0074 a0001c0001t0001g0087 a0001c0001t0001g0089 others(13): Show |
16 | HG00738.hp2 HG01070.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.16-25621A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68619539 | |||||||
| chr15:68619707 | G | T | 1 | a0001c0001t0010g0252 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.16-25453G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68619707 | |||||||
| chr15:68619747 | G | T | 32 | a0001c0001t0001g0074 a0001c0001t0001g0087 a0001c0001t0001g0089 others(29): Show |
32 | HG00738.hp2 HG01070.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.16-25413G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68619747 | |||||||
| chr15:68619754 | C | CGT | 23 | a0001c0001t0001g0039 a0001c0001t0001g0042 a0001c0001t0001g0044 others(20): Show |
23 | HG01109.hp2 HG01346.hp2 HG02083.hp1 others(20): Show |
intron_variant | MODIFIER | c.16-25394_16-25393d others(4): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68619754 | ||||||
| chr15:68619771 | G | A | 2 | a0001c0001t0007g0193 a0001c0003t0006g0145 |
2 | HG02145.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.16-25389G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68619771 | |||||||
| chr15:68619944 | C | T | 1 | a0001c0001t0002g0091 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.16-25216C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68619944 | |||||||
| chr15:68619969 | T | A | 2 | a0001c0001t0002g0219 a0001c0001t0002g0220 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.16-25191T>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68619969 | |||||||
| chr15:68620033 | T | C | 1 | a0001c0001t0002g0167 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.16-25127T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68620033 | |||||||
| chr15:68620086 | A | AT | 3 | a0001c0001t0001g0042 a0001c0001t0002g0081 a0001c0001t0008g0001 |
3 | HG02559.hp2 HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.16-25069dupT | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68620086 | ||||||
| chr15:68620599 | G | A | 1 | a0001c0001t0002g0167 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.16-24561G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68620599 | |||||||
| chr15:68620639 | T | G | 4 | a0001c0001t0005g0164 a0001c0001t0006g0004 a0001c0001t0006g0237 others(1): Show |
4 | HG01109.hp2 HG02886.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-24521T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68620639 | |||||||
| chr15:68620788 | T | C | 1 | a0001c0001t0002g0167 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.16-24372T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68620788 | |||||||
| chr15:68620816 | T | C | 1 | a0001c0001t0002g0167 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.16-24344T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68620816 | |||||||
| chr15:68621077 | A | G | 4 | a0001c0001t0001g0042 a0001c0001t0002g0081 a0001c0001t0008g0001 others(1): Show |
4 | HG02451.hp1 HG02559.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-24083A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68621077 | |||||||
| chr15:68621131 | G | A | 1 | a0001c0002t0003g0256 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.16-24029G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68621131 | |||||||
| chr15:68621152 | G | A | 5 | a0001c0001t0002g0002 a0001c0001t0002g0091 a0001c0001t0004g0024 others(2): Show |
5 | HG02451.hp2 HG02572.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.16-24008G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68621152 | |||||||
| chr15:68621164 | G | A | 1 | a0001c0002t0006g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.16-23996G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68621164 | |||||||
| chr15:68621164 | G | T | 1 | a0001c0001t0002g0167 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.16-23996G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68621164 | |||||||
| chr15:68621177 | C | T | 1 | a0001c0001t0002g0167 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.16-23983C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68621177 | |||||||
| chr15:68621268 | A | G | 1 | a0001c0001t0002g0002 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.16-23892A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68621268 | |||||||
| chr15:68621331 | G | T | 1 | a0001c0002t0006g0248 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.16-23829G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68621331 | |||||||
| chr15:68621353 | C | T | 1 | a0001c0001t0004g0092 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.16-23807C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68621353 | |||||||
| chr15:68621360 | G | C | 1 | a0001c0001t0001g0085 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.16-23800G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68621360 | |||||||
| chr15:68621404 | C | T | 9 | a0001c0001t0001g0048 a0001c0001t0004g0229 a0001c0001t0005g0015 others(6): Show |
9 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.16-23756C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68621404 | |||||||
| chr15:68621466 | G | A | 9 | a0001c0001t0001g0048 a0001c0001t0004g0229 a0001c0001t0005g0015 others(6): Show |
9 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.16-23694G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68621466 | |||||||
| chr15:68621593 | T | C | 1 | a0001c0001t0003g0059 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.16-23567T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68621593 | |||||||
| chr15:68621743 | C | T | 1 | a0001c0001t0002g0167 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.16-23417C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68621743 | |||||||
| chr15:68621767 | C | CT | 55 | a0001c0001t0001g0039 a0001c0001t0001g0044 a0001c0001t0001g0052 others(52): Show |
55 | HG00597.hp1 HG00642.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.16-23376dupT | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68621767 | ||||||
| chr15:68621767 | CT | C | 17 | a0001c0001t0001g0037 a0001c0001t0001g0048 a0001c0001t0001g0087 others(14): Show |
17 | HG01070.hp2 HG01256.hp1 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.16-23376delT | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68621767 | ||||||
| chr15:68621864 | C | G | 13 | a0001c0001t0001g0048 a0001c0001t0004g0229 a0001c0001t0005g0015 others(10): Show |
13 | HG01109.hp2 HG02109.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.16-23296C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68621864 | |||||||
| chr15:68622126 | G | A | 1 | a0001c0001t0004g0216 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.16-23034G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68622126 | |||||||
| chr15:68622145 | C | T | 10 | a0001c0001t0001g0179 a0001c0001t0002g0022 a0001c0001t0004g0077 others(7): Show |
10 | HG01074.hp1 HG01175.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.16-23015C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68622145 | |||||||
| chr15:68622204 | C | T | 17 | a0001c0001t0001g0074 a0001c0001t0001g0087 a0001c0001t0001g0089 others(14): Show |
17 | HG00738.hp2 HG01192.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.16-22956C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68622204 | |||||||
| chr15:68622469 | G | A | 10 | a0001c0001t0001g0179 a0001c0001t0002g0022 a0001c0001t0004g0077 others(7): Show |
10 | HG01074.hp1 HG01175.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.16-22691G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68622469 | |||||||
| chr15:68622667 | C | A | 9 | a0001c0001t0001g0048 a0001c0001t0004g0229 a0001c0001t0005g0015 others(6): Show |
9 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.16-22493C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68622667 | |||||||
| chr15:68622762 | CA | C | 9 | a0001c0001t0001g0048 a0001c0001t0004g0229 a0001c0001t0005g0015 others(6): Show |
9 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.16-22397delA | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68622762 | |||||||
| chr15:68622785 | A | G | 1 | a0001c0001t0003g0127 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.16-22375A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68622785 | |||||||
| chr15:68622824 | C | T | 10 | a0001c0001t0001g0048 a0001c0001t0002g0167 a0001c0001t0004g0229 others(7): Show |
10 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.16-22336C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68622824 | |||||||
| chr15:68623047 | C | A | 1 | a0001c0001t0002g0167 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.16-22113C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68623047 | |||||||
| chr15:68623186 | A | C | 2 | a0001c0001t0003g0158 a0001c0001t0004g0058 |
2 | NA18975.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.16-21974A>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68623186 | |||||||
| chr15:68623329 | G | A | 5 | a0001c0001t0001g0094 a0001c0001t0004g0017 a0001c0001t0004g0141 others(2): Show |
5 | HG02886.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-21831G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68623329 | |||||||
| chr15:68623379 | T | C | 1 | a0001c0001t0002g0167 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.16-21781T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68623379 | |||||||
| chr15:68623418 | G | T | 1 | a0001c0001t0002g0167 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.16-21742G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68623418 | |||||||
| chr15:68623440 | A | C | 1 | a0001c0001t0002g0167 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.16-21720A>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68623440 | |||||||
| chr15:68623471 | C | T | 1 | a0001c0002t0001g0006 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.16-21689C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68623471 | |||||||
| chr15:68623542 | C | T | 9 | a0001c0001t0001g0179 a0001c0001t0002g0022 a0001c0001t0004g0077 others(6): Show |
9 | HG01074.hp1 HG01175.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.16-21618C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68623542 | |||||||
| chr15:68623558 | A | G | 2 | a0001c0001t0004g0117 a0001c0001t0005g0113 |
2 | HG03239.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.16-21602A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68623558 | |||||||
| chr15:68623577 | G | A | 2 | a0001c0001t0003g0163 a0001c0001t0003g0214 |
2 | HG03017.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.16-21583G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68623577 | |||||||
| chr15:68623747 | C | T | 37 | a0001c0001t0001g0060 a0001c0001t0001g0066 a0001c0001t0001g0095 others(34): Show |
37 | HG00597.hp1 HG00642.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.16-21413C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68623747 | |||||||
| chr15:68623822 | T | C | 1 | a0001c0002t0002g0224 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.16-21338T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68623822 | |||||||
| chr15:68623888 | G | A | 9 | a0001c0001t0001g0048 a0001c0001t0004g0229 a0001c0001t0005g0015 others(6): Show |
9 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.16-21272G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68623888 | |||||||
| chr15:68624271 | C | T | 1 | a0001c0001t0005g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.16-20889C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68624271 | |||||||
| chr15:68624272 | G | A | 2 | a0001c0005t0002g0043 a0001c0005t0003g0130 |
2 | HG00741.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.16-20888G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68624272 | |||||||
| chr15:68624388 | C | T | 1 | a0001c0001t0004g0129 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.16-20772C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68624388 | |||||||
| chr15:68624425 | G | A | 3 | a0001c0001t0002g0148 a0001c0001t0004g0207 a0001c0002t0003g0107 |
3 | NA18947.hp2 NA19012.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.16-20735G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68624425 | |||||||
| chr15:68624610 | A | G | 1 | a0001c0001t0001g0128 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.16-20550A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68624610 | |||||||
| chr15:68624616 | T | C | 9 | a0001c0001t0001g0048 a0001c0001t0004g0229 a0001c0001t0005g0015 others(6): Show |
9 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.16-20544T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68624616 | |||||||
| chr15:68624680 | TTTTTTC | T | 9 | a0001c0001t0001g0048 a0001c0001t0004g0229 a0001c0001t0005g0015 others(6): Show |
9 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.16-20475_16-20470d others(8): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68624680 | ||||||
| chr15:68624719 | G | C | 4 | a0001c0001t0001g0042 a0001c0001t0002g0081 a0001c0001t0008g0001 others(1): Show |
4 | HG02451.hp1 HG02559.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-20441G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68624719 | |||||||
| chr15:68624793 | T | C | 70 | a0001c0001t0001g0039 a0001c0001t0001g0042 a0001c0001t0001g0044 others(67): Show |
70 | HG00738.hp2 HG01070.hp2 HG01071.hp2 others(67): Show |
intron_variant | MODIFIER | c.16-20367T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68624793 | |||||||
| chr15:68624824 | G | A | 10 | a0001c0001t0001g0048 a0001c0001t0002g0167 a0001c0001t0004g0229 others(7): Show |
10 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.16-20336G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68624824 | |||||||
| chr15:68624903 | G | A | 4 | a0001c0001t0005g0164 a0001c0001t0006g0004 a0001c0001t0006g0237 others(1): Show |
4 | HG01109.hp2 HG02886.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-20257G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68624903 | |||||||
| chr15:68625256 | C | T | 3 | a0001c0001t0002g0234 a0001c0001t0003g0235 a0001c0002t0002g0224 |
3 | NA18944.hp2 NA18960.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.16-19904C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68625256 | |||||||
| chr15:68625270 | A | AT | 29 | a0001c0001t0001g0039 a0001c0001t0001g0042 a0001c0001t0001g0044 others(26): Show |
29 | HG01109.hp2 HG01258.hp1 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.16-19879dupT | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68625270 | ||||||
| chr15:68625270 | AT | A | 10 | a0001c0001t0001g0048 a0001c0001t0004g0229 a0001c0001t0005g0015 others(7): Show |
10 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.16-19879delT | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68625270 | ||||||
| chr15:68625295 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.16-19865C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68625295 | |||||||
| chr15:68625308 | AC | A | 32 | a0001c0001t0001g0074 a0001c0001t0001g0087 a0001c0001t0001g0089 others(29): Show |
32 | HG00738.hp2 HG01070.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.16-19851delC | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68625308 | |||||||
| chr15:68625323 | AC | A | 4 | a0001c0001t0002g0091 a0001c0001t0004g0024 a0001c0001t0004g0026 others(1): Show |
4 | HG02451.hp2 HG02717.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-19836delC | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68625323 | |||||||
| chr15:68625574 | C | A | 1 | a0001c0001t0001g0144 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.16-19586C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68625574 | |||||||
| chr15:68625730 | A | G | 16 | a0001c0001t0001g0039 a0001c0001t0001g0044 a0001c0001t0001g0052 others(13): Show |
16 | HG01346.hp2 HG02083.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.16-19430A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68625730 | |||||||
| chr15:68625852 | C | G | 38 | a0001c0001t0001g0060 a0001c0001t0001g0066 a0001c0001t0001g0095 others(35): Show |
38 | HG00597.hp1 HG00642.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.16-19308C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68625852 | |||||||
| chr15:68625875 | G | A | 1 | a0001c0001t0006g0218 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.16-19285G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68625875 | |||||||
| chr15:68626150 | T | A | 9 | a0001c0001t0001g0048 a0001c0001t0004g0229 a0001c0001t0005g0015 others(6): Show |
9 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.16-19010T>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68626150 | |||||||
| chr15:68626232 | G | A | 9 | a0001c0001t0001g0048 a0001c0001t0004g0229 a0001c0001t0005g0015 others(6): Show |
9 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.16-18928G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68626232 | |||||||
| chr15:68626359 | T | G | 13 | a0001c0001t0001g0048 a0001c0001t0002g0091 a0001c0001t0004g0024 others(10): Show |
13 | HG02109.hp2 HG02280.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.16-18801T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68626359 | |||||||
| chr15:68626572 | G | A | 15 | a0001c0001t0001g0039 a0001c0001t0001g0044 a0001c0001t0001g0052 others(12): Show |
15 | HG01346.hp2 HG02083.hp1 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.16-18588G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68626572 | |||||||
| chr15:68626763 | G | A | 4 | a0001c0001t0005g0164 a0001c0001t0006g0004 a0001c0001t0006g0237 others(1): Show |
4 | HG01109.hp2 HG02886.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-18397G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68626763 | |||||||
| chr15:68626982 | G | A | 37 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0037 others(34): Show |
37 | HG00280.hp2 HG00408.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.16-18178G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68626982 | |||||||
| chr15:68626987 | G | A | 1 | a0001c0001t0027g0034 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.16-18173G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68626987 | |||||||
| chr15:68627076 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.16-18084C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68627076 | |||||||
| chr15:68627086 | A | G | 1 | a0001c0003t0008g0178 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.16-18074A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68627086 | |||||||
| chr15:68627152 | T | C | 2 | a0001c0003t0008g0178 a0001c0004t0005g0003 |
2 | HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.16-18008T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68627152 | |||||||
| chr15:68627237 | G | T | 1 | a0001c0003t0008g0178 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.16-17923G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68627237 | |||||||
| chr15:68627248 | G | A | 1 | a0001c0001t0005g0015 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.16-17912G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68627248 | |||||||
| chr15:68627311 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.16-17849C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68627311 | |||||||
| chr15:68627370 | G | T | 1 | a0001c0001t0005g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.16-17790G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68627370 | |||||||
| chr15:68627399 | C | G | 46 | a0001c0001t0001g0060 a0001c0001t0001g0066 a0001c0001t0001g0095 others(43): Show |
46 | HG00597.hp1 HG00642.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.16-17761C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68627399 | |||||||
| chr15:68627519 | G | A | 23 | a0001c0001t0001g0074 a0001c0001t0001g0087 a0001c0001t0001g0089 others(20): Show |
23 | HG00738.hp2 HG01070.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.16-17641G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68627519 | |||||||
| chr15:68627681 | A | G | 2 | a0001c0001t0005g0046 a0001c0003t0012g0047 |
2 | HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.16-17479A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68627681 | |||||||
| chr15:68627805 | T | C | 107 | a0001c0001t0001g0039 a0001c0001t0001g0042 a0001c0001t0001g0044 others(104): Show |
107 | HG00597.hp1 HG00642.hp1 HG00673.hp1 others(104): Show |
intron_variant | MODIFIER | c.16-17355T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68627805 | |||||||
| chr15:68627853 | C | T | 1 | a0001c0001t0007g0232 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.16-17307C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68627853 | |||||||
| chr15:68627886 | A | AG | 3 | a0001c0001t0004g0024 a0001c0001t0004g0026 a0001c0001t0008g0025 |
3 | HG02451.hp2 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.16-17274_16-17273i others(3): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68627886 | |||||||
| chr15:68628094 | G | A | 3 | a0001c0001t0005g0164 a0001c0001t0006g0004 a0001c0001t0006g0237 |
3 | HG01109.hp2 HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.16-17066G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68628094 | |||||||
| chr15:68628110 | A | G | 1 | a0001c0001t0006g0237 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.16-17050A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68628110 | |||||||
| chr15:68628229 | G | A | 100 | a0001c0001t0001g0039 a0001c0001t0001g0042 a0001c0001t0001g0044 others(97): Show |
100 | HG00597.hp1 HG00642.hp1 HG00673.hp1 others(97): Show |
intron_variant | MODIFIER | c.16-16931G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68628229 | |||||||
| chr15:68628391 | G | A | 4 | a0001c0001t0001g0087 a0001c0001t0001g0089 a0001c0002t0001g0069 others(1): Show |
4 | HG00738.hp2 HG01243.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-16769G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68628391 | |||||||
| chr15:68628550 | T | C | 1 | a0001c0001t0002g0221 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.16-16610T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68628550 | |||||||
| chr15:68628707 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.16-16453A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68628707 | |||||||
| chr15:68628740 | T | A | 1 | a0001c0001t0003g0154 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.16-16420T>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68628740 | |||||||
| chr15:68628865 | A | C | 2 | a0001c0003t0008g0178 a0001c0004t0005g0003 |
2 | HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.16-16295A>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68628865 | |||||||
| chr15:68628879 | C | A | 7 | a0001c0001t0001g0179 a0001c0001t0002g0022 a0001c0001t0004g0180 others(4): Show |
7 | HG01175.hp2 HG02258.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.16-16281C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68628879 | |||||||
| chr15:68629088 | G | T | 24 | a0001c0001t0001g0039 a0001c0001t0001g0044 a0001c0001t0001g0052 others(21): Show |
24 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.16-16072G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68629088 | |||||||
| chr15:68629117 | C | T | 1 | a0001c0001t0010g0249 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.16-16043C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68629117 | |||||||
| chr15:68629185 | C | G | 109 | a0001c0001t0001g0039 a0001c0001t0001g0042 a0001c0001t0001g0044 others(106): Show |
109 | HG00597.hp1 HG00642.hp1 HG00673.hp1 others(106): Show |
intron_variant | MODIFIER | c.16-15975C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68629185 | |||||||
| chr15:68629395 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.16-15765C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68629395 | |||||||
| chr15:68629612 | G | A | 1 | a0001c0001t0005g0073 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.16-15548G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68629612 | |||||||
| chr15:68629613 | G | A | 1 | a0001c0002t0002g0038 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.16-15547G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68629613 | |||||||
| chr15:68629677 | G | A | 17 | a0001c0001t0001g0039 a0001c0001t0001g0044 a0001c0001t0001g0052 others(14): Show |
17 | HG00642.hp1 HG01346.hp2 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.16-15483G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68629677 | |||||||
| chr15:68629709 | G | A | 5 | a0001c0002t0001g0206 a0001c0002t0002g0045 a0001c0005t0002g0043 others(2): Show |
5 | HG00741.hp1 HG01071.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-15451G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68629709 | |||||||
| chr15:68629826 | G | A | 109 | a0001c0001t0001g0039 a0001c0001t0001g0042 a0001c0001t0001g0044 others(106): Show |
109 | HG00597.hp1 HG00642.hp1 HG00673.hp1 others(106): Show |
intron_variant | MODIFIER | c.16-15334G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68629826 | |||||||
| chr15:68629911 | T | A | 25 | a0001c0001t0001g0074 a0001c0001t0001g0087 a0001c0001t0001g0089 others(22): Show |
25 | HG00738.hp2 HG01070.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.16-15249T>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68629911 | |||||||
| chr15:68629966 | G | A | 7 | a0001c0001t0001g0228 a0001c0001t0002g0080 a0001c0001t0002g0195 others(4): Show |
7 | HG02145.hp2 HG02615.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.16-15194G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68629966 | |||||||
| chr15:68630081 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.16-15079G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68630081 | |||||||
| chr15:68630113 | T | C | 1 | a0001c0001t0004g0112 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.16-15047T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68630113 | |||||||
| chr15:68630138 | C | T | 64 | a0001c0001t0001g0039 a0001c0001t0001g0044 a0001c0001t0001g0052 others(61): Show |
64 | HG00597.hp1 HG00642.hp1 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.16-15022C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68630138 | |||||||
| chr15:68630231 | G | A | 3 | a0001c0001t0002g0078 a0001c0001t0002g0079 a0001c0001t0005g0035 |
3 | HG02257.hp1 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.16-14929G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68630231 | |||||||
| chr15:68630278 | A | G | 1 | a0001c0003t0008g0178 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.16-14882A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68630278 | |||||||
| chr15:68630281 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.16-14879G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68630281 | |||||||
| chr15:68630422 | G | GT | 70 | a0001c0001t0001g0039 a0001c0001t0001g0044 a0001c0001t0001g0048 others(67): Show |
70 | HG00642.hp1 HG00738.hp2 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.16-14728dupT | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68630422 | ||||||
| chr15:68630422 | G | GTT | 40 | a0001c0001t0001g0060 a0001c0001t0001g0066 a0001c0001t0001g0095 others(37): Show |
40 | HG00597.hp1 HG00673.hp1 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.16-14729_16-14728d others(4): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68630422 | ||||||
| chr15:68630871 | G | C | 112 | a0001c0001t0001g0039 a0001c0001t0001g0042 a0001c0001t0001g0044 others(109): Show |
112 | HG00597.hp1 HG00642.hp1 HG00673.hp1 others(109): Show |
intron_variant | MODIFIER | c.16-14289G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68630871 | |||||||
| chr15:68630889 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.16-14271C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68630889 | |||||||
| chr15:68630901 | A | G | 2 | a0001c0001t0005g0035 a0001c0003t0006g0145 |
2 | HG02145.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.16-14259A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68630901 | |||||||
| chr15:68631061 | C | T | 2 | a0001c0001t0009g0238 a0001c0004t0007g0023 |
2 | NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.16-14099C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68631061 | |||||||
| chr15:68631199 | C | G | 10 | a0001c0001t0001g0132 a0001c0001t0002g0135 a0001c0001t0004g0216 others(7): Show |
10 | HG02809.hp1 HG03041.hp1 HG03130.hp2 others(7): Show |
intron_variant | MODIFIER | c.16-13961C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68631199 | |||||||
| chr15:68631201 | A | G | 37 | a0001c0001t0001g0048 a0001c0001t0001g0074 a0001c0001t0001g0087 others(34): Show |
37 | HG00738.hp2 HG01070.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.16-13959A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68631201 | |||||||
| chr15:68631222 | C | T | 1 | a0001c0001t0004g0092 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.16-13938C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68631222 | |||||||
| chr15:68631334 | G | A | 1 | a0001c0001t0010g0249 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.16-13826G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68631334 | |||||||
| chr15:68631355 | T | G | 1 | a0001c0003t0008g0178 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.16-13805T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68631355 | |||||||
| chr15:68631478 | C | T | 1 | a0001c0003t0006g0145 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.16-13682C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68631478 | |||||||
| chr15:68631514 | C | G | 1 | a0001c0001t0005g0015 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.16-13646C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68631514 | |||||||
| chr15:68631613 | G | C | 2 | a0001c0001t0001g0074 a0001c0001t0005g0018 |
2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.16-13547G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68631613 | |||||||
| chr15:68631691 | T | G | 114 | a0001c0001t0001g0039 a0001c0001t0001g0042 a0001c0001t0001g0044 others(111): Show |
114 | HG00597.hp1 HG00642.hp1 HG00673.hp1 others(111): Show |
intron_variant | MODIFIER | c.16-13469T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68631691 | |||||||
| chr15:68631775 | C | T | 1 | a0001c0002t0002g0038 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.16-13385C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68631775 | |||||||
| chr15:68631869 | G | A | 2 | a0001c0001t0004g0026 a0001c0001t0008g0025 |
2 | HG02451.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.16-13291G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68631869 | |||||||
| chr15:68631985 | G | A | 16 | a0001c0001t0001g0039 a0001c0001t0001g0044 a0001c0001t0001g0052 others(13): Show |
16 | HG00642.hp1 HG01346.hp2 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.16-13175G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68631985 | |||||||
| chr15:68632101 | A | G | 39 | a0001c0001t0001g0060 a0001c0001t0001g0066 a0001c0001t0001g0095 others(36): Show |
39 | HG00597.hp1 HG00673.hp1 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.16-13059A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68632101 | |||||||
| chr15:68632229 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.16-12931C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68632229 | |||||||
| chr15:68632371 | T | A | 1 | a0001c0001t0002g0091 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.16-12789T>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68632371 | |||||||
| chr15:68632624 | T | C | 1 | a0001c0002t0005g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.16-12536T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68632624 | |||||||
| chr15:68632739 | C | T | 101 | a0001c0001t0001g0039 a0001c0001t0001g0042 a0001c0001t0001g0044 others(98): Show |
101 | HG00597.hp1 HG00642.hp1 HG00673.hp1 others(98): Show |
intron_variant | MODIFIER | c.16-12421C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68632739 | |||||||
| chr15:68632838 | C | T | 1 | a0001c0001t0004g0019 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.16-12322C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68632838 | |||||||
| chr15:68632893 | A | G | 1 | a0001c0001t0005g0018 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.16-12267A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68632893 | |||||||
| chr15:68633186 | T | C | 64 | a0001c0001t0001g0039 a0001c0001t0001g0042 a0001c0001t0001g0044 others(61): Show |
64 | HG00140.hp2 HG00642.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.16-11974T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68633186 | |||||||
| chr15:68633367 | G | A | 1 | a0001c0001t0004g0017 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.16-11793G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68633367 | |||||||
| chr15:68633442 | G | A | 14 | a0001c0001t0001g0048 a0001c0001t0001g0159 a0001c0001t0001g0228 others(11): Show |
14 | HG02074.hp2 HG02083.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.16-11718G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68633442 | |||||||
| chr15:68633514 | T | TAC | 3 | a0001c0001t0001g0212 a0001c0001t0002g0241 a0001c0001t0006g0191 |
3 | HG01433.hp2 HG02004.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.16-11615_16-11614d others(4): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68633514 | ||||||
| chr15:68633514 | T | TACAC | 7 | a0001c0001t0002g0080 a0001c0001t0002g0081 a0001c0001t0003g0059 others(4): Show |
7 | HG02080.hp2 HG02145.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.16-11617_16-11614d others(6): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68633514 | ||||||
| chr15:68633514 | T | TACACAC | 6 | a0001c0001t0001g0189 a0001c0001t0004g0017 a0001c0001t0005g0194 others(3): Show |
6 | HG00621.hp1 HG00642.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.16-11619_16-11614d others(8): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68633514 | ||||||
| chr15:68633514 | T | TACACACA others(1): Show |
11 | a0001c0001t0001g0179 a0001c0001t0002g0078 a0001c0001t0002g0079 others(8): Show |
11 | HG00741.hp2 HG01496.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.16-11621_16-11614d others(10): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68633514 | ||||||
| chr15:68633514 | T | TACACACA others(3): Show |
97 | a0001c0001t0001g0010 a0001c0001t0001g0039 a0001c0001t0001g0048 others(94): Show |
97 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.16-11623_16-11614d others(12): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68633514 | ||||||
| chr15:68633514 | T | TACACACA others(5): Show |
27 | a0001c0001t0001g0044 a0001c0001t0001g0133 a0001c0001t0001g0168 others(24): Show |
27 | HG01074.hp1 HG01891.hp2 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.16-11625_16-11614d others(14): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68633514 | ||||||
| chr15:68633514 | T | TACACACA others(7): Show |
13 | a0001c0001t0001g0095 a0001c0001t0002g0022 a0001c0001t0003g0111 others(10): Show |
13 | HG01361.hp2 HG02083.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.16-11627_16-11614d others(16): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68633514 | ||||||
| chr15:68633514 | T | TACACACA others(9): Show |
3 | a0001c0001t0001g0115 a0001c0001t0002g0121 a0001c0001t0004g0180 |
3 | HG03540.hp2 HG04204.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.16-11629_16-11614d others(18): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68633514 | ||||||
| chr15:68633514 | T | TACACACA others(13): Show |
2 | a0001c0001t0001g0074 a0001c0003t0001g0057 |
2 | HG02109.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.16-11633_16-11614d others(22): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68633514 | ||||||
| chr15:68633514 | TAC | T | 8 | a0001c0001t0001g0042 a0001c0001t0005g0015 a0001c0001t0005g0046 others(5): Show |
8 | HG01099.hp2 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.16-11615_16-11614d others(4): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68633514 | ||||||
| chr15:68633514 | TACAC | T | 8 | a0001c0001t0002g0002 a0001c0001t0005g0029 a0001c0001t0006g0021 others(5): Show |
8 | HG01109.hp2 HG01884.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.16-11617_16-11614d others(6): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68633514 | ||||||
| chr15:68633514 | TACACACA others(9): Show |
T | 2 | a0001c0001t0006g0020 a0001c0001t0017g0251 |
2 | HG02630.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.16-11629_16-11614d others(18): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68633514 | ||||||
| chr15:68633547 | T | A | 4 | a0001c0001t0001g0179 a0001c0001t0006g0191 a0001c0001t0021g0033 others(1): Show |
4 | HG02615.hp1 HG02647.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-11613T>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68633547 | |||||||
| chr15:68633627 | A | G | 12 | a0001c0001t0002g0002 a0001c0001t0002g0022 a0001c0001t0002g0078 others(9): Show |
12 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.16-11533A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68633627 | |||||||
| chr15:68633713 | TCA | T | 9 | a0001c0001t0002g0002 a0001c0001t0002g0022 a0001c0001t0002g0078 others(6): Show |
9 | HG01884.hp2 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.16-11444_16-11443d others(4): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68633713 | ||||||
| chr15:68633776 | G | A | 117 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0039 others(114): Show |
117 | HG00140.hp1 HG00408.hp1 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.16-11384G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68633776 | |||||||
| chr15:68633784 | G | A | 3 | a0001c0001t0005g0035 a0001c0001t0008g0025 a0001c0001t0010g0249 |
3 | HG02451.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.16-11376G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68633784 | |||||||
| chr15:68633784 | G | C | 114 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0039 others(111): Show |
114 | HG00140.hp1 HG00408.hp1 HG00597.hp2 others(111): Show |
intron_variant | MODIFIER | c.16-11376G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68633784 | |||||||
| chr15:68633816 | A | G | 1 | a0001c0001t0003g0217 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.16-11344A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68633816 | |||||||
| chr15:68634244 | T | C | 38 | a0001c0001t0001g0132 a0001c0001t0001g0179 a0001c0001t0002g0135 others(35): Show |
38 | HG01109.hp2 HG01175.hp2 HG01258.hp1 others(35): Show |
intron_variant | MODIFIER | c.16-10916T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68634244 | |||||||
| chr15:68634309 | C | T | 1 | a0001c0001t0001g0048 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.16-10851C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68634309 | |||||||
| chr15:68634348 | G | A | 1 | a0001c0001t0005g0194 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.16-10812G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68634348 | |||||||
| chr15:68634484 | T | A | 1 | a0001c0001t0004g0110 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.16-10676T>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68634484 | |||||||
| chr15:68634605 | G | A | 2 | a0001c0001t0001g0095 a0001c0001t0003g0064 |
2 | HG01361.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.16-10555G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68634605 | |||||||
| chr15:68634705 | C | T | 2 | a0001c0001t0006g0236 a0001c0001t0027g0034 |
2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.16-10455C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68634705 | |||||||
| chr15:68634851 | G | A | 19 | a0001c0001t0002g0242 a0001c0001t0003g0160 a0001c0001t0003g0244 others(16): Show |
19 | HG01175.hp2 HG01258.hp1 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.16-10309G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68634851 | |||||||
| chr15:68635073 | C | T | 6 | a0001c0001t0001g0042 a0001c0001t0002g0081 a0001c0001t0005g0035 others(3): Show |
6 | HG02451.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.16-10087C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68635073 | |||||||
| chr15:68635118 | C | T | 3 | a0001c0001t0001g0042 a0001c0001t0002g0081 a0001c0001t0008g0001 |
3 | HG02559.hp2 HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.16-10042C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68635118 | |||||||
| chr15:68635541 | G | A | 10 | a0001c0001t0001g0056 a0001c0001t0001g0101 a0001c0001t0001g0108 others(7): Show |
10 | HG00280.hp1 HG00597.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.16-9619G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68635541 | |||||||
| chr15:68635664 | T | A | 6 | a0001c0001t0001g0042 a0001c0001t0002g0081 a0001c0001t0005g0035 others(3): Show |
6 | HG02451.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.16-9496T>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68635664 | |||||||
| chr15:68635731 | T | C | 3 | a0001c0001t0002g0181 a0001c0001t0005g0194 a0001c0003t0012g0076 |
3 | HG02109.hp1 HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.16-9429T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68635731 | |||||||
| chr15:68635818 | G | A | 18 | a0001c0001t0002g0242 a0001c0001t0003g0244 a0001c0001t0003g0245 others(15): Show |
18 | HG01175.hp2 HG01258.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.16-9342G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68635818 | |||||||
| chr15:68635965 | C | G | 2 | a0001c0001t0005g0007 a0001c0002t0003g0198 |
2 | HG00280.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.16-9195C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68635965 | |||||||
| chr15:68636031 | C | G | 20 | a0001c0001t0001g0074 a0001c0001t0002g0091 a0001c0001t0002g0242 others(17): Show |
20 | HG01175.hp2 HG01258.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.16-9129C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68636031 | |||||||
| chr15:68636067 | C | T | 3 | a0001c0001t0003g0217 a0001c0002t0001g0006 a0001c0002t0002g0170 |
3 | HG00738.hp1 HG01978.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.16-9093C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68636067 | |||||||
| chr15:68636331 | G | A | 1 | a0001c0001t0004g0129 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.16-8829G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68636331 | |||||||
| chr15:68636424 | G | A | 23 | a0001c0001t0001g0048 a0001c0001t0001g0094 a0001c0001t0001g0132 others(20): Show |
23 | HG01109.hp2 HG01884.hp2 HG02615.hp1 others(20): Show |
intron_variant | MODIFIER | c.16-8736G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68636424 | |||||||
| chr15:68636553 | G | A | 1 | a0001c0001t0002g0242 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.16-8607G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68636553 | |||||||
| chr15:68636620 | A | G | 7 | a0001c0001t0001g0159 a0001c0001t0002g0146 a0001c0001t0002g0234 others(4): Show |
7 | HG03017.hp2 HG03710.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.16-8540A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68636620 | |||||||
| chr15:68636697 | T | C | 5 | a0001c0001t0001g0042 a0001c0001t0002g0081 a0001c0001t0005g0035 others(2): Show |
5 | HG02559.hp2 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-8463T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68636697 | |||||||
| chr15:68636744 | G | A | 1 | a0001c0001t0002g0146 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.16-8416G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68636744 | |||||||
| chr15:68637374 | C | G | 158 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0037 others(155): Show |
158 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.16-7786C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68637374 | |||||||
| chr15:68637396 | C | G | 1 | a0001c0002t0002g0142 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.16-7764C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68637396 | |||||||
| chr15:68637457 | G | A | 58 | a0001c0001t0001g0048 a0001c0001t0001g0074 a0001c0001t0001g0094 others(55): Show |
58 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(55): Show |
intron_variant | MODIFIER | c.16-7703G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68637457 | |||||||
| chr15:68637603 | A | G | 2 | a0001c0001t0006g0004 a0001c0001t0006g0053 |
2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.16-7557A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68637603 | |||||||
| chr15:68637744 | TCC | T | 152 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0037 others(149): Show |
152 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.16-7411_16-7410del others(2): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68637744 | ||||||
| chr15:68637764 | G | C | 158 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0037 others(155): Show |
158 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.16-7396G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68637764 | |||||||
| chr15:68637999 | G | A | 1 | a0001c0001t0022g0049 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.16-7161G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68637999 | |||||||
| chr15:68638254 | T | C | 158 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0037 others(155): Show |
158 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.16-6906T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68638254 | |||||||
| chr15:68638321 | G | A | 58 | a0001c0001t0001g0048 a0001c0001t0001g0074 a0001c0001t0001g0094 others(55): Show |
58 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(55): Show |
intron_variant | MODIFIER | c.16-6839G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68638321 | |||||||
| chr15:68638405 | G | A | 7 | a0001c0001t0001g0074 a0001c0001t0004g0019 a0001c0001t0005g0164 others(4): Show |
7 | HG02109.hp2 HG02145.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.16-6755G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68638405 | |||||||
| chr15:68639123 | A | T | 1 | a0001c0001t0007g0151 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.16-6037A>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68639123 | |||||||
| chr15:68639276 | G | A | 1 | a0001c0001t0004g0104 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.16-5884G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68639276 | |||||||
| chr15:68639319 | G | C | 1 | a0001c0001t0002g0148 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.16-5841G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68639319 | |||||||
| chr15:68639611 | C | T | 4 | a0001c0001t0002g0022 a0001c0001t0002g0078 a0001c0001t0002g0079 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-5549C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68639611 | |||||||
| chr15:68639704 | G | C | 163 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(160): Show |
163 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.16-5456G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68639704 | |||||||
| chr15:68639712 | A | C | 1 | a0001c0001t0021g0033 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.16-5448A>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68639712 | |||||||
| chr15:68639779 | TTCAAAAC others(18): Show |
T | 1 | a0001c0001t0009g0238 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.16-5369_16-5345del others(25): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68639779 | ||||||
| chr15:68639790 | T | C | 1 | a0001c0001t0005g0007 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.16-5370T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68639790 | |||||||
| chr15:68639820 | C | T | 82 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0037 others(79): Show |
82 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.16-5340C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68639820 | |||||||
| chr15:68639931 | G | A | 2 | a0001c0001t0001g0066 a0001c0001t0003g0116 |
2 | NA19085.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.16-5229G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68639931 | |||||||
| chr15:68640080 | C | A | 4 | a0001c0001t0001g0074 a0001c0003t0001g0057 a0001c0003t0006g0145 others(1): Show |
4 | HG02109.hp2 HG02145.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-5080C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68640080 | |||||||
| chr15:68640081 | G | A | 1 | a0001c0001t0006g0041 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.16-5079G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68640081 | |||||||
| chr15:68640144 | AC | A | 4 | a0001c0001t0001g0074 a0001c0003t0001g0057 a0001c0003t0006g0145 others(1): Show |
4 | HG02109.hp2 HG02145.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-5013delC | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68640144 | ||||||
| chr15:68640149 | G | A | 4 | a0001c0001t0001g0074 a0001c0003t0001g0057 a0001c0003t0006g0145 others(1): Show |
4 | HG02109.hp2 HG02145.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-5011G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68640149 | |||||||
| chr15:68640150 | C | T | 4 | a0001c0001t0001g0074 a0001c0003t0001g0057 a0001c0003t0006g0145 others(1): Show |
4 | HG02109.hp2 HG02145.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-5010C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68640150 | |||||||
| chr15:68640206 | C | A | 1 | a0001c0001t0006g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.16-4954C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68640206 | |||||||
| chr15:68640233 | C | T | 4 | a0001c0001t0001g0074 a0001c0003t0001g0057 a0001c0003t0006g0145 others(1): Show |
4 | HG02109.hp2 HG02145.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-4927C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68640233 | |||||||
| chr15:68640304 | C | T | 1 | a0001c0002t0002g0230 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.16-4856C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68640304 | |||||||
| chr15:68640511 | TA | T | 148 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0037 others(145): Show |
148 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.16-4635delA | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68640511 | ||||||
| chr15:68640541 | G | A | 2 | a0001c0001t0003g0086 a0001c0001t0003g0138 |
2 | HG00673.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.16-4619G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68640541 | |||||||
| chr15:68640603 | T | C | 59 | a0001c0001t0001g0048 a0001c0001t0001g0094 a0001c0001t0001g0132 others(56): Show |
59 | HG01109.hp2 HG01175.hp2 HG01258.hp1 others(56): Show |
intron_variant | MODIFIER | c.16-4557T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68640603 | |||||||
| chr15:68640738 | C | T | 39 | a0001c0001t0001g0048 a0001c0001t0001g0094 a0001c0001t0001g0132 others(36): Show |
39 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(36): Show |
intron_variant | MODIFIER | c.16-4422C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68640738 | |||||||
| chr15:68640758 | T | C | 9 | a0001c0001t0001g0094 a0001c0001t0004g0026 a0001c0001t0004g0216 others(6): Show |
9 | HG02615.hp1 HG02896.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.16-4402T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68640758 | |||||||
| chr15:68640874 | G | A | 1 | a0001c0001t0002g0242 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.16-4286G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68640874 | |||||||
| chr15:68640924 | G | A | 1 | a0001c0001t0003g0068 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.16-4236G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68640924 | |||||||
| chr15:68640950 | C | T | 1 | a0001c0001t0004g0112 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.16-4210C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68640950 | |||||||
| chr15:68641021 | C | T | 106 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0037 others(103): Show |
106 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.16-4139C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68641021 | |||||||
| chr15:68641133 | C | G | 1 | a0001c0001t0004g0180 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.16-4027C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68641133 | |||||||
| chr15:68641264 | C | T | 1 | a0001c0002t0002g0170 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.16-3896C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68641264 | |||||||
| chr15:68641265 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.16-3895G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68641265 | |||||||
| chr15:68641321 | G | T | 1 | a0001c0001t0003g0214 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.16-3839G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68641321 | |||||||
| chr15:68641443 | G | T | 28 | a0001c0001t0001g0037 a0001c0001t0001g0139 a0001c0001t0001g0228 others(25): Show |
28 | HG00280.hp2 HG00738.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.16-3717G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68641443 | |||||||
| chr15:68641474 | G | A | 1 | a0001c0002t0002g0170 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.16-3686G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68641474 | |||||||
| chr15:68641608 | G | A | 9 | a0001c0001t0001g0009 a0001c0001t0001g0098 a0001c0001t0001g0161 others(6): Show |
9 | HG00738.hp2 HG01070.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.16-3552G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68641608 | |||||||
| chr15:68641821 | T | TCAAG | 5 | a0001c0001t0001g0153 a0001c0001t0001g0192 a0001c0001t0003g0239 others(2): Show |
5 | HG00408.hp2 HG00621.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.16-3337_16-3334dup others(4): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68641821 | ||||||
| chr15:68641865 | A | G | 6 | a0001c0001t0001g0094 a0001c0001t0005g0035 a0001c0001t0006g0191 others(3): Show |
6 | HG02615.hp1 HG02896.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.16-3295A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68641865 | |||||||
| chr15:68641975 | C | T | 2 | a0001c0001t0006g0053 a0001c0002t0005g0016 |
2 | HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.16-3185C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68641975 | |||||||
| chr15:68642035 | C | CT | 116 | a0001c0001t0001g0010 a0001c0001t0001g0028 a0001c0001t0001g0037 others(113): Show |
116 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.16-3106dupT | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68642035 | ||||||
| chr15:68642035 | C | CTT | 120 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0039 others(117): Show |
120 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.16-3107_16-3106dup others(2): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68642035 | ||||||
| chr15:68642035 | C | CTTT | 9 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0175 others(6): Show |
9 | HG00597.hp2 HG00735.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.16-3108_16-3106dup others(3): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68642035 | ||||||
| chr15:68642091 | C | T | 1 | a0002c0008t0002g0093 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.16-3069C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68642091 | |||||||
| chr15:68642097 | C | T | 1 | a0001c0001t0005g0015 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.16-3063C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68642097 | |||||||
| chr15:68642134 | T | C | 3 | a0001c0001t0001g0094 a0001c0001t0022g0049 a0003c0007t0006g0186 |
3 | HG02896.hp1 HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.16-3026T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68642134 | |||||||
| chr15:68642190 | C | T | 1 | a0001c0001t0004g0063 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.16-2970C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68642190 | |||||||
| chr15:68642235 | C | T | 2 | a0001c0001t0002g0091 a0001c0001t0006g0053 |
2 | HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.16-2925C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68642235 | |||||||
| chr15:68642269 | C | T | 2 | a0001c0001t0002g0054 a0001c0001t0026g0055 |
2 | HG02735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.16-2891C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68642269 | |||||||
| chr15:68642342 | G | A | 25 | a0001c0001t0001g0133 a0001c0001t0001g0212 a0001c0001t0002g0234 others(22): Show |
25 | HG00280.hp2 HG00738.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.16-2818G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68642342 | |||||||
| chr15:68642359 | G | A | 1 | a0001c0002t0002g0071 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.16-2801G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68642359 | |||||||
| chr15:68642529 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.16-2631G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68642529 | |||||||
| chr15:68642587 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.16-2573A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68642587 | |||||||
| chr15:68642759 | C | T | 2 | a0001c0001t0004g0017 a0001c0001t0009g0014 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.16-2401C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68642759 | |||||||
| chr15:68642805 | A | G | 247 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(244): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.16-2355A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68642805 | |||||||
| chr15:68642915 | G | A | 1 | a0001c0001t0003g0214 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.16-2245G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68642915 | |||||||
| chr15:68643314 | T | C | 4 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0196 others(1): Show |
4 | HG03130.hp2 HG03225.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-1846T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68643314 | |||||||
| chr15:68643501 | C | A | 1 | a0001c0001t0004g0119 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.16-1659C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68643501 | |||||||
| chr15:68643553 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.16-1607C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68643553 | |||||||
| chr15:68643629 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.16-1531G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68643629 | |||||||
| chr15:68643676 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.16-1484C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68643676 | |||||||
| chr15:68643704 | T | C | 14 | a0001c0001t0001g0074 a0001c0001t0002g0022 a0001c0001t0002g0078 others(11): Show |
14 | HG01496.hp1 HG02109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.16-1456T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68643704 | |||||||
| chr15:68643898 | G | A | 3 | a0001c0001t0004g0017 a0001c0001t0005g0164 a0001c0001t0009g0014 |
3 | HG02886.hp2 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.16-1262G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68643898 | |||||||
| chr15:68643954 | T | C | 210 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(207): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.16-1206T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68643954 | |||||||
| chr15:68643972 | G | A | 1 | a0001c0001t0002g0079 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.16-1188G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68643972 | |||||||
| chr15:68644014 | G | A | 1 | a0001c0001t0009g0238 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.16-1146G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68644014 | |||||||
| chr15:68644031 | AAAAC | A | 27 | a0001c0001t0001g0132 a0001c0001t0002g0234 a0001c0001t0003g0217 others(24): Show |
27 | HG00280.hp2 HG00738.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.16-1117_16-1114del others(4): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 68644031 | ||||||
| chr15:68644341 | T | G | 1 | a0001c0001t0004g0019 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.16-819T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68644341 | |||||||
| chr15:68644459 | G | C | 4 | a0001c0001t0002g0181 a0001c0001t0005g0194 a0001c0001t0017g0251 others(1): Show |
4 | HG02109.hp1 HG02630.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-701G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68644459 | |||||||
| chr15:68644461 | T | C | 1 | a0001c0002t0002g0045 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.16-699T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68644461 | |||||||
| chr15:68644467 | G | T | 1 | a0001c0001t0006g0011 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.16-693G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68644467 | |||||||
| chr15:68644592 | T | C | 5 | a0001c0001t0001g0179 a0001c0001t0001g0228 a0001c0001t0002g0091 others(2): Show |
5 | HG01891.hp2 HG02615.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.16-568T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68644592 | |||||||
| chr15:68644617 | T | C | 2 | a0001c0001t0004g0017 a0001c0001t0009g0014 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.16-543T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68644617 | |||||||
| chr15:68644654 | G | A | 1 | a0001c0003t0011g0247 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.16-506G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68644654 | |||||||
| chr15:68644898 | G | A | 1 | a0001c0002t0006g0248 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.16-262G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68644898 | |||||||
| chr15:68645078 | G | A | 1 | a0001c0001t0005g0018 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.16-82G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68645078 | |||||||
| chr15:68645102 | C | T | 48 | a0001c0001t0001g0074 a0001c0001t0001g0094 a0001c0001t0001g0132 others(45): Show |
48 | HG00280.hp2 HG00738.hp1 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.16-58C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68645102 | |||||||
| chr15:68645129 | C | G | 2 | a0001c0001t0004g0017 a0001c0001t0009g0014 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.16-31C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 1/11 | chr15 | 68645129 | |||||||
| chr15:68645757 | G | A | 15 | a0001c0001t0001g0052 a0001c0001t0001g0105 a0001c0001t0001g0199 others(12): Show |
15 | HG02015.hp1 HG02040.hp1 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.216+397G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68645757 | |||||||
| chr15:68645779 | AT | A | 10 | a0001c0001t0001g0098 a0001c0001t0001g0139 a0001c0001t0001g0202 others(7): Show |
10 | HG01074.hp1 HG01109.hp2 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.216+431delT | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68645779 | ||||||
| chr15:68645921 | G | A | 9 | a0001c0001t0001g0108 a0001c0001t0001g0132 a0001c0001t0003g0036 others(6): Show |
9 | HG02040.hp2 HG02074.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.216+561G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68645921 | |||||||
| chr15:68645953 | C | T | 248 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(245): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.216+593C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68645953 | |||||||
| chr15:68645963 | G | A | 21 | a0001c0001t0002g0234 a0001c0001t0003g0217 a0001c0001t0003g0235 others(18): Show |
21 | HG00280.hp2 HG00738.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.216+603G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68645963 | |||||||
| chr15:68646076 | C | G | 2 | a0001c0001t0002g0121 a0001c0001t0004g0240 |
2 | HG02698.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.216+716C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68646076 | |||||||
| chr15:68646079 | A | G | 1 | a0001c0001t0002g0091 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.216+719A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68646079 | |||||||
| chr15:68646248 | C | T | 2 | a0001c0001t0001g0065 a0001c0001t0006g0218 |
2 | HG01106.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.216+888C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68646248 | |||||||
| chr15:68646249 | G | A | 4 | a0001c0001t0001g0094 a0001c0001t0006g0191 a0001c0001t0022g0049 others(1): Show |
4 | HG02615.hp1 HG02896.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.216+889G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68646249 | |||||||
| chr15:68646292 | G | C | 6 | a0001c0001t0001g0132 a0001c0001t0004g0229 a0001c0001t0006g0020 others(3): Show |
6 | HG02486.hp2 HG02809.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.216+932G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68646292 | |||||||
| chr15:68646702 | A | G | 6 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0196 others(3): Show |
6 | HG01884.hp2 HG03130.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.216+1342A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68646702 | |||||||
| chr15:68646769 | A | G | 1 | a0001c0001t0002g0181 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.216+1409A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68646769 | |||||||
| chr15:68646776 | C | T | 6 | a0001c0001t0002g0181 a0001c0001t0005g0164 a0001c0001t0005g0194 others(3): Show |
6 | HG02109.hp1 HG02630.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.216+1416C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68646776 | |||||||
| chr15:68646940 | G | A | 1 | a0001c0001t0002g0002 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.216+1580G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68646940 | |||||||
| chr15:68647139 | T | A | 51 | a0001c0001t0001g0052 a0001c0001t0001g0074 a0001c0001t0001g0094 others(48): Show |
51 | HG01496.hp1 HG01884.hp2 HG02015.hp1 others(48): Show |
intron_variant | MODIFIER | c.216+1779T>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68647139 | |||||||
| chr15:68647142 | G | C | 6 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0196 others(3): Show |
6 | HG01884.hp2 HG03130.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.216+1782G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68647142 | |||||||
| chr15:68647262 | C | T | 28 | a0001c0001t0001g0074 a0001c0001t0001g0094 a0001c0001t0002g0022 others(25): Show |
28 | HG01496.hp1 HG01884.hp2 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.216+1902C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68647262 | |||||||
| chr15:68647278 | A | G | 2 | a0001c0001t0003g0059 a0001c0001t0003g0154 |
2 | HG02080.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.216+1918A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68647278 | |||||||
| chr15:68647372 | A | G | 4 | a0001c0001t0001g0044 a0001c0001t0001g0168 a0001c0001t0001g0169 others(1): Show |
4 | HG03490.hp1 HG03490.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.216+2012A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68647372 | |||||||
| chr15:68647640 | A | G | 21 | a0001c0001t0001g0074 a0001c0001t0001g0094 a0001c0001t0002g0022 others(18): Show |
21 | HG01496.hp1 HG02109.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.216+2280A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68647640 | |||||||
| chr15:68647689 | C | CA | 22 | a0001c0001t0002g0234 a0001c0001t0003g0217 a0001c0001t0003g0235 others(19): Show |
22 | HG00280.hp2 HG00642.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.216+2342dupA | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68647689 | ||||||
| chr15:68647689 | C | CAA | 12 | a0001c0001t0001g0132 a0001c0001t0002g0181 a0001c0001t0004g0229 others(9): Show |
12 | HG02109.hp1 HG02486.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.216+2341_216+2342d others(4): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68647689 | ||||||
| chr15:68647689 | C | CAAA | 22 | a0001c0001t0001g0052 a0001c0001t0001g0105 a0001c0001t0001g0122 others(19): Show |
22 | HG01884.hp2 HG02015.hp1 HG02040.hp1 others(19): Show |
intron_variant | MODIFIER | c.216+2340_216+2342d others(5): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68647689 | ||||||
| chr15:68647689 | C | CAAAA | 82 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0042 others(79): Show |
82 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.216+2339_216+2342d others(6): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68647689 | ||||||
| chr15:68647689 | C | CAAAAA | 25 | a0001c0001t0001g0074 a0001c0001t0001g0094 a0001c0001t0001g0175 others(22): Show |
25 | HG00735.hp1 HG01175.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.216+2338_216+2342d others(7): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68647689 | ||||||
| chr15:68647737 | G | A | 1 | a0001c0001t0003g0163 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.216+2377G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68647737 | |||||||
| chr15:68647764 | T | C | 6 | a0001c0001t0002g0181 a0001c0001t0005g0164 a0001c0001t0005g0194 others(3): Show |
6 | HG02109.hp1 HG02630.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.216+2404T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68647764 | |||||||
| chr15:68647770 | G | A | 16 | a0001c0001t0001g0052 a0001c0001t0001g0105 a0001c0001t0001g0122 others(13): Show |
16 | HG02015.hp1 HG02040.hp1 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.216+2410G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68647770 | |||||||
| chr15:68647857 | T | G | 5 | a0001c0001t0002g0181 a0001c0001t0005g0164 a0001c0001t0005g0194 others(2): Show |
5 | HG02109.hp1 HG02630.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.216+2497T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68647857 | |||||||
| chr15:68647857 | T | TA | 240 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(237): Show |
240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.216+2511dupA | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68647857 | ||||||
| chr15:68647885 | C | T | 1 | a0001c0001t0003g0064 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.216+2525C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68647885 | |||||||
| chr15:68647900 | G | C | 1 | a0001c0001t0005g0073 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.216+2540G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68647900 | |||||||
| chr15:68647999 | C | G | 135 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0042 others(132): Show |
135 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.216+2639C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68647999 | |||||||
| chr15:68648029 | C | CA | 74 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0042 others(71): Show |
74 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.216+2688dupA | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68648029 | ||||||
| chr15:68648029 | C | CAA | 86 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0037 others(83): Show |
86 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.216+2687_216+2688d others(4): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68648029 | ||||||
| chr15:68648045 | AAAAG | A | 20 | a0001c0001t0001g0074 a0001c0001t0001g0094 a0001c0001t0002g0022 others(17): Show |
20 | HG01496.hp1 HG02109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.216+2687_216+2690d others(6): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68648045 | ||||||
| chr15:68648070 | C | T | 22 | a0001c0001t0002g0234 a0001c0001t0003g0217 a0001c0001t0003g0235 others(19): Show |
22 | HG00280.hp2 HG00642.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.216+2710C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68648070 | |||||||
| chr15:68648281 | G | A | 2 | a0001c0001t0004g0184 a0001c0001t0004g0185 |
2 | NA18949.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.216+2921G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68648281 | |||||||
| chr15:68648330 | T | TA | 32 | a0001c0001t0001g0074 a0001c0001t0001g0094 a0001c0001t0001g0215 others(29): Show |
32 | HG01496.hp1 HG01884.hp2 HG02080.hp1 others(29): Show |
intron_variant | MODIFIER | c.216+2986dupA | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68648330 | ||||||
| chr15:68648330 | TA | T | 83 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0042 others(80): Show |
83 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.216+2986delA | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68648330 | ||||||
| chr15:68648370 | G | A | 1 | a0001c0001t0002g0022 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.216+3010G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68648370 | |||||||
| chr15:68648474 | A | G | 1 | a0001c0001t0003g0059 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.216+3114A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68648474 | |||||||
| chr15:68648575 | A | G | 3 | a0001c0001t0001g0044 a0001c0001t0001g0168 a0001c0001t0001g0169 |
3 | HG03490.hp1 HG03492.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.216+3215A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68648575 | |||||||
| chr15:68648581 | T | C | 248 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(245): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.216+3221T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68648581 | |||||||
| chr15:68648645 | G | A | 2 | a0001c0001t0003g0140 a0001c0001t0005g0072 |
2 | HG01099.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.216+3285G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68648645 | |||||||
| chr15:68648658 | G | T | 1 | a0001c0001t0007g0151 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.216+3298G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68648658 | |||||||
| chr15:68648688 | G | A | 1 | a0001c0002t0002g0045 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.216+3328G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68648688 | |||||||
| chr15:68648833 | C | T | 245 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(242): Show |
245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.216+3473C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68648833 | |||||||
| chr15:68648877 | C | A | 1 | a0001c0001t0002g0091 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.216+3517C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68648877 | |||||||
| chr15:68649003 | A | G | 5 | a0001c0001t0002g0181 a0001c0001t0005g0194 a0001c0001t0009g0238 others(2): Show |
5 | HG02109.hp1 HG02630.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.216+3643A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68649003 | |||||||
| chr15:68649099 | C | T | 21 | a0001c0001t0001g0074 a0001c0001t0001g0094 a0001c0001t0002g0022 others(18): Show |
21 | HG01496.hp1 HG02109.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.216+3739C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68649099 | |||||||
| chr15:68649118 | G | A | 21 | a0001c0001t0001g0074 a0001c0001t0001g0094 a0001c0001t0002g0022 others(18): Show |
21 | HG01496.hp1 HG02109.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.216+3758G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68649118 | |||||||
| chr15:68649181 | TATGTCTA others(2): Show |
T | 21 | a0001c0001t0001g0074 a0001c0001t0001g0094 a0001c0001t0002g0022 others(18): Show |
21 | HG01496.hp1 HG02109.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.216+3822_216+3830d others(11): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68649181 | |||||||
| chr15:68649239 | C | A | 3 | a0001c0001t0006g0020 a0001c0001t0006g0041 a0001c0001t0014g0254 |
3 | HG02486.hp2 HG03098.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.216+3879C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68649239 | |||||||
| chr15:68649619 | G | T | 21 | a0001c0001t0001g0074 a0001c0001t0001g0094 a0001c0001t0002g0022 others(18): Show |
21 | HG01496.hp1 HG02109.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.216+4259G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68649619 | |||||||
| chr15:68649620 | T | G | 1 | a0001c0001t0007g0193 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.216+4260T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68649620 | |||||||
| chr15:68649747 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.216+4387A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68649747 | |||||||
| chr15:68649749 | A | T | 1 | a0001c0001t0004g0106 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.216+4389A>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68649749 | |||||||
| chr15:68650079 | G | A | 27 | a0001c0001t0001g0074 a0001c0001t0001g0094 a0001c0001t0002g0022 others(24): Show |
27 | HG01496.hp1 HG01884.hp2 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.216+4719G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68650079 | |||||||
| chr15:68650281 | T | G | 1 | a0001c0002t0003g0198 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.216+4921T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68650281 | |||||||
| chr15:68650311 | C | G | 21 | a0001c0001t0001g0074 a0001c0001t0001g0094 a0001c0001t0002g0022 others(18): Show |
21 | HG01496.hp1 HG02109.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.216+4951C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68650311 | |||||||
| chr15:68650355 | CTAAAAAA others(11): Show |
C | 1 | a0001c0001t0010g0252 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.216+4996_216+5013d others(20): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68650355 | |||||||
| chr15:68650355 | CTAAAAAA others(12): Show |
C | 3 | a0001c0001t0001g0139 a0001c0001t0001g0215 a0001c0001t0004g0134 |
3 | HG02486.hp1 HG03130.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.216+4996_216+5014d others(21): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68650355 | |||||||
| chr15:68650355 | CTAAAAAA others(13): Show |
C | 15 | a0001c0001t0001g0039 a0001c0001t0001g0098 a0001c0001t0001g0133 others(12): Show |
15 | HG00597.hp1 HG00673.hp1 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.216+4996_216+5015d others(22): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68650355 | |||||||
| chr15:68650355 | CTAAAAAA others(14): Show |
C | 15 | a0001c0001t0001g0009 a0001c0001t0001g0048 a0001c0001t0001g0118 others(12): Show |
15 | HG01070.hp2 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.216+4996_216+5016d others(23): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68650355 | |||||||
| chr15:68650355 | CTAAAAAA others(15): Show |
C | 36 | a0001c0001t0001g0037 a0001c0001t0001g0067 a0001c0001t0001g0084 others(33): Show |
36 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.216+4996_216+5017d others(24): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68650355 | |||||||
| chr15:68650355 | CTAAAAAA others(16): Show |
C | 8 | a0001c0001t0002g0167 a0001c0001t0003g0082 a0001c0001t0003g0116 others(5): Show |
8 | HG01074.hp1 HG01099.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.216+4996_216+5018d others(25): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68650355 | |||||||
| chr15:68650355 | CTAAAAAA others(17): Show |
C | 6 | a0001c0001t0001g0044 a0001c0001t0001g0066 a0001c0001t0001g0168 others(3): Show |
6 | HG02896.hp2 HG03490.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.216+4996_216+5019d others(26): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68650355 | |||||||
| chr15:68650356 | TAAAAAAA others(7): Show |
T | 2 | a0001c0001t0004g0017 a0001c0001t0009g0014 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.216+5033_216+5046d others(16): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68650356 | ||||||
| chr15:68650356 | TAAAAAAA others(17): Show |
T | 2 | a0001c0001t0002g0121 a0001c0003t0006g0145 |
2 | HG02145.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.216+5023_216+5046d others(26): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68650356 | ||||||
| chr15:68650356 | TAAAAAAA others(18): Show |
T | 23 | a0001c0001t0001g0074 a0001c0001t0001g0094 a0001c0001t0002g0022 others(20): Show |
23 | HG01496.hp1 HG02109.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.216+5022_216+5046d others(27): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68650356 | ||||||
| chr15:68650356 | TAAAAAAA others(19): Show |
T | 3 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0196 |
3 | HG03130.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.216+5021_216+5046d others(28): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68650356 | ||||||
| chr15:68650356 | TAAAAAAA others(20): Show |
T | 17 | a0001c0001t0001g0052 a0001c0001t0001g0105 a0001c0001t0001g0122 others(14): Show |
17 | HG01884.hp2 HG02015.hp1 HG02040.hp1 others(14): Show |
intron_variant | MODIFIER | c.216+5020_216+5046d others(29): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68650356 | ||||||
| chr15:68650356 | TAAAAAAA others(21): Show |
T | 4 | a0001c0001t0002g0102 a0001c0001t0004g0103 a0001c0001t0005g0164 others(1): Show |
4 | HG02886.hp2 NA18906.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.216+5019_216+5046d others(30): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68650356 | ||||||
| chr15:68650356 | TAAAAAAA others(22): Show |
T | 5 | a0001c0002t0005g0016 a0001c0002t0006g0223 a0001c0003t0006g0051 others(2): Show |
5 | HG02572.hp2 HG02647.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.216+5018_216+5046d others(31): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68650356 | ||||||
| chr15:68650356 | TAAAAAAA others(23): Show |
T | 30 | a0001c0001t0001g0010 a0001c0001t0001g0176 a0001c0001t0002g0080 others(27): Show |
30 | HG00280.hp2 HG00642.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.216+5017_216+5046d others(32): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68650356 | ||||||
| chr15:68650356 | TAAAAAAA others(24): Show |
T | 73 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0042 others(70): Show |
73 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.216+5016_216+5046d others(33): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68650356 | ||||||
| chr15:68650373 | AAAAAAAA others(27): Show |
A | 4 | a0001c0001t0002g0181 a0001c0001t0005g0194 a0001c0001t0017g0251 others(1): Show |
4 | HG02109.hp1 HG02630.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.216+5014_216+5047d others(36): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68650373 | |||||||
| chr15:68650378 | A | C | 1 | a0001c0001t0001g0084 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.216+5018A>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68650378 | |||||||
| chr15:68650406 | A | T | 55 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0056 others(52): Show |
55 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.216+5046A>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68650406 | |||||||
| chr15:68650407 | T | C | 1 | a0001c0001t0010g0252 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.216+5047T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68650407 | |||||||
| chr15:68650440 | C | T | 1 | a0001c0001t0003g0150 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.216+5080C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68650440 | |||||||
| chr15:68650453 | A | C | 78 | a0001c0001t0001g0037 a0001c0001t0001g0039 a0001c0001t0001g0044 others(75): Show |
78 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.216+5093A>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68650453 | |||||||
| chr15:68650495 | C | G | 4 | a0001c0001t0001g0094 a0001c0001t0006g0191 a0001c0001t0022g0049 others(1): Show |
4 | HG02615.hp1 HG02896.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.216+5135C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68650495 | |||||||
| chr15:68650566 | C | T | 2 | a0001c0001t0004g0205 a0001c0001t0005g0208 |
2 | HG02015.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.216+5206C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68650566 | |||||||
| chr15:68650612 | A | G | 11 | a0001c0001t0002g0181 a0001c0001t0005g0164 a0001c0001t0005g0194 others(8): Show |
11 | HG02109.hp1 HG02572.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.216+5252A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68650612 | |||||||
| chr15:68650760 | G | C | 2 | a0001c0004t0007g0023 a0001c0004t0007g0172 |
2 | HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.216+5400G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68650760 | |||||||
| chr15:68651092 | C | T | 1 | a0001c0001t0003g0125 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.216+5732C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68651092 | |||||||
| chr15:68651219 | C | A | 23 | a0001c0001t0003g0217 a0001c0001t0005g0007 a0001c0001t0008g0025 others(20): Show |
23 | HG00280.hp2 HG00642.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.216+5859C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68651219 | |||||||
| chr15:68651231 | C | T | 1 | a0001c0003t0006g0145 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.216+5871C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68651231 | |||||||
| chr15:68651248 | A | G | 78 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0028 others(75): Show |
78 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.216+5888A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68651248 | |||||||
| chr15:68651301 | A | T | 2 | a0001c0001t0004g0017 a0001c0001t0009g0014 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.216+5941A>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68651301 | |||||||
| chr15:68651687 | C | T | 2 | a0001c0001t0001g0037 a0001c0002t0002g0152 |
2 | HG03704.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.216+6327C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68651687 | |||||||
| chr15:68651892 | T | A | 1 | a0001c0003t0012g0076 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.216+6532T>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68651892 | |||||||
| chr15:68652213 | G | A | 73 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0028 others(70): Show |
73 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.216+6853G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68652213 | |||||||
| chr15:68652221 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.216+6861G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68652221 | |||||||
| chr15:68652318 | C | T | 1 | a0001c0002t0003g0256 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.216+6958C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68652318 | |||||||
| chr15:68652334 | C | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0161 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.216+6974C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68652334 | |||||||
| chr15:68652610 | C | T | 4 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0196 others(1): Show |
4 | HG03130.hp2 HG03225.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.216+7250C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68652610 | |||||||
| chr15:68652747 | C | T | 4 | a0001c0001t0002g0181 a0001c0001t0005g0194 a0001c0001t0017g0251 others(1): Show |
4 | HG02109.hp1 HG02630.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.216+7387C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68652747 | |||||||
| chr15:68652818 | A | G | 1 | a0001c0001t0015g0222 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.216+7458A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68652818 | |||||||
| chr15:68653057 | A | C | 4 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0196 others(1): Show |
4 | HG03130.hp2 HG03225.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.216+7697A>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68653057 | |||||||
| chr15:68653064 | C | T | 2 | a0001c0001t0002g0234 a0001c0001t0003g0235 |
2 | NA18944.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.216+7704C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68653064 | |||||||
| chr15:68653442 | A | C | 1 | a0001c0001t0005g0018 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.216+8082A>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68653442 | |||||||
| chr15:68653586 | G | A | 24 | a0001c0001t0001g0074 a0001c0001t0001g0094 a0001c0001t0001g0179 others(21): Show |
24 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.216+8226G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68653586 | |||||||
| chr15:68653618 | T | G | 3 | a0001c0001t0005g0046 a0001c0001t0006g0236 a0001c0001t0027g0034 |
3 | HG02818.hp1 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.216+8258T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68653618 | |||||||
| chr15:68653755 | ATT | A | 74 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0028 others(71): Show |
74 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.216+8398_216+8399d others(4): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68653755 | ||||||
| chr15:68653776 | C | T | 1 | a0001c0001t0005g0164 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.216+8416C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68653776 | |||||||
| chr15:68653800 | G | C | 5 | a0001c0001t0002g0181 a0001c0001t0005g0194 a0001c0001t0009g0238 others(2): Show |
5 | HG02109.hp1 HG02630.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.216+8440G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68653800 | |||||||
| chr15:68653860 | GA | G | 242 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(239): Show |
242 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.216+8513delA | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68653860 | ||||||
| chr15:68653876 | C | A | 2 | a0001c0004t0007g0023 a0001c0004t0007g0172 |
2 | HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.216+8516C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68653876 | |||||||
| chr15:68653905 | G | A | 247 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(244): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.216+8545G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68653905 | |||||||
| chr15:68653912 | G | A | 5 | a0001c0001t0002g0241 a0001c0001t0003g0225 a0001c0001t0003g0226 others(2): Show |
5 | HG01070.hp1 HG01081.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.216+8552G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68653912 | |||||||
| chr15:68654124 | C | T | 74 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0028 others(71): Show |
74 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.216+8764C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68654124 | |||||||
| chr15:68654255 | G | A | 2 | a0001c0001t0004g0019 a0001c0001t0006g0053 |
2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.216+8895G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68654255 | |||||||
| chr15:68654258 | T | C | 247 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(244): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.216+8898T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68654258 | |||||||
| chr15:68654259 | G | A | 1 | a0001c0001t0003g0126 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.216+8899G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68654259 | |||||||
| chr15:68654280 | G | C | 5 | a0001c0002t0005g0016 a0001c0002t0006g0223 a0001c0003t0006g0051 others(2): Show |
5 | HG02572.hp2 HG02647.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.216+8920G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68654280 | |||||||
| chr15:68654405 | C | T | 4 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0196 others(1): Show |
4 | HG03130.hp2 HG03225.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.216+9045C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68654405 | |||||||
| chr15:68654511 | G | C | 78 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0028 others(75): Show |
78 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.216+9151G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68654511 | |||||||
| chr15:68654767 | G | T | 1 | a0001c0001t0003g0155 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.216+9407G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68654767 | |||||||
| chr15:68654771 | G | C | 13 | a0001c0001t0001g0009 a0001c0001t0001g0098 a0001c0001t0001g0139 others(10): Show |
13 | HG01070.hp2 HG01071.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.216+9411G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68654771 | |||||||
| chr15:68654906 | C | T | 74 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0028 others(71): Show |
74 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.216+9546C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68654906 | |||||||
| chr15:68654966 | G | T | 1 | a0001c0001t0006g0004 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.216+9606G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68654966 | |||||||
| chr15:68655068 | C | A | 74 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0028 others(71): Show |
74 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.216+9708C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68655068 | |||||||
| chr15:68655182 | G | A | 1 | a0001c0001t0006g0053 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.216+9822G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68655182 | |||||||
| chr15:68655226 | T | C | 74 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0028 others(71): Show |
74 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.216+9866T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68655226 | |||||||
| chr15:68655295 | G | A | 5 | a0001c0001t0002g0181 a0001c0001t0005g0194 a0001c0001t0009g0238 others(2): Show |
5 | HG02109.hp1 HG02630.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.216+9935G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68655295 | |||||||
| chr15:68655358 | C | T | 5 | a0001c0001t0001g0179 a0001c0001t0001g0228 a0001c0001t0002g0091 others(2): Show |
5 | HG01891.hp2 HG02615.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.216+9998C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68655358 | |||||||
| chr15:68655424 | C | T | 1 | a0001c0001t0001g0052 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.216+10064C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68655424 | |||||||
| chr15:68655476 | C | T | 3 | a0001c0002t0006g0223 a0001c0003t0006g0051 a0001c0003t0012g0047 |
3 | HG02572.hp2 HG02647.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.216+10116C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68655476 | |||||||
| chr15:68655976 | G | A | 6 | a0001c0001t0001g0094 a0001c0001t0006g0191 a0001c0001t0008g0001 others(3): Show |
6 | HG02559.hp2 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.216+10616G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68655976 | |||||||
| chr15:68656075 | A | C | 2 | a0001c0001t0002g0121 a0001c0001t0004g0240 |
2 | HG02698.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.216+10715A>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68656075 | |||||||
| chr15:68656103 | G | C | 247 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(244): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.216+10743G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68656103 | |||||||
| chr15:68656154 | C | A | 6 | a0001c0001t0001g0094 a0001c0001t0006g0191 a0001c0001t0008g0001 others(3): Show |
6 | HG02559.hp2 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.216+10794C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68656154 | |||||||
| chr15:68656168 | GT | G | 79 | a0001c0001t0001g0010 a0001c0001t0001g0028 a0001c0001t0001g0042 others(76): Show |
79 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.216+10809delT | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68656168 | |||||||
| chr15:68656169 | T | C | 9 | a0001c0001t0001g0027 a0001c0001t0001g0056 a0001c0001t0001g0067 others(6): Show |
9 | HG00597.hp2 HG00621.hp1 HG00642.hp1 others(6): Show |
intron_variant | MODIFIER | c.216+10809T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68656169 | |||||||
| chr15:68656177 | GCC | G | 88 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0028 others(85): Show |
88 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.216+10822_216+1082 others(6): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68656177 | ||||||
| chr15:68656289 | A | C | 172 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(169): Show |
172 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.216+10929A>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68656289 | |||||||
| chr15:68656415 | G | A | 6 | a0001c0001t0001g0094 a0001c0001t0006g0191 a0001c0001t0008g0001 others(3): Show |
6 | HG02559.hp2 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.216+11055G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68656415 | |||||||
| chr15:68656423 | G | T | 1 | a0001c0001t0006g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.216+11063G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68656423 | |||||||
| chr15:68656562 | G | T | 5 | a0001c0001t0002g0181 a0001c0001t0005g0164 a0001c0001t0005g0194 others(2): Show |
5 | HG02109.hp1 HG02630.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.216+11202G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68656562 | |||||||
| chr15:68656563 | C | T | 5 | a0001c0001t0002g0181 a0001c0001t0005g0164 a0001c0001t0005g0194 others(2): Show |
5 | HG02109.hp1 HG02630.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.216+11203C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68656563 | |||||||
| chr15:68657177 | TAA | T | 22 | a0001c0001t0005g0007 a0001c0001t0008g0025 a0001c0002t0001g0006 others(19): Show |
22 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.216+11819_216+1182 others(6): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68657177 | ||||||
| chr15:68657207 | C | T | 2 | a0001c0001t0004g0017 a0001c0001t0009g0014 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.216+11847C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68657207 | |||||||
| chr15:68657224 | T | A | 113 | a0001c0001t0001g0010 a0001c0001t0001g0028 a0001c0001t0001g0042 others(110): Show |
113 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.216+11864T>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68657224 | |||||||
| chr15:68657441 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.216+12081C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68657441 | |||||||
| chr15:68657517 | C | CA | 22 | a0001c0001t0001g0105 a0001c0001t0001g0122 a0001c0001t0001g0199 others(19): Show |
22 | HG01070.hp1 HG02015.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.216+12176dupA | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68657517 | ||||||
| chr15:68657517 | C | CAA | 83 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0037 others(80): Show |
83 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.216+12175_216+1217 others(6): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68657517 | ||||||
| chr15:68657517 | CA | C | 8 | a0001c0001t0004g0117 a0001c0001t0005g0012 a0001c0001t0005g0013 others(5): Show |
8 | HG01074.hp1 HG03130.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.216+12176delA | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68657517 | ||||||
| chr15:68657562 | C | T | 133 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0037 others(130): Show |
133 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(130): Show |
intron_variant | MODIFIER | c.216+12202C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68657562 | |||||||
| chr15:68657605 | G | A | 120 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0037 others(117): Show |
120 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(117): Show |
intron_variant | MODIFIER | c.216+12245G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68657605 | |||||||
| chr15:68657618 | G | A | 1 | a0001c0001t0006g0004 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.216+12258G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68657618 | |||||||
| chr15:68657777 | A | G | 1 | a0001c0001t0009g0238 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.216+12417A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68657777 | |||||||
| chr15:68657792 | G | A | 16 | a0001c0001t0001g0052 a0001c0001t0001g0105 a0001c0001t0001g0122 others(13): Show |
16 | HG02015.hp1 HG02040.hp1 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.216+12432G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68657792 | |||||||
| chr15:68658080 | C | G | 4 | a0001c0001t0001g0048 a0001c0001t0003g0086 a0001c0001t0003g0127 others(1): Show |
4 | HG00673.hp2 HG02015.hp2 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.216+12720C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68658080 | |||||||
| chr15:68658113 | A | G | 2 | a0001c0001t0001g0204 a0001c0001t0003g0213 |
2 | HG01256.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.216+12753A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68658113 | |||||||
| chr15:68658265 | G | A | 2 | a0001c0004t0007g0023 a0001c0004t0007g0172 |
2 | HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.216+12905G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68658265 | |||||||
| chr15:68658281 | C | G | 1 | a0001c0001t0007g0162 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.216+12921C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68658281 | |||||||
| chr15:68658300 | T | TGGA | 253 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(250): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.216+12949_216+1295 others(7): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68658300 | ||||||
| chr15:68658313 | C | T | 83 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0037 others(80): Show |
83 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.216+12953C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68658313 | |||||||
| chr15:68658314 | G | A | 19 | a0001c0001t0001g0074 a0001c0001t0001g0179 a0001c0001t0001g0228 others(16): Show |
19 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.216+12954G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68658314 | |||||||
| chr15:68658319 | G | A | 1 | a0001c0001t0007g0193 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.216+12959G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68658319 | |||||||
| chr15:68658368 | G | A | 79 | a0001c0001t0001g0010 a0001c0001t0001g0028 a0001c0001t0001g0042 others(76): Show |
79 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.216+13008G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68658368 | |||||||
| chr15:68658404 | G | T | 1 | a0001c0001t0001g0179 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.216+13044G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68658404 | |||||||
| chr15:68658412 | A | G | 246 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(243): Show |
246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.216+13052A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68658412 | |||||||
| chr15:68658425 | G | A | 2 | a0001c0001t0002g0080 a0001c0001t0002g0135 |
2 | HG02145.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.216+13065G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68658425 | |||||||
| chr15:68658563 | G | A | 2 | a0001c0004t0007g0023 a0001c0004t0007g0172 |
2 | HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.216+13203G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68658563 | |||||||
| chr15:68658611 | C | T | 1 | a0001c0002t0003g0256 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.216+13251C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68658611 | |||||||
| chr15:68658671 | T | G | 1 | a0001c0001t0002g0181 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.216+13311T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68658671 | |||||||
| chr15:68658686 | A | G | 17 | a0001c0001t0001g0074 a0001c0001t0001g0179 a0001c0001t0001g0228 others(14): Show |
17 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.216+13326A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68658686 | |||||||
| chr15:68658842 | A | G | 59 | a0001c0001t0001g0052 a0001c0001t0001g0074 a0001c0001t0001g0105 others(56): Show |
59 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.216+13482A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68658842 | |||||||
| chr15:68658864 | T | C | 4 | a0001c0001t0002g0181 a0001c0001t0005g0194 a0001c0001t0017g0251 others(1): Show |
4 | HG02109.hp1 HG02630.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.216+13504T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68658864 | |||||||
| chr15:68658889 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.216+13529G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68658889 | |||||||
| chr15:68658936 | C | T | 147 | a0001c0001t0001g0010 a0001c0001t0001g0028 a0001c0001t0001g0042 others(144): Show |
147 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.216+13576C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68658936 | |||||||
| chr15:68659111 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.216+13751C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68659111 | |||||||
| chr15:68659229 | G | T | 2 | a0001c0001t0006g0236 a0001c0001t0027g0034 |
2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.216+13869G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68659229 | |||||||
| chr15:68659230 | A | C | 54 | a0001c0001t0001g0028 a0001c0001t0001g0056 a0001c0001t0001g0067 others(51): Show |
54 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.216+13870A>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68659230 | |||||||
| chr15:68659543 | T | C | 97 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0037 others(94): Show |
97 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.216+14183T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68659543 | |||||||
| chr15:68659750 | A | G | 3 | a0001c0001t0001g0037 a0001c0001t0001g0088 a0001c0002t0002g0152 |
3 | HG01361.hp1 HG03704.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.216+14390A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68659750 | |||||||
| chr15:68659806 | C | T | 15 | a0001c0001t0001g0052 a0001c0001t0001g0105 a0001c0001t0001g0199 others(12): Show |
15 | HG02015.hp1 HG02040.hp1 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.216+14446C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68659806 | |||||||
| chr15:68659900 | G | A | 2 | a0001c0004t0007g0023 a0001c0004t0007g0172 |
2 | HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.216+14540G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68659900 | |||||||
| chr15:68659902 | G | A | 4 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0196 others(1): Show |
4 | HG03130.hp2 HG03225.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.216+14542G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68659902 | |||||||
| chr15:68659981 | G | A | 34 | a0001c0001t0001g0052 a0001c0001t0001g0074 a0001c0001t0001g0105 others(31): Show |
34 | HG01884.hp2 HG01891.hp2 HG02015.hp1 others(31): Show |
intron_variant | MODIFIER | c.216+14621G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68659981 | |||||||
| chr15:68660005 | A | G | 5 | a0001c0002t0005g0016 a0001c0002t0006g0223 a0001c0003t0006g0051 others(2): Show |
5 | HG02572.hp2 HG02647.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.216+14645A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68660005 | |||||||
| chr15:68660138 | C | T | 1 | a0001c0001t0009g0238 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.216+14778C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68660138 | |||||||
| chr15:68660278 | A | G | 1 | a0001c0001t0006g0011 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.216+14918A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68660278 | |||||||
| chr15:68660349 | C | G | 3 | a0001c0001t0008g0025 a0001c0002t0006g0137 a0001c0002t0006g0248 |
3 | HG01496.hp1 HG02451.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.216+14989C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68660349 | |||||||
| chr15:68660864 | A | G | 173 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(170): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.216+15504A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68660864 | |||||||
| chr15:68660913 | A | T | 2 | a0001c0004t0007g0023 a0001c0004t0007g0172 |
2 | HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.216+15553A>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68660913 | |||||||
| chr15:68660976 | C | CTT | 138 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.216+15627_216+1562 others(6): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68660976 | ||||||
| chr15:68660976 | CT | C | 62 | a0001c0001t0001g0074 a0001c0001t0001g0105 a0001c0001t0001g0179 others(59): Show |
62 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(59): Show |
intron_variant | MODIFIER | c.216+15628delT | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68660976 | ||||||
| chr15:68661034 | C | T | 34 | a0001c0001t0001g0052 a0001c0001t0001g0074 a0001c0001t0001g0105 others(31): Show |
34 | HG01884.hp2 HG01891.hp2 HG02015.hp1 others(31): Show |
intron_variant | MODIFIER | c.216+15674C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68661034 | |||||||
| chr15:68661107 | G | A | 34 | a0001c0001t0001g0052 a0001c0001t0001g0074 a0001c0001t0001g0105 others(31): Show |
34 | HG01884.hp2 HG01891.hp2 HG02015.hp1 others(31): Show |
intron_variant | MODIFIER | c.216+15747G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68661107 | |||||||
| chr15:68661121 | G | T | 13 | a0001c0001t0001g0085 a0001c0001t0001g0143 a0001c0001t0001g0159 others(10): Show |
13 | HG01192.hp1 HG02523.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.216+15761G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68661121 | |||||||
| chr15:68661167 | G | A | 1 | a0001c0003t0008g0178 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.216+15807G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68661167 | |||||||
| chr15:68661236 | C | G | 26 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0065 others(23): Show |
26 | HG01106.hp2 HG01175.hp2 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.216+15876C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68661236 | |||||||
| chr15:68661363 | GA | G | 4 | a0001c0001t0001g0048 a0001c0001t0003g0086 a0001c0001t0003g0127 others(1): Show |
4 | HG00673.hp2 HG02015.hp2 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.216+16005delA | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68661363 | ||||||
| chr15:68661389 | A | G | 246 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(243): Show |
246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.216+16029A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68661389 | |||||||
| chr15:68661510 | T | G | 1 | a0001c0001t0010g0252 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.216+16150T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68661510 | |||||||
| chr15:68661533 | G | A | 33 | a0001c0001t0001g0009 a0001c0001t0001g0037 a0001c0001t0001g0060 others(30): Show |
33 | HG00408.hp1 HG00597.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.216+16173G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68661533 | |||||||
| chr15:68661603 | A | G | 1 | a0001c0001t0007g0162 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.216+16243A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68661603 | |||||||
| chr15:68661762 | T | G | 14 | a0001c0001t0001g0098 a0001c0001t0001g0139 a0001c0001t0001g0202 others(11): Show |
14 | HG01074.hp1 HG01109.hp2 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.216+16402T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68661762 | |||||||
| chr15:68661900 | A | C | 28 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0065 others(25): Show |
28 | HG01106.hp2 HG01175.hp2 HG01258.hp1 others(25): Show |
intron_variant | MODIFIER | c.216+16540A>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68661900 | |||||||
| chr15:68661957 | A | C | 1 | a0001c0001t0003g0213 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.216+16597A>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68661957 | |||||||
| chr15:68662006 | C | CAATA | 29 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0042 others(26): Show |
29 | HG01070.hp2 HG01071.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.216+16666_216+1666 others(8): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68662006 | ||||||
| chr15:68662006 | C | CAATAAAT others(1): Show |
2 | a0001c0001t0001g0115 a0001c0004t0006g0032 |
2 | HG02622.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.216+16662_216+1666 others(12): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68662006 | ||||||
| chr15:68662022 | A | AAATT | 4 | a0001c0001t0001g0098 a0001c0001t0005g0073 a0001c0001t0006g0021 others(1): Show |
4 | HG01978.hp1 HG02615.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.216+16665_216+1666 others(8): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68662022 | ||||||
| chr15:68662022 | A | T | 7 | a0001c0001t0001g0028 a0001c0001t0001g0067 a0001c0001t0001g0090 others(4): Show |
7 | HG01243.hp2 HG02056.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.216+16662A>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68662022 | |||||||
| chr15:68662026 | A | AAATT | 12 | a0001c0001t0001g0094 a0001c0001t0001g0139 a0001c0001t0001g0202 others(9): Show |
12 | HG01074.hp1 HG01109.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.216+16678_216+1668 others(8): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68662026 | ||||||
| chr15:68662026 | A | T | 144 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0037 others(141): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.216+16666A>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68662026 | |||||||
| chr15:68662030 | T | A | 21 | a0001c0001t0001g0010 a0001c0001t0001g0115 a0001c0001t0001g0132 others(18): Show |
21 | HG01258.hp1 HG01261.hp1 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.216+16670T>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68662030 | |||||||
| chr15:68662034 | T | A | 1 | a0001c0001t0006g0004 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.216+16674T>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68662034 | |||||||
| chr15:68662333 | A | C | 4 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0196 others(1): Show |
4 | HG03130.hp2 HG03225.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.216+16973A>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68662333 | |||||||
| chr15:68662440 | A | G | 1 | a0001c0001t0018g0255 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.216+17080A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68662440 | |||||||
| chr15:68662597 | A | G | 1 | a0001c0001t0024g0120 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.216+17237A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68662597 | |||||||
| chr15:68662769 | T | C | 246 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(243): Show |
246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.216+17409T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68662769 | |||||||
| chr15:68662832 | C | T | 4 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0196 others(1): Show |
4 | HG03130.hp2 HG03225.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.216+17472C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68662832 | |||||||
| chr15:68662857 | T | C | 27 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0065 others(24): Show |
27 | HG01106.hp2 HG01175.hp2 HG01258.hp1 others(24): Show |
intron_variant | MODIFIER | c.216+17497T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68662857 | |||||||
| chr15:68662930 | A | AT | 6 | a0001c0001t0001g0039 a0001c0001t0001g0061 a0001c0001t0001g0114 others(3): Show |
6 | HG01261.hp2 HG01346.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.216+17580dupT | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68662930 | ||||||
| chr15:68662979 | T | A | 88 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0074 others(85): Show |
88 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(85): Show |
intron_variant | MODIFIER | c.216+17619T>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68662979 | |||||||
| chr15:68663040 | G | A | 88 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0074 others(85): Show |
88 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(85): Show |
intron_variant | MODIFIER | c.216+17680G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68663040 | |||||||
| chr15:68663044 | T | A | 53 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0074 others(50): Show |
53 | HG01070.hp2 HG01071.hp2 HG01074.hp1 others(50): Show |
intron_variant | MODIFIER | c.216+17684T>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68663044 | |||||||
| chr15:68663099 | C | T | 53 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0074 others(50): Show |
53 | HG01070.hp2 HG01071.hp2 HG01074.hp1 others(50): Show |
intron_variant | MODIFIER | c.216+17739C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68663099 | |||||||
| chr15:68663129 | C | T | 53 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0074 others(50): Show |
53 | HG01070.hp2 HG01071.hp2 HG01074.hp1 others(50): Show |
intron_variant | MODIFIER | c.216+17769C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68663129 | |||||||
| chr15:68663163 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.216+17803C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68663163 | |||||||
| chr15:68663206 | T | C | 220 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(217): Show |
220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.216+17846T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68663206 | |||||||
| chr15:68663449 | G | A | 1 | a0001c0001t0010g0252 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.216+18089G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68663449 | |||||||
| chr15:68663526 | A | C | 246 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(243): Show |
246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.216+18166A>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68663526 | |||||||
| chr15:68663544 | A | G | 1 | a0001c0002t0001g0006 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.216+18184A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68663544 | |||||||
| chr15:68663611 | C | T | 2 | a0001c0001t0004g0058 a0001c0001t0004g0109 |
2 | HG00408.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.216+18251C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68663611 | |||||||
| chr15:68663836 | C | T | 47 | a0001c0001t0001g0052 a0001c0001t0001g0074 a0001c0001t0001g0098 others(44): Show |
47 | HG01074.hp1 HG01109.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.216+18476C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68663836 | |||||||
| chr15:68663968 | G | T | 1 | a0001c0005t0003g0210 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.216+18608G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68663968 | |||||||
| chr15:68664052 | T | G | 47 | a0001c0001t0001g0052 a0001c0001t0001g0074 a0001c0001t0001g0098 others(44): Show |
47 | HG01074.hp1 HG01109.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.216+18692T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68664052 | |||||||
| chr15:68664107 | G | A | 1 | a0001c0001t0004g0119 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.216+18747G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68664107 | |||||||
| chr15:68664354 | CTG | C | 47 | a0001c0001t0001g0052 a0001c0001t0001g0074 a0001c0001t0001g0098 others(44): Show |
47 | HG01074.hp1 HG01109.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.216+18995_216+1899 others(6): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68664354 | |||||||
| chr15:68664368 | C | T | 1 | a0001c0001t0005g0164 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.216+19008C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68664368 | |||||||
| chr15:68664374 | A | G | 245 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(242): Show |
245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.216+19014A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68664374 | |||||||
| chr15:68664430 | G | A | 17 | a0001c0001t0001g0052 a0001c0001t0001g0066 a0001c0001t0001g0105 others(14): Show |
17 | HG02015.hp1 HG02040.hp1 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.216+19070G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68664430 | |||||||
| chr15:68664589 | G | A | 20 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0065 others(17): Show |
20 | HG01106.hp2 HG01175.hp2 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.216+19229G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68664589 | |||||||
| chr15:68664646 | C | CA | 8 | a0001c0001t0001g0200 a0001c0001t0002g0181 a0001c0001t0003g0036 others(5): Show |
8 | HG02074.hp1 HG02109.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.216+19295dupA | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68664646 | ||||||
| chr15:68664764 | A | T | 1 | a0001c0002t0002g0170 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.216+19404A>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68664764 | |||||||
| chr15:68664803 | A | G | 172 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(169): Show |
172 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.216+19443A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68664803 | |||||||
| chr15:68664814 | C | T | 2 | a0001c0001t0006g0236 a0001c0001t0027g0034 |
2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.216+19454C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68664814 | |||||||
| chr15:68665011 | G | GTCTTT | 246 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(243): Show |
246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.216+19653_216+1965 others(9): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68665011 | ||||||
| chr15:68665090 | G | A | 1 | a0001c0001t0016g0250 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.216+19730G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68665090 | |||||||
| chr15:68665274 | G | A | 1 | a0001c0004t0005g0003 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.216+19914G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68665274 | |||||||
| chr15:68665414 | T | G | 5 | a0001c0001t0002g0181 a0001c0001t0005g0164 a0001c0001t0005g0194 others(2): Show |
5 | HG02109.hp1 HG02630.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.216+20054T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68665414 | |||||||
| chr15:68665545 | ATAAAT | A | 29 | a0001c0001t0001g0052 a0001c0001t0001g0098 a0001c0001t0001g0105 others(26): Show |
29 | HG01074.hp1 HG01109.hp2 HG01978.hp1 others(26): Show |
intron_variant | MODIFIER | c.216+20190_216+2019 others(9): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68665545 | ||||||
| chr15:68665657 | T | G | 13 | a0001c0001t0001g0098 a0001c0001t0001g0139 a0001c0001t0001g0202 others(10): Show |
13 | HG01074.hp1 HG01109.hp2 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.216+20297T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68665657 | |||||||
| chr15:68665706 | A | G | 172 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(169): Show |
172 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.216+20346A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68665706 | |||||||
| chr15:68665737 | G | A | 15 | a0001c0001t0001g0052 a0001c0001t0001g0105 a0001c0001t0001g0199 others(12): Show |
15 | HG02015.hp1 HG02040.hp1 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.216+20377G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68665737 | |||||||
| chr15:68665899 | G | A | 33 | a0001c0001t0004g0017 a0001c0001t0005g0007 a0001c0001t0005g0012 others(30): Show |
33 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.216+20539G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68665899 | |||||||
| chr15:68666170 | A | C | 1 | a0001c0001t0004g0058 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.216+20810A>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68666170 | |||||||
| chr15:68666251 | G | T | 1 | a0001c0001t0009g0238 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.216+20891G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68666251 | |||||||
| chr15:68666324 | G | A | 6 | a0001c0001t0004g0017 a0001c0001t0005g0012 a0001c0001t0005g0013 others(3): Show |
6 | HG02976.hp1 HG03130.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.216+20964G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68666324 | |||||||
| chr15:68666338 | C | G | 2 | a0001c0004t0007g0023 a0001c0004t0007g0172 |
2 | HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.216+20978C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68666338 | |||||||
| chr15:68666444 | T | G | 1 | a0001c0004t0006g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.216+21084T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68666444 | |||||||
| chr15:68666663 | G | A | 33 | a0001c0001t0004g0017 a0001c0001t0005g0007 a0001c0001t0005g0012 others(30): Show |
33 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.216+21303G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68666663 | |||||||
| chr15:68666798 | C | T | 30 | a0001c0001t0001g0052 a0001c0001t0001g0098 a0001c0001t0001g0105 others(27): Show |
30 | HG01074.hp1 HG01109.hp2 HG01978.hp1 others(27): Show |
intron_variant | MODIFIER | c.216+21438C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68666798 | |||||||
| chr15:68666834 | G | A | 246 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(243): Show |
246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.216+21474G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68666834 | |||||||
| chr15:68667030 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.216+21670G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68667030 | |||||||
| chr15:68667233 | TCTTCTAC others(9): Show |
T | 1 | a0001c0001t0001g0098 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.216+21879_216+2189 others(20): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68667233 | ||||||
| chr15:68667337 | C | T | 45 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0065 others(42): Show |
45 | HG01106.hp2 HG01175.hp2 HG01258.hp1 others(42): Show |
intron_variant | MODIFIER | c.216+21977C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68667337 | |||||||
| chr15:68667423 | G | A | 1 | a0001c0001t0005g0164 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.216+22063G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68667423 | |||||||
| chr15:68667514 | G | A | 6 | a0001c0001t0004g0017 a0001c0001t0005g0012 a0001c0001t0005g0013 others(3): Show |
6 | HG02976.hp1 HG03130.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.216+22154G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68667514 | |||||||
| chr15:68667608 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.216+22248G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68667608 | |||||||
| chr15:68667675 | C | T | 35 | a0001c0001t0001g0212 a0001c0001t0004g0017 a0001c0001t0005g0007 others(32): Show |
35 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.216+22315C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68667675 | |||||||
| chr15:68667814 | G | C | 1 | a0001c0001t0003g0036 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.216+22454G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68667814 | |||||||
| chr15:68667839 | T | C | 15 | a0001c0001t0001g0052 a0001c0001t0001g0105 a0001c0001t0001g0199 others(12): Show |
15 | HG02015.hp1 HG02040.hp1 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.216+22479T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68667839 | |||||||
| chr15:68667848 | G | A | 19 | a0001c0001t0001g0074 a0001c0001t0001g0179 a0001c0001t0001g0228 others(16): Show |
19 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.216+22488G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68667848 | |||||||
| chr15:68667879 | T | G | 246 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(243): Show |
246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.216+22519T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68667879 | |||||||
| chr15:68667919 | C | T | 27 | a0001c0001t0005g0007 a0001c0001t0008g0025 a0001c0002t0001g0006 others(24): Show |
27 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.216+22559C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68667919 | |||||||
| chr15:68667920 | G | A | 27 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0065 others(24): Show |
27 | HG01106.hp2 HG01175.hp2 HG01258.hp1 others(24): Show |
intron_variant | MODIFIER | c.216+22560G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68667920 | |||||||
| chr15:68667947 | C | T | 5 | a0001c0001t0002g0241 a0001c0001t0003g0225 a0001c0001t0003g0226 others(2): Show |
5 | HG01070.hp1 HG01081.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.216+22587C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68667947 | |||||||
| chr15:68668015 | G | A | 4 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0196 others(1): Show |
4 | HG03130.hp2 HG03225.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.216+22655G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68668015 | |||||||
| chr15:68668057 | G | C | 4 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0196 others(1): Show |
4 | HG03130.hp2 HG03225.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.216+22697G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68668057 | |||||||
| chr15:68668116 | C | T | 2 | a0001c0001t0005g0194 a0001c0001t0017g0251 |
2 | HG02630.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.216+22756C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68668116 | |||||||
| chr15:68668180 | A | G | 35 | a0001c0001t0001g0212 a0001c0001t0004g0017 a0001c0001t0005g0007 others(32): Show |
35 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.216+22820A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68668180 | |||||||
| chr15:68668210 | G | A | 2 | a0001c0001t0006g0236 a0001c0001t0027g0034 |
2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.216+22850G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68668210 | |||||||
| chr15:68668281 | A | AG | 50 | a0001c0001t0001g0052 a0001c0001t0001g0105 a0001c0001t0001g0199 others(47): Show |
50 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.216+22927dupG | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68668281 | ||||||
| chr15:68668288 | C | T | 1 | a0001c0001t0009g0238 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.216+22928C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68668288 | |||||||
| chr15:68668414 | AC | A | 35 | a0001c0001t0001g0212 a0001c0001t0004g0017 a0001c0001t0005g0007 others(32): Show |
35 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.216+23055delC | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68668414 | |||||||
| chr15:68668455 | T | A | 1 | a0001c0001t0001g0183 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.216+23095T>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68668455 | |||||||
| chr15:68668513 | G | A | 5 | a0001c0001t0001g0094 a0001c0001t0006g0191 a0001c0001t0008g0001 others(2): Show |
5 | HG02559.hp2 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.216+23153G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68668513 | |||||||
| chr15:68668550 | C | T | 15 | a0001c0001t0001g0052 a0001c0001t0001g0105 a0001c0001t0001g0199 others(12): Show |
15 | HG02015.hp1 HG02040.hp1 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.216+23190C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68668550 | |||||||
| chr15:68668671 | C | T | 45 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0065 others(42): Show |
45 | HG01106.hp2 HG01175.hp2 HG01258.hp1 others(42): Show |
intron_variant | MODIFIER | c.216+23311C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68668671 | |||||||
| chr15:68668806 | T | C | 97 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0052 others(94): Show |
97 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(94): Show |
intron_variant | MODIFIER | c.216+23446T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68668806 | |||||||
| chr15:68668895 | G | A | 1 | a0001c0001t0006g0218 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.216+23535G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68668895 | |||||||
| chr15:68669019 | G | A | 2 | a0001c0001t0004g0017 a0001c0001t0009g0014 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.216+23659G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68669019 | |||||||
| chr15:68669065 | GAGAA | G | 5 | a0001c0001t0001g0179 a0001c0001t0001g0228 a0001c0001t0002g0091 others(2): Show |
5 | HG01891.hp2 HG02615.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.216+23709_216+2371 others(8): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68669065 | ||||||
| chr15:68669069 | A | AAG | 29 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0065 others(26): Show |
29 | HG01106.hp2 HG01175.hp2 HG01258.hp1 others(26): Show |
intron_variant | MODIFIER | c.216+23727_216+2372 others(6): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68669069 | ||||||
| chr15:68669085 | G | A | 2 | a0001c0001t0006g0236 a0001c0001t0027g0034 |
2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.216+23725G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68669085 | |||||||
| chr15:68669090 | A | AGAAG | 6 | a0001c0001t0001g0039 a0001c0001t0001g0061 a0001c0001t0001g0114 others(3): Show |
6 | HG01261.hp2 HG01346.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.216+23749_216+2375 others(8): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68669090 | ||||||
| chr15:68669164 | G | GAAAGA | 5 | a0001c0001t0001g0095 a0001c0001t0002g0234 a0001c0001t0003g0064 others(2): Show |
5 | HG01361.hp2 NA18944.hp2 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.216+23817_216+2382 others(9): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68669164 | ||||||
| chr15:68669187 | G | GAAGC | 48 | a0001c0001t0001g0052 a0001c0001t0001g0105 a0001c0001t0001g0199 others(45): Show |
48 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.216+23848_216+2385 others(8): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68669187 | ||||||
| chr15:68669187 | G | GAAGCAAG others(1): Show |
2 | a0001c0001t0004g0017 a0001c0001t0009g0014 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.216+23844_216+2385 others(12): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68669187 | ||||||
| chr15:68669213 | G | A | 4 | a0001c0001t0002g0096 a0001c0001t0002g0097 a0001c0001t0002g0219 others(1): Show |
4 | HG00735.hp2 HG01106.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.216+23853G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68669213 | |||||||
| chr15:68669225 | C | T | 50 | a0001c0001t0001g0052 a0001c0001t0001g0105 a0001c0001t0001g0199 others(47): Show |
50 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.216+23865C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68669225 | |||||||
| chr15:68669378 | C | G | 15 | a0001c0001t0001g0052 a0001c0001t0001g0105 a0001c0001t0001g0199 others(12): Show |
15 | HG02015.hp1 HG02040.hp1 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.216+24018C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68669378 | |||||||
| chr15:68669420 | G | T | 3 | a0001c0001t0003g0244 a0001c0001t0003g0245 a0001c0001t0003g0246 |
3 | HG01261.hp1 HG01433.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.216+24060G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68669420 | |||||||
| chr15:68669517 | G | C | 5 | a0001c0001t0001g0094 a0001c0001t0006g0191 a0001c0001t0008g0001 others(2): Show |
5 | HG02559.hp2 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.216+24157G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68669517 | |||||||
| chr15:68669526 | C | T | 2 | a0001c0001t0006g0236 a0001c0001t0027g0034 |
2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.216+24166C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68669526 | |||||||
| chr15:68669600 | G | A | 46 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0065 others(43): Show |
46 | HG01106.hp2 HG01175.hp2 HG01258.hp1 others(43): Show |
intron_variant | MODIFIER | c.216+24240G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68669600 | |||||||
| chr15:68669674 | G | C | 3 | a0001c0001t0001g0074 a0001c0003t0001g0057 a0001c0003t0011g0247 |
3 | HG02109.hp2 HG03139.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.216+24314G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68669674 | |||||||
| chr15:68669798 | T | TA | 50 | a0001c0001t0001g0052 a0001c0001t0001g0105 a0001c0001t0001g0199 others(47): Show |
50 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.216+24439dupA | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68669798 | ||||||
| chr15:68669822 | C | T | 17 | a0001c0001t0001g0074 a0001c0001t0001g0179 a0001c0001t0001g0228 others(14): Show |
17 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.216+24462C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68669822 | |||||||
| chr15:68670058 | G | GA | 140 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0037 others(137): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.216+24708dupA | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68670058 | ||||||
| chr15:68670068 | A | AC | 8 | a0001c0001t0001g0009 a0001c0001t0001g0098 a0001c0001t0001g0139 others(5): Show |
8 | HG01070.hp2 HG01071.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.216+24708_216+2470 others(5): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68670068 | |||||||
| chr15:68670074 | G | A | 1 | a0001c0001t0004g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.216+24714G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68670074 | |||||||
| chr15:68670075 | GA | G | 30 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0065 others(27): Show |
30 | HG01106.hp2 HG01175.hp2 HG01258.hp1 others(27): Show |
intron_variant | MODIFIER | c.216+24720delA | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68670075 | ||||||
| chr15:68670076 | A | G | 3 | a0001c0001t0002g0002 a0001c0001t0005g0029 a0001c0001t0005g0166 |
3 | HG02258.hp2 HG02559.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.216+24716A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68670076 | |||||||
| chr15:68670164 | C | T | 1 | a0001c0002t0002g0038 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.216+24804C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68670164 | |||||||
| chr15:68670206 | G | T | 4 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0196 others(1): Show |
4 | HG03130.hp2 HG03225.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.216+24846G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68670206 | |||||||
| chr15:68670236 | G | A | 4 | a0001c0001t0001g0042 a0001c0001t0002g0081 a0001c0001t0009g0238 others(1): Show |
4 | HG02451.hp1 HG02622.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.216+24876G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68670236 | |||||||
| chr15:68670325 | C | A | 2 | a0001c0001t0004g0017 a0001c0001t0009g0014 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.217-24815C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68670325 | |||||||
| chr15:68670405 | CCTGGG | C | 45 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0065 others(42): Show |
45 | HG01106.hp2 HG01175.hp2 HG01258.hp1 others(42): Show |
intron_variant | MODIFIER | c.217-24732_217-2472 others(9): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68670405 | ||||||
| chr15:68670417 | T | A | 1 | a0001c0001t0002g0182 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.217-24723T>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68670417 | |||||||
| chr15:68670470 | G | A | 20 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0065 others(17): Show |
20 | HG01106.hp2 HG01175.hp2 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.217-24670G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68670470 | |||||||
| chr15:68670807 | G | A | 15 | a0001c0001t0001g0052 a0001c0001t0001g0105 a0001c0001t0001g0199 others(12): Show |
15 | HG02015.hp1 HG02040.hp1 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.217-24333G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68670807 | |||||||
| chr15:68670834 | C | T | 15 | a0001c0001t0001g0052 a0001c0001t0001g0105 a0001c0001t0001g0199 others(12): Show |
15 | HG02015.hp1 HG02040.hp1 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.217-24306C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68670834 | |||||||
| chr15:68671109 | G | A | 26 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0065 others(23): Show |
26 | HG01106.hp2 HG01175.hp2 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.217-24031G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68671109 | |||||||
| chr15:68671129 | G | A | 1 | a0001c0001t0004g0092 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.217-24011G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68671129 | |||||||
| chr15:68671211 | C | T | 15 | a0001c0001t0001g0052 a0001c0001t0001g0105 a0001c0001t0001g0199 others(12): Show |
15 | HG02015.hp1 HG02040.hp1 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.217-23929C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68671211 | |||||||
| chr15:68671262 | G | T | 2 | a0001c0004t0007g0023 a0001c0004t0007g0172 |
2 | HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.217-23878G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68671262 | |||||||
| chr15:68671310 | G | T | 1 | a0001c0001t0003g0160 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.217-23830G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68671310 | |||||||
| chr15:68671553 | G | C | 1 | a0001c0003t0001g0057 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.217-23587G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68671553 | |||||||
| chr15:68671900 | A | C | 2 | a0001c0001t0001g0060 a0001c0001t0001g0147 |
2 | HG01081.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.217-23240A>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68671900 | |||||||
| chr15:68671958 | G | T | 5 | a0001c0002t0005g0016 a0001c0002t0006g0223 a0001c0003t0006g0051 others(2): Show |
5 | HG02572.hp2 HG02647.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.217-23182G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68671958 | |||||||
| chr15:68672043 | C | T | 48 | a0001c0001t0001g0052 a0001c0001t0001g0105 a0001c0001t0001g0199 others(45): Show |
48 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.217-23097C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68672043 | |||||||
| chr15:68672058 | G | A | 5 | a0001c0001t0002g0181 a0001c0001t0005g0164 a0001c0001t0005g0194 others(2): Show |
5 | HG02109.hp1 HG02630.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.217-23082G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68672058 | |||||||
| chr15:68672154 | C | T | 1 | a0001c0002t0001g0188 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.217-22986C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68672154 | |||||||
| chr15:68672155 | G | A | 1 | a0001c0001t0004g0119 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.217-22985G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68672155 | |||||||
| chr15:68672158 | A | T | 1 | a0001c0001t0004g0119 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.217-22982A>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68672158 | |||||||
| chr15:68672159 | G | GGT | 6 | a0001c0002t0001g0008 a0001c0002t0002g0071 a0001c0002t0002g0142 others(3): Show |
6 | HG03471.hp1 HG03491.hp1 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.217-22956_217-2295 others(6): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68672159 | ||||||
| chr15:68672159 | G | GGTGTGT | 6 | a0001c0001t0001g0094 a0001c0001t0006g0191 a0001c0001t0006g0218 others(3): Show |
6 | HG01175.hp2 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.217-22960_217-2295 others(10): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68672159 | ||||||
| chr15:68672159 | G | GGTGTGTG others(1): Show |
4 | a0001c0001t0001g0215 a0001c0001t0003g0068 a0001c0001t0005g0073 others(1): Show |
4 | HG02155.hp1 HG02486.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.217-22962_217-2295 others(12): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68672159 | ||||||
| chr15:68672159 | G | GGTGTGTG others(3): Show |
27 | a0001c0001t0001g0010 a0001c0001t0001g0065 a0001c0001t0001g0115 others(24): Show |
27 | HG01070.hp1 HG01081.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.217-22964_217-2295 others(14): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68672159 | ||||||
| chr15:68672159 | G | GGTGTGTG others(5): Show |
28 | a0001c0001t0001g0042 a0001c0001t0001g0052 a0001c0001t0001g0074 others(25): Show |
28 | HG00280.hp2 HG01891.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.217-22966_217-2295 others(16): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68672159 | ||||||
| chr15:68672159 | G | GGTGTGTG others(7): Show |
90 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0039 others(87): Show |
90 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.217-22968_217-2295 others(18): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68672159 | ||||||
| chr15:68672159 | G | GGTGTGTG others(9): Show |
46 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0084 others(43): Show |
46 | HG00280.hp1 HG00408.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.217-22970_217-2295 others(20): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68672159 | ||||||
| chr15:68672159 | G | GGTGTGTG others(11): Show |
24 | a0001c0001t0001g0028 a0001c0001t0001g0087 a0001c0001t0001g0089 others(21): Show |
24 | HG00140.hp2 HG00621.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.217-22972_217-2295 others(22): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68672159 | ||||||
| chr15:68672159 | G | GGTGTGTG others(13): Show |
14 | a0001c0001t0001g0037 a0001c0001t0001g0090 a0001c0001t0001g0100 others(11): Show |
14 | HG01109.hp1 HG01243.hp2 HG02004.hp2 others(11): Show |
intron_variant | MODIFIER | c.217-22974_217-2295 others(24): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68672159 | ||||||
| chr15:68672159 | G | GTGTGTGT others(6): Show |
1 | a0001c0001t0004g0119 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.217-22981_217-2298 others(17): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68672159 | |||||||
| chr15:68672247 | A | T | 5 | a0001c0002t0005g0016 a0001c0002t0006g0223 a0001c0003t0006g0051 others(2): Show |
5 | HG02572.hp2 HG02647.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.217-22893A>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68672247 | |||||||
| chr15:68672257 | A | G | 45 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0065 others(42): Show |
45 | HG01106.hp2 HG01175.hp2 HG01258.hp1 others(42): Show |
intron_variant | MODIFIER | c.217-22883A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68672257 | |||||||
| chr15:68672274 | C | T | 149 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(146): Show |
149 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.217-22866C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68672274 | |||||||
| chr15:68672444 | G | A | 1 | a0001c0001t0003g0140 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.217-22696G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68672444 | |||||||
| chr15:68672531 | G | A | 44 | a0001c0001t0001g0052 a0001c0001t0001g0105 a0001c0001t0001g0199 others(41): Show |
44 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.217-22609G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68672531 | |||||||
| chr15:68673017 | A | T | 1 | a0004c0006t0002g0136 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.217-22123A>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68673017 | |||||||
| chr15:68673036 | G | A | 2 | a0001c0001t0006g0236 a0001c0001t0027g0034 |
2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.217-22104G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68673036 | |||||||
| chr15:68673051 | T | C | 3 | a0001c0001t0006g0236 a0001c0001t0009g0238 a0001c0001t0027g0034 |
3 | HG02970.hp2 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.217-22089T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68673051 | |||||||
| chr15:68673160 | A | T | 1 | a0001c0001t0003g0155 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.217-21980A>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68673160 | |||||||
| chr15:68673375 | A | G | 2 | a0001c0001t0004g0017 a0001c0001t0009g0014 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.217-21765A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68673375 | |||||||
| chr15:68673625 | G | A | 28 | a0001c0001t0001g0212 a0001c0001t0005g0007 a0001c0001t0008g0025 others(25): Show |
28 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.217-21515G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68673625 | |||||||
| chr15:68673834 | C | CGT | 3 | a0001c0001t0004g0017 a0001c0001t0009g0014 a0001c0001t0009g0238 |
3 | HG02976.hp1 HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.217-21306_217-2130 others(6): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68673834 | |||||||
| chr15:68673835 | T | A | 3 | a0001c0001t0004g0017 a0001c0001t0009g0014 a0001c0001t0009g0238 |
3 | HG02976.hp1 HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.217-21305T>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68673835 | |||||||
| chr15:68673835 | T | TA | 7 | a0001c0001t0002g0181 a0001c0001t0005g0164 a0001c0001t0005g0194 others(4): Show |
7 | HG01884.hp2 HG02109.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.217-21282dupA | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68673835 | ||||||
| chr15:68673835 | TA | T | 60 | a0001c0001t0001g0009 a0001c0001t0001g0067 a0001c0001t0001g0074 others(57): Show |
60 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.217-21282delA | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68673835 | ||||||
| chr15:68673835 | TAA | T | 155 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0028 others(152): Show |
155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.217-21283_217-2128 others(6): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68673835 | ||||||
| chr15:68673888 | C | T | 2 | a0001c0004t0007g0023 a0001c0004t0007g0172 |
2 | HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.217-21252C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68673888 | |||||||
| chr15:68674105 | G | A | 1 | a0001c0001t0007g0232 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.217-21035G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68674105 | |||||||
| chr15:68674193 | A | T | 3 | a0001c0001t0001g0204 a0001c0001t0003g0171 a0001c0001t0003g0213 |
3 | HG00140.hp1 HG01256.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.217-20947A>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68674193 | |||||||
| chr15:68674395 | C | G | 67 | a0001c0001t0001g0052 a0001c0001t0001g0074 a0001c0001t0001g0105 others(64): Show |
67 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.217-20745C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68674395 | |||||||
| chr15:68674473 | T | C | 15 | a0001c0001t0001g0052 a0001c0001t0001g0105 a0001c0001t0001g0199 others(12): Show |
15 | HG02015.hp1 HG02040.hp1 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.217-20667T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68674473 | |||||||
| chr15:68674520 | A | C | 2 | a0001c0001t0006g0236 a0001c0001t0027g0034 |
2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.217-20620A>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68674520 | |||||||
| chr15:68674542 | G | A | 1 | a0001c0001t0002g0197 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.217-20598G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68674542 | |||||||
| chr15:68674707 | C | T | 29 | a0001c0001t0001g0212 a0001c0001t0005g0007 a0001c0001t0008g0025 others(26): Show |
29 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.217-20433C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68674707 | |||||||
| chr15:68674795 | C | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.217-20345C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68674795 | |||||||
| chr15:68674796 | A | G | 247 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(244): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.217-20344A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68674796 | |||||||
| chr15:68674821 | G | C | 145 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(142): Show |
145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.217-20319G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68674821 | |||||||
| chr15:68674936 | G | T | 13 | a0001c0001t0001g0052 a0001c0001t0001g0105 a0001c0001t0001g0199 others(10): Show |
13 | HG02015.hp1 HG02040.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.217-20204G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68674936 | |||||||
| chr15:68674944 | C | T | 18 | a0001c0001t0001g0074 a0001c0001t0001g0179 a0001c0001t0001g0228 others(15): Show |
18 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.217-20196C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68674944 | |||||||
| chr15:68674950 | G | A | 2 | a0001c0005t0002g0043 a0001c0005t0003g0130 |
2 | HG00741.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.217-20190G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68674950 | |||||||
| chr15:68675048 | T | A | 1 | a0001c0001t0001g0065 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.217-20092T>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68675048 | |||||||
| chr15:68675225 | C | T | 1 | a0001c0001t0009g0014 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.217-19915C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68675225 | |||||||
| chr15:68675241 | C | G | 1 | a0001c0001t0002g0091 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.217-19899C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68675241 | |||||||
| chr15:68675613 | C | T | 3 | a0001c0001t0002g0002 a0001c0001t0005g0029 a0001c0001t0005g0166 |
3 | HG02258.hp2 HG02559.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.217-19527C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68675613 | |||||||
| chr15:68675650 | T | C | 174 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(171): Show |
174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.217-19490T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68675650 | |||||||
| chr15:68675944 | ATATAG | A | 3 | a0001c0001t0004g0017 a0001c0001t0009g0014 a0001c0001t0009g0238 |
3 | HG02976.hp1 HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.217-19191_217-1918 others(9): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68675944 | ||||||
| chr15:68675979 | TATAGA | T | 3 | a0001c0001t0004g0017 a0001c0001t0009g0014 a0001c0001t0009g0238 |
3 | HG02976.hp1 HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.217-19147_217-1914 others(9): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68675979 | ||||||
| chr15:68676005 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.217-19135G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68676005 | |||||||
| chr15:68676307 | G | A | 1 | a0001c0001t0002g0181 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.217-18833G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68676307 | |||||||
| chr15:68676325 | C | G | 1 | a0001c0001t0003g0214 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.217-18815C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68676325 | |||||||
| chr15:68676394 | C | T | 5 | a0001c0001t0001g0133 a0001c0001t0004g0026 a0001c0001t0004g0134 others(2): Show |
5 | HG03130.hp1 HG03139.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.217-18746C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68676394 | |||||||
| chr15:68676478 | C | G | 5 | a0001c0002t0005g0016 a0001c0002t0006g0223 a0001c0003t0006g0051 others(2): Show |
5 | HG02572.hp2 HG02647.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.217-18662C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68676478 | |||||||
| chr15:68676481 | T | C | 174 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(171): Show |
174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.217-18659T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68676481 | |||||||
| chr15:68676492 | G | A | 1 | a0001c0001t0011g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.217-18648G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68676492 | |||||||
| chr15:68676624 | G | A | 2 | a0001c0001t0001g0042 a0001c0001t0002g0081 |
2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.217-18516G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68676624 | |||||||
| chr15:68676663 | C | T | 13 | a0001c0001t0001g0052 a0001c0001t0001g0105 a0001c0001t0001g0199 others(10): Show |
13 | HG02015.hp1 HG02040.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.217-18477C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68676663 | |||||||
| chr15:68676839 | AC | A | 15 | a0001c0001t0001g0042 a0001c0001t0001g0094 a0001c0001t0001g0115 others(12): Show |
15 | HG02145.hp2 HG02451.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.217-18300delC | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68676839 | |||||||
| chr15:68677098 | C | T | 1 | a0001c0001t0002g0146 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.217-18042C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68677098 | |||||||
| chr15:68677157 | G | A | 42 | a0001c0001t0001g0009 a0001c0001t0001g0074 a0001c0001t0001g0098 others(39): Show |
42 | HG01070.hp2 HG01071.hp2 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.217-17983G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68677157 | |||||||
| chr15:68677256 | G | A | 1 | a0001c0001t0003g0213 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.217-17884G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68677256 | |||||||
| chr15:68677389 | A | G | 43 | a0001c0001t0001g0009 a0001c0001t0001g0074 a0001c0001t0001g0098 others(40): Show |
43 | HG01070.hp2 HG01071.hp2 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.217-17751A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68677389 | |||||||
| chr15:68677390 | G | A | 9 | a0001c0001t0004g0017 a0001c0001t0009g0014 a0001c0001t0009g0238 others(6): Show |
9 | HG02109.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.217-17750G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68677390 | |||||||
| chr15:68677397 | G | T | 43 | a0001c0001t0001g0009 a0001c0001t0001g0074 a0001c0001t0001g0098 others(40): Show |
43 | HG01070.hp2 HG01071.hp2 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.217-17743G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68677397 | |||||||
| chr15:68677519 | A | T | 1 | a0001c0001t0006g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.217-17621A>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68677519 | |||||||
| chr15:68677526 | A | G | 1 | a0001c0001t0005g0131 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.217-17614A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68677526 | |||||||
| chr15:68677534 | G | A | 1 | a0001c0001t0006g0021 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.217-17606G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68677534 | |||||||
| chr15:68677669 | C | T | 1 | a0001c0003t0011g0247 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.217-17471C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68677669 | |||||||
| chr15:68677780 | C | G | 129 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0037 others(126): Show |
129 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.217-17360C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68677780 | |||||||
| chr15:68677858 | A | G | 4 | a0001c0001t0002g0022 a0001c0001t0002g0078 a0001c0001t0002g0079 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.217-17282A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68677858 | |||||||
| chr15:68677933 | G | A | 2 | a0001c0001t0004g0184 a0001c0001t0004g0185 |
2 | NA18949.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.217-17207G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68677933 | |||||||
| chr15:68677983 | C | T | 2 | a0001c0004t0007g0023 a0001c0004t0007g0172 |
2 | HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.217-17157C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68677983 | |||||||
| chr15:68678067 | A | AG | 43 | a0001c0001t0001g0009 a0001c0001t0001g0074 a0001c0001t0001g0098 others(40): Show |
43 | HG01070.hp2 HG01071.hp2 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.217-17071dupG | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68678067 | ||||||
| chr15:68678117 | A | G | 43 | a0001c0001t0001g0009 a0001c0001t0001g0074 a0001c0001t0001g0098 others(40): Show |
43 | HG01070.hp2 HG01071.hp2 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.217-17023A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68678117 | |||||||
| chr15:68678130 | A | G | 2 | a0001c0001t0003g0111 a0001c0001t0004g0112 |
2 | NA18964.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.217-17010A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68678130 | |||||||
| chr15:68678143 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.217-16997C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68678143 | |||||||
| chr15:68678148 | T | C | 236 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(233): Show |
236 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.217-16992T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68678148 | |||||||
| chr15:68678233 | G | A | 39 | a0001c0001t0001g0052 a0001c0001t0001g0105 a0001c0001t0001g0199 others(36): Show |
39 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.217-16907G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68678233 | |||||||
| chr15:68678402 | G | A | 4 | a0001c0001t0002g0096 a0001c0001t0002g0097 a0001c0001t0002g0219 others(1): Show |
4 | HG00735.hp2 HG01106.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.217-16738G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68678402 | |||||||
| chr15:68678412 | A | G | 43 | a0001c0001t0001g0009 a0001c0001t0001g0074 a0001c0001t0001g0098 others(40): Show |
43 | HG01070.hp2 HG01071.hp2 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.217-16728A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68678412 | |||||||
| chr15:68678433 | G | A | 128 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0037 others(125): Show |
128 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.217-16707G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68678433 | |||||||
| chr15:68678711 | G | A | 14 | a0001c0001t0001g0098 a0001c0001t0001g0139 a0001c0001t0001g0202 others(11): Show |
14 | HG01074.hp1 HG01109.hp2 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.217-16429G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68678711 | |||||||
| chr15:68678849 | G | A | 2 | a0001c0001t0006g0236 a0001c0001t0027g0034 |
2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.217-16291G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68678849 | |||||||
| chr15:68679115 | G | A | 22 | a0001c0001t0001g0074 a0001c0001t0001g0179 a0001c0001t0001g0228 others(19): Show |
22 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.217-16025G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68679115 | |||||||
| chr15:68679256 | G | A | 1 | a0001c0001t0001g0028 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.217-15884G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68679256 | |||||||
| chr15:68679284 | C | A | 1 | a0001c0003t0011g0247 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.217-15856C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68679284 | |||||||
| chr15:68679617 | T | A | 169 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(166): Show |
169 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.217-15523T>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68679617 | |||||||
| chr15:68679879 | C | T | 25 | a0001c0001t0001g0212 a0001c0001t0004g0207 a0001c0001t0005g0007 others(22): Show |
25 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.217-15261C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68679879 | |||||||
| chr15:68679923 | T | C | 3 | a0001c0001t0004g0180 a0001c0001t0006g0021 a0001c0001t0006g0237 |
3 | HG01109.hp2 HG02896.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.217-15217T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68679923 | |||||||
| chr15:68679942 | T | C | 22 | a0001c0001t0001g0074 a0001c0001t0001g0179 a0001c0001t0001g0228 others(19): Show |
22 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.217-15198T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68679942 | |||||||
| chr15:68680071 | C | T | 13 | a0001c0001t0001g0052 a0001c0001t0001g0105 a0001c0001t0001g0199 others(10): Show |
13 | HG02015.hp1 HG02040.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.217-15069C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68680071 | |||||||
| chr15:68680097 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.217-15043G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68680097 | |||||||
| chr15:68680168 | T | G | 1 | a0001c0001t0005g0164 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.217-14972T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68680168 | |||||||
| chr15:68680236 | A | T | 2 | a0001c0001t0002g0096 a0001c0001t0002g0097 |
2 | HG00735.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.217-14904A>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68680236 | |||||||
| chr15:68680249 | TTG | T | 2 | a0001c0001t0002g0096 a0001c0001t0002g0097 |
2 | HG00735.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.217-14887_217-1488 others(6): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68680249 | ||||||
| chr15:68680253 | G | T | 2 | a0001c0001t0002g0096 a0001c0001t0002g0097 |
2 | HG00735.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.217-14887G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68680253 | |||||||
| chr15:68680257 | G | T | 2 | a0001c0001t0002g0096 a0001c0001t0002g0097 |
2 | HG00735.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.217-14883G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68680257 | |||||||
| chr15:68680365 | A | C | 25 | a0001c0001t0001g0074 a0001c0001t0001g0179 a0001c0001t0001g0228 others(22): Show |
25 | HG01884.hp2 HG01891.hp2 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.217-14775A>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68680365 | |||||||
| chr15:68680593 | A | C | 1 | a0001c0001t0005g0164 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.217-14547A>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68680593 | |||||||
| chr15:68680634 | G | A | 9 | a0001c0001t0004g0017 a0001c0001t0009g0014 a0001c0001t0009g0238 others(6): Show |
9 | HG02109.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.217-14506G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68680634 | |||||||
| chr15:68680636 | T | C | 1 | a0001c0001t0016g0250 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.217-14504T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68680636 | |||||||
| chr15:68680994 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.217-14146G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68680994 | |||||||
| chr15:68681105 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.217-14035C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68681105 | |||||||
| chr15:68681111 | C | A | 25 | a0001c0001t0001g0212 a0001c0001t0004g0207 a0001c0001t0005g0007 others(22): Show |
25 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.217-14029C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68681111 | |||||||
| chr15:68681127 | CG | C | 25 | a0001c0001t0001g0212 a0001c0001t0004g0207 a0001c0001t0005g0007 others(22): Show |
25 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.217-14012delG | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68681127 | |||||||
| chr15:68681129 | C | T | 25 | a0001c0001t0001g0212 a0001c0001t0004g0207 a0001c0001t0005g0007 others(22): Show |
25 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.217-14011C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68681129 | |||||||
| chr15:68681198 | G | A | 1 | a0001c0001t0003g0083 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.217-13942G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68681198 | |||||||
| chr15:68681225 | AAT | A | 12 | a0001c0001t0001g0052 a0001c0001t0001g0105 a0001c0001t0001g0199 others(9): Show |
12 | HG02015.hp1 HG02040.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.217-13914_217-1391 others(6): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68681225 | |||||||
| chr15:68681226 | AT | A | 222 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(219): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.217-13905delT | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68681226 | ||||||
| chr15:68681240 | A | G | 18 | a0001c0001t0001g0074 a0001c0001t0001g0179 a0001c0001t0001g0228 others(15): Show |
18 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.217-13900A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68681240 | |||||||
| chr15:68681365 | G | A | 9 | a0001c0001t0001g0048 a0001c0001t0001g0098 a0001c0001t0001g0139 others(6): Show |
9 | HG00673.hp2 HG01978.hp1 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.217-13775G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68681365 | |||||||
| chr15:68681401 | GC | G | 25 | a0001c0001t0001g0212 a0001c0001t0004g0207 a0001c0001t0005g0007 others(22): Show |
25 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.217-13734delC | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68681401 | ||||||
| chr15:68681480 | G | T | 25 | a0001c0001t0001g0212 a0001c0001t0004g0207 a0001c0001t0005g0007 others(22): Show |
25 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.217-13660G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68681480 | |||||||
| chr15:68681481 | T | C | 25 | a0001c0001t0001g0212 a0001c0001t0004g0207 a0001c0001t0005g0007 others(22): Show |
25 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.217-13659T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68681481 | |||||||
| chr15:68681504 | G | A | 1 | a0001c0001t0004g0106 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.217-13636G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68681504 | |||||||
| chr15:68681515 | A | G | 19 | a0001c0001t0001g0074 a0001c0001t0001g0179 a0001c0001t0001g0228 others(16): Show |
19 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.217-13625A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68681515 | |||||||
| chr15:68681542 | C | T | 18 | a0001c0001t0001g0074 a0001c0001t0001g0179 a0001c0001t0001g0228 others(15): Show |
18 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.217-13598C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68681542 | |||||||
| chr15:68681550 | T | C | 1 | a0001c0004t0006g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.217-13590T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68681550 | |||||||
| chr15:68681568 | A | G | 2 | a0001c0001t0001g0165 a0001c0001t0002g0167 |
2 | HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.217-13572A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68681568 | |||||||
| chr15:68681586 | C | T | 18 | a0001c0001t0001g0074 a0001c0001t0001g0179 a0001c0001t0001g0228 others(15): Show |
18 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.217-13554C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68681586 | |||||||
| chr15:68681726 | GCTGA | G | 9 | a0001c0001t0004g0017 a0001c0001t0009g0014 a0001c0001t0009g0238 others(6): Show |
9 | HG02109.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.217-13411_217-1340 others(8): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68681726 | ||||||
| chr15:68681928 | A | C | 12 | a0001c0001t0001g0052 a0001c0001t0001g0105 a0001c0001t0001g0199 others(9): Show |
12 | HG02015.hp1 HG02040.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.217-13212A>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68681928 | |||||||
| chr15:68681960 | C | T | 18 | a0001c0001t0001g0074 a0001c0001t0001g0179 a0001c0001t0001g0228 others(15): Show |
18 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.217-13180C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68681960 | |||||||
| chr15:68682040 | C | T | 3 | a0001c0001t0003g0225 a0001c0001t0003g0226 a0001c0001t0003g0227 |
3 | HG01070.hp1 HG01081.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.217-13100C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68682040 | |||||||
| chr15:68682068 | A | G | 1 | a0001c0002t0001g0006 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.217-13072A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68682068 | |||||||
| chr15:68682089 | A | G | 236 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(233): Show |
236 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.217-13051A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68682089 | |||||||
| chr15:68682138 | C | A | 1 | a0001c0001t0005g0164 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.217-13002C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68682138 | |||||||
| chr15:68682139 | C | A | 1 | a0001c0001t0005g0164 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.217-13001C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68682139 | |||||||
| chr15:68682272 | A | G | 2 | a0001c0001t0001g0212 a0001c0002t0002g0099 |
2 | HG00741.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.217-12868A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68682272 | |||||||
| chr15:68682299 | C | T | 1 | a0001c0001t0006g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.217-12841C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68682299 | |||||||
| chr15:68682445 | G | GT | 18 | a0001c0001t0001g0074 a0001c0001t0001g0179 a0001c0001t0001g0228 others(15): Show |
18 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.217-12694dupT | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68682445 | ||||||
| chr15:68682521 | G | A | 55 | a0001c0001t0001g0028 a0001c0001t0001g0056 a0001c0001t0001g0067 others(52): Show |
55 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.217-12619G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68682521 | |||||||
| chr15:68682521 | G | C | 18 | a0001c0001t0001g0074 a0001c0001t0001g0179 a0001c0001t0001g0228 others(15): Show |
18 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.217-12619G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68682521 | |||||||
| chr15:68682630 | G | A | 1 | a0001c0001t0002g0182 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.217-12510G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68682630 | |||||||
| chr15:68682752 | G | A | 148 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(145): Show |
148 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.217-12388G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68682752 | |||||||
| chr15:68682800 | G | T | 25 | a0001c0001t0001g0212 a0001c0001t0004g0207 a0001c0001t0005g0007 others(22): Show |
25 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.217-12340G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68682800 | |||||||
| chr15:68682826 | T | C | 2 | a0001c0004t0007g0023 a0001c0004t0007g0172 |
2 | HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.217-12314T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68682826 | |||||||
| chr15:68682963 | C | T | 26 | a0001c0001t0001g0212 a0001c0001t0004g0207 a0001c0001t0005g0007 others(23): Show |
26 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.217-12177C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68682963 | |||||||
| chr15:68683011 | G | C | 4 | a0001c0001t0002g0181 a0001c0001t0005g0194 a0001c0001t0017g0251 others(1): Show |
4 | HG02109.hp1 HG02630.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.217-12129G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68683011 | |||||||
| chr15:68683153 | G | A | 1 | a0001c0001t0005g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.217-11987G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68683153 | |||||||
| chr15:68683257 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.217-11883C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68683257 | |||||||
| chr15:68683563 | C | A | 3 | a0001c0001t0001g0143 a0001c0001t0003g0125 a0001c0001t0003g0126 |
3 | NA18968.hp2 NA19057.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.217-11577C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68683563 | |||||||
| chr15:68683565 | A | AC | 18 | a0001c0001t0001g0074 a0001c0001t0001g0179 a0001c0001t0001g0228 others(15): Show |
18 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.217-11571dupC | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68683565 | ||||||
| chr15:68683655 | C | T | 164 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(161): Show |
164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.217-11485C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68683655 | |||||||
| chr15:68683726 | T | C | 18 | a0001c0001t0001g0074 a0001c0001t0001g0179 a0001c0001t0001g0228 others(15): Show |
18 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.217-11414T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68683726 | |||||||
| chr15:68683748 | G | A | 18 | a0001c0001t0001g0074 a0001c0001t0001g0179 a0001c0001t0001g0228 others(15): Show |
18 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.217-11392G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68683748 | |||||||
| chr15:68683830 | G | A | 18 | a0001c0001t0001g0074 a0001c0001t0001g0179 a0001c0001t0001g0228 others(15): Show |
18 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.217-11310G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68683830 | |||||||
| chr15:68683875 | T | C | 10 | a0001c0001t0004g0017 a0001c0001t0005g0164 a0001c0001t0009g0014 others(7): Show |
10 | HG02109.hp2 HG02572.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.217-11265T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68683875 | |||||||
| chr15:68683956 | A | G | 2 | a0001c0001t0003g0062 a0001c0001t0004g0110 |
2 | HG02523.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.217-11184A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68683956 | |||||||
| chr15:68683999 | AG | A | 25 | a0001c0001t0001g0212 a0001c0001t0004g0207 a0001c0001t0005g0007 others(22): Show |
25 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.217-11140delG | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68683999 | |||||||
| chr15:68684057 | A | T | 1 | a0001c0001t0002g0197 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.217-11083A>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68684057 | |||||||
| chr15:68684069 | G | A | 6 | a0001c0002t0005g0016 a0001c0002t0006g0223 a0001c0003t0001g0057 others(3): Show |
6 | HG02109.hp2 HG02572.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.217-11071G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68684069 | |||||||
| chr15:68684310 | A | C | 1 | a0001c0001t0005g0073 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.217-10830A>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68684310 | |||||||
| chr15:68684489 | C | T | 9 | a0001c0001t0004g0180 a0001c0001t0005g0012 a0001c0001t0005g0013 others(6): Show |
9 | HG01074.hp1 HG01109.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.217-10651C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68684489 | |||||||
| chr15:68684492 | A | G | 27 | a0001c0001t0001g0212 a0001c0001t0004g0207 a0001c0001t0005g0007 others(24): Show |
27 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.217-10648A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68684492 | |||||||
| chr15:68684543 | G | A | 27 | a0001c0001t0001g0212 a0001c0001t0004g0207 a0001c0001t0005g0007 others(24): Show |
27 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.217-10597G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68684543 | |||||||
| chr15:68684830 | G | A | 9 | a0001c0001t0004g0180 a0001c0001t0005g0012 a0001c0001t0005g0013 others(6): Show |
9 | HG01074.hp1 HG01109.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.217-10310G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68684830 | |||||||
| chr15:68684923 | C | G | 139 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(136): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.217-10217C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68684923 | |||||||
| chr15:68685132 | C | A | 18 | a0001c0001t0001g0074 a0001c0001t0001g0179 a0001c0001t0001g0228 others(15): Show |
18 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.217-10008C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68685132 | |||||||
| chr15:68685543 | C | G | 18 | a0001c0001t0001g0074 a0001c0001t0001g0179 a0001c0001t0001g0228 others(15): Show |
18 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.217-9597C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68685543 | |||||||
| chr15:68685663 | G | A | 18 | a0001c0001t0001g0074 a0001c0001t0001g0179 a0001c0001t0001g0228 others(15): Show |
18 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.217-9477G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68685663 | |||||||
| chr15:68685699 | A | G | 18 | a0001c0001t0001g0074 a0001c0001t0001g0179 a0001c0001t0001g0228 others(15): Show |
18 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.217-9441A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68685699 | |||||||
| chr15:68685769 | G | GATTA | 220 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(217): Show |
220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.217-9369_217-9366d others(6): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68685769 | ||||||
| chr15:68685837 | C | T | 18 | a0001c0001t0001g0074 a0001c0001t0001g0179 a0001c0001t0001g0228 others(15): Show |
18 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.217-9303C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68685837 | |||||||
| chr15:68685958 | G | A | 9 | a0001c0001t0004g0180 a0001c0001t0005g0012 a0001c0001t0005g0013 others(6): Show |
9 | HG01074.hp1 HG01109.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.217-9182G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68685958 | |||||||
| chr15:68686007 | A | C | 28 | a0001c0001t0001g0212 a0001c0001t0004g0207 a0001c0001t0005g0007 others(25): Show |
28 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.217-9133A>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68686007 | |||||||
| chr15:68686009 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.217-9131C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68686009 | |||||||
| chr15:68686020 | GT | G | 29 | a0001c0001t0001g0094 a0001c0001t0001g0105 a0001c0001t0001g0179 others(26): Show |
29 | HG01884.hp2 HG02015.hp1 HG02040.hp1 others(26): Show |
intron_variant | MODIFIER | c.217-9103delT | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68686020 | ||||||
| chr15:68686020 | GTT | G | 175 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(172): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.217-9104_217-9103d others(4): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68686020 | ||||||
| chr15:68686036 | T | C | 3 | a0001c0001t0003g0086 a0001c0001t0003g0154 a0001c0001t0005g0013 |
3 | HG02027.hp1 NA18522.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.217-9104T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68686036 | |||||||
| chr15:68686037 | T | C | 1 | a0001c0001t0001g0052 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.217-9103T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68686037 | |||||||
| chr15:68686037 | TC | T | 3 | a0001c0001t0003g0086 a0001c0001t0003g0154 a0001c0001t0005g0013 |
3 | HG02027.hp1 NA18522.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.217-9102delC | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68686037 | |||||||
| chr15:68686038 | C | T | 2 | a0001c0001t0001g0052 a0001c0001t0004g0141 |
2 | HG02965.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.217-9102C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68686038 | |||||||
| chr15:68686039 | T | C | 1 | a0001c0001t0008g0025 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.217-9101T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68686039 | |||||||
| chr15:68686098 | C | T | 29 | a0001c0001t0001g0115 a0001c0001t0001g0212 a0001c0001t0004g0207 others(26): Show |
29 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.217-9042C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68686098 | |||||||
| chr15:68686099 | G | A | 18 | a0001c0001t0001g0074 a0001c0001t0001g0179 a0001c0001t0001g0228 others(15): Show |
18 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.217-9041G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68686099 | |||||||
| chr15:68686131 | G | A | 7 | a0001c0001t0001g0087 a0001c0001t0001g0089 a0001c0001t0001g0183 others(4): Show |
7 | HG00140.hp2 HG00738.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.217-9009G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68686131 | |||||||
| chr15:68686190 | C | T | 12 | a0001c0001t0001g0052 a0001c0001t0001g0105 a0001c0001t0001g0199 others(9): Show |
12 | HG02015.hp1 HG02040.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.217-8950C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68686190 | |||||||
| chr15:68686223 | A | AG | 29 | a0001c0001t0001g0115 a0001c0001t0001g0212 a0001c0001t0004g0207 others(26): Show |
29 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.217-8912dupG | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68686223 | ||||||
| chr15:68686514 | A | G | 2 | a0001c0001t0006g0236 a0001c0001t0027g0034 |
2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.217-8626A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68686514 | |||||||
| chr15:68686554 | A | G | 1 | a0001c0001t0007g0232 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.217-8586A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68686554 | |||||||
| chr15:68686669 | C | A | 12 | a0001c0001t0001g0052 a0001c0001t0001g0105 a0001c0001t0001g0199 others(9): Show |
12 | HG02015.hp1 HG02040.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.217-8471C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68686669 | |||||||
| chr15:68686760 | A | G | 13 | a0001c0001t0001g0094 a0001c0001t0002g0080 a0001c0001t0002g0135 others(10): Show |
13 | HG02145.hp2 HG02451.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.217-8380A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68686760 | |||||||
| chr15:68686829 | G | A | 18 | a0001c0001t0001g0074 a0001c0001t0001g0179 a0001c0001t0001g0228 others(15): Show |
18 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.217-8311G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68686829 | |||||||
| chr15:68686841 | G | A | 12 | a0001c0001t0001g0052 a0001c0001t0001g0105 a0001c0001t0001g0199 others(9): Show |
12 | HG02015.hp1 HG02040.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.217-8299G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68686841 | |||||||
| chr15:68686887 | G | A | 1 | a0001c0001t0001g0027 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.217-8253G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68686887 | |||||||
| chr15:68686895 | G | A | 9 | a0001c0001t0004g0180 a0001c0001t0005g0012 a0001c0001t0005g0013 others(6): Show |
9 | HG01074.hp1 HG01109.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.217-8245G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68686895 | |||||||
| chr15:68686899 | C | CA | 10 | a0001c0001t0002g0231 a0001c0001t0004g0017 a0001c0001t0009g0014 others(7): Show |
10 | HG02109.hp2 HG02572.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.217-8228dupA | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68686899 | ||||||
| chr15:68687008 | A | G | 165 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(162): Show |
165 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.217-8132A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68687008 | |||||||
| chr15:68687209 | G | A | 2 | a0001c0004t0007g0023 a0001c0004t0007g0172 |
2 | HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.217-7931G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68687209 | |||||||
| chr15:68687315 | G | C | 1 | a0001c0001t0001g0101 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.217-7825G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68687315 | |||||||
| chr15:68687371 | G | A | 1 | a0001c0001t0003g0140 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.217-7769G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68687371 | |||||||
| chr15:68687520 | C | T | 68 | a0001c0001t0001g0027 a0001c0001t0001g0037 a0001c0001t0001g0039 others(65): Show |
68 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.217-7620C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68687520 | |||||||
| chr15:68687764 | A | G | 235 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(232): Show |
235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.217-7376A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68687764 | |||||||
| chr15:68687845 | A | G | 2 | a0001c0004t0007g0023 a0001c0004t0007g0172 |
2 | HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.217-7295A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68687845 | |||||||
| chr15:68687847 | A | C | 1 | a0001c0001t0001g0048 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.217-7293A>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68687847 | |||||||
| chr15:68687862 | C | T | 1 | a0001c0002t0005g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.217-7278C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68687862 | |||||||
| chr15:68688002 | G | A | 1 | a0001c0003t0006g0145 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.217-7138G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68688002 | |||||||
| chr15:68688031 | G | A | 2 | a0001c0001t0001g0066 a0001c0001t0003g0116 |
2 | NA19085.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.217-7109G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68688031 | |||||||
| chr15:68688226 | T | G | 3 | a0001c0001t0011g0075 a0001c0001t0014g0254 a0001c0004t0005g0003 |
3 | HG02280.hp2 HG02486.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.217-6914T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68688226 | |||||||
| chr15:68688307 | T | C | 15 | a0001c0001t0001g0074 a0001c0001t0001g0179 a0001c0001t0001g0228 others(12): Show |
15 | HG01891.hp2 HG02257.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.217-6833T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68688307 | |||||||
| chr15:68688324 | T | C | 18 | a0001c0001t0001g0074 a0001c0001t0001g0179 a0001c0001t0001g0228 others(15): Show |
18 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.217-6816T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68688324 | |||||||
| chr15:68688330 | G | C | 216 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(213): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.217-6810G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68688330 | |||||||
| chr15:68688406 | C | G | 216 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(213): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.217-6734C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68688406 | |||||||
| chr15:68688485 | A | G | 6 | a0001c0002t0005g0016 a0001c0002t0006g0223 a0001c0003t0001g0057 others(3): Show |
6 | HG02109.hp2 HG02572.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.217-6655A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68688485 | |||||||
| chr15:68688540 | A | G | 2 | a0001c0001t0003g0062 a0001c0001t0004g0110 |
2 | HG02523.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.217-6600A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68688540 | |||||||
| chr15:68688582 | T | G | 2 | a0001c0001t0006g0236 a0001c0001t0027g0034 |
2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.217-6558T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68688582 | |||||||
| chr15:68688624 | C | T | 7 | a0001c0001t0001g0087 a0001c0001t0001g0089 a0001c0001t0001g0183 others(4): Show |
7 | HG00140.hp2 HG00738.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.217-6516C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68688624 | |||||||
| chr15:68688638 | C | T | 204 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(201): Show |
204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.217-6502C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68688638 | |||||||
| chr15:68688798 | G | A | 204 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(201): Show |
204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.217-6342G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68688798 | |||||||
| chr15:68688875 | G | A | 1 | a0001c0001t0004g0109 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.217-6265G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68688875 | |||||||
| chr15:68688920 | C | T | 204 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(201): Show |
204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.217-6220C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68688920 | |||||||
| chr15:68688985 | ACT | A | 12 | a0001c0001t0001g0052 a0001c0001t0001g0105 a0001c0001t0001g0199 others(9): Show |
12 | HG02015.hp1 HG02040.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.217-6152_217-6151d others(4): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68688985 | ||||||
| chr15:68688994 | G | A | 1 | a0001c0001t0005g0113 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.217-6146G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68688994 | |||||||
| chr15:68689106 | A | G | 27 | a0001c0001t0001g0115 a0001c0001t0001g0212 a0001c0001t0004g0207 others(24): Show |
27 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.217-6034A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68689106 | |||||||
| chr15:68689120 | ACC | A | 204 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(201): Show |
204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.217-6019_217-6018d others(4): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68689120 | |||||||
| chr15:68689205 | TC | T | 9 | a0001c0001t0004g0180 a0001c0001t0005g0012 a0001c0001t0005g0013 others(6): Show |
9 | HG01074.hp1 HG01109.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.217-5933delC | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68689205 | ||||||
| chr15:68689257 | G | T | 56 | a0001c0001t0001g0042 a0001c0001t0001g0094 a0001c0001t0001g0115 others(53): Show |
56 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.217-5883G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68689257 | |||||||
| chr15:68689370 | G | A | 160 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(157): Show |
160 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.217-5770G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68689370 | |||||||
| chr15:68689519 | A | G | 56 | a0001c0001t0001g0042 a0001c0001t0001g0094 a0001c0001t0001g0115 others(53): Show |
56 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.217-5621A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68689519 | |||||||
| chr15:68689627 | C | T | 56 | a0001c0001t0001g0042 a0001c0001t0001g0094 a0001c0001t0001g0115 others(53): Show |
56 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.217-5513C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68689627 | |||||||
| chr15:68689630 | T | C | 216 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(213): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.217-5510T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68689630 | |||||||
| chr15:68689640 | G | A | 56 | a0001c0001t0001g0042 a0001c0001t0001g0094 a0001c0001t0001g0115 others(53): Show |
56 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.217-5500G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68689640 | |||||||
| chr15:68689714 | G | C | 1 | a0001c0001t0002g0002 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.217-5426G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68689714 | |||||||
| chr15:68689808 | T | A | 43 | a0001c0001t0001g0042 a0001c0001t0001g0115 a0001c0001t0001g0212 others(40): Show |
43 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.217-5332T>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68689808 | |||||||
| chr15:68689890 | T | C | 1 | a0001c0001t0003g0064 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.217-5250T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68689890 | |||||||
| chr15:68689899 | G | A | 43 | a0001c0001t0001g0042 a0001c0001t0001g0115 a0001c0001t0001g0212 others(40): Show |
43 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.217-5241G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68689899 | |||||||
| chr15:68689993 | G | A | 216 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(213): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.217-5147G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68689993 | |||||||
| chr15:68690104 | C | A | 56 | a0001c0001t0001g0042 a0001c0001t0001g0094 a0001c0001t0001g0115 others(53): Show |
56 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.217-5036C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68690104 | |||||||
| chr15:68690112 | T | G | 149 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(146): Show |
149 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.217-5028T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68690112 | |||||||
| chr15:68690186 | G | A | 1 | a0001c0003t0008g0178 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.217-4954G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68690186 | |||||||
| chr15:68690637 | G | A | 3 | a0001c0001t0002g0080 a0001c0001t0002g0135 a0001c0001t0021g0033 |
3 | HG02145.hp2 HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.217-4503G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68690637 | |||||||
| chr15:68690646 | C | CT | 5 | a0001c0001t0003g0059 a0001c0001t0003g0213 a0001c0001t0004g0092 others(2): Show |
5 | HG01256.hp1 HG02080.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.217-4473dupT | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68690646 | ||||||
| chr15:68690646 | C | CTTTCT | 9 | a0001c0001t0001g0094 a0001c0001t0005g0007 a0001c0001t0006g0004 others(6): Show |
9 | HG00280.hp2 HG01099.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.217-4491_217-4490i others(7): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68690646 | ||||||
| chr15:68690646 | CT | C | 29 | a0001c0001t0001g0065 a0001c0001t0001g0179 a0001c0001t0001g0183 others(26): Show |
29 | HG01074.hp1 HG01074.hp2 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.217-4473delT | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68690646 | ||||||
| chr15:68690646 | CTT | C | 5 | a0001c0001t0001g0074 a0001c0001t0002g0022 a0001c0001t0002g0078 others(2): Show |
5 | HG02257.hp1 HG02258.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.217-4474_217-4473d others(4): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68690646 | ||||||
| chr15:68690649 | T | TC | 11 | a0001c0001t0001g0052 a0001c0001t0001g0199 a0001c0001t0002g0102 others(8): Show |
11 | HG02015.hp1 HG02040.hp1 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.217-4491_217-4490i others(3): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68690649 | |||||||
| chr15:68690649 | T | TCTTTTC | 46 | a0001c0001t0001g0042 a0001c0001t0001g0115 a0001c0001t0001g0212 others(43): Show |
46 | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.217-4491_217-4490i others(8): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68690649 | |||||||
| chr15:68690650 | T | C | 10 | a0001c0001t0001g0094 a0001c0001t0001g0105 a0001c0001t0005g0007 others(7): Show |
10 | HG00280.hp2 HG01099.hp2 HG02155.hp2 others(7): Show |
intron_variant | MODIFIER | c.217-4490T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68690650 | |||||||
| chr15:68690654 | T | C | 1 | a0001c0001t0001g0042 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.217-4486T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68690654 | |||||||
| chr15:68690736 | G | A | 12 | a0001c0001t0001g0052 a0001c0001t0001g0105 a0001c0001t0001g0199 others(9): Show |
12 | HG02015.hp1 HG02040.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.217-4404G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68690736 | |||||||
| chr15:68690759 | C | T | 1 | a0001c0004t0005g0003 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.217-4381C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68690759 | |||||||
| chr15:68690875 | G | C | 56 | a0001c0001t0001g0042 a0001c0001t0001g0094 a0001c0001t0001g0115 others(53): Show |
56 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.217-4265G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68690875 | |||||||
| chr15:68690921 | CCAAG | C | 50 | a0001c0001t0001g0042 a0001c0001t0001g0094 a0001c0001t0001g0115 others(47): Show |
50 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.217-4218_217-4215d others(6): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68690921 | |||||||
| chr15:68690983 | G | A | 1 | a0001c0001t0006g0237 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.217-4157G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68690983 | |||||||
| chr15:68691032 | T | C | 7 | a0001c0001t0002g0080 a0001c0001t0002g0135 a0001c0001t0004g0141 others(4): Show |
7 | HG02145.hp2 HG02451.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.217-4108T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68691032 | |||||||
| chr15:68691047 | C | T | 50 | a0001c0001t0001g0042 a0001c0001t0001g0094 a0001c0001t0001g0115 others(47): Show |
50 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.217-4093C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68691047 | |||||||
| chr15:68691058 | G | A | 27 | a0001c0001t0001g0115 a0001c0001t0001g0212 a0001c0001t0004g0207 others(24): Show |
27 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.217-4082G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68691058 | |||||||
| chr15:68691063 | C | T | 11 | a0001c0001t0001g0052 a0001c0001t0001g0199 a0001c0001t0002g0102 others(8): Show |
11 | HG02015.hp1 HG02040.hp1 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.217-4077C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68691063 | |||||||
| chr15:68691101 | G | C | 50 | a0001c0001t0001g0042 a0001c0001t0001g0094 a0001c0001t0001g0115 others(47): Show |
50 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.217-4039G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68691101 | |||||||
| chr15:68691135 | C | G | 2 | a0001c0001t0001g0028 a0001c0001t0003g0154 |
2 | NA18947.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.217-4005C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68691135 | |||||||
| chr15:68691202 | G | A | 138 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.217-3938G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68691202 | |||||||
| chr15:68691212 | T | C | 211 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(208): Show |
211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.217-3928T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68691212 | |||||||
| chr15:68691262 | A | G | 50 | a0001c0001t0001g0042 a0001c0001t0001g0094 a0001c0001t0001g0115 others(47): Show |
50 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.217-3878A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68691262 | |||||||
| chr15:68691296 | C | G | 2 | a0001c0002t0001g0069 a0001c0002t0001g0070 |
2 | HG00738.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.217-3844C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68691296 | |||||||
| chr15:68691314 | C | T | 161 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(158): Show |
161 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.217-3826C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68691314 | |||||||
| chr15:68691327 | CAAAAAAA others(292): Show |
C | 5 | a0001c0001t0008g0001 a0001c0002t0001g0188 a0001c0002t0002g0038 others(2): Show |
5 | HG00642.hp2 HG01891.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.217-3796_217-3498d others(2): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68691327 | ||||||
| chr15:68691327 | CAAAAAAA others(293): Show |
C | 46 | a0001c0001t0001g0042 a0001c0001t0001g0094 a0001c0001t0001g0115 others(43): Show |
46 | HG00280.hp2 HG00738.hp2 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.217-3796_217-3497d others(2): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68691327 | ||||||
| chr15:68691330 | AAAAAAAA others(287): Show |
A | 6 | a0001c0001t0001g0187 a0001c0001t0003g0083 a0001c0001t0004g0063 others(3): Show |
6 | HG00140.hp2 HG00408.hp2 HG00597.hp1 others(3): Show |
intron_variant | MODIFIER | c.217-3796_217-3503d others(2): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68691330 | ||||||
| chr15:68691331 | AAAAAAAA others(286): Show |
A | 107 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(104): Show |
107 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.217-3796_217-3504d others(2): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68691331 | ||||||
| chr15:68691332 | AAAAAAAA others(285): Show |
A | 42 | a0001c0001t0001g0048 a0001c0001t0001g0056 a0001c0001t0001g0066 others(39): Show |
42 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.217-3796_217-3505d others(2): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68691332 | ||||||
| chr15:68691333 | AAAAAAAA others(284): Show |
A | 5 | a0001c0001t0001g0052 a0001c0001t0001g0199 a0001c0001t0002g0097 others(2): Show |
5 | HG01106.hp1 NA18968.hp1 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.217-3796_217-3506d others(2): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68691333 | ||||||
| chr15:68691485 | C | T | 6 | a0001c0001t0002g0181 a0001c0001t0005g0194 a0001c0001t0017g0251 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.217-3655C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68691485 | |||||||
| chr15:68691580 | C | G | 6 | a0001c0001t0002g0181 a0001c0001t0005g0194 a0001c0001t0017g0251 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.217-3560C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68691580 | |||||||
| chr15:68691603 | C | A | 6 | a0001c0001t0002g0181 a0001c0001t0005g0194 a0001c0001t0017g0251 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.217-3537C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68691603 | |||||||
| chr15:68691606 | CAG | C | 6 | a0001c0001t0002g0181 a0001c0001t0005g0194 a0001c0001t0017g0251 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.217-3531_217-3530d others(4): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68691606 | ||||||
| chr15:68691622 | C | A | 1 | a0001c0001t0006g0020 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.217-3518C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68691622 | |||||||
| chr15:68691624 | C | CAA | 14 | a0001c0001t0001g0065 a0001c0001t0001g0132 a0001c0001t0001g0215 others(11): Show |
14 | HG01106.hp2 HG01175.hp2 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.217-3495_217-3494d others(4): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68691624 | ||||||
| chr15:68691624 | C | CAAA | 14 | a0001c0001t0001g0010 a0001c0001t0001g0074 a0001c0001t0002g0022 others(11): Show |
14 | HG01261.hp1 HG01433.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.217-3496_217-3494d others(5): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68691624 | ||||||
| chr15:68691624 | C | CAAAA | 7 | a0001c0001t0001g0179 a0001c0001t0001g0228 a0001c0001t0002g0091 others(4): Show |
7 | HG02615.hp2 HG02647.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.217-3497_217-3494d others(6): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68691624 | ||||||
| chr15:68691624 | CAAA | C | 5 | a0001c0001t0005g0194 a0001c0001t0017g0251 a0001c0003t0012g0076 others(2): Show |
5 | HG01884.hp2 HG02630.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.217-3496_217-3494d others(5): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68691624 | ||||||
| chr15:68691735 | T | C | 13 | a0001c0001t0001g0094 a0001c0001t0002g0080 a0001c0001t0002g0135 others(10): Show |
13 | HG02145.hp2 HG02451.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.217-3405T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68691735 | |||||||
| chr15:68691757 | T | C | 161 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(158): Show |
161 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.217-3383T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68691757 | |||||||
| chr15:68691786 | G | C | 43 | a0001c0001t0001g0042 a0001c0001t0001g0115 a0001c0001t0001g0212 others(40): Show |
43 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.217-3354G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68691786 | |||||||
| chr15:68691848 | G | A | 52 | a0001c0001t0001g0028 a0001c0001t0001g0056 a0001c0001t0001g0067 others(49): Show |
52 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.217-3292G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68691848 | |||||||
| chr15:68691930 | A | G | 56 | a0001c0001t0001g0042 a0001c0001t0001g0094 a0001c0001t0001g0115 others(53): Show |
56 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.217-3210A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68691930 | |||||||
| chr15:68692049 | G | A | 1 | a0001c0003t0001g0057 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.217-3091G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68692049 | |||||||
| chr15:68692102 | A | G | 1 | a0001c0001t0004g0119 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.217-3038A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68692102 | |||||||
| chr15:68692105 | C | T | 1 | a0001c0001t0003g0126 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.217-3035C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68692105 | |||||||
| chr15:68692242 | G | C | 43 | a0001c0001t0001g0042 a0001c0001t0001g0115 a0001c0001t0001g0212 others(40): Show |
43 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.217-2898G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68692242 | |||||||
| chr15:68692290 | G | C | 1 | a0001c0001t0002g0146 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.217-2850G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68692290 | |||||||
| chr15:68692507 | C | T | 161 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(158): Show |
161 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.217-2633C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68692507 | |||||||
| chr15:68692515 | G | A | 12 | a0001c0001t0001g0052 a0001c0001t0001g0105 a0001c0001t0001g0199 others(9): Show |
12 | HG02015.hp1 HG02040.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.217-2625G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68692515 | |||||||
| chr15:68692516 | C | T | 2 | a0001c0004t0007g0023 a0001c0004t0007g0172 |
2 | HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.217-2624C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68692516 | |||||||
| chr15:68692548 | A | G | 161 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(158): Show |
161 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.217-2592A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68692548 | |||||||
| chr15:68692563 | C | T | 27 | a0001c0001t0001g0115 a0001c0001t0001g0212 a0001c0001t0004g0207 others(24): Show |
27 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.217-2577C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68692563 | |||||||
| chr15:68692598 | T | TA | 161 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(158): Show |
161 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.217-2534dupA | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68692598 | ||||||
| chr15:68692632 | C | CTT | 13 | a0001c0001t0001g0052 a0001c0001t0001g0105 a0001c0001t0001g0199 others(10): Show |
13 | HG01256.hp1 HG02015.hp1 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.217-2499_217-2498d others(4): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68692632 | ||||||
| chr15:68692632 | C | CTTT | 146 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0037 others(143): Show |
146 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.217-2500_217-2498d others(5): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68692632 | ||||||
| chr15:68692826 | T | G | 217 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(214): Show |
217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.217-2314T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68692826 | |||||||
| chr15:68692840 | T | G | 235 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(232): Show |
235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.217-2300T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68692840 | |||||||
| chr15:68692842 | T | C | 161 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(158): Show |
161 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.217-2298T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68692842 | |||||||
| chr15:68692858 | T | C | 12 | a0001c0001t0001g0052 a0001c0001t0001g0105 a0001c0001t0001g0199 others(9): Show |
12 | HG02015.hp1 HG02040.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.217-2282T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68692858 | |||||||
| chr15:68692865 | C | T | 161 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(158): Show |
161 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.217-2275C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68692865 | |||||||
| chr15:68693040 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.217-2100C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68693040 | |||||||
| chr15:68693076 | C | T | 57 | a0001c0001t0001g0042 a0001c0001t0001g0094 a0001c0001t0001g0115 others(54): Show |
57 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.217-2064C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68693076 | |||||||
| chr15:68693130 | T | C | 3 | a0001c0001t0004g0017 a0001c0001t0009g0014 a0001c0001t0009g0238 |
3 | HG02976.hp1 HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.217-2010T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68693130 | |||||||
| chr15:68693260 | C | T | 217 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(214): Show |
217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.217-1880C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68693260 | |||||||
| chr15:68693569 | C | T | 28 | a0001c0001t0001g0115 a0001c0001t0001g0212 a0001c0001t0004g0207 others(25): Show |
28 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.217-1571C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68693569 | |||||||
| chr15:68693645 | A | C | 1 | a0001c0001t0001g0027 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.217-1495A>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68693645 | |||||||
| chr15:68693667 | G | A | 3 | a0001c0001t0001g0044 a0001c0001t0001g0168 a0001c0001t0001g0169 |
3 | HG03490.hp1 HG03492.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.217-1473G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68693667 | |||||||
| chr15:68693689 | A | G | 187 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(184): Show |
187 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.217-1451A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68693689 | |||||||
| chr15:68693825 | A | ATTTG | 20 | a0001c0001t0001g0074 a0001c0001t0001g0179 a0001c0001t0001g0228 others(17): Show |
20 | HG01884.hp2 HG01891.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.217-1291_217-1288d others(6): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68693825 | ||||||
| chr15:68693825 | ATTTG | A | 215 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(212): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.217-1291_217-1288d others(6): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 68693825 | ||||||
| chr15:68693893 | C | T | 48 | a0001c0001t0001g0052 a0001c0001t0001g0115 a0001c0001t0001g0199 others(45): Show |
48 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.217-1247C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68693893 | |||||||
| chr15:68694083 | G | A | 1 | a0001c0001t0016g0250 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.217-1057G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68694083 | |||||||
| chr15:68694241 | T | C | 1 | a0001c0001t0003g0155 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.217-899T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68694241 | |||||||
| chr15:68694352 | A | G | 1 | a0001c0001t0002g0148 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.217-788A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68694352 | |||||||
| chr15:68694390 | G | A | 20 | a0001c0001t0001g0074 a0001c0001t0001g0179 a0001c0001t0001g0228 others(17): Show |
20 | HG01884.hp2 HG01891.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.217-750G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68694390 | |||||||
| chr15:68694478 | G | T | 49 | a0001c0001t0001g0052 a0001c0001t0001g0105 a0001c0001t0001g0115 others(46): Show |
49 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.217-662G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68694478 | |||||||
| chr15:68694524 | G | A | 9 | a0001c0001t0001g0042 a0001c0001t0002g0181 a0001c0002t0005g0016 others(6): Show |
9 | HG02109.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.217-616G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68694524 | |||||||
| chr15:68694613 | A | G | 189 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(186): Show |
189 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.217-527A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68694613 | |||||||
| chr15:68694683 | G | A | 1 | a0001c0001t0005g0073 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.217-457G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68694683 | |||||||
| chr15:68694730 | G | A | 6 | a0001c0001t0001g0179 a0001c0001t0001g0228 a0001c0001t0002g0091 others(3): Show |
6 | HG01891.hp2 HG02615.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.217-410G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68694730 | |||||||
| chr15:68694744 | A | G | 189 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(186): Show |
189 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.217-396A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68694744 | |||||||
| chr15:68694865 | T | C | 253 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(250): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.217-275T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68694865 | |||||||
| chr15:68694922 | T | C | 215 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(212): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.217-218T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68694922 | |||||||
| chr15:68694976 | A | C | 235 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(232): Show |
235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.217-164A>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68694976 | |||||||
| chr15:68695002 | A | G | 217 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(214): Show |
217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.217-138A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 2/11 | chr15 | 68695002 | |||||||
| chr15:68695300 | T | C | 1 | a0001c0001t0006g0031 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.333+44T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68695300 | |||||||
| chr15:68695319 | C | A | 3 | a0001c0001t0005g0164 a0001c0001t0005g0194 a0001c0001t0017g0251 |
3 | HG02630.hp1 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.333+63C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68695319 | |||||||
| chr15:68695401 | G | T | 147 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(144): Show |
147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.333+145G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68695401 | |||||||
| chr15:68695584 | A | G | 1 | a0001c0002t0003g0256 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.333+328A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68695584 | |||||||
| chr15:68695730 | G | C | 26 | a0001c0001t0001g0042 a0001c0001t0001g0094 a0001c0001t0002g0080 others(23): Show |
26 | HG02109.hp1 HG02109.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.333+474G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68695730 | |||||||
| chr15:68696086 | TA | T | 229 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(226): Show |
229 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.333+844delA | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68696086 | ||||||
| chr15:68696111 | G | T | 1 | a0001c0001t0001g0088 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.333+855G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68696111 | |||||||
| chr15:68696189 | G | T | 1 | a0001c0001t0004g0019 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.333+933G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68696189 | |||||||
| chr15:68696249 | CA | C | 10 | a0001c0001t0002g0079 a0001c0001t0003g0062 a0001c0001t0003g0125 others(7): Show |
10 | HG01256.hp1 HG01496.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.333+1008delA | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68696249 | ||||||
| chr15:68696286 | T | C | 3 | a0001c0004t0005g0003 a0001c0004t0007g0023 a0001c0004t0007g0172 |
3 | HG01884.hp2 HG03098.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.333+1030T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68696286 | |||||||
| chr15:68696306 | C | T | 1 | a0001c0001t0003g0155 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.333+1050C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68696306 | |||||||
| chr15:68696309 | G | A | 5 | a0001c0001t0002g0241 a0001c0001t0003g0225 a0001c0001t0003g0226 others(2): Show |
5 | HG01070.hp1 HG01081.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+1053G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68696309 | |||||||
| chr15:68696409 | C | A | 142 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(139): Show |
142 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.333+1153C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68696409 | |||||||
| chr15:68696550 | T | A | 3 | a0001c0001t0002g0080 a0001c0001t0002g0135 a0001c0001t0021g0033 |
3 | HG02145.hp2 HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.333+1294T>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68696550 | |||||||
| chr15:68696557 | C | CAA | 38 | a0001c0001t0001g0042 a0001c0001t0001g0115 a0001c0001t0001g0212 others(35): Show |
38 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.333+1317_333+1318d others(4): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68696557 | ||||||
| chr15:68696557 | C | CAAA | 21 | a0001c0001t0001g0052 a0001c0001t0001g0105 a0001c0001t0001g0199 others(18): Show |
21 | HG01109.hp2 HG02015.hp1 HG02040.hp1 others(18): Show |
intron_variant | MODIFIER | c.333+1316_333+1318d others(5): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68696557 | ||||||
| chr15:68696557 | C | CAAAA | 21 | a0001c0001t0001g0048 a0001c0001t0001g0094 a0001c0001t0001g0108 others(18): Show |
21 | HG02040.hp2 HG02145.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.333+1315_333+1318d others(6): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68696557 | ||||||
| chr15:68696557 | C | CAAAAA | 125 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(122): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.333+1314_333+1318d others(7): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68696557 | ||||||
| chr15:68696557 | C | CAAAAAA | 15 | a0001c0001t0001g0153 a0001c0001t0001g0204 a0001c0001t0002g0097 others(12): Show |
15 | HG00673.hp1 HG00673.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.333+1313_333+1318d others(8): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68696557 | ||||||
| chr15:68696886 | C | T | 25 | a0001c0001t0001g0061 a0001c0001t0001g0085 a0001c0001t0001g0087 others(22): Show |
25 | HG00140.hp2 HG00280.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.333+1630C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68696886 | |||||||
| chr15:68696891 | G | T | 142 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(139): Show |
142 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.333+1635G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68696891 | |||||||
| chr15:68696986 | A | T | 1 | a0001c0001t0003g0111 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.333+1730A>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68696986 | |||||||
| chr15:68697010 | C | A | 10 | a0001c0001t0004g0180 a0001c0001t0005g0012 a0001c0001t0005g0013 others(7): Show |
10 | HG01109.hp2 HG02280.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.333+1754C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68697010 | |||||||
| chr15:68697082 | T | C | 29 | a0001c0001t0001g0115 a0001c0001t0001g0212 a0001c0001t0004g0207 others(26): Show |
29 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.333+1826T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68697082 | |||||||
| chr15:68697210 | A | ATGGATGG others(45): Show |
3 | a0001c0001t0005g0164 a0001c0001t0005g0194 a0001c0001t0017g0251 |
3 | HG02630.hp1 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.333+1955_333+1956i others(54): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68697210 | ||||||
| chr15:68697212 | T | G | 3 | a0001c0001t0005g0164 a0001c0001t0005g0194 a0001c0001t0017g0251 |
3 | HG02630.hp1 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.333+1956T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68697212 | |||||||
| chr15:68697214 | T | A | 3 | a0001c0001t0005g0164 a0001c0001t0005g0194 a0001c0001t0017g0251 |
3 | HG02630.hp1 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.333+1958T>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68697214 | |||||||
| chr15:68697214 | T | TTGGA | 12 | a0001c0001t0001g0052 a0001c0001t0001g0105 a0001c0001t0001g0199 others(9): Show |
12 | HG02015.hp1 HG02040.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.333+1984_333+1987d others(6): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68697214 | ||||||
| chr15:68697279 | C | T | 8 | a0001c0001t0001g0094 a0001c0001t0004g0017 a0001c0001t0006g0191 others(5): Show |
8 | HG02559.hp2 HG02615.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.333+2023C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68697279 | |||||||
| chr15:68697409 | A | G | 1 | a0001c0001t0011g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.333+2153A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68697409 | |||||||
| chr15:68697611 | G | T | 1 | a0001c0001t0004g0063 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.333+2355G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68697611 | |||||||
| chr15:68697733 | G | A | 29 | a0001c0001t0001g0115 a0001c0001t0001g0212 a0001c0001t0004g0207 others(26): Show |
29 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.333+2477G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68697733 | |||||||
| chr15:68697786 | T | C | 4 | a0001c0001t0001g0060 a0001c0001t0001g0147 a0001c0001t0002g0123 others(1): Show |
4 | HG01081.hp1 HG01975.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.333+2530T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68697786 | |||||||
| chr15:68697968 | A | G | 1 | a0001c0001t0001g0179 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.333+2712A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68697968 | |||||||
| chr15:68698297 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.333+3041G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68698297 | |||||||
| chr15:68698356 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.333+3100A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68698356 | |||||||
| chr15:68698424 | C | T | 1 | a0001c0002t0006g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.333+3168C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68698424 | |||||||
| chr15:68698526 | C | T | 1 | a0001c0002t0003g0198 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.333+3270C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68698526 | |||||||
| chr15:68698808 | T | G | 227 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(224): Show |
227 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.333+3552T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68698808 | |||||||
| chr15:68698872 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.333+3616C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68698872 | |||||||
| chr15:68698889 | C | T | 1 | a0001c0001t0002g0221 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.333+3633C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68698889 | |||||||
| chr15:68699028 | T | G | 15 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(12): Show |
15 | HG01891.hp2 HG02145.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.333+3772T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68699028 | |||||||
| chr15:68699321 | G | A | 16 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(13): Show |
16 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.333+4065G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68699321 | |||||||
| chr15:68699332 | A | G | 2 | a0001c0001t0011g0075 a0001c0001t0014g0254 |
2 | HG02280.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.333+4076A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68699332 | |||||||
| chr15:68699356 | G | T | 2 | a0001c0004t0007g0023 a0001c0004t0007g0172 |
2 | HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.333+4100G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68699356 | |||||||
| chr15:68699388 | A | C | 17 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(14): Show |
17 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.333+4132A>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68699388 | |||||||
| chr15:68699412 | A | G | 18 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(15): Show |
18 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.333+4156A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68699412 | |||||||
| chr15:68699655 | C | T | 28 | a0001c0001t0001g0115 a0001c0001t0001g0212 a0001c0001t0004g0207 others(25): Show |
28 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.333+4399C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68699655 | |||||||
| chr15:68699723 | G | A | 199 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(196): Show |
199 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.333+4467G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68699723 | |||||||
| chr15:68699728 | C | T | 1 | a0001c0003t0006g0145 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.333+4472C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68699728 | |||||||
| chr15:68699909 | G | A | 2 | a0001c0004t0007g0023 a0001c0004t0007g0172 |
2 | HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.333+4653G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68699909 | |||||||
| chr15:68700004 | G | C | 7 | a0001c0003t0006g0145 a0001c0003t0008g0178 a0001c0003t0011g0247 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.333+4748G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68700004 | |||||||
| chr15:68700013 | G | A | 10 | a0001c0001t0001g0052 a0001c0001t0001g0199 a0001c0001t0002g0102 others(7): Show |
10 | HG02015.hp1 HG02040.hp1 NA18947.hp2 others(7): Show |
intron_variant | MODIFIER | c.333+4757G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68700013 | |||||||
| chr15:68700070 | G | T | 7 | a0001c0003t0006g0145 a0001c0003t0008g0178 a0001c0003t0011g0247 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.333+4814G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68700070 | |||||||
| chr15:68700086 | C | T | 17 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(14): Show |
17 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.333+4830C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68700086 | |||||||
| chr15:68700204 | T | G | 17 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(14): Show |
17 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.333+4948T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68700204 | |||||||
| chr15:68700214 | G | C | 28 | a0001c0001t0001g0115 a0001c0001t0001g0212 a0001c0001t0004g0207 others(25): Show |
28 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.333+4958G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68700214 | |||||||
| chr15:68700216 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.333+4960C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68700216 | |||||||
| chr15:68700380 | C | CAAAACAT others(279): Show |
2 | a0001c0001t0001g0094 a0001c0001t0006g0237 |
2 | HG01109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.333+5138_333+5139i others(288): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68700380 | ||||||
| chr15:68700380 | C | CAAAACAT others(278): Show |
7 | a0001c0001t0002g0135 a0001c0001t0004g0180 a0001c0001t0005g0018 others(4): Show |
7 | HG01891.hp2 HG02886.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.333+5138_333+5139i others(287): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68700380 | ||||||
| chr15:68700380 | C | CAAAACAT others(277): Show |
8 | a0001c0001t0001g0179 a0001c0001t0001g0228 a0001c0001t0002g0080 others(5): Show |
8 | HG02145.hp2 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.333+5138_333+5139i others(286): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68700380 | ||||||
| chr15:68700481 | G | A | 2 | a0001c0001t0001g0204 a0001c0001t0003g0213 |
2 | HG01256.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.333+5225G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68700481 | |||||||
| chr15:68700494 | C | T | 2 | a0001c0001t0003g0062 a0001c0001t0004g0110 |
2 | HG02523.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.333+5238C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68700494 | |||||||
| chr15:68700544 | C | T | 1 | a0001c0001t0021g0033 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.333+5288C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68700544 | |||||||
| chr15:68700580 | C | T | 17 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(14): Show |
17 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.333+5324C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68700580 | |||||||
| chr15:68700803 | GGA | G | 233 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(230): Show |
233 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.333+5559_333+5560d others(4): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68700803 | ||||||
| chr15:68700830 | T | C | 17 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(14): Show |
17 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.333+5574T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68700830 | |||||||
| chr15:68700942 | C | T | 1 | a0001c0001t0004g0117 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.333+5686C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68700942 | |||||||
| chr15:68701001 | C | T | 1 | a0001c0002t0003g0107 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.333+5745C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68701001 | |||||||
| chr15:68701155 | C | A | 3 | a0001c0002t0006g0223 a0001c0003t0006g0051 a0001c0003t0012g0047 |
3 | HG02572.hp2 HG02647.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.333+5899C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68701155 | |||||||
| chr15:68701155 | C | T | 226 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(223): Show |
226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.333+5899C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68701155 | |||||||
| chr15:68701211 | C | A | 1 | a0001c0001t0001g0202 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.333+5955C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68701211 | |||||||
| chr15:68701239 | CT | C | 17 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(14): Show |
17 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.333+5985delT | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68701239 | ||||||
| chr15:68701297 | G | GTTTCTTT others(11): Show |
2 | a0001c0001t0005g0131 a0003c0007t0006g0186 |
2 | HG02257.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.333+6054_333+6071d others(20): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68701297 | ||||||
| chr15:68701297 | GTTTCTTT others(2): Show |
G | 17 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(14): Show |
17 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.333+6063_333+6071d others(11): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68701297 | ||||||
| chr15:68701343 | G | T | 17 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(14): Show |
17 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.333+6087G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68701343 | |||||||
| chr15:68701416 | A | G | 1 | a0001c0003t0011g0247 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.333+6160A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68701416 | |||||||
| chr15:68701468 | C | A | 5 | a0001c0001t0001g0042 a0001c0001t0001g0133 a0001c0001t0004g0026 others(2): Show |
5 | HG02630.hp2 HG03130.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.333+6212C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68701468 | |||||||
| chr15:68701472 | C | T | 5 | a0001c0001t0002g0022 a0001c0001t0002g0078 a0001c0001t0002g0079 others(2): Show |
5 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.333+6216C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68701472 | |||||||
| chr15:68701478 | A | AT | 20 | a0001c0001t0001g0042 a0001c0001t0001g0048 a0001c0001t0001g0074 others(17): Show |
20 | HG01175.hp2 HG02257.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.333+6247dupT | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68701478 | ||||||
| chr15:68701478 | A | ATT | 59 | a0001c0001t0001g0028 a0001c0001t0001g0061 a0001c0001t0001g0084 others(56): Show |
59 | HG00408.hp2 HG00621.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.333+6246_333+6247d others(4): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68701478 | ||||||
| chr15:68701478 | A | ATTT | 76 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0037 others(73): Show |
76 | HG00140.hp2 HG00597.hp2 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.333+6245_333+6247d others(5): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68701478 | ||||||
| chr15:68701478 | A | ATTTT | 16 | a0001c0001t0001g0039 a0001c0001t0001g0169 a0001c0001t0002g0096 others(13): Show |
16 | HG00140.hp1 HG00280.hp1 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.333+6244_333+6247d others(6): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68701478 | ||||||
| chr15:68701478 | A | ATTTTT | 6 | a0001c0001t0001g0085 a0001c0001t0003g0086 a0001c0001t0003g0127 others(3): Show |
6 | HG00408.hp1 HG00673.hp2 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.333+6243_333+6247d others(7): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68701478 | ||||||
| chr15:68701478 | A | ATTTTTTT | 14 | a0001c0001t0001g0115 a0001c0001t0001g0212 a0001c0001t0005g0007 others(11): Show |
14 | HG00280.hp2 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.333+6241_333+6247d others(9): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68701478 | ||||||
| chr15:68701478 | A | ATTTTTTT others(1): Show |
8 | a0001c0002t0001g0006 a0001c0002t0001g0206 a0001c0002t0002g0045 others(5): Show |
8 | HG00741.hp2 HG01071.hp1 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.333+6240_333+6247d others(10): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68701478 | ||||||
| chr15:68701478 | ATTT | A | 16 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0002g0080 others(13): Show |
16 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.333+6245_333+6247d others(5): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68701478 | ||||||
| chr15:68701546 | C | G | 1 | a0001c0001t0001g0084 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.333+6290C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68701546 | |||||||
| chr15:68701572 | G | A | 1 | a0001c0004t0005g0233 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.333+6316G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68701572 | |||||||
| chr15:68701578 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.333+6322C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68701578 | |||||||
| chr15:68701630 | T | C | 70 | a0001c0001t0001g0052 a0001c0001t0001g0094 a0001c0001t0001g0115 others(67): Show |
70 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.333+6374T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68701630 | |||||||
| chr15:68701635 | G | A | 145 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(142): Show |
145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.333+6379G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68701635 | |||||||
| chr15:68701684 | T | C | 17 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(14): Show |
17 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.333+6428T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68701684 | |||||||
| chr15:68701699 | C | T | 38 | a0001c0001t0001g0052 a0001c0001t0001g0115 a0001c0001t0001g0199 others(35): Show |
38 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.333+6443C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68701699 | |||||||
| chr15:68701701 | A | G | 38 | a0001c0001t0001g0052 a0001c0001t0001g0115 a0001c0001t0001g0199 others(35): Show |
38 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.333+6445A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68701701 | |||||||
| chr15:68701811 | C | G | 1 | a0001c0001t0002g0148 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.333+6555C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68701811 | |||||||
| chr15:68702043 | G | A | 10 | a0001c0001t0001g0052 a0001c0001t0001g0199 a0001c0001t0002g0102 others(7): Show |
10 | HG02015.hp1 HG02040.hp1 NA18947.hp2 others(7): Show |
intron_variant | MODIFIER | c.333+6787G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68702043 | |||||||
| chr15:68702050 | C | G | 28 | a0001c0001t0001g0115 a0001c0001t0001g0212 a0001c0001t0005g0007 others(25): Show |
28 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.333+6794C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68702050 | |||||||
| chr15:68702141 | G | C | 1 | a0001c0001t0005g0164 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.333+6885G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68702141 | |||||||
| chr15:68702169 | G | A | 7 | a0001c0003t0006g0145 a0001c0003t0008g0178 a0001c0003t0011g0247 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.333+6913G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68702169 | |||||||
| chr15:68702251 | C | G | 157 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(154): Show |
157 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.333+6995C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68702251 | |||||||
| chr15:68702290 | T | C | 8 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0046 others(5): Show |
8 | HG02280.hp2 HG02486.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.333+7034T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68702290 | |||||||
| chr15:68702385 | C | A | 8 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0046 others(5): Show |
8 | HG02280.hp2 HG02486.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.333+7129C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68702385 | |||||||
| chr15:68702407 | A | T | 1 | a0001c0001t0003g0068 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.333+7151A>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68702407 | |||||||
| chr15:68702465 | C | T | 157 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(154): Show |
157 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.333+7209C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68702465 | |||||||
| chr15:68702488 | G | A | 6 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0046 others(3): Show |
6 | HG02615.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.333+7232G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68702488 | |||||||
| chr15:68702494 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.333+7238A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68702494 | |||||||
| chr15:68702773 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.333+7517T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68702773 | |||||||
| chr15:68702818 | TTTC | T | 5 | a0001c0003t0006g0145 a0001c0003t0008g0178 a0001c0004t0005g0233 others(2): Show |
5 | HG01884.hp2 HG02145.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.333+7565_333+7567d others(5): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68702818 | ||||||
| chr15:68702821 | C | CT | 16 | a0001c0001t0001g0056 a0001c0001t0001g0101 a0001c0001t0001g0157 others(13): Show |
16 | HG00597.hp2 HG01175.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.333+7588dupT | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68702821 | ||||||
| chr15:68702821 | C | CTT | 27 | a0001c0001t0001g0115 a0001c0001t0001g0212 a0001c0001t0005g0007 others(24): Show |
27 | HG00280.hp2 HG00642.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.333+7587_333+7588d others(4): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68702821 | ||||||
| chr15:68702821 | CT | C | 25 | a0001c0001t0001g0074 a0001c0001t0001g0087 a0001c0001t0001g0094 others(22): Show |
25 | HG01109.hp2 HG01256.hp2 HG01516.hp1 others(22): Show |
intron_variant | MODIFIER | c.333+7588delT | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68702821 | ||||||
| chr15:68702821 | CTT | C | 8 | a0001c0001t0002g0080 a0001c0001t0002g0135 a0001c0001t0004g0017 others(5): Show |
8 | HG02145.hp2 HG02559.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.333+7587_333+7588d others(4): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68702821 | ||||||
| chr15:68702827 | T | C | 1 | a0001c0001t0001g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.333+7571T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68702827 | |||||||
| chr15:68702868 | C | A | 1 | a0003c0007t0006g0186 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.333+7612C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68702868 | |||||||
| chr15:68702868 | C | T | 17 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(14): Show |
17 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.333+7612C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68702868 | |||||||
| chr15:68703056 | G | A | 17 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(14): Show |
17 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.334-7676G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68703056 | |||||||
| chr15:68703057 | A | C | 17 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(14): Show |
17 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.334-7675A>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68703057 | |||||||
| chr15:68703062 | A | G | 17 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(14): Show |
17 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.334-7670A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68703062 | |||||||
| chr15:68703069 | C | T | 17 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(14): Show |
17 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.334-7663C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68703069 | |||||||
| chr15:68703070 | A | G | 17 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(14): Show |
17 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.334-7662A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68703070 | |||||||
| chr15:68703074 | G | A | 17 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(14): Show |
17 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.334-7658G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68703074 | |||||||
| chr15:68703076 | C | CT | 17 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(14): Show |
17 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.334-7655dupT | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68703076 | ||||||
| chr15:68703078 | C | G | 17 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(14): Show |
17 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.334-7654C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68703078 | |||||||
| chr15:68703081 | A | C | 17 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(14): Show |
17 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.334-7651A>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68703081 | |||||||
| chr15:68703150 | CT | C | 14 | a0001c0001t0002g0022 a0001c0001t0002g0078 a0001c0001t0002g0079 others(11): Show |
14 | HG02257.hp1 HG02258.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.334-7563delT | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68703150 | ||||||
| chr15:68703150 | CTT | C | 164 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(161): Show |
164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.334-7564_334-7563d others(4): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68703150 | ||||||
| chr15:68703150 | CTTT | C | 31 | a0001c0001t0001g0087 a0001c0001t0001g0115 a0001c0001t0001g0124 others(28): Show |
31 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.334-7565_334-7563d others(5): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68703150 | ||||||
| chr15:68703150 | CTTTTTTT others(12): Show |
C | 1 | a0001c0001t0002g0231 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.334-7581_334-7563d others(21): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68703150 | |||||||
| chr15:68703154 | T | C | 17 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(14): Show |
17 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.334-7578T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68703154 | |||||||
| chr15:68703162 | T | C | 1 | a0001c0001t0014g0254 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.334-7570T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68703162 | |||||||
| chr15:68703200 | T | C | 1 | a0001c0001t0006g0218 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.334-7532T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68703200 | |||||||
| chr15:68703274 | C | T | 63 | a0001c0001t0001g0028 a0001c0001t0001g0056 a0001c0001t0001g0061 others(60): Show |
63 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.334-7458C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68703274 | |||||||
| chr15:68703300 | G | A | 1 | a0001c0003t0012g0047 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.334-7432G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68703300 | |||||||
| chr15:68703442 | C | T | 7 | a0001c0003t0006g0145 a0001c0003t0008g0178 a0001c0003t0011g0247 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.334-7290C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68703442 | |||||||
| chr15:68703559 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.334-7173C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68703559 | |||||||
| chr15:68703615 | C | T | 17 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(14): Show |
17 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.334-7117C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68703615 | |||||||
| chr15:68703791 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.334-6941A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68703791 | |||||||
| chr15:68703858 | T | C | 7 | a0001c0003t0006g0145 a0001c0003t0008g0178 a0001c0003t0011g0247 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.334-6874T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68703858 | |||||||
| chr15:68703880 | G | A | 17 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(14): Show |
17 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.334-6852G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68703880 | |||||||
| chr15:68703903 | A | G | 157 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(154): Show |
157 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.334-6829A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68703903 | |||||||
| chr15:68703978 | G | C | 2 | a0001c0001t0006g0236 a0001c0001t0027g0034 |
2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.334-6754G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68703978 | |||||||
| chr15:68703988 | G | A | 17 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(14): Show |
17 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.334-6744G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68703988 | |||||||
| chr15:68704010 | A | G | 28 | a0001c0001t0001g0115 a0001c0001t0001g0212 a0001c0001t0005g0007 others(25): Show |
28 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.334-6722A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68704010 | |||||||
| chr15:68704014 | CA | C | 17 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(14): Show |
17 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.334-6713delA | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68704014 | ||||||
| chr15:68704039 | T | TAC | 3 | a0001c0001t0002g0182 a0001c0001t0011g0075 a0001c0001t0014g0254 |
3 | HG02280.hp2 HG02486.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.334-6653_334-6652d others(4): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68704039 | ||||||
| chr15:68704039 | TAC | T | 62 | a0001c0001t0001g0009 a0001c0001t0001g0028 a0001c0001t0001g0044 others(59): Show |
62 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.334-6653_334-6652d others(4): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68704039 | ||||||
| chr15:68704039 | TACAC | T | 93 | a0001c0001t0001g0027 a0001c0001t0001g0037 a0001c0001t0001g0039 others(90): Show |
93 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.334-6655_334-6652d others(6): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68704039 | ||||||
| chr15:68704039 | TACACAC | T | 25 | a0001c0001t0001g0042 a0001c0001t0001g0067 a0001c0001t0001g0084 others(22): Show |
25 | HG00408.hp2 HG00621.hp1 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.334-6657_334-6652d others(8): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68704039 | ||||||
| chr15:68704039 | TACACACA others(3): Show |
T | 1 | a0001c0001t0001g0074 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.334-6661_334-6652d others(12): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68704039 | ||||||
| chr15:68704039 | TACACACA others(7): Show |
T | 1 | a0001c0001t0006g0004 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.334-6665_334-6652d others(16): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68704039 | ||||||
| chr15:68704039 | TACACACA others(9): Show |
T | 16 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(13): Show |
16 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.334-6667_334-6652d others(18): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68704039 | ||||||
| chr15:68704041 | C | CAA | 6 | a0001c0001t0001g0199 a0001c0001t0002g0102 a0001c0001t0002g0231 others(3): Show |
6 | HG02015.hp1 HG02040.hp1 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.334-6690_334-6689i others(4): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68704041 | ||||||
| chr15:68704043 | C | A | 7 | a0001c0002t0001g0069 a0001c0002t0001g0070 a0001c0002t0001g0206 others(4): Show |
7 | HG00738.hp2 HG00741.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.334-6689C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68704043 | |||||||
| chr15:68704045 | C | A | 21 | a0001c0001t0001g0115 a0001c0001t0001g0212 a0001c0001t0005g0007 others(18): Show |
21 | HG00280.hp2 HG00642.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.334-6687C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68704045 | |||||||
| chr15:68704077 | CACA | C | 3 | a0001c0001t0001g0147 a0001c0001t0001g0173 a0001c0001t0003g0226 |
3 | HG01070.hp1 HG01070.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.334-6653_334-6651d others(5): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68704077 | ||||||
| chr15:68704102 | T | C | 144 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(141): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.334-6630T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68704102 | |||||||
| chr15:68704111 | G | A | 17 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(14): Show |
17 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.334-6621G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68704111 | |||||||
| chr15:68704151 | G | A | 17 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(14): Show |
17 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.334-6581G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68704151 | |||||||
| chr15:68704175 | G | A | 2 | a0001c0001t0005g0194 a0001c0001t0017g0251 |
2 | HG02630.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.334-6557G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68704175 | |||||||
| chr15:68704232 | C | T | 8 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0046 others(5): Show |
8 | HG02280.hp2 HG02486.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.334-6500C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68704232 | |||||||
| chr15:68704239 | GA | G | 17 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(14): Show |
17 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.334-6482delA | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68704239 | ||||||
| chr15:68704250 | A | G | 18 | a0001c0001t0001g0212 a0001c0001t0005g0007 a0001c0002t0001g0006 others(15): Show |
18 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.334-6482A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68704250 | |||||||
| chr15:68704299 | G | T | 1 | a0001c0002t0005g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.334-6433G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68704299 | |||||||
| chr15:68704355 | C | T | 1 | a0001c0001t0002g0221 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.334-6377C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68704355 | |||||||
| chr15:68704567 | C | T | 235 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(232): Show |
235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.334-6165C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68704567 | |||||||
| chr15:68704688 | C | G | 7 | a0001c0003t0006g0145 a0001c0003t0008g0178 a0001c0003t0011g0247 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.334-6044C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68704688 | |||||||
| chr15:68704689 | G | C | 17 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(14): Show |
17 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.334-6043G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68704689 | |||||||
| chr15:68704923 | A | G | 17 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(14): Show |
17 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.334-5809A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68704923 | |||||||
| chr15:68705088 | G | A | 1 | a0001c0001t0006g0031 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.334-5644G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68705088 | |||||||
| chr15:68705135 | T | C | 7 | a0001c0003t0006g0145 a0001c0003t0008g0178 a0001c0003t0011g0247 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.334-5597T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68705135 | |||||||
| chr15:68705143 | G | A | 17 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(14): Show |
17 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.334-5589G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68705143 | |||||||
| chr15:68705170 | A | G | 2 | a0001c0001t0011g0075 a0001c0001t0014g0254 |
2 | HG02280.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.334-5562A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68705170 | |||||||
| chr15:68705174 | A | G | 151 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(148): Show |
151 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.334-5558A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68705174 | |||||||
| chr15:68705258 | C | T | 17 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(14): Show |
17 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.334-5474C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68705258 | |||||||
| chr15:68705275 | T | C | 1 | a0001c0003t0008g0178 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.334-5457T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68705275 | |||||||
| chr15:68705276 | A | T | 1 | a0001c0003t0008g0178 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.334-5456A>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68705276 | |||||||
| chr15:68705299 | G | A | 145 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(142): Show |
145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.334-5433G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68705299 | |||||||
| chr15:68705311 | G | A | 17 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(14): Show |
17 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.334-5421G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68705311 | |||||||
| chr15:68705417 | A | G | 17 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(14): Show |
17 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.334-5315A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68705417 | |||||||
| chr15:68705435 | TC | T | 5 | a0001c0002t0006g0223 a0001c0003t0001g0057 a0001c0003t0006g0051 others(2): Show |
5 | HG02109.hp2 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-5296delC | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68705435 | |||||||
| chr15:68705436 | C | CA | 141 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(138): Show |
141 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.334-5278dupA | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68705436 | ||||||
| chr15:68705436 | C | CAA | 17 | a0001c0001t0001g0042 a0001c0001t0001g0052 a0001c0001t0001g0133 others(14): Show |
17 | HG02015.hp1 HG02040.hp1 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.334-5279_334-5278d others(4): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68705436 | ||||||
| chr15:68705436 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0004g0180 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.334-5287_334-5278d others(12): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68705436 | ||||||
| chr15:68705436 | C | CAAAAAAA others(4): Show |
9 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(6): Show |
9 | HG01109.hp2 HG02615.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.334-5288_334-5278d others(13): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68705436 | ||||||
| chr15:68705436 | C | CAAAAAAA others(5): Show |
6 | a0001c0001t0002g0080 a0001c0001t0002g0135 a0001c0001t0005g0018 others(3): Show |
6 | HG01891.hp2 HG02145.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.334-5289_334-5278d others(14): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68705436 | ||||||
| chr15:68705436 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0005g0164 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.334-5290_334-5278d others(15): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68705436 | ||||||
| chr15:68705436 | C | T | 1 | a0001c0004t0006g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.334-5296C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68705436 | |||||||
| chr15:68705436 | CAA | C | 7 | a0001c0003t0006g0145 a0001c0003t0008g0178 a0001c0003t0011g0247 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.334-5279_334-5278d others(4): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68705436 | ||||||
| chr15:68705437 | A | T | 5 | a0001c0002t0006g0223 a0001c0003t0001g0057 a0001c0003t0006g0051 others(2): Show |
5 | HG02109.hp2 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-5295A>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68705437 | |||||||
| chr15:68705450 | A | G | 7 | a0001c0003t0006g0145 a0001c0003t0008g0178 a0001c0003t0011g0247 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.334-5282A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68705450 | |||||||
| chr15:68705490 | G | A | 1 | a0001c0004t0006g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.334-5242G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68705490 | |||||||
| chr15:68705500 | T | A | 28 | a0001c0001t0001g0115 a0001c0001t0001g0212 a0001c0001t0005g0007 others(25): Show |
28 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.334-5232T>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68705500 | |||||||
| chr15:68705512 | A | G | 1 | a0001c0002t0005g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.334-5220A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68705512 | |||||||
| chr15:68705529 | G | A | 8 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0046 others(5): Show |
8 | HG02280.hp2 HG02486.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.334-5203G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68705529 | |||||||
| chr15:68705758 | A | G | 1 | a0001c0001t0002g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.334-4974A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68705758 | |||||||
| chr15:68706015 | C | T | 5 | a0001c0001t0001g0094 a0001c0001t0004g0180 a0001c0001t0006g0021 others(2): Show |
5 | HG01109.hp2 HG02896.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-4717C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68706015 | |||||||
| chr15:68706190 | T | C | 7 | a0001c0003t0006g0145 a0001c0003t0008g0178 a0001c0003t0011g0247 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.334-4542T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68706190 | |||||||
| chr15:68706204 | C | T | 7 | a0001c0003t0006g0145 a0001c0003t0008g0178 a0001c0003t0011g0247 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.334-4528C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68706204 | |||||||
| chr15:68706208 | C | T | 227 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(224): Show |
227 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.334-4524C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68706208 | |||||||
| chr15:68706211 | C | A | 1 | a0001c0001t0004g0180 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.334-4521C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68706211 | |||||||
| chr15:68706301 | A | G | 1 | a0001c0001t0001g0074 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.334-4431A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68706301 | |||||||
| chr15:68706385 | C | G | 7 | a0001c0003t0006g0145 a0001c0003t0008g0178 a0001c0003t0011g0247 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.334-4347C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68706385 | |||||||
| chr15:68706434 | G | T | 1 | a0001c0002t0005g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.334-4298G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68706434 | |||||||
| chr15:68706529 | T | C | 7 | a0001c0003t0006g0145 a0001c0003t0008g0178 a0001c0003t0011g0247 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.334-4203T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68706529 | |||||||
| chr15:68706537 | G | A | 1 | a0001c0003t0011g0247 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.334-4195G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68706537 | |||||||
| chr15:68706657 | A | T | 62 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0037 others(59): Show |
62 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.334-4075A>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68706657 | |||||||
| chr15:68706751 | C | T | 7 | a0001c0003t0006g0145 a0001c0003t0008g0178 a0001c0003t0011g0247 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.334-3981C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68706751 | |||||||
| chr15:68706813 | G | A | 8 | a0001c0001t0021g0033 a0001c0003t0006g0145 a0001c0003t0008g0178 others(5): Show |
8 | HG01884.hp2 HG02145.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.334-3919G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68706813 | |||||||
| chr15:68706984 | A | G | 8 | a0001c0001t0021g0033 a0001c0003t0006g0145 a0001c0003t0008g0178 others(5): Show |
8 | HG01884.hp2 HG02145.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.334-3748A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68706984 | |||||||
| chr15:68707064 | G | A | 3 | a0001c0001t0002g0002 a0001c0001t0005g0029 a0001c0001t0005g0166 |
3 | HG02258.hp2 HG02559.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.334-3668G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68707064 | |||||||
| chr15:68707066 | T | C | 8 | a0001c0001t0021g0033 a0001c0003t0006g0145 a0001c0003t0008g0178 others(5): Show |
8 | HG01884.hp2 HG02145.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.334-3666T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68707066 | |||||||
| chr15:68707109 | C | T | 10 | a0001c0001t0001g0052 a0001c0001t0001g0199 a0001c0001t0002g0102 others(7): Show |
10 | HG02015.hp1 HG02040.hp1 NA18947.hp2 others(7): Show |
intron_variant | MODIFIER | c.334-3623C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68707109 | |||||||
| chr15:68707112 | C | T | 4 | a0001c0001t0001g0192 a0001c0001t0003g0086 a0001c0001t0003g0127 others(1): Show |
4 | HG00673.hp2 HG02015.hp2 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.334-3620C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68707112 | |||||||
| chr15:68707117 | C | T | 8 | a0001c0001t0021g0033 a0001c0003t0006g0145 a0001c0003t0008g0178 others(5): Show |
8 | HG01884.hp2 HG02145.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.334-3615C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68707117 | |||||||
| chr15:68707129 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.334-3603G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68707129 | |||||||
| chr15:68707278 | T | A | 2 | a0001c0001t0006g0236 a0001c0001t0027g0034 |
2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.334-3454T>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68707278 | |||||||
| chr15:68707409 | G | A | 247 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(244): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.334-3323G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68707409 | |||||||
| chr15:68707415 | C | T | 1 | a0001c0001t0014g0254 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.334-3317C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68707415 | |||||||
| chr15:68707677 | G | A | 143 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(140): Show |
143 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.334-3055G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68707677 | |||||||
| chr15:68707782 | A | T | 1 | a0001c0001t0003g0171 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.334-2950A>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68707782 | |||||||
| chr15:68707824 | C | G | 28 | a0001c0001t0001g0115 a0001c0001t0001g0212 a0001c0001t0005g0007 others(25): Show |
28 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.334-2908C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68707824 | |||||||
| chr15:68708197 | G | A | 1 | a0001c0001t0002g0231 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.334-2535G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68708197 | |||||||
| chr15:68708323 | A | G | 6 | a0001c0001t0001g0074 a0001c0001t0004g0017 a0001c0001t0008g0001 others(3): Show |
6 | HG02559.hp2 HG02976.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.334-2409A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68708323 | |||||||
| chr15:68708357 | C | CT | 32 | a0001c0001t0001g0115 a0001c0001t0001g0212 a0001c0001t0003g0239 others(29): Show |
32 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.334-2354dupT | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68708357 | ||||||
| chr15:68708357 | C | CTTT | 8 | a0001c0001t0001g0052 a0001c0001t0001g0199 a0001c0001t0002g0102 others(5): Show |
8 | HG02015.hp1 HG02040.hp1 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.334-2356_334-2354d others(5): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68708357 | ||||||
| chr15:68708357 | CT | C | 9 | a0001c0001t0001g0027 a0001c0001t0001g0153 a0001c0001t0001g0187 others(6): Show |
9 | HG00140.hp2 HG01516.hp1 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.334-2354delT | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68708357 | ||||||
| chr15:68708357 | CTTTTTTT others(9): Show |
C | 1 | a0001c0002t0002g0099 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.334-2369_334-2354d others(18): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68708357 | ||||||
| chr15:68708360 | T | C | 1 | a0001c0001t0001g0048 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.334-2372T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68708360 | |||||||
| chr15:68708422 | G | A | 21 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(18): Show |
21 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.334-2310G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68708422 | |||||||
| chr15:68708537 | A | AT | 6 | a0001c0002t0006g0223 a0001c0003t0001g0057 a0001c0003t0006g0051 others(3): Show |
6 | HG02109.hp2 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.334-2188dupT | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68708537 | ||||||
| chr15:68708613 | C | T | 2 | a0001c0001t0001g0027 a0001c0001t0004g0104 |
2 | NA19060.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.334-2119C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68708613 | |||||||
| chr15:68708624 | A | G | 1 | a0001c0001t0001g0074 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.334-2108A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68708624 | |||||||
| chr15:68708680 | C | CT | 27 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(24): Show |
27 | HG01109.hp2 HG01891.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.334-2042dupT | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68708680 | ||||||
| chr15:68709110 | A | G | 20 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(17): Show |
20 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.334-1622A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68709110 | |||||||
| chr15:68709278 | A | G | 1 | a0001c0003t0012g0076 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.334-1454A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68709278 | |||||||
| chr15:68709448 | T | A | 218 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(215): Show |
218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.334-1284T>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68709448 | |||||||
| chr15:68709459 | G | GT | 5 | a0001c0001t0008g0025 a0001c0001t0009g0030 a0001c0001t0021g0033 others(2): Show |
5 | HG02451.hp1 HG02451.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-1252dupT | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68709459 | ||||||
| chr15:68709459 | GT | G | 23 | a0001c0001t0001g0052 a0001c0001t0001g0175 a0001c0001t0001g0176 others(20): Show |
23 | HG00408.hp1 HG00735.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.334-1252delT | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68709459 | ||||||
| chr15:68709459 | GTT | G | 194 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(191): Show |
194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.334-1253_334-1252d others(4): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68709459 | ||||||
| chr15:68709644 | G | A | 218 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(215): Show |
218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.334-1088G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68709644 | |||||||
| chr15:68709647 | C | T | 6 | a0001c0001t0001g0074 a0001c0001t0004g0017 a0001c0001t0008g0001 others(3): Show |
6 | HG02559.hp2 HG02976.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.334-1085C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68709647 | |||||||
| chr15:68709887 | A | AC | 26 | a0001c0001t0001g0115 a0001c0001t0005g0007 a0001c0002t0001g0006 others(23): Show |
26 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.334-843dupC | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 68709887 | ||||||
| chr15:68710216 | C | A | 144 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(141): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.334-516C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68710216 | |||||||
| chr15:68710312 | A | G | 31 | a0001c0001t0001g0052 a0001c0001t0001g0094 a0001c0001t0001g0179 others(28): Show |
31 | HG01109.hp2 HG01891.hp2 HG02015.hp1 others(28): Show |
intron_variant | MODIFIER | c.334-420A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68710312 | |||||||
| chr15:68710556 | A | C | 6 | a0001c0001t0005g0035 a0001c0001t0005g0046 a0001c0001t0006g0191 others(3): Show |
6 | HG02280.hp2 HG02486.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.334-176A>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 3/11 | chr15 | 68710556 | |||||||
| chr15:68710940 | G | A | 1 | a0001c0002t0003g0107 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.483+59G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 4/11 | chr15 | 68710940 | |||||||
| chr15:68710979 | A | G | 1 | a0001c0001t0009g0238 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.483+98A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 4/11 | chr15 | 68710979 | |||||||
| chr15:68711004 | T | TATTC | 9 | a0001c0001t0001g0009 a0001c0001t0001g0098 a0001c0001t0001g0139 others(6): Show |
9 | HG01070.hp1 HG01070.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.483+140_483+143dup others(4): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr15 | 68711004 | ||||||
| chr15:68711031 | C | T | 21 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(18): Show |
21 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.483+150C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 4/11 | chr15 | 68711031 | |||||||
| chr15:68711032 | G | A | 2 | a0001c0004t0007g0023 a0001c0004t0007g0172 |
2 | HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.483+151G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 4/11 | chr15 | 68711032 | |||||||
| chr15:68711243 | T | C | 220 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(217): Show |
220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.484-299T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 4/11 | chr15 | 68711243 | |||||||
| chr15:68711291 | T | G | 6 | a0001c0001t0001g0074 a0001c0001t0004g0017 a0001c0001t0008g0001 others(3): Show |
6 | HG02559.hp2 HG02976.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.484-251T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 4/11 | chr15 | 68711291 | |||||||
| chr15:68711449 | G | A | 34 | a0001c0001t0001g0052 a0001c0001t0001g0199 a0001c0001t0002g0102 others(31): Show |
34 | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.484-93G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 4/11 | chr15 | 68711449 | |||||||
| chr15:68711494 | G | C | 6 | a0001c0001t0005g0035 a0001c0001t0005g0046 a0001c0001t0006g0191 others(3): Show |
6 | HG02280.hp2 HG02486.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.484-48G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 4/11 | chr15 | 68711494 | |||||||
| chr15:68711525 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.484-17T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 4/11 | chr15 | 68711525 | |||||||
| chr15:68711532 | G | T | 151 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(148): Show |
151 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.484-10G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 4/11 | chr15 | 68711532 | |||||||
| chr15:68711934 | C | G | 1 | a0001c0001t0001g0144 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.648+228C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 5/11 | chr15 | 68711934 | |||||||
| chr15:68712131 | C | T | 3 | a0001c0001t0004g0180 a0001c0001t0006g0021 a0001c0001t0006g0237 |
3 | HG01109.hp2 HG02896.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.648+425C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 5/11 | chr15 | 68712131 | |||||||
| chr15:68712194 | G | A | 1 | a0001c0001t0003g0214 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.648+488G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 5/11 | chr15 | 68712194 | |||||||
| chr15:68712251 | A | G | 25 | a0001c0001t0005g0007 a0001c0002t0001g0006 a0001c0002t0001g0008 others(22): Show |
25 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.648+545A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 5/11 | chr15 | 68712251 | |||||||
| chr15:68712338 | C | A | 1 | a0001c0002t0005g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.648+632C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 5/11 | chr15 | 68712338 | |||||||
| chr15:68712376 | T | C | 21 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(18): Show |
21 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.648+670T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 5/11 | chr15 | 68712376 | |||||||
| chr15:68712760 | C | A | 1 | a0001c0001t0001g0124 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.648+1054C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 5/11 | chr15 | 68712760 | |||||||
| chr15:68712770 | G | T | 10 | a0001c0001t0001g0052 a0001c0001t0001g0199 a0001c0001t0002g0102 others(7): Show |
10 | HG02015.hp1 HG02040.hp1 NA18947.hp2 others(7): Show |
intron_variant | MODIFIER | c.648+1064G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 5/11 | chr15 | 68712770 | |||||||
| chr15:68712788 | T | G | 30 | a0001c0001t0001g0052 a0001c0001t0001g0094 a0001c0001t0001g0179 others(27): Show |
30 | HG01109.hp2 HG01891.hp2 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.648+1082T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 5/11 | chr15 | 68712788 | |||||||
| chr15:68712812 | C | T | 208 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(205): Show |
208 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.648+1106C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 5/11 | chr15 | 68712812 | |||||||
| chr15:68712826 | C | A | 12 | a0001c0001t0001g0074 a0001c0001t0002g0022 a0001c0001t0002g0078 others(9): Show |
12 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.649-1099C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 5/11 | chr15 | 68712826 | |||||||
| chr15:68712827 | C | T | 12 | a0001c0001t0001g0074 a0001c0001t0002g0022 a0001c0001t0002g0078 others(9): Show |
12 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.649-1098C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 5/11 | chr15 | 68712827 | |||||||
| chr15:68712848 | C | T | 1 | a0001c0002t0001g0206 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.649-1077C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 5/11 | chr15 | 68712848 | |||||||
| chr15:68712968 | T | C | 35 | a0001c0001t0001g0052 a0001c0001t0001g0199 a0001c0001t0002g0102 others(32): Show |
35 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.649-957T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 5/11 | chr15 | 68712968 | |||||||
| chr15:68712995 | G | A | 207 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(204): Show |
207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.649-930G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 5/11 | chr15 | 68712995 | |||||||
| chr15:68713103 | C | T | 1 | a0001c0001t0002g0054 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.649-822C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 5/11 | chr15 | 68713103 | |||||||
| chr15:68713286 | C | A | 20 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(17): Show |
20 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.649-639C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 5/11 | chr15 | 68713286 | |||||||
| chr15:68713308 | T | C | 35 | a0001c0001t0001g0052 a0001c0001t0001g0199 a0001c0001t0002g0102 others(32): Show |
35 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.649-617T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 5/11 | chr15 | 68713308 | |||||||
| chr15:68713309 | G | A | 20 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(17): Show |
20 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.649-616G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 5/11 | chr15 | 68713309 | |||||||
| chr15:68713312 | G | A | 1 | a0001c0001t0003g0214 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.649-613G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 5/11 | chr15 | 68713312 | |||||||
| chr15:68714087 | G | A | 2 | a0001c0001t0001g0067 a0001c0001t0001g0118 |
2 | HG02056.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.765+46G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 6/11 | chr15 | 68714087 | |||||||
| chr15:68714128 | G | A | 20 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(17): Show |
20 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.765+87G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 6/11 | chr15 | 68714128 | |||||||
| chr15:68714132 | G | A | 20 | a0001c0001t0001g0094 a0001c0001t0001g0179 a0001c0001t0001g0228 others(17): Show |
20 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.765+91G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 6/11 | chr15 | 68714132 | |||||||
| chr15:68714144 | C | A | 4 | a0001c0004t0005g0003 a0001c0004t0005g0233 a0001c0004t0007g0023 others(1): Show |
4 | HG01884.hp2 HG03098.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.765+103C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 6/11 | chr15 | 68714144 | |||||||
| chr15:68714268 | G | A | 10 | a0001c0001t0001g0052 a0001c0001t0001g0199 a0001c0001t0002g0102 others(7): Show |
10 | HG02015.hp1 HG02040.hp1 NA18947.hp2 others(7): Show |
intron_variant | MODIFIER | c.765+227G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 6/11 | chr15 | 68714268 | |||||||
| chr15:68714394 | C | T | 1 | a0001c0001t0003g0140 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.766-165C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 6/11 | chr15 | 68714394 | |||||||
| chr15:68714688 | G | A | 1 | a0001c0001t0004g0180 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.870+25G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 7/11 | chr15 | 68714688 | |||||||
| chr15:68715011 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.871-204C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 7/11 | chr15 | 68715011 | |||||||
| chr15:68715012 | A | G | 28 | a0001c0001t0001g0074 a0001c0001t0001g0094 a0001c0001t0001g0179 others(25): Show |
28 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.871-203A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 7/11 | chr15 | 68715012 | |||||||
| chr15:68715317 | T | G | 234 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(231): Show |
234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
splice_region_variant&intron_variant | LOW | c.967+6T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 8/11 | chr15 | 68715317 | |||||||
| chr15:68715682 | G | A | 2 | a0001c0003t0006g0145 a0001c0003t0008g0178 |
2 | HG02145.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.967+371G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 8/11 | chr15 | 68715682 | |||||||
| chr15:68715782 | G | A | 1 | a0001c0001t0004g0117 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.967+471G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 8/11 | chr15 | 68715782 | |||||||
| chr15:68715888 | C | G | 24 | a0001c0002t0001g0006 a0001c0002t0001g0008 a0001c0002t0001g0069 others(21): Show |
24 | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.967+577C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 8/11 | chr15 | 68715888 | |||||||
| chr15:68715912 | A | G | 24 | a0001c0001t0001g0085 a0001c0001t0001g0087 a0001c0001t0001g0089 others(21): Show |
24 | HG00140.hp2 HG00280.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.967+601A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 8/11 | chr15 | 68715912 | |||||||
| chr15:68715924 | G | A | 1 | a0001c0002t0002g0224 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.967+613G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 8/11 | chr15 | 68715924 | |||||||
| chr15:68715976 | C | T | 24 | a0001c0002t0001g0006 a0001c0002t0001g0008 a0001c0002t0001g0069 others(21): Show |
24 | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.967+665C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 8/11 | chr15 | 68715976 | |||||||
| chr15:68715983 | G | A | 1 | a0001c0003t0008g0178 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.967+672G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 8/11 | chr15 | 68715983 | |||||||
| chr15:68716372 | C | T | 201 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(198): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.967+1061C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 8/11 | chr15 | 68716372 | |||||||
| chr15:68716473 | G | A | 1 | a0001c0001t0003g0171 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.967+1162G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 8/11 | chr15 | 68716473 | |||||||
| chr15:68716514 | A | G | 1 | a0001c0001t0001g0074 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.967+1203A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 8/11 | chr15 | 68716514 | |||||||
| chr15:68716537 | A | G | 1 | a0001c0001t0001g0212 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.967+1226A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 8/11 | chr15 | 68716537 | |||||||
| chr15:68716676 | G | A | 178 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(175): Show |
178 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.967+1365G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 8/11 | chr15 | 68716676 | |||||||
| chr15:68716891 | C | T | 178 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(175): Show |
178 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.967+1580C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 8/11 | chr15 | 68716891 | |||||||
| chr15:68717129 | C | T | 10 | a0001c0001t0001g0052 a0001c0001t0001g0199 a0001c0001t0002g0102 others(7): Show |
10 | HG02015.hp1 HG02040.hp1 NA18947.hp2 others(7): Show |
intron_variant | MODIFIER | c.968-1569C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 8/11 | chr15 | 68717129 | |||||||
| chr15:68717311 | C | CA | 27 | a0001c0001t0001g0052 a0001c0001t0001g0199 a0001c0001t0002g0022 others(24): Show |
27 | HG02015.hp1 HG02040.hp1 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.968-1372dupA | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 68717311 | ||||||
| chr15:68717374 | G | A | 183 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(180): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.968-1324G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 8/11 | chr15 | 68717374 | |||||||
| chr15:68717449 | C | T | 1 | a0001c0001t0017g0251 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.968-1249C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 8/11 | chr15 | 68717449 | |||||||
| chr15:68717461 | T | G | 193 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(190): Show |
193 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.968-1237T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 8/11 | chr15 | 68717461 | |||||||
| chr15:68717512 | G | A | 1 | a0001c0001t0008g0025 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.968-1186G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 8/11 | chr15 | 68717512 | |||||||
| chr15:68717531 | G | T | 10 | a0001c0001t0001g0052 a0001c0001t0001g0199 a0001c0001t0002g0102 others(7): Show |
10 | HG02015.hp1 HG02040.hp1 NA18947.hp2 others(7): Show |
intron_variant | MODIFIER | c.968-1167G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 8/11 | chr15 | 68717531 | |||||||
| chr15:68717548 | G | A | 183 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(180): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.968-1150G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 8/11 | chr15 | 68717548 | |||||||
| chr15:68717548 | G | T | 3 | a0001c0003t0006g0145 a0001c0003t0008g0178 a0001c0003t0011g0247 |
3 | HG02145.hp1 HG02451.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.968-1150G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 8/11 | chr15 | 68717548 | |||||||
| chr15:68717650 | A | C | 1 | a0001c0001t0006g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.968-1048A>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 8/11 | chr15 | 68717650 | |||||||
| chr15:68717688 | CAGA | C | 183 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(180): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.968-1002_968-1000d others(5): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 68717688 | ||||||
| chr15:68717766 | G | A | 183 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(180): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.968-932G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 8/11 | chr15 | 68717766 | |||||||
| chr15:68717875 | C | T | 1 | a0001c0004t0005g0233 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.968-823C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 8/11 | chr15 | 68717875 | |||||||
| chr15:68717909 | A | G | 26 | a0001c0001t0005g0007 a0001c0002t0001g0006 a0001c0002t0001g0008 others(23): Show |
26 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.968-789A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 8/11 | chr15 | 68717909 | |||||||
| chr15:68717981 | G | A | 5 | a0001c0001t0004g0017 a0001c0001t0008g0001 a0001c0001t0009g0014 others(2): Show |
5 | HG02559.hp2 HG02976.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.968-717G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 8/11 | chr15 | 68717981 | |||||||
| chr15:68717986 | A | G | 183 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(180): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.968-712A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 8/11 | chr15 | 68717986 | |||||||
| chr15:68718039 | C | T | 6 | a0001c0001t0001g0087 a0001c0001t0001g0089 a0001c0001t0001g0187 others(3): Show |
6 | HG00140.hp2 HG00738.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.968-659C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 8/11 | chr15 | 68718039 | |||||||
| chr15:68718165 | G | T | 183 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(180): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.968-533G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 8/11 | chr15 | 68718165 | |||||||
| chr15:68718290 | C | A | 183 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(180): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.968-408C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 8/11 | chr15 | 68718290 | |||||||
| chr15:68718311 | C | T | 5 | a0001c0001t0004g0017 a0001c0001t0008g0001 a0001c0001t0009g0014 others(2): Show |
5 | HG02559.hp2 HG02976.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.968-387C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 8/11 | chr15 | 68718311 | |||||||
| chr15:68718464 | T | G | 1 | a0001c0001t0002g0231 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.968-234T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 8/11 | chr15 | 68718464 | |||||||
| chr15:68718476 | A | G | 4 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0196 others(1): Show |
4 | HG03130.hp2 HG03225.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.968-222A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 8/11 | chr15 | 68718476 | |||||||
| chr15:68718840 | G | A | 1 | a0001c0001t0025g0149 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1080+30G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 9/11 | chr15 | 68718840 | |||||||
| chr15:68718916 | A | G | 192 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(189): Show |
192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.1080+106A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 9/11 | chr15 | 68718916 | |||||||
| chr15:68718925 | C | G | 1 | a0001c0001t0004g0184 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1080+115C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 9/11 | chr15 | 68718925 | |||||||
| chr15:68719050 | A | C | 162 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(159): Show |
162 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.1081-94A>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 9/11 | chr15 | 68719050 | |||||||
| chr15:68719050 | A | G | 31 | a0001c0002t0001g0006 a0001c0002t0001g0008 a0001c0002t0001g0069 others(28): Show |
31 | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.1081-94A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 9/11 | chr15 | 68719050 | |||||||
| chr15:68719055 | C | T | 193 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(190): Show |
193 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.1081-89C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 9/11 | chr15 | 68719055 | |||||||
| chr15:68719066 | T | G | 1 | a0001c0001t0004g0240 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1081-78T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 9/11 | chr15 | 68719066 | |||||||
| chr15:68719579 | C | T | 29 | a0001c0001t0003g0225 a0001c0001t0003g0226 a0001c0001t0003g0227 others(26): Show |
29 | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.1311+27C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68719579 | |||||||
| chr15:68719806 | A | G | 174 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(171): Show |
174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1311+254A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68719806 | |||||||
| chr15:68719823 | C | T | 1 | a0001c0001t0006g0031 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1311+271C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68719823 | |||||||
| chr15:68719880 | C | T | 2 | a0001c0001t0005g0164 a0001c0001t0005g0194 |
2 | HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1311+328C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68719880 | |||||||
| chr15:68719917 | G | A | 29 | a0001c0001t0003g0225 a0001c0001t0003g0226 a0001c0001t0003g0227 others(26): Show |
29 | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.1311+365G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68719917 | |||||||
| chr15:68719970 | G | A | 4 | a0001c0001t0001g0044 a0001c0001t0001g0168 a0001c0001t0001g0169 others(1): Show |
4 | HG03490.hp1 HG03490.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.1311+418G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68719970 | |||||||
| chr15:68720117 | A | G | 16 | a0001c0001t0001g0094 a0001c0001t0001g0228 a0001c0001t0002g0091 others(13): Show |
16 | HG01109.hp2 HG01891.hp2 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.1311+565A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68720117 | |||||||
| chr15:68720168 | T | C | 175 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(172): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1311+616T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68720168 | |||||||
| chr15:68720383 | C | T | 204 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(201): Show |
204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.1311+831C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68720383 | |||||||
| chr15:68720466 | C | T | 16 | a0001c0001t0001g0094 a0001c0001t0001g0228 a0001c0001t0002g0091 others(13): Show |
16 | HG01109.hp2 HG01891.hp2 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.1311+914C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68720466 | |||||||
| chr15:68720532 | G | C | 30 | a0001c0001t0003g0225 a0001c0001t0003g0226 a0001c0001t0003g0227 others(27): Show |
30 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.1311+980G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68720532 | |||||||
| chr15:68720552 | C | T | 29 | a0001c0001t0003g0225 a0001c0001t0003g0226 a0001c0001t0003g0227 others(26): Show |
29 | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.1311+1000C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68720552 | |||||||
| chr15:68720588 | T | A | 2 | a0001c0001t0002g0080 a0001c0001t0002g0135 |
2 | HG02145.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1311+1036T>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68720588 | |||||||
| chr15:68720733 | G | C | 5 | a0001c0001t0001g0061 a0001c0001t0001g0114 a0001c0001t0001g0156 others(2): Show |
5 | HG01261.hp2 HG01346.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.1311+1181G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68720733 | |||||||
| chr15:68720815 | G | T | 174 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(171): Show |
174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1311+1263G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68720815 | |||||||
| chr15:68720920 | T | G | 3 | a0001c0001t0002g0197 a0001c0001t0003g0083 a0001c0001t0023g0209 |
3 | HG00597.hp1 HG00673.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.1311+1368T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68720920 | |||||||
| chr15:68721134 | G | C | 30 | a0001c0001t0003g0225 a0001c0001t0003g0226 a0001c0001t0003g0227 others(27): Show |
30 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.1311+1582G>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68721134 | |||||||
| chr15:68721185 | TA | T | 174 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(171): Show |
174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1311+1635delA | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr15 | 68721185 | ||||||
| chr15:68721341 | G | A | 174 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(171): Show |
174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1311+1789G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68721341 | |||||||
| chr15:68721368 | G | A | 174 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(171): Show |
174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1311+1816G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68721368 | |||||||
| chr15:68721420 | T | C | 204 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(201): Show |
204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.1311+1868T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68721420 | |||||||
| chr15:68721445 | C | T | 29 | a0001c0001t0003g0225 a0001c0001t0003g0226 a0001c0001t0003g0227 others(26): Show |
29 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.1311+1893C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68721445 | |||||||
| chr15:68721477 | G | A | 5 | a0001c0001t0011g0075 a0001c0003t0001g0057 a0001c0003t0006g0051 others(2): Show |
5 | HG02109.hp2 HG02145.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1311+1925G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68721477 | |||||||
| chr15:68721566 | C | T | 1 | a0002c0008t0002g0093 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1311+2014C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68721566 | |||||||
| chr15:68721577 | G | A | 30 | a0001c0001t0003g0225 a0001c0001t0003g0226 a0001c0001t0003g0227 others(27): Show |
30 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.1311+2025G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68721577 | |||||||
| chr15:68721578 | C | T | 152 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(149): Show |
152 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.1311+2026C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68721578 | |||||||
| chr15:68721712 | T | C | 1 | a0001c0002t0002g0071 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1311+2160T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68721712 | |||||||
| chr15:68721744 | G | GTATT | 173 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(170): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.1311+2204_1311+220 others(8): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr15 | 68721744 | ||||||
| chr15:68721760 | G | T | 30 | a0001c0001t0003g0225 a0001c0001t0003g0226 a0001c0001t0003g0227 others(27): Show |
30 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.1311+2208G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68721760 | |||||||
| chr15:68721761 | T | TATTTATG | 30 | a0001c0001t0003g0225 a0001c0001t0003g0226 a0001c0001t0003g0227 others(27): Show |
30 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.1311+2209_1311+221 others(11): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68721761 | |||||||
| chr15:68721810 | C | T | 1 | a0001c0001t0009g0238 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1311+2258C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68721810 | |||||||
| chr15:68721812 | A | G | 174 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(171): Show |
174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1311+2260A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68721812 | |||||||
| chr15:68721834 | A | C | 7 | a0001c0001t0001g0179 a0001c0001t0006g0004 a0001c0001t0021g0033 others(4): Show |
7 | HG02451.hp1 HG02647.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1311+2282A>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68721834 | |||||||
| chr15:68721877 | A | G | 204 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(201): Show |
204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.1311+2325A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68721877 | |||||||
| chr15:68721984 | C | G | 28 | a0001c0001t0003g0225 a0001c0001t0003g0226 a0001c0001t0003g0227 others(25): Show |
28 | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.1311+2432C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68721984 | |||||||
| chr15:68722380 | G | A | 204 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(201): Show |
204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.1311+2828G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68722380 | |||||||
| chr15:68722429 | C | T | 6 | a0001c0001t0004g0017 a0001c0001t0008g0001 a0001c0001t0008g0025 others(3): Show |
6 | HG02451.hp2 HG02559.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1311+2877C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68722429 | |||||||
| chr15:68722430 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1311+2878G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68722430 | |||||||
| chr15:68722432 | A | G | 204 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(201): Show |
204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.1311+2880A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68722432 | |||||||
| chr15:68722442 | G | A | 4 | a0001c0001t0001g0132 a0001c0001t0004g0019 a0001c0001t0004g0134 others(1): Show |
4 | HG02809.hp1 HG02886.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1311+2890G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68722442 | |||||||
| chr15:68722486 | C | T | 1 | a0001c0001t0013g0253 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1311+2934C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68722486 | |||||||
| chr15:68722580 | G | A | 1 | a0001c0001t0008g0025 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1311+3028G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68722580 | |||||||
| chr15:68722586 | T | G | 43 | a0001c0001t0001g0094 a0001c0001t0001g0228 a0001c0001t0002g0091 others(40): Show |
43 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.1311+3034T>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68722586 | |||||||
| chr15:68722704 | A | G | 3 | a0001c0001t0001g0028 a0001c0001t0003g0059 a0001c0001t0003g0154 |
3 | HG02080.hp2 NA18947.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1312-3139A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68722704 | |||||||
| chr15:68722792 | G | T | 1 | a0001c0001t0007g0151 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1312-3051G>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68722792 | |||||||
| chr15:68722822 | C | T | 16 | a0001c0001t0001g0179 a0001c0001t0002g0022 a0001c0001t0002g0078 others(13): Show |
16 | HG01109.hp2 HG02109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.1312-3021C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68722822 | |||||||
| chr15:68722839 | G | A | 3 | a0001c0001t0003g0225 a0001c0001t0003g0226 a0001c0001t0003g0227 |
3 | HG01070.hp1 HG01081.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1312-3004G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68722839 | |||||||
| chr15:68722849 | C | T | 2 | a0001c0002t0006g0137 a0001c0002t0006g0248 |
2 | HG01496.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1312-2994C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68722849 | |||||||
| chr15:68722863 | T | C | 30 | a0001c0001t0003g0225 a0001c0001t0003g0226 a0001c0001t0003g0227 others(27): Show |
30 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.1312-2980T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68722863 | |||||||
| chr15:68722907 | A | C | 1 | a0001c0002t0002g0224 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1312-2936A>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68722907 | |||||||
| chr15:68723047 | ACAAGAGT others(12): Show |
A | 10 | a0001c0001t0001g0052 a0001c0001t0001g0199 a0001c0001t0002g0102 others(7): Show |
10 | HG02015.hp1 HG02040.hp1 NA18947.hp2 others(7): Show |
intron_variant | MODIFIER | c.1312-2792_1312-277 others(23): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr15 | 68723047 | ||||||
| chr15:68723062 | C | T | 1 | a0001c0001t0008g0025 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1312-2781C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68723062 | |||||||
| chr15:68723063 | G | A | 1 | a0001c0001t0006g0218 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1312-2780G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68723063 | |||||||
| chr15:68723116 | CT | C | 167 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(164): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.1312-2703delT | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr15 | 68723116 | ||||||
| chr15:68723116 | CTTTTTTT others(2): Show |
C | 30 | a0001c0001t0003g0225 a0001c0001t0003g0226 a0001c0001t0003g0227 others(27): Show |
30 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.1312-2711_1312-270 others(13): Show |
CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr15 | 68723116 | ||||||
| chr15:68723163 | C | A | 1 | a0001c0001t0005g0164 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1312-2680C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68723163 | |||||||
| chr15:68723184 | C | A | 5 | a0001c0001t0011g0075 a0001c0003t0001g0057 a0001c0003t0006g0051 others(2): Show |
5 | HG02109.hp2 HG02145.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1312-2659C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68723184 | |||||||
| chr15:68723212 | C | G | 1 | a0001c0001t0008g0025 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1312-2631C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68723212 | |||||||
| chr15:68723280 | C | T | 1 | a0001c0001t0002g0123 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1312-2563C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68723280 | |||||||
| chr15:68723411 | G | A | 1 | a0001c0001t0008g0025 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1312-2432G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68723411 | |||||||
| chr15:68723414 | G | A | 6 | a0001c0001t0004g0017 a0001c0001t0008g0001 a0001c0001t0008g0025 others(3): Show |
6 | HG02451.hp2 HG02559.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1312-2429G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68723414 | |||||||
| chr15:68723440 | C | T | 30 | a0001c0001t0003g0225 a0001c0001t0003g0226 a0001c0001t0003g0227 others(27): Show |
30 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.1312-2403C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68723440 | |||||||
| chr15:68723542 | C | G | 1 | a0001c0001t0001g0074 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1312-2301C>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68723542 | |||||||
| chr15:68723562 | C | T | 13 | a0001c0001t0001g0094 a0001c0001t0001g0228 a0001c0001t0002g0091 others(10): Show |
13 | HG01891.hp2 HG02615.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.1312-2281C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68723562 | |||||||
| chr15:68723578 | C | T | 30 | a0001c0001t0003g0225 a0001c0001t0003g0226 a0001c0001t0003g0227 others(27): Show |
30 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.1312-2265C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68723578 | |||||||
| chr15:68723652 | C | T | 5 | a0001c0001t0004g0229 a0001c0001t0006g0053 a0001c0002t0005g0016 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1312-2191C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68723652 | |||||||
| chr15:68723665 | A | G | 250 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(247): Show |
250 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.1312-2178A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68723665 | |||||||
| chr15:68723680 | C | T | 30 | a0001c0001t0003g0225 a0001c0001t0003g0226 a0001c0001t0003g0227 others(27): Show |
30 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.1312-2163C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68723680 | |||||||
| chr15:68723703 | T | C | 30 | a0001c0001t0003g0225 a0001c0001t0003g0226 a0001c0001t0003g0227 others(27): Show |
30 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.1312-2140T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68723703 | |||||||
| chr15:68723804 | T | C | 177 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(174): Show |
177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.1312-2039T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68723804 | |||||||
| chr15:68724058 | C | T | 177 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(174): Show |
177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.1312-1785C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68724058 | |||||||
| chr15:68724161 | C | T | 1 | a0001c0001t0002g0148 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1312-1682C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68724161 | |||||||
| chr15:68724294 | C | A | 48 | a0001c0001t0001g0027 a0001c0001t0001g0039 a0001c0001t0001g0060 others(45): Show |
48 | HG00140.hp1 HG00597.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.1312-1549C>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68724294 | |||||||
| chr15:68724445 | A | G | 6 | a0001c0001t0004g0017 a0001c0001t0008g0001 a0001c0001t0008g0025 others(3): Show |
6 | HG02451.hp2 HG02559.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1312-1398A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68724445 | |||||||
| chr15:68724621 | T | C | 194 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(191): Show |
194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.1312-1222T>C | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68724621 | |||||||
| chr15:68724909 | C | T | 177 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(174): Show |
177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.1312-934C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68724909 | |||||||
| chr15:68725082 | G | A | 194 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(191): Show |
194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.1312-761G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68725082 | |||||||
| chr15:68725090 | C | T | 2 | a0001c0001t0003g0082 a0001c0001t0003g0239 |
2 | HG02135.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1312-753C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68725090 | |||||||
| chr15:68725091 | G | A | 3 | a0001c0002t0002g0071 a0001c0002t0002g0224 a0001c0002t0002g0230 |
3 | NA18944.hp1 NA18971.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1312-752G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68725091 | |||||||
| chr15:68725348 | G | A | 42 | a0001c0001t0001g0042 a0001c0001t0001g0098 a0001c0001t0001g0143 others(39): Show |
42 | HG00738.hp2 HG00741.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.1312-495G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68725348 | |||||||
| chr15:68725352 | A | T | 46 | a0001c0001t0001g0042 a0001c0001t0001g0074 a0001c0001t0001g0098 others(43): Show |
46 | HG00280.hp2 HG00738.hp2 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.1312-491A>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68725352 | |||||||
| chr15:68725482 | G | A | 1 | a0001c0001t0006g0011 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1312-361G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68725482 | |||||||
| chr15:68725660 | G | A | 200 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(197): Show |
200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.1312-183G>A | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68725660 | |||||||
| chr15:68725677 | A | G | 1 | a0001c0001t0024g0120 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1312-166A>G | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68725677 | |||||||
| chr15:68725798 | C | T | 5 | a0001c0001t0001g0084 a0001c0001t0004g0106 a0001c0001t0007g0151 others(2): Show |
5 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(2): Show |
intron_variant | MODIFIER | c.1312-45C>T | CORO2B | ENSG00000103647.13 | transcript | ENST00000261861.10 | protein_coding | 11/11 | chr15 | 68725798 |