Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 840 |
| ensemblid | ENSG00000165806.21 |
| hgncid | 1508 |
| symbol | CASP7 |
| name | caspase 7 |
| refseq_nuc | NM_001227.5 |
| refseq_prot | NP_001218.1 |
| ensembl_nuc | ENST00000369318.8 |
| ensembl_prot | ENSP00000358324.4 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 113679912 |
| end | 113730905 |
| strand | + |
| ver | v1.2 |
| region | chr10:113679912-113730905 |
| region5000 | chr10:113674912-113735905 |
| regionname0 | CASP7_chr10_113679912_113730905 |
| regionname5000 | CASP7_chr10_113674912_113735905 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 303 | 250 | 68 | 42 | 99 | 9 | 30 | 70 | CASP7_chr10_113674912_113735905 | CASP7 | MADDQ others(298): Show |
chr10 | 113674912 | 113735905 |
| a0002 | 0/0 | 303 | 112 | 14 | 24 | 62 | 3 | 9 | 48 | CASP7_chr10_113674912_113735905 | CASP7 | MADDQ others(298): Show |
chr10 | 113674912 | 113735905 |
| a0003 | 0/0 | 303 | 39 | 10 | 11 | 14 | 2 | 2 | 11 | CASP7_chr10_113674912_113735905 | CASP7 | MADEQ others(298): Show |
chr10 | 113674912 | 113735905 |
| a0004 | 0/0 | 303 | 3 | 1 | 0 | 1 | 0 | 1 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | MADEQ others(298): Show |
chr10 | 113674912 | 113735905 |
| a0005 | 0/0 | 303 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | MADDQ others(298): Show |
chr10 | 113674912 | 113735905 |
| a0006 | 0/0 | 309 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | MADDQ others(304): Show |
chr10 | 113674912 | 113735905 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 909 | 243 | 64 | 41 | 99 | 9 | 28 | CASP7_chr10_113674912_113735905 | CASP7 | ATGGC others(904): Show |
chr10 | 113674912 | 113735905 | ||
| a0001c0005 | 0/0 | 909 | 2 | 2 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | ATGGC others(904): Show |
chr10 | 113674912 | 113735905 | ||
| a0001c0008 | 0/0 | 909 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | ATGGC others(904): Show |
chr10 | 113674912 | 113735905 | ||
| a0001c0010 | 0/0 | 909 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | ATGGC others(904): Show |
chr10 | 113674912 | 113735905 | ||
| a0001c0011 | 0/0 | 909 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | ATGGC others(904): Show |
chr10 | 113674912 | 113735905 | ||
| a0001c0012 | 0/0 | 909 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | ATGGC others(904): Show |
chr10 | 113674912 | 113735905 | ||
| a0001c0013 | 0/0 | 909 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | ATGGC others(904): Show |
chr10 | 113674912 | 113735905 | ||
| a0002c0002 | 0/0 | 909 | 110 | 12 | 24 | 62 | 3 | 9 | CASP7_chr10_113674912_113735905 | CASP7 | ATGGC others(904): Show |
chr10 | 113674912 | 113735905 | ||
| a0002c0006 | 0/0 | 909 | 2 | 2 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | ATGGC others(904): Show |
chr10 | 113674912 | 113735905 | ||
| a0003c0003 | 0/0 | 909 | 39 | 10 | 11 | 14 | 2 | 2 | CASP7_chr10_113674912_113735905 | CASP7 | ATGGC others(904): Show |
chr10 | 113674912 | 113735905 | ||
| a0004c0004 | 0/0 | 909 | 3 | 1 | 0 | 1 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | ATGGC others(904): Show |
chr10 | 113674912 | 113735905 | ||
| a0005c0007 | 0/0 | 909 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | ATGGC others(904): Show |
chr10 | 113674912 | 113735905 | ||
| a0006c0009 | 0/0 | 927 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | ATGGC others(922): Show |
chr10 | 113674912 | 113735905 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 2344 | 39 | 10 | 3 | 19 | 2 | 5 | CASP7_chr10_113674912_113735905 | CASP7 | AGACC others(2339): Show |
chr10 | 113674912 | 113735905 |
| a0001c0001t0003 | 0/0 | 2344 | 71 | 26 | 6 | 25 | 2 | 12 | CASP7_chr10_113674912_113735905 | CASP7 | AGACC others(2339): Show |
chr10 | 113674912 | 113735905 |
| a0001c0001t0004 | 0/1 | 2344 | 60 | 17 | 20 | 14 | 3 | 5 | CASP7_chr10_113674912_113735905 | CASP7 | AGACC others(2339): Show |
chr10 | 113674912 | 113735905 |
| a0001c0001t0005 | 1/0 | 2344 | 50 | 6 | 10 | 25 | 2 | 6 | CASP7_chr10_113674912_113735905 | CASP7 | AGACC others(2339): Show |
chr10 | 113674912 | 113735905 |
| a0001c0001t0006 | 0/0 | 2344 | 6 | 0 | 0 | 6 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | AGACC others(2339): Show |
chr10 | 113674912 | 113735905 |
| a0001c0001t0007 | 0/0 | 2344 | 6 | 0 | 0 | 6 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | AGACC others(2339): Show |
chr10 | 113674912 | 113735905 |
| a0001c0001t0008 | 0/0 | 2344 | 2 | 2 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | AGACC others(2339): Show |
chr10 | 113674912 | 113735905 |
| a0001c0001t0009 | 0/0 | 2344 | 2 | 2 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | AGACC others(2339): Show |
chr10 | 113674912 | 113735905 |
| a0001c0001t0010 | 0/0 | 2344 | 2 | 1 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | AGACC others(2339): Show |
chr10 | 113674912 | 113735905 |
| a0001c0001t0011 | 0/0 | 2344 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | AGACC others(2339): Show |
chr10 | 113674912 | 113735905 |
| a0001c0001t0014 | 0/0 | 2344 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | AGACC others(2339): Show |
chr10 | 113674912 | 113735905 |
| a0001c0001t0015 | 0/0 | 2344 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | AGACC others(2339): Show |
chr10 | 113674912 | 113735905 |
| a0001c0001t0016 | 0/0 | 2344 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | AGACC others(2339): Show |
chr10 | 113674912 | 113735905 |
| a0001c0001t0018 | 0/0 | 2344 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | AGACC others(2339): Show |
chr10 | 113674912 | 113735905 |
| a0001c0005t0002 | 0/0 | 2344 | 2 | 2 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | AGACC others(2339): Show |
chr10 | 113674912 | 113735905 |
| a0001c0008t0002 | 0/0 | 2344 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | AGACC others(2339): Show |
chr10 | 113674912 | 113735905 |
| a0001c0010t0005 | 0/0 | 2344 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | AGACC others(2339): Show |
chr10 | 113674912 | 113735905 |
| a0001c0011t0017 | 0/0 | 2344 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | AGACC others(2339): Show |
chr10 | 113674912 | 113735905 |
| a0001c0012t0002 | 0/0 | 2344 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | AGACC others(2339): Show |
chr10 | 113674912 | 113735905 |
| a0001c0013t0005 | 0/0 | 2344 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | AGACC others(2339): Show |
chr10 | 113674912 | 113735905 |
| a0002c0002t0001 | 0/0 | 2344 | 108 | 12 | 23 | 61 | 3 | 9 | CASP7_chr10_113674912_113735905 | CASP7 | AGACC others(2339): Show |
chr10 | 113674912 | 113735905 |
| a0002c0002t0012 | 0/0 | 2344 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | AGACC others(2339): Show |
chr10 | 113674912 | 113735905 |
| a0002c0002t0013 | 0/0 | 2344 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | AGACC others(2339): Show |
chr10 | 113674912 | 113735905 |
| a0002c0006t0001 | 0/0 | 2344 | 2 | 2 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | AGACC others(2339): Show |
chr10 | 113674912 | 113735905 |
| a0003c0003t0002 | 0/0 | 2344 | 33 | 4 | 11 | 14 | 2 | 2 | CASP7_chr10_113674912_113735905 | CASP7 | AGACC others(2339): Show |
chr10 | 113674912 | 113735905 |
| a0003c0003t0005 | 0/0 | 2344 | 5 | 5 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | AGACC others(2339): Show |
chr10 | 113674912 | 113735905 |
| a0003c0003t0019 | 0/0 | 2344 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | AGACC others(2339): Show |
chr10 | 113674912 | 113735905 |
| a0004c0004t0001 | 0/0 | 2344 | 3 | 1 | 0 | 1 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | AGACC others(2339): Show |
chr10 | 113674912 | 113735905 |
| a0005c0007t0004 | 0/0 | 2344 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | AGACC others(2339): Show |
chr10 | 113674912 | 113735905 |
| a0006c0009t0003 | 0/0 | 2362 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | AGACC others(2357): Show |
chr10 | 113674912 | 113735905 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0002g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0017 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0003g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0158 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0004g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0001 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0044 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0005g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0006g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0006g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0006g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0006g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0006g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0006g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0007g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0007g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0007g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0007g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0008g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0009g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0009g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0010g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0010g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0011g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0014g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0015g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0016g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0001t0018g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0005t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0005t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0008t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0010t0005g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0011t0017g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0012t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0001c0013t0005g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0006 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0012g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0002t0013g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0006t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0002c0006t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0005g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0005g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0005g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0003c0003t0019g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0004c0004t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0004c0004t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0004c0004t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0005c0007t0004g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| a0006c0009t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0326 | EUR | GBR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0106 | EUR | GBR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0165 | EUR | FIN | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0081 | EUR | FIN | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0070 | EUR | FIN | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0186 | EUR | FIN | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | CHS | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0368 | EAS | CHS | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0300 | EAS | CHS | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00423 | hp2 | a0001 | c0001 | t0004 | g0033 | EAS | CHS | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | CHS | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0360 | EAS | CHS | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0353 | EAS | CHS | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | CHS | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00558 | hp1 | a0003 | c0003 | t0002 | g0140 | EAS | CHS | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0190 | EAS | CHS | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00597 | hp2 | a0001 | c0001 | t0006 | g0099 | EAS | CHS | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | CHS | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00621 | hp2 | a0001 | c0001 | t0004 | g0034 | EAS | CHS | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00639 | hp1 | a0001 | c0001 | t0005 | g0001 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0341 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00642 | hp1 | a0003 | c0003 | t0002 | g0143 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0072 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0105 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00733 | hp2 | a0001 | c0001 | t0005 | g0011 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00735 | hp1 | a0005 | c0007 | t0004 | g0069 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0346 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0225 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0084 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0151 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0036 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01069 | hp1 | a0003 | c0003 | t0002 | g0126 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0182 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0071 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0025 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0025 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01071 | hp2 | a0003 | c0003 | t0002 | g0127 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0245 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01081 | hp2 | a0001 | c0001 | t0005 | g0114 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01099 | hp1 | a0001 | c0001 | t0005 | g0045 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0351 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01106 | hp1 | a0003 | c0003 | t0002 | g0119 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0347 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0366 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01109 | hp2 | a0001 | c0001 | t0014 | g0153 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01168 | hp1 | a0003 | c0003 | t0002 | g0003 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0239 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01169 | hp1 | a0003 | c0003 | t0002 | g0003 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0354 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0175 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01175 | hp2 | a0003 | c0003 | t0002 | g0003 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0074 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0160 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01243 | hp1 | a0003 | c0003 | t0002 | g0144 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01243 | hp2 | a0001 | c0001 | t0010 | g0227 | AMR | PUR | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0338 | AMR | CLM | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0311 | AMR | CLM | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0339 | AMR | CLM | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01256 | hp2 | a0001 | c0001 | t0005 | g0001 | AMR | CLM | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0285 | AMR | CLM | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01257 | hp2 | a0001 | c0001 | t0004 | g0161 | AMR | CLM | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01258 | hp1 | a0001 | c0001 | t0005 | g0001 | AMR | CLM | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0157 | AMR | CLM | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0096 | AMR | CLM | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01261 | hp2 | a0003 | c0003 | t0002 | g0146 | AMR | CLM | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01346 | hp1 | a0003 | c0003 | t0002 | g0145 | AMR | CLM | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01346 | hp2 | a0001 | c0001 | t0005 | g0063 | AMR | CLM | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0203 | AMR | CLM | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0089 | AMR | CLM | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0355 | AMR | CLM | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0064 | AMR | CLM | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0263 | AMR | CLM | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0238 | AMR | CLM | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0087 | AMR | CLM | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0291 | AMR | CLM | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0242 | EUR | IBS | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01515 | hp2 | a0003 | c0003 | t0002 | g0142 | EUR | IBS | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01517 | hp1 | a0003 | c0003 | t0002 | g0149 | EUR | IBS | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0274 | EUR | IBS | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0020 | AFR | ACB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0292 | AFR | ACB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0154 | AFR | ACB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0295 | AFR | ACB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0038 | AMR | PEL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01928 | hp2 | a0002 | c0002 | t0012 | g0342 | AMR | PEL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0269 | AMR | PEL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01943 | hp2 | a0001 | c0001 | t0005 | g0029 | AMR | PEL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01952 | hp1 | a0001 | c0010 | t0005 | g0104 | AMR | PEL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0090 | AMR | PEL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0010 | AMR | PEL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0359 | AMR | PEL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01978 | hp1 | a0001 | c0001 | t0005 | g0042 | AMR | PEL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01978 | hp2 | a0001 | c0001 | t0004 | g0043 | AMR | PEL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0024 | AMR | PEL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01981 | hp2 | a0001 | c0001 | t0005 | g0091 | AMR | PEL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02004 | hp1 | a0001 | c0001 | t0004 | g0010 | AMR | PEL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0344 | AMR | PEL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0304 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0348 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0218 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0309 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0261 | AFR | ACB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0327 | AFR | ACB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0345 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0178 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02071 | hp2 | a0001 | c0001 | t0005 | g0049 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0216 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02074 | hp2 | a0001 | c0001 | t0005 | g0324 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02080 | hp1 | a0001 | c0001 | t0005 | g0052 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0333 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0196 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0075 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02129 | hp1 | a0001 | c0001 | t0005 | g0009 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02129 | hp2 | a0003 | c0003 | t0002 | g0134 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0332 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02132 | hp2 | a0001 | c0001 | t0018 | g0176 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02135 | hp1 | a0001 | c0001 | t0004 | g0080 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0289 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0228 | AFR | ACB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0020 | AFR | ACB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | CDX | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0323 | EAS | CDX | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0267 | EAS | CDX | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02165 | hp2 | a0001 | c0001 | t0005 | g0191 | EAS | CDX | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02257 | hp1 | a0004 | c0004 | t0001 | g0115 | AFR | ACB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0286 | AFR | ACB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0362 | AFR | ACB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02258 | hp2 | a0001 | c0001 | t0008 | g0027 | AFR | ACB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02273 | hp1 | a0001 | c0001 | t0004 | g0085 | AMR | PEL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0290 | AMR | PEL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02293 | hp1 | a0001 | c0001 | t0004 | g0086 | AMR | PEL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02293 | hp2 | a0001 | c0001 | t0004 | g0039 | AMR | PEL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02300 | hp1 | a0001 | c0001 | t0004 | g0214 | AMR | PEL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0162 | AMR | PEL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0293 | AFR | ACB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0200 | AFR | ACB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02523 | hp1 | a0001 | c0001 | t0005 | g0056 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | KHV | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02572 | hp1 | a0001 | c0001 | t0009 | g0370 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0256 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0181 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02602 | hp2 | a0001 | c0001 | t0005 | g0041 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0152 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02622 | hp2 | a0001 | c0001 | t0009 | g0361 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02630 | hp1 | a0003 | c0003 | t0019 | g0147 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0226 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02647 | hp1 | a0003 | c0003 | t0005 | g0123 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02647 | hp2 | a0002 | c0006 | t0001 | g0111 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0006 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0006 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0287 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0156 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02717 | hp1 | a0003 | c0003 | t0005 | g0002 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0013 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0330 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0265 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0211 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0213 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0257 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0229 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0030 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0224 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0260 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0364 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0363 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0204 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02922 | hp1 | a0003 | c0003 | t0005 | g0002 | AFR | ESN | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02922 | hp2 | a0003 | c0003 | t0002 | g0125 | AFR | ESN | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0208 | AFR | ESN | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0317 | AFR | ESN | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0316 | AFR | ESN | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0026 | AFR | ESN | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02976 | hp1 | a0001 | c0011 | t0017 | g0369 | AFR | ESN | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0319 | AFR | ESN | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03017 | hp1 | a0001 | c0008 | t0002 | g0236 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0159 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03041 | hp1 | a0003 | c0003 | t0002 | g0117 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0210 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03098 | hp1 | a0001 | c0012 | t0002 | g0113 | AFR | MSL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0331 | AFR | MSL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03130 | hp1 | a0003 | c0003 | t0002 | g0116 | AFR | ESN | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0352 | AFR | ESN | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03139 | hp1 | a0006 | c0009 | t0003 | g0201 | AFR | ESN | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0026 | AFR | ESN | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0241 | AFR | ESN | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0014 | AFR | ESN | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0205 | AFR | MSL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | MSL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03225 | hp1 | a0003 | c0003 | t0005 | g0130 | AFR | MSL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03225 | hp2 | a0001 | c0001 | t0010 | g0202 | AFR | MSL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03239 | hp1 | a0001 | c0001 | t0005 | g0050 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0179 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0240 | AFR | MSL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0296 | AFR | MSL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0155 | AFR | MSL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0199 | AFR | MSL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03490 | hp1 | a0001 | c0001 | t0005 | g0001 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0321 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03491 | hp1 | a0001 | c0001 | t0004 | g0356 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0221 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0322 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0222 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0350 | AFR | ESN | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03516 | hp2 | a0001 | c0005 | t0002 | g0254 | AFR | ESN | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03540 | hp2 | a0002 | c0006 | t0001 | g0110 | AFR | GWD | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0328 | AFR | MSL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0223 | AFR | MSL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03654 | hp1 | a0001 | c0001 | t0005 | g0060 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03654 | hp2 | a0004 | c0004 | t0001 | g0136 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0246 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0167 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0357 | SAS | STU | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03688 | hp2 | a0001 | c0013 | t0005 | g0054 | SAS | STU | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0180 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03704 | hp2 | a0003 | c0003 | t0002 | g0124 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0284 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03710 | hp2 | a0001 | c0001 | t0004 | g0088 | SAS | PJL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0301 | SAS | BEB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0017 | SAS | BEB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0187 | SAS | BEB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0318 | SAS | BEB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03927 | hp1 | a0001 | c0001 | t0005 | g0061 | SAS | BEB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0163 | SAS | BEB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0170 | SAS | BEB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0298 | SAS | BEB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0171 | SAS | STU | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0082 | SAS | STU | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0302 | SAS | BEB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0197 | SAS | BEB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG04199 | hp1 | a0003 | c0003 | t0002 | g0131 | SAS | STU | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0248 | SAS | STU | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0212 | AFR | YRI | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0232 | AFR | YRI | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18612 | hp1 | a0001 | c0001 | t0006 | g0078 | EAS | CHB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18612 | hp2 | a0003 | c0003 | t0002 | g0132 | EAS | CHB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | CHB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0281 | EAS | CHB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0198 | AFR | YRI | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | YRI | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18943 | hp2 | a0001 | c0001 | t0004 | g0068 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18945 | hp2 | a0003 | c0003 | t0002 | g0129 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0358 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0276 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0288 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18947 | hp2 | a0001 | c0001 | t0004 | g0097 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18948 | hp1 | a0002 | c0002 | t0001 | g0183 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0234 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18956 | hp1 | a0001 | c0001 | t0005 | g0092 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0280 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18960 | hp1 | a0001 | c0001 | t0005 | g0059 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18960 | hp2 | a0003 | c0003 | t0002 | g0121 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18963 | hp2 | a0001 | c0001 | t0005 | g0058 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0303 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18964 | hp2 | a0003 | c0003 | t0002 | g0141 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0320 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18965 | hp2 | a0001 | c0001 | t0005 | g0035 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18966 | hp1 | a0001 | c0001 | t0005 | g0279 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18969 | hp1 | a0001 | c0001 | t0007 | g0005 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18969 | hp2 | a0001 | c0001 | t0005 | g0037 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18970 | hp1 | a0001 | c0001 | t0005 | g0062 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18971 | hp1 | a0001 | c0001 | t0006 | g0077 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18971 | hp2 | a0001 | c0001 | t0007 | g0019 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18973 | hp1 | a0001 | c0001 | t0007 | g0217 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0294 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18974 | hp2 | a0001 | c0001 | t0005 | g0093 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0336 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18978 | hp1 | a0003 | c0003 | t0002 | g0133 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0272 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18979 | hp1 | a0001 | c0001 | t0011 | g0100 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0308 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18981 | hp1 | a0001 | c0001 | t0015 | g0016 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18981 | hp2 | a0003 | c0003 | t0002 | g0150 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0164 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0305 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18985 | hp2 | a0001 | c0001 | t0004 | g0083 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0278 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18986 | hp2 | a0003 | c0003 | t0002 | g0135 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18988 | hp2 | a0001 | c0001 | t0005 | g0048 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18990 | hp1 | a0003 | c0003 | t0002 | g0148 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18991 | hp1 | a0001 | c0001 | t0004 | g0095 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18992 | hp1 | a0002 | c0002 | t0001 | g0337 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18993 | hp1 | a0001 | c0001 | t0004 | g0073 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18998 | hp1 | a0002 | c0002 | t0013 | g0266 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18998 | hp2 | a0001 | c0001 | t0005 | g0040 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0270 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0046 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19000 | hp1 | a0001 | c0001 | t0006 | g0032 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0334 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0249 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19004 | hp1 | a0001 | c0001 | t0007 | g0220 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0282 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19006 | hp1 | a0001 | c0001 | t0005 | g0067 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19007 | hp1 | a0001 | c0001 | t0016 | g0047 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0255 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0310 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19009 | hp2 | a0001 | c0001 | t0007 | g0019 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19012 | hp1 | a0001 | c0001 | t0005 | g0009 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19012 | hp2 | a0003 | c0003 | t0002 | g0128 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0109 | AFR | LWK | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0209 | AFR | LWK | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | LWK | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0365 | AFR | LWK | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0297 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19054 | hp2 | a0003 | c0003 | t0002 | g0120 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19055 | hp1 | a0003 | c0003 | t0002 | g0122 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19055 | hp2 | a0001 | c0001 | t0005 | g0065 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0184 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19062 | hp2 | a0001 | c0001 | t0005 | g0066 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0307 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19067 | hp1 | a0001 | c0001 | t0004 | g0299 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19067 | hp2 | a0001 | c0001 | t0005 | g0028 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19072 | hp1 | a0001 | c0001 | t0004 | g0102 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19072 | hp2 | a0002 | c0002 | t0001 | g0283 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19074 | hp1 | a0001 | c0001 | t0007 | g0005 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0306 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19075 | hp1 | a0001 | c0001 | t0005 | g0057 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19075 | hp2 | a0002 | c0002 | t0001 | g0343 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19077 | hp1 | a0004 | c0004 | t0001 | g0137 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19077 | hp2 | a0002 | c0002 | t0001 | g0264 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19079 | hp1 | a0001 | c0001 | t0006 | g0098 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0273 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19080 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19080 | hp2 | a0003 | c0003 | t0002 | g0138 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0268 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19085 | hp1 | a0001 | c0001 | t0005 | g0055 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0262 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19088 | hp1 | a0001 | c0001 | t0005 | g0053 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0275 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0271 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19090 | hp2 | a0001 | c0001 | t0006 | g0079 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0277 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0230 | AFR | YRI | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0258 | AFR | YRI | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA20129 | hp1 | a0001 | c0001 | t0008 | g0027 | AFR | ASW | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0169 | AFR | ASW | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0335 | EUR | TSI | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA20752 | hp2 | a0001 | c0001 | t0005 | g0107 | EUR | TSI | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA20805 | hp1 | a0001 | c0001 | t0005 | g0011 | EUR | TSI | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0237 | EUR | TSI | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA20905 | hp1 | a0001 | c0001 | t0005 | g0094 | SAS | GIH | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0243 | SAS | GIH | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0340 | AMR | CLM | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG01123 | hp2 | a0003 | c0003 | t0002 | g0139 | AMR | CLM | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0206 | AFR | ACB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0329 | AFR | ACB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0051 | AFR | ACB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0014 | AFR | ACB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02559 | hp1 | a0001 | c0005 | t0002 | g0031 | AFR | ACB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0108 | AFR | ACB | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0367 | AFR | MSL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG03471 | hp2 | a0003 | c0003 | t0002 | g0118 | AFR | MSL | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG06807 | hp1 | a0003 | c0003 | t0005 | g0002 | AFR | USA | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0325 | AFR | USA | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18955 | hp1 | a0001 | c0001 | t0005 | g0076 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0349 | AFR | USA | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0101 | AFR | USA | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0103 | AFR | LWK | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0207 | AFR | LWK | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0158 | REF | REF | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0005 | g0044 | REF | REF | CASP7_chr10_113674912_113735905 | CASP7 | chr10 | 113674912 | 113735905 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:113697505 | T | G | 2 | a0003 a0004 |
42 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(39): Show |
missense_variant | MODERATE | c.12T>G | p.Asp4Glu | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/7 | 79/2344 | 12/912 | 4/303 | chr10 | 113697505 | |||
| chr10:113726320 | G | A | 1 | a0005 | 1 | HG00735.hp1 | missense_variant | MODERATE | c.568G>A | p.Glu190Lys | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/7 | 635/2344 | 568/912 | 190/303 | chr10 | 113726320 | |||
| chr10:113729393 | C | G | 2 | a0002 a0004 |
115 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(112): Show |
missense_variant | MODERATE | c.765C>G | p.Asp255Glu | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 7/7 | 832/2344 | 765/912 | 255/303 | chr10 | 113729393 | |||
| chr10:113729503 | T | TCTCCATG others(11): Show |
1 | a0006 | 1 | HG03139.hp1 | conservative_inframe_insertion | MODERATE | c.885_886insCGCAGGTA others(10): Show |
p.Leu295_Thr296insAr others(16): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 7/7 | 953/2344 | 886/912 | 296/303 | INFO_REALIGN_3_PRIME | chr10 | 113729503 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:113721712 | C | T | 1 | a0002c0006 | 2 | HG02647.hp2 HG03540.hp2 |
synonymous_variant | LOW | c.309C>T | p.Ser103Ser | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/7 | 376/2344 | 309/912 | 103/303 | chr10 | 113721712 | |||
| chr10:113725399 | C | T | 1 | a0001c0013 | 1 | HG03688.hp2 | synonymous_variant | LOW | c.414C>T | p.Ala138Ala | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 5/7 | 481/2344 | 414/912 | 138/303 | chr10 | 113725399 | |||
| chr10:113725480 | C | T | 1 | a0001c0012 | 1 | HG03098.hp1 | synonymous_variant | LOW | c.495C>T | p.His165His | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 5/7 | 562/2344 | 495/912 | 165/303 | chr10 | 113725480 | |||
| chr10:113725519 | C | T | 1 | a0001c0011 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.534C>T | p.Pro178Pro | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 5/7 | 601/2344 | 534/912 | 178/303 | chr10 | 113725519 | |||
| chr10:113729321 | G | A | 1 | a0001c0005 | 2 | HG02559.hp1 HG03516.hp2 |
synonymous_variant | LOW | c.693G>A | p.Ser231Ser | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 7/7 | 760/2344 | 693/912 | 231/303 | chr10 | 113729321 | |||
| chr10:113729408 | G | A | 3 | a0002c0002 a0002c0006 a0004c0004 |
115 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(112): Show |
synonymous_variant | LOW | c.780G>A | p.Gln260Gln | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 7/7 | 847/2344 | 780/912 | 260/303 | chr10 | 113729408 | |||
| chr10:113729495 | C | T | 1 | a0001c0010 | 1 | HG01952.hp1 | synonymous_variant | LOW | c.867C>T | p.Pro289Pro | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 7/7 | 934/2344 | 867/912 | 289/303 | chr10 | 113729495 | |||
| chr10:113729537 | A | G | 1 | a0001c0008 | 1 | HG03017.hp1 | synonymous_variant | LOW | c.909A>G | p.Gln303Gln | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 7/7 | 976/2344 | 909/912 | 303/303 | chr10 | 113729537 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:113679932 | C | A | 1 | a0001c0001t0011 | 1 | NA18979.hp1 | 5_prime_UTR_variant | MODIFIER | c.-47C>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/7 | 17562 | chr10 | 113679932 | ||||||
| chr10:113679959 | G | T | 1 | a0003c0003t0019 | 1 | HG02630.hp1 | 5_prime_UTR_variant | MODIFIER | c.-20G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/7 | 17535 | chr10 | 113679959 | ||||||
| chr10:113729705 | A | G | 1 | a0001c0001t0018 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*165A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 7/7 | 165 | chr10 | 113729705 | ||||||
| chr10:113729725 | A | G | 1 | a0001c0001t0010 | 2 | HG01243.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*185A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 7/7 | 185 | chr10 | 113729725 | ||||||
| chr10:113729830 | T | C | 5 | a0002c0002t0001 a0002c0002t0012 a0002c0002t0013 others(2): Show |
115 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*290T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 7/7 | 290 | chr10 | 113729830 | ||||||
| chr10:113729891 | T | G | 11 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(8): Show |
150 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*351T>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 7/7 | 351 | chr10 | 113729891 | ||||||
| chr10:113729913 | C | T | 1 | a0001c0011t0017 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*373C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 7/7 | 373 | chr10 | 113729913 | ||||||
| chr10:113729923 | C | G | 1 | a0001c0001t0016 | 1 | NA19007.hp1 | 3_prime_UTR_variant | MODIFIER | c.*383C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 7/7 | 383 | chr10 | 113729923 | ||||||
| chr10:113730102 | G | A | 1 | a0001c0001t0008 | 2 | HG02258.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*562G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 7/7 | 562 | chr10 | 113730102 | ||||||
| chr10:113730228 | G | A | 1 | a0001c0001t0006 | 6 | HG00597.hp2 NA18612.hp1 NA18971.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*688G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 7/7 | 688 | chr10 | 113730228 | ||||||
| chr10:113730247 | A | G | 1 | a0002c0002t0013 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*707A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 7/7 | 707 | chr10 | 113730247 | ||||||
| chr10:113730301 | G | A | 5 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0010 others(2): Show |
81 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*761G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 7/7 | 761 | chr10 | 113730301 | ||||||
| chr10:113730306 | G | A | 1 | a0001c0001t0015 | 1 | NA18981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*766G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 7/7 | 766 | chr10 | 113730306 | ||||||
| chr10:113730314 | A | G | 1 | a0001c0001t0014 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*774A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 7/7 | 774 | chr10 | 113730314 | ||||||
| chr10:113730350 | G | A | 9 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0015 others(6): Show |
81 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*810G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 7/7 | 810 | chr10 | 113730350 | ||||||
| chr10:113730540 | A | G | 1 | a0001c0001t0007 | 6 | NA18969.hp1 NA18971.hp2 NA18973.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1000A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 7/7 | 1000 | chr10 | 113730540 | ||||||
| chr10:113730665 | A | G | 1 | a0001c0001t0009 | 2 | HG02572.hp1 HG02622.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1125A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 7/7 | 1125 | chr10 | 113730665 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:113680019 | G | T | 1 | a0001c0001t0008g0027 | 2 | HG02258.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-1+41G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113680019 | |||||||
| chr10:113680025 | C | T | 1 | a0001c0001t0009g0370 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-1+47C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113680025 | |||||||
| chr10:113680160 | G | T | 285 | a0001c0001t0002g0016 a0001c0001t0002g0021 a0001c0001t0002g0109 others(282): Show |
311 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(308): Show |
intron_variant | MODIFIER | c.-1+182G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113680160 | |||||||
| chr10:113680174 | A | G | 1 | a0001c0001t0005g0107 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-1+196A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113680174 | |||||||
| chr10:113680321 | C | T | 1 | a0001c0011t0017g0369 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-1+343C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113680321 | |||||||
| chr10:113680349 | C | G | 1 | a0002c0002t0001g0368 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-1+371C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113680349 | |||||||
| chr10:113680654 | T | G | 1 | a0001c0001t0005g0028 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-1+676T>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113680654 | |||||||
| chr10:113680663 | A | G | 1 | a0001c0001t0004g0026 | 2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-1+685A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113680663 | |||||||
| chr10:113680828 | G | T | 3 | a0001c0001t0005g0365 a0001c0001t0005g0367 a0002c0002t0001g0366 |
3 | HG01109.hp1 HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-1+850G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113680828 | |||||||
| chr10:113680846 | A | G | 4 | a0001c0001t0002g0362 a0001c0001t0002g0363 a0001c0001t0002g0364 others(1): Show |
4 | HG02258.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1+868A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113680846 | |||||||
| chr10:113680897 | A | C | 1 | a0001c0001t0009g0361 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-1+919A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113680897 | |||||||
| chr10:113680898 | G | C | 1 | a0001c0001t0009g0361 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-1+920G>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113680898 | |||||||
| chr10:113680907 | T | G | 1 | a0001c0001t0005g0028 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-1+929T>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113680907 | |||||||
| chr10:113680934 | C | T | 2 | a0001c0001t0004g0105 a0001c0001t0004g0106 |
2 | HG00140.hp2 HG00733.hp1 |
intron_variant | MODIFIER | c.-1+956C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113680934 | |||||||
| chr10:113681032 | T | C | 10 | a0001c0001t0002g0109 a0001c0001t0002g0112 a0001c0001t0002g0362 others(7): Show |
11 | HG02258.hp1 HG02559.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1+1054T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113681032 | |||||||
| chr10:113681084 | G | T | 4 | a0001c0001t0002g0109 a0001c0001t0002g0112 a0002c0006t0001g0110 others(1): Show |
4 | HG02647.hp2 HG03540.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1+1106G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113681084 | |||||||
| chr10:113681172 | T | C | 2 | a0001c0001t0005g0114 a0001c0012t0002g0113 |
2 | HG01081.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-1+1194T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113681172 | |||||||
| chr10:113681283 | G | A | 10 | a0001c0001t0002g0109 a0001c0001t0002g0112 a0001c0001t0002g0362 others(7): Show |
11 | HG02258.hp1 HG02559.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1+1305G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113681283 | |||||||
| chr10:113681323 | A | G | 108 | a0001c0001t0002g0287 a0001c0001t0002g0298 a0001c0001t0002g0312 others(105): Show |
118 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.-1+1345A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113681323 | |||||||
| chr10:113681363 | A | G | 1 | a0002c0002t0001g0360 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-1+1385A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113681363 | |||||||
| chr10:113681370 | C | T | 1 | a0001c0001t0003g0261 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-1+1392C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113681370 | |||||||
| chr10:113681383 | G | A | 38 | a0003c0003t0002g0003 a0003c0003t0002g0116 a0003c0003t0002g0117 others(35): Show |
42 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.-1+1405G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113681383 | |||||||
| chr10:113681472 | A | T | 1 | a0001c0001t0005g0114 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-1+1494A>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113681472 | |||||||
| chr10:113681545 | G | C | 1 | a0004c0004t0001g0115 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-1+1567G>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113681545 | |||||||
| chr10:113681562 | T | C | 1 | a0001c0001t0003g0151 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-1+1584T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113681562 | |||||||
| chr10:113681601 | A | G | 280 | a0001c0001t0002g0016 a0001c0001t0002g0021 a0001c0001t0002g0109 others(277): Show |
305 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(302): Show |
intron_variant | MODIFIER | c.-1+1623A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113681601 | |||||||
| chr10:113681716 | A | G | 1 | a0002c0002t0001g0359 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-1+1738A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113681716 | |||||||
| chr10:113681904 | T | C | 1 | a0002c0002t0001g0262 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-1+1926T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113681904 | |||||||
| chr10:113681924 | A | C | 275 | a0001c0001t0002g0016 a0001c0001t0002g0021 a0001c0001t0002g0109 others(272): Show |
300 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(297): Show |
intron_variant | MODIFIER | c.-1+1946A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113681924 | |||||||
| chr10:113681954 | T | C | 2 | a0001c0001t0005g0029 a0001c0001t0005g0107 |
2 | HG01943.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-1+1976T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113681954 | |||||||
| chr10:113682076 | A | G | 3 | a0002c0002t0001g0008 a0002c0002t0001g0262 a0002c0002t0001g0358 |
5 | NA18946.hp1 NA18955.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1+2098A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113682076 | |||||||
| chr10:113682111 | A | G | 1 | a0001c0001t0005g0028 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-1+2133A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113682111 | |||||||
| chr10:113682112 | G | A | 1 | a0001c0001t0005g0028 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-1+2134G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113682112 | |||||||
| chr10:113682338 | G | C | 1 | a0001c0001t0005g0028 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-1+2360G>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113682338 | |||||||
| chr10:113682339 | C | G | 1 | a0001c0001t0005g0028 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-1+2361C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113682339 | |||||||
| chr10:113682343 | A | C | 1 | a0001c0001t0005g0028 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-1+2365A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113682343 | |||||||
| chr10:113682456 | T | TTCTCTCT others(5): Show |
1 | a0003c0003t0002g0150 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-1+2479_-1+2490dup others(12): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113682456 | ||||||
| chr10:113682481 | C | G | 1 | a0001c0001t0003g0260 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-1+2503C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113682481 | |||||||
| chr10:113682485 | C | T | 1 | a0001c0001t0002g0259 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-1+2507C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113682485 | |||||||
| chr10:113682578 | A | G | 1 | a0001c0001t0003g0260 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-1+2600A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113682578 | |||||||
| chr10:113682612 | C | A | 2 | a0001c0001t0004g0105 a0001c0001t0004g0106 |
2 | HG00140.hp2 HG00733.hp1 |
intron_variant | MODIFIER | c.-1+2634C>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113682612 | |||||||
| chr10:113682627 | A | G | 83 | a0001c0001t0002g0021 a0001c0001t0002g0109 a0001c0001t0002g0112 others(80): Show |
91 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.-1+2649A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113682627 | |||||||
| chr10:113682651 | T | C | 2 | a0001c0001t0005g0114 a0001c0012t0002g0113 |
2 | HG01081.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-1+2673T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113682651 | |||||||
| chr10:113682767 | A | T | 1 | a0001c0010t0005g0104 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-1+2789A>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113682767 | |||||||
| chr10:113682814 | T | G | 1 | a0001c0001t0005g0028 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-1+2836T>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113682814 | |||||||
| chr10:113682924 | A | C | 1 | a0001c0001t0005g0028 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-1+2946A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113682924 | |||||||
| chr10:113682943 | T | C | 1 | a0001c0001t0005g0028 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-1+2965T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113682943 | |||||||
| chr10:113682944 | C | T | 1 | a0001c0001t0005g0028 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-1+2966C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113682944 | |||||||
| chr10:113682945 | A | C | 1 | a0001c0001t0005g0028 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-1+2967A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113682945 | |||||||
| chr10:113682995 | A | G | 4 | a0001c0001t0004g0026 a0001c0001t0004g0257 a0001c0001t0004g0258 others(1): Show |
5 | HG02572.hp2 HG02886.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1+3017A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113682995 | |||||||
| chr10:113683039 | G | A | 1 | a0001c0001t0003g0162 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-1+3061G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113683039 | |||||||
| chr10:113683160 | A | G | 275 | a0001c0001t0002g0016 a0001c0001t0002g0021 a0001c0001t0002g0109 others(272): Show |
300 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(297): Show |
intron_variant | MODIFIER | c.-1+3182A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113683160 | |||||||
| chr10:113683268 | C | T | 1 | a0001c0001t0005g0028 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-1+3290C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113683268 | |||||||
| chr10:113683269 | T | C | 1 | a0001c0001t0005g0028 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-1+3291T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113683269 | |||||||
| chr10:113683284 | A | C | 1 | a0001c0001t0005g0028 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-1+3306A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113683284 | |||||||
| chr10:113683298 | C | G | 1 | a0001c0001t0004g0103 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-1+3320C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113683298 | |||||||
| chr10:113683331 | G | A | 84 | a0001c0001t0002g0016 a0001c0001t0002g0168 a0001c0001t0002g0174 others(81): Show |
91 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.-1+3353G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113683331 | |||||||
| chr10:113683404 | G | A | 2 | a0001c0001t0005g0030 a0001c0005t0002g0031 |
2 | HG02559.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-1+3426G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113683404 | |||||||
| chr10:113683431 | A | G | 84 | a0001c0001t0002g0016 a0001c0001t0002g0168 a0001c0001t0002g0174 others(81): Show |
91 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.-1+3453A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113683431 | |||||||
| chr10:113683629 | C | T | 1 | a0001c0001t0003g0232 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-1+3651C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113683629 | |||||||
| chr10:113683630 | G | A | 1 | a0001c0001t0006g0032 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-1+3652G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113683630 | |||||||
| chr10:113683636 | T | C | 275 | a0001c0001t0002g0016 a0001c0001t0002g0021 a0001c0001t0002g0109 others(272): Show |
300 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(297): Show |
intron_variant | MODIFIER | c.-1+3658T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113683636 | |||||||
| chr10:113683673 | T | C | 1 | a0001c0001t0005g0028 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-1+3695T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113683673 | |||||||
| chr10:113683731 | TTATC | T | 39 | a0002c0002t0001g0255 a0003c0003t0002g0003 a0003c0003t0002g0116 others(36): Show |
43 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.-1+3757_-1+3760del others(4): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113683731 | ||||||
| chr10:113683770 | A | G | 1 | a0001c0001t0004g0102 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-1+3792A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113683770 | |||||||
| chr10:113684054 | T | TAC | 234 | a0001c0001t0002g0016 a0001c0001t0002g0021 a0001c0001t0002g0168 others(231): Show |
256 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(253): Show |
intron_variant | MODIFIER | c.-1+4094_-1+4095dup others(2): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113684054 | ||||||
| chr10:113684054 | T | TACAC | 40 | a0001c0001t0002g0233 a0001c0001t0005g0256 a0003c0003t0002g0003 others(37): Show |
44 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.-1+4092_-1+4095dup others(4): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113684054 | ||||||
| chr10:113684135 | C | T | 149 | a0001c0001t0002g0287 a0001c0001t0002g0298 a0001c0001t0002g0312 others(146): Show |
163 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(160): Show |
intron_variant | MODIFIER | c.-1+4157C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113684135 | |||||||
| chr10:113684239 | A | AT | 65 | a0001c0001t0002g0352 a0001c0001t0004g0012 a0001c0001t0004g0034 others(62): Show |
66 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.-1+4285dupT | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113684239 | ||||||
| chr10:113684239 | A | ATT | 13 | a0001c0001t0004g0096 a0001c0001t0004g0097 a0001c0001t0004g0101 others(10): Show |
14 | HG00597.hp2 HG01192.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-1+4284_-1+4285dup others(2): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113684239 | ||||||
| chr10:113684239 | AT | A | 39 | a0001c0001t0003g0228 a0001c0001t0004g0014 a0001c0001t0005g0256 others(36): Show |
44 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.-1+4285delT | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113684239 | ||||||
| chr10:113684239 | ATT | A | 27 | a0001c0001t0002g0112 a0001c0001t0002g0215 a0001c0001t0002g0226 others(24): Show |
31 | HG00438.hp1 HG00738.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.-1+4284_-1+4285del others(2): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113684239 | ||||||
| chr10:113684239 | ATTT | A | 69 | a0001c0001t0002g0016 a0001c0001t0002g0109 a0001c0001t0002g0168 others(66): Show |
74 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.-1+4283_-1+4285del others(3): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113684239 | ||||||
| chr10:113684239 | ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0005g0030 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-1+4276_-1+4285del others(10): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113684239 | ||||||
| chr10:113684349 | A | G | 1 | a0001c0001t0003g0231 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-1+4371A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113684349 | |||||||
| chr10:113684362 | T | C | 280 | a0001c0001t0002g0016 a0001c0001t0002g0021 a0001c0001t0002g0109 others(277): Show |
306 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(303): Show |
intron_variant | MODIFIER | c.-1+4384T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113684362 | |||||||
| chr10:113684364 | G | A | 38 | a0003c0003t0002g0003 a0003c0003t0002g0116 a0003c0003t0002g0117 others(35): Show |
42 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.-1+4386G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113684364 | |||||||
| chr10:113684408 | T | A | 103 | a0001c0001t0002g0016 a0001c0001t0002g0109 a0001c0001t0002g0112 others(100): Show |
113 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.-1+4430T>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113684408 | |||||||
| chr10:113684522 | T | G | 1 | a0001c0001t0005g0035 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-1+4544T>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113684522 | |||||||
| chr10:113684586 | G | A | 56 | a0001c0001t0002g0016 a0001c0001t0002g0168 a0001c0001t0002g0174 others(53): Show |
62 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.-1+4608G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113684586 | |||||||
| chr10:113684660 | A | G | 64 | a0001c0001t0002g0021 a0001c0001t0002g0233 a0001c0001t0002g0235 others(61): Show |
70 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.-1+4682A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113684660 | |||||||
| chr10:113684715 | T | C | 6 | a0001c0001t0003g0198 a0001c0001t0003g0199 a0001c0001t0003g0200 others(3): Show |
6 | HG02451.hp2 HG02896.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1+4737T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113684715 | |||||||
| chr10:113684994 | T | A | 1 | a0001c0001t0005g0035 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-1+5016T>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113684994 | |||||||
| chr10:113684995 | G | T | 1 | a0001c0001t0005g0035 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-1+5017G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113684995 | |||||||
| chr10:113685077 | G | T | 2 | a0002c0002t0001g0332 a0002c0002t0001g0333 |
2 | HG02080.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.-1+5099G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113685077 | |||||||
| chr10:113685425 | G | T | 38 | a0003c0003t0002g0003 a0003c0003t0002g0116 a0003c0003t0002g0117 others(35): Show |
42 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.-1+5447G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113685425 | |||||||
| chr10:113685455 | A | C | 1 | a0001c0001t0010g0227 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-1+5477A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113685455 | |||||||
| chr10:113685650 | G | C | 26 | a0001c0001t0002g0021 a0001c0001t0002g0233 a0001c0001t0002g0235 others(23): Show |
28 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.-1+5672G>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113685650 | |||||||
| chr10:113685767 | G | T | 34 | a0001c0001t0002g0021 a0001c0001t0002g0109 a0001c0001t0002g0112 others(31): Show |
36 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.-1+5789G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113685767 | |||||||
| chr10:113685919 | C | T | 2 | a0001c0001t0005g0066 a0001c0001t0005g0067 |
2 | NA19006.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.-1+5941C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113685919 | |||||||
| chr10:113686251 | G | A | 1 | a0001c0001t0003g0163 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-1+6273G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113686251 | |||||||
| chr10:113686510 | A | G | 1 | a0001c0001t0003g0223 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-1+6532A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113686510 | |||||||
| chr10:113686589 | T | C | 39 | a0001c0001t0004g0012 a0001c0001t0004g0068 a0001c0001t0004g0070 others(36): Show |
40 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.-1+6611T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113686589 | |||||||
| chr10:113686617 | G | A | 185 | a0001c0001t0002g0021 a0001c0001t0002g0109 a0001c0001t0002g0112 others(182): Show |
201 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.-1+6639G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113686617 | |||||||
| chr10:113686759 | C | T | 1 | a0001c0005t0002g0254 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-1+6781C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113686759 | |||||||
| chr10:113686839 | T | C | 1 | a0001c0001t0004g0154 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-1+6861T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113686839 | |||||||
| chr10:113687144 | T | C | 3 | a0003c0003t0002g0116 a0003c0003t0002g0117 a0003c0003t0002g0118 |
3 | HG03041.hp1 HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-1+7166T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687144 | |||||||
| chr10:113687344 | G | GTGTATGT others(27): Show |
1 | a0001c0001t0004g0089 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-1+7405_-1+7438dup others(34): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687344 | ||||||
| chr10:113687344 | GTGTATGT others(27): Show |
G | 279 | a0001c0001t0002g0016 a0001c0001t0002g0021 a0001c0001t0002g0109 others(276): Show |
305 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(302): Show |
intron_variant | MODIFIER | c.-1+7405_-1+7438del others(34): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687344 | ||||||
| chr10:113687378 | A | G | 1 | a0001c0001t0003g0197 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-1+7400A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687378 | |||||||
| chr10:113687383 | T | C | 1 | a0001c0001t0003g0197 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-1+7405T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687383 | |||||||
| chr10:113687415 | T | C | 1 | a0002c0002t0001g0267 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-1+7437T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687415 | |||||||
| chr10:113687417 | C | T | 8 | a0001c0001t0002g0109 a0001c0001t0002g0112 a0001c0001t0002g0362 others(5): Show |
8 | HG02258.hp1 HG02647.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1+7439C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687417 | |||||||
| chr10:113687424 | A | G | 6 | a0001c0001t0003g0196 a0001c0001t0004g0101 a0001c0001t0005g0365 others(3): Show |
6 | HG01109.hp1 HG01346.hp1 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1+7446A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687424 | |||||||
| chr10:113687448 | A | G | 1 | a0001c0001t0002g0226 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-1+7470A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687448 | |||||||
| chr10:113687580 | T | G | 1 | a0001c0001t0004g0155 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-1+7602T>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687580 | |||||||
| chr10:113687721 | C | A | 2 | a0001c0001t0004g0013 a0001c0001t0004g0108 |
3 | HG02559.hp2 HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-1+7743C>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687721 | |||||||
| chr10:113687729 | A | G | 38 | a0003c0003t0002g0003 a0003c0003t0002g0116 a0003c0003t0002g0117 others(35): Show |
42 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.-1+7751A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687729 | |||||||
| chr10:113687794 | C | CTCTT | 7 | a0001c0001t0003g0204 a0001c0001t0003g0224 a0001c0001t0004g0095 others(4): Show |
8 | HG00733.hp2 HG02559.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1+7855_-1+7858dup others(4): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687794 | ||||||
| chr10:113687794 | C | CTCTTCTT others(8): Show |
1 | a0001c0001t0004g0068 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-1+7820_-1+7821ins others(15): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687794 | ||||||
| chr10:113687794 | C | CTCTTTCT others(1): Show |
24 | a0001c0001t0003g0205 a0001c0001t0004g0080 a0001c0001t0004g0157 others(21): Show |
24 | HG00597.hp2 HG01109.hp1 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.-1+7851_-1+7858dup others(8): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687794 | ||||||
| chr10:113687794 | C | CTCTTTCT others(5): Show |
30 | a0001c0001t0002g0226 a0001c0001t0002g0312 a0001c0001t0002g0313 others(27): Show |
33 | HG00280.hp2 HG00544.hp1 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.-1+7847_-1+7858dup others(12): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687794 | ||||||
| chr10:113687794 | C | CTCTTTCT others(9): Show |
25 | a0001c0001t0002g0016 a0001c0001t0002g0319 a0001c0001t0003g0017 others(22): Show |
26 | HG00140.hp2 HG00597.hp1 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.-1+7843_-1+7858dup others(16): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687794 | ||||||
| chr10:113687794 | C | CTCTTTCT others(13): Show |
11 | a0001c0001t0003g0193 a0001c0001t0004g0087 a0001c0001t0004g0088 others(8): Show |
11 | HG00558.hp1 HG01123.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.-1+7839_-1+7858dup others(20): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687794 | ||||||
| chr10:113687794 | C | CTCTTTCT others(17): Show |
10 | a0001c0001t0003g0194 a0001c0001t0003g0221 a0001c0001t0003g0222 others(7): Show |
10 | HG00642.hp1 HG01243.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.-1+7835_-1+7858dup others(24): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687794 | ||||||
| chr10:113687794 | C | CTCTTTCT others(21): Show |
2 | a0001c0001t0003g0195 a0001c0001t0005g0324 |
2 | HG02074.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.-1+7831_-1+7858dup others(28): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687794 | ||||||
| chr10:113687794 | C | CTTTCTTT others(7): Show |
1 | a0002c0002t0001g0328 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-1+7817_-1+7818ins others(14): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687794 | ||||||
| chr10:113687794 | C | CTTTCTTT others(11): Show |
1 | a0001c0001t0003g0329 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-1+7817_-1+7818ins others(18): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687794 | ||||||
| chr10:113687794 | C | CTTTCTTT others(15): Show |
2 | a0001c0001t0003g0331 a0001c0001t0004g0330 |
2 | HG02809.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-1+7817_-1+7818ins others(22): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687794 | ||||||
| chr10:113687794 | CTCTT | C | 5 | a0001c0001t0004g0010 a0001c0001t0004g0103 a0001c0001t0005g0040 others(2): Show |
7 | HG01952.hp1 HG01975.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1+7855_-1+7858del others(4): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687794 | ||||||
| chr10:113687794 | CTCTTTCT others(1): Show |
C | 4 | a0001c0001t0004g0014 a0001c0001t0004g0154 a0001c0001t0004g0155 others(1): Show |
5 | HG01891.hp1 HG02486.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1+7851_-1+7858del others(8): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687794 | ||||||
| chr10:113687794 | CTCTTTCT others(5): Show |
C | 1 | a0001c0001t0002g0109 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-1+7847_-1+7858del others(12): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687794 | ||||||
| chr10:113687800 | C | CTTT | 3 | a0001c0001t0002g0246 a0001c0001t0002g0247 a0001c0001t0002g0248 |
3 | HG00408.hp1 HG03669.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-1+7823_-1+7825dup others(3): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687800 | ||||||
| chr10:113687803 | TC | T | 7 | a0001c0001t0002g0233 a0001c0001t0002g0250 a0001c0001t0002g0251 others(4): Show |
7 | HG00544.hp2 HG02015.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1+7826delC | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687803 | |||||||
| chr10:113687803 | TCTTTCTT others(2): Show |
T | 15 | a0001c0001t0002g0021 a0001c0001t0002g0235 a0001c0001t0002g0237 others(12): Show |
17 | HG01081.hp1 HG01168.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.-1+7826_-1+7834del others(9): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687803 | |||||||
| chr10:113687812 | C | CTTTCTTT others(3): Show |
2 | a0002c0002t0001g0301 a0002c0002t0001g0346 |
2 | HG00735.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-1+7836_-1+7845dup others(10): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687812 | ||||||
| chr10:113687816 | C | CTTTCTT | 4 | a0002c0002t0001g0325 a0002c0002t0001g0326 a0002c0002t0001g0327 others(1): Show |
4 | HG00140.hp1 HG01361.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1+7840_-1+7845dup others(6): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687816 | ||||||
| chr10:113687823 | T | TC | 3 | a0001c0001t0002g0246 a0001c0001t0002g0247 a0001c0001t0002g0248 |
3 | HG00408.hp1 HG03669.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-1+7846dupC | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687823 | ||||||
| chr10:113687827 | T | TC | 9 | a0001c0001t0002g0233 a0001c0001t0002g0250 a0001c0001t0002g0251 others(6): Show |
9 | HG00544.hp2 HG02015.hp1 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.-1+7850dupC | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687827 | ||||||
| chr10:113687827 | T | TCTTTC | 3 | a0001c0001t0004g0064 a0001c0001t0005g0065 a0001c0001t0005g0067 |
3 | HG01361.hp2 NA19006.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.-1+7850_-1+7854dup others(5): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687827 | ||||||
| chr10:113687833 | T | C | 12 | a0001c0001t0004g0033 a0001c0001t0004g0034 a0001c0001t0004g0036 others(9): Show |
13 | HG00423.hp2 HG00621.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.-1+7855T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687833 | |||||||
| chr10:113687835 | TC | T | 39 | a0001c0001t0003g0151 a0001c0001t0003g0163 a0001c0001t0003g0182 others(36): Show |
41 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.-1+7859delC | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687835 | ||||||
| chr10:113687836 | C | CTTT | 69 | a0001c0001t0002g0215 a0001c0001t0002g0298 a0001c0001t0003g0004 others(66): Show |
71 | HG00280.hp1 HG00639.hp2 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.-1+7858_-1+7859ins others(3): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687836 | |||||||
| chr10:113687836 | C | CTTTCTTT | 29 | a0001c0001t0002g0168 a0001c0001t0003g0018 a0001c0001t0003g0171 others(26): Show |
31 | HG01081.hp2 HG01123.hp1 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.-1+7858_-1+7859ins others(7): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687836 | |||||||
| chr10:113687836 | C | CTTTCTTT others(4): Show |
21 | a0001c0001t0002g0174 a0001c0001t0003g0004 a0001c0001t0003g0167 others(18): Show |
23 | HG00323.hp1 HG00408.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.-1+7858_-1+7859ins others(11): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687836 | |||||||
| chr10:113687836 | C | CTTTCTTT others(18): Show |
1 | a0001c0001t0004g0097 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-1+7858_-1+7859ins others(25): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687836 | |||||||
| chr10:113687836 | C | CTTTCTTT others(22): Show |
1 | a0001c0001t0004g0075 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-1+7858_-1+7859ins others(29): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687836 | |||||||
| chr10:113687836 | C | CTTTCTTT others(8): Show |
6 | a0001c0001t0002g0287 a0001c0001t0003g0004 a0001c0001t0003g0175 others(3): Show |
6 | HG00558.hp2 HG01175.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1+7858_-1+7859ins others(15): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687836 | |||||||
| chr10:113687836 | C | CTTTCTTT others(12): Show |
1 | a0001c0001t0004g0101 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-1+7858_-1+7859ins others(19): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687836 | |||||||
| chr10:113687836 | C | CTTTCTTT others(34): Show |
1 | a0001c0001t0004g0299 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-1+7858_-1+7859ins others(41): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687836 | |||||||
| chr10:113687836 | C | T | 15 | a0001c0001t0002g0246 a0001c0001t0002g0247 a0001c0001t0002g0248 others(12): Show |
16 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.-1+7858C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687836 | |||||||
| chr10:113687837 | C | T | 23 | a0001c0001t0002g0112 a0001c0001t0002g0233 a0001c0001t0002g0250 others(20): Show |
25 | HG00140.hp1 HG00544.hp2 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.-1+7859C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687837 | |||||||
| chr10:113687840 | T | C | 8 | a0001c0001t0005g0060 a0002c0002t0001g0007 a0002c0002t0001g0303 others(5): Show |
10 | HG00140.hp1 HG01361.hp1 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.-1+7862T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687840 | |||||||
| chr10:113687840 | T | TC | 4 | a0001c0001t0005g0365 a0002c0002t0001g0268 a0002c0002t0001g0305 others(1): Show |
4 | HG00735.hp1 NA18984.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1+7863dupC | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687840 | ||||||
| chr10:113687845 | C | T | 16 | a0001c0001t0002g0112 a0001c0001t0002g0363 a0001c0001t0002g0364 others(13): Show |
17 | HG00423.hp2 HG00621.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.-1+7867C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687845 | |||||||
| chr10:113687845 | CT | C | 14 | a0001c0001t0002g0233 a0001c0001t0002g0246 a0001c0001t0002g0247 others(11): Show |
16 | HG00408.hp1 HG00544.hp2 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.-1+7871delT | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687845 | ||||||
| chr10:113687846 | T | C | 116 | a0001c0001t0002g0112 a0001c0001t0002g0168 a0001c0001t0002g0215 others(113): Show |
126 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.-1+7868T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687846 | |||||||
| chr10:113687846 | T | TTTC | 5 | a0001c0001t0002g0248 a0001c0001t0004g0075 a0001c0001t0004g0299 others(2): Show |
5 | HG01515.hp2 HG02083.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1+7870_-1+7871ins others(3): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687846 | ||||||
| chr10:113687846 | T | TTTCCTTT others(14): Show |
1 | a0001c0001t0002g0298 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-1+7870_-1+7871ins others(21): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687846 | ||||||
| chr10:113687846 | T | TTTCTTTC others(14): Show |
1 | a0002c0002t0001g0345 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-1+7870_-1+7871ins others(21): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687846 | ||||||
| chr10:113687846 | T | TTTCTTTC others(22): Show |
1 | a0002c0002t0001g0074 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-1+7870_-1+7871ins others(29): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687846 | ||||||
| chr10:113687846 | T | TTTCTTTC others(26): Show |
1 | a0002c0002t0001g0332 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-1+7870_-1+7871ins others(33): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687846 | ||||||
| chr10:113687846 | T | TTTTC | 28 | a0001c0001t0002g0317 a0001c0001t0002g0319 a0001c0001t0003g0329 others(25): Show |
31 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.-1+7909_-1+7912dup others(4): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687846 | ||||||
| chr10:113687846 | T | TTTTCTTT others(1): Show |
9 | a0001c0001t0003g0331 a0001c0001t0005g0056 a0001c0001t0005g0057 others(6): Show |
9 | HG02523.hp1 HG03098.hp2 NA18612.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1+7905_-1+7912dup others(8): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687846 | ||||||
| chr10:113687846 | T | TTTTCTTT others(5): Show |
4 | a0001c0001t0004g0068 a0001c0001t0004g0080 a0001c0001t0005g0058 others(1): Show |
4 | HG02135.hp1 NA18943.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1+7901_-1+7912dup others(12): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687846 | ||||||
| chr10:113687846 | TTTTCTTT others(1): Show |
T | 2 | a0001c0001t0004g0026 a0002c0002t0001g0300 |
3 | HG00423.hp1 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-1+7905_-1+7912del others(8): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687846 | ||||||
| chr10:113687849 | T | C | 58 | a0001c0001t0002g0174 a0001c0001t0003g0004 a0001c0001t0003g0018 others(55): Show |
66 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.-1+7871T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687849 | |||||||
| chr10:113687850 | C | CTT | 2 | a0001c0001t0004g0013 a0001c0001t0004g0108 |
3 | HG02559.hp2 HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-1+7874_-1+7875dup others(2): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687850 | ||||||
| chr10:113687850 | C | CTTTCT | 22 | a0001c0001t0003g0292 a0001c0001t0004g0070 a0001c0001t0004g0071 others(19): Show |
23 | HG00323.hp1 HG00642.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.-1+7875_-1+7879dup others(5): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687850 | ||||||
| chr10:113687850 | C | T | 11 | a0001c0001t0003g0223 a0001c0001t0005g0060 a0001c0001t0005g0365 others(8): Show |
11 | HG00140.hp1 HG00735.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.-1+7872C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687850 | |||||||
| chr10:113687851 | TTTC | T | 2 | a0002c0002t0001g0007 a0002c0002t0001g0303 |
4 | NA18943.hp1 NA18962.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1+7876_-1+7878del others(3): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687851 | ||||||
| chr10:113687853 | T | C | 1 | a0001c0001t0003g0223 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-1+7875T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687853 | |||||||
| chr10:113687853 | TC | T | 5 | a0001c0001t0004g0014 a0001c0001t0004g0154 a0001c0001t0004g0155 others(2): Show |
6 | HG01109.hp2 HG01891.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1+7876delC | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687853 | |||||||
| chr10:113687854 | C | CT | 67 | a0001c0001t0002g0168 a0001c0001t0002g0215 a0001c0001t0002g0287 others(64): Show |
74 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.-1+7879dupT | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687854 | ||||||
| chr10:113687855 | TTTC | T | 7 | a0001c0001t0003g0151 a0001c0001t0003g0163 a0001c0001t0003g0182 others(4): Show |
7 | HG00741.hp1 HG01069.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1+7880_-1+7882del others(3): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687855 | ||||||
| chr10:113687858 | C | CT | 43 | a0001c0001t0002g0174 a0001c0001t0003g0004 a0001c0001t0003g0018 others(40): Show |
51 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.-1+7883dupT | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687858 | ||||||
| chr10:113687859 | TTTC | T | 4 | a0001c0001t0003g0211 a0001c0001t0003g0212 a0003c0003t0002g0126 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1+7884_-1+7886del others(3): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687859 | ||||||
| chr10:113687870 | C | CT | 3 | a0001c0001t0002g0112 a0001c0001t0003g0180 a0001c0001t0003g0181 |
3 | HG02602.hp1 HG03704.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-1+7895dupT | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687870 | ||||||
| chr10:113687889 | TC | T | 74 | a0001c0001t0002g0016 a0001c0001t0002g0239 a0001c0001t0003g0004 others(71): Show |
78 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.-1+7913delC | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687889 | ||||||
| chr10:113687890 | C | CTTT | 58 | a0001c0001t0002g0168 a0001c0001t0002g0174 a0001c0001t0002g0215 others(55): Show |
62 | HG00280.hp1 HG00408.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.-1+7912_-1+7913ins others(3): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687890 | |||||||
| chr10:113687890 | C | CTTTCTTT | 4 | a0001c0001t0004g0084 a0003c0003t0002g0131 a0003c0003t0002g0133 others(1): Show |
4 | HG00738.hp2 HG04199.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1+7912_-1+7913ins others(7): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687890 | |||||||
| chr10:113687890 | C | CTTTCTTT others(4): Show |
1 | a0003c0003t0002g0134 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-1+7912_-1+7913ins others(11): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687890 | |||||||
| chr10:113687890 | C | CTTTCTTT others(8): Show |
1 | a0003c0003t0002g0120 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-1+7912_-1+7913ins others(15): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687890 | |||||||
| chr10:113687890 | C | T | 8 | a0001c0001t0002g0109 a0001c0001t0004g0014 a0001c0001t0004g0154 others(5): Show |
9 | HG01109.hp2 HG01891.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-1+7912C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687890 | |||||||
| chr10:113687891 | C | T | 38 | a0001c0001t0002g0021 a0001c0001t0002g0233 a0001c0001t0002g0235 others(35): Show |
40 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.-1+7913C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687891 | |||||||
| chr10:113687894 | T | C | 20 | a0001c0001t0002g0235 a0001c0001t0002g0237 a0001c0001t0002g0238 others(17): Show |
20 | HG00280.hp2 HG00735.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.-1+7916T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687894 | |||||||
| chr10:113687894 | T | TC | 6 | a0001c0001t0004g0084 a0001c0001t0005g0011 a0001c0001t0005g0029 others(3): Show |
7 | HG00733.hp2 HG00738.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1+7917dupC | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687894 | ||||||
| chr10:113687895 | C | T | 5 | a0001c0001t0002g0235 a0001c0001t0002g0237 a0001c0001t0002g0238 others(2): Show |
5 | HG01433.hp2 HG03017.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1+7917C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687895 | |||||||
| chr10:113687896 | TTTCTTTC others(5): Show |
T | 1 | a0001c0001t0002g0112 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-1+7922_-1+7933del others(12): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687896 | ||||||
| chr10:113687898 | T | TC | 5 | a0001c0001t0003g0203 a0001c0001t0004g0258 a0002c0002t0001g0296 others(2): Show |
5 | HG01358.hp1 HG03453.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1+7921dupC | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687898 | ||||||
| chr10:113687900 | T | C | 1 | a0001c0012t0002g0113 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-1+7922T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687900 | |||||||
| chr10:113687902 | T | TC | 9 | a0001c0001t0002g0215 a0001c0001t0003g0178 a0001c0001t0003g0188 others(6): Show |
9 | HG01243.hp2 HG02040.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1+7925dupC | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687902 | ||||||
| chr10:113687904 | T | C | 4 | a0001c0001t0002g0363 a0001c0001t0002g0364 a0001c0005t0002g0254 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1+7926T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687904 | |||||||
| chr10:113687908 | C | CT | 96 | a0001c0001t0002g0016 a0001c0001t0002g0109 a0001c0001t0002g0168 others(93): Show |
105 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.-1+7932dupT | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687908 | ||||||
| chr10:113687908 | C | CTTTCT | 4 | a0001c0001t0003g0177 a0001c0001t0003g0179 a0002c0006t0001g0110 others(1): Show |
4 | HG02647.hp2 HG03239.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1+7932_-1+7933ins others(5): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687908 | ||||||
| chr10:113687908 | C | T | 51 | a0001c0001t0002g0215 a0001c0001t0002g0235 a0001c0001t0002g0237 others(48): Show |
54 | HG00280.hp2 HG00733.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.-1+7930C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687908 | |||||||
| chr10:113687909 | TTCC | T | 26 | a0001c0001t0002g0021 a0001c0001t0002g0233 a0001c0001t0002g0240 others(23): Show |
29 | HG00408.hp1 HG00544.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.-1+7933_-1+7935del others(3): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687909 | ||||||
| chr10:113687911 | CCTT | C | 4 | a0001c0001t0002g0235 a0002c0002t0001g0234 a0003c0003t0005g0002 others(1): Show |
4 | HG03225.hp1 HG06807.hp1 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1+7937_-1+7939del others(3): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687911 | ||||||
| chr10:113687912 | C | CT | 9 | a0001c0001t0002g0362 a0001c0001t0003g0170 a0001c0001t0003g0171 others(6): Show |
9 | HG01106.hp1 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1+7936dupT | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687912 | ||||||
| chr10:113687912 | C | T | 116 | a0001c0001t0002g0016 a0001c0001t0002g0109 a0001c0001t0002g0168 others(113): Show |
126 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.-1+7934C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687912 | |||||||
| chr10:113687913 | TTCTTTCC others(4): Show |
T | 2 | a0001c0001t0002g0237 a0001c0001t0002g0238 |
2 | HG01433.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-1+7937_-1+7947del others(11): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687913 | ||||||
| chr10:113687914 | T | TC | 2 | a0003c0003t0005g0002 a0003c0003t0005g0123 |
3 | HG02647.hp1 HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-1+7937dupC | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687914 | ||||||
| chr10:113687916 | T | C | 36 | a0001c0001t0002g0109 a0001c0001t0002g0112 a0001c0001t0002g0312 others(33): Show |
37 | HG00280.hp2 HG00733.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.-1+7938T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687916 | |||||||
| chr10:113687916 | T | TTTCC | 32 | a0001c0001t0002g0319 a0001c0001t0003g0331 a0001c0001t0004g0010 others(29): Show |
36 | HG00639.hp2 HG00642.hp2 HG01256.hp1 others(33): Show |
intron_variant | MODIFIER | c.-1+7985_-1+7988dup others(4): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687916 | ||||||
| chr10:113687916 | T | TTTCCTTC others(1): Show |
6 | a0001c0001t0004g0156 a0001c0001t0004g0159 a0001c0001t0005g0091 others(3): Show |
6 | HG01081.hp2 HG01123.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1+7981_-1+7988dup others(8): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687916 | ||||||
| chr10:113687916 | T | TTTCCTTC others(5): Show |
1 | a0001c0001t0005g0367 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-1+7977_-1+7988dup others(12): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687916 | ||||||
| chr10:113687916 | T | TTTCCTTC others(9): Show |
1 | a0001c0001t0005g0365 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-1+7973_-1+7988dup others(16): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687916 | ||||||
| chr10:113687916 | TTTCC | T | 6 | a0001c0001t0004g0088 a0001c0001t0004g0089 a0001c0001t0005g0063 others(3): Show |
6 | HG01192.hp1 HG01346.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1+7985_-1+7988del others(4): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687916 | ||||||
| chr10:113687916 | TTTCCTTC others(5): Show |
T | 1 | a0001c0001t0005g0030 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-1+7977_-1+7988del others(12): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687916 | ||||||
| chr10:113687916 | TTTCCTTC others(9): Show |
T | 1 | a0001c0001t0004g0026 | 2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-1+7973_-1+7988del others(16): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687916 | ||||||
| chr10:113687920 | C | T | 107 | a0001c0001t0002g0016 a0001c0001t0002g0168 a0001c0001t0002g0174 others(104): Show |
117 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.-1+7942C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687920 | |||||||
| chr10:113687924 | C | T | 11 | a0001c0001t0003g0170 a0001c0001t0003g0171 a0001c0001t0003g0203 others(8): Show |
13 | HG01358.hp1 HG02647.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.-1+7946C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687924 | |||||||
| chr10:113687928 | C | T | 38 | a0001c0001t0002g0215 a0001c0001t0002g0237 a0001c0001t0002g0238 others(35): Show |
40 | HG00558.hp1 HG01069.hp1 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.-1+7950C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687928 | |||||||
| chr10:113687932 | C | T | 78 | a0001c0001t0002g0016 a0001c0001t0002g0168 a0001c0001t0002g0174 others(75): Show |
85 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.-1+7954C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687932 | |||||||
| chr10:113687936 | C | T | 6 | a0001c0001t0003g0170 a0001c0001t0003g0171 a0002c0002t0001g0184 others(3): Show |
8 | HG02647.hp1 HG02717.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1+7958C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687936 | |||||||
| chr10:113687955 | CCTTCCTT others(5): Show |
C | 5 | a0001c0001t0002g0242 a0001c0001t0002g0243 a0001c0001t0002g0245 others(2): Show |
5 | HG01081.hp1 HG01515.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1+7981_-1+7992del others(12): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687955 | ||||||
| chr10:113687959 | CCTTCCTT others(1): Show |
C | 12 | a0001c0001t0002g0287 a0002c0002t0001g0007 a0002c0002t0001g0264 others(9): Show |
14 | HG00423.hp1 HG00438.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-1+7985_-1+7992del others(8): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687959 | ||||||
| chr10:113687963 | CCTTT | C | 51 | a0001c0001t0002g0021 a0001c0001t0002g0233 a0001c0001t0002g0244 others(48): Show |
53 | HG00140.hp1 HG00408.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.-1+7998_-1+8001del others(4): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113687963 | ||||||
| chr10:113687967 | T | C | 70 | a0001c0001t0002g0235 a0001c0001t0002g0237 a0001c0001t0002g0238 others(67): Show |
75 | HG00544.hp1 HG00639.hp2 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.-1+7989T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113687967 | |||||||
| chr10:113688035 | C | T | 26 | a0001c0001t0002g0021 a0001c0001t0002g0233 a0001c0001t0002g0235 others(23): Show |
28 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.-1+8057C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113688035 | |||||||
| chr10:113688410 | T | C | 1 | a0001c0001t0003g0188 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-1+8432T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113688410 | |||||||
| chr10:113688419 | C | G | 1 | a0001c0001t0003g0171 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-1+8441C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113688419 | |||||||
| chr10:113688422 | T | C | 13 | a0001c0001t0002g0109 a0001c0001t0002g0112 a0001c0001t0002g0362 others(10): Show |
14 | HG01109.hp2 HG01891.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-1+8444T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113688422 | |||||||
| chr10:113688506 | A | G | 1 | a0001c0001t0003g0197 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-1+8528A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113688506 | |||||||
| chr10:113688546 | A | G | 2 | a0001c0001t0005g0048 a0001c0001t0005g0055 |
2 | NA18988.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-1+8568A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113688546 | |||||||
| chr10:113688552 | A | G | 1 | a0001c0001t0002g0287 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-1+8574A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113688552 | |||||||
| chr10:113688604 | T | C | 39 | a0001c0001t0002g0021 a0001c0001t0002g0109 a0001c0001t0002g0112 others(36): Show |
42 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.-1+8626T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113688604 | |||||||
| chr10:113688644 | T | C | 39 | a0001c0001t0002g0021 a0001c0001t0002g0109 a0001c0001t0002g0112 others(36): Show |
42 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.-1+8666T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113688644 | |||||||
| chr10:113688699 | C | T | 84 | a0001c0001t0002g0016 a0001c0001t0002g0168 a0001c0001t0002g0174 others(81): Show |
91 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.-1+8721C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113688699 | |||||||
| chr10:113688824 | T | C | 2 | a0002c0006t0001g0110 a0002c0006t0001g0111 |
2 | HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1-8670T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113688824 | |||||||
| chr10:113689005 | GT | G | 4 | a0002c0002t0001g0022 a0002c0002t0001g0288 a0002c0002t0001g0305 others(1): Show |
5 | NA18947.hp1 NA18951.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.1-8488delT | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113689005 | |||||||
| chr10:113689057 | C | T | 3 | a0002c0002t0001g0293 a0002c0002t0001g0295 a0002c0002t0001g0350 |
3 | HG01891.hp2 HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1-8437C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113689057 | |||||||
| chr10:113689081 | T | C | 1 | a0002c0002t0001g0347 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1-8413T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113689081 | |||||||
| chr10:113689085 | A | C | 3 | a0001c0001t0003g0163 a0001c0001t0003g0169 a0001c0001t0003g0186 |
3 | HG00323.hp2 HG03927.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1-8409A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113689085 | |||||||
| chr10:113689180 | C | T | 8 | a0001c0001t0002g0109 a0001c0001t0002g0112 a0001c0001t0002g0362 others(5): Show |
8 | HG02258.hp1 HG02647.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1-8314C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113689180 | |||||||
| chr10:113689210 | T | C | 1 | a0004c0004t0001g0115 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1-8284T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113689210 | |||||||
| chr10:113689238 | C | T | 1 | a0001c0001t0002g0168 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1-8256C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113689238 | |||||||
| chr10:113689432 | G | A | 2 | a0003c0003t0002g0126 a0003c0003t0002g0127 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1-8062G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113689432 | |||||||
| chr10:113689573 | T | C | 3 | a0001c0001t0003g0329 a0001c0001t0003g0331 a0001c0001t0004g0330 |
3 | HG02109.hp2 HG02809.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1-7921T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113689573 | |||||||
| chr10:113689576 | T | C | 1 | a0001c0001t0002g0362 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1-7918T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113689576 | |||||||
| chr10:113689681 | A | C | 26 | a0001c0001t0002g0021 a0001c0001t0002g0233 a0001c0001t0002g0235 others(23): Show |
28 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.1-7813A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113689681 | |||||||
| chr10:113689717 | G | A | 90 | a0001c0001t0002g0016 a0001c0001t0002g0168 a0001c0001t0002g0174 others(87): Show |
99 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.1-7777G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113689717 | |||||||
| chr10:113690040 | C | CCCGAAGG others(118): Show |
62 | a0001c0001t0002g0016 a0001c0001t0002g0168 a0001c0001t0002g0174 others(59): Show |
68 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.1-7454_1-7453insCC others(123): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113690040 | |||||||
| chr10:113690058 | G | A | 5 | a0001c0001t0004g0014 a0001c0001t0004g0154 a0001c0001t0004g0155 others(2): Show |
6 | HG01109.hp2 HG01891.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1-7436G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113690058 | |||||||
| chr10:113690096 | T | C | 1 | a0001c0001t0002g0168 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1-7398T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113690096 | |||||||
| chr10:113690198 | T | C | 1 | a0003c0003t0019g0147 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1-7296T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113690198 | |||||||
| chr10:113690264 | G | GT | 160 | a0001c0001t0002g0109 a0001c0001t0002g0112 a0001c0001t0002g0287 others(157): Show |
175 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(172): Show |
intron_variant | MODIFIER | c.1-7221dupT | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113690264 | ||||||
| chr10:113690264 | GT | G | 5 | a0001c0001t0005g0114 a0001c0001t0005g0365 a0001c0001t0005g0367 others(2): Show |
5 | HG01081.hp2 HG01109.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1-7221delT | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr10 | 113690264 | ||||||
| chr10:113690265 | T | G | 2 | a0001c0001t0005g0049 a0001c0001t0005g0056 |
2 | HG02071.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.1-7229T>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113690265 | |||||||
| chr10:113690288 | A | G | 84 | a0001c0001t0002g0016 a0001c0001t0002g0168 a0001c0001t0002g0174 others(81): Show |
91 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1-7206A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113690288 | |||||||
| chr10:113690368 | C | T | 1 | a0003c0003t0002g0125 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1-7126C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113690368 | |||||||
| chr10:113690400 | A | G | 2 | a0001c0001t0005g0091 a0001c0001t0005g0094 |
2 | HG01981.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1-7094A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113690400 | |||||||
| chr10:113690755 | C | G | 364 | a0001c0001t0002g0016 a0001c0001t0002g0021 a0001c0001t0002g0109 others(361): Show |
398 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(395): Show |
intron_variant | MODIFIER | c.1-6739C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113690755 | |||||||
| chr10:113691013 | G | A | 1 | a0001c0001t0003g0203 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1-6481G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113691013 | |||||||
| chr10:113691424 | A | T | 4 | a0002c0002t0001g0338 a0002c0002t0001g0339 a0002c0002t0001g0340 others(1): Show |
4 | HG00639.hp2 HG01123.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.1-6070A>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113691424 | |||||||
| chr10:113691464 | G | T | 1 | a0003c0003t0002g0125 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1-6030G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113691464 | |||||||
| chr10:113691641 | C | A | 3 | a0001c0001t0005g0365 a0001c0001t0005g0367 a0002c0002t0001g0366 |
3 | HG01109.hp1 HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1-5853C>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113691641 | |||||||
| chr10:113691673 | G | A | 26 | a0001c0001t0002g0021 a0001c0001t0002g0233 a0001c0001t0002g0235 others(23): Show |
28 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.1-5821G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113691673 | |||||||
| chr10:113691702 | C | T | 1 | a0001c0001t0006g0077 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1-5792C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113691702 | |||||||
| chr10:113691878 | T | C | 2 | a0001c0001t0004g0157 a0001c0001t0004g0161 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1-5616T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113691878 | |||||||
| chr10:113691887 | G | A | 8 | a0001c0001t0002g0109 a0001c0001t0002g0112 a0001c0001t0002g0362 others(5): Show |
8 | HG02258.hp1 HG02647.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1-5607G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113691887 | |||||||
| chr10:113691941 | G | T | 1 | a0002c0002t0001g0358 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1-5553G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113691941 | |||||||
| chr10:113691946 | A | G | 1 | a0001c0001t0004g0154 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1-5548A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113691946 | |||||||
| chr10:113692022 | C | T | 26 | a0001c0001t0002g0021 a0001c0001t0002g0233 a0001c0001t0002g0235 others(23): Show |
28 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.1-5472C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113692022 | |||||||
| chr10:113692245 | G | T | 1 | a0002c0002t0001g0323 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1-5249G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113692245 | |||||||
| chr10:113692246 | G | A | 2 | a0001c0001t0005g0037 a0001c0001t0005g0052 |
2 | HG02080.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.1-5248G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113692246 | |||||||
| chr10:113692269 | G | A | 1 | a0001c0001t0008g0027 | 2 | HG02258.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1-5225G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113692269 | |||||||
| chr10:113692525 | G | C | 7 | a0001c0001t0004g0356 a0002c0002t0001g0269 a0002c0002t0001g0334 others(4): Show |
7 | HG01099.hp2 HG01928.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.1-4969G>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113692525 | |||||||
| chr10:113692543 | G | A | 1 | a0001c0001t0003g0203 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1-4951G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113692543 | |||||||
| chr10:113692624 | G | A | 26 | a0001c0001t0002g0021 a0001c0001t0002g0233 a0001c0001t0002g0235 others(23): Show |
28 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.1-4870G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113692624 | |||||||
| chr10:113692684 | T | A | 34 | a0001c0001t0002g0021 a0001c0001t0002g0109 a0001c0001t0002g0112 others(31): Show |
36 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.1-4810T>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113692684 | |||||||
| chr10:113692693 | A | T | 1 | a0001c0001t0003g0171 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1-4801A>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113692693 | |||||||
| chr10:113692914 | C | T | 2 | a0001c0001t0005g0365 a0001c0001t0005g0367 |
2 | HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1-4580C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113692914 | |||||||
| chr10:113693366 | G | A | 1 | a0001c0001t0005g0052 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1-4128G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113693366 | |||||||
| chr10:113693366 | G | C | 39 | a0001c0001t0002g0021 a0001c0001t0002g0109 a0001c0001t0002g0112 others(36): Show |
42 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.1-4128G>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113693366 | |||||||
| chr10:113693492 | C | T | 1 | a0001c0001t0003g0210 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1-4002C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113693492 | |||||||
| chr10:113693509 | T | C | 26 | a0001c0001t0002g0021 a0001c0001t0002g0233 a0001c0001t0002g0235 others(23): Show |
28 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.1-3985T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113693509 | |||||||
| chr10:113693590 | G | A | 38 | a0003c0003t0002g0003 a0003c0003t0002g0116 a0003c0003t0002g0117 others(35): Show |
42 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.1-3904G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113693590 | |||||||
| chr10:113693610 | T | A | 1 | a0001c0001t0002g0240 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1-3884T>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113693610 | |||||||
| chr10:113693682 | G | A | 1 | a0003c0003t0002g0150 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1-3812G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113693682 | |||||||
| chr10:113693922 | A | G | 2 | a0001c0001t0003g0292 a0002c0002t0001g0316 |
2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1-3572A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113693922 | |||||||
| chr10:113693961 | A | G | 1 | a0003c0003t0002g0138 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1-3533A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113693961 | |||||||
| chr10:113694004 | G | A | 26 | a0001c0001t0002g0021 a0001c0001t0002g0233 a0001c0001t0002g0235 others(23): Show |
28 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.1-3490G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113694004 | |||||||
| chr10:113694140 | C | T | 1 | a0001c0001t0008g0027 | 2 | HG02258.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1-3354C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113694140 | |||||||
| chr10:113694173 | G | T | 1 | a0001c0001t0008g0027 | 2 | HG02258.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1-3321G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113694173 | |||||||
| chr10:113694226 | A | G | 1 | a0001c0001t0003g0179 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1-3268A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113694226 | |||||||
| chr10:113694230 | A | C | 322 | a0001c0001t0002g0016 a0001c0001t0002g0021 a0001c0001t0002g0109 others(319): Show |
350 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.1-3264A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113694230 | |||||||
| chr10:113694265 | G | A | 10 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0003g0208 others(7): Show |
10 | HG01243.hp2 HG02109.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1-3229G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113694265 | |||||||
| chr10:113694447 | C | T | 2 | a0001c0001t0004g0013 a0001c0001t0004g0108 |
3 | HG02559.hp2 HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1-3047C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113694447 | |||||||
| chr10:113694554 | G | A | 1 | a0003c0003t0019g0147 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1-2940G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113694554 | |||||||
| chr10:113694779 | T | C | 3 | a0001c0001t0003g0329 a0001c0001t0003g0331 a0001c0001t0004g0330 |
3 | HG02109.hp2 HG02809.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1-2715T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113694779 | |||||||
| chr10:113694784 | T | G | 26 | a0001c0001t0002g0021 a0001c0001t0002g0233 a0001c0001t0002g0235 others(23): Show |
28 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.1-2710T>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113694784 | |||||||
| chr10:113694789 | T | C | 2 | a0001c0001t0005g0048 a0001c0001t0005g0055 |
2 | NA18988.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1-2705T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113694789 | |||||||
| chr10:113694839 | G | A | 1 | a0002c0002t0001g0270 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1-2655G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113694839 | |||||||
| chr10:113694879 | G | A | 1 | a0001c0001t0004g0330 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1-2615G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113694879 | |||||||
| chr10:113694937 | T | C | 4 | a0001c0001t0004g0026 a0001c0001t0004g0257 a0001c0001t0004g0258 others(1): Show |
5 | HG02572.hp2 HG02886.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1-2557T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113694937 | |||||||
| chr10:113694974 | T | A | 4 | a0001c0001t0002g0109 a0001c0001t0002g0112 a0002c0006t0001g0110 others(1): Show |
4 | HG02647.hp2 HG03540.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1-2520T>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113694974 | |||||||
| chr10:113695031 | C | T | 2 | a0003c0003t0002g0129 a0004c0004t0001g0137 |
2 | NA18945.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1-2463C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113695031 | |||||||
| chr10:113695103 | C | A | 108 | a0001c0001t0002g0287 a0001c0001t0002g0298 a0001c0001t0002g0312 others(105): Show |
118 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.1-2391C>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113695103 | |||||||
| chr10:113695278 | C | T | 2 | a0003c0003t0002g0126 a0003c0003t0002g0127 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1-2216C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113695278 | |||||||
| chr10:113695407 | C | T | 4 | a0001c0001t0002g0109 a0001c0001t0002g0112 a0002c0006t0001g0110 others(1): Show |
4 | HG02647.hp2 HG03540.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1-2087C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113695407 | |||||||
| chr10:113695455 | G | A | 1 | a0001c0001t0003g0225 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1-2039G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113695455 | |||||||
| chr10:113695481 | G | A | 1 | a0003c0003t0002g0125 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1-2013G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113695481 | |||||||
| chr10:113695494 | T | C | 2 | a0001c0001t0004g0020 a0001c0001t0004g0241 |
3 | HG01884.hp1 HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1-2000T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113695494 | |||||||
| chr10:113695532 | G | A | 34 | a0001c0001t0002g0021 a0001c0001t0002g0109 a0001c0001t0002g0112 others(31): Show |
36 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.1-1962G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113695532 | |||||||
| chr10:113695542 | C | T | 8 | a0001c0001t0002g0109 a0001c0001t0002g0112 a0001c0001t0002g0362 others(5): Show |
8 | HG02258.hp1 HG02647.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1-1952C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113695542 | |||||||
| chr10:113695777 | G | T | 26 | a0001c0001t0002g0021 a0001c0001t0002g0233 a0001c0001t0002g0235 others(23): Show |
28 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.1-1717G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113695777 | |||||||
| chr10:113696122 | G | A | 8 | a0001c0001t0002g0109 a0001c0001t0002g0112 a0001c0001t0002g0362 others(5): Show |
8 | HG02258.hp1 HG02647.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1-1372G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113696122 | |||||||
| chr10:113696208 | A | G | 1 | a0001c0001t0005g0030 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1-1286A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113696208 | |||||||
| chr10:113696414 | C | T | 1 | a0001c0001t0002g0253 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1-1080C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113696414 | |||||||
| chr10:113696469 | C | A | 1 | a0002c0002t0001g0357 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1-1025C>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113696469 | |||||||
| chr10:113696507 | A | C | 108 | a0001c0001t0002g0287 a0001c0001t0002g0298 a0001c0001t0002g0312 others(105): Show |
118 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.1-987A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113696507 | |||||||
| chr10:113696623 | C | A | 1 | a0001c0001t0005g0053 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1-871C>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113696623 | |||||||
| chr10:113697086 | A | C | 1 | a0002c0002t0001g0350 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1-408A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113697086 | |||||||
| chr10:113697088 | A | G | 1 | a0001c0008t0002g0236 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1-406A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113697088 | |||||||
| chr10:113697134 | C | T | 1 | a0003c0003t0002g0117 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1-360C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113697134 | |||||||
| chr10:113697208 | C | T | 3 | a0001c0001t0002g0362 a0001c0001t0002g0363 a0001c0001t0002g0364 |
3 | HG02258.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1-286C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113697208 | |||||||
| chr10:113697355 | G | A | 26 | a0001c0001t0002g0021 a0001c0001t0002g0233 a0001c0001t0002g0235 others(23): Show |
28 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.1-139G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113697355 | |||||||
| chr10:113697410 | C | A | 1 | a0001c0001t0003g0190 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1-84C>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 1/6 | chr10 | 113697410 | |||||||
| chr10:113697628 | T | C | 2 | a0002c0002t0001g0285 a0002c0002t0001g0286 |
2 | HG01257.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.110+25T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113697628 | |||||||
| chr10:113697691 | G | A | 26 | a0001c0001t0002g0021 a0001c0001t0002g0233 a0001c0001t0002g0235 others(23): Show |
28 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.110+88G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113697691 | |||||||
| chr10:113697745 | G | A | 1 | a0003c0003t0002g0124 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.110+142G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113697745 | |||||||
| chr10:113697838 | G | A | 26 | a0001c0001t0002g0021 a0001c0001t0002g0233 a0001c0001t0002g0235 others(23): Show |
28 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.110+235G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113697838 | |||||||
| chr10:113697930 | T | C | 1 | a0003c0003t0002g0116 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.110+327T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113697930 | |||||||
| chr10:113698130 | T | C | 37 | a0001c0001t0002g0021 a0001c0001t0002g0109 a0001c0001t0002g0112 others(34): Show |
39 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.110+527T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113698130 | |||||||
| chr10:113698146 | T | A | 1 | a0001c0001t0005g0062 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.110+543T>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113698146 | |||||||
| chr10:113698209 | C | A | 2 | a0001c0001t0004g0013 a0001c0001t0004g0108 |
3 | HG02559.hp2 HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.110+606C>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113698209 | |||||||
| chr10:113698378 | A | C | 6 | a0001c0001t0006g0032 a0001c0001t0006g0077 a0001c0001t0006g0078 others(3): Show |
6 | HG00597.hp2 NA18612.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.110+775A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113698378 | |||||||
| chr10:113698465 | C | T | 1 | a0001c0001t0004g0154 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.110+862C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113698465 | |||||||
| chr10:113698513 | G | A | 5 | a0001c0001t0003g0172 a0001c0001t0003g0173 a0001c0001t0003g0177 others(2): Show |
5 | HG02074.hp1 HG02300.hp1 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.110+910G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113698513 | |||||||
| chr10:113698555 | G | A | 280 | a0001c0001t0002g0016 a0001c0001t0002g0021 a0001c0001t0002g0109 others(277): Show |
306 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(303): Show |
intron_variant | MODIFIER | c.110+952G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113698555 | |||||||
| chr10:113698610 | A | T | 1 | a0002c0002t0001g0023 | 2 | NA18966.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.110+1007A>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113698610 | |||||||
| chr10:113698666 | G | GT | 94 | a0001c0001t0002g0016 a0001c0001t0002g0174 a0001c0001t0002g0215 others(91): Show |
104 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.110+1074dupT | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr10 | 113698666 | ||||||
| chr10:113698666 | G | GTT | 39 | a0001c0001t0002g0168 a0003c0003t0002g0003 a0003c0003t0002g0116 others(36): Show |
43 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.110+1073_110+1074d others(4): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr10 | 113698666 | ||||||
| chr10:113698666 | G | T | 33 | a0001c0001t0002g0021 a0001c0001t0002g0109 a0001c0001t0002g0112 others(30): Show |
35 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.110+1063G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113698666 | |||||||
| chr10:113698761 | A | G | 1 | a0002c0002t0001g0327 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.110+1158A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113698761 | |||||||
| chr10:113698866 | G | A | 1 | a0001c0001t0004g0026 | 2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.110+1263G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113698866 | |||||||
| chr10:113698927 | G | T | 2 | a0001c0001t0005g0365 a0001c0001t0005g0367 |
2 | HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.110+1324G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113698927 | |||||||
| chr10:113699177 | A | G | 109 | a0001c0001t0002g0287 a0001c0001t0002g0298 a0001c0001t0002g0312 others(106): Show |
119 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.110+1574A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113699177 | |||||||
| chr10:113699222 | A | G | 26 | a0001c0001t0002g0021 a0001c0001t0002g0233 a0001c0001t0002g0235 others(23): Show |
28 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.110+1619A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113699222 | |||||||
| chr10:113699241 | T | C | 1 | a0002c0002t0001g0311 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.110+1638T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113699241 | |||||||
| chr10:113699280 | C | G | 1 | a0006c0009t0003g0201 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.110+1677C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113699280 | |||||||
| chr10:113699347 | T | C | 13 | a0001c0001t0002g0109 a0001c0001t0002g0112 a0001c0001t0002g0362 others(10): Show |
14 | HG01109.hp2 HG01891.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.110+1744T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113699347 | |||||||
| chr10:113699536 | A | G | 2 | a0003c0003t0002g0135 a0003c0003t0002g0141 |
2 | NA18964.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.110+1933A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113699536 | |||||||
| chr10:113699553 | C | G | 1 | a0002c0002t0001g0269 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.110+1950C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113699553 | |||||||
| chr10:113699576 | A | G | 1 | a0001c0001t0018g0176 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.110+1973A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113699576 | |||||||
| chr10:113699698 | A | T | 1 | a0001c0012t0002g0113 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.110+2095A>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113699698 | |||||||
| chr10:113699742 | T | G | 1 | a0001c0001t0005g0256 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.110+2139T>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113699742 | |||||||
| chr10:113699850 | A | C | 1 | a0001c0005t0002g0254 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.110+2247A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113699850 | |||||||
| chr10:113699881 | TA | T | 1 | a0001c0001t0005g0001 | 4 | HG00639.hp1 HG01256.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.110+2279delA | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113699881 | |||||||
| chr10:113700020 | T | C | 1 | a0001c0001t0004g0064 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.110+2417T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113700020 | |||||||
| chr10:113700053 | A | G | 4 | a0001c0001t0002g0109 a0001c0001t0002g0112 a0002c0006t0001g0110 others(1): Show |
4 | HG02647.hp2 HG03540.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.110+2450A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113700053 | |||||||
| chr10:113700054 | T | A | 1 | a0003c0003t0002g0120 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.110+2451T>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113700054 | |||||||
| chr10:113700218 | G | T | 1 | a0002c0002t0001g0265 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.110+2615G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113700218 | |||||||
| chr10:113700432 | A | G | 1 | a0001c0005t0002g0254 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.110+2829A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113700432 | |||||||
| chr10:113700449 | C | T | 25 | a0001c0001t0002g0021 a0001c0001t0002g0233 a0001c0001t0002g0235 others(22): Show |
27 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.110+2846C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113700449 | |||||||
| chr10:113700701 | G | C | 13 | a0001c0001t0002g0109 a0001c0001t0002g0112 a0001c0001t0002g0362 others(10): Show |
14 | HG01109.hp2 HG01891.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.110+3098G>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113700701 | |||||||
| chr10:113700729 | CATG | C | 332 | a0001c0001t0002g0016 a0001c0001t0002g0021 a0001c0001t0002g0109 others(329): Show |
362 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(359): Show |
intron_variant | MODIFIER | c.110+3127_110+3129d others(5): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113700729 | |||||||
| chr10:113700766 | G | T | 2 | a0001c0001t0004g0013 a0001c0001t0004g0108 |
3 | HG02559.hp2 HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.110+3163G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113700766 | |||||||
| chr10:113700784 | T | C | 1 | a0002c0002t0001g0288 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.110+3181T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113700784 | |||||||
| chr10:113700815 | G | A | 5 | a0001c0001t0005g0114 a0001c0001t0005g0365 a0001c0001t0005g0367 others(2): Show |
5 | HG01081.hp2 HG01109.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.110+3212G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113700815 | |||||||
| chr10:113700844 | C | T | 38 | a0001c0001t0002g0021 a0001c0001t0002g0109 a0001c0001t0002g0112 others(35): Show |
41 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.110+3241C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113700844 | |||||||
| chr10:113700954 | C | T | 25 | a0001c0001t0004g0012 a0001c0001t0004g0043 a0001c0001t0004g0068 others(22): Show |
26 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.110+3351C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113700954 | |||||||
| chr10:113700955 | G | A | 109 | a0001c0001t0002g0287 a0001c0001t0002g0298 a0001c0001t0002g0312 others(106): Show |
119 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.110+3352G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113700955 | |||||||
| chr10:113701011 | C | T | 25 | a0001c0001t0002g0021 a0001c0001t0002g0233 a0001c0001t0002g0235 others(22): Show |
27 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.110+3408C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113701011 | |||||||
| chr10:113701078 | A | C | 1 | a0003c0003t0005g0123 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.110+3475A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113701078 | |||||||
| chr10:113701169 | G | A | 185 | a0001c0001t0002g0016 a0001c0001t0002g0168 a0001c0001t0002g0174 others(182): Show |
202 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.110+3566G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113701169 | |||||||
| chr10:113701207 | C | CA | 90 | a0001c0001t0002g0016 a0001c0001t0002g0168 a0001c0001t0002g0174 others(87): Show |
99 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.110+3605dupA | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr10 | 113701207 | ||||||
| chr10:113701312 | C | CT | 99 | a0001c0001t0002g0287 a0001c0001t0002g0298 a0001c0001t0002g0312 others(96): Show |
109 | HG00140.hp1 HG00423.hp1 HG00639.hp2 others(106): Show |
intron_variant | MODIFIER | c.110+3725dupT | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr10 | 113701312 | ||||||
| chr10:113701312 | CT | C | 39 | a0001c0001t0002g0021 a0001c0001t0002g0233 a0001c0001t0002g0235 others(36): Show |
42 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.110+3725delT | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr10 | 113701312 | ||||||
| chr10:113701353 | C | G | 1 | a0001c0001t0005g0062 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.110+3750C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113701353 | |||||||
| chr10:113701360 | G | T | 1 | a0001c0001t0003g0185 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.110+3757G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113701360 | |||||||
| chr10:113701466 | C | T | 25 | a0001c0001t0002g0021 a0001c0001t0002g0233 a0001c0001t0002g0235 others(22): Show |
27 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.110+3863C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113701466 | |||||||
| chr10:113701509 | T | C | 2 | a0001c0001t0002g0109 a0001c0001t0002g0112 |
2 | NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.110+3906T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113701509 | |||||||
| chr10:113701698 | C | G | 2 | a0003c0003t0002g0142 a0003c0003t0002g0149 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.110+4095C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113701698 | |||||||
| chr10:113701726 | A | G | 109 | a0001c0001t0002g0287 a0001c0001t0002g0298 a0001c0001t0002g0312 others(106): Show |
119 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.110+4123A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113701726 | |||||||
| chr10:113701761 | A | G | 1 | a0002c0002t0001g0347 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.110+4158A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113701761 | |||||||
| chr10:113702038 | A | G | 90 | a0001c0001t0002g0016 a0001c0001t0002g0168 a0001c0001t0002g0174 others(87): Show |
99 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.110+4435A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113702038 | |||||||
| chr10:113702055 | A | G | 2 | a0002c0006t0001g0110 a0002c0006t0001g0111 |
2 | HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.110+4452A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113702055 | |||||||
| chr10:113702399 | A | G | 1 | a0003c0003t0019g0147 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.110+4796A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113702399 | |||||||
| chr10:113702415 | C | A | 5 | a0001c0001t0005g0114 a0001c0001t0005g0365 a0001c0001t0005g0367 others(2): Show |
5 | HG01081.hp2 HG01109.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.110+4812C>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113702415 | |||||||
| chr10:113702655 | A | G | 332 | a0001c0001t0002g0016 a0001c0001t0002g0021 a0001c0001t0002g0109 others(329): Show |
362 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(359): Show |
intron_variant | MODIFIER | c.110+5052A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113702655 | |||||||
| chr10:113702684 | C | T | 1 | a0002c0002t0001g0291 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.110+5081C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113702684 | |||||||
| chr10:113702714 | C | T | 1 | a0001c0001t0004g0068 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.110+5111C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113702714 | |||||||
| chr10:113702727 | C | T | 2 | a0001c0001t0005g0114 a0001c0012t0002g0113 |
2 | HG01081.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.110+5124C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113702727 | |||||||
| chr10:113702770 | A | G | 5 | a0001c0001t0003g0172 a0001c0001t0003g0173 a0001c0001t0003g0177 others(2): Show |
5 | HG02074.hp1 HG02300.hp1 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.110+5167A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113702770 | |||||||
| chr10:113703058 | A | G | 2 | a0001c0001t0005g0029 a0001c0001t0005g0107 |
2 | HG01943.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.110+5455A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113703058 | |||||||
| chr10:113703238 | T | C | 9 | a0002c0002t0001g0264 a0002c0002t0001g0268 a0002c0002t0001g0273 others(6): Show |
9 | HG00423.hp1 HG01257.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.110+5635T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113703238 | |||||||
| chr10:113703323 | G | A | 332 | a0001c0001t0002g0016 a0001c0001t0002g0021 a0001c0001t0002g0109 others(329): Show |
362 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(359): Show |
intron_variant | MODIFIER | c.110+5720G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113703323 | |||||||
| chr10:113703493 | C | T | 1 | a0002c0002t0001g0310 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.110+5890C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113703493 | |||||||
| chr10:113703556 | G | C | 1 | a0001c0001t0004g0081 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.110+5953G>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113703556 | |||||||
| chr10:113703630 | CT | C | 211 | a0001c0001t0002g0016 a0001c0001t0002g0021 a0001c0001t0002g0168 others(208): Show |
230 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.110+6051delT | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr10 | 113703630 | ||||||
| chr10:113703654 | T | A | 8 | a0001c0001t0004g0356 a0002c0002t0001g0183 a0002c0002t0001g0264 others(5): Show |
8 | HG01255.hp1 HG01517.hp2 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.110+6051T>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113703654 | |||||||
| chr10:113703654 | T | TA | 60 | a0001c0001t0002g0312 a0001c0001t0002g0314 a0001c0001t0002g0315 others(57): Show |
69 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.110+6053dupA | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr10 | 113703654 | ||||||
| chr10:113703909 | A | G | 21 | a0001c0001t0005g0279 a0002c0002t0001g0007 a0002c0002t0001g0023 others(18): Show |
25 | HG00438.hp2 HG01433.hp1 HG01981.hp1 others(22): Show |
intron_variant | MODIFIER | c.110+6306A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113703909 | |||||||
| chr10:113703920 | G | A | 22 | a0001c0001t0002g0021 a0001c0001t0002g0233 a0001c0001t0002g0235 others(19): Show |
23 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.110+6317G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113703920 | |||||||
| chr10:113703948 | A | G | 1 | a0001c0001t0005g0059 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.110+6345A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113703948 | |||||||
| chr10:113703977 | G | A | 1 | a0001c0001t0005g0030 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.110+6374G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113703977 | |||||||
| chr10:113704093 | G | C | 1 | a0001c0001t0008g0027 | 2 | HG02258.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.110+6490G>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113704093 | |||||||
| chr10:113704138 | C | T | 3 | a0001c0001t0002g0240 a0001c0001t0004g0020 a0001c0001t0004g0241 |
4 | HG01884.hp1 HG02145.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.110+6535C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113704138 | |||||||
| chr10:113704260 | C | T | 2 | a0002c0002t0001g0326 a0002c0002t0001g0327 |
2 | HG00140.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.110+6657C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113704260 | |||||||
| chr10:113704274 | T | C | 25 | a0001c0001t0002g0021 a0001c0001t0002g0233 a0001c0001t0002g0235 others(22): Show |
27 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.110+6671T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113704274 | |||||||
| chr10:113704342 | C | T | 1 | a0002c0002t0001g0341 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.110+6739C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113704342 | |||||||
| chr10:113704373 | G | A | 90 | a0001c0001t0004g0010 a0001c0001t0004g0012 a0001c0001t0004g0033 others(87): Show |
98 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.110+6770G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113704373 | |||||||
| chr10:113704378 | C | T | 1 | a0001c0001t0005g0093 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.110+6775C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113704378 | |||||||
| chr10:113704412 | A | G | 180 | a0001c0001t0002g0016 a0001c0001t0002g0168 a0001c0001t0002g0174 others(177): Show |
197 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.110+6809A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113704412 | |||||||
| chr10:113704517 | A | G | 13 | a0001c0001t0002g0109 a0001c0001t0002g0112 a0001c0001t0002g0362 others(10): Show |
14 | HG01109.hp2 HG01891.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.110+6914A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113704517 | |||||||
| chr10:113704677 | A | G | 1 | a0001c0001t0004g0258 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.110+7074A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113704677 | |||||||
| chr10:113704710 | C | G | 2 | a0001c0001t0002g0317 a0001c0001t0002g0319 |
2 | HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.110+7107C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113704710 | |||||||
| chr10:113704716 | C | A | 1 | a0001c0001t0002g0246 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.110+7113C>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113704716 | |||||||
| chr10:113704782 | T | C | 2 | a0001c0001t0005g0114 a0001c0012t0002g0113 |
2 | HG01081.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.110+7179T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113704782 | |||||||
| chr10:113704931 | C | T | 107 | a0001c0001t0002g0287 a0001c0001t0002g0298 a0001c0001t0002g0312 others(104): Show |
117 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.110+7328C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113704931 | |||||||
| chr10:113704952 | G | GC | 217 | a0001c0001t0002g0016 a0001c0001t0002g0168 a0001c0001t0002g0174 others(214): Show |
237 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.110+7359dupC | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr10 | 113704952 | ||||||
| chr10:113704952 | G | GCC | 42 | a0001c0001t0003g0167 a0001c0001t0003g0171 a0001c0001t0003g0175 others(39): Show |
42 | HG00280.hp2 HG00423.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.110+7358_110+7359d others(4): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr10 | 113704952 | ||||||
| chr10:113705018 | T | C | 5 | a0001c0001t0004g0014 a0001c0001t0004g0154 a0001c0001t0004g0155 others(2): Show |
6 | HG01109.hp2 HG01891.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+7415T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113705018 | |||||||
| chr10:113705109 | C | T | 1 | a0002c0002t0001g0302 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.110+7506C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113705109 | |||||||
| chr10:113705115 | A | G | 1 | a0003c0003t0002g0135 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.110+7512A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113705115 | |||||||
| chr10:113705118 | C | T | 1 | a0001c0001t0003g0225 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.110+7515C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113705118 | |||||||
| chr10:113705225 | CT | C | 329 | a0001c0001t0002g0016 a0001c0001t0002g0021 a0001c0001t0002g0109 others(326): Show |
358 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(355): Show |
intron_variant | MODIFIER | c.110+7631delT | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr10 | 113705225 | ||||||
| chr10:113705378 | AC | A | 3 | a0001c0001t0002g0362 a0001c0001t0002g0363 a0001c0001t0002g0364 |
3 | HG02258.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.110+7776delC | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113705378 | |||||||
| chr10:113705459 | C | T | 1 | a0001c0005t0002g0254 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.110+7856C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113705459 | |||||||
| chr10:113705500 | G | T | 1 | a0001c0001t0003g0194 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.110+7897G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113705500 | |||||||
| chr10:113705727 | G | T | 1 | a0003c0003t0002g0124 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.110+8124G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113705727 | |||||||
| chr10:113705729 | G | C | 1 | a0001c0001t0004g0103 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.110+8126G>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113705729 | |||||||
| chr10:113705736 | CAG | C | 7 | a0001c0001t0003g0208 a0001c0001t0003g0210 a0001c0001t0003g0211 others(4): Show |
7 | HG01243.hp2 HG02818.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.110+8134_110+8135d others(4): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113705736 | |||||||
| chr10:113705805 | G | T | 5 | a0001c0001t0004g0014 a0001c0001t0004g0154 a0001c0001t0004g0155 others(2): Show |
6 | HG01109.hp2 HG01891.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+8202G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113705805 | |||||||
| chr10:113705808 | T | G | 2 | a0001c0001t0005g0037 a0001c0001t0005g0052 |
2 | HG02080.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.110+8205T>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113705808 | |||||||
| chr10:113705840 | G | A | 1 | a0003c0003t0002g0146 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.110+8237G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113705840 | |||||||
| chr10:113705926 | C | T | 2 | a0001c0001t0003g0188 a0001c0001t0003g0196 |
2 | HG02040.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.110+8323C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113705926 | |||||||
| chr10:113705971 | G | A | 4 | a0002c0002t0001g0338 a0002c0002t0001g0339 a0002c0002t0001g0340 others(1): Show |
4 | HG00639.hp2 HG01123.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.110+8368G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113705971 | |||||||
| chr10:113706080 | C | T | 1 | a0001c0001t0005g0191 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.110+8477C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113706080 | |||||||
| chr10:113706166 | G | T | 70 | a0001c0001t0002g0312 a0001c0001t0002g0314 a0001c0001t0002g0315 others(67): Show |
79 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.110+8563G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113706166 | |||||||
| chr10:113706408 | C | T | 2 | a0002c0002t0001g0285 a0002c0002t0001g0286 |
2 | HG01257.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.110+8805C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113706408 | |||||||
| chr10:113706409 | G | A | 1 | a0001c0001t0003g0331 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.110+8806G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113706409 | |||||||
| chr10:113706557 | G | A | 1 | a0002c0002t0001g0366 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.110+8954G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113706557 | |||||||
| chr10:113706696 | T | C | 1 | a0003c0003t0002g0125 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.110+9093T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113706696 | |||||||
| chr10:113706740 | T | G | 14 | a0001c0001t0002g0109 a0001c0001t0002g0112 a0001c0001t0002g0362 others(11): Show |
14 | HG01081.hp2 HG01109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.110+9137T>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113706740 | |||||||
| chr10:113706793 | G | A | 1 | a0001c0001t0004g0154 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.110+9190G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113706793 | |||||||
| chr10:113706889 | C | G | 25 | a0001c0001t0002g0021 a0001c0001t0002g0233 a0001c0001t0002g0235 others(22): Show |
27 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.110+9286C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113706889 | |||||||
| chr10:113707077 | T | G | 25 | a0001c0001t0002g0021 a0001c0001t0002g0233 a0001c0001t0002g0235 others(22): Show |
27 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.110+9474T>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113707077 | |||||||
| chr10:113707184 | C | T | 2 | a0001c0001t0004g0020 a0001c0001t0004g0241 |
3 | HG01884.hp1 HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.110+9581C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113707184 | |||||||
| chr10:113707309 | A | G | 134 | a0001c0001t0002g0021 a0001c0001t0002g0233 a0001c0001t0002g0235 others(131): Show |
146 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.110+9706A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113707309 | |||||||
| chr10:113707506 | C | G | 2 | a0002c0002t0001g0272 a0002c0002t0001g0277 |
2 | NA18978.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.110+9903C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113707506 | |||||||
| chr10:113707549 | C | G | 25 | a0001c0001t0002g0021 a0001c0001t0002g0233 a0001c0001t0002g0235 others(22): Show |
27 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.110+9946C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113707549 | |||||||
| chr10:113707652 | A | G | 1 | a0001c0001t0004g0299 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.110+10049A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113707652 | |||||||
| chr10:113707862 | G | C | 2 | a0001c0001t0005g0114 a0001c0012t0002g0113 |
2 | HG01081.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.110+10259G>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113707862 | |||||||
| chr10:113707898 | C | T | 38 | a0001c0001t0005g0001 a0001c0001t0005g0009 a0001c0001t0005g0011 others(35): Show |
43 | HG00639.hp1 HG00733.hp2 HG01099.hp1 others(40): Show |
intron_variant | MODIFIER | c.110+10295C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113707898 | |||||||
| chr10:113707987 | C | CAGATTAC others(6): Show |
3 | a0002c0002t0001g0293 a0002c0002t0001g0295 a0002c0002t0001g0350 |
3 | HG01891.hp2 HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.110+10386_110+1038 others(17): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr10 | 113707987 | ||||||
| chr10:113708081 | G | A | 1 | a0001c0001t0003g0151 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.110+10478G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113708081 | |||||||
| chr10:113708147 | C | T | 3 | a0001c0001t0004g0013 a0001c0001t0004g0108 a0003c0003t0002g0150 |
4 | HG02559.hp2 HG02717.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.110+10544C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113708147 | |||||||
| chr10:113708239 | A | G | 11 | a0001c0001t0004g0010 a0001c0001t0004g0033 a0001c0001t0004g0034 others(8): Show |
12 | HG00423.hp2 HG00621.hp2 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.110+10636A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113708239 | |||||||
| chr10:113708277 | G | T | 4 | a0001c0001t0004g0026 a0001c0001t0004g0257 a0001c0001t0004g0258 others(1): Show |
5 | HG02572.hp2 HG02886.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.110+10674G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113708277 | |||||||
| chr10:113708356 | T | C | 1 | a0001c0001t0005g0050 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.110+10753T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113708356 | |||||||
| chr10:113708535 | A | G | 1 | a0002c0002t0001g0344 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.110+10932A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113708535 | |||||||
| chr10:113708567 | C | T | 1 | a0003c0003t0002g0124 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.110+10964C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113708567 | |||||||
| chr10:113708928 | G | C | 51 | a0001c0001t0004g0010 a0001c0001t0004g0012 a0001c0001t0004g0033 others(48): Show |
53 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.110+11325G>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113708928 | |||||||
| chr10:113709009 | T | C | 90 | a0001c0001t0004g0010 a0001c0001t0004g0012 a0001c0001t0004g0033 others(87): Show |
98 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.110+11406T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113709009 | |||||||
| chr10:113709013 | CCT | C | 90 | a0001c0001t0004g0010 a0001c0001t0004g0012 a0001c0001t0004g0033 others(87): Show |
98 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.110+11411_110+1141 others(6): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113709013 | |||||||
| chr10:113709018 | C | T | 5 | a0001c0001t0004g0014 a0001c0001t0004g0154 a0001c0001t0004g0155 others(2): Show |
6 | HG01109.hp2 HG01891.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+11415C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113709018 | |||||||
| chr10:113709049 | C | T | 37 | a0001c0001t0005g0001 a0001c0001t0005g0009 a0001c0001t0005g0011 others(34): Show |
42 | HG00639.hp1 HG00733.hp2 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.110+11446C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113709049 | |||||||
| chr10:113709090 | C | G | 1 | a0001c0001t0004g0154 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.110+11487C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113709090 | |||||||
| chr10:113709184 | G | A | 1 | a0001c0001t0004g0095 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.110+11581G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113709184 | |||||||
| chr10:113709225 | C | T | 1 | a0002c0002t0001g0276 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.110+11622C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113709225 | |||||||
| chr10:113709603 | C | T | 1 | a0001c0001t0002g0240 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.111-11429C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113709603 | |||||||
| chr10:113709791 | G | A | 1 | a0002c0002t0001g0283 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.111-11241G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113709791 | |||||||
| chr10:113709866 | C | G | 204 | a0001c0001t0002g0016 a0001c0001t0002g0109 a0001c0001t0002g0112 others(201): Show |
223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.111-11166C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113709866 | |||||||
| chr10:113709951 | G | A | 125 | a0001c0001t0002g0021 a0001c0001t0002g0233 a0001c0001t0002g0235 others(122): Show |
136 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.111-11081G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113709951 | |||||||
| chr10:113710005 | A | G | 3 | a0001c0001t0003g0198 a0001c0001t0003g0200 a0001c0001t0003g0223 |
3 | HG02451.hp2 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.111-11027A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113710005 | |||||||
| chr10:113710131 | G | A | 61 | a0001c0001t0002g0016 a0001c0001t0002g0168 a0001c0001t0002g0174 others(58): Show |
67 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.111-10901G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113710131 | |||||||
| chr10:113710233 | C | T | 53 | a0001c0001t0003g0329 a0001c0001t0003g0331 a0001c0001t0004g0010 others(50): Show |
55 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.111-10799C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113710233 | |||||||
| chr10:113710309 | C | T | 1 | a0001c0005t0002g0254 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.111-10723C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113710309 | |||||||
| chr10:113710335 | T | C | 2 | a0001c0001t0005g0048 a0001c0001t0005g0055 |
2 | NA18988.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.111-10697T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113710335 | |||||||
| chr10:113710344 | T | G | 1 | a0001c0001t0003g0172 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.111-10688T>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113710344 | |||||||
| chr10:113710685 | G | A | 3 | a0001c0001t0005g0365 a0001c0001t0005g0367 a0002c0002t0001g0366 |
3 | HG01109.hp1 HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.111-10347G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113710685 | |||||||
| chr10:113710697 | C | G | 2 | a0002c0002t0001g0272 a0002c0002t0001g0277 |
2 | NA18978.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.111-10335C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113710697 | |||||||
| chr10:113710735 | A | T | 1 | a0001c0001t0003g0175 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.111-10297A>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113710735 | |||||||
| chr10:113710831 | A | G | 5 | a0001c0001t0004g0071 a0001c0001t0004g0088 a0001c0001t0004g0096 others(2): Show |
5 | HG00735.hp1 HG01070.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.111-10201A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113710831 | |||||||
| chr10:113711257 | T | G | 124 | a0001c0001t0002g0021 a0001c0001t0002g0233 a0001c0001t0002g0235 others(121): Show |
135 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.111-9775T>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113711257 | |||||||
| chr10:113711270 | T | C | 1 | a0001c0001t0002g0240 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.111-9762T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113711270 | |||||||
| chr10:113711310 | C | G | 1 | a0001c0001t0004g0299 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.111-9722C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113711310 | |||||||
| chr10:113711523 | G | A | 1 | a0003c0003t0019g0147 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.111-9509G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113711523 | |||||||
| chr10:113711802 | A | G | 329 | a0001c0001t0002g0016 a0001c0001t0002g0021 a0001c0001t0002g0109 others(326): Show |
359 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.111-9230A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113711802 | |||||||
| chr10:113712014 | A | G | 329 | a0001c0001t0002g0016 a0001c0001t0002g0021 a0001c0001t0002g0109 others(326): Show |
359 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.111-9018A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113712014 | |||||||
| chr10:113712039 | C | T | 3 | a0001c0001t0004g0020 a0001c0001t0004g0241 a0001c0005t0002g0254 |
4 | HG01884.hp1 HG02145.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.111-8993C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113712039 | |||||||
| chr10:113712161 | C | T | 1 | a0002c0002t0001g0338 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.111-8871C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113712161 | |||||||
| chr10:113712354 | G | C | 38 | a0001c0001t0005g0001 a0001c0001t0005g0009 a0001c0001t0005g0011 others(35): Show |
43 | HG00639.hp1 HG00733.hp2 HG01099.hp1 others(40): Show |
intron_variant | MODIFIER | c.111-8678G>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113712354 | |||||||
| chr10:113712523 | T | C | 5 | a0003c0003t0002g0003 a0003c0003t0002g0126 a0003c0003t0002g0127 others(2): Show |
7 | HG01069.hp1 HG01071.hp2 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.111-8509T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113712523 | |||||||
| chr10:113712562 | C | G | 2 | a0001c0001t0004g0013 a0001c0001t0004g0108 |
3 | HG02559.hp2 HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.111-8470C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113712562 | |||||||
| chr10:113712575 | C | G | 1 | a0002c0002t0001g0290 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.111-8457C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113712575 | |||||||
| chr10:113712683 | T | G | 1 | a0002c0002t0001g0296 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.111-8349T>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113712683 | |||||||
| chr10:113712691 | C | T | 2 | a0002c0002t0001g0281 a0002c0002t0001g0282 |
2 | NA18747.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.111-8341C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113712691 | |||||||
| chr10:113712698 | G | A | 1 | a0002c0002t0001g0339 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.111-8334G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113712698 | |||||||
| chr10:113712802 | G | A | 1 | a0001c0001t0003g0171 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.111-8230G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113712802 | |||||||
| chr10:113712833 | A | G | 1 | a0001c0011t0017g0369 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.111-8199A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113712833 | |||||||
| chr10:113712838 | G | A | 1 | a0001c0001t0003g0212 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.111-8194G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113712838 | |||||||
| chr10:113712960 | G | A | 270 | a0001c0001t0002g0016 a0001c0001t0002g0021 a0001c0001t0002g0109 others(267): Show |
293 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(290): Show |
intron_variant | MODIFIER | c.111-8072G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113712960 | |||||||
| chr10:113713029 | C | T | 1 | a0002c0002t0001g0309 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.111-8003C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113713029 | |||||||
| chr10:113713153 | C | G | 24 | a0001c0001t0002g0021 a0001c0001t0002g0233 a0001c0001t0002g0235 others(21): Show |
25 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.111-7879C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113713153 | |||||||
| chr10:113713216 | T | TA | 107 | a0001c0001t0002g0287 a0001c0001t0002g0298 a0001c0001t0002g0317 others(104): Show |
118 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.111-7807dupA | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr10 | 113713216 | ||||||
| chr10:113713497 | C | G | 86 | a0001c0001t0002g0016 a0001c0001t0002g0168 a0001c0001t0002g0174 others(83): Show |
94 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.111-7535C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113713497 | |||||||
| chr10:113713628 | C | CTGT | 36 | a0001c0001t0002g0312 a0001c0001t0002g0314 a0001c0001t0002g0315 others(33): Show |
38 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.111-7403_111-7402i others(5): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr10 | 113713628 | ||||||
| chr10:113713628 | CT | C | 331 | a0001c0001t0002g0016 a0001c0001t0002g0021 a0001c0001t0002g0109 others(328): Show |
361 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.111-7394delT | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr10 | 113713628 | ||||||
| chr10:113713637 | T | C | 1 | a0001c0001t0004g0258 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.111-7395T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113713637 | |||||||
| chr10:113713736 | G | C | 1 | a0001c0001t0004g0154 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.111-7296G>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113713736 | |||||||
| chr10:113713832 | A | C | 1 | a0001c0001t0005g0049 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.111-7200A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113713832 | |||||||
| chr10:113713933 | T | C | 1 | a0001c0001t0003g0187 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.111-7099T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113713933 | |||||||
| chr10:113714206 | C | T | 1 | a0002c0006t0001g0111 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.111-6826C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113714206 | |||||||
| chr10:113714277 | C | G | 36 | a0001c0001t0002g0312 a0001c0001t0002g0314 a0001c0001t0002g0315 others(33): Show |
38 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.111-6755C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113714277 | |||||||
| chr10:113714362 | G | A | 1 | a0001c0001t0002g0242 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.111-6670G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113714362 | |||||||
| chr10:113714475 | G | T | 5 | a0001c0001t0004g0014 a0001c0001t0004g0154 a0001c0001t0004g0155 others(2): Show |
6 | HG01109.hp2 HG01891.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.111-6557G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113714475 | |||||||
| chr10:113714590 | A | G | 87 | a0001c0001t0002g0016 a0001c0001t0002g0168 a0001c0001t0002g0174 others(84): Show |
96 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.111-6442A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113714590 | |||||||
| chr10:113714804 | T | TA | 16 | a0001c0001t0002g0109 a0001c0001t0002g0112 a0001c0001t0002g0226 others(13): Show |
17 | HG01081.hp2 HG01109.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.111-6228_111-6227i others(3): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113714804 | |||||||
| chr10:113714805 | T | A | 98 | a0001c0001t0002g0312 a0001c0001t0002g0314 a0001c0001t0002g0315 others(95): Show |
104 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.111-6227T>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113714805 | |||||||
| chr10:113714806 | T | A | 13 | a0001c0001t0002g0109 a0001c0001t0002g0112 a0001c0001t0002g0226 others(10): Show |
14 | HG01081.hp2 HG01109.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.111-6226T>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113714806 | |||||||
| chr10:113714807 | T | A | 96 | a0001c0001t0002g0312 a0001c0001t0002g0314 a0001c0001t0002g0315 others(93): Show |
101 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.111-6225T>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113714807 | |||||||
| chr10:113714808 | T | A | 6 | a0001c0001t0002g0240 a0001c0001t0004g0014 a0001c0001t0004g0154 others(3): Show |
7 | HG01109.hp2 HG01891.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.111-6224T>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113714808 | |||||||
| chr10:113714809 | T | A | 40 | a0001c0001t0002g0312 a0001c0001t0002g0314 a0001c0001t0002g0315 others(37): Show |
42 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.111-6223T>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113714809 | |||||||
| chr10:113714811 | T | A | 36 | a0001c0001t0002g0312 a0001c0001t0002g0314 a0001c0001t0002g0315 others(33): Show |
38 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.111-6221T>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113714811 | |||||||
| chr10:113715033 | G | A | 1 | a0001c0001t0004g0012 | 2 | NA18945.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.111-5999G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113715033 | |||||||
| chr10:113715362 | C | T | 5 | a0001c0001t0004g0014 a0001c0001t0004g0154 a0001c0001t0004g0155 others(2): Show |
6 | HG01109.hp2 HG01891.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.111-5670C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113715362 | |||||||
| chr10:113715363 | G | A | 3 | a0001c0001t0005g0030 a0001c0005t0002g0031 a0002c0002t0001g0271 |
3 | HG02559.hp1 HG02895.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.111-5669G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113715363 | |||||||
| chr10:113715455 | G | A | 36 | a0001c0001t0002g0312 a0001c0001t0002g0314 a0001c0001t0002g0315 others(33): Show |
38 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.111-5577G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113715455 | |||||||
| chr10:113715472 | A | C | 1 | a0003c0003t0002g0116 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.111-5560A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113715472 | |||||||
| chr10:113715588 | A | G | 367 | a0001c0001t0002g0016 a0001c0001t0002g0021 a0001c0001t0002g0109 others(364): Show |
399 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(396): Show |
intron_variant | MODIFIER | c.111-5444A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113715588 | |||||||
| chr10:113715639 | A | G | 2 | a0001c0001t0003g0166 a0001c0001t0003g0193 |
2 | NA18991.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.111-5393A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113715639 | |||||||
| chr10:113715682 | G | A | 70 | a0001c0001t0004g0356 a0001c0001t0005g0279 a0002c0002t0001g0006 others(67): Show |
79 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.111-5350G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113715682 | |||||||
| chr10:113715748 | G | A | 1 | a0001c0001t0002g0226 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.111-5284G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113715748 | |||||||
| chr10:113715864 | A | C | 56 | a0001c0001t0003g0018 a0001c0001t0003g0206 a0001c0001t0003g0230 others(53): Show |
59 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.111-5168A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113715864 | |||||||
| chr10:113715869 | T | C | 56 | a0001c0001t0003g0018 a0001c0001t0003g0206 a0001c0001t0003g0230 others(53): Show |
59 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.111-5163T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113715869 | |||||||
| chr10:113715870 | C | T | 56 | a0001c0001t0003g0018 a0001c0001t0003g0206 a0001c0001t0003g0230 others(53): Show |
59 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.111-5162C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113715870 | |||||||
| chr10:113716043 | C | T | 1 | a0003c0003t0002g0116 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.111-4989C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113716043 | |||||||
| chr10:113716045 | A | G | 35 | a0001c0001t0002g0312 a0001c0001t0002g0314 a0001c0001t0002g0315 others(32): Show |
37 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.111-4987A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113716045 | |||||||
| chr10:113716053 | G | A | 1 | a0002c0002t0001g0339 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.111-4979G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113716053 | |||||||
| chr10:113716069 | A | G | 2 | a0001c0001t0004g0013 a0001c0001t0004g0108 |
3 | HG02559.hp2 HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.111-4963A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113716069 | |||||||
| chr10:113716283 | C | T | 147 | a0001c0001t0002g0021 a0001c0001t0002g0109 a0001c0001t0002g0112 others(144): Show |
159 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.111-4749C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113716283 | |||||||
| chr10:113716348 | TTGTC | T | 147 | a0001c0001t0002g0021 a0001c0001t0002g0109 a0001c0001t0002g0112 others(144): Show |
159 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.111-4678_111-4675d others(6): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr10 | 113716348 | ||||||
| chr10:113716379 | C | T | 147 | a0001c0001t0002g0021 a0001c0001t0002g0109 a0001c0001t0002g0112 others(144): Show |
159 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.111-4653C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113716379 | |||||||
| chr10:113716510 | G | A | 1 | a0001c0001t0003g0197 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.111-4522G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113716510 | |||||||
| chr10:113716642 | G | A | 1 | a0001c0001t0004g0085 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.111-4390G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113716642 | |||||||
| chr10:113716769 | C | T | 1 | a0001c0001t0002g0243 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.111-4263C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113716769 | |||||||
| chr10:113716831 | A | G | 1 | a0002c0002t0001g0347 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.111-4201A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113716831 | |||||||
| chr10:113716849 | T | C | 1 | a0002c0002t0001g0038 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.111-4183T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113716849 | |||||||
| chr10:113716858 | T | C | 1 | a0002c0002t0001g0328 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.111-4174T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113716858 | |||||||
| chr10:113716860 | T | C | 37 | a0001c0001t0002g0312 a0001c0001t0002g0314 a0001c0001t0002g0315 others(34): Show |
40 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.111-4172T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113716860 | |||||||
| chr10:113716931 | C | T | 1 | a0002c0002t0001g0282 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.111-4101C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113716931 | |||||||
| chr10:113717101 | A | G | 11 | a0001c0001t0002g0109 a0001c0001t0002g0112 a0001c0001t0002g0226 others(8): Show |
12 | HG01109.hp2 HG01891.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.111-3931A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113717101 | |||||||
| chr10:113717404 | G | A | 142 | a0001c0001t0002g0021 a0001c0001t0002g0109 a0001c0001t0002g0112 others(139): Show |
153 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.111-3628G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113717404 | |||||||
| chr10:113717544 | A | AAAAT | 6 | a0001c0001t0004g0043 a0001c0001t0004g0072 a0001c0001t0004g0085 others(3): Show |
6 | HG00642.hp2 HG01358.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.111-3472_111-3469d others(6): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr10 | 113717544 | ||||||
| chr10:113717680 | T | A | 35 | a0001c0001t0002g0312 a0001c0001t0002g0314 a0001c0001t0002g0315 others(32): Show |
37 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.111-3352T>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113717680 | |||||||
| chr10:113717811 | T | C | 2 | a0002c0002t0001g0288 a0002c0002t0001g0305 |
2 | NA18947.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.111-3221T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113717811 | |||||||
| chr10:113717817 | A | C | 1 | a0001c0012t0002g0113 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.111-3215A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113717817 | |||||||
| chr10:113717860 | T | C | 2 | a0001c0001t0005g0030 a0001c0005t0002g0031 |
2 | HG02559.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.111-3172T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113717860 | |||||||
| chr10:113717947 | T | C | 1 | a0002c0002t0001g0327 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.111-3085T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113717947 | |||||||
| chr10:113718049 | A | C | 1 | a0001c0001t0005g0114 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.111-2983A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113718049 | |||||||
| chr10:113718095 | C | A | 2 | a0002c0002t0001g0296 a0004c0004t0001g0115 |
2 | HG02257.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.111-2937C>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113718095 | |||||||
| chr10:113718142 | C | A | 1 | a0004c0004t0001g0136 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.111-2890C>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113718142 | |||||||
| chr10:113718255 | A | G | 1 | a0001c0001t0005g0028 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.111-2777A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113718255 | |||||||
| chr10:113718367 | T | C | 37 | a0001c0001t0002g0312 a0001c0001t0002g0314 a0001c0001t0002g0315 others(34): Show |
40 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.111-2665T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113718367 | |||||||
| chr10:113718411 | C | G | 272 | a0001c0001t0002g0016 a0001c0001t0002g0021 a0001c0001t0002g0109 others(269): Show |
296 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(293): Show |
intron_variant | MODIFIER | c.111-2621C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113718411 | |||||||
| chr10:113718863 | C | T | 37 | a0001c0001t0002g0312 a0001c0001t0002g0314 a0001c0001t0002g0315 others(34): Show |
40 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.111-2169C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113718863 | |||||||
| chr10:113718864 | A | C | 37 | a0001c0001t0002g0312 a0001c0001t0002g0314 a0001c0001t0002g0315 others(34): Show |
40 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.111-2168A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113718864 | |||||||
| chr10:113718918 | A | G | 37 | a0001c0001t0002g0312 a0001c0001t0002g0314 a0001c0001t0002g0315 others(34): Show |
40 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.111-2114A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113718918 | |||||||
| chr10:113719069 | G | A | 1 | a0002c0002t0001g0164 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.111-1963G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113719069 | |||||||
| chr10:113719194 | G | A | 2 | a0001c0001t0004g0014 a0001c0001t0004g0155 |
3 | HG02486.hp2 HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.111-1838G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113719194 | |||||||
| chr10:113719221 | G | A | 35 | a0001c0001t0002g0312 a0001c0001t0002g0314 a0001c0001t0002g0315 others(32): Show |
37 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.111-1811G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113719221 | |||||||
| chr10:113719232 | G | A | 1 | a0003c0003t0002g0132 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.111-1800G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113719232 | |||||||
| chr10:113719402 | G | A | 1 | a0001c0001t0003g0205 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.111-1630G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113719402 | |||||||
| chr10:113719509 | C | T | 21 | a0001c0001t0002g0021 a0001c0001t0002g0233 a0001c0001t0002g0235 others(18): Show |
22 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.111-1523C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113719509 | |||||||
| chr10:113719607 | A | C | 1 | a0001c0001t0002g0240 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.111-1425A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113719607 | |||||||
| chr10:113720025 | C | A | 24 | a0001c0001t0002g0021 a0001c0001t0002g0233 a0001c0001t0002g0235 others(21): Show |
25 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.111-1007C>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113720025 | |||||||
| chr10:113720316 | C | G | 2 | a0002c0002t0001g0272 a0002c0002t0001g0277 |
2 | NA18978.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.111-716C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113720316 | |||||||
| chr10:113720323 | G | A | 2 | a0002c0002t0001g0326 a0002c0002t0001g0327 |
2 | HG00140.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.111-709G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113720323 | |||||||
| chr10:113720391 | A | G | 1 | a0004c0004t0001g0115 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.111-641A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113720391 | |||||||
| chr10:113720468 | G | C | 1 | a0003c0003t0002g0148 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.111-564G>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113720468 | |||||||
| chr10:113720501 | C | T | 1 | a0002c0002t0001g0347 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.111-531C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113720501 | |||||||
| chr10:113720764 | C | T | 1 | a0002c0002t0001g0289 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.111-268C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113720764 | |||||||
| chr10:113720823 | T | C | 272 | a0001c0001t0002g0016 a0001c0001t0002g0021 a0001c0001t0002g0109 others(269): Show |
296 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(293): Show |
intron_variant | MODIFIER | c.111-209T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113720823 | |||||||
| chr10:113720998 | C | T | 5 | a0001c0001t0002g0109 a0001c0001t0002g0112 a0001c0001t0002g0226 others(2): Show |
5 | HG02630.hp2 HG02647.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.111-34C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113720998 | |||||||
| chr10:113721005 | T | C | 1 | a0003c0003t0002g0131 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.111-27T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 2/6 | chr10 | 113721005 | |||||||
| chr10:113721171 | G | A | 1 | a0001c0001t0005g0040 | 1 | NA18998.hp2 | splice_region_variant&intron_variant | LOW | c.247+3G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 3/6 | chr10 | 113721171 | |||||||
| chr10:113721177 | G | A | 5 | a0001c0001t0002g0109 a0001c0001t0002g0112 a0001c0001t0002g0226 others(2): Show |
5 | HG02630.hp2 HG02647.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.247+9G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 3/6 | chr10 | 113721177 | |||||||
| chr10:113721259 | C | T | 107 | a0001c0001t0002g0287 a0001c0001t0002g0298 a0001c0001t0002g0317 others(104): Show |
117 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.247+91C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 3/6 | chr10 | 113721259 | |||||||
| chr10:113721308 | A | T | 2 | a0002c0002t0001g0280 a0002c0002t0001g0337 |
2 | NA18956.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.247+140A>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 3/6 | chr10 | 113721308 | |||||||
| chr10:113721537 | G | T | 1 | a0001c0001t0006g0099 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.248-114G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 3/6 | chr10 | 113721537 | |||||||
| chr10:113721547 | G | A | 11 | a0002c0002t0001g0249 a0002c0002t0001g0255 a0002c0002t0001g0264 others(8): Show |
11 | HG00423.hp1 HG01257.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.248-104G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 3/6 | chr10 | 113721547 | |||||||
| chr10:113721551 | C | T | 1 | a0001c0001t0004g0026 | 2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.248-100C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 3/6 | chr10 | 113721551 | |||||||
| chr10:113721586 | G | A | 1 | a0004c0004t0001g0136 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.248-65G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 3/6 | chr10 | 113721586 | |||||||
| chr10:113721599 | A | G | 1 | a0001c0001t0003g0190 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.248-52A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 3/6 | chr10 | 113721599 | |||||||
| chr10:113721907 | AT | A | 38 | a0001c0001t0003g0221 a0001c0001t0004g0010 a0001c0001t0004g0012 others(35): Show |
40 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.376+143delT | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr10 | 113721907 | ||||||
| chr10:113722028 | A | C | 37 | a0001c0001t0002g0312 a0001c0001t0002g0314 a0001c0001t0002g0315 others(34): Show |
40 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.376+249A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113722028 | |||||||
| chr10:113722069 | G | A | 1 | a0001c0001t0004g0214 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.376+290G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113722069 | |||||||
| chr10:113722099 | C | T | 1 | a0002c0002t0001g0286 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.376+320C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113722099 | |||||||
| chr10:113722138 | G | T | 1 | a0001c0005t0002g0254 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.376+359G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113722138 | |||||||
| chr10:113722150 | A | G | 1 | a0001c0001t0004g0101 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.376+371A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113722150 | |||||||
| chr10:113722229 | G | T | 1 | a0002c0006t0001g0110 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.376+450G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113722229 | |||||||
| chr10:113722233 | A | G | 35 | a0001c0001t0002g0312 a0001c0001t0002g0314 a0001c0001t0002g0315 others(32): Show |
37 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.376+454A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113722233 | |||||||
| chr10:113722558 | C | T | 1 | a0002c0002t0001g0359 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.376+779C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113722558 | |||||||
| chr10:113722847 | G | A | 1 | a0001c0001t0004g0241 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.376+1068G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113722847 | |||||||
| chr10:113722878 | A | T | 1 | a0001c0001t0002g0315 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.376+1099A>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113722878 | |||||||
| chr10:113722897 | AAAAAT | A | 8 | a0001c0001t0005g0028 a0001c0001t0005g0057 a0001c0001t0005g0058 others(5): Show |
8 | HG02647.hp2 HG03540.hp2 NA18956.hp1 others(5): Show |
intron_variant | MODIFIER | c.376+1128_376+1132d others(7): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr10 | 113722897 | ||||||
| chr10:113722970 | C | T | 2 | a0001c0001t0004g0014 a0001c0001t0004g0155 |
3 | HG02486.hp2 HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.376+1191C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113722970 | |||||||
| chr10:113723145 | C | G | 1 | a0001c0001t0004g0097 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.376+1366C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113723145 | |||||||
| chr10:113723173 | A | C | 1 | a0001c0001t0006g0079 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.376+1394A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113723173 | |||||||
| chr10:113723174 | C | A | 1 | a0001c0001t0006g0079 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.376+1395C>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113723174 | |||||||
| chr10:113723202 | CT | C | 263 | a0001c0001t0002g0016 a0001c0001t0002g0021 a0001c0001t0002g0109 others(260): Show |
285 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(282): Show |
intron_variant | MODIFIER | c.376+1436delT | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr10 | 113723202 | ||||||
| chr10:113723214 | T | A | 1 | a0003c0003t0002g0141 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.376+1435T>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113723214 | |||||||
| chr10:113723215 | T | A | 37 | a0001c0001t0002g0312 a0001c0001t0002g0314 a0001c0001t0002g0315 others(34): Show |
40 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.376+1436T>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113723215 | |||||||
| chr10:113723224 | G | A | 1 | a0001c0001t0005g0041 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.376+1445G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113723224 | |||||||
| chr10:113723363 | G | A | 1 | a0001c0001t0006g0078 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.376+1584G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113723363 | |||||||
| chr10:113723367 | C | A | 1 | a0001c0001t0005g0041 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.376+1588C>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113723367 | |||||||
| chr10:113723504 | G | C | 2 | a0001c0001t0004g0020 a0001c0001t0004g0241 |
3 | HG01884.hp1 HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.376+1725G>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113723504 | |||||||
| chr10:113723676 | A | C | 1 | a0001c0001t0002g0226 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.377-1686A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113723676 | |||||||
| chr10:113723689 | G | T | 1 | a0001c0001t0002g0243 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.377-1673G>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113723689 | |||||||
| chr10:113723725 | A | ATTTT | 53 | a0001c0001t0003g0018 a0001c0001t0003g0206 a0001c0001t0003g0230 others(50): Show |
54 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.377-1622_377-1619d others(6): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr10 | 113723725 | ||||||
| chr10:113723725 | AT | A | 6 | a0001c0001t0003g0017 a0001c0001t0004g0356 a0001c0001t0005g0001 others(3): Show |
6 | HG01069.hp1 HG01256.hp2 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.377-1619delT | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr10 | 113723725 | ||||||
| chr10:113723853 | C | T | 37 | a0001c0001t0002g0312 a0001c0001t0002g0314 a0001c0001t0002g0315 others(34): Show |
40 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.377-1509C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113723853 | |||||||
| chr10:113723854 | G | A | 1 | a0001c0001t0003g0172 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.377-1508G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113723854 | |||||||
| chr10:113724247 | C | T | 24 | a0001c0001t0002g0021 a0001c0001t0002g0233 a0001c0001t0002g0235 others(21): Show |
25 | HG00408.hp1 HG00544.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.377-1115C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113724247 | |||||||
| chr10:113724271 | A | G | 5 | a0002c0002t0001g0249 a0002c0002t0001g0255 a0002c0002t0001g0264 others(2): Show |
5 | HG00423.hp1 NA19003.hp2 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.377-1091A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113724271 | |||||||
| chr10:113724370 | C | T | 5 | a0001c0001t0002g0237 a0001c0001t0002g0238 a0001c0001t0002g0239 others(2): Show |
5 | HG01081.hp1 HG01168.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.377-992C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113724370 | |||||||
| chr10:113724424 | T | C | 180 | a0001c0001t0002g0021 a0001c0001t0002g0109 a0001c0001t0002g0112 others(177): Show |
194 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.377-938T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113724424 | |||||||
| chr10:113724441 | T | G | 143 | a0001c0001t0002g0021 a0001c0001t0002g0109 a0001c0001t0002g0112 others(140): Show |
154 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.377-921T>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113724441 | |||||||
| chr10:113724477 | T | C | 1 | a0001c0001t0003g0292 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.377-885T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113724477 | |||||||
| chr10:113724667 | TTTTG | T | 6 | a0001c0001t0004g0012 a0001c0001t0004g0068 a0001c0001t0004g0075 others(3): Show |
7 | HG02083.hp2 NA18943.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.377-691_377-688del others(4): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr10 | 113724667 | ||||||
| chr10:113724690 | C | T | 42 | a0001c0001t0002g0312 a0001c0001t0002g0314 a0001c0001t0002g0315 others(39): Show |
45 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.377-672C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113724690 | |||||||
| chr10:113724785 | C | CT | 2 | a0001c0001t0004g0013 a0001c0001t0004g0108 |
3 | HG02559.hp2 HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.377-574dupT | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr10 | 113724785 | ||||||
| chr10:113724900 | A | G | 43 | a0001c0001t0002g0109 a0001c0001t0002g0312 a0001c0001t0002g0314 others(40): Show |
45 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.377-462A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113724900 | |||||||
| chr10:113724901 | G | A | 188 | a0001c0001t0002g0016 a0001c0001t0002g0021 a0001c0001t0002g0109 others(185): Show |
202 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.377-461G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113724901 | |||||||
| chr10:113725017 | G | A | 4 | a0001c0001t0004g0014 a0001c0001t0004g0020 a0001c0001t0004g0155 others(1): Show |
6 | HG01884.hp1 HG02145.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.377-345G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113725017 | |||||||
| chr10:113725059 | C | T | 1 | a0001c0001t0005g0191 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.377-303C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113725059 | |||||||
| chr10:113725254 | C | T | 1 | a0003c0003t0002g0140 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.377-108C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 4/6 | chr10 | 113725254 | |||||||
| chr10:113725541 | ATCTCTTT others(11): Show |
A | 1 | a0006c0009t0003g0201 | 1 | HG03139.hp1 | splice_region_variant&intron_variant | LOW | c.552+5_552+22delTCT others(15): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 5/6 | chr10 | 113725541 | |||||||
| chr10:113725582 | G | GCAGAGTG others(79): Show |
3 | a0001c0001t0002g0362 a0001c0001t0002g0363 a0001c0001t0002g0364 |
3 | HG02258.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.552+121_552+206dup others(86): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr10 | 113725582 | ||||||
| chr10:113725641 | T | C | 44 | a0001c0001t0002g0109 a0001c0001t0002g0312 a0001c0001t0002g0314 others(41): Show |
46 | HG00558.hp1 HG00642.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.552+104T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 5/6 | chr10 | 113725641 | |||||||
| chr10:113725651 | T | C | 3 | a0001c0001t0004g0026 a0001c0001t0004g0257 a0001c0001t0004g0258 |
4 | HG02886.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.552+114T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 5/6 | chr10 | 113725651 | |||||||
| chr10:113725687 | A | G | 2 | a0001c0001t0004g0033 a0001c0001t0004g0034 |
2 | HG00423.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.552+150A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 5/6 | chr10 | 113725687 | |||||||
| chr10:113725695 | T | C | 6 | a0002c0002t0001g0183 a0002c0002t0001g0271 a0002c0002t0001g0275 others(3): Show |
6 | HG02027.hp1 NA18946.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.552+158T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 5/6 | chr10 | 113725695 | |||||||
| chr10:113725728 | A | G | 4 | a0001c0001t0003g0208 a0001c0001t0003g0210 a0001c0001t0003g0232 others(1): Show |
4 | HG01884.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.552+191A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 5/6 | chr10 | 113725728 | |||||||
| chr10:113725857 | G | A | 1 | a0001c0001t0002g0242 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.552+320G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 5/6 | chr10 | 113725857 | |||||||
| chr10:113725961 | A | G | 4 | a0001c0001t0004g0014 a0001c0001t0004g0154 a0001c0001t0004g0155 others(1): Show |
5 | HG01109.hp2 HG01891.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.553-344A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 5/6 | chr10 | 113725961 | |||||||
| chr10:113725966 | T | C | 2 | a0001c0001t0005g0049 a0001c0001t0005g0056 |
2 | HG02071.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.553-339T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 5/6 | chr10 | 113725966 | |||||||
| chr10:113726064 | G | A | 5 | a0001c0001t0003g0005 a0001c0001t0007g0005 a0001c0001t0007g0019 others(2): Show |
7 | NA18969.hp1 NA18971.hp2 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.553-241G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 5/6 | chr10 | 113726064 | |||||||
| chr10:113726131 | T | C | 2 | a0001c0001t0004g0020 a0001c0001t0004g0241 |
3 | HG01884.hp1 HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.553-174T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 5/6 | chr10 | 113726131 | |||||||
| chr10:113726269 | C | G | 1 | a0001c0001t0004g0070 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.553-36C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 5/6 | chr10 | 113726269 | |||||||
| chr10:113726475 | C | T | 1 | a0001c0001t0003g0151 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.682+41C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113726475 | |||||||
| chr10:113726837 | A | C | 2 | a0001c0001t0004g0020 a0001c0001t0004g0241 |
3 | HG01884.hp1 HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.682+403A>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113726837 | |||||||
| chr10:113726851 | G | A | 324 | a0001c0001t0002g0016 a0001c0001t0002g0021 a0001c0001t0002g0109 others(321): Show |
350 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.682+417G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113726851 | |||||||
| chr10:113727115 | G | A | 46 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0015 others(43): Show |
52 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.682+681G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113727115 | |||||||
| chr10:113727194 | G | A | 1 | a0001c0001t0005g0052 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.682+760G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113727194 | |||||||
| chr10:113727293 | C | T | 1 | a0001c0001t0004g0102 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.682+859C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113727293 | |||||||
| chr10:113727294 | G | A | 1 | a0003c0003t0019g0147 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.682+860G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113727294 | |||||||
| chr10:113727318 | CTATT | C | 188 | a0001c0001t0002g0016 a0001c0001t0002g0021 a0001c0001t0002g0109 others(185): Show |
201 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.682+887_682+890del others(4): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr10 | 113727318 | ||||||
| chr10:113727712 | C | T | 1 | a0001c0001t0004g0039 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.682+1278C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113727712 | |||||||
| chr10:113727723 | A | G | 326 | a0001c0001t0002g0016 a0001c0001t0002g0021 a0001c0001t0002g0109 others(323): Show |
353 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.682+1289A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113727723 | |||||||
| chr10:113727734 | C | G | 134 | a0001c0001t0002g0016 a0001c0001t0002g0021 a0001c0001t0002g0168 others(131): Show |
145 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.682+1300C>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113727734 | |||||||
| chr10:113727818 | A | T | 1 | a0001c0001t0008g0027 | 2 | HG02258.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.682+1384A>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113727818 | |||||||
| chr10:113727828 | C | CA | 65 | a0001c0001t0002g0112 a0001c0001t0002g0226 a0001c0001t0002g0250 others(62): Show |
71 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.682+1409dupA | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr10 | 113727828 | ||||||
| chr10:113727828 | C | CAA | 6 | a0001c0001t0003g0198 a0001c0001t0003g0199 a0001c0001t0003g0200 others(3): Show |
6 | HG02451.hp2 HG02896.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.682+1408_682+1409d others(4): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr10 | 113727828 | ||||||
| chr10:113727991 | C | CA | 168 | a0001c0001t0002g0016 a0001c0001t0002g0021 a0001c0001t0002g0112 others(165): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.683-1299dupA | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr10 | 113727991 | ||||||
| chr10:113727991 | C | CAA | 54 | a0001c0001t0002g0109 a0001c0001t0002g0174 a0001c0001t0002g0215 others(51): Show |
56 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.683-1300_683-1299d others(4): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr10 | 113727991 | ||||||
| chr10:113727991 | CAA | C | 70 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0015 others(67): Show |
77 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.683-1300_683-1299d others(4): Show |
CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr10 | 113727991 | ||||||
| chr10:113728456 | A | T | 1 | a0001c0001t0003g0171 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.683-855A>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113728456 | |||||||
| chr10:113728478 | C | T | 1 | a0001c0012t0002g0113 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.683-833C>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113728478 | |||||||
| chr10:113728572 | G | A | 105 | a0002c0002t0001g0006 a0002c0002t0001g0007 a0002c0002t0001g0008 others(102): Show |
115 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.683-739G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113728572 | |||||||
| chr10:113728613 | G | C | 1 | a0001c0001t0007g0217 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.683-698G>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113728613 | |||||||
| chr10:113728691 | G | A | 1 | a0003c0003t0002g0124 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.683-620G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113728691 | |||||||
| chr10:113728815 | A | G | 3 | a0002c0002t0001g0269 a0002c0002t0001g0335 a0002c0002t0012g0342 |
3 | HG01928.hp2 HG01943.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.683-496A>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113728815 | |||||||
| chr10:113729056 | G | A | 4 | a0001c0001t0005g0114 a0001c0001t0005g0256 a0001c0001t0005g0365 others(1): Show |
4 | HG01081.hp2 HG02572.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.683-255G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113729056 | |||||||
| chr10:113729060 | T | G | 2 | a0001c0005t0002g0031 a0001c0005t0002g0254 |
2 | HG02559.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.683-251T>G | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113729060 | |||||||
| chr10:113729172 | A | T | 1 | a0001c0012t0002g0113 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.683-139A>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113729172 | |||||||
| chr10:113729219 | G | A | 1 | a0001c0001t0005g0030 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.683-92G>A | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113729219 | |||||||
| chr10:113729259 | A | T | 1 | a0001c0001t0003g0179 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.683-52A>T | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113729259 | |||||||
| chr10:113729298 | T | C | 1 | a0001c0001t0004g0026 | 2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.683-13T>C | CASP7 | ENSG00000165806.21 | transcript | ENST00000369318.8 | protein_coding | 6/6 | chr10 | 113729298 |