Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10241 |
| ensemblid | ENSG00000136436.15 |
| hgncid | 29912 |
| symbol | CALCOCO2 |
| name | calcium binding and coiled-coil domain 2 |
| refseq_nuc | NM_005831.5 |
| refseq_prot | NP_005822.1 |
| ensembl_nuc | ENST00000258947.8 |
| ensembl_prot | ENSP00000258947.3 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 48831035 |
| end | 48865245 |
| strand | + |
| ver | v1.2 |
| region | chr17:48831035-48865245 |
| region5000 | chr17:48826035-48870245 |
| regionname0 | CALCOCO2_chr17_48831035_48865245 |
| regionname5000 | CALCOCO2_chr17_48826035_48870245 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 446 | 103 | 30 | 29 | 34 | 4 | 6 | 26 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | MEETI others(441): Show |
chr17 | 48826035 | 48870245 |
| a0002 | 1/1 | 446 | 86 | 26 | 24 | 12 | 7 | 15 | 8 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | MEETI others(441): Show |
chr17 | 48826035 | 48870245 |
| a0003 | 0/0 | 446 | 87 | 3 | 12 | 63 | 1 | 8 | 41 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | MEETI others(441): Show |
chr17 | 48826035 | 48870245 |
| a0004 | 0/0 | 446 | 51 | 25 | 5 | 12 | 2 | 7 | 8 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | MEETI others(441): Show |
chr17 | 48826035 | 48870245 |
| a0005 | 0/0 | 436 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | MEETI others(431): Show |
chr17 | 48826035 | 48870245 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1338 | 103 | 30 | 29 | 34 | 4 | 6 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | ATGGA others(1333): Show |
chr17 | 48826035 | 48870245 | ||
| a0002c0003 | 1/1 | 1338 | 81 | 21 | 24 | 12 | 7 | 15 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | ATGGA others(1333): Show |
chr17 | 48826035 | 48870245 | ||
| a0002c0005 | 0/0 | 1338 | 3 | 3 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | ATGGA others(1333): Show |
chr17 | 48826035 | 48870245 | ||
| a0002c0006 | 0/0 | 1338 | 2 | 2 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | ATGGA others(1333): Show |
chr17 | 48826035 | 48870245 | ||
| a0003c0002 | 0/0 | 1338 | 87 | 3 | 12 | 63 | 1 | 8 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | ATGGA others(1333): Show |
chr17 | 48826035 | 48870245 | ||
| a0004c0004 | 0/0 | 1338 | 51 | 25 | 5 | 12 | 2 | 7 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | ATGGA others(1333): Show |
chr17 | 48826035 | 48870245 | ||
| a0005c0007 | 0/0 | 1308 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | ATGGA others(1303): Show |
chr17 | 48826035 | 48870245 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 3636 | 87 | 23 | 25 | 30 | 3 | 6 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | ACTCT others(3631): Show |
chr17 | 48826035 | 48870245 |
| a0001c0001t0006 | 0/0 | 3635 | 8 | 3 | 3 | 2 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | ACTCT others(3630): Show |
chr17 | 48826035 | 48870245 |
| a0001c0001t0007 | 0/0 | 3637 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | ACTCT others(3632): Show |
chr17 | 48826035 | 48870245 |
| a0001c0001t0014 | 0/0 | 3637 | 3 | 1 | 1 | 0 | 1 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | ACTCT others(3632): Show |
chr17 | 48826035 | 48870245 |
| a0001c0001t0020 | 0/0 | 3636 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | ACTCT others(3631): Show |
chr17 | 48826035 | 48870245 |
| a0001c0001t0021 | 0/0 | 3635 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | ACTCT others(3630): Show |
chr17 | 48826035 | 48870245 |
| a0001c0001t0022 | 0/0 | 3636 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | ACTCT others(3631): Show |
chr17 | 48826035 | 48870245 |
| a0001c0001t0027 | 0/0 | 3636 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | ACTCT others(3631): Show |
chr17 | 48826035 | 48870245 |
| a0002c0003t0001 | 0/1 | 3636 | 48 | 7 | 21 | 6 | 6 | 7 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | ACTCT others(3631): Show |
chr17 | 48826035 | 48870245 |
| a0002c0003t0004 | 1/0 | 3635 | 15 | 13 | 0 | 0 | 1 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | ACTCT others(3630): Show |
chr17 | 48826035 | 48870245 |
| a0002c0003t0007 | 0/0 | 3637 | 4 | 1 | 2 | 0 | 0 | 1 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | ACTCT others(3632): Show |
chr17 | 48826035 | 48870245 |
| a0002c0003t0008 | 0/0 | 3636 | 5 | 0 | 0 | 5 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | ACTCT others(3631): Show |
chr17 | 48826035 | 48870245 |
| a0002c0003t0009 | 0/0 | 3637 | 6 | 0 | 0 | 1 | 0 | 5 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | ACTCT others(3632): Show |
chr17 | 48826035 | 48870245 |
| a0002c0003t0025 | 0/0 | 3636 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | ACTCT others(3631): Show |
chr17 | 48826035 | 48870245 |
| a0002c0003t0028 | 0/0 | 3637 | 1 | 0 | 0 | 0 | 0 | 1 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | ACTCT others(3632): Show |
chr17 | 48826035 | 48870245 |
| a0002c0003t0029 | 0/0 | 3636 | 1 | 0 | 0 | 0 | 0 | 1 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | ACTCT others(3631): Show |
chr17 | 48826035 | 48870245 |
| a0002c0005t0004 | 0/0 | 3635 | 3 | 3 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | ACTCT others(3630): Show |
chr17 | 48826035 | 48870245 |
| a0002c0006t0015 | 0/0 | 3636 | 2 | 2 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | ACTCT others(3631): Show |
chr17 | 48826035 | 48870245 |
| a0003c0002t0001 | 0/0 | 3636 | 75 | 3 | 7 | 57 | 0 | 8 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | ACTCT others(3631): Show |
chr17 | 48826035 | 48870245 |
| a0003c0002t0004 | 0/0 | 3635 | 2 | 0 | 0 | 2 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | ACTCT others(3630): Show |
chr17 | 48826035 | 48870245 |
| a0003c0002t0007 | 0/0 | 3637 | 2 | 0 | 0 | 2 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | ACTCT others(3632): Show |
chr17 | 48826035 | 48870245 |
| a0003c0002t0013 | 0/0 | 3636 | 3 | 0 | 2 | 0 | 1 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | ACTCT others(3631): Show |
chr17 | 48826035 | 48870245 |
| a0003c0002t0017 | 0/0 | 3635 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | ACTCT others(3630): Show |
chr17 | 48826035 | 48870245 |
| a0003c0002t0018 | 0/0 | 3636 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | ACTCT others(3631): Show |
chr17 | 48826035 | 48870245 |
| a0003c0002t0023 | 0/0 | 3635 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | ACTCT others(3630): Show |
chr17 | 48826035 | 48870245 |
| a0003c0002t0024 | 0/0 | 3636 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | ACTCT others(3631): Show |
chr17 | 48826035 | 48870245 |
| a0003c0002t0026 | 0/0 | 3636 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | ACTCT others(3631): Show |
chr17 | 48826035 | 48870245 |
| a0004c0004t0003 | 0/0 | 3634 | 21 | 1 | 3 | 10 | 2 | 5 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | ACTCT others(3629): Show |
chr17 | 48826035 | 48870245 |
| a0004c0004t0005 | 0/0 | 3634 | 15 | 13 | 2 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | ACTCT others(3629): Show |
chr17 | 48826035 | 48870245 |
| a0004c0004t0010 | 0/0 | 3634 | 4 | 4 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | ACTCT others(3629): Show |
chr17 | 48826035 | 48870245 |
| a0004c0004t0011 | 0/0 | 3634 | 3 | 3 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | ACTCT others(3629): Show |
chr17 | 48826035 | 48870245 |
| a0004c0004t0012 | 0/0 | 3635 | 3 | 3 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | ACTCT others(3630): Show |
chr17 | 48826035 | 48870245 |
| a0004c0004t0016 | 0/0 | 3634 | 2 | 0 | 0 | 0 | 0 | 2 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | ACTCT others(3629): Show |
chr17 | 48826035 | 48870245 |
| a0004c0004t0019 | 0/0 | 3634 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | ACTCT others(3629): Show |
chr17 | 48826035 | 48870245 |
| a0004c0004t0030 | 0/0 | 3635 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | ACTCT others(3630): Show |
chr17 | 48826035 | 48870245 |
| a0004c0004t0031 | 0/0 | 3634 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | ACTCT others(3629): Show |
chr17 | 48826035 | 48870245 |
| a0005c0007t0008 | 0/0 | 3606 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | ACTCT others(3601): Show |
chr17 | 48826035 | 48870245 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0006g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0006g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0006g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0006g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0006g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0006g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0006g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0006g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0007g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0014g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0014g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0014g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0020g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0021g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0022g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0001c0001t0027g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0065 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0004g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0004g0126 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0004g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0004g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0004g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0004g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0004g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0004g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0007g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0007g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0007g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0007g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0008g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0008g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0008g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0008g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0008g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0009g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0009g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0009g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0009g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0009g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0009g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0025g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0028g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0003t0029g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0005t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0005t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0005t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0006t0015g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0002c0006t0015g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0007g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0007g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0013g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0013g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0013g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0017g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0018g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0023g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0024g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0003c0002t0026g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0003g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0005g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0005g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0005g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0005g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0005g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0005g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0005g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0005g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0005g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0005g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0005g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0005g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0005g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0005g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0005g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0010g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0010g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0010g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0010g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0011g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0011g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0011g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0012g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0012g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0012g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0016g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0019g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0030g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0004c0004t0031g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| a0005c0007t0008g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0003 | t0001 | g0038 | EUR | GBR | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG00099 | hp2 | a0002 | c0003 | t0001 | g0036 | EUR | GBR | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG00140 | hp1 | a0002 | c0003 | t0001 | g0047 | EUR | GBR | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0253 | EUR | GBR | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0309 | EUR | FIN | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG00323 | hp2 | a0002 | c0003 | t0001 | g0052 | EUR | FIN | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG00408 | hp1 | a0003 | c0002 | t0001 | g0207 | EAS | CHS | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | CHS | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG00423 | hp1 | a0003 | c0002 | t0001 | g0224 | EAS | CHS | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | CHS | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG00438 | hp1 | a0002 | c0003 | t0001 | g0019 | EAS | CHS | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG00438 | hp2 | a0003 | c0002 | t0001 | g0318 | EAS | CHS | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG00558 | hp1 | a0004 | c0004 | t0030 | g0082 | EAS | CHS | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG00558 | hp2 | a0003 | c0002 | t0001 | g0151 | EAS | CHS | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG00609 | hp1 | a0003 | c0002 | t0001 | g0222 | EAS | CHS | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG00609 | hp2 | a0003 | c0002 | t0001 | g0186 | EAS | CHS | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG00639 | hp1 | a0002 | c0003 | t0001 | g0249 | AMR | PUR | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG00639 | hp2 | a0002 | c0003 | t0001 | g0033 | AMR | PUR | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG00642 | hp1 | a0002 | c0003 | t0001 | g0063 | AMR | PUR | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0254 | AMR | PUR | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG00673 | hp1 | a0004 | c0004 | t0003 | g0118 | EAS | CHS | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG00673 | hp2 | a0003 | c0002 | t0001 | g0146 | EAS | CHS | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG00735 | hp1 | a0002 | c0003 | t0001 | g0049 | AMR | PUR | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0257 | AMR | PUR | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | PUR | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG00741 | hp1 | a0004 | c0004 | t0003 | g0079 | AMR | PUR | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG00741 | hp2 | a0002 | c0003 | t0001 | g0051 | AMR | PUR | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01069 | hp1 | a0001 | c0001 | t0006 | g0263 | AMR | PUR | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01069 | hp2 | a0004 | c0004 | t0005 | g0098 | AMR | PUR | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01070 | hp1 | a0001 | c0001 | t0006 | g0271 | AMR | PUR | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01070 | hp2 | a0003 | c0002 | t0017 | g0307 | AMR | PUR | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01071 | hp1 | a0004 | c0004 | t0005 | g0111 | AMR | PUR | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01071 | hp2 | a0003 | c0002 | t0018 | g0199 | AMR | PUR | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01074 | hp1 | a0002 | c0003 | t0001 | g0054 | AMR | PUR | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0264 | AMR | PUR | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01081 | hp1 | a0002 | c0003 | t0001 | g0043 | AMR | PUR | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01081 | hp2 | a0002 | c0003 | t0025 | g0053 | AMR | PUR | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01099 | hp1 | a0003 | c0002 | t0001 | g0154 | AMR | PUR | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01099 | hp2 | a0002 | c0003 | t0001 | g0056 | AMR | PUR | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0261 | AMR | PUR | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01106 | hp2 | a0002 | c0003 | t0001 | g0034 | AMR | PUR | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01167 | hp1 | a0002 | c0003 | t0001 | g0030 | AMR | PUR | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0245 | AMR | PUR | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0248 | AMR | PUR | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01169 | hp2 | a0003 | c0002 | t0001 | g0204 | AMR | PUR | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01175 | hp1 | a0002 | c0003 | t0001 | g0022 | AMR | PUR | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0281 | AMR | PUR | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0164 | AMR | PUR | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01192 | hp2 | a0002 | c0003 | t0001 | g0041 | AMR | PUR | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | PUR | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01243 | hp2 | a0001 | c0001 | t0014 | g0321 | AMR | PUR | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01255 | hp1 | a0003 | c0002 | t0001 | g0218 | AMR | CLM | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01255 | hp2 | a0004 | c0004 | t0003 | g0093 | AMR | CLM | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01256 | hp1 | a0001 | c0001 | t0006 | g0241 | AMR | CLM | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01256 | hp2 | a0002 | c0003 | t0001 | g0050 | AMR | CLM | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01257 | hp1 | a0002 | c0003 | t0007 | g0064 | AMR | CLM | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01257 | hp2 | a0003 | c0002 | t0001 | g0133 | AMR | CLM | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0251 | AMR | CLM | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01258 | hp2 | a0002 | c0003 | t0007 | g0062 | AMR | CLM | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | CLM | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0161 | AMR | CLM | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01346 | hp2 | a0002 | c0003 | t0001 | g0058 | AMR | CLM | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01358 | hp1 | a0002 | c0003 | t0001 | g0025 | AMR | CLM | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0155 | AMR | CLM | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0163 | AMR | CLM | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0158 | AMR | CLM | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01496 | hp2 | a0003 | c0002 | t0024 | g0149 | AMR | CLM | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01515 | hp1 | a0003 | c0002 | t0013 | g0215 | EUR | IBS | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01515 | hp2 | a0004 | c0004 | t0003 | g0077 | EUR | IBS | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01517 | hp1 | a0002 | c0003 | t0004 | g0040 | EUR | IBS | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01517 | hp2 | a0004 | c0004 | t0003 | g0078 | EUR | IBS | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01891 | hp1 | a0002 | c0003 | t0001 | g0139 | AFR | ACB | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01891 | hp2 | a0001 | c0001 | t0014 | g0276 | AFR | ACB | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01952 | hp1 | a0003 | c0002 | t0013 | g0216 | AMR | PEL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01952 | hp2 | a0003 | c0002 | t0013 | g0214 | AMR | PEL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0160 | AMR | PEL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0159 | AMR | PEL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01981 | hp1 | a0002 | c0003 | t0001 | g0039 | AMR | PEL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01981 | hp2 | a0002 | c0003 | t0001 | g0045 | AMR | PEL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0157 | AMR | PEL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG01993 | hp2 | a0003 | c0002 | t0001 | g0198 | AMR | PEL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0156 | AMR | PEL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02004 | hp2 | a0002 | c0003 | t0001 | g0037 | AMR | PEL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02015 | hp1 | a0003 | c0002 | t0001 | g0142 | EAS | KHV | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02015 | hp2 | a0003 | c0002 | t0001 | g0180 | EAS | KHV | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02040 | hp1 | a0003 | c0002 | t0001 | g0208 | EAS | KHV | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | KHV | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02055 | hp1 | a0002 | c0003 | t0004 | g0128 | AFR | ACB | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02055 | hp2 | a0002 | c0003 | t0001 | g0027 | AFR | ACB | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02056 | hp1 | a0003 | c0002 | t0001 | g0210 | EAS | KHV | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | KHV | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02071 | hp1 | a0003 | c0002 | t0001 | g0225 | EAS | KHV | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02071 | hp2 | a0002 | c0003 | t0009 | g0238 | EAS | KHV | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02074 | hp1 | a0003 | c0002 | t0001 | g0213 | EAS | KHV | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02074 | hp2 | a0002 | c0003 | t0001 | g0059 | EAS | KHV | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02080 | hp1 | a0003 | c0002 | t0001 | g0147 | EAS | KHV | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | KHV | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02129 | hp1 | a0003 | c0002 | t0001 | g0212 | EAS | KHV | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02129 | hp2 | a0001 | c0001 | t0021 | g0255 | EAS | KHV | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02132 | hp1 | a0003 | c0002 | t0001 | g0201 | EAS | KHV | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02132 | hp2 | a0004 | c0004 | t0003 | g0088 | EAS | KHV | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02135 | hp1 | a0003 | c0002 | t0001 | g0184 | EAS | KHV | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | KHV | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02145 | hp1 | a0001 | c0001 | t0027 | g0278 | AFR | ACB | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02145 | hp2 | a0004 | c0004 | t0012 | g0075 | AFR | ACB | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02148 | hp1 | a0002 | c0003 | t0001 | g0042 | AMR | PEL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0301 | AMR | PEL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02155 | hp1 | a0003 | c0002 | t0001 | g0189 | EAS | CDX | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02155 | hp2 | a0003 | c0002 | t0001 | g0211 | EAS | CDX | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02165 | hp1 | a0001 | c0001 | t0022 | g0252 | EAS | CDX | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02165 | hp2 | a0003 | c0002 | t0007 | g0196 | EAS | CDX | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0265 | AFR | ACB | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02257 | hp2 | a0003 | c0002 | t0001 | g0202 | AFR | ACB | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02273 | hp1 | a0003 | c0002 | t0001 | g0132 | AMR | PEL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02273 | hp2 | a0002 | c0003 | t0001 | g0028 | AMR | PEL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02280 | hp1 | a0004 | c0004 | t0005 | g0113 | AFR | ACB | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02280 | hp2 | a0002 | c0003 | t0004 | g0325 | AFR | ACB | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0270 | AMR | PEL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02293 | hp2 | a0004 | c0004 | t0003 | g0089 | AMR | PEL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02300 | hp1 | a0003 | c0002 | t0001 | g0192 | AMR | PEL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02300 | hp2 | a0002 | c0003 | t0001 | g0057 | AMR | PEL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0236 | AFR | ACB | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0243 | AFR | ACB | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02523 | hp1 | a0003 | c0002 | t0001 | g0188 | EAS | KHV | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02523 | hp2 | a0002 | c0003 | t0001 | g0029 | EAS | KHV | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02572 | hp1 | a0002 | c0005 | t0004 | g0124 | AFR | GWD | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0311 | AFR | GWD | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02615 | hp1 | a0001 | c0001 | t0020 | g0327 | AFR | GWD | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0262 | AFR | GWD | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02622 | hp1 | a0004 | c0004 | t0005 | g0105 | AFR | GWD | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02622 | hp2 | a0002 | c0003 | t0004 | g0323 | AFR | GWD | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02630 | hp1 | a0004 | c0004 | t0011 | g0102 | AFR | GWD | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02630 | hp2 | a0002 | c0003 | t0004 | g0324 | AFR | GWD | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02647 | hp1 | a0004 | c0004 | t0005 | g0103 | AFR | GWD | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0299 | AFR | GWD | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02698 | hp1 | a0002 | c0003 | t0001 | g0060 | SAS | PJL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02698 | hp2 | a0002 | c0003 | t0001 | g0026 | SAS | PJL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02738 | hp1 | a0002 | c0003 | t0007 | g0023 | SAS | PJL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02738 | hp2 | a0002 | c0003 | t0009 | g0240 | SAS | PJL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02809 | hp1 | a0004 | c0004 | t0005 | g0114 | AFR | GWD | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02809 | hp2 | a0002 | c0003 | t0001 | g0315 | AFR | GWD | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02818 | hp1 | a0002 | c0003 | t0004 | g0136 | AFR | GWD | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02818 | hp2 | a0001 | c0001 | t0007 | g0228 | AFR | GWD | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0317 | AFR | GWD | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02886 | hp2 | a0003 | c0002 | t0001 | g0220 | AFR | GWD | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02896 | hp1 | a0002 | c0003 | t0004 | g0326 | AFR | GWD | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02896 | hp2 | a0001 | c0001 | t0006 | g0004 | AFR | GWD | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02897 | hp2 | a0004 | c0004 | t0012 | g0097 | AFR | GWD | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0297 | AFR | ESN | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02922 | hp2 | a0002 | c0003 | t0004 | g0127 | AFR | ESN | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02965 | hp1 | a0004 | c0004 | t0010 | g0087 | AFR | ESN | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02965 | hp2 | a0002 | c0003 | t0004 | g0129 | AFR | ESN | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02976 | hp1 | a0004 | c0004 | t0005 | g0109 | AFR | ESN | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0246 | AFR | ESN | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03017 | hp1 | a0004 | c0004 | t0016 | g0001 | SAS | PJL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03017 | hp2 | a0002 | c0003 | t0009 | g0312 | SAS | PJL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0260 | AFR | GWD | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03041 | hp2 | a0004 | c0004 | t0011 | g0073 | AFR | GWD | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03098 | hp1 | a0004 | c0004 | t0011 | g0108 | AFR | MSL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0298 | AFR | MSL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03130 | hp1 | a0002 | c0005 | t0004 | g0125 | AFR | ESN | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0247 | AFR | ESN | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03139 | hp1 | a0002 | c0003 | t0007 | g0141 | AFR | ESN | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03139 | hp2 | a0002 | c0006 | t0015 | g0011 | AFR | ESN | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03195 | hp1 | a0001 | c0001 | t0006 | g0302 | AFR | ESN | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0310 | AFR | ESN | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0319 | AFR | MSL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03209 | hp2 | a0004 | c0004 | t0010 | g0080 | AFR | MSL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03225 | hp1 | a0004 | c0004 | t0005 | g0104 | AFR | MSL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03225 | hp2 | a0002 | c0005 | t0004 | g0123 | AFR | MSL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03239 | hp1 | a0003 | c0002 | t0001 | g0217 | SAS | PJL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0289 | SAS | PJL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03486 | hp1 | a0002 | c0003 | t0001 | g0131 | AFR | MSL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0320 | AFR | MSL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03492 | hp1 | a0002 | c0003 | t0029 | g0031 | SAS | PJL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03492 | hp2 | a0003 | c0002 | t0001 | g0233 | SAS | PJL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03516 | hp1 | a0004 | c0004 | t0005 | g0112 | AFR | ESN | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0150 | AFR | ESN | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03540 | hp1 | a0004 | c0004 | t0005 | g0101 | AFR | GWD | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03540 | hp2 | a0004 | c0004 | t0005 | g0110 | AFR | GWD | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0242 | AFR | MSL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03579 | hp2 | a0004 | c0004 | t0005 | g0106 | AFR | MSL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03654 | hp1 | a0004 | c0004 | t0003 | g0094 | SAS | PJL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03654 | hp2 | a0003 | c0002 | t0001 | g0187 | SAS | PJL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03669 | hp1 | a0002 | c0003 | t0028 | g0316 | SAS | PJL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0303 | SAS | PJL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03688 | hp1 | a0003 | c0002 | t0001 | g0145 | SAS | STU | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03688 | hp2 | a0002 | c0003 | t0001 | g0061 | SAS | STU | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03704 | hp1 | a0004 | c0004 | t0016 | g0001 | SAS | PJL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03704 | hp2 | a0002 | c0003 | t0009 | g0239 | SAS | PJL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03710 | hp1 | a0003 | c0002 | t0001 | g0194 | SAS | PJL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03710 | hp2 | a0002 | c0003 | t0001 | g0035 | SAS | PJL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03834 | hp1 | a0002 | c0003 | t0009 | g0313 | SAS | BEB | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0266 | SAS | BEB | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03927 | hp1 | a0004 | c0004 | t0003 | g0083 | SAS | BEB | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03927 | hp2 | a0002 | c0003 | t0001 | g0024 | SAS | BEB | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03942 | hp1 | a0004 | c0004 | t0003 | g0081 | SAS | BEB | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03942 | hp2 | a0002 | c0003 | t0001 | g0021 | SAS | BEB | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0258 | SAS | STU | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG04115 | hp2 | a0002 | c0003 | t0009 | g0148 | SAS | STU | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG04184 | hp1 | a0003 | c0002 | t0001 | g0227 | SAS | BEB | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0162 | SAS | BEB | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0268 | SAS | STU | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG04204 | hp2 | a0004 | c0004 | t0003 | g0092 | SAS | STU | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG04228 | hp1 | a0004 | c0004 | t0003 | g0086 | SAS | STU | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG04228 | hp2 | a0003 | c0002 | t0001 | g0203 | SAS | STU | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0259 | AFR | YRI | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18522 | hp2 | a0002 | c0003 | t0004 | g0130 | AFR | YRI | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18612 | hp1 | a0004 | c0004 | t0003 | g0072 | EAS | CHB | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18612 | hp2 | a0003 | c0002 | t0001 | g0234 | EAS | CHB | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18906 | hp1 | a0002 | c0003 | t0001 | g0140 | AFR | YRI | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18906 | hp2 | a0002 | c0006 | t0015 | g0012 | AFR | YRI | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18939 | hp1 | a0003 | c0002 | t0001 | g0308 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18940 | hp2 | a0003 | c0002 | t0001 | g0226 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18941 | hp1 | a0003 | c0002 | t0001 | g0153 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18942 | hp1 | a0003 | c0002 | t0001 | g0175 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18942 | hp2 | a0003 | c0002 | t0001 | g0229 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18944 | hp2 | a0003 | c0002 | t0001 | g0177 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18945 | hp1 | a0003 | c0002 | t0001 | g0069 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18945 | hp2 | a0002 | c0003 | t0008 | g0017 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18946 | hp1 | a0003 | c0002 | t0004 | g0173 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18946 | hp2 | a0004 | c0004 | t0031 | g0085 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18947 | hp1 | a0003 | c0002 | t0001 | g0197 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18947 | hp2 | a0005 | c0007 | t0008 | g0014 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18951 | hp1 | a0003 | c0002 | t0001 | g0200 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18951 | hp2 | a0001 | c0001 | t0006 | g0291 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18952 | hp1 | a0002 | c0003 | t0008 | g0013 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18953 | hp1 | a0003 | c0002 | t0001 | g0305 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18954 | hp1 | a0003 | c0002 | t0023 | g0134 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18954 | hp2 | a0003 | c0002 | t0001 | g0172 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18960 | hp1 | a0004 | c0004 | t0003 | g0117 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18960 | hp2 | a0003 | c0002 | t0001 | g0306 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18964 | hp1 | a0003 | c0002 | t0001 | g0209 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18964 | hp2 | a0002 | c0003 | t0008 | g0018 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18966 | hp1 | a0003 | c0002 | t0001 | g0219 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18966 | hp2 | a0004 | c0004 | t0003 | g0120 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18968 | hp1 | a0002 | c0003 | t0001 | g0044 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18968 | hp2 | a0003 | c0002 | t0001 | g0191 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18969 | hp2 | a0003 | c0002 | t0001 | g0179 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18971 | hp2 | a0001 | c0001 | t0006 | g0009 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18972 | hp2 | a0003 | c0002 | t0026 | g0181 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18975 | hp1 | a0004 | c0004 | t0003 | g0095 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18977 | hp1 | a0003 | c0002 | t0001 | g0171 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18977 | hp2 | a0004 | c0004 | t0003 | g0090 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18978 | hp2 | a0003 | c0002 | t0001 | g0071 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18980 | hp1 | a0003 | c0002 | t0001 | g0178 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18981 | hp1 | a0004 | c0004 | t0003 | g0119 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18981 | hp2 | a0003 | c0002 | t0001 | g0144 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18982 | hp1 | a0003 | c0002 | t0001 | g0235 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18982 | hp2 | a0003 | c0002 | t0004 | g0223 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18984 | hp1 | a0003 | c0002 | t0001 | g0193 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18984 | hp2 | a0004 | c0004 | t0003 | g0116 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18989 | hp1 | a0002 | c0003 | t0008 | g0016 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18990 | hp2 | a0003 | c0002 | t0001 | g0190 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18999 | hp1 | a0002 | c0003 | t0008 | g0015 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA19010 | hp1 | a0003 | c0002 | t0001 | g0195 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA19010 | hp2 | a0003 | c0002 | t0001 | g0070 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA19011 | hp2 | a0003 | c0002 | t0001 | g0168 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA19030 | hp1 | a0004 | c0004 | t0010 | g0096 | AFR | LWK | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA19030 | hp2 | a0002 | c0003 | t0004 | g0322 | AFR | LWK | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA19043 | hp1 | a0002 | c0003 | t0001 | g0138 | AFR | LWK | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA19043 | hp2 | a0004 | c0004 | t0010 | g0084 | AFR | LWK | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA19056 | hp1 | a0003 | c0002 | t0001 | g0067 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA19058 | hp2 | a0003 | c0002 | t0001 | g0221 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA19060 | hp1 | a0002 | c0003 | t0001 | g0020 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA19060 | hp2 | a0003 | c0002 | t0001 | g0185 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA19066 | hp2 | a0003 | c0002 | t0001 | g0206 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA19067 | hp2 | a0003 | c0002 | t0007 | g0183 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA19068 | hp2 | a0003 | c0002 | t0001 | g0174 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA19074 | hp1 | a0003 | c0002 | t0001 | g0068 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA19077 | hp1 | a0003 | c0002 | t0001 | g0205 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA19083 | hp1 | a0003 | c0002 | t0001 | g0232 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA19083 | hp2 | a0002 | c0003 | t0001 | g0046 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA19084 | hp2 | a0003 | c0002 | t0001 | g0176 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA19087 | hp1 | a0004 | c0004 | t0003 | g0091 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA19087 | hp2 | a0003 | c0002 | t0001 | g0143 | EAS | JPT | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0296 | AFR | YRI | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA19240 | hp2 | a0002 | c0003 | t0004 | g0135 | AFR | YRI | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA20129 | hp1 | a0004 | c0004 | t0005 | g0115 | AFR | ASW | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA20129 | hp2 | a0003 | c0002 | t0001 | g0182 | AFR | ASW | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA20752 | hp1 | a0002 | c0003 | t0001 | g0066 | EUR | TSI | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0280 | EUR | TSI | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA20805 | hp1 | a0002 | c0003 | t0001 | g0048 | EUR | TSI | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA20805 | hp2 | a0001 | c0001 | t0014 | g0284 | EUR | TSI | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA20905 | hp1 | a0002 | c0003 | t0001 | g0055 | SAS | GIH | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA20905 | hp2 | a0003 | c0002 | t0001 | g0230 | SAS | GIH | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02109 | hp1 | a0002 | c0003 | t0004 | g0137 | AFR | ACB | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02109 | hp2 | a0004 | c0004 | t0019 | g0099 | AFR | ACB | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0250 | AFR | ACB | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02486 | hp2 | a0004 | c0004 | t0005 | g0100 | AFR | ACB | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02559 | hp1 | a0004 | c0004 | t0003 | g0074 | AFR | ACB | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG02559 | hp2 | a0004 | c0004 | t0005 | g0107 | AFR | ACB | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0244 | AFR | MSL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| HG03471 | hp2 | a0002 | c0003 | t0004 | g0122 | AFR | MSL | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0273 | AFR | USA | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA20300 | hp2 | a0002 | c0003 | t0001 | g0032 | AFR | USA | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0282 | AFR | LWK | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| NA21309 | hp2 | a0004 | c0004 | t0012 | g0076 | AFR | LWK | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| homoSapiens | chm13v2 | a0002 | c0003 | t0001 | g0065 | REF | REF | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| homoSapiens | grch38p0 | a0002 | c0003 | t0004 | g0126 | REF | REF | CALCOCO2_chr17_48826035_48870245 | CALCOCO2 | chr17 | 48826035 | 48870245 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:48849253 | G | A | 1 | a0003 | 87 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(84): Show |
missense_variant&splice_region_variant | MODERATE | c.419G>A | p.Gly140Glu | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 5/13 | 473/3635 | 419/1341 | 140/446 | chr17 | 48849253 | |||
| chr17:48852546 | T | C | 1 | a0004 | 51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
missense_variant | MODERATE | c.743T>C | p.Val248Ala | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 8/13 | 797/3635 | 743/1341 | 248/446 | chr17 | 48852546 | |||
| chr17:48852574 | GTTAGAGC others(23): Show |
G | 1 | a0005 | 1 | NA18947.hp2 | conservative_inframe_deletion | MODERATE | c.772_801delTTAGAGCA others(22): Show |
p.Leu258_His267del | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 8/13 | 826/3635 | 772/1341 | 258/446 | chr17 | 48852574 | |||
| chr17:48852915 | T | TTTTTGTG others(13): Show |
1 | a0002 | 1 | NA18968.hp1 | frameshift_variant | HIGH | c.826-10_835dupTTTTG others(15): Show |
p.Gln279fs | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/13 | 890/3635 | 836/1341 | 279/446 | INFO_REALIGN_3_PRIME | chr17 | 48852915 | ||
| chr17:48862296 | C | G | 1 | a0001 | 103 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(100): Show |
missense_variant | MODERATE | c.1165C>G | p.Pro389Ala | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 12/13 | 1219/3635 | 1165/1341 | 389/446 | chr17 | 48862296 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:48849287 | G | A | 1 | a0002c0006 | 2 | HG03139.hp2 NA18906.hp2 |
synonymous_variant | LOW | c.453G>A | p.Glu151Glu | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 5/13 | 507/3635 | 453/1341 | 151/446 | chr17 | 48849287 | |||
| chr17:48862921 | T | C | 1 | a0002c0005 | 3 | HG02572.hp1 HG03130.hp1 HG03225.hp2 |
synonymous_variant | LOW | c.1257T>C | p.Cys419Cys | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 13/13 | 1311/3635 | 1257/1341 | 419/446 | chr17 | 48862921 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:48831043 | C | T | 1 | a0004c0004t0031 | 1 | NA18946.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-46C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/13 | chr17 | 48831043 | |||||||
| chr17:48863054 | A | G | 4 | a0004c0004t0003 a0004c0004t0016 a0004c0004t0030 others(1): Show |
25 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*49A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 13/13 | 49 | chr17 | 48863054 | ||||||
| chr17:48863107 | T | C | 1 | a0004c0004t0011 | 3 | HG02630.hp1 HG03041.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*102T>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 13/13 | 102 | chr17 | 48863107 | ||||||
| chr17:48863238 | C | T | 1 | a0002c0006t0015 | 2 | HG03139.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*233C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 13/13 | 233 | chr17 | 48863238 | ||||||
| chr17:48863459 | C | T | 1 | a0002c0003t0029 | 1 | HG03492.hp1 | 3_prime_UTR_variant | MODIFIER | c.*454C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 13/13 | 454 | chr17 | 48863459 | ||||||
| chr17:48863554 | T | A | 2 | a0003c0002t0017 a0003c0002t0018 |
2 | HG01070.hp2 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*549T>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 13/13 | 549 | chr17 | 48863554 | ||||||
| chr17:48863633 | C | T | 1 | a0002c0006t0015 | 2 | HG03139.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*628C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 13/13 | 628 | chr17 | 48863633 | ||||||
| chr17:48863883 | G | A | 9 | a0004c0004t0003 a0004c0004t0005 a0004c0004t0010 others(6): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*878G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 13/13 | 878 | chr17 | 48863883 | ||||||
| chr17:48863969 | T | C | 1 | a0001c0001t0020 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*964T>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 13/13 | 964 | chr17 | 48863969 | ||||||
| chr17:48864009 | G | A | 2 | a0001c0001t0021 a0001c0001t0022 |
2 | HG02129.hp2 HG02165.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1004G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 13/13 | 1004 | chr17 | 48864009 | ||||||
| chr17:48864057 | G | T | 17 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0014 others(14): Show |
154 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(151): Show |
3_prime_UTR_variant | MODIFIER | c.*1052G>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 13/13 | 1052 | chr17 | 48864057 | ||||||
| chr17:48864058 | C | A | 1 | a0003c0002t0023 | 1 | NA18954.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1053C>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 13/13 | 1053 | chr17 | 48864058 | ||||||
| chr17:48864066 | C | CT | 15 | a0001c0001t0002 a0001c0001t0020 a0001c0001t0022 others(12): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
3_prime_UTR_variant | MODIFIER | c.*1080dupT | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 13/13 | 1081 | INFO_REALIGN_3_PRIME | chr17 | 48864066 | |||||
| chr17:48864066 | C | CTT | 6 | a0001c0001t0007 a0001c0001t0014 a0002c0003t0007 others(3): Show |
17 | HG01243.hp2 HG01257.hp1 HG01258.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1079_*1080dupTT | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 13/13 | 1081 | INFO_REALIGN_3_PRIME | chr17 | 48864066 | |||||
| chr17:48864066 | CT | C | 7 | a0004c0004t0003 a0004c0004t0005 a0004c0004t0010 others(4): Show |
47 | HG00673.hp1 HG00741.hp1 HG01069.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*1080delT | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 13/13 | 1080 | INFO_REALIGN_3_PRIME | chr17 | 48864066 | |||||
| chr17:48864127 | G | A | 1 | a0001c0001t0027 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1122G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 13/13 | 1122 | chr17 | 48864127 | ||||||
| chr17:48864185 | T | C | 3 | a0002c0003t0009 a0002c0003t0028 a0002c0006t0015 |
9 | HG02071.hp2 HG02738.hp2 HG03017.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1180T>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 13/13 | 1180 | chr17 | 48864185 | ||||||
| chr17:48864211 | G | A | 1 | a0003c0002t0024 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1206G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 13/13 | 1206 | chr17 | 48864211 | ||||||
| chr17:48864216 | G | A | 11 | a0002c0003t0008 a0004c0004t0003 a0004c0004t0005 others(8): Show |
57 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*1211G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 13/13 | 1211 | chr17 | 48864216 | ||||||
| chr17:48864300 | G | A | 1 | a0004c0004t0019 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1295G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 13/13 | 1295 | chr17 | 48864300 | ||||||
| chr17:48864320 | G | C | 9 | a0004c0004t0003 a0004c0004t0005 a0004c0004t0010 others(6): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*1315G>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 13/13 | 1315 | chr17 | 48864320 | ||||||
| chr17:48864455 | C | T | 9 | a0004c0004t0003 a0004c0004t0005 a0004c0004t0010 others(6): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*1450C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 13/13 | 1450 | chr17 | 48864455 | ||||||
| chr17:48864534 | G | A | 1 | a0002c0003t0025 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1529G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 13/13 | 1529 | chr17 | 48864534 | ||||||
| chr17:48864541 | C | T | 1 | a0003c0002t0013 | 3 | HG01515.hp1 HG01952.hp1 HG01952.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1536C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 13/13 | 1536 | chr17 | 48864541 | ||||||
| chr17:48864734 | C | T | 1 | a0004c0004t0016 | 2 | HG03017.hp1 HG03704.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1729C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 13/13 | 1729 | chr17 | 48864734 | ||||||
| chr17:48864874 | C | T | 3 | a0004c0004t0005 a0004c0004t0011 a0004c0004t0012 |
21 | HG01069.hp2 HG01071.hp1 HG02145.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1869C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 13/13 | 1869 | chr17 | 48864874 | ||||||
| chr17:48865049 | C | T | 1 | a0003c0002t0026 | 1 | NA18972.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2044C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 13/13 | 2044 | chr17 | 48865049 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:48831268 | G | A | 1 | a0001c0001t0002g0002 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-11+190G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48831268 | |||||||
| chr17:48831289 | G | A | 2 | a0001c0001t0002g0003 a0001c0001t0006g0004 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-11+211G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48831289 | |||||||
| chr17:48831319 | G | C | 3 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 |
3 | NA18980.hp2 NA19058.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.-11+241G>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48831319 | |||||||
| chr17:48831378 | G | A | 3 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0006g0009 |
3 | HG01261.hp2 HG01433.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.-11+300G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48831378 | |||||||
| chr17:48831494 | T | G | 2 | a0002c0006t0015g0011 a0002c0006t0015g0012 |
2 | HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-11+416T>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48831494 | |||||||
| chr17:48831626 | A | T | 1 | a0001c0001t0020g0327 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-11+548A>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48831626 | |||||||
| chr17:48831642 | C | T | 5 | a0002c0003t0004g0322 a0002c0003t0004g0323 a0002c0003t0004g0324 others(2): Show |
5 | HG02280.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+564C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48831642 | |||||||
| chr17:48831931 | A | G | 3 | a0001c0001t0002g0319 a0001c0001t0002g0320 a0001c0001t0014g0321 |
3 | HG01243.hp2 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-11+853A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48831931 | |||||||
| chr17:48832015 | G | T | 1 | a0003c0002t0001g0318 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-11+937G>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48832015 | |||||||
| chr17:48832028 | C | G | 1 | a0001c0001t0002g0317 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-11+950C>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48832028 | |||||||
| chr17:48832121 | G | A | 53 | a0002c0003t0001g0019 a0002c0003t0001g0020 a0002c0003t0001g0021 others(50): Show |
53 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(50): Show |
intron_variant | MODIFIER | c.-11+1043G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48832121 | |||||||
| chr17:48832228 | T | C | 6 | a0002c0003t0008g0013 a0002c0003t0008g0015 a0002c0003t0008g0016 others(3): Show |
6 | NA18945.hp2 NA18947.hp2 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11+1150T>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48832228 | |||||||
| chr17:48832327 | G | A | 5 | a0003c0002t0001g0067 a0003c0002t0001g0068 a0003c0002t0001g0069 others(2): Show |
5 | NA18945.hp1 NA18978.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+1249G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48832327 | |||||||
| chr17:48832372 | C | T | 1 | a0002c0003t0028g0316 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-11+1294C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48832372 | |||||||
| chr17:48832389 | G | A | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.-11+1311G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48832389 | |||||||
| chr17:48832705 | T | C | 1 | a0001c0001t0002g0121 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-11+1627T>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48832705 | |||||||
| chr17:48833196 | A | G | 317 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(314): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.-11+2118A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48833196 | |||||||
| chr17:48833385 | T | C | 1 | a0002c0003t0001g0131 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-11+2307T>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48833385 | |||||||
| chr17:48833546 | CA | C | 67 | a0002c0003t0001g0019 a0002c0003t0001g0020 a0002c0003t0001g0021 others(64): Show |
67 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(64): Show |
intron_variant | MODIFIER | c.-11+2484delA | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 48833546 | ||||||
| chr17:48833546 | CAA | C | 246 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(243): Show |
247 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.-11+2483_-11+2484d others(4): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 48833546 | ||||||
| chr17:48833567 | GA | G | 6 | a0002c0003t0001g0131 a0002c0003t0001g0138 a0002c0003t0001g0139 others(3): Show |
6 | HG01891.hp1 HG02809.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11+2496delA | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 48833567 | ||||||
| chr17:48833667 | T | A | 1 | a0003c0002t0001g0067 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-11+2589T>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48833667 | |||||||
| chr17:48833869 | A | G | 6 | a0002c0003t0004g0137 a0002c0003t0004g0322 a0002c0003t0004g0323 others(3): Show |
6 | HG02109.hp1 HG02280.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11+2791A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48833869 | |||||||
| chr17:48833991 | A | T | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.-11+2913A>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48833991 | |||||||
| chr17:48834066 | A | G | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.-11+2988A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48834066 | |||||||
| chr17:48834106 | C | CA | 14 | a0002c0003t0001g0131 a0002c0003t0001g0138 a0002c0003t0001g0139 others(11): Show |
14 | HG00673.hp2 HG01891.hp1 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.-11+3053dupA | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 48834106 | ||||||
| chr17:48834106 | CA | C | 140 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0006 others(137): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.-11+3053delA | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 48834106 | ||||||
| chr17:48834106 | CAAAAA | C | 42 | a0004c0004t0003g0077 a0004c0004t0003g0078 a0004c0004t0003g0079 others(39): Show |
43 | HG00558.hp1 HG00741.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.-11+3049_-11+3053d others(7): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 48834106 | ||||||
| chr17:48834106 | CAAAAAA | C | 6 | a0004c0004t0003g0072 a0004c0004t0003g0116 a0004c0004t0003g0117 others(3): Show |
6 | HG00673.hp1 NA18612.hp1 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11+3048_-11+3053d others(8): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 48834106 | ||||||
| chr17:48834159 | G | T | 1 | a0003c0002t0001g0067 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-11+3081G>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48834159 | |||||||
| chr17:48834253 | A | T | 1 | a0004c0004t0005g0115 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-11+3175A>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48834253 | |||||||
| chr17:48834255 | GT | G | 4 | a0002c0003t0001g0138 a0002c0003t0001g0139 a0002c0003t0001g0140 others(1): Show |
4 | HG01891.hp1 HG02809.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11+3178delT | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48834255 | |||||||
| chr17:48834351 | T | G | 1 | a0002c0003t0001g0026 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-11+3273T>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48834351 | |||||||
| chr17:48834392 | C | A | 2 | a0002c0003t0004g0135 a0002c0003t0004g0136 |
2 | HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-11+3314C>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48834392 | |||||||
| chr17:48834567 | G | T | 1 | a0003c0002t0001g0235 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-11+3489G>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48834567 | |||||||
| chr17:48834698 | C | T | 6 | a0002c0003t0001g0131 a0002c0003t0001g0138 a0002c0003t0001g0139 others(3): Show |
6 | HG01891.hp1 HG02809.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11+3620C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48834698 | |||||||
| chr17:48834712 | G | C | 1 | a0002c0003t0001g0027 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-11+3634G>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48834712 | |||||||
| chr17:48834875 | C | T | 1 | a0001c0001t0002g0314 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-11+3797C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48834875 | |||||||
| chr17:48835033 | G | A | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.-11+3955G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48835033 | |||||||
| chr17:48835041 | G | GC | 199 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(196): Show |
199 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.-11+3970dupC | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 48835041 | ||||||
| chr17:48835049 | G | A | 1 | a0001c0001t0002g0236 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-11+3971G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48835049 | |||||||
| chr17:48835049 | G | C | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.-11+3971G>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48835049 | |||||||
| chr17:48835050 | C | G | 49 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(46): Show |
50 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(47): Show |
intron_variant | MODIFIER | c.-11+3972C>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48835050 | |||||||
| chr17:48835051 | A | C | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.-11+3973A>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48835051 | |||||||
| chr17:48835074 | A | G | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.-11+3996A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48835074 | |||||||
| chr17:48835189 | G | A | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.-11+4111G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48835189 | |||||||
| chr17:48835211 | G | T | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.-11+4133G>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48835211 | |||||||
| chr17:48835372 | C | T | 1 | a0002c0003t0009g0313 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-11+4294C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48835372 | |||||||
| chr17:48835505 | T | C | 6 | a0002c0003t0001g0131 a0002c0003t0001g0138 a0002c0003t0001g0139 others(3): Show |
6 | HG01891.hp1 HG02809.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11+4427T>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48835505 | |||||||
| chr17:48835605 | C | G | 1 | a0002c0003t0009g0312 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-11+4527C>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48835605 | |||||||
| chr17:48835657 | G | A | 1 | a0003c0002t0001g0142 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-11+4579G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48835657 | |||||||
| chr17:48835659 | T | C | 1 | a0001c0001t0002g0237 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-11+4581T>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48835659 | |||||||
| chr17:48835720 | TTTTTCTT others(3): Show |
T | 310 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(307): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.-11+4672_-11+4681d others(12): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 48835720 | ||||||
| chr17:48835720 | TTTTTCTT others(8): Show |
T | 1 | a0001c0001t0014g0321 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-11+4667_-11+4681d others(17): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 48835720 | ||||||
| chr17:48835720 | TTTTTCTT others(13): Show |
T | 6 | a0002c0003t0001g0131 a0002c0003t0001g0138 a0002c0003t0001g0139 others(3): Show |
6 | HG01891.hp1 HG02809.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11+4662_-11+4681d others(22): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 48835720 | ||||||
| chr17:48835749 | T | C | 1 | a0002c0003t0001g0028 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-11+4671T>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48835749 | |||||||
| chr17:48835755 | C | T | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.-11+4677C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48835755 | |||||||
| chr17:48835911 | G | A | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.-11+4833G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48835911 | |||||||
| chr17:48836225 | GT | G | 6 | a0002c0003t0001g0131 a0002c0003t0001g0138 a0002c0003t0001g0139 others(3): Show |
6 | HG01891.hp1 HG02809.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11+5149delT | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 48836225 | ||||||
| chr17:48836284 | A | G | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.-11+5206A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48836284 | |||||||
| chr17:48836501 | T | G | 2 | a0004c0004t0003g0077 a0004c0004t0003g0078 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-10-5197T>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48836501 | |||||||
| chr17:48836601 | T | C | 9 | a0002c0003t0009g0148 a0002c0003t0009g0238 a0002c0003t0009g0239 others(6): Show |
9 | HG02071.hp2 HG02738.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.-10-5097T>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48836601 | |||||||
| chr17:48836731 | G | A | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.-10-4967G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48836731 | |||||||
| chr17:48836758 | C | CT | 8 | a0001c0001t0002g0231 a0001c0001t0002g0237 a0002c0003t0001g0024 others(5): Show |
8 | HG01358.hp1 HG02738.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-10-4920dupT | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 48836758 | ||||||
| chr17:48836758 | CT | C | 14 | a0001c0001t0002g0121 a0001c0001t0002g0150 a0001c0001t0002g0236 others(11): Show |
14 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-10-4920delT | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 48836758 | ||||||
| chr17:48837371 | A | G | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.-10-4327A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48837371 | |||||||
| chr17:48837383 | G | A | 27 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(24): Show |
28 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.-10-4315G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48837383 | |||||||
| chr17:48837393 | C | T | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.-10-4305C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48837393 | |||||||
| chr17:48837480 | A | T | 61 | a0002c0003t0001g0019 a0002c0003t0001g0020 a0002c0003t0001g0021 others(58): Show |
61 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(58): Show |
intron_variant | MODIFIER | c.-10-4218A>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48837480 | |||||||
| chr17:48837632 | C | T | 9 | a0002c0003t0009g0148 a0002c0003t0009g0238 a0002c0003t0009g0239 others(6): Show |
9 | HG02071.hp2 HG02738.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.-10-4066C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48837632 | |||||||
| chr17:48837940 | T | C | 53 | a0002c0003t0001g0019 a0002c0003t0001g0020 a0002c0003t0001g0021 others(50): Show |
53 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(50): Show |
intron_variant | MODIFIER | c.-10-3758T>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48837940 | |||||||
| chr17:48837975 | G | A | 1 | a0004c0004t0010g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-10-3723G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48837975 | |||||||
| chr17:48838046 | G | T | 1 | a0003c0002t0001g0071 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-10-3652G>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838046 | |||||||
| chr17:48838149 | T | C | 250 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(247): Show |
251 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.-10-3549T>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838149 | |||||||
| chr17:48838373 | C | T | 1 | a0002c0003t0001g0066 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-10-3325C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838373 | |||||||
| chr17:48838571 | G | A | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.-10-3127G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838571 | |||||||
| chr17:48838720 | T | A | 7 | a0002c0003t0004g0137 a0002c0003t0004g0322 a0002c0003t0004g0323 others(4): Show |
7 | HG00558.hp2 HG02109.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10-2978T>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838720 | |||||||
| chr17:48838838 | A | AAAAATCC others(9): Show |
1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2860_-10-2859i others(18): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838838 | |||||||
| chr17:48838842 | T | A | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2856T>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838842 | |||||||
| chr17:48838843 | C | A | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2855C>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838843 | |||||||
| chr17:48838845 | G | T | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2853G>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838845 | |||||||
| chr17:48838846 | T | G | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2852T>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838846 | |||||||
| chr17:48838847 | G | A | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2851G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838847 | |||||||
| chr17:48838848 | T | G | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2850T>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838848 | |||||||
| chr17:48838861 | T | A | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2837T>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838861 | |||||||
| chr17:48838862 | T | A | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2836T>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838862 | |||||||
| chr17:48838864 | T | A | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2834T>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838864 | |||||||
| chr17:48838873 | C | T | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2825C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838873 | |||||||
| chr17:48838874 | C | G | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2824C>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838874 | |||||||
| chr17:48838877 | G | C | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2821G>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838877 | |||||||
| chr17:48838878 | T | A | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2820T>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838878 | |||||||
| chr17:48838879 | A | C | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2819A>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838879 | |||||||
| chr17:48838881 | A | G | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2817A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838881 | |||||||
| chr17:48838883 | C | A | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2815C>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838883 | |||||||
| chr17:48838884 | C | G | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2814C>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838884 | |||||||
| chr17:48838885 | C | A | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2813C>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838885 | |||||||
| chr17:48838887 | A | G | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2811A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838887 | |||||||
| chr17:48838890 | T | G | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2808T>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838890 | |||||||
| chr17:48838891 | T | A | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2807T>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838891 | |||||||
| chr17:48838892 | G | A | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2806G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838892 | |||||||
| chr17:48838896 | A | G | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2802A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838896 | |||||||
| chr17:48838897 | T | C | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2801T>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838897 | |||||||
| chr17:48838902 | G | T | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2796G>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838902 | |||||||
| chr17:48838905 | T | A | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2793T>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838905 | |||||||
| chr17:48838908 | C | T | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2790C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838908 | |||||||
| chr17:48838909 | T | G | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2789T>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838909 | |||||||
| chr17:48838910 | A | C | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2788A>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838910 | |||||||
| chr17:48838918 | G | T | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2780G>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838918 | |||||||
| chr17:48838921 | C | T | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2777C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838921 | |||||||
| chr17:48838923 | G | T | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2775G>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838923 | |||||||
| chr17:48838924 | C | A | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2774C>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838924 | |||||||
| chr17:48838927 | G | A | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2771G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838927 | |||||||
| chr17:48838929 | C | A | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2769C>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838929 | |||||||
| chr17:48838930 | A | T | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2768A>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838930 | |||||||
| chr17:48838931 | T | C | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2767T>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838931 | |||||||
| chr17:48838935 | G | C | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2763G>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838935 | |||||||
| chr17:48838944 | G | T | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2754G>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838944 | |||||||
| chr17:48838949 | T | C | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2749T>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838949 | |||||||
| chr17:48838950 | G | T | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2748G>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838950 | |||||||
| chr17:48838954 | T | G | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2744T>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838954 | |||||||
| chr17:48838957 | T | A | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2741T>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838957 | |||||||
| chr17:48838963 | G | T | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2735G>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838963 | |||||||
| chr17:48838966 | A | T | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2732A>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838966 | |||||||
| chr17:48838982 | C | A | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2716C>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838982 | |||||||
| chr17:48838983 | A | C | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2715A>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838983 | |||||||
| chr17:48838987 | A | T | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2711A>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838987 | |||||||
| chr17:48838988 | T | A | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2710T>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838988 | |||||||
| chr17:48838989 | T | C | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2709T>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838989 | |||||||
| chr17:48838991 | A | G | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2707A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838991 | |||||||
| chr17:48838992 | A | G | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2706A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838992 | |||||||
| chr17:48838993 | A | C | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2705A>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838993 | |||||||
| chr17:48838994 | T | A | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2704T>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48838994 | |||||||
| chr17:48839004 | T | A | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2694T>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48839004 | |||||||
| chr17:48839005 | C | CTT | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.-10-2682_-10-2681d others(4): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 48839005 | ||||||
| chr17:48839005 | C | T | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2693C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48839005 | |||||||
| chr17:48839018 | G | A | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2680G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48839018 | |||||||
| chr17:48839023 | G | A | 1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-2675G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48839023 | |||||||
| chr17:48839100 | C | T | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.-10-2598C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48839100 | |||||||
| chr17:48839169 | G | A | 1 | a0004c0004t0012g0097 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-10-2529G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48839169 | |||||||
| chr17:48839353 | C | CT | 46 | a0001c0001t0002g0309 a0001c0001t0002g0311 a0001c0001t0006g0310 others(43): Show |
46 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.-10-2328dupT | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 48839353 | ||||||
| chr17:48839353 | C | CTT | 8 | a0004c0004t0003g0077 a0004c0004t0003g0078 a0004c0004t0003g0092 others(5): Show |
9 | HG01255.hp2 HG01515.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.-10-2329_-10-2328d others(4): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 48839353 | ||||||
| chr17:48839353 | CT | C | 89 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(86): Show |
89 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.-10-2328delT | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 48839353 | ||||||
| chr17:48839353 | CTTTTTT | C | 61 | a0002c0003t0001g0019 a0002c0003t0001g0020 a0002c0003t0001g0021 others(58): Show |
61 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(58): Show |
intron_variant | MODIFIER | c.-10-2333_-10-2328d others(8): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 48839353 | ||||||
| chr17:48839644 | C | T | 53 | a0002c0003t0001g0019 a0002c0003t0001g0020 a0002c0003t0001g0021 others(50): Show |
53 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(50): Show |
intron_variant | MODIFIER | c.-10-2054C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48839644 | |||||||
| chr17:48839645 | G | A | 1 | a0001c0001t0002g0152 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-10-2053G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48839645 | |||||||
| chr17:48839654 | TCTTTG | T | 3 | a0002c0003t0004g0127 a0002c0003t0004g0128 a0002c0003t0004g0129 |
3 | HG02055.hp1 HG02922.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-10-2029_-10-2025d others(7): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 48839654 | ||||||
| chr17:48839670 | C | CT | 41 | a0001c0001t0002g0002 a0001c0001t0002g0169 a0001c0001t0002g0170 others(38): Show |
41 | HG00423.hp1 HG00673.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.-10-2004dupT | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 48839670 | ||||||
| chr17:48839670 | C | CTT | 6 | a0002c0003t0001g0029 a0002c0003t0004g0326 a0002c0003t0009g0148 others(3): Show |
6 | HG01069.hp2 HG02523.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-2005_-10-2004d others(4): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 48839670 | ||||||
| chr17:48839670 | C | CTTT | 78 | a0002c0003t0001g0019 a0002c0003t0001g0020 a0002c0003t0001g0021 others(75): Show |
79 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(76): Show |
intron_variant | MODIFIER | c.-10-2006_-10-2004d others(5): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 48839670 | ||||||
| chr17:48839670 | C | CTTTT | 19 | a0002c0003t0001g0022 a0002c0003t0001g0025 a0002c0003t0001g0057 others(16): Show |
19 | HG00642.hp1 HG01071.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.-10-2007_-10-2004d others(6): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 48839670 | ||||||
| chr17:48839670 | C | T | 1 | a0004c0004t0005g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-10-2028C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48839670 | |||||||
| chr17:48839670 | CTTTTTTT others(6): Show |
C | 1 | a0003c0002t0001g0171 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-10-2016_-10-2004d others(15): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 48839670 | ||||||
| chr17:48839832 | C | T | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.-10-1866C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48839832 | |||||||
| chr17:48839894 | C | T | 3 | a0003c0002t0001g0171 a0003c0002t0001g0229 a0003c0002t0004g0223 |
3 | NA18942.hp2 NA18977.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.-10-1804C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48839894 | |||||||
| chr17:48839905 | C | A | 53 | a0002c0003t0001g0019 a0002c0003t0001g0020 a0002c0003t0001g0021 others(50): Show |
53 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(50): Show |
intron_variant | MODIFIER | c.-10-1793C>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48839905 | |||||||
| chr17:48840325 | T | C | 2 | a0001c0001t0002g0309 a0001c0001t0002g0311 |
2 | HG00323.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-10-1373T>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48840325 | |||||||
| chr17:48840422 | T | C | 317 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(314): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.-10-1276T>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48840422 | |||||||
| chr17:48840488 | A | G | 1 | a0004c0004t0003g0088 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-10-1210A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48840488 | |||||||
| chr17:48840591 | C | G | 112 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(109): Show |
112 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.-10-1107C>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48840591 | |||||||
| chr17:48840611 | C | T | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.-10-1087C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48840611 | |||||||
| chr17:48840655 | A | G | 21 | a0004c0004t0005g0098 a0004c0004t0005g0100 a0004c0004t0005g0101 others(18): Show |
21 | HG01069.hp2 HG01071.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.-10-1043A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48840655 | |||||||
| chr17:48840842 | A | G | 200 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(197): Show |
200 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.-10-856A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48840842 | |||||||
| chr17:48841006 | C | G | 1 | a0003c0002t0001g0222 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-10-692C>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48841006 | |||||||
| chr17:48841139 | A | T | 16 | a0004c0004t0005g0101 a0004c0004t0005g0103 a0004c0004t0005g0104 others(13): Show |
16 | HG02145.hp2 HG02280.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.-10-559A>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48841139 | |||||||
| chr17:48841278 | T | G | 1 | a0001c0001t0002g0250 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-10-420T>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48841278 | |||||||
| chr17:48841359 | A | G | 1 | a0001c0001t0006g0310 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-10-339A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48841359 | |||||||
| chr17:48841412 | A | G | 88 | a0002c0003t0001g0249 a0003c0002t0001g0067 a0003c0002t0001g0068 others(85): Show |
88 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.-10-286A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48841412 | |||||||
| chr17:48841500 | A | C | 1 | a0003c0002t0001g0308 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-10-198A>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48841500 | |||||||
| chr17:48841523 | T | C | 2 | a0001c0001t0002g0251 a0001c0001t0006g0241 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-10-175T>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48841523 | |||||||
| chr17:48841616 | G | A | 5 | a0004c0004t0005g0098 a0004c0004t0005g0100 a0004c0004t0005g0110 others(2): Show |
5 | HG01069.hp2 HG01071.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-82G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 1/12 | chr17 | 48841616 | |||||||
| chr17:48842154 | C | CT | 54 | a0002c0003t0001g0019 a0002c0003t0001g0020 a0002c0003t0001g0021 others(51): Show |
54 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(51): Show |
intron_variant | MODIFIER | c.180+286dupT | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 48842154 | ||||||
| chr17:48842154 | CT | C | 9 | a0002c0003t0004g0127 a0002c0003t0004g0130 a0002c0003t0004g0137 others(6): Show |
9 | HG01069.hp2 HG02109.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.180+286delT | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 48842154 | ||||||
| chr17:48842154 | CTTTTTT | C | 7 | a0002c0003t0009g0148 a0002c0003t0009g0238 a0002c0003t0009g0239 others(4): Show |
7 | HG02071.hp2 HG02738.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.180+281_180+286del others(6): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 48842154 | ||||||
| chr17:48842154 | CTTTTTTT | C | 192 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(189): Show |
192 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.180+280_180+286del others(7): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 48842154 | ||||||
| chr17:48842493 | C | G | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.180+606C>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48842493 | |||||||
| chr17:48842571 | C | T | 6 | a0002c0003t0004g0137 a0002c0003t0004g0322 a0002c0003t0004g0323 others(3): Show |
6 | HG02109.hp1 HG02280.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.180+684C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48842571 | |||||||
| chr17:48842621 | A | AAAACAAT others(3): Show |
1 | a0001c0001t0020g0327 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.180+734_180+735ins others(10): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48842621 | |||||||
| chr17:48842622 | G | GAACAATG others(3): Show |
249 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(246): Show |
250 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.180+739_180+748dup others(10): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 48842622 | ||||||
| chr17:48842622 | G | T | 1 | a0001c0001t0020g0327 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.180+735G>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48842622 | |||||||
| chr17:48842646 | C | CTT | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.180+771_180+772dup others(2): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 48842646 | ||||||
| chr17:48842730 | T | C | 5 | a0004c0004t0005g0098 a0004c0004t0005g0100 a0004c0004t0005g0110 others(2): Show |
5 | HG01069.hp2 HG01071.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.180+843T>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48842730 | |||||||
| chr17:48842755 | C | G | 1 | a0002c0003t0001g0131 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.180+868C>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48842755 | |||||||
| chr17:48842885 | C | T | 1 | a0002c0003t0001g0131 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.180+998C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48842885 | |||||||
| chr17:48842899 | AAATTAAA others(10): Show |
A | 6 | a0002c0003t0001g0131 a0002c0003t0001g0138 a0002c0003t0001g0139 others(3): Show |
6 | HG01891.hp1 HG02809.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.180+1014_180+1030d others(19): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 48842899 | ||||||
| chr17:48842969 | A | T | 1 | a0003c0002t0001g0220 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.180+1082A>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48842969 | |||||||
| chr17:48843237 | C | T | 1 | a0002c0006t0015g0012 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.180+1350C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48843237 | |||||||
| chr17:48843273 | C | T | 6 | a0002c0003t0001g0131 a0002c0003t0001g0138 a0002c0003t0001g0139 others(3): Show |
6 | HG01891.hp1 HG02809.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.180+1386C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48843273 | |||||||
| chr17:48843313 | T | C | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.180+1426T>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48843313 | |||||||
| chr17:48843373 | C | T | 1 | a0003c0002t0001g0219 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.180+1486C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48843373 | |||||||
| chr17:48843825 | A | G | 88 | a0002c0003t0001g0249 a0003c0002t0001g0067 a0003c0002t0001g0068 others(85): Show |
88 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.180+1938A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48843825 | |||||||
| chr17:48843960 | C | T | 1 | a0002c0003t0001g0056 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.180+2073C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48843960 | |||||||
| chr17:48844179 | G | A | 1 | a0003c0002t0001g0172 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.180+2292G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48844179 | |||||||
| chr17:48844183 | T | C | 1 | a0002c0003t0029g0031 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.180+2296T>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48844183 | |||||||
| chr17:48844198 | T | C | 1 | a0001c0001t0002g0242 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.180+2311T>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48844198 | |||||||
| chr17:48844371 | C | A | 1 | a0004c0004t0010g0080 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.180+2484C>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48844371 | |||||||
| chr17:48844457 | C | T | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.180+2570C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48844457 | |||||||
| chr17:48845135 | C | CA | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.181-2919dupA | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 48845135 | ||||||
| chr17:48845153 | T | A | 1 | a0002c0003t0004g0135 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.181-2911T>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48845153 | |||||||
| chr17:48845192 | G | A | 1 | a0001c0001t0022g0252 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.181-2872G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48845192 | |||||||
| chr17:48845320 | G | GGT | 113 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(110): Show |
113 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.181-2715_181-2714d others(4): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 48845320 | ||||||
| chr17:48845320 | G | GGTGT | 17 | a0001c0001t0002g0002 a0001c0001t0002g0167 a0001c0001t0002g0296 others(14): Show |
17 | HG00738.hp1 HG00738.hp2 HG02071.hp2 others(14): Show |
intron_variant | MODIFIER | c.181-2717_181-2714d others(6): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 48845320 | ||||||
| chr17:48845320 | GGT | G | 88 | a0002c0003t0001g0028 a0002c0003t0001g0033 a0002c0003t0001g0034 others(85): Show |
88 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.181-2715_181-2714d others(4): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 48845320 | ||||||
| chr17:48845320 | GGTGT | G | 4 | a0002c0003t0004g0326 a0002c0006t0015g0012 a0003c0002t0001g0153 others(1): Show |
4 | HG02896.hp1 NA18906.hp2 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.181-2717_181-2714d others(6): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 48845320 | ||||||
| chr17:48845320 | GGTGTGTG others(3): Show |
G | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.181-2723_181-2714d others(12): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 48845320 | ||||||
| chr17:48845322 | T | G | 1 | a0002c0003t0001g0032 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.181-2742T>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48845322 | |||||||
| chr17:48845370 | A | ACT | 7 | a0001c0001t0002g0003 a0001c0001t0002g0277 a0001c0001t0002g0279 others(4): Show |
7 | HG02145.hp1 HG02647.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.181-2693_181-2692d others(4): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 48845370 | ||||||
| chr17:48845371 | C | CTCTG | 5 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0158 others(2): Show |
5 | HG01175.hp2 HG01496.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.181-2692_181-2691i others(6): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 48845371 | ||||||
| chr17:48845371 | C | CTCTGTG | 3 | a0001c0001t0002g0282 a0001c0001t0002g0283 a0001c0001t0014g0284 |
3 | HG02135.hp2 NA20805.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.181-2692_181-2691i others(8): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 48845371 | ||||||
| chr17:48845371 | C | CTG | 8 | a0001c0001t0002g0309 a0002c0003t0001g0026 a0002c0003t0001g0063 others(5): Show |
8 | HG00323.hp1 HG00642.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.181-2643_181-2642d others(4): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 48845371 | ||||||
| chr17:48845371 | C | CTGTG | 6 | a0002c0003t0001g0027 a0002c0003t0004g0127 a0002c0003t0004g0128 others(3): Show |
6 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.181-2645_181-2642d others(6): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 48845371 | ||||||
| chr17:48845371 | CTG | C | 38 | a0001c0001t0002g0002 a0001c0001t0002g0010 a0001c0001t0002g0121 others(35): Show |
38 | HG00099.hp1 HG00140.hp1 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.181-2643_181-2642d others(4): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 48845371 | ||||||
| chr17:48845371 | CTGTG | C | 46 | a0001c0001t0002g0150 a0001c0001t0002g0155 a0001c0001t0002g0156 others(43): Show |
46 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.181-2645_181-2642d others(6): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 48845371 | ||||||
| chr17:48845371 | CTGTGTG | C | 15 | a0001c0001t0002g0256 a0001c0001t0002g0296 a0001c0001t0002g0297 others(12): Show |
15 | HG00438.hp1 HG00639.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.181-2647_181-2642d others(8): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 48845371 | ||||||
| chr17:48845371 | CTGTGTGT others(3): Show |
C | 4 | a0002c0003t0001g0140 a0002c0006t0015g0011 a0004c0004t0003g0119 others(1): Show |
4 | HG02965.hp1 HG03139.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.181-2651_181-2642d others(12): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 48845371 | ||||||
| chr17:48845371 | CTGTGTGT others(5): Show |
C | 27 | a0002c0003t0001g0315 a0002c0003t0004g0135 a0002c0006t0015g0012 others(24): Show |
27 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.181-2653_181-2642d others(14): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 48845371 | ||||||
| chr17:48845371 | CTGTGTGT others(7): Show |
C | 17 | a0002c0003t0001g0060 a0002c0003t0004g0136 a0002c0003t0004g0137 others(14): Show |
18 | HG01496.hp2 HG01515.hp1 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.181-2655_181-2642d others(16): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 48845371 | ||||||
| chr17:48845371 | CTGTGTGT others(9): Show |
C | 78 | a0002c0003t0001g0249 a0003c0002t0001g0067 a0003c0002t0001g0068 others(75): Show |
78 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.181-2657_181-2642d others(18): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 48845371 | ||||||
| chr17:48845371 | CTGTGTGT others(11): Show |
C | 2 | a0001c0001t0006g0009 a0003c0002t0001g0174 |
2 | NA18971.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.181-2659_181-2642d others(20): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 48845371 | ||||||
| chr17:48845371 | CTGTGTGT others(13): Show |
C | 1 | a0003c0002t0001g0235 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.181-2661_181-2642d others(22): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 48845371 | ||||||
| chr17:48845371 | CTGTGTGT others(15): Show |
C | 1 | a0001c0001t0002g0008 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.181-2663_181-2642d others(24): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 48845371 | ||||||
| chr17:48845371 | CTGTGTGT others(17): Show |
C | 22 | a0002c0003t0009g0148 a0002c0003t0009g0238 a0002c0003t0009g0239 others(19): Show |
22 | HG02071.hp2 HG02280.hp1 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.181-2665_181-2642d others(26): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 48845371 | ||||||
| chr17:48845373 | G | C | 30 | a0001c0001t0002g0007 a0001c0001t0002g0152 a0001c0001t0002g0159 others(27): Show |
30 | HG00408.hp2 HG00642.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.181-2691G>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48845373 | |||||||
| chr17:48845375 | G | C | 26 | a0001c0001t0002g0002 a0001c0001t0002g0010 a0001c0001t0002g0121 others(23): Show |
26 | HG00738.hp2 HG01070.hp1 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.181-2689G>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48845375 | |||||||
| chr17:48845377 | G | C | 24 | a0001c0001t0002g0150 a0001c0001t0002g0155 a0001c0001t0002g0156 others(21): Show |
24 | HG00140.hp2 HG00423.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.181-2687G>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48845377 | |||||||
| chr17:48845379 | G | C | 5 | a0001c0001t0002g0256 a0001c0001t0002g0296 a0001c0001t0002g0297 others(2): Show |
5 | HG02129.hp2 HG02165.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.181-2685G>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48845379 | |||||||
| chr17:48845391 | G | C | 1 | a0001c0001t0006g0009 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.181-2673G>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48845391 | |||||||
| chr17:48845395 | G | C | 1 | a0001c0001t0002g0008 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.181-2669G>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48845395 | |||||||
| chr17:48845557 | CTG | C | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.181-2505_181-2504d others(4): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 48845557 | ||||||
| chr17:48845715 | C | T | 5 | a0004c0004t0005g0098 a0004c0004t0005g0100 a0004c0004t0005g0110 others(2): Show |
5 | HG01069.hp2 HG01071.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.181-2349C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48845715 | |||||||
| chr17:48845728 | C | CA | 6 | a0001c0001t0002g0319 a0001c0001t0002g0320 a0002c0003t0004g0135 others(3): Show |
6 | HG00423.hp1 HG01257.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.181-2320dupA | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 48845728 | ||||||
| chr17:48845728 | C | CAA | 52 | a0002c0003t0001g0019 a0002c0003t0001g0020 a0002c0003t0001g0021 others(49): Show |
52 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(49): Show |
intron_variant | MODIFIER | c.181-2321_181-2320d others(4): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 48845728 | ||||||
| chr17:48845728 | CA | C | 49 | a0001c0001t0002g0152 a0004c0004t0003g0072 a0004c0004t0003g0074 others(46): Show |
50 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(47): Show |
intron_variant | MODIFIER | c.181-2320delA | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 48845728 | ||||||
| chr17:48846022 | G | A | 88 | a0002c0003t0001g0249 a0003c0002t0001g0067 a0003c0002t0001g0068 others(85): Show |
88 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.181-2042G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48846022 | |||||||
| chr17:48846063 | C | T | 2 | a0003c0002t0001g0210 a0003c0002t0001g0211 |
2 | HG02056.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.181-2001C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48846063 | |||||||
| chr17:48846204 | T | TG | 6 | a0002c0003t0004g0137 a0002c0003t0004g0322 a0002c0003t0004g0323 others(3): Show |
6 | HG02109.hp1 HG02280.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.181-1857dupG | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 48846204 | ||||||
| chr17:48846266 | A | T | 1 | a0001c0001t0006g0310 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.181-1798A>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48846266 | |||||||
| chr17:48846470 | G | A | 2 | a0001c0001t0002g0309 a0001c0001t0002g0311 |
2 | HG00323.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.181-1594G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48846470 | |||||||
| chr17:48846473 | CAAGAACT others(55): Show |
C | 1 | a0002c0003t0001g0055 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.181-1590_181-1529d others(64): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48846473 | |||||||
| chr17:48846537 | T | C | 1 | a0002c0003t0001g0061 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.181-1527T>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48846537 | |||||||
| chr17:48846551 | TA | T | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.181-1511delA | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 48846551 | ||||||
| chr17:48846722 | G | A | 3 | a0004c0004t0003g0079 a0004c0004t0003g0092 a0004c0004t0003g0093 |
3 | HG00741.hp1 HG01255.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.181-1342G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48846722 | |||||||
| chr17:48846856 | G | T | 13 | a0001c0001t0002g0121 a0001c0001t0002g0150 a0001c0001t0002g0242 others(10): Show |
13 | HG00323.hp1 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.181-1208G>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48846856 | |||||||
| chr17:48847074 | C | T | 3 | a0003c0002t0001g0172 a0003c0002t0001g0224 a0003c0002t0001g0306 |
3 | HG00423.hp1 NA18954.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.181-990C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48847074 | |||||||
| chr17:48847238 | T | G | 1 | a0004c0004t0016g0001 | 2 | HG03017.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.181-826T>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48847238 | |||||||
| chr17:48847241 | T | C | 7 | a0002c0003t0009g0148 a0002c0003t0009g0238 a0002c0003t0009g0239 others(4): Show |
7 | HG02071.hp2 HG02738.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.181-823T>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48847241 | |||||||
| chr17:48847278 | C | T | 1 | a0003c0002t0001g0209 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.181-786C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48847278 | |||||||
| chr17:48847618 | G | T | 61 | a0002c0003t0001g0019 a0002c0003t0001g0020 a0002c0003t0001g0021 others(58): Show |
61 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(58): Show |
intron_variant | MODIFIER | c.181-446G>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48847618 | |||||||
| chr17:48847679 | G | A | 88 | a0002c0003t0001g0249 a0003c0002t0001g0067 a0003c0002t0001g0068 others(85): Show |
88 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.181-385G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48847679 | |||||||
| chr17:48847725 | G | A | 2 | a0003c0002t0001g0229 a0003c0002t0004g0223 |
2 | NA18942.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.181-339G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48847725 | |||||||
| chr17:48847808 | A | G | 3 | a0001c0001t0002g0251 a0001c0001t0002g0268 a0001c0001t0006g0241 |
3 | HG01256.hp1 HG01258.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.181-256A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48847808 | |||||||
| chr17:48847874 | C | G | 88 | a0002c0003t0001g0249 a0003c0002t0001g0067 a0003c0002t0001g0068 others(85): Show |
88 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.181-190C>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48847874 | |||||||
| chr17:48847912 | C | T | 2 | a0002c0003t0004g0135 a0002c0003t0004g0136 |
2 | HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.181-152C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48847912 | |||||||
| chr17:48847926 | A | T | 1 | a0002c0003t0001g0029 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.181-138A>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48847926 | |||||||
| chr17:48847950 | C | T | 2 | a0003c0002t0001g0207 a0003c0002t0001g0208 |
2 | HG00408.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.181-114C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 2/12 | chr17 | 48847950 | |||||||
| chr17:48848497 | G | A | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.417+42G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 4/12 | chr17 | 48848497 | |||||||
| chr17:48848506 | A | ATAGGATA others(75): Show |
1 | a0002c0003t0001g0055 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.417+52_417+133dupT others(81): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 48848506 | ||||||
| chr17:48848930 | A | ACACTGTC others(8): Show |
1 | a0002c0003t0001g0054 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.418-319_418-305dup others(15): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 48848930 | ||||||
| chr17:48848987 | G | A | 1 | a0004c0004t0012g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.418-265G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 4/12 | chr17 | 48848987 | |||||||
| chr17:48849410 | A | G | 316 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(313): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.543+33A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 5/12 | chr17 | 48849410 | |||||||
| chr17:48849445 | C | A | 1 | a0001c0001t0006g0310 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.543+68C>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 5/12 | chr17 | 48849445 | |||||||
| chr17:48849568 | C | T | 2 | a0004c0004t0005g0098 a0004c0004t0005g0111 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.543+191C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 5/12 | chr17 | 48849568 | |||||||
| chr17:48849592 | A | G | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.543+215A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 5/12 | chr17 | 48849592 | |||||||
| chr17:48849695 | G | T | 7 | a0002c0003t0009g0148 a0002c0003t0009g0238 a0002c0003t0009g0239 others(4): Show |
7 | HG02071.hp2 HG02738.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.543+318G>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 5/12 | chr17 | 48849695 | |||||||
| chr17:48849724 | G | A | 53 | a0002c0003t0001g0019 a0002c0003t0001g0020 a0002c0003t0001g0021 others(50): Show |
53 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(50): Show |
intron_variant | MODIFIER | c.543+347G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 5/12 | chr17 | 48849724 | |||||||
| chr17:48849856 | G | A | 1 | a0003c0002t0001g0175 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.543+479G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 5/12 | chr17 | 48849856 | |||||||
| chr17:48849987 | G | A | 1 | a0002c0003t0001g0029 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.543+610G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 5/12 | chr17 | 48849987 | |||||||
| chr17:48849992 | T | C | 1 | a0002c0003t0004g0136 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.543+615T>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 5/12 | chr17 | 48849992 | |||||||
| chr17:48850176 | G | A | 1 | a0001c0001t0006g0310 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.543+799G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 5/12 | chr17 | 48850176 | |||||||
| chr17:48850225 | G | A | 1 | a0001c0001t0002g0253 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.543+848G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 5/12 | chr17 | 48850225 | |||||||
| chr17:48850342 | G | A | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.544-747G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 5/12 | chr17 | 48850342 | |||||||
| chr17:48850429 | C | T | 1 | a0004c0004t0003g0095 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.544-660C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 5/12 | chr17 | 48850429 | |||||||
| chr17:48850874 | C | T | 1 | a0004c0004t0019g0099 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.544-215C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 5/12 | chr17 | 48850874 | |||||||
| chr17:48850917 | TA | T | 10 | a0001c0001t0002g0159 a0001c0001t0002g0167 a0001c0001t0006g0009 others(7): Show |
10 | HG00738.hp1 HG01891.hp1 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.544-156delA | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr17 | 48850917 | ||||||
| chr17:48850917 | TAA | T | 247 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(244): Show |
248 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.544-157_544-156del others(2): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr17 | 48850917 | ||||||
| chr17:48851064 | C | T | 1 | a0003c0002t0001g0206 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.544-25C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 5/12 | chr17 | 48851064 | |||||||
| chr17:48851677 | C | A | 11 | a0001c0001t0002g0002 a0001c0001t0002g0157 a0001c0001t0002g0160 others(8): Show |
11 | HG00738.hp2 HG01070.hp1 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.702+49C>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 7/12 | chr17 | 48851677 | |||||||
| chr17:48851720 | G | A | 1 | a0002c0003t0001g0035 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.702+92G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 7/12 | chr17 | 48851720 | |||||||
| chr17:48851788 | A | C | 1 | a0002c0003t0001g0059 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.702+160A>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 7/12 | chr17 | 48851788 | |||||||
| chr17:48851898 | A | G | 1 | a0002c0003t0001g0043 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.702+270A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 7/12 | chr17 | 48851898 | |||||||
| chr17:48851992 | C | T | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.702+364C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 7/12 | chr17 | 48851992 | |||||||
| chr17:48852057 | G | T | 1 | a0002c0003t0009g0313 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.702+429G>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 7/12 | chr17 | 48852057 | |||||||
| chr17:48852098 | A | G | 6 | a0002c0003t0001g0131 a0002c0003t0001g0138 a0002c0003t0001g0139 others(3): Show |
6 | HG01891.hp1 HG02809.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.703-408A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 7/12 | chr17 | 48852098 | |||||||
| chr17:48852142 | G | GA | 6 | a0001c0001t0002g0152 a0001c0001t0002g0257 a0001c0001t0002g0258 others(3): Show |
6 | HG00735.hp2 HG02074.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.703-349dupA | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr17 | 48852142 | ||||||
| chr17:48852142 | G | GAA | 47 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(44): Show |
48 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.703-350_703-349dup others(2): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr17 | 48852142 | ||||||
| chr17:48852142 | GA | G | 7 | a0002c0003t0001g0131 a0002c0003t0001g0138 a0002c0003t0001g0139 others(4): Show |
7 | HG01891.hp1 HG02080.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.703-349delA | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr17 | 48852142 | ||||||
| chr17:48852213 | A | G | 1 | a0004c0004t0010g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.703-293A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 7/12 | chr17 | 48852213 | |||||||
| chr17:48852265 | C | A | 6 | a0002c0003t0004g0137 a0002c0003t0004g0322 a0002c0003t0004g0323 others(3): Show |
6 | HG02109.hp1 HG02280.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.703-241C>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 7/12 | chr17 | 48852265 | |||||||
| chr17:48852418 | T | A | 1 | a0001c0001t0002g0243 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.703-88T>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 7/12 | chr17 | 48852418 | |||||||
| chr17:48852501 | T | C | 4 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0282 others(1): Show |
4 | HG01261.hp2 HG01433.hp1 NA18971.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.703-5T>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 7/12 | chr17 | 48852501 | |||||||
| chr17:48852717 | A | G | 1 | a0004c0004t0005g0109 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.825+89A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 8/12 | chr17 | 48852717 | |||||||
| chr17:48852743 | G | GAAAGGGC others(13): Show |
1 | a0005c0007t0008g0014 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.825+116_825+135dup others(20): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 48852743 | ||||||
| chr17:48853049 | C | A | 1 | a0001c0001t0022g0252 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.912+37C>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48853049 | |||||||
| chr17:48853167 | A | G | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.912+155A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48853167 | |||||||
| chr17:48853191 | CATTTCTA others(3): Show |
C | 5 | a0004c0004t0005g0098 a0004c0004t0005g0100 a0004c0004t0005g0110 others(2): Show |
5 | HG01069.hp2 HG01071.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.912+180_912+189del others(10): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48853191 | |||||||
| chr17:48853257 | A | C | 1 | a0001c0001t0002g0282 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.912+245A>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48853257 | |||||||
| chr17:48853338 | G | C | 1 | a0004c0004t0003g0072 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.912+326G>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48853338 | |||||||
| chr17:48853493 | G | T | 317 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(314): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.912+481G>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48853493 | |||||||
| chr17:48853520 | G | A | 1 | a0002c0003t0001g0039 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.912+508G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48853520 | |||||||
| chr17:48853545 | G | A | 73 | a0003c0002t0001g0067 a0003c0002t0001g0068 a0003c0002t0001g0069 others(70): Show |
73 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.912+533G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48853545 | |||||||
| chr17:48853813 | G | A | 317 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(314): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.912+801G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48853813 | |||||||
| chr17:48853821 | G | A | 4 | a0002c0003t0004g0322 a0002c0003t0004g0323 a0002c0003t0004g0324 others(1): Show |
4 | HG02280.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.912+809G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48853821 | |||||||
| chr17:48853857 | G | A | 3 | a0001c0001t0002g0319 a0001c0001t0002g0320 a0001c0001t0014g0321 |
3 | HG01243.hp2 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.912+845G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48853857 | |||||||
| chr17:48853929 | G | A | 317 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(314): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.912+917G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48853929 | |||||||
| chr17:48853987 | C | T | 9 | a0002c0003t0009g0148 a0002c0003t0009g0238 a0002c0003t0009g0239 others(6): Show |
9 | HG02071.hp2 HG02738.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.912+975C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48853987 | |||||||
| chr17:48854019 | ATGATCTA others(33): Show |
A | 1 | a0002c0003t0001g0035 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.912+1008_912+1047d others(42): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48854019 | |||||||
| chr17:48854054 | G | A | 1 | a0003c0002t0001g0187 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.912+1042G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48854054 | |||||||
| chr17:48854114 | G | A | 6 | a0001c0001t0002g0319 a0001c0001t0002g0320 a0001c0001t0014g0321 others(3): Show |
6 | HG01243.hp2 HG02572.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.912+1102G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48854114 | |||||||
| chr17:48854128 | C | T | 1 | a0003c0002t0001g0151 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.912+1116C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48854128 | |||||||
| chr17:48854222 | A | G | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.912+1210A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48854222 | |||||||
| chr17:48854271 | G | A | 1 | a0003c0002t0001g0176 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.912+1259G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48854271 | |||||||
| chr17:48854294 | C | T | 7 | a0002c0003t0009g0148 a0002c0003t0009g0238 a0002c0003t0009g0239 others(4): Show |
7 | HG02071.hp2 HG02738.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.912+1282C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48854294 | |||||||
| chr17:48854315 | C | CA | 162 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(159): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.912+1320dupA | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854315 | ||||||
| chr17:48854315 | C | CAA | 142 | a0001c0001t0002g0010 a0001c0001t0002g0152 a0001c0001t0002g0155 others(139): Show |
143 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.912+1319_912+1320d others(4): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854315 | ||||||
| chr17:48854315 | C | CAAA | 13 | a0001c0001t0002g0159 a0002c0003t0001g0140 a0002c0003t0007g0023 others(10): Show |
13 | HG01978.hp2 HG02056.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.912+1318_912+1320d others(5): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854315 | ||||||
| chr17:48854378 | T | TTTTATAT others(9): Show |
1 | a0003c0002t0013g0214 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.912+1367_912+1368i others(18): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854378 | ||||||
| chr17:48854380 | A | T | 66 | a0002c0003t0001g0249 a0003c0002t0001g0133 a0003c0002t0001g0142 others(63): Show |
66 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.912+1368A>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48854380 | |||||||
| chr17:48854382 | T | A | 88 | a0002c0003t0001g0249 a0003c0002t0001g0067 a0003c0002t0001g0068 others(85): Show |
88 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.912+1370T>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48854382 | |||||||
| chr17:48854382 | T | TTATATA | 6 | a0001c0001t0002g0121 a0001c0001t0002g0150 a0001c0001t0002g0244 others(3): Show |
6 | HG01243.hp1 HG02738.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.912+1380_912+1385d others(8): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854382 | ||||||
| chr17:48854382 | T | TTATATAT others(1): Show |
6 | a0001c0001t0002g0242 a0001c0001t0002g0243 a0001c0001t0002g0245 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.912+1378_912+1385d others(10): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854382 | ||||||
| chr17:48854382 | T | TTATATAT others(3): Show |
1 | a0004c0004t0019g0099 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.912+1376_912+1385d others(12): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854382 | ||||||
| chr17:48854382 | T | TTATATAT others(5): Show |
1 | a0002c0003t0001g0131 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.912+1374_912+1385d others(14): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854382 | ||||||
| chr17:48854382 | T | TTATATAT others(11): Show |
1 | a0001c0001t0002g0259 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.912+1385_912+1386i others(20): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854382 | ||||||
| chr17:48854382 | T | TTATATAT others(13): Show |
1 | a0004c0004t0003g0077 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.912+1385_912+1386i others(22): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854382 | ||||||
| chr17:48854396 | A | ATATATAT others(8): Show |
1 | a0001c0001t0006g0004 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.912+1385_912+1386i others(17): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(10): Show |
2 | a0001c0001t0022g0252 a0003c0002t0013g0216 |
2 | HG01952.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.912+1385_912+1386i others(19): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(12): Show |
6 | a0001c0001t0002g0250 a0001c0001t0002g0260 a0001c0001t0002g0277 others(3): Show |
6 | HG02486.hp1 HG03041.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.912+1385_912+1386i others(21): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(14): Show |
1 | a0004c0004t0003g0078 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.912+1385_912+1386i others(23): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(16): Show |
2 | a0001c0001t0007g0228 a0002c0003t0004g0136 |
2 | HG02818.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.912+1385_912+1386i others(25): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(40): Show |
1 | a0003c0002t0001g0318 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.912+1385_912+1386i others(49): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(41): Show |
1 | a0003c0002t0001g0225 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.912+1385_912+1386i others(50): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(39): Show |
2 | a0003c0002t0001g0145 a0003c0002t0001g0174 |
2 | HG03688.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.912+1385_912+1386i others(48): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(35): Show |
1 | a0003c0002t0024g0149 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.912+1385_912+1386i others(44): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(36): Show |
1 | a0003c0002t0001g0178 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.912+1385_912+1386i others(45): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(37): Show |
3 | a0003c0002t0001g0230 a0003c0002t0001g0235 a0003c0002t0004g0223 |
3 | NA18982.hp1 NA18982.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.912+1385_912+1386i others(46): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(38): Show |
1 | a0003c0002t0001g0207 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.912+1385_912+1386i others(47): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(39): Show |
3 | a0003c0002t0001g0143 a0003c0002t0001g0179 a0003c0002t0001g0184 |
3 | HG02135.hp1 NA18969.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.912+1385_912+1386i others(48): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(41): Show |
2 | a0003c0002t0001g0172 a0003c0002t0001g0185 |
2 | NA18954.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.912+1385_912+1386i others(50): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(34): Show |
3 | a0003c0002t0001g0186 a0003c0002t0001g0209 a0003c0002t0001g0308 |
3 | HG00609.hp2 NA18939.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.912+1385_912+1386i others(43): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(36): Show |
2 | a0003c0002t0001g0210 a0003c0002t0001g0219 |
2 | HG02056.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.912+1385_912+1386i others(45): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(43): Show |
1 | a0003c0002t0001g0212 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.912+1385_912+1386i others(52): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(31): Show |
1 | a0003c0002t0001g0144 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.912+1385_912+1386i others(40): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(32): Show |
1 | a0003c0002t0001g0221 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.912+1385_912+1386i others(41): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(33): Show |
3 | a0003c0002t0001g0132 a0003c0002t0001g0180 a0003c0002t0001g0306 |
3 | HG02015.hp2 HG02273.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.912+1385_912+1386i others(42): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(34): Show |
3 | a0003c0002t0001g0213 a0003c0002t0001g0226 a0003c0002t0001g0233 |
3 | HG02074.hp1 HG03492.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.912+1385_912+1386i others(43): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(35): Show |
3 | a0003c0002t0001g0151 a0003c0002t0001g0208 a0003c0002t0001g0211 |
3 | HG00558.hp2 HG02040.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.912+1385_912+1386i others(44): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(36): Show |
3 | a0003c0002t0001g0153 a0003c0002t0001g0187 a0003c0002t0001g0188 |
3 | HG02523.hp1 HG03654.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.912+1385_912+1386i others(45): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(37): Show |
1 | a0003c0002t0001g0189 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.912+1385_912+1386i others(46): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(38): Show |
1 | a0003c0002t0004g0173 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.912+1385_912+1386i others(47): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(29): Show |
1 | a0003c0002t0001g0070 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.912+1385_912+1386i others(38): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(30): Show |
4 | a0003c0002t0001g0190 a0003c0002t0001g0191 a0003c0002t0001g0218 others(1): Show |
4 | HG00423.hp1 HG01255.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.912+1385_912+1386i others(39): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(31): Show |
3 | a0003c0002t0001g0154 a0003c0002t0001g0168 a0003c0002t0001g0192 |
3 | HG01099.hp1 HG02300.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.912+1385_912+1386i others(40): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(32): Show |
2 | a0003c0002t0001g0175 a0003c0002t0026g0181 |
2 | NA18942.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.912+1385_912+1386i others(41): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(36): Show |
1 | a0003c0002t0001g0177 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.912+1385_912+1386i others(45): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(27): Show |
2 | a0002c0006t0015g0012 a0003c0002t0001g0193 |
2 | NA18906.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.912+1385_912+1386i others(36): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(30): Show |
1 | a0003c0002t0001g0068 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.912+1385_912+1386i others(39): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(31): Show |
2 | a0003c0002t0001g0200 a0003c0002t0001g0222 |
2 | HG00609.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.912+1385_912+1386i others(40): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(32): Show |
1 | a0003c0002t0001g0201 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.912+1385_912+1386i others(41): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(33): Show |
3 | a0003c0002t0001g0069 a0003c0002t0001g0182 a0003c0002t0001g0194 |
3 | HG03710.hp1 NA18945.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.912+1385_912+1386i others(42): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(35): Show |
1 | a0003c0002t0001g0195 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.912+1385_912+1386i others(44): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(36): Show |
1 | a0003c0002t0001g0142 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.912+1385_912+1386i others(45): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(25): Show |
1 | a0003c0002t0001g0067 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.912+1385_912+1386i others(34): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(30): Show |
1 | a0003c0002t0001g0171 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.912+1385_912+1386i others(39): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(33): Show |
1 | a0003c0002t0001g0147 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.912+1385_912+1386i others(42): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(36): Show |
1 | a0003c0002t0001g0232 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.912+1385_912+1386i others(45): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(26): Show |
1 | a0003c0002t0001g0305 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.912+1385_912+1386i others(35): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(30): Show |
2 | a0003c0002t0007g0183 a0003c0002t0007g0196 |
2 | HG02165.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.912+1385_912+1386i others(39): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(31): Show |
1 | a0003c0002t0001g0229 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.912+1385_912+1386i others(40): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(22): Show |
1 | a0002c0003t0004g0323 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.912+1385_912+1386i others(31): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(23): Show |
2 | a0002c0003t0004g0324 a0003c0002t0001g0197 |
2 | HG02630.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.912+1385_912+1386i others(32): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(24): Show |
2 | a0002c0006t0015g0011 a0003c0002t0001g0198 |
2 | HG01993.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.912+1385_912+1386i others(33): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(28): Show |
1 | a0003c0002t0001g0202 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.912+1385_912+1386i others(37): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(17): Show |
2 | a0001c0001t0002g0002 a0001c0001t0002g0275 |
2 | HG00738.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.912+1385_912+1386i others(26): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(18): Show |
1 | a0001c0001t0002g0301 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.912+1385_912+1386i others(27): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(19): Show |
1 | a0002c0003t0001g0060 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.912+1385_912+1386i others(28): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(20): Show |
1 | a0002c0003t0004g0325 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.912+1385_912+1386i others(29): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(22): Show |
1 | a0002c0003t0004g0137 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.912+1385_912+1386i others(31): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(27): Show |
1 | a0003c0002t0001g0071 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.912+1385_912+1386i others(36): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(15): Show |
6 | a0001c0001t0002g0269 a0001c0001t0002g0319 a0001c0001t0006g0310 others(3): Show |
6 | HG01069.hp2 HG01071.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.912+1385_912+1386i others(24): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(16): Show |
3 | a0003c0002t0001g0234 a0004c0004t0003g0089 a0004c0004t0003g0116 |
3 | HG02293.hp2 NA18612.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.912+1385_912+1386i others(25): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(17): Show |
1 | a0002c0003t0001g0027 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.912+1385_912+1386i others(26): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(18): Show |
1 | a0004c0004t0010g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.912+1385_912+1386i others(27): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(21): Show |
1 | a0002c0003t0004g0322 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.912+1385_912+1386i others(30): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(13): Show |
4 | a0001c0001t0002g0157 a0001c0001t0002g0257 a0001c0001t0002g0261 others(1): Show |
4 | HG00735.hp2 HG01106.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.912+1385_912+1386i others(22): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(14): Show |
7 | a0001c0001t0002g0152 a0001c0001t0002g0161 a0004c0004t0003g0074 others(4): Show |
7 | HG00558.hp1 HG00741.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.912+1385_912+1386i others(23): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(15): Show |
9 | a0002c0003t0001g0054 a0002c0003t0001g0249 a0004c0004t0003g0081 others(6): Show |
10 | HG00639.hp1 HG01074.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.912+1385_912+1386i others(24): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(16): Show |
5 | a0001c0001t0002g0160 a0002c0003t0001g0045 a0004c0004t0003g0083 others(2): Show |
5 | HG01978.hp1 HG01981.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.912+1385_912+1386i others(25): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(17): Show |
2 | a0001c0001t0002g0162 a0002c0003t0001g0056 |
2 | HG01099.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.912+1385_912+1386i others(26): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(18): Show |
1 | a0003c0002t0001g0203 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.912+1385_912+1386i others(27): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(11): Show |
5 | a0001c0001t0002g0279 a0001c0001t0002g0283 a0001c0001t0002g0314 others(2): Show |
5 | HG02129.hp2 HG02135.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.912+1385_912+1386i others(20): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(12): Show |
3 | a0001c0001t0002g0288 a0001c0001t0002g0296 a0004c0004t0011g0073 |
3 | HG03041.hp2 NA18971.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.912+1385_912+1386i others(21): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(13): Show |
10 | a0001c0001t0002g0169 a0001c0001t0002g0285 a0001c0001t0006g0271 others(7): Show |
10 | HG00099.hp2 HG01070.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.912+1385_912+1386i others(22): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(14): Show |
12 | a0001c0001t0002g0156 a0001c0001t0002g0159 a0001c0001t0002g0300 others(9): Show |
12 | HG01069.hp1 HG01517.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.912+1385_912+1386i others(23): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(15): Show |
10 | a0001c0001t0002g0163 a0001c0001t0002g0164 a0001c0001t0002g0231 others(7): Show |
10 | HG01192.hp1 HG01255.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.912+1385_912+1386i others(24): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(16): Show |
5 | a0001c0001t0002g0158 a0001c0001t0002g0167 a0001c0001t0002g0264 others(2): Show |
5 | HG00738.hp1 HG01074.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.912+1385_912+1386i others(25): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(17): Show |
6 | a0001c0001t0002g0251 a0001c0001t0002g0258 a0001c0001t0002g0265 others(3): Show |
6 | HG01256.hp1 HG01258.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.912+1385_912+1386i others(26): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(9): Show |
1 | a0001c0001t0002g0003 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.912+1385_912+1386i others(18): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(11): Show |
6 | a0001c0001t0002g0237 a0001c0001t0002g0289 a0001c0001t0002g0290 others(3): Show |
6 | HG02922.hp1 HG03239.hp2 NA18941.hp2 others(3): Show |
intron_variant | MODIFIER | c.912+1385_912+1386i others(20): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(12): Show |
9 | a0001c0001t0002g0292 a0001c0001t0006g0291 a0001c0001t0014g0284 others(6): Show |
9 | HG01257.hp1 HG01258.hp2 HG03492.hp1 others(6): Show |
intron_variant | MODIFIER | c.912+1385_912+1386i others(21): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(13): Show |
13 | a0001c0001t0002g0006 a0001c0001t0002g0256 a0001c0001t0002g0273 others(10): Show |
13 | HG00642.hp1 HG00735.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.912+1385_912+1386i others(22): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(14): Show |
17 | a0001c0001t0002g0005 a0001c0001t0002g0155 a0001c0001t0002g0274 others(14): Show |
17 | HG00099.hp1 HG00140.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.912+1385_912+1386i others(23): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(15): Show |
11 | a0001c0001t0002g0165 a0001c0001t0002g0266 a0001c0001t0014g0276 others(8): Show |
11 | HG00741.hp2 HG01070.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.912+1385_912+1386i others(24): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(16): Show |
4 | a0001c0001t0002g0253 a0002c0003t0001g0024 a0002c0003t0001g0037 others(1): Show |
4 | HG00140.hp2 HG01169.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.912+1385_912+1386i others(25): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(9): Show |
2 | a0001c0001t0002g0236 a0002c0003t0001g0032 |
2 | HG02451.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.912+1385_912+1386i others(18): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(10): Show |
2 | a0001c0001t0002g0281 a0004c0004t0012g0075 |
2 | HG01175.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.912+1385_912+1386i others(19): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(11): Show |
2 | a0001c0001t0002g0280 a0001c0001t0002g0294 |
2 | HG00408.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.912+1385_912+1386i others(20): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(12): Show |
6 | a0001c0001t0002g0254 a0002c0003t0001g0028 a0002c0003t0001g0030 others(3): Show |
6 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(3): Show |
intron_variant | MODIFIER | c.912+1385_912+1386i others(21): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(13): Show |
8 | a0001c0001t0002g0007 a0001c0001t0002g0295 a0002c0003t0001g0019 others(5): Show |
8 | HG00438.hp1 HG01081.hp2 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.912+1385_912+1386i others(22): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(14): Show |
2 | a0001c0001t0002g0166 a0001c0001t0020g0327 |
2 | HG02615.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.912+1385_912+1386i others(23): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(15): Show |
1 | a0004c0004t0005g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.912+1385_912+1386i others(24): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(6): Show |
1 | a0002c0003t0001g0315 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.912+1385_912+1386i others(15): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(12): Show |
2 | a0001c0001t0002g0267 a0003c0002t0001g0176 |
2 | HG00423.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.912+1385_912+1386i others(21): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(3): Show |
1 | a0002c0003t0001g0138 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.912+1385_912+1386i others(12): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(4): Show |
1 | a0002c0003t0007g0141 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.912+1385_912+1386i others(13): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(11): Show |
1 | a0001c0001t0002g0170 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.912+1385_912+1386i others(20): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(3): Show |
1 | a0002c0003t0001g0140 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.912+1385_912+1386i others(12): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(4): Show |
2 | a0002c0003t0001g0139 a0002c0003t0009g0238 |
2 | HG01891.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.912+1385_912+1386i others(13): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATAT others(5): Show |
1 | a0003c0002t0001g0206 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.912+1385_912+1386i others(14): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATATTT others(7): Show |
1 | a0004c0004t0005g0115 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.912+1385_912+1386i others(16): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATGTAT others(15): Show |
1 | a0002c0003t0004g0135 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.912+1385_912+1386i others(24): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854396 | A | ATATTTTT others(3): Show |
1 | a0003c0002t0001g0146 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.912+1385_912+1386i others(12): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854396 | ||||||
| chr17:48854397 | T | TA | 4 | a0002c0003t0004g0122 a0002c0003t0004g0128 a0002c0003t0004g0129 others(1): Show |
4 | HG00673.hp1 HG02055.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.912+1385_912+1386i others(3): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48854397 | |||||||
| chr17:48854397 | T | TATA | 4 | a0004c0004t0003g0072 a0004c0004t0003g0117 a0004c0004t0003g0119 others(1): Show |
4 | NA18612.hp1 NA18960.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.912+1385_912+1386i others(5): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48854397 | |||||||
| chr17:48854397 | T | TATATATA others(8): Show |
1 | a0003c0002t0013g0215 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.912+1385_912+1386i others(17): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48854397 | |||||||
| chr17:48854397 | T | TATATATA others(12): Show |
3 | a0001c0001t0002g0309 a0001c0001t0002g0311 a0001c0001t0014g0321 |
3 | HG00323.hp1 HG01243.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.912+1385_912+1386i others(21): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48854397 | |||||||
| chr17:48854398 | T | A | 13 | a0001c0001t0002g0121 a0001c0001t0002g0150 a0001c0001t0002g0242 others(10): Show |
13 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.912+1386T>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48854398 | |||||||
| chr17:48854399 | T | A | 8 | a0001c0001t0002g0311 a0001c0001t0002g0317 a0001c0001t0014g0321 others(5): Show |
8 | HG00673.hp1 HG01243.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.912+1387T>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48854399 | |||||||
| chr17:48854400 | T | A | 12 | a0001c0001t0002g0121 a0001c0001t0002g0150 a0001c0001t0002g0242 others(9): Show |
12 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.912+1388T>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48854400 | |||||||
| chr17:48854401 | T | A | 7 | a0001c0001t0002g0311 a0001c0001t0002g0317 a0004c0004t0003g0072 others(4): Show |
7 | HG00673.hp1 HG02572.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.912+1389T>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48854401 | |||||||
| chr17:48854402 | T | A | 11 | a0001c0001t0002g0121 a0001c0001t0002g0150 a0001c0001t0002g0242 others(8): Show |
11 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.912+1390T>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48854402 | |||||||
| chr17:48854403 | T | A | 6 | a0001c0001t0002g0317 a0004c0004t0003g0072 a0004c0004t0003g0117 others(3): Show |
6 | HG00673.hp1 HG02886.hp1 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.912+1391T>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48854403 | |||||||
| chr17:48854404 | T | A | 11 | a0001c0001t0002g0121 a0001c0001t0002g0150 a0001c0001t0002g0242 others(8): Show |
11 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.912+1392T>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48854404 | |||||||
| chr17:48854405 | T | A | 6 | a0001c0001t0002g0317 a0004c0004t0003g0072 a0004c0004t0003g0117 others(3): Show |
6 | HG00673.hp1 HG02886.hp1 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.912+1393T>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48854405 | |||||||
| chr17:48854406 | T | A | 9 | a0001c0001t0002g0121 a0001c0001t0002g0150 a0001c0001t0002g0242 others(6): Show |
9 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.912+1394T>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48854406 | |||||||
| chr17:48854407 | T | A | 6 | a0001c0001t0002g0317 a0004c0004t0003g0072 a0004c0004t0003g0117 others(3): Show |
6 | HG00673.hp1 HG02886.hp1 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.912+1395T>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48854407 | |||||||
| chr17:48854408 | T | A | 9 | a0001c0001t0002g0121 a0001c0001t0002g0150 a0001c0001t0002g0242 others(6): Show |
9 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.912+1396T>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48854408 | |||||||
| chr17:48854409 | T | A | 6 | a0001c0001t0002g0317 a0004c0004t0003g0072 a0004c0004t0003g0117 others(3): Show |
6 | HG00673.hp1 HG02886.hp1 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.912+1397T>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48854409 | |||||||
| chr17:48854410 | T | A | 8 | a0001c0001t0002g0121 a0001c0001t0002g0150 a0001c0001t0002g0243 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.912+1398T>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48854410 | |||||||
| chr17:48854411 | T | A | 2 | a0004c0004t0003g0118 a0004c0004t0003g0119 |
2 | HG00673.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.912+1399T>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48854411 | |||||||
| chr17:48854412 | T | A | 1 | a0001c0001t0002g0244 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.912+1400T>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48854412 | |||||||
| chr17:48854413 | T | A | 1 | a0004c0004t0003g0118 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.912+1401T>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48854413 | |||||||
| chr17:48854461 | G | A | 1 | a0002c0003t0009g0312 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.912+1449G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48854461 | |||||||
| chr17:48854461 | G | T | 2 | a0002c0003t0001g0035 a0002c0003t0001g0059 |
2 | HG02074.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.912+1449G>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48854461 | |||||||
| chr17:48854485 | G | A | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.912+1473G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48854485 | |||||||
| chr17:48854703 | G | A | 3 | a0002c0003t0007g0023 a0002c0003t0007g0062 a0002c0003t0007g0064 |
3 | HG01257.hp1 HG01258.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.913-1389G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48854703 | |||||||
| chr17:48854713 | TTAGTTTT others(43): Show |
T | 1 | a0002c0003t0008g0016 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.913-1375_913-1326d others(52): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48854713 | ||||||
| chr17:48854832 | GGAGCCTA others(18): Show |
G | 1 | a0002c0003t0001g0054 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.913-1259_913-1235d others(27): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48854832 | |||||||
| chr17:48854833 | G | A | 4 | a0001c0001t0002g0254 a0001c0001t0002g0257 a0001c0001t0002g0280 others(1): Show |
4 | HG00642.hp2 HG00735.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.913-1259G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48854833 | |||||||
| chr17:48854936 | A | G | 53 | a0002c0003t0001g0019 a0002c0003t0001g0020 a0002c0003t0001g0021 others(50): Show |
53 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(50): Show |
intron_variant | MODIFIER | c.913-1156A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48854936 | |||||||
| chr17:48854943 | C | T | 1 | a0004c0004t0010g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.913-1149C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48854943 | |||||||
| chr17:48854988 | G | A | 9 | a0002c0003t0009g0148 a0002c0003t0009g0238 a0002c0003t0009g0239 others(6): Show |
9 | HG02071.hp2 HG02738.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.913-1104G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48854988 | |||||||
| chr17:48855109 | GCACTAAA others(11): Show |
G | 1 | a0003c0002t0001g0308 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.913-982_913-965del others(18): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48855109 | |||||||
| chr17:48855362 | G | GCATTACT others(18): Show |
1 | a0002c0003t0001g0055 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.913-726_913-702dup others(25): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48855362 | ||||||
| chr17:48855420 | T | G | 1 | a0003c0002t0001g0217 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.913-672T>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48855420 | |||||||
| chr17:48855527 | T | C | 1 | a0004c0004t0003g0086 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.913-565T>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48855527 | |||||||
| chr17:48855679 | T | C | 317 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(314): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.913-413T>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48855679 | |||||||
| chr17:48855690 | T | TA | 6 | a0002c0003t0004g0137 a0002c0003t0004g0322 a0002c0003t0004g0323 others(3): Show |
6 | HG02109.hp1 HG02280.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.913-400dupA | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48855690 | ||||||
| chr17:48855702 | G | C | 9 | a0002c0003t0009g0148 a0002c0003t0009g0238 a0002c0003t0009g0239 others(6): Show |
9 | HG02071.hp2 HG02738.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.913-390G>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48855702 | |||||||
| chr17:48855718 | C | T | 2 | a0001c0001t0002g0003 a0001c0001t0006g0004 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.913-374C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48855718 | |||||||
| chr17:48855863 | C | CA | 56 | a0001c0001t0002g0163 a0001c0001t0002g0166 a0001c0001t0002g0169 others(53): Show |
57 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.913-210dupA | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48855863 | ||||||
| chr17:48855863 | CA | C | 6 | a0001c0001t0002g0292 a0002c0003t0001g0052 a0002c0003t0004g0326 others(3): Show |
6 | HG00323.hp2 HG02896.hp1 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.913-210delA | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 48855863 | ||||||
| chr17:48856069 | C | T | 1 | a0003c0002t0001g0205 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.913-23C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 9/12 | chr17 | 48856069 | |||||||
| chr17:48856330 | A | G | 1 | a0002c0003t0009g0313 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1008+143A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48856330 | |||||||
| chr17:48856560 | T | C | 1 | a0002c0003t0001g0131 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1008+373T>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48856560 | |||||||
| chr17:48856639 | GCATT | G | 60 | a0002c0003t0001g0019 a0002c0003t0001g0020 a0002c0003t0001g0021 others(57): Show |
60 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(57): Show |
intron_variant | MODIFIER | c.1008+481_1008+484d others(6): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48856639 | ||||||
| chr17:48856639 | GCATTCAT others(5): Show |
G | 1 | a0004c0004t0019g0099 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1008+473_1008+484d others(14): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48856639 | ||||||
| chr17:48856645 | A | C | 200 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(197): Show |
200 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.1008+458A>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48856645 | |||||||
| chr17:48856646 | TTCATTCA others(32): Show |
T | 1 | a0002c0003t0025g0053 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1008+462_1008+500d others(41): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48856646 | ||||||
| chr17:48856778 | CT | C | 11 | a0001c0001t0002g0237 a0002c0003t0001g0020 a0002c0003t0001g0029 others(8): Show |
11 | HG02071.hp2 HG02523.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.1008+605delT | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48856778 | ||||||
| chr17:48856965 | AT | A | 104 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(101): Show |
104 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.1008+788delT | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48856965 | ||||||
| chr17:48857008 | C | CCCAAGCT others(3): Show |
1 | a0002c0003t0004g0040 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1008+823_1008+832d others(12): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857008 | ||||||
| chr17:48857198 | C | CT | 7 | a0002c0003t0001g0021 a0002c0003t0001g0131 a0002c0003t0001g0138 others(4): Show |
7 | HG01891.hp1 HG02809.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1008+1027dupT | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857198 | ||||||
| chr17:48857198 | CT | C | 239 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(236): Show |
240 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1008+1027delT | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857198 | ||||||
| chr17:48857198 | CTT | C | 6 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0248 others(3): Show |
6 | HG01169.hp1 HG01261.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1008+1026_1008+102 others(6): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857198 | ||||||
| chr17:48857300 | C | T | 1 | a0001c0001t0002g0299 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1008+1113C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48857300 | |||||||
| chr17:48857301 | G | A | 66 | a0001c0001t0002g0121 a0001c0001t0002g0150 a0001c0001t0002g0242 others(63): Show |
67 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(64): Show |
intron_variant | MODIFIER | c.1008+1114G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48857301 | |||||||
| chr17:48857386 | G | T | 1 | a0004c0004t0019g0099 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1008+1199G>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48857386 | |||||||
| chr17:48857414 | C | T | 2 | a0003c0002t0001g0145 a0003c0002t0001g0230 |
2 | HG03688.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1008+1227C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48857414 | |||||||
| chr17:48857497 | C | CTTT | 7 | a0002c0003t0009g0238 a0002c0003t0009g0239 a0002c0003t0009g0313 others(4): Show |
7 | HG00408.hp1 HG02040.hp1 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.1008+1331_1008+133 others(7): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857497 | ||||||
| chr17:48857497 | C | CTTTT | 7 | a0002c0003t0001g0033 a0002c0003t0004g0040 a0002c0003t0009g0148 others(4): Show |
7 | HG00639.hp2 HG01517.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.1008+1330_1008+133 others(8): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857497 | ||||||
| chr17:48857497 | C | CTTTTT | 39 | a0002c0003t0001g0019 a0002c0003t0001g0020 a0002c0003t0001g0022 others(36): Show |
39 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.1008+1329_1008+133 others(9): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857497 | ||||||
| chr17:48857497 | C | CTTTTTT | 18 | a0001c0001t0002g0320 a0001c0001t0014g0321 a0002c0003t0001g0021 others(15): Show |
18 | HG00099.hp2 HG01167.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.1008+1328_1008+133 others(10): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857497 | ||||||
| chr17:48857497 | C | CTTTTTTT others(3): Show |
4 | a0002c0003t0004g0322 a0002c0003t0004g0323 a0003c0002t0001g0190 others(1): Show |
4 | HG02622.hp2 NA18990.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1008+1324_1008+133 others(14): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857497 | ||||||
| chr17:48857497 | C | CTTTTTTT others(4): Show |
11 | a0001c0001t0002g0243 a0001c0001t0002g0245 a0001c0001t0002g0246 others(8): Show |
11 | HG01167.hp2 HG01169.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1008+1323_1008+133 others(15): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857497 | ||||||
| chr17:48857497 | C | CTTTTTTT others(5): Show |
6 | a0001c0001t0002g0121 a0001c0001t0002g0242 a0001c0001t0002g0244 others(3): Show |
6 | HG01243.hp1 HG02109.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1008+1322_1008+133 others(16): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857497 | ||||||
| chr17:48857497 | C | CTTTTTTT others(6): Show |
3 | a0001c0001t0002g0150 a0001c0001t0002g0247 a0003c0002t0001g0203 |
3 | HG03130.hp2 HG03516.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1008+1321_1008+133 others(17): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857497 | ||||||
| chr17:48857497 | C | CTTTTTTT others(7): Show |
2 | a0003c0002t0001g0176 a0003c0002t0001g0179 |
2 | NA18969.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1008+1320_1008+133 others(18): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857497 | ||||||
| chr17:48857497 | C | CTTTTTTT others(8): Show |
10 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0275 others(7): Show |
10 | HG01175.hp2 HG02015.hp1 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.1008+1319_1008+133 others(19): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857497 | ||||||
| chr17:48857497 | C | CTTTTTTT others(9): Show |
35 | a0001c0001t0002g0002 a0001c0001t0002g0156 a0001c0001t0002g0157 others(32): Show |
35 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.1008+1318_1008+133 others(20): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857497 | ||||||
| chr17:48857497 | C | CTTTTTTT others(10): Show |
33 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0152 others(30): Show |
33 | HG00408.hp2 HG00423.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.1008+1317_1008+133 others(21): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857497 | ||||||
| chr17:48857497 | C | CTTTTTTT others(11): Show |
7 | a0001c0001t0002g0008 a0001c0001t0002g0162 a0001c0001t0002g0262 others(4): Show |
7 | HG01069.hp1 HG01433.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1008+1316_1008+133 others(22): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857497 | ||||||
| chr17:48857497 | C | CTTTTTTT others(13): Show |
4 | a0001c0001t0002g0170 a0003c0002t0001g0151 a0003c0002t0001g0175 others(1): Show |
4 | HG00558.hp2 NA18942.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.1008+1314_1008+133 others(24): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857497 | ||||||
| chr17:48857497 | C | CTTTTTTT others(14): Show |
7 | a0001c0001t0006g0009 a0003c0002t0001g0174 a0003c0002t0001g0200 others(4): Show |
7 | HG00438.hp2 HG02129.hp1 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.1008+1313_1008+133 others(25): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857497 | ||||||
| chr17:48857497 | C | CTTTTTTT others(15): Show |
1 | a0001c0001t0002g0270 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1008+1312_1008+133 others(26): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857497 | ||||||
| chr17:48857497 | C | CTTTTTTT others(16): Show |
2 | a0001c0001t0002g0003 a0001c0001t0006g0004 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1008+1311_1008+133 others(27): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857497 | ||||||
| chr17:48857497 | C | CTTTTTTT others(17): Show |
2 | a0003c0002t0001g0187 a0003c0002t0001g0308 |
2 | HG03654.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.1008+1333_1008+133 others(28): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857497 | ||||||
| chr17:48857497 | C | CTTTTTTT others(20): Show |
6 | a0002c0006t0015g0011 a0003c0002t0001g0067 a0003c0002t0001g0154 others(3): Show |
6 | HG01099.hp1 HG03139.hp2 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.1008+1333_1008+133 others(31): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857497 | ||||||
| chr17:48857497 | C | CTTTTTTT others(21): Show |
21 | a0002c0003t0001g0249 a0003c0002t0001g0068 a0003c0002t0001g0070 others(18): Show |
21 | HG00423.hp1 HG00609.hp1 HG00609.hp2 others(18): Show |
intron_variant | MODIFIER | c.1008+1333_1008+133 others(32): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857497 | ||||||
| chr17:48857497 | C | CTTTTTTT others(22): Show |
11 | a0003c0002t0001g0146 a0003c0002t0001g0178 a0003c0002t0001g0191 others(8): Show |
11 | HG00673.hp2 HG02155.hp2 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.1008+1333_1008+133 others(33): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857497 | ||||||
| chr17:48857497 | C | CTTTTTTT others(23): Show |
4 | a0003c0002t0001g0171 a0003c0002t0001g0188 a0003c0002t0001g0194 others(1): Show |
4 | HG02523.hp1 HG03710.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.1008+1333_1008+133 others(34): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857497 | ||||||
| chr17:48857497 | C | CTTTTTTT others(24): Show |
1 | a0003c0002t0001g0069 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1008+1333_1008+133 others(35): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857497 | ||||||
| chr17:48857497 | C | CTTTTTTT others(25): Show |
1 | a0003c0002t0001g0210 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1008+1333_1008+133 others(36): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857497 | ||||||
| chr17:48857497 | C | CTTTTTTT others(26): Show |
1 | a0003c0002t0001g0235 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1008+1333_1008+133 others(37): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857497 | ||||||
| chr17:48857497 | C | CTTTTTTT others(33): Show |
1 | a0003c0002t0001g0306 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1008+1333_1008+133 others(44): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857497 | ||||||
| chr17:48857497 | C | T | 1 | a0003c0002t0001g0229 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1008+1310C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48857497 | |||||||
| chr17:48857497 | CTTT | C | 9 | a0001c0001t0002g0253 a0001c0001t0002g0311 a0004c0004t0003g0086 others(6): Show |
9 | HG00140.hp2 HG02293.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1008+1331_1008+133 others(7): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857497 | ||||||
| chr17:48857497 | CTTTT | C | 43 | a0001c0001t0002g0309 a0004c0004t0003g0072 a0004c0004t0003g0074 others(40): Show |
44 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.1008+1330_1008+133 others(8): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857497 | ||||||
| chr17:48857525 | C | T | 2 | a0003c0002t0001g0144 a0003c0002t0001g0190 |
2 | NA18981.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1008+1338C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48857525 | |||||||
| chr17:48857589 | A | G | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.1008+1402A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48857589 | |||||||
| chr17:48857610 | A | G | 6 | a0002c0003t0001g0131 a0002c0003t0001g0138 a0002c0003t0001g0139 others(3): Show |
6 | HG01891.hp1 HG02809.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1008+1423A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48857610 | |||||||
| chr17:48857673 | G | A | 3 | a0002c0003t0001g0026 a0002c0003t0009g0148 a0002c0003t0009g0240 |
3 | HG02698.hp2 HG02738.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1008+1486G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48857673 | |||||||
| chr17:48857794 | G | A | 10 | a0003c0002t0001g0151 a0003c0002t0001g0174 a0003c0002t0001g0175 others(7): Show |
10 | HG00438.hp2 HG00558.hp2 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.1008+1607G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48857794 | |||||||
| chr17:48857818 | C | CA | 87 | a0002c0003t0001g0249 a0003c0002t0001g0067 a0003c0002t0001g0068 others(84): Show |
87 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1008+1641dupA | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857818 | ||||||
| chr17:48857835 | A | C | 2 | a0003c0002t0001g0153 a0003c0002t0004g0173 |
2 | NA18941.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.1008+1648A>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48857835 | |||||||
| chr17:48857894 | G | A | 1 | a0002c0003t0004g0136 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1008+1707G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48857894 | |||||||
| chr17:48857930 | TCGTGCCA others(3): Show |
T | 1 | a0002c0003t0001g0066 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1008+1745_1008+175 others(14): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857930 | ||||||
| chr17:48857974 | C | CAATAG | 22 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0156 others(19): Show |
22 | HG01175.hp2 HG01255.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.1008+1855_1008+185 others(9): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857974 | ||||||
| chr17:48857974 | C | CAATAGAA others(3): Show |
17 | a0001c0001t0002g0162 a0001c0001t0002g0257 a0001c0001t0002g0265 others(14): Show |
17 | HG00673.hp2 HG00735.hp2 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.1008+1850_1008+185 others(14): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857974 | ||||||
| chr17:48857974 | C | CAATAGAA others(8): Show |
10 | a0001c0001t0002g0003 a0001c0001t0002g0253 a0001c0001t0002g0261 others(7): Show |
10 | HG00140.hp2 HG01074.hp2 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.1008+1845_1008+185 others(19): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857974 | ||||||
| chr17:48857974 | C | CAATAGAA others(13): Show |
3 | a0001c0001t0002g0301 a0002c0003t0007g0141 a0003c0002t0001g0221 |
3 | HG02148.hp2 HG03139.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1008+1840_1008+185 others(24): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857974 | ||||||
| chr17:48857974 | C | CAATAGAA others(18): Show |
1 | a0001c0001t0002g0320 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1008+1835_1008+185 others(29): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857974 | ||||||
| chr17:48857974 | C | CAATAGAA others(23): Show |
1 | a0001c0001t0002g0236 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1008+1830_1008+185 others(34): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857974 | ||||||
| chr17:48857974 | C | CAATAGAA others(48): Show |
2 | a0001c0001t0002g0268 a0001c0001t0002g0319 |
2 | HG03209.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1008+1805_1008+185 others(59): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857974 | ||||||
| chr17:48857974 | C | CAATAGAA others(168): Show |
1 | a0001c0001t0002g0259 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(179): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857974 | ||||||
| chr17:48857974 | C | CAATAGAA others(268): Show |
1 | a0001c0001t0002g0262 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(279): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857974 | ||||||
| chr17:48857974 | C | CAATAGAA others(293): Show |
1 | a0002c0003t0001g0048 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1008+1802_1008+180 others(304): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857974 | ||||||
| chr17:48857974 | C | G | 59 | a0001c0001t0006g0291 a0002c0003t0001g0039 a0002c0003t0009g0148 others(56): Show |
60 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.1008+1787C>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48857974 | |||||||
| chr17:48857974 | CAATAG | C | 36 | a0001c0001t0002g0121 a0001c0001t0002g0150 a0001c0001t0002g0155 others(33): Show |
36 | HG00558.hp2 HG01099.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.1008+1855_1008+185 others(9): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857974 | ||||||
| chr17:48857974 | CAATAGAA others(3): Show |
C | 25 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0242 others(22): Show |
25 | HG00423.hp1 HG00609.hp1 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.1008+1850_1008+185 others(14): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857974 | ||||||
| chr17:48857974 | CAATAGAA others(8): Show |
C | 3 | a0002c0003t0001g0138 a0002c0003t0001g0139 a0003c0002t0001g0168 |
3 | HG01891.hp1 NA19011.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1008+1845_1008+185 others(19): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857974 | ||||||
| chr17:48857974 | CAATAGAA others(13): Show |
C | 4 | a0002c0003t0004g0128 a0002c0003t0004g0129 a0003c0002t0001g0220 others(1): Show |
4 | HG02055.hp1 HG02886.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1008+1840_1008+185 others(24): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48857974 | ||||||
| chr17:48857978 | A | T | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.1008+1791A>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48857978 | |||||||
| chr17:48857983 | A | T | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.1008+1796A>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48857983 | |||||||
| chr17:48857988 | A | T | 49 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(46): Show |
50 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(47): Show |
intron_variant | MODIFIER | c.1008+1801A>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48857988 | |||||||
| chr17:48857993 | A | T | 5 | a0004c0004t0003g0094 a0004c0004t0005g0110 a0004c0004t0010g0084 others(2): Show |
5 | HG02630.hp1 HG02897.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1008+1806A>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48857993 | |||||||
| chr17:48858000 | A | G | 2 | a0002c0003t0001g0022 a0002c0003t0001g0052 |
2 | HG00323.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1008+1813A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858000 | |||||||
| chr17:48858006 | A | ATAGAGTA others(58): Show |
2 | a0001c0001t0002g0277 a0001c0001t0002g0300 |
2 | HG02056.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1008+1823_1008+182 others(69): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48858006 | ||||||
| chr17:48858006 | A | ATAGAGTA others(93): Show |
1 | a0001c0001t0002g0275 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1008+1823_1008+182 others(104): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48858006 | ||||||
| chr17:48858009 | G | GAATAGAA others(90): Show |
1 | a0001c0001t0002g0152 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1008+1833_1008+183 others(101): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48858009 | ||||||
| chr17:48858011 | A | ATAGAGTA others(43): Show |
1 | a0001c0001t0002g0270 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1008+1828_1008+182 others(54): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48858011 | ||||||
| chr17:48858011 | A | ATAGAGTA others(53): Show |
1 | a0001c0001t0002g0269 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1008+1828_1008+182 others(64): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48858011 | ||||||
| chr17:48858011 | A | ATAGAGTA others(58): Show |
1 | a0001c0001t0002g0287 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1008+1828_1008+182 others(69): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48858011 | ||||||
| chr17:48858011 | A | ATAGAGTA others(68): Show |
1 | a0001c0001t0002g0157 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1008+1828_1008+182 others(79): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48858011 | ||||||
| chr17:48858011 | A | ATAGAGTA others(88): Show |
1 | a0001c0001t0002g0274 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1008+1828_1008+182 others(99): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48858011 | ||||||
| chr17:48858011 | A | G | 3 | a0001c0001t0002g0275 a0001c0001t0002g0277 a0001c0001t0002g0300 |
3 | HG02056.hp2 NA18999.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1008+1824A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858011 | |||||||
| chr17:48858014 | G | GAATAGAG others(95): Show |
1 | a0001c0001t0002g0256 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1008+1833_1008+183 others(106): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48858014 | ||||||
| chr17:48858016 | A | ATAGAGTA others(53): Show |
2 | a0001c0001t0002g0169 a0001c0001t0002g0285 |
2 | NA19011.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1008+1833_1008+183 others(64): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48858016 | ||||||
| chr17:48858016 | A | ATAGAGTA others(58): Show |
2 | a0001c0001t0002g0273 a0001c0001t0002g0288 |
2 | NA18971.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1008+1833_1008+183 others(69): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48858016 | ||||||
| chr17:48858016 | A | ATAGAGTA others(63): Show |
2 | a0001c0001t0002g0160 a0001c0001t0002g0286 |
2 | HG01978.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.1008+1833_1008+183 others(74): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48858016 | ||||||
| chr17:48858016 | A | ATAGAGTA others(68): Show |
1 | a0001c0001t0006g0271 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1008+1833_1008+183 others(79): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48858016 | ||||||
| chr17:48858016 | A | G | 8 | a0001c0001t0002g0157 a0001c0001t0002g0269 a0001c0001t0002g0270 others(5): Show |
8 | HG01993.hp1 HG02056.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.1008+1829A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858016 | |||||||
| chr17:48858019 | GAATAGAA others(20): Show |
G | 1 | a0004c0004t0010g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1008+1860_1008+188 others(31): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48858019 | ||||||
| chr17:48858021 | A | ATAGAGTA others(48): Show |
1 | a0001c0001t0002g0002 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1008+1838_1008+183 others(59): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48858021 | ||||||
| chr17:48858021 | A | ATAGAGTA others(58): Show |
1 | a0001c0001t0002g0272 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1008+1838_1008+183 others(69): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48858021 | ||||||
| chr17:48858021 | A | ATAGAGTA others(68): Show |
1 | a0001c0001t0002g0304 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1008+1838_1008+183 others(79): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48858021 | ||||||
| chr17:48858021 | A | ATAGAGTA others(73): Show |
1 | a0001c0001t0002g0314 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1008+1838_1008+183 others(84): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48858021 | ||||||
| chr17:48858021 | A | G | 15 | a0001c0001t0002g0157 a0001c0001t0002g0160 a0001c0001t0002g0169 others(12): Show |
15 | HG01070.hp1 HG01978.hp1 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.1008+1834A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858021 | |||||||
| chr17:48858022 | T | TAGAATAG others(10): Show |
1 | a0002c0003t0001g0025 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1008+1837_1008+185 others(21): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48858022 | ||||||
| chr17:48858024 | GAATAGAA others(15): Show |
G | 3 | a0004c0004t0005g0107 a0004c0004t0005g0114 a0004c0004t0016g0001 |
3 | HG02559.hp2 HG02809.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1008+1860_1008+188 others(26): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48858024 | ||||||
| chr17:48858026 | A | ATAGAATA others(173): Show |
1 | a0001c0001t0002g0283 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(184): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48858026 | ||||||
| chr17:48858026 | A | ATAGAATA others(148): Show |
1 | a0001c0001t0022g0252 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(159): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48858026 | ||||||
| chr17:48858026 | A | ATAGAATA others(128): Show |
1 | a0001c0001t0002g0279 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(139): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48858026 | ||||||
| chr17:48858026 | A | ATAGAATA others(108): Show |
1 | a0001c0001t0021g0255 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(119): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48858026 | ||||||
| chr17:48858026 | A | ATAGAATA others(68): Show |
1 | a0001c0001t0002g0290 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1008+1848_1008+184 others(79): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48858026 | ||||||
| chr17:48858026 | A | G | 19 | a0001c0001t0002g0002 a0001c0001t0002g0157 a0001c0001t0002g0160 others(16): Show |
19 | HG00738.hp2 HG01070.hp1 HG01978.hp1 others(16): Show |
intron_variant | MODIFIER | c.1008+1839A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858026 | |||||||
| chr17:48858029 | G | GAATAGAA others(5): Show |
1 | a0003c0002t0001g0153 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1008+1843_1008+185 others(16): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48858029 | ||||||
| chr17:48858029 | GAATAGAA others(10): Show |
G | 13 | a0004c0004t0003g0077 a0004c0004t0003g0078 a0004c0004t0003g0083 others(10): Show |
13 | HG00673.hp1 HG01515.hp2 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.1008+1860_1008+187 others(21): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48858029 | ||||||
| chr17:48858031 | A | G | 3 | a0001c0001t0002g0002 a0001c0001t0002g0270 a0001c0001t0002g0314 |
3 | HG00738.hp2 HG02293.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1008+1844A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858031 | |||||||
| chr17:48858034 | GAATAGAA others(5): Show |
G | 17 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0079 others(14): Show |
17 | HG00741.hp1 HG02132.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1008+1860_1008+187 others(16): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48858034 | ||||||
| chr17:48858039 | GAATAGAA | G | 9 | a0004c0004t0003g0090 a0004c0004t0003g0093 a0004c0004t0003g0094 others(6): Show |
9 | HG00558.hp1 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1008+1860_1008+186 others(11): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48858039 | ||||||
| chr17:48858044 | GAA | G | 7 | a0002c0003t0001g0042 a0004c0004t0003g0116 a0004c0004t0005g0103 others(4): Show |
7 | HG02148.hp1 HG02280.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1008+1860_1008+186 others(6): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48858044 | ||||||
| chr17:48858045 | A | G | 1 | a0002c0003t0001g0049 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1008+1858A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858045 | |||||||
| chr17:48858046 | A | AAATAG | 4 | a0002c0003t0001g0138 a0002c0003t0001g0139 a0002c0003t0001g0140 others(1): Show |
4 | HG01891.hp1 HG02809.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1008+1883_1008+188 others(9): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48858046 | ||||||
| chr17:48858046 | A | AAATAGAA others(3): Show |
14 | a0001c0001t0002g0121 a0001c0001t0002g0242 a0001c0001t0002g0243 others(11): Show |
14 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.1008+1878_1008+188 others(14): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48858046 | ||||||
| chr17:48858046 | A | AAATAGAA others(8): Show |
5 | a0001c0001t0002g0262 a0003c0002t0001g0306 a0003c0002t0013g0214 others(2): Show |
5 | HG01515.hp1 HG01952.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.1008+1873_1008+188 others(19): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48858046 | ||||||
| chr17:48858046 | A | AAATAGAA others(13): Show |
54 | a0001c0001t0002g0251 a0001c0001t0002g0268 a0001c0001t0002g0314 others(51): Show |
54 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.1008+1868_1008+188 others(24): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48858046 | ||||||
| chr17:48858046 | A | AAATAGAA others(18): Show |
42 | a0001c0001t0002g0002 a0001c0001t0002g0156 a0001c0001t0002g0157 others(39): Show |
42 | HG00423.hp1 HG00738.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.1008+1863_1008+188 others(29): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48858046 | ||||||
| chr17:48858046 | A | AAATAGAA others(23): Show |
39 | a0001c0001t0002g0007 a0001c0001t0002g0160 a0001c0001t0002g0162 others(36): Show |
39 | HG00140.hp2 HG00639.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.1008+1887_1008+188 others(34): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48858046 | ||||||
| chr17:48858046 | A | AAATAGAA others(28): Show |
10 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(7): Show |
10 | HG02148.hp2 HG02257.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1008+1887_1008+188 others(39): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48858046 | ||||||
| chr17:48858046 | A | AAATAGAA others(33): Show |
8 | a0001c0001t0002g0010 a0001c0001t0002g0155 a0001c0001t0002g0236 others(5): Show |
8 | HG00323.hp1 HG01261.hp2 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.1008+1887_1008+188 others(44): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48858046 | ||||||
| chr17:48858046 | A | AAATAGAA others(38): Show |
1 | a0001c0001t0002g0008 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1008+1887_1008+188 others(49): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48858046 | ||||||
| chr17:48858046 | A | AAATAGAA others(43): Show |
1 | a0001c0001t0006g0302 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1008+1887_1008+188 others(54): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48858046 | ||||||
| chr17:48858046 | A | ATAG | 10 | a0001c0001t0002g0152 a0001c0001t0002g0256 a0001c0001t0002g0293 others(7): Show |
10 | HG01358.hp1 HG02040.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1008+1859_1008+186 others(7): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(16): Show |
1 | a0001c0001t0002g0163 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(27): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(21): Show |
1 | a0002c0003t0001g0052 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(32): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(26): Show |
1 | a0002c0003t0001g0022 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(37): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(73): Show |
1 | a0001c0001t0002g0260 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(84): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(88): Show |
1 | a0001c0001t0002g0250 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(99): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(56): Show |
1 | a0002c0003t0004g0136 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(67): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(76): Show |
1 | a0002c0003t0001g0059 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(87): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(123): Show |
1 | a0002c0003t0001g0030 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(134): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(109): Show |
1 | a0001c0001t0002g0295 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(120): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(111): Show |
1 | a0002c0003t0004g0135 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(122): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(131): Show |
1 | a0002c0003t0009g0240 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(142): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(166): Show |
1 | a0002c0003t0004g0326 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(177): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(174): Show |
1 | a0001c0001t0002g0294 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(185): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(176): Show |
1 | a0002c0003t0028g0316 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(187): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(186): Show |
1 | a0001c0001t0002g0282 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(197): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(191): Show |
2 | a0002c0003t0004g0324 a0002c0003t0009g0148 |
2 | HG02630.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1008+1859_1008+186 others(202): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(206): Show |
1 | a0002c0003t0004g0325 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(217): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(216): Show |
1 | a0002c0003t0004g0323 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(227): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(231): Show |
2 | a0002c0003t0001g0026 a0002c0003t0007g0064 |
2 | HG01257.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1008+1859_1008+186 others(242): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(236): Show |
1 | a0002c0003t0001g0051 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(247): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(241): Show |
3 | a0002c0003t0004g0137 a0002c0003t0007g0023 a0002c0003t0007g0062 |
3 | HG01258.hp2 HG02109.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1008+1859_1008+186 others(252): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(246): Show |
1 | a0002c0003t0001g0060 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(257): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(256): Show |
3 | a0001c0001t0002g0237 a0002c0003t0001g0058 a0002c0003t0008g0015 |
3 | HG01346.hp2 NA18999.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1008+1859_1008+186 others(267): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(266): Show |
1 | a0002c0003t0001g0055 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(277): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(271): Show |
4 | a0001c0001t0014g0284 a0002c0003t0001g0034 a0002c0003t0001g0039 others(1): Show |
4 | HG01106.hp2 HG01981.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.1008+1859_1008+186 others(282): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(276): Show |
1 | a0002c0003t0001g0043 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(287): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(281): Show |
1 | a0002c0003t0001g0056 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(292): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(286): Show |
2 | a0002c0003t0001g0037 a0002c0003t0001g0054 |
2 | HG01074.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1008+1859_1008+186 others(297): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(291): Show |
3 | a0002c0003t0001g0027 a0002c0003t0001g0045 a0002c0003t0004g0040 |
3 | HG01517.hp1 HG01981.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1008+1859_1008+186 others(302): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(296): Show |
3 | a0002c0003t0001g0028 a0002c0003t0001g0033 a0002c0003t0001g0066 |
3 | HG00639.hp2 HG02273.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1008+1859_1008+186 others(307): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(301): Show |
2 | a0001c0001t0002g0170 a0002c0003t0009g0239 |
2 | HG03704.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.1008+1859_1008+186 others(312): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(306): Show |
1 | a0002c0003t0001g0029 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(317): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(311): Show |
1 | a0002c0003t0001g0019 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(322): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(316): Show |
4 | a0002c0003t0001g0021 a0002c0003t0001g0044 a0002c0003t0008g0017 others(1): Show |
4 | HG03834.hp1 HG03942.hp2 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.1008+1859_1008+186 others(327): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(321): Show |
2 | a0002c0003t0004g0322 a0002c0003t0009g0238 |
2 | HG02071.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1008+1859_1008+186 others(332): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(326): Show |
1 | a0001c0001t0002g0267 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(337): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(331): Show |
1 | a0002c0003t0008g0016 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(342): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(336): Show |
1 | a0002c0003t0008g0013 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(347): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(336): Show |
2 | a0002c0003t0009g0312 a0002c0003t0029g0031 |
2 | HG03017.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1008+1859_1008+186 others(347): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(341): Show |
1 | a0002c0003t0001g0032 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(352): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(346): Show |
2 | a0002c0003t0025g0053 a0003c0002t0001g0070 |
2 | HG01081.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1008+1859_1008+186 others(357): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(351): Show |
1 | a0002c0003t0001g0057 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(362): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(366): Show |
1 | a0002c0003t0001g0036 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(377): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(371): Show |
1 | a0005c0007t0008g0014 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(382): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(386): Show |
1 | a0002c0003t0001g0020 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(397): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(396): Show |
1 | a0002c0003t0001g0035 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(407): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(401): Show |
1 | a0002c0003t0001g0046 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(412): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(426): Show |
1 | a0001c0001t0002g0292 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(437): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(466): Show |
1 | a0001c0001t0002g0231 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(477): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(474): Show |
1 | a0001c0001t0006g0291 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(485): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(310): Show |
1 | a0002c0003t0001g0063 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(321): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(183): Show |
1 | a0002c0003t0001g0024 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(194): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(173): Show |
1 | a0002c0003t0001g0038 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(184): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(148): Show |
1 | a0002c0003t0001g0050 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(159): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858046 | A | ATAGAATA others(78): Show |
1 | a0002c0003t0001g0047 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1008+1859_1008+186 others(89): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858046 | |||||||
| chr17:48858047 | A | T | 1 | a0002c0003t0001g0049 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1008+1860A>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858047 | |||||||
| chr17:48858049 | T | C | 1 | a0002c0003t0008g0013 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1008+1862T>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858049 | |||||||
| chr17:48858049 | T | G | 1 | a0002c0003t0001g0049 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1008+1862T>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858049 | |||||||
| chr17:48858050 | A | AGAATAGA others(177): Show |
1 | a0002c0003t0001g0061 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1008+1887_1008+188 others(188): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48858050 | ||||||
| chr17:48858051 | G | C | 2 | a0001c0001t0006g0291 a0005c0007t0008g0014 |
2 | NA18947.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.1008+1864G>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858051 | |||||||
| chr17:48858054 | T | TAG | 3 | a0002c0003t0001g0041 a0002c0003t0001g0042 a0002c0003t0001g0059 |
3 | HG01192.hp2 HG02074.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1008+1869_1008+187 others(6): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48858054 | ||||||
| chr17:48858056 | G | C | 2 | a0001c0001t0002g0294 a0001c0001t0002g0295 |
2 | HG00408.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.1008+1869G>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858056 | |||||||
| chr17:48858057 | A | G | 2 | a0002c0003t0004g0135 a0002c0003t0004g0136 |
2 | HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1008+1870A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858057 | |||||||
| chr17:48858061 | G | C | 1 | a0002c0003t0008g0015 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1008+1874G>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858061 | |||||||
| chr17:48858071 | G | C | 2 | a0002c0003t0009g0148 a0002c0003t0009g0240 |
2 | HG02738.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1008+1884G>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858071 | |||||||
| chr17:48858071 | G | GAATAGAA others(137): Show |
1 | a0001c0001t0002g0293 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1008+1887_1008+188 others(148): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48858071 | ||||||
| chr17:48858073 | A | ATAGAATA others(14): Show |
1 | a0003c0002t0001g0308 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1008+1887_1008+188 others(25): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48858073 | ||||||
| chr17:48858477 | G | A | 2 | a0002c0003t0004g0135 a0002c0003t0004g0136 |
2 | HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1009-1837G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858477 | |||||||
| chr17:48858572 | C | T | 1 | a0002c0003t0001g0032 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1009-1742C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858572 | |||||||
| chr17:48858626 | G | A | 1 | a0002c0003t0001g0027 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1009-1688G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858626 | |||||||
| chr17:48858700 | G | T | 1 | a0003c0002t0001g0222 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1009-1614G>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858700 | |||||||
| chr17:48858758 | T | G | 1 | a0003c0002t0001g0179 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1009-1556T>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858758 | |||||||
| chr17:48858792 | C | T | 103 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(100): Show |
103 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.1009-1522C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858792 | |||||||
| chr17:48858814 | G | C | 4 | a0004c0004t0003g0072 a0004c0004t0003g0117 a0004c0004t0003g0119 others(1): Show |
4 | NA18612.hp1 NA18960.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.1009-1500G>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858814 | |||||||
| chr17:48858977 | G | A | 1 | a0001c0001t0006g0310 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1009-1337G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48858977 | |||||||
| chr17:48859024 | C | T | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.1009-1290C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48859024 | |||||||
| chr17:48859045 | C | CA | 27 | a0001c0001t0002g0005 a0001c0001t0002g0150 a0001c0001t0002g0152 others(24): Show |
27 | HG00735.hp2 HG01106.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.1009-1241dupA | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48859045 | ||||||
| chr17:48859045 | C | CAAA | 48 | a0002c0003t0001g0019 a0002c0003t0001g0020 a0002c0003t0001g0021 others(45): Show |
48 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(45): Show |
intron_variant | MODIFIER | c.1009-1243_1009-124 others(7): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48859045 | ||||||
| chr17:48859045 | C | CAAAA | 9 | a0002c0003t0001g0022 a0002c0003t0001g0026 a0002c0003t0001g0041 others(6): Show |
9 | HG00741.hp2 HG01081.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.1009-1244_1009-124 others(8): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48859045 | ||||||
| chr17:48859045 | CA | C | 80 | a0001c0001t0002g0008 a0001c0001t0002g0282 a0001c0001t0006g0009 others(77): Show |
80 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.1009-1241delA | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48859045 | ||||||
| chr17:48859045 | CAA | C | 54 | a0002c0003t0009g0148 a0002c0003t0009g0238 a0002c0003t0009g0239 others(51): Show |
55 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.1009-1242_1009-124 others(6): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 48859045 | ||||||
| chr17:48859127 | T | C | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.1009-1187T>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48859127 | |||||||
| chr17:48859254 | C | A | 317 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(314): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.1009-1060C>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48859254 | |||||||
| chr17:48859470 | C | T | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.1009-844C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48859470 | |||||||
| chr17:48859612 | A | G | 2 | a0003c0002t0001g0153 a0003c0002t0004g0173 |
2 | NA18941.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.1009-702A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48859612 | |||||||
| chr17:48859678 | G | A | 2 | a0002c0003t0004g0135 a0002c0003t0004g0136 |
2 | HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1009-636G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48859678 | |||||||
| chr17:48859764 | T | C | 2 | a0001c0001t0002g0299 a0001c0001t0020g0327 |
2 | HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1009-550T>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48859764 | |||||||
| chr17:48859884 | C | T | 3 | a0002c0003t0001g0041 a0002c0003t0001g0042 a0002c0003t0001g0049 |
3 | HG00735.hp1 HG01192.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1009-430C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48859884 | |||||||
| chr17:48859893 | G | A | 1 | a0004c0004t0003g0095 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1009-421G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48859893 | |||||||
| chr17:48859960 | A | G | 103 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(100): Show |
103 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.1009-354A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48859960 | |||||||
| chr17:48860120 | T | C | 2 | a0003c0002t0001g0153 a0003c0002t0004g0173 |
2 | NA18941.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.1009-194T>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48860120 | |||||||
| chr17:48860311 | T | C | 1 | a0001c0001t0014g0284 | 1 | NA20805.hp2 | splice_region_variant&intron_variant | LOW | c.1009-3T>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 10/12 | chr17 | 48860311 | |||||||
| chr17:48860655 | C | T | 1 | a0002c0003t0029g0031 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1144+206C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 11/12 | chr17 | 48860655 | |||||||
| chr17:48860790 | G | GA | 4 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0163 others(1): Show |
4 | HG01261.hp2 HG01433.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.1144+342dupA | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 48860790 | ||||||
| chr17:48860819 | A | G | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.1144+370A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 11/12 | chr17 | 48860819 | |||||||
| chr17:48860978 | G | C | 1 | a0002c0003t0004g0122 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1144+529G>C | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 11/12 | chr17 | 48860978 | |||||||
| chr17:48861083 | T | G | 1 | a0002c0003t0001g0249 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1144+634T>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 11/12 | chr17 | 48861083 | |||||||
| chr17:48861090 | G | A | 1 | a0003c0002t0004g0223 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1144+641G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 11/12 | chr17 | 48861090 | |||||||
| chr17:48861094 | G | A | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.1144+645G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 11/12 | chr17 | 48861094 | |||||||
| chr17:48861178 | G | A | 2 | a0001c0001t0002g0003 a0001c0001t0006g0004 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1144+729G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 11/12 | chr17 | 48861178 | |||||||
| chr17:48861249 | C | A | 2 | a0001c0001t0002g0279 a0001c0001t0002g0283 |
2 | HG02135.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1144+800C>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 11/12 | chr17 | 48861249 | |||||||
| chr17:48861276 | C | T | 3 | a0001c0001t0002g0319 a0001c0001t0002g0320 a0001c0001t0014g0321 |
3 | HG01243.hp2 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1144+827C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 11/12 | chr17 | 48861276 | |||||||
| chr17:48861307 | C | T | 7 | a0002c0003t0009g0148 a0002c0003t0009g0238 a0002c0003t0009g0239 others(4): Show |
7 | HG02071.hp2 HG02738.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.1144+858C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 11/12 | chr17 | 48861307 | |||||||
| chr17:48861360 | C | T | 1 | a0001c0001t0006g0302 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1144+911C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 11/12 | chr17 | 48861360 | |||||||
| chr17:48861500 | C | T | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.1145-776C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 11/12 | chr17 | 48861500 | |||||||
| chr17:48861651 | A | G | 4 | a0001c0001t0002g0299 a0001c0001t0020g0327 a0002c0003t0001g0026 others(1): Show |
4 | HG02615.hp1 HG02647.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.1145-625A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 11/12 | chr17 | 48861651 | |||||||
| chr17:48861651 | ATG | A | 87 | a0002c0003t0001g0249 a0003c0002t0001g0067 a0003c0002t0001g0068 others(84): Show |
87 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1145-615_1145-614d others(4): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 48861651 | ||||||
| chr17:48861659 | G | GTA | 62 | a0002c0003t0001g0019 a0002c0003t0001g0020 a0002c0003t0001g0021 others(59): Show |
62 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(59): Show |
intron_variant | MODIFIER | c.1145-616_1145-615i others(4): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 48861659 | ||||||
| chr17:48861659 | G | GTATA | 97 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(94): Show |
97 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(94): Show |
intron_variant | MODIFIER | c.1145-616_1145-615i others(6): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 48861659 | ||||||
| chr17:48861659 | G | GTATATA | 7 | a0001c0001t0002g0259 a0001c0001t0002g0267 a0001c0001t0002g0309 others(4): Show |
7 | HG00323.hp1 HG00423.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1145-616_1145-615i others(8): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 48861659 | ||||||
| chr17:48861659 | G | GTATATAT others(1): Show |
13 | a0001c0001t0002g0121 a0001c0001t0002g0150 a0001c0001t0002g0242 others(10): Show |
13 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.1145-616_1145-615i others(10): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 48861659 | ||||||
| chr17:48861659 | G | GTATATAT others(5): Show |
4 | a0004c0004t0003g0079 a0004c0004t0003g0092 a0004c0004t0003g0093 others(1): Show |
4 | HG00741.hp1 HG01255.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.1145-616_1145-615i others(14): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 48861659 | ||||||
| chr17:48861659 | G | GTATATAT others(7): Show |
23 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(20): Show |
24 | HG00558.hp1 HG00673.hp1 HG01515.hp2 others(21): Show |
intron_variant | MODIFIER | c.1145-616_1145-615i others(16): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 48861659 | ||||||
| chr17:48861659 | G | GTATATAT others(9): Show |
1 | a0004c0004t0012g0075 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1145-616_1145-615i others(18): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 48861659 | ||||||
| chr17:48861659 | G | GTATATAT others(15): Show |
3 | a0004c0004t0005g0098 a0004c0004t0005g0100 a0004c0004t0005g0111 |
3 | HG01069.hp2 HG01071.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1145-616_1145-615i others(24): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 48861659 | ||||||
| chr17:48861659 | G | GTATATAT others(17): Show |
1 | a0004c0004t0005g0110 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1145-616_1145-615i others(26): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 48861659 | ||||||
| chr17:48861659 | G | GTATATAT others(19): Show |
3 | a0004c0004t0005g0101 a0004c0004t0010g0096 a0004c0004t0012g0076 |
3 | HG03540.hp1 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1145-616_1145-615i others(28): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 48861659 | ||||||
| chr17:48861659 | G | GTATATAT others(21): Show |
5 | a0004c0004t0005g0103 a0004c0004t0005g0107 a0004c0004t0005g0112 others(2): Show |
5 | HG02559.hp2 HG02647.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1145-616_1145-615i others(30): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 48861659 | ||||||
| chr17:48861659 | G | GTATATAT others(23): Show |
4 | a0004c0004t0005g0109 a0004c0004t0005g0115 a0004c0004t0011g0073 others(1): Show |
4 | HG02976.hp1 HG03041.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1145-616_1145-615i others(32): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 48861659 | ||||||
| chr17:48861659 | G | GTATATAT others(25): Show |
5 | a0004c0004t0005g0104 a0004c0004t0005g0105 a0004c0004t0005g0106 others(2): Show |
5 | HG02280.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1145-616_1145-615i others(34): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 48861659 | ||||||
| chr17:48861661 | G | A | 229 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(226): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1145-615G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 11/12 | chr17 | 48861661 | |||||||
| chr17:48861675 | A | G | 1 | a0004c0004t0019g0099 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1145-601A>G | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 11/12 | chr17 | 48861675 | |||||||
| chr17:48861677 | A | ATATATAT others(30): Show |
1 | a0004c0004t0019g0099 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1145-599_1145-598i others(39): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 11/12 | chr17 | 48861677 | |||||||
| chr17:48861682 | C | CTG | 10 | a0002c0003t0001g0066 a0002c0003t0001g0131 a0002c0003t0001g0138 others(7): Show |
10 | HG00408.hp1 HG01891.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.1145-571_1145-570d others(4): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 48861682 | ||||||
| chr17:48861682 | CTG | C | 156 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0006 others(153): Show |
157 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.1145-571_1145-570d others(4): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 48861682 | ||||||
| chr17:48862013 | C | T | 1 | a0002c0005t0004g0125 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1145-263C>T | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 11/12 | chr17 | 48862013 | |||||||
| chr17:48862048 | CA | C | 246 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(243): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.1145-212delA | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 48862048 | ||||||
| chr17:48862048 | CAA | C | 12 | a0001c0001t0006g0310 a0003c0002t0001g0151 a0003c0002t0001g0174 others(9): Show |
12 | HG00438.hp2 HG00558.hp2 HG02132.hp1 others(9): Show |
intron_variant | MODIFIER | c.1145-213_1145-212d others(4): Show |
CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 48862048 | ||||||
| chr17:48862064 | AT | A | 3 | a0002c0003t0001g0028 a0002c0003t0001g0033 a0002c0003t0001g0057 |
3 | HG00639.hp2 HG02273.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1145-211delT | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 11/12 | chr17 | 48862064 | |||||||
| chr17:48862065 | T | A | 4 | a0002c0003t0001g0020 a0002c0003t0001g0034 a0002c0003t0001g0044 others(1): Show |
4 | HG01106.hp2 NA18968.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.1145-211T>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 11/12 | chr17 | 48862065 | |||||||
| chr17:48862133 | G | A | 50 | a0004c0004t0003g0072 a0004c0004t0003g0074 a0004c0004t0003g0077 others(47): Show |
51 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.1145-143G>A | CALCOCO2 | ENSG00000136436.15 | transcript | ENST00000258947.8 | protein_coding | 11/12 | chr17 | 48862133 |